Saturday, May 25, 2013

EMBASE Cardiac Update AutoAlert: EPICORE Cardiac Surgery Blogger2

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<1>
Accession Number
2013283385
Authors
Ozaydin M. Erdogan D. Yucel H. Peker O. Icli A. Akcay S. Etli M. Ceyhan
B.M. Sutcu R. Varol E. Dogan A. Yavuz T.
Institution
(Ozaydin, Erdogan, Yucel, Icli, Akcay, Varol, Dogan) Department of
Cardiology, Suleyman Demirel University, Isparta, Turkey
(Peker, Etli, Yavuz) Department of Cardiovascular Surgery, Suleyman
Demirel University, Isparta, Turkey
(Ceyhan, Sutcu) Department of Biochemistry, Suleyman Demirel University,
Isparta, Turkey
Title
N-acetyl cysteine for the conversion of atrial fibrillation into sinus
rhythm after cardiac surgery: A prospective, randomized, double-blind,
placebo-controlled pilot study.
Source
International Journal of Cardiology. 165 (3) (pp 580-583), 2013. Date of
Publication: 2013.
Publisher
Elsevier Ireland Ltd (P.O. Box 85, Limerick, Ireland)

<2>
Accession Number
2013298983
Authors
Sadaka M. Loutfy M. Sobhy M.
Institution
(Sadaka, Loutfy, Sobhy) Cardiovascular Department, Faculty of Medicine,
Alexandria University, Egypt
Title
Partial revascularization plus medical treatment versus medical treatment
alone in patients with multivessel coronary artery disease not eligible
for CABG.
Source
Egyptian Heart Journal. 65 (2) (pp 57-64), 2013. Date of Publication: June
2013.
Publisher
Egyptian Society of Cardiology (Egypt)
Abstract
Aim: The purpose of this study was to compare the impact of incomplete
revascularization (IR) plus optimal medical therapy (OMT) to OMT alone on
1. year clinical outcomes in patients with multivessel coronary artery
disease (MVD) who were not eligible for coronary bypass graft surgery
(CABG). Methods: This is a prospective randomized study conducted on 50
selected patients with chronic stable angina with documented MVD and CABG
was refused by the surgeon due to poor distal vessel quality. Patients
were randomized 1:1 into two groups, group (I): 25 patients were subjected
to OMT alone and group (II): 25 patients were subjected to IR plus OMT.
All patients were subjected to 1. year follow up. Results: The baseline
patients' details were matched. At 1. year; death occurred slightly more
in group II (16% versus 12%; p=. 1.000), ACS occurred more in the group I
(32% versus 16%; p=. 0.321) while freedom from angina occurred more in
group II (20% versus 4%; p=. 0.189). The OMT alone did not affect neither
the level of angina class nor EI while the IR plus OMT markedly improved
the decline in the level of angina class (p=. 0.011), but it did not
improve EF significantly (p=. 0.326). Conclusion: In patients with MVD who
were not eligible for CABG; IR plus OMT was not superior to OMT alone in
improving the 1year clinical outcomes except the improvement in the level
of angina class, which could be the adopted strategy to improve the
quality of life in such patients 2012 .

<3>
Accession Number
2013291280
Authors
Haghjooy Javanmard S. Ziaei A. Ziaei S. Ziaei E. Mirmohammad-Sadeghi M.
Institution
(Haghjooy Javanmard, Ziaei) Department of Physiology, Physiology Research
Centre, Isfahan University of Medical Sciences, Hezar Jerib Avenue,
Isfahan 73461-8174, Iran, Islamic Republic of
(Ziaei) Medical Research Center, Medical School, Isfahan University of
Medical Sciences, Isfahan 73461-8174, Iran, Islamic Republic of
(Ziaei) Shahid Beheshti University of Medical Sciences, Tehran, Iran,
Islamic Republic of
(Ziaei) Medical Research Center, Medical School, Shahrekord University of
Medical Sciences, Shahrekord, Iran, Islamic Republic of
(Mirmohammad-Sadeghi) Department of Cardiac Surgery, Isfahan Medical
School, Isfahan University of Medical Sciences, Isfahan 73461-8174, Iran,
Islamic Republic of
Title
The effect of preoperative melatonin on nuclear erythroid 2-related factor
2 activation in patients undergoing coronary artery bypass grafting
surgery.
Source
Oxidative Medicine and Cellular Longevity. , 2013. Article Number:
676829. Date of Publication: 2013.
Publisher
Hindawi Publishing Corporation (410 Park Avenue, 15th Floor, 287 pmb, New
York NY 10022, United States)
Abstract
During and after coronary artery bypass grafting (CABG), oxidative stress
occurs. Finding an effective way to improveantioxidant response is
important in CABG surgery. It has been shown that patients with coronary
heart disease have a low Melatonin production rate. The present study
aimed to investigate the effects ofMelatoninon nuclear erythroid 2-related
factor 2(Nrf2) activity in patients undergoing CABG surgery. Thirty
volunteers undergoing CABG were randomized to receive 10 mg oral Melatonin
(Melatonin group, n=15) or placebo (placebo group, n=15) before sleeping
for 1 month before surgery. The activatedNrf2 was measured twice by
DNA-based ELISA method in the nuclear extract of peripheral blood
mononuclear cells of patients before aortic clumps and 45 minutes after
CABG operation. Melatonin administration was associated with a
significantincrease in both plasma levels of Melatonin and Nrf2
concentration in Melatonin group compared to placebo group, respectively
(15.2+/-4.6 pmol/L, 0.28+/-0.01 versus 1.1+/-0.59 pmol/L, 0.20+/-0.07,
P<0.05). The findings of the present study provide preliminary data
suggesting that Melatoninmay play a significant role in the potentiation
of the antioxidant defense and attenuate cellular damages resulting from
CABG surgery via theNrf2 pathway. 2013 Shaghayegh Haghjooy Javanmard et
al.

<4>
Accession Number
2013289153
Authors
Imantalab V. Seddighinejad A. Mir Mansouri A. Sadeghi Meibodi A. Dadkhah
H. Farzam S. Forghan-Parast K.
Institution
(Imantalab, Seddighinejad, Mir Mansouri) Guilan University of Medical
Sciences, Department of Cardiac Anesthesia, Rasht University of Medical
Sciences, Heshmat Hospital, Iran, Islamic Republic of
(Sadeghi Meibodi, Dadkhah, Farzam, Forghan-Parast) Guilan University of
Medical Sciences, Iran, Islamic Republic of
Title
Effect of calcium gluconate on mean arterial pressure (MAP) after
induction of anesthesia with propofol in patients undergoing coronary
artery bypass graft surgery.
Source
Iranian Heart Journal. 13 (4) (pp 49-56), 2013. Date of Publication: 2013.
Publisher
Iranian Heart Association (P.O. Box 15745-1341, Tehran, Iran, Islamic
Republic of)
Abstract
Introduction: A combination of Propofol and Fentanyl is used as a method
to induce general anesthesia. Although Propofol is widely used for the
induction and maintenance of anesthesia, it has a significant effect on
reducing the arterial blood pressure.It has been suggested that calcium
gluconate, when administered simultaneously with Propofol, may reduce the
inotrope negative effect of Propofolon the heart function. Objective: We
sought to determine the efficacy of calcium gluconate in decreasing the
negative effect of Propofol. Materials and Methods: This randomized,
controlled, double-blind clinical trial, divided 70 patients undergoing
elective coronary artery bypass graft surgery (CABG) into two groups:
Group A (calcium gluconate) and Group B (placebo group).Each patient was
injected with Fentanyl (4 mug/kg) andPancuronium (0.1 mg/kg),followed by
Propofol(1.5mg/kg) during 60 secondsviaa CVline. Calcium gluconate (30
mg/kg) was administered to Group A and saline (placebo) was given to Group
B as well. Homodynamic data were obtained at baseline (T0), 4 minutes
after anesthesia induction (T1), and 2 minutes after tracheal intubation
(T2).The data were analyzed using descriptive statistics and repeated
measurement as well as t tests. A p value <0.05 was considered
statistically significant. Results: The mean and standard deviation (SD)
of the mean arterial pressure(MAP) at T0 was 101.11+/- 13.63 for Group A
and 107.142+/-14.59 for Group B (non-significant). These data for T1 (4
minutes after anesthesia induction) and T2 (2 minutes after tracheal
intubation) were 70.14+/-14.67 and 80.22+/- 23.29 for Group A and
72.05+/-15.45 and 82.42+/-14.86 for Group B, respectively
(non-significant). Conclusion: The findings of this research indicated no
differences between the two groups. Moreover, calcium gluconate appeared
to have no efficacy in reducing the negative effect of Propofol. (Iranian
Heart Journal 2013; 13(4):49-56).

<5>
Accession Number
2013261151
Authors
Dearden A.S. Sammon P.M. Matthew E.F.
Institution
(Dearden, Sammon, Matthew) Department of Cardiothoracic surgery, Royal
Infirmary of Edinburgh, Edinburgh EH16 4SA, United Kingdom
Title
In patients undergoing video-assisted thoracic surgery for pleurodesis in
primary spontaneous pneumothorax, how long should chest drains remain in
place prior to safe removal and subsequent discharge from hospital?.
Source
Interactive Cardiovascular and Thoracic Surgery. 16 (5) (pp 686-691),
2013. Date of Publication: May 2013.
Publisher
Oxford University Press (Great Clarendon Street, Oxford OX2 6DP, United
Kingdom)
Abstract
A best evidence topic in thoracic surgery was written according to a
structured protocol. The question addressed was how long chest drains
should be left in place following video-assisted thoracic surgery (VATS)
pleurodesis for primary spontaneous pneumothorax. Altogether, a total of
730 papers were found using the reported search, of which eight
represented the best evidence to answer the clinical question. The
authors, journal, date and country of publication, patient group studied,
study type, relevant outcomes and results of these papers are tabulated.
We report that the main determining factor for the length of hospital stay
following VATS pleurodesis is chest-drain duration. Providing no
postoperative complications occur, and chest X-ray appearances of lung
inflation are satisfactory, there is no documented contraindication to
removing chest drains as early as 2 days postoperatively, with discharge
the following day. Furthermore, leaving chest drains on water seal after a
brief period of suction has been shown to benefit in reducing
postoperative chest-drain duration and subsequent hospital stay. There is
a paucity of literature directly addressing early vs late chest-drain
removal protocols in this patient group. Hence, we conclude that, in
clinical practice, the decision of when to remove chest drains
postoperatively should remain guided empirically towards the individual
patient. 2013 The Author 2013.

<6>
Accession Number
2013261146
Authors
Wang W. Buehler D. Wang X. Yuan X.
Institution
(Wang, Buehler) Department of Cardiac Surgery, Scripps Memorial Hospital,
9850 Genesee Ave. Suite 560, San Diego, CA 92037, United States
(Wang, Wang, Yuan) Department of Cardiac Surgery, Shanxi Cardiovascular
Hospital, Taiyuan, Shanxi, China
Title
Effectiveness of biatrial pacing in reducing early postoperative atrial
fibrillation after the maze procedure.
Source
Interactive Cardiovascular and Thoracic Surgery. 16 (5) (pp 589-594),
2013. Date of Publication: May 2013.
Publisher
Oxford University Press (Great Clarendon Street, Oxford OX2 6DP, United
Kingdom)
Abstract
OBJECTIVESInteratrial conduction abnormalities have an important role in
the initiation of recurrent atrial fibrillation (AF) after the maze
procedure. Biatrial pacing or single atrial pacing alters the site and
timing of atrial depolarization and may improve restoration of sinus
rhythm after the maze procedure. To further evaluate whether biatrial
pacing is superior to single atrial or no pacing, we performed a
randomized prospective study on 240 patients with a full maze procedure to
compare the effectiveness with different pacing approaches in the
postoperative period.METHODSBetween 2002 and 2010, 240 patients undergoing
mitral +/- tricuspid valve surgery concomitant with the maze procedure
were randomized into three equal groups: Group I using overdrive biatrial
pacing, Group II utilizing single atrial pacing and Group III without
pacing. The atria were paced continuously in Atrium paced, Atrium sensed,
and pacemaker Inhibited in response to sensed beat (AAI) mode at a rate of
80 pulses per minute or 10 pulses above the underlying rate for 5 days.
The endpoints were the onset of AF or discharge.RESULTSThe incidence of
recurrent postoperative atrial fibrillation was significantly less in
Group I with 9 of 80 patients (11%) incurring atrial fibrillation compared
with 23 of 80 patients (28%) in Group II (P < 0.01) and 29 of 80 patients
in Group III (P < 0.01). The length of hospital stay and the mean costs of
hospital stay were significantly lower in the biatrial pacing group (P <
0.05). CONCLUSIONSBiatrial overdrive pacing is well tolerated and more
effective in preventing the early recurrence of atrial fibrillation after
the maze procedure. The impacts of the long-term results with the maze
procedure require further study. 2013 The Author 2013.

<7>
Accession Number
2013261144
Authors
Lenkin A.I. Zaharov V.I. Lenkin P.I. Smetkin A.A. Bjertnaes L.J. Kirov
M.Y.
Institution
(Lenkin) Department of Anesthesiology and Intensive Care Medicine, City
Hospital 1 of Arkhangelsk, Arkhangelsk, Russian Federation
(Zaharov, Lenkin, Smetkin, Kirov) Department of Anesthesiology and
Intensive Care Medicine, Northern State Medical University, Troitsky
Avenue 51, Arkhangelsk 163000, Russian Federation
(Bjertnaes) Department of Clinical Medicine (Anesthesiology), Faculty of
Medicine, University of Tromsoe, Tromsoe, Norway
Title
Normothermic cardiopulmonary bypass increases cerebral tissue oxygenation
during combined valve surgery: A single-centre, randomized trial.
Source
Interactive Cardiovascular and Thoracic Surgery. 16 (5) (pp 595-601),
2013. Date of Publication: May 2013.
Publisher
Oxford University Press (Great Clarendon Street, Oxford OX2 6DP, United
Kingdom)
Abstract
OBJECTIVESIn cardiac surgery, the choice of temperature regimen during
cardiopulmonary bypass (CPB) remains a subject of debate. Hypothermia
reduces tissue metabolic demands, but may impair the autoregulation of
cerebral blood flow and contribute to neurological morbidity. The aim of
this study was to evaluate the effect of two different temperature
regimens during CPB on the systemic oxygen transport and the cerebral
oxygenation during surgical correction of acquired heart
diseases.METHODSIn a prospective study, we randomized 40 adult patients
with combined valvular disorders requiring surgical correction of two or
more valves into two groups: (i) a normothermic (NMTH) group (n = 20), in
which the body core temperature was maintained at 36.6degreeC during CPB
and (ii) a hypothermic (HPTH) group (n = 20), in which the body was cooled
to a core temperature of 32degreeC maintained throughout the period of
CPB. The systemic oxygen transport and the cerebral oxygen saturation
(SctO <sub>2</sub>) were assessed by means of a PiCCO<sub>2</sub>
haemodynamic monitor and a cerebral oximeter, respectively. All the
patients received standard perioperative monitoring. We assessed
haemodynamic and oxygen transport parameters, the duration of mechanical
ventilation and the length of the ICU and the hospital stays.RESULTSDuring
CPB, central venous oxygen saturation was significantly higher in the HPTH
group but SctO<sub>2</sub> was increased in the NMTH group (P < 0.05).
Cardiac index, systemic oxygen delivery and consumption increased
postoperatively in both groups. However, oxygen delivery and consumption
were significantly higher in the NMTH group (P < 0.05). The duration of
respiratory support and the length of ICU and hospital stays did not
differ between the groups.CONCLUSIONSDuring combined valve surgery,
normothermic CPB provides lower central venous oxygen saturation, but
increases cerebral tissue oxygenation when compared with the hypothermic
regimen.TRIAL REGISTRATION NUMBERNCT01685554. 2013 The Author 2013.

<8>
Accession Number
2013261138
Authors
Llewellyn-Bennett R. Wotton R. West D.
Institution
(Llewellyn-Bennett, Wotton, West) Department of Thoracic Surgery, Bristol
Royal Infirmary, Upper Maudlin Street, Bristol BS2 8HW, United Kingdom
Title
Prophylactic flap coverage and the incidence of bronchopleural fistulae
after pneumonectomy.
Source
Interactive Cardiovascular and Thoracic Surgery. 16 (5) (pp 681-685),
2013. Date of Publication: May 2013.
Publisher
Oxford University Press (Great Clarendon Street, Oxford OX2 6DP, United
Kingdom)
Abstract
A best evidence topic in thoracic surgery was written according to a
structured protocol. The question addressed was 'In pneumonectomy
patients, is buttressing the bronchial stump associated with a reduced
incidence of bronchopleural fistula?'. Fifty-seven papers were found using
the reported search, of which 12 represented the best evidence to answer
the clinical question. The authors, journal, date and country of
publication, patient group studied, study type, relevant outcomes and
results of these papers are tabulated. One prospective randomized
controlled trial was identified, which found significantly lower rates of
bronchopleural fistula and empyema after pneumonectomy with the use of
pedicled intercostal flap buttressing. Intercostal muscle flaps and
pericardial flaps have been used in case series of high-risk patients,
e.g. those with neoadjuvant therapy or extended resections, with low rates
of subsequent bronchopleural fistulae. There is the least-reported
evidence for thoracodorsal artery perforator and omental flaps. There is
relatively little published evidence beyond the single randomized trial
identified, with only a few comparison studies to guide clinicians. We
conclude that there is evidence for flap buttressing in reducing the risk
of bronchopleural fistulae after pneumonectomy in diabetic patients. Flap
coverage in other high-risk situations, such as extrapleural or completion
pneumonectomy, has been reported in case series with good results. Of the
reported techniques, the evidence is strongest for the pedicled
inter-costal flap. 2013 The Author 2013.

<9>
Accession Number
2013261137
Authors
Rajakaruna C. Rogers C. Pike K. Alwair H. Cohen A. Tomkins S. Angelini
G.D. Caputo M.
Institution
(Rajakaruna) Section of Cardiac Surgery, Yale School of Medicine, New
Haven, CT, United States
(Rogers, Pike, Alwair, Cohen, Tomkins, Angelini, Caputo) Bristol Heart
Institute, University of Bristol, Bristol BS2 8HW, United Kingdom
Title
Superior haemodynamic stability during off-pump coronary surgery with
thoracic epidural anaesthesia: Results from a prospective randomized
controlled trial.
Source
Interactive Cardiovascular and Thoracic Surgery. 16 (5) (pp 602-607),
2013. Date of Publication: May 2013.
Publisher
Oxford University Press (Great Clarendon Street, Oxford OX2 6DP, United
Kingdom)
Abstract
OBJECTIVESOff-pump coronary artery bypass (OPCAB) surgery is a technically
more demanding strategy of myocardial revascularization compared with the
standard on-pump technique. Thoracic epidural anaesthesia, by reducing
sympathetic stress, may ameliorate the haemodynamic changes occurring
during OPCAB surgery. The aim of this randomized controlled trial was to
evaluate the impact of thoracic epidural anaesthesia on intraoperative
haemodynamics in patients undergoing OPCAB surgery.METHODSTwo hundred and
twenty-six patients were randomized to either general anaesthesia plus
epidural (GAE) (n = 109) or general anaesthesia (GA) only (n = 117). Mean
arterial blood pressure (MAP), heart rate (HR) and central venous pressure
(CVP) were measured before sternotomy and subsequently after positioning
the heart for each distal anastomosis.RESULTSBoth groups were well
balanced with respect to baseline characteristics and received a
standardized anaesthesia. The MAP decreased in both groups with no
significant difference (mean difference (GAE minus GA) -1.11, 95% CI -3.06
to 0.84, P = 0.26). The HR increased in both groups after sternotomy but
was significantly less in the GAE group (mean difference (GAE minus GA)
-4.29, 95% CI -7.10 to -1.48, P = 0.003). The CVP also increased in both
groups after sternotomy, but the difference between the groups varied over
time (P = 0.05). A difference was observed at the third anastomosis when
the heart was in position for the revascularization of the circumflex
artery (mean difference (GAE minus GA) +2.09, 95% CI 0.21-3.96, P = 0.03),
but not at other time points. The incidence of new arrhythmias was also
significantly lower in the GAE compared with the GA group (OR = 0.41, 95%
CI 0.22-0.78, P = 0.01).CONCLUSIONThoracic epidural with general
anaesthesia minimizes the intraoperative haemodynamic changes that occur
during heart positioning and stabilization for distal coronary anastomosis
in OPCAB surgery. 2013 The Author 2013.

<10>
Accession Number
2013261135
Authors
Filosso P.L. Ruffini E. Sandri A. Lausi P.O. Giobbe R. Oliaro A.
Institution
(Filosso, Ruffini, Sandri, Lausi, Giobbe, Oliaro) Department of Thoracic
Surgery, University of Torino, San Giovanni Battista Hospital, Via Genova
3, 10126 Turin, Italy
Title
Efficacy and safety of human fibrinogen-thrombin patch (TachoSil) in the
treatment of postoperative air leakage in patients submitted to redo
surgery for lung malignancies: A randomized trial.
Source
Interactive Cardiovascular and Thoracic Surgery. 16 (5) (pp 661-666),
2013. Date of Publication: May 2013.
Publisher
Oxford University Press (Great Clarendon Street, Oxford OX2 6DP, United
Kingdom)
Abstract
OBJECTIVESPrevious studies of the human fibrinogen-thrombin patch TachoSil
for air leak management in thoracic surgery have excluded patients
undergoing redo surgery, a group at high risk of persistent air leaks.
This is the first study to assess TachoSil in patients undergoing redo
surgery.METHODSPatients who had undergone pulmonary resection for primary
lung cancer or lung metastasis and were scheduled for completion lobectomy
plus lymphadenectomy due to tumour recurrence were eligible. After
complete lobectomy, patients with intraoperative Macchiarini grade 3 air
leaks (or >30% of the tidal volume at plethysmographic assessment) were
randomized to receive either TachoSil or further lung parenchymal
stapling/suturing procedures according to standard surgical
practice.RESULTSA total of 24 patients were randomized to TachoSil (n =
13) or standard treatment (n = 11). Mean duration of surgery was
significantly shorter in the TachoSil group than in the standard group
(3.6 vs 4.0 h; P = 0.023). The mean duration of air leaks was also
significantly reduced in the TachoSil group (4.7 vs 10.0 days; P < 0.001),
and the removal of both the first and the second chest tubes occurred
earlier (mean 3.8 vs 5.5 days; P = 0.005; and 6.1 vs 10.8 days; P < 0.001,
respectively). TachoSil was also effective in reducing persistent (>=9
days) air leaks (1 vs 7 patients; P = 0.008). There were no significant
differences between groups in other postoperative complications. Mean
length of hospital stay was significantly shorter in TachoSil-treated
patients (6.9 vs 9.5 days; P < 0.001).CONCLUSIONSTachoSil was superior to
standard stapling and suturing aerostatic techniques in reducing
postoperative air leaks in patients undergoing redo thoracic surgery.
2013 The Author 2013.

<11>
Accession Number
2013301637
Authors
McAteer J.P. LaRiviere C.A. Drugas G.T. Abdullah F. Oldham K.T. Goldin
A.B.
Institution
(McAteer, Drugas, Goldin) Division of Pediatric General and Thoracic
Surgery, Seattle Children's Hospital, 4800 Sand Point Way NE, Seattle, WA
98105, United States
(McAteer, Drugas, Goldin) Department of Surgery, University of Washington
School of Medicine, Seattle, United States
(LaRiviere) Department of Surgery, Louisiana State University, New
Orleans, United States
(Abdullah) Department of Surgery, Johns Hopkins University, Baltimore, MD,
United States
(Oldham) Division of Pediatric Surgery, Children's Hospital of Wisconsin,
Milwaukee, United States
Title
Influence of surgeon experience, hospital volume, and specialty
designation on outcomes in pediatric surgery.
Source
JAMA Pediatrics. 167 (5) (pp 468-475), 2013. Date of Publication: May
2013.
Publisher
American Medical Association (515 North State Street, Chicago IL 60654,
United States)
Abstract
Importance: Analyses of volume-outcome relationships in adult surgery have
found that hospital and physician characteristics affect patient outcomes,
such as length of stay, hospital charges, complications, and mortality.
Similar investigations in children's surgical specialties are fewer in
number, and their conclusions are less clear. Objective: To review the
evidence regarding surgeon or hospital experience and their influence on
outcomes in children's surgery. Evidence Review: A MEDLINE and EMBASE
search was conducted for English-language studies published from January
1, 1980, through April 13, 2012. Titles and abstracts were screened in a
standardized manner by 2 reviewers. Studies selected for inclusion had to
use ameasure of hospital or surgeon experience as a predictor variable and
had to report postoperative outcomes as dependent response variables.
Included studies were reviewed with regard to methodologic quality, and
study results were extracted. Findings: Sixty-three studies were reviewed.
Significant heterogeneity was detected in exposure definitions, outcome
measures, and risk adjustment, with the greatest heterogeneity seen in
appendectomy studies. Various ex- exposure levels were examined: hospital
level in 48 (68%) studies, surgeon level in 11 (17%), and both in 9 (14%).
Nineteen percent of studies did not adjust for confounding, and 57% did
not adjust for sample clustering. The most consistent methods and
reproducible results were seen in the pediatric cardiac surgical
literature. Forty-nine studies (78%) showed positive correlation between
experience and most primary outcomes, but differences in outcomes and
exposure definitions made comparisons between studies difficult. In
general, hospital-level factors tended to correlate with outcomes for
high-complexity procedures, whereas surgeon-level factors tended to
correlate with outcomes for more common procedures. Conclusions and
Relevance: Data on experiencerelated outcomes in children's surgery are
limited in number and vary widely in methodologic quality. Future studies
should seek both to standardize definitions, making results more
applicable, and to differentiate procedures affected by surgeon experience
from those more affected by hospital resources and system-level variables.
2013 American Medical Association. All rights reserved.

<12>
Accession Number
2013286699
Authors
Song J. Park J. Kim J.-Y. Kim J.-D. Kang W.-S. Muhammad H.B. Kwon M.-Y.
Kim S.-H. Yoon T.G. Kim T.-Y. Chung J.W.
Institution
(Song) Department of Anesthesiology, CHA Bundang Medical Center, CHA
University, Seongnam, South Korea
(Park, Kim, Kim, Kang, Muhammad, Kim, Yoon, Kim) Department of
Anesthesiology, Konkuk University Medical Center, Research Institute of
Biomedical Science, Konkuk University School of Medicine, Seoul, South
Korea
(Kwon) Department of Anesthesiology, National Medical Center, Seoul, South
Korea
(Chung) Department of Thoracic Surgery, Konkuk University Medical Center,
Konkuk University School of Medicine, Seoul, South Korea
Title
Effect of ulinastatin on perioperative organ function and systemic
inflammatory reaction during cardiac surgery: A randomized double-blinded
study.
Source
Korean Journal of Anesthesiology. 64 (4) (pp 334-340), 2013. Date of
Publication: April 2013.
Publisher
Korean Society of Anesthesiologists (314-1,2-Ga Hangangro, Yongsan-gu,
Seoul 140-871, South Korea)
Abstract
Background: This study evaluated the efficacy of ulinastatin for
attenuating organ injury and the release of proinflammatory cytokines due
to cardiopulmonary bypass (CPB) during cardiac surgery. Methods: Patients
undergoing valvular heart surgery employing CPB were assigned to receive
either ulinastatin (group U, n = 13) or a placebo (group C, n = 11) before
the commencement of CPB. Hemodynamic data, parameters of major organ
injury and function, and proinflammatory cytokines were measured after the
induction of anesthesia (T1), after CPB (T2), at the end of anesthesia
(T3), and at 24 hours after surgery (POD). Results: The demographic data,
CPB duration, and perioperative transfusions were not different between
the groups. PaO2/FiO2 in group U was significantly higher than that in
group C at T3 (3.8 +/- 0.8 vs. 2.8 +/- 0.7, P = 0.005) and at POD (4.0 +/-
0.7 vs. 2.8 +/- 0.7, P < 0.001). Creatine kinase-MB at POD in group U was
significantly lower than that in group C (17.7 +/- 8.3 vs. 33.7 +/- 22.1,
P = 0.03), whereas troponin I at POD was not different between the groups.
Creatinine clearance and the extubation time were not different between
the groups at POD. The dopamine infusion rate during the post-CPB period
in group U was significantly lower than that in group C (1.6 +/- 1.6 vs.
5.5 +/- 3.3 mug/kg/min, P = 0.003). The interleukin-6 and tumor necrosis
factor-alpha concentrations at T1, T2, and T3 as well as the incidences of
postoperative cardiac, pulmonary and kidney injuries were not different
between the groups. Conclusions: Ulinastatin pretreatment resulted in an
improved oxygenation profile and reduced inotropic support, probably by
attenuating the degree of cardiopulmonary injury; however, it did not
reduce the levels of proinflammatory cytokines. the Korean Society of
Anesthesiologists, 2013.

<13>
Accession Number
2013275425
Authors
Westwood M.E. Raatz H.D.I. Misso K. Burgers L. Redekop K. Lhachimi S.K.
Armstrong N. Kleijnen J.
Institution
(Westwood, Misso, Armstrong) Kleijnen Systematic Reviews Ltd, Escrick
Business Park, Escrick, York YO19 6FD, United Kingdom
(Raatz) Basel Institute of Clinical Epidemiology and Biostatistics,
University Hospital Basel, Basel, Switzerland
(Burgers, Redekop, Lhachimi) Institute of Health Policy and Management,
Erasmus University Rotterdam, Rotterdam, Netherlands
(Kleijnen) School for Public Health and Primary Care, Maastricht
University, Maastricht, Netherlands
Title
Systematic review of the accuracy of dual-source cardiacct for detection
of arterial stenosis in difficult to image patient groups.
Source
Radiology. 267 (2) (pp 387-395), 2013. Date of Publication: May 2013.
Publisher
Radiological Society of North America Inc. (820 Jorie Boulevard, Oak Brook
IL 60523-2251, United States)
Abstract
Purpose: To assess the diagnostic performance of dual-source cardiac (DSC)
computed tomography (CT) newer-generation CT instruments for identifying
anatomically significant coronary artery disease (CAD) in patients who are
difficult to image by using 64-section CT. Materials and Methods: A
literature search comprised bibliographic databases (January 1, 2000, to
March 22, 2011, with a pragmatic update on September 6, 2012), trial
registries, and conference proceedings. Only studies using invasive
coronary angiography as reference standard were included. Risk of bias was
assessed (QUADAS-2). Results were stratified according to patient group on
the basis of clinical characteristics. Summary estimates of sensitivity
and specificity of DSC CT for detecting 50% or greater arterial stenosis
were calculated by using a bivariate summary receiver operating
characteristic or random-effects model. Results: Twenty-five studies
reported accuracy of DSC CT for diagnosing CAD in difficult to image
patients; in 22 studies, one of two CT units of the same manufacturer
(Somatom Definition or Somatom Definition Flash) was used, and in the
remaining three, a different CT unit of another manufacturer (Aquilion
One) was used. The pooled, per-patient estimates of sensitivity were 97.7%
(95% confidence interval [CI]: 88.0%, 99.9%) and 97.7% (95% CI: 93.2%,
99.3%) for patients with arrhythmias and high heart rates, respectively.
The corresponding pooled estimates of specificity were 81.7% (95% CI:
71.6%, 89.4%) and 86.3% (95% CI: 80.2%, 90.7%), respectively. All data
were acquired by using Somatom Definition. In two studies with Somatom and
one study with Aquilion One, sensitivity estimates of 90% or greater were
reported in patients with previous stent implantations; specificities were
81.7% and 89.5% for Somatom and 81.0% for Aquilion One. In patients with
high coronary calcium scores, previous bypass grafts, or obesity, only
per-segment or per-artery data were available. Sensitivity estimates
remained high (.90% in all but one study), and specificities ranged from
79.1% to 100%. All data were acquired by using Somatom Definition.
Conclusion: DSC CT may be sufficiently accurate to diagnose clinically
significant CAD in some or all difficult to image patients. RSNA, 2013.

<14>
Accession Number
2013282338
Authors
Kikkert W.J. Claessen B.E. Stone G.W. Mehran R. Witzenbichler B. Brodie
B.R. Wohrle J. Witkowski A. Guagliumi G. Zmudka K. Henriques J.P.S.
Tijssen J.G.P. Sanidas E.A. Chantziara V. Xu K. Dangas G.D.
Institution
(Claessen, Stone, Mehran, Sanidas, Chantziara, Xu, Dangas) Cardiovascular
Research Foundation, New York, NY, United States
(Stone, Sanidas, Chantziara) Columbia University Medical Center, New York,
NY, United States
(Mehran, Dangas) Mount Sinai Medical Center, New York, NY, United States
(Kikkert, Claessen, Henriques, Tijssen) Academic Medical Center,
University of Amsterdam, Amsterdam, Netherlands
(Guagliumi) Ospedali Reuniti di Bergamo, Bergamo, Italy
(Witzenbichler) Charite Universitatsmedizin Campus Benjamin Franklin,
Berlin, Germany
(Wohrle) University of Ulm, Ulm, Germany
(Brodie) LeBauer CV Research Foundation, Greensboro, NC, United States
(Witkowski) National Institute of Cardiology, Warsaw, Poland
(Zmudka) Szpital Jana Pawla II, Krakow, Poland
(Dangas) Mount Sinai Medical Center, Cardiovascular Institute, One Gustave
L. Levy Place, New York, NY 10029, United States
Title
Relationship between biomarkers and subsequent bleeding risk in ST-segment
elevation myocardial infarction patients treated with paclitaxel-eluting
stents: A HORIZONS-AMI substudy.
Source
Journal of Thrombosis and Thrombolysis. 35 (2) (pp 200-208), 2013. Date of
Publication: February 2013.
Publisher
Springer Netherlands (Van Godewijckstraat 30, Dordrecht 3311 GZ,
Netherlands)
Abstract
Major bleeding complications in STEMI patients result in significant
mortality, morbidity and healthcare cost. Identification of patients at
increased risk of bleeding is therefore essential. New biomarkers might be
of incremental value to identify patients at risk for bleeding after
primary PCI. A total of 26 biomarkers were measured at enrolment and
analyzed at a central core laboratory in 464 STEMI patients in the
HORIZONS-AMI trial. We investigated the relationship between tertiles of
biomarker and in hospital non-CABG major bleeding. In hospital non-CABG
major bleeding occurred in 3.7 % of patients (n = 17). Increasing levels
of cystatin C and D-dimer at admission were associated with higher rates
of in hospital major bleeding. After adjustment for a risk score for
bleeding, the odds ratio for in hospital major bleeding was 3.13 for
cystatin C > 2.04 mg/L (p = 0.046) and 3.28 for ESAM > 34 ng/mL (p =
0.037). In this exploratory analysis of the HORIZONS-AMI biomarker
substudy, high cystatin C and ESAM levels were associated with a higher
risk of major bleeding. Larger studies are warranted to confirm the
prognostic value of cystatin C and ESAM for major bleeding in STEMI
patients. 2012 Springer Science+Business Media New York.

<15>
Accession Number
2013283349
Authors
Henrard V. Ducharme A. Khairy P. Gisbert A. Roy D. Levesque S. Talajic M.
Thibault B. Racine N. White M. Guerra P.G. Tardif J.-C.
Institution
(Henrard, Ducharme, Khairy, Gisbert, Roy, Talajic, Thibault, Racine,
White, Guerra, Tardif) Montreal Heart Institute, Universite de Montreal,
Research Center, 5000 Belanger East, Montreal, QC H1T-1C8, Canada
(Ducharme, Khairy, Roy, Levesque, Talajic, Thibault, White, Tardif)
Montreal Heart Institute Coordinating Center (MHICC), Montreal, QC, Canada
Title
Cardiac remodeling with rhythm versus rate control strategies for atrial
fibrillation in patients with heart failure: Insights from the AF-CHF
echocardiographic sub-study.
Source
International Journal of Cardiology. 165 (3) (pp 430-436), 2013. Date of
Publication: 2013.
Publisher
Elsevier Ireland Ltd (P.O. Box 85, Limerick, Ireland)
Abstract
Background: In patients with heart failure and atrial fibrillation, the
AF-CHF (Atrial Fibrillation and Congestive Heart Failure) trial did not
demonstrate the superiority of rhythm control (RhyC) over a rate control
(RaC) strategy on cardiovascular mortality. Nevertheless, deleterious
hemodynamic effects of atrial fibrillation can lead to further decrease in
left ventricular (LV) function and progression of symptoms. This
echocardiographic sub-study was designed to compare the effects of the two
treatment strategies on LV ejection fraction (LVEF), chamber volumes and
dimensions, valvular regurgitation and functional status. Methods and
results: A total of 59 patients (29 RhyC, 30 RaC) aged 67 +/- 8 years (14%
women), enrolled in the AF-CHF trial at the Montreal Heart Institute
underwent standardized echocardiograms at baseline and at 12 months. Mean
LVEF at baseline was severely depressed (RhyC: 27.0 +/- 4.9% and RaC: 27.6
+/- 7.4%, p = 0.73), and improved to a similar degree in both groups
(RhyC: + 8.0 +/- 10.4% and RaC: + 4.5 +/- 10.6, both p < 0.05; p = 0.19
for RhyC versus RaC). Other echocardiographic parameters, such as LV
end-systolic volume index and degree of mitral and tricuspid
regurgitation, remained unchanged. New York Heart Association functional
class and distance walked in 6 min improved significantly in both groups
(RhyC: + 48.9 +/- 78.7 m and RaC: + 47.2 +/- 96.7 m, both p <= 0.01), with
no difference between RhyC and RaC strategies. Conclusions: Improvements
in LVEF and functional status are observed after 12 months in patients
with heart failure and atrial fibrillation, regardless of whether rate or
rhythm control strategies are used. 2011 Elsevier Ireland Ltd.

<16>
Accession Number
2013296397
Authors
Casida J.M. Yaremchuk K.L. Shpakoff L. Marrocco A. Babicz G. Yarandi H.
Institution
(Casida) University of Michigan School of Nursing, 400 North Ingalls, Ann
Arbor, MI 48109, United States
(Yaremchuk) Head and Neck Surgery/Otolaryngology, Henry Ford Hospital, Ann
Arbor, MI, United States
(Shpakoff, Yarandi) Wayne State University College of Nursing, Detroit,
MI, United States
(Marrocco, Babicz) Cardiothoracic Surgery Department, Detroit, MI, United
States
Title
The effects of guided imagery on sleep and inflammatory response in
cardiac surgery: A pilot randomized controlled trial.
Source
Journal of Cardiovascular Surgery. 54 (2) (pp 269-279), 2013. Date of
Publication: April 2013.
Publisher
Edizioni Minerva Medica (Corso Bramante 83-85, Torino 10126, Italy)

<17>
Accession Number
2013289008
Authors
Veljovic M. Popadic A. Vukic Z. Ilic R. Trifunovic Z. Antunovic M.
Mandaric V. Tisma S. Markovic Z.
Institution
(Veljovic, Popadic, Vukic) Clinic of Anesthesiology and Intensive Care,
Belgrade, Serbia
(Ilic, Trifunovic, Mandaric, Tisma, Markovic) Clinic of Cardiac Surgery,
Military Medical Academy, Belgrade, Serbia
(Antunovic) Sector of Pharmacy, Military Medical Academy, Belgrade, Serbia
(Veljovic, Ilic, Antunovic) University of Defence, Belgrade, Serbia
Title
Myocardial protection during elective coronary artery bypasses grafting by
pretreatment with omega-3 polyunsaturated fatty acids.
Source
Vojnosanitetski Pregled. 70 (5) (pp 484-492), 2013. Date of Publication:
May 2013.
Publisher
Vojnomedicinske akademija (Crnotravska 17, Belgrade 11040, Serbia)
Abstract
Background/Aim. Despite recent advances in coronary artery bypass grafting
(CABG), cardioplegic cardiac arrest and cardiopulmonary bypass (CPB) are
still associated with myo-cardial injury. Accordingly, the efforts have
been made lately to improve the outcome of CPB by
glucose-insulin-potassium, adenosine, Ca<sup>2+</sup>-channel antagonists,
L-arginine, N-acetylcysteine, coenzyme Q10, diazoxide,
Na<sup>+</sup>/H<sup>+</sup> exchange inhibitors, but with an unequal
results. Since omega-3 polyunsatutated fatty acids (PUFAs) have shown
remarkable cardioprotection in preclinical researches, the aim of our
study was to check their effects in prevention of ischemia re-perfusion
injury in patients with CPB. Methods. This prospective, randomized,
placebo-controlled study was performed with parallel groups. The patients
undergoing elective CABG were randomized to receive preoperative
intravenous omega-3 PUFAs infusion (n = 20) or the same volume of 0.9%
saline solution infusion (n = 20). Blood samples were collected
simultaneously from the radial artery and the coronary sinus before
starting CPB and at 10, 20 and 30 min after the release of the aortic
cross clamp. Lactate extraction/excretion and myo-cardial oxygen
extraction were calculated and compared between the two groups. The levels
of troponin I (TnT) and cre-atine kinase-myocardial band (CK-MB) were
determined before starting CPB and 4 and 24 h postoperatively. Results.
Demographic and operative characteristics, including CPB and aortic
cross-clamp time, were similar between the two groups of patients. The
level of lactate extraction 10 and 20 min after aortic cross-clamp time
has shown negative values in the control group, but positive values in the
PUFAs group with statistically significant differences (-19.6% vs 7.9%; p
< 0.0001 and -19.9% vs 8.2%; p < 0.0008, respectively). The level of
lactate extraction 30 minutes after reperfusion was not statistically
different between the two groups (6.9% vs 4.2%; p < 0.54). Oxygen
extraction in the PUFAs group was statistically significantly higher
compared to the control group after 10, 20 and 30 min of reperfusion
(35.5% vs 50.4%, p < 0.0004; 25.8% vs 48.7%, p 0.0001 and 25.8% vs 45.6%,
p < 0.0002, respectively). The level of TnT, 4 and 24 h after CPB, was
significantly higher in the control group compared to PUFAs group, with
statistically significant differences (11.4 vs 6.6, p < 0.009 and 12.7 vs
5.9, p < 0.008, respectively). The level of CK-MB, 4 h after CPB, was
significantly higher in the control group compared to PUFAs group (61.9 vs
37.7, p < 0.008), but its level, 24 h after CPB, was not statistically
different between the two groups (58.9 vs 40.6, p 0.051). Conclusion.
Treatment with omega-3 PUFAs administered preoperatively promoted early
metabolic recovery of the heart after elective CABG and improved
myocardial protection. This study showed that omega-3 emulsion should not
be considered only as a nutritional supplement but also as a clinically
safe and potent cardioprotective adjunct during CPB.

<18>
Accession Number
2013264980
Authors
Rathnayake N. Akerman S. Klinge B. Lundegren N. Jansson H. Tryselius Y.
Sorsa T. Gustafsson A.
Institution
(Rathnayake, Klinge, Tryselius, Gustafsson) Karolinska Institutet,
Department of Dental Medicine, Division of Periodontology, Stockholm,
Sweden
(Akerman, Lundegren) Malmo University, Faculty of Odontology, Department
of Oral Diagnostics, Malmo, Sweden
(Klinge, Jansson) Malmo University, Faculty of Odontology, Department of
Periodontology, Malmo, Sweden
(Sorsa) University of Helsinki, Helsinki University Central Hospital,
Department of Oral and Maxillofacial Diseases, Helsinki, Finland
Title
Salivary Biomarkers for Detection of Systemic Diseases.
Source
PLoS ONE. 8 (4) , 2013. Article Number: e61356. Date of Publication: 24
Apr 2013.
Publisher
Public Library of Science (185 Berry Street, Suite 1300, San Francisco CA
94107, United States)
Abstract
Background and Objective:Analysis of inflammatory biomarkers in saliva
could offer an attractive opportunity for the diagnosis of different
systemic conditions specifically in epidemiological surveys. The aim of
this study was to investigate if certain salivary biomarkers could be used
for detection of common systemic diseases.Materials and Methods:A randomly
selected sample of 1000 adults living in Skane, a county in the southern
part of Sweden, was invited to participate in a clinical study of oral
health. 451 individuals were enrolled in this investigation, 51% women.
All participants were asked to fill out a questionnaire, history was
taken, a clinical examination was made and stimulated saliva samples were
collected. Salivary concentrations of IL-1beta, -6, -8, TNF-alpha,
lysozyme, MMP-8 and TIMP-1 were determined using ELISA, IFMA or Luminex
assays.Results:Salivary IL-8 concentration was found to be twice as high
in subjects who had experience of tumour diseases. In addition, IL-8
levels were also elevated in patients with bowel disease. MMP-8 levels
were elevated in saliva from patients after cardiac surgery or suffering
from diabetes, and muscle and joint diseases. The levels of IL-1beta, IL-8
and MMP-8, as well as the MMP-8/TIMP-1 ratio were higher in subjects with
muscle and joint diseases.Conclusion:Biomarkers in saliva have the
potential to be used for screening purposes in epidemiological studies.
The relatively unspecific inflammatory markers used in this study can not
be used for diagnosis of specific diseases but can be seen as markers for
increased systemic inflammation. 2013 Rathnayake et al.

<19>
Accession Number
2013279671
Authors
Panza J.A. Holly T.A. Asch F.M. She L. Pellikka P.A. Velazquez E.J. Lee
K.L. Borges-Neto S. Farsky P.S. Jones R.H. Berman D.S. Bonow R.O.
Institution
(Panza, Asch) Division of Cardiology, MedStar Washington Hospital Center,
110 Irving Street, NW, Washington, DC 20010, United States
(Holly, Bonow) Northwestern University Feinberg School of Medicine,
Chicago, IL, United States
(She, Velazquez, Lee, Borges-Neto, Jones) Duke Clinical Research
Institute, Duke University Medical Center, Durham, NC, United States
(Pellikka) Mayo Clinic College of Medicine, Rochester, MN, United States
(Farsky) Instituto Dante Pazzanese de Cardiologia, Sao Paulo, Brazil
(Berman) Cedars-Sinai Medical Center, Los Angeles, CA, United States
Title
Inducible myocardial ischemia and outcomes in patients with coronary
artery disease and left ventricular dysfunction.
Source
Journal of the American College of Cardiology. 61 (18) (pp 1860-1870),
2013. Date of Publication: 07 May 2013.
Publisher
Elsevier USA (6277 Sea Harbor Drive, Orlando FL 32862 8239, United States)
Abstract
Objectives: The study objectives were to test the hypotheses that ischemia
during stress testing has prognostic value and identifies those patients
with coronary artery disease (CAD) with left ventricular (LV) dysfunction
who derive the greatest benefit from coronary artery bypass grafting
(CABG) compared with medical therapy. Background: The clinical
significance of stress-induced ischemia in patients with CAD and
moderately to severely reduced LV ejection fraction (EF) is largely
unknown. Methods: The STICH (Surgical Treatment for IsChemic Heart
Failure) trial randomized patients with CAD and EF <=35% to CABG or
medical therapy. In the current study, we assessed the outcomes of those
STICH patients who underwent a radionuclide (RN) stress test or a
dobutamine stress echocardiogram (DSE). A test was considered positive for
ischemia by RN testing if the summed difference score (difference in
tracer activity between stress and rest) was >=4 or if >=2 of 16 segments
were ischemic during DSE. Clinical endpoints were assessed by intention to
treat during a median follow-up of 56 months. Results: Of the 399 study
patients (51 women, mean EF 26 +/- 8%), 197 were randomized to CABG and
202 were randomized to medical therapy. Myocardial ischemia was induced
during stress testing in 256 patients (64% of the study population).
Patients with and without ischemia were similar in age, multivessel CAD,
previous myocardial infarction, LV EF, LV volumes, and treatment
allocation (all p = NS). There was no difference between patients with and
without ischemia in all-cause mortality (hazard ratio: 1.08; 95%
confidence interval: 0.77 to 1.50; p = 0.66), cardiovascular mortality, or
all-cause mortality plus cardiovascular hospitalization. There was no
interaction between ischemia and treatment for any clinical endpoint.
Conclusions: In CAD with severe LV dysfunction, inducible myocardial
ischemia does not identify patients with worse prognosis or those with
greater benefit from CABG over optimal medical therapy. (Comparison of
Surgical and Medical Treatment for Congestive Heart Failure and Coronary
Artery Disease [STICH]; NCT00023595) 2013 American College of Cardiology
Foundation.

<20>
Accession Number
2013279132
Authors
Vohra H.A. Whistance R.N. De kerchove L. Punjabi P. El khoury G.
Institution
(Vohra, De kerchove, El khoury) Divisions of Cardiothoracic and Vascular
Surgery, Universite Catholique de Louvain, Cliniques Universitaires
Saint-Luc, Brussels, Belgium
(Whistance) Academic Unit of Surgical Research, School of Social and
Community Medicine, University of Bristol, Bristol, United Kingdom
(Punjabi) Imperial College Heathcare NHS Trust, Imperial College School of
Medicine, London, United Kingdom
Title
Valve-preserving surgery on the bicuspid aortic valve.
Source
European Journal of Cardio-thoracic Surgery. 43 (5) (pp 888-898), 2013.
Article Number: ezs664. Date of Publication: May 2013.
Publisher
Oxford University Press (Great Clarendon Street, Oxford OX2 6DP, United
Kingdom)
Abstract
Valve repair has emerged as an important intervention for the management
of bicuspid aortic valve disease. This systematic review aims to assess
the safety, efficacy and durability of bicuspid aortic valve repair.
Initial searches yielded 682 abstracts, reduced by de-duplication to 370,
of which 56 full papers were accessed and 30 met the inclusion criteria.
Overall, 163 unique outcomes for bicuspid aortic valve-preserving surgery
were reported on 280 occasions. Bicuspid aortic valve-preserving surgery
exhibited low operative mortality (0.0-5.2%), excellent 5-year survival
(82-100%) and 43-100% 5-year freedom from reoperation. Bicuspid aortic
valve repair is safe and efficacious, but concerns regarding its
durability necessitate further standardized outcome assessments. The
Author 2013. Published by Oxford University Press on behalf of the
European Association for Cardio-Thoracic Surgery. All rights reserved.

<21>
Accession Number
2013279077
Authors
Haase M. Haase-Fielitz A. Plass M. Kuppe H. Hetzer R. Hannon C. Murray
P.T. Bailey M.J. Bellomo R. Bagshaw S.M.
Institution
(Haase, Haase-Fielitz) Department of Nephrology and Hypertension,
Diabetes, and Endocrinology, Otto-von-Guericke-University Magdeburg,
Germany
(Plass, Kuppe) Department of Anesthesiology, The German Heart Center,
Berlin, Germany
(Hetzer) Department of Cardiothoracic Surgery, The German Heart Center,
Berlin, Germany
(Hannon, Murray) Nephrology and Clinical Pharmacology, University College
Dublin School of Medicine and Medical Science, Dublin, Ireland
(Bailey) The Australian and New Zealand Intensive Care Research Centre,
Department of Epidemiology and Preventive Medicine, Monash University,
Melbourne, Australia
(Bellomo) Department of Intensive Care, The Austin Hospital, Melbourne,
Australia
(Bagshaw) Division of Critical Care Medicine, Faculty of Medicine and
Dentistry, University of Alberta, Alberta, Canada
Title
Prophylactic Perioperative Sodium Bicarbonate to Prevent Acute Kidney
Injury Following Open Heart Surgery: A Multicenter Double-Blinded
Randomized Controlled Trial.
Source
PLoS Medicine. 10 (4) , 2013. Article Number: e1001426. Date of
Publication: April 2013.
Publisher
Public Library of Science (185 Berry Street, Suite 1300, San Francisco CA
94107, United States)
Abstract
Background: Preliminary evidence suggests a nephroprotective effect of
urinary alkalinization in patients at risk of acute kidney injury. In this
study, we tested whether prophylactic bicarbonate-based infusion reduces
the incidence of acute kidney injury and tubular damage in patients
undergoing open heart surgery. Methods and Findings: In a multicenter,
double-blinded (patients, clinical and research personnel), randomized
controlled trial we enrolled 350 adult patients undergoing open heart
surgery with the use of cardiopulmonary bypass. At induction of
anesthesia, patients received either 24 hours of intravenous infusion of
sodium bicarbonate (5.1 mmol/kg) or sodium chloride (5.1 mmol/kg). The
primary endpoint was the proportion of patients developing acute kidney
injury. Secondary endpoints included the magnitude of acute tubular damage
as measured by urinary neutrophil gelatinase-associated lipocalin (NGAL),
initiation of acute renal replacement therapy, and mortality. The study
was stopped early under recommendation of the Data Safety and Monitoring
Committee because interim analysis suggested likely lack of efficacy and
possible harm. Groups were non-significantly different at baseline except
that a greater proportion of patients in the sodium bicarbonate group
(66/174 [38%]) presented with preoperative chronic kidney disease compared
to control (44/176 [25%]; p = 0.009). Sodium bicarbonate increased urinary
pH (from 6.0 to 7.5, p<0.001). More patients receiving bicarbonate (83/174
[47.7%]) developed acute kidney injury compared with control patients
(64/176 [36.4%], odds ratio [OR] 1.60 [95% CI 1.04-2.45]; unadjusted p =
0.032). After multivariable adjustment, a non-significant unfavorable
group difference affecting patients receiving sodium bicarbonate was found
for the primary endpoint (OR 1.45 [0.90-2.33], p = 0.120]). A greater
postoperative increase in urinary NGAL in patients receiving bicarbonate
infusion was observed compared to control patients (p = 0.011). The
incidence of postoperative renal replacement therapy was similar but
hospital mortality was increased in patients receiving sodium bicarbonate
compared with control (11/174 [6.3%] versus 3/176 [1.7%], OR 3.89
[1.07-14.2], p = 0.031). Conclusions: Urinary alkalinization using sodium
bicarbonate infusion was not found to reduce the incidence of acute kidney
injury or attenuate tubular damage following open heart surgery; however,
it was associated with a possible increase in mortality. On the basis of
these findings we do not recommend the prophylactic use of sodium
bicarbonate infusion to reduce the risk of acute kidney injury.
Discontinuation of growing implementation of this therapy in this setting
seems to be justified. Trial registration: ClinicalTrials.gov NCT00672334
Please see later in the article for the Editors' Summary. 2013 Haase et
al.

<22>
Accession Number
2013278968
Authors
Li X.-D. Yang Y.-J. Hao Y.-C. Yang Y. Zhao J.-L. Dou K.-F. Gu D.-F.
Institution
(Li, Yang, Hao, Yang) Department of Evidence Based Medicine, Fuwai
Hospital and Cardiovascular Institute, Peking Union Medical College and
Chinese Academy of Medical Sciences, Beijing 100037, China
(Zhao, Dou, Gu) Department of and Cardiology, Fuwai Hospital and
Cardiovascular Institute, Peking Union Medical College and Chinese Academy
of Medical Sciences, Beijing 100037, China
Title
Effect of pre-procedural statin therapy on myocardial no-reflow following
percutaneous coronary intervention: A meta analysis.
Source
Chinese Medical Journal. 126 (9) (pp 1755-1760), 2013. Date of
Publication: 05 May 2013.
Publisher
Chinese Medical Association (42 Dongsi Xidajie, Beijing 100710, China)
Abstract
Background Successful revascularization of coronary artery disease,
especially ST-elevation myocardial infarction (STEMI), does not always
mean optimal myocardial reperfusion in a portion of patients because of
no-reflow phenomenon. We hypothesized that statins might attenuate the
incidence of myocardial no-reflow when used before percutaneous coronary
intervention (PCI). The purpose of this study was to summarize the
evidence of pre-procedural statin therapy to reduce myocardial no-reflow
after PCI. Methods We searched the MEDLINE, Cochrane, and
clinicaltrials.gov databases from inception to October 2012 for clinical
trials that examined statin therapy before PCI. We required that studies
initiated statins before PCI and reported myocardial no-reflow. A
DerSimonian-Laird model was used to construct random-effects summary risk
ratios. Results In all, 7 studies with 3086 patients met our selection
criteria. The use of pre-procedural statins significantly reduced
post-procedural no-reflow by 4.2% in all PCI patients (risk ratio (RR)
0.56, 95% confidence interval (CI) 0.35 to 0.90, P=0.016), and attenuated
by 5.0% in non-STEMI patients (RR 0.41, 95% CI 0.18 to 0.94, P=0.035).
This benefit was mainly observed in the early or acute intensive statin
therapy populations (RR 0.43, 95% CI 0.26 to 0.71, P=0.001). Conclusions
Acute intensive statin therapy before PCI significantly reduces the hazard
of post-procedural no-reflow phenomenon. The routine use of statins before
PCI should be considered.

<23>
Accession Number
2013277256
Authors
Harskamp R.E. Park D.-W.
Institution
(Harskamp) Academic Medical Center, University of Amsterdam, Netherlands
(Park) Department of Cardiology, University of Ulsan College of Medicine,
Asan Medical Center, Seoul, South Korea
(Harskamp, Park) Duke Clinical Research Institute, Duke University,
Durham, NC, United States
Title
Percutaneous coronary intervention in diabetic patients: Should choice of
stents be influenced?.
Source
Expert Review of Cardiovascular Therapy. 11 (5) (pp 541-553), 2013. Date
of Publication: May 2013.
Publisher
Expert Reviews Ltd. (2 Albert Place, London N3 1QB, United Kingdom)
Abstract
Patients with diabetes mellitus are prone to a diffuse and rapidly
progressive form of coronary artery disease. As a result, diabetic
patients undergoing coronary revascularization are at higher risk of
cardiovascular events compared with nondiabetic patients. Due to marked
advances of stent device technology and adjunctive pharmacology,
percutaneous coronary intervention has been regarded as an efficient
revascularization strategy in diabetic patients. Numerous randomized
trials and large observational registries have compared the efficacy and
safety of bare-metal stents and drug-eluting stents, as well as several DE
platforms. This article systematically reviews the cumulative evidence
from key clinical studies and tries to help guide the physician in making
informed decisions on the optimal stent type for patients with diabetes
mellitus. 2013 2013 Expert Reviews Ltd.

<24>
Accession Number
2013258027
Authors
Curtis A.B. Worley S.J. Adamson P.B. Chung E.S. Niazi I. Sherfesee L.
Shinn T. Sutton M.St.J.
Institution
(Curtis) Department of Medicine, University at Buffalo, Buffalo General
Medical Center, 100 High St., D2-76, Buffalo, NY 14203, United States
(Worley) Lancaster General Hospital, Lancaster, PA, United States
(Adamson) Oklahoma Foundation for Cardiovascular Research, Oklahoma City,
OK, United States
(Chung) Heart and Vascular Center at Christ Hospital, Cincinnati, United
States
(Niazi) St. Luke's Medical Center, Milwaukee, United States
(Sherfesee) Medtronic, Minneapolis, United States
(Shinn) St. Joseph Mercy, Ann Arbor, MI, United States
(Sutton) University of Pennsylvania Medical Center, Philadelphia, PA,
United States
Title
Biventricular pacing for atrioventricular block and systolic dysfunction.
Source
New England Journal of Medicine. 368 (17) (pp 1585-1593), 2013. Date of
Publication: 25 Apr 2013.
Publisher
Massachussetts Medical Society (860 Winter Street, Waltham MA 02451-1413,
United States)
Abstract
BACKGROUND: Right ventricular pacing restores an adequate heart rate in
patients with atrioventricular block, but high percentages of right
ventricular apical pacing may promote left ventricular systolic
dysfunction. We evaluated whether biventricular pacing might reduce
mortality, morbidity, and adverse left ventricular remodeling in such
patients. METHODS: We enrolled patients who had indications for pacing
with atrioventricular block; New York Heart Association (NYHA) class I,
II, or III heart failure; and a left ventricular ejection fraction of 50%
or less. Patients received a cardiac-resynchronization pacemaker or
implantable cardioverter-defibrillator (ICD) (the latter if the patient
had an indication for defibrillation therapy) and were randomly assigned
to standard right ventricular pacing or biventricular pacing. The primary
outcome was the time to death from any cause, an urgent care visit for
heart failure that required intravenous therapy, or a 15% or more increase
in the left ventricular end-systolic volume index. RESULTS: Of 918
patients enrolled, 691 underwent randomization and were followed for an
average of 37 months. The primary outcome occurred in 190 of 342 patients
(55.6%) in the right-ventricular-pacing group, as compared with 160 of 349
(45.8%) in the biventricular-pacing group. Patients randomly assigned to
biventricular pacing had a significantly lower incidence of the primary
outcome over time than did those assigned to right ventricular pacing
(hazard ratio, 0.74; 95% credible interval, 0.60 to 0.90); results were
similar in the pacemaker and ICD groups. Left ventricular lead-related
complications occurred in 6.4% of patients. CONCLUSIONS: Biventricular
pacing was superior to conventional right ventricular pacing in patients
with atrioventricular block and left ventricular systolic dysfunction with
NYHA class I, II, or III heart failure. (Funded by Medtronic; BLOCK HF
ClinicalTrials.gov number, NCT00267098.) Copyright 2013 Massachusetts
Medical Society.

<25>
Accession Number
2013280136
Authors
Rosa R.F.M. Rosa R.C.M. Zen P.R.G. Graziadio C. Paskulin G.A.
Institution
(Rosa) UFCSPA, Geneticista Clinico, Hospital Materno Infantil Presidente
Vargas (HMIPV), Porto Alegre, RS, Brazil
(Rosa) UFCSPA, Porto Alegre, RS, Brazil
(Zen, Graziadio) UFCSPA, Disciplina de Genetica Clinica da UFCSPA, Porto
Alegre, RS, Brazil
(Paskulin) Universidade Federal do Rio Grande do Sul (UFRGS), Disciplina
de Genetica Clinica da UFCSPA, Porto Alegre, RS, Brazil
Title
Trisomy 18: Review of the clinical, etiologic, prognostic, and ethical
aspects.
Source
Revista Paulista de Pediatria. 31 (1) (pp 111-120), 2013. Date of
Publication: January-March 2013.
Publisher
Sao Paulo Pediatric Society (Alameda Santos 211, Cerq cesar, Sao Paulo
01419-000, Brazil)
Abstract
Objective: To review the clinical, etiological, diagnostic, and prognostic
characteristics of trisomy 18 (Edwards syndrome). Data sources: Scientific
articles in the MedLine, Lilacs, and SciELO databases were searched using
the descriptors 'trisomy 18' and 'Edwards syndrome'. The research was not
limited to a specific time period and included all articles in such
databases. Data synthesis: Edwards syndrome is a disease characterized by
a broad clinical picture and a very reserved prognosis. There are
descriptions of more than 130 different anomalies, which can involve
virtually all organs and systems. Its findings are the result of the
presence of three copies of chromosome 18. The main chromosomal
constitution observed among these patients is a free trisomy of chromosome
18, which is associated with the phenomenon of nondisjunction, especially
in maternal gametogenesis. Most fetuses with Edwards syndrome die during
the embryonic and fetal life. The median of survival among live births has
usually varied between 2.5 and 14.5 days. Conclusions: Knowledge on the
clinical picture and on the prognosis of Edwards syndrome patients is of
great importance regarding the neonatal care and the decisions about
invasive treatments. The speed to have a confirmed diagnosis is important
for making decisions about medical procedures. Often, interventions are
performed under emergency conditions, without many opportunities for
discussion, and they involve difficult medical and ethical issues.

<26>
Accession Number
71061360
Authors
Meads D.M. Fairbairn T.A. Hulme C.T. Mather A.N. Plein S. Blackman D.J.
Greenwood J.P.
Institution
(Meads, Fairbairn, Hulme, Mather, Plein, Greenwood) University of Leeds,
Leeds, United Kingdom
(Blackman) Leeds General Infirmary, Leeds, United Kingdom
Title
The cost-effectiveness of transcatheter aortic valve implantation versus
surgical aortic valve replacement in patients with severe aortic stenosis
at high operative risk.
Source
Value in Health. Conference: ISPOR 18th Annual International Meeting New
Orleans, LA United States. Conference Start: 20130518 Conference End:
20130522. Conference Publication: (var.pagings). 16 (3) (pp A294), 2013.
Date of Publication: May 2013.
Publisher
Elsevier Ltd
Abstract
OBJECTIVES: To determine the cost-effectiveness of Transcatheter aortic
valve implantation (TAVI) compared to surgical aortic valve replacement
(SAVR) in a high-risk aortic stenosis (AS) population from the perspective
of the UK health and personal social services. METHODS: A Markov model was
developed to enable a cost-utility analysis employing NICE reference case
methods. A systematic review was conducted to identify model parameter
values. Mean utility values per NYHA category were derived from a UK
high-risk AS population. Two-year TAVI and SAVR effectiveness was taken
from the PARTNER A trial. Costs and effects were modelled from two years
over a 10 year horizon via NYHA health state transitions. Incremental
cost-effectiveness ratios (ICER) and cost effectiveness acceptability
curves (CEAC) were calculated and deterministic and probabilistic
sensitivity analyses conducted. RESULTS: Despite greater procedural costs
(16,500 vs. 9,256), TAVI was cost-effective compared to SAVR over 10 years
(costs 52,593 vs. 53,943 and QALYs 2.81 vs 2.75), indicating TAVI
dominated SAVR. This appeared to be due to greater SAVR post-surgical
costs and attendant length and cost of hospital stay. The results appeared
robust to a number of deterministic sensitivity (including high stroke
rates, worst case scenario complication rates, alternative utility values
and higher costs) and probabilistic analyses. Given modest cost savings
and QALY benefits conferred by TAVI, results were sensitive to some
parameter changes when incurred by one arm in isolation. The CEAC
indicated that at a 20,000 incremental QALY willingness to pay threshold,
TAVI had a 64.6% likelihood of being cost-effective. CONCLUSIONS: This
economic evaluation is the first to incorporate two year data comparing
TAVI and SAVR in elderly high risk AS patients. TAVI is likely to be a
cost-effective option compared to SAVR. However, uncertainty surrounding
the long-term outcomes for TAVI patients remains; this could have a
substantive impact on estimates of cost-effectiveness.

<27>
[Use Link to view the full text]
Accession Number
71058379
Authors
Cholette J. Powers K. Alfieris G. Angona R. Henrichs K. Blumberg N.
Institution
(Cholette, Powers) Golisano Children's Hospital, University of Rochester,
United States
(Alfieris, Angona, Henrichs, Blumberg) University of Rochester, United
States
Title
Cell saver for volume replacement in children following cardiopulmonary
bypass reduces the number of RBC and blood product transfusions and donor
exposures.
Source
Critical Care Medicine. Conference: Critical Care Congress 2012 Houston,
TX United States. Conference Start: 20120204 Conference End: 20120208.
Conference Publication: (var.pagings). 39 (pp 7), 2011. Date of
Publication: December 2011.
Publisher
Lippincott Williams and Wilkins
Abstract
Introduction: Children typically require large numbers of red blood cell
(RBC) and blood component therapy following repair or palliation of
cardiac defects with cardiopulmonary bypass (CPB). Cell savers remove
heparin and cytokines from CPB salvage, and are now available for
pediatrics. The impact of cell saver infusion on RBC and component therapy
in pediatric cardiac surgery has not been explored. Hypothesis:
Utilization of cell saver for volume replacement in children undergoing
cardiac surgery for congenital heart defects with CPB reduces
post-operative allogeneic RBC and blood component transfusions, and donor
exposures. Methods: A prospective, randomized controlled trial of cell
saver v. allogeneic RBC and crystalloid/colloid for post-operative volume
replacement in children undergoing cardiac surgery with CPB.Subjects:
Children 20 kg undergoing CPB, stratified by weight and surgical
severity.Study Group: Residual CPB volume was processed by the Fresinius
Continuous Auto Transfusion System and collected as cell saver. Cell saver
was infused for anemia, or for volume replacement if hemoglobin (Hb) < 13
g/dL. Albumin or crystalloid was given for volume replacement if Hb >/= 13
g/dL.Control Group: Allogeneic RBC, albumin, or crystalloid was given for
anemia or volume replacement per the current standard of care. Blood
component therapy was transfused in each group per the standard of care.
Results: 34 cell saver and 31 control subjects were studied.
Post-operatively until hospital discharge, the cell saver group received a
mean of 1.9 +/<sup>-</sup> 1.5 allogeneic RBC transfusions v. 3.6
+/<sup>-</sup> 2.5 in the control group (p<0.001). The cell saver group
received 2.1 +/- 1.6 total post-operative transfusions (FFP, cryo, plts)
v. 4.3 +/<sup>-</sup> 3.2 in the control group (p<0.001). Mean
post-operative donor exposures were 1.6 +/- 1.6 for the cell saver group
and 3.2 +/- 2.8 for the control group (p<0.001). There was no significant
difference in RBC storage age or clinical outcomes. Conclusions: Infusion
of cell saver for volume replacement in children following CPB reduces the
number of allogeneic RBC and blood product transfusions and donor
exposures, and may reduce complications from blood product transfusions.

Saturday, May 18, 2013

EMBASE Cardiac Update AutoAlert: EPICORE Cardiac Surgery Blogger2

Total documents retrieved: 30

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<1>
Accession Number
2013285031
Authors
Tefikow S. Barth J. Maichrowitz S. Beelmann A. Strauss B. Rosendahl J.
Institution
(Tefikow, Strauss, Rosendahl) Jena University Hospital, Friedrich Schiller
University Jena, Institute of Psychosocial Medicine and Psychotherapy,
Jena, Germany
(Barth) University of Bern, Institute of Social and Preventive Medicine,
Bern, Switzerland
(Maichrowitz, Beelmann) Friedrich Schiller University Jena, Institute of
Psychology, Department of Research Synthesis, Intervention and Evaluation,
Jena, Germany
Title
Efficacy of hypnosis in adults undergoing surgery or medical procedures: A
meta-analysis of randomized controlled trials.
Source
Clinical Psychology Review. 33 (5) (pp 623-636), 2013. Date of
Publication: July 2013.
Publisher
Elsevier Inc. (360 Park Avenue South, New York NY 10010, United States)
Abstract
This meta-analysis investigates the efficacy of hypnosis in adults
undergoing surgical or medical procedures compared to standard care alone
or an attention control. Through a comprehensive literature search N=. 34
eligible randomized controlled trials (RCTs) were included, comprising a
total of 2597 patients. Random effects meta-analyses revealed positive
treatment effects on emotional distress (g=. 0.53, CI 95% [0.37; 0.69]),
pain (g=. 0.44, CI 95% [0.26; 0.61]), medication consumption (g=. 0.38, CI
95% [0.20; 0.56]), physiological parameters (g=. 0.10, CI 95% [0.02;
0.18]), recovery (g=. 0.25, CI 95% [0.04; 0.46]), and surgical procedure
time (g=. 0.25, CI 95% [0.12; 0.38]). In conclusion, benefits of hypnosis
on various surgically relevant outcomes were demonstrated. However, the
internal validity of RCTs seems limited and further high methodological
quality RCTs are needed to strengthen the promising evidence of hypnosis
for adults undergoing surgery or medical procedures. 2013 Elsevier Ltd.

<2>
Accession Number
2013265274
Authors
Gijsen V.M.G.J. Hesselink D.A. Croes K. Koren G. De Wildt S.N.
Institution
(Gijsen, Croes, De Wildt) Clinical Pharmacologist, Erasmus MC - Sophia
Childrens Hospital, Department of Pediatric Surgery and Intensive Care, Dr
Molewaterplein 60, 3015 GJ Rotterdam, Netherlands
(Gijsen, Koren) Division of Clinical Pharmacology and Toxicology, Hospital
for Sick Children, Toronto, ON, Canada
(Hesselink) Division of Nephrology and Renal Transplantation, Department
of Internal Medicine, Erasmus MC, Rotterdam, Netherlands
(Koren) Department of Medicine, University of Western Ontario, London, ON,
Canada
Title
Prevalence of renal dysfunction in tacrolimus-treated pediatric transplant
recipients: A systematic review.
Source
Pediatric Transplantation. 17 (3) (pp 205-215), 2013. Date of Publication:
May 2013.
Publisher
Blackwell Publishing Ltd (9600 Garsington Road, Oxford OX4 2XG, United
Kingdom)
Abstract
Renal dysfunction after non-renal transplantation in adult
tacrolimus-treated transplant patients is well documented. Little is known
about its prevalence in children. Age-related changes in both disposition
and effect of tacrolimus as well as renal function may preclude
extrapolation of adult data to children. To systematically review the
literature on renal dysfunction in non-renal pediatric transplant
recipients treated with tacrolimus. PubMed/Medline, Embase, and Google
were searched from their inception until April 19, 2012, with the search
terms "tacrolimus," "renal function," "transplantation," and "children."
Eighteen of 385 retrieved papers were considered relevant. Twelve dealt
with liver, four with heart transplant, one with heart and lung
transplant, and one with intestinal recipients. Reported prevalences of
mild and severe chronic kidney disease ranged from 0% to 39% and 0% to
71.4%, respectively, for liver, and from 22.7% to 40% and 6.8% to 46%,
respectively, for heart and/or lung transplant recipients. Ranges remained
wide after adjusting for follow-up time and disease severity. Possible
explanations are inclusion bias and definitions used for renal
dysfunction. A considerable proportion of pediatric non-renal transplant
patients who receive tacrolimus-based immunosuppression, appear to suffer
from chronic kidney disease. This conclusion warrants further research
into the real risk, its risk factors, and individualization of
immunosuppressant therapy. 2013 John Wiley & Sons A/S.

<3>
Accession Number
2013274682
Authors
Potter B.J. Deverenne B. Doucette S. Fergusson D. Magder S.
Institution
(Potter, Deverenne, Magder) McGill University Health Center, Montreal QC,
Canada
(Doucette, Fergusson) Ottawa Hospital Research Institute, Ottawa, ON,
Canada
Title
Cardiac output responses in a flow-driven protocol of resuscitation
following cardiac surgery.
Source
Journal of Critical Care. 28 (3) (pp 265-269), 2013. Date of Publication:
June 2013.
Publisher
W.B. Saunders (Independence Square West, Philadelphia PA 19106-3399,
United States)
Abstract
Objective: Determine the role of cardiac output and central venous
pressure (CVP) measurements in the clinical decisions that were based on
the algorithm used in a randomized trial that compared a colloid to a
crystalloid solution in the management of patients early after cardiac
surgery (FACS trial, NCT00337805, Crit Care Med 2010; 38:2117). Methods:
We analyzed the changes in CVP and cardiac index (CI) in 729 fluid
challenges from the FACS trial in which 119 patients were randomized to
colloid and 118 to crystalloid boluses in a flow-based protocol. A fluid
challenge was defined as being positive if CI increased by <0.3
L/min<sup>-1</sup>m<sup>-2</sup> and negative if CI increased by <0.3
L/min<sup>-1</sup>m<sup>-2</sup> but CVP increased by <2 mmHg. Results: As
defined in the protocol, 26% of boluses were given for a low CI (<2.2
L/min<sup>-1</sup>m<sup>-2</sup>). CI did not increase in 20% of boluses
despite an adequate increase in CVP; in the protocol this meant that
further volume boluses were not given. In another 34% of boluses in which
CI did not increase, CVP increased by < 2 mmHg, which meant that volume
responsiveness could not be ruled out and another bolus was indicated. 43%
of the boluses were given for hypotension, but surprisingly in 90% of
these instances, CI was in the acceptable range indicating that the low
arterial pressure was due to decreased systemic vascular resistance.
Conclusion: Measurement of cardiac output and CVP significantly influenced
clinical decisions in the FACS algorithm. 2013 Elsevier Inc.

<4>
Accession Number
22958313
Authors
Tewarie L.S. Menon A.K. Hatam N. Amerini A. Moza A.K. Autschbach R.
Goetzenich A.
Institution
(Tewarie) Department of Cardiothoracic and Vascular Surgery, University
Hospital RWTH Aachen, Pauwelsstrasse 30, 52074 Aachen, Germany.
Title
Prevention of sternal dehiscence with the sternum external fixation
(Stern-E-Fix) corset--randomized trial in 750 patients.
Source
Journal of cardiothoracic surgery. 7 (pp 85), 2012. Date of Publication:
2012.
Abstract
The main objective of this study will be to determine the effects of a new
advanced sternum external fixation (Stern-E-Fix) corset on prevention of
sternal instability and mediastinitis in high-risk patients. This
prospective, randomized study (January 2009 - June 2011) comprised 750
male patients undergoing standard median sternotomy for cardiac procedures
(78% CABG). Patients were divided in two randomized groups (A, n = 380:
received a Stern-E-Fix corset postoperatively for 6 weeks and B, n = 370:
control group received a standard elastic thorax bandage). In both groups,
risk factors for sternal dehiscence and preoperative preparations were
similar. Wound infections occurred in n = 13 (3.42%) pts. in group A vs. n
= 35 (9.46%) in group B. In group A, only 1 patient presented with sternal
dehiscence vs. 22 pts. in group B. In all 22 patients, sternal rewiring
followed by antibiotic therapy was needed. Mediastinitis related mortality
was none in A versus two in B. Treatment failure in group B was more than
five times higher than in A (p = 0.01); the mean length of stay in
hospital was 12.5 +/- 7.4 days (A) versus 18 +/- 15.1 days (B) (p=0.002).
Re-operation for sternal infection was 4 times higher in group B. Mean
ventilation time was relatively longer in B (2.5 vs. 1.28 days) (p =
0.01). The mean follow-up period was 8 weeks (range 6 - 12 weeks). We
demonstrated that using an external supportive sternal corset
(Stern-E-Fix) yields a significantly better and effective prevention
against development of sternal dehiscence and secondary sternal infection
in high-risk poststernotomy patients.

<5>
Accession Number
2013278473
Authors
Wu Y.-C. Zhang J.-F. Shen W.-F. Zhao Q.
Institution
(Wu, Zhang, Zhao) Department of Cardiac Surgery, Rui Jin Hospital,
Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China
(Shen) Department of Cardiology, Rui Jin Hospital, Shanghai Jiao Tong
University School of Medicine, Shanghai 200025, China
Title
Transcatheter aortic valve implantation versus surgical aortic valve
replacement for severe aortic stenosis: A meta analysis.
Source
Chinese Medical Journal. 126 (6) (pp 1171-1177), 2013. Date of
Publication: 20 Mar 2013.
Publisher
Chinese Medical Association (42 Dongsi Xidajie, Beijing 100710, China)
Abstract
Background Transcatheter aortic valve implantation (TAVI) has emerged as
the treatment choice for non-operable patients with severe symptomatic
aortic stenosis (AS) and may be a good alternative to surgery for those at
very high or prohibitive surgical risk. We performed a meta-analysis to
evaluate the comparative benefits of TAVI versus surgical aortic valve
replacement (SAVR) in patients with severe AS. Methods A comprehensive
literature search of PubMed, Embase, ScienceDirect and Cochrane Central
Register of Controlled trials was performed, and randomized trials as well
as cohort studies with propensity score analysis were included. Results
One randomized trial (n=699) and six retrospective cohort studies (n=781)
were selected for meta-analysis. Mortality at 30-day and 1-year follow-up
was comparable between TAVI and SAVR. Despite similar incidences of
stroke, myocardial infarction, re-operation for bleeding, and renal
failure requiring dialysis, TAVI was associated with a lower occurrence
rate of new-onset atrial fibrillation (OR 0.51, 95% CI 0.33-0.78) and
shorter procedural time (mean difference -67.50 minutes, 95% CI -87.20 to
-47.81 minutes). Post-operative aortic regurgitation and permanent
pacemaker implantation were more common in patients after TAVI than in
those with SAVR (OR 5.53, 95% CI 3.41-8.97; OR 1.71, 95% CI 1.02-2.84,
respectively). Conclusion In patients with severe symptomatic AS, TAVI and
SAVR did not differ with respect to short- and mid-term survival, but the
incidence of permanent pacemaker implantation and post-procedural aortic
regurgitation remain relatively high after TAVI.

<6>
Accession Number
2013272421
Authors
Abdel-Meguid M.E.
Institution
(Abdel-Meguid) Department of Anesthesia, Faculty of Medicine, Ain Shams
University, Egypt
(Abdel-Meguid) King Fahad Specialist Hospital, Saudi Arabia
Title
Dexmedetomidine as anesthetic adjunct for fast tracking and pain control
in off-pump coronary artery bypass.
Source
Saudi Journal of Anaesthesia. 7 (1) (pp 6-8), 2013. Date of Publication:
January-March 2013.
Publisher
Medknow Publications and Media Pvt. Ltd (B9, Kanara Business Centre, off
Link Road, Ghatkopar (E), Mumbai 400 075, India)
Abstract
Objective: This study was designed to determine the efficacy of
dexmedetomidine (a highly selective alpha-2 agonist) in achieving fast
tracking and improved postoperative pain control in off-pump coronary
artery bypass (OPCAB) patients. Methods: Thirty patients scheduled for
elective OPCAB were prospectively randomized into two groups: Group I (15
patients) started dexmedetomidine at 0.5 ug/kg/hour after the induction of
anesthesia; this was reduced to 0.3 ug/kg/hour on admission in the cardiac
intensive care unit and continued for 12 hours post extubation. Group II
(15 patients) received a similar volume and infusion rate of normal
saline. Visual analog scale (VAS) of 10-100 was explained thoroughly to
the patients during the preoperative visit. Postoperative pain was managed
with morphine. The total dose of morphine was recorded. Extubation time
and VAS was recorded every two hours for 12 hours post extubation.
Results: Extubation time in group I was 72+/-8 minutes and 186+/-22
minutes in group II. Mean total use of narcotics in group II was
23.5+/-20.7 mg compared to 11.4+/-6.3 mg in group I. VAS median figures
were lower at all data points in group I than in group II. Conclusion:
Dexmedetomidine showed an effective and safe profile as an anesthetic
adjunct in OPCAB, achieving fast tracking of patients and higher quality
of pain control with a lower consumption of narcotics.

<7>
[Use Link to view the full text]
Accession Number
23400891
Authors
Li X. Qi Y. Li Y. Zhang S. Guo S. Chu S. Gao P. Zhu D. Wu Z. Lu L. Shen W.
Jia N. Niu W.
Institution
(Li) State Key Laboratory of Medical Genomics, Ruijin Hospital, School of
Medicine, Shanghai Jiao Tong University, Shanghai, China.
Title
Impact of mineralocorticoid receptor antagonists on changes in cardiac
structure and function of left ventricular dysfunction: a meta-analysis of
randomized controlled trials.
Source
Circulation. Heart failure. 6 (2) (pp 156-165), 2013. Date of Publication:
Mar 2013.
Abstract
A comprehensive evaluation of the benefits of mineralocorticoid receptor
antagonists on cardiac remodeling is lacking. We aimed to evaluate the
impact of mineralocorticoid receptor antagonists on changes in cardiac
structure and function of left ventricular dysfunction. Articles were
identified by online searches in PubMed, EMBASE, Cochrane, and
ClinicalTrials.gov databases before June 2012, by hand searches of reviews
and relevant journals, and by contact with the authors. Qualified articles
were restricted to randomized controlled trials. There were, respectively,
12, 4, and 3 qualified trials that randomized 572, 647, and 407 patients
to spironolactone, canrenoate, and eplerenone, and 531, 655, and 395
patients to placebo or active treatment, respectively. Overall, under
mineralocorticoid receptor antagonist treatment there was improvement in
left ventricular ejection fraction (weighted mean difference, 2.97; 95%
confidence interval [95% CI], 2.26-3.67; P<0.0005), left ventricular
end-systolic and end-diastolic volume index (weighted mean difference,
-5.64; 95% CI, -7.94 to -3.34; P<0.0005 and weighted mean difference,
-7.46; 95% CI, -11.63 to -3.3; P<0.0005), serum amino-terminal peptide of
procollagen type-III (weighted mean difference, -1.12; 95% CI, -1.49 to
-0.74; P<0.0005), B-type natriuretic peptide (weighted mean difference,
-67.06; 95% CI, -91.24 to -42.88; P<0.0005), peak velocities of early
mitral inflow (E; weighted mean difference, -9.57; 95% CI, -12.98 to
-6.17; P<0.0005), and E wave deceleration time (weighted mean difference,
7.08; 95% CI, 4.07-10.09; P<0.0005). There was low probability of
heterogeneity and publication bias. Our findings demonstrate that
mineralocorticoid receptor antagonist treatment may exert beneficial
effects on the reversal of cardiac remodeling and improvement of left
ventricular function.

<8>
[Use Link to view the full text]
Accession Number
23258574
Authors
Maurer M.S. Teruya S. Chakraborty B. Helmke S. Mancini D.
Institution
(Maurer) Columbia University Medical Center, New York, NY, USA.
Title
Treating anemia in older adults with heart failure with a preserved
ejection fraction with epoetin alfa: single-blind randomized clinical
trial of safety and efficacy.
Source
Circulation. Heart failure. 6 (2) (pp 254-263), 2013. Date of Publication:
Mar 2013.
Abstract
Anemia is a common comorbidity in older adults with heart failure and a
preserved ejection fraction and is associated with worse outcomes. We
hypothesized that treating anemia with subcutaneous epoetin alfa would be
associated with reverse ventricular remodeling and improved exercise
capacity and health status compared with placebo. Prospective, randomized,
single-blind, 24-week study with blinded end point assessment among anemic
(average hemoglobin of 10.4+/-1 g/dL) older adult patients (n=56; 77+/-11
years; 68% women) with heart failure and a preserved ejection fraction
(ejection fraction=63+/-15%; B-type natriuretic peptide=431+/-366 pg/mL)
was conducted. Treatment with epoetin alfa resulted in significant
increases in hemoglobin (P<0.0001). Changes in end-diastolic volume
(-6+/-14 versus -4+/-16 mL; P=0.67) at 6 months did not differ between
epoetin alfa and placebo, but declines in stroke volume (-5+/-8 versus
2+/-10 mL; P=0.09) without significant changes in left ventricular mass
were observed. Changes in 6-minute walk distance (16+/-11 versus 5+/-12 m;
P=0.52) did not differ. Although quality of life improved by the Kansas
City Cardiomyopathy Questionnaire and the Minnesota Living with Heart
Failure Questionnaire in both cohorts, there were no significant
differences between groups. Administration of epoetin alfa to older adult
patients with heart failure and a preserved ejection fraction compared
with placebo did not change left ventricular end-diastolic volume and left
ventricular mass nor did it improve submaximal exercise capacity or
quality of life. URL: http://www.clinicaltrials.gov. UNIQUE IDENTIFIER:
NCT00286182.

<9>
Accession Number
2013271803
Authors
Sun Y. Ji B. Zhu X. Zheng Z.
Institution
(Sun, Ji, Zhu) Department of Cardiopulmonary Bypass, State Key Laboratory
of Cardiovascular Disease, Fuwai Hospital, National Center for
Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking
Union Medical College, Beijing, China
(Zheng) Department of Cardiovascular Surgery, State Key Laboratory of
Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular
Diseases, Chinese Academy of Medical Sciences and Peking Union Medical
College, Beijing, China
Title
Efficacy of Carbon Dioxide Insufflation for Cerebral and Cardiac
Protection During Open Heart Surgery: A Systematic Review and
Meta-Analysis.
Source
Artificial Organs. 37 (5) (pp 439-446), 2013. Date of Publication: May
2013.
Publisher
Blackwell Publishing Inc. (350 Main Street, Malden MA 02148, United
States)
Abstract
In spite of widespread application around the world, there has been
controversy on the cerebral and cardiac protection efficacy of carbon
dioxide insufflation (CDI) during open heart surgery. To make a
comprehensive evaluation, we screened all relevant published randomized
controlled trials to perform the first systematic review and meta-analysis
for CDI during open heart surgery. We searched PubMed, EMBASE, the
Cochrane Controlled Clinical Trial register, WANFAN, CQVIP, and CNKI
database for published articles. Randomized controlled trials were
included when the research provided data of neurological complications
postoperatively, creatinine kinase, MB isoenzyme (CK-MB) on the first
postoperative day, or all-cause mortality. We chose a fixed-effects model
when the trials showed low heterogeneity, otherwise a random effects model
was used. The quality of studies was assessed by modified Jadad scale.
Four studies were included in this meta-analysis. The overall pooled
relative risk (RR) for neurological complications was 1.59, 95% confidence
interval (CI)=[0.57, 4.46], and the z-score for overall effect was 0.89
(P=0.37). The standardized mean difference of the CK-MB between groups was
1.15, 95% CI=[-1.27, 3.56], and the z-score for overall effect was 0.93
(P=0.35). The overall pooled RR for all-cause mortality was 0.5, 95%
CI=[0.16, 1.64], and the z-score for overall effect was 1.14 (P=0.25).
There was no significant difference between groups. Because of the
insufficiency of powerful evidences, the cerebral and cardiac protection
efficacy of CDI during open heart surgery needs to be further verified by
more high-quality trials. 2013, International Center for Artificial
Organs and Transplantation and Wiley Periodicals, Inc.

<10>
Accession Number
2013276735
Authors
Taylor S. Margolick J. Abughosh Z. Goldenberg S.L. Lange D. Bowie W.R.
Bell R. Roscoe D. MacHan L. Black P.
Institution
(Taylor, Margolick, Abughosh, Goldenberg, Lange, Bell, Black) Department
of Urologic Sciences, University of British Columbia, Gordon and Leslie
Diamond Health Care Centre, 2775 Laurel Street, Vancouver, BC V5Z 1M9,
Canada
(Bowie) Department of Medicine, University of British Columbia, Vancouver,
Canada
(Roscoe) Department of Pathology and Laboratory Medicine, University of
British Columbia, Vancouver, Canada
(MacHan) Department of Radiology, University of British Columbia,
Vancouver, Canada
Title
Ciprofloxacin resistance in the faecal carriage of patients undergoing
transrectal ultrasound guided prostate biopsy.
Source
BJU International. 111 (6) (pp 946-953), 2013. Date of Publication: May
2013.
Publisher
Blackwell Publishing Ltd (9600 Garsington Road, Oxford OX4 2XG, United
Kingdom)
Abstract
What's known on the subject? and What does the study add? * Transrectal
ultrasound guided prostate biopsies (TRUSBx) are associated with a
spectrum of complications, including most significantly infection, which
affects up to 5% of patients. In the most severe cases, infection leads to
sepsis, a life-threatening complication. Escherichia coli is the primary
responsible pathogen. Although antibiotic prophylaxis with
fluoroquinolones is routinely used, there is evidence that the infection
rate after TRUSBx is increasing, and this appears to be due to an
increasing prevalence of ciprofloxacin-resistant rectal flora. * This is
the largest prospective clinical trial to date analysing the rectal flora
of men undergoing prostate biopsies. We determined the microbial and
antibiotic sensitivity profiles from 849 patients. Ciprofloxacin-resistant
Gram-negative organisms were identified in the rectal flora of 19.0% of
men. Furthermore, fluoroquinolone use within 6 months preceding a TRUSBx
and the presence of a prosthetic heart valve were significant predictors
of ciprofloxacin resistance on rectal swab. Determining the prevalence of
rectal fluoroquinolone resistance has important implications in evaluation
of the suitability of prophylactic regimens. Antimicrobial profiles
derived from rectal swabs pre-biopsy may prove useful in guiding targeted
antibiotic prophylaxis. Objectives To establish the prevalence of
ciprofloxacin-resistant bacteria in patients undergoing transrectal
ultrasound guided prostate biopsies (TRUSBx) and to determine whether this
predicts subsequent infectious complications. To identify risk factors for
harbouring ciprofloxacin-resistant flora. Patients and Methods Any patient
undergoing a TRUSBx from 2009 to 2011 was eligible for enrolment in this
prospective study. Pre-biopsy rectal and urine cultures and post-biopsy
urine cultures were obtained and antimicrobial susceptibility was
determined. Univariate and multivariate analyses were performed to
identify independent patient risk factors associated with
ciprofloxacin-resistant rectal flora. Results A total of 865 patients
underwent TRUSBx, of whom 19.0% were found to have ciprofloxacin-resistant
Gram-negative coliforms. Escherichia coli was the most prevalent
Gram-negative rectal isolate (80.9%) and accounted for 90.6% of
ciprofloxacin resistance. Patient characteristics that conferred an
increased risk of harbouring ciprofloxacin-resistant organisms included a
history of a heart valve replacement (P < 0.05) and ciprofloxacin use in
the past 3 months (P < 0.05). Infectious complications were observed in
3.6% (n = 31) of the patient population and 48% of these patients grew
ciprofloxacin-resistant organisms on the pre-biopsy rectal swab (P <
0.001). Conclusions Antimicrobial resistance to ciprofloxacin in the
rectal flora was common, particularly in patients with recent
ciprofloxacin use and a heart valve replacement. Despite a significant
correlation between those patients who developed infections and the
detection of ciprofloxacin-resistant organisms, only 9.0% (n = 15) of the
total group with ciprofloxacin resistance developed an infectious
complication. Future studies will need to evaluate the cost effectiveness
and clinical utility of a pre-biopsy rectal culture in targeting
antibiotic prophylaxis. 2013 BJU International.

<11>
Accession Number
2013276783
Authors
Eisen H.J. Kobashigawa J. Starling R.C. Pauly D.F. Kfoury A. Ross H. Wang
S.-S. Cantin B. Van Bakel A. Ewald G. Hirt S. Lehmkuhl H. Keogh A. Rinaldi
M. Potena L. Zuckermann A. Dong G. Cornu-Artis C. Lopez P.
Institution
(Eisen) Division of Cardiology, Drexel University College of Medicine,
Hahnemann University Hospital, Philadelphia, PA, United States
(Kobashigawa) Cedars-Sinai Heart Institute, Los Angeles, CA, United States
(Starling) Kaufman Center for Heart Failure, Heart and Vascular Institute,
Cleveland Clinic Foundation, Cleveland, OH, United States
(Pauly) Division of Cardiovascular Medicine, University of Florida,
College of Medicine, Gainesville, FL, United States
(Kfoury) Intermountain Medical Center, Salt Lake City, UT, United States
(Ross) Department of Cardiology/Heart Transplant, University Health
Network, Toronto General Hospital, Toronto, ON, Canada
(Wang) Division of Cardiovascular Surgery, National Taiwan University,
Taipei, Taiwan (Republic of China)
(Cantin) Quebec Heart Institute, Quebec, QC, Canada
(Van Bakel) Medical University of South Carolina, Charleston, SC, United
States
(Ewald) Washington University, School of Medicine, St. Louis, MO, United
States
(Hirt) University Hospital Regensburg, Regensburg, Germany
(Lehmkuhl) German Heart Center Berlin, Berlin, Germany
(Keogh) Heart and Lung Transplant Unit, St. Vincents Hospital,
Darlinghurst, Sydney, Australia
(Rinaldi) Az.Ospedaliero-Universitaria, S.Giovanni Battista di Torino,
Torino, Italy
(Potena) School of Medicine, University of Bologna, Bologna, Italy
(Zuckermann) Department of Cardiothoracic Surgery, University of Vienna,
Vienna, Austria
(Dong) Novartis Pharmaceuticals, East Hanover, NJ, United States
(Cornu-Artis, Lopez) Novartis Pharma AG, Basel, Switzerland
Title
Everolimus versus mycophenolate mofetil in heart transplantation: A
randomized, multicenter trial.
Source
American Journal of Transplantation. 13 (5) (pp 1203-1216), 2013. Date of
Publication: May 2013.
Publisher
Blackwell Publishing Ltd (9600 Garsington Road, Oxford OX4 2XG, United
Kingdom)
Abstract
In an open-label, 24-month trial, 721 de novo heart transplant recipients
were randomized to everolimus 1.5 mg or 3.0 mg with reduced-dose
cyclosporine, or mycophenolate mofetil (MMF) 3 g/day with standard-dose
cyclosporine (plus corticosteroids +/- induction). Primary efficacy
endpoint was the 12-month composite incidence of biopsy-proven acute
rejection, acute rejection associated with hemodynamic compromise, graft
loss/retransplant, death or loss to follow-up. Everolimus 1.5 mg was
noninferior to MMF for this endpoint at month 12 (35.1% vs. 33.6%;
difference 1.5% [97.5% CI: -7.5%, 10.6%]) and month 24. Mortality to month
3 was higher with everolimus 1.5 mg versus MMF in patients receiving
rabbit antithymocyte globulin (rATG) induction, mainly due to infection,
but 24-month mortality was similar (everolimus 1.5 mg 10.6% [30/282], MMF
9.2% [25/271]). Everolimus 3.0 mg was terminated prematurely due to higher
mortality. The mean (SD) 12-month increase in maximal intimal thickness
was 0.03 (0.05) mm with everolimus 1.5 mg versus 0.07 (0.11) mm with MMF
(p < 0.001). Everolimus 1.5 mg was inferior to MMF for renal function but
comparable in patients achieving predefined reduced cyclosporine trough
concentrations. Nonfatal serious adverse events were more frequent with
everolimus 1.5 mg versus MMF. Everolimus 1.5 mg with reduced-dose
cyclosporine offers similar efficacy to MMF with standard-dose
cyclosporine and reduces intimal proliferation at 12 months in de novo
heart transplant recipients. In this study comparing cardiac transplant
recipients receiving one of two doses of everolimus with reduced dose
cyclosporine to patients receiving mycophenolate mofetil with standard
dose cyclosporine, the authors find no effect on acute cellular rejection,
modestly reduced renal function, and a reduction in the incidence and
severity of lesions defined by intravascular ultrasound. See editorial by
Mehra on page 1119. 2013 The American Society of Transplantation and the
American Society of Transplant Surgeons.

<12>
Accession Number
2013273380
Authors
Aghadavoudi O. Ameli Zamani K. Farajzadegan Z.
Institution
(Aghadavoudi) Department of Anesthesiology, School of Medicine, Isfahan
University of Medical Sciences, Isfahan, Iran, Islamic Republic of
(Ameli Zamani) School of Medicine AND Student Research Committee, Isfahan
University of Medical Sciences, Isfahan, Iran, Islamic Republic of
(Farajzadegan) Department of Community Medicine, School of Medicine,
Isfahan University of Medical Sciences, Isfahan, Iran, Islamic Republic of
Title
Comparing the effects of hydroxy ethyl starch 6% and gelatin as
replacement for prime during coronary artery bypass graft surgery.
Source
Journal of Isfahan Medical School. 31 (223) , 2013. Date of Publication:
April 2013.
Publisher
Isfahan University of Medical Sciences (Hezar Jerib Avenue, P.O. Box
81745-319, Isfahan, Iran, Islamic Republic of)
Abstract
Background: Several fluids have been used in priming the cardiopulmonary
pump in coronary artery bypass graft surgery (CABG). Hydroxy-ethyl starch
6% (HES 6%) is a new colloid fluid which is widely used as a substitute
for intraoperative fluid. Gelatin is also a commonly used colloid fluid
for priming. However, it has some adverse effects, especially on the
coagulation system. Methods: In this clinical trial, patients were
randomized into two groups of HES 6% and gelatin. Prothrombin time (PT),
partial thromboplastin time (PTT), and international normalized ratio
(INR) were measured before surgery and immediately and 24 hours after the
operation. Chest drainage (CD) was measured 24 hours after the operation.
Urine output (UO) was measured during the first 24 postoperative hours.
Blood urea nitrogen (BUN) and creatinine were measured before and 24 hours
after surgery. Data was analyzed with SPSS. Findings: Totally 100 patients
were recruited for this study. CD was not significantly different between
HES 6% and gelatin groups. In the HES and gelatin groups the UO was also
not significantly different. PT and INR did not show any significant
difference betwean the two groups before, at the end and 24 hours after
surgery, however PTT was significantly higher(p-value=0.05) in gelatin
group only at the end of surgery(30.6+/- 5.7,44 +/- 27,37 +/- 19 for HES
vs 30.5 +/- 5.7,56 +/- 35,37 +/- 23 for gelatin respectively). BUN was
only significantly higher in HES group 24 hours after surgery (19.9 +/-9.8
vs 16.4 +/- 7.6, Pvalue = 0.05). Cr did not differ. Conclusion: HES and
gelatine are both options for prime in cardiopulmonary pomp,with adverse
effect on renal function and coagulation respectively.more studies with
larger sample sizes are recommended.

<13>
Accession Number
2013274154
Authors
Head S.J. Osnabrugge R.L.J. Howell N.J. Freemantle N. Bridgewater B.
Pagano D. Pieter Kappetein A.
Institution
(Head, Osnabrugge, Pieter Kappetein) Department of Cardiothoracic Surgery,
Erasmus University Medical Center, Rotterdam, Netherlands
(Howell, Pagano) Department of Cardiothoracic Surgery and Quality and
Outcomes Research Unit, University Hospital Birmingham, Birmingham, United
Kingdom
(Howell) School of Clinical and Experimental Medicine, University of
Birmingham, Birmingham, United Kingdom
(Freemantle) Department of Primary Care and Population Health, University
College London, London, United Kingdom
(Bridgewater) Department of Cardiothoracic Surgery, Manchester Academic
Health Science Centre University of Manchester, University Hospital of
South Manchester, Manchester, United Kingdom
Title
A systematic review of risk prediction in adult cardiac surgery:
Considerations for future model development.
Source
European Journal of Cardio-thoracic Surgery. 43 (5) (pp e121-e129), 2013.
Article Number: ezt044. Date of Publication: May 2013.
Publisher
Oxford University Press (Great Clarendon Street, Oxford OX2 6DP, United
Kingdom)
Abstract
Objectives: Risk prediction in adult patients undergoing cardiac surgery
remains inaccurate and should be further improved. Therefore, we aimed to
identify risk factors that are predictive of mortality, stroke, renal
failure and/or length of stay after adult cardiac surgery in contemporary
practice. Methods: We searched the Medline database for English-language
original contributions from January 2000 to December 2011 to identify
preoperative independent risk factors of one of the following outcomes
after adult cardiac surgery: death, stroke, renal failure and/or length of
stay. Two investigators independently screened the studies. Inclusion
criteria were (i) the study described an adult cardiac patient population;
(ii) the study was an original contribution; (iii) multivariable analyses
were performed to identify independent predictors; (iv) >=1 of the
predefined outcomes was analysed; (v) at least one variable was an
independent predictor, or a variable was included in a risk model that was
developed. Results: The search yielded 5768 studies. After the initial
title screening, a second screening of the full texts of 1234 studies was
performed. Ultimately, 844 studies were included in the systematic review.
In these studies, we identified a large number of independent predictors
of mortality, stroke, renal failure and length of stay, which could be
categorized into variables related to: disease pathology, planned surgical
procedure, patient demographics, patient history, patient comorbidities,
patient status, blood values, urine values, medication use and gene
mutations. Many of these variables are frequently not considered as
predictive of outcomes. Conclusions: Risk estimates of mortality, stroke,
renal failure and length of stay may be improved by the inclusion of
additional (non-traditional) innovative risk factors. Current and future
databases should consider collecting these variables. The Author 2013.
Published by Oxford University Press on behalf of the European Association
for Cardio-Thoracic Surgery. All rights reserved.

<14>
Accession Number
2013274116
Authors
Brunelli A. Salati M. Pompili C. Refai M. Sabbatini A.
Institution
(Brunelli, Salati, Pompili, Refai, Sabbatini) Division of Thoracic
Surgery, Ospedali Riuniti Ancona, Ancona, Italy
(Brunelli) Section of Minimally Invasive Thoracic Surgery, Division of
Thoracic Surgery, Ospedali Riuniti Ancona, Ancona, Italy
Title
Regulated tailored suction vs regulated seal: A prospective randomized
trial on air leak duration.
Source
European Journal of Cardio-thoracic Surgery. 43 (5) (pp 899-904), 2013.
Article Number: ezs518. Date of Publication: May 2013.
Publisher
Oxford University Press (Great Clarendon Street, Oxford OX2 6DP, United
Kingdom)
Abstract
Objective: The objective of this study was to compare the air leak
duration of two regulated chest tube modes following pulmonary lobectomy.
Methods: This is a prospective randomized trial on 100 consecutive
pulmonary lobectomies (2010-11) performed for lung cancer. A single
24-French chest tube was connected to an electronic system capable of
maintaining the pleural pressure within preset values (regulated suction
mode) or within a physiological range (regulated seal mode). Patients were
randomized to two groups: Group 1, regulated individualized suction
(range: -11 to -20 cmH<sub>2</sub>O, according to lobectomy type); Group
2, regulated seal (-2 cmH<sub>2</sub>O). The main endpoint was the
duration of air leak (h) calculated from the end of the operation to a
value consistently below 20 ml/min. Patients with prolonged air leak (>168
h) were connected to a portable device before discharge. Their air leak
duration was considered as 192 h. The sample size was calculated to detect
1-day difference in air leak duration with a statistical power of 80%.
Results: The two groups were well matched for several baseline and
surgical characteristics. No crossovers occurred between groups. The
average air leak duration (Group 1: 28 vs Group 2: 22.2, P = 0.6), and the
number of patients with prolonged air leak (Group 1: 5 vs Group 2: 4, P =
0.7) and with other complications (Group 1: 6 patients vs Group 2: 7
patients, P = 0.9) were similar between the groups. Sixteen patients of
Group 1 and 21 of Group 2 had an air leak present immediately after
extubation. Among them, patients of Group 2 (regulated seal) had an air
leak lasting 34.5 h less than those of Group 1 (regulated suction) (52.9
vs 87.4, P = 0.07). Conclusions: Regulated seal is as effective and safe
as regulated suction in managing chest tubes following lobectomy. This
information demonstrates with objective data the non-superiority of
regulated suction vs regulated seal and may assist in future
investigations on regulated pleural pressure. The Author 2012. Published
by Oxford University Press on behalf of the European Association for
Cardio-Thoracic Surgery. All rights reserved.

<15>
Accession Number
2013255898
Authors
Prasad A. Gossl M. Hoyt J. Lennon R.J. Polk L. Simari R. Holmes Jr. D.R.
Rihal C.S. Lerman A.
Institution
(Prasad, Gossl, Hoyt, Polk, Simari, Holmes Jr., Rihal, Lerman) Division of
Cardiovascular Diseases, Department of Internal Medicine, Mayo Clinic and
Mayo Foundation, 200 First Street SW, Rochester, MN 55905, United States
(Lennon) Division of Biomedical Statistics and Informatics, Mayo Clinic
and Mayo Foundation, Rochester MN, United States
Title
Remote ischemic preconditioning immediately before percutaneous coronary
intervention does not impact myocardial necrosis, inflammatory response,
and circulating endothelial progenitor cell counts: A single center
randomized sham controlled trial.
Source
Catheterization and Cardiovascular Interventions. 81 (6) (pp 930-936),
2013. Date of Publication: May 2013.
Publisher
Wiley-Liss Inc. (111 River Street, Hoboken NJ 07030-5774, United States)
Abstract
Aims: Percutaneous coronary intervention (PCI) is frequently accompanied
by myocardial injury. The present study was performed to determine whether
remote ischemic preconditioning (IP) induces cardioprotection during PCI.
Methods: We enrolled 95 patients requiring nonemergency PCI for stable
disease or unstable angina into this prospective clinical trial. Patients
were randomized to either remote IP (induced by three 3-min cycles of
blood pressure cuff inflations to 200 mm Hg around the upper arm, followed
by 3-min of reperfusion n = 47) or sham control (n = 48) immediately
preceding PCI. The primary outcome measure was the frequency of post-PCI
myonecrosis, defined as a peak postprocedural cTnT T >=0.03 ng/dL.
Secondary outcome measures were the change in plasma high-sensitivity
C-reactive protein (hsCRP) levels following PCI and in endothelial
progenitor cells (EPC) counts following IP. Results: There was no
difference in the primary endpoint of the frequency of PCI related
myonecrosis which occurred in 22 (47%) and 19 (40%) patients in the remote
IP and control groups, respectively, P = 0.42. There was significant
increase in hsCRP post-PCI in both groups (P < 0.001), but there was no
difference between the groups (median %change in hsCRP 46% vs. 54%, P =
0.73). There was no significant change in circulating early (CD34
-/CD133+/KDR+), intermediate (CD34+/CD133+/KDR+), or late
(CD34+/CD133-/KDR+) EPC in the two groups immediately following IP. The
composite rate of death, myocardial infarction, and target lesion
revascularization at 1 year was 14.1% versus 13.7% (P = 0.90).
Conclusions: Our study indicates that remote IP immediately before PCI
does not induce cardioprotection in low to moderate risk patients. 2012
Wiley Periodicals, Inc.

<16>
[Use Link to view the full text]
Accession Number
23460569
Authors
Moerman A. Bove T. Francois K. Jacobs S. Deblaere I. Wouters P. De Hert S.
Institution
(Moerman) Department of Anesthesiology, Ghent University Hospital, De
Pintelaan 185, 9000 Gent, Belgium.
Title
Society of cardiovascular anesthesiologists: the effect of blood pressure
regulation during aortic coarctation repair on brain, kidney, and muscle
oxygen saturation measured by near-infrared spectroscopy: a randomized,
clinical trial.
Source
Anesthesia and analgesia. 116 (4) (pp 760-766), 2013. Date of Publication:
Apr 2013.
Abstract
In this study, we compared the effects of 3 frequently used arterial blood
pressure-regulating agents on brain (rScO2), renal (SrO2), and muscle
(SmO2) oxygen saturation, during aortic coarctation repair in children.
Based on the reported adverse effect of sodium nitroprusside (SNP) on
left-sided rScO2 during aortic coarctation repair, we tested the
hypothesis that the alterations in left rScO2 occurring with SNP would not
be present with sevoflurane and nitroglycerin (NTG). Additionally, we
explored the effects of blood pressure regulation with SNP, NTG, or
sevoflurane on right-sided rScO2, SrO2, and SmO2. Children with isolated
aortic coarctation undergoing surgical repair through a left thoracotomy
without the use of cardiopulmonary bypass were considered eligible for the
study. During aortic cross-clamping, control of mean arterial blood
pressure (MAP) was conducted according to randomization by the use of SNP,
NTG, or sevoflurane to obtain a mean target right brachial blood pressure
of 120% to 150% of the MAP value before cross-clamping. Bilateral rScO2,
SrO2, and SmO2 were recorded continuously with near-infrared spectroscopy.
As a primary end point, the maximal relative change in left-sided rScO2 in
response to aortic cross-clamping was compared among treatment groups. Ten
patients per group were included. No significant difference among
treatment groups was observed in maximal relative change in left-sided
rScO2 (SNP versus sevoflurane: mean difference -0.7%, 99% confidence
interval [CI] -31% to 29%, P = 1.0; SNP versus NTG: mean difference -1.8%,
99% CI -32% to 28%, P = 1.0; sevoflurane versus NTG: mean difference
-1.1%, 99% CI -31% to 29%, P = 1.0). Additional analyses also detected no
difference between groups in right rScO2 (P = 0.4). Compared with NTG,
treatment with SNP resulted in a significantly larger (-64% +/- 17% vs
-34% +/- 25%, P = 0.01) and faster (-9 +/- 4 %min(-1) vs -4 +/- 3
%min(-1), P = 0.004) decrease in SmO2. Right-sided rScO2 and MAP showed a
poor correlation for NTG (r = -0.2, P = 0.93), whereas borderline for
sevoflurane (r = 0.44, P = 0.09) and SNP (r = 0.56, P = 0.04). The mean
differences in left-sided rScO2 among the patients treated with SNP, NTG,
or sevoflurane for proximal hypertension during aortic cross-clamping were
no more than 32%. Additional analysis demonstrated a low MAP-rScO2
dependence with the use of NTG. Because NTG also resulted in a smaller and
slower decrease of oxygen saturation in peripheral tissues, our data
suggest that its use might be preferable for proximal blood pressure
control during surgical procedures involving aortic cross-clamping.

<17>
Accession Number
2013130259
Authors
Navarese E.P. Gurbel P.A. Andreotti F. Tantry U. Jeong Y.-H. Kozinski M.
Engstrom T. di Pasquale G. Kochman W. Ardissino D. Kedhi E. Stone G.W.
Kubica J.
Institution
(Navarese, Kozinski, Kubica) Department of Cardiology and Internal
Medicine, Ludwik Rydygier Collegium Medicum, Nicolaus Copernicus
University, Sklodowskiej-Curie Street No. 9, 85-094 Bydgoszcz, Poland
(Gurbel, Tantry, Jeong) Center for Thrombosis Research, Cardiac
Catheterization Laboratory, 2401 West Belvedere Avenue, Baltimore, MD
21215, United States
(Andreotti) Department of Cardiovascular Sciences, Catholic University,
Largo A. Gemelli 8, 00168 Rome, Italy
(Engstrom) Cardiac Catheterization Laboratory, Department of Cardiology,
The Heart Center, Rigshospitalet, Copenhagen 2100, Denmark
(di Pasquale) Unita Operativa di Cardiologia, Ospedale Maggiore, Largo
Bartolo Nigrisoli 2, 40133 Bologna, Italy
(Kochman) Faculty of Health Sciences, Medical University of Gdansk,
Swissmed Hospital, 44 Wilenska Street, 80-215 Gdansk, Poland
(Ardissino) Unita Operativa di Cardiologia, Azienda Ospedaliero
Universitaria di Parma, Via Gramsci 14, 43100 Parma, Italy
(Kedhi) Department of Cardiology, Maasstadziekenhuis, Maasstadweg, 3079DZ
Rotterdam, Netherlands
(Stone) Columbia University Medical Center, New York-Presbyterian
Hospital, The Cardiovascular Research Foundation, New York, NY 10022,
United States
Title
Optimal timing of coronary invasive strategy in non-ST-segment elevation
acute coronary syndromes: A systematic review and meta-analysis.
Source
Annals of Internal Medicine. 158 (4) (pp 261-270), 2013. Date of
Publication: 19 Feb 2013.
Publisher
American College of Physicians (190 N. Indenpence Mall West, Philadelphia
PA 19106-1572, United States)
Abstract
Background: The optimal timing of coronary intervention in patients with
non-ST-segment elevation acute coronary syndromes (NSTE-ACSs) is a matter
of debate. Conflicting results among published studies partly relate to
different risk profiles of the studied populations. Purpose: To do the
most comprehensive meta-analysis of current evidence on early versus
delayed invasive treatment in NSTE-ACS. Data Sources: MEDLINE, PubMed
Central, and Google Scholar databases; conference proceedings;
ClinicalTrials.gov registry; and Current Controlled Trials registry
through May 2012. Study Selection: Available randomized, controlled trials
(RCTs) and observational studies comparing early versus delayed
intervention in the NSTE-ACS population. Data Extraction: Data were
extracted for populations, interventions, outcomes, and risk of bias.
All-cause mortality was the prespecified primary end point. The longest
follow-up available in each study was chosen. The odds ratio with 95% CI
was the effect measure. Data Synthesis: Seven RCTs (5370 patients) and 4
observational studies (77 499 patients) were included. Early intervention
was less than 20 hours after hospitalization or randomization for RCTs and
24 hours or less for observational studies. Meta-analysis of the RCTs was
inconclusive for a survival benefit associated with the early invasive
strategy (odds ratio, 0.83 [95% CI, 0.64 to 1.09]; P = 0.180); a similar
result emerged from the observational studies. With early versus late
intervention, the odds ratios in the RCTs were 1.15 (CI, 0.65 to 2.01; P =
0.63) and 0.76 (CI, 0.56 to 1.04; P = 0.090) for myocardial infarction and
major bleeding during follow-up, respectively. Limitation: Current
evidence from RCTs is limited by the small overall sample size, low
numbers of events in some trials, and heterogeneity in the timing of
intervention and in patient risk profiles. Conclusion: At present, there
is insufficient evidence either in favor of or against an early invasive
approach in the NSTE-ACS population. A more definitive RCT is warranted to
guide clinical practice. Primary Funding Source: None. 2013 American
College of Physicians.

<18>
Accession Number
2013271639
Authors
Lomivorotov V.V. Efremov S.M. Shmirev V.A. Ponomarev D.N. Svyatchenko A.V.
Deryagin M.N. Lomivorotov V.N. Karaskov A.M.
Institution
(Lomivorotov, Efremov, Shmirev, Ponomarev, Svyatchenko, Deryagin,
Lomivorotov, Karaskov) Research Institute of Circulation Pathology,
Rechkunovskaya Street 15, Novosibirsk 630055, Russian Federation
Title
Does Glutamine Promote Benefits for Patients With Diabetes Mellitus
Scheduled for Cardiac Surgery?.
Source
Heart Lung and Circulation. 22 (5) (pp 360-365), 2013. Date of
Publication: May 2013.
Publisher
Elsevier Ltd (Langford Lane, Kidlington, Oxford OX5 1GB, United Kingdom)
Abstract
Background: We hypothesised, that perioperative use of
N(2)-l-alanyl-l-glutamine confers cardioprotection and improves insulin
resistance in diabetic patients with coronary artery disease operated
under cardiopulmonary bypass. Methods: This double-blind,
placebo-controlled, randomised study included 64 patients with diabetes
mellitus type 2 who were scheduled for on-pump coronary artery bypass
graft surgery. The protocol group (32 patients) and the control group (32
patients) glutamine (0.4g/kg/day of 20% solution of
N(2)-l-alanyl-l-glutamine (" Dipeptiven<sup></sup>" Fresenius Kabi,
Germany)) and placebo (0.9% NaCl), respectively. Perioperative
concentration of troponin I in plasma was considered as the primary
end-point. Whereas the secondary end-points were insulin resistance,
insulin sensitivity, beta-cell function, blood glucose, plasma
triglycerides and free fatty acids concentrations. Insulin resistance,
insulin sensitivity and beta-cell function were measured using HOMA
equation. Thermodilution method was used to measure haemodynamics in all
the patients. Results: No differences have been found in perioperative
dynamics of troponin I, insulin resistance, insulin sensitivity, beta-cell
function, blood glucose, plasma triglycerides free fatty acids
concentrations and haemodynamics. Conclusion: Our results have failed to
confirm the cardioprotective properties and modulatory effect on
perioperative insulin resistance that are thought to be attributable to
parenteral glutamine administration in dose 0.4. g/kg/day among cardiac
patients with DM operated on under CPB. 2012 Australian and New Zealand
Society of Cardiac and Thoracic Surgeons (ANZSCTS) and the Cardiac Society
of Australia and New Zealand (CSANZ).

<19>
Accession Number
23488362
Authors
Cossette S. Frasure-Smith N. Robert M. Chouinard M.C. Juneau M. Guertin
M.C. Cournoyer A. Mailhot T. Kayser J.W.
Institution
(Cossette) Montreal Heart Institute Research Centre, R-2231, 5000,
Belanger est, Montreal, QC H1T 1C8.
Title
A pilot randomized trial of a smoking cessation nursing intervention in
cardiac patients after hospital discharge.
Source
Canadian journal of cardiovascular nursing = Journal canadien en soins
infirmiers cardio-vasculaires. 22 (4) (pp 16-26), 2012. Date of
Publication: 2012 Fall.
Abstract
One fifth of Canadians are smokers despite the availability of
community-based smoking cessation programs. It was hypothesized that
offering a post-discharge smoking cessation program to cardiac patients
would decrease smoking rates at six months. This pilot randomized study
explored the feasibility, acceptability and preliminary efficacy of a
smoking cessation intervention delivered by a smoking cessation nurse
specialist (SCNS) to cardiac patients after hospital discharge.
Participants (N=40) were randomized to either a postdischarge telephone
intervention delivered weekly for the first month and then monthly until
the third month (experimental group [EG]), or referral to usual community
care (control group [CG]). The researchers confirmed the feasibility of
recruitment and acceptability of the intervention, but dfficulty with
follow-up. The intention-to-treat analysis showed similar smoking
cessation rates in both groups at six months (25% EG versus 30% CG; p =
0.72). An intensifed follow-up protocol, or a more intensive,
comprehensive and multidisciplinary intervention might be required, given
the characteristics of the smokers.

<20>
Accession Number
23488361
Authors
Goldie C.L. Prodan-Bhalla N. Mackay M.
Institution
(Goldie) School of Nursing, University of British Columbia, 302-6190
Agronomy Road, Vancouver, BC V6T 1Z3.
Title
Nurse practitioners in postoperative cardiac surgery: are they effective?.
Source
Canadian journal of cardiovascular nursing = Journal canadien en soins
infirmiers cardio-vasculaires. 22 (4) (pp 8-15), 2012. Date of
Publication: 2012 Fall.
Abstract
High demand for acute care nurse practitioners (ACNPs) in Canadian
postoperative cardiac surgery settings has outpaced methodologically
rigorous research to support the role. To compare the effectiveness of
ACNP-led care to hospitalist-led care in a postoperative cardiac surgery
unit in a Canadian, university-affiliated, tertiary care hospital.
Patients scheduled for urgent or elective coronary artery bypass and/or
valvular surgery were randomly assigned to either ACNP-led (n=22) or
hospitalist-led (n=81) postoperative care. Both ACNPs and hospitalists
worked in collaboration with a cardiac surgeon. Outcome variables included
length of hospital stay, hospital readmission rate, postoperative
complications, adherence to follow-up appointments, attendance at cardiac
rehabilitation and both patient and health care team satisfaction.
Baseline demographic characteristics were similar between groups except
more patients in the ACNP-led group had had surgery on an urgent basis (p
< or = 0.01), and had undergone more complicated surgical procedures (p <
or =0.01). After discharge, more patients in the hospitalist-led group had
visited their family doctor within a week (p < or =0.02) and measures of
satisfaction relating to teaching, answering questions, listening and pain
management were higher in the ACNP-led group. Although challenges in
recruitment yielded a lower than anticipated sample size, this study
contributes to our knowledge of the ACNP role in postoperative cardiac
surgery. Our findings provide support for the ACNP role in this setting as
patients who received care from an ACNP had similar outcomes to
hospitalist-led care and reported greater satisfaction in some measures of
care.

<21>
Accession Number
71058023
Authors
Kobashigawa J. Kittleson M. Rafiei M. Osborne A. Chang D. Czer L. Patel J.
Institution
(Kobashigawa, Kittleson, Rafiei, Osborne, Chang, Czer, Patel) Cedars-Sinai
Heart Institute, Los Angeles, CA, United States
Title
Atg induction for sensitized patients who have undergone heart transplant:
Is it beneficial?.
Source
American Journal of Transplantation. Conference: 13th American Transplant
Congress, ATC 2013 Seattle, WA United States. Conference Start: 20130518
Conference End: 20130522. Conference Publication: (var.pagings). 13 (pp
457), 2013. Date of Publication: April 2013.
Publisher
Blackwell Publishing Ltd
Abstract
BACKGROUND: Heart transplant recipients who are sensitized pre-transplant
are at increased risk for the development of antibody mediated and
cellular rejection post transplantation. The use of induction therapy with
anti-thymocyte globulin (ATG) may reduce the incidence of antibody
mediated rejection (AMR), but this has not been formally studied in a
randomized controlled trial. The purpose of this study was to determine
the impact of ATG induction on the incidence of AMR in a large
single-center experience.METHODS: We identified 170 heart transplant (HTx)
patients transplanted between January 1994 and October 2011, with
pre-transplant panel reactive antibodies (PRA) >10%. Induction therapy was
given based on the treating physician's preference. One-year outcomes were
assessed, including the incidence of treated rejection and
pathology-defined AMR.RESULTS: Of the 170 HTx, 91 received ATG induction
and 79 did not. The mean pre-transplant PRA was significantly higher in
the ATG group (59 +/- 31% vs 43 +/- 32%, p=0.0015). In the ATG induction
group, there were fewer treated rejection episodes (14% vs 30%, p= 0.010)
and fewer pathology-defined AMR episodes (12% vs 26%, p=0.016). There was
no difference in the incidence of cellular rejection (12% in both groups).
CONCLUSION: ATG induction therapy for sensitized patients results in fewer
treated rejection episodes and a decreased incidence of pathology-defined
AMR. This suggests that ATG induction may be beneficial in sensitized
patients, but the results should be confirmed with a randomized trial.f.

<22>
Accession Number
71057353
Authors
Guo Z. Ju W. Wang P. He M. Deng S. He X.
Institution
(Guo, Ju, Wang, He, Deng, He) Organ Transplant Center, First Affiliated
Hospital, Sun Yat-sen University, Guangzhou, China
Title
The effect of gender on transplant outcomes: A meta-analysis.
Source
American Journal of Transplantation. Conference: 13th American Transplant
Congress, ATC 2013 Seattle, WA United States. Conference Start: 20130518
Conference End: 20130522. Conference Publication: (var.pagings). 13 (pp
264-265), 2013. Date of Publication: April 2013.
Publisher
Blackwell Publishing Ltd
Abstract
Purpose: Although the effects of donor-recipient gender matching on
transplant outcomes have been discussed for long, no widely-accepted
consensus has been reached. We conducted a meta-analysis to
comprehensively reevaluate how gender matching affects transplant outcomes
in major organ transplantations. 18Methods: PubMed/Medline, Embase, and
Cochrane library databases were searched for relevant studies. Twelve
studies (174177 patients) for kidney, 3 studies (28812 patients) for
liver, and 4 studies (19184 patients) for heart transplantation comparing
transplant outcomes between gender match and mismatch groups, or among the
four donor to recipient gender pairs were included. The primary outcome
were graft and patient survival.Results: We found it consistent in kidney,
heart, liver transplantation that compared with donor/recipient gender
match group, donor/recipient gender mismatch was associated with
significantly worse 1-, 3-, 5-year graft or patient survival. However,
gender mismatch had no deleterious effects on delayed graft function (DGF)
in kidney transplantation. The interaction between donor and recipient
gender is responsible for transplant outcomes. Male donor to male
recipient pairing is most advantageous for 5-year outcome, while female
donor to male recipient pairing have worst prognosis in both kidney and
liver transplantation.Conclusion: Gender matching greatly affects
transplant outcomes in major organ transplantation, which should be
considered when organs are allocated. (Table presented).

<23>
Accession Number
71053282
Authors
Corley A. Caruana L. Barnett A. Fraser J.
Institution
(Corley, Caruana, Barnett, Fraser) Prince Charles Hospital, Institute of
Health and Biomedical Innovation, Queensland University of Technology,
Brisbane, QLD, Australia
Title
Open and closed suctioning result in significant lung derecruitment: A
randomised controlled study using electrical impedance tomography.
Source
Anaesthesia and Intensive Care. Conference: Intensive Care Annual
Scientific Meeting of the Australian and New Zealand Intensive Care
Society, ANZICS and Australian College of Critical Care Nurses, ACCN 2010
Melbourne, VIC Australia. Conference Start: 20101014 Conference End:
20101016. Conference Publication: (var.pagings). 38 (6) (pp 1119-1120),
2010. Date of Publication: November 2010.
Publisher
Australian Society of Anaesthetists
Abstract
Airway suctioning is essential in airway management for mechanically
ventilated patients but is associated with lung de-recruitment. There is a
deficiency of high quality evidence investigating the effects of open
suction (OS) compared to closed suction (CS) in the area of lung volume
loss. Lung volumes can be safely and accurately determined by measuring
lung impedance using electrical impedance tomography (EIT). The aim of
this prospective observational randomised controlled study was to compare
lung volume changes during OS and CS, and end expiratory lung volume
(EELV) 30 minutes post each suction. Twenty post-cardiac surgical patients
were recruited. Both OS and CS were tested in randomised order for each
participant. Baseline end expiratory lung impedance (EELI) measures were
compared with EELI measures during each suction manoeuvre in addition to
30 minutes post-suction to determine lung volume loss. A mixed model using
a pair-wise estimate of means was used to determine the effect of OS and
CS on EELI. EELI reduced by -2405 impedance units (95% CI 2103, 2708; P
value <0.001) from baseline during OS and by -1645 (95% CI 1360, 1930; P
value <0.001) during CS. Thirty minutes after suctioning, EELI was 452
impedance units (95% CI 273, 633; P value <0.001) lower than baseline in
OS, and 726 units (95% CI 548, 904; P value <0.001) lower than baseline in
CS. Both OS and CS reduce expiratory lung volumes by a significant amount.
CS appears not to be protective against de-recruitment, even after 30
minutes. Consideration should be given to restoring EELV after suctioning
via a recruitment manoeuvre.

<24>
Accession Number
71052652
Authors
Shorrock D. Michael T. Patel V. Rangan B. Abdullah S. Banerjee S. Brilakis
E.
Institution
(Shorrock, Rangan) Dallas Veterans Affairs Medical Center, United States
(Michael, Patel, Abdullah) University of Texas Southwestern Medical
Center, United States
(Banerjee, Brilakis) VA North Texas Healthcare System, University of Texas
Southwestern Medical Ce, United States
Title
Frequency and outcomes of aortocoronary dissection during percutaneous
coronary intervention of chronic total occlusions: A case series and
systematic review of the literature.
Source
Catheterization and Cardiovascular Interventions. Conference: 36th Annual
Scientific Sessions of the Society for Cardiovascular Angiography and
Interventions', SCAI Orlando, FL United States. Conference Start: 20130508
Conference End: 20130511. Conference Publication: (var.pagings). 81 (pp
S48), 2013. Date of Publication: May 2013.
Publisher
Wiley-Liss Inc.
Abstract
Background: Aortocoronary dissection can complicate percutaneous coronary
intervention (PCI) of chronic total occlusions (CTOs). Methods: We
retrospectively examined the frequency and outcomes of aortocoronary
dissection among 336 consecutive CTO PCIs performed at our institution
between 2005 and 2012 and performed a systematic review of the published
literature. Results: Aortocoronary dissection occurred in 6 patients
(1.8%, 95% confidence intervals 0.7%, 3.8%). All aortocoronary dissections
occurred in the right coronary artery (CTO target vessel in 5 patients and
donor vessel in 1 patient. The baseline clinical characteristics of
patients with and without aortocoronary dissection were similar. Compared
to patients without, those with aortocoronary dissection were more likely
to undergo crossing attempts using the retrograde approach (25% vs. 67%, P
= 0.036) and experience a major complication (2.4% vs. 33.3%, p = 008).
Technical and procedural success rates were similar in both groups. Of the
6 patients with aortocoronary dissection one underwent emergency coronary
bypass graft surgery, 4 were treated with ostial stenting and one was
treated conservatively without subsequent adverse clinical outcomes.
Systematic literature review provided 107 published cases of aortocoronary
dissection during PCI, that occurred mainly in the right coronary artery
(74.8%) and were treated with stenting (49.5%), emergency coronary bypass
graft surgery (29%) or conservatively (21.5%). Conclusion: Aortocoronary
dissection is an infrequent complication of retrograde CTO PCI and
although it can be treated with stents in most patients it may
infrequently require emergency coronary artery bypass graft surgery.

<25>
Accession Number
71052638
Authors
Garg N. Uretsky B. Ahmed Z. Hakeem A.
Institution
(Garg, Uretsky, Ahmed, Hakeem) UAMS, United States
Title
Comparative effectiveness of PCI with drug eluting stents vs. CABG for
multi-vessel CAD in diabetic patients- meta analysis of randomized
controlled trials.
Source
Catheterization and Cardiovascular Interventions. Conference: 36th Annual
Scientific Sessions of the Society for Cardiovascular Angiography and
Interventions', SCAI Orlando, FL United States. Conference Start: 20130508
Conference End: 20130511. Conference Publication: (var.pagings). 81 (pp
S39), 2013. Date of Publication: May 2013.
Publisher
Wiley-Liss Inc.
Abstract
Background: Coronary artery bypass grafting (CABG) has been compared to
percutaneous coronary intervention (PCI) for multi-vessel disease (MVD)
using drug eluting stents (DES) in diabetic patients in recent randomized
clinical trials (RCTs). We performed meta-analysis of these RCTs. Methods:
RCTs comparing PCI with DES vs. CABG in diabetic patients with MVD were
included. The primary endpoint was a composite of death, MI and stroke as
reported in the primary trials. Effects of both revascularization
strategies were analyzed by calculating pooled estimates for death from
any cause, MI, repeat revascularization, and stroke. Separate analyses
were performed for each outcome by using risk ratio (RR) by fixed and
random effects models. Heterogeneity among studies was assessed by
calculating I<sup>2</sup> measure of inconsistency. Results: Three studies
with a total of 2862 patients met inclusion criteria (1440 PCI vs. 1422 in
CABG arm). Incidence of the primary outcome was 18.8% in PCI arm and 14%
in CABG arm, (RR-1.33, 95%CI 1.12-1.57, P = 0.0008), at a mean follow up
of three years. Similar results were obtained for death (10.6% vs. 7.5%,
RR 1.39, 95% CI 1.10-1.75, P = 0.006), and MI (9.4% vs. 5%, RR 2.71; 95%
CI 1.41-2.46, P < 0.0001). Stroke risk was significantly higher in the
CABG group (1.8% vs. 3.6%, RR 0.52; 95% CI 0.33-0.84, P < 0.007). PCI was
associated with several fold higher risk of subsequent revascularization
compared to CABG (14% vs. 5.1%, OR 3.0 (95% CI 2.27-3.98; p < 0.00001).
There was no heterogeneity amongst the trials for any of these endpoints
(I<sup>2</sup> = 0% for all comparisons). Conclusion: These data strongly
suggest thatCABG in diabetic patients with MVD is superior to MVD PCI with
DES. CABG decreased overall death, non-fatal myocardial infarction, and
repeat revasculariza-tion at the expense of increase in stroke risk.

<26>
Accession Number
71052629
Authors
Khan M. Wendel C. Thai H. Movahed M.
Institution
(Khan, Wendel, Thai, Movahed) Southern Arizona VA Health Care System,
United States
Title
Failed percutaneous recanalization of chronic total occlusion is
associated with higher in-hospital mortality: A systematic review and
meta-analysis of the literature.
Source
Catheterization and Cardiovascular Interventions. Conference: 36th Annual
Scientific Sessions of the Society for Cardiovascular Angiography and
Interventions', SCAI Orlando, FL United States. Conference Start: 20130508
Conference End: 20130511. Conference Publication: (var.pagings). 81 (pp
S33-S34), 2013. Date of Publication: May 2013.
Publisher
Wiley-Liss Inc.
Abstract
Background: Chronic total occlusions (CTOs) are the most complex and
challenging coronary lesions for percutaneous coronary intervention (PCI).
As compared to non-CTO interventions, PCI for CTO is a higher risk
procedure. Additionally, unsuccessful CTO-PCI may result in significant
mechanical trauma to coronaries due to multiple attempts to pass the
guide-wire along with higher radiation and contrast exposures. All of
these measures might result in higher rates of peri-procedural
complications and in-hospital cardiac events. The goal of this analysis is
to compare the rates of complications between the patients with successful
and failed PCI for CTOs. Methods: Using major electronic data bases, we
searched for studies comparing peri-procedural complications and
in-hospital events [death, major adverse cardiovascular events (MACE) and
urgent CABG (coronary artery bypass grafting)] between the patients who
underwent successful PCI recanalization of CTOs versus those who had
failed PCI attempts for CTOs. Results: We identified 18 observational
studies (10,566 patients) reporting in-hospital deaths for successful and
failed PCI-CTO groups. Of those studies, in-hospital MACE was reported in
10 studies and urgent CABG was reported in 13 studies. Compared to failed
intervention, successful PCI recanalization of a CTO was associated with
lower in-hospital mortality (RR of 0.355, 95% CI (0.221-0.569) with a
p-value < 0.001) (figure 1), lower overall risk of in-hospital MACE (RR of
0.458, 95% CI (0.324-0.647) p-value < 0.001) and a reduced need for urgent
CABG (RR of 0.144, 95% CI (0.097-0.215) p-value < 0.001). The analysis of
the pooled data showed higher rates of coronary perforations (81/1328
[6.1%] versus 24/2758 [0.90%]) and cardiac tamponade (10/678 [1.5%] versus
0/1589 [0%]) in patients with unsuccessful CTO PCI. Conclusion: As
compared to successful interventions, failed PCI attempts for CTOs appear
to be associated with higher rates of peri-procedural complications and
in-hospital events. (Table Presented) (Graph Presented).

<27>
Accession Number
71051493
Authors
Imazio M. Brucato A. Cemin R. Belli R. Spodick D.H. Adler Y.
Institution
(Imazio, Belli) Cardiology, Maria Vittoria Hospital, Torino, Italy
(Brucato) Medicine, Ospedali Riuniti, Bergamo, Italy
(Cemin) Cardiology, San Maurizio Regional Hospital, Bolzano, Italy
(Spodick) Medicine, St. Vincent Hospital, University of Massachusetts,
Worcester, United States
(Adler) Cardiology, Chaim Sheba Medical Center, Tel-Hashomer, Israel
Title
Prevention of the post-pericardiotomy syndrome. A meta-analysis of
published randomized trials.
Source
Circulation. Conference: World Congress of Cardiology Scientific Sessions
2012, WCC 2012 Dubai United Arab Emirates. Conference Start: 20120418
Conference End: 20120421. Conference Publication: (var.pagings). 125 (19)
(pp e770-e771), 2012. Date of Publication: 15 May 2012.
Publisher
Lippincott Williams and Wilkins
Abstract
Introduction: The natural history of the post-pericardiotomy syndrome
(PPS), a relatively common complication of cardiac surgery, is variable
ranging from mild, self-limited episodes to cases with protracted courses,
recurrences and readmissions. Preventive strategies may be valuable to
reduce morbidity and management costs. Objectives: Systematic review on
available data for the pharmacologic prevention of the PPS. Methods:
Controlled clinical studies were searched in several databases and were
included provided they focused on the pharmacologic primary prevention of
the PPS. Random-effect odds ratios (ORs) were computed for the occurrence
of the PPS. Results: From the initial sample of 343 citations, 4
controlled clinical trials for the primary prevention of the PPS were
finally included (894 patients); 3 studies were double-blind randomised
controlled trials (RCT). Treatment comparisons were as follows: colchicine
vs. placebo (2 RCTs enrolling a total of 471 patients), methylprednisolone
vs. placebo (a single RCT on 246 pediatric patients), and aspirin vs.
historical controls (a single non-randomised study on 177 pediatric
patients). Meta-analytic pooling showed that colchicine was associated
with a reduced risk of PPS (OR= 0.38 [0.22- 0.65]). Data either on
methylpredisolone (OR= 1.13 [0.57-2.25]), or aspirin (OR= 1.00
[0.16-6.11]) were negative but inconclusive because based on a single
study and/or a non-randomised design. Conclusion: Clinical evidence for
the primary prevention of the PPS is still limited to few studies of
variable quality. Nevertheless, available data suggest a beneficial
profile for colchicine, at present the only efficacious agent for PPS
primary prevention.

<28>
Accession Number
71053062
Authors
Chen Q. Sheikh A. Sheppard S. Gibbs R. Smith D. Haw M.
Institution
(Chen, Sheikh) Univ College of London Hosps, London, United Kingdom
(Sheppard, Smith, Haw) Southampton General Hosp, Southampton, United
Kingdom
(Gibbs) Univ of Portsmouth, Portsmouth, United Kingdom
Title
Combination of blood cardioplegic and strategic reperfusion period
leucodepletion during cardiopulmonary bypass preserves the cardiac and
pulmonary function: A prospective randomized controlled study.
Source
Circulation Research. Conference: Basic Cardiovascular Sciences 2012
Scientific Sessions New Orleans, LA United States. Conference Start:
20120723 Conference End: 20120726. Conference Publication: (var.pagings).
111 (4 MeetingAbstract) , 2012. Date of Publication: 03 Aug 2012.
Publisher
Lippincott Williams and Wilkins
Abstract
Objectives: Leucocytes activation during cardiopulmonary bypass (CPB)
contributes to postoperative organ dysfunction. We compared the outcomes
of various leucodepletion strategies in patients undergoing coronary
artery bypass grafting (CABG). Methods: One hundred-twenty low-risk
patients undergoing first time CABG were prospectively randomized to six
groups: 1 non-leucodepletion arterial filtration; 2 continuous arterial
leucodepletion; 3 reperfusion period leucodepletion; 4 leucodepletion of
blood cardioplegia; 5 combination of continuous arterial and blood
cardioplegic leucodepletion; 6 combination of blood cardioplegic and
reperfusion period leucodepletion. Blood samples were taken 5 min before
CPB, 5 and 30 min on CPB, 5, 60 min after aortic X-clamp removal and 6 h
post-CPB. Activated leucocytes were identified with Nitroblue Tetrazolium
staining. Exhaled nitro oxide (NO) was measured pre- and post-CPB using
real-time chemiluminescense analyzer. Respiratory index (alveolar-arterial
oxygenation index, AaOI) was calculated 5 min before CPB and 5 min on CPB,
1, 2, 4, 8 and 18 h post-CPB. Results: Activated white cell counts were
similar before CPB in all groups, but reduced significantly 5, 60 min
following aortic X-clamp removal, and 6 h post-CPB in groups 2, 3, 5 and
6, compared with group 1 (ANOVA p=0.02). Post-CPB, NO increased in all
groups (p<0.05) except in Group 6 (3.17+/-0.64 vs. 3.63+/-0.79 ppb/s,
p=0.22). Group 6 exhibited a lower AaOI than group 1 over all time points
post-CPB (ANOVA, p=0.02). Postoperatively, there was a significant
reduction in inotropic requirement, ventilation time and atrial
fibrillation in group 6 (p=0.045, 0.04 and 0.043, respectively). There was
no difference in chest drain output, length of ICU and hospital stay among
all groups. Conclusions: Combination of blood cardioplegic and reperfusion
period leucodepletion appeared to be most effective in attenuating
activated leucocytes during CPB, which was associated with better
preservation of cardiac and pulmonary function compared with other
leucodepletion strategies.

<29>
Accession Number
71048979
Authors
Vierling W.
Institution
(Vierling) Institute of Pharmacology, Technical University Munich, Munich,
Germany
Title
Is magnesium important for the prevention and therapy of cardiac
arrhythmias?.
Source
Trace Elements and Electrolytes. Conference: 32nd Symposium of the Society
for Magnesium Research Herne Germany. Conference Start: 20120906
Conference End: 20120908. Conference Publication: (var.pagings). 30 (2)
(pp 85), 2013. Date of Publication: 2013.
Publisher
Dustri-Verlag Dr. Karl Feistle
Abstract
Based on the physiological and pharmacodynamic effects of magnesium, it
can be concluded that magnesium deficiency favors cardiac arrhythmias
while magnesium supply can prevent or abolish arrhythmias. The efficiency
of parenteral administration of magnesium for the treatment of certain
cardiac arrhythmias is acknowledged by cardiological societies and is
incorporated in guidelines to treat arrhythmias. Besides therapeutics the
preventive effect of magnesium is very important. In the Framingham study,
it was already detected that the appearance of dangerous arrhythmias was
inversely related to the serum concentrations of magnesium and potassium.
In a recent study, it was shown that sudden cardiac death, which in most
cases is related to arrhythmias, is more frequent if magnesium intake and
serum concentrations are low. An important question is whether magnesium
is suited for the prevention of atrial fibrillation in patients who
undergo cardiac surgery. The heart and thorax surgeons stated that
parenteral administration of magnesium can reduce the incidence of atrial
fibrillations after such an intervention. However, in a recent
meta-analysis, it was demonstrated that a beneficial effect of magnesium
only resulted if low quality studies were included, but was absent if only
studies with higher quality were selected. In contrast, in another study
where also only studies with higher quality were considered, it was
concluded that magnesium has indeed a preventive effect. Although there is
no final clarity, it can be stated that in each case, magnesium deficiency
has to be corrected to avoid cardiac arrhythmias and finally sudden
cardiac death. This is particularly important if predisposing factors like
intake of certain drugs, but also cardiac surgery, play a role.

<30>
Accession Number
71050858
Authors
Samat M. Hong Z.
Institution
(Samat, Hong) Department of Anesthesiology, First Affiliated Hospital of
Xinjiang Medical University, Urumqi, Xinjiang, China
Title
Tight heart rate control is needed for perioperative cardioprotection.
Source
British Journal of Anaesthesia. Conference: Joint Meeting of the
Anaesthetic Research Society and the Chinese Society of Anesthesiology
2011 Ji'nan, Shandong China. Conference Start: 20110910 Conference End:
20110910. Conference Publication: (var.pagings). 108 (3) (pp 546p), 2012.
Date of Publication: March 2012.
Publisher
Oxford University Press
Abstract
Recent meta-analyses assessing the efficacy of perioperative b-blockade
trials have failed to show a reduction in postoperative morbidity and
mortality. Tight control of heart rate (HR) has been suggested to improve
these outcomes. Meta-analyses have not considered the influence of tight
HR control on the efficacy of perioperative b-blockade. We identified all
randomized trials evaluating perioperative beta-blockers after non-cardiac
surgery and yielded 13 trials with 11 590 patients. We used the data from
these studies to correlate measures of HR control with major postoperative
outcomes, primarily in-hospital myocardial infarction. Odds ratios (ORs),
95% confidence limits (CLs), and heterogeneity were calculated. The
combined results of all studies show cardioprotective effect of
beta-blockers (OR=0.64, 95% CL=0.50-0.80, P<0.0001), but there was
considerable heterogeneity among the studies (57%). However, grouping the
trials on the basis of maximal HR showed that trials where the estimated
maximal HR was ,100 beats min<sup>-1</sup> were associated with
cardioprotection (OR=0.37, 95% CL=0.26-0.52, P<0.00001) and no
heterogeneity (Fig. 9), whereas those trials where the estimated maximal
HR was <100 beats min<sup>-1</sup> did not show cardioprotection. The
large heterogeneity in HR response to b-blockade was found to be related,
in part, to the type of b-blocker, specifically, metoprolol, and the
concomitant use of calcium channel blockers. Calcium channel blocker use
and beta-blockers other than metoprolol resulted in more effective control
of HR. The results suggest that effective control of HR is important for
achieving cardioprotection and demonstrates that administration of
beta-blockers does not reliably increase HR in all patients. Combination
therapy with other drugs and adequate control of anaesthesia may be
necessary for effective postoperative control of HR.