Saturday, May 8, 2010

EMBASE Cardiac Update AutoAlert: EPICORE Cardiac Surgery Blogger2

Total documents retrieved: 10

Results Generated From:
EMBASE <1980 to 2010 Week 18>
EMBASE (updates since 2010-04-29)


<1>
Accession Number
2010235977
Authors
Sadoh W.E.
Institution
(Sadoh) Paediatric Cardiology Unit, Department of Child Health, University
of Benin Teaching Hospital, Benin City, Edo State, Nigeria.
Title
Natural history of ventricular septal defects in Nigerian children.
Source
SAJCH South African Journal of Child Health. 4(1)(pp 16-19), 2010. Date
of Publication: 2010.
Publisher
Health and Medical Publishing Group
Abstract
Introduction. Ventricular septal defect (VSD) is a common congenital heart
disease (CHD). Spontaneous closure of the VSD may occur, depending on the
type and size of defects. This study was conducted to determine the
natural history of VSD in a group of Nigerian children. Subjects and
methods. Sixty-one children diagnosed with VSD were prospectively studied
at a tertiary centre in Nigeria until they were 2 years old. They had
regular two-dimensional (2D) and Doppler echocardiography evaluations for
the VSD size and closure. Results. Most (35 - 57.4%) of the patients were
female, their mean age at presentation was 11.2+/-5.2 months, and the most
common type of VSD was the perimembranous (39 - 63.9%). Almost half (28 -
45.9%) of the patients had spontaneous closure. The spontaneous closure
rate was highest in muscular VSD (82.4%) and in small defects (95.0%).
Incidental presence of a murmur, absence of heart failure and
bronchopneumonia were good clinical predictors of closure. Only 3 (4.9%)
patients had surgery abroad. There were 2 (3.3%) deaths from
bronchopneumonia and bacterial endocarditis. Conclusion. Spontaneous
closure readily occurs in small-sized defects and muscular VSDs. However,
most patients with moderate to large VSDs are confined to long-term
medical management, highlighting the need for indigenous surgical capacity
in Nigeria.

<2>
Accession Number
0020231678
Authors
Pisters K.M. Vallieres E. Crowley J.J. Franklin W.A. Bunn Jr. P.A.
Ginsberg R.J. Putnam Jr. J.B. Chansky K. Gandara D.
Institution
(Pisters, Vallieres, Crowley, Franklin, Bunn Jr., Ginsberg, Putnam Jr.,
Chansky, Gandara) The University of Texas M. D. Anderson Cancer Center, PO
Box 301402, Unit 432, Houston, TX 77230-1402, USA.
Title
Surgery with or without preoperative paclitaxel and carboplatin in
early-stage non-small-cell lung cancer: Southwest Oncology Group Trial
S9900, an intergroup, randomized, phase III trial..
Source
Journal of clinical oncology : official journal of the American Society of
Clinical Oncology. 28(11)(pp 1843-1849), 2010. Date of Publication: 10
Apr 2010.
Abstract
PURPOSE Patients with early-stage non-small-cell lung cancer (NSCLC) have
a poor prognosis even after complete resection. Earlier studies of
preoperative (induction) chemotherapy in resectable NSCLC demonstrated
feasibility and encouraging survival data. This randomized phase III trial
compared overall survival (OS) for preoperative paclitaxel and carboplatin
followed by surgery with surgery alone in patients with early-stage NSCLC.
PATIENTS AND METHODS Patients with clinical stage IB-IIIA NSCLC (excluding
superior sulcus tumors and N2 disease) were eligible. Patients were
randomly assigned to surgery alone or to three cycles of paclitaxel (225
mg/m(2)) and carboplatin (area under curve, 6) followed by surgical
resection. The primary end point was OS; secondary end points were
progression-free survival (PFS), chemotherapy response, and toxicity.
RESULTS The trial closed early with 354 patients after reports of a
survival benefit for postoperative chemotherapy in other studies. The
median OS was 41 months in the surgery-only arm and 62 months in the
preoperative chemotherapy arm (hazard ratio, 0.79; 95% CI, 0.60 to 1.06; P
= .11.) The median PFS was 20 months for surgery alone and 33 months for
preoperative chemotherapy (hazard ratio, 0.80; 95% CI, 0.61 to 1.04; P =
.10.) Major response to chemotherapy was seen in 41% of patients; no
unexpected toxicity was observed. CONCLUSION This trial closed prematurely
after compelling evidence supporting postoperative chemotherapy emerged.
Although OS and PFS were higher with preoperative chemotherapy, the
differences did not reach statistical significance. At present, stronger
evidence exists for postoperative chemotherapy in early-stage NSCLC.

<3>
Accession Number
0020387748
Authors
Akbarzadeh F. Kazemi-Arbat B. Golmohammadi A. Pourafkari L.
Institution
(Akbarzadeh, Kazemi-Arbat, Golmohammadi, Pourafkari) Department of
Cardiology, Shahid Madani Cardiovascular Research Center, Tabriz
University of Medical Sciences, Tabriz, Iran, Islamic Republic of.
Title
Biatrial pacing vs. intravenous amiodarone in prevention of atrial
fibrillation after coronary artery bypass surgery.
Source
Pakistan Journal of Biological Sciences. 12(19)(pp 1325-1329), 2009. Date
of Publication: 2009.
Publisher
Asian Network for Scientific Information
Abstract
This study was aimed to compare the results of post operative biatrial
pacing and IV amiodarone in prevention of AF. In a single blind randomized
clinical trial, 210 patients scheduled for elective CABG surgery were
randomized either to receive overdrive biatrial pacing, IV amiodarone or
no intervention. Incidence of AF postoperatively evaluated. Pacing was
successful in 83% of patients and 80% of patients in amiodarone group
could receive their drug. Twenty and one patients developed AF. Incidence
of AF in pace, amiodarone and control group was 10.7, 5.3 and 17.9%,
respectively (p = 0.08). Comparing incidence of AF between pacing and
control group, the difference was not significant (p = 0.2), but the
difference between amiodarone and control groups was significant
statistically (p = 0.03). Patients who developed AF were older but their
left ventricular ejection fraction was not different with patients without
AF. The ICU stay was higher in patients with AF. Use of IV amiodarone was
more effective than biatrial pacing in prevention of post operative AF and
we recommend use of this drug in high risk patients. copyright 2009 Asian
Network for Scientific Information.

<4>
Accession Number
2010069638
Authors
Brown J.R. Toler A.W.J. Kramer R.S. Clive Landis R.
Institution
(Brown, Toler) Dartmouth Institute for Health Policy and Clinical
Practice, Dartmouth Medical School, Lebanon, NH, United States.
(Kramer) Division of Cardiothoracic Surgery, Maine Medical Center,
Portland, ME, United States.
(Clive Landis) Edmund Cohen Laboratory for Vascular Research, University
of the West Indies, Barbados.
Title
Anti-inflammatory effect of aprotinin: A meta-analysis.
Source
Journal of Extra-Corporeal Technology. 41(2)(pp 79-86), 2009. Date of
Publication: June 2009.
Publisher
American Society of Extra-Corporeal Technology
Abstract
It is important to define the extent, and any limitations, of potential
anti-inflammatory regimens used in cardiac surgery to guide the rational
combination of drugs to suppress the systemic inflammatory response.
Aprotinin (Trasylol) is an anti-fibrinolytic agent with reported
anti-inflammatory properties. In this study, we investigated the published
data on aprotinin's effect on acute phase protein and cytokine levels in
cardiac surgery patients. Randomized placebo-controlled trials of
aprotinin published between 1985 and 2007, in adult cardiac surgery using
cardiopulmonary bypass, reporting tumor necrosis factor-alpha (TNF-alpha),
interleukin-6 (IL-6), IL-8, and IL-10 levels were included for review. Two
independent reviewers graded each paper and collected information on
inflammatory markers. RevMan 4.3 statistical software was used to
calculate and plot the weighted mean difference between placebo and
aprotinin groups. Thirteen studies met the review criteria. None of the
inflammatory markers were reduced by high-dose aprotinin treatment.
Low-dose aprotinin significantly reduced IL-10 levels after protamine
administration (?41.3 pg/ mL; 95% CI: ?59.5, ?23.1), but this result was
gone by the first post-operative day. These meta-analyses showed no
significant effect of aprotinin on acute phase proteins or systemic
cytokine markers of inflammation during clinical adult cardiac surgery
using cardiopulmonary bypass. While recognizing that other host defense
systems, such as coagulation and complement, contribute to the overall
systemic inflammatory response, the evidence presented here does not
support the clinical use of aprotinin as an anti-inflammatory agent on its
own.

<5>
Accession Number
2010065040
Authors
Neyt M. Vinck I. Gewillig M. Van Brabandt H.
Institution
(Neyt, Vinck, Van Brabandt) BelgianHealth Care Knowledge Centre,
Kruidtuinlaan 55, 1000 Brussels, Belgium.
(Gewillig) Department of Paediatric Cardiology, University Hospital
Gasthuisberg, Herestraat 49, 3000 Leuven, Belgium.
Title
Percutaneous pulmonary and aortic valve insertion in Belgium: Going for
conditional reimbursement or waiting for further evidence?.
Source
International Journal of Technology Assessment in Health Care. 25(3)(pp
281-289), 2009. Date of Publication: July 2009.
Publisher
Cambridge University Press
Abstract
Objectives: The aim of this study was to assess current evidence
supporting the use of percutaneous heart valves (PHV) in degenerative
aortic valve and congenital pulmonary outflow tract disease, as compared
to conservative medical therapy or traditional surgical valve replacement.
Methods: A systematic review of the literature on PHV was performed.
Results: No randomized controlled trials (RCT) on PHV have been published
so far. Only observational data from series and data presented at
cardiology meetings are available. Both percutaneous aortic valve (PAV)
and percutaneous pulmonary valve (PPV) seem feasible in the hands of an
experienced team. Safety, however, seems to be a problem in PAV, as shown
by the high 30-day and 6-month mortality rates. Conclusions: Due to safety
concerns, PAV reimbursement is not recommended and patients should only be
subjected to PAV insertion within the boundaries of an RCT. In contrast,
PPV implantation seems to be a safe and promising technology for which
reimbursement under strict conditions may be recommended. copyright 2009
Cambridge University Press.

<6>
Accession Number
2010191781
Authors
Axelsson B. Arbeus M. Magnuson A. Hultman J.
Institution
(Axelsson, Arbeus) Department of Cardiothoracic Surgery and
Anesthesiology, Orebro University Hospital, Orebro, Sweden.
(Magnuson) Statistical and Epidemiological Unit, Orebro University
Hospital, Orebro, Sweden.
(Hultman) Thoracic Clinic, Karolinska University Hospital, Stockholm,
Sweden.
Title
Milrinone Improves Diastolic Function in Coronary Artery Bypass Surgery as
Assessed by Acoustic Quantification and Peak Filling Rate: A Prospective
Randomized Study.
Source
Journal of Cardiothoracic and Vascular Anesthesia. 24(2)(pp 244-249),
2010. Date of Publication: April 2010.
Publisher
W.B. Saunders
Abstract
Objective: To compare the effects of a bolus dose of milrinone, 50 mug/kg,
to placebo on diastolic function (active relaxation) in patients
undergoing on-pump coronary artery bypass grafting (CABG). Design:
Prospective, randomized, double-blind, placebo-controlled study. Setting:
University hospital. Participants: Twenty-four patients with stable angina
and left ventricular ejection fraction >30%, scheduled for elective CABG
using cardiopulmonary bypass (CPB), were included. Intervention: Patients
were randomized to receive either 50 mug/kg of milrinone (n = 12) or
placebo (n = 12) after aortic declamping. Measurements and Main Results:
The diastolic function of the left ventricle (LV) was measured as peak
filling rate (dA/dt [maximal diastolic area change over time]) with
transesophageal echocardiography (TEE) using acoustic quantification (AQ)
before CPB and 10 minutes after termination of CPB. The normalized peak
filling rate (dA/dt)/EDA was also calculated. Active relaxation was
statistically significantly increased in the milrinone group compared with
the placebo group after CPB. Conclusion: Patients undergoing CABG surgery
and treated with milrinone after aortic declamping had better diastolic
function following cardiopulmonary bypass. copyright 2010 Elsevier Inc.
All rights reserved.

<7>
Accession Number
2010191777
Authors
Hasija S. Makhija N. Choudhury M. Hote M. Chauhan S. Kiran U.
Institution
(Hasija, Makhija, Choudhury, Chauhan, Kiran) Department of Cardiac
Anaesthesia, Cardiothoracic Centre, All India Institute of Medical
Sciences, Ansari Nagar, New Delhi, India.
(Hote) Department of Cardiothoracic and Vascular Surgery, Cardiothoracic
Centre, All India Institute of Medical Sciences, Ansari Nagar, New Delhi,
India.
Title
Prophylactic Vasopressin in Patients Receiving the Angiotensin-Converting
Enzyme Inhibitor Ramipril Undergoing Coronary Artery Bypass Graft Surgery.
Source
Journal of Cardiothoracic and Vascular Anesthesia. 24(2)(pp 230-238),
2010. Date of Publication: April 2010.
Publisher
W.B. Saunders
Abstract
Objective: The purpose of this study was to compare the effects of
continuation versus discontinuation of the angiotensin-converting enzyme
(ACE) inhibitor ramipril and assess the efficacy of prophylactic
vasopressin infusion on hemodynamic stability and vasoactive drug
requirements in patients undergoing coronary artery bypass graft (CABG)
surgery. Design: A prospective, randomized, double-blinded, single-center
clinical study. Setting: Tertiary care hospital. Participants: Forty-seven
patients on the ACE inhibitor ramipril for 6 weeks before undergoing
elective primary CABG surgery on cardiopulmonary bypass (CPB).
Interventions: Patients were randomly divided into 3 groups: group A (n =
16), patients discontinued ramipril 24 hours before surgery; group B (n =
16), patients continued ramipril until the morning of surgery; and group C
(n = 15), patients continued ramipril until the morning of surgery and
received vasopressin infusion (0.03 U/min) from the onset of rewarming
until the hemodynamics were stable without vasopressor agents. The
anesthetic technique and conduct of CPB were standardized for all the
groups. Hemodynamic parameters and vasoactive drug requirements were
recorded for 3 days postoperatively. Measurements and Main Results:
Patients in group A maintained stable mean arterial pressure (MAP) and
systemic vascular resistance (SVR). In group B, MAP and SVR decreased
after the induction of anesthesia and remained so throughout surgery (p <
0.05). In group C, MAP and SVR decreased upon the induction of anesthesia
(p < 0.05) but normalized after CPB. Conclusions: Preoperative ACE
inhibitor continuation predisposed to hypotension upon the induction of
anesthesia and in the post-CPB period. Prophylactic low-dose vasopressin
infusion prevented post-CPB hypotension. Low-dose vasopressin can be
considered as potential therapy in these patients. copyright 2010 Elsevier
Inc. All rights reserved.

<8>
Accession Number
2010065029
Authors
Quenneville S.P. Xie X. Brophy J.M.
Institution
(Quenneville, Xie, Brophy) Technology Assessment Unit, Royal Victoria
Hospital, McGill University, 687 Pine Avenue West, R4.14, Montreal, QC H3A
1A1, Canada.
(Brophy) Department of Medicine and Epidemiology (McGill), McGill
University, Royal Victoria Hospital, 687 Pine Avenue West, Ross 4.12,
Montreal, QC H3A 1A1, Canada.
Title
The cost-effectiveness of Maze procedures using ablation techniques at the
time of mitral valve surgery.
Source
International Journal of Technology Assessment in Health Care. 25(4)(pp
485-496), 2009. Date of Publication: October 2009.
Publisher
Cambridge University Press
Abstract
Background: The classic cut and sew surgical Maze procedure has been shown
to reduce atrial fibrillation (AF), and recently newer surgical ablation
techniques with reduced technical complexity have been introduced. This
study sought to systematically review the efficacy and safety of these
newer techniques and to evaluate their long-term cost-effectiveness at the
time of scheduled mitral valve (MV) surgery. Methods: A systematic
literature search and meta-analysis was performed to generate the most
reliable efficacy and safety parameter estimates for a Markov decision
analysis model comparing MV surgery alone to MV surgery plus an ablation
Maze procedure. Both basic and probabilistic sensitivity analyses were
conducted. Results: Based on the six randomized controlled trials (RCTs)
identified, the pooled 1-year estimate of AF after surgery alone was 71
percent (95 percent confidence interval [CI], 64 percent to 78 percent).
The pooled risk ratio of AF after surgical ablation treatment at the time
of mitral valve surgery relative to valve surgery alone was 0.33 (95
percent CI, 0.19 to 0.55). The pooled analyses showed that no statistical
significant increases in operative mortality, permanent pacemaker
implantation, and postoperative bleeding with the ablative Maze
procedures. An ablation-based Maze procedure at the time of mitral valve
surgery had an incremental cost-effectiveness ratio (ICER) of $4,446CAD
($3,850US) per quality-adjusted life-year (QALY) compared with valve
surgery alone. Specifically costs were an extra $900CAD but with improved
clinical outcomes (0.20 QALYs), including a prolonged life expectancy of
0.10 life-years. In one-way sensitivity analyses, survival time after MV
surgery had the largest impact on ICER. Other variables influencing the
ICER included the risk ratio of AF, utility, and cost estimates.
Probabilistic sensitivity analysis suggests that 58.1 percent, 73.9
percent, and 89.3 percent of the simulations of the Maze strategy are
cost-effective at willingness to pay thresholds of $20,000, $50,000, and
$100,000CAD per QALY gained, respectively. Conclusions: Our meta-analysis
suggests that a Maze surgical ablation procedure at the time of MV surgery
is associated with a reduced postoperative AF risk. Our economic model
further suggests that the surgical ablation strategy at the time of mitral
valve surgery is likely a cost-effective intervention, provided patients
have a good long-term postsurgical prognosis. copyright 2009 Cambridge
University Press.

<9>
Accession Number
2010192128
Authors
Landoni G. Turi S. Biondi-Zoccai G. Bignami E. Testa V. Belloni I. Cornero
G. Zangrillo A.
Institution
(Landoni, Turi, Bignami, Testa, Belloni, Cornero, Zangrillo) Department of
Anesthesia and Intensive Care, Universita Vita-Salute San Raffaele, Milan,
Italy.
(Biondi-Zoccai) Interventional Cardiology, Division of Cardiology,
University of Turin, Turin, Italy.
Title
Esmolol Reduces Perioperative Ischemia in Noncardiac Surgery: A
Meta-analysis of Randomized Controlled Studies.
Source
Journal of Cardiothoracic and Vascular Anesthesia. 24(2)(pp 219-229),
2010. Date of Publication: April 2010.
Publisher
W.B. Saunders
Abstract
Objective: Literature increasingly has suggested how beta-blockers could
be associated with reductions of mortality and morbidity in noncardiac
surgery. Recently, the POISE trial showed that beta-blockers could be
harmful in the perioperative period. The authors performed a meta-analysis
to evaluate the clinical effects of esmolol in noncardiac surgery. Design:
Meta-analysis. Setting: Hospitals. Participants: A total of 1765 patients
from 32 randomized trials. Interventions: None. Measurements and Main
Results: Three investigators independently searched BioMedCentral and
PubMed. Inclusion criteria were random allocation to treatment and
comparison of esmolol versus placebo, other drugs, or standard of care in
noncardiac surgery. Exclusion criteria were duplicate publications,
nonhuman experimental studies, and no data on clinical outcomes. The use
of esmolol was associated with a significant reduction of myocardial
ischemia episodes (5/283 [1.76%] in the esmolol group v 16/265 [6.03%] in
the control arm, odds ratio [OR] = 0.16 [0.05-0.54], p = 0.003). The
authors did not observe significant differences regarding episodes of
arrhythmias (8/236 [3.38%] v 22/309 [7.11%], OR = 0.52 [0.23-1.18], p =
0.12) and in the incidence of myocardial infarction (0/148 [0%] v 1/169
[0.59%], OR = 0.23 [0.01-6.09], p = 0.38). Esmolol-treated patients did
not experience more episodes of hypotension (17/384 [4.42%] v 38/439
[8.65%], OR = 0.41 [0.22-0.79], p = 0.17) and bradycardia (25/342 [7.30%]
v 17/406 [4.18%], OR = 1.42 [0.74-2.74], p = 0.42). Conclusions: Esmolol
seemed to reduce the incidence of myocardial ischemia in noncardiac
surgery without increasing the episodes of hypotension and bradycardia.
Large randomized trials are necessary to confirm these promising results.
copyright 2010 Elsevier Inc. All rights reserved.

<10>
Accession Number
2010166060
Authors
Rutter M.K. Nesto R.W.
Institution
(Rutter) Cardiovascular Research Group, School of Clinical and Laboratory
Sciences, University of Manchester, Manchester, United Kingdom.
(Rutter) Manchester Diabetes Centre, Manchester Academic Health Science
Centre, Manchester NIHR Biomedical Research Centre, Manchester, United
Kingdom.
(Nesto) Lahey Clinic, Burlington, United States.
(Nesto) Tufts Medical School, MA, United States.
(Rutter) Cardiovascular Research Group, Core Technology Facility, 46
Grafton Street, Manchester M13 9NT, United Kingdom.
Title
The BARI 2D study: A randomised trial of therapies for type 2 diabetes and
coronary artery disease.
Source
Diabetes and Vascular Disease Research. 7(1)(pp 69-72), 2010. Date of
Publication: 2010.
Publisher
SAGE Publications Ltd
Abstract
The Bypass Angioplasty Revascularization Investigation 2 Diabetes (BARI
2D) trial randomized 2368 patients with type 2 diabetes (T2DM) and
coronary artery disease to either prompt revascularization or intensive
medical therapy alone; and to either insulin-sensitization or
insulin-provision diabetes therapy. Randomization was stratified by
proposed revascularization method. Five-year survival and major
cardiovascular events (MACE) were similar in study subgroups except in the
coronary bypass surgery (CABG) stratum where there were fewer MACE after
revascularization. There was less hypoglycaemia and weight gain, and
greater apparent benefit from CABG in the insulin sensitization group.
BARI 2D has provided important data for clinicians. copyright The
Author(s) 2010.

Saturday, May 1, 2010

EMBASE Cardiac Update AutoAlert: EPICORE Cardiac Surgery Blogger2

Total documents retrieved: 21

Results Generated From:
EMBASE <1980 to 2010 Week 17>
EMBASE (updates since 2010-04-22)


<1>
Accession Number
0020238333
Authors
Hoenig M.R. Aroney C.N. Scott I.A.
Institution
(Hoenig, Aroney, Scott) Royal Brisbane and Women's Hospital, Herston,
Brisbane, Australia, 4029.
Title
Early invasive versus conservative strategies for unstable angina and
non-ST elevation myocardial infarction in the stent era..
Source
Cochrane database of systematic reviews (Online). 3(pp CD004815), 2010.
Date of Publication: 2010.
Abstract
BACKGROUND: In patients with unstable angina and non-ST elevation
myocardial infarction (UA/NSTEMI) two strategies are possible, either a
routine invasive strategy where all patients undergo coronary angiography
shortly after admission and, if indicated, coronary revascularization; or
a conservative strategy where medical therapy alone is used initially,
with selection of patients for angiography based on clinical symptoms or
investigational evidence of persistent myocardial ischemia. OBJECTIVES: To
determine the benefits of an invasive compared to conservative strategy
for treating UA/NSTEMI in the stent era. SEARCH STRATEGY: The Cochrane
Central Register of Controlled Trials (CENTRAL) (The Cochrane Library
2008, Issue 1), MEDLINE and EMBASE were searched (1996 to February 2008)
with no language restrictions. SELECTION CRITERIA: Included studies were
prospective trials comparing invasive with conservative strategies in
UA/NSTEMI. DATA COLLECTION AND ANALYSIS: We identified five studies (7818
participants). Using intention-to-treat analysis with random-effects
models, summary estimates of relative risk (RR) with 95% confidence
interval (CI) were determined for primary end-points of all-cause death,
fatal and non-fatal myocardial infarction, all-cause death or non-fatal
myocardial infarction, and refractory angina. Further analysis of included
studies was undertaken based on whether glycoprotein IIb/IIIa receptor
antagonists were used routinely. Heterogeneity was assessed using Chi(2)
and variance (I(2) statistic) methods. MAIN RESULTS: In the all-study
analysis, mortality during initial hospitalization showed a trend to
hazard with an invasive strategy (RR 1.59, 95% CI 0.96 to 2.64). The
invasive strategy did not reduce death on longer-term follow up.
Myocardial infarction rates assessed at 6 to 12 months (5 trials) and 3 to
5 years (3 trials) were significantly decreased by an invasive strategy
(RR 0.73, 95% CI 0.62 to 0.86; and RR 0.78, 95% CI 0.67 to 0.92
respectively). The incidence of early (< 4 month) and intermediate (6 to
12 month) refractory angina were both significantly decreased by an
invasive strategy (RR 0.47, 95% CI 0.32 to 0.68; and RR 0.67, 95% CI 0.55
to 0.83 respectively), as were early and intermediate rehospitalization
rates (RR 0.60, 95% CI 0.41to 0.88; and RR 0.67, 95% CI 0.61 to 0.74
respectively). The invasive strategy was associated with a two-fold
increase in the RR of peri-procedural myocardial infarction (as variably
defined) and a 1.7-fold increase in the RR of (minor) bleeding with no
hazard of stroke. AUTHORS' CONCLUSIONS: Compared to a conservative
strategy for UA/NSTEMI, an invasive strategy is associated with reduced
rates of refractory angina and rehospitalization in the shorter term and
myocardial infarction in the longer term. However, the invasive strategy
is associated with a doubled risk of procedure-related heart attack and
increased risk of bleeding and procedural biomarker leaks. Available data
suggest that an invasive strategy may be particularly useful in those at
high risk for recurrent events.

<2>
Accession Number
0020238316
Authors
Carless P.A. Henry D.A. Moxey A.J. O'Connell D. Brown T. Fergusson D.A.
Institution
(Carless, Henry, Moxey, O'Connell, Brown, Fergusson) Discipline of
Clinical Pharmacology, Faculty of Health, University of Newcastle, Level
5, Clinical Sciences Building, Newcastle Mater Hospital, Edith Street,
Waratah, Newcastle, New South Wales, Australia, 2298.
Title
Cell salvage for minimising perioperative allogeneic blood transfusion..
Source
Cochrane database of systematic reviews (Online). 3(pp CD001888), 2010.
Date of Publication: 2010.
Abstract
BACKGROUND: Concerns regarding the safety of transfused blood, have
prompted reconsideration of the use of allogeneic (blood from an unrelated
donor) red blood cell (RBC) transfusion, and a range of techniques to
minimise transfusion requirements. OBJECTIVES: To examine the evidence for
the efficacy of cell salvage in reducing allogeneic blood transfusion and
the evidence for any effect on clinical outcomes. SEARCH STRATEGY: We
identified studies by searching CENTRAL (The Cochrane Library 2009, Issue
2), MEDLINE (1950 to June 2009), EMBASE (1980 to June 2009), the Internet
(to August 2009) and bibliographies of published articles. SELECTION
CRITERIA: Randomised controlled trials with a concurrent control group in
which adult patients, scheduled for non-urgent surgery, were randomised to
cell salvage (autotransfusion), or to a control group, who did not receive
the intervention. DATA COLLECTION AND ANALYSIS: Data were independently
extracted and the risk of bias assessed. Relative risks (RR) and weighted
mean differences (WMD) with 95% confidence intervals (CIs) were
calculated. Data were pooled using a random effects model. The primary
outcomes were the number of patients exposed to allogeneic red cell
transfusion, and the amount of blood transfused. Other clinical outcomes
are detailed in the review. MAIN RESULTS: A total of 75 trials were
included. Overall, the use of cell salvage reduced the rate of exposure to
allogeneic RBC transfusion by a relative 38% (RR=0.62: 95% CI 0.55 to
0.70). The absolute reduction in risk (ARR) of receiving an allogeneic RBC
transfusion was 21% (95% CI 15% to 26%). In orthopaedic procedures the RR
of exposure to RBC transfusion was 0.46 (95% CI 0.37 to 0.57) compared to
0.77 (95% CI 0.69 to 0.86) for cardiac procedures. The use of cell salvage
resulted in an average saving of 0.68 units of allogeneic RBC per patient
(WMD=-0.68; 95% CI -0.88 to -0.49). Cell salvage did not appear to impact
adversely on clinical outcomes. AUTHORS' CONCLUSIONS: The results suggest
cell salvage is efficacious in reducing the need for allogeneic red cell
transfusion in adult elective cardiac and orthopaedic surgery. The use of
cell salvage did not appear to impact adversely on clinical outcomes.
However, the methodological quality of trials was poor. As the trials were
unblinded and lacked adequate concealment of treatment allocation,
transfusion practices may have been influenced by knowledge of the
patients' treatment status potentially biasing the results in favour of
cell salvage.

<3>
Accession Number
2010207022
Authors
Serebruany V.L. Atar D.
Institution
(Serebruany) HeartDrugTM Research Laboratories, Johns Hopkins University,
Towson, MD 21204, United States.
(Atar) Division of Cardiology, Oslo University Hospital Aker, Faculty of
Medicine, Norway.
Title
The PLATO trial: Do you believe in magic?.
Source
European Heart Journal. 31(7)(pp 764-767), 2010. Date of Publication:
April 2010.
Publisher
Oxford University Press
Abstract
The recently published and presented PLATelet Inhibition and Clinical
Outcomes (PLATO) trial was a pivotal Phase III, randomized, double-blind,
parallel-group, multinational, clinical study.1 The trial compared
head-to-head the efficacy of the experimental antiplatelet agent
ticagrelor (formerly known as AZD6140, to be marketed as Brilintaw) vs.
standard care with clopidogrel. Patients (n = 18 624) with moderate to
high risk acute coronary syndromes undergoing coronary intervention were
randomized to ticagrelor 180 mg loading dose followed by 90 mg twice daily
thereafter, or clopidogrel 300-600 mg loading dose followed by 75 mg once
daily for 6-12 months. The primary endpoint was the time of the first
event of death from vascular causes, myocardial infarction (MI), or
stroke, and occurred in 11.7% of patients treated with clopidogrel vs.
9.8% of patients randomized to ticagrelor, representing a highly
significant benefit [hazard ratio (HR)=0.84; confidence interval (CI)
=0.77-0.92; P<0.001] of the experimental drug.1 Triaging these three
components of the combined endpoint suggests that the difference in favour
of ticagrelor was driven by the reduction of vascular death (P<0.001) and
MI (P<0.005), but not stroke (P=0.22). There were significantly more fatal
intracranial bleedings (11 vs. 1, P=0.02), but numerically less overall
fatal bleeding (20 vs. 23) after ticagrelor. Among side effects associated
with ticagrelor, dyspnoea (already recognized in the earlier studies with
AZD6140, and probably caused by transitory bronchoconstriction) was the
most prominent one (HR=1.84; CI=1.68-2.02; P<0.001), followed by
ventricular pauses (P,0.01), and laboratory findings of increased uric
acid as well as elevated creatinine (P<0.001 for both). Obviously the
PLATO data will undergo detailed scrutiny and verification during the
assessment by regulatory authorities; however, some considerations already
seem appropriate.

<4>
Accession Number
2010207978
Authors
Conte J.
Institution
(Conte) Division of Cardiac Surgery, The Johns Hopkins Hospital,
Baltimore, MD, United States.
Title
An indictment of the STICH trial: "True, true, and unrelated".
Source
Journal of Heart and Lung Transplantation. 29(5)(pp 491-496), 2010. Date
of Publication: May 2010.
Publisher
Elsevier USA

<5>
Accession Number
2010222827
Authors
Weir R.A.P. Murphy C.A. Petrie C.J. Martin T.N. Clements S. Steedman T.
Wagner G.S. McMurray J.J.V. Dargie H.J.
Institution
(Weir, Murphy, Petrie, Martin, Clements, Steedman, McMurray, Dargie)
Cardiology Department, Western Infirmary, Glasgow G11 6NT, Scotland,
United Kingdom.
(Wagner) Duke University Medical Center, Durham, NC, United States.
Title
Monocyte chemoattractant protein-1: A dichotomous role in cardiac
remodeling following acute myocardial infarction in man?.
Source
Cytokine. 50(2)(pp 158-162), 2010. Date of Publication: May 2010.
Publisher
Academic Press
Abstract
Introduction: Monocyte chemoattractant protein-1 (MCP-1) is elevated after
acute myocardial infarction (AMI), and potentiates left ventricular (LV)
remodeling in murine models of AMI. We examined the relationships between
serum MCP-1, change in LV function and biomarkers related to remodeling in
a cohort of AMI patients. Methods: Serum MCP-1 concentrations were
measured in 100 patients (age 58.9 +/- 12.0. years, 77% male) admitted
with AMI and LV dysfunction, at baseline (mean 46. h), 12 and 24. weeks;
cardiac magnetic resonance imaging and measurement of matrix
metalloproteinase-2 (MMP-2), MMP-3 and MMP-9 occurred at each time-point.
Results: MCP-1 increased significantly from 697 [483, 997]. pg/mL at
baseline to 878 [678, 1130]. pg/mL at 24. weeks (p<0.001). MMP-3
concentration increased while MMP-9 decreased significantly over time;
MMP-2 concentration did not change significantly. Baseline MCP-1
correlated with change in (Delta) LV end-systolic volume index
(DeltaLVESVI; r=-0.48, p=0.01) and with DeltaLV ejection fraction
(DeltaLVEF; r=0.50, p=0.02). However, DeltaMCP-1 correlated positively
with DeltaLVESVI (r=0.40, p=0.006) and negatively with DeltaLVEF (r=-0.36,
p=0.004). MCP-1 had no relationship with any MMP. Conclusions: MCP-1 may
have a dichotomous role following AMI, aiding early infarct healing but
potentiating later remodeling, which merits further study before any
therapeutic trials of MCP-1 modulation in humans. copyright 2010 Elsevier
Ltd.

<6>
Accession Number
2010217444
Authors
van de Gevel D.F.D. Soliman Hamad M.A. Elenbaas T.W.O. Ostertag J.U.
Schonberger J.P.A.M.
Institution
(van de Gevel, Soliman Hamad, Elenbaas, Schonberger) Department of
Cardio-thoracic Surgery, Catharina Hospital, Eindhoven, Michelangelolaan
2, 5623 EJ Eindhoven, Netherlands.
(Ostertag) Department of Dermatology, Catharina Hospital, Eindhoven,
Michelangelolaan 2, 5623 EJ Eindhoven, Netherlands.
Title
Is the use of Steri-Strip[trademark] S for wound closure after coronary
artery bypass grafting better than intracuticular suture?.
Source
Interactive Cardiovascular and Thoracic Surgery. 10(4)(pp 561-564), 2010.
Date of Publication: April 2010.
Publisher
European Association for Cardio-Thoracis Surgery
Abstract
Several methods have been used in wound closure after coronary artery
bypass grafting (CABG). In this study, the safety and efficacy of one of
these methods, Steri-Strip[trademark] S is compared with the traditional
intracuticular suture method. Eighty-one patients undergoing CABG were
prospectively randomized into two groups according to the method of skin
closure: Steri-Strip[trademark] S group and traditional suture group.
Comparison between the two methods was done with regards to the length of
the wound and the time needed to close it. The median closure time with
Steri-Strip[trademark] S was 5.45+/-3.35 min vs. 7.53+/-3.41 min in the
suture group. A pain score of [greater-than or equal to]6 at the first
postoperative day was found in 30% of the patients in the suture group vs.
14% of the patients in the Steri-Strip[trademark] S group (P=0.07).
Cosmetic evaluation showed a non-significant difference in the linear
visual analogue score in favor of Steri-Strip[trademark] S group compared
to the intracuticular suture group (73.1 vs. 70.1) (P=0.07).
Steri-Strip[trademark] S is a fast, safe alternative for wound closure of
the sternotomy incision and graft harvesting site. A larger study is
needed to establish the potential beneficial effect of
Steri-Strip[trademark] S on wound infection prevention. copyright 2010
Published by European Association for Cardio-thoracic Surgery.

<7>
Accession Number
2010217433
Authors
Hoffmann M. Bruch H.-P. Kujath P. Limmer S.
Institution
(Hoffmann, Bruch, Kujath, Limmer) Surgical Clinic, University Clinic
Schleswig-Holstein, Campus Luebeck, Ratzeburger Allee 160, 23538 Luebeck,
Germany.
Title
Cold-plasma coagulation in the treatment of malignant pleural
mesothelioma: Results of a combined approach.
Source
Interactive Cardiovascular and Thoracic Surgery. 10(4)(pp 502-505), 2010.
Date of Publication: April 2010.
Publisher
European Association for Cardio-Thoracis Surgery
Abstract
Malignant pleural mesothelioma is on a continuous rise throughout the
Western countries. It is associated with asbestos fibre exposition in the
past. Surgical approaches include extrapleural pneumonectomy and
pleurectomy/decortication (PyD). We investigated the feasability of the
implementation of cold-plasma coagulation (CPC) on the pleura, pericardium
and diaphragm into an established therapeutic algorithm consisting of PyD
and hyperthermic intrathoracal chemoperfusion (HITHOC) therapy. The
underlying rationale was the prevention of cardiotoxic effects during
HITHOC as well as accidental translocation of malignant cells to the
abdomen. CPC was done as part of a multimodal therapy in stage III
mesothelioma patients. Histologic examinations of pleural excisates after
CPC were done. The patients were followed up in three-month intervals.
Neither parenchymal fistulas, nor cardiotoxic effects were observed. The
histologic examination of the pleural excisates showed complete
predictable necrosis. Moreover, until now (median time after operation 1
year) no relapse of the disease was observed. CPC proved to be a safe
technique when used on the pleura, pericardium and diaphragm. We consider
our trial as a pilot-study. To evaluate potential survival benefits using
this technique larger trials are mandatory. copyright 2010 Published by
European Association for Cardio-Thoracic Surgery.

<8>
Accession Number
2010217102
Authors
Crowe E. Lovibond K. Gray H. Henderson R. Krause T. Camm J.
Institution
(Crowe, Lovibond, Krause) National Clinical Guideline Centre, Royal
College of Physicians of London, London NW1 4LE, United Kingdom.
(Gray) Southampton University Hospital, Southampton SO16 6YD, United
Kingdom.
(Henderson) Nottingham University Hospitals, Nottingham NG5 1PB, United
Kingdom.
(Camm) St. George's, University of London, London SW17 0RE, United
Kingdom.
Title
Early management of unstable angina and non-ST segment elevation
myocardial infarction: Summary of NICE guidance.
Source
BMJ. 340(7750)(pp 805-807), 2010. Date of Publication: 10 Apr 2010.
Publisher
BMJ Publishing Group

<9>
Accession Number
2010211230
Authors
Chong E. Poh K.K. Liang S. Lee R.C.-H. Low A. Teo S.-G. Tan H.C.
Institution
(Chong) Cardiac Department, Alexandra Hospital, National University,
Singapore.
(Poh, Lee, Low, Teo, Tan) National University, Heart Center, National
University Hospital, Singapore.
(Poh, Lee, Low, Teo, Tan) Yong Loo Lin School of Medicine, National
University of Singapore, Singapore.
(Liang) Biostatistics Unit, National University of Singapore, Yong Loo Lin
School of Medicine, Singapore.
Title
Two-year clinical registry follow-up of endothelial progenitor cell
capture stent versus sirolimus-eluting bioabsorbable polymer-coated stent
versus bare metal stents in patients undergoing primary percutaneous
coronary intervention for ST elevation myocardial infarction: ACUTE
CORONARY SYNDROME.
Source
Journal of Interventional Cardiology. 23(2)(pp 101-108), 2010. Date of
Publication: April 2010.
Publisher
Blackwell Publishing Inc.
Abstract
Background: Endothelial progenitor cell (EPC) capture stent is designed to
promote rapid endothelization and healing and is potentially useful in
patients undergoing primary percutaneous coronary intervention (PCI) for
acute myocardial infarction (AMI). We studied the intermediate-term
efficacy and safety of EPC stent and compared that with sirolimus-eluting
bioabsorbable polymer stent (CURA) and bare metal stent (BMS) in AMI
patients. Methodology: Patients presenting with AMI who underwent primary
PCI with the respective stents between January 2004 and June 2006 were
enrolled in the single-center clinical registry. The study end-points were
major adverse cardiac events (MACE) and stent thrombosis. Results: A total
of 366 patients (EPC = 95, CURA = 53, BMS 218) were enrolled. Baseline
demographics including age, gender, diabetes, renal impairment,
predischarge left ventricular ejection fraction, and creatinine kinase
level were comparable among the groups. Procedural success rate was 99.5%.
Post-procedural thrombolysis in myocardial infarction (TIMI) 3 flow was
achieved in EPC 91.6%, CURA 96.2%, and BMS 88.5% (P = 0.209). At 2 years,
the MACE rate was EPC 13.7%, CURA 15.1%, and BMS 19.7% (P = 0.383). Target
vessel revascularizations (TVR) were EPC 4.2%, CURA 9.4%, and BMS 6.0% (P
= 0.439). Nonfatal myocardial infarctions were EPC 1.1%, CURA 3.8%, and
BMS 4.1% (P = 0.364). One patient in the EPC group had acute stent
thrombosis. There was no late stent thrombosis in the EPC group.
Conclusion: EPC stent appeared to be safe and had comparable clinical
efficacy with a BMS when used in the AMI setting. At 2-year follow-up, the
EPC group showed favorable, single-digit TVR rate and stent thrombosis
remained a low-event occurrence. copyright 2010, Wiley Periodicals, Inc.

<10>
Accession Number
2010211223
Authors
Galassi A.R. Tomasello S.D. Costanzo L. Campisano M.B. MarzA F. Tamburino
C.
Institution
(Galassi, Tomasello, Costanzo, Campisano, MarzA, Tamburino) Department of
Internal Medicine and Systemic Disease, Ferrarotto Hospital, University of
Catania, Catania, Italy.
Title
Recanalization of complex coronary chronic total occlusions using
high-frequency vibrational energy CROSSER catheter as first-line therapy:
A single center experience.
Source
Journal of Interventional Cardiology. 23(2)(pp 130-138), 2010. Date of
Publication: April 2010.
Publisher
Blackwell Publishing Inc.
Abstract
Background: Several studies have illustrated the safety and the procedural
outcome of high-frequency vibrational energy in guidewire refractory
chronic total occlusions (CTOs). Aim: To evaluate the advantage of
high-frequency vibrational energy device (CROSSER Catheter) use in
coronary complex CTO revascularization as primary strategy. Methods:
CROSSER was used as a primary approach if four or more unfavorable
angiographic features were observed in the CTO lesions. Results: From May
2007 to February 2009, a CTO percutaneous intervention attempt was
performed in 178 lesions of 171 patients (60.1 +/- 8.9 age with 49.4 +/-
7.2% in ejection fraction). Among these, the CROSSER was used in 46
complex CTO lesions of 45 patients (25.8% of cases) and in the remaining
cases, typical CTO percutaneous coronary intervention techniques were
employed. Clinical success was 84.8% in CROSSER group. Moreover, in the
CROSSER group, no periprocedural myocardial infarction, perforation, or 30
days MACE was observed. In addition, the use of CROSSER was associated
with lower time of procedure, time of fluoroscopy, and contrast load
administration as compared with conventional techniques [88 +/- 27 minutes
vs 109 +/- 38 minutes (P = 0.045), 39 +/- 12 minutes vs 50 +/- 27 minutes
(P = 0.032), and 334 +/- 122cc vs 408 +/- 198cc (P = 0.05), respectively].
Conclusion: In the present study, the CROSSER System was safe and obtained
a high rate of success in complex CTO similar to conventional dedicated
guidewire techniques for noncomplex CTO; however, the CROSSER Catheter
obtained CTO recanalization with lower contrast load administration, less
time of procedure, and lower fluoroscopy exposure. copyright 2010, Wiley
Periodicals, Inc.

<11>
Accession Number
2010211219
Authors
Fernandez-Guerrero J.C. Herrador-Fuentes J. Sanchez-Gila J. Guzman-Herrera
M. Lozano C.
Institution
(Fernandez-Guerrero, Herrador-Fuentes, Sanchez-Gila, Guzman-Herrera,
Lozano) Unidad de Hemodinamica, Servicio de Cardiologia, Complejo
Hospitalario de Jaen, C/Avenida Ejercito Espanol, 10, 23007 Jaen, Spain.
Title
In-hospital and 12-month postprocedural clinical outcome of coronary
bifurcational lesion treatment with the endeavor stent.
Source
Journal of Interventional Cardiology. 23(2)(pp 188-194), 2010. Date of
Publication: April 2010.
Publisher
Blackwell Publishing Inc.
Abstract
Background: The zotarolimus-eluting stent (ZES) has been documented as
significantly reducing restenosis and target lesion revascularization
(TLR) requirement compared to bare metal stents (BMS). Methods: In this
single-centered, prospective study we sought to evaluate the short- and
medium-term outcomes of ZES placement in bifurcated coronary artery
lesions. Between August 2006 and December 2007, 107 consecutive patients
(110 bifurcations) were recruited to have ZES placement in the lesion. The
provisional T stenting (PTS) technique was used in 96.3%. Angiographic
success was 100% in main vessel (MV) cases and 97.2% in that of side
branch (SB). Results: With a mean follow-up of 12.4 +/- 1.77 (mean +/- SD)
months there were four deaths, three from cardiac cause (2.85%). There
were 18 patients (19 bifurcations) requiring TLR (17.59%) for clinical
reasons. The only predictor of TLR was the use diameter of ZES [less-than
or equal to]3 mm. Conclusion: ZES can be used for bifurcation lesions
using the PTS technique with a high rate of intraprocedural success;
however, frequency of TLR is high, especially for stents with a diameter
[less-than or equal to]3 mm. copyright 2010, Wiley Periodicals, Inc.

<12>
Accession Number
2010207451
Authors
Angeli F. Verdecchia P. Karthikeyan G. Mazzotta G. Repaci S. Del Pinto M.
Gentile G. Cavallini C. Reboldi G.
Institution
(Angeli, Verdecchia, Mazzotta, Repaci, Del Pinto, Cavallini) Department of
Cardiology, Hospital 'Santa Maria della Misericordia', Perugia, Italy.
(Angeli, Verdecchia) Fondazione Umbra Cuore e Ipertensione, AUCI-ONLUS,
06126 Perugia, Italy.
(Karthikeyan) Departement of Cardiology, All India Institute of Medical
Sciences, New Delhi, India.
(Gentile, Reboldi) Department of Internal Medicine, University of Perugia,
Perugia, Italy.
Title
beta-blockers and risk of all-cause mortality in non-cardiac surgery.
Source
Therapeutic Advances in Cardiovascular Disease. 4(2)(pp 109-118), 2010.
Date of Publication: April 2010.
Publisher
SAGE Publications Ltd
Abstract
Myocardial ischemia is a frequent complication in patients undergoing
non-cardiac surgery and beta-blockers may exert a protective effect. The
main benefit of beta-blockers in perioperative cardiovascular morbidity
and mortality is believed to be linked to specific effects on myocardial
oxygen supply and demand. beta-blockers may exert anti-inflammatory and
anti-arrhythmic effects. Randomized clinical trials which evaluated the
effects of beta-blockers on all-cause mortality in patients undergoing
non-cardiac surgery have yielded conflicting results. In 9 trials, 10,544
patients with non-cardiac surgery were randomized to beta-blockers (n =
5274) or placebo (n = 5270) and there were a total of 304 deaths. Patients
randomized to beta-blockers group showed a 19% increased risk of all-cause
mortality (odds ratio [OR] 1.19, 95% confidence interval (CI) 0.95-1.50; p
= 0.135). However, trials included in the meta-analysis differed in
several aspects, and a significant degree of heterogeneity (I2 = 46.5%)
was noted. A recent analysis showed that the surgical risk category had a
substantial influence on the overall estimate of the effect of
beta-blockers. Compared with patients in the
intermediate-high-surgical-risk category, those in the high-risk category
showed a 73% reduction in the risk of total mortality with beta-blockers
compared with placebo (OR 0.27, 95% CI 0.10-0.71, p = 0.016). These data
suggest that perioperative beta-blockers confer a benefit which is mostly
limited to patients undergoing high-risk surgery. copyright The Author(s),
2010.

<13>
Accession Number
2010173773
Authors
Onorati F. Rubino A.S. Nucera S. Foti D. Sica V. Santini F. Gulletta E.
Renzulli A.
Institution
(Onorati, Rubino, Nucera, Renzulli) Cardiac Surgery Unit, Magna Graecia
University of Catanzaro, Catanzaro, Italy.
(Foti, Gulletta) Pathology Unit, Magna Graecia University of Catanzaro,
Catanzaro, Italy.
(Santini) Cardiac Surgery Unit, University of Verona, Verona, Italy.
(Sica) Institute of Pathology, Second University of Naples, Naples, Italy.

Title
Off-pump coronary artery bypass surgery versus standard linear or
pulsatile cardiopulmonary bypass: endothelial activation and inflammatory
response.
Source
European Journal of Cardio-thoracic Surgery. 37(4)(pp 897-904), 2010.
Date of Publication: April 2010.
Publisher
Elsevier
Abstract
Objective: Poor outcomes after coronary artery bypass grafting (CABG) have
been linked to perioperative endothelial activation and systemic
inflammatory responses. The use of pulsatile cardiopulmonary bypass (PCPB)
or off-pump CABG (OPCABG) may minimise these phenomena. We compared
biochemical and clinical outcomes among patients who underwent CABG with
PCPB, CABG with linear CPB (LCPB) or OPCABG. Methods: Sixty consecutive
patients undergoing isolated elective CABG were prospectively randomised
trial to receive pulsatile CPB (group A, 20 patients), linear CPB (group
B, 20 patients) or OPCABG (group C, 20 patients). Levels of
proinflammatory cytokines (interleukins-2, -6, and -8), anti-inflammatory
cytokines (interleukin-10) and endothelial markers (vascular endothelial
growth factor (VEGF), monocyte chemo-attractant protein (MCP)-1) were
measured before, during and after surgery. Results: VEGF and MCP-1 levels
increased significantly during surgery in all groups, but they increased
the least and were the lowest overall with OPCABG. They rose most and
peaked overall with LCPB. Interleukin-2 levels remained stable during
OPCABG but decreased equally during PCPB and LCPB. Interleukin-6 and -8
levels rose significantly during both types of CPB versus OPCABG.
Interleukin-10 levels increased significantly in all groups during
surgery, but they rose least and were the lowest overall with OPCABG and
rose most and were the highest overall with PCPB. Intubation times,
intensive care unit (ICU) stay and hospital stay were significantly longer
in the LCPB group than the other two groups. Conclusions: LCPB appears to
promote endothelial activation and cytokine secretion, which may delay
recovery. OPCABG was associated with slight endothelial activation and
cytokine response. PCPB significantly attenuates endothelial/cytokine
leakage, resulting in hospital outcomes comparable with those after
OPCABG. copyright 2009 European Association for Cardio-Thoracic Surgery.

<14>
Accession Number
2010177833
Authors
Wu N. Yan S. Wang X. Lv C. Wang J. Zheng Q. Feng Y. Yang Y.
Institution
(Wu, Yan, Wang, Lv, Wang, Zheng, Feng, Yang) Key laboratory of
Carcinogenesis and Translational Research (Ministry of Education),
Department of Thoracic Surgery II, Peking University School of Oncology,
No. 52, Fucheng Avenue, Haidian District, Beijing 100142, China.
Title
A prospective, single-blind randomised study on the effect of intercostal
nerve protection on early post-thoracotomy pain relief.
Source
European Journal of Cardio-thoracic Surgery. 37(4)(pp 840-845), 2010.
Date of Publication: April 2010.
Publisher
Elsevier
Abstract
Objectives: Intracostal suture or intercostal muscle flap can reduce
post-thoracotomy pain through the preservation of intercostal nerves below
or above the incision. This study aims to test whether combining
intracostal suture with intercostal muscle flap might achieve better pain
relief than intracostal suture alone. Methods: This study included 144
consecutive patients who underwent pulmonary resection. Eighty patients
entered the trial but eight were excluded. Seventy-two patients were
randomly assigned to a muscle flap group, in which the fifth intercostal
muscle and neurovascular bundle were raised and intracostal suture on the
sixth rib was applied. For the control group, only intracostal suturing on
the sixth rib was done. All patients had a functional epidural placed,
which were removed 24 h after surgery. Differences on average numeric
rating scale (aNRS) scores were assessed in an early post-operative period
from day 1 to day 7 and a later period from week 2 to week 12, when
patients were resting or coughing. The doses of oxycodone demand and
hyperalgesia-related intercostal dermatomes (HIDs) were recorded for
analysis. Results: No differences were noted between the two groups in
terms of length and width of the incision, or duration of rib retraction.
Neither in different time periods (early or late) nor the activity status
(while resting or coughing) yielded a statistical difference on aNRS
scores between the muscle flap group and the control group (muscle flap
group vs control group: mean (95% confidence intervals) from d ay 1 to day
7, 4.42 (1.56-7.28) vs 4.79 (2.03-7.55) on coughing (p = 0.282); median
(inter-quartile range, IQR) from day 1 to day 7, 1.71 (0.86-3) vs 2.50
(1.16-3.12) while resting (p = 0.279); median (IQR) from week 2 to week
12, 0.43 (0-0.86) vs 0.48 (0.06-1.20) on coughing (p = 0.595); median
(IQR) from week 2 to week 12, 0 (0-0.14) vs 0.05 (0-0.14) while resting (p
= 0.856)). No differences were found in total oxycodone consumption from
day 1 to day 7 between the two groups (Z = -1.821, p = 0.069). The rate of
HIDs in each intercostal space and median number of HIDs were similar
between the two groups on day 1 (p > 0.05) and day 7 (p > 0.05).
Conclusions: The combination of intracostal suture with intercostal muscle
flap may not necessarily achieve better post-thoracotomy pain control than
using intracostal suture alone. copyright 2009 European Association for
Cardio-Thoracic Surgery.

<15>
Accession Number
2010177832
Authors
Cardillo G. Carleo F. Giunti R. Lopergolo M.G. Salvadori L. De Massimi
A.R. Petrella L. Martelli M.
Institution
(Cardillo, Carleo, Giunti, Lopergolo, Salvadori, De Massimi, Martelli)
Unit of Thoracic Surgery, Carlo Forlanini Hospital, Azienda Ospedaliera
San Camillo-Forlanini, Via Portuense 332, 00149 Rome, Italy.
(Petrella) Department of Studi Geoeconomici, Linguistici, Statistici,
Storici per l'Analisi Regionale, Sapienza University of Rome, Rome, Italy.

Title
Predictors of survival in patients with locally advanced thymoma and
thymic carcinoma (Masaoka stages III and IVa).
Source
European Journal of Cardio-thoracic Surgery. 37(4)(pp 819-823), 2010.
Date of Publication: April 2010.
Publisher
Elsevier
Abstract
Objective: We sought to evaluate factors influencing long-term survival of
patients with locally advanced thymoma/thymic carcinoma (Masaoka stages
III and IVa) treated by immediate surgery or induction therapy plus
surgery. Methods: From January 1991 to April 2007, we surgically treated
61 patients with locally advanced thymoma/thymic carcinoma (Masaoka stages
III and IVa). Staging included total body computed tomography (CT) scan in
all patients, and chest magnetic resonance imaging (MRI) in 27 selected
patients. All patients had histological confirmation before surgery.
Thirty-one patients (group A) underwent induction chemotherapy followed by
surgery. Thirty patients (group B) underwent immediate surgery.
Thirty-four patients (group A: 13; group B: 17) received postoperative
radiation therapy. Results: No intra-operative mortality was reported.
World Health Organization (WHO) histological classification included 19
AB, four B1, seven B2 and 13 B3 thymomas and 18 thymic carcinomas.
Thirty-four patients were Masaoka stage III (group A: 18; group B: 16) and
27 patients were stage IVa (group A: 13; group B: 14). After a median
follow-up of 77 months, six patients of group A and seven patients of
group B died of disease. The overall 10-year survival rate was 50.6%. The
10-year survival rate was 57.9% in group A and 38.1% in group B (p =
0.03). Multivariate analysis showed complete resection (p = 0.02), Masaoka
stage (III vs IVa) (p = 0.02), induction chemotherapy (group A vs group B)
(p = 0.003) and histological WHO subtype (AB vs B1, B2 and B3) (p = 0.01)
to be statistically significant independent predictors of survival. Sex,
age and adjuvant radiation therapy showed no statistically significant
difference. Conclusions: Complete resection, Masaoka stage, induction
chemotherapy and histological WHO classification showed to be independent
predictors of survival in locally advanced thymoma/thymic carcinoma.
copyright 2009 European Association for Cardio-Thoracic Surgery.

<16>
Accession Number
2010173724
Authors
Fan Y. Zhang A.-M. Xiao Y.-B. Weng Y.-G. Hetzer R.
Institution
(Fan, Xiao) Department of Cardiothoracic and Vascular Surgery, Chongqing
Xinqiao Hospital, Third Military Medical University, Chongqing, China.
(Zhang) Department of Oncology, Chongqing Xinqiao Hospital, Third Military
Medical University, Chongqing, China.
(Weng, Hetzer) Department of Cardiothoracic and Vascular Surgery,
Deutsches Herzzentrum Berlin, Berlin, Germany.
Title
Warm versus cold cardioplegia for heart surgery: a meta-analysis.
Source
European Journal of Cardio-thoracic Surgery. 37(4)(pp 912-919), 2010.
Date of Publication: April 2010.
Publisher
Elsevier
Abstract
Much controversy persists regarding the optimal techniques for myocardial
protection during heart surgery. Numerous studies have compared warm
cardioplegia with cold cardioplegia for myocardial preservation, but the
outcomes were inconclusive. The aim of this meta-analysis of randomised
controlled trials (RCTs) was to compare the beneficial and harmful effects
of warm and cold cardioplegia during heart surgery. Electronic databases
and manual bibliographical searches were conducted. A meta-analysis of all
RCTs comparing warm cardioplegia to cold cardioplegia perfusion during
cardiac surgery was performed. Data for clinical events (in-hospital
death, myocardial infarction (MI), low output syndrome, postoperative use
of intra-aortic balloon pump, stroke and atrial fibrillation),
postoperative cardiac index, postoperative creatine kinase-MB (CK-MB) and
cardiac troponin release were extracted, and we summarised the combined
results of the data of the RCTs as relative risk (RR), with 95% confidence
intervals. A total of 41 RCTs including 5879 patients were assessed in
this study. We found that there was no statistical difference between
patients receiving warm cardioplegia and cold cardioplegia in the
incidences of clinical events. Warm cardioplegia was associated with
improved postoperative cardiac index. CK-MB and cardiac troponin
concentrations after surgery were significantly lower in the warm group as
compared with the cold group. Using warm cardioplegia for myocardial
protection during heart surgery resulted in similar incidences of clinical
events, significant improvement in postoperative cardiac index and
reduction in postoperative enzyme release as compared with cold
cardioplegia. copyright 2009 European Association for Cardio-Thoracic
Surgery.

<17>
Accession Number
2010218092
Authors
Ovrum E. Tangen G. Tollofsrud S. Ringdal M.-A.L. Oystese R. Istad R.
Institution
(Ovrum, Tangen, Tollofsrud, Ringdal, Oystese, Istad) Division of
Cardiovascular and Respiratory Medicine and Surgery, Oslo Heart Center,
Oslo University Hospital, Rikshospitalet, Norway.
Title
Low postoperative dose of aprotinin reduces bleeding and is safe in
patients receiving clopidogrel before coronary artery bypass surgery. A
prospective randomized study.
Source
Interactive Cardiovascular and Thoracic Surgery. 10(4)(pp 545-548), 2010.
Date of Publication: April 2010.
Publisher
European Association for Cardio-Thoracis Surgery
Abstract
Clopidogrel (Plavix) given before the operation increases bleeding
complications following coronary artery bypass grafting (CABG). High
perioperative doses of aprotinin (Trasylol) are known to reduce bleeding
and transfusions after cardiac surgery, but may increase the risk of
thrombosis, renal impairment, and mortality. The aim of the study was to
evaluate the clinical effects of aprotinin given in high doses intra- and
postoperatively vs. a low postoperative dose in patients on clopidogrel.
Patients admitted for first-time CABG and receiving clopidogrel with or
without aspirin, were prospectively randomized either to receive a total
of 75,000 kallikrein inhibitor unit (KIU)/kg aprotinin given intra- and
postoperatively or 25,000 KIU/kg aprotinin after the operation. Three
hundred and ninety-nine patients aged 32-87 years (median 67 years) were
included. Postoperative bleeding was slightly different, but moderate in
both groups. The transfusion rate was similar, as were the incidences of
postoperative neurological disturbances and myocardial infarction. Renal
impairment and need for inotropic drugs were more frequent in the high
dose group. Thirty-day mortality was similar (high dose 2%, low dose 0.5%,
P=0.22). A low postoperative dose of aprotinin in patients receiving
clopidogrel is safe and has comparable effects regarding postoperative
bleeding complications as a high dose. copyright 2010 Published by
European Association for Cardio-Thoracic Surgery.

<18>
Accession Number
2010210919
Authors
Piscione F. Piccolo R. Cassese S. Galasso G. D'Andrea C. De Rosa R.
Chiariello M.
Institution
(Piscione, Piccolo, Cassese, Galasso, D'Andrea, De Rosa, Chiariello)
Department of Clinical Medicine, Cardiovascular Sciences and Immunology,
Federico II University, Naples, Italy.
Title
Is direct stenting superior to stenting with predilation in patients
treated with percutaneous coronary intervention? Results from a
meta-analysis of 24 randomised controlled trials.
Source
Heart. 96(8)(pp 588-594), 2010. Date of Publication: April 2010.
Publisher
BMJ Publishing Group
Abstract
Background: In the last decade, direct stenting has been proposed as an
alternative strategy to conventional stenting with balloon predilation.
The aim of this study was to perform a meta-analysis of randomised trials
comparing a direct stenting strategy versus a conventional one. Methods: A
literature search was performed using Medline, EMBASE, the Cochrane
Central Register of Controlled Trials, scientific session abstracts and
relevant websites, from inception of each database to June 2009. Included
studies comprised randomised controlled trials evaluating direct versus
conventional stenting in patients undergoing percutaneous coronary
intervention. Primary endpoint was the composite of death or myocardial
infarction and secondary endpoints were myocardial infarction and
target-vessel revascularisation occurrence. Results: 24 trials met
inclusion criteria, with 6803 patients enrolled (3412 or 50.15% randomised
to direct stenting and 3391 or 49.85% randomised to conventional
stenting). Up to 6-month follow-up, the composite of death or myocardial
infarction was significantly reduced with direct stenting compared with
conventional stenting (3.95% versus 5.10% respectively, OR=0.76 (95% CI
0.60 to 0.96), p=0.02). This reduction was primarily driven by a lower
myocardial infarction occurrence (3.16% versus 4.04%, respectively,
OR=0.77 (0.59 to 0.99), p=0.04). Furthermore, direct stenting was not
associated with a reduction in target-vessel revascularisation (6.50%
versus 6.96%, respectively, OR=0.92 (0.76 to 1.12), p=0.42). Conclusion:
This meta-analysis demonstrates that, in selected coronary lesions, direct
stenting improves outcome in patients undergoing percutaneous coronary
intervention, primarily reducing myocardial infarction incidence.

<19>
Accession Number
2010210670
Authors
Flores G.
Title
Racial and ethnic disparities in the health and health care of children.
Source
Pediatrics. 125(4)(pp e979-e1020), 2010. Date of Publication: April 2010.
Publisher
American Academy of Pediatrics
Abstract
OBJECTIVE: This technical report reviews and synthesizes the published
literature on racial/ethnic disparities in children's health and health
care. METHODS: A systematic review of the literature was conducted for
articles published between 1950 and March 2007. Inclusion criteria were
peer-reviewed, original research articles in English on racial/ ethnic
disparities in the health and health care of US children. Search terms
used included "child," "disparities," and the Index Medicus terms for each
racial/ethnic minority group. RESULTS: Of 781 articles initially reviewed,
111 met inclusion criteria and constituted the final database. Review of
the literature revealed that racial/ethnic disparities in children's
health and health care are quite extensive, pervasive, and persistent.
Disparities were noted across the spectrum of health and health care,
including in mortality rates, access to care and use of services,
prevention and population health, health status, adolescent health,
chronic diseases, special health care needs, quality of care, and organ
transplantation. Mortality-rate disparities were noted for children in all
4 major US racial/ethnic minority groups, including substantially greater
risks than white children of all-cause mortality; death from drowning,
from acute lymphoblastic leukemia, and after congenital heart defect
surgery; and an earlier median age at death for those with Down syndrome
and congenital heart defects. Certain methodologic flaws were commonly
observed among excluded studies, including failure to evaluate children
separately from adults (22%), combining all nonwhite children into 1 group
(9%), and failure to provide a white comparison group (8%). Among studies
in the final database, 22% did not perform multivariable or stratified
analyses to ensure that disparities persisted after adjustment for
potential confounders. CONCLUSIONS: Racial/ethnic disparities in
children's health and health care are extensive, pervasive, and
persistent, and occur across the spectrum of health and health care.
Methodologie flaws were identified in how such disparities are sometimes
documented and analyzed. Optimal health and health care for all children
will require recognition of disparities as pervasive problems,
methodologically sound disparities studies, and rigorous evaluation of
disparities interventions.

<20>
Accession Number
2010210628
Authors
Snookes S.H. Gunn J.K. Eldridge B.J. Donath S.M. Hunt R.W. Galea M.P.
Shekerdemian L.
Institution
(Snookes, Eldridge) Physiotherapy Department, Melbourne, VIC, Australia.
(Gunn, Hunt) Department of Neonatal Medicine, Melbourne, VIC, Australia.
(Donath) Clinical Epidemiology and Biostatistics Unit, Melbourne, VIC,
Australia.
(Shekerdemian) Paediatric Intensive Care Unit, Royal Children's Hospital,
Melbourne, VIC, Australia.
(Snookes, Galea) School of Physiotherapy, Melbourne, VIC, Australia.
(Gunn, Donath, Hunt, Shekerdemian) Department of Paediatrics, University
of Melbourne, Melbourne, VIC, Australia.
(Gunn, Hunt, Shekerdemian) Critical Care and Neurosciences, Melbourne,
VIC, Australia.
(Donath) Clinical Epidemiology and Biostatistics Unit, Murdoch Children's
Research Institute, Melbourne, VIC, Australia.
Title
A systematic review of motor and cognitive outcomes after early surgery
for congenital heart disease.
Source
Pediatrics. 125(4)(pp e818-e827), 2010. Date of Publication: April 2010.
Publisher
American Academy of Pediatrics
Abstract
CONTEXT: Brain injury is the most common long-term complication of
congenital heart disease requiring surgery during infancy. It is clear
that the youngest patients undergoing cardiac surgery, primarily neo-nates
and young infants, are at the greatest risk for brain injury.
Develop-mental anomalies sustained early in life have lifelong
repercussions. OBJECTIVE: We conducted a systematic reviewto examine
longitudinal studies of cognitive and/or motor outcome after cardiac
surgery dur-ing early infancy. METHODS: Electronic searches were performed
in Medline, the Cumu-lative Index to Nursing and Allied Health Literature
(Cinahl), and Em-base (1998-2008). The search strategy yielded 327
articles, of which 65 were reviewed. Eight cohorts provided prospective
data regarding the cognitive and/or motor outcome of infants who had
undergone surgery for congenital heart disease before 6 months of age. Two
authors, Ms Snookes and Dr Gunn, independently extracted data and
presented results according to 3 subgroups for age of follow-up: early
develop-ment (1 to <3 years); preschool age (3-5 years); and school age
(>5 to 17 years). Weighted analysis was undertaken to pool the results of
studies when appropriate. RESULTS: All of the identified studies reported
results of the Bayley Scales of Infant Development for children younger
than the age of 3. Outcome data as reported by the Bayley Scales were
combined for infants assessed at 1 year of age, revealing a weighted mean
Mental Development Index of 90.3 (95% confidence interval: 88.9-91.6) and
Psychomotor Development Index of 78.1 (95% confidence interval:
76.4-79.7). Additional analysis was limited by a lack of data at
pre-school and school age. CONCLUSIONS: With this review we identified a
limited number of pro-spective studies that systematically addressed
outcome in patients at the highest risk. These studies consistently
revealed cognitive and mo-tor delay in children after cardiac surgery
during early infancy. Addi-tional investigation is required to ascertain
the consequences of such impairment during later childhood and into adult
life.

<21>
[Use Link to view the full text]
Accession Number
2010172125
Authors
Eder B. Hofmann P. Von Duvillard S.P. Brandt D. Schmid J.-P. Pokan R.
Wonisch M.
Institution
(Eder, Brandt, Wonisch) Center for Cardiac Rehabilitation, PVA SKA,
Quellenstr.1, Graz, A-8061 St Radegund, Austria.
(Hofmann) Institute of Sports Sciences, Human Performance Research,
Karl-Franzens University Graz, Austria.
(Von Duvillard) Department of Sport Science and Kinesiology, University of
Salzburg, Austria.
(Schmid) Swiss Cardiovascular Centre Bern, Cardiovascular Prevention and
Rehabilitation, University Hospital, Switzerland.
(Pokan) Institute of Sports Science, University of Vienna, Austria.
Title
Early 4-week cardiac rehabilitation exercise training in elderly patients
after heart surgery.
Source
Journal of Cardiopulmonary Rehabilitation and Prevention. 30(2)(pp
85-92), 2010. Date of Publication: March-April 2010.
Publisher
Lippincott Williams and Wilkins
Abstract
Purpose: The aim of this study was to assess the effects on exercise
performance of supplementing a standard cardiac rehabilitation program
with additional exercise programming compared to the standard cardiac
rehabilitation program alone in elderly patients after heart surgery.
Methods: In this prospective, randomized controlled trial, 60 patients (32
men and 28 women, mean age 73.1 +/- 4.7 years) completed cardiac
rehabilitation (initiated 12.2 +/- 4.9 days postsurgery). Subjects were
assigned to either a control group (CG, standard cardiac rehabilitation
program [n = 19]), or an intervention group (IG, additional walking [n =
19], or cycle ergometry training [n = 22]). A symptom limited
cardiopulmonary exercise test and 6-minute walk test (6MWT) were performed
before and after 4 weeks of cardiac rehabilitation. The MacNew
questionnaire was used to assess quality of life (QOL). Results: At
baseline, no significant differences for peak oxygen uptake (V[dot]2),
maximal power output, or the 6MWT were detected between IG and CG. Global
QOL was significantly higher in IG. After 4 weeks of cardiac
rehabilitation, patients significantly improved in absolute values of the
cardiopulmonary exercise test, 6MWT, and QOL scores. Significant
differences between groups were found for peak V[dot]2 (IG: 18.2 +/- 3.1
mL*kg-1*min -1 vs. CG: 16.5 +/- 2.2 mL*kg*min, P < .05); maximal power
output (IG: 72.2 +/- 16 W vs. CG: 60.7 +/- 15 W, P < .05); 6MWT (IG: 454.8
+/- 76.3 m vs. CG: 400.5 +/- 75.5 m, P < .05); and QOL global (IG: 6.5 +/-
0.5 vs. CG: 6.3 +/- 0.6, P < .05). Conclusion: The supplementation of
additional walking or cycle exercise training to standard cardiac
rehabilitation programming compared to standard cardiac rehabilitation
alone in elderly patients after heart surgery leads to significantly
better exercise tolerance.

Saturday, April 24, 2010

EMBASE Cardiac Update AutoAlert: EPICORE Cardiac Surgery Blogger2

Total documents retrieved: 18

Results Generated From:
EMBASE <1980 to 2010 Week 16>
EMBASE (updates since 2010-04-15)


<1>
Accession Number
0020237039
Authors
Abraham A. Nichol G. Williams K.A. Guo A. deKemp R.A. Garrard L. Davies
R.A. Duchesne L. Haddad H. Chow B. DaSilva J. Beanlands R.S.
Institution
(Abraham, Nichol, Williams, Guo, deKemp, Garrard, Davies, Duchesne,
Haddad, Chow, DaSilva, Beanlands) National Cardiac PET Centre and Division
of Cardiology, Cardiovascular Research Methods Centre, University of
Ottawa Heart Institute, Ottawa, Ontario, Canada.
Title
18F-FDG PET imaging of myocardial viability in an experienced center with
access to 18F-FDG and integration with clinical management teams: the
Ottawa-FIVE substudy of the PARR 2 trial..
Source
Journal of nuclear medicine : official publication, Society of Nuclear
Medicine. 51(4)(pp 567-574), 2010. Date of Publication: Apr 2010.
Abstract
(18)F-FDG PET may assist decision making in ischemic cardiomyopathy. The
PET and Recovery Following Revascularization (PARR 2) trial demonstrated a
trend toward beneficial outcomes with PET-assisted management. The
substudy of PARR 2 that we call Ottawa-FIVE, described here, was a post
hoc analysis to determine the benefit of PET in a center with experience,
ready access to (18)F-FDG, and integration with clinical teams. METHODS:
Included were patients with left ventricular dysfunction and suspected
coronary artery disease being considered for revascularization. The
patients had been randomized in PARR 2 to PET-assisted management (group
1) or standard care (group 2) and had been enrolled in Ottawa after August
1, 2002 (the date that on-site (18)F-FDG was initiated) (n = 111). The
primary outcome was the composite endpoint of cardiac death, myocardial
infarction, or cardiac rehospitalization within 1 y. Data were compared
with the rest of PARR 2 (PET-assisted management [group 3] or standard
care [group 4]). RESULTS: In the Ottawa-FIVE subgroup of PARR 2, the
cumulative proportion of patients experiencing the composite event was 19%
(group 1), versus 41% (group 2). Multivariable Cox proportional hazards
regression showed a benefit for the PET-assisted strategy (hazard ratio,
0.34; 95% confidence interval, 0.16-0.72; P = 0.005). Compared with other
patients in PARR 2, Ottawa-FIVE patients had a lower ejection fraction
(25% +/- 7% vs. 27% +/- 8%, P = 0.04), were more often female (24% vs.
13%, P = 0.006), tended to be older (64 +/- 10 y vs. 62 +/- 10 y, P =
0.07), and had less previous coronary artery bypass grafting (13% vs. 21%,
P = 0.07). For patients in the rest of PARR 2, there was no significant
difference in events between groups 3 and 4. The observed effect of
(18)F-FDG PET-assisted management in the 4 groups in the context of
adjusted survival curves demonstrated a significant interaction (P =
0.016). Comparisons of the 2 arms in Ottawa-FIVE to the 2 arms in the rest
of PARR 2 demonstrated a trend toward significance (standard care, P =
0.145; PET-assisted management, P = 0.057). CONCLUSION: In this post hoc
group analysis, a significant reduction in cardiac events was observed in
patients with (18)F-FDG PET-assisted management, compared with patients
who received standard care. The results suggest that outcome may be
benefited using (18)F-FDG PET in an experienced center with ready access
to (18)F-FDG and integration with imaging, heart failure, and
revascularization teams.

<2>
Accession Number
2010217625
Authors
Hemingway H. Henriksson M. Chen R. Damant J. Fitzpatrick N. Abrams K.
Hingorani A. Janzon M. Shipley M. Feder G. Keogh B. Stenestrand U.
McAllister K. Kaski J.-C. Timmis A. Palmer S. Sculpher M.
Institution
(Hemingway, Chen, Damant, Fitzpatrick, Hingorani, Shipley, McAllister)
Department of Epidemiology and Public Health, University College London,
United Kingdom.
(Henriksson) Centre for Medical Technology Assessment, Linkoping
University, Sweden.
(Henriksson, Palmer, Sculpher) Centre for Health Economics, University of
York, United Kingdom.
(Abrams) Department of Health Sciences, University of Leicester, United
Kingdom.
(Janzon, Stenestrand) Department of Cardiology, Linkoping University,
Sweden.
(Feder) Department of Primary Health Care, University of Bristol, United
Kingdom.
(Keogh) Department of Health, London, United Kingdom.
(Kaski) Cardiovascular Biology Research Centre, St George's, University of
London, United Kingdom.
(Timmis) Barts and the London NHS Trust, London, United Kingdom.
Title
The effectiveness and costeffectiveness of biomarkers for the
prioritisation of patients awaiting coronary revascularisation: A
systematic review and decision model.
Source
Health Technology Assessment. 14(9)(pp 1-178), 2010. Date of Publication:
2010.
Publisher
National Co-ordinating Centre for HTA
Abstract
Objective: To determine the effectiveness and cost-effectiveness of a
range of strategies based on conventional clinical information and novel
circulating biomarkers for prioritising patients with stable angina
awaiting coronary artery bypass grafting (CABG). Data sources: MEDLINE and
EMBASE were searched from 1966 until 30 November 2008. Review methods: We
carried out systematic reviews and meta-analyses of literature-based
estimates of the prognostic effects of circulating biomarkers in stable
coronary disease. We assessed five routinely measured biomarkers and the
eight emerging (i.e. not currently routinely measured) biomarkers
recommended by the European Society of Cardiology Angina guidelines. The
cost-effectiveness of prioritising patients on the waiting list for CABG
using circulating biomarkers was compared against a range of alternative
formal approaches to prioritisation as well as no formal prioritisation. A
decision-analytic model was developed to synthesise data on a range of
effectiveness, resource use and value parameters necessary to determine
costeffectiveness. A total of seven strategies was evaluated in the final
model. Results: We included 390 reports of biomarker effects in our
review. The quality of individual study reports was variable, with
evidence of small study (publication) bias and incomplete adjustment for
simple clinical information such as age, sex, smoking, diabetes and
obesity. The risk of cardiovascular events while on the waiting list for
CABG was 3 per 10,000 patients per day within the first 90 days (184
events in 9935 patients with a mean of 59 days at risk). Risk factors
associated with an increased risk, and included in the basic risk
equation, were age, diabetes, heart failure, previous myocardial
infarction and involvement of the left main coronary artery or
three-vessel disease. The optimal strategy in terms of cost-effectiveness
considerations was a prioritisation strategy employing biomarker
information. Evaluating shorter maximum waiting times did not alter the
conclusion that a prioritisation strategy with a risk score using
estimated glomerular filtration rate (eGFR) was cost-effective. These
results were robust to most alternative scenarios investigating other
sources of uncertainty. However, the cost-effectiveness of the strategy
using a risk score with both eGFR and Creactive protein (CRP) was
potentially sensitive to the cost of the CRP test itself (assumed to be
[pounds]6 in the base-case scenario). Conclusions: Formally employing more
information in the prioritisation of patients awaiting CABG appears to be
a cost-effective approach and may result in improved health outcomes. The
most robust results relate to a strategy employing a risk score using
conventional clinical information together with a single biomarker (eGFR).
The additional prognostic information conferred by collecting the more
costly novel circulating biomarker CRP, singly or in combination with
other biomarkers, in terms of waiting list prioritisation is unlikely to
be cost-effective. copyright 2010 Queen's Printer and Controller of HMSO.

<3>
Accession Number
0020091633
Authors
Hollands G.J. Hankins M. Marteau T.M.
Institution
(Hollands, Hankins, Marteau) Health Psychology Section, King's College
London, 5th Floor, Bermondsey Wing, Guy's Campus, London, UK, SE1 9RT.
Title
Visual feedback of individuals' medical imaging results for changing
health behaviour..
Source
Cochrane database of systematic reviews (Online). (1)(pp CD007434), 2010.
Date of Publication: 2010.
Abstract
BACKGROUND: Feedback of medical imaging results can reveal visual evidence
of actual bodily harm attributable to a given behaviour. This may offer a
particularly promising approach to motivating changes in health behaviour
to decrease risk. Applicable behaviours include smoking cessation, skin
self-examination, sun protection behaviour, dietary intake, physical
activity and medication usage. The current review assembles and evaluates
the evidence concerning the behavioural impact of showing and explaining
images, in order to determine whether their communication is an effective
intervention approach. OBJECTIVES: To assess the extent to which feedback
to individuals of images of their own bodies created during medical
imaging procedures increases or decreases a range of health behaviours.
SEARCH STRATEGY: We searched the Cochrane Central Register of Controlled
Trials (CENTRAL, The Cochrane Library, Issue 3 2009), MEDLINE (1950 to 14
September 2009), EMBASE (1980 to 14 September 2009), CINAHL (1982 to 9
October 2009), PsycINFO (1806 to 14 September 2009) and reference lists of
articles. We also contacted authors of selected papers, and searched the
ProQuest Dissertations and Theses database on 1 October 2009 for grey
literature. SELECTION CRITERIA: Randomised or quasi-randomised controlled
trials involving adult (18 years and over) non-pregnant individuals
undergoing medical imaging procedures assessing risk of disease or of an
existing condition, for which personal risk may be reduced by modification
of behaviour. The sole or principal component of included interventions is
visual feedback of individuals' medical imaging results, defined as
individuals being shown, and having explained, source images (still or
moving images) of their bodies generated by the procedure. DATA COLLECTION
AND ANALYSIS: Two authors searched for studies and independently extracted
data from included studies, with disagreements resolved by consensus and a
third author acting as arbiter. The risk of bias of included studies was
assessed and reported in accordance with the guidelines in the Cochrane
Handbook for Systematic Reviews of Interventions. We conducted a narrative
synthesis of the included studies, dividing them into clinical and
non-clinical population groups and presenting major characteristics and
results. Where the studies were sufficiently similar in terms of
population, inclusion criteria, interventions and/or outcomes, we pooled
the data statistically. MAIN RESULTS: We included nine trials involving
1371 participants. Overall, results were mixed. Regarding five trials in
clinical populations, three assessed smoking cessation behaviours, all
featuring arterial scanning procedures to assess cardiovascular risk, and
reported a statistically significant effect favouring the intervention,
producing a pooled odds ratio (OR) of 2.81 (95% confidence interval (CI)
1.23 to 6.41, P = 0.01). One of these trials also measured physical
activity and reported no statistically significant difference between the
groups. A further trial measured skin examination behaviour following a
skin photography procedure for assessing moles, and reported a
statistically significant increase in favour of the intervention, with an
OR of 4.86 (95% CI 1.95 to 12.10, P = 0.0007). The final clinical
population trial measured a range of dietary intake and medication usage
behaviours and featured an arterial scanning procedure assessing
cardiovascular risk, and reported no statistically significant
effects.Among the four trials in non-clinical populations, all featuring
ultraviolet (UV) photography to highlight UV-related skin damage, a
statistically significant result favouring the intervention was found in
one trial for reducing tanning booth use, producing a mean difference (MD)
of -1.10 (95% CI -1.90 to -0.30, P = .007) and one trial reported an
outcome on which the control condition was favoured, with an MD of 0.45
(95% CI 0.04 to 0.86, P = 0.03) on intentional hours spent in the sun. In
two further trials, no statistically significant behavioral effects were
reported regarding time spent in the sun or sun protection
behaviours.There was no evidence of significant adverse effects in the
included trials, although this was not well reported. AUTHORS'
CONCLUSIONS: Due to the limited nature of the available evidence and the
mixed results that were found, no strong statements can be made about the
effectiveness of communicating medical imaging results to change health
behaviour. Only three trials in clinical populations were similar enough
in term of setting, intervention and outcome to allow meta-analysis. We
suggest, however, that targeted interventions using medical imaging
technologies may be effective in certain contexts, or as applied to
certain behaviours, but that this should be considered on an intervention
by intervention basis, and not assumed as a general principle.

<4>
Accession Number
0020091618
Authors
Taylor R.S. Dalal H. Jolly K. Moxham T. Zawada A.
Institution
(Taylor, Dalal, Jolly, Moxham, Zawada) PenTAG, Peninsula Medical School,
University of Exeter, Noy Scott House, Barrack Road, Exeter, UK, EX2 5DW.

Title
Home-based versus centre-based cardiac rehabilitation..
Source
Cochrane database of systematic reviews (Online). (1)(pp CD007130), 2010.
Date of Publication: 2010.
Abstract
BACKGROUND: The burden of cardiovascular disease world-wide is one of
great concern to patients and health care agencies alike. Traditionally
centre-based cardiac rehabilitation (CR) programmes are offered to
individuals after cardiac events to aid recovery and prevent further
cardiac illness. Home-based cardiac rehabilitation programmes have been
introduced in an attempt to widen access and participation. OBJECTIVES: To
determine the effectiveness of home-based cardiac rehabilitation
programmes compared with supervised centre-based cardiac rehabilitation on
mortality and morbidity, health-related quality of life and modifiable
cardiac risk factors in patients with coronary heart disease. SEARCH
STRATEGY: We updated the search of a previous review by searching the
Cochrane Central Register of Controlled Trials (CENTRAL) in The Cochrane
Library (2007, Issue 4), MEDLINE, EMBASE and CINAHL from 2001 to January
2008. We checked reference lists and sought advice from experts. No
language restrictions were applied. SELECTION CRITERIA: Randomised
controlled trials (RCTs) that compared centre-based cardiac rehabilitation
(e.g. hospital, gymnasium, sports centre) with home-based programmes, in
adults with myocardial infarction, angina, heart failure or who had
undergone revascularisation. DATA COLLECTION AND ANALYSIS: Studies were
selected independently by two reviewers, and data extracted by a single
reviewer and checked by a second one. Authors were contacted where
possible to obtain missing information. MAIN RESULTS: Twelve studies
(1,938 participants) met the inclusion criteria. The majority of studies
recruited a lower risk patient following an acute myocardial infarction
(MI) and revascularisation. There was no difference in outcomes of home-
versus centre-based cardiac rehabilitation in mortality risk ratio (RR)
was1.31 (95% confidence interval (C) 0.65 to 2.66), cardiac events,
exercise capacity standardised mean difference (SMD) -0.11 (95% CI -0.35
to 0.13), as well as in modifiable risk factors (systolic blood pressure;
diastolic blood pressure; total cholesterol; HDL-cholesterol;
LDL-cholesterol) or proportion of smokers at follow up or health-related
quality of life. There was no consistent difference in the healthcare
costs of the two forms of cardiac rehabilitation. AUTHORS' CONCLUSIONS:
Home- and centre-based cardiac rehabilitation appear to be equally
effective in improving the clinical and health-related quality of life
outcomes in acute MI and revascularisation patients. This finding,
together with an absence of evidence of difference in healthcare costs
between the two approaches, would support the extension of home-based
cardiac rehabilitation programmes such as the Heart Manual to give
patients a choice in line with their preferences, which may have an impact
on uptake of cardiac rehabilitation in the individual case.

<5>
Accession Number
0020091510
Authors
Toomtong P. Suksompong S.
Institution
(Toomtong, Suksompong) Department of Anesthesiology, Faculty of Medicine,
Siriraj Hospital, Mahidol University, 2 Prannok Road, Siriraj,
Bangkok-noi, Bangkok, Thailand, 10700.
Title
Intravenous fluids for abdominal aortic surgery..
Source
Cochrane database of systematic reviews (Online). (1)(pp CD000991), 2010.
Date of Publication: 2010.
Abstract
BACKGROUND: Surgery on the abdominal aorta to treat aneurysms or occlusive
disease is a major undertaking which requires intensive physiological
support and fluid management. Blood products are often used but the main
fluid replacement is with crystalloids or colloids. For years there has
been controversy over which fluid is optimal and a number of studies have
examined the subject. This is an update of a Cochrane review first
published in 2000 and previously updated in 2002. OBJECTIVES: To determine
the effectiveness of different non-blood replacement fluids used in
abdominal aorta procedures with a view to identifying the optimal fluid
for use. SEARCH STRATEGY: The Cochrane Peripheral Vascular Diseases Group
searched their Specialised Register (August 2009) and the Cochrane Central
Register of Controlled Trials (CENTRAL) (The Cochrane Library 2009, Issue
3) for publications describing randomised controlled trials of non-blood
replacement fluids in abdominal aortic surgery. In addition, the reference
lists from retrieved trials were screened for further information about
trials. SELECTION CRITERIA: Randomised controlled trials assessing the
effects of at least one specific non-blood fluid used for replacement
therapy in operations on, and confined to, the abdominal aorta. DATA
COLLECTION AND ANALYSIS: Data were extracted and then entered into the
Review Manager software where statistical analyses were performed. MAIN
RESULTS: Thirty-eight trials involving 1589 patients were included.
Patients undergoing aortic surgery had various physiological parameters
measured before and after their operation (these were cardiac,
respiratory, haematological, and biochemical). Patients were randomised to
a fluid type. This review demonstrated that no single fluid affects any
outcome measure significantly more than another fluid across a range of
outcomes. The death rate in these studies was 2.45% (39 patients).
AUTHORS' CONCLUSIONS: Despite the confirmed beneficial effects of colloids
in this review, further studies are still required. There are no studies
examining the effects of combination fluid therapy. The primary research
outcome was death, for which results were limited; therefore, future
studies should pay more attention to short-term outcomes such as
minimising the need for allogenic blood transfusion, complications (organ
failure), and length of stay in both the intensive care unit and hospital.

<6>
Accession Number
2010174269
Authors
Ma Y. Liu Y. Zuo J.
Institution
(Ma, Liu) Department of Thoracic Surgery, General Hospital of the People's
Liberation Army, Beijing 100853, China.
(Zuo) Department of Thoracic Surgery, Military General Hospital of Beijing
PLA, Beijing 100700, China.
Title
Cryoanalgesia of intercostal nerves following thoracotomy: Clinical trial
based on animal experiment.
Source
Neural Regeneration Research. 4(12)(pp 1083-1087), 2009. Date of
Publication: December 2009.
Publisher
Editorial Board of Neural Regeneration Research
Abstract
BACKGROUND: Cryoanalgesia at -50 degreesC for 90 seconds yields effective
pain relief following thoracotomy. In China, -50 degreesC is a common
temperature for intercostal cryoanalgesia following thoracotomy. However,
experimental results vary. OBJECTIVE: To explore intercostal nerve
pathological changes at -70 degreesC for various freezing times by
studying canines, and to evaluate long-term clinical efficacy of
intercostal nerve cryoanalgesia for postoperative pain relief based on the
animal experiments. DESIGN, TIME AND SETTING: A comparative animal study
was performed at the Animal Experimental Center of the General Hospital of
the People's Liberation Army. Based on results from the animal study, a
randomized, controlled, clinical trial was performed at the Department of
Thoracic Surgery of the General Hospital of the People's Liberation Army
between October 2006 and October 2008. PARTICIPANTS: A total of 120
patients undergoing posterolateral single incision lobectomy at the
Department of Thoracic Surgery of PLA General Hospital between October
2006 and October 2008 were selected. Nervous system diseases were
excluded. METHODS: Animal experiment: 8 anaesthetized, mixed-breed dogs
were used. The intercostal nerves (costal bone 6-10) were frozen at -70
degreesC for varying times (30, 60, 90, 120, and 180 seconds). Clinical
study: 120 patients were randomly assigned to 2 groups (n = 60). In the
cryoanalgesia group, the intercostal nerves were frozen prior to chest
closure, and 4 costal nerves (1 at incision level, 2 above and below
incision, and 1 at drainage tube level) were frozen for 90 seconds at -70
degreesC, respectively. Intercostal nerves were not frozen in the control
group patients. Dolantin was used to relieve postoperative pain in
patients from both groups. MAIN OUTCOME MEASURES: Pathological changes in
frozen intercostal nerves were examined at days 1, 10, 30, and 60
following freezing. Following surgery, the degree of postoperative pain in
all patients was evaluated by visual analogue scale at days 1, 3, 5, 9,
30, 60, 90, and 180. Dolantin doses at days 1, 3, 5, 9 post-surgery and
postoperative complications were noted. RESULTS: Nerve damage
progressively increased with length of freezing time at -70 degreesC, and
recovery time from damage was gradually increased. After freezing for 90
seconds, the nerves exhibited obvious histopathological damage, and then
completely recovered. In addition, after freezing for 180 seconds, the
histopathological changes in nerves were reversible. In the clinical
study, visual analogue scale scores were significantly less in the
cryoanalgesia group compared with the control group (P < 0.01), which was
maintained over 30 days. In the cryoanalgesia group, the mean dolantin
dose administered and postoperative complications were significantly
reduced compared with the control group (P < 0.01). CONCLUSION: Freezing
of the intercostal nerve at -70 degreesC for 90 seconds is a safe and
long-term effective method for relieving post-thoracotomy pain.

<7>
Accession Number
2010155544
Authors
Alghamdi A.A. Elmistekawy E.M. Singh S.K. Latter D.A.
Institution
(Alghamdi, Elmistekawy, Singh, Latter) Division of Cardiac Surgery, St.
Michael's Hospital, University of Toronto, Toronto, Canada.
Title
Is concomitant surgery for moderate functional Mitral regurgitation
indicated during aortic valve replacement for aortic stenosis? a
systematic review and evidence-based recommendations.
Source
Journal of Cardiac Surgery. 25(2)(pp 182-187), 2010. Date of Publication:
March 2010.
Publisher
Blackwell Publishing Inc.
Abstract
Background: Mitral regurgitation (MR) is associated with poor clinical
outcomes. Functional MR is often associated with aortic stenosis (AS) and
may resolve after aortic valve replacement (AVR). The objective of this
study was to derive evidence-based recommendations regarding surgical
intervention for moderate functional MR at the time of AVR for AS.
Methods: An exhaustive literature search strategy including Medline,
Embase, the Cochrane library, and meeting abstracts was performed. Studies
meeting inclusion criteria were critically appraised and data pooled
according to accepted meta-analysis techniques. The primary outcome was
change in moderate MR after isolated AVR. Secondary outcomes were the
impact of functional MR on survival and identifying factors that predict
progression of MR, in patients undergoing isolated AVR for AS. Results:
Thirteen nonrandomized studies including 2113 patients were reviewed. A
total of 268 patients had preoperative moderate functional MR and AS. All
studies were appraised as poor methodological quality. After isolated AVR
a trend toward improvement in MR was observed. Left ventricular
dysfunction, left atrial enlargement, and atrial fibrillation were
associated with progression of MR after AVR. However, the impact of
residual MR on late survival was not consistent. Conclusion: Pooling
current evidence provided inconclusive evidence to make clinical practice
recommendations for or against routine surgical intervention of moderate
MR at the time of AVR for AS. The incidence of this pathology makes
further clinical trial studies warranted. copyright 2009 Wiley
Periodicals, Inc.

<8>
Accession Number
2010152641
Authors
Ramadan A.S.E. Stefanidis C. N'Gatchou W. El Oumeiri B. Jansens J.-L. De
Smet J.-M. Antoine M. De Canniere D.
Institution
(Ramadan, Stefanidis, N'Gatchou, El Oumeiri, Jansens, De Smet, Antoine, De
Canniere) Department of Cardiac Surgery, Erasme Hospital, University of
Brussels (ULB), 808, Route de Lennik, 1070 Brussels, Belgium.
Title
Five years follow-up after Y-graft arterial revascularization: On pump
versus off pump; prospective clinical trial.
Source
Interactive Cardiovascular and Thoracic Surgery. 10(3)(pp 423-427), 2010.
Date of Publication: March 2010.
Publisher
European Association for Cardio-Thoracis Surgery
Abstract
Objectives: We report our comparative experience of on-pump and off-pump
full arterial coronary artery bypass grafting (CABG) using both internal
mammary arteries (IMAs) anastomosed as a Y-graft. Methods: A single-center
clinical study was conducted prospectively between January 2003 and May
2008. It compared the short- and mid-term clinical outcomes of on- and
off-pump arterial revascularization where the left internal mammary artery
(LIMA) was anastomosed to the left anterior descending (LAD) artery while
the free right internal mammary artery (RIMA) graft taking off from the
LIMA was used to bypass different coronary targets. Results: One hundred
and ninety-two patients were divided into 77 on-pump and 115 off-pump
procedures based on the intention to treat. The mean age in both groups
was 60.2+/-11.7 and 68.1+/-10.6 years, respectively (P<0.05). Mean
predictive logistic EuroSCORE was 3.5+/-6.7% for the on-pump group and
7.3+/-8.6% for the off-pump group (P<0.0001). Mean number of distal
anastomoses were 2.7+/-0.6 (group ON) and 2.5+/-0.6 (group OFF) (P=NS).
Postoperative mortality was two patients (2.6%) in the on-pump group and
four patients (3.4%) in the off-pump group (P=0.63). No major adverse
cardiac event, no stroke and no late death were reported during the
follow-up that averaged 36.5+/-18.6 months. Angina recurrence was three
patients (2.6%) in off-pump and two patients (3.5%) in on-pump group
(P=NS). Conclusions: The use of a free RIMA as Y-graft from the LIMA
performed off pump eradicates aortic manipulations and provides complete
revascularization to high-risk patients with mortality similar to the one
of a lower risk population operated on pump. The morbidity and cost was
lower in the off-pump group. This advocates for the widespread usage of
the technique in high-risk patients.

<9>
Accession Number
2010152626
Authors
Gunaydin S. McCusker K. Sari T. Onur M.A. Zorlutuna Y.
Institution
(Gunaydin) University of Kirikkale, Angora Evleri G-8 Bl. No: 1, Ankara
06800, Turkey.
(McCusker) New York Medical College, NY, United States.
(Sari, Zorlutuna) Bayindir Hospital, Ankara, Turkey.
(Onur) Hacettepe University, Ankara, Turkey.
Title
Clinical performance and biocompatibility of hyaluronan-based
heparin-bonded extracorporeal circuits in different risk cohorts.
Source
Interactive Cardiovascular and Thoracic Surgery. 10(3)(pp 371-376), 2010.
Date of Publication: March 2010.
Publisher
European Association for Cardio-Thoracis Surgery
Abstract
This prospective randomized study compares novel hyaluronan-based
heparin-bonded circuits vs. uncoated controls across EuroSCORE patient
risk strata including biomaterial evaluation. Over a two-year period, 90
patients undergoing coronary artery bypass grafting were prospectively
randomized to one of the two perfusion protocols: Group 1 was treated with
hyaluronan-based heparin-bonded preconnected circuits (Vision
HFO-GBS[trademark], Gish, CA, USA) and Group 2 with identical uncoated
controls. Each group was composed of three subgroups (n=15) with respect
to preoperative evaluation of low (EuroSCORE 0-2), medium (3-5) and high
(6+) risk patients. Blood samples were collected after induction (T1) and
heparinization (T2), 15 min after cardiopulmonary bypass start (T3),
before cessation of CPB (T4), 15 min after reversal (T5), and the first
postoperative day (T6). In high-risk patients, platelet counts
demonstrated significant preservation at T4, T5 and leukocyte counts were
lower at T5 in hyaluronan group (P[less-than or equal to]0.05 vs.
control). C3a (ng.ml -1) levels were significantly lower at T3 (0.2+/-0.04
vs. 0.31+/-0.05), T4 (0.25+/-0.04 vs. 0.51+/-0.05), T5 (0.38+/-0.04 vs.
0.56+/-0.05) and interleukin-6 (pg.ml -1 ) at T4 (91+/-18 vs. 124+/-20),
T5 (110+/-20 vs. 220+/-25) in coated group vs. control (P[less-than or
equal to]0.05). Protein desorption (microalbumin) on fibers (mg.mm-3) was
less in hyaluronan vs. control groups (P[less-than or equal to]0.05).
Hyaluronan coating reduced platelet adhesion and cell adsorption, and
modulated inflammatory response in high-risk patients.

<10>
[Use Link to view the full text]
Accession Number
2010102114
Authors
Bolognese L. Falsini G. Grotti S. Limbruno U. Liistro F. Carrera A.
Angioli P. Picchi A. Ducci K. Pierli C.
Institution
(Bolognese, Falsini, Grotti, Liistro, Angioli, Ducci) Cardiovascular
Department, San Donato Hospital, Arezzo, Italy.
(Limbruno, Picchi) Department of Cardiology, Misericordia Hospital,
Grosseto, Italy.
(Carrera, Pierli) Cardiovascular Department, University Hospital of Siena,
Siena, Italy.
Title
The contrast media and nephrotoxicity following coronary revascularization
by primary angioplasty for acute myocardial infarction study: Design and
rationale of the CONTRAST-AMI study.
Source
Journal of Cardiovascular Medicine. 11(3)(pp 199-206), 2010. Date of
Publication: March 2010.
Publisher
Lippincott Williams and Wilkins
Abstract
Background: Contrast-induced acute kidney injury (CI-AKI) is a complex
syndrome of acute renal failure occurring after the administration of
contrast media and contributing to prolonged hospital stay and mortality.
The risk of CI-AKI is higher among patients undergoing primary
percutaneous coronary interventions for acute myocardial infarction (AMI),
but its clinical relevance in such setting has only been evaluated by
small sample size single-center studies and retrospective or observational
analyses. Furthermore, whereas high-osmolar contrast media was shown to
have direct nephrotoxicity, the role of low-osmolar and iso-osmolar agents
is still debated. Study design: The CONTRAST-AMI study is a prospective,
multicenter, controlled, randomized, single-blind, parallel-group trial,
designed to show the noninferiority of the effects of iopromide
(low-osmolar) compared with iodixanol (iso-osmolar) contrast media on the
incidence of CI-AKI and tissue-level perfusion in patients with AMI. All
consecutive patients admitted to participating centers for ST-segment
elevation AMI undergoing primary percutaneous coronary intervention will
be enrolled. All patients will be treated with high-dose N-acetylcysteine
(1200 mg intravenously during the procedure and 1200 mg orally two times
daily for the next 48 h after percutaneous coronary intervention) and
hydration according to a standardized protocol. The primary endpoint is
the proportion of patients with a relative increase in serum creatinine
(sCr) of at least 25% from baseline to 72 h after agent administration.
The secondary endpoints are absolute and relative increases in sCr of at
least 50%, thrombolysis in myocardial infarction (TIMI) perfusion grade,
and major adverse cardiac events at 1, 6, and 12 months. Conclusion: The
CONTRAST-AMI study will provide information on the effects of iodixanol
and iopromide on the incidence of CI-AKI and tissue-level perfusion in
patients with AMI. copyright 2010 Italian Federation of Cardiology.

<11>
Accession Number
2010205250
Authors
Tanveer R. Khan A.-R. Siddiqi T.A. Siddique S. Nasreen A. Salman-ur-Rehman
Badar S.
Institution
(Tanveer, Khan, Siddiqi, Siddique, Nasreen, Salman-ur-Rehman, Badar)
National Institute of Cardiovascular Diseases (NICVD), Karachi, Pakistan.

Title
Continuous versus interrupted technique of ventricular septal defect (VSD)
closure in total correction for tetrology of fallot pertaining to residal
VSD.
Source
Journal of the Pakistan Medical Association. 64(4)(pp 253-256), 2010.
Date of Publication: April, 2010.
Publisher
Pakistan Medical Association
Abstract
Objective: To analyze the outcome of continuous versus interrupted closure
technique of ventricular septal defect (VSD) closure in Tetrology of
Fallot with reference to postoperative residual VSD after total
correction. Methods: A randomised control study was conducted between
January 2008 to December 2008 at The Department of Cardiac Surgery,
National Institute of Cardiovascular Diseases (NICVD), Karachi. The
results of total correction (T.C) of VSD in patients with Tetralogy of
Fallot, with emphasis on the suturing technique and eventually on the
occurrence of residual ventricular septal defect(VSD) were analyzed.
Transventricular as well as transatrial route was used to approach VSD. In
thirty patients VSD was closed with 5/0 proline continuous double ended
suture while in remaining 30(50%) patients VSD was closed with interrupted
5/0 prolene double ended sutures. Postoperative echocardiography was done
in all patients as a routine on second postoperative day, to document
residual VSD. Results: The study included 60 (100%) patients with T.O.F.
There were 20 (33.3%) females and 40 (66.6%) males with ages ranging
between 04 to 18 years (mean 13.025 +/- 2.123 years). Postoperative
echocardiography showed residual VSD in 05 (8.3%) patients at
posteroinferior rim of VSD. Of these 05 cases, in four VSD had been closed
with continuous 5/0 proline double ended sutures, and one had VSD closed
with interrupted 5/0 double ended sutures. Conclusion: Residual VSD is
common with continuous suturing technique as compared to interrupted
suturing technique. This is perhaps because of poor myocardium quality and
higher RV pressures in our patients presenting at a late age. Small (less
than 05 milimeter) residual VSD can be treated conservatively in
haemodynamically stable patients.

<12>
Accession Number
2010171374
Authors
Neumann F.-J.
Institution
(Neumann) Herz-Zentrum, Bad Krozingen, Germany.
Title
Balancing efficacy and safety in the TRITON-TIMI 38 trial.
Source
European Heart Journal, Supplement. 11(G)(pp G14-G17), 2009. Date of
Publication: 2009.
Publisher
Oxford University Press
Abstract
The TRITON-TIMI 38 study tested the hypothesis that prasugrel compared
with clopidogrel is more efficacious in prevention of ischaemic events in
patients undergoing percutaneous coronary intervention (PCI) for either
ST-elevation myocardial infarction or for non-ST-elevation acute coronary
syndromes. In a double-blind design, 13 608 patients were randomly
assigned to receive prasugrel or clopidogrel. During 15-month follow-up,
prasugrel compared with clopidogrel significantly reduced the incidence of
the primary endpoint, the composite of the rate of cardiovascular death,
myocardial infarction, or stroke from 12.1 to 9.9% (hazard ratio: 0.81; P
< 0.001). Significant benefit of prasugrel was found during the first 3
days (hazard ratio: 0.82; P = 0.01) and from day 4 to the end of the study
(hazard ratio: 0.8; P = 0.003). Of the patients treated with prasugrel,
2.4% experienced at least one TIMI major haemorrhage unrelated to coronary
artery bypass graft, compared with 1.8% treated with clopidogrel (hazard
ratio: 1.32; P = 0.03). Thus, in the entire study group, the balance of
efficacy and safety was in favour of prasugrel with an absolute 2.2%
reduction in the primary efficacy endpoint by prasugrel when compared with
clopidogrel that was opposed by an only 0.6% increase in major
haemorrhage. In conclusion, in patients with acute coronary syndromes
undergoing PCI prasugrel significantly reduced the incidence of ischaemic
events, both in the acute and long term. Prasugrel was associated with an
increased risk of bleeding. In the entire cohort, the superior efficacy of
prasugrel outweighed the increased risk of bleeding. copyright The Author
2009.

<13>
Accession Number
2010115239
Authors
Alavi S.M. Kish R.F. Farsad F. Imani F. Sheikhvatan M.
Institution
(Alavi, Kish, Farsad, Imani, Sheikhvatan) Iran University of Medical
Sciences, P.O.Box: 13185-1678, Tehran, Iran, Islamic Republic of.
Title
Intravenous sufentanil and morphine for post-cardiac surgery pain relief
using patient-controlled analgesia (PCA) device: A randomized double-blind
clinical trial.
Source
Pakistan Journal of Medical Sciences. 26(1)(pp 137-141), 2010. Date of
Publication: January-March 2010.
Publisher
Professional Medical Publications
Abstract
Background: Selection of the best analgesic technique in patients
undergoing major surgeries can result in lower morbidity and satisfactory
postoperative pain relief. In the present study, we tried to compare the
effect of morphine and sufentanil on postoperative pain severity and
hemodynamic changes by using patient-controlled analgesia (PCA) device in
patients who were candidate for coronary artery bypass surgery (CABG).
Methodology: It was a randomized double-blinded clinical trial in which
120 patients aged 30-65 years, ASA physical status I-III, candidate for
CABG in Shahid Rajaee hospital in Tehran were included. Before anesthesia,
patients were randomly assigned to one of three groups to receive
sufentanil (n=40), morphine (n=40) or normal saline (n=40). After tracheal
extubation at intensive care unit, PCA was started by, sufentanil 4mg for
the first group, morphine 2mg for the second group and normal saline, at
same volume for the third group, intravenously with 10 minute lockout
interval. Postoperative pain was evaluated by VAS scale, 1, 6, 12, 18 and
24 hours after extubation and systolic blood pressure, arterial oxygen
saturation, PCO2 and PO2 were recorded 24 hours after extubation. Results:
VAS scores at rest revealed significantly less pain for patients in
sufentanil and morphine groups than normal saline group, throughout the
twenty-four hours after operation (P<0.001). However, there were no
significant differences in the means of VAS scores between sufentanil and
morphine groups. Among studied hemodynamic parameters, only systolic blood
pressure was reduced more in morphine than sufentanil group (P<0.001).
Conclusion: After CABG surgery, administration of intravenous sufentanil
and morphine using PCA can lead to similar reduction of postoperative pain
severity.

<14>
Accession Number
2010205284
Authors
Landoni G. Mizzi A. Biondi-Zoccai G. Bignami E. Prati P. Ajello V. Marino
G. Guarracino F. Zangrillo A.
Institution
(Landoni, Mizzi, Bignami, Prati, Ajello, Marino, Zangrillo) Department of
Anesthesiology and Intensive Care, Vita-Salute San Raffaele University,
via Olgettina 60, Milan, 20132, Italy.
(Biondi-Zoccai) Interventional Cardiology, Division of Cardiology,
University of Turin, Turin, Italy.
(Guarracino) Department of Cardiothoracic Surgery, University Hospital of
Pisa, Pisa, Italy.
Title
Levosimendan reduces mortality in critically ill patients. A meta-analysis
of randomized controlled studies.
Source
Minerva Anestesiologica. 76(4)(pp 276-286), 2010. Date of Publication:
April, 2010.
Publisher
Edizioni Minerva Medica S.p.A.
Abstract
Aim. Critically ill patients often need catecholamines, but these agents
could be associated with an increased risk of death and other adverse
cardiac events. Levosimendan is a calcium sensitizer that is able to
enhance myocardial contractility without increasing myocardial oxygen use.
We conducted a meta-analysis to determine the impact of levosimendan on
mortality in critically ill patients. Methods. Four investigators
independently searched BioMedCentral and PubMed to identify all randomized
trials that compared levosimendan vs. control with no restriction in dose
or time of administration. Exclusion criteria were duplicate publications,
non-human experimental studies, and no information on the primary outcome
(mortality). Results. Data from a total of 3,350 patients from 27
randomized controlled studies were included in the analysis. Levosimendan
was associated with a significant reduction in mortality (333/1893 [17.6%]
in the levosimendan group vs. 326/1457 [22.4%] in the control arm, OR=0.74
[0.62-0.89], P for effect=0.001) and in the rate of myocardial infarction
(3/493 [0.6%] in the levosimendan group vs. 14/356 [3.9%] in the control
arm P=0.007), with a significant increase in the rate of hypotension
(164/1484 [11.1%] in the levosimendan group vs. 106/1093 [9.7%] in the
control arm P=0.02). Conclusion. Levosimendan has cardioprotective effects
that could result in a reduced mortality in critically ill patients. A
large randomized controlled study is warranted in this setting.

<15>
Accession Number
2010205281
Authors
Ranucci M. de Benedetti D. Bianchini C. Castelvecchio S. Ballotta A.
Frigiola A. Menicanti L.
Institution
(Ranucci, de Benedetti, Bianchini, Castelvecchio, Ballotta) Department of
Cardiothoracic-Vascular Anesthesia and Intensive Care, IRCCS S. Donato
Policlinic, Milan, Italy.
(Frigiola, Menicanti) Department of Cardiac Surgery, IRCCS S. Donato
Policlinic, Milan, Italy.
Title
Effects of fenoldopam infusion in complex cardiac surgical operations: A
prospective, randomized, double-blind, placebo-controlled study.
Source
Minerva Anestesiologica. 76(4)(pp 249-259), 2010. Date of Publication:
April, 2010.
Publisher
Edizioni Minerva Medica S.p.A.
Abstract
Aim. Fenoldopam mesylate is a short-acting dopamine-1 agonist that has
been suggested to be a possible reno-protective agent in patients
undergoing cardiac surgery. The present study is a prospective,
randomized, double-blind placebo controlled trial conducted to determine
the effects of fenoldopam in a population of patients undergoing complex
cardiac operations. Methods. Eighty subjects undergoing complex cardiac
operations with cardiopulmonary bypass (CPB) were enrolled in the study.
Patients were randomly assigned either to the fenoldopam (0.1 mug. kg-1.
min-1) or the placebo group. Fenoldopam infusion started at the onset of
CPB and was maintained for the first twelve postoperative hours. CPB
parameters and renal outcome data were collected. Results. Patients in the
fenoldopam group had higher oxygen delivery during CPB and a significantly
lower perfusion pressure, although this parameter was still within the
normal range. Blood lactate concentrations during CPB were similar in the
two groups. Urine output during and after CPB did not differ between
groups, nor did the renal function parameters. There was a significantly
higher rate of acute kidney injury (AKI) in the placebo group (10% vs 0%).
In the subgroup of patients requiring inotropic support for more than 48
hours, renal function parameters were significantly better, the peak
arterial blood lactate was significantly lower, and the major morbidity
rate was significantly lower (36% vs100%) for patients who received
fenoldopam. Conclusion. Fenoldopam improves the quality of perfusion
during CPB. In patients receiving catecholamines to treat a postoperative
low cardiac output state, fenoldopam significantly improves renal function
and prevents AKI and major morbidity.

<16>
Accession Number
2010190100
Authors
Sanz J. Moreno P.R. Fuster V.
Institution
(Sanz, Moreno, Fuster) The Zena and Michael A. Wiener Cardiovascular
Institute, Marie-Josee and Henry R. Kravis Center for Cardiovascular
Health, Mount Sinai School of Medicine, New York, NY, United States.
(Fuster) Centro Nacional de Investigaciones Cardiovasculares, Madrid,
Spain.
Title
The Year in Atherothrombosis.
Source
Journal of the American College of Cardiology. 55(14)(pp 1487-1498),
2010. Date of Publication: 06 Apr 2010.
Publisher
Elsevier USA

<17>
Accession Number
2010190093
Authors
Sorajja P. Gersh B.J. Cox D.A. McLaughlin M.G. Zimetbaum P. Costantini C.
Stuckey T. Tcheng J.E. Mehran R. Lansky A.J. Grines C.L. Stone G.W.
Institution
(Sorajja, Gersh) Division of Cardiovascular Diseases and Internal
Medicine, Mayo Clinic, Mayo Foundation, Rochester, MN, United States.
(McLaughlin, Zimetbaum) Beth Israel Deaconess Medical Center, Boston, MA,
United States.
(Cox) Mid Carolina Cardiology, Charlotte, NC, United States.
(Stuckey) Moses Cone Health System, Greensboro, NC, United States.
(Tcheng) Duke University Medical Center, Durham, NC, United States.
(Grines) William Beaumont Hospital, Royal Oak, MI, United States.
(Costantini, Mehran, Lansky, Stone) College of Physicians and Surgeons,
Columbia University Medical Center, New York, NY, United States.
(Costantini, Mehran, Lansky, Stone) Cardiovascular Research Foundation,
New York, NY, United States.
Title
Impact of Delay to Angioplasty in Patients With Acute Coronary Syndromes
Undergoing Invasive Management. Analysis From the ACUITY (Acute
Catheterization and Urgent Intervention Triage strategY) Trial.
Source
Journal of the American College of Cardiology. 55(14)(pp 1416-1424),
2010. Date of Publication: 06 Apr 2010.
Publisher
Elsevier USA
Abstract
Objectives: The aim of this study was to determine the impact of delay to
angioplasty in patients with acute coronary syndromes (ACS). Background:
There is a paucity of data on the impact of delays to percutaneous
coronary intervention (PCI) in patients with non-ST-segment elevation
acute coronary syndromes (NSTE-ACS) undergoing an invasive management
strategy. Methods: Patients undergoing PCI in the ACUITY (Acute
Catheterization and Urgent Intervention Triage strategY) trial were
stratified according to timing of PCI after clinical presentation for
outcome analysis. Results: Percutaneous coronary intervention was
performed in 7,749 patients (median age 63 years; 73% male) with NSTE-ACS
at a median of 19.5 h after presentation (<8 h [n = 2,197], 8 to 24 h [n =
2,740], and >24 h [n = 2,812]). Delay to PCI >24 h after clinical
presentation was significantly associated with increased 30-day mortality,
myocardial infarction (MI), and composite ischemia (death, MI, and
unplanned revascularization). By multivariable analysis, delay to PCI of
>24 h was a significant independent predictor of 30-day and 1-year
mortality. The incremental risk of death attributable to PCI delay >24 h
was greatest in those patients presenting with high-risk features.
Conclusions: In this large-scale study, delaying revascularization with
PCI >24 h in patients with NSTE-ACS was an independent predictor of early
and late mortality and adverse ischemic outcomes. These findings suggest
that urgent angiography and triage to revascularization should be a
priority in NSTE-ACS patients. copyright 2010 American College of
Cardiology Foundation.

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Accession Number
2010181877
Authors
Taleska G. Trajkovska T. Kokareva A. Popovska A. Naumoska M. Gavrilovska
A. Dzhambazovska-Trajkovska V. Toleska M. Dimov A.
Institution
(Taleska, Trajkovska, Kokareva, Popovska, Naumoska, Gavrilovska,
Dzhambazovska-Trajkovska, Toleska, Dimov) Clinic of Anesthesiology,
Reanimation and Intensive Care, Faculty of Medicine, University Ss Kiril
and Metodij, Skopje, Macedonia.
Title
Preemptive epidural analgesia with bupivacaine and sufentanyl and the
effects of epiduraly added epinephrine for thoracic surgery.
Source
Macedonian Journal of Medical Sciences. 3(1)(pp 46-53), 2010. Date of
Publication: 15 Mar 2010.
Publisher
Institute of Immunobiology and Human Genetics
Abstract
Aim. The aim of the study was to determine if preemptive epidural
analgesia in thoracic surgery reduces postoperative pain, and to compare
these effects in relation to the usage of epinephrine. Material and
Methods. Sixty patients admitted for thoracic surgery were randomly
allocated into three groups (n = 20 each). Group A received bupivacaine
and sufentanyl epiduraly prior to skin incision, followed by infusion of
bupivacaine and sufentanyl. Group B (control) received saline in the
epidural. In both groups patients received bupivacaine and sufentanyl
epiduraly at the time of the chest closure. In Group C the same doses of
bupivacaine and sufentanyl as in Group A were given to the patients
including epinephrine in the epidural mixture. The level of statistical
significance was pointed at p < 0.05. Results. The patients in Group A had
lower intraoperative isofluran requirements, lower postoperative epidural
infusion rates and lower pain scores in first eight postoperative hours,
compared with the control. In the epinephrine group patients had lower
pain intensity and smaller needs for postoperative epidural infusion rate
than those in Group A. Conclusion. The usage of epinephrine has caused
less nausea and easier mobilization. While there was a beneficial effect
of the reduced intraoperative anesthetic requirements, any lasting effect
of preemptive analgesia did not extend beyond eight hours after the
operation. copyright 2010 Taleska G.