<?xml version="1.0" encoding="utf-8"?>
<journal>
	<language>en</language>
	<journal_id_issn></journal_id_issn>
	<journal_id_issn_online>2008-2290</journal_id_issn_online>
	<journal_id_pii></journal_id_pii>
	<journal_id_doi></journal_id_doi>
	<journal_id_isnet></journal_id_isnet>
	<journal_id_iranmedex></journal_id_iranmedex>
	<journal_id_magiran></journal_id_magiran>
	<journal_id_sid></journal_id_sid>
	<pubdate>
		<type>gregorian</type>
		<year>2009</year>
		<month>8</month>
		<day>1</day>
	</pubdate>
	<pubdate>
		<type>jalali</type>
		<year></year>
		<month></month>
		<day></day>
	</pubdate>
	<volume>2</volume>
	<number>4</number>
	<publish_type>print</publish_type>
	<publish_edition>8</publish_edition>
	<article_type>fulltext</article_type>
	<articleset>
		
		<article>
			<language></language>
			<article_id_issn></article_id_issn>
			<article_id_issn_online></article_id_issn_online>
			<article_id_pubmed></article_id_pubmed>
			<article_id_pii></article_id_pii>
			<article_id_doi></article_id_doi>
			<article_id_iranmedex></article_id_iranmedex>
			<article_id_magiran></article_id_magiran>
			<article_id_sid></article_id_sid>
			<title_fa></title_fa>
			<title>﻿Pulmonary Thromboendarterectomy 	 </title>
			<subject_fa></subject_fa>
			<subject></subject>
			<content_type_fa></content_type_fa>
			<content_type>Case Report</content_type>
			<abstract_fa></abstract_fa>
			<abstract></abstract>
			<keyword_fa></keyword_fa>
			<keyword>Pulmonary emboli,Respiratory failure,﻿Thromboendarterectomy 	 </keyword>
			<start_page>38</start_page>
			<end_page>40</end_page>
			<web_url>http://www.iscs.org.ir/journals/vol.2/no.4/56/</web_url>
			<author_list>
				
			</author_list>
		</article>
		
		<article>
			<language></language>
			<article_id_issn></article_id_issn>
			<article_id_issn_online></article_id_issn_online>
			<article_id_pubmed></article_id_pubmed>
			<article_id_pii></article_id_pii>
			<article_id_doi></article_id_doi>
			<article_id_iranmedex></article_id_iranmedex>
			<article_id_magiran></article_id_magiran>
			<article_id_sid></article_id_sid>
			<title_fa></title_fa>
			<title>﻿Cardiac Transplantation for ﻿Doxorubicin-induced Heart Failure ﻿after Chemotherapy of Ewing’s Sarcoma 	 </title>
			<subject_fa></subject_fa>
			<subject></subject>
			<content_type_fa></content_type_fa>
			<content_type>Case Report</content_type>
			<abstract_fa></abstract_fa>
			<abstract>﻿Abstract: 	 
A 30-year-old woman presented with doxorubicin-induced heart failure. 	 
She had been treated due to Ewing’s sarcoma five years ago. Traditional heart failure treatment has been 	 
performed but its effect was mostly very limits. We, therefore, decided to perform heart transplantation for her. 	 
</abstract>
			<keyword_fa></keyword_fa>
			<keyword>﻿doxorubicin-induced heart ﻿failure, Heart transplantation, Ewing’s ﻿sarcoma 	 </keyword>
			<start_page>35</start_page>
			<end_page>37</end_page>
			<web_url>http://www.iscs.org.ir/journals/vol.2/no.4/55/</web_url>
			<author_list>
				
			</author_list>
		</article>
		
		<article>
			<language></language>
			<article_id_issn></article_id_issn>
			<article_id_issn_online></article_id_issn_online>
			<article_id_pubmed></article_id_pubmed>
			<article_id_pii></article_id_pii>
			<article_id_doi></article_id_doi>
			<article_id_iranmedex></article_id_iranmedex>
			<article_id_magiran></article_id_magiran>
			<article_id_sid></article_id_sid>
			<title_fa></title_fa>
			<title>﻿Cerebrospinal Fluid Drainage During ﻿Thoracic Aortic Repair: Safety and Current Management 	 </title>
			<subject_fa></subject_fa>
			<subject></subject>
			<content_type_fa></content_type_fa>
			<content_type>Original Article</content_type>
			<abstract_fa></abstract_fa>
			<abstract>﻿Background: The benefit of cerebrospinal fluid 	 
(CSF) drainage during thoracic aortic repair has been 	 
established. Few studies, however, report management 	 
and safety of CSF drainage. 	 
Methods: Between September 1992 and August 2007, 	 
1,353 repairs of the thoracic aorta were performed, 	 
with 82% using CSF drainage. The CSF drainage was 	 
not used in cases of rupture, acute trauma, infection, 	 
or prior paraplegia. Thirty-one percent (76 of 246) 	 
of patients without CSF drainage were repaired prior 	 
to standardized use. All drains were inserted by 	 
cardiovascular anesthesia staff. Repairs were performed 	 
using distal aortic perfusion with heparinization. Early 	 
management involved free drainage to maintain CSF 	 
pressure less than10 mm Hg, but was later modified to 	 
limit CSF drainage unless neurologic deficit occurred. 	 
Results: Cerebrospinal fluid drainage was technically 	 
achieved in 99.8% (1,105 of 1,107) of cases. The 	 
CSF catheter-related complications occurred in 1.5% 	 
﻿(17 of 1,107) of patients. No spinal hematomas were 	 
observed. The CSF leaks with spinal headache, 	 
CSF leak without spinal headache, spinal headache, 	 
intracranial hemorrhage, catheter fracture, and 	 
meningitis occurred in 6 (0.54%), 1 (0.1%), 2 (0.2%), 	 
5 (0.45%), 1 (0.1%), and 2 (0.2%) cases, respectively. 	 
Mortality from subdural hematoma was 40% (2 of 5), 	 
and from meningitis was 50% (1 of 2). Spinal headaches 	 
resolved with conservative management. All CSF leaks 	 
resolved, but 71% (5/7) required blood patches. Since 	 
implementation of a limited CSF drainage protocol, no 	 
subdural hematomas have been observed. 	 
Conclusions: Cerebrospinal fluid drainage for thoracic 	 
aortic repairs can be performed safely with excellent 	 
technical success. Perioperative management of CSF 	 
drains requires diligent monitoring and judicious 	 
drainage. Standardizing CSF management may be 	 
beneficial. 	 
</abstract>
			<keyword_fa></keyword_fa>
			<keyword>Brain Protection,CSF,Aortic surgery,Aortic Aneurgsm</keyword>
			<start_page>34</start_page>
			<end_page>0</end_page>
			<web_url>http://www.iscs.org.ir/journals/vol.2/no.4/54/</web_url>
			<author_list>
				
			</author_list>
		</article>
		
		<article>
			<language></language>
			<article_id_issn></article_id_issn>
			<article_id_issn_online></article_id_issn_online>
			<article_id_pubmed></article_id_pubmed>
			<article_id_pii></article_id_pii>
			<article_id_doi></article_id_doi>
			<article_id_iranmedex></article_id_iranmedex>
			<article_id_magiran></article_id_magiran>
			<article_id_sid></article_id_sid>
			<title_fa></title_fa>
			<title>﻿Aortic and mitral valve replacement in children:﻿is there any role for biologic and bioprosthetic substitutes? 	  </title>
			<subject_fa></subject_fa>
			<subject></subject>
			<content_type_fa></content_type_fa>
			<content_type>Original Article</content_type>
			<abstract_fa></abstract_fa>
			<abstract>﻿Objective: The ideal valve substitute in children does not 	 
exist. Biologic and bioprosthetic valves do not require 	 
anticoagulation, however their use is complicated 	 
by accelerated degeneration and requirement for 	 
reoperation. We examine results following mitral 	 
(MVR) or aortic (AVR) replacement with biologic 	 
and bioprosthetic valves at our institution. Methods: 	 
﻿Medical records of children who underwent AVR 	 
or MVR from 1986 to 2006 were reviewed. Median 	 
follow-up duration was 10.5 years. Competing-risks 	 
methodology determined time-related prevalence and 	 
associated factors for three mutually exclusive end 	 
states: death, valve reoperation, and survival without 	 
subsequent reoperation. Results: One hundred and ten 	 
﻿children (age 15.6 ± 2.6 years, 80% females) underwent 	 
123 valve replacements with biologic and bioprosthetic 	 
substitutes including 87 MVR and 36 AVR (13 had 	 
both). Underlying pathology was mainly rheumatic 	 
fever (91%). Thirty-nine patients (35%) had undergone 	 
a previous cardiac surgery. Most common mitral 	 
substitute was Hancock (73%) and homograft (8%); 	 
most common aortic substitute was homograft (41%) and 	 
Carpentier–Edwards (39%). Competing-risks analysis 	 
showed that 15 years after valve replacement, 16% of 	 
patients had died without subsequent reoperation, 66% 	 
underwent valve reoperations, and only 18% remained 	 
alive without further reoperation. Factors associated 	 
with increased reoperation risk included younger age at 	 
surgery (p = 0.005), AVR (p = 0.005), male gender (p 	 
= 0.02) and homograft use (p = 0.007) especially in the 	 
mitral position (p = 0.002). Fifteen-year freedom from 	 
﻿endocarditis was 97% while freedom from bleeding and 	 
thrombo-embolic complications was 100%. Majority of 	 
patients (95%) were in NYHA functional classes I/II at 	 
last follow-up. Conclusion: While valve reoperation is 	 
inevitable following AVR and MVR with biologic and 	 
bioprosthetic substitutes; favorable results such as low 	 
valve-related morbidity rate, good long-term survival 	 
and functional status encourage their consideration 	 
as valid replacement alternatives in selected children 	 
especially females. Valve durability is higher in the 	 
mitral position and longevity of bioprosthetic valves is 	 
greater than that of homografts especially in the mitral 	 
position. 	 
</abstract>
			<keyword_fa></keyword_fa>
			<keyword>﻿Mitral valve replacement 	• Aortic valve﻿replacement • Rheumatic fever • Homograft • Pulmonary ﻿autograft • Bioprosthetic valve 	  </keyword>
			<start_page>33</start_page>
			<end_page>34</end_page>
			<web_url>http://www.iscs.org.ir/journals/vol.2/no.4/53/</web_url>
			<author_list>
				
			</author_list>
		</article>
		
		<article>
			<language></language>
			<article_id_issn></article_id_issn>
			<article_id_issn_online></article_id_issn_online>
			<article_id_pubmed></article_id_pubmed>
			<article_id_pii></article_id_pii>
			<article_id_doi></article_id_doi>
			<article_id_iranmedex></article_id_iranmedex>
			<article_id_magiran></article_id_magiran>
			<article_id_sid></article_id_sid>
			<title_fa></title_fa>
			<title>Current strategies in tetralogy of Fallot repair:﻿pulmonary valve sparing and evolution of right ventricle/left ventricle pressures ratio 	 </title>
			<subject_fa></subject_fa>
			<subject></subject>
			<content_type_fa></content_type_fa>
			<content_type>Original Article</content_type>
			<abstract_fa></abstract_fa>
			<abstract>﻿Objective: Chronic volume overload in repair of 	 
tetralogy of Fallot (TOF) with transannular patch leads 	 
to significant late morbidity and mortality. Preserving 	 
pulmonary valve integrity offers a better long-term 	 
prognosis, despite a risk of residual stenosis. In our 	 
study we analyzed the evolution of pressure gradients 	 
in patients operated with conservative approaches, with 	 
particular regard to those babies with an immediate 	 
postoperative Prv/Plv ratio 0.70. 	 
Methods: Between January 2000 and June 2008, 24 	 
patients with TOF underwent reparative surgery with 	 
a valve sparing procedure (median age 8.1 months, 	 
range 1.1–86.6). The intraoperative post-repair 	 
echocardiography showed a Prv/Plv ratio 0.70 in 	 
eight patients (33%, group A) and &lt;0.70 in 16 patients 	 
(67%, group B). We realized a retrospective study of 	 
pre-, intra-, and postoperative data and of clinical and 	 
echocardiographic follow-up data. 	 
﻿Results: There was no early or late mortality, nor 	 
functional or rhythmic disturbances. One patient required 	 
re-operation for residual stenosis at annular level at one 	 
year. After a median follow-up of 32.8 months (range 	 
0.6–73.1), the Prv/Plv ratio decreased by 16% (p = 0.001) 	 
in all patients. In group A the reduction was 28% (p = 	 
0.018) and in group B it was 12% (p = 0.14). 	 
Conclusions: After a valve sparing procedure there is a 	 
reduction of Prv/Plv ratio at medium-term follow-up; 	 
in our study this reduction was statistically significant 	 
in all patients and in the subgroup with higher 	 
postoperative ratios. A valve sparing strategy reduces 	 
pulmonary regurgitation, preserves RV function and 	 
decreases the incidence of late arrhythmias, which are 	 
the determinants of long-term outcome. 	 
</abstract>
			<keyword_fa></keyword_fa>
			<keyword>﻿Tetralogy of Fallot • Pulmonary valve ﻿sparing • Cardiac congenital 	 </keyword>
			<start_page>33</start_page>
			<end_page>0</end_page>
			<web_url>http://www.iscs.org.ir/journals/vol.2/no.4/52/</web_url>
			<author_list>
				
			</author_list>
		</article>
		
		<article>
			<language></language>
			<article_id_issn></article_id_issn>
			<article_id_issn_online></article_id_issn_online>
			<article_id_pubmed></article_id_pubmed>
			<article_id_pii></article_id_pii>
			<article_id_doi></article_id_doi>
			<article_id_iranmedex></article_id_iranmedex>
			<article_id_magiran></article_id_magiran>
			<article_id_sid></article_id_sid>
			<title_fa></title_fa>
			<title>Reoperations After Initial Repair of ﻿Complete Atrioventricular Septal Defect 	 </title>
			<subject_fa></subject_fa>
			<subject></subject>
			<content_type_fa></content_type_fa>
			<content_type>Original Article</content_type>
			<abstract_fa></abstract_fa>
			<abstract>﻿Background: Excellent surgical results have been 	 
reported after repair of complete atrioventricular 	 
septal defects (CAVSD); however, 5% to 10% require 	 
reoperation. We examine causes leading to reoperation 	 
and evaluate long-term outcome. 	 
Methods: Between 1972 and 2007, 50 patients (26 male) 	 
underwent reoperation at our institution after initial 	 
repair of CAVSD (median interval, 15 months; range, 	 
3 days to 29 years). Median age at first reoperation was 	 
4.5 years (range, 53 days to 38 years). Indications for
first reoperation included left atrioventricular valve
(LAVV) regurgitation in 41 patients, subaortic stenosis
in 5, and LAVV stenosis, residual atrial septal defect
(ASD), pulmonary artery (PA) stenosis, and aortic
coarctation in 1 each.
Results: The first reoperation included LAVV repair
in 21 patients and replacement in 21, modified
Konno procedure in 3, septal myectomy in 2, and PA
reconstruction, coarctation repair, and ASD re-repair in
1 each. After LAVV repair (n = 21) 5 patients required
a second reoperation, and after LAVV replacement
(n = 21) 6 patients required a second reoperation.
Overall freedom from further reoperation after the first
reoperation was 63%, 48%, and 42% at 5, 10, and 15
years, respectively. There were 2 early deaths (4%) after
first reoperation, and none after subsequent reoperations.
During late follow-up (median 10.7 years, maximum 30
﻿years), actuarial overall survival was 91%, 91%, and 	 
86% at 5, 10, and 15 years, respectively. 	 
Conclusions: The most common indication for 	 
reoperation after CAVSD repair is LAVV regurgitation. 	 
LAVV re-repair offers good durability, and LAVV 	 
replacement does not preclude additional reoperations. 	 
Long-term survival is very good despite need for 	 
multiple reoperations in some. 	 
</abstract>
			<keyword_fa></keyword_fa>
			<keyword>Congenital heart disease,Re-operation,AV Septal Defect</keyword>
			<start_page>32</start_page>
			<end_page>33</end_page>
			<web_url>http://www.iscs.org.ir/journals/vol.2/no.4/51/</web_url>
			<author_list>
				
			</author_list>
		</article>
		
		<article>
			<language></language>
			<article_id_issn></article_id_issn>
			<article_id_issn_online></article_id_issn_online>
			<article_id_pubmed></article_id_pubmed>
			<article_id_pii></article_id_pii>
			<article_id_doi></article_id_doi>
			<article_id_iranmedex></article_id_iranmedex>
			<article_id_magiran></article_id_magiran>
			<article_id_sid></article_id_sid>
			<title_fa></title_fa>
			<title>﻿Predictors of impaired neurodevelopmental ﻿outcomes at one year of age after infant cardiac surgery 	 </title>
			<subject_fa></subject_fa>
			<subject></subject>
			<content_type_fa></content_type_fa>
			<content_type>Original Article</content_type>
			<abstract_fa></abstract_fa>
			<abstract>﻿Objective: For most newborns, congenital heart defects 	 
(CHD) appear to be isolated anomalies and the brain 	 
is presumed to have normal developmental potential. 	 
Most studies of neurodevelopmental outcomes have 	 
focused on operative management strategies. 	 
Methods: Infants with complex CHD and no identified 	 
syndromes other than 22q11 microdeletions enrolled 	 
in a study of apolipoprotein E (APOE) polymorphisms 	 
and developmental outcome were evaluated at one year 	 
of age; including genetic evaluation and the Bayley 	 
Scales of Infant Development-II [mental (MDI) and 	 
psychomotor developmental indices (PDI)]. 	 
Results: Five hundred and fifty infants enrolled and 	 
359 (20 with 22q11) of 501 survivors (72%) returned. 	 
Mean MDI was 90 ± 15 and PDI was 78 ± 18. Genetic 	 
syndromes not identified at birth were confirmed in 28 	 
(8.1%) and suspected in 51 (15.0%). By multivariable 	 
analysis, suspected/confirmed genetic syndromes and 	 
APOE 2 allele predicted lower MDI and PDI, all p &lt; 	 
0.04. Lower birth weight (p &lt; 0.001) and preoperative 	 
intubation (p = 0.012) predicted lower MDI. Higher 	 
hematocrit during the initial operation was associated 	 
with higher MDI (p = 0.007). Longer postoperative 	 
length of stay was predictive of lower PDI (p = 0.002). 	 
Additional operations with cardiopulmonary bypass 	 
﻿were associated with lower MDI and PDI (both p &lt; 	 
0.002), but use of deep hypothermic circulatory arrest 	 
was not. 	 
Conclusions: Patient factors (birth weight and 	 
preoperative status) are significant determinants of 	 
neurodevelopmental outcomes as opposed to operative 	 
management strategies. In this cohort, genetic syndromes 	 
unsuspected at birth were surprisingly common and 	 
correlate with poor neurodevelopmental outcomes. 	 
Without multiple congenital anomalies, syndromes 	 
may be missed in infancy. Genetic evaluation should be 	 
considered in all infants with CHD. 	 
Abbreviations: APOE = apolipoprotein E • BCAS = 	 
Boston Circulatory Arrest Study • CHD = congenital 	 
heart defect • CPB = cardiopulmonary bypass • 	 
DHCA = deep hypothermic circulatory arrest • MDI 	 
= mental developmental index • PDI = psychomotor 	 
developmental index • TGA = transposition of the great 	 
arteries • TOF = tetralogy of Fallot • VSD = ventricular 	 
septal defect 	 
</abstract>
			<keyword_fa></keyword_fa>
			<keyword>﻿Heart defects • Congenital • Genetic ﻿predisposition to disease • Apolipoprotein E ﻿Neurodevelopmental outcomes 	 	 </keyword>
			<start_page>32</start_page>
			<end_page>0</end_page>
			<web_url>http://www.iscs.org.ir/journals/vol.2/no.4/50/</web_url>
			<author_list>
				
			</author_list>
		</article>
		
		<article>
			<language></language>
			<article_id_issn></article_id_issn>
			<article_id_issn_online></article_id_issn_online>
			<article_id_pubmed></article_id_pubmed>
			<article_id_pii></article_id_pii>
			<article_id_doi></article_id_doi>
			<article_id_iranmedex></article_id_iranmedex>
			<article_id_magiran></article_id_magiran>
			<article_id_sid></article_id_sid>
			<title_fa></title_fa>
			<title>Short-term systolic and diastolic ventricular performance aftersurgical ventricular restoration for dilated ischemic cardiomyopathy</title>
			<subject_fa></subject_fa>
			<subject></subject>
			<content_type_fa></content_type_fa>
			<content_type>Original Article</content_type>
			<abstract_fa></abstract_fa>
			<abstract>﻿Objective: Based on the adverse relationship between 	 
left ventricular (LV) remodeling and clinical outcome 	 
in ischemic cardiomyopathy, surgical ventricular 	 
restoration (SVR) is proposed as a valuable adjunct 	 
procedure. This study reports on the short-term clinical 	 
and hemodynamical performance of SVR. 	 
Methods: Using end-systolic LV volume as indication 	 
for SVR, 78 patients with ischemic cardiomyopathy are 	 
divided in two groups: group 1 comprised 55 patients 	 
treated by coronary revascularization and mitral 	 
annuloplasty, group 2 comprised 23 patients undergoing 	 
additional SVR. Hemodynamic investigation included 	 
echocardiographic assessment of systolic and diastolic 	 
function. Clinical follow-up focused on survival and 	 
functional status with exercise performance. 	 
Results: Both surgical approaches resulted in 	 
improvement of NYHA class (2.9–1.6 in group 1; 3.3– 	 
1.5 in group 2, p &lt; 0.001), achieving similar exercise 	 
performance (peak VO2 13.7 vs 15.4 ml/kg min in 	 
groups 1 and 2, p = 0.25) and plasma BNP values (group 	 
1: 1350 pg/ml and group 2: 767 pg/ml, p = 0.23). SVR 	 
provided additional benefit as patients basically had a 	 
worse NYHA class (2.9 in group 1 vs 3.3 in group 2, p 	 
= 0.03). Within mean follow-up of 20 months, survival 	 
rate was 84% in group 1 and 74% in group 2 (p = 0.11), 	 
including operative mortality of 7% and 13% (p = 	 
﻿0.42). Through effective volume reduction (LVEDVI 	 
41%; LVESVI 49%) systolic function improved 	 
immediately after SVR (LVEF 27–39% in group 2, p &lt; 	 
0.05). Worsening of diastolic function was specifically 	 
observed after SVR within the first year (E/A-ratio 1.38– 	 
1.74 cm/s, p = 0.02). Recurrent mitral regurgitation (p = 	 
0.004) and secondary remodeling (p = 0.01) were major 	 
determinants of decreasing LV compliance. Clinical 	 
outcome in terms of cardiac events and survival was 	 
compromised by restrictive diastolic function (p = 0.02) 	 
and increased LV volumes (p = 0.04). 	 
Conclusion:SVRinadditiontocoronaryrevascularization 	 
and restrictive mitral annuloplasty results in significant 	 
clinical improvement in selected patients with advanced 	 
ischemic heart disease and severely dilated ventricles. 	 
SVRentailsimmediateimprovementofsystolicfunction, 	 
which remains sustained during short-term follow-up. 	 
Serial assessment of diastolic function is mandatory as 	 
LV compliance seems more sensitive to early changes 	 
induced by recurrence of mitral regurgitation and 	 
secondary ventricular dilation. Moreover, worsening 	 
of diastolic dysfunction should be timely recognized 	 
because of its adverse clinical impact. 	 
</abstract>
			<keyword_fa></keyword_fa>
			<keyword>﻿Ischemic cardiac disease • Surgical ﻿ventricular restoration • Heart failure 	 	 </keyword>
			<start_page>31</start_page>
			<end_page>0</end_page>
			<web_url>http://www.iscs.org.ir/journals/vol.2/no.4/49/</web_url>
			<author_list>
				
			</author_list>
		</article>
		
		<article>
			<language></language>
			<article_id_issn></article_id_issn>
			<article_id_issn_online></article_id_issn_online>
			<article_id_pubmed></article_id_pubmed>
			<article_id_pii></article_id_pii>
			<article_id_doi></article_id_doi>
			<article_id_iranmedex></article_id_iranmedex>
			<article_id_magiran></article_id_magiran>
			<article_id_sid></article_id_sid>
			<title_fa></title_fa>
			<title>﻿Epicardial off-pump pulmonary vein isolation and vagal denervation ﻿improve long-term outcome and quality of life in patients with atrial fibrillation 	 </title>
			<subject_fa></subject_fa>
			<subject></subject>
			<content_type_fa></content_type_fa>
			<content_type>Original Article</content_type>
			<abstract_fa></abstract_fa>
			<abstract>﻿Objectives: The limited information available on 	 
thoracoscopic pulmonary vein isolation combined with 	 
ganglionated plexi ablation and the lack of studies 	 
regarding its effect on quality of life and physical 	 
capacity urged us to study its acute and long-term results 	 
in patients with atrial fibrillation. 	 
Methods: Forty-three patients (mean age 57.1 	 
years) with symptomatic atrial fibrillation referred 	 
﻿for thoracoscopic off-pump epicardial pulmonary 	 
vein isolation and ganglionated plexi ablation using 	 
radiofrequency energy were included. 	 
Results: The physical capacity improved significantly 	 
at 6-month follow-up compared with baseline (mean ± 	 
standard deviation, 165.2 ± 65 Watt versus 155.9 ± 57 	 
Watt, P = .02). Quality of life (Short Form-36 health 	 
survey) significantly improved 12 months after surgery 	 
﻿compared with baseline in all subscales except for 	 
bodily pain. The symptom severity questionnaire score 	 
decreased significantly from mean 15.2 ± 4.0 points to 	 
10.7 ± 4.8 points (P = .02). Overall, 25 of 33 patients 	 
(76%) followed up for 12 months had no symptomatic 	 
atrialfibrillationrecurrencesoratrialfibrillationepisodes 	 
on 24-hour Holter recordings. The corresponding figures 	 
were 79% (19/24) for patients with paroxysmal atrial 	 
fibrillation, 100% (2/2) for persistent atrial fibrillation, 	 
and 57% (4/7) for permanent atrial fibrillation. The 	 
most common complication was bleeding events (9%) 	 
during pulmonary vein dissection. 	 
Conclusions: Epicardial off-pump pulmonary vein 	 
﻿isolation combined with ganglionated plexi ablation 	 
improved quality of life, symptoms, and exercise 	 
capacity and therefore may be considered for patients 	 
with atrial fibrillation who fail endocardial pulmonary 	 
vein ablation or as a first-line procedure if left atrial 	 
appendage exclusion is warranted. 	 
Abbreviations and Acronyms AAD = antiarrhythmic 	 
drug; AF = atrial fibrillation; CT = contrast tomography; 	 
ECG = electrocardiogram; GP = ganglionated plexi; 	 
LAA = left atrial appendage; PV = pulmonary vein; QoL 	 
= quality of life; RF = radiofrequency; SSQ = symptom 	 
severity questionnaire 	 
</abstract>
			<keyword_fa></keyword_fa>
			<keyword>Atrial firillation,Pulmonary Vein Isolation ,Quality of life,Radiofiegueney</keyword>
			<start_page>30</start_page>
			<end_page>31</end_page>
			<web_url>http://www.iscs.org.ir/journals/vol.2/no.4/48/</web_url>
			<author_list>
				
			</author_list>
		</article>
		
		<article>
			<language></language>
			<article_id_issn></article_id_issn>
			<article_id_issn_online></article_id_issn_online>
			<article_id_pubmed></article_id_pubmed>
			<article_id_pii></article_id_pii>
			<article_id_doi></article_id_doi>
			<article_id_iranmedex></article_id_iranmedex>
			<article_id_magiran></article_id_magiran>
			<article_id_sid></article_id_sid>
			<title_fa></title_fa>
			<title>﻿Effects of Preoperative Statin Treatment on the Incidence of Postoperative ﻿Atrial Fibrillation in Patients Undergoing Coronary Artery Bypass Grafting 	 </title>
			<subject_fa></subject_fa>
			<subject></subject>
			<content_type_fa></content_type_fa>
			<content_type>Original Article</content_type>
			<abstract_fa></abstract_fa>
			<abstract>﻿Background: Postoperative atrial fibrillation is still a 	 
common complication in patients undergoing coronary 	 
artery bypass grafting. The aim of this study was to 	 
evaluate the effect of preoperative statin therapy on 	 
new onset of postoperative atrial fibrillation in patients 	 
undergoing coronary artery bypass grafting. 	 
Methods: Of 8,946 patients undergoing isolated coronary 	 
artery bypass grafting at the Bristol Heart Institute from 	 
April 1996 to September 2006, 6,321 (70.6%) received 	 
preoperative statins. Of these, 2,152 patients (statin 	 
group) were matched to a control group (no statin) by 	 
propensity score analysis. 	 
Results: Preoperative characteristics, number of distal 	 
anastomoses, and the use of off -pump procedures were 	 
similar in both groups. Hospital mortality was 1.3% (56 	 
patients) with no difference between the two groups. 	 
Postoperative atrial fibrillation was significantly higher 	 
﻿in the statin compared with the no statin group (411, 	 
19.5%, versus 336; 15.8% respectively; p = 0.002). 	 
In a multivariate regression analysis, age (odds ratio 	 
[OR], 1.04; 95% confidence interval [CI], 1.02 to 1.05), 	 
pulmonary disease (OR, 1.42; 95% CI, 1.12–1.82), 	 
history of paroxysmal atrial fibrillation (OR, 3; 95% 	 
CI, 2.13 to 4.19), preoperative angiotensin-converting 	 
enzyme inhibitor therapy (OR, 1.26; 95% CI, 1.07 to 	 
1.49), ejection fraction less than 0.30 (OR, 1.71; 95% 	 
CI, 1.22 to 2.38), emergency operations (OR, 4.5; 	 
95% CI, 2 to 10.12), and preoperative statin treatment 	 
(OR, 1.31; 95% CI, 1.11 to 1.55) were all independent 	 
predictors of postoperative atrial fibrillation. 	 
Conclusions: Preoperative statin is associated with a 	 
significantly higher incidence of postoperative atrial 	 
fibrillation compared with no statin treatment in patients 	 
undergoing isolated coronary artery bypass grafting. 	 
</abstract>
			<keyword_fa></keyword_fa>
			<keyword>Coronary Artery disease,CABG,Atrial fibrillation,statin	 </keyword>
			<start_page>30</start_page>
			<end_page>0</end_page>
			<web_url>http://www.iscs.org.ir/journals/vol.2/no.4/47/</web_url>
			<author_list>
				
			</author_list>
		</article>
		
		<article>
			<language></language>
			<article_id_issn></article_id_issn>
			<article_id_issn_online></article_id_issn_online>
			<article_id_pubmed></article_id_pubmed>
			<article_id_pii></article_id_pii>
			<article_id_doi></article_id_doi>
			<article_id_iranmedex></article_id_iranmedex>
			<article_id_magiran></article_id_magiran>
			<article_id_sid></article_id_sid>
			<title_fa></title_fa>
			<title>﻿pulmonary endarterectomy for ﻿chronic thromboembolic pulmonary hypertension: a single institution experience 	 </title>
			<subject_fa></subject_fa>
			<subject></subject>
			<content_type_fa></content_type_fa>
			<content_type>Original Article</content_type>
			<abstract_fa></abstract_fa>
			<abstract>﻿Objective: Pulmonary endarterectomy (PEA) for 	 
chronic thromboembolic pulmonary hypertension 	 
(CTEPH) is the first treatment of choice with good 	 
short-term results. Only limited data are available 	 
concerning the long-term outcome after PEA. The 	 
purpose of this study is to evaluate the long-term 	 
survival and functional outcome after PEA with nearly 	 
10 years experience. 	 
Method: In the period of December 1998 and December 	 
2007 120 patients with CTEPH were referred to the 	 
St Antonius Hospital (Nieuwegein, The Netherlands) 	 
﻿of whom 72 underwent PEA. The clinical data are 	 
collected retrospectively. 	 
Results: In-hospital mortality was (5/72) 6.9%. Since 	 
2004 one patient died in the hospital (1/38, 2.9%). 	 
Two patients died during long-term follow-up with a 	 
median observation of 3 years. The overall 1-, 3-and 	 
5-year survival rates were 93.1%, 91.2% and 88.7% 	 
respectively. Prior to surgery patients were in New 	 
York Heart Association functional class III (58) and 	 
IV (14) with a mean pulmonary vascular resistance 	 
of 572 ± 313 dynes s cm–5. The following data were 	 
﻿compared before and after operation: mean pulmonary 	 
artery pressure (mPAP) decreased from 42 ± 11 to 22 	 
± 7 mmHg (p = 0.0001), NT-pro BNP improved from 	 
1527 ± 1652 to 160 ± 3 pg/ml (p = 0.0001), 6 min walk 	 
distance (6MWD) from 359 ± 124 to 518 ± 11 m (p = 	 
0.0001), and almost all patients returned to functional 	 
class I or II (p = 0.0001). Conclusion: Pulmonary 	 
﻿endarterectomy for patients with CTEPH has shown a 	 
dramatic improvement of clinical status with excellent 	 
long-term survival. 	 
</abstract>
			<keyword_fa></keyword_fa>
			<keyword>﻿Pulmonary 	endarterectomy • Pulmonary﻿hypertension • Survival • Surgical outcomes 	  	 </keyword>
			<start_page>29</start_page>
			<end_page>30</end_page>
			<web_url>http://www.iscs.org.ir/journals/vol.2/no.4/46/</web_url>
			<author_list>
				
			</author_list>
		</article>
		
		<article>
			<language></language>
			<article_id_issn></article_id_issn>
			<article_id_issn_online></article_id_issn_online>
			<article_id_pubmed></article_id_pubmed>
			<article_id_pii></article_id_pii>
			<article_id_doi></article_id_doi>
			<article_id_iranmedex></article_id_iranmedex>
			<article_id_magiran></article_id_magiran>
			<article_id_sid></article_id_sid>
			<title_fa></title_fa>
			<title>﻿Prophylactic intra-aortic balloon pump in high-risk ﻿patients undergoing coronary artery bypass grafting: a propensity score analysis 	 </title>
			<subject_fa></subject_fa>
			<subject></subject>
			<content_type_fa></content_type_fa>
			<content_type>Original Article</content_type>
			<abstract_fa></abstract_fa>
			<abstract>﻿The optimal use of prophylactic intra-aortic balloon pump 	 
(IABP) to prevent postcardiotomy low cardiac output 	 
syndrome (LCOS) is still debated and poorly defined. The 	 
aim of this study was to evaluate whether prophylactic 	 
IABP reduces the rate of postcardiotomy LCOS and 	 
improves the early outcome in hemodynamically stable, 	 
high-risk patients undergoing coronary artery bypass 	 
grafting (CABG). From May 2004 to August 2007, 141 	 
consecutive risk patients underwent CABG. Of these 38 	 
(27%) received prophylactic IABP. The remaining 103 	 
patientsunderwentoperationwithoutpreoperativeinsertion 	 
of the device. Prophylactic IABP patients were more 	 
likely to be younger (p&lt;0.0001), had a recent myocardial 	 
infarction (p&lt;0.0001), lower ejection fraction (p=0.006), 	 
﻿and higher NYHA functional class (p=0.05). After risk-	 
adjusting for propensity score, prophylactic IABP patients 	 
had a lower incidence of postcardiotomy LCOS (adjusted 	 
OR 0.07, p=0.006), postoperative myocardial infarction 	 
(adjusted OR 0.04, p=0.04), a shorter length of hospital stay 	 
(10.4±0.8 versus 12.2±0.6 days, p&lt;0.0001) than those who 	 
did not receive IABP. This study shows that prophylactic 	 
IABP treatment for hemodynamically stable high-risk 	 
patients undergoing CABG may improve postoperative 	 
course reducing postcardiotomy LCOS, postoperative 	 
myocardial infarction and length of hospital stay. 	 
</abstract>
			<keyword_fa></keyword_fa>
			<keyword>﻿Intra-aortic balloon pump; Low output cardiac ﻿syndrome; High-risk patients 	 </keyword>
			<start_page>29</start_page>
			<end_page>0</end_page>
			<web_url>http://www.iscs.org.ir/journals/vol.2/no.4/45/</web_url>
			<author_list>
				
			</author_list>
		</article>
		
		<article>
			<language></language>
			<article_id_issn></article_id_issn>
			<article_id_issn_online></article_id_issn_online>
			<article_id_pubmed></article_id_pubmed>
			<article_id_pii></article_id_pii>
			<article_id_doi></article_id_doi>
			<article_id_iranmedex></article_id_iranmedex>
			<article_id_magiran></article_id_magiran>
			<article_id_sid></article_id_sid>
			<title_fa></title_fa>
			<title>﻿Extra-corporeal life support following cardiac surgery﻿in children: analysis of risk factors and survival in a single institution 	 </title>
			<subject_fa></subject_fa>
			<subject></subject>
			<content_type_fa></content_type_fa>
			<content_type>Original Article</content_type>
			<abstract_fa></abstract_fa>
			<abstract>﻿Objective: Application of extra-corporeal life support 	 
(ECLS) following pediatric cardiac surgery varies between 	 
different institutions based on manpower availability and 	 
philosophy towards ECLS utilization. We examined a 	 
large single institution experience with postoperative 	 
ECLS in children aiming to identify outcome predictors. 	 
Methods: Hospital records of all children who required 	 
postoperative ECLS at our institution were reviewed. 	 
Patients’ demographics, cardiac anatomy, surgical and 	 
ECLS support details were entered into a multivariable 	 
regression analysis to determine factors associated with 	 
survival. Results: Between 1990 and 2007, 180 consecutive 	 
children, median age 109 days (range: 1 day–16.9 years), 	 
required postoperative ECLS. Sixty-nine children (38%) 	 
had undergone palliative treatment for single ventricle 	 
pathology.ECLSsupportwasrequiredforfailuretoseparate 	 
from cardiopulmonary bypass (n = 83) or for postoperative 	 
low cardiac output state (n = 97). Forty-eight patients (27%) 	 
received rescue extra-corporeal membrane oxygenation 	 
(ECMO) support during active chest compression for 	 
﻿refractory cardiac arrest. Under ECLS support, 37 patients 	 
required surgical revision and 20 received orthotopic 	 
heart transplantation. One hundred and nine patients 	 
(61%) survived &gt;24 h following ECLS discontinuation 	 
and 68 (38%) were discharged alive. Hospital survivors 	 
required shorter ECLS support duration compared to non-	 
survivors (median 3 vs 5 days, respectively, p = 0.05) 	 
however survival occurred after up to 16 days of ECLS 	 
support. ECLS indication (OR: 0.85 for failure to separate 	 
from bypass vs postoperative low cardiac output 95% CI 	 
(0.47–1.56), p = 0.62) and rescue ECMO (OR: 0.63 for 	 
rescue ECMO vs not 95%CI (0.32–1.24), p = 0.18) were 	 
not associated with risk of mortality. In a multivariable 	 
logistic regression model, neurological complications (p 	 
= 0.0007), prolonged ECLS duration (p = 0.003), repeat 	 
ECLS requirement (p = 0.02), renal dysfunction (p = 0.04) 	 
and not performing heart transplantation (p = 0.04) were 	 
significant factors for hospital death. Conclusion: ECLS 	 
plays a valuable role in children with low cardiac output 	 
state following cardiac surgery. More than one third of 	 
﻿those patients, including young neonates, older children, 	 
patients with single ventricle, or those requiring rescue 	 
ECMO can be salvaged. Although prognosis worsens with 	 
prolonged ECLS duration, survival can be noted up to 16 	 
days of support. Heart transplantation is often an important 	 
ECLS exit strategy and should be considered early in 	 
﻿selected children. Patients’ survival could improve if renal 	 
and neurological complications are avoided. 	 
</abstract>
			<keyword_fa></keyword_fa>
			<keyword>﻿Congenital heart disease • Cardiac arrest Extra-corporeal life support • Single ventricle</keyword>
			<start_page>29</start_page>
			<end_page>0</end_page>
			<web_url>http://www.iscs.org.ir/journals/vol.2/no.4/44/</web_url>
			<author_list>
				
			</author_list>
		</article>
		
		<article>
			<language></language>
			<article_id_issn></article_id_issn>
			<article_id_issn_online></article_id_issn_online>
			<article_id_pubmed></article_id_pubmed>
			<article_id_pii></article_id_pii>
			<article_id_doi></article_id_doi>
			<article_id_iranmedex></article_id_iranmedex>
			<article_id_magiran></article_id_magiran>
			<article_id_sid></article_id_sid>
			<title_fa></title_fa>
			<title>﻿Diazoxide protects myocardial mitochondria, metabolism, and function during cardiac ﻿surgery: A double-blind randomized feasibility study of diazoxide-supplemented cardioplegia 	 </title>
			<subject_fa></subject_fa>
			<subject></subject>
			<content_type_fa></content_type_fa>
			<content_type>Original Article</content_type>
			<abstract_fa></abstract_fa>
			<abstract>﻿Objectives: The study was designed to assess whether diazoxide-mediated cardioprotection might be used in human 	 
subjects during cardiac surgery. 	 
Methods: Forty patients undergoing coronary artery bypass grafting were randomized to receive intermittent warm 	 
﻿blood antegrade cardioplegia supplemented with either 	 
diazoxide (100 μmol/L) or placebo (n = 20 in each group). 	 
Mitochondria were assessed before and after ischemia and 	 
reperfusion in myocardial biopsy specimens. Myocardial 	 
oxygen and glucose and lactic acid extraction ratios were 	 
measured before ischemia and in the first 20 minutes 	 
of reperfusion. Hemodynamic data were collected, 	 
and troponin I, creatine kinase–MB, and N-terminal 	 
prohormone brain natriuretic peptide levels were 	 
measured. All outcomes were analyzed by using mixed-	 
effects modeling for repeated measures. 	 
Results: No deaths, strokes, or infarcts were observed. 	 
Patients received, on average, 36.2 ± 1.2 mg of diazoxide 	 
and 37.3 ± 1.9 mg of placebo (P = .6). Diazoxide added 	 
to cardioplegia prevented mitochondrial swelling (8899 ± 	 
474 vs 9273 ± 688 pixels before and after the procedure, 	 
respectively; P = .6) compared with that seen in the placebo 	 
group (8474 ± 163 vs 11,357 ± 759 pixels, P = .004). 	 
No oxygen debt was observed in the diazoxide group. 	 
Glucose consumption and lactic acid production returned 	 
to preischemic values faster in the diazoxide group. The 	 
﻿following hemodynamic parameters differed between 	 
the diazoxide and placebo groups, respectively, in the 	 
postoperative period: cardiac index, 3.0 ± 0.09 versus 2.6 	 
± 0.09 L • min–1 • m–2 (P = .002); left cardiac work index, 	 
2.81 ± 0.07 versus 2.31 ± 0.07 kg/m2 (P &lt; .001); oxygen 	 
delivery index, 420 ± 14 versus 377 ± 13 mL • min–1 • 	 
m–2 (P = .03); and oxygen extraction ratio, 29.3% ± 1.1% 	 
versus 32.6% ± 1.1% (P = .02). Postoperative myocardial 	 
enzyme levels did not differ, but N-terminal prohormone 	 
brain natriuretic peptide levels were lower in the diazoxide 	 
group (120 ± 27 vs 192 ± 29 pg/mL, P = .04). 	 
Conclusions: Supplementing blood cardioplegia with 	 
diazoxide is safe and improves myocardial protection 	 
during cardiac surgery, possibly through its influence on 	 
the mitochondria. 	 
Abbreviations andAcronymsAXC = aortic crossclamping; 	 
CK-MB = creatine kinase–MB; CPB = cardiopulmonary 	 
bypass; KATP = adenosine triphosphate–sensitive 	 
potassium; NT-proBNP = N-terminal prohormone brain 	 
natriuretic peptide; O2ER = oxygen extraction ratio 	 
</abstract>
			<keyword_fa></keyword_fa>
			<keyword>﻿myocardial Protection,Cardiac Surgery,Cardioplegia,Cardiopulmonary bypass</keyword>
			<start_page>27</start_page>
			<end_page>0</end_page>
			<web_url>http://www.iscs.org.ir/journals/vol.2/no.4/43/</web_url>
			<author_list>
				
			</author_list>
		</article>
		
		<article>
			<language></language>
			<article_id_issn></article_id_issn>
			<article_id_issn_online></article_id_issn_online>
			<article_id_pubmed></article_id_pubmed>
			<article_id_pii></article_id_pii>
			<article_id_doi></article_id_doi>
			<article_id_iranmedex></article_id_iranmedex>
			<article_id_magiran></article_id_magiran>
			<article_id_sid></article_id_sid>
			<title_fa></title_fa>
			<title>﻿opoietin protects from reperfusion-induced ﻿myocardial injury by enhancing coronary endothelial nitric oxide production 	 </title>
			<subject_fa></subject_fa>
			<subject></subject>
			<content_type_fa></content_type_fa>
			<content_type>Original Article</content_type>
			<abstract_fa></abstract_fa>
			<abstract>﻿Objective: Cardioprotective properties of recombinant 	 
human Erythropoietin (rhEpo) have been shown in in vivo 	 
regional or ex vivo global models of ischemia–reperfusion 	 
(I/R) injury. The aim of this study was to characterize 	 
the cardioprotective potential of rhEPO in an in vivo 	 
experimental model of global I/R approximating the 	 
clinical cardiac surgical setting and to gain insights into 	 
the myocardial binding sites of rhEpo and the mechanism 	 
involved in its cardioprotective effect. 	 
Methods: Hearts of donor Lewis rats were arrested with 	 
cold crystalloid cardioplegia and after 45 min of cold 	 
global ischemia grafted heterotopically into the abdomen 	 
of recipient Lewis rats. Recipients were randomly assigned 	 
to control non-treated or Epo-treated group receiving 5000 	 
U/kg of rhEpo intravenously 20 min prior to reperfusion.At 	 
5 time points 5–1440 min after reperfusion, the recipients 	 
(n = 6–8 at each point) were sacrificed, blood and native 	 
and grafted hearts harvested for subsequent analysis. 	 
Results: Treatment with rhEpo resulted in a significant 	 
reduction in myocardial I/R injury (plasma troponin T) in 	 
correlation with preservation of the myocardial redox state 	 
(reduced glutathione). The extent of apoptosis (activity 	 
of caspase 3 and caspase 9, TUNEL test) in our model 	 
﻿was very modest and not significantly affected by rhEpo. 	 
Immunostaining of the heart tissue with anti-Epo antibodies 	 
showed an exclusive binding of rhEpo to the coronary 	 
endothelium with no binding of rhEpo to cardiomyocytes. 	 
Administration of rhEpo resulted in a significant increase 	 
in nitric oxide (NO) production assessed by plasma nitrite 	 
levels. Immunostaining of heart tissue with anti-phospho-	 
eNOS antibodies showed that after binding to the coronary 	 
endothelium, rhEpo increased the phosphorylation and 	 
thus activation of endothelial nitric oxide synthase (eNOS) 	 
in coronary vessels. There was no activation of eNOS in 	 
cardiomyocytes. Conclusions: Intravenous administration 	 
of rhEpo protects the heart against cold global I/R. 	 
Apoptosis does not seem to play a major role in the 	 
process of tissue injury in this model. After binding to the 	 
coronary endothelium, rhEpo enhances NO production by 	 
phosphorylation and thus activation of eNOS in coronary 	 
vessels. Our results suggest that cardioprotective properties 	 
of rhEpo are at least partially mediated by NO released by 	 
the coronary endothelium. 	 
</abstract>
			<keyword_fa></keyword_fa>
			<keyword>﻿Erythropoietin • Myocardial ischemia– ﻿reperfusion injury 	 	 </keyword>
			<start_page>27</start_page>
			<end_page>0</end_page>
			<web_url>http://www.iscs.org.ir/journals/vol.2/no.4/42/</web_url>
			<author_list>
				
			</author_list>
		</article>
		
		<article>
			<language></language>
			<article_id_issn></article_id_issn>
			<article_id_issn_online></article_id_issn_online>
			<article_id_pubmed></article_id_pubmed>
			<article_id_pii></article_id_pii>
			<article_id_doi></article_id_doi>
			<article_id_iranmedex></article_id_iranmedex>
			<article_id_magiran></article_id_magiran>
			<article_id_sid></article_id_sid>
			<title_fa></title_fa>
			<title>﻿Cavopulmonary anastomosis improves left ﻿ventricular assist device support in acute biventricular failure 	 </title>
			<subject_fa></subject_fa>
			<subject></subject>
			<content_type_fa></content_type_fa>
			<content_type>Original Article</content_type>
			<abstract_fa></abstract_fa>
			<abstract>﻿Objective: Right ventricular failure during left ventricular 	 
assist device (LVAD) support can result in severe 	 
hemodynamic compromise with high mortality. This 	 
study investigated the acute effects of cavopulmonary 	 
anastomosis on right ventricular loading and LVAD 	 
performance in a model of severe biventricular failure. 	 
Methods: LVAD support was performed by means of 	 
centrifugal pump implantation in 14 anesthetized dogs 	 
(20–30 kg) with severe biventricular failure obtained by 	 
ventricularfibrillationinduction.Animalswererandomized 	 
to be submitted to classical cavopulmonary anastomosis 	 
(Glenn shunt) or to control group and were maintained 	 
﻿under LVAD support for 2 h. Left and right atrial, right 	 
ventricular and systemic pressures were monitored, while 	 
total pulmonary flow was simultaneously recorded by 	 
transonic flowmeters located on the superior vena cava 	 
and pulmonary trunk. Blood gas and venous lactate 	 
determinations were also obtained. 	 
Results: Ventricular fibrillation maintenance resulted in 	 
acute LVAD performance impairment after 90 min in the 	 
control group, while animals with Glenn circuit maintained 	 
normal LVAD pump flow (55 ± 13 ml kg–1 min–1 vs 21 ± 4 	 
ml kg–1 min–1, p &lt; 0.001) and better peripheral perfusion 	 
(blood lactate of 29 ± 10 pg/ml vs 46 ± 9 pg/ml, p &lt; 0.001). 	 
﻿Left and right atrial pressures did not change significantly, 	 
while right ventricular pressure was lower in animals with 	 
Glenn circuit (13 ± 3 mmHg vs 22 ± 8 mmHg, p = 0.005). 	 
Right ventricular unloading with Glenn shunt also resulted 	 
in superior total pulmonary flow (59 ± 13 ml kg–1 min–1 	 
vs 17 ± 3 ml kg–1 min–1, p &lt; 0.001). Conclusion: The 	 
concomitant use of cavopulmonary anastomosis during 	 
﻿LVAD support in a model of severe biventricular failure 	 
limited right ventricular overloading and resulted in better 	 
hemodynamic performance. 	 
</abstract>
			<keyword_fa></keyword_fa>
			<keyword>﻿Circulatory support • Assisted circulation ﻿Biventricular failure • Cavopulmonary anastomosis ﻿Right ventricle 	 	 </keyword>
			<start_page>26</start_page>
			<end_page>0</end_page>
			<web_url>http://www.iscs.org.ir/journals/vol.2/no.4/41/</web_url>
			<author_list>
				
			</author_list>
		</article>
		
		<article>
			<language></language>
			<article_id_issn></article_id_issn>
			<article_id_issn_online></article_id_issn_online>
			<article_id_pubmed></article_id_pubmed>
			<article_id_pii></article_id_pii>
			<article_id_doi></article_id_doi>
			<article_id_iranmedex></article_id_iranmedex>
			<article_id_magiran></article_id_magiran>
			<article_id_sid></article_id_sid>
			<title_fa></title_fa>
			<title>Is bicaval orthotopic heart ﻿transplantation superior to the biatrial technique? 	 </title>
			<subject_fa></subject_fa>
			<subject></subject>
			<content_type_fa></content_type_fa>
			<content_type>Original Article</content_type>
			<abstract_fa></abstract_fa>
			<abstract>﻿A best evidence topic in cardiac surgery was written 	 
according to a structured protocol. The question addressed 	 
was whether the bicaval heart transplantation technique is 	 
superior to biatrial orthotopic heart transplantation (OTH). 	 
Altogether, 175 papers were found using the reported 	 
search, of which 20 presented the best evidence to answer 	 
the clinical question. The authors, journal, date and country 	 
of publication, patient group studied, study type, relevant 	 
outcomes and results of these papers are tabulated. We 	 
concludethatmany papers have documented the superiority 	 
of the bicaval technique over the biatrial technique for 	 
short-term outcomes. A meta-analysis of 41 papers on this 	 
topic found significant benefits for early atrial pressure, 	 
tricuspid valve regurgitation, return to sinus rhythm and 	 
﻿even perioperative mortality. But for longer-term outcome, 	 
the largest series of 11,931 patients found no difference 	 
in survival between the two groups and the meta-analysis 	 
found no mortality differences at 1 or 3 years. The bicaval 	 
technique is also more demanding technically and has a 	 
slightly longer bypass and ischemic time. The United 	 
Network for Organ Sharing (UNOS) database showed that 	 
in 2005 in the USA the bicaval technique has now become 	 
more popular than the biatrial technique (1083 procedures 	 
versus 806). 	 
</abstract>
			<keyword_fa></keyword_fa>
			<keyword>﻿Evidence-based medicine; 	Orthotopic ﻿transplantation; Bicaval anastomosis; Biatrial anastomosis; ﻿Survival; Arrhythmia 	 	 </keyword>
			<start_page>26</start_page>
			<end_page>0</end_page>
			<web_url>http://www.iscs.org.ir/journals/vol.2/no.4/40/</web_url>
			<author_list>
				
			</author_list>
		</article>
		
		<article>
			<language></language>
			<article_id_issn></article_id_issn>
			<article_id_issn_online></article_id_issn_online>
			<article_id_pubmed></article_id_pubmed>
			<article_id_pii></article_id_pii>
			<article_id_doi></article_id_doi>
			<article_id_iranmedex></article_id_iranmedex>
			<article_id_magiran></article_id_magiran>
			<article_id_sid></article_id_sid>
			<title_fa></title_fa>
			<title>﻿eatment of multivalvular ﻿endocarditis: Twenty-one–year single center experience 	 </title>
			<subject_fa></subject_fa>
			<subject></subject>
			<content_type_fa></content_type_fa>
			<content_type>Original Article</content_type>
			<abstract_fa></abstract_fa>
			<abstract>﻿Objective: Little information is available about surgical 	 
outcomes in patients with multivalvular endocarditis. 	 
The aim of this article is to review the 21-year experience 	 
with surgical treatment of patients with multivalvular 	 
endocarditis at our institution and, in particular, to 	 
determine the incidence, pathologic status, diagnosis, 	 
surgical strategies, and outcomes of patients with this 	 
disease. 	 
Methods: From January 1986 to December 2006, a total 	 
of 48 patients (40 men, 8 women), with a mean age of 	 
42 ± 12 years, underwent surgery for multivalvular 	 
endocarditis. Endocarditis was active in 32 patients and 	 
healed in 16. Preoperative transthoracic echocardiographic 	 
evaluation was performed in all 48 patients with addition 	 
of transesophageal echocardiography in 22 (45.8%). 	 
Intraoperative findings showed that the endocarditis 	 
involved mostly the mitral and aortic valves (40/48 	 
patients). Triple or quadruple valve involvement was 	 
found in 1 and 2 patients, respectively. Preoperative, 	 
﻿perioperative, and postoperative data were retrospectively 	 
analyzed and risk factors for early and late survival were 	 
determined. 	 
Results: In only 24 (50.0%) patients was multivalvular 	 
endocarditis diagnosed by preoperative transthoracic 	 
echocardiography; 17 (77.3%) patients had multivalvular 	 
endocarditis confirmed by preoperative transesophageal 	 
echocardiography. The 30-day hospital mortality was 	 
12.5% (n = 6). Preoperative renal failure, New York Heart 	 
AssociationclassIV,andemergencysurgerywereidentified 	 
as independent risk factors for hospital mortality. Overall 	 
long-term survival was 74% ± 6% at 5 years and 62% ± 	 
3% at 10 years. Multivariate analysis revealed that renal 	 
failure and recurrent endocarditis were associated with 	 
increased late mortality. Ten-year freedom from recurrent 	 
endocarditis was 74% ± 5% and 10-year freedom from 	 
reoperation was 73% ± 6%. 	 
Conclusions: In our institution, multivalvular endocarditis 	 
was diagnosed by transthoracic echocardiography in 	 
﻿only half of the patients. Intraoperative transesophageal 	 
echocardiography provided a more effective means to 	 
identify this disease. Radical resection of all infected 	 
tissues for patients with multivalvular endocarditis and 	 
additional intraoperative interventions, depending on the 	 
intraoperative pathologic condition, produced satisfactory 	 
in-hospital and long-term results, similar to those in 	 
﻿patients with a single infected heart valve. 	 
Abbreviations and Acronyms CHD = congenital heart 	 
disease; CI = confidence interval; MVE = multivalvular 	 
endocarditis; NVE = native valve endocarditis; OR = odds 	 
ratio; TEE = transesophageal echocardiography; TTE = 	 
transthoracic echocardiography 	 
</abstract>
			<keyword_fa></keyword_fa>
			<keyword>Heart Valve,Endo Carditis,Valve Surgery</keyword>
			<start_page>25</start_page>
			<end_page>26</end_page>
			<web_url>http://www.iscs.org.ir/journals/vol.2/no.4/39/</web_url>
			<author_list>
				
			</author_list>
		</article>
		
		<article>
			<language></language>
			<article_id_issn></article_id_issn>
			<article_id_issn_online></article_id_issn_online>
			<article_id_pubmed></article_id_pubmed>
			<article_id_pii></article_id_pii>
			<article_id_doi></article_id_doi>
			<article_id_iranmedex></article_id_iranmedex>
			<article_id_magiran></article_id_magiran>
			<article_id_sid></article_id_sid>
			<title_fa></title_fa>
			<title>﻿Repair of Ischemic Mitral Regurgitation: ﻿Comparison between Flexible and Rigid Annuloplasty Rings 	 </title>
			<subject_fa></subject_fa>
			<subject></subject>
			<content_type_fa></content_type_fa>
			<content_type>Original Article</content_type>
			<abstract_fa></abstract_fa>
			<abstract>﻿Background: The surgical treatment of ischemic mitral 	 
regurgitation (MR) usually involves implantation of an 	 
annuloplasty ring. We compared results of mitral valve 	 
repair using a flexible or a rigid annuloplasty ring in 	 
patients with ischemic MR undergoing coronary artery 	 
bypass graft surgery. 	 
Methods: There were 169 patients. A flexible ring was 	 
implanted in 117 and a rigid ring in 52. Age and clinical 	 
profile, degree of left ventricular dysfunction, and degree 	 
of MR (mean 3.2) were similar between groups. 	 
Results: Operative mortality was 9% in each group. Follow-	 
up (58 ± 30 months for flexible group and 14 ± 7 months 	 
for rigid group) was available for 91%. For the flexible 	 
and rigid ring groups, respectively, mean New York Heart 	 
Association functional class was 1.9 and 1.6, with 33% and 	 
14% in classes III to IV (p = 0.03); mean MR grade was 	 
﻿1.25 and 0.7 (p = 0.006). There was no difference in left 	 
ventricle function or dimensions. At follow-up, 29 patients 	 
(34%) in the flexible group had residual MR of moderate 	 
degree or greater compared with 6 (15%) in the rigid 	 
group (p = 0.03). Mean tricuspid incompetence gradient 	 
was 39 and 34 mm Hg (p = nonsignificant); however, the 	 
degree of reduction was greater in the rigid group (p = 	 
0.001). Late mortality was observed in 32 patients, all in 	 
the flexible group. 	 
Conclusions: Clinical and hemodynamic results are 	 
better with rigid mitral annuloplasty rings compared with 	 
flexible rings. That result may be due to ring design, which 	 
dictates not only the annular diameter but also annular 	 
configuration. Longer follow-up is needed to determine 	 
differences in survival 	 
</abstract>
			<keyword_fa></keyword_fa>
			<keyword>Mitral Valve,Ischemic MR,Ring Annuloplasty	 </keyword>
			<start_page>25</start_page>
			<end_page>0</end_page>
			<web_url>http://www.iscs.org.ir/journals/vol.2/no.4/38/</web_url>
			<author_list>
				
			</author_list>
		</article>
		
		<article>
			<language></language>
			<article_id_issn></article_id_issn>
			<article_id_issn_online></article_id_issn_online>
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			<article_id_pii></article_id_pii>
			<article_id_doi></article_id_doi>
			<article_id_iranmedex></article_id_iranmedex>
			<article_id_magiran></article_id_magiran>
			<article_id_sid></article_id_sid>
			<title_fa></title_fa>
			<title>Aortic and mitral valve disease in ﻿the United States: A trend of change in surgical practice between 1998 and 2005 	 </title>
			<subject_fa></subject_fa>
			<subject></subject>
			<content_type_fa></content_type_fa>
			<content_type>Original Article</content_type>
			<abstract_fa></abstract_fa>
			<abstract>&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;</abstract>
			<keyword_fa></keyword_fa>
			<keyword>Aortic Valve,mitral valve,valve replacement,mitral valve repair</keyword>
			<start_page>24</start_page>
			<end_page>0</end_page>
			<web_url>http://www.iscs.org.ir/journals/vol.2/no.4/37/</web_url>
			<author_list>
				
			</author_list>
		</article>
		
		<article>
			<language></language>
			<article_id_issn></article_id_issn>
			<article_id_issn_online></article_id_issn_online>
			<article_id_pubmed></article_id_pubmed>
			<article_id_pii></article_id_pii>
			<article_id_doi></article_id_doi>
			<article_id_iranmedex></article_id_iranmedex>
			<article_id_magiran></article_id_magiran>
			<article_id_sid></article_id_sid>
			<title_fa></title_fa>
			<title>Long-term follow-up of elderly patients ﻿subjected to aortic valve replacement with mechanical prostheses 	 </title>
			<subject_fa></subject_fa>
			<subject></subject>
			<content_type_fa></content_type_fa>
			<content_type>Original Article</content_type>
			<abstract_fa></abstract_fa>
			<abstract>﻿We propose to analyse the long-term follow-up in patients 	 
older than 65 years of age who received a mechanical valve 	 
in the aortic position, using death and prosthetic-related 	 
complications as endpoints. From April 1988 to December 	 
1995, 144 consecutive patients 65-75 years of age (mean 	 
67.7±2.5) were enrolled. Total duration of follow-up was 	 
1663 patient-years (median 13.0 years) and was complete 	 
for 99% of the patients. Thirty-day mortality was 1.4% 	 
(n=2). At the end of the study, 77 patients (53.8%) were 	 
alive, with ages ranging from 77 to 91 years (mean 82.1±3.2 	 
years). The overall 5-, 10-and 15-year actuarial survival 	 
was 87.4%±3.0, 67.7%±4.3 and 58.5%±4.5, respectively. 	 
Freedom from stroke was 93.3±3.1%, 84.6±3.3% and 	 
71.7±4.5%, respectively, after identical periods. Freedom 	 
﻿from major bleeding was 97.2±1.1%, 90.4±3.5% and 	 
86.4±4.0%, respectively. Freedom from endocarditis was 	 
95.7±2.3%, 95.0±2.1% and 94.4±2.5%, respectively, and 	 
freedom from reoperation was 98.0±1.2%, 97.6±1.3%, 	 
96.9±2.4% and 96.4±2.6%, respectively. Freedom from 	 
major valve-related events was 87.7±2.6%, 73.9±3.4% and 	 
61.5±4.6%, respectively. Nearly two-thirds of the patients 	 
were alive and free from major adverse valve-related 	 
events. Hence, we consider implantation of a mechanical 	 
prosthesis in elderly patients safe and appropriate, but the 	 
choice must be tailored for each specific patient. 	 
</abstract>
			<keyword_fa></keyword_fa>
			<keyword>﻿Aortic valve replacement; Elderly; Mechanical ﻿prostheses; Bioprostheses 	 </keyword>
			<start_page>24</start_page>
			<end_page>0</end_page>
			<web_url>http://www.iscs.org.ir/journals/vol.2/no.4/36/</web_url>
			<author_list>
				
			</author_list>
		</article>
		
		<article>
			<language></language>
			<article_id_issn></article_id_issn>
			<article_id_issn_online></article_id_issn_online>
			<article_id_pubmed></article_id_pubmed>
			<article_id_pii></article_id_pii>
			<article_id_doi></article_id_doi>
			<article_id_iranmedex></article_id_iranmedex>
			<article_id_magiran></article_id_magiran>
			<article_id_sid></article_id_sid>
			<title_fa></title_fa>
			<title>﻿Fifteen years of ﻿experience in repair of 	 ﻿aortopulmonary window in children 	 </title>
			<subject_fa></subject_fa>
			<subject></subject>
			<content_type_fa></content_type_fa>
			<content_type>Original Article</content_type>
			<abstract_fa></abstract_fa>
			<abstract>﻿Introduction: 	 
Aorto-pulmonary window is a very rare 	 
Malformation which accounts for about 	 
0.15% of all cardiac anomalies. There 	 
is no tendency for AP windows to close 	 
spontaneously. The natural history of infants 	 
with large AP windows is as unfavorable 	 
rarely they survive to childhood and 	 
those who survive beyond early life have 	 
important pulmonary vascular disease (1). 	 
The Richardson classification system for 	 
aorto-pulmonary window includes simple 	 
defects between the ascending aorta and 	 
pulmonary trunk (type I), defects extending 	 
distally to include the origin of the right main 	 
pulmonary artery (type II), and anomalous 	 
origin of the right main pulmonary artery 	 
from the ascending aorta with no other 	 
aorto-pulmonary communication (type III). 	 
Material and Methods: 	 
We reviewed our cases of aorto-pulmonary 	 
window who underwent surgical repair 	 
From 1992 to 2007 at Sahid Rajee Heat 	 
center, Tehran, Iran. There were 30 	 
children with male to female ratio of 2:1 	 
.We evaluated demographic information 	 
of the patients.We used different operative 	 
techniques . The approach for AP Window 	 
repair was ligation without CPB in two 	 
cases, division and suturing using CPB 	 
in one patient, trans-window in 17 (PTFE 	 
patch in16; Dacron in 1), trans-aortic in 9 (in 	 
8 PTFE patch, in one simple suturing) and 	 
trans-pulmonary in 2 (both with PTFE) 	 
Among 15 patients with associated cardiac 	 
anomalies, 13 (87%) underwent single 	 
stage repair with the IAA repair was the 	 
most common (2 cases) .Factors such as 	 
cross-clamp and bypass time, mortality, 	 
early and late morbidity, ICU stay, hospital 	 
stay, duration of ventilator support were 	 
compared between groups with various 	 
methods of repair using “SPSS 16”. 	 
﻿Resullts: 	 
In among 30 patients male to female ratio 	 
was 2:1 .Mean age of the opatients was 	 
28± 9 months ;range 2-90 months,weight 	 
8.6±4.6;range 2-17 kg . Most patients 	 
(73%) had sub-systemic or systemic 	 
pulmonary hypertension (23% and 50% 	 
respectively) .Morphology of Ap windows 	 
was type I (87%, n=26), type II (10%, n=3) 	 
distal and one type III (3%), This agree 	 
with other reportsres. 63% of patients were 	 
symptomatic, most commonly dyspnea and 	 
43% were in heart failure on admission. 	 
Preoperative EF was 0.66 ± 0.07 which 	 
increased to 0.75 ± 0.07 post-operatively 	 
apparently duo to elimination of shunt and 	 
resultant increase in forward flow of aorta. 	 
Preoperative pulmonary artery pressure 	 
was 63 ± 13 mm Hg. 19 (63%) of patients 	 
had associated cardiac anomalies most 	 
frequently various forms of Aortic stenosis 	 
(23%) fallowed by interrupted aortic arch 	 
(IAA), coronary anomalies and VSD (each 	 
about 7%). In most other series IAAhas been 	 
most common associated anomaly (6), (7). 	 
The overall in-hospital mortality was 10% 	 
(3 patients), two of whom had associated 	 
anomaly, one had undergone arterial 	 
switch operation for TGA who couldn’t be 	 
separated from CPB, and the other one had 	 
simultaneous repair for interrupted aortic 	 
arch. The mortality was no different among 	 
patients with or without associated anomaly 	 
(10% each). Among the 27 survivors, the 	 
mean ICU stay was 4.4 days (range 3 -12 	 
days) and the mean post-operative hospital 	 
stay was 10.7 days (range 7 -16 days). 	 
Early complications were bleeding (two 	 
cases), pneumonia (one) and CVA (one). 	 
Mean follow-up was 49 months (range 2 – 	 
280 months) and there was no re-operation 	 
or late death. There were 4 cases of residual 	 
AP Window detected by echocardiography; 	 
none of them required re-intervention. 	 
Among patients with residual AP Window 	 
﻿two cases were seen with banding technique (100%) one with 	 
trans-aortic patch repair (11%) and one case with trans-window 	 
patch repair (5%). 	 
Discussion: 	 
An aorto-pulmonary window is a communication between the 	 
pulmonary artery (PA) and the ascending aorta in the presence 	 
of two separate semilunar valves. There is no tendency for 	 
AP Windows to close spontaneously [8] Since the early 	 
1990s, diagnosis has relied exclusively on two-dimensional 	 
echocardiography [9] but type II and III lesions are difficult 	 
to differentiate from PDA [10]. Cardiac catheterization and 	 
cineangiography with retrograde aortography is done in infants 	 
6 months of age for evaluating the presence of irreversible 	 
pulmonary vascular disease and in case of complex APW for 	 
delineating the 	 
exact morphology. In our series in 27% (8) of patients the 	 
diagnosis was made only through echocardiography, remainder 	 
of the cases was diagnosed via both echocardiography and 	 
angiography.Using multivariate analysis, we assessed the 	 
effects of (1) patient related factors (age, sex, weight and type 	 
of aorto-pulmonary window) and (2) procedural factors (type 	 
of approach) on post-operative course (ICU stay, Post-operative 	 
hospital stay, duration of ventilator support and post-operative 	 
EF). Age ,sex and weight had no clear impact on post operative 	 
course. As mentioned earlier the overall in-hospital mortality 	 
was 10% (3 patients). The reported mortality among other 	 
series ranged from 7.6% to 27%).The mortality was no different 	 
among patients with or without associated anomaly (3% each). 	 
Also there was no difference among various methods of repair 	 
in respect of morbidity, ICU stay; ventilator support and post 	 
operative EF . 	 
Conclusion: 	 
In our view Trans aortic or transwindow repair is the procedure 	 
of choice for APW repair and, simple ligation without CPB 	 
should be avoided due to the possibility of residual APW and 	 
distortion of pulmonary artery. 	 
</abstract>
			<keyword_fa></keyword_fa>
			<keyword>﻿Aortopulmonary window,Transaortic ﻿repair,Cardiopulmonary bypass 	 </keyword>
			<start_page>18</start_page>
			<end_page>23</end_page>
			<web_url>http://www.iscs.org.ir/journals/vol.2/no.4/35/</web_url>
			<author_list>
				
			</author_list>
		</article>
		
		<article>
			<language></language>
			<article_id_issn></article_id_issn>
			<article_id_issn_online></article_id_issn_online>
			<article_id_pubmed></article_id_pubmed>
			<article_id_pii></article_id_pii>
			<article_id_doi></article_id_doi>
			<article_id_iranmedex></article_id_iranmedex>
			<article_id_magiran></article_id_magiran>
			<article_id_sid></article_id_sid>
			<title_fa></title_fa>
			<title>﻿RoleofEpsilonAminocaproicacid&amp;Tranexamic ﻿Acid, vs Placebo in Reduction of mediastinal ﻿Bleeding following Open Heart Surgery 	 </title>
			<subject_fa></subject_fa>
			<subject></subject>
			<content_type_fa></content_type_fa>
			<content_type>Original Article</content_type>
			<abstract_fa></abstract_fa>
			<abstract>﻿Background: Post-operative bleeding 	 
is one of the Challenging issues in 	 
cardiacsurgery. The Excessive bleeding 	 
and need for transfusion of blood 	 
products may increases the patients’ 	 
mortality and morbidity. Although use 	 
of antifibrinolytics has long been the 	 
issue of interest but recently according 	 
to some reports of sudden death after 	 
use of aprotinin has encountered great 	 
limitations. So we decided to find an 	 
alternative drug for aprotinin. 	 
Methods and Materials: This 	 
study was performed as a Double blind 	 
Randomized clinical traial. Three hundred 	 
patients underwent open heart surgery using 	 
CPB to Shahid Rajaee Heart Center. The 	 
patients were divided into 3 groups; each 	 
containing 100 patients. Group A Amicar 	 
(Caproamin) , group B (Tranexamic acid) 	 
and group C (Control). The mean age was 	 
56.5 yr. (Ranged 16-79). 65.3% were male 	 
and 85.7% underwent CABG. Need for 	 
blood and blood products transfusion in 	 
operating room, ICU &amp; ward, as well ad 	 
post-op drainage volume during 6, 12, 24 	 
hours were evaluated. The probable post-op 	 
complications including post-op myocardial 	 
infarction or CNS, renal complications were 	 
also recorded. 	 
Results: 	 
The average volume of hemorrhage in group 	 
A was 427 cc, 558 cc in group B &amp; 659 cc, 	 
in group C, but these differences were not 	 
significant statistically (P=0.55). In group A 	 
46% of patients need 1-8 unit of blood, in 	 
group B this rate was 60% and in group C 	 
was 69% (P=0.093). Prevalence of post op 	 
MI was zero in group A 2% in group B and 	 
3% in group C (P=0.377). Incidence of Re-	 
explorationwas 4% in group A, 5% in group 	 
B &amp; 6% in group C (P=0.810). The length 	 
of hospital stay was the least in group A and 	 
﻿was the most in group B, but this difference 	 
was also not as significant (P=0.964) 	 
Comment: 	 
Antifibrinolytics, particularly Caproamin 	 
can play a role in decreasing post operative 	 
mediastinal bleeding, especially non surgical 	 
bleeding. 	 
Both Transamin and Caproamin are safe 	 
and do not increase thromboembolic events 	 
and other complications. These drugs do 	 
not cause significant reduction in volume 	 
of postoperative bleeding and transfusion 	 
requirements in OR and ICU, but when just 	 
CABG cases are considered, Caproamin 	 
causes significant reduction in post op 	 
hemorrhage and as a result reduction in 	 
transfusion requirements of blood products. 	 
</abstract>
			<keyword_fa></keyword_fa>
			<keyword>﻿CABG, Mediastinal bleeding, ﻿Antifibrinolytic, Open Heart Surgery 	 </keyword>
			<start_page>13</start_page>
			<end_page>17</end_page>
			<web_url>http://www.iscs.org.ir/journals/vol.2/no.4/34/</web_url>
			<author_list>
				
			</author_list>
		</article>
		
		<article>
			<language></language>
			<article_id_issn></article_id_issn>
			<article_id_issn_online></article_id_issn_online>
			<article_id_pubmed></article_id_pubmed>
			<article_id_pii></article_id_pii>
			<article_id_doi></article_id_doi>
			<article_id_iranmedex></article_id_iranmedex>
			<article_id_magiran></article_id_magiran>
			<article_id_sid></article_id_sid>
			<title_fa></title_fa>
			<title>﻿Assessment of protective effects of ﻿Warm Terminal Blood Cardioplegia ﻿on Myocardial Protection in CABG. 	 </title>
			<subject_fa></subject_fa>
			<subject></subject>
			<content_type_fa></content_type_fa>
			<content_type>Original Article</content_type>
			<abstract_fa></abstract_fa>
			<abstract>&lt;p&gt;﻿Abstract: Introduction: Coronary artery disease A significant metabolic derangement occurs in the ischaemic-reperfused heart of patients undergoing coronary artery bypass surgery using cold blood cardioplegia . It has been reported that up to one forth of deaths after coronary artery bypass grafting surgery may be caused by Reperfusion injury especially in patients with higher NYHA classes. There are evidences that in adult cardiac operations, a warm cardioplegic reperfusate (hot shot) before removing the aortic cross-clamp improves postbypass myocardial function and metabolic recovery . We randomly assigned 41 consecutive patients undergoing primary, elective CABG into two groups; TWBC Group who received Terminal Warm Blood Cardioplegia just before removing of Aortic cross clamp (n=24) and second group (Control) did not received TWBC (n=17). Among patients in CONTROL group 41% (95% CL: 19-62%) received at least one inotrope, but only 17% (95% CL:&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; &amp;nbsp;0 - 35%) of patients in TWBC group did so (p = 0.085). Also in respect to EF there was superiority in TWBC group only in patients with low pre operative EF. There was higher rate of spontaneous beating in TWBC group (21 of 24 or 88%) versus Control group (12 of 17 or 70%; P&amp;lt;0.1). Conclusion: it seems prudent to routinely use Terminal Warm Blood Cardioplegia in patients undergoing coronary bypass graft especially in those with reduced ventricular function.&lt;/p&gt;</abstract>
			<keyword_fa></keyword_fa>
			<keyword>﻿Cardioplegia, CABG, ﻿Myocardial Protection 	 </keyword>
			<start_page>9</start_page>
			<end_page>12</end_page>
			<web_url>http://www.iscs.org.ir/journals/vol.2/no.4/33/</web_url>
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		</article>
		
		<article>
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			<article_id_issn_online></article_id_issn_online>
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			<article_id_doi></article_id_doi>
			<article_id_iranmedex></article_id_iranmedex>
			<article_id_magiran></article_id_magiran>
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			<title_fa></title_fa>
			<title>﻿Continuous Local Infusion of ﻿Bupivacaine with ON-Q Pump System for Pain Management after Median Sternotomy</title>
			<subject_fa></subject_fa>
			<subject></subject>
			<content_type_fa></content_type_fa>
			<content_type>Original Article</content_type>
			<abstract_fa></abstract_fa>
			<abstract>﻿Background: Postoperative pain 	 
remains as a challenging case despite 	 
improvement of analgesic techniques. It 	 
may also increase the rate of morbidity 	 
and even mortality. Local anesthesia may 	 
decrease the consumption of opioids and 	 
its potential side effects. This study was 	 
aimed to show the role of local anesthesia 	 
in post-sternotomy pain. 	 
Methods: This prospective randomized 	 
clinical trial includes 40 candidates for 	 
elective coronary artery bypass graft 	 
(CABG) surgery. Patients with diabetic 	 
mellitus and other major co-morbidities 	 
were excluded. In group A (20 patiens) 	 
Bupivacaine 0.25% was continuously 	 
infused into subcutaneous tissue using 	 
the ON-Q system (I-flow Corporation, 	 
Lake Firest CA, USA) (2ml/h for 72h). 	 
Group B patients did not receive local 	 
anesthetics. The intensity of pain in 	 
was measured using Visual Analogue 	 
Scale (0-10). Need for narcotics or other 	 
analgesics, hemodynamic and arterial 	 
blood gas profiles were also recorded. 	 
Results: Both groups were similar 	 
regarding age, sex, body mass index, 	 
smoking and drug addiction and operative 	 
characteristics. The mean visual analogue 	 
scale (VAS) was significantly lower in 	 
G.A than G.B (2.1+/-1.7 versus 4.3+/-	 
2.7) (P=0.005). Narcotics requirement in 	 
G.A had decreased 25% compared to G.B 	 
(P= 0.041) but the mean doses of opioids 	 
consumption had no significant difference 	 
in two groups. Most of the patients in G.A 	 
(85%) were fully satisfied from his pain 	 
control, while this rate was only 45% in 	 
G.B (P= 0.029). Regarding other post-	 
operative complications, both groups were 	 
identical and no significant difference 	 
﻿was observed. Days of stay in hospital 	 
was reduced 1.4 days in average which 	 
is not significant (P=0.06). Drug addicts 	 
required higher doses of narcotics. 	 
Conclusion: Continuous local infusion of 	 
Bupivacain with ON-Q pump system can be 	 
useful and safe for pain management after 	 
median sternotomies. Bupivacaine not only 	 
reduces the pain intensty, but also reduces 	 
the consumption of opioids and other 	 
analgesics when compared to the control 	 
group. It also seems that this method may 	 
reduce the length of hospitalization and 	 
hence the hospital charges. 	 
</abstract>
			<keyword_fa></keyword_fa>
			<keyword>﻿Pain, CABG, Local Anesthesia, ﻿ON-Q Pump, Bupivacaine 	 	 </keyword>
			<start_page>3</start_page>
			<end_page>8</end_page>
			<web_url>http://www.iscs.org.ir/journals/vol.2/no.4/32/</web_url>
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		</article>
		
	</articleset>
</journal>

