<?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>﻿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>
		
	</articleset>
</journal>

