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Tenuous Airway in Children With Trisomy 21

Identifieur interne : 000018 ( Istex/Corpus ); précédent : 000017; suivant : 000019

Tenuous Airway in Children With Trisomy 21

Auteurs : Andrew L. De Jong ; Marcelle Sulek ; Michael Nihill ; Newton O. Duncan ; Ellen M. Friedman

Source :

RBID : ISTEX:0B46AE6A37A8A498573D625E527B7276AB364233

Abstract

Multiple congenital anomalies are closely linked to Down syndrome(trisomy 21). Cardiac malformations are found in 40% of patients, a large number of whom will require a major surgical procedure. The importance of postextubation stridor in these children is frequently underestimated. A retrospective review of 99 trisomy 21 patients who underwent cardiovascular surgery revealed postextubation stridor in 24 (24.2%). Significant factors for the development of stridor included younger age (P=0.04), lower growth percentile for weight (P=0.03), and increased frequency of reintubation(P=0.04). Subglottic stenosis was found in 6 (6.1%). In 4 of these patients, an endotracheal tube of larger diameter than predicted for age was used. All 6 patients were less than the 10th percentile for weight. We conclude that Down syndrome patients deserve special considerations and modifications of standard intubation techniques for successful airway management.

Url:
DOI: 10.1097/00005537-199703000-00013

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ISTEX:0B46AE6A37A8A498573D625E527B7276AB364233

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</titleInfo>
<name type="personal">
<namePart type="given">Andrew L.</namePart>
<namePart type="family">de Jong</namePart>
<namePart type="termsOfAddress">MD</namePart>
<affiliation>Department of Otolaryngology, Baylor College of Medicine and Texas Children's Hospital, Department of Otolaryngology, Houston, TX.</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Marcelle</namePart>
<namePart type="family">Sulek</namePart>
<namePart type="termsOfAddress">MD</namePart>
<affiliation>Department of Otolaryngology, Baylor College of Medicine and Texas Children's Hospital, Department of Otolaryngology, Houston, TX.</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Michael</namePart>
<namePart type="family">Nihill</namePart>
<namePart type="termsOfAddress">MD</namePart>
<affiliation>Department of Cardiology, Baylor College of Medicine and Texas Children's Hospital, Department of Otolaryngology, Houston, TX.</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Newton O.</namePart>
<namePart type="family">Duncan</namePart>
<namePart type="termsOfAddress">MD</namePart>
<affiliation>Department of Otolaryngology, Baylor College of Medicine and Texas Children's Hospital, Department of Otolaryngology, Houston, TX.</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Ellen M.</namePart>
<namePart type="family">Friedman</namePart>
<namePart type="termsOfAddress">MD</namePart>
<affiliation>Department of Otolaryngology, Baylor College of Medicine and Texas Children's Hospital, Department of Otolaryngology, Houston, TX.</affiliation>
<affiliation>Ellen M. Friedman, MD, Pediatric Otolaryngology, Texas Children's Hospital, 6621 Fannin St., Houston, TX 77030, U.S.A.</affiliation>
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<publisher>John Wiley & Sons, Inc.</publisher>
<place>
<placeTerm type="text">Hoboken, NJ</placeTerm>
</place>
<dateIssued encoding="w3cdtf">1997-03</dateIssued>
<dateValid encoding="w3cdtf">1996-10-14</dateValid>
<copyrightDate encoding="w3cdtf">1997</copyrightDate>
</originInfo>
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<languageTerm type="code" authority="rfc3066">en</languageTerm>
<languageTerm type="code" authority="iso639-2b">eng</languageTerm>
</language>
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<internetMediaType>text/html</internetMediaType>
<extent unit="figures">1</extent>
<extent unit="tables">2</extent>
<extent unit="references">19</extent>
</physicalDescription>
<abstract lang="en">Multiple congenital anomalies are closely linked to Down syndrome(trisomy 21). Cardiac malformations are found in 40% of patients, a large number of whom will require a major surgical procedure. The importance of postextubation stridor in these children is frequently underestimated. A retrospective review of 99 trisomy 21 patients who underwent cardiovascular surgery revealed postextubation stridor in 24 (24.2%). Significant factors for the development of stridor included younger age (P=0.04), lower growth percentile for weight (P=0.03), and increased frequency of reintubation(P=0.04). Subglottic stenosis was found in 6 (6.1%). In 4 of these patients, an endotracheal tube of larger diameter than predicted for age was used. All 6 patients were less than the 10th percentile for weight. We conclude that Down syndrome patients deserve special considerations and modifications of standard intubation techniques for successful airway management.</abstract>
<relatedItem type="host">
<titleInfo>
<title>The Laryngoscope</title>
</titleInfo>
<titleInfo type="abbreviated">
<title>The Laryngoscope</title>
</titleInfo>
<genre type="journal">journal</genre>
<subject>
<genre>article-category</genre>
<topic>Article</topic>
</subject>
<identifier type="ISSN">0023-852X</identifier>
<identifier type="eISSN">1531-4995</identifier>
<identifier type="DOI">10.1002/(ISSN)1531-4995</identifier>
<identifier type="PublisherID">LARY</identifier>
<part>
<date>1997</date>
<detail type="volume">
<caption>vol.</caption>
<number>107</number>
</detail>
<detail type="issue">
<caption>no.</caption>
<number>3</number>
</detail>
<extent unit="pages">
<start>345</start>
<end>350</end>
<total>6</total>
</extent>
</part>
</relatedItem>
<identifier type="istex">0B46AE6A37A8A498573D625E527B7276AB364233</identifier>
<identifier type="DOI">10.1097/00005537-199703000-00013</identifier>
<identifier type="ArticleID">LARY5541070313</identifier>
<accessCondition type="use and reproduction" contentType="copyright">Copyright © 1997 The Triological Society</accessCondition>
<recordInfo>
<recordContentSource>WILEY</recordContentSource>
<recordOrigin>John Wiley & Sons, Inc.</recordOrigin>
</recordInfo>
</mods>
</metadata>
<serie></serie>
</istex>
</record>

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