Long-term outcomes after fetal therapy for congenital high airway obstructive syndrome

Abstract Background/Purpose Congenital high airway obstructive syndrome (CHAOS) is a rare and devastating condition that is uniformly fatal without fetal intervention. We sought to describe fetal treatment and long-term outcomes of CHAOS at a single referral center. Methods The medical records of pa...

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Veröffentlicht in:Journal of pediatric surgery 2012-06, Vol.47 (6), p.1095-1100
Hauptverfasser: Saadai, Payam, Jelin, Eric B, Nijagal, Amar, Schecter, Samuel C, Hirose, Shinjiro, MacKenzie, Tippi C, Rand, Larry, Goldstein, Ruth, Farrell, Jody, Harrison, Michael, Lee, Hanmin
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container_end_page 1100
container_issue 6
container_start_page 1095
container_title Journal of pediatric surgery
container_volume 47
creator Saadai, Payam
Jelin, Eric B
Nijagal, Amar
Schecter, Samuel C
Hirose, Shinjiro
MacKenzie, Tippi C
Rand, Larry
Goldstein, Ruth
Farrell, Jody
Harrison, Michael
Lee, Hanmin
description Abstract Background/Purpose Congenital high airway obstructive syndrome (CHAOS) is a rare and devastating condition that is uniformly fatal without fetal intervention. We sought to describe fetal treatment and long-term outcomes of CHAOS at a single referral center. Methods The medical records of patients with fetal CHAOS evaluated at our center between 1993 and 2011 were reviewed. Maternal history, radiographic findings, antenatal management, and postnatal outcomes were compared. Results Twelve fetuses with CHAOS were identified. Eleven had concomitant hydrops at diagnosis. Six were electively terminated, and 2 had intra- or peripartum demise. Four patients underwent fetal intervention. Two underwent delivery via ex utero intrapartum treatment (EXIT) procedure with tracheostomy placement only, and 2 underwent fetal bronchoscopy with attempted wire tracheoplasty followed by EXIT with tracheostomy at delivery. All 4 patients who underwent EXIT were alive at last follow-up. One patient was ventilator and tracheostomy free and feeding by mouth. Conclusion Long-term and tracheostomy-free survival is possible with appropriate fetal intervention even in the presence of hydrops. Fetal intervention earlier in pregnancy may improve long-term outcomes, but patient selection for intervention remains challenging. Magnetic resonance imaging may help select those patients for whom fetal intervention before EXIT delivery may be beneficial.
doi_str_mv 10.1016/j.jpedsurg.2012.03.015
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We sought to describe fetal treatment and long-term outcomes of CHAOS at a single referral center. Methods The medical records of patients with fetal CHAOS evaluated at our center between 1993 and 2011 were reviewed. Maternal history, radiographic findings, antenatal management, and postnatal outcomes were compared. Results Twelve fetuses with CHAOS were identified. Eleven had concomitant hydrops at diagnosis. Six were electively terminated, and 2 had intra- or peripartum demise. Four patients underwent fetal intervention. Two underwent delivery via ex utero intrapartum treatment (EXIT) procedure with tracheostomy placement only, and 2 underwent fetal bronchoscopy with attempted wire tracheoplasty followed by EXIT with tracheostomy at delivery. All 4 patients who underwent EXIT were alive at last follow-up. One patient was ventilator and tracheostomy free and feeding by mouth. Conclusion Long-term and tracheostomy-free survival is possible with appropriate fetal intervention even in the presence of hydrops. Fetal intervention earlier in pregnancy may improve long-term outcomes, but patient selection for intervention remains challenging. Magnetic resonance imaging may help select those patients for whom fetal intervention before EXIT delivery may be beneficial.</description><identifier>ISSN: 0022-3468</identifier><identifier>EISSN: 1531-5037</identifier><identifier>DOI: 10.1016/j.jpedsurg.2012.03.015</identifier><identifier>PMID: 22703776</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Abnormalities, Multiple ; Abortion, Eugenic ; Adult ; Airway Obstruction - congenital ; Airway Obstruction - embryology ; Airway Obstruction - surgery ; Bronchoscopy ; CHAOS ; Ex utero intrapartum treatment ; EXIT ; Female ; Fetal Death - etiology ; Fetal surgery ; Fetal Therapies - methods ; Fetal Therapies - statistics &amp; numerical data ; Gestational Age ; Humans ; Hydrops Fetalis ; Infant, Newborn ; Larynx - abnormalities ; Larynx - embryology ; Magnetic Resonance Imaging ; Male ; Patient Selection ; Pediatrics ; Pregnancy ; Surgery ; Syndrome ; Trachea - abnormalities ; Trachea - embryology ; Trachea - surgery ; Tracheostomy ; Treatment Outcome ; Young Adult</subject><ispartof>Journal of pediatric surgery, 2012-06, Vol.47 (6), p.1095-1100</ispartof><rights>Elsevier Inc.</rights><rights>2012 Elsevier Inc.</rights><rights>Copyright © 2012 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c493t-8aa71edcae5a2a31615384294e3c283623c26269e10c95951aa4eafdcf1377c3</citedby><cites>FETCH-LOGICAL-c493t-8aa71edcae5a2a31615384294e3c283623c26269e10c95951aa4eafdcf1377c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jpedsurg.2012.03.015$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27929,27930,46000</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22703776$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Saadai, Payam</creatorcontrib><creatorcontrib>Jelin, Eric B</creatorcontrib><creatorcontrib>Nijagal, Amar</creatorcontrib><creatorcontrib>Schecter, Samuel C</creatorcontrib><creatorcontrib>Hirose, Shinjiro</creatorcontrib><creatorcontrib>MacKenzie, Tippi C</creatorcontrib><creatorcontrib>Rand, Larry</creatorcontrib><creatorcontrib>Goldstein, Ruth</creatorcontrib><creatorcontrib>Farrell, Jody</creatorcontrib><creatorcontrib>Harrison, Michael</creatorcontrib><creatorcontrib>Lee, Hanmin</creatorcontrib><title>Long-term outcomes after fetal therapy for congenital high airway obstructive syndrome</title><title>Journal of pediatric surgery</title><addtitle>J Pediatr Surg</addtitle><description>Abstract Background/Purpose Congenital high airway obstructive syndrome (CHAOS) is a rare and devastating condition that is uniformly fatal without fetal intervention. We sought to describe fetal treatment and long-term outcomes of CHAOS at a single referral center. Methods The medical records of patients with fetal CHAOS evaluated at our center between 1993 and 2011 were reviewed. Maternal history, radiographic findings, antenatal management, and postnatal outcomes were compared. Results Twelve fetuses with CHAOS were identified. Eleven had concomitant hydrops at diagnosis. Six were electively terminated, and 2 had intra- or peripartum demise. Four patients underwent fetal intervention. Two underwent delivery via ex utero intrapartum treatment (EXIT) procedure with tracheostomy placement only, and 2 underwent fetal bronchoscopy with attempted wire tracheoplasty followed by EXIT with tracheostomy at delivery. All 4 patients who underwent EXIT were alive at last follow-up. One patient was ventilator and tracheostomy free and feeding by mouth. Conclusion Long-term and tracheostomy-free survival is possible with appropriate fetal intervention even in the presence of hydrops. Fetal intervention earlier in pregnancy may improve long-term outcomes, but patient selection for intervention remains challenging. Magnetic resonance imaging may help select those patients for whom fetal intervention before EXIT delivery may be beneficial.</description><subject>Abnormalities, Multiple</subject><subject>Abortion, Eugenic</subject><subject>Adult</subject><subject>Airway Obstruction - congenital</subject><subject>Airway Obstruction - embryology</subject><subject>Airway Obstruction - surgery</subject><subject>Bronchoscopy</subject><subject>CHAOS</subject><subject>Ex utero intrapartum treatment</subject><subject>EXIT</subject><subject>Female</subject><subject>Fetal Death - etiology</subject><subject>Fetal surgery</subject><subject>Fetal Therapies - methods</subject><subject>Fetal Therapies - statistics &amp; numerical data</subject><subject>Gestational Age</subject><subject>Humans</subject><subject>Hydrops Fetalis</subject><subject>Infant, Newborn</subject><subject>Larynx - abnormalities</subject><subject>Larynx - embryology</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Patient Selection</subject><subject>Pediatrics</subject><subject>Pregnancy</subject><subject>Surgery</subject><subject>Syndrome</subject><subject>Trachea - abnormalities</subject><subject>Trachea - embryology</subject><subject>Trachea - surgery</subject><subject>Tracheostomy</subject><subject>Treatment Outcome</subject><subject>Young Adult</subject><issn>0022-3468</issn><issn>1531-5037</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUU1v1DAQtRCILm3_QuUjl6QeO3E2FwSqyoe0Ug-tuFquM9l1SOLFTlrl3zPRthy4cJoPvfdm5g1jVyByEKCvu7w7YpPmuM-lAJkLlQso37ANlAqyUqjqLdsIIWWmCr09Yx9S6oSgtoD37EzKitJKb9jPXRj32YRx4GGeXBgwcdtSzVucbM-nA0Z7XHgbIncExdGv7YPfH7j18dkuPDymKc5u8k_I0zI2kUQu2LvW9gkvX-I5e_h6-3DzPdvdfftx82WXuaJWU7a1tgJsnMXSSqtA0_bbQtYFKie3SksKWuoaQbi6rEuwtkDbNq4FWt-pc_bxJHuM4feMaTKDTw773o4Y5mRASAC6VVcE1SeoiyGliK05Rj_YuBDIrJaazrxaalZLjVCGLCXi1cuM-XHA5i_t1UMCfD4BkA598hhNch5Hh42P6CbTBP__GZ_-kXC9H72z_S9cMHVhjiPZaMAk4pj79bHrX0FSVpZS_QGFKqDx</recordid><startdate>20120601</startdate><enddate>20120601</enddate><creator>Saadai, Payam</creator><creator>Jelin, Eric B</creator><creator>Nijagal, Amar</creator><creator>Schecter, Samuel C</creator><creator>Hirose, Shinjiro</creator><creator>MacKenzie, Tippi C</creator><creator>Rand, Larry</creator><creator>Goldstein, Ruth</creator><creator>Farrell, Jody</creator><creator>Harrison, Michael</creator><creator>Lee, Hanmin</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20120601</creationdate><title>Long-term outcomes after fetal therapy for congenital high airway obstructive syndrome</title><author>Saadai, Payam ; Jelin, Eric B ; Nijagal, Amar ; Schecter, Samuel C ; Hirose, Shinjiro ; MacKenzie, Tippi C ; Rand, Larry ; Goldstein, Ruth ; Farrell, Jody ; Harrison, Michael ; Lee, Hanmin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c493t-8aa71edcae5a2a31615384294e3c283623c26269e10c95951aa4eafdcf1377c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Abnormalities, Multiple</topic><topic>Abortion, Eugenic</topic><topic>Adult</topic><topic>Airway Obstruction - congenital</topic><topic>Airway Obstruction - embryology</topic><topic>Airway Obstruction - surgery</topic><topic>Bronchoscopy</topic><topic>CHAOS</topic><topic>Ex utero intrapartum treatment</topic><topic>EXIT</topic><topic>Female</topic><topic>Fetal Death - etiology</topic><topic>Fetal surgery</topic><topic>Fetal Therapies - methods</topic><topic>Fetal Therapies - statistics &amp; numerical data</topic><topic>Gestational Age</topic><topic>Humans</topic><topic>Hydrops Fetalis</topic><topic>Infant, Newborn</topic><topic>Larynx - abnormalities</topic><topic>Larynx - embryology</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Patient Selection</topic><topic>Pediatrics</topic><topic>Pregnancy</topic><topic>Surgery</topic><topic>Syndrome</topic><topic>Trachea - abnormalities</topic><topic>Trachea - embryology</topic><topic>Trachea - surgery</topic><topic>Tracheostomy</topic><topic>Treatment Outcome</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Saadai, Payam</creatorcontrib><creatorcontrib>Jelin, Eric B</creatorcontrib><creatorcontrib>Nijagal, Amar</creatorcontrib><creatorcontrib>Schecter, Samuel C</creatorcontrib><creatorcontrib>Hirose, Shinjiro</creatorcontrib><creatorcontrib>MacKenzie, Tippi C</creatorcontrib><creatorcontrib>Rand, Larry</creatorcontrib><creatorcontrib>Goldstein, Ruth</creatorcontrib><creatorcontrib>Farrell, Jody</creatorcontrib><creatorcontrib>Harrison, Michael</creatorcontrib><creatorcontrib>Lee, Hanmin</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of pediatric surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Saadai, Payam</au><au>Jelin, Eric B</au><au>Nijagal, Amar</au><au>Schecter, Samuel C</au><au>Hirose, Shinjiro</au><au>MacKenzie, Tippi C</au><au>Rand, Larry</au><au>Goldstein, Ruth</au><au>Farrell, Jody</au><au>Harrison, Michael</au><au>Lee, Hanmin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Long-term outcomes after fetal therapy for congenital high airway obstructive syndrome</atitle><jtitle>Journal of pediatric surgery</jtitle><addtitle>J Pediatr Surg</addtitle><date>2012-06-01</date><risdate>2012</risdate><volume>47</volume><issue>6</issue><spage>1095</spage><epage>1100</epage><pages>1095-1100</pages><issn>0022-3468</issn><eissn>1531-5037</eissn><abstract>Abstract Background/Purpose Congenital high airway obstructive syndrome (CHAOS) is a rare and devastating condition that is uniformly fatal without fetal intervention. We sought to describe fetal treatment and long-term outcomes of CHAOS at a single referral center. Methods The medical records of patients with fetal CHAOS evaluated at our center between 1993 and 2011 were reviewed. Maternal history, radiographic findings, antenatal management, and postnatal outcomes were compared. Results Twelve fetuses with CHAOS were identified. Eleven had concomitant hydrops at diagnosis. Six were electively terminated, and 2 had intra- or peripartum demise. Four patients underwent fetal intervention. Two underwent delivery via ex utero intrapartum treatment (EXIT) procedure with tracheostomy placement only, and 2 underwent fetal bronchoscopy with attempted wire tracheoplasty followed by EXIT with tracheostomy at delivery. All 4 patients who underwent EXIT were alive at last follow-up. One patient was ventilator and tracheostomy free and feeding by mouth. Conclusion Long-term and tracheostomy-free survival is possible with appropriate fetal intervention even in the presence of hydrops. Fetal intervention earlier in pregnancy may improve long-term outcomes, but patient selection for intervention remains challenging. Magnetic resonance imaging may help select those patients for whom fetal intervention before EXIT delivery may be beneficial.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>22703776</pmid><doi>10.1016/j.jpedsurg.2012.03.015</doi><tpages>6</tpages></addata></record>
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subjects Abnormalities, Multiple
Abortion, Eugenic
Adult
Airway Obstruction - congenital
Airway Obstruction - embryology
Airway Obstruction - surgery
Bronchoscopy
CHAOS
Ex utero intrapartum treatment
EXIT
Female
Fetal Death - etiology
Fetal surgery
Fetal Therapies - methods
Fetal Therapies - statistics & numerical data
Gestational Age
Humans
Hydrops Fetalis
Infant, Newborn
Larynx - abnormalities
Larynx - embryology
Magnetic Resonance Imaging
Male
Patient Selection
Pediatrics
Pregnancy
Surgery
Syndrome
Trachea - abnormalities
Trachea - embryology
Trachea - surgery
Tracheostomy
Treatment Outcome
Young Adult
title Long-term outcomes after fetal therapy for congenital high airway obstructive syndrome
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