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...
Gespeichert in:
Veröffentlicht in: | Journal of pediatric surgery 2012-06, Vol.47 (6), p.1095-1100 |
---|---|
Hauptverfasser: | , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
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 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1021127067</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0022346812002552</els_id><sourcerecordid>1021127067</sourcerecordid><originalsourceid>FETCH-LOGICAL-c493t-8aa71edcae5a2a31615384294e3c283623c26269e10c95951aa4eafdcf1377c3</originalsourceid><addsrcrecordid>eNqFUU1v1DAQtRCILm3_QuUjl6QeO3E2FwSqyoe0Ug-tuFquM9l1SOLFTlrl3zPRthy4cJoPvfdm5g1jVyByEKCvu7w7YpPmuM-lAJkLlQso37ANlAqyUqjqLdsIIWWmCr09Yx9S6oSgtoD37EzKitJKb9jPXRj32YRx4GGeXBgwcdtSzVucbM-nA0Z7XHgbIncExdGv7YPfH7j18dkuPDymKc5u8k_I0zI2kUQu2LvW9gkvX-I5e_h6-3DzPdvdfftx82WXuaJWU7a1tgJsnMXSSqtA0_bbQtYFKie3SksKWuoaQbi6rEuwtkDbNq4FWt-pc_bxJHuM4feMaTKDTw773o4Y5mRASAC6VVcE1SeoiyGliK05Rj_YuBDIrJaazrxaalZLjVCGLCXi1cuM-XHA5i_t1UMCfD4BkA598hhNch5Hh42P6CbTBP__GZ_-kXC9H72z_S9cMHVhjiPZaMAk4pj79bHrX0FSVpZS_QGFKqDx</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1021127067</pqid></control><display><type>article</type><title>Long-term outcomes after fetal therapy for congenital high airway obstructive syndrome</title><source>MEDLINE</source><source>Access via ScienceDirect (Elsevier)</source><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</creator><creatorcontrib>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</creatorcontrib><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><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 & 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 & 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 & 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> |
fulltext | fulltext |
identifier | ISSN: 0022-3468 |
ispartof | Journal of pediatric surgery, 2012-06, Vol.47 (6), p.1095-1100 |
issn | 0022-3468 1531-5037 |
language | eng |
recordid | cdi_proquest_miscellaneous_1021127067 |
source | MEDLINE; Access via ScienceDirect (Elsevier) |
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 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-16T07%3A46%3A53IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Long-term%20outcomes%20after%20fetal%20therapy%20for%20congenital%20high%20airway%20obstructive%20syndrome&rft.jtitle=Journal%20of%20pediatric%20surgery&rft.au=Saadai,%20Payam&rft.date=2012-06-01&rft.volume=47&rft.issue=6&rft.spage=1095&rft.epage=1100&rft.pages=1095-1100&rft.issn=0022-3468&rft.eissn=1531-5037&rft_id=info:doi/10.1016/j.jpedsurg.2012.03.015&rft_dat=%3Cproquest_cross%3E1021127067%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1021127067&rft_id=info:pmid/22703776&rft_els_id=S0022346812002552&rfr_iscdi=true |