Intrauterine aortic valvuloplasty in fetuses with critical aortic stenosis: experience and results of 24 procedures
Objective Valvuloplasty of the fetal aortic valve has the potential to prevent progression of critical aortic stenosis (AS) to hypoplastic left heart syndrome (HLHS). The aim of the study was to assess 24 aortic valvuloplasties regarding indications, success rate, procedure‐related risks and outcome...
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creator | Arzt, W. Wertaschnigg, D. Veit, I. Klement, F. Gitter, R. Tulzer, G. |
description | Objective
Valvuloplasty of the fetal aortic valve has the potential to prevent progression of critical aortic stenosis (AS) to hypoplastic left heart syndrome (HLHS). The aim of the study was to assess 24 aortic valvuloplasties regarding indications, success rate, procedure‐related risks and outcome.
Methods
Between January 2001 and December 2009 we performed 24 aortic valvuloplasties in 23 fetuses with critical AS at a median gestational age of 26 + 4 (range, 21 + 3 to 32 + 5) weeks by a transabdominal ultrasound‐guided approach. Four fetuses had hydrops as a late sign of heart failure.
Results
In 16/24 procedures (66.7%) corresponding to 16/23 fetuses (69.6%) the procedures were technically successful, with one intrauterine death in this group. After an initial learning curve, success rate improved to 78.6% (11 of the last 14 interventions were successful). In 10 out of the 15 (66.7%) successfully‐treated and liveborn fetuses a biventricular circulation could be achieved postnatally. All four fetuses with hydrops had successful interventions, hydrops disappearing within 5 weeks. In 8/24 interventions (33.3%) the aortic valve could not be treated successfully, with intrauterine fetal death in two of these cases. In one fetus a repeat procedure was successful. All surviving fetuses with unsuccessful (n = 5) or no (n = 5) procedure performed developed HLHS until delivery.
Conclusions
Fetal aortic valvuloplasty could be performed successfully in selected fetuses with critical AS and evolving HLHS, with a biventricular outcome in two thirds of the patients. Safety and success rate were dependent on patient selection and the level of experience of the whole interventional team. In fetuses with AS and hydrops, aortic valvuloplasty could reverse end‐stage heart failure and hydrops and ensure fetal survival. Copyright © 2011 ISUOG. Published by John Wiley & Sons, Ltd. |
doi_str_mv | 10.1002/uog.8927 |
format | Article |
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Valvuloplasty of the fetal aortic valve has the potential to prevent progression of critical aortic stenosis (AS) to hypoplastic left heart syndrome (HLHS). The aim of the study was to assess 24 aortic valvuloplasties regarding indications, success rate, procedure‐related risks and outcome.
Methods
Between January 2001 and December 2009 we performed 24 aortic valvuloplasties in 23 fetuses with critical AS at a median gestational age of 26 + 4 (range, 21 + 3 to 32 + 5) weeks by a transabdominal ultrasound‐guided approach. Four fetuses had hydrops as a late sign of heart failure.
Results
In 16/24 procedures (66.7%) corresponding to 16/23 fetuses (69.6%) the procedures were technically successful, with one intrauterine death in this group. After an initial learning curve, success rate improved to 78.6% (11 of the last 14 interventions were successful). In 10 out of the 15 (66.7%) successfully‐treated and liveborn fetuses a biventricular circulation could be achieved postnatally. All four fetuses with hydrops had successful interventions, hydrops disappearing within 5 weeks. In 8/24 interventions (33.3%) the aortic valve could not be treated successfully, with intrauterine fetal death in two of these cases. In one fetus a repeat procedure was successful. All surviving fetuses with unsuccessful (n = 5) or no (n = 5) procedure performed developed HLHS until delivery.
Conclusions
Fetal aortic valvuloplasty could be performed successfully in selected fetuses with critical AS and evolving HLHS, with a biventricular outcome in two thirds of the patients. Safety and success rate were dependent on patient selection and the level of experience of the whole interventional team. In fetuses with AS and hydrops, aortic valvuloplasty could reverse end‐stage heart failure and hydrops and ensure fetal survival. Copyright © 2011 ISUOG. Published by John Wiley & Sons, Ltd.</description><identifier>ISSN: 0960-7692</identifier><identifier>ISSN: 1469-0705</identifier><identifier>EISSN: 1469-0705</identifier><identifier>DOI: 10.1002/uog.8927</identifier><identifier>PMID: 21229549</identifier><identifier>CODEN: UOGYFJ</identifier><language>eng</language><publisher>Chichester, UK: John Wiley & Sons, Ltd</publisher><subject>Aorta ; Aortic valve ; Aortic Valve Stenosis - diagnostic imaging ; Aortic Valve Stenosis - embryology ; Aortic Valve Stenosis - therapy ; Biological and medical sciences ; Cardiology. Vascular system ; Catheterization - methods ; Edema ; Edema - diagnostic imaging ; Edema - embryology ; Edema - therapy ; Endocardial and cardiac valvular diseases ; Female ; fetal aortic stenosis ; Fetal Heart - diagnostic imaging ; Fetal Therapies - methods ; Fetuses ; Gestational Age ; Gynecology ; Gynecology. Andrology. Obstetrics ; Heart ; Heart diseases ; Hemodynamics ; Humans ; intrauterine valvuloplasty ; Learning ; Medical sciences ; Obstetrics ; Pregnancy ; Pregnancy Outcome ; Stenosis ; Survival ; Ultrasonography, Prenatal ; Ultrasound</subject><ispartof>Ultrasound in obstetrics & gynecology, 2011-06, Vol.37 (6), p.689-695</ispartof><rights>Copyright © 2011 ISUOG. Published by John Wiley & Sons, Ltd.</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4457-d1f823b980ae954b43fc2c12c2515475d35baa353f13cacdfcbd461cfd851dc83</citedby><cites>FETCH-LOGICAL-c4457-d1f823b980ae954b43fc2c12c2515475d35baa353f13cacdfcbd461cfd851dc83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fuog.8927$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fuog.8927$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,1428,27905,27906,45555,45556,46390,46814</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24212438$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21229549$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Arzt, W.</creatorcontrib><creatorcontrib>Wertaschnigg, D.</creatorcontrib><creatorcontrib>Veit, I.</creatorcontrib><creatorcontrib>Klement, F.</creatorcontrib><creatorcontrib>Gitter, R.</creatorcontrib><creatorcontrib>Tulzer, G.</creatorcontrib><title>Intrauterine aortic valvuloplasty in fetuses with critical aortic stenosis: experience and results of 24 procedures</title><title>Ultrasound in obstetrics & gynecology</title><addtitle>Ultrasound Obstet Gynecol</addtitle><description>Objective
Valvuloplasty of the fetal aortic valve has the potential to prevent progression of critical aortic stenosis (AS) to hypoplastic left heart syndrome (HLHS). The aim of the study was to assess 24 aortic valvuloplasties regarding indications, success rate, procedure‐related risks and outcome.
Methods
Between January 2001 and December 2009 we performed 24 aortic valvuloplasties in 23 fetuses with critical AS at a median gestational age of 26 + 4 (range, 21 + 3 to 32 + 5) weeks by a transabdominal ultrasound‐guided approach. Four fetuses had hydrops as a late sign of heart failure.
Results
In 16/24 procedures (66.7%) corresponding to 16/23 fetuses (69.6%) the procedures were technically successful, with one intrauterine death in this group. After an initial learning curve, success rate improved to 78.6% (11 of the last 14 interventions were successful). In 10 out of the 15 (66.7%) successfully‐treated and liveborn fetuses a biventricular circulation could be achieved postnatally. All four fetuses with hydrops had successful interventions, hydrops disappearing within 5 weeks. In 8/24 interventions (33.3%) the aortic valve could not be treated successfully, with intrauterine fetal death in two of these cases. In one fetus a repeat procedure was successful. All surviving fetuses with unsuccessful (n = 5) or no (n = 5) procedure performed developed HLHS until delivery.
Conclusions
Fetal aortic valvuloplasty could be performed successfully in selected fetuses with critical AS and evolving HLHS, with a biventricular outcome in two thirds of the patients. Safety and success rate were dependent on patient selection and the level of experience of the whole interventional team. In fetuses with AS and hydrops, aortic valvuloplasty could reverse end‐stage heart failure and hydrops and ensure fetal survival. Copyright © 2011 ISUOG. Published by John Wiley & Sons, Ltd.</description><subject>Aorta</subject><subject>Aortic valve</subject><subject>Aortic Valve Stenosis - diagnostic imaging</subject><subject>Aortic Valve Stenosis - embryology</subject><subject>Aortic Valve Stenosis - therapy</subject><subject>Biological and medical sciences</subject><subject>Cardiology. Vascular system</subject><subject>Catheterization - methods</subject><subject>Edema</subject><subject>Edema - diagnostic imaging</subject><subject>Edema - embryology</subject><subject>Edema - therapy</subject><subject>Endocardial and cardiac valvular diseases</subject><subject>Female</subject><subject>fetal aortic stenosis</subject><subject>Fetal Heart - diagnostic imaging</subject><subject>Fetal Therapies - methods</subject><subject>Fetuses</subject><subject>Gestational Age</subject><subject>Gynecology</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Heart</subject><subject>Heart diseases</subject><subject>Hemodynamics</subject><subject>Humans</subject><subject>intrauterine valvuloplasty</subject><subject>Learning</subject><subject>Medical sciences</subject><subject>Obstetrics</subject><subject>Pregnancy</subject><subject>Pregnancy Outcome</subject><subject>Stenosis</subject><subject>Survival</subject><subject>Ultrasonography, Prenatal</subject><subject>Ultrasound</subject><issn>0960-7692</issn><issn>1469-0705</issn><issn>1469-0705</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kV1rFDEUhoModq2Cv0ACInozbT5nJt5J0Voo9Ka9HjL50JRssuZMWvffm7VbC4V6FQgPz3vOeRF6S8kRJYQd1_zjaFRseIZWVPSqIwORz9GKqJ50Q6_YAXoFcE0I6QXvX6IDRhlTUqgVgrO0FF0XV0JyWOeyBINvdLypMW-ihmWLQ8LeLRUc4Nuw_MSmhAbpeE_D4lKGAJ-x-71pHpdMMyWLi4MaF8DZYybwpmTjbG2fr9ELryO4N_v3EF19-3p58r07vzg9O_ly3hkh5NBZ6kfGZzUS7dqws-DeMEOZYZJKMUjL5aw1l9xTbrSx3sxW9NR4O0pqzcgP0cc7b4v-VR0s0zqAcTHq5HKFaexHpYZ2q0Z--i9JCR1Uz3s-NPT9I_Q615LaHhOVdGiDCyoehKZkgOL8tClhrcu2qaZdZVOrbNpV1tB3e2Gd187-A-87asCHPaChnd0XnUyAB040UvDdut0ddxui2z4ZOF1dnP4N_gOoOa4R</recordid><startdate>201106</startdate><enddate>201106</enddate><creator>Arzt, W.</creator><creator>Wertaschnigg, D.</creator><creator>Veit, I.</creator><creator>Klement, F.</creator><creator>Gitter, R.</creator><creator>Tulzer, G.</creator><general>John Wiley & Sons, Ltd</general><general>Wiley</general><general>Wiley Subscription Services, Inc</general><scope>IQODW</scope><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>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>201106</creationdate><title>Intrauterine aortic valvuloplasty in fetuses with critical aortic stenosis: experience and results of 24 procedures</title><author>Arzt, W. ; Wertaschnigg, D. ; Veit, I. ; Klement, F. ; Gitter, R. ; Tulzer, G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4457-d1f823b980ae954b43fc2c12c2515475d35baa353f13cacdfcbd461cfd851dc83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Aorta</topic><topic>Aortic valve</topic><topic>Aortic Valve Stenosis - diagnostic imaging</topic><topic>Aortic Valve Stenosis - embryology</topic><topic>Aortic Valve Stenosis - therapy</topic><topic>Biological and medical sciences</topic><topic>Cardiology. Vascular system</topic><topic>Catheterization - methods</topic><topic>Edema</topic><topic>Edema - diagnostic imaging</topic><topic>Edema - embryology</topic><topic>Edema - therapy</topic><topic>Endocardial and cardiac valvular diseases</topic><topic>Female</topic><topic>fetal aortic stenosis</topic><topic>Fetal Heart - diagnostic imaging</topic><topic>Fetal Therapies - methods</topic><topic>Fetuses</topic><topic>Gestational Age</topic><topic>Gynecology</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Heart</topic><topic>Heart diseases</topic><topic>Hemodynamics</topic><topic>Humans</topic><topic>intrauterine valvuloplasty</topic><topic>Learning</topic><topic>Medical sciences</topic><topic>Obstetrics</topic><topic>Pregnancy</topic><topic>Pregnancy Outcome</topic><topic>Stenosis</topic><topic>Survival</topic><topic>Ultrasonography, Prenatal</topic><topic>Ultrasound</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Arzt, W.</creatorcontrib><creatorcontrib>Wertaschnigg, D.</creatorcontrib><creatorcontrib>Veit, I.</creatorcontrib><creatorcontrib>Klement, F.</creatorcontrib><creatorcontrib>Gitter, R.</creatorcontrib><creatorcontrib>Tulzer, G.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Ultrasound in obstetrics & gynecology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Arzt, W.</au><au>Wertaschnigg, D.</au><au>Veit, I.</au><au>Klement, F.</au><au>Gitter, R.</au><au>Tulzer, G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intrauterine aortic valvuloplasty in fetuses with critical aortic stenosis: experience and results of 24 procedures</atitle><jtitle>Ultrasound in obstetrics & gynecology</jtitle><addtitle>Ultrasound Obstet Gynecol</addtitle><date>2011-06</date><risdate>2011</risdate><volume>37</volume><issue>6</issue><spage>689</spage><epage>695</epage><pages>689-695</pages><issn>0960-7692</issn><issn>1469-0705</issn><eissn>1469-0705</eissn><coden>UOGYFJ</coden><abstract>Objective
Valvuloplasty of the fetal aortic valve has the potential to prevent progression of critical aortic stenosis (AS) to hypoplastic left heart syndrome (HLHS). The aim of the study was to assess 24 aortic valvuloplasties regarding indications, success rate, procedure‐related risks and outcome.
Methods
Between January 2001 and December 2009 we performed 24 aortic valvuloplasties in 23 fetuses with critical AS at a median gestational age of 26 + 4 (range, 21 + 3 to 32 + 5) weeks by a transabdominal ultrasound‐guided approach. Four fetuses had hydrops as a late sign of heart failure.
Results
In 16/24 procedures (66.7%) corresponding to 16/23 fetuses (69.6%) the procedures were technically successful, with one intrauterine death in this group. After an initial learning curve, success rate improved to 78.6% (11 of the last 14 interventions were successful). In 10 out of the 15 (66.7%) successfully‐treated and liveborn fetuses a biventricular circulation could be achieved postnatally. All four fetuses with hydrops had successful interventions, hydrops disappearing within 5 weeks. In 8/24 interventions (33.3%) the aortic valve could not be treated successfully, with intrauterine fetal death in two of these cases. In one fetus a repeat procedure was successful. All surviving fetuses with unsuccessful (n = 5) or no (n = 5) procedure performed developed HLHS until delivery.
Conclusions
Fetal aortic valvuloplasty could be performed successfully in selected fetuses with critical AS and evolving HLHS, with a biventricular outcome in two thirds of the patients. Safety and success rate were dependent on patient selection and the level of experience of the whole interventional team. In fetuses with AS and hydrops, aortic valvuloplasty could reverse end‐stage heart failure and hydrops and ensure fetal survival. Copyright © 2011 ISUOG. Published by John Wiley & Sons, Ltd.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><pmid>21229549</pmid><doi>10.1002/uog.8927</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Wiley Online Library Journals Frontfile Complete; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Wiley Free Content |
subjects | Aorta Aortic valve Aortic Valve Stenosis - diagnostic imaging Aortic Valve Stenosis - embryology Aortic Valve Stenosis - therapy Biological and medical sciences Cardiology. Vascular system Catheterization - methods Edema Edema - diagnostic imaging Edema - embryology Edema - therapy Endocardial and cardiac valvular diseases Female fetal aortic stenosis Fetal Heart - diagnostic imaging Fetal Therapies - methods Fetuses Gestational Age Gynecology Gynecology. Andrology. Obstetrics Heart Heart diseases Hemodynamics Humans intrauterine valvuloplasty Learning Medical sciences Obstetrics Pregnancy Pregnancy Outcome Stenosis Survival Ultrasonography, Prenatal Ultrasound |
title | Intrauterine aortic valvuloplasty in fetuses with critical aortic stenosis: experience and results of 24 procedures |
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