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Dilatable Pulmonary Artery Banding Palliation in Congenital Heart Disease
Background: Surgical pulmonary artery banding (PAB) has been limited in practice because of later requirement for surgical removal or adjustment. The aim of this study is to describe our experience creating a dilatable PAB via transcatheter balloon dilation (TCBD) in congenital heart disease (CHD) p...
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Published in: | World journal for pediatric & congenital heart surgery 2021-03, Vol.12 (2), p.213-219 |
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container_title | World journal for pediatric & congenital heart surgery |
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creator | Ligon, R. Allen Latson, Larry A. Ruzmetov, Mark M. Chan, Kak-Chen Turner, Immanuel I. Scholl, Frank G. Bibevski, Steve |
description | Background:
Surgical pulmonary artery banding (PAB) has been limited in practice because of later requirement for surgical removal or adjustment. The aim of this study is to describe our experience creating a dilatable PAB via transcatheter balloon dilation (TCBD) in congenital heart disease (CHD) patients.
Methods:
Retrospective chart review of adjustable PAB—outline anatomical variants palliated and patient outcomes.
Results:
Sixteen patients underwent dilatable PAB—median age 52 days (range 4-215) and weight 3.12 kg (1.65-5.8). Seven (44%) of the patients were premature, 11 (69%) had ventricular septal defect(s) with pulmonary over-circulation, four (25%) atrioventricular septal defects, and four (25%) single ventricle physiology. Subsequent to the index procedure: five patients have undergone intracardiac complete repair, six patients remain well palliated with no additional intervention, and four single ventricles await their next palliation. One patient died from necrotizing enterocolitis (unrelated to PAB) and one patient required a pericardiocentesis postoperatively. Five patients underwent TCBD of the PAB without complication—Two had one TCBD, two had two TCBD, and another had three TCBD. The median change in saturation was 14% (complete range 6-22) and PAB diameter 1.7 mm (complete range 1.1-5.2). Median time from PAB to most recent outpatient follow-up was 868 days (interquartile range 190-1,079).
Conclusions:
Our institution has standardized a PAB technique that allows for transcatheter incremental increases in pulmonary blood flow over time. This methodology has proven safe and effective enough to supplant other institutional techniques of limiting pulmonary blood flow in most patients—allowing for interval growth or even serving as the definitive palliation. |
doi_str_mv | 10.1177/2150135120975763 |
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Surgical pulmonary artery banding (PAB) has been limited in practice because of later requirement for surgical removal or adjustment. The aim of this study is to describe our experience creating a dilatable PAB via transcatheter balloon dilation (TCBD) in congenital heart disease (CHD) patients.
Methods:
Retrospective chart review of adjustable PAB—outline anatomical variants palliated and patient outcomes.
Results:
Sixteen patients underwent dilatable PAB—median age 52 days (range 4-215) and weight 3.12 kg (1.65-5.8). Seven (44%) of the patients were premature, 11 (69%) had ventricular septal defect(s) with pulmonary over-circulation, four (25%) atrioventricular septal defects, and four (25%) single ventricle physiology. Subsequent to the index procedure: five patients have undergone intracardiac complete repair, six patients remain well palliated with no additional intervention, and four single ventricles await their next palliation. One patient died from necrotizing enterocolitis (unrelated to PAB) and one patient required a pericardiocentesis postoperatively. Five patients underwent TCBD of the PAB without complication—Two had one TCBD, two had two TCBD, and another had three TCBD. The median change in saturation was 14% (complete range 6-22) and PAB diameter 1.7 mm (complete range 1.1-5.2). Median time from PAB to most recent outpatient follow-up was 868 days (interquartile range 190-1,079).
Conclusions:
Our institution has standardized a PAB technique that allows for transcatheter incremental increases in pulmonary blood flow over time. This methodology has proven safe and effective enough to supplant other institutional techniques of limiting pulmonary blood flow in most patients—allowing for interval growth or even serving as the definitive palliation.</description><identifier>ISSN: 2150-1351</identifier><identifier>EISSN: 2150-136X</identifier><identifier>DOI: 10.1177/2150135120975763</identifier><identifier>PMID: 33684011</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><subject>Female ; Heart Defects, Congenital - physiopathology ; Heart Defects, Congenital - surgery ; Humans ; Infant ; Infant, Newborn ; Male ; Palliative Care - methods ; Pulmonary Artery - physiopathology ; Pulmonary Artery - surgery ; Pulmonary Circulation - physiology ; Retrospective Studies ; Treatment Outcome ; Vascular Surgical Procedures - methods</subject><ispartof>World journal for pediatric & congenital heart surgery, 2021-03, Vol.12 (2), p.213-219</ispartof><rights>The Author(s) 2020</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c220t-290283e273a6de1510f8cbf617ec0247a9f8b6a71ea33dad46974bca2994e9093</cites><orcidid>0000-0003-4530-8984 ; 0000-0002-1022-3430</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924,79235</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33684011$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ligon, R. Allen</creatorcontrib><creatorcontrib>Latson, Larry A.</creatorcontrib><creatorcontrib>Ruzmetov, Mark M.</creatorcontrib><creatorcontrib>Chan, Kak-Chen</creatorcontrib><creatorcontrib>Turner, Immanuel I.</creatorcontrib><creatorcontrib>Scholl, Frank G.</creatorcontrib><creatorcontrib>Bibevski, Steve</creatorcontrib><title>Dilatable Pulmonary Artery Banding Palliation in Congenital Heart Disease</title><title>World journal for pediatric & congenital heart surgery</title><addtitle>World J Pediatr Congenit Heart Surg</addtitle><description>Background:
Surgical pulmonary artery banding (PAB) has been limited in practice because of later requirement for surgical removal or adjustment. The aim of this study is to describe our experience creating a dilatable PAB via transcatheter balloon dilation (TCBD) in congenital heart disease (CHD) patients.
Methods:
Retrospective chart review of adjustable PAB—outline anatomical variants palliated and patient outcomes.
Results:
Sixteen patients underwent dilatable PAB—median age 52 days (range 4-215) and weight 3.12 kg (1.65-5.8). Seven (44%) of the patients were premature, 11 (69%) had ventricular septal defect(s) with pulmonary over-circulation, four (25%) atrioventricular septal defects, and four (25%) single ventricle physiology. Subsequent to the index procedure: five patients have undergone intracardiac complete repair, six patients remain well palliated with no additional intervention, and four single ventricles await their next palliation. One patient died from necrotizing enterocolitis (unrelated to PAB) and one patient required a pericardiocentesis postoperatively. Five patients underwent TCBD of the PAB without complication—Two had one TCBD, two had two TCBD, and another had three TCBD. The median change in saturation was 14% (complete range 6-22) and PAB diameter 1.7 mm (complete range 1.1-5.2). Median time from PAB to most recent outpatient follow-up was 868 days (interquartile range 190-1,079).
Conclusions:
Our institution has standardized a PAB technique that allows for transcatheter incremental increases in pulmonary blood flow over time. This methodology has proven safe and effective enough to supplant other institutional techniques of limiting pulmonary blood flow in most patients—allowing for interval growth or even serving as the definitive palliation.</description><subject>Female</subject><subject>Heart Defects, Congenital - physiopathology</subject><subject>Heart Defects, Congenital - surgery</subject><subject>Humans</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Male</subject><subject>Palliative Care - methods</subject><subject>Pulmonary Artery - physiopathology</subject><subject>Pulmonary Artery - surgery</subject><subject>Pulmonary Circulation - physiology</subject><subject>Retrospective Studies</subject><subject>Treatment Outcome</subject><subject>Vascular Surgical Procedures - methods</subject><issn>2150-1351</issn><issn>2150-136X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp1kM1Lw0AQxRdRbKm9e5IcvUT3K7vZY23VFgr2oOAtTJJJ2bLZ1Gxy8L83pbUHwbm8YfjNg_cIuWX0gTGtHzlLKBMJ49ToRCtxQcaHU8yE-rw87wkbkWkIOzqMVEJIeU1GQqhUUsbGZLWwDjrIHUab3tWNh_Y7mrUdDvIEvrR-G23AOQudbXxkfTRv_Ba97cBFS4S2ixY2IAS8IVcVuIDTk07Ix8vz-3wZr99eV_PZOi44p13MDeWpQK4FqBJZwmiVFnmlmMaCcqnBVGmuQDMEIUoopTJa5gVwYyQaasSE3B99923z1WPostqGAp0Dj00fMi6NEalO9QGlR7RomxBarLJ9a-shYcZodugw-9vh8HJ3cu_zGsvzw29jAxAfgQBbzHZN3_oh7f-GP1-Hd28</recordid><startdate>202103</startdate><enddate>202103</enddate><creator>Ligon, R. Allen</creator><creator>Latson, Larry A.</creator><creator>Ruzmetov, Mark M.</creator><creator>Chan, Kak-Chen</creator><creator>Turner, Immanuel I.</creator><creator>Scholl, Frank G.</creator><creator>Bibevski, Steve</creator><general>SAGE Publications</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><orcidid>https://orcid.org/0000-0003-4530-8984</orcidid><orcidid>https://orcid.org/0000-0002-1022-3430</orcidid></search><sort><creationdate>202103</creationdate><title>Dilatable Pulmonary Artery Banding Palliation in Congenital Heart Disease</title><author>Ligon, R. Allen ; Latson, Larry A. ; Ruzmetov, Mark M. ; Chan, Kak-Chen ; Turner, Immanuel I. ; Scholl, Frank G. ; Bibevski, Steve</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c220t-290283e273a6de1510f8cbf617ec0247a9f8b6a71ea33dad46974bca2994e9093</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Female</topic><topic>Heart Defects, Congenital - physiopathology</topic><topic>Heart Defects, Congenital - surgery</topic><topic>Humans</topic><topic>Infant</topic><topic>Infant, Newborn</topic><topic>Male</topic><topic>Palliative Care - methods</topic><topic>Pulmonary Artery - physiopathology</topic><topic>Pulmonary Artery - surgery</topic><topic>Pulmonary Circulation - physiology</topic><topic>Retrospective Studies</topic><topic>Treatment Outcome</topic><topic>Vascular Surgical Procedures - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ligon, R. Allen</creatorcontrib><creatorcontrib>Latson, Larry A.</creatorcontrib><creatorcontrib>Ruzmetov, Mark M.</creatorcontrib><creatorcontrib>Chan, Kak-Chen</creatorcontrib><creatorcontrib>Turner, Immanuel I.</creatorcontrib><creatorcontrib>Scholl, Frank G.</creatorcontrib><creatorcontrib>Bibevski, Steve</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>World journal for pediatric & congenital heart surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ligon, R. Allen</au><au>Latson, Larry A.</au><au>Ruzmetov, Mark M.</au><au>Chan, Kak-Chen</au><au>Turner, Immanuel I.</au><au>Scholl, Frank G.</au><au>Bibevski, Steve</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dilatable Pulmonary Artery Banding Palliation in Congenital Heart Disease</atitle><jtitle>World journal for pediatric & congenital heart surgery</jtitle><addtitle>World J Pediatr Congenit Heart Surg</addtitle><date>2021-03</date><risdate>2021</risdate><volume>12</volume><issue>2</issue><spage>213</spage><epage>219</epage><pages>213-219</pages><issn>2150-1351</issn><eissn>2150-136X</eissn><abstract>Background:
Surgical pulmonary artery banding (PAB) has been limited in practice because of later requirement for surgical removal or adjustment. The aim of this study is to describe our experience creating a dilatable PAB via transcatheter balloon dilation (TCBD) in congenital heart disease (CHD) patients.
Methods:
Retrospective chart review of adjustable PAB—outline anatomical variants palliated and patient outcomes.
Results:
Sixteen patients underwent dilatable PAB—median age 52 days (range 4-215) and weight 3.12 kg (1.65-5.8). Seven (44%) of the patients were premature, 11 (69%) had ventricular septal defect(s) with pulmonary over-circulation, four (25%) atrioventricular septal defects, and four (25%) single ventricle physiology. Subsequent to the index procedure: five patients have undergone intracardiac complete repair, six patients remain well palliated with no additional intervention, and four single ventricles await their next palliation. One patient died from necrotizing enterocolitis (unrelated to PAB) and one patient required a pericardiocentesis postoperatively. Five patients underwent TCBD of the PAB without complication—Two had one TCBD, two had two TCBD, and another had three TCBD. The median change in saturation was 14% (complete range 6-22) and PAB diameter 1.7 mm (complete range 1.1-5.2). Median time from PAB to most recent outpatient follow-up was 868 days (interquartile range 190-1,079).
Conclusions:
Our institution has standardized a PAB technique that allows for transcatheter incremental increases in pulmonary blood flow over time. This methodology has proven safe and effective enough to supplant other institutional techniques of limiting pulmonary blood flow in most patients—allowing for interval growth or even serving as the definitive palliation.</abstract><cop>Los Angeles, CA</cop><pub>SAGE Publications</pub><pmid>33684011</pmid><doi>10.1177/2150135120975763</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0003-4530-8984</orcidid><orcidid>https://orcid.org/0000-0002-1022-3430</orcidid></addata></record> |
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subjects | Female Heart Defects, Congenital - physiopathology Heart Defects, Congenital - surgery Humans Infant Infant, Newborn Male Palliative Care - methods Pulmonary Artery - physiopathology Pulmonary Artery - surgery Pulmonary Circulation - physiology Retrospective Studies Treatment Outcome Vascular Surgical Procedures - methods |
title | Dilatable Pulmonary Artery Banding Palliation in Congenital Heart Disease |
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