Evidence map›Paper›PMID 41577181›Full record

ArticleIndian heart journal

Balloon pulmonary valvuloplasty as a palliative strategy for late presenting adolescents and adult patients with cyanotic congenital heart disease.

Amit Kumar Pandey, Anu Cyriac, Navaneetha Sasikumar, Raman Krishna Kumar

Abstract read
In one paragraph

Article in Indian heart journal. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Amit Kumar PandeyDepartment of Pediatric Cardiology, Amrita Institute of Medical Sciences, Amrita Hospital, Ponekkara, AIMS P.O, Kochi, Kerala, 682 041, India. Electronic address: amit952.pandey@gmail.com.
Anu CyriacCardiovascular Technology, Amrita Institute of Medical Sciences, Amrita Hospital, Ponekkara, AIMS P.O, Kochi, Kerala, 682 041, India. Electronic address: anucyriac727@gmail.com.
Navaneetha SasikumarAdult Congenital Heart Disease Clinic, Department of Pediatric Cardiology, Amrita Institute of Medical Sciences, Amrita Hospital, Ponekkara, AIMS P.O, Kochi, Kerala, 682 041, India. Electronic address: drnavni@yahoo.com.
Raman Krishna KumarDepartment of Pediatric Cardiology, Amrita Institute of Medical Sciences, Amrita Hospital, Ponekkara, AIMS P.O, Kochi, Kerala, 682 041, India. Electronic address: kumar_rk@yahoo.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundManagement of late presenters with cyanotic congenital heart disease (CCHD) and reduced pulmonary blood flow is challenged by multi-system derangements from longstanding hypoxia in addition to anatomic factors. Balloon pulmonary valvuloplasty (BPV) is a potentially viable palliative option for selected patients with severely stenotic pulmonary valve and are unsuitable for definitive surgical repair

methodsA retrospective chart review was conducted (2002-2024, age >12 years). BPV was considered for those with a significant component of valvular pulmonary stenosis (PS) on echocardiography. A strategy of stepwise dilation using progressively larger balloon sizes, andmonitoring pulmonary artery pressures between each dilation, was adapted.

resultsThirty patients [TOF (n = 13), DORV/DILV (n = 7/2), single ventricle/Unbalanced AVCD (n = 3), and corrected transposition (n = 5)] with median age: 20.5 years (IQR: 14.0-26.8), weight: 49 kg (IQR: 44.1-57.7) underwent BPV. The fluoroscopy and procedure times were 17.8 min (IQR:12.7-25.7) and 71 ± 26 min (mean ± SD), respectively. The balloon-to-annulus ratio was 1.01 (0.96-1.2). Saturation improved significantly from 76.7 ± 9.6 % to 90.2 ± 4.4 %. Complications included transient arrhythmias in five patients and fatal re-perfusion pulmonary edema during repeat BPV in one. At a median follow-up of 51 months (IQR: 26.75-139.25 months), majority of patients demonstrated sustained symptomatic relief. Seven patients underwent corrective surgery, and four required repeat BPV.

conclusionIn a selected subgroup of anatomically suited patients with CCHD and PS, stepwise dilatation of the pulmonary valve resulted in improved oxygenation and symptomatic relief, which was sustained on follow-up, making it an attractive low-resource option for palliation, particularly in resource constrained LMIC settings.

Indexed as

Balloon ValvuloplastyCyanosisHeart Defects, CongenitalPalliative CarePulmonary ValvePulmonary Valve StenosisAdolescentAdultChildEchocardiographyFemaleFollow-Up StudiesHumansMaleRetrospective StudiesTreatment OutcomeBalloon valvuloplastyCongenitalCyanosisDeveloping countriesHeart defectsPalliative carePulmonary valve stenosis

Identifiers

PMID41577181
PMCPMC13315977

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.