Evidence map›Paper›PMID 36793501›Full record

ArticleFrontiers in pediatrics2022

Outcome of patients with tetralogy of Fallot with pulmonary atresia.

Eva Sames-Dolzer, Anna Fahrnberger, Michaela Kreuzer, Roland Mair, Gregor Gierlinger, Andreas Tulzer, Roland Gitter, Christoph Prandstetter, Gerald Tulzer, Rudolf Mair

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pediatrics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
1.1field-weighted citation impact, top 23% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Eva Sames-DolzerDivision of Pediatric and Congenital Heart Surgery, Kepler University Hospital, Linz, Austria.
Anna FahrnbergerDivision of Pediatric and Congenital Heart Surgery, Kepler University Hospital, Linz, Austria.
Michaela KreuzerDivision of Pediatric and Congenital Heart Surgery, Kepler University Hospital, Linz, Austria.
Roland MairDivision of Pediatric and Congenital Heart Surgery, Kepler University Hospital, Linz, Austria.
Gregor GierlingerDivision of Pediatric and Congenital Heart Surgery, Kepler University Hospital, Linz, Austria.
Andreas TulzerMedical Faculty, Johannes Kepler University Linz, Linz, Austria.
Roland GitterDepartment of Pediatric Cardiology, Kepler University Hospital, Linz, Austria.
Christoph PrandstetterMedical Faculty, Johannes Kepler University Linz, Linz, Austria.
Gerald TulzerMedical Faculty, Johannes Kepler University Linz, Linz, Austria.
Rudolf MairDivision of Pediatric and Congenital Heart Surgery, Kepler University Hospital, Linz, Austria.
Kepler Universitätsklinikum · ATJohannes Kepler University of Linz · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Tetralogy of Fallot patients with pulmonary atresia (TOFPA) have a largely varying source of pulmonary perfusion with often hypoplastic and even absent central pulmonary arteries. A retrospective single center study was undertaken to assess outcome of these patients regarding type of surgical procedures, long-term mortality, achievement of VSD closure and analysis of postoperative interventions. Methods: 76 consecutive patients with TOFPA operated between 01.01.2003 and 31.12.2019 are included in this single center study. Patients with ductus dependent pulmonary circulation underwent primary single stage full correction including VSD closure and right ventricular to pulmonary conduit implantation (RVPAC) or transanular patch reconstruction. Children with hypoplastic pulmonary arteries and MAPCAs without double supply were predominantly treated by unifocalization and RVPAC implantation. The follow up period ranges between 0 and 16,5 years. Results: 31 patients (41%) underwent single stage full correction at a median age of 12 days, 15 patients could be treated by a transanular patch. 30 days mortality rate in this group was 6%. In the remaining 45 patients the VSD could not be closed during their first surgery which was performed at a median age of 89 days. A VSD closure was achieved later in 64% of these patients after median 178 days. 30 days mortality rate after the first surgery was 13% in this group. The estimated 10-year-survival rate after the first surgery is 80,5% ± 4,7% showing no significant difference between the groups with and without MAPCAs ( Conclusions: A VSD closure could be achieved in 79% of the total cohort. In patients without MAPCAs this was possible at a significant earlier age (

Indexed as

aorto-pulmonary collateralspulmonary atresiarehabilitationstaged repairtetralogy of Fallotunifocalization

Identifiers

PMID36793501
PMCPMC9922747
OpenAlexW4318590610

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.