Evidence map›Paper›PMID 39713600›Full record

ArticleInternational journal of cardiology. Congenital heart disease2022

Outcome of humanitarian patients with late complete repair of tetralogy of Fallot: A 13-year long single-center experience.

Damien Schaffner, Guillaume Maitre, Sebastiano A G Lava, Yann Boegli, Mirko Dolci, Raymond Pfister, Nicole Sekarski, Perez Marie-Hélène, Stefano Di Bernardo

Abstract read
In one paragraph

Article in International journal of cardiology. Congenital heart disease, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Humanitarian Congenital Cardiac Surgery: Late is better than never.International journal of cardiology. Congenital heart disease · 2023
    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

9 authors.

Damien SchaffnerPediatric Cardiology Unit, Women Mother and Child Department, Lausanne University Hospital, Switzerland.
Guillaume MaitreIntensive Care Unit, Women Mother and Child Department, Lausanne University Hospital, Switzerland.
Sebastiano A G LavaPediatric Cardiology Unit, Women Mother and Child Department, Lausanne University Hospital, Switzerland.
Yann BoegliPediatric Anesthesiologic Unit, Anesthesiologic Department, Lausanne University Hospital, Switzerland.
Mirko DolciPediatric Anesthesiologic Unit, Anesthesiologic Department, Lausanne University Hospital, Switzerland.
Raymond PfisterCardiac Surgery Department, Lausanne University Hospital, Switzerland.
Nicole SekarskiPediatric Cardiology Unit, Women Mother and Child Department, Lausanne University Hospital, Switzerland.
Perez Marie-HélèneIntensive Care Unit, Women Mother and Child Department, Lausanne University Hospital, Switzerland.
Stefano Di BernardoPediatric Cardiology Unit, Women Mother and Child Department, Lausanne University Hospital, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Surgical repair of tetralogy of Fallot is usually performed between 3 and 6 months of age with pulmonary valve-sparing repair promoted for the best long-term result. Through a humanitarian program from developing countries, late complete surgical repair of tetralogy of Fallot has been performed at our institution for many years. Methods: Retrospective analysis of pre- and perioperative data, as well as 30-days outcome of patients older than one year with a confirmed diagnosis of tetralogy of Fallot who had a complete surgical repair between 2005 and 2018 at our institution. Results: One hundred sixty-five patients were included with a median age of 4.5 years [3.0-6.3], median weight of 13.5 kg [10.9 to 16.5], median transcutaneous oximetry of 78% [70 to 85] and median pulmonary valve annulus Z-score of -1.8 [-3.4 to -0.8]. There was no early surgical mortality. By multivariate analysis, only severe right ventricular hypertrophy, severe right ventricle outflow tract obstruction, and hypoplasia of the main pulmonary artery were independent predictors of failure to preserve the pulmonary annulus at surgical repair. Conclusions: Late complete surgical repair of tetralogy of Fallot has low mortality and morbidity even when pulmonary valve-sparing repair cannot be successfully performed. The preservation of the pulmonary valve function is significantly associated with shorter ventilation time, ICU and hospital lengths of stay. In the analyzed group of patients, a pulmonary valve-sparing repair cannot be predicted exclusively based on the dimension of the pulmonary valve annulus.

Indexed as

Humanitarian patientsLate complete surgical repairPostoperative outcomePulmonary valve annulusPulmonary valve-sparing repairTetralogy of Fallot

Identifiers

PMID39713600
PMCPMC11658541

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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.