Evidence map›Paper›PMID 35260893›Full record

ArticleInteractive cardiovascular and thoracic surgery2022

Short-term outcomes of EXCOR Paediatric implantation.

Motoki Komori, Takaya Hoashi, Heima Sakaguchi, Kenta Imai, Naoki Okuda, Norihide Fukushima, Kenichi Kurosaki, Hajime Ichikawa

Abstract read
In one paragraph

Article in Interactive cardiovascular and thoracic surgery, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–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

3 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Myocardial recovery in children supported with a durable ventricular assist device-a systematic review.European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery · 2023
    Pooled it
  2. Article
  3. 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

8 authors.

Motoki KomoriDepartment of Pediatric Cardiovascular Surgery, National Cerebral and Cardiovascular Center, Osaka, Japan.ORCID 0000-0002-8321-7277
Takaya HoashiDepartment of Pediatric Cardiovascular Surgery, National Cerebral and Cardiovascular Center, Osaka, Japan.ORCID 0000-0003-0320-3682
Heima SakaguchiDepartment of Pediatric Cardiology, National Cerebral and Cardiovascular Center, Osaka, Japan.
Kenta ImaiDepartment of Pediatric Cardiovascular Surgery, National Cerebral and Cardiovascular Center, Osaka, Japan.
Naoki OkudaDepartment of Pediatric Cardiovascular Surgery, National Cerebral and Cardiovascular Center, Osaka, Japan.
Norihide FukushimaDepartment of Pediatric Transplantation, National Cerebral and Cardiovascular Center, Osaka, Japan.ORCID 0000-0003-1367-4066
Kenichi KurosakiDepartment of Pediatric Cardiology, National Cerebral and Cardiovascular Center, Osaka, Japan.
Hajime IchikawaDepartment of Pediatric Cardiovascular Surgery, National Cerebral and Cardiovascular Center, Osaka, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThe aim of this study was to review a single institution's experience with EXCOR Paediatric implantation.

methodsPatients <15 years old who underwent EXCOR implantation as a bridge to transplantation between 2015 and 2021 were enrolled. Major adverse events included death, cerebrovascular event resulting in sequelae, major infection (sepsis or surgical site infection requiring open sternal irrigation or device removal) and device malfunction requiring surgical treatment.

resultsOverall median age and weight for all 20 children at implantation were 10.8 (interquartile range, 7.9-33.2) months and 6.3 (4.6-10.2) kg. Ten patients (50%) weighed <5 kg. Primary diagnoses were dilated cardiomyopathy in 13 patients, fulminant myocarditis in 3, restrictive cardiomyopathy in 2 and congenital heart disease in 2. Two patients required biventricular assist support. The median support time was 365 (241-636) days. Six patients (30%) were supported for >20 months. One patient died. Seven patients underwent heart transplant. Heart transplant has not been performed in the last 1.5 years. Five patients were weaned from EXCOR support after native myocardial recovery, including a patient with dilated cardiomyopathy who recovered after 24 months of EXCOR support. Major complication-free survival at 6, 12 and 18 months were 79.3%, 49.6% and 38.6%, respectively. Body weight <5 kg at implantation was a risk factor for decreased major complication-free survival.

conclusionsSurvival during EXCOR Paediatric support was good, but it prolonged the wait time for a heart transplant. The number of major complications increased over time and was not negligible, especially in small children.

Indexed as

Cardiomyopathy, DilatedHeart-Assist DevicesHeart FailureHeart TransplantationAdolescentChildHumansTreatment Outcome

Identifiers

PMID35260893
PMCPMC9252124

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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.