Evidence map›Paper›PMID 39552869›Full record

ArticleJournal of thoracic disease2024

Comparison of the use of venovenous extracorporeal membrane oxygenation in anti-melanoma differentiation-associated protein 5 positive dermatomyositis and other systemic rheumatic diseases associated with acute respiratory failure based on a single-center retrospective study.

Lifeng Wang, Xueling Wu, Shuangjun He, Xiaodong Wang, Weijun Wang, Yi Chen, Cuiying Xie

Abstract read
In one paragraph

Article in Journal of thoracic disease, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  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

7 authors.

Lifeng Wang *Department of Emergency, Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Xueling Wu *Department of Pulmonology, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
Shuangjun HeDepartment of Emergency, Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Xiaodong WangDepartment of Rheumatology, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
Weijun WangDepartment of Cardiovascular Surgery, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
Yi ChenDepartment of Emergency, Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Cuiying XieDepartment of Emergency, Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Systemic rheumatic diseases (SRDs), particularly anti-melanoma differentiation-associated protein 5 positive dermatomyositis (MDA5 Methods: A single-center retrospective study of patients with SRD who received VV-ECMO between June 2017 and February 2022 was conducted. Demographic and laboratory data, treatments, extracorporeal membrane oxygenation (ECMO) parameters, and clinical outcomes were extracted from electronic medical records and compared between patients with MDA5 Results: Seven patients with MDA5 Conclusions: Treatment by VV-ECMO could be safely applied to patients with SRDs to maintain normal respiration and oxygenation. However, patients with MDA5

Indexed as

acute respiratory failure (ARF)anti-melanoma differentiation-associated protein 5 positive dermatomyositis (MDA5+ DM)systemic rheumatic diseases (SRDs)Venovenous extracorporeal membrane oxygenation (VV-ECMO)

Identifiers

PMID39552869
PMCPMC11565323

What OpenQuestion holds

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Registered trials

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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.