Evidence map›Paper›PMID 35229229›Full record

ReviewGeneral thoracic and cardiovascular surgery2022

Immunocompetent cells in durable ventricular assist device-implanted non-ischaemic dilated cardiomyopathy.

Ayumi Koga-Ikuta, Satsuki Fukushima, Hatsue Ishibashi-Ueda, Naoki Tadokoro, Takashi Kakuta, Takurya Watanabe, Norihide Fukushima, Ken Suzuki, Toshihiro Fukui, Tomoyuki Fujita

Open access · hybridAbstract readReview
In one paragraph

Review in General thoracic and cardiovascular surgery, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 60% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Molecular mechanisms and intervention approaches of heart failure (Review).International journal of molecular medicine · 2025
    Review
  2. Review
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 3 institutions in 2 countries.

Ayumi Koga-IkutaDepartment of Cardiac Surgery, National Cerebral and Cardiovascular Center, Osaka, Japan.
Satsuki FukushimaDepartment of Cardiac Surgery, National Cerebral and Cardiovascular Center, Osaka, Japan. s.fukushima@ncvc.go.jp.ORCID http://orcid.org/0000-0002-9481-8860
Hatsue Ishibashi-UedaDepartment of Pathology, National Cerebral and Cardiovascular Center, Osaka, Japan.
Naoki TadokoroDepartment of Cardiac Surgery, National Cerebral and Cardiovascular Center, Osaka, Japan.
Takashi KakutaDepartment of Cardiac Surgery, National Cerebral and Cardiovascular Center, Osaka, Japan.
Takurya WatanabeDepartment of Transplantation, National Cerebral and Cardiovascular Center, Osaka, Japan.
Norihide FukushimaDepartment of Transplantation, National Cerebral and Cardiovascular Center, Osaka, Japan.
Ken SuzukiTranslational Therapeutics, William Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, UK.
Toshihiro FukuiDepartment of Cardiovascular Surgery, Kumamoto University Graduate School of Medical Sciences, Kumamoto, Japan.
Tomoyuki FujitaDepartment of Cardiac Surgery, National Cerebral and Cardiovascular Center, Osaka, Japan.
National Cerebral and Cardiovascular Center · JPKumamoto University · JPQueen Mary University of London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveBecause the presence of immunocompetent cells in the myocardium is associated with the pathological stage and/or myocardial viability, we explored relationships between functional recovery after left ventricular assist device implantation and the distribution of immunocompetent cells in non-ischaemic dilated cardiomyopathy patients.

methodsWe reviewed 50 consecutive dilated cardiomyopathy patients implanted with HeartMate II at our institute between April 2013 and December 2018 who were treated with optimal medical therapy during left ventricular assist device support. Patients were stratified by improvement of the left ventricular ejection fraction at 6 months after implantation: ≥ 10% increase (Gr ≥ 10%), 5-10% (Gr 5-10%), and ≤ 5% (Gr ≤ 5%). T cells and macrophages were evaluated in the apical myocardium after left ventricular assist device implantation.

resultsDuring left ventricular assist device support, 12 patients underwent heart transplantation and 2 patients died. Four patients with Gr ≤ 5% were readmitted because of congestive heart failure, but none with Gr ≥ 10%. Macrophages and T cells in the left ventricular myocardium with Gr ≥ 10% were significantly more present compared to those in other groups.

conclusionsThe distribution of immunocompetent cells in the left ventricular myocardium might predict myocardial viability of this pathology after implantation.

Indexed as

Cardiomyopathy, DilatedHeart-Assist DevicesHeart FailureHumansStroke VolumeVentricular Function, LeftImmunocompetent cellsLeft ventricular assist deviceNon-ischaemic dilated cardiomyopathy

Identifiers

PMID35229229
PMCPMC9300518
OpenAlexW4214771333

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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.