Evidence map›Paper›PMID 35882521›Full record

ArticleHeart (British Cardiac Society)2023

Long-term outcomes in distinct phenogroups of patients with primary mitral regurgitation undergoing valve surgery.

Soongu Kwak, Seung-Ah Lee, Jaehyun Lim, Seokhun Yang, Hong-Mi Choi, In-Chang Hwang, Sahmin Lee, Yeonyee Elizabeth Yoon, Jun-Bean Park, Hyung-Kwan Kim and 7 more

Open access · hybridAbstract read
In one paragraph

Article in Heart (British Cardiac Society), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 2 institutions in 1 country.

Soongu Kwak *Division of Cardiology, Department of Internal Medicine, Seoul National University Hospital, Seoul, Korea (the Republic of).
Seung-Ah Lee *Division of Cardiology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea (the Republic of).
Jaehyun LimDivision of Cardiology, Department of Internal Medicine, Seoul National University Hospital, Seoul, Korea (the Republic of).
Seokhun YangDivision of Cardiology, Department of Internal Medicine, Seoul National University Hospital, Seoul, Korea (the Republic of).
Hong-Mi ChoiDepartment of Internal Medicine, Seoul National University College of Medicine, Seoul, Korea (the Republic of).
In-Chang HwangDepartment of Internal Medicine, Seoul National University College of Medicine, Seoul, Korea (the Republic of).
Sahmin LeeDivision of Cardiology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea (the Republic of).
Yeonyee Elizabeth YoonDepartment of Internal Medicine, Seoul National University College of Medicine, Seoul, Korea (the Republic of).ORCID 0000-0002-8479-9889
Jun-Bean ParkDivision of Cardiology, Department of Internal Medicine, Seoul National University Hospital, Seoul, Korea (the Republic of).ORCID 0000-0003-4053-8713
Hyung-Kwan KimDivision of Cardiology, Department of Internal Medicine, Seoul National University Hospital, Seoul, Korea (the Republic of).ORCID 0000-0001-7950-2131
Yong-Jin KimDivision of Cardiology, Department of Internal Medicine, Seoul National University Hospital, Seoul, Korea (the Republic of).
Jong-Min SongDivision of Cardiology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea (the Republic of).ORCID 0000-0002-6754-8199
Goo-Yeong ChoDepartment of Internal Medicine, Seoul National University College of Medicine, Seoul, Korea (the Republic of).
Kyung-Hwan KimDepartment of Thoracic and Cardiovascular Surgery, Seoul National University Hospital, Seoul, Korea (the Republic of).
Duk-Hyun KangDivision of Cardiology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea (the Republic of).ORCID 0000-0003-4031-8649
Dae-Hee KimDivision of Cardiology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea (the Republic of) sproll1@snu.ac.kr daehee74@amc.seoul.kr.ORCID 0000-0002-8275-4871
Seung-Pyo LeeDivision of Cardiology, Department of Internal Medicine, Seoul National University Hospital, Seoul, Korea (the Republic of) sproll1@snu.ac.kr daehee74@amc.seoul.kr.ORCID 0000-0002-5502-3977
Ulsan College · KRSeoul National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesPatients with mitral regurgitation (MR) may be heterogeneous with different risk profiles. We aimed to identify distinct phenogroups of patients with severe primary MR and investigate their long-term prognosis after mitral valve (MV) surgery.

methodsThe retrospective cohort of patients with severe primary MR undergoing MV surgery (derivation, n=1629; validation, n=692) was analysed. Latent class analysis was used to classify patients into subgroups using 15 variables. The primary outcome was all-cause mortality after MV surgery.

resultsDuring follow-up (median 6.0 years), 149 patients (9.1%) died in the derivation cohort. In the univariable Cox analysis, age, female, atrial fibrillation, left ventricular (LV) end-systolic dimension/volumes, LV ejection fraction, left atrial dimension and tricuspid regurgitation peak velocity were significant predictors of mortality following MV surgery. Five distinct phenogroups were identified, three younger groups (group 1-3) and two older groups (group 4-5): group 1, least comorbidities; group 2, men with LV enlargement; group 3, predominantly women with rheumatic MR; group 4, low-risk older patients; and group 5, high-risk older patients. Cumulative survival was the lowest in group 5, followed by groups 3 and 4 (5-year survival for groups 1-5: 98.5%, 96.0%, 91.7%, 95.6% and 83.4%; p<0.001). Phenogroups had similar predictive performance compared with the Mitral Regurgitation International Database score in patients with degenerative MR (3-year C-index, 0.763 vs 0.750, p=0.602). These findings were reproduced in the validation cohort.

conclusionFive phenogroups of patients with severe primary MR with different risk profiles and outcomes were identified. This phenogrouping strategy may improve risk stratification when optimising the timing and type of interventions for severe MR.

Indexed as

Mitral Valve InsufficiencyFemaleHumansMaleMitral ValveRetrospective StudiesStroke VolumeTreatment OutcomeVentricular Function, LeftMitral Valve Insufficiency

Identifiers

PMID35882521
PMCPMC9887360
OpenAlexW4288074954

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LicenceCC BY-NC
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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.