Evidence map›Paper›PMID 39355918›Full record

ArticleCirculation2024

Long-Term Outcomes After Septal Reduction Therapies in Obstructive Hypertrophic Cardiomyopathy: Insights From the SHARE Registry.

Niccolò Maurizi, Panagiotis Antiochos, Anjali Owens, Neal Lakdawala, Sara Saberi, Mark W Russell, Carlo Fumagalli, Ioannis Skalidis, Kimberly Y Lin, Ashwin S Nathan and 19 more

Abstract readMulticenter Study
In one paragraph

Article in Circulation, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing 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

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

  1. Pooled it
  2. Article
  3. Atrial electrophysiology in hypertrophic cardiomyopathy: current insights and knowledge gaps.Journal of interventional cardiac electrophysiology : an international journal of arrhythmias and pacing · 2026
    Review
  4. Article
  5. Observational
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Heart Failure in Hypertrophic Cardiomyopathy.Cardiac failure review · 2026
    Review
  14. Observational
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. 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

29 authors.

Niccolò MauriziCardiomyopathy Unit, Careggi University Hospital, Florence, Italy (N.M., C.F., I.O.).ORCID 0000-0001-5819-204X
Panagiotis AntiochosService of Cardiology, University Hospital of Lausanne, Switzerland (N.M., P.A., I.S.).ORCID 0000-0001-8466-7360
Anjali OwensPenn Center for Inherited Cardiovascular Disease, Hospital of the University of Pennsylvania and the Perelman School of Medicine at the University of Pennsylvania, Philadelphia (A.O., A.S.N., A.D.F.A., N.R., S.M.D.).ORCID 0000-0002-9669-8495
Neal LakdawalaCardiovascular Division, Brigham and Women's Hospital, Boston, MA (N.L., C.Y.H.).ORCID 0000-0001-6458-5421
Sara SaberiDepartments of Internal Medicine (S.S., A.S.H.), University of Michigan, Ann Arbor.ORCID 0000-0003-4473-6725
Mark W RussellPediatrics (M.W.R.), University of Michigan, Ann Arbor.
Carlo FumagalliCardiomyopathy Unit, Careggi University Hospital, Florence, Italy (N.M., C.F., I.O.).ORCID 0000-0001-7963-5049
Ioannis SkalidisService of Cardiology, University Hospital of Lausanne, Switzerland (N.M., P.A., I.S.).
Kimberly Y LinDepartment of Pediatrics, Children's Hospital of Philadelphia, PA (K.Y.L., R.L., J.R.).ORCID 0000-0003-1582-9797
Ashwin S NathanPenn Center for Inherited Cardiovascular Disease, Hospital of the University of Pennsylvania and the Perelman School of Medicine at the University of Pennsylvania, Philadelphia (A.O., A.S.N., A.D.F.A., N.R., S.M.D.).ORCID 0000-0002-7227-6423
Alejandro De Feria AlsinaPenn Center for Inherited Cardiovascular Disease, Hospital of the University of Pennsylvania and the Perelman School of Medicine at the University of Pennsylvania, Philadelphia (A.O., A.S.N., A.D.F.A., N.R., S.M.D.).
Nosheen RezaPenn Center for Inherited Cardiovascular Disease, Hospital of the University of Pennsylvania and the Perelman School of Medicine at the University of Pennsylvania, Philadelphia (A.O., A.S.N., A.D.F.A., N.R., S.M.D.).ORCID 0000-0002-2942-3731
John C StendahlSection of Cardiovascular Medicine, Yale University School of Medicine, New Haven, CT (J.C.S.).ORCID 0000-0002-1568-9280
Dominic AbramsCenter for Cardiovascular Genetics, Boston Children's Hospital, MA (D.A.).ORCID 0000-0001-5266-2805
Christopher SemsarianAgnes Ginges Centre for Molecular Cardiology at Centenary Institute, The University of Sydney, New South Wales, Australia (C.S.).ORCID 0000-0001-6441-274X
Brian ClaggetDepartment of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, MA (B.C.).ORCID 0000-0002-4215-9218
Rachel LampertDepartment of Pediatrics, Children's Hospital of Philadelphia, PA (K.Y.L., R.L., J.R.).ORCID 0000-0003-3313-0939
Matthew WheelerCenter for Inherited Cardiovascular Disease, Falk Cardiovascular Research Building, Stanford Medicine, CA (M.W., V.N.P., E.A.).ORCID 0000-0001-8721-3022
Victoria N ParikhCenter for Inherited Cardiovascular Disease, Falk Cardiovascular Research Building, Stanford Medicine, CA (M.W., V.N.P., E.A.).ORCID 0000-0002-5138-5559
Euan AshleyCenter for Inherited Cardiovascular Disease, Falk Cardiovascular Research Building, Stanford Medicine, CA (M.W., V.N.P., E.A.).ORCID 0000-0001-9418-9577
Michelle MichelsErasmus Medical Center, Cardiovascular Institute, Thoraxcenter, Department of Cardiology, Rotterdam, the Netherlands (M.M.).ORCID 0000-0001-6432-0431
Joseph RossanoDepartment of Pediatrics, Children's Hospital of Philadelphia, PA (K.Y.L., R.L., J.R.).ORCID 0000-0002-8284-0673
Thomas D RyanHeart Institute, Cincinnati Children's Hospital Medical Center and Department of Pediatrics, University of Cincinnati College of Medicine, OH (T.D.R.).ORCID 0000-0003-4237-576X
Jodie InglesGenomics and Inherited Diseases Program, Garvan Institute of Medical Research and UNSW Sydney, Australia (J.I.).ORCID 0000-0002-4846-7676
James WareNational Heart and Lung Institute and Royal Brompton Cardiovascular Research Centre, Imperial College London, UK (J.W.).
Carolyn Y HoCardiovascular Division, Brigham and Women's Hospital, Boston, MA (N.L., C.Y.H.).
Adam S HelmsDepartments of Internal Medicine (S.S., A.S.H.), University of Michigan, Ann Arbor.
Sharlene M Day *Penn Center for Inherited Cardiovascular Disease, Hospital of the University of Pennsylvania and the Perelman School of Medicine at the University of Pennsylvania, Philadelphia (A.O., A.S.N., A.D.F.A., N.R., S.M.D.).ORCID 0000-0001-9802-7188
Iacopo Olivotto *Cardiomyopathy Unit, Careggi University Hospital, Florence, Italy (N.M., C.F., I.O.).ORCID 0000-0003-1751-9266

Funding

Hypertrophic Cardiomyopathy: Understanding the Heterogeneity of Disease Expression and OutcomesR01HL155568 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI HO, CAROLYN Y · 2021 to 2024
$5.9M
Missense Variants in Myosin Binding Protein C that Cause Hypertrophic CardiomyopathyR01HL167524 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI Sharlene M Day · 2023 to 2026
$2.8M
Risk Alleles in Protein Quality Control Genes as Modifiers of Hypertrophic CardiomyopathyR01HL168841 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI Sharlene M Day · 2024 to 2026
$2.2M
SGLT-inhibitors in patients with hypertrophic cardiomyopathyR33HL164376 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI Sharlene M Day · 2024 to 2026
$2.0M
Improving the Detection of Hypertrophic Cardiomyopathy Using Machine Learning Applied to Electronic Health Record DataK23HL166961 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI Nosheen Reza · 2023 to 2026
$691k
NHLBI NIH HHS K23 HL166961NHLBI NIH HHS R01 HL155568NHLBI NIH HHS R01 HL167524NHLBI NIH HHS R01 HL168841NHLBI NIH HHS R33 HL164376Wellcome Trust
6 · The paper itself

Abstract

backgroundSeptal reduction therapy (SRT) provides substantial symptomatic improvement in patients with obstructive hypertrophic cardiomyopathy (HCM). However, long-term disease course after SRT and predictors of adverse outcomes have not been systematically examined.

methodsData from 13 high clinical volume HCM centers from the international SHARE (Sarcomeric Human Cardiomyopathy Registry) were analyzed. Patients were followed from the time of SRT until last follow-up or occurrence of heart failure (HF) composite outcome (cardiac transplantation, implantation of a left ventricular assist device, left ventricular ejection fraction <35%, development of New York Heart Association class III or IV symptoms), ventricular arrhythmias composite outcome (sudden cardiac death, resuscitated cardiac arrest, or appropriate implantable cardioverter defibrillator therapy), or HCM-related death. Cox proportional hazards models were used to identify predictors of outcome.

resultsOf the 10 225 patients in SHARE, 1832 (18%; 968 [53%] male) underwent SRT, including 455 (25%) with alcohol septal ablation and 1377 (75%) with septal myectomy. The periprocedural 30-day mortality rate was 0.4% (8 of 1832) and 1499 of 1565 (92%) had a maximal left ventricular outflow tract gradient <50 mm Hg at 1 year. After 6.8 years (range, 3.4-9.8 years; 12 565 person-years) from SRT, 77 (4%) experienced HCM-related death (0.6% per year), 236 (13%) a composite HF outcome (1.9% per year), and 87 (5%) a composite ventricular arrhythmia outcome (0.7% per year). Among adults, older age at SRT was associated with a higher incidence of HCM death (hazard ratio, 1.22 [95 CI, 1.1-1.3];

conclusionsSuccessful short- and long-term relief of outflow tract obstruction was observed in experienced multidisciplinary HCM centers. A subset of patients progressed to develop HF, but event-free survival at 10 years was 83% and ventricular arrhythmias were rare. Older age, female sex, and SRT during childhood were associated with a greater risk of developing HF.

Indexed as

Cardiomyopathy, HypertrophicRegistriesAdultAgedFemaleFollow-Up StudiesHeart SeptumHumansMaleMiddle AgedTime FactorsTreatment Outcomecardiomyopathy, hypertrophicheart failurehypertrophy, left ventricularmyectomy

Identifiers

PMID39355918
PMCPMC11493522

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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.