Evidence map›Paper›PMID 41823908›Full record

ArticleJACC. Case reports2026

Mavacamten Reduces LVOT Obstruction Risk, Enabling Transseptal Mitral Valve-in-Valve for Degenerated Bioprosthesis.

Alexander Hoss, Fabian Voß, Amin Polzin

Abstract readCase Reports
In one paragraph

Article in JACC. Case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Alexander HossDivision of Cardiology, Pulmonology, and Vascular Medicine, Department of Internal Medicine, Medical Faculty and University Hospital, Heinrich-Heine-University, Düsseldorf, Germany.
Fabian VoßDivision of Cardiology, Pulmonology, and Vascular Medicine, Department of Internal Medicine, Medical Faculty and University Hospital, Heinrich-Heine-University, Düsseldorf, Germany.
Amin PolzinDivision of Cardiology, Pulmonology, and Vascular Medicine, Department of Internal Medicine, Medical Faculty and University Hospital, Heinrich-Heine-University, Düsseldorf, Germany. Electronic address: amin.polzin@med.uni-duesseldorf.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTranscatheter mitral valve replacement (TMVR) is an alternative to redo surgery for failed mitral bioprostheses, but left ventricular outflow tract (LVOT) obstruction remains a major limitation. CASE SUMMARY: An 86-year-old woman presented with heart failure due to severe prosthetic mitral restenosis. Screening computed tomography (CT) predicted a critically small neo-LVOT, rendering TMVR prohibitive. Given prohibitive surgical risk and no feasible LVOT obstruction-mitigation procedure, off-label mavacamten 2.5 mg daily was initiated. After 4 months, repeat CT showed neo-LVOT enlargement, enabling transseptal valve-in-valve TMVR without complications. Invasive hemodynamics excluded a relevant LVOT gradient; echocardiography confirmed excellent valve function without LVOT obstruction. WHY BEYOND THE GUIDELINES: No guideline-endorsed pharmacologic strategy exists to enlarge predicted neo-LVOT before TMVR. DISCUSSION: Myosin inhibition may offer a noninvasive LVOT obstruction-mitigation bridge when procedural options are unsuitable. TAKE-HOME MESSAGE: In selected patients with prohibitive neo-LVOT, short-term mavacamten may convert CT screening to a feasible TMVR pathway.

Indexed as

LVOT obstructionmavacamtenneo-LVOTstructural heart interventiontranscatheter mitral valve replacement (TMVR)

Identifiers

PMID41823908
PMCPMC13104045

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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.