Initial experience with percutaneous mitral valve repair in patients with cardiac amyloidosis.


Journal

European journal of clinical investigation
ISSN: 1365-2362
Titre abrégé: Eur J Clin Invest
Pays: England
ID NLM: 0245331

Informations de publication

Date de publication:
Jun 2021
Historique:
revised: 07 12 2020
received: 20 10 2020
accepted: 12 12 2020
pubmed: 17 12 2020
medline: 31 12 2021
entrez: 16 12 2020
Statut: ppublish

Résumé

Percutaneous mitral valve repair (PMVR) is a therapeutic option for severe mitral regurgitation (MR) in patients with heart failure due to differential aetiologies. However, only little is known about the safety and efficacy of this procedure in patients with amyloid cardiomyopathy. Five patients with cardiac amyloidosis and moderate to severe or severe MR undergoing PMVR were analysed retrospectively and compared to seven patients with cardiac amyloidosis and severe MR without intervention. Clinical and functional data, renal function and cardiac biomarkers as well as established risk scores for cardiac amyloidosis were assessed. Primary endpoint was the reduction in MR one year after PMVR. Secondary endpoints were safety, overall mortality after 12 months compared with the control group, as well as changes in clinical and functional parameters. Amyloidosis risk assessment documented amyloid cardiomyopathy at an advanced stage in all patients. Procedural, technical and device success of PMVR were all 100% and residual MR remained mild to moderate at 12 months follow-up (P = .038 vs before PMVR). Differences in survival compared with the control (no PMVR) group pointed to a possible survival benefit in the PMVR group (P = .02). PMVR is a feasible and safe procedure in patients with cardiac amyloidosis and might carry a possible survival benefit in this patient group.

Sections du résumé

BACKGROUND BACKGROUND
Percutaneous mitral valve repair (PMVR) is a therapeutic option for severe mitral regurgitation (MR) in patients with heart failure due to differential aetiologies. However, only little is known about the safety and efficacy of this procedure in patients with amyloid cardiomyopathy.
METHODS METHODS
Five patients with cardiac amyloidosis and moderate to severe or severe MR undergoing PMVR were analysed retrospectively and compared to seven patients with cardiac amyloidosis and severe MR without intervention. Clinical and functional data, renal function and cardiac biomarkers as well as established risk scores for cardiac amyloidosis were assessed. Primary endpoint was the reduction in MR one year after PMVR. Secondary endpoints were safety, overall mortality after 12 months compared with the control group, as well as changes in clinical and functional parameters.
RESULTS RESULTS
Amyloidosis risk assessment documented amyloid cardiomyopathy at an advanced stage in all patients. Procedural, technical and device success of PMVR were all 100% and residual MR remained mild to moderate at 12 months follow-up (P = .038 vs before PMVR). Differences in survival compared with the control (no PMVR) group pointed to a possible survival benefit in the PMVR group (P = .02).
CONCLUSION CONCLUSIONS
PMVR is a feasible and safe procedure in patients with cardiac amyloidosis and might carry a possible survival benefit in this patient group.

Identifiants

pubmed: 33326601
doi: 10.1111/eci.13473
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e13473

Informations de copyright

© 2020 The Authors. European Journal of Clinical Investigation published by John Wiley & Sons Ltd on behalf of Stichting European Society for Clinical Investigation Journal Foundation.

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Auteurs

Martin J Volz (MJ)

Division of Cardiology, Department of Internal Medicine III, University of Heidelberg, Heidelberg, Germany.

Sven T Pleger (ST)

Division of Cardiology, Department of Internal Medicine III, University of Heidelberg, Heidelberg, Germany.

Andreas Weber (A)

Division of Cardiology, Department of Internal Medicine III, University of Heidelberg, Heidelberg, Germany.

Nicolas A Geis (NA)

Division of Cardiology, Department of Internal Medicine III, University of Heidelberg, Heidelberg, Germany.

Sonja Hamed (S)

Division of Cardiology, Department of Internal Medicine III, University of Heidelberg, Heidelberg, Germany.

Derliz Mereles (D)

Division of Cardiology, Department of Internal Medicine III, University of Heidelberg, Heidelberg, Germany.

Ute Hegenbart (U)

Division of Hematology and Oncology, Department of Internal Medicine V, University of Heidelberg, Heidelberg, Germany.

Hugo A Katus (HA)

Division of Cardiology, Department of Internal Medicine III, University of Heidelberg, Heidelberg, Germany.
DZHK (German Center for Cardiovascular Research), partner site Heidelberg/Mannheim, Heidelberg, Germany.

Norbert Frey (N)

Division of Cardiology, Department of Internal Medicine III, University of Heidelberg, Heidelberg, Germany.
DZHK (German Center for Cardiovascular Research), partner site Heidelberg/Mannheim, Heidelberg, Germany.

Philip W Raake (PW)

Division of Cardiology, Department of Internal Medicine III, University of Heidelberg, Heidelberg, Germany.
DZHK (German Center for Cardiovascular Research), partner site Heidelberg/Mannheim, Heidelberg, Germany.

Michael M Kreusser (MM)

Division of Cardiology, Department of Internal Medicine III, University of Heidelberg, Heidelberg, Germany.
DZHK (German Center for Cardiovascular Research), partner site Heidelberg/Mannheim, Heidelberg, Germany.

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