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Age‐related survival after alcohol septal ablation in hypertrophic obstructive cardiomyopathy

AIMS: Since its introduction, alcohol septal ablation (PTSMA) was discussed as treatment option only in elderly symptomatic patients with hypertrophic obstructive cardiomyopathy (HOCM). We report on long‐term follow‐up after PTSMA with respect to patient's age. METHODS AND RESULTS: Between May...

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Autores principales: Batzner, Angelika, Aicha, Diaa, Pfeiffer, Barbara, Neugebauer, Anna, Seggewiss, Hubert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8788038/
https://www.ncbi.nlm.nih.gov/pubmed/34904378
http://dx.doi.org/10.1002/ehf2.13750
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author Batzner, Angelika
Aicha, Diaa
Pfeiffer, Barbara
Neugebauer, Anna
Seggewiss, Hubert
author_facet Batzner, Angelika
Aicha, Diaa
Pfeiffer, Barbara
Neugebauer, Anna
Seggewiss, Hubert
author_sort Batzner, Angelika
collection PubMed
description AIMS: Since its introduction, alcohol septal ablation (PTSMA) was discussed as treatment option only in elderly symptomatic patients with hypertrophic obstructive cardiomyopathy (HOCM). We report on long‐term follow‐up after PTSMA with respect to patient's age. METHODS AND RESULTS: Between May 2000 and June 2017, we treated 952 consecutive HOCM patients with PTSMA; 133 (14.0%) patients were <40 years of age (Group A; mean age 30.3 ± 7.6; 26.3% female), 422 (44.3%) patients were between ≥40 and <60 years of age (Group B; mean age 50.6 ± 5.8; 27.0% female), and 397 (41.7%) patients were ≥60 years of age (Group C; 69.7 ± 6.1; 60.2% female). After PTSMA, need of pacemaker implantation was lowest in Group A (3.8%, P < 0.01 each) compared with Group B (9.2%) and Group C (14.1%) during hospital stay. One patient in Groups A and C died during hospital stay, each. Follow‐up was longer in Group A (7.4 ± 5.5 years) compared with Group C (5.6 ± 4.8 years; P < 0.001) and comparable with Group B (6.5 ± 5.1 years). Mortality was highest in Group C (13.1%; P < 0.0001 each) compared with Group A (1.5%) and Group B (4.3%). In Group A, no patient died from cardiac reason, whereas five patients died from cardiac reasons in Group B and seven patients in Group C. Sudden cardiac death was not observed in Group A, whereas three patients in Group B and one patient in Group C suffered sudden cardiac death. CONCLUSIONS: Mortality after PTSMA is predominantly due to non‐cardiac reasons and mainly observed in elderly patients. Survival in young patients is not affected by cardiac mortality. In experienced centres with careful patient selection, PTSMA is safe in young patients.
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spelling pubmed-87880382022-01-31 Age‐related survival after alcohol septal ablation in hypertrophic obstructive cardiomyopathy Batzner, Angelika Aicha, Diaa Pfeiffer, Barbara Neugebauer, Anna Seggewiss, Hubert ESC Heart Fail Original Articles AIMS: Since its introduction, alcohol septal ablation (PTSMA) was discussed as treatment option only in elderly symptomatic patients with hypertrophic obstructive cardiomyopathy (HOCM). We report on long‐term follow‐up after PTSMA with respect to patient's age. METHODS AND RESULTS: Between May 2000 and June 2017, we treated 952 consecutive HOCM patients with PTSMA; 133 (14.0%) patients were <40 years of age (Group A; mean age 30.3 ± 7.6; 26.3% female), 422 (44.3%) patients were between ≥40 and <60 years of age (Group B; mean age 50.6 ± 5.8; 27.0% female), and 397 (41.7%) patients were ≥60 years of age (Group C; 69.7 ± 6.1; 60.2% female). After PTSMA, need of pacemaker implantation was lowest in Group A (3.8%, P < 0.01 each) compared with Group B (9.2%) and Group C (14.1%) during hospital stay. One patient in Groups A and C died during hospital stay, each. Follow‐up was longer in Group A (7.4 ± 5.5 years) compared with Group C (5.6 ± 4.8 years; P < 0.001) and comparable with Group B (6.5 ± 5.1 years). Mortality was highest in Group C (13.1%; P < 0.0001 each) compared with Group A (1.5%) and Group B (4.3%). In Group A, no patient died from cardiac reason, whereas five patients died from cardiac reasons in Group B and seven patients in Group C. Sudden cardiac death was not observed in Group A, whereas three patients in Group B and one patient in Group C suffered sudden cardiac death. CONCLUSIONS: Mortality after PTSMA is predominantly due to non‐cardiac reasons and mainly observed in elderly patients. Survival in young patients is not affected by cardiac mortality. In experienced centres with careful patient selection, PTSMA is safe in young patients. John Wiley and Sons Inc. 2021-12-13 /pmc/articles/PMC8788038/ /pubmed/34904378 http://dx.doi.org/10.1002/ehf2.13750 Text en © 2021 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Batzner, Angelika
Aicha, Diaa
Pfeiffer, Barbara
Neugebauer, Anna
Seggewiss, Hubert
Age‐related survival after alcohol septal ablation in hypertrophic obstructive cardiomyopathy
title Age‐related survival after alcohol septal ablation in hypertrophic obstructive cardiomyopathy
title_full Age‐related survival after alcohol septal ablation in hypertrophic obstructive cardiomyopathy
title_fullStr Age‐related survival after alcohol septal ablation in hypertrophic obstructive cardiomyopathy
title_full_unstemmed Age‐related survival after alcohol septal ablation in hypertrophic obstructive cardiomyopathy
title_short Age‐related survival after alcohol septal ablation in hypertrophic obstructive cardiomyopathy
title_sort age‐related survival after alcohol septal ablation in hypertrophic obstructive cardiomyopathy
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8788038/
https://www.ncbi.nlm.nih.gov/pubmed/34904378
http://dx.doi.org/10.1002/ehf2.13750
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