The DOI matches its Crossref record; 50 of the 52 references it cites were found in a registry or an index.
Multicenter study of the efficacy and safety of disopyramide in obstructive hypertrophic cardiomyopathy
Open accessAbstract
Objectives In this study we assessed the long-term efficacy and safety of disopyramide for patients with obstructive hypertrophic cardiomyopathy (HCM).Background It has been reported that disopyramide may reduce left ventricular outflow gradient and improve symptoms in patients with HCM. However, long-term efficacy and safety of disopyramide has not been shown in a large cohort.Methods Clinical and echocardiographic data were evaluated in 118 obstructive HCM patients treated with disopyramide at 4 HCM treatment centers. Mortality in the disopyramide-treated patients was compared with 373 obstructive HCM patients not treated with disopyramide.Results Patients were followed with disopyramide for 3.1 +/- 2.6 years; dose 432 +/- 181 mg/day (97% also received beta-blockers). Seventy-eight patients (66%) were maintained with disopyramide without the necessity for major non-pharmacologic intervention with surgical myectomy, alcohol ablation, or pacing; outflow gradient at rest decreased from 75 +/- 33 to 40 +/- 32 mm Hg (p < 0.0001) and mean New York Heart Association functional class from 2.3 +/- 0.7 to 1.7 +/- 0.6 (p < 0.0001). Forty other patients (34%) could not be satisfactorily managed with disopyramide and required major invasive interventions because of inadequate symptom and gradient control or vagolytic side effects. All-cause annual cardiac death rate between disopyramide and non-disopyramide-treated patients did not differ significantly, 1.4% versus 2.6%/year (p = 0.07). There was also no difference in sudden death rate, 1.0%/year versus 1.8%/year (p = 0.08).Conclusions Two-thirds of obstructed HCM patients treated with disopyramide could be managed medically with amelioration of symptoms and about 50% reduction in subaortic gradient over >/=3 years. Disopyramide therapy does not appear to be proarrhythmic in HCM and should be considered before proceeding to surgical myectomy or alternate strategies.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Disopyramide has been shown in retrospective studies to be safe and associated with an improvement in both LVOT gradient and symptoms when used in combination with β blockers or non-dihydropyridine CCBs.”
From Current management of hypertrophic cardiomyopathy (2025) · cites this paper as [30]
Experimental — accuracy not yet measuredIn the citing paper
“has been shown to reduce LV outflow gradient and improve symptoms in patients with hypertrophic cardiomyopathy.[662][663][664]”
From 2016 ESC Guidelines for the management of atrial fibrillation developed in collaboration with EACTS (2016) · cites this paper as [662]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Hypertrophic Cardiomyopathy: A Systematic Review
Maron, B. J. (2002) · JAMA · doi:10.1001/jama.287.10.1308 · Cited by 2,224
Self-citationHypertensive, Y., & Chin, K. (1982) · Springer eBooks · doi:10.1007/978-3-642-68282-7 · Cited by 1,757
Maron, B. J., McKenna, W. J., Danielson, G. K., KAPPENBERGER, L. J., Kuhn, H. J., Seidman, C. E., Shah, P. M., Spencer, W. H., Spirito, P., ten Cate, F. J., et al. (2003) · Journal of the American College of Cardiology · doi:10.1016/s0735-1097(03)00941-0 · Cited by 1,572
Maron, M. S., Olivotto, I., Betocchi, S., Casey, S. A., Lesser, J. R., Losi, M. A., Cecchi, F., & Maron, B. J. (2003) · New England Journal of Medicine · doi:10.1056/nejmoa021332 · Cited by 1,259
Magnitude of Left Ventricular Hypertrophy and Risk of Sudden Death in Hypertrophic Cardiomyopathy
Spirito, P., Bellone, P., Harris, K. M., Bernabò, P., Bruzzi, P., & Maron, B. J. (2000) · New England Journal of Medicine · doi:10.1056/nejm200006153422403 · Cited by 1,142
Hypertrophic cardiomyopathy. The importance of the site and the extent of hypertrophy. A review
Wigle, E. D., Sasson, Z., Henderson, M. A., Ruddy, T. D., Fulop, J. C., Rakowski, H., & Williams, W. G. (1985) · Progress in Cardiovascular Diseases · doi:10.1016/0033-0620(85)90024-6 · Cited by 822
Wigle, E. D., Rakowski, H., Kimball, B. P., & Williams, W. G. (1995) · Circulation · doi:10.1161/01.cir.92.7.1680 · Cited by 775
D, E. B. M., Lambrew, C. T., Rockoff, S. D., Ross, J., & Morrow, A. G. (1964) · Circulation · doi:10.1161/01.cir.29.5s4.iv-3 · Cited by 758
Elliot, P. M., Gimeno, J. R., Mahon, N., Poloniecki, J. D., & McKenna, W. J. (2001) · The Lancet · doi:10.1016/s0140-6736(00)04005-8 · Cited by 517
Behr, E. R., & McKenna, W. J. (2002) · Current Treatment Options in Cardiovascular Medicine · doi:10.1007/s11936-002-0039-8 · Cited by 407
Flagged first, then by citations
2 of the 52 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
Items 201–300 of 409
Banthiya, S., Check, L., & Atkins, J. (2024) · US Cardiology Review · doi:10.15420/usc.2023.21 · Cited by 10
“49 However, it should be used in combination with a atrioventricular nodal blocking agent, such as a β-blocker or calcium channel blocker, because this drug can increase the risk of AF with rapid ventricular rate by enhancing conduction through the atrioventricular node CMIs are a novel class of…”
Elliot, P. M., Anastasakis, A., Borger, M. A., Borggrefe, M., Cecchi, F., Charron, P., Hagège, A. A., Lafont, A. M., Limongelli, G., Mahrholdt, H., et al. (2014) · Revista Española de Cardiología · doi:10.1016/j.recesp.2014.12.001 · Cited by 10
Surgical Management of Hypertrophic Cardiomyopathy in 2007: What is New?
Brown, M. L., & Schaff, H. V. (2008) · World Journal of Surgery · doi:10.1007/s00268-007-9412-9 · Cited by 10
“In a multicenter study, 66% of patients treated with disopyramide had improvement of symptoms and had a 50% reduction in the LVOT gradient after 3 years of follow-up [15].”
BackgroundNon-surgical septal reduction therapy in hypertrophic cardiomyopathy
Cooper, R. M., & Stables, R. (2017) · Heart · doi:10.1136/heartjnl-2016-309952 · Cited by 10
Wang, A., Lakdawala, N. K., Abraham, T. P., Nilles, E. K., WOJDYLA, D. M., OWENS, A. T., Bach, R. G., Saberi, S., Sehnert, A. J., & Cresci, S. (2024) · Journal of Cardiac Failure · doi:10.1016/j.cardfail.2024.10.449 · Cited by 9
Tian, Z., Li, L., Li, X., Zhang, Q., Peng, D., Ma, W., Yang, P. C., Wang, F., Cheng, X. C., Fu, Y., et al. (2025) · JACC Asia · doi:10.1016/j.jacasi.2025.05.015 · Cited by 9
Sandín, M., Marín, F. R., Cambronero, F., Climent, V. E., Caro, C., Martı́nez, J. G., García‐Honrubia, A., Alberola, A. G., de la Morena, G., Valdés, M., et al. (2009) · Revista Española de Cardiología · doi:10.1016/s0300-8932(09)73075-1 · Cited by 9
“Terapia combinada con BB + antagonista del calcio, 22 (30,6%); con BB + disopiramida, previo a la implantación de 87 [61,5-115,2] mmHg, pasó a 30 [18-54,5] mmHg en la primera ecocardiografía y a 17,5 [9,5-47] mmHg en el último estudio ecocardiográfico (todos, p < 0,01).”
BackgroundInfluentialFaber, L. (2014) · Advances in Medicine · doi:10.1155/2014/464851 · Cited by 9
“Medical therapy with negatively inotropic drugs (betablockers, calcium antagonists of the verapamil type, and disopyramide) is the first line of treatment in order to reduce symptoms and improve quality of life [83–86] in patients with HOCM.”
BackgroundThe Brockenbrough – Braunwald – Morrow Sign
Trevino, A. R., & Buergler, J. M. (2014) · Methodist DeBakey Cardiovascular Journal · doi:10.14797/mdcj-10-1-34 · Cited by 9
State-of-the-Art Treatments for Atrial Fibrillation in Patients with Hypertrophic Cardiomyopathy
Penela, D., Sorgente, A., & Cappato, R. (2021) · Journal of Clinical Medicine · doi:10.3390/jcm10143025 · Cited by 9
Gomes, J. A. (2020) · Springer eBooks · doi:10.1007/978-3-030-45066-3_22 · Cited by 9
Maron, B. J., Ommen, S. R., Nishimura, R. A., McKenna, W. J., Rakowski, H., Sherrid, M. V., Olivotto, I., Braunwald, E., & Maron, M. S. (2026) · Journal of the American Heart Association · doi:10.1161/jaha.125.047462 · Cited by 9
Evolving Strategies for the Management of Obstructive Hypertrophic Cardiomyopathy
Liang, L. W., Lumish, H. S., Sewanan, L. R., Shimada, Y. J., Maurer, M. S., Weiner, S. D., & Clerkin, K. J. (2024) · Journal of Cardiac Failure · doi:10.1016/j.cardfail.2024.04.024 · Cited by 8
Hálasz, G., Dei, L., Moroni, F., Ayers, M. P., Ciacci, P., Giacalone, G., Mistrulli, R., Redivo, M., Orellana, S., Gabrielli, D., et al. (2024) · European Journal of Preventive Cardiology · doi:10.1093/eurjpc/zwae198 · Cited by 8
Pinto, G., Chiarito, M., Puscas, T., Bacher, A., Donal, E., Réant, P., Condorelli, G., & Hagège, A. A. (2024) · The American Journal of Cardiology · doi:10.1016/j.amjcard.2024.10.029 · Cited by 8
Dahlström, U. (2019) · Cardiovascular medicine · doi:10.1007/978-3-319-98184-0_1 · Cited by 8
Markers of responsiveness to disopyramide in patients with hypertrophic cardiomyopathy
Habib, M., Hoss, S., Bruchal-Garbicz, B., Chan, R. H. M., Rakowski, H., Williams, L. K., & Adler, A. (2019) · International Journal of Cardiology · doi:10.1016/j.ijcard.2019.09.066 · Cited by 8
Stefàno, P., Argirò, A., Bacchi, B., Iannone, L., Bertini, A., Zampieri, M., Cerillo, A. G., & Olivotto, I. (2022) · International Journal of Cardiology · doi:10.1016/j.ijcard.2022.09.036 · Cited by 8
Awad, K., Pereyra, M., Farina, J., Pathangey, G., Abbas, M. T., Scalia, I. G., Couteur, D. G. L., Wilanksy, S., Lester, S. J., Ommen, S. R., et al. (2025) · European Heart Journal - Cardiovascular Pharmacotherapy · doi:10.1093/ehjcvp/pvaf036 · Cited by 8
Current and emerging medical and surgical therapy in hypertrophic cardiomyopathy
Kim, K. A., & Jung, M. (2025) · Journal of Cardiovascular Imaging · doi:10.1186/s44348-025-00050-9 · Cited by 8
Does Disopyramide Still Have a Place in the Management of Obstructive Hypertrophic Cardiomyopathy?
Corriveau, S., Heydari, B., & Garceau, P. (2024) · CJC Open · doi:10.1016/j.cjco.2024.03.006 · Cited by 7
Medical, Surgical and Interventional Management of Hypertrophic Cardiomyopathy With Obstruction
Elmariah, S., & Fifer, M. A. (2012) · Current Treatment Options in Cardiovascular Medicine · doi:10.1007/s11936-012-0206-5 · Cited by 8
Anti-arrhythmic therapy in patients with non-ischemic cardiomyopathy
Proietti, R., Russo, V., & AlTurki, A. (2019) · Pharmacological Research · doi:10.1016/j.phrs.2019.03.004 · Cited by 7
Disopyramide for Hypertrophic Cardiomyopathy
Sánchez-Nadales, A., Guzman, A. A., & Khan, A. (2019) · Cureus · doi:10.7759/cureus.4526 · Cited by 7
Pharmacotherapy for the treatment of obstructive hypertrophic cardiomyopathy
Spoladore, R., Fragasso, G., Pannone, L., Slavich, M., & Margonato, A. (2020) · Expert Opinion on Pharmacotherapy · doi:10.1080/14656566.2019.1702023 · Cited by 7
“demonstrated in a large multicentre registry [37].”
Hori, Y., Fujimoto, E., Nishikawa, Y., & Nakamura, T. (2020) · Journal of Veterinary Cardiology · doi:10.1016/j.jvc.2020.04.002 · Cited by 7
Medical Management of Hypertrophic Cardiomyopathy
Naghi, J. J., & Siegel, R. J. (2010) · Reviews in Cardiovascular Medicine · doi:10.3909/ricm0546 · Cited by 7
Östman‐Smith, I., Rossano, J. W., & Shaddy, R. E. (2013) · Current Opinion in Cardiology · doi:10.1097/hco.0b013e32835dd020 · Cited by 7
“It does not appear to have pro-arrhythmic effects in a HCM population [36].”
BackgroundTowbin, J. A., Udelson, J. E., Nishimura, R. A., Ommen, S. R., Rakowski, H., Bonow, R. O., Dearani, J. A., Fifer, M. A., Gersh, B. J., & Maron, B. J. (2011) · Cited by 7
Refaat, M. M., Fahed, A. C., Hassanieh, S., Hotait, M., Arabi, M. T., Skouri, H. N., Seidman, J. G., Seidman, C. E., Bitar, F. F., & Nemer, G. M. (2016) · Cardiac Electrophysiology Clinics · doi:10.1016/j.ccep.2015.10.034 · Cited by 7
Rodríguez‐González, M., Castellano‐Martínez, A., Grujic, B., & Prieto-Heredia, M. A. (2017) · Journal of Cardiology Cases · doi:10.1016/j.jccase.2017.03.004 · Cited by 7
“However, beta-blocking therapy should only decrease exercise gradient, but not reduce outflow gradient at rest, and it may not control symptoms satisfactorily in some patients [4,6].”
BackgroundInfluentialMateo, J. J. S., Molina, M. S., & Gimeno, J. R. (2018) · Medicina Clínica (English Edition) · doi:10.1016/j.medcle.2017.09.029 · Cited by 7
Cardiac Myosin Inhibitors in Hypertrophic Cardiomyopathy: From Sarcomere to Clinic
Nakamura, K., Okumura, T., Kato, S., Onoue, K., Kubo, T., Kouzu, H., Yano, T., & Inomata, T. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26199347 · Cited by 6
“Disopyramide, a sodium channel blocker with negative inotropic effects, is often added in refractory cases but requires careful monitoring owing to potential QT prolongation and anticholinergic side effects [24].”
An overview of the treatments for hypertrophic cardiomyopathy
Xu, W., Zhu, F., Zhang, Y., Li, P., & Sheng, Y. (2024) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2024.1387596 · Cited by 6
Class I Antiarrhythmic Drugs: Na+ Channel Blockers
Shenasa, M., Shenasa, M.-A., & Smith, M. (2020) · Springer eBooks · doi:10.1007/978-3-030-34893-9_2 · Cited by 6
Treatment of hypertrophic cardiomyopathy in childhood
Colan, S. D. (2011) · Progress in Pediatric Cardiology · doi:10.1016/j.ppedcard.2010.11.004 · Cited by 6
“A number of case reports documenting a fall in outflow tract obstruction and symptomatic improvement have appeared, including a relatively recent observational series in 118 adults with obstructive HCM [33] documenting symptomatic improvement in 2/3 and no evidence of a proarrhythmic effect.”
BackgroundMaron, B. J. (2012) · Elsevier eBooks · doi:10.1016/b978-1-4377-0398-6.00069-x · Cited by 6
Fool Me Once, Fool Me Twice: Hypertrophic Cardiomyopathy with Aortic Stenosis
Vanichsarn, C. T., & Siegel, R. J. (2015) · The American Journal of Medicine · doi:10.1016/j.amjmed.2015.05.003 · Cited by 6
Atrial Fibrillation in Hypertrophic Obstructive Cardiomyopathy - Antiarrhythmics, Ablation and More!
Malasana, G., Day, J. D., & Bunch, T. J. (2009) · Europe PMC (PubMed Central) · doi:10.4022/jafib.210 · Cited by 6
Güler, A., Erata, Y. E., Demirtola, A. İ., Türkmen, I., Atmaca, S., Şahin, H., Aydın, S. G., Almasri, M., Tekin, M., Coşkun, G., et al. (2024) · International Journal of Cardiology · doi:10.1016/j.ijcard.2024.132913 · Cited by 5
Rate Versus Rhythm Control for Atrial Fibrillation: From Affirm to EAST-AFNET 4 – a Paradigm Shift
Roman, S., Patel, K. B., Hana, D., Guice, K. C., Patel, J. D., Stadnick, C., Basta, A., & Khouzam, R. N. (2022) · Future Cardiology · doi:10.2217/fca-2021-0034 · Cited by 6
Parodi, A., Puscas, T., Réant, P., Donal, E., M’Barek, D. R., Billon, C., Bacher, A., Hachmi, M. E., Wahbi, K., Jeunemaı̂tre, X., et al. (2024) · Archives of cardiovascular diseases · doi:10.1016/j.acvd.2024.04.001 · Cited by 5
Badr, A., Roehl, K. M., Suppah, M., Abdullah, H. A., Arsanjani, R., Siontis, K. C., Geske, J. B., Ommen, S. R., Giudicessi, J. R., & Alsidawi, S. (2025) · Biomedicines · doi:10.3390/biomedicines13041005 · Cited by 5
“Disopyramide improves clinical symptoms, however it has not been associated with improved survival or reduced cardiovascular deaths, including sudden arrhyth-mic death [23,24].”
Echocardiography in the treatment of hypertrophic cardiomyopathy.
Musat, D. L., & Sherrid, M. V. (2006) · PubMed · Cited by 5
Can Pharmacologic Gradient Reduction Decrease Mortality in Hypertrophic Cardiomyopathy?
Musat, D. L., Marineci, S., & Sherrid, M. V. (2012) · Progress in Cardiovascular Diseases · doi:10.1016/j.pcad.2012.05.003 · Cited by 5
Atrioventricular Sequential Pacing for Hypertrophic Cardiomyopathy During Liver Transplantation
Ramos, J., Pai, S., Perry, D. K., Blackshear, J. L., & Aniskevich, S. (2015) · A & A Case Reports · doi:10.1213/xaa.0000000000000219 · Cited by 5
Arunachalam, K., Maan, A., & Chu, A. F. (2020) · Critical Pathways in Cardiology A Journal of Evidence-Based Medicine · doi:10.1097/hpc.0000000000000210 · Cited by 5
Atrial Fibrillation in Hypertrophic Cardiomyopathy
Игнатенко, Г. А., Тарадин, Г. Г., Ватутин, Н. Т., Kaluga, A. A., & Kostyamin, Y. D. (2021) · The Russian Archives of Internal Medicine · doi:10.20514/2226-6704-2021-11-3-173-185 · Cited by 5
“Альтернативными антиаритмическими препаратами при ФП у больных с ГКМП являются соталол и дизопирамид [30, 73-75].”
Diagnosis and Treatment of Obstructive Hypertrophic Cardiomyopathy
Todde, G., Canciello, G., Borrelli, F., Perillo, E. F., Esposito, G., Lombardi, R., & Losi, M. A. (2023) · Cardiogenetics · doi:10.3390/cardiogenetics13020008 · Cited by 5
“The safety and efficacy of disopyramide were demonstrated in a large multicenter registry [34].”
BackgroundHaruki, S., Minami, Y., Kajimoto, K., Yashiro, B., Suzuki, T., Kawana, M., & Hagiwara, N. (2009) · European Journal of Heart Failure · doi:10.1093/eurjhf/hfp166 · Cited by 5
Hosokawa, Y., Takano, H., Ohno, T., Takayama, M., & Takano, T. (2008) · Angiology · doi:10.1177/0003319707305406 · Cited by 5
“These drugs not only act as antiarrhythmic agents by modifying ion channels but also suppress hypercontraction of LV by their negative inotropic effect, resulting in the reduction of intracavity pressure gradients.(16-18) However, the effectiveness of these drugs practically varies among patients.”
BackgroundSelection of hypertrophic cardiomyopathy patients for myectomy or alcohol septal ablation.
Lever, H. M. (2006) · PubMed · Cited by 5
Chu, E. L.-W., Kim, D. S., & Masri, A. (2025) · Cardiac failure review · doi:10.15420/cfr.2025.08 · Cited by 4
Scalone, G., & Niccoli, G. (2015) · Expert Review of Cardiovascular Therapy · doi:10.1586/14779072.2015.1077114 · Cited by 4
“In this context, disopyramide represents the most reliable drug for reducing outflow gradients at rest in HCM [59].”
BackgroundInfluentialKehl, D. W., Rader, F., Pollick, C., Trento, A., & Siegel, R. J. (2016) · The American Journal of Cardiology · doi:10.1016/j.amjcard.2016.07.046 · Cited by 4
Imaging in Hypertrophic Cardiomyopathy: Beyond Risk Stratification
Nealy, Z., & Kramer, C. M. (2023) · Heart Failure Clinics · doi:10.1016/j.hfc.2023.03.004 · Cited by 4
Hypertrophic Cardiomyopathy: From Medical Treatment to Advanced Heart Failure Therapies
Mazur, M. M., Braksator, W., & Popjes, E. D. (2024) · Current Cardiology Reports · doi:10.1007/s11886-024-02095-6 · Cited by 4
“%) serving as an option to delay elective myectomy (or alcohol septal ablation) [37].”
Advancements in the Diagnosis and Treatment of Hypertrophic Cardiomyopathy: A Comprehensive Review
Gill, R. S., Siddiqui, A. K., Yee, B., Dicaro, M. V., Houshmand, N., & Tak, T. (2024) · Journal of Cardiovascular Development and Disease · doi:10.3390/jcdd11090290 · Cited by 7
“Disopyramide has been shown in symptomatic HOCM patients to decrease resting LVOT gradient and improve NYHA functional class [67–69].”
BackgroundLong QT syndrome caused by N-acetyl procainamide in a patient on hemodialysis
Ashida, K., Mine, T., Kodani, T., Kishima, H., & Masuyama, T. (2015) · Journal of Cardiology Cases · doi:10.1016/j.jccase.2015.02.005 · Cited by 4
“One observational study, however, revealed that there were no significant differences in cardiac events between class 1A drug arm and the other arm [4].”
BackgroundPreventing Recurrences: Classic and Modern Antiarrhythmic Drugs in Atrial Fibrillation
Víctor, F., Ramos, T., & Lozano, F. (2014) · Cardiovascular Pharmacology Open Access · doi:10.4172/2329-6607.1000130 · Cited by 2
“The negative inotropic effects of this drug also make it a viable option for patients with AF and hypertrophic cardiomyopathy [24].”
BackgroundNovel Pharmacotherapy for Hypertrophic Cardiomyopathy
Wong, T. C., & Martinez, M. W. (2018) · Cardiology Clinics · doi:10.1016/j.ccl.2018.08.008 · Cited by 4
Computational Modeling of Sarcomere Protein Mutations and Drug Effects on Cardiac Muscle Behavior
Prodanović, M., Stojanovic, B. S., Prodanovic, D., Filipović, N., & Mijailovich, S. M. (2021) · IEEE International Conference on Bioinformatics and Bioengineering (BIBE) · doi:10.1109/bibe52308.2021.9635428 · Cited by 4
“It has been used to decrease left ventricular outflow tract obstruction in obstructive HCM since first reports in the early 1980’s [26], [27].”
MethodBatzner, A., & Seggewiß, H. (2020) · Herz · doi:10.1007/s00059-020-04899-y · Cited by 4
“DynamischeundsymptomatischeTherapieerfolge werden auch durch den Einsatz von Disopyramid beschrieben [27], allerdings ist dieses ursprünglich als Antiarrhythmikum eingesetzte Medikament mit negativer Inotropie in Deutschland nicht mehr zugelassen.”
BackgroundMaron, B. J., Maron, M. S., Sherrid, M. V., Ommen, S. R., & Rowin, E. J. (2022) · The American Journal of Cardiology · doi:10.1016/j.amjcard.2022.07.033 · Cited by 4
Efthimiadis, G. K., Pagourelias, E. D., Zegkos, T., Parcharidou, D. G., Panagiotidis, T., Arvanitaki, A., Rouskas, P., & Karvounis, H. I. (2016) · Reviews in Cardiovascular Medicine · doi:10.3909/ricm0816 · Cited by 4
Thirty Controversies and Considerations in Hypertrophic Cardiomyopathy
Masri, A., Nazer, B., Al‐Rashdan, L., Mannello, M., Fischer, K. L., Akhavein, R., Divanji, P., Song, H. K., & Heitner, S. B. (2020) · Structural Heart · doi:10.1080/24748706.2020.1844926 · Cited by 4
A complex unit for a complex disease: the HCM-Family Unit
Vriz, O., Alsergani, H., Elshaer, A. N., Shaik, A., Mushtaq, A. H., Lioncino, M., Alamro, B., Monda, E., Caiazza, M., Mauro, C., et al. (2021) · Monaldi Archives for Chest Disease · doi:10.4081/monaldi.2021.2147 · Cited by 5
Cardiovascular causes of complex breathlessness
Kerrigan, W. J., Murphy, T. M., & Lyon, A. R. (2022) · European Respiratory Society eBooks · doi:10.1183/2312508x.10013521 · Cited by 4
Hypertrophic Cardiomyopathy in Infants and Children
Luís, E., & Moreyr, E. (2012) · InTech eBooks · doi:10.5772/29763 · Cited by 4
Saito, M., Okayama, H., Yoshii, T., Hiasa, G., Sumimoto, T., Inaba, S., Nishimura, K., Inoue, K., Ogimoto, A., Shigematsu, Y., et al. (2010) · Journal of Cardiovascular Pharmacology · doi:10.1097/fjc.0b013e318203830d · Cited by 4
“In summary, all the above drugs are probably effective in improving LV diastolic function in patients with HOCM.”
BackgroundInfluentialEchocardiography in the Evaluation and Management of Patients with Hypertrophic Cardiomyopathy
Woo, A., Wigle, E. D., & Rakowski, H. (2007) · Elsevier eBooks · doi:10.1016/b978-1-4160-3640-1.50032-0 · Cited by 4
Lifestyle Modification and Medical Management of Hypertrophic Cardiomyopathy
Heitner, S. B., & Fischer, K. L. (2019) · Cardiology Clinics · doi:10.1016/j.ccl.2018.08.004 · Cited by 3
Alfarano, M., Ciccarelli, F., Marchionni, G., Ballatore, F., Costantino, J., Lattanzio, A., Pecci, G., Stavagna, S., Iannelli, L., Galardo, G., et al. (2025) · Journal of Clinical Medicine · doi:10.3390/jcm14124228 · Cited by 3
“ESC guidelines [2] suggest mavacamten as an intermediate option compared to surgery; instead, AHA/ACC guidelines [14] consider CMIs on the same level, as an alternative to invasive therapies.”
Panichella, G., Garofalo, M., Ragagnin, M., Fanizzi, A. I., Zampieri, M., Franco, A. D., Cappelli, F., Pieroni, M., & Olivotto, I. (2025) · Current Cardiology Reports · doi:10.1007/s11886-025-02316-6 · Cited by 3
“Disopyramide, historically considered the most potent negative inotrope for oHCM, has demonstrated efficacy in reducing LVOT gradients and deferring SRT in long-term observational studies [80].”
Rowin, E. J., Siontis, K. C., OWENS, A. T., Olivotto, I., Moussavi‐Harami, F., Michels, M., Ommen, S. R., García‐Pavía, P., Nazer, B., Silver, J., et al. (2026) · Heart Rhythm · doi:10.1016/j.hrthm.2026.03.1961 · Cited by 3
Baseline and Longitudinal Imaging of Hypertrophic Cardiomyopathy in the Era of Emerging Therapeutics
Altibi, A. M. A., Alani, A., Zhao, Y., & Masri, A. (2023) · Current Cardiology Reports · doi:10.1007/s11886-023-01883-w · Cited by 3
Concomitant Aficamten and Disopyramide in Symptomatic Obstructive Hypertrophic Cardiomyopathy
Masri, A., Maron, M. S., Abraham, T. P., Nassif, M. E., Villa, R. B., Bilen, O., COATS, C. J., Elliott, P., García‐Pavía, P., Massera, D., et al. (2025) · JACC Heart Failure · doi:10.1016/j.jchf.2025.03.008 · Cited by 3
Chen, F., Feng, L.-Y., Zhao, A.-Q., Zhang, Y., Li, J., Zhu, Y.-J., Jia, Y., Zhang, Y.-N., Zheng, Y., Lv, Y., et al. (2025) · The Journal of Organic Chemistry · doi:10.1021/acs.joc.5c00677 · Cited by 3
Gaballa, A., Jadam, S., & Desai, M. Y. (2024) · Expert Opinion on Pharmacotherapy · doi:10.1080/14656566.2024.2362902 · Cited by 3
“However, this difference was not statistically significant [23].”
BackgroundHarano, Y., Kawase, Y., & Matsuo, H. (2022) · European Heart Journal - Case Reports · doi:10.1093/ehjcr/ytac311 · Cited by 3
“To manage the pressure gradient, beta-blockade with Class 1A anti-arrhythmic drugs have been recommended.(3,4) In this case, intravenous propranolol .”
BackgroundTherapeutic options in hypertrophic cardiomyopathy: A pediatric perspective
Rhee, E. K., Nigro, J. J., & Pophal, S. G. (2008) · Current Treatment Options in Cardiovascular Medicine · doi:10.1007/s11936-008-0035-8 · Cited by 3
HYPERTROPHIC OBSTRUCTIVE CARDIOMYOPATHY
Осиев, А. Г., Naydenov, R., Kretov, E. I., Obedinskaya, N. R., & Kurbatov, V. P. (2016) · Almanac of Clinical Medicine · doi:10.18786/2072-0505-2015-38-95-104 · Cited by 3
Faber, L. (2017) · Elsevier eBooks · doi:10.1016/b978-0-323-47870-0.00024-6 · Cited by 3
Colan, S. D., & Margossian, R. E. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-802393-8.00019-3 · Cited by 3
Pacing for drug-refractory or drug-intolerant hypertrophic cardiomyopathy
Qintar, M., Morad, A., Charbaji, K., Alhawasli, H., Essali, A., & Kadro, W. Y. (2010) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd008523 · Cited by 3
Nair, A. P., Xie, L. X., & Enciso, J. S. (2023) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2022.10.018 · Cited by 3
Stereoselective block of the hERG potassium channel by the Class Ia antiarrhythmic drug disopyramide
Zhang, Y., Harchi, A. E., James, A. F., Oiki, S., Dempsey, C. E., & Hancox, J. C. (2024) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-024-05498-4 · Cited by 2
Zakynthinos, G. Ε., Gialamas, I., Tsolaki, V., Pantelidis, P., Goliopoulou, A., Gounaridi, M. I., Tzima, I. G., Xanthopoulos, A. V., Kalogeras, K. I., Siasos, G., et al. (2024) · Journal of Cardiovascular Development and Disease · doi:10.3390/jcdd11120401 · Cited by 2
“Disopyramide is an effective antiarrhythmic drug used in the management of HCM, particularly for reducing LVOTO [72].”
54-Year-Old Woman With Progressive Dyspnea on Exertion and Syncopal Episodes
Sánchez-Álvarez, C., Oluleye, O. W., & Blackshear, J. L. (2017) · Mayo Clinic Proceedings · doi:10.1016/j.mayocp.2016.10.021 · Cited by 2
Diagnosis and Treatment of Hypertrophic Cardiomyopathy
Saraiva, F., Fernandes, F., Romano, M. M. D., Cardoso, J. N., Soliani, M. T., Madison, M. M., Schmidt, A., & Simões, M. V. (2023) · ABC Heart Failure & Cardiomyopathy · doi:10.36660/abchf.20230040 · Cited by 2
Alharbi, T. Y., Alnadawi, H. A., Almutairi, G. M., Altheyab, F. Y., Aldoweesh, O. H., Alfehaid, O. S., Alhaj, A. A., Alotaibi, A. M., & Zweihary, A. M. A. (2024) · Cureus · doi:10.7759/cureus.70550 · Cited by 2
Harada, P. H. N., Morita, F., Arteaga, E., Shiozaki, A. A., & Castelli, J. B. (2008) · Arquivos Brasileiros de Cardiologia · doi:10.1590/s0066-782x2008000100010 · Cited by 2
Nomura, T., Kojima, A., Urakabe, Y., Enomoto, S., Nishikawa, S., Keira, N., Matsubara, H., & Tatsumi, T. (2010) · International Journal of Cardiology · doi:10.1016/j.ijcard.2010.09.001 · Cited by 2
“The class Ia antiarrhythmic agent, disopyramide has been demonstrated to reduce the LVOT pressure gradient and improve the clinical prognosis of the patients with hypertrophic obstructive cardiomyopathy [4].”
BackgroundRecent Advances in the Pharmacological Management of Atrial Fibrillation
Gooden, J. Y., Powell, B. D., Akogyeram, C. O., & Melduni, R. M. (2013) · American Journal of Therapeutics · doi:10.1097/mjt.0b013e31828d4532 · Cited by 2
“Disopyramide is also useful for reducing LV outflow gradients in patients with hypertrophic cardiomyopathy, especially when BB treatment is contraindicated.(43) It is noted to have more adverse effects, including heart failure, although efficacy for maintaining sinus rhythm 6 months after cardioversion was comparable…”
BackgroundSandín, M., Marín, F. R., Cambronero, F., Climent, V. E., Martínez, C. C., Martı́nez, J. G., García‐Honrubia, A., Alberola, A. G., de la Morena, G., Valdés, M., et al. (2009) · Revista Española de Cardiología (English Edition) · doi:10.1016/s1885-5857(09)73350-x · Cited by 2
“8 A fair number of patients will continue to have disabling symptoms despite optimized medical therapy, however.”
BackgroundHeart Failure as a Consequence of Hypertrophic Cardiomyopathy
Marian, A. J. (2020) · Elsevier eBooks · doi:10.1016/b978-0-323-60987-6.00023-5 · Cited by 2
Anti-arrhythmic Drugs—a Review and Comment on Relevance in the Current Era: Part 1
Hanayneh, S., Panna, M. E., Miles, W. M., & Goel, R. (2021) · Current Treatment Options in Cardiovascular Medicine · doi:10.1007/s11936-021-00940-3 · Cited by 2
“More importantly, disopyramide had found a niche use in patients with hypertrophic obstructive cardiomyopathy (HOCM) due to its negative inotropic effects on the LV myocardium which can result in up to 50% drop in the dynamic ventriculo-aortic outflow gradient in two-thirds of patients [27].”
BackgroundElliot, P. M., Noutsias, M., & Anastasakis, A. (2023) · doi:10.1093/med/9780198891628.003.0008 · Cited by 2
Hypertrophic Cardiomyopathy in Childhood
Maron, B. J., & Maron, M. S. (2013) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2011.12.064 · Cited by 2
Hanna, E. B. (2017) · doi:10.1002/9781119233503.ch7 · Cited by 2
Metadata
- Authors
- Sherrid, M. V., Barac, I., McKenna, W. J., Elliott, P. M., Dickie, S., Chojnowska, L., Casey, S., & Maron, B. J.
- Affiliations
- St. Luke's-Roosevelt Hospital Center (US)
- St George's, University of London (GB)
- Institute of Cardiology (PL)
- Minneapolis Heart Institute Foundation (US)
- Corresponding author
- Sherrid, Mark V.
- Venue
- Journal of the American College of Cardiology
- Publisher
- Elsevier BV
- Published
- 2005-04
- Volume
- 45
- Issue
- 8
- Pages
- 1251-1258
- ISSN
- 0735-1097 (ISSN-L)
- OpenAlex
- W1992100033
- Cited by
- 410
- References
- 52
- Citations by year
- 2026: 12 · 2025: 35 · 2024: 34 · 2023: 24 · 2022: 23 · 2021: 23 · 2020: 20 · 2019: 14 · 2018: 19 · 2017: 16 · 2016: 15 · 2015: 17 · 2014: 27 · 2013: 18 · 2012: 22
- FWCI
- 8.45
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Journal of the American College of Cardiology (publishedVersion)
- PubMed (publishedVersion)
- UCL Discovery (University College London) (submittedVersion)
- Topics
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiomyopathy and Myosin Studies
- Health Sciences › Medicine › Infectious Diseases › Viral Infections and Immunology Research
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Blood Pressure and Hypertension Studies
- Keywords
- disopyramide, hypertrophic obstructive cardiomyopathy, left ventricular outflow tract gradient, long-term efficacy, drug safety, sudden cardiac death, cardiac mortality, drug-induced arrhythmia, beta-blockers, myectomy, alcohol septal ablation, NYHA functional class
- MeSH terms
- Administration, Oral, Adrenergic beta-Antagonists, Anti-Arrhythmia Agents, Cardiomyopathy, Hypertrophic, Disopyramide, Echocardiography, Female, Humans, Male, Middle Aged, Myocardial Contraction, Safety, Death, Sudden, Cardiac, Treatment Outcome
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review