The DOI matches its Crossref record; 5 of the 5 references it cites were found in a registry or an index.
Mavacamten for treatment of symptomatic obstructive hypertrophic cardiomyopathy (EXPLORER-HCM): health status analysis of a randomised, double-blind, placebo-controlled, phase 3 trial
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
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?
Mavacamten was associated with a significant reduction in left ventricular outflow tract gradient and improvement in quality of life as measured by the Kansas City Cardiomyopathy Questionnaire compared with placebo.
“Mavacamten was associated with a significant reduction in LVOT gradient and improvement in quality of life as measured by the Kansas City Cardiomyopathy Questionnaire, compared with placebo.47”
From Current management of hypertrophic cardiomyopathy (2025) · cites this paper as [47]
Citations
Cites
Osterberg, L., & Blaschke, T. (2005) · New England Journal of Medicine · doi:10.1056/nejmra050100 · Cited by 7,974
An Assessment of Clinically Useful Measures of the Consequences of Treatment
Laupacis, A., Sackett, D. L., & Roberts, R. S. (1988) · New England Journal of Medicine · doi:10.1056/nejm198806303182605 · Cited by 1,681
Hypertrophic Cardiomyopathy: Genetics, Pathogenesis, Clinical Manifestations, Diagnosis, and Therapy
Marian, A. J., & Braunwald, E. (2017) · Circulation Research · doi:10.1161/circresaha.117.311059 · Cited by 1,403
Kosiborod, M. N., Jhund, P. S., Docherty, K. F., Diez, M., Petrie, M. C., Verma, S., Nicolau, J. C., Merkely, B., Kitakaze, M., DeMets, D. L., et al. (2020) · Circulation · doi:10.1161/circulationaha.119.044138 · Cited by 350
Reynolds, M. R., Magnuson, E. A., Wang, K., Thourani, V. H., Williams, M., Zajarias, A., Rihal, C. S., Brown, D. L., Smith, C. R., Leon, M. B., et al. (2012) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2012.03.075 · Cited by 295
Flagged first, then by citations
Research works printed but not linked: 30
- Maron, 2018, Clinical Course and management of hypertrophic cardiomyopathy, N Engl J Med, 379, 655, 10.1056/NEJMra1710575 · DOI · Paper page
- Zaiser, 2020, Patient experiences with hypertrophic cardiomyopathy: a conceptual model of symptoms and impacts on quality of life, J Patient Rep Outcomes, 4, 102, 10.1186/s41687-020-00269-8 · DOI
- Elliott, 2014, 2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy: the Task Force for the Diagnosis and Management of Hypertrophic Cardiomyopathy of the European Society of Cardiology (ESC), Eur Heart J, 35, 2733, 10.1093/eurheartj/ehu284 · DOI · Paper page
- Ommen, 2020, 2020 AHA/ACC guideline for the diagnosis and treatment of patients with hypertrophic cardiomyopathy: executive summary: a report of the American College of Cardiology/American Heart Association Joint Committee on clinical practice guidelines, Circulation, 142, e533
- Rastegar, 2017, Results of surgical septal myectomy for obstructive hypertrophic cardiomyopathy: the Tufts experience, Ann Cardiothorac Surg, 6, 353, 10.21037/acs.2017.07.07 · DOI
- Khalil, 2017, Hypertrophic obstructive cardiomyopathy-the Leipzig experience, Ann Cardiothorac Surg, 6, 337, 10.21037/acs.2017.07.09 · DOI
- Fortunato de Cano, 2016, Long-term clinical follow-up of patients undergoing percutaneous alcohol septal reduction for symptomatic obstructive hypertrophic cardiomyopathy, Catheter Cardiovasc Interv, 88, 953
- Green, 2016, A small-molecule inhibitor of sarcomere contractility suppresses hypertrophic cardiomyopathy in mice, Science, 351, 617, 10.1126/science.aad3456 · DOI
- Papadakis, 2020, Mavacamten: treatment aspirations in hypertrophic cardiomyopathy, Lancet, 396, 736, 10.1016/S0140-6736(20)31793-1 · DOI
- Ho, 2020, Study design and rationale of EXPLORER-HCM: evaluation of mavacamten in adults with symptomatic obstructive hypertrophic cardiomyopathy, Circ Heart Fail, 13, 10.1161/CIRCHEARTFAILURE.120.006853 · DOI
- Olivotto, 2020, Mavacamten for treatment of symptomatic obstructive hypertrophic cardiomyopathy (EXPLORER-HCM): a randomised, double-blind, placebo-controlled, phase 3 trial, Lancet, 396, 759, 10.1016/S0140-6736(20)31792-X · DOI · Paper page
- Green, 2000, Development and evaluation of the Kansas City Cardiomyopathy Questionnaire: a new health status measure for heart failure, J Am Coll Cardiol, 35, 1245, 10.1016/S0735-1097(00)00531-3 · DOI · Paper page
- Huff, 2013, Correlations between physician-perceived functional status, patient-perceived health status, and cardiopulmonary exercise results in hypertrophic cardiomyopathy, Qual Life Res, 22, 647, 10.1007/s11136-012-0182-y · DOI
- Heidenreich, 2006, Health status identifies heart failure outpatients at risk for hospitalization or death, J Am Coll Cardiol, 47, 752, 10.1016/j.jacc.2005.11.021 · DOI
- Soto, 2004, Prognostic value of health status in patients with heart failure after acute myocardial infarction, Circulation, 110, 546, 10.1161/01.CIR.0000136991.85540.A9 · DOI
- Chan, 2009, Patient health status and costs in heart failure: insights from the eplerenone post-acute myocardial infarction heart failure efficacy and survival study (EPHESUS), Circulation, 119, 398, 10.1161/CIRCULATIONAHA.108.820472 · DOI
- Spertus, 2005, Monitoring clinical changes in patients with heart failure: a comparison of methods, Am Heart J, 150, 707, 10.1016/j.ahj.2004.12.010 · DOI
- Dreyer, 2016, Quantifying clinical change: discrepancies between patients' and providers' perspectives, Qual Life Res, 25, 2213, 10.1007/s11136-016-1267-9 · DOI
- Spertus, 2020, Interpreting the Kansas City Cardiomyopathy Questionnaire in clinical trials and clinical care: JACC state-of-the-art review, J Am Coll Cardiol, 76, 2379, 10.1016/j.jacc.2020.09.542 · DOI · Paper page
- Kosiborod, 2007, Identifying heart failure patients at high risk for near-term cardiovascular events with serial health status assessments, Circulation, 115, 1975, 10.1161/CIRCULATIONAHA.106.670901 · DOI
- Pokharel, 2017, Association of serial Kansas City Cardiomyopathy Questionnaire assessments with death and hospitalization in patients with heart failure with preserved and reduced ejection fraction: a secondary analysis of 2 randomized clinical trials, JAMA Cardiol, 2, 1315, 10.1001/jamacardio.2017.3983 · DOI
- Ho, 2021, Guidelines on the verge of a more evidence-based era for hypertrophic cardiomyopathy, Circulation, 143, 295, 10.1161/CIRCULATIONAHA.120.050608 · DOI
- Heidenreich, 2020, 2020 ACC/AHA clinical performance and quality measures for adults with heart failure: a report of the American College of Cardiology/American Heart Association Task Force on Performance Measures, J Am Coll Cardiol, 76, 2527, 10.1016/j.jacc.2020.07.023 · DOI
- Flynn, 2012, Relationships between changes in patient-reported health status and functional capacity in outpatients with heart failure, Am Heart J, 163, 88, 10.1016/j.ahj.2011.09.027 · DOI
- Arnold, 2020, Health status changes and outcomes in patients with heart failure and mitral regurgitation: COAPT trial, J Am Coll Cardiol, 75, 2099, 10.1016/j.jacc.2020.03.002 · DOI
- Solomon, 2019, Angiotensin-neprilysin inhibition in heart failure with preserved ejection fraction, N Engl J Med, 381, 1609, 10.1056/NEJMoa1908655 · DOI · Paper page
- Teerlink, 2021, Cardiac myosin activation with omecamtiv mecarbil in systolic heart failure, N Engl J Med, 384, 105, 10.1056/NEJMoa2025797 · DOI · Paper page
- Maurer, 2018, Tafamidis Treatment for patients with transthyretin amyloid cardiomyopathy, N Engl J Med, 379, 1007, 10.1056/NEJMoa1805689 · DOI · Paper page
- Greene, 2018, Medical therapy for heart failure with reduced ejection fraction: the CHAMP-HF registry, J Am Coll Cardiol, 72, 351, 10.1016/j.jacc.2018.04.070 · DOI
- Haynes, 2002, Helping patients follow prescribed treatment: clinical applications, JAMA, 288, 2880, 10.1001/jama.288.22.2880 · DOI · Paper page
Cited by
Sorted by citations
Current management of hypertrophic cardiomyopathy
Sikand, N., Stendahl, J., Sen, S., Lampert, R., & Day, S. (2025) · BMJ · doi:10.1136/bmj-2023-077274 · Cited by 26
Metadata
- Authors
- Spertus, J. A., Fine, J. T., Elliott, P., Ho, C. Y., Olivotto, I., Saberi, S., Li, W., Dolan, C., Reaney, M., Sehnert, A. J., & Jacoby, D.
- Venue
- The Lancet
- Publisher
- Elsevier BV
- Published
- 2021-06
- Volume
- 397
- Issue
- 10293
- Pages
- 2467-2475
- ISSN
- 0140-6736
- Cited by
- 220
- References
- 5
- Language
- en
- Licence
- Funders
- MyoKardia
- Shire
- Sanofi Genzyme
- Bayer Fund
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