The challenges in diagnosing hypertrophic cardiomyopathy in the presence of arterial hypertension: a clinical case
DOI:
https://doi.org/10.14739/2310-1210.2024.4.300534Keywords:
hypertrophic cardiomyopathy, hypertension, clinical case, left ventricle hypertrophyAbstract
Aim. To describe a clinical case and analyze the challenges in diagnosing hypertrophic cardiomyopathy (HCM) in a patient with concomitant arterial hypertension (AH).
Materials and methods. The article presents the clinical case of HCM in the patient with concomitant AH that was observed in an ambulatory setting in the Municipal Enterprise “Dnipropetrovsk Regional Clinical Center for Diagnostics and Treatment” of Dnipropetrovsk Regional Council.
Results. A 66-year-old woman N., diagnosed by her family physician with coronary artery disease (CAD): stable angina FC II, grade 2 AH, chronic heart failure FC II NYHA, was referred to a cardiologist because of experiencing exertional dyspnea, chest pain, and uncontrolled blood pressure despite treatment compliance.
Echocardiography identified concentric left ventricular hypertrophy with the left ventricular outflow tract (LVOT) obstruction (a mean gradient of 35 mmHg as per catheterization). Cardiac MRI confirmed the diagnosis and coronary angiography ruled out CAD. Adjustments to the treatment regimen, taking into account HCM with LVOT obstruction, effectively alleviated the patient’s symptoms and stabilized her blood pressure.
Conclusions. It is especially important to follow the guidelines of AH management and perform echocardiography in all patients with high blood pressure, so as not to miss the signs of concomitant HCM, particularly with LVOT obstruction. In addition, in the case of HCM, it is necessary to timely detect, provide prevention and manage patients at risk for sudden cardiac death. Since HCM encompasses various diagnoses with different pathogenesis and distinct management, cardiac MRI, enzymatic or genetic testing may be needed according to guidelines.
As HCM is a relatively common inherited cardiac disease, general practitioners could often encounter such patients in everyday clinical practice. Hence, they should have a certain suspicion of this diagnosis in persons with AH whose left ventricular mass meets the criteria for HCM.
References
Maron BJ. Clinical Course and Management of Hypertrophic Cardiomyopathy. N Engl J Med. 2018 Aug 16;379(7):655-668. doi: https://doi.org/10.1056/NEJMra1710575
Pasqualucci D, Iacovoni A, Palmieri V, De Maria R, Iacoviello M, Battistoni I, et al. Epidemiology of cardiomyopathies: essential context knowledge for a tailored clinical work-up. Eur J Prev Cardiol. 2022;29(8):1190-9. doi: https://doi.org/10.1093/eurjpc/zwaa035
Arbelo E, Protonotarios A, Gimeno JR, Arbustini E, Barriales-Villa R, Basso C, et al. 2023 ESC Guidelines for the management of cardiomyopathies. Eur Heart J. 2023;44(37):3503-626. doi: https://doi.org/10.1093/eurheartj/ehad194
Ommen SR, Mital S, Burke MA, Day SM, Deswal A, Elliott P, et al. 2020 AHA/ACC Guideline for the Diagnosis and Treatment of Patients With Hypertrophic Cardiomyopathy: A Report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice Guidelines. Circulation. 2020;142(25):e558-631. doi: https://doi.org/10.1161/cir.0000000000000937
Sayin BY, Oto A. Left Ventricular Hypertrophy: Etiology-Based Therapeutic Options. Cardiol Ther. 2022;11(2):203-30. doi: https://doi.org/10.1007/s40119-022-00260-y
Mancia G, Kreutz R, Brunström M, Burnier M, Grassi G, Januszewicz A, et al. 2023 ESH Guidelines for the management of arterial hypertension The Task Force for the management of arterial hypertension of the European Society of Hypertension: Endorsed by the International Society of Hypertension and the European Renal Association. J Hypertens. 2023;41(12):1874. doi: https://doi.org/10.1097/hjh.0000000000003480
Arabadjian M, Nicolas B, Montgomery S, Pleasure M, Collins M, Reuter M, et al. Clinical course and outcomes in adults with co-occurring hypertrophic cardiomyopathy and hypertension: a scoping review protocol. BMJ Open. 2023;13(7):e075087. doi: https://doi.org/10.1136/bmjopen-2023-075087
Seferović PM, Polovina M, Bauersachs J, Arad M, Ben Gal T, Lund LH, et al. Heart failure in cardiomyopathies: a position paper from the Heart Failure Association of the European Society of Cardiology. Eur J Heart Fail. 2019;21(5):553-76. doi: https://doi.org/10.1002/ejhf.1461
Nielsen JC, Lin YJ, de Oliveira Figueiredo MJ, Sepehri Shamloo A, Alfie A, Boveda S, et al. European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) expert consensus on risk assessment in cardiac arrhythmias: use the right tool for the right outcome, in the right population. EP Eur. 2020;22(8):1147-8. doi: https://doi.org/10.1002/joa3.12338
Menghoum N, Vos JL, Pouleur AC, Nijveldt R, Gerber BL. How to evaluate cardiomyopathies by cardiovascular magnetic resonance parametric mapping and late gadolinium enhancement. Eur Heart J Cardiovasc Imaging. 2022;23(5):587-9. doi: https://doi.org/10.1093/ehjci/jeac051
Visseren FL, Mach F, Smulders YM, Carballo D, Koskinas KC, Bäck M, et al. 2021 ESC Guidelines on cardiovascular disease prevention in clinical practice. Eur Heart J. 2021;42(34):3227-337. doi: https://doi.org/10.1093/eurheartj/ehab484
Shin YJ, Lee JH, Yoo JY, Kim JA, Jeon Y, Yoon YE, et al. Clinical significance of evaluating coronary atherosclerosis in adult patients with hypertrophic cardiomyopathy who have chest pain. Eur Radiol. 2019;29(9):4593-602. doi: https://doi.org/10.1007/s00330-018-5951-8
Klopotowski M, Kukula K, Jamiolkowski J, Oreziak A, Dabrowski M, Chmielak Z, et al. Sudden cardiac death risk over time in HCM patients with implantable cardioverter-defibrillator. J Clin Med. 2022;11(6):1633. doi: https://doi.org/10.3390%2Fjcm11061633
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