Independent predictors of hypertrophic cardiomyopathy-related mortality or life-threatening events were younger age at diagnosis (P < .001), female sex (P …
A few of the common treatment include:Managing hypertrophic cardiomyopathy varies from one patient to another. and L.G. The results for each group showed similar trends compared with the overall results but the statistic power was lower.
The prognostic role of FHSD varied in previous studies (significant as an independent factorLarge wall thickness (MWTh) ≥30 mm and non-sustained ventricular tachycardia in Holter monitoring of electrocardiography also appeared to be important prognostic factors in both cardiovascular death and sudden cardiac death, as suggested in previous studiesPrevious studies indicated male patients had a 3:2 predominance (59%)Advanced heart failure (NYHA III/IV) was reported as an independent predictor of cardiovascular mortality in end-stage HCMLeft atrial diameter (LAD) and left ventricle ejection fraction (LVEF) are routine echocardiographic parameters used to assess cardiac function, but previous studiesOur study has several limitations.
This makes it hard for the heart to relax and reduces the amount of blood the ventricle can hold and send to the body with each heartbeat.People with hypertrophic cardiomyopathy also have an abnormal arrangement of heart muscle cells (myofiber disarray).
Hypertrophic cardiomyopathy or HCM is a condition where hypertrophy or thickening of the heart muscle occurs.
[{Review}]. The pooled 1-, 3-, 5- and 10-year survival rates were 98.0%, 94.3%, 82.2% and 75.0%, respectively.
D.L. Cardiomyopathy life expectancy depends on the causes, types and severity of the cardiomyopathy. Our articles are resourced from reputable online pages. The situation leads to enlargement of the muscle cells, and the scarring grows between the cells.
Until now, experts associated with cardiology studies have unable to know the exact numbers of years a woman may survive with the problem of cardiomyopathy. Among patients with HCM, age, NYHA functional class, family history of sudden death (FHSD), syncope, atrial fibrillation, non-sustained ventricular tachycardia (nsVT), maximum left ventricular wall thickness and obstruction were significant prognostic factors for cardiovascular death.
Shin, D. G., Son, J., Park, J. Y., Choi, J. W. & Ryu, S. K. Impact of Coronary Artery Anatomy on Clinical Course and Prognosis in Apical Hypertrophic Cardiomyopathy: Analysis of Coronary Angiography and Computed Tomography.
McKenna, W. J., Franklin, R. C., Nihoyannopoulos, P., Robinson, K. C. & Deanfield, J. E. Arrhythmia and prognosis in infants, children and adolescents with hypertrophic cardiomyopathy.
Arteaga, E., Ianni, B. M., Fernandes, F. & Mady, C. Benign outcome in a long-term follow-up of patients with hypertrophic cardiomyopathy in Brazil. Losi, M. A., Betocchi, S. & Barbati, G. Prognostic Significance of Left Atrial Volume Dilatation in Patients with Hypertrophic Cardiomyopathy. Spectrum and prognostic significance of arrhythmias on ambulatory Holter electrocardiogram in hypertrophic cardiomyopathy. & Altman, D. G. Academia and Clinic Annals of Internal Medicine Preferred Reporting Items for Systematic Reviews and Meta-Analyses: Karlson, B. W., Sjolin, M., Lindqvist, J., Caidahl, K. & Herlitz, J. Ten-year mortality rate in relation to observations at a bicycle exercise test in patients with a suspected or confirmed ischemic event but no or only minor myocardial damage: influence of subsequent revascularization. A single copy of these materials may be reprinted for noncommercial personal use only.
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