Læknablaðið : fylgirit - 01.06.1982, Qupperneq 26

Læknablaðið : fylgirit - 01.06.1982, Qupperneq 26
14 CARDIAC ARRHYTHÍ-IIAS IN HYPERTROPHIC CARDIOMYOPT'THY. Ingvar Bjamason, Thordur Hardarson, Stefan Jonsson, Reykjavik City Hospital, Itedical Departinent. Patients with hypertrophic cardioiryopathy (HC) frequently die suddenly and unexpectedly, presumably from cardiac arrhythinias. We studied by 24-hour Holter ambulatory monitor- ing 51 close relatives of eight patients with HC v/ho came to autopsy in Iceland during the years 1966 to 1577. A total of 11 patients with the disease were autopsied during these years. Twenty two of the relatives had HC as defined by an echocardio- graphic demonstration of inordinate septal thickening ( 1.3cm) Nineteen of them were asymptomatic, tv.o were in New York Heart Association Class III and one in Class IV. Twenty nine relatives and 40 normal subjects served as control groups. All were without symptoms.Seven patients had >. 50 supraventric- ular extrasystoles per day, but only one subject in the group of relatives and one in the control group. Eight patients with hypertrophic cardiomyopathy had supraventricular arrhythm- ias. Three patients with hypertrophic cardiomyopathy had runs of ventricular tachycardia but none in the two other groups. TWo patients with hypertrophic cardiomyopathy had coupled ventricular ectopic beats, one in the normal control group. Nine patients with hypertrophic cardioiryopathy had multiform ventricular ectopics, one in the normal group. Twelve patients with hypeirtrophic cardiomyopathy had more than 10 ventricular extrasystoles per day as conpared with four in the control group and two in the group of relatives. This study shows: 1) A strong correlation between in- ordinate septal thickening and arrhythmia in a (mostly) asymptomatic group of relatives of patients with HC, suggesting that they do also suffer from HC. 2) That many relatives of patients with HC have an unexpectedly hich incidence of arrhythmias, perhaps putting them at risk of dying suddenly. Relatives of patients with HC should be studied by echocardio- graphy and subsequently Holter monitoring if a thickened inter- ventricular septum is demonstrated.
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