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拡張型心筋症(dilated cardiomyopathy,DCM)の予後は明らかに不良で,死亡例の約半数は突然死である1)。その機序については必ずしも明らかではないが,ほとんどが重篤な不整脈によるものと考えられている。
本症の心筋には,変性,線維化および肥大などの病変を広範に認めるが,これらの心筋病変の広がりや程度によっては,刺激伝導系にも種々の障害を起こし得る2)。
Electrophysiological study was performed in 29 cases with dilated cardiomyopathy (DCM). Prolongations of maximum corrected sinus node recovery time and sino-atrial conduction time were found in 7(24.1%) and 8 cases (27.6%), respectively. Prolongations of PA, AH, H, HV interval and QRS duration were found in 4 (13.8%), 8 (27.6%), 16 (57.1%*), 17 (60.7%*) and 17 (60.7%), respectively.
The mean value of HRAmax/HRAc in DCM group was higher than in control group significantly (p< 0.001). Atrial fibrillation after rapid atrial pacing (< 250/m) or atrial extrastimulus method appeared in 6 cases (20.7%) in DCM group and none in control group. These results showed the enhanced atrial vulnera-bility in DCM group.
A-V nodal conduction disturbance was found in 12 cases (41.4%) when these disturbances were evaluated by prolongation of AH interval in His bundle electro-gram and latent conduction disturbance judged by atrial pacing
During the follow up period, 8 of 29 cases (27.6%) were suddenly dead, A-V conduction disturbance, espe-cially in His-purkinje system was highly demonstrated in their His bundle electrograms.
*except a case with complete A-V block
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