here are 2 types of hypertrophic obstructive cardiomyopathy (HOCM): obstruction at the subaorta, called idiopathic hypertrophic subaortic stenosis (IHSS), 1 and obstruction at the mid left ventricle. 2 In contrast to the many studies of IHSS, only a few studies, other than case reports, have focused on midventricular obstruction (MVO). Two patients with MVO were reported for the first time in 1976 by Falicov et al, 2 one of whom suddenly died shortly after unsuccessful myectomy. Maron et al elucidated that the left ventricular pressure gradient (LVPG) was related to even prognosis in patients with hypertrophic cardiomyopathy (HCM). 3 Thus, attenuation of the LVPG has recently become an important strategy in the management of patients with HOCM.In the clinical setting, patients with MVO may often be overlooked. Very recently we reported that there are 2 specific patterns of carotid pulse tracing in these patients, 4 by which they may be diagnosed with ease. As to the treatment of patients with MVO, Hintringer et al reported the usefulness of permanent DDD pacing to alleviate LVPG and symptoms in an 85-year-old woman with MVO who did not respond to pharmacological therapy. 5 In patients with MVO, unlike those with IHSS, therapies involving myotomy or myectomy and alcohol septal ablation require great caution to prevent the induction or deterioration of mitral regurgitation. Both -blockers and calcium antagonists are often insufficient for attenuating LVPG. In 1982, Pollick reported the usefulness of the antiarrhythmic drug disopyramide in attenuating LVPG in IHSS. 6 Unfortunately sustained use of disopyramide is difficult owing to the thirst, dysuria and so on related to its strong anticholinergic action. We previously reported the usefulness of the antiarrhythmic drug, cibenzoline, the anticholinergic action of which is very weak, 7 to attenuate LVPG in IHSS. 8 In the present study, therefore, we examined the acute and chronic effect of cibenzoline on LVPG and left ventricular (LV) diastolic dysfunction in patients with MVO.
Methods
Study SubjectsTwenty-three patients with MVO participated in this study after giving written informed consent. Twenty healthy control subjects served as the comparison of the hemo-