Classification of the Site of Ventricular Septal Defect with 2-Dimensional Doppler Echocardiography.
10.4070/kcj.1990.20.1.19
- Author:
Duk Kyung KIM
;
Young Dae KIM
;
Dong Jin OH
;
Chee Jeong KIM
;
Myoung Mook LEE
;
Young Bae PARK
;
Yun Shik CHOI
;
Jung Don SEO
;
Young Woo LEE
- Publication Type:Original Article
- Keywords:
Apical hypertrophic cardiomyopathy
- MeSH:
Asian Continental Ancestry Group;
Atrial Fibrillation;
Blood Pressure;
Cardiac Catheterization;
Cardiac Catheters;
Cardiomyopathy, Hypertrophic;
Classification*;
Diagnosis;
Echocardiography;
Echocardiography, Doppler*;
Follow-Up Studies;
Heart Septal Defects, Ventricular*;
Humans;
Hypertrophy;
Phenotype;
Prevalence;
Systole;
Thorax
- From:Korean Circulation Journal
1990;20(1):19-28
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Seventeen cases of apical hypertrophic cardiomyopthy were reviewed to clarify whether there is any racial difference in phenotypic expression of apical hypertrophic cardiomopathy and to study whether there is any clinical or morphological difference between apical hypertrophic cardiomyopathy of Japanese type (J-APH) and apical hypertrophic cardiomyophthy of non-Japanese type (NJ-APH). The diagnosis was made by cardiac catheterization, left ventriculography and echocardiography. Seventeen patients were divided into 9 (53%) patients with J-APH and 8 (47%) patients with NJ-APH. Mean ages of patients with J-APH and NJ-APH were 55 years and 57 years, respectively. The most common clinical symptoms were chest pain(100%), dyspnea(59%) and palpitation(35%). Mean values of S1+R5 and T wave depth were 58+/-16mm and 16+/-6mm in J-APH and 42+/-11mm and 7+/-3mm in NJ-APH(p<0.05, respectively). Seven patients experienced transient or permanent atrial fibrillation without significant symptoms. Seven patients showed progression or regression of T wave depth greater than 5mm during the period of follow-ups. On echocardiography IVS/LVPW thickness(mm) at the base were 11+/-2/10+/-2 in J-APH and 17+/-7/11+/-2 in NJ-APH, and IVS/LVPW thickness(mm) at the apex were 25+/-7/24+/-5 in J-APH and 26+/-3/26+/-2 in NJ-APH. Three patients with NJ-APH showed asymmetrical septal hypertrophy, cardiac catheterization disclosed elevated left ventricular end diastolic pressure in 11 out of 19 patients. Dye entrapment at the apex during systole was noted in 5 out of 18 patients. In conclusion, our study showed high prevalence rate expression of J-APH in contrast to the Western countries, there may be racial difference in phenotype of apical hypertrophic cardiomyopathy. Considering progression or regression of T-wave depth, NJ-APH may be a forme fruste or regressed form of J-APH.
