After proper patients were selected from among those who were candidates for CRT implantation and their informed consent was obtained, their personal and medical information, including age, gender, and cardiac risk factors (smoking, hypertension, hyperlipidemia, diabetes, and family history), and the results of angiography were recorded in the study forms. Subsequently, the patients’ history was recorded to precisely determine NYHA function class, and a 12-lead electrocardiogram was performed. Among patients with LBBB and intraventricular conduction delay, the presence of two or more R waves or a notch on the R or S wave in at least two consecutive leads was considered as notched QRS complex (nQRS). Patients without a notch in the QRS complex were considered as smooth QRS complex (sQRS) (
Figures 1 and
2). According to the location of nQRS (lateral, inferior, and anterior leads) and absence of a notch, the patients were divided into four subgroups. Echocardiographic criteria, including LVESV and LVEF for each patient, were recorded in the study form based on transthoracic echocardiography and the Simpson method. Six months after CRT implantation, the patients’ detailed history was collected again to determine NYHA function class, echocardiography was conducted again, and the difference between LVESV and LVEF was measured. A decrease in LVESV of 15% or more, an increase in LVEF of 5% or more, or at least one class improvement in NYHA function class was considered a positive therapeutic response. Subsequently, the positive therapeutic response among individuals with nQRS and sQRS was analyzed according to the location of nQRS in lateral, inferior, and anterior leads. Inclusion criteria are as follows: Symptomatic congestive HF according to the criteria issued by NYHA class II to IV that has not responded to medical therapies, LVEF of less than or equal to 35%, QRS complex of over 120 ms, and age over 18 years. Exclusion criteria are as follows: Right branch block, presence of a pacemaker, expected lifetime of less than 1 year, severe kidney dysfunction (serum creatinine over 3 mg/dL), atrial fibrillation rhythm, and lack of consent to participate in the study.