4-8 The Resynchronization-Defibrillation for Ambulatory Heart Failure Trial (RAFT) reported that patients with mild to moderate HF and depressed left ventricular systolic function in association with an intraventricular conduction delay randomized to an implantable cardioverter-defibrillator (ICD) plus CRT experienced improved survival and were significantly less likely to be hospitalized for HF compared with the group randomized to ICD therapy alone. 8 This prespecified study within RAFT presents a detailed analysis of the causes of hospitalization, hospitalization rates, and hospitalization lengths of stay in the RAFT cohort.
Clinical Perspective on p 2030
MethodsThe study design 9 and results of RAFT 8 have previously been published. Patients were enrolled at 24 centers in Canada, 8 centers inBackground-This study reports the impact of cardiac resynchronization therapy (CRT) on hospitalizations in patients randomized to implantable cardioverter-defibrillator (ICD) or ICD-CRT in the Resynchronization-Defibrillation for Ambulatory Heart Failure Trial (RAFT). Methods and Results-Hospitalization rates and lengths of hospital stay were compared between the 2 groups. At the 18-month follow-up, the numbers of patients hospitalized for any cause were similar in the ICD (n=351, 38.8%) and ICD-CRT (n=331, 30.0%) groups. The number of patients hospitalized for heart failure was significantly lower in the ICD-CRT (n=101, 11.3%) compared with the ICD (n=141, 15.6%; P=0.003) group. The number of patients hospitalized for a device-related indication was similar in the ICD-CRT group (n=147, 16.4%) and ICD group (n=126, 13.9%; P=0.148). The total number of hospitalizations for any cause (n=1448 versus n=1553; P=0.042), any cardiovascular cause (n=667 versus n=790; P=0.017), and any heart failure cause (n=385 versus n=505; P<0.0001) was significantly lower in ICD-CRT group compared with the ICD group, whereas the number of hospitalizations for device-related causes was significantly higher in the ICD-CRT group compared with the ICD group (246 versus 159; P<0.001). Although the reduction in hospitalizations for heart failure in the CRT-ICD group was offset by an increased number of hospitalizations for device-related indications, the length of hospital stay for any cause was significantly shorter in the ICD-CRT group (8.83±13.30 days) compared with the ICD group (9.59±14.40 days; P=0.005). Conclusion-ICD-CRT therapy significantly reduces hospitalizations and total days in hospital in patients with New York Heart Association class II/III heart failure compared with ICD therapy despite increased admissions for device-related indications. Clinical Trial Registration-URL: http://www.clinicaltrials.gov. Unique identifier: NCT00251251.