Introduction
Little is known about the effects of cardiac resynchronization therapy (CRT-D) on
hospitalizations during long-term follow up. We assessed the impact of CRT-D on CV
and non-CV hospitalizations in patients randomized to implantable cardioverter-defibrillator
(ICD) or CRT-D in the MADIT-CRT trial.
Methods and Results
MADIT-CRT randomized 1820 patients with mild heart failure (HF), low ejection fraction
and a wide QRS to ICD or CRT-D. Hospitalization rates and lengths of hospital stay
were compared. At an average of 5.6 years follow-up, there was a lower rate of all-cause
hospitalizations in the CRT-D arm compared with the ICD group (72.6 events per 100
pt-years versus 82.6 events per 100 pt-years, p=0.020). This was driven by a reduction
in CV-hospitalizations with CRT-D vs. ICD (28.8 events per 100 pt-years vs. 42.6 events
per 100 pt-years, p<0.001), and a reduction in HF hospitalizations (11.9 events per
100 pt-years vs. 22.4 events per 100 pt-years, p<0.001). There was no significant
difference in non-CV hospitalizations in the CRT-D group compared to ICD (43.8 vs.
39.9 events per 100 pt-years, p=0.166). The length of hospital stay for any cause
was similar with CRT-D (14.8±1.06 days) compared with the ICD group (14.7±0.95 days;
p=0.06). The length of stay for cardiovascular hospitalizations was shorter for the
CRT-D group (6.7±0.89 days) compared with the ICD group (7.7±0.68 days); p<0.001.
The length of stay for heart failure related hospitalizations was shorter for the
CRT-D group (4.2±0.79 days) compared with the ICD group (4.8±0.58 days); p<0.001.
The length of stay for non-cardiovascular hospitalizations was not significantly different
(8.1 vs. 7 days, p=0.08). Any hospital admission was associated with an increased
risk of death (HR 8.97 95%CI 6.17-13.05).
Conclusions
Among patients with NYHA class I/II heart failure, CRT-D therapy significantly reduces
all-cause hospitalizations, HF, and CV hospitalizations with reductions in hospital
length of stay. Any hospitalization was associated with an increased risk of death.
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Copyright
© 2020 Published by Elsevier Inc.