From: In ®Entresto we trust
Clinical trial | No. of patients | Follow-up (months) | End point | Event rate (%) | HR (95% CI) | P value | |
---|---|---|---|---|---|---|---|
Intervention | Control | ||||||
PARADIGM-HF | 8442 | 27 | All-cause mortality | 17.0 | 19.8 | 0.84 (0.76–0.93) | <.001 |
CV death, HF hospitalization | 21.8 | 26.5 | 0.80 (0.73–0.87) | <.001 | |||
HF hospitalization | 12.8 | 15.6 | 0.81 (0.71–0.89) | <.001 | |||
PIONEER-HF | 881 | 2 | HF hospitalization | 8.0 | 13.8 | 0.56 (0.37–0.84) | – |
All-cause mortality | 2.3 | 3.4 | 0.66 (0.30 to 1.48) | – | |||
NT-proBNP reduction | 46.7 | 25.3 | 0.71b (0.63–0.81) | < 0.001 | |||
TRANSITION | 1002 | 2.5 | Proportion of patients attaining 97/103 mg bid target dose after 10 weeks | 45.4 | 50.7 | 0.90c (0.79–1.02) | 0.099 |
PROVE-HF | 654 | 12 | Correlation between log2–NT-proBNP changes in patients treated with S/V and changes in measures of cardiac volume and function | LVEF (r = −0.381 [IQR, −0.448 to −0.310]; P < .001), LVEDVI (r = 0.320 [IQR, 0.246 to 0.391]; P < .001), LVESVI (r = 0.405 [IQR, 0.335 to 0.470]; P < .001), LAVI (r = 0.263 [IQR, 0.186 to 0.338]; P < .001), E/e′ ratio (r = 0.269 [IQR, 0.182 to 0.353]; P < .001). |