Levosimendan | acute heart failure, in all type of patients | vs placebo | all NS | Endpoint | TE [95% CI] | p val | I2 | n | k | |
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Amelioration of Dyspnea at 6 h | no data | amelioration of Dyspnea at 24 h | no data | 30-day death | no data | Death from any cause or hospitalization for heart failure | no data | hospitalisation for heart failure | no data | All cause death | no data |
Trial | Studied treatment | Control | Patients |
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REVIVE II, 2013 | Intravenous Levosimendan | placebo | patients with decompensated chronic heart failure | REVIVE-I, 2003 | levosimendan 0.1–0.2 mg/kg/min | placebo | patienst with HF andsymptoms at rest | RUSSLAN, 2002 | Levosimendan at different doses (0.1-0.4 microg x kg(-1) x min(-1)) for 6h | placebo | patients with left ventricular failure complicating acute myocardial infarction |
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