1. To evaluate the efficacy and safety of levosimendan in the treatment of heart failure ; 2. Guide patients to apply levosimendan individually and establish a dose adjustment program.
The efficacy and safety of levosimendan in Chinese patients with different acetylmetabolites and CrCl(Creatine clreance) were re-evaluated after marketing. The population pharmacokinetics of different populations was studied, and the patients were guided to apply levosimendan individually and establish a dose adjustment program.
Study Type
OBSERVATIONAL
Enrollment
352
First Affiliated Hospital of Shandong First Medical University ( Qianfoshan Hospital of Shandong Province )
Jinan, Shandong, China
RECRUITING35-day survival rate
Survival of patients at 35 days
Time frame: 35-day
The changes of plasma BNP(brain natriuretic peptide) / NT-proBNP(N-terminal B-type natriuretic peptide) before and after treatment.
Measurement of BNP(brain natriuretic peptide) / NT-proBNP(N-terminal B-type natriuretic peptide)
Time frame: 35-day
The improvement rate of patients ' health status
EQ-5D scale(EuroQol Five Dimensions Questionnaire) was used to assess health status
Time frame: 35-day
The incidence of composite endpoint events ( within 35 days ) included mortality, unplanned readmission, transfer to ICU, and rescue.
Incidence of composite endpoint events within 35 days
Time frame: 35-day
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