Liu 1999.

Methods	RCT design: Parallel‐group trial Total N randomised: unclear Length of follow‐up: 4 weeks Analysis: unclear
Participants	Location: China Number of study centres and setting: Patients from 1 hospital CAD diagnosis: Myocardial infarction (MI) as confirmed by electrocardiography Depression diagnosis: Center for Epidemiologic Studies Depression Scale (CES‐D), Hamilton Depression Rating Scale (HAMD), diagnosis according to Chinese Classification of Mental Disorders, Second Edition, Revised (CCMD‐2‐R) Other entry criteria: unclear Exclusion criteria: unclear Treatment N: 31 (32% female, mean age unclear) Control N: 37 (27% female, mean age unclear) Comparability of groups: No significant differences
Interventions	Treatment: Fluoxetine Control: Placebo Duration of treatment: 4 weeks
Outcomes	Review outcomes: HAM‐D, Mortality Other Outcomes: Ventricular Tachycardia (VT), Heart Rate Variability (HRV)
Funding	unclear
Notes
Risk of bias
Bias	Authors' judgement	Support for judgement
Random sequence generation (selection bias)	Unclear risk	not applicable
Allocation concealment (selection bias)	Unclear risk	not applicable
Blinding (performance bias and detection bias) All outcomes	Unclear risk	not applicable
Incomplete outcome data (attrition bias) All outcomes	Unclear risk	not applicable
Selective reporting (reporting bias)	Unclear risk	not applicable
Other bias	Unclear risk	not applicable