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. 2000 Nov 11;321(7270):1183–1187. doi: 10.1136/bmj.321.7270.1183

Table.

Characteristics of studies included in meta-analysis

Study Year Aspirin formulation Dose (mg/day) Average treatment duration (months) Indication for aspirin therapy
Diener et alw1 w2 1996 Unspecified 50 24 Transient ischaemic attack or stroke
Hansson et alw3 1998 Standard 75 45 Hypertension
Petersen et alw4 1989 Unspecified 75 24 Atrial fibrillation
SALTw5 1991 Standard 75 32 Transient ischaemic attack or stroke
TPTw6 1998 Modified release 75 81 Cardiovascular risk factors
Wallentinw7 1991 Unspecified 75 12 Unstable angina
Silagy et alw8 1993 Standard 100 12 Primary prevention
USPHSw9 1989 Standard 162.5 60 Primary prevention
EAFTw10 1993 Unspecified 300 28 Transient ischaemic attack or stroke
Elwood et alw11 1974 Standard 300 12 Myocardial infarction
UK-TIAw12 1991 Various 300, 1200 48 Transient ischaemic attack
Gavaghan et alw13 1991 Standard 324 12 Coronary artery bypass grafting
Olivotto et alw14 1996 Modified release 325 12 Breast cancer
Elwood et alw15 1979 Standard 900 12 Myocardial infarction
CDPAw16 1976 Unspecified 972 22 Myocardial infarction
PARISw17 1980 Unspecified 972 41 Myocardial infarction
Hess et alw18 1985 Unspecified 990 24 Peripheral vascular disease
AMISw19 1980 Standard 1000 36 Myocardial infarction
Breddin et alw20 1980 Modified release 1000 24 Myocardial infarction
CCSGw21 1978 Standard 1300 26 Transient ischaemic attack
Fields et alw22 1977 Standard 1300 24 Transient ischaemic attack
Fields et alw23 1978 Standard 1300 24 Transient ischaemic attack
Brittonw24 1987 Modified release 1500 24 Stroke
Ehresman et alw25 1977 Modified release 1500 12 Peripheral vascular disease

SALT=Swedish aspirin low dose trial; TPT=thrombosis prevention trial; USPHS=US physicians health study; EAFT=European atrial fibrillation trial; UK-TIA=UK transient ischaemic attack aspirin trial; CDPA=coronary drug project aspirin study; PARIS=persantine-aspirin reinfarction study; AMIS=aspirin myocardial infarction study; CCSG=Canadian Cooperative Study Group.