Table 1. Characteristics of Included Trials.
Source | Demographic characteristics | Key conditions | BP eligibility requirements, mm Hg | More intensive BP treatment assignment | Less intensive BP treatment assignment | BP measurement | Length of follow-up, median, y | Definition of cardiovascular disease event or all-cause mortality |
---|---|---|---|---|---|---|---|---|
BP treatment goal trials | ||||||||
AASK (n = 1094)18 | African American patients aged 18-70 y | Hypertensive kidney disease without diabetes | Seated DBP ≥95 |
|
Goal: MAP of 102-107 mm Hg |
|
|
Any definite or probable cardiovascular outcomes (nonfatal myocardial infarction, stroke, heart failure) or death due to any cause |
ACCORD BP (n = 4733)19 | Patients aged ≥40 y | Diabetes, CVD, or CVD risk factors | Seated SBP 130-180a |
|
Goal: SBP <140 mm Hg |
|
|
Primary end point (nonfatal myocardial infarction, nonfatal stroke, or death due to cardiovascular causes), nonfatal heart failure, or death due to any cause |
SPRINT (n = 9361)16 | Patients aged ≥50 y | High risk for CVD without prior stroke or diabetes | Seated SBP 130-180a and standing SBP <110 |
|
Goal: SBP <140 mm Hg |
|
|
Primary end point (myocardial infarction, acute coronary syndrome, stroke, heart failure, or death due to cardiovascular causes) or death due to any cause |
SPS3 (n = 3020)20 | Patients aged ≥30 y | Recent lacunar stroke and hypertension | Seated SBP ≥140 or seated DBP ≥90 |
|
Goal: SBP 130-149 mm Hg |
|
|
Primary end point (recurrent fatal and nonfatal stroke) or acute myocardial infarction, heart failure event, or death due to any cause |
UKPDS (n = 1148)15 | Patients aged 25-65 y | Diabetes and hypertension | Seated SBP ≥150 or seated DBP ≥85 (≥160/≥85 if taking medication for hypertension) |
|
Goal: BP <180/105 mm Hg |
|
|
Any myocardial infarction, any stroke, any heart failure, or death due to any cause |
Placebo-controlled trials | ||||||||
HYVET (n = 3845)17 | Patients aged ≥80 y | Hypertension | Seated SBP 160-199, standing SBP ≥140, seated DBP 90-109c |
|
Placebo |
|
|
Primary end point (fatal or nonfatal stroke), any myocardial infarction, any heart failure, or death due to any cause |
SHEP (n = 4736)21 | Patients aged ≥60 y | Isolated systolic hypertension | Seated SBP 160-219,d standing SBP ≥140, seated DBP <90 |
|
Placebo |
|
|
Any stroke, any coronary heart disease, any left ventricular heart failure, or death due to any cause |
SYST-EUR (n = 4695)22 | Patients aged ≥60 y | Isolated systolic hypertension | Seated SBP <220, standing SBP ≥140, seated DBP <95 |
|
Placebo |
|
|
Nonfatal myocardial infarction, nonfatal stroke, nonfatal heart failure, or death due to any cause |
TOMHS (n = 902)23 | Patients aged 45-69 y | Mild hypertension | DBP 90-99 |
|
|
|
|
Primary end point (major coronary heart disease events, including myocardial infarction and heart failure), nonfatal stroke, or death due to any cause |
Abbreviations: BP, blood pressure; CVD, cardiovascular disease; DBP, diastolic blood pressure; MAP, mean arterial pressure; SBP, systolic blood pressure.
Range varied based on baseline antihypertensive medication use: SBP 130-160 mm Hg with 0-3 antihypertensives, SBP 161-170 with 0-2 antihypertensives, or SBP 171-180 with 0-1 antihypertensives.
Of 4 measures, the first was discarded and the mean of the next 3 consecutive readings with a coefficient of variation below 15% was used in the study.
The average seated DBP was later changed to <110 mm Hg to be able to recruit participants with isolated systolic hypertension.
Range was 130-219 mm Hg and DBP <85 mm Hg if taking antihypertensive medications.
These groups were combined to represent the “intensive blood pressure treatment group” in our extended pooled meta-analysis, which included the 4 placebo-controlled studies.