SPRINT
Study design
- Multicenter randomized open-label trial
- N = 9,361
- Increased cardiovascular risk + hypertension
- SBP target <120 vs <140 mmHg
- Median follow-up 3.26 years
- Stopped early for cardiovascular benefit
Population
- Age ≥50 years
- SBP 130–180 mmHg
- Increased CV risk
- Clinical/subclinical CVD, CKD, ≥15% Framingham risk or age ≥75
- Diabetes
- Prior stroke
- Symptomatic HF or LVEF <35%
- Standing SBP <110 mmHg
- Nursing home residence
Interventions
- Target SBP <120 mmHg
- Mean SBP at 1 year: 121.4 mmHg
- Mean antihypertensives: 2.8
- Target SBP <140 mmHg
- Mean SBP at 1 year: 136.2 mmHg
- Mean antihypertensives: 1.8
Primary outcome
SBP <120 vs <140 mmHg
Annualized primary cardiovascular event rate
Intensive BP control reduced the primary cardiovascular outcome by 25% relative
Secondary outcomes
1.03%/yr vs 1.40%/yr
HR 0.73, P = 0.003
0.25%/yr vs 0.43%/yr
HR 0.57, P = 0.005
0.41%/yr vs 0.67%/yr
HR 0.62
90 over 3.26 years
To prevent one death
Safety
2.4% vs 1.4%
Increased with intensive therapy
2.3% vs 1.7%
Increased with intensive therapy
3.1% vs 2.3%
Increased with intensive therapy
4.1% vs 2.5%
Increased with intensive therapy
2.2% vs 2.3%
No increase
Clinical interpretation
- Lower SBP targets reduce cardiovascular events and mortality in selected high-risk adults
- Benefits were particularly notable for HF, cardiovascular death and all-cause mortality
- Intensive control requires more medication and closer monitoring
- Watch for orthostasis, hypotension, electrolyte changes and AKI
- SPRINT does not directly apply to diabetes or prior stroke
Limitations
- Excluded diabetes and prior stroke
- Excluded symptomatic HF and LVEF <35%
- Trial stopped early for benefit
- Intensive BP management required frequent structured follow-up
- BP measurement protocol differed from many routine clinic workflows