ESPIRIT Trial: Does Lowering Systolic BP Targets to 120 mm Hg Reduce Risk for Cardiovascular Events Among Hypertensive Patients?
BACKGROUND AND PURPOSE:
- Liu et al. (The Lancet, 2024) compared the efficacy and safety of intensive blood pressure lowering treatment targeting systolic BP of <120 mm Hg among participants with high cardiovascular risk and with or without diabetes or previous stroke
METHODS:
- Open-label, blinded-outcome, randomized controlled trial
- Effects of Intensive Systolic Blood Pressure Lowering Treatment in Reducing Risk of Vascular Events (ESPRIT) trial
- 116 hospitals or communities in China
- Participants
- ≥50 years
- High cardiovascular risk: Established cardiovascular disease or ≥2 major cardiovascular risk factors
- Interventions
- Intensive treatment: Systolic BP <120 mm Hg
- Standard treatment: Systolic BP <140 mm Hg
- Study design
- Follow up: Months 1, 2, and 3 and then every 3 months
- Medications based on standard office BP measurement
- Free medications were made available to improve adherence
- Analysis was by intention-to-treat
- Primary outcome
- Composite of major vascular events
- Myocardial infarction | Revascularization | Hospitalization for heart failure | Stroke | Death from cardiovascular causes
- Composite of major vascular events
RESULTS:
- Intensive treatment: 5624 | Standard treatment: 5631
- Patients with diabetes: 4359 | Patients with previous stroke: 3022
- Mean age: 64.6 (SD, 7.1) years
- Median follow-up: 3.4 years
- Mean systolic BP through follow-up
- Intensive: 119.1 (SD, 11.1) mm Hg
- Standard: 134.8 (SD, 10.5) mm Hg
- Over the follow-up period, the primary outcome occurred in fewer patients in the intensive treatment group
- Intensive: 9.7% | Standard: 11.11%
- Hazard ratio (HR) 0.88 (95% CI, 0.78 to 0.99) | P=0.028
- There was no heterogeneity of effects due to
- Diabetes status | Duration of diabetes | History of stroke
- Syncope occurred more frequently in the intensive treatment group
- Intensive: 0.4% | Standard: 0.1%
- HR 3.00 (95% CI, 1.35 to 6.68)
- There was no significant between-group difference in other serious adverse events
- Hypotension | Electrolyte abnormality | Injurious fall | Acute kidney injury
- Intention-to-treat analysis
- To prevent a primary outcome event: 75 patients need to be treated
- To prevent a cardiovascular death: 148 patients need to be treated
CONCLUSION:
- A target systolic BP of 120 mm Hg vs 140 mm Hg reduced adverse cardiovascular events among high-risk hypertensive patients with a slight increase in syncope risk
- Other adverse events did not differ between the groups
- The authors state
Our findings provide new evidence about the benefit and harm of treatment targeting systolic blood pressure of less than 120 mm Hg
Learn More – Primary Sources:
Want to share this with your colleagues?
SPECIALTY AREAS
- Alerts
- Allergy And Immunology
- Cancer Screening
- Cardiology
- Cervical Cancer Screening
- Dermatology
- Diabetes
- Endocrine
- ENT
- Evidence Matters
- General Internal Medicine
- Genetics
- Geriatrics
- GI
- GU
- Hematology
- ID
- Medical Legal
- Mental Health
- MSK
- Nephrology
- Neurology
- PcMED Connect
- PrEP for Patients
- PrEP for Physicians
- Preventive Medicine
- Pulmonary
- Rheumatology
- Vaccinations
- Women's Health
- Your Practice