The Systolic Blood Pressure Intervention Trial (SPRINT) 1 is a large National Institutes of Health-sponsored multicenter randomized controlled trial that enrolled 9361 patients with a systolic blood pressure (SBP) of at least 130 mm Hg. The primary goal of SPRINT was to test whether reducing SBP to a lower goal (<120 mm Hg) than currently recommended (<140 mm Hg) would reduce the occurrence of cardio-vascular disease (CVD) and chronic kidney disease (CKD) events. Enrolled patients were 50 years or older with an SBP ≥130 mm Hg and at least one of the following: a history of CVD, stage 3 CKD (estimated glomerular filtration rate 20-59 mL/min/1.73 m 2), an intermediate to high risk for CVD other than stroke, or age 75 years or older. A patient was defined as having CVD if they had a prior myocardial infarction, percu-taneous coronary intervention, coronary artery bypass grafting, carotid endarterectomy or carotid stenting, peripheral arterial disease with revascularization, acute coronary syndrome, abdominal aortic aneurysm ≥5 cm with or without repair, a coronary calcium score >400, or left ventricular hypertrophy. Patients were defined as at intermediate or high risk for CVD based on the following: Framingham Risk Score for 10-year CVD risk of 15% based on laboratory work performed for lipids within the past 12 months. The primary outcome was a composite of cardiovascular events. The SPRINT study was terminated early after 3.26 years on advisory of the data safety monitoring board. The results of the SPRINT study showed a 25% reduction in the primary combined cardiovascular outcome and a 27% reduction in mortality in the group randomized to SBP <120 mm Hg. 1,2 This obviously has important implications for blood pressure (BP) guidelines in this population. The baseline mean systolic and diastolic BPs were 139.7 mm Hg and 78.1 mm Hg, respectively. At 1 year, the mean SBP was 121.4 mm Hg in the intensive treatment group and 136.2 mm Hg in the standard treatment group. The SPRINT study included 28% of patients with CKD, 28% of patients were older than 75 years, 36% were women, and 20% had prior CVD. The sample was diverse and included 29.9% black, 10.5% Hispanic, and 57.7% white patients.