O ne of the great successes of modern medicine is the development of effective pharmacological treatments to lower blood pressure (BP). Of the modifiable risk factors for cardiovascular disease, elevated BP or hypertension has the highest population attributable risk, 1 and a near continuous relationship with rates of stroke and coronary heart disease from levels of 115 mm Hg systolic and 75 mm Hg diastolic BP.2 Overviews of randomized trials are consistent in showing that lowering systolic BP by 5 to 10 mm Hg reduces the risk of stroke by one third, irrespective of disease history, initial BP level, or type of agent used.3-5 Moreover, more intensive longterm BP lowering can result in additional benefits proportional to the size of fall in BP. [4][5][6] Despite this body of evidence, there has been longstanding controversy (and consternation) over the levels to which BP should be brought down by treatment for the prevention of cardiovascular disease. Because there has been limited randomized evidence, guideline committees have been challenged in defining BP targets below 130 to 140 mm Hg to manage individual patients.7 Concerns over diminishing net benefit being overtaking by excessive harm with increasing reductions in BP is supported by a physiological argument over critical thresholds for organ perfusion and secondary analysis of randomized trials suggesting a J-shaped relationship with cardiovascular events.8 Moreover, recent trials of more intensive BP lowering, including the Action to Control Cardiovascular Risk on Type 2 Diabetes (ACCORD) 9 and Secondary Prevention of Small Subcortical Strokes (SPS3), 10 failed to show significant reductions in rates of ischemic stroke with systolic BP reductions below 120 and 130 mm Hg, respectively.The main result of the Systolic Blood Pressure Intervention Trial (SPRINT) 11 has, therefore, created a new paradigm in hypertension management and is affecting on hypertension management guidelines around the world. The headline summary was that people at high cardiovascular risk who received more intensive BP-lowering treatment to target systolic levels below 120 mm Hg had fewer cardiovascular events than those who were treated to a target of below 140 mm Hg. For stroke physicians, the key question is whether these results apply to their patients.SPRINT was a carefully conducted clinical trial, sponsored by the National Heart, Lung and Blood Institute of the United States, that involved 9361 hypertensive patients (mean age, 68 years) who were treated to 2 systolic BP treatment targets (<120 versus <140 mm Hg). The key inclusion criteria were an age ≥50 years, systolic BP of 130 to 180 mm Hg, and evidence of increased cardiovascular risk based on either a 10-year Framingham risk estimate of at least 15% or markers of vascular disease including chronic renal disease in approximately one third of participants; but people with diabetes mellitus or stroke were specifically excluded. The study was stopped earlier than planned after a mean follow-up of 3.26 years, on the recommend...