Inclusion criteria | Exclusion criteria | |
---|---|---|
Aim | Screening for hypertension in a primary care setting | Studies measuring blood pressure for reasons other than screening or confirmation of a hypertension diagnosis; mathematical transformation of blood pressure results (e.g., pulse pressure, variability) or diurnal variations (e.g., morning surge, dipping) for use as additional diagnostic criteria, predicting risk, or both |
Population | Adults age ≥ 18 years | Pregnant women, children (age < 18 years), inpatients, persons in institutions, patients with secondary hypertension, and highly selected groups of patients (e.g., those with chronic kidney disease or renal transplant) who do not represent a primary screening population Patients treated for hypertension with medication |
Interventions | Benefits & harms: Clinic-based, noninvasive brachial blood pressure measurement (manual or attended/unattended automated) using any common device or screening protocol during a single encounter Harms: HBPM and ABPM | Benefits & harms: Blood pressure measurement with wrist and finger monitors, forearm cuffs, or ankle and toe measures; any method not commonly used in routine blood pressure screening (e.g., invasive methods, noninvasive method of central blood pressure measurement); Osler’s maneuver Benefits: HBPM and ABPM |
Comparator | No blood pressure measurement with the intention of screening | |
Outcomes | Potential benefits of the following: 1. Reduced all-cause mortality 2. Reduced CVD-related mortality 3. Reduced macrovascular CVD events (cardiovascular disease events, including myocardial infarction, sudden cardiac death, stroke, heart failure, and hospitalization for coronary heart disease, symptomatic peripheral arterial disease) 4. Reduced microvascular CVD events (end-stage renal disease, vascular dementia) Potential harms: 5. Increased harms of screening (e.g., labeling, absenteeism, quality of life measures, tolerability of ABPM devices) 6. Increased overdiagnosisa Potential benefits or harms: 7. Increased/decreased quality of life | Cardiovascular symptoms (e.g., palpitations), angina pectoris (chest pain), revascularization, carotid intima-media thickness, left ventricular hypertrophy, or patient satisfaction |
Timing of outcome assessment | No restrictions | No restrictions |
Setting | Eligible primary care settings must have physicians or personnel trained in blood pressure measurement, established blood pressure measurement protocols, and ongoing documentation procedures | Settings not generalizable to primary care, inpatient/residential facilities |
Study design | Benefits: Randomized controlled trials (RCTs) CTs and controlled clinical trials (CCTs) Harms: RCTs, CCTs, and cohort studies | Benefits & harms: Before-after studies, time series, case series, case reports, case–control studies, and simulation studies Harms: Cross-sectional studies |
Country | Studies conducted in countries categorized as “very high” on the 2015 Human Development Index (as defined by the United Nations Development Programme) | Studies conducted in countries not categorized as “very high” on the 2015 Human Development Index |
Language | Englishb | N/A |
Study quality | Fair or good qualityb | N/A |