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Blood pressure control by home monitoring: meta-analysis of randomised trials
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     1 Department of Community Health Sciences, St George's Hospital Medical School, London SW17 0RE, 2 Bazian Ltd, London N1 1QP

    Correspondence to: F P Cappuccio f.cappuccio@sghms.ac.uk

    Abstract

    High blood pressure is one of the most readily preventable causes of stroke and other cardiovascular complications.1-4 It can be easily detected, and most cases have no underlying detectable cause; the most effective way to reduce the associated risk is to reduce the blood pressure. Unlike many other common, chronic conditions, we have very effective ways of treating high blood pressure and we have clear evidence of the benefits of such interventions.1 However, despite a great deal of time and effort, hypertension is still underdiagnosed and undertreated.5 Furthermore, losses to follow up are high and are responsible for avoidable vascular deaths.6

    Blood pressure is usually measured and monitored in the healthcare system by doctors or nurses in hospital outpatient departments and, increasingly, in primary care settings. New electronic devices have been introduced and validated in the clinical setting to replace the mercury sphygmomanometer and to overcome the large variations in measurement due to variability between observers. Ambulatory blood pressure monitoring is also being used more often to assess individuals' blood pressures outside the clinical setting.

    Measuring blood pressure at home is becoming increasingly popular with both doctors and patients.7 8 Some national and international guidelines also recommend home monitoring in certain circumstances.9 A recent qualitative review of the role of home blood pressure measurement in managing hypertension concluded that no evidence exists as to whether home monitoring leads to better control of high blood pressure.10

    We reviewed the literature on home blood pressure monitoring and did a meta-analysis of the effect of home monitoring on blood pressure levels and the control of hypertension in randomised trials that compared home or "self" blood pressure monitoring and usual blood pressure monitoring in the healthcare system.

    Methods

    We identified 18 randomised controlled trials that compared blood pressure control or the proportion of people with blood pressure above target. The table shows the characteristics of the analysed trials. Six were based in hospital outpatient clinics,14 19 21 22 25 31 eight in communities and general practices,16 18 23 24 26-29 and four in mixed settings.15 17 20 30 Treatment in the "control" group was mainly "usual" or "standard" care,15-19 21 22 24-29 31 but some trials had nurse clinics,14 30 educational interventions,20 or flagged medical records.23 Trials used different methods of home or self blood pressure monitoring. In total, 1359 people were randomised to home or self blood pressure monitoring and 1355 to a control group of blood pressure monitoring by health professionals in clinical settings. Two trials used a factorial design,16 18 four had more than two randomised groups,17 19 20 29 and one was randomised in clusters.23 Only in eight trials was outcome assessment stated to have been blind,14-16 24 25 29 31 and only in nine was randomisation concealed.15-18 20 21 24 29 31 The duration of the intervention varied between two months31 and 36 months.19

    Characteristics of trials included in meta-analysis of home or self blood pressure monitoring

    Systolic blood pressure

    Thirteen studies reported systolic blood pressure at follow up and baseline or the change from baseline (see appendix D1 on bmj.com), but only five of these studies reported full data on means and the standard deviation of the difference. For the remaining seven studies we estimated standard deviations. The overall effect of intervention was 4.2 (95% confidence interval 1.5 to 6.9) mm Hg, with highly significant heterogeneity between studies (P < 0.001) (fig 2, top panel). The funnel plot showed some asymmetry, and Egger's test for publication bias was significant (P = 0.038) (fig 3, top panel). The trim and fill method estimated three missing studies and gave a revised estimate of 2.2 (-0.9 to 5.3) mm Hg.

    Fig 2 Standardised mean differences (95% confidence interval) in systolic (top), diastolic (middle), and mean (bottom) blood pressures achieved in people monitoring blood pressure at home compared with people whose blood pressure was monitored by health professionals in clinical settings

    Fig 3 Funnel plots for systolic and diastolic blood pressure

    Diastolic blood pressure

    Sixteen studies reported diastolic blood pressure at follow up and baseline or the change from baseline (see appendix D2 on bmj.com), but only eight of these studies reported full data on means and the standard deviation of the difference. For the remaining eight studies we estimated standard deviations. One study had multiple endpoints.19 We included results from the one year endpoint. Use of the two year endpoint did not make an important difference to the results (2.2 (1.0 to 3.3) mm Hg). The overall effect of intervention was 2.4 (1.2 to 3.5) mm Hg, with significant heterogeneity between studies (P = 0.014) (fig 2, middle panel). The funnel plot showed some asymmetry (fig 3, bottom panel) (Egger's test for publication bias, P = 0.095). The trim and fill method estimated two missing studies and gave a revised estimate of 1.9 (0.6 to 3.2) mm Hg.

    Mean arterial pressure

    Three studies reported mean arterial pressure, one of which did not report either systolic or diastolic blood pressure.25 All studies reported change from baseline (see appendix D3 on bmj.com) with standard deviation of the difference. The overall effect was 4.4 (2.0 to 6.8) mm Hg, with no significant heterogeneity (P = 0.319) (fig 2, bottom panel).

    Blood pressure above target

    Six studies reported the number of patients whose blood pressure was controlled at follow up. Different definitions of blood pressure control were used (see appendix C on bmj.com). Two studies reported the outcome at more than one time point. The analysis reported here is for the one year outcome in both studies. The overall relative risk was 0.90 (0.80 to 1.00), with no significant heterogeneity between studies (P = 0.34) (fig 4). Inclusion of the two year outcomes for Earp17 and Stahl19 slightly reduced the effect—relative risk 0.92 (0.83 to 1.04).

    Fig 4 Standardised relative risk of blood pressure above target in people monitoring blood pressure at home compared with people whose blood pressure was monitored by health professionals in clinical settings

    Discussion

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