In an individual patient data meta-analysis of randomized trials, Katherine Tucker and colleagues examine the evidence for the effectiveness of self-monitoring of blood pressure in hypertension.
Treatment of hypertension results in significant reductions in risk of subsequent cardiovascular disease [1,2]. Despite strong evidence for such treatment, international epidemiological studies suggest that many people remain suboptimally controlled . Self-monitoring of blood pressure (BP), where individuals measure their own blood pressure, usually in a home environment, can improve BP control and is an increasingly common part of hypertension management. Such monitoring can be accompanied by additional support such as from a nurse or pharmacist .
Self-monitoring is well tolerated by patients and has been shown to be a better predictor of end organ damage than clinic measurement [5–8]. This is despite potential issues with quality control of self-measurement such as poor technique or withholding of results [9,10]. The latter can be reduced to an extent by the use of telemonitoring .
Previous meta-analyses have shown that self-monitoring reduces clinic BP by a small but significant amount compared to conventional care (around 4/1.5 mmHg) [4,12–14]. Analysis by Bray and colleagues suggested that when self-monitoring was accompanied by a co-intervention, participants were more likely to meet target BP, but it remains unclear which interventions are most effective and what specific populations (if any) should be targeted .
The aim of this work was therefore to use individual patient data (IPD) from relevant trials to assess the effectiveness of BP self-monitoring on BP reduction and hypertension control, evaluating how best to utilise self-monitoring of BP and to determine which subpopulation is most likely to benefit.
Materials and methods
This study systematically reviewed the existing literature to identify randomised trials examining the efficacy of self-monitoring of BP compared to control. Authors of all eligible trials were approached for access to IPD. A protocol with detailed methods has been published previously . The methods used are summarised below.
Data sources and searches
Medline, Embase, and the Cochrane Library were searched for trials using BP self-monitoring in hypertensive patients (S2 Fig; search date June 2016).
Two reviewers (RM and KT) independently assessed the articles for eligibility and inclusion; disagreements were resolved by discussion. Randomised trials were eligible that recruited patients with hypertension being managed as outpatients using an intervention that included self-measurement of BP. Self-monitoring had to be without medical professional input (i.e., by patient with or without carer support) and using a validated monitor, with or without other co-interventions, and where a comparator group had no organised self-measurement of BP. Included studies were required to have involved at least 100 patients, followed up for at least 24 weeks, and to have been published since 2000. This was to ensure that self-monitoring equipment was likely to be relevant to contemporary medical management (i.e., automated oscillometric monitors). Relevant outcomes were systolic blood pressure (sBP) and/or diastolic blood pressure (dBP) measured in clinic, by researcher or by ambulatory measurement, and achievement of BP control.
Data extraction and quality assessment
Authors whose trials met the inclusion criteria were approached for provision of IPD including demographic details, comorbidities, antihypertensive medications, lifestyle factors, and BP end points (clinic and/or ambulatory). Study-level data were extracted where available from published articles and checked by the original authors. In particular, any co-interventions were carefully documented and prospectively allocated to 1 of 4 levels of interventional support based on a previous classification  (S1 Table).
Study quality was assessed in terms of potential bias from randomisation, blinding, outcome assessment, and method of analysis using an adaptation of the Cochrane tool .
Original data were kept on a secure server and assembled in a consistent format for all trials. Three researchers (KT, RM, and JS) cross-checked trial details, summary measures, major outcomes, and definitions against published articles. Any apparent inconsistencies were checked with the original trial authors. Overall ethical approval was not required as this study does not include identifiable data; collaborating groups gained individual approval where required for data sharing.
Data synthesis and analysis
A 2-stage IPD meta-analysis was conducted using linear regression for continuous outcomes and logistic regression for proportions, aggregated across studies by random-effects inverse variance methods. Intention-to-treat comparisons of outcomes between the self-monitoring and comparator arms were summarised with forest plots using the I-squared (I2) statistic for heterogeneity. Regression models were adjusted for age, sex, baseline clinic BP, and diabetic status (the latter due to the lower BP target generally used in a diabetic population).
The primary outcomes were change in sBP and dBP at 12 months and likelihood of uncontrolled BP below target at 12 months (control as defined by each trial). Analyses are reported in subgroups, by pre-specified level of self-monitoring intervention as described in Table 1 and in the published protocol .
Subgroup analyses examined the effect of self-monitoring on BP mean and control by age, sex, baseline sBP, the presence and number of antihypertensive medications prescribed, and comorbidities (myocardial infarction [MI], stroke, diabetes mellitus [DM], chronic kidney disease [CKD], and obesity [defined as a body mass index (BMI) ≥ 30 kg/m2]). All subgroup analyses were adjusted for age, sex, baseline clinic BP, level of intervention, and individual study (contributing to each analysis).
Sensitivity analyses included incorporation of aggregate data from studies that did not contribute IPD [17–23], exclusion of individual patients for whom a lower home BP target was not used (due to study design or the presence of comorbidities such as diabetes) [24–27], influence of BP inclusion criteria (clinic or ambulatory) from ambulatory outcome studies, different assumptions regarding BP of patients lost to follow-up (controlled or uncontrolled), and influence of adjusting for medication changes (in those studies which recorded changes in medication). Finally, the influence of each study on the overall results was assessed using an influence analysis. Egger’s test for funnel plot asymmetry was applied to consider possible publication bias (S21 Fig) .
There were no deviations from the protocol . Five post-hoc analyses were undertaken: firstly, an additional subgroup analysis was carried out (resistant hypertension [defined as BP > 140/90 mmHg and 3 medications at baseline or any BP level and 4 or more medications at baseline]); secondly, the distribution of baseline antihypertensive medications was compared in patients with and without a history of stroke using Pearson’s chi-squared; thirdly, the effectiveness of self-monitoring in stroke was assessed controlling for the number of baseline medications; fourthly, the influence of blinding was assessed; and finally, sBP was plotted against medication changes.
Statistical software and presentation
All analyses were conducted using STATA version 13.1 (MP parallel edition, StataCorp, College Station, Texas, USA), using the ipdmetan package . Data are presented as proportions of the total study population, means with standard deviation or relative risk (RR) with 95% confidence intervals unless otherwise stated.
Of 2,846 unique studies from the combined searches, 132 were assessed in full and 36 studies were deemed potentially eligible (S1 Fig). One study which would otherwise have been eligible was excluded because the comparator group used ambulatory monitoring to guide treatment, a control intervention that had not been anticipated in the protocol but which was not comparable to any other included studies . Of the 36 potentially eligible studies, 19 had published data at 12 months, the primary outcome. Authors from 24 of the potentially eligible studies provided IPD, with 1 group submitting additional data from an unpublished study. These 25 studies were published from 2005–2014, were conducted in North America and Europe (11 United States; 6 United Kingdom; 3 Italy; 1 each from the Netherlands, Australia, Spain, Finland, and Canada), and included a wide range of self-monitoring protocols, co-interventions, and populations (Table 1) [23–27,31–48]. Authors from the remaining 12 studies were either unable to provide IPD (2 studies) or did not respond to the request for data (10 studies). Four studies which followed up patients for 12 months did not provide IPD, so that data for the primary outcome were available from 15/19 studies (7,138/8,292 [86%], of potential participants) (S2 Table) [17,18,22,49]. A total of 838 patients (12%) were lost to follow-up across all included studies, and a further 227 patients from the potentially available studies were lost to follow-up, leaving 6,300/7,227 patients (87%) for inclusion in the final analysis of the primary outcome (12 months follow-up).
Overall, the information from the included trials was judged to be at low risk of bias: most studies used computerised generation of randomisation sequences (23/25, 92%), appropriate allocation concealment (24/25, 96%), and all used an intention-to-treat approach with either multiple imputation for missing data or analysis of complete cases. Most studies (19/25, 76%) followed up more than 80% of participants, but only 12/25 (48%) used blinded assessment of outcome (S3 Table). An influence analysis assessed the impact of each individual study on the overall results. Included studies were predominantly publically funded (S4 Table).
Overall, self-monitoring was associated with reduced clinic sBP between baseline and 12-months follow-up compared to usual care (systolic −3.2 mmHg, 95% CI −4.9 to −1.6 mmHg) (Fig 1). Significant heterogeneity was present between studies: I2 = 76%, P < 0.001. Self-monitoring was also associated with reduced dBP at 12-months follow-up (diastolic −1.5 mmHg, 95% CI −2.2 to −0.8 mmHg) and significant heterogeneity remained (I2 = 62%, P < 0.001) (Fig 2). Similar reductions in BP were seen after 6-months follow-up, but the point estimates after 18-months follow-up were smaller, albeit from only 5 studies (S3, S4, S6 and S7 Figs).
Clinic BP control
Clinic BP control was improved at 12-months follow-up (RR of uncontrolled BP 0.7 [95% CI 0.56 to 0.86]) again with significant heterogeneity between groups (Fig 3). Similar results were seen at 6 and 18 months (S5 and S8 Figs, respectively).
Intensity of co-intervention
The reductions in clinic sBP varied with different levels of intervention: level 1 (with no co-intervention) −1.0 mmHg, [95% CI −3.3 to 1.2 mmHg]; level 4 (personal support throughout the trial) −6.1 mmHg, [95% CI −9.0 to −3.2 mmHg] (Fig 1) (heterogeneity in outcome between different levels of intervention P < 0.001). Within predefined categories of intensity of co-intervention, significant heterogeneity remained, apart from within level 2.
A similar pattern of reductions was seen in dBP: level 1 (with no co-intervention) −1.1 mmHg, [95% CI −2.4 to 0.2 mmHg]; level 4 (personal support throughout the trial) −2.3 mmHg, [95% CI −4.0 to −0.6 mmHg] (Fig 2) (heterogeneity in outcome between different levels of intervention P < 0.001). Within predefined categories of intensity of co-intervention, significant heterogeneity remained in levels 1 and 4.
BP control (defined according to individual study targets, Table 1) at 12 months also differed by level of intensity. The RR of having uncontrolled BP with a self-monitoring intervention at 12 months varied from level 1 (RR 1.0, 95% CI 0.7 to 1.4) to level 4 (RR 0.4, 95% CI 0.3 to 0.6) (Fig 3) (heterogeneity between levels of intervention P < 0.001). Heterogeneity within levels of intervention in this analysis was low for levels 2 and 4 of co-intervention, although the I2 remained above 50% for level 1. Similar results were seen at 6-months follow-up (21 studies) and at 18-months follow-up (5 studies) (S5 and S8 Figs, respectively).
Four studies had data at 12 months using ambulatory BP as the outcome (1,478 participants); these were studies with no co-intervention (level 1; n = 3) or automated feedback only (level 2; n = 1). No change was seen in ambulatory sBP associated with self-monitoring (1.1 mmHg [−0.3, 2.5]) (Fig 4) or ambulatory dBP (0.8 mmHg [−0.2, 1.9]), and there was no significant heterogeneity between studies in either case (Fig 5). At 6 months, data were available for 5 studies with no difference seen in ambulatory sBP (−1.0 mmHg [−2.8, 0.9]) or dBP (−0.4 mmHg [−1.6, 0.8]) (S9 and S10 Figs, respectively). The additional study, which used a level 3–intensity intervention, increased heterogeneity as it had a significant outcome.
No ambulatory data were available at 18 months.
Subgroup analyses using data from 12-months follow-up showed little difference in either reduction of systolic or diastolic clinic BP or likelihood of uncontrolled BP depending on history of MI or presence of CKD or diabetes (Figs 6, 7 and 8) (I2 ≤ 20% for all subgroups).
However, a history of stroke was associated with a reduced effectiveness of self-monitoring in terms of clinic sBP lowering (I2 = 77%, P = 0.04), though this difference was not observed for dBP or maintained in the likelihood of control analysis (RR I2 = 42%, P = 0.19). Post-hoc analyses showed that the distribution of number of medications between stroke and non-stroke patients was similar (S5 Table), and adjusting for baseline medication use did not explain the lack of effectiveness in patients with stroke. There was moderate heterogeneity between age groups for the effect of self-monitoring on systolic and diastolic clinic BP (I2 = 31%, P = 0.20 and I2 = 33, P = 0.19, respectively) but not in the likelihood of uncontrolled BP (I2 = 0.0%, P = 0.60). Considering the effect of obesity, there was no difference in the effect on systolic clinic BP reduction (I2 = 0, P = 0.72) but there was some evidence of heterogeneity of effect for dBP (I2 = 63, P = 0.10) and the risk of uncontrolled BP (I2 = 61%, P = 0.11).
Fewer baseline antihypertensive medications were associated with larger reductions of BP and better control (Figs 6–8). Post-hoc analyses, comparing those with resistant hypertension to those without, suggested that self-monitoring was less effective at achieving BP control in the former (RR of uncontrolled BP = 0.62, 95% CI 0.54–0.71 [non-resistant hypertension] versus RR of uncontrolled BP = 0.94, 95% CI 0.65–1.36 [resistant hypertension], I2 = 76%, P = 0.04). Similarly, the post-hoc analysis plotting change in sBP against medication changes was consistent with the hypothesis that self-monitoring interventions resulted in BP decreases via increases in prescribed medication (S22 Fig).
Inclusion of aggregate data for clinic BP at 12 months from the 4 eligible studies that did not contribute IPD (S2 Table) and exclusion of studies that did not use a lower home BP threshold did not materially change the results (S11 and S12 Figs). The exclusion of studies that randomised on the basis of ambulatory BP monitoring (ABPM) or studies that randomised on clinic BP did not change the impact of clinic or ambulatory measurement of sBP at 12 months (S13 and S14 Figs). Assuming patients lost to follow-up had uncontrolled BP attenuated the results, whereas assuming that they had controlled BP accentuated them (S15 and S16 Figs, respectively). Exclusion of patients with controlled BP at baseline also accentuated the results (S17 Fig). A post-hoc comparison of studies with blinded outcome (2,829 patients) versus unblinded (3,257 patients) showed that blinding was associated with a reduced point estimate for the change in sBP at 12 months in those studies examining higher-level interventions, albeit with overlapping confidence intervals (level 1 & 2 intervention studies: −1.51, 95% CI −4.06 to 1.04 [blinded] versus −0.83, 95% CI −2.38 to 0.73 [unblinded]; level 3 & 4 intervention studies: −4.67, 95% CI −7.51 to −1.84 [blinded] versus −6.16, 95% CI −9.36 to −2.95 [unblinded]).
Where studies had measured changes in antihypertensive medication over time, there was evidence of attenuation of the change in sBP when the analysis was adjusted for change in medication (S18 and S19 Figs). The influence analysis did not suggest that any one study was materially influencing the results (S20 Fig and Egger’s test found no evidence of asymmetry in the funnel plot (P = 0.9, S21 Fig).
Using IPD from 25 studies totalling 10,487 patients, this meta-analysis provides strong evidence that the degree of BP lowering is related to the intensity of the co-intervention (i.e., additional support) combined with self-monitoring, with little or no effect from self-monitoring alone.
These results held whether systolic or diastolic clinic BP or clinic BP control were assessed and were consistent at both 6 and 12 months. No data were available from studies with intensive co-interventions which used ambulatory BP monitoring to measure outcomes at 12 months or longer, and those with little or no co-intervention showed similar effects to the clinic BP data (no effect in either case). There was a suspicion of attenuation of the effect of self-monitoring in the few studies to date that have followed up patients for longer than 1 year but data were sparse. Future research might be directed towards longer studies with ambulatory BP measurement (or other measurements to reduce the white coat effect) for outcomes. Self-monitoring appeared most effective at lowering BP in people on fewer BP medications at baseline, and there was a suggestion of a greater effect with higher BP—provided BP was not 170 mmHg or above. Analyses considering those with apparent resistant hypertension at baseline suggested that self-monitoring works less well in this group, but this analysis was not prespecified, could not take into account dose of antihypertensive medication, and should be interpreted with caution. In terms of comorbidities, the effects of self-monitoring were similar whether or not an individual had a history of MI, diabetes, or CKD. In people with previous stroke, there may be a reduced effect of self-monitoring but this did not reflect more intensive treatment prior to randomisation.
Strengths and weaknesses
To our knowledge, this is the first analysis of self-monitoring of BP to use IPD from a wide range of self-monitoring trials from North America, Australia, and Europe and including both specialist and primary care settings. IPD allowed for standardised adjustment of outcomes and sufficient power to detect differences between subgroups.
An important issue in IPD analysis is selection of studies. The BP—SMART collaboration has gained access to a large number of datasets; nevertheless, some studies were not available due to unavailability of data or lack of response. Despite this, only 4 studies eligible for the primary outcome (14% of available patient data) were unable to provide data, and sensitivity analyses suggested no material change in the results when the published aggregate data from these studies were included.
Quality of included studies was adequate in terms of randomisation sequences, appropriate allocation concealment, and analyses. Follow-up was high for most studies but only half used blinded assessment of outcome. However, a post-hoc sensitivity analysis showed no difference in results from blinding, perhaps because in most studies BP was assessed using automated monitors reducing the chance of bias.
Despite the use of IPD and the division of studies into subgroups, significant heterogeneity remained, which limited the ability to do meta-analysis. However, this does not negate the conclusion that the evidence for both BP reduction and control is stronger for higher-intensity interventions and weak for self-monitoring alone. The hypothesis that effect would vary with level of intervention was prespecified and the categorisation of studies into 4 levels of intervention was agreed to by all study investigators before results were available.
Whilst all included studies compared self-monitoring of BP to control groups without self-monitoring, inevitably different investigators used different protocols and therefore studies differed in inclusion criteria, self-monitoring regime, and target BPs. These issues could at least in part explain the remaining heterogeneity between studies. The exclusion of studies which did not use lower BP targets for self-monitored BP did not change the results, but even IPD analysis is unable to take differences between studies entirely into account and this may be reflected in the heterogeneity which remained. Significance tests should be interpreted with caution when, as in Figs 6 and 7, multiple coequal exposures are under test; however, the 3 P values ≤ 5% for heterogeneity across these 18 tests are unlikely to be all due to chance alone and the tests were prespecified.
Most outcome data were based on clinic measurement of BP, which is what was used by the majority of trials of outcome of hypertension treatment . Ambulatory monitoring might reduce any attenuation to the white coat effect from repeated habituation to measurement but, whilst 6 studies used ambulatory BP as an outcome [25,32,33,43,45] (including 1 unpublished study), all but 1 of these used less intensive or no co-interventions. The single intensive study with an ambulatory outcome had data to 6 months and a positive result, whereas the remaining 4 studies showed no impact on ambulatory BP in common with the pooled results for clinic BP. Other studies have used multiple automated BP measurements in the clinic to assess habituation and have found no evidence that the BP differences are removed when the white coat effect is reduced, though further studies examining the effects of self-monitoring with intensive co-interventions on outcomes which reduce white coat effects are arguably needed  .
Even with IPD, issues such as loss to follow-up may be important. Included studies had rates of follow-up between 58% and 98% at 12 months with most studies following-up around 90%. In the main analysis, formal methods for handling missing data were not used since methods for imputation in IPD meta-analysis are in their infancy; however, the impact of each individual study on the overall results as assessed by the influence analysis suggests that factors such as differential follow-up between studies were unlikely to have affected the results .
The outcomes included in this review are all related to BP. Whilst BP is directly related to stroke and coronary heart disease risk, it is nevertheless an intermediate outcome. Ideally, such hard outcomes would be directly measured in trials. However, because of relatively short follow-up and small numbers of participants, few included individual trials did so.
Comparison with the previous literature
There have been previous systematic reviews of trials of self-monitoring [4,13,14,53], including those focussing on specific outcomes such as adherence  or processes such as telemonitoring , but all previous analyses have relied on summary statistics rather than IPD. Compared to the most recent and comprehensive summary data review, the current study has provided pooled estimates of the effect of self-monitoring with different levels of co-intervention, suggests that self-monitoring alone has little impact on BP, and provides new evidence that the level of BP reduction is related to the intensity of the co-intervention .
Self-monitoring in the absence of such a co-intervention had little effect on BP. This is not to say that self-monitoring alone should be discouraged, for it brings other advantages both theoretical (better estimation of the underlying BP, increased self-efficacy for the patient)  and practical (increased adherence, reduced need for monitoring within the clinic, and identification of white coat and masked hypertension) [24,54]. These advantages are despite any potential inaccuracy caused by individuals not conforming to the recommended self-monitoring regime [9,10].
Obese patients had similar BP reductions to non-obese individuals but greater chance of BP control, which does not reflect differences in mean BP. The findings concerning patients with previous stroke and resistant hypertension require some caution, particularly the latter which was a post-hoc analysis, but have not been previously described. In the case of stroke, the results do not appear to be due to baseline intensity of antihypertensive treatment and warrant further study as more data become available.
Meaning of the study
Combining self-monitoring with increased collaboration between patient and either a nurse, physician, or pharmacist can result in important decreases in BP (6 mmHg systolic on average for the more intensive co-interventions) and improved control. The mechanisms for these reductions in BP could include lifestyle changes (no data available); increased adherence to medication (no data available) ; or increased prescription of medications, i.e., overcoming clinical inertia (data available from 11 studies). In order to assess the impact of enhanced medication prescription, number of medication changes was plotted against changes in BP and showed that increased numbers of medication changes were weakly correlated with reduced BP (S22 Fig). Whatever the mechanism, the literature suggests that a 6 mmHg reduction in sBP, as observed in higher-intensity interventions, would reduce subsequent stroke by more than 20% . Considering the content of such interventions is an important part of decision-making in the implementation of self-monitoring. Table 1 and S1 Table describe the key characteristics of effective interventions which depend on actively intervening in terms of medication titration and/or health behaviours. Much of the effect appears to be associated with one-to-one intervention combined with medication intensification. Self-monitoring can therefore facilitate significant improvements in BP level and control but should not necessarily be seen as reducing clinical input because clinical input within the co-interventions is often required for effective BP lowering.
The recent SPRINT trial results suggest that more intensive BP interventions are likely to be important in terms of morbidity and mortality . Increasing the level or intensity of intervention also increases the cost of an intervention, both directly to the health provider and also in terms of patients’ time. Understanding the relative cost-effectiveness of the different co-interventions is likely to be important in deciding policy in this area and will require further work.
The effects appear to be independent of age, sex, and a range of comorbidities (such as MI, CKD, diabetes, and obesity), but there was a suggestion that people receiving less intensive antihypertensive treatment, and those with the highest BPs (up to 170 mmHg systolic), may have the most to gain, presumably because they are not already receiving sufficient doses of medication. Conversely, with resistant hypertension there appeared to be little effect from self-monitoring. Similar results for stroke should be interpreted cautiously and warrant further study.
The data presented appear to indicate a potential attenuation of the beneficial effects of self-monitoring over time (see S6, S7 and S8 Figs). We believe that the key issue is a need for longer studies (at least 2 years, and preferably 5 years or more) that are accompanied by investigation of how best to administer a self-monitoring—based intervention in the long term, including whether it should be perhaps “topped up” with additional training over time.
Finally, we know from the individual trials that only a proportion of those with hypertension will be suitable for self-monitoring. Despite this, the numbers of people with hypertension and access to their own BP monitor are likely to be well into the tens of millions internationally and represent an important population to engage with [58,59].
Several unanswered questions remain. Ultimately, trials including cardiovascular endpoints would provide the strongest evidence for self-monitoring in the management of hypertension but may not be appropriate given the strong evidence linking BP to outcome. Further consideration of self-monitoring in the presence of comorbidities seems warranted, particularly for stroke. Furthermore, this review has not included economic outcomes (available from 6 of the included studies) or quality of life measures (available in 8 of the included studies), and these outcomes form part of the next series of investigations for this collaboration.
Self-monitoring of BP combined with co-interventions involving individually tailored support lowers clinic BP but has little effect on its own. Self-monitoring supported by such co-interventions should be recommended as part of routine clinical practice in international guidelines and further research should determine the most cost-effective means of supporting implementation.
1. Law MR, Morris JK, Wald NJ. Use of blood pressure lowering drugs in the prevention of cardiovascular disease: meta-analysis of 147 randomised trials in the context of expectations from prospective epidemiological studies. BMJ. 2009;338: b1665. doi: 10.1136/bmj.b1665 19454737
2. Collins R, Peto R, MacMahon S, Hebert P, Fiebach NH, Eberlein KA, et al. Blood pressure, stroke, and coronary heart disease. Part 2, Short-term reductions in blood pressure: overview of randomised drug trials in their epidemiological context. Lancet. 1990;335: 827–38. 1969567
3. Wolf-Maier K, Cooper RS, Kramer H, Banegas JR, Giampaoli S, Joffres MR, et al. Hypertension treatment and control in five European countries, Canada, and the United States. Hypertension. 2004;43: 10–17. Epub 2003/11/26. doi: 10.1161/01.HYP.0000103630.72812.10 14638619
4. Uhlig K, Patel K, Ip S, Kitsios GD, Balk EM. Self-measured blood pressure monitoring in the management of hypertension: a systematic review and meta-analysis. Ann Intern Med. 2013;159: 185–94. Epub 2013/08/08. doi: 10.7326/0003-4819-159-3-201308060-00008 23922064
5. Little P, Barnett J, Barnsley L, Marjoram J, Fitzgerald-Barron A, Mant D. Comparison of acceptability of and preferences for different methods of measuring blood pressure in primary care. BMJ. 2002;325: 258–9. Epub 2002/08/03. 12153924
6. Bobrie G, Chatellier G, Genes N, Clerson P, Vaur L, Vaisse B, et al. Cardiovascular prognosis of "masked hypertension" detected by blood pressure self-measurement in elderly treated hypertensive patients. JAMA. 2004;291: 1342–9. doi: 10.1001/jama.291.11.1342 15026401
7. Grant RW, Pandiscio JC, Pajolek H, Woulfe A, Pelletier A, Kvedar J, et al. Implementation of a web-based tool for patient medication self-management: the Medication Self-titration Evaluation Programme (Med-STEP) for blood pressure control. Inform Prim Care. 2012;20: 57–67. Epub 2013/01/23. 23336836
8. Hypertension: the clinical management of primary hypertension in adults. (2011) NICE clinical guideline 127.
9. Mengden T, Hernandez Medina RM, Beltran B, Alvarez E, Kraft K, Vetter H. Reliability of reporting self-measured blood pressure values by hypertensive patients. Am J Hypertens. 1998;11: 1413–7. Epub 1999/01/08. 9880121
11. Omboni S, Ferrari R. The role of telemedicine in hypertension management: focus on blood pressure telemonitoring. Curr Hypertens Rep. 2015;17: 535. Epub 2015/03/21. doi: 10.1007/s11906-015-0535-3 25790799
12. Fahey T, Schroeder K, Ebrahim S. Interventions used to improve control of blood pressure in patients with hypertension. Cochrane Database Syst Rev. 2005: CD005182. Epub 2005/01/18. doi: 10.1002/14651858.CD005182 15654709
13. Cappuccio FP, Kerry SM, Forbes L, Donald A. Blood pressure control by home monitoring: meta-analysis of randomised trials. BMJ. 2004;329: 145. Epub 2004/06/15. doi: 10.1136/bmj.38121.684410.AE 15194600
14. Bray EP, Holder R, Mant J, McManus RJ. Does self-monitoring reduce blood pressure? Meta-analysis with meta-regression of randomized controlled trials. Ann Med. 2010;42: 371–86. Epub 2010/05/28. doi: 10.3109/07853890.2010.489567 20504241
15. Tucker KL, Sheppard JP, Stevens R, Bosworth HB, Bove A, Bray EP, et al. Individual patient data meta-analysis of self-monitoring of blood pressure (BP-SMART): a protocol. BMJ Open. 2015;5: 008532.
16. Mangesi L, Dowswell T. Treatments for breast engorgement during lactation. Cochrane Database Syst Rev. 2010: CD006946. Epub 2010/09/09. doi: 10.1002/14651858.CD006946.pub2 20824853
17. Varis J, Kantola I. The choice of home blood pressure result reporting method is essential: Results mailed to physicians did not improve hypertension control compared with ordinary office-based blood pressure treatment. Blood Press. 2010;19: 319–24. Epub 2010/04/07. doi: 10.3109/08037051003718457 20367560
18. Artinian NT, Flack JM, Nordstrom CK, Hockman EM, Washington OG, Jen KL, et al. Effects of nurse-managed telemonitoring on blood pressure at 12-month follow-up among urban African Americans. Nurs Res. 2007;56: 312–22. Epub 2007/09/12. doi: 10.1097/01.NNR.0000289501.45284.6e 17846552
19. Rudd P, Miller NH, Kaufman J, Kraemer HC, Bandura A, Greenwald G, et al. Nurse management for hypertension. A systems approach. Am J Hypertens. 2004;17: 921–7. Epub 2004/10/16. doi: 10.1016/j.amjhyper.2004.06.006 15485755
20. Marquez-Contreras E, Martell-Claros N, Gil-Guillen V, de la Figuera-Von Wichmann M, Casado-Martinez JJ, Martin-de Pablos JL, et al. Efficacy of a home blood pressure monitoring programme on therapeutic compliance in hypertension: the EAPACUM-HTA study. J Hypertens. 2006;24: 169–75. Epub 2005/12/07. 16331115
21. Madsen LB, Kirkegaard P, Pedersen EB. Blood pressure control during telemonitoring of home blood pressure. A randomized controlled trial during 6 months. Blood Press. 2008;17: 78–86. doi: 10.1080/08037050801915468 18568696
22. Rinfret S, Lussier MT, Peirce A, Duhamel F, Cossette S, Lalonde L, et al. The impact of a multidisciplinary information technology-supported program on blood pressure control in primary care. Circ Cardiovasc Qual Outcomes. 2009;2: 170–7. Epub 2009/12/25. doi: 10.1161/CIRCOUTCOMES.108.823765 20031834
23. Earle K. In people with poorly controlled hypertension, self-management including telemonitoring is more effective than usual care for reducing systolic blood pressure at 6 and 12 months. Evid Based Med. 2011;16: 17–8. Epub 2010/11/27. doi: 10.1136/ebm1148 21109677
24. McManus RJ, Mant J, Roalfe A, Oakes RA, Bryan S, Pattison HM, et al. Targets and self monitoring in hypertension: randomised controlled trial and cost effectiveness analysis. BMJ. 2005;331: 493. Epub 2005/08/24. doi: 10.1136/bmj.38558.393669.E0 16115830
25. Verberk WJ, Thien T, Kroon AA, Lenders JW, van Montfrans GA, Smit AJ, et al. Prevalence and persistence of masked hypertension in treated hypertensive patients. Am J Hypertens. 2007;20: 1258–65. Epub 2007/12/01. doi: 10.1016/j.amjhyper.2007.08.002 18047914
26. Bosworth HB, Olsen MK, McCant F, Harrelson M, Gentry P, Rose C, et al. Hypertension Intervention Nurse Telemedicine Study (HINTS): testing a multifactorial tailored behavioral/educational and a medication management intervention for blood pressure control. Am Heart J. 2007;153: 918–24. Epub 2007/06/02. doi: 10.1016/j.ahj.2007.03.004 17540191
27. Bosworth HB, Olsen MK, Grubber JM, Neary AM, Orr MM, Powers BJ, et al. Two self-management interventions to improve hypertension control: a randomized trial. Ann Intern Med. 2009;151: 687–95. Epub 2009/11/19. 19920269
28. Yu SM, Tzou WS, Lo WS, Kuo YH, Lee HT, Wu R. Regulation of alpha-amylase-encoding gene expression in germinating seeds and cultured cells of rice. Gene. 1992;122: 247–53. Epub 1992/12/15. 1339378
29. Fisher D. Two-stage individual participant data meta-analysis and generalised forest plots. Stata Journal. 2015;15: 369–96.
30. Stergiou GS, Karpettas N, Destounis A, Tzamouranis D, Nasothimiou E, Kollias A, et al. Home blood pressure monitoring alone vs. combined clinic and ambulatory measurements in following treatment-induced changes in blood pressure and organ damage. Am J Hypertens. 2014;27: 184–92. Epub 2013/11/06. doi: 10.1093/ajh/hpt206 24190902
31. Wakefield BJ, Holman JE, Ray A, Scherubel M, Adams MR, Hillis SL, et al. Effectiveness of home telehealth in comorbid diabetes and hypertension: a randomized, controlled trial. Telemed J E Health. 2011;17: 254–61. Epub 2011/04/12. doi: 10.1089/tmj.2010.0176 21476945
32. Parati G, Omboni S, Compare A, Grossi E, Callus E, Venco A, et al. Blood pressure control and treatment adherence in hypertensive patients with metabolic syndrome: protocol of a randomized controlled study based on home blood pressure telemonitoring vs. conventional management and assessment of psychological determinants of adherence (TELEBPMET Study). Trials. 2013;14: 22. Epub 2013/01/25. doi: 10.1186/1745-6215-14-22 23343138
33. Parati G, Omboni S, Albini F, Piantoni L, Giuliano A, Revera M, et al. Home blood pressure telemonitoring improves hypertension control in general practice. The TeleBPCare study. J Hypertens. 2009;27: 198–203. Epub 2009/01/17. 19145785
34. Ogedegbe G, Tobin JN, Fernandez S, Cassells A, Diaz-Gloster M, Khalida C, et al. Counseling African Americans to Control Hypertension: cluster-randomized clinical trial main effects. Circulation. 2014;129: 2044–51. Epub 2014/03/25. doi: 10.1161/CIRCULATIONAHA.113.006650 24657991
35. McManus RJ, Mant J, Haque MS, Bray EP, Bryan S, Greenfield SM, et al. Effect of self-monitoring and medication self-titration on systolic blood pressure in hypertensive patients at high risk of cardiovascular disease: the TASMIN-SR randomized clinical trial. JAMA. 2014;312: 799–808. Epub 2014/08/27. doi: 10.1001/jama.2014.10057 25157723
36. McManus RJ, Mant J, Bray EP, Holder R, Jones MI, Greenfield S, et al. Telemonitoring and self-management in the control of hypertension (TASMINH2): a randomised controlled trial. Lancet. 2010;376: 163–72. Epub 2010/07/14. doi: 10.1016/S0140-6736(10)60964-6 20619448
37. Margolis KL, Asche SE, Bergdall AR, Dehmer SP, Groen SE, Kadrmas HM, et al. Effect of home blood pressure telemonitoring and pharmacist management on blood pressure control: a cluster randomized clinical trial. JAMA. 2013;310: 46–56. Epub 2013/07/04. doi: 10.1001/jama.2013.6549 23821088
38. Magid DJ, Ho PM, Olson KL, Brand DW, Welch LK, Snow KE, et al. A multimodal blood pressure control intervention in 3 healthcare systems. Am J Manag Care. 2011;17: e96–103. Epub 2011/07/21. 21774100
39. Kerry SM, Markus HS, Khong TK, Cloud GC, Tulloch J, Coster D, et al. Home blood pressure monitoring with nurse-led telephone support among patients with hypertension and a history of stroke: a community-based randomized controlled trial. CMAJ. 2013;185: 23–31. Epub 2012/11/07. doi: 10.1503/cmaj.120832 23128283
40. Hebert PL, Sisk JE, Tuzzio L, Casabianca JM, Pogue VA, Wang JJ, et al. Nurse-led disease management for hypertension control in a diverse urban community: a randomized trial. J Gen Intern Med. 2012;27: 630–9. Epub 2011/12/07. doi: 10.1007/s11606-011-1924-1 22143452
41. Halme L, Vesalainen R, Kaaja M, Kantola I. Self-monitoring of blood pressure promotes achievement of blood pressure target in primary health care. Am J Hypertens. 2005;18: 1415–20. Epub 2005/11/11. doi: 10.1016/j.amjhyper.2005.05.017 16280273
42. Green BB, Ralston JD, Fishman PA, Catz SL, Cook A, Carlson J, et al. Electronic Communications and Home Blood Pressure Monitoring (e-BP) study: Design, delivery, and evaluation framework. Contemp Clin Trials. 2008;29: 376–95. doi: 10.1016/j.cct.2007.09.005 17974502
43. Godwin M, Lam M, Birtwhistle R, Delva D, Seguin R, Casson I, et al. A primary care pragmatic cluster randomized trial of the use of home blood pressure monitoring on blood pressure levels in hypertensive patients with above target blood pressure. Fam Pract. 2010;27: 135–42. Epub 2009/12/25. doi: 10.1093/fampra/cmp094 20032170
44. Bove AA, Homko CJ, Santamore WP, Kashem M, Kerper M, Elliott DJ. Managing hypertension in urban underserved subjects using telemedicine—a clinical trial. Am Heart J. 2013;165: 615–21. Epub 2013/03/30. doi: 10.1016/j.ahj.2013.01.004 23537980
45. McKinstry B, Hanley J, Wild S, Pagliari C, Paterson M, Lewis S, et al. Telemonitoring based service redesign for the management of uncontrolled hypertension: multicentre randomised controlled trial. BMJ. 2013;346: f3030. Epub 2013/05/28. doi: 10.1136/bmj.f3030 23709583
46. Leiva A, Aguilo A, Fajo-Pascual M, Moreno L, Martin MC, Garcia EM, et al. Efficacy of a brief multifactorial adherence-based intervention in reducing blood pressure: a randomized clinical trial. Patient Prefer Adherence. 2014;8: 1683–90. Epub 2014/12/20. doi: 10.2147/PPA.S66927 25525344
47. Yi SS, Tabaei BP, Angell SY, Rapin A, Buck MD, Pagano WG, et al. Self-blood pressure monitoring in an urban, ethnically diverse population: a randomized clinical trial utilizing the electronic health record. Circ Cardiovasc Qual Outcomes. 2015;8: 138–45. Epub 2015/03/05. doi: 10.1161/CIRCOUTCOMES.114.000950 25737487
48. Stewart K, George J, Mc Namara KP, Jackson SL, Peterson GM, Bereznicki LR, et al. A multifaceted pharmacist intervention to improve antihypertensive adherence: a cluster-randomized, controlled trial (HAPPy trial). J Clin Pharm Ther. 2014;39: 527–34. Epub 2014/06/20. doi: 10.1111/jcpt.12185 24943987
49. Kim KB, Han HR, Huh B, Nguyen T, Lee H, Kim MT. The effect of a community-based self-help multimodal behavioral intervention in Korean American seniors with high blood pressure. Am J Hypertens. 2014;27: 1199–208. Epub 2014/03/29. doi: 10.1093/ajh/hpu041 24671049
50. Magid DJ, Olson KL, Billups SJ, Wagner NM, Lyons EE, Kroner BA. A pharmacist-led, American Heart Association Heart360 Web-enabled home blood pressure monitoring program. Circ Cardiovasc Qual Outcomes. 2013;6: 157–63. Epub 2013/03/07. doi: 10.1161/CIRCOUTCOMES.112.968172 23463811
51. Green BB, Anderson ML, Cook AJ, Catz S, Fishman PA, McClure JB, et al. e-Care for heart wellness: a feasibility trial to decrease blood pressure and cardiovascular risk. Am J Prev Med. 2014;46: 368–77. Epub 2014/03/22. doi: 10.1016/j.amepre.2013.11.009 24650839
52. Sterne JA, White IR, Carlin JB, Spratt M, Royston P, Kenward MG, et al. Multiple imputation for missing data in epidemiological and clinical research: potential and pitfalls. BMJ. 2009;338: b2393. Epub 2009/07/01. doi: 10.1136/bmj.b2393 19564179
53. Agarwal R, Bills JE, Hecht TJ, Light RP. Role of home blood pressure monitoring in overcoming therapeutic inertia and improving hypertension control: a systematic review and meta-analysis. Hypertension. 2011;57: 29–38. Epub 2010/12/01. doi: 10.1161/HYPERTENSIONAHA.110.160911 21115879
54. Fletcher BR, Hartmann-Boyce J, Hinton L, McManus RJ. The Effect of Self-Monitoring of Blood Pressure on Medication Adherence and Lifestyle Factors: A Systematic Review and Meta-Analysis. Am J Hypertens. 2015;28: 1209–21. Epub 2015/03/01. doi: 10.1093/ajh/hpv008 25725092
55. Omboni S, Gazzola T, Carabelli G, Parati G. Clinical usefulness and cost effectiveness of home blood pressure telemonitoring: meta-analysis of randomized controlled studies. J Hypertens. 2013;31: 455–67; discussion 467–8. Epub 2013/01/10. doi: 10.1097/HJH.0b013e32835ca8dd 23299557
56. Wald DS, Law M, Mills S, Bestwick JP, Morris JK, Wald NJ. A 16-week, randomized, double-blind, placebo-controlled, crossover trial to quantify the combined effect of an angiotensin-converting enzyme inhibitor and a beta-blocker on blood pressure reduction. Clin Ther. 2008;30: 2030–9. Epub 2008/12/26. doi: 10.1016/j.clinthera.2008.11.003 19108791
57. Group SR, Wright JT Jr., Williamson JD, Whelton PK, Snyder JK, Sink KM, et al. A Randomized Trial of Intensive versus Standard Blood-Pressure Control. N Engl J Med. 2015;373: 2103–16. doi: 10.1056/NEJMoa1511939 26551272
58. Baral-Grant S, Haque MS, Nouwen A, Greenfield SM, McManus RJ. Self-Monitoring of Blood Pressure in Hypertension: A UK Primary Care Survey. Int J Hypertens. 2012;2012: 582068. Epub 2011/10/21. doi: 10.1155/2012/582068 22013510
59. Joffres M, Falaschetti E, Gillespie C, Robitaille C, Loustalot F, Poulter N, et al. Hypertension prevalence, awareness, treatment and control in national surveys from England, the USA and Canada, and correlation with stroke and ischaemic heart disease mortality: a cross-sectional study. BMJ Open. 2013;3: e003423. Epub 2013/09/03. doi: 10.1136/bmjopen-2013-003423 23996822