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. 2019 Feb 13;57(3):230–236. doi: 10.1097/MLR.0000000000001064

Effect of Home Medication Titration on Blood Pressure Control in Patients With Hypertension

A Meta-Analysis of Randomized Controlled Trials

Ting-Yu Chen *,, Chi-Wen Kao ‡,§,, Shu-Meng Cheng ∥,, Yue-Cune Chang #
PMCID: PMC6410972  PMID: 30762831

Supplemental Digital Content is available in the text.

Key Words: medication titration, hypertension, meta-analysis

Abstract

Background:

Medication titration has been used in home blood pressure (BP) control, with the expectation of enabling patients with hypertension to better manage their BP.

Objective:

The study goal was to estimate the effects of medication titration intervention in lowering the systolic blood pressure and diastolic blood pressure of patients with hypertension.

Methods:

The meta-analysis included randomized controlled trials on adults diagnosed with hypertension and BP≧130/80 mm Hg, having a medication-titration intervention, and using a home BP measurement. We systematically searched PubMed, CINAHL, Ovid-Medline, and the Cochrane Library, for studies published from 1997 to 2017. The quality of the studies was evaluated by the Modified Jadad scale. Statistical heterogeneity among the trials was evaluated using Q statistics and I2. Publication bias was assessed with the funnel plot and Rosenthal’s fail-safe N.

Results:

The meta-analysis included 4 studies randomizing 1335 participants. Medication-titration intervention significantly assisted hypertensive patients to improve BP control; systolic blood pressure was reduced by 6.86 mm Hg [95% confidence interval (CI), 4.80-8.93, P<0.0001] and diastolic blood pressure by 3.03 mm Hg (95% CI, 2.07-3.99, P<0.0001), did not significantly affect EQ-5D scores (mean difference, 0.02; 95% CI, −0.01 to 0.04, P=0.13).

Conclusions:

Our findings suggest home medication titration of antihypertensive medication for hypertensive patients significantly improved home BP control. However, the strategy did not enhance quality of life in patients with hypertension.


Hypertension affects ~40% of the adult population worldwide and is one of the leading causes of disease-related death and disability.1,2 In the United States, 1 in every 3 adults has hypertension;3 in Canada, ~1 in 4 adults is affected.4 In Taiwan, hypertension has been one of the top 10 causes of death for more than 10 years. In 2015, the death rate from hypertension was 23.6 per 10,000 people, compared to 8.3 per 10,000 people in 2005, indicating a significant increase in death due to hypertension in the past 10 years.5 It is estimated that the percentage of the global population suffering from hypertension will increase to 29.2% in 2025.6 Effective control of blood pressure (BP) can lower the incident rate of cerebrovascular accidents by 35%–40%, myocardial infarctions by 20%–25%, and heart failures by 50%.7

Uncontrolled BP not only causes target organ damage,4 but also influences patients’ quality of life (QoL).8,9 Home BP monitoring can be used to assess the treatment responses in patients with hypertension.10 The findings of a meta-analysis showed that home BP monitoring combined with other strategies resulted in more effective and lasting impact on home BP control, and medication titration is one of these strategies.11

Medication titration is a novel strategy, which allows patients or medical professionals to adjust their medicine (additional, maintain, or decrease dose) depending on a medication titration plan.12 This strategy has been widely used to assist patients with asthma,13 diabetes,14 and those receiving long-term anticoagulant treatment to self-manage and adhere to their treatments.15 In recent years, medication titration has been used for BP control, with the expectation of enabling patients with hypertension to better manage their BP at home. The medication titration plan for hypertensive patients involves setting target BP, self-monitoring BP, and constructing a medication titration schedule.16 Each medication titration step is conducted based on the average home BP measurement readings.17 Several randomized controlled trials (RCTs) identified that medication titration strategy through a step-by-step approach can remind patients about their BP readings and target goals.16,1820 The strategy filled the gap of patient’s insufficiency of the BP readings and target, which is one of the main causes of poor BP control.21 However, some studies has significantly decreased in systolic blood pressure (SBP) and diastolic blood pressure (DBP) between groups;16,19 some studies conversely.18,20

No meta-analysis has been conducted that examines the effects of medication titration on BP control. Therefore, the purpose of this systematic review and meta-analysis was to investigate the overall effectiveness of a medication titration strategy on lowering the SBP and DBP of patients with hypertension.

METHODS

This analysis followed the guidelines of the Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA).22

Search Strategy

We searched PubMed, CINAHL, Ovid-Medline, and the Cochrane Library, for studies published from 1997 to 2017. The keywords used were “blood pressure,” “hypertension,” “self-titration,” “medication-titration,” and “home-titration.” We also used Medical Subject Headings to identify the terminology of keywords.

Study Selection

Studies for review were included if they met the following criteria: (1) RCT; (2) subjects were adult patients with an existing diagnosis of hypertension by a physician, and BP≧130/80 mm Hg; (3) a medication-titration intervention was provided to the intervention group; (4) use of a home BP measurement; (5) written in English or Chinese; and (6) presented adequate data to calculate the effect size (eg, sample size, mean, SD, 95% confidence interval, and P-value).

Quality Assessment

The methodological quality of included studies was independently evaluated by 2 reviewers (C.W.K. and T.Y.C.) using the Modified Jadad scale.23 The scale includes 8 items: (1) Was the study designed as randomized? (2) Was the method of randomization appropriate? (3) Was the study designed as blind? (4) Was the method of blinding appropriate? (5) Was there a description of withdrawals and drop outs? (6) Was there a clear description of the inclusion and exclusion criteria? (7) Was the method used to assess adverse effects described? (8) Was the method of statistical analysis described? The questions are evaluated as yes (1-point) or no (0-point) for a maximum total score of 8. Scores higher than 4 points reflect favorable quality. Any disagreements between the 2 reviewers regarding the quality evaluation were resolved by discussion.

Data Extraction

C.W.K. and T.Y.C. independently reviewed full-text articles and extracted the data, which included authors, publication year, title of study, sample size of intervention and control groups, participants’ age, gender and body mass index, percentage of current smokers, comorbidity, baseline and post antihypertensive medicine dose, baseline and postintervention SBP and DBP, follow-up times and intervention context, and the scores of the State-Trait Anxiety Inventory (STAI-6) and the EuroQol 5 dimensions questionnaire (EQ-5D). The 2 reviewers discussed any inconsistency in the data they extracted to achieve consensus.

Data Analysis and Synthesis

This meta-analysis was conducted using Comprehensive Meta-Analysis version 2.0 software. The BP data were reported as the mean and SD in each original study. When necessary, we estimated SD from the 95% confidence intervals provided. Statistical heterogeneity among the trials was evaluated using Q statistics and I2. If I2>75%, high heterogeneity was indicated.24 On the basis of the findings of the heterogeneity analysis, we used a random-effects or fixed-effects model to pool data and estimate the overall effect.25 A fixed-effects model is based on the assumption that the sole source of variation in observed outcomes is that occurring within the study; that is, the effect expected from each study is the same. A random-effects model assume that each of the included trials may estimate a different treatment effect. Therefore, need to be taken into account the variance within trials and the variance between trials.

Potential publication bias was assessed with a funnel plot and Rosenthal’s fail-safe N. An asymmetrical funnel plot indicates publication bias.26 The Rosenthal’s method estimates the number of unpublished studies with a zero-effect size that would be needed to reduce the overall effect size to cause it become nonsignificant. If only a few studies are needed to negate the effect, publication bias should be considered. Conversely, if a large number of studies are needed to negate the effect, there is less reason for the consideration of publication bias.27

RESULTS

Characteristics of Included Trials

A PRISMA flow diagram (Fig. 1) illustrates the study selection process of clinical trials for the meta-analysis, based on the inclusion and exclusion criteria. In total, 50 titles and abstracts were identified through database screening, and 5 studies were found through hand searches. A total of 33 studies were removed due to duplication. Of the remaining 22 studies retrieved, we excluded 4 studies with a non-RCT design,17,2830 4 due to study protocols, which were not present in the BP readings,3134 1 study providing titration intervention for both arms,35 1 study recruiting patients with BP <130/80 mm Hg,36 1 study presenting an unclear titration plan,37 1 study reporting mean arterial pressure,15 and 6 commentary articles.3843 Finally, we recruited 4 RCTs for meta-analysis (Table 1).16,1820 These 4 studies included 1335 participants with hypertension; 670 and 665 patients were randomly assigned to the intervention and control groups, respectively. In the intervention group the pooled mean SBP at baseline was 149.72 (SD=12.99) mm Hg and DBP was 83.20 (SD=8.61) mm Hg. In the control group the pooled mean SBP at baseline was 149.45 (SD=13.67) mm Hg and DBP was 82.83 (SD=9.83) mm Hg.

FIGURE 1.

FIGURE 1

PRISMA flow diagram for the selection process of clinical trials for meta-analysis, showing inclusion and exclusion criteria, selection, and inclusion process. RCT indicates randomized controlled trial.

TABLE 1.

Characteristics of Participants and Interventions for Included Studies

graphic file with name mlr-57-230-g002.jpg

We evaluated methodological quality of these 4 studies by using the 8-item Modified Jadad scale (eTable 1, Supplemental Digital Content 1, http://links.lww.com/MLR/B700). The Jadad scores for these 4 studies were >4 points, which indicated favorable quality.23 Two studies evaluated received a score of 8.16,19 One study scored 5 points because it did not describe the double blinding, and did not report adverse effects.18 One study scored 6 points because it did not use the double-blind design.20

Effect on BP Control

We used a random-effects model for examining the effects of medication titration on SBP control because of the heterogeneity among trials (χ2=5.39, P=0.15; I2=44.29%). The pooled mean effect size of SBP was estimated as 6.86 [95% confidence interval (CI), 4.80-8.93; P<0.0001], a statistically significant difference between the intervention and control groups (Fig. 2). The results indicated that medication titration strategy significantly assisted hypertension patients to improve their SBP control.

FIGURE 2.

FIGURE 2

Forest plot of random-effects model for studies examining the effects of medication titration on systolic blood pressure between intervention and nonintervention groups: mean differences between groups. CI indicates confidence intervals.

Because no heterogeneity among trials in DBP was detected (χ2=1.24, P=0.74; I2=0%), we used a fixed-effects model to examine the effect of self-titration of medication on DBP control. The pooled mean effect size of DBP was estimated as 3.03 (95% CI, 2.07-3.99; P<0.0001), a statistically significant difference between the intervention and control groups (Fig. 3), indicating medication titration strategy also significantly improved DBP control in hypertensive patients.

FIGURE 3.

FIGURE 3

Forest plot of fixed-effects model on studies looking at the effect of self-titration of medication on diastolic blood pressure between intervention and nonintervention groups: mean differences between groups. CI indicates confidence intervals.

Effect on QoL

To examine the effect of medication titration strategy on improving QoL in patients with hypertension, we conducted a subgroup analysis of 2 RCTs that used the EQ-5D to evaluate QoL.16,19 We used the random-effects model to determine the effect of medication titration strategy on QoL because homogeneity was detected among trials (χ2=10.20, P=0.001; I2=90.19%). The pooled mean difference of EQ-5D scores was estimated as 0.02 (95% CI, −0.01 to 0.04; P=0.13) (Fig. 4), indicating no difference in improvement of QoL between hypertensive patients receiving or not receiving a medication-titration strategy.

FIGURE 4.

FIGURE 4

Forest plot of fixed-effects model for on studies looking at the effects of a medication titration strategy on quality of life. Mean differences in EQ-5D scores between intervention and nonintervention groups. CI indicates confidence intervals.

Publication Bias

The funnel plot of the 4 RCTs detected no severe publication bias (eFigure 1, Supplemental Digital Content 1, http://links.lww.com/MLR/B700). The results of Rosenthal’s fail-safe N analysis showed that 91 studies with zero-effect would be needed to be published to render the mean effect size of SBP as nonsignificant. Visual inspection of the funnel plot for DBP also showed no severe publication bias and the findings of Rosenthal’s fail-safe N indicated that 34 studies with zero-effect would be needed to render the mean effect size of DBP as nonsignificant (eFigure 2, Supplemental Digital Content 1, http://links.lww.com/MLR/B700). These findings suggest that publication bias was unlikely to interfere with the explanation of the main results of this meta-analysis.

DISCUSSION

This meta-analysis contributes to knowledge about using a titration strategy for antihypertensive medication to improve home BP control in patients with hypertension. This the first meta-analysis to evaluate the effects of medication titration for home BP control. This meta-analysis provides evidence that using medication titration can significantly reduce SBP and DBP, but does not significantly improve QoL scores. These findings suggest that medication titration is beneficial for BP control in patients with hypertension; additionally, 3 studies reported no harmful events.16,19,20

The hypertensive patients in the 4 included studies were guided by a medication titration plan to control their home BP. The medication titration plan was comprised of setting home BP goals with medical professionals, measuring and monitoring home BP, and titrating antihypertensive medications according to their average home BP, either by the patient themselves16,19 or health care professionals.18,20 Both patients and medical professionals evaluated home BP readings and shared the decision-making for how to titrate the antihypertensive medications. The TASMINH2 trial compared with the control group, the intervention group had significantly more decreases in SBP by 3.7 mm Hg (95% CI, 0.8-6.6) and DBP by 1.3 mm Hg (95% CI, 0.3-2.6).19 The TASMIN-SR trial recruited high-risk patients compared with the control group, the intervention groups had significant differences in SBP 8.8 mm Hg (95% CI, 4.9-12.7) and DBP 3.1 mm Hg (95% CI, 0.7-5.5) at 12 months, respectively.

The patients who received the medication titration plan have to self-measure and report BP every day. The strategy of self-monitor BP increased reliability of BP values, absence of white-coat and masked hypertension, and a more accurate reflection of cardiovascular prognosis compared with BP readings completed at the clinic.33 Furthermore, a meta-analysis examining the effect of self-monitored BP at home on BP control reported that patients with self-monitoring BP at home had a significant decrease in both SBP and DBP at 6 months, compared with the patients without self-monitoring BP (weighted mean difference, 3.9 and 2.4 mm Hg, respectively). The authors suggested that home-based BP monitoring with co-intervention (eg, providing educational materials, tele-counseling, phone monitoring, or medication management with decision support) may achieve long-term efficacy on BP control.11 According to a previous qualitative study, the medication titration process can alert participants as to whether they are, or are not, on the right track.28 The researchers found when patients not only measured their own BP, but also understood the implications of the BP readings. Therefore, patients may engage in their disease management.1620 The strategy of medication titration enhances patient motivation to take more responsibility to maintain better BP control.28 The medication titration strategy may also effectively influence patients’ behavior.44

In addition, all of the presented studies provided lifestyle modification education for the patients.16,1820 The guidelines in American Heart Association for management of hypertension has identified lifestyle modification as a key to prevention and control of hypertension.45 Previous study suggested that the clinical professionals may provide the education through the internet for hypertension patients to modify their lifestyle and prevent long-term risk of cardiovascular diseases.46 The 4 studies also used internet-based system16,19 or telephone calls18,20 to follow-up patient safety and adherence.

There are some limitations to this meta-analysis. First, we found few recent RCTs which used medication titration for control of hypertension. Although we contacted many authors and conducted hand searches from the reference lists of all the collected articles, we were only able to include 4 RCTs, which fit the inclusion criteria and had adequate quality for this meta-analysis. Second, this meta-analysis showed no significant improvement in scores for QoL, which is most likely due to the small sample size resulting in low statistical power. One meta-analysis study indicated that patients with hypertension had a lower QoL for both physical and mental components (mean difference, −2.43; 95% CI, −4.77 to −0.08 and mean difference, −1.68; 95% CI, −2.14 to −1.23, respectively) compared with normotensive.47 Issues associated with how to improve QoL in patients with hypertension are important and, as such, require further investigation. Last, not all of the included studies had baseline data for anxiety status and medication dosages in hypertension patients, therefore, we cannot present subgroup analysis.

CONCLUSIONS

The results of this systematic review and meta-analysis provide evidence that medication titration could assist hypertension patients in controlling their SBP and DBP; however, there were no significant findings on QoL score. Medication titration is a novel home BP control strategy. We recommend that the health professionals be designated to assist hypertensive patients with managing their home BP through the use of medication titration in clinical practice.

Supplementary Material

SUPPLEMENTARY MATERIAL
mlr-57-230-s001.docx (23.5KB, docx)

Supplemental Digital Content is available for this article. Direct URL citations appear in the printed text and are provided in the HTML and PDF versions of this article on the journal's website, www.lww-medicalcare.com.

ACKNOWLEDGMENTS

The authors thank the Research Center for Testing and Assessment of the National Academy for Educational Research, Taiwan, and Associate Research Fellow Jin-Chang Hsieh for providing statistical consultation.

Footnotes

Present address: Ting-Yu Chen, MD and Chi-Wen Kao, PhD, No. 161, Section 6, Minquan East Road, Neihu District, Taipei City, Taiwan.

Present address: Shu-Meng Cheng, PhD, No. 325, Section 2, Chenggong Road, Neihu District, Taipei City, Taiwan.

Present address: Yue-Cune Chang, PhD, No. 151, Yingzhuan Road, Tamsui District, New Taipei City, Taiwan.

The authors declare no conflict of interest.

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Associated Data

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Supplementary Materials

SUPPLEMENTARY MATERIAL
mlr-57-230-s001.docx (23.5KB, docx)

Supplemental Digital Content is available for this article. Direct URL citations appear in the printed text and are provided in the HTML and PDF versions of this article on the journal's website, www.lww-medicalcare.com.


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