Mobile phone text messaging for medication adherence in secondary prevention of cardiovascular disease
- PMID: 38533994
- PMCID: PMC10966941
- DOI: 10.1002/14651858.CD011851.pub3
Mobile phone text messaging for medication adherence in secondary prevention of cardiovascular disease
Abstract
Background: Cardiovascular diseases (CVDs) are the leading cause of death globally, accounting for almost 18 million deaths annually. People with CVDs have a five times greater chance of suffering a recurrent cardiovascular event than people without known CVDs. Although drug interventions have been shown to be cost-effective in reducing the risk of recurrent cardiovascular events, adherence to medication remains suboptimal. As a scalable and cost-effective approach, mobile phone text messaging presents an opportunity to convey health information, deliver electronic reminders, and encourage behaviour change. However, it is uncertain whether text messaging can improve medication adherence and clinical outcomes. This is an update of a Cochrane review published in 2017.
Objectives: To evaluate the benefits and harms of mobile phone text messaging for improving medication adherence in people with CVDs compared to usual care.
Search methods: We searched CENTRAL, MEDLINE, Embase, four other databases, and two trial registers. We also checked the reference lists of all primary included studies and relevant systematic reviews and meta-analyses. The date of the latest search was 30 August 2023.
Selection criteria: We included randomised controlled trials (RCTs) with participants with established arterial occlusive events. We included trials investigating interventions using short message service (SMS) or multimedia messaging service (MMS) with the aim of improving adherence to medication for the secondary prevention of cardiovascular events. The comparator was usual care. We excluded cluster-RCTs and quasi-RCTs.
Data collection and analysis: We used standard Cochrane methods. Our primary outcomes were medication adherence, fatal cardiovascular events, non-fatal cardiovascular events, and combined CVD event. Secondary outcomes were low-density lipoprotein cholesterol for the effect of statins, blood pressure for antihypertensive drugs, heart rate for the effect of beta-blockers, urinary 11-dehydrothromboxane B2 for the antiplatelet effects of aspirin, adverse effects, and patient-reported experience. We used GRADE to assess the certainty of the evidence for each outcome.
Main results: We included 18 RCTs involving a total of 8136 participants with CVDs. We identified 11 new studies in the review update and seven studies in the previous version of the review. Participants had various CVDs including acute coronary syndrome, coronary heart disease, stroke, myocardial infarction, and angina. All studies were conducted in middle- and high-income countries, with no studies conducted in low-income countries. The mean age of participants was 53 to 64 years. Participants were recruited from hospitals or cardiac rehabilitation facilities. Follow-up ranged from one to 12 months. There was variation in the characteristics of text messages amongst studies (e.g. delivery method, frequency, theoretical grounding, content used, personalisation, and directionality). The content of text messages varied across studies, but generally included medication reminders and healthy lifestyle information such as diet, physical activity, and weight loss. Text messages offered advice, motivation, social support, and health education to promote behaviour changes and regular medication-taking. We assessed risk of bias for all studies as high, as all studies had at least one domain at unclear or high risk of bias. Medication adherence Due to different evaluation score systems and inconsistent definitions applied for the measurement of medication adherence, we did not conduct meta-analysis for medication adherence. Ten out of 18 studies showed a beneficial effect of mobile phone text messaging for medication adherence compared to usual care, whereas the other eight studies showed either a reduction or no difference in medication adherence with text messaging compared to usual care. Overall, the evidence is very uncertain about the effects of mobile phone text messaging for medication adherence when compared to usual care. Fatal cardiovascular events Text messaging may have little to no effect on fatal cardiovascular events compared to usual care (odds ratio 0.83, 95% confidence interval (CI) 0.47 to 1.45; 4 studies, 1654 participants; low-certainty evidence). Non-fatal cardiovascular events We found very low-certainty evidence that text messaging may have little to no effect on non-fatal cardiovascular events. Two studies reported non-fatal cardiovascular events, neither of which found evidence of a difference between groups. Combined CVD events We found very low-certainty evidence that text messaging may have little to no effect on combined CVD events. Only one study reported combined CVD events, and did not find evidence of a difference between groups. Low-density lipoprotein cholesterol Text messaging may have little to no effect on low-density lipoprotein cholesterol compared to usual care (mean difference (MD) -1.79 mg/dL, 95% CI -4.71 to 1.12; 8 studies, 4983 participants; very low-certainty evidence). Blood pressure Text messaging may have little to no effect on systolic blood pressure (MD -0.93 mmHg, 95% CI -3.55 to 1.69; 8 studies, 5173 participants; very low-certainty evidence) and diastolic blood pressure (MD -1.00 mmHg, 95% CI -2.49 to 0.50; 5 studies, 3137 participants; very low-certainty evidence) when compared to usual care. Heart rate Text messaging may have little to no effect on heart rate compared to usual care (MD -0.46 beats per minute, 95% CI -1.74 to 0.82; 4 studies, 2946 participants; very low-certainty evidence).
Authors' conclusions: Due to limited evidence, we are uncertain if text messaging reduces medication adherence, fatal and non-fatal cardiovascular events, and combined cardiovascular events in people with cardiovascular diseases when compared to usual care. Furthermore, text messaging may result in little or no effect on low-density lipoprotein cholesterol, blood pressure, and heart rate compared to usual care. The included studies were of low methodological quality, and no studies assessed the effects of text messaging in low-income countries or beyond the 12-month follow-up. Long-term and high-quality randomised trials are needed, particularly in low-income countries.
Copyright © 2024 The Authors. Cochrane Database of Systematic Reviews published by John Wiley & Sons, Ltd. on behalf of The Cochrane Collaboration.
Conflict of interest statement
JR holds a National Health and Medical Research Council (NHMRC) Fellowship (investigator‐initiated), which supports part of her salary that includes academic time spent working on this review; and an NHMRC Synergy Grant, paid to institution. JR was one of the authors of Chow 2015 and Chow 2022. JR was not involved in assessing the eligibility of the studies, extracting data, or assessing risk of bias or the certainty of the evidence for this review update. These tasks were performed by two independent review authors (QT, NH). Chow 2015 was supported by grants from the National Heart Foundation of Australia Grant‐in‐Aid (G10S5110) and a BUPA Foundation Grant. Chow 2022 was supported by the NHMRC (APP1042290). JR retained complete control over the design, methods, data analysis, and reporting of both studies. JR did not receive the funds personally for either study and did not benefit financially from the payment or have access to or control of the funds. JR reports a trademark for the TEXTCARE software that delivers text message programmes for research, which is owned by the University of Sydney. It is not patented and was not used to deliver any of the research projects for this Cochrane review. JR has not benefitted financially from the trademark, and the University of Sydney does not intend to commercialise it.
QT: none known.
KH reports a grant from the National Health and Medical Research Council, which is a government‐funded fellowship and is not related to the topic. KH retains complete control over all study designs, methods, data analysis, and reporting related to her grant.
MH: none known.
NH: none known.
CZ: none known.
CF is a former editor of Cochrane Heart but was not an editor of Cochrane Heart in the 36 months prior to this review update. CF was not involved in the editorial process for this review. CF was also involved in a study eligible for inclusion in the review (Bermon 2021). The study was supported by the Ministerio de Ciencia Tecnología e Innovación (code: 656672553352; grants 899‐2015 and 753 de 2016); Fundación Cardiovascular de Colombia, Floridablanca; UK Medical Research Council Funded Reference (reference number: MR/N021304/1); and the Universidad Pontificia Bolivariana, Bucaramanga. However, CF was not involved in assessing the eligibility of the study, extracting data, or assessing risk of bias or the certainty of the evidence for this review update; these tasks were performed by two independent review authors (QT, NH). CF’s institution did not receive any payments for this study, and CF had complete control over the study design, methods, data analysis, and reporting.
PP has published an opinion on the topic of text messaging, Adler 2018, and several editorials, but these were unrelated to the current review. PP is affiliated with the World Heart Federation, and was and remains affiliated to London School of Hygiene & Tropical Medicine, but the organisation received no financial contribution for PP's work on this Cochrane review and had no involvement in the protocol or published work. PP is a former editorial advisor of the Cochrane Heart Group and was not involved in the editorial process for this review update. PP was also involved in the Bermon 2021 study, which was eligible for inclusion in the review. The study was supported by the Ministerio de Ciencia Tecnología e Innovación (code: 656672553352; grants 899‐2015 and 753 de 2016); Fundación Cardiovascular de Colombia, Floridablanca; and UK Medical Research Council Funded Reference (reference number: MR/N021304/1). However, PP was not involved in assessing the eligibility of the study, extracting data, or assessing risk of bias or the certainty of the evidence for this review update; these tasks were performed by two independent review authors (QT, NH). PP’s institution did not receive any payments for this study, and PP had complete control over the study design, methods, data analysis, and reporting.
CKC was one of the authors of Chow 2015 and Chow 2022. CKC was not involved in assessing the eligibility of the studies, extracting data, or assessing risk of bias or the certainty of the evidence for this review update. These tasks were performed by two independent review authors (QT, NH). Chow 2015 was supported by grants from the National Heart Foundation of Australia Grant‐in‐Aid (G10S5110) and a BUPA Foundation Grant. Chow 2022 was supported by the National Health and Medical Research Council (NHMRC) (APP1042290). CKC was the Principal Investigator for both of these studies, and, as such, payments were made to her institution, University of Sydney, for delivery of the research projects (such as paying research assistants and to perform measurements and analyses). However, both studies were investigator‐initiated, and CKC received no direct financial gain and retained complete control over the study design, methods, data analysis, and reporting. CKC holds an NHMRC Fellowship (investigator‐initiated), which supports part of her salary that includes academic time spent working on this review; paid to institution, but CKC benefitted or had control over the funds. CKC is a Cardiologist at Westmead Hospital in Australia. CKC reports a trademark for the TEXTCARE software that delivers text message programmes for research, which is owned by the University of Sydney. It is not patented and was not used to deliver any of the research projects for this Cochrane review. CKC has not benefitted financially from the trademark, and the University of Sydney does not intend to commercialise it. CKC has also published an opinion piece on the topic of text messaging (Klimis 2021).
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Update of
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Mobile phone text messaging to improve medication adherence in secondary prevention of cardiovascular disease.Cochrane Database Syst Rev. 2017 Apr 29;4(4):CD011851. doi: 10.1002/14651858.CD011851.pub2. Cochrane Database Syst Rev. 2017. Update in: Cochrane Database Syst Rev. 2024 Mar 27;3:CD011851. doi: 10.1002/14651858.CD011851.pub3. PMID: 28455948 Free PMC article. Updated.
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Acevedo 2023 {published data only}
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References to ongoing studies
ACTRN12621000754842 {published data only}
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- ACTRN12621000754842. Efficacy and safety of adjunctive virtual models of care in the secondary prevention of cardiovascular events in adults discharged from hospital after myocardial infarction or decompensated heart failure. anzctr.org.au/ACTRN12621000754842.aspx (first received 16 June 2021).
CTRI/2021/06/034463 {published data only}
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- CTRI/2021/06/034463. Drug adherence in persons after stunting and the effect of text messages on drug adherence. trialsearch.who.int/Trial2.aspx?TrialID=CTRI/2021/06/034463 (first received 29 June 2021).
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- CTRI/2021/10/037432. Prevention of secondary stroke by risk factor control and medication adherence. trialsearch.who.int/Trial2.aspx?TrialID=CTRI/2021/10/037432 (first received 21 October 2021).
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- IRCT2014050617596N1. Comparison of telephone and SMS follow up on treatment regimen adherence in patients with coronary artery bypass surgery. trialsearch.who.int/Trial2.aspx?TrialID=IRCT2014050617596N1 (first received 7 August 2014).
IRCT2016011025937N1 {published data only}
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- IRCT2016011025937N1. The effect of follow up using short message service on illness perception and medication adherence in patients under coronary angioplasty. trialsearch.who.int/Trial2.aspx?TrialID=IRCT2016011025937N1 (first received 20 February 2016).
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- IRCT2016081125937N2. Effect of a reminder system on medication adherence. trialsearch.who.int/Trial2.aspx?TrialID=IRCT2016081125937N2 (first received 29 August 2016).
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- ISRCTN10549665. Improving medication taking in patients with coronary heart disease using a mobile health technology, a feasibility study. www.isrctn.com/ISRCTN10549665 (first received 26 November 2019). [DOI: 10.1186/ISRCTN10549665] - DOI
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