Digital interventions to improve adherence to maintenance medication in asthma.

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dc.contributor.author Chan, Amy
dc.contributor.author De Simoni, Anna
dc.contributor.author Wileman, Vari
dc.contributor.author Holliday, Lois
dc.contributor.author Newby, Chris J
dc.contributor.author Chisari, Claudia
dc.contributor.author Ali, Sana
dc.contributor.author Zhu, Natalee
dc.contributor.author Padakanti, Prathima
dc.contributor.author Pinprachanan, Vasita
dc.contributor.author Ting, Victoria
dc.contributor.author Griffiths, Chris J
dc.coverage.spatial England
dc.date.accessioned 2023-03-16T01:45:21Z
dc.date.available 2023-03-16T01:45:21Z
dc.date.issued 2022-06
dc.identifier.citation (2022). Cochrane Database of Systematic Reviews, 6(6), CD013030-.
dc.identifier.issn 1469-493X
dc.identifier.uri https://hdl.handle.net/2292/63391
dc.description.abstract <h4>Background</h4>Asthma is the most common chronic lung condition worldwide, affecting 334 million adults and children globally. Despite the availability of effective treatment, such as inhaled corticosteroids (ICS), adherence to maintenance medication remains suboptimal. Poor ICS adherence leads to increased asthma symptoms, exacerbations, hospitalisations, and healthcare utilisation. Importantly, suboptimal use of asthma medication is a key contributor to asthma deaths. The impact of digital interventions on adherence and asthma outcomes is unknown.<h4>Objectives</h4>To determine the effectiveness of digital interventions for improving adherence to maintenance treatments in asthma.<h4>Search methods</h4>We identified trials from the Cochrane Airways Trials Register, which contains studies identified through multiple electronic searches and handsearches of other sources. We also searched trial registries and reference lists of primary studies. We conducted the most recent searches on 1 June 2020, with no restrictions on language of publication. A further search was run in October 2021, but studies were not fully incorporated.<h4>Selection criteria</h4>We included randomised controlled trials (RCTs) including cluster- and quasi-randomised trials of any duration in any setting, comparing a digital adherence intervention with a non-digital adherence intervention or usual care. We included adults and children with a clinical diagnosis of asthma, receiving maintenance treatment.<h4>Data collection and analysis</h4>We used standard methodological procedures for data collection. We used GRADE to assess quantitative outcomes where data were available.<h4>Main results</h4>We included 40 parallel randomised controlled trials (RCTs) involving adults and children with asthma (n = 15,207), of which eight are ongoing studies. Of the included studies, 30 contributed data to at least one meta-analysis. The total number of participants ranged from 18 to 8517 (median 339). Intervention length ranged from two to 104 weeks. Most studies (n = 29) reported adherence to maintenance medication as their primary outcome; other outcomes such as asthma control and quality of life were also commonly reported. Studies had low or unclear risk of selection bias but high risk of performance and detection biases due to inability to blind the participants, personnel, or outcome assessors. A quarter of the studies had high risk of attrition bias and selective outcome reporting. We examined the effect of digital interventions using meta-analysis for the following outcomes: adherence (16 studies); asthma control (16 studies); asthma exacerbations (six studies); unscheduled healthcare utilisation (four studies); lung function (seven studies); and quality of life (10 studies). Pooled results showed that patients receiving digital interventions may have increased adherence (mean difference of 14.66 percentage points, 95% confidence interval (CI) 7.74 to 21.57; low-certainty evidence); this is likely to be clinically significant in those with poor baseline medication adherence. Subgroup analysis by type of intervention was significant (P = 0.001), with better adherence shown with electronic monitoring devices (EMDs) (23 percentage points over control, 95% CI 10.84 to 34.16; seven studies), and with short message services (SMS) (12 percentage points over control, 95% CI 6.22 to 18.03; four studies). No significant subgroup differences were seen for interventions having an in-person component versus fully digital interventions, adherence feedback, one or multiple digital components to the intervention, or participant age. Digital interventions were likely to improve asthma control (standardised mean difference (SMD) 0.31 higher, 95% CI 0.17 to 0.44; moderate-certainty evidence) - a small but likely clinically significant effect. They may reduce asthma exacerbations (risk ratio 0.53, 95% CI 0.32 to 0.91; low-certainty evidence). Digital interventions may result in a slight change in unscheduled healthcare utilisation, although some studies reported no or a worsened effect. School or work absence data could not be included for meta-analysis due to the heterogeneity in reporting and the low number of studies. They may result in little or no difference in lung function (forced expiratory volume in one second (FEV<sub>1</sub>)): there was an improvement of 3.58% predicted FEV<sub>1</sub>, 95% CI 1.00% to 6.17%; moderate-certainty evidence); however, this is unlikely to be clinically significant as the FEV<sub>1</sub> change is below 12%. Digital interventions likely increase quality of life (SMD 0.26 higher, 95% CI 0.07 to 0.45; moderate-certainty evidence); however, this is a small effect that may not be clinically significant. Acceptability data showed positive attitudes towards digital interventions. There were no data on cost-effectiveness or adverse events. Our confidence in the evidence was reduced by risk of bias and inconsistency.<h4>Authors' conclusions</h4>Overall, digital interventions may result in a large increase in adherence (low-certainty evidence). There is moderate-certainty evidence that digital adherence interventions likely improve asthma control to a degree that is clinically significant, and likely increase quality of life, but there is little or no improvement in lung function. The review found low-certainty evidence that digital interventions may reduce asthma exacerbations. Subgroup analyses show that EMDs may improve adherence by 23% and SMS interventions by 12%, and interventions with an in-person element and adherence feedback may have greater benefits for asthma control and adherence, respectively. Future studies should include percentage adherence as a routine outcome measure to enable comparison between studies and meta-analysis, and use validated questionnaires to assess adherence and outcomes.
dc.format.medium Electronic
dc.language eng
dc.publisher Wiley
dc.relation.ispartofseries The Cochrane database of systematic reviews
dc.rights Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher.
dc.rights This Cochrane Review was published in the Cochrane Database of Systematic Reviews 2022, Issue 6. Cochrane Reviews are regularly updated as new evidence emerges and in response to feedback, and the Cochrane Database of Systematic Reviews should be consulted for the most recent version of the Cochrane Review.
dc.rights.uri https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm
dc.rights.uri https://documentation.cochrane.org/display/EPPR/Standard+%7C+Cochrane+Review
dc.subject Humans
dc.subject Asthma
dc.subject Adrenal Cortex Hormones
dc.subject Forced Expiratory Volume
dc.subject Quality of Life
dc.subject Adult
dc.subject Child
dc.subject Medication Adherence
dc.subject Clinical Research
dc.subject Prevention
dc.subject Lung
dc.subject Clinical Trials and Supportive Activities
dc.subject 7 Management of diseases and conditions
dc.subject 7.1 Individual care needs
dc.subject Respiratory
dc.subject 11 Medical and Health Sciences
dc.subject 17 Psychology and Cognitive Sciences
dc.title Digital interventions to improve adherence to maintenance medication in asthma.
dc.type Journal Article
dc.identifier.doi 10.1002/14651858.cd013030.pub2
pubs.issue 6
pubs.begin-page CD013030
pubs.volume 6
dc.date.updated 2023-02-26T13:05:59Z
dc.rights.holder Copyright: The Cochrane Collaboration en
dc.identifier.pmid 35691614 (pubmed)
pubs.author-url https://www.ncbi.nlm.nih.gov/pubmed/35691614
pubs.publication-status Published
dc.rights.accessrights http://purl.org/eprint/accessRights/OpenAccess en
pubs.subtype Research Support, Non-U.S. Gov't
pubs.subtype Systematic Review
pubs.subtype Review
pubs.subtype Journal Article
pubs.elements-id 911157
pubs.org-id Medical and Health Sciences
pubs.org-id Pharmacy
dc.identifier.eissn 1469-493X
pubs.record-created-at-source-date 2023-02-27
pubs.online-publication-date 2022-06-13


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