Medication Adherence Evaluated Through Electronic Monitors During the 2020 COVID-19 Pandemic Lockdown in Switzerland: A Longitudinal Analysis.

COVID-19 SARS-CoV-2 electronic adherence monitoring implementation adherence interprofessional adherence intervention medication adherence patient compliance

Journal

Patient preference and adherence
ISSN: 1177-889X
Titre abrégé: Patient Prefer Adherence
Pays: New Zealand
ID NLM: 101475748

Informations de publication

Date de publication:
2022
Historique:
received: 08 06 2022
accepted: 09 08 2022
entrez: 1 9 2022
pubmed: 2 9 2022
medline: 2 9 2022
Statut: epublish

Résumé

During the 2020 COVID-19 lockdown, patients included in the Interprofessional Medication Adherence Program (IMAP) in Switzerland continued to use electronic monitors (EMs) that registered daily drug-dose intake. We aimed to understand to what extent patients' medication implementation (ie, the extent to which the patient took the prescribed medicine), measured with EMs, was impacted by the lockdown. Patients participating in the IMAP were diagnosed with diabetic kidney disease (DKD), solid cancer, human immunodeficiency virus (HIV) and miscellaneous long-term diseases (MLTD). Patient implementation was defined through a proxy: if all patient EMs were opened at least once daily, implementation was considered active (=1), and no implementation was considered (=0) otherwise. Implementation before (from December 2019 to March 2020), during (March to June 2020) and after (June to September 2020) the lockdown was compared. Subanalyses were performed according to the patients' diseases. Subanalyses were performed in patients who used at least one EM in 2018-2019 during the same periods (defined as winter, spring and summer). The logistic regression models used to estimate medication implementation according to the period were fitted using generalized estimating equations. In 2020, patient implementation (n = 118) did not differ significantly before versus during (OR = 0.98, 95% CI: 0.84-1.15, p = 0.789) and before versus after (OR = 0.91, 95% CI: 0.79-1.06, p = 0.217) the lockdown. These findings remained stable when separately analyzing the implementation of patients with HIV (n = 61), DKD (n = 25) or MLTD (n = 22). Too few patients with cancer were included (n = 10) to interpret the results. In 2019, the implementation of 61/118 (51.7%) patients was significantly lower during summertime versus wintertime (OR = 0.73, 95% CI: 0.60-0.89, p = 0.002). Medication implementation remained steady before, during and after the lockdown in 2020. The IMAP before, during and after the lockdown may have supported the adherence of most patients, by ensuring continuity of care during periods of routine disturbances.

Sections du résumé

Background UNASSIGNED
During the 2020 COVID-19 lockdown, patients included in the Interprofessional Medication Adherence Program (IMAP) in Switzerland continued to use electronic monitors (EMs) that registered daily drug-dose intake. We aimed to understand to what extent patients' medication implementation (ie, the extent to which the patient took the prescribed medicine), measured with EMs, was impacted by the lockdown.
Methods UNASSIGNED
Patients participating in the IMAP were diagnosed with diabetic kidney disease (DKD), solid cancer, human immunodeficiency virus (HIV) and miscellaneous long-term diseases (MLTD). Patient implementation was defined through a proxy: if all patient EMs were opened at least once daily, implementation was considered active (=1), and no implementation was considered (=0) otherwise. Implementation before (from December 2019 to March 2020), during (March to June 2020) and after (June to September 2020) the lockdown was compared. Subanalyses were performed according to the patients' diseases. Subanalyses were performed in patients who used at least one EM in 2018-2019 during the same periods (defined as winter, spring and summer). The logistic regression models used to estimate medication implementation according to the period were fitted using generalized estimating equations.
Results UNASSIGNED
In 2020, patient implementation (n = 118) did not differ significantly before versus during (OR = 0.98, 95% CI: 0.84-1.15, p = 0.789) and before versus after (OR = 0.91, 95% CI: 0.79-1.06, p = 0.217) the lockdown. These findings remained stable when separately analyzing the implementation of patients with HIV (n = 61), DKD (n = 25) or MLTD (n = 22). Too few patients with cancer were included (n = 10) to interpret the results. In 2019, the implementation of 61/118 (51.7%) patients was significantly lower during summertime versus wintertime (OR = 0.73, 95% CI: 0.60-0.89, p = 0.002).
Conclusion UNASSIGNED
Medication implementation remained steady before, during and after the lockdown in 2020. The IMAP before, during and after the lockdown may have supported the adherence of most patients, by ensuring continuity of care during periods of routine disturbances.

Identifiants

pubmed: 36046500
doi: 10.2147/PPA.S377780
pii: 377780
pmc: PMC9423122
doi:

Types de publication

Journal Article

Langues

eng

Pagination

2313-2320

Informations de copyright

© 2022 Bandiera et al.

Déclaration de conflit d'intérêts

Prof. Dr. Grégoire Wuerzner reports consultancy and/or advisory board from Aktiia, Bayer, Servier and AstraZeneca, outside the submitted work. Prof. Dr. Gilles Wandeler reports grants, Speaker and advisory board fees paid to their institution from Gilead Sciences and MSD, grants from Roche Diagnostics, advisory board fees paid to their institution from ViiV, outside the submitted work. Dr Anna Dorothea Wagner reports personal fees, non-financial support from Merck, personal fees from Lily, personal fees from Pierre-Fabre Pharma, is coordinating investigator of EORTC trial 1203 “INNOVATION”, which is supported by an educational grant to EORTC from Hoffmann La Roche, personal fees from Sanofi, personal fees from Daiichi Sankyo, personal fees from Dragonfly Therapeutics, personal fees from Servier, personal fees from Bristol-Myers Squibb, personal fees from Astellas Pharma, outside the submitted work. Professor Chantal Csajka reports grants from Swiss Cancer Research, during the conduct of the study. Prof. Dr. Matthias Cavassini reports grants from Gilead, ViiV and MSD, outside the submitted work. Professor Marie Schneider reports grants from Swiss Cancer Research Foundation, grants from Research and quality fund of Santésuisse, Curafutura and PharmaSuisse, during the conduct of the study. The authors declare that they have no other competing interests.

Références

Indian J Ophthalmol. 2021 May;69(5):1264-1270
pubmed: 33913874
BMC Health Serv Res. 2018 Nov 20;18(1):874
pubmed: 30458844
Br J Clin Pharmacol. 2012 May;73(5):691-705
pubmed: 22486599
Ann Rheum Dis. 2021 Jun;80(6):e85
pubmed: 32576568
Res Social Adm Pharm. 2022 Apr;18(4):2706-2710
pubmed: 34154930
Front Pharmacol. 2013 Jul 25;4:91
pubmed: 23898295
Ann Transl Med. 2020 Sep;8(18):1179
pubmed: 33241028
Int J Environ Res Public Health. 2022 Jan 20;19(3):
pubmed: 35162159
Biomed Res Int. 2015;2015:103546
pubmed: 26839879
J Allergy Clin Immunol Pract. 2020 Jul - Aug;8(7):2384-2385
pubmed: 32371047
JMIR Res Protoc. 2021 Mar 19;10(3):e25966
pubmed: 33739292
JMIR Res Protoc. 2021 Jun 29;10(6):e30090
pubmed: 34185020
Pediatr Res. 2021 Sep;90(3):637-641
pubmed: 33446913
Health Psychol. 2006 Jul;25(4):462-73
pubmed: 16846321
Rheumatology (Oxford). 2021 Oct 9;60(SI):SI51-SI58
pubmed: 33704418

Auteurs

Carole Bandiera (C)

School of Pharmaceutical Sciences, University of Geneva, Geneva, Switzerland.
Institute of Pharmaceutical Sciences of Western Switzerland, University of Geneva, University of Lausanne, Geneva, Switzerland.
Center for Primary Care and Public Health (Unisanté), University of Lausanne, Lausanne, Switzerland.

Jérôme Pasquier (J)

Center for Primary Care and Public Health (Unisanté), University of Lausanne, Lausanne, Switzerland.

Isabella Locatelli (I)

Center for Primary Care and Public Health (Unisanté), University of Lausanne, Lausanne, Switzerland.

Anne Niquille (A)

Institute of Pharmaceutical Sciences of Western Switzerland, University of Geneva, University of Lausanne, Geneva, Switzerland.
Center for Primary Care and Public Health (Unisanté), University of Lausanne, Lausanne, Switzerland.

Grégoire Wuerzner (G)

Service of Nephrology and Hypertension, Department of Medicine, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.

Jennifer Dotta-Celio (J)

Center for Primary Care and Public Health (Unisanté), University of Lausanne, Lausanne, Switzerland.

Anna Hachfeld (A)

Department of Infectious Diseases, Bern University Hospital, University of Bern, Bern, Switzerland.

Gilles Wandeler (G)

Department of Infectious Diseases, Bern University Hospital, University of Bern, Bern, Switzerland.

Anna Dorothea Wagner (AD)

Service of Oncology, Department of Medicine, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.

Chantal Csajka (C)

School of Pharmaceutical Sciences, University of Geneva, Geneva, Switzerland.
Institute of Pharmaceutical Sciences of Western Switzerland, University of Geneva, University of Lausanne, Geneva, Switzerland.
Center for Research and Innovation in Clinical Pharmaceutical Sciences, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.

Anne Zanchi (A)

Service of Nephrology and Hypertension, Department of Medicine, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
Service of Endocrinology, Diabetes and Metabolism, Department of Medicine, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.

Matthias Cavassini (M)

Service of Infectious Diseases, Department of Medicine, Lausanne University Hospital, University of Lausanne, Lausanne, Switzerland.

Marie P Schneider (MP)

School of Pharmaceutical Sciences, University of Geneva, Geneva, Switzerland.
Institute of Pharmaceutical Sciences of Western Switzerland, University of Geneva, University of Lausanne, Geneva, Switzerland.

Classifications MeSH