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Retention rate of a novel autoinjector e-Device introduced to patients with chronic arthritis treated with certolizumab pegol in clinical practice: an observational implementation study
Copenhagen Univ Hosp, Denmark.
Copenhagen Univ Hosp, Denmark.
Sint Maartensliniek, Netherlands; Radboud Univ Nijmegen, Netherlands.
Sint Maartensliniek, Netherlands; Radboud Univ Nijmegen, Netherlands.
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2025 (English)In: Scandinavian Journal of Rheumatology, ISSN 0300-9742, E-ISSN 1502-7732, Vol. 54, no 1, p. 25-32Article in journal (Refereed) Published
Abstract [en]

ObjectivesThe objectives were to explore the clinical retention rate of an e-Device aimed at empowering chronic arthritis patients using certolizumab pegol (CZP) and to analyse beliefs about medication in the Danish population.MethodPatients treated with CZP were recruited from the Netherlands, Denmark, and Sweden through rheumatology clinics at initiation of, or switching to, the e-Device. Patients were adults (aged 18-85 years) diagnosed with rheumatoid arthritis, axial spondyloarthritis, or psoriatic arthritis. Patients administered three consecutive self-injections at home. Descriptive statistics regarding baseline characteristics, retention rates, and reasons for withdrawal were assessed, along with the Beliefs about Medicines Questionnaire.ResultsIn total, 59 patients participated (Netherlands 25, Denmark 15, Sweden 19). Most subjects (71%) were women, with a mean +/- sd age of 55 +/- 16.2 years and mean disease duration 12 +/- 8.8 years. Six patients (10%) started CZP de novo and the remaining patients switched device. The overall retention rate was 42% after 52 weeks, declining to 38% after 104 weeks. A sharp decline, 34%, was seen at week 8. Between weeks 32 and 112, only four patients (6.8%) withdrew from the study. The primary reason for withdrawal was the patient's request. Stratification by country showed significant differences for some outcomes.ConclusionAn initial large dropout was evident within the first 8 weeks, with almost no dropouts thereafter. The reasons for withdrawal were primarily patient requests. Thus, the injection experience must be tailored carefully when selecting patients for new autoinjector e-Devices to enhance retention rates and patient satisfaction.

Place, publisher, year, edition, pages
TAYLOR & FRANCIS LTD , 2025. Vol. 54, no 1, p. 25-32
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Clinical Medicine
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URN: urn:nbn:se:liu:diva-206367DOI: 10.1080/03009742.2024.2365508ISI: 001264716500001PubMedID: 38975797Scopus ID: 2-s2.0-85197709334OAI: oai:DiVA.org:liu-206367DiVA, id: diva2:1889792
Available from: 2024-08-16 Created: 2024-08-16 Last updated: 2025-06-27

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Sjöwall, Christopher
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Division of Inflammation and InfectionFaculty of Medicine and Health SciencesDepartment of Rheumatology
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