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Adherence Management for Cancer Patients on Capecitabine

dc.contributor.advisorJaehde, Ulrich
dc.contributor.authorKrolop, Linda
dc.date.accessioned2020-04-19T03:04:11Z
dc.date.available2020-04-19T03:04:11Z
dc.date.issued13.01.2014
dc.identifier.urihttp://hdl.handle.net/20.500.11811/5818
dc.description.abstractThe oral anticancer drug capecitabine is given twice daily for 14 days followed by a seven day rest period. Adequate patient adherence is essential for treatment success.
The present study aimed at developing and evaluating a multiprofessional modular medication management to assure adherence to capecitabine.
The study was conducted as a prospective, multicentred observational cohort study. All participants received pharmaceutical care consisting of oral and written information. Daily adherence was defined as percentage of days with correctly administered doses and assessed using medication event monitoring. According to their daily adherence during the first cycle, patients were identified as initially non-adherent (<90% adherence) or adherent (≥90% adherence). Initially non-adherent patients received additional adherence support. Secondary endpoints included quality of life, patient satisfaction with information, occurrence of hand-foot syndrome (HFS), pharmacist’s working time, and patients’ evaluation of capecitabine treatment.
Seventy-three patients with various tumour entities were enrolled, 58 were initially adherent and 15 non-adherent. Median daily adherence of initially non-adherent patients increased from 85.7% to 97.6% during the observation period of six cycles. Throughout all cycles, median daily adherence of initially adherent patients was 100.0%. Daily adherence was not associated with sociodemographic and disease-related factors. No patient was non-persistent. Quality of life was stable and patient satisfaction was high and increased over the cycles. Median HFS severity grade did not exceed a well tolerable level. Pharmacist’s working time for provision of medication management was kept within reasonable limits. Patient evaluation of treatment by initially adherent patients was good, whereas initially non-adherent patients expressed a worse impression.
An early adherence screening effectively distinguishes between patients adhering and non-adhering to capecitabine. The provision of specific adherence support is associated with enhanced adherence of initially non-adherent patients, whereas initially adherent patients remain adherent for at least six cycles without specific support. Our needs-based approach helps to use available resources for adherence management efficiently. The present results show a beneficial impact of pharmaceutical care on further patient-related endpoints.
dc.language.isoeng
dc.relation.ispartofseriesKlinische Pharmazie
dc.rightsIn Copyright
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/
dc.subjectadherence
dc.subjectcompliance
dc.subjectcapecitabine
dc.subjectpharmaceutical care
dc.subjectoral chemotherapy
dc.subject.ddc500 Naturwissenschaften
dc.titleAdherence Management for Cancer Patients on Capecitabine
dc.typeDissertation oder Habilitation
dc.publisher.nameUniversitäts- und Landesbibliothek Bonn
dc.publisher.locationBonn
dc.rights.accessRightsopenAccess
dc.identifier.urnhttps://nbn-resolving.org/urn:nbn:de:hbz:5n-34718
dc.relation.isbn978-3-8439-1274-7
ulbbn.pubtypeZweitveröffentlichung
ulbbnediss.affiliation.nameRheinische Friedrich-Wilhelms-Universität Bonn
ulbbnediss.affiliation.locationBonn
ulbbnediss.thesis.levelDissertation
ulbbnediss.dissID3471
ulbbnediss.date.accepted2013-08-30
ulbbnediss.fakultaetMathematisch-Naturwissenschaftliche Fakultät
dc.contributor.coRefereeKo, Yon-Dschun


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