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Development and validation of an instrument to assess treatment adherence for each individual drug taken by a patient
OBJECTIVE: To develop and validate an instrument to assess adherence to each individual drug taken by patients undergoing long-term treatment. DESIGN: Multicentre prospective observational validation study. SETTING: Six general practitioners' clinics and 6 university hospitals in Paris, France....
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4874131/ https://www.ncbi.nlm.nih.gov/pubmed/27165645 http://dx.doi.org/10.1136/bmjopen-2015-010510 |
Sumario: | OBJECTIVE: To develop and validate an instrument to assess adherence to each individual drug taken by patients undergoing long-term treatment. DESIGN: Multicentre prospective observational validation study. SETTING: Six general practitioners' clinics and 6 university hospitals in Paris, France. PARTICIPANTS: Patients 18 years and older receiving at least one long-term treatment. METHODS: The instrument was developed from a literature search and interviews with experts. Clarity and wording were assessed during pilot testing with 51 patients. The tool was validated in a sample of consecutive patients. We assessed agreement between adherence measured with our tool and drug diaries and compared measurements from our instrument with (1) the Lu instrument; (2) the Adherence Estimator (AE); (3) patient's adherence assessed by physicians; (4) the Morisky Medication Adherence Scale-4 items (MMAS-4); and (5) the Treatment Burden Questionnaire (TBQ). Reliability was assessed by a test–retest method. RESULTS: A total of 243 patients taking 961 drugs were recruited in 2014. We found good agreement between adherence measured by our tool and drug diaries (intraclass correlation coefficient (ICC) 0.69, 95% CI 0.34 to 0.91) and a linear relationship between measurement with our tool and (1) the Lu instrument (p<0.01); (2) 2 items of the AE (perceived need for medication (p<0.01) and concerns about medication (p<0.01)); (3) patients' adherence assessed by their physicians (p<0.01); (4) the MMAS-4 (p<0.01) and (5) the TBQ (p<0.01). Reliability of the retest was good (ICC 0.67, 95% CI 0.42 to 0.85). CONCLUSIONS: We developed an instrument with acceptable validity and reliability to assess adherence for each drug taken by patients, usable in hospital and primary care settings. |
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