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Review

A systematic review of patient-reported measures of burden of treatment in three chronic diseases

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Pages 7-20 | Published online: 05 Jun 2013

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Anne Møller, Kristine Henderson Bissenbakker, Anne Beiter Arreskov & John Brodersen. (2020) Specific Measures of Quality of Life in Patients with Multimorbidity in Primary Healthcare: A Systematic Review on Patient-Reported Outcome Measures’ Adequacy of Measurement. Patient Related Outcome Measures 11, pages 1-10.
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Barbra Katusiime, Sarah A Corlett & Janet Krska. (2018) Development and validation of a revised instrument to measure burden of long-term medicines use: the Living with Medicines Questionnaire version 3. Patient Related Outcome Measures 9, pages 155-168.
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Elizabeth A Rogers, Kathleen J Yost, Jordan K Rosedahl, Mark Linzer, Deborah H Boehm, Azra Thakur, Sara Poplau, Roger T Anderson & David T Eton. (2017) Validating the Patient Experience with Treatment and Self-Management (PETS), a patient-reported measure of treatment burden, in people with diabetes. Patient Related Outcome Measures 8, pages 143-156.
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Janet Krska, Barbra Katusiime & Sarah A Corlett. (2017) Validation of an instrument to measure patients’ experiences of medicine use: the Living with Medicines Questionnaire. Patient Preference and Adherence 11, pages 671-679.
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Ana-Carolina Vieira Gonçalves, Cristina Isabel Oliveira Jácome, Sara Holtum Demain, Katherine J. Hunt & Alda Sofia Pires de Dias Marques. (2017) Burden of treatment in the light of the international classification of functioning, disability and health: a “best fit” framework synthesis. Disability and Rehabilitation 39:13, pages 1253-1261.
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Barbra Katusiime, Sarah Corlett, Joanne Reeve & Janet Krska. (2016) Measuring medicine-related experiences from the patient perspective: a systematic review. Patient Related Outcome Measures 7, pages 157-171.
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David T Eton, Jennifer L Ridgeway, Jason S Egginton, Kristina Tiedje, Mark Linzer, Deborah H Boehm, Sara Poplau, Djenane Ramalho de Oliveira, Laura Odell, Victor M Montori, Carl R May & Roger T Anderson. (2015) Finalizing a measurement framework for the burden of treatment in complex patients with chronic conditions. Patient Related Outcome Measures 6, pages 117-126.
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Inger Miriam Janssen, Ansgar Gerhardus, Gero D von Gersdorff, Conrad August Baldamus, Mathias Schaller, Claudia Barth & Fueloep Scheibler. (2015) Preferences of patients undergoing hemodialysis – results from a questionnaire-based study with 4,518 patients. Patient Preference and Adherence 9, pages 847-855.
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David T Eton, Timothy J Beebe, Philip T Hagen, Michele Y Halyard, Victor M Montori, James M Naessens, Jeff A Sloan, Carrie A Thompson & Douglas L Wood. (2014) Harmonizing and consolidating the measurement of patient-reported information at health care institutions: a position statement of the Mayo Clinic. Patient Related Outcome Measures 5, pages 7-15.
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