Evaluation of Noncompletion Bias and Long-Term Adherence in a 10-Year Patient-Reported Outcome Monitoring Program in Clinical Routine

被引:9
作者
Gamper, Eva Maria [1 ,2 ]
Nerich, Virginie [3 ,4 ]
Sztankay, Monika [1 ]
Martini, Caroline [1 ]
Giesinger, Johannes M. [1 ]
Scarpa, Lorenza [5 ]
Buxbaum, Sabine [5 ]
Jeller, Martin [5 ]
Holzner, Bernhard [1 ]
Virgolini, Irene [5 ]
机构
[1] Med Univ Innsbruck, Dept Psychiat & Psychotherapy, Anichstr 35, A-6020 Innsbruck, Austria
[2] Innsbruck Inst Patient Ctr Outcome Res, Innsbruck, Austria
[3] Univ Franche Comte, INSERM, Unit 1098, Besancon, France
[4] Uniuers Hosp Besancon, Dept Pharm, Besancon, France
[5] Med Univ Innsbruck, Dept Nucl Med, Innsbruck, Austria
基金
奥地利科学基金会;
关键词
clinical routine; evaluation; mode of assessment; patient reported outcomes; QUALITY-OF-LIFE; HEALTH-CARE; TRIALS; RECOMMENDATIONS; IMPLEMENTATION; PERSPECTIVE; EXPERIENCES; IMPROVEMENT; ONCOLOGY; DESIGN;
D O I
10.1016/j.jval.2017.01.009
中图分类号
F [经济];
学科分类号
02 ;
摘要
Background: Currently there is little knowledge on real-life sustain ability of routine patient-reported outcome (PRO) measurement and the representativeness of collected data. Objectives: The investigation of routine PRO with regard to noncompletion bias and long-term adher- ence, considering the potential impact of mode of assessment (MOA) (paper-pencil vs. electronic PRO [ePRO]) and patient characteristics. Methods: At our department, routine PRO measurement in oncological patients is being done since 2005 using different MOA (paper-pencil assessment until 2011 and ePRO assessment from 2011 onward). We analyzed two different patient groups: patients eligible in both periods (both-MOA group) and patients eligible in only one period (one-MOA group). The primary outcome was PRO noncompletion (100% missing questionnaires). The secondary outcome was poor PRO adherence (>20% missing questionnaires). Multivariate logistic regression models were developed, testing the impact of MOA and patient characteristics on the outcomes in the different patient groups. Results: Data from 1484 eligible patients were included in the analyses. Most of the patients could be included in PRO assessment at least once. PRO noncompletion rates were clearly higher during paper-pencil assessment (odds ratios between 2.72 and 4.31), as were poor PRO adherence rates (odd ratio 2.23). Analyses of potential bias by patient characteristics showed that male patients had a higher risk of poor adherence. Other factors with significant impact were age, country, and cancer diagnosis, but results were indecisive. Conclusions: ePRO increased the feasibility of our clinical routine PRO data for retrospective analyses by increasing completion rates. In general, potential completion bias regarding certain patient characteristics requires attention before generalizing results to the respective populations. Copyright (C) 2017, International Society for Pharmacoeconomics and Outcomes Research (ISPOR). Published by Elsevier Inc.
引用
收藏
页码:610 / 617
页数:8
相关论文
共 29 条
[11]   Patient-reported outcomes in randomized clinical trials: development of ISOQOL reporting standards [J].
Brundage, Michael ;
Blazeby, Jane ;
Revicki, Dennis ;
Bass, Brenda ;
de Vet, Henrica ;
Duffy, Helen ;
Efficace, Fabio ;
King, Madeleine ;
Lam, Cindy L. K. ;
Moher, David ;
Scott, Jane ;
Sloan, Jeff ;
Snyder, Claire ;
Yount, Susan ;
Calvert, Melanie .
QUALITY OF LIFE RESEARCH, 2013, 22 (06) :1161-1175
[12]  
CEBM O, 2009, OXFORD CTR EVIDENCE
[13]   Use of patient-reported outcomes to measure symptoms and health related quality of life in the clinic [J].
Gilbert, Alexandra ;
Sebag-Montefiore, David ;
Davidson, Susan ;
Velikova, Galina .
GYNECOLOGIC ONCOLOGY, 2015, 136 (03) :429-439
[14]   Practical clinical trials for translating research to practice - Design and measurement recommendations [J].
Glasgow, RE ;
Magid, DJ ;
Beck, A ;
Ritzwoller, D ;
Estabrooks, PA .
MEDICAL CARE, 2005, 43 (06) :551-557
[15]  
Holzner B, 2005, COMPUTER BASED HLTH
[16]   Patient-reported outcomes in routine cancer clinical practice: a scoping review of use, impact on health outcomes, and implementation factors [J].
Howell, D. ;
Molloy, S. ;
Wilkinson, K. ;
Green, E. ;
Orchard, K. ;
Wang, K. ;
Liberty, J. .
ANNALS OF ONCOLOGY, 2015, 26 (09) :1846-1858
[17]   Loss to follow-up after total hip replacement: a source of bias in patient reported outcome measures and registry datasets? [J].
Imam, Mohamed A. ;
Barke, Samuel ;
Stafford, Giles H. ;
Parkin, David ;
Field, Richard E. .
HIP INTERNATIONAL, 2014, 24 (05) :465-472
[18]   Issues in the design of Internet-based systems for collecting patient-reported outcomes [J].
Jones, James B. ;
Snyder, Claire F. ;
Wu, Albert W. .
QUALITY OF LIFE RESEARCH, 2007, 16 (08) :1407-1417
[19]   What Is the Value of the Routine Use of Patient-Reported Outcome Measures Toward Improvement of Patient Outcomes, Processes of Care, and Health Service Outcomes in Cancer Care? A Systematic Review of Controlled Trials [J].
Kotronoulas, Grigorios ;
Kearney, Nora ;
Maguire, Roma ;
Harrow, Alison ;
Di Domenico, David ;
Croy, Suzanne ;
MacGillivray, Stephen .
JOURNAL OF CLINICAL ONCOLOGY, 2014, 32 (14) :1480-+
[20]   Increasing Patient Involvement in Drug Development [J].
Lowe, Maria M. ;
Blaser, David A. ;
Cone, Lisa ;
Arcona, Steve ;
Ko, John ;
Sasane, Rahul ;
Wicks, Paul .
VALUE IN HEALTH, 2016, 19 (06) :869-878