Disability meanings according to patients and clinicians: imagined recovery choice pathways
- PMID: 19190999
- PMCID: PMC2862634
- DOI: 10.1007/s11136-009-9441-y
Disability meanings according to patients and clinicians: imagined recovery choice pathways
Abstract
Objective: The purpose of this study was to explore how the meaning of disability varies between patients with acute-onset activity limitations and clinicians, and between males and females.
Methods: Seventy-nine patients undergoing inpatient rehabilitation and 93 practicing rehabilitation clinicians in the USA developed personal recovery choice pathways through recovery preference exploration (RPE). Imagining complete dependence in 18 activities as diverse as eating and expression, each individual determined an optimal sequence of recovery. This sequence was used to determine the relative value of each activity compared with the other 17. Three comparisons were made by calculating the mean absolute difference (MAD) in median utilities, including patients versus clinicians, male versus female patients, and male versus female clinicians. The MAD shows the relative magnitude of disparity between each pair.
Results: The MAD value between patients and clinicians was 3.4 times larger and 4.8 times larger than the MAD values between male and female patients and male and female clinicians, respectively.
Conclusions: The much larger difference in recovery preferences between patients and clinicians compared with differences between genders suggests that life contexts of being a patient with disabilities versus a clinician are more potent determinants of activity limitation perspectives than being a man or woman.
Figures




References
-
- Baron J, Asch DA, Fagerlin A, Jepson C, Loewenstein G, Riis J, et al. Effect of assessment method on the discrepancy between judgments of health disorders people have and do not have: A web study. Medical Decision Making. 2003;23:422–434. doi:10.1177/0272989X03257277. - PubMed
-
- Sprangers MA, Aaronson NK. The role of health care providers and significant others in evaluating the quality of life of patients with chronic disease: A review. Journal of Clinical Epidemiology. 1992;45:743–760. doi:10.1016/0895-4356 (92)90052-O. - PubMed
-
- Ubel PA, Loewenstein G, Jepson C. Whose quality of life? A commentary exploring discrepancies between health state evaluations of patients and the general public. Quality of Life Research. 2003;12:599–607. doi:10.1023/A:1025119931010. - PubMed
-
- Bach JR, Barnett V. Ethical considerations in the management of individuals with severe neuromuscular disorders. American Journal of Physical Medicine and Rehabilitation. 1994;73:134–140. doi:10.1097/00002060-199404000-00012. - PubMed
-
- Bach JR, Tilton MC. Life satisfaction and well-being measures in ventilator assisted individuals with traumatic tetraplegia. Archives of Physical Medicine and Rehabilitation. 1994;75:626–632. doi:10.1016/0003-9993(94)90183-X. - PubMed
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources