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Journal ArticleDOI

The Use of Proxies in Health Surveys: Substantive and Policy Implications

Ray R. Mosely, +1 more
- 01 Jun 1986 - 
- Vol. 24, Iss: 6, pp 496-510
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TLDR
Using data on the 78,439 adults interviewed in person or by proxy as part of the 1978 Health Interview Survey, the authors examine whether the use of proxy respondents alters the results of empirical assessments of the behavioral model of health services utilization or the policy implications that can be derived from it.
Abstract
It has traditionally been assumed that obtaining health and illness behavior data by proxy on household members who are not present during the actual interview presents no significant threats to the internal validity of subsequent analyses. Using data on the 78,439 adults interviewed in person or by proxy (about 37% of the total adult sample) as part of the 1978 Health Interview Survey, the authors examine whether the use of proxy respondents alters the results of empirical assessments of the behavioral model of health services utilization or the policy implications that can be derived from it. Two important findings emerge from these analyses. On the one hand, failing to consider explicitly the possibility of a proxy effect (i.e., including a proxy variable in the analyses) does not alter the effect parameters estimated for the behavioral model. On the other hand, failing to consider explicitly the effect of using proxies appears to underestimate slightly physician and hospital contact rates (by 4% and 2%, respectively), as well as the volume of physician utilization. The substantive and policy implications of these findings are discussed, as are two alternative explanations that suggest that proxy-respondents simply use fewer health services either because they are "too busy" or because they are in slightly better health.

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Journal ArticleDOI

The role of health care providers and significant others in evaluating the quality of life of patients with chronic disease: A review

TL;DR: There is need for more methodologically sound studies that incorporate head-to-head comparisons of health care providers and significant others as proxy raters and employ well-validated quality-of-life measures and employ a longitudinal design in order to examine the effect of changes in patients' health status over time on the ability of proxies to provide valid quality- of-life assessments.
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Using proxies to evaluate quality of life. Can they provide valid information about patients' health status and satisfaction with medical care?

TL;DR: The results suggest that use of proxies intermingled with subjects to measure health status through interview may lead to biased results.
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The use of significant others as proxy raters of the quality of life of patients with brain cancer.

TL;DR: In general, patients and their significant others provide similar ratings of the patients' quality of life and discrepancies between patient-proxy ratings should not be interpreted, a priori, as evidence of the inaccuracy or biased nature of proxy-generated data.
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Use, Type, and Efficacy of Assistance for Disability

TL;DR: Severe disability in a task and poor overall health/disability status increase use of assistance for the task, and especially both types rather than one, and equipment is more efficacious than personal assistance.
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