Original CommunicationsEvaluation of the construct validity of the DASH questionnaire by correlation to the SF-36☆,☆☆
Section snippets
Study design
The study sample consisted of patients presenting to the upper-extremity clinic at a tertiary referral center over a period of 4 months. All patients were given a study packet and asked to complete an informed consent form on initial and follow-up visits. All patients were included if they were able to read English and complete the packet. The informed consent form and protocol were approved by the institutional review board before enrollment of patients. Participating patients completed the
Results
A total of 872 patients were scheduled to be seen in the upper-extremity clinic from October 30, 1997, through February 27, 1998. Review of charts identified 105 patients with diagnoses not related to the upper extremity. Of the remaining 767 scheduled visits, 167 packets were returned with completed informed consent and at least partial completion of questionnaires; this represents 22% of scheduled visits.
Of the patients returning packets, 77 did not respond to sufficient numbers of items to
Discussion
Several outcomes instruments have been proposed for use in patients with musculoskeletal complaints. The SF-36 has been validated in this population and is used widely for measuring health outcomes.2, 4, 11 The SF-36 is a generic questionnaire, however, and has the potential disadvantage of being less sensitive to clinical change in patients with complaints specific to an anatomic region or disease process. The DASH and a variety of region-specific and disease-specific questionnaires have been
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No benefits in any form have been received or will be received from a commercial party related directly or indirectly to the subject of this article.
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Reprint requests: Nelson Fong SooHoo, MD, Balance Orthopaedic Foot and Ankle Center, 2651 Elm Ave, Ste 205, Long Beach, CA 90806.