A model for conducting clinical-outcome research: an adaptation of the standard protocol for use in aphasiology

被引:160
作者
Robey, RR
Schultz, MC
机构
[1] Univ Virginia, Commun Disorders Program, Charlottesville, VA 22903 USA
[2] Univ New Mexico, Albuquerque, NM 87131 USA
关键词
D O I
10.1080/02687039808249573
中图分类号
R36 [病理学]; R76 [耳鼻咽喉科学];
学科分类号
100104 ; 100213 ;
摘要
Communication disorders scientists and practitioners face critical fiscal pressures to establish the efficacy and effectiveness of treatments. The pressures come about from (a) increasing demands from reimbursers that a variety of professions test the effectiveness of their treatments, thereby generating demands for the resources to do so; (b) increasing demands for reimbursement of those same clinical services provided by the same variety of professions; and (c) a general recision in available funds for each. While there is strong evidence that the treatments of speech-language pathologists and audiologists have generally proved patent as they have been tested, the accepted standards for clinical-outcome testing used throughout the research community (e.g. by other clinical disciplines, regulatory agencies of the federal government, and third-party payers) have been mostly ignored. In a marketplace of competition for scarce resources, and a recognized set of procedures for demonstrating the efficacy of intervention, it seems obvious that this profession cannot continue to depend on idiosyncratic approaches to clinical-outcome research. Ensuring successful claims for reimbursement requires that assertions of efficacy be justified on the basis of broadly accepted criteria of the general outcome-research community. Critical aspects of accepted standards are described, including prospective adaptations to the clinical-outcome research of our own discipline. A plausible means for conforming to the standard model is proposed in the context of treatment for aphasia.
引用
收藏
页码:787 / 810
页数:24
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