Document 0874 DOCN M95A0874 TI The Bristol-Myers Anorexia/Cachexia Recovery Instrument (BACRI): a brief assessment of patients' subjective response to treatment for anorexia/cachexia. DT 9510 AU Cella DF; VonRoenn J; Lloyd S; Browder HP; Division of Psychosocial Oncology, Rush Cancer Institute,; Chicago, IL 60612, USA. SO Qual Life Res. 1995 Jun;4(3):221-31. Unique Identifier : AIDSLINE MED/95338196 AB A brief visual analogue instrument was developed and tested in the context of a multicentre randomized double-blinded four-dose trial of megestrol acetate for the treatment of AIDS-related anorexia/cachexia. This nine-item instrument, the Bristol-Myers Anorexia/Cachexia Recovery Instrument (BACRI), was administered every 4 weeks after initiation of study drug (placebo vs 100 mg, 400 mg or 800 mg of drug). The purpose of the instrument was to quantify patient perception of benefit in areas such as decreased concern over weight, decreased concern over appearance, increased pleasure in eating and increase in global perception of quality of life. Post-trial psychometric evaluation of the instrument strongly supported the use of a seven-item index of subjective recovery from symptoms of anorexia/cachexia (BACRI-7) and a single criterion item depicting patient perception of benefit (BACRI-1). The BACRI-7 and BACRI-1 scales showed significant improvement over 12 weeks in patients who received higher dose active drug (400 and 800 mg) compared with the placebo and 100 mg doses. Further differentiation of 400 vs 800 mg arms was seen in the BACRI-7 results, consistent with dose-response improvements in weight and lean body mass changes. Quadratic trends over time in lean body mass change and provider-rated appetite grade suggested peak therapeutic effect at 8 weeks for these endpoints, whereas the absence of these trends in overall weight and patient-reported BACRI scores suggested that these benefits are more persistent. Although subjective (patient-reported) benefit is strongly associated with objective indicators of improvement, there remains the possibility that there is some added, independent benefit of megestrol acetate to subjective well-being. DE Acquired Immunodeficiency Syndrome/*COMPLICATIONS Adult Aged Anorexia/*DRUG THERAPY Appetite/DRUG EFFECTS Body Weight/DRUG EFFECTS Cachexia/*DRUG THERAPY Dose-Response Relationship, Drug Double-Blind Method Human Karnofsky Performance Status Megestrol/*ANALOGS & DERIVATIVES/ADMINISTRATION & DOSAGE/ THERAPEUTIC USE Middle Age Psychometrics *Quality of Life Questionnaires CLINICAL TRIAL JOURNAL ARTICLE MULTICENTER STUDY RANDOMIZED CONTROLLED TRIAL SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).