Literature DB >> 1727616

Quality of life in persons with human immunodeficiency virus infection: measurement by the Medical Outcomes Study instrument.

T Wachtel1, J Piette, V Mor, M Stein, J Fleishman, C Carpenter.   

Abstract

OBJECTIVE: To assess the reliability and validity of the Medical Outcomes Study (MOS) Short Form Health Survey as an indicator for quality of life in patients infected with the human immunodeficiency virus (HIV).
DESIGN: Patient interview survey.
SETTING: The AIDS Health Services Program in seven sites: Newark and Jersey City, New Jersey; Nassau County, New York; Atlanta, Georgia; Dallas, Texas; Fort Lauderdale and Miami, Florida; New Orleans, Louisiana; and Seattle, Washington. PATIENTS: Patients (520) with HIV infection receiving health services at one of the above sites. MEASUREMENTS: All components of the MOS Short Form Health Survey were included in the interview. Minor modifications were made to adapt the survey to the particular circumstances of the study. Measured sociodemographic characteristics included age, sex, race, intravenous drug use, and education. Symptoms were assessed by closed-ended questions concerning memory, seizure, weakness or numbness, fever, chills, diaphoreses, dyspnea, diarrhea, and weight loss. Information on the frequency of symptoms was also collected. History of Pneumocystis carinii pneumonia and Kaposi sarcoma was noted. MAIN
RESULTS: The sociodemographic characteristics resemble those of patients with the acquired immunodeficiency syndrome (AIDS) reported to the Centers for Disease Control (CDC): mean age, 36; men, 89%; nonwhite, 31%; intravenous drug use, 34%. Neurologic symptoms (memory trouble, seizures, weakness or numbness) occurred in 71% of patients; constitutional symptoms (fever, chills, night sweats, weight loss) in 69%; dyspnea in 50%; and diarrhea in 47%. Although older age, female sex, nonwhite race, and intravenous drug use were associated with lower MOS scores in several areas, the strongest single or adjusted indicator of lower MOS scores was the presence of symptoms. Finally, patients with HIV infection had significantly lower scores than did previously reported patients with other chronic medical conditions (P less than 0.001).
CONCLUSIONS: The MOS survey is a reliable measure of quality of life for patients with HIV infection. These patients tend to have low scores, suggesting validity of the survey. The MOS survey is extremely sensitive to the effect of symptoms, which suggests that it might be useful as a quality-of-life indicator for AIDS clinical drug trials.

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Year:  1992        PMID: 1727616     DOI: 10.7326/0003-4819-116-2-129

Source DB:  PubMed          Journal:  Ann Intern Med        ISSN: 0003-4819            Impact factor:   25.391


  75 in total

1.  Continued high prevalence and adverse clinical impact of human immunodeficiency virus-associated sensory neuropathy in the era of combination antiretroviral therapy: the CHARTER Study.

Authors:  Ronald J Ellis; Debralee Rosario; David B Clifford; Justin C McArthur; David Simpson; Terry Alexander; Benjamin B Gelman; Florin Vaida; Ann Collier; Christina M Marra; Beau Ances; J Hampton Atkinson; Robert H Dworkin; Susan Morgello; Igor Grant
Journal:  Arch Neurol       Date:  2010-05

2.  Identification of patient attitudes and preferences regarding treatment of depression.

Authors:  L Cooper-Patrick; N R Powe; M W Jenckes; J J Gonzales; D M Levine; D E Ford
Journal:  J Gen Intern Med       Date:  1997-07       Impact factor: 5.128

3.  Asking patients about their treatment.

Authors:  T Sensky; J Catalan
Journal:  BMJ       Date:  1992-11-07

4.  Assessment of quality of life among HIV-infected persons in Pune, India.

Authors:  Rewa M Kohli; Suvarna Sane; Kishore Kumar; Ramesh S Paranjape; Sanjay M Mehendale
Journal:  Qual Life Res       Date:  2005-08       Impact factor: 4.147

5.  Putting Wilson and Cleary to the test: analysis of a HRQOL conceptual model using structural equation modeling.

Authors:  Karen H Sousa; Oi-Man Kwok
Journal:  Qual Life Res       Date:  2006-05       Impact factor: 4.147

6.  Development of a culturally appropriate health-related quality of life measure for human immunodeficiency virus-infected children in Thailand.

Authors:  Warunee Punpanich; Ron D Hays; Roger Detels; Kulkanya Chokephaibulkit; Umaporn Chantbuddhiwet; Pimsiri Leowsrisook; Wasana Prasitsuebsai
Journal:  J Paediatr Child Health       Date:  2010-10-26       Impact factor: 1.954

Review 7.  Conceptualizing a quality plan for healthcare. A philosophical reflection on the relevance of the health profession to society.

Authors:  S Mehrdad Mohammadi; S Farzad Mohammadi; Jerris R Hedges
Journal:  Health Care Anal       Date:  2007-12

8.  Acupuncture/Moxibustion RCT for Distal Sensory Peripheral Neuropathy in HIV/AIDS: Rationale, Design, Methods, Procedure and Logistics.

Authors:  Joyce K Anastasi; Bernadette Capili; Ann M Chung; Richard Hammerschlag
Journal:  EJOM       Date:  2010

9.  Social support mediates the relationship between HIV stigma and depression/quality of life among people living with HIV in Beijing, China.

Authors:  D Rao; W T Chen; C R Pearson; J M Simoni; K Fredriksen-Goldsen; K Nelson; H Zhao; F Zhang
Journal:  Int J STD AIDS       Date:  2012-07       Impact factor: 1.359

10.  Describing the health-related quality of life impact of HIV infection: findings from a study using the HIV Overview of Problems--Evaluation System (HOPES).

Authors:  P A Ganz; C A Coscarelli Schag; B Kahn; L Petersen; K Hirji
Journal:  Qual Life Res       Date:  1993-04       Impact factor: 4.147

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