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DOI 10.1097/00002030-199312000-00011

Медицинская библиотека · AIDS (London, England) · 1993

Evaluation of two staging systems for HIV infection for use in developing countries.

Vandenbruaene M, Colebunders R, Goeman J, Alary M, Farber C M, Kestens L, van Ham G, Van den Ende J, Van Gompel A, Van den Enden E

Сравнительное исследованиеСтатьяПеревод пока не подготовлен

Аннотация

OBJECTIVE

To evaluate the clinical axis of the World Health Organization (WHO) clinical staging system and the modified WHO staging system proposed by Montaner et al. using the lymphocyte strata > 1500, 1500-1000 and < 1000 cells x 10(6)/l.

DESIGN

Cross-sectional study.

PATIENTS: Four hundred and fifteen consecutive patients with HIV infection attending three HIV reference centres in Belgium.

METHODS

Absolute CD4 lymphocyte counts were compared between stages within the two staging systems.

RESULTS

Median CD4 lymphocyte counts decreased with increasing stage of disease in both staging systems. Differences in median CD4 lymphocyte counts between stages of each staging system were statistically significant (Kruskal-Wallis one-way analysis of variance, P < 0.001). The WHO clinical stage 1 and the modified WHO stage I had positive predictive values of 56 and 58%, respectively, for identifying patients with CD4 lymphocyte levels > 500 cells x 10(6)/l. The WHO clinical stage 4 and the modified WHO stage IV had positive predictive values of 79 and 80%, respectively, for identifying patients with CD4 lymphocyte levels < 200 cells x 10(6)/l.

CONCLUSIONS

The WHO clinical staging system or a modified version of this system using lymphocytes stratification may be a good alternative in developing countries to the CD4 lymphocyte count-based HIV staging system used in the developed world. Cohort studies in developing countries are needed to assess their prognostic value.

Для цитирования: Vandenbruaene M, Colebunders R, Goeman J, Alary M, Farber C M, Kestens L, van Ham G, Van den Ende J, Van Gompel A, Van den Enden E. Evaluation of two staging systems for HIV infection for use in developing countries.. AIDS (London, England). 1993. DOI: 10.1097/00002030-199312000-00011.

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