NYMC Faculty Publications

Over-Reported Peripheral Neuropathy Symptoms in a Cohort of HIV Infected and Uninfected Rwandan Women: The Need for Validated Locally Appropriate Questionnaires

Author Type(s)

Faculty

DOI

10.4314/ahs.v14i2.24

Journal Title

African Health Sciences

First Page

460

Last Page

467

Document Type

Article

Publication Date

6-1-2014

Department

Medicine

Keywords

Adult, Aged, CD4 Lymphocyte Count, Female, HIV Infections, HIV Seronegativity, HIV-1, Health Services Needs and Demand, Humans, Logistic Models, Middle Aged, Peripheral Nervous System Diseases, Prevalence, Prospective Studies, Risk Factors, Rwanda, Severity of Illness Index, Surveys and Questionnaires, Women's Health, Young Adult

Disciplines

Medicine and Health Sciences

Abstract

BACKGROUND: Peripheral neuropathy symptoms (PNS) are commonly manifested in HIV-infected (HIV+) individuals, although data are limited on the prevalence and predictors of PNS in HIV+ patients from sub-Saharan Africa.

OBJECTIVE: To determine the prevalence and predictors of PNS in HIV+ and HIV-uninfected (HIV-) Rwandan women.

METHODS: Data were analysed from 936 (710 HIV+ and 226 HIV-) women from the Rwanda Women Interassociation Study and Assessment (RWISA), an observational prospective cohort study investigating the effectiveness and toxicity of ART in HIV+ women.

RESULTS: Of 936 enrolled, 920 (98.3%) were included in this analysis with 44% of HIV- and 52% of the HIV+ women reporting PNS (p=0.06). CD4+ count was not associated with PNS, although there was a non-significant trend towards higher prevalence in those with lower CD4+ counts. For the HIV- women, only alcohol and co-trimoxazole use were independently associated with PNS. WHO HIV stage IV illness and albumin ≤ 3.5 were associated with PNS in HIV+ women.

CONCLUSIONS: The rate of peripheral neuropathy symptoms reported in this cohort of HIV-infected African women seems implausible, and rather suggests that the screening tool for peripheral neuropathy in culturally diverse African settings be locally validated.

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