Self‐reported alcohol use versus phosphatidylethanol in behavioral trials: A study of people living with HIV in Tshwane, South Africa

Author:

Parry Charles D. H.12ORCID,Myers Bronwyn134ORCID,Londani Mukhethwa5,Shuper Paul A.167ORCID,Nkosi Sebenzile5,Hahn Judith A.8ORCID,Kekwaletswe Connie5,Morojele Neo K.591011ORCID

Affiliation:

1. Alcohol, Tobacco and Other Drug Research Unit South African Medical Research Council Cape Town South Africa

2. Department of Psychiatry University of Stellenbosch Cape Town South Africa

3. Curtin enAble Institute, Faculty of Health Sciences Curtin University Perth Western Australia Australia

4. Division of Addiction Psychiatry, Department of Psychiatry and Mental Health University of Cape Town Cape Town 7700 South Africa

5. Alcohol, Tobacco and Other Drug Research Unit South African Medical Research Council Pretoria South Africa

6. Institute for Mental Health Policy Research and Campbell Family Mental Health Research Institute Centre for Addiction and Mental Health Toronto Ontario Canada

7. Dalla Lana School of Public Health University of Toronto Toronto Ontario Canada

8. Department of Medicine University of California San Francisco San Francisco California USA

9. Department of Psychology University of Johannesburg Johannesburg South Africa

10. School of Public Health University of the Witwatersrand Johannesburg South Africa

11. School of Family Medicine and Public Health University of Cape Town Johannesburg South Africa

Abstract

AbstractBackgroundAccurately quantifying alcohol use among persons with HIV (PWH) is important for validly assessing the efficacy of alcohol reduction interventions.MethodsWe used data from a randomized controlled trial of an intervention to reduce alcohol use among PWH who were receiving antiretroviral therapy in Tshwane, South Africa. We calculated agreement between self‐reported hazardous alcohol use measured by the Alcohol Use Disorders Identification Test (AUDIT; score ≥8) and AUDIT‐Consumption (AUDIT‐C; score ≥3 for females and ≥4 for males), heavy episodic drinking (HED) in the past 30 days, and heavy drinking in the past 7 days with a gold standard biomarker‐‐phosphatidylethanol (PEth) level (≥50 ng/mL)‐‐among 309 participants. We used multiple logistic regression to assess whether underreporting of hazardous drinking (AUDIT‐C vs. PEth) differed by sex, study arm, and assessment time point.ResultsParticipants' mean age was 40.6 years, 43% were males, and 48% were in the intervention arm. At 6 months, 51% had PEth ≥50 ng/mL, 38% and 76% had scores indicative of hazardous drinking on the AUDIT and AUDIT‐C, respectively, 11% reported past 30‐day HED, and 13% reported past 7‐day heavy drinking. At 6 months, there was low agreement between AUDIT‐C scores and past 7‐day heavy drinking relative to PEth ≥50 (sensitivities of 83% and 20% and negative predictive values of 62% and 51%, respectively). Underreporting of hazardous drinking at 6 months was associated with sex (OR = 3.504. 95% CI: 1.080 to 11.364), with odds of underreporting being greater for females.ConclusionsSteps should be taken to decrease underreporting of alcohol use in clinical trials.

Funder

National Institutes of Health

South African Medical Research Council

Publisher

Wiley

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