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AIDS Care
Psychological and Socio-medical Aspects of AIDS/HIV
Volume 29, 2017 - Issue 4
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Articles

Co-calibration of two self-reported measures of adherence to antiretroviral therapy

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Pages 464-468 | Received 12 Apr 2016, Accepted 15 Nov 2016, Published online: 02 Dec 2016
 

ABSTRACT

Adherence to antiretroviral therapy (ART) is an important determinant of clinical success assessed in many HIV studies. Harmonizing adherence data from studies that use different measures is difficult without a co-calibration equation to convert between validated instruments. Our purpose was to co-calibrate two commonly used adherence measures: the AIDS Clinical Trials Group (ACTG) questionnaire and the Visual Analog Scale (VAS). We used robust linear regression to develop a co-calibration equation in a clinical care cohort. The outcome was the 30-day VAS percentage of ART taken and the predictors were ACTG questions. We evaluated the equation’s goodness of fit in five STTR (Seek, Test, Treat, Retain) consortium studies where individuals completed both measures: 2 criminal justice; 2 international; and 1 other high-risk vulnerable population. We developed a three-phase decision rule to convert ACTG to VAS in 1045 participants. First, when the last missed dose on the ACTG was reported as >30 days ago, the VAS was set to 100% (N = 582). Second, if “doses missed” was zero for all items, VAS was 100% (N = 104). Third, among remaining participants (N = 359), VAS was estimated as 96.8% minus 2.9% times the number of missed doses (“doses per day” was non-significant). Correlation between predicted and reported VAS was r = 0.80 in the criminal justice group (N = 446), r = 0.46 in the international group (N = 311), r = 0.32 in the other vulnerable population (N = 63), and r = 0.66 overall. When outliers due to inversion of the VAS scale were excluded (n = 25), these correlations were 0.88, 0.78, 0.80, and 0.86, respectively. We concluded that a simple decision rule and equation allowed us to co-calibrate between two widely used adherence measures thus combining data from studies with different instruments. This study highlighted issues with VAS inversions and its limitations as a single item. Combining studies using different instrument facilitates larger pooled datasets to address key research questions.

Acknowledgements

The authors thank the other investigators, the staff, and particularly the participants of the individual STTR studies for their valuable contributions. A full list of participating STTR investigators and institutions can be found at http://www.sttr-hiv.org.

Findings have been presented in part at the 9th International Conference on HIV Treatment and Prevention Adherence.

Disclosure statement

No potential conflict of interest was reported by the authors.

Additional information

Funding

Research presented in this paper is the result of secondary data analysis and was supported by 5U01DA037702 from the National Institute on Drug Abuse (NIDA) of the National Institutes of Health. Primary data collection for STTR studies was supported by grants: 5R01DA030768, 5R01DA030747, 5R01DA030781, 5R01DA030771, 5R01MH094090, 5R01DA030796, 5R01DA030778, 1R01DA030766, 7R01DA030770, 5R01DA030762, 5R01DA030776, 5R01DA030793, 1R01DA032059, 1R01DA032083, 1R01DA032106, 1R01DA032061, 1R01DA032110, 1R01DA032080, 1R01DA032082, 5R01DA032057, 1R01DA032098, 1R01DA032100; National Institute of Allergy and Infectious Diseases [P30AI127757, R24AI067039]. This work was also supported by the University of Washington Center for AIDS Research NIAID Grant (AI-027757) and the Centers for AIDS Research Network of Integrated Clinical Systems (CNICS) grant (R24 AI-067039).

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