Abstract

To the Editor:
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We analyzed data collected from the Medical Monitoring Project (MMP), a national HIV surveillance system that produces annual, cross-sectional estimates of behavioral and clinical characteristics of HIV-positive adults in medical care. 7 Informed consent was obtained from all interviewed participants. For the 2013–2014 data collection cycles, MMP used a three-stage design to sample HIV-positive adults receiving outpatient medical care (states, outpatient HIV care facilities, and patients). Data were collected from June 2013 to May 2015 via face-to-face or telephone interviews. All sampled states and territories participated; facility response rates ranged 85–86%, and patient response rates ranged 55–56%. Data were weighted based on known probabilities of selection at state or territory, facility, and patient levels and weighted to adjust for patient and facility nonresponse.
Using pooled annual cross-sectional interview data from patients with diagnosed HIV infection in the past 5 years (N = 1653), we calculated weighted percentages and associated 95% confidence intervals (CIs) of (1) persons being offered PS following one's HIV diagnosis, (2) acceptance of PS among those offered, and (3) reasons for not accepting PS among those who reported having partners and declined PS for all of their partners. We used Rao–Scott chi-square tests to assess differences in selected characteristics between patients: (1) offered versus not offered PS, and (2) accepting for some or all of their partners versus none of their partners. We assessed differences overall and by selected characteristics, and patients' self-reported main reason for not accepting PS. All analyses accounted for the complex sample design and weights.
Among patients with diagnosed HIV in the past 5 years, 68% (95% CI: 63–72) were offered PS following their diagnosis. Among those offered PS, 44% (95% CI: 38–50) accepted for all partners, 8% (95% CI: 5–10) accepted for some partners, 34% (95% CI: 28–40) declined PS for all partners, and 15% (95% CI: 12–18) did not report any partners (results not reported in table). Among those who were offered PS and reported having partners, 61% accepted PS for some or all of their partners. Among those declining PS for all of their partners, 71% (95% CI: 65–78) wanted to notify their partners personally, 9% (6–12) did not know their partners' contact information, 7% (3–10) reported only HIV-positive partners, 4% (2–5) were afraid of their partners' reaction to PS, and 7% (95% CI: 3–10) reported other reasons for declining PS (results not reported in table). The remaining persons reported that they either did not trust the health department or provider to notify their partners or that they were afraid their partners would find out who may have infected them as reasons for refusing PS, but these estimates were too small and unstable to report.
Being offered PS was significantly associated with age, with 76% of those aged 18–29 years reporting being offered PS compared with 60% of those ≥50 years (Table 1). Overall, being offered PS was not significantly associated with a gender-stratified racial/ethnic group; non-Hispanic black men reported the highest prevalence of being offered PS and Hispanic/Latina women reported the lowest. Gay or bisexual persons were significantly more likely to be offered PS compared with persons who were not gay or bisexual. HIV testing location of the index-case patient was significantly associated with being offered PS; the prevalence was 84% in health departments and 60% in private doctor's offices, and varied substantially across MMP areas.
Prevalence of Being Offered and Accepting Partner Services Among Recently Diagnosed Persons Receiving HIV Medical Care—United States, 2013–2014
Unweighted numbers and weighted percentages are presented.
Coefficient of variation >0.30, estimate may be unstable.
Estimate for negative response (not presented) has a coefficient of variation >0.30 and may be unstable.
CI, confidence interval; MMP, Medical Monitoring Project; PS, partner services.
Among those who were offered PS and reported having partners, 61% accepted PS for some or all of their partners (Table 1). Accepting PS was associated with a gender-stratified racial/ethnic group, with 78% of Hispanic/Latina women accepting PS compared with 44% of non-Hispanic white women (Table 1). PS acceptance was significantly higher among persons who were not gay or bisexual compared with gay or bisexual persons. The prevalence of PS acceptance was highest in other medical settings and lowest in private doctor's offices, and varied substantially across MMP areas.
Consistent with prior findings, 8 our analysis showed that being diagnosed with HIV at a health department clinic—where DIS are readily available to facilitate PS—was associated with higher likelihood of being offered PS; persons diagnosed at private doctor's offices and hospital inpatient settings were least likely to have been offered PS. PS is a complex task, requiring time and expertise, and is therefore potentially difficult and time-consuming for clinicians to routinely integrate into a patient's clinical visit in addition to providing medical care and treatment. Studies have shown that the integration of DIS in clinical settings increases the number of persons offered PS, partners elicited and tested, and new HIV cases identified. 9–10
Despite CDC recommendations that all persons with diagnosed HIV be offered PS, 3 our analysis found vast differences in the proportion of patients offered PS among MMP areas. Factors such as the volume of HIV diagnoses by medical providers, the burden of new HIV diagnosis within a jurisdiction, completeness and permissible legal use of surveillance data to offer PS, and resources available to a health department may help to explain geographic variation in offering PS. 11,12 For example, between June 2008 and April 2014, PS for newly diagnosed PWH in Philadelphia were only available by provider referral.
Our analysis shows that declining an offer of PS was most commonly associated with patients' desires to personally inform their own partners of potential exposure. However, people may be unaware that PS includes options for self-notification with support from the DIS. Studies have consistently found that provider- and DIS-facilitated PS yielded significantly higher proportions of partners elicited, notified, or tested for HIV. 9,10 In addition to ensuring that potentially exposed partners are notified, provider- or DIS-facilitated PS can benefit notified partners by allowing them to access the benefits of PS beyond exposure notification, such as access to prevention, medical, and social services.
The limitations of this analysis include the following: (1) PS experiences were self-reported and thus may be subject to biases inherent to self-reported information; and (2) we did not assess whether partners were actually notified of their exposure to HIV or received other components of PS.
There is a wide variation in the offering of PS to patients with newly diagnosed HIV. More research is needed to assess the extent of, and barriers to, offering PS by public health jurisdictions. Fostering complementary and collaborative relationships between public health departments and medical providers can enhance each group's ability to offer and facilitate PS for a higher proportion of PWH.
Footnotes
Acknowledgments
We thank MMP participants, area staff, and Provider and Community Advisory Board members. We also acknowledge the contributions of the Clinical Outcomes Team and Behavioral and Clinical Surveillance Branch at CDC.
Author Disclosure Statement
No competing financial interests exist.
Funding Information
Funding for the MMP is provided by the CDC through cooperative agreement PS09-937.
