Abstract
Non-occupational post-exposure prophylaxis (nPEP) has often relied on the joint work of emergency physicians and infectious disease specialists in busy emergency departments and human immunodeficiency virus (HIV)/sexually transmitted infections clinics abroad, where adherence education and follow-up are invariably reactive. In our pilot study, community-based organizations (CBOs) were invited to together implement the nPEP tailored to men who have sex with men (MSM) in 2 cities of Guangxi in Southwestern China, of which experiences and lessons drawn from would be provided to the promotion of nPEP in China.
The study population enrolled MSM individuals prescribed nPEP from September 2017 to December 2019. One-to-one follow-ups by CBOs were applied through the treatment. Predictors of treatment completion were assessed by logistic regression.
Of 271 individuals presented for nPEP, 266 MSM with documented treatment completion or non-completion, 93.6% completed the 28-day course of medication. Completion was associated with reporting side effects (aOR = .10; 95% CI: 0.02–0.38; P = .001). The follow-up rate of 91.9% was achieved based on the definition of loss to follow-up. No documented nPEP failures were found, although 1 MSM subsequently seroconverted to HIV due to ongoing high-risk behavior.
CBOs’ engagement in HIV nPEP, especially the “one-to-one” follow-up supports by peer educators partly ensure adherence and retention to nPEP. Tailored interventions are needed to address the subsequent high-risk behaviors among the MSM population.
Keywords: community-based organization, HIV, men who have sex with men, non-occupational post-exposure prophylaxis
1. Introduction
Over 30 years, China's human immunodeficiency virus (HIV) epidemic has kept increasing that contributed to 0.958 million survival cases as of October 2019,[1] but disparities remain across various regions. Most HIV diagnoses occurred in southwest China, which comprises largely cases from Sichuan, Yunnan, and Guangxi.[2] The fast escalating epidemic among men who have sex with men (MSM) is of particular concern in recent years.[3] Overall, HIV prevalence among the MSM group was approximately 8% in 2015, with a three-time higher prevalence observed in five provinces including Guangxi of southwest China, according to a scoping review.[4] In 2017, among newly diagnosed cases in China, 25.5% were MSM,[5] and this figure rapidly rose from the rate of 2.5%, reported in 2006.[6] In addition, studies in China show that 2% to 5% of sexually active men have sex with other men in the nation, accounting a total of 2 to 8million male population across the country.[7]
Neighboring on the provinces of Guangdong in the east, Hunan in the northeast, and Yunnan in the west, Guizhou in the northwest, the Guangxi Zhuang Autonomous Region (Guangxi) links to Hong Kong and Macao by the waterway of the Xijiang River and shares a borderline of 637 kilometers in the southwest with Vietnam. Due to its location along a major heroin trafficking route connecting Guangxi with Yunnan and Vietnam as well as its close proximity to the world's major heroin-producing base, famous for the Golden Triangle, HIV transmission in Guangxi was triggered initially by intravenous drug use.[8] In 1996, the first case of HIV infection was discovered among local intravenous drug users in Pingxiang city of Guangxi, bordering Vietnam.[9] After then, HIV prevalence via injecting drugs climbed and accounted for 69% of the total reported cases across the region in 2003.[10] With passing years, sexual transmission becomes the dominant mode of HIV spread in Guangxi.[11] Guangxi has occupied the second position in the largest number of reported HIV cases in China.[12,13] MSM are now recognized as a disproportionately affected group in this area of which the proportion of HIV infections among MSM increased from 0.1% in 2005 to 7.27% in 2018 in a total reported number.[14] HIV surveillance data published by Guangxi Center for Disease Control and Prevention (CDC) indicated a trend of rapid HIV incidence among MSM in recent years that HIV positive rate among them ascended from 3.9% in 2010 to 9.67% in 2018.[15]
HIV non-occupational post-exposure prophylaxis (nPEP) is a 28-day prescription of antiretroviral therapy (ART) provided within 72 hours of exposure to prevent the infection.[16–18] nPEP is an evidence-based HIV prevention strategy that has been implemented in most countries for decades, of which lessons drawn from suggesting its completion rates are of major concern.[19] Meta-analyses indicate 25.7% to 67.2% of patients who accepted nPEP completed the full course.[20,21] nPEP awareness, access (eg, cost and where available), side effects (SEs), follow-up retention, and drug regimens are associated with lower rates of nPEP completion.[22–25] As a result, the efficacy of nPEP may depend on a comprehensive health service mechanism, including sustainable antiretroviral adherence education, SEs observation, psychological, and follow-up supports during the implementation. In many countries, nPEP services have often relied on the joint work of emergency physicians and infectious disease specialists (IDS) in busy emergency departments and HIV/sexually transmitted infections (STI) clinics, where compliance education and follow-up are invariably reactive.[26,27] A prospective study suggested that funded additional staff could support counseling and follow-up activities.[28]
Over the years, nPEP in China has been limited to some surveys on awareness and demands[29,30] and to date, there has not been a comprehensive guideline developed due to lack of domestic research data, despite clinicians in some areas tried to offer nPEP.[31] Supported by the “Technical Collaboration with the People's Republic of China on Innovative Approach on AIDS between U.S. CDC” and “Guangxi Natural Science Foundation,” a cooperative pilot program of HIV nPEP tailored to MSM in 2 cities of Guangxi in Southwestern China was established in 2017, by taking experience and lessons abroad. We invited gay-oriented community-based organizations (CBOs) as our partner to involve in this culturally appropriate and lesbian, gay, bisexual, and transgender (LGBT)-friendly program, given CBOs helpful to retaining MSM in care and treatment in the public health system and decreasing stigma[32] while non-community-based care providers difficultly reach the hidden population.[33] The program addressed nPEP through linkage to counseling, treatment, and follow-up management by close cooperation between CBOs, CDCs/hospitals, and pharmacies. Specifically, we described the efficacy through medication adherence, follow-up retention, and HIV seroconversion among MSM consulting for nPEP under this model. Experiences and lessons drawn from the analysis would be provided to the promotion of nPEP in China.
2. Methods
We conducted research from September 2017 to December 2019 in Nanning and Liuzhou cities in Guangxi, southwest China, based on the aforementioned survey[29] finding that MSM in the 2 cities had potential demands for HIV nPEP. Our study was carried out with reference to international nPEP guidelines, including WHO, Canadian, and American guidelines.[34–37]
2.1. Inclusion and exclusion criteria
MSM, who were 18 years or older, tested HIV-negative, lived in Nanning and Liuzhou. Eligibility assessment should be based on the HIV status of the source whenever possible and may include consideration of background prevalence and local epidemiological patterns. Exposures that may warrant nPEP include: (1) having sex without condoms (including homosexual and heterosexual behaviors), (2) sharing needles with HIV-infected drug users, (3) blood, semen, genital secretions, blood-stained saliva, and wound exudate splashing to eye, nose, and oral cavity or damaged mucosa. Exposures that do not require nPEP include: (1) when the exposed individual is HIV already positive, (2) when the source is established to be HIV negative, and window period is excluded, (3) exposures to bodily fluids that do not pose a significant risk, that is, tears, non-blood-stained saliva, urine, and sweat, and (4) exposure time exceeds 72 hours.
2.2. Recommended regimens
HIV nPEP should be offered and initiated as early as possible in all individuals with an exposure that has the potential for HIV transmission, and ideally within 72 hours. A full 28-day prescription of antiretrovirals (ARVs) would be provided for nPEP following the initial risk assessment.[38] Participants should bear the cost of medication sold by commercial pharmacies or pharmacies within hospitals, and doctors in the research explained all regimens available and specifications to them before the prescription. Participants would choose the preferred and affordable regimen:
Regimen 1: Tenofovir fumarate/emtricitabine (TDF/FTC) 300/200 mg once daily + raltegravir (RAL) 400 mg twice daily,[39] RMB 3960 ($ 573.91) for a full 28-day prescription.
Regimen 2: Tenofovir fumarate/emtricitabine (TDF/FTC) 300/200 mg once daily + dolutegravir (DTG) 50 mg once daily,[36] RMB 3960 ($ 573.91) for a full 28-day prescription.
Regimen 3: Elvitegravir/cobicistat/emtricitabine/tenofovir alafenamide (E/C/F/TAF) single tablet once daily,[19] RMB 2980 ($ 431.88) for a full 28-day prescription.
Regimen 4: Tenofovir fumarate/emtricitabine (TDF/FTC) 300/200 mg once daily,[34] RMB 1980 ($ 286.96) for a full 28-day prescription.
According to the availability of medications locally, alternatives would be made with reference to relevant guidelines, for example, abacavir/lamivudine/dolutegravir (ABC/3TC/DTG) 50/600/300 mg combination tablet once daily,[40] RMB 2880 ($ 417.39) for a full 28-day prescription.
2.3. Laboratory testing and follow-up
Baseline testing: (1) patients being initiated on nPEP should be tested for HIV antibodies and antigens, fourth-generation screening and (2) tests for syphilis serology, hepatitis B screen, and hepatitis C antibody, complete blood count (CBC), renal, and liver function. Follow-up testing: (1) repeating HIV serology at week-4 to week-6 and 3 months after exposure as well as at 6 months after exposure if hepatitis C infection was acquired from the exposure and (2) repeating CBC, renal, and liver function at week-4 to week-6 after exposure. Other testing: those tested positive for HIV were referred to CDC for western-blot, CD4 count, and viral load tests, and started on ART.
2.4. Determination of completing a full 28-day medication, loss to follow-up
Adherence to nPEP: Information on treatment completion was self-reported by the patients at subsequent follow-up or via phone call by CBO staff for conforming. We defined patients who completed 28 days of treatment as adherent. Loss to follow-up (LTFU): Patients had scheduled follow-up at 4 to 6 weeks, 3 months post-exposure as well as 6 months if hepatitis C infection was acquired from the exposure. LTFU was determined if patients did not return to CBOs for HIV tests at least once within the follow-up schedule.[26]
2.5. Measures to guarantee adherence and retention in nPEP
(1) Training on adherence to medication for CBOs was provided by ART clinics of CDC and hospitals time after time, which covered risk assessment of HIV exposure, medication use, and ways to improve adherence and retention in care. (2) Budget was specially developed for supporting CBOs to carry out compliance education. Participants who showed lab testing reports during follow-up visits obtained RMB 100 ($ 14.49) for transportation. (3) CBOs used the standardized form for documenting nPEP regimens, adherence, SEs, and follow-up tests. A reminder system was established between peer educators and patients, reminding participants to take drugs and return for HIV tests on time though phone calls and social media, for example, WeChat, QQ. (4) The informed consent form included the provisions of drug adherence and follow-up that participants should abide.
2.6. Study procedures
To scale up nPEP awareness, we made community publicity and advocacy before the recruitments by the platform of MSM CBOs – Nanning Yitongxing Healthcare Center and Liuzhou Hongying Working Group, and Nanning/Liuzhou CDCs in the 2 cities as well as the provincial CDC of Guangxi. Online publicity via social media of WeChat, MicroBlog, Blued, QQ, and offline advocacy through cards, posters, and brochures were implemented to address nPEP knowledge, and inform the way of seeking services.
A collaboration mechanism between CBOs, CDC/hospitals, and pharmacies were established. Firstly, ART clinic doctors of CDC and hospitals organized training on research protocol for MSM peer educators, emphasizing adherence and psychological support, monitoring of SEs, retention in care, and laboratory tests. As the first providers contacted participants, patients’ consulting for nPEP in CBOs was available 24/7 on the protocol basis, which trained peer educators conducted a preliminary risk assessment for MSM to be consulted after exposure, including HIV rapid test of a 4th-generation antibody/antigen combo assay.[35] For those who met eligible recruits, CBOs referred them to ART clinics of CDC and/or hospitals for further risk assessment and baseline testing. For patients seeking nPEP out of normal working hours, CBOs would refer them to on-call physicians in the ART clinic of hospitals. With prescriptions given by doctors, pharmacies in hospitals, or commercial pharmacies would sell medications to patients. One-to-one service was encouraged in our study, that is, the first counselor (peer educator) who received the patient would then accompany him for referral service to ART clinics, and subsequently, assist doctors in offering follow-up services included adherence education, SEs monitoring, psychological support, and follow-up testing throughout the nPEP. In addition, CBOs were responsible for the registration of medical records which covered patients’ basic information, the outcome of the risk assessment, drug uptake, and results of laboratory tests (Fig. 1).
Figure 1.
Study flow (1) intra-city transportation from CBOs to ART clinics takes about 15 minutes. (2) Information on the risk of acquiring HIV, safe sex behaviors, risks, and benefits of nPEP were provided. (3) Patients had the option of purchasing prescribed regimens in commercial pharmacy if were in short supply in ART clinic pharmacy. ART = antiretroviral therapy, CBO = community-based organization, HIV = human immunodeficiency virus, nPEP = non-occupational post-exposure prophylaxis.
2.7. Data collection and analysis
Data were extracted from clinical records onto standardized casebooks, structured according to the Chinese national guidelines for diagnosis and treatment of HIV/AIDS.[40] Information was extracted from the records of the initial consultation and follow-up visits and included: sociodemographic characteristics, risk profile including exposure type that led to nPEP, time of exposure to nPEP, types of ARV prescribed, and the occurrence of SEs, treatment completion, and laboratory test results. Data were stored in the EPI 3.1 Database (EpiData Association, Odense, Denmark).
Outside China, the findings of the previous systematic review have highlighted that adherence remains a challenge across populations including MSM, female sex workers, and victims of sexual assault.[21] However, associated factors impacting adherence have yet to be fully explored,[41] and adverse events of treatment are a well-known reason for nPEP withdrawal in studies on mixed groups.[21,25,42–44] For this study we analyzed the demographics, correlates of SEs associated with nPEP among the only MSM group, and predictors of adherence extended to sociodemographic characteristics, knowing HIV status of source contact, Ses, substance abuse, and nPEP frequency, to further verify whether completion rate for nPEP and associated factors, when prescribed between CBOs, CDCs/hospitals, and pharmacies, are in line with or go beyond previous reports.
For our first aim to assess factors associated with treatment completion vs. non-completion, we performed bivariate analyses using χ2 test and Fisher exact test and to evaluate the difference between the 2 groups on socio-demographic, knowing HIV status of the source patient, SEs, substance abuse, and nPEP frequency. Wilcoxon–Mann–Whitney rank-sum test was conducted for continuous variables or abnormal distributions of data, as appropriate. Significant variables were then analyzed in multivariate logistic regression (odds ratios, 95% confidence intervals) to evaluate independent factors associated with adherence to nPEP. Variables with P value <.30 in the bivariate analyses were further considered for inclusion in the model. All data analyses were completed using IBM SPSS Statistics 23 (IBM Corporation, Armonk, NY, USA). We considered a two-tailed alpha error of 0.05 throughout the analysis.
3. Results
From September 2017 to December 2019, a total of 370 MSM presented LGBT-friendly CBOs for nPEP counseling in the two cities, 281 of them eligible for nPEP uptake, and 271 were enrolled in the study while 9 abandoned the treatment on account of drug burden, 1 rejected to join in the research; 89 were not qualified for nPEP, including 15 presented later than 72 hours after exposure, 4 baseline HIV positive and referred to CDC, 46 evaluated as no risk of HIV acquisition (5 source contacts’ HIV negative, out of window period), 22 only received counseling but refused HIV tests, and 2 were 17 years old, not meet the age for the study.
3.1. Socio-demographics and exposure characteristics
A total of 271 participants ranged from 18 to 56 years old (M = 29.8, SD = 7.3), and 21 to 40 years old occupied dominantly of 84.1% (n = 228). 86.3% (n = 234) self-reported as single. More than half of the participants were Han ethnic group (68.6%, n = 186), and 90.4% (n = 261) were from Guangxi. Most patients sought nPEP for the reason of unprotected anal intercourse (UAI) between men and 3.7% (n = 10) experienced condom failure, defined as a broken, torn, or slipped-off condom. 17.0% (n = 46) were with a known HIV-positive source (Table 1).
Table 1.
Socio-demographic and exposure characteristics of MSM uptake nPEP in Southwestern China (N = 271).
| Characteristics | n | % |
| Age group (years) | ||
| ≤20 | 19 | 7.0 |
| 21– | 228 | 84.1 |
| >40 | 24 | 8.9 |
| Marital status | ||
| Single | 234 | 86.3 |
| Married | 33 | 12.2 |
| Divorced | 4 | 1.5 |
| Ethnic groups | ||
| Han | 186 | 68.6 |
| Ethnic minorities | 85 | 31.4 |
| Residency status | ||
| Guangxi | 245 | 90.4 |
| Out of Guangxi | 22 | 8.1 |
| Unknown | 4 | 1.5 |
| Source contact's HIV status | ||
| Positive | 46 | 17.0 |
| Negative (window period not excluded) | 8 | 3.0 |
| Unknown | 217 | 80.1 |
| Exposure type | ||
| Insertive anal (“1”) | 19 | 7.0 |
| Receptive anal (“0”) | 89 | 32.8 |
| Insertive/receptive anal (“0.5”) | 3 | 1.1 |
| Unsure anal position | 149 | 55.0 |
| Insertive/receptive oral | 11 | 4.1 |
| Condon use | ||
| Not use | 261 | 96.3 |
| Torn/slipped | 10 | 3.7 |
3.2. nPEP medication uptake
A 89.7% (243/271) MSM consulted nPEP at CBOs during the daytime while 7.4% (20/271) at 0:00 to 6:00 and 26.9% (73/271) during 18:00 to 0:00. All patients were prescribed nPEP within 72 hours. The time between exposure and medication prescription was less than 24 hours in 177 (65.3%) episodes, 24 to 48 hours in 76 (28.0%) episodes, and 48 to 72 hours in 18 (6.6%) episodes. A 6.3% (17/271) initiated ART at 0:00 to 6:00, and 38.4% (104/271) during 18:00 to 0:00. A 50.9% (138/271) participants were prescribed with TDF/FTC, 34.3% (93/271) and 7.7% (21/271), respectively, with ABC/3TC/DTG and E/C/F/TAF. A 88.6% (240/271) the first time presented for nPEP, and 11.4% (31/271) were nPEP repeat presenters (Table 2). A total of 18 were with documented SEs reporting, with nausea, headache, fatigue, and lethargy/malaise being the most commonly reported. In bivariate analysis, we found no statistically significant association between age, marital status, residency status, ethnic groups or substance/stimulants abuse, time to initiate ART, frequency of nPEP uptake, types of ARV prescribed, and SEs to nPEP; however, treatment completion (P = .006) was found statistically significant associated with SEs by the χ2 test (Table 3).
Table 2.
Intervention, follow-up, and compliance to nPEP among MSM in Southwestern China (N = 271).
| Characteristic | n | % |
| Time to receive counselling in CBOs | ||
| 0:00– | 20 | 7.4 |
| 6:00– | 60 | 22.1 |
| 12:00– | 110 | 40.6 |
| 18:00– | 73 | 26.9 |
| Unknown | 8 | 3.0 |
| Time to initiate ART | ||
| 0:00– | 17 | 6.3 |
| 6:00– | 30 | 11.1 |
| 12:00– | 112 | 41.3 |
| 18:00– | 104 | 38.4 |
| Unknown | 8 | 3.0 |
| Exposure to nPEP time | ||
| <24 h | 177 | 65.3 |
| 24– | 76 | 28.0 |
| 48–72 | 18 | 6.6 |
| Types of ARV prescribed | ||
| TDF + FTC | 138 | 50.9 |
| ABC + 3TC + DTG | 93 | 34.3 |
| E/C/F/TAF | 21 | 7.7 |
| TDF + FTC + DTG | 15 | 5.5 |
| TDF + FTC + RAL | 4 | 1.5 |
| nPEP repeat presenters | ||
| Twice | 27 | 10.0 |
| The third time | 2 | 0.7 |
| The fourth time | 2 | 0.7 |
| None | 240 | 88.6 |
| Side effects | ||
| Yes | 18 | 6.6 |
| No | 244 | 90.0 |
| Unknown | 9 | 3.3 |
| Baseline HIV tests results | ||
| Negative | 265 | 97.8 |
| Positive | 0 | 0.0 |
| Results not sure | 6 | 2.2 |
| HIV test results at week-4–week-6 after exposure | ||
| Negative | 237 | 87.5 |
| Positive | 0 | 0.0 |
| Tests not done | 34 | 12.5 |
| HIV test results 3–6 months after exposure | ||
| Negative | 216 | 79.7 |
| Positive | 1 | 0.4 |
| Tests not done | 54 | 19.9 |
| Follow up (at least once within 1 to 6 months post-exposure) | ||
| Yes | 249 | 91.9 |
| No | 22 | 8.1 |
Table 3.
Correlates of SEs associated with nPEP among MSM in Southwestern China (N = 262).
| Factors | SEs n (%) | Non-SEs n (%) | P | Overall (N = 262) |
| Age group (years) | ||||
| ≤20 | 0 (0.0) | 18 (100.0) | .768 | 18 |
| 21– | 17 (7.7) | 203 (92.3) | 220 | |
| >40 | 1 (4.2) | 23 (95.8) | 24 | |
| Marital status | ||||
| Single | 14 (6.2) | 212 (93.8) | .366 | 226 |
| Married | 4 (11.8) | 30 (88.2) | 34 | |
| Divorced | 0 (0.0) | 2 (100.0) | 2 | |
| Residency status | ||||
| Guangxi | 15 (6.4) | 221 (93.6) | .222 | 236 |
| Out of Guangxi | 2 (9.1) | 20 (90.9) | 22 | |
| Unknown | 1 (25.0) | 3 (75.0) | 4 | |
| Ethnic groups | ||||
| Han | 9 (4.9) | 173 (95.1) | .070 | 182 |
| Ethnic minorities | 9 (11.3) | 71 (88.7) | 80 | |
| Knowing source contact was HIV positive | ||||
| Yes | 3 (7.0) | 40 (93.0) | 1.000 | 43 |
| Unknown | 15 (6.8) | 204 (93.2) | 219 | |
| Substance or stimulants abuse | ||||
| Yes | 2 (3.6) | 54 (96.4) | .378 | 56 |
| No | 16 (7.8) | 190 (92.2) | 206 | |
| Time to initiate ART | ||||
| 0:00– | 2 (8.7) | 21 (91.3) | .311 | 23 |
| 6:00– | 4 (14.3) | 24 (85.7) | 28 | |
| 12:00– | 7 (6.4) | 102 (93.6) | 109 | |
| 18:00– | 5 (4.9) | 97 (95.1) | 102 | |
| Frequency of nPEP uptake | ||||
| The first time | 17 (7.6) | 206 (92.4) | .824 | 223 |
| Twice | 1 (3.1) | 31 (96.9) | 32 | |
| Third time | 0 (0.0) | 5 (100.0) | 5 | |
| Fourth time | 0 (0.0) | 2 (100.0) | 2 | |
| Types of ARV prescribed | ||||
| TDF/FTC | 9 (6.9) | 122 (93.1) | .314 | 131 |
| ABC/3TC/DTG | 5 (5.4) | 87 (94.6) | 92 | |
| E/C/F/TAF | 1 (5.0) | 19 (95.0) | 20 | |
| TDF/FTC + DTG | 2 (13.3) | 13 (86.7) | 15 | |
| TDF/FTC + RAL | 1 (25.0) | 3 (75.0) | 4 | |
| Treatment completion | ||||
| Yes | 14 (5.6) | 234 (94.4) | .006 | 248 |
| No | 4 (33.3) | 8 (66.7) | 12∗ | |
3.3. Adherence to nPEP and factors independently associated with adherence
Five MSM could not be confirmed whether or not completed the full course of ART due to loss of contact. 266 (98.2%) MSM with documented treatment completion or non-completion, and 93.6% (249/266) of them completed the 28-day course of medication. For the patients discontinued treatment, 7 due to sex partners being tested negative and 5 without specific reasons. Three stopped treatments because of medication SEs. One patient defaulted treatment on account of busy work and 1 could not afford a whole ART course. In a multivariate model, including age, residency status, and SEs (of which P < .3 in univariate analysis), only SEs retained a statistically significant association with adherence to nPEP (aOR = .10; 95% CI: .02–.38; P = .001) (Tables 4 and 5).
Table 4.
Predictors of adherence to nPEP among MSM in Southwestern China.
| Factors | Treatment completion n (%) 249 (93.6) | Treatment non-completion n (%) 17 (6.4) | P ∗ | Overall (N = 266) |
| Age group (years) | ||||
| ≤20 | 16 (84.2) | 3 (15.8) | .191 | 19 |
| 21– | 210 (94.2) | 13 (5.8) | 223 | |
| >40 | 23 (95.8) | 1 (4.2) | 24 | |
| Marital status | ||||
| Single | 214 (93.4) | 15 (6.6) | 1.000 | 229 |
| Married | 33 (94.3) | 2 (5.7) | 35 | |
| Divorced | 2 (100.0) | 0 (0.0) | 2 | |
| Residency status | ||||
| Guangxi | 225 (93.7) | 15 (6.3) | .266 | 240 |
| Out of Guangxi | 21 (95.5) | 1 (4.5) | 22 | |
| Unknown | 3 (75.0) | 1 (25.0) | 4 | |
| Ethnic groups | ||||
| Han | 173 (94.5) | 10 (5.5) | .419 | 183 |
| Ethnic minorities | 76 (91.6) | 7 (8.4) | 83 | |
| Knowing source contact was HIV positive | ||||
| Yes | 43 (93.5) | 3 (6.5) | 1.000 | 46 |
| Unknown | 206 (93.6) | 14 (6.4) | 220 | |
| SEs | ||||
| Yes | 14 (77.8) | 4 (22.2) | .020 | 18 |
| No/unknown | 235 (94.8) | 13 (5.2) | 248 | |
| Substance or stimulants abuse | ||||
| Yes | 54 (94.7) | 3 (5.3) | 1.000 | 57 |
| No | 195 (93.3) | 14 (6.7) | 209 | |
| nPEP uptake the first time | ||||
| Yes | 212 (93.4) | 15 (6.6) | 1.000 | 227 |
| No | 37 (94.9) | 2 (5.1) | 39 | |
Table 5.
Factors associated with adherence to nPEP (N = 266).
| Predictors | Crude OR (95% CI) | P | Adjusted OR (95% CI) | P |
| Age group (years) | ||||
| ≤20 | 1 | |||
| 21– | 0.20 (0.04–1.08) | .061 | 0.21 (0.04–1.12) | .068 |
| >40 | 0.19 (0.02–2.40) | .200 | 0.21 (0.02–2.62) | .228 |
| Residency status | ||||
| Guangxi | 1 | |||
| Out of Guangxi | 0.91 (0.10–7.98) | .931 | ||
| Unknown | 5.96 (0.41–85.95) | .190 | ||
| SEs | ||||
| Yes | 1 | |||
| No/unknown | 0.10 (0.03–0.42) | .002 | 0.10 (0.02–0.38) | .001 |
3.4. Laboratory tests, seroconversion, and follow-up retention
At the baseline testing, all participants received HIV tests before nPEP uptake, 97.8% (265/271) were found negative, and 6 (2.2%) MSM showed uncertain HIV antibody test results but were confirmed as negative while further testing was applied (Table 2). A 95.9% (260/271) received syphilis TP rapid tests and 10 MSM were found positive, of which 6 were new infections and referred to STI clinics for treatment. A 82.3% (223/271) had tests for CBC, renal, and liver function. 70.1% (190/271) received hepatitis B tests, 12 were found positive for HBsAg but no liver abnormalities caused by ARVs after 3 months’ follow-up. A 47.6% (129/271) had hepatitis C tests, and 2 patients were found with hepatitis C infection and abided by follow-up for 6 months.
For the follow-up assessment at week-4 to week-6 after exposure, 87.5% (237/271) received tests by the SD Bioline Syphilis/HIV Duo assay, and none of the patients seronegative at baseline had seroconverted for HIV and syphilis infections. A 55.4% (150/271) had tests for CBC, renal, and liver function, no abnormal outcomes and indicators were found.
As for the follow-up tests at 3-month and/or 6-month after exposure, 79.7% (216/271) had tests for both HIV and syphilis, 1 case of HIV seroconversion was reported. Documented information indicated this seroconversion patient was tested as negative at the 6-week after exposure though he discontinued medication 2 weeks later due to sex partner not living with HIV, however, he had ongoing high-risk behaviors (UAI, oral penetration) and was confirmed as positive at the 82nd day within the follow-up schedule, not ascribed as nPEP failure.
When it came to follow-up retention based on the definition of LTFU, our research realized an overall follow-up rate of 91.9% (249/271), with the calculation from 205 participants coming back to CBOs for HIV tests both at week-4 to week-6 and 3-month and/or 6-month after exposure, as well as 32 and 12 MSM, respectively had test only 1 time at week-4 to week-6, and at 3-month and/or 6-month after exposure. Likewise, the follow-up rate of participants completing a full 28-day medication reached 92.8% (231/249).
4. Discussion
HIV transmission persists, particularly in MSM who usually retain UAI behaviors, and some may experience condom failure even though kept condom use. As a result, nPEP is an imperative component of public health strategy for HIV prevention in this group. Using almost one and a half years of clinical data, we described nPEP practices in two cities of Southwestern China through partnerships with CBOs. Most participants prescribed with nPEP at ART clinics were young men (84.1%) potentially exposed to HIV through high-risk sexual behaviors, and a certain number of patients (32.8%) were identified as a sex role of receptive anal (“0”) which had been ranked the second for HIV transmission risk.[45] Our research indicated 11.4% nPEP repeat presenters, similar to other studies,[27,46] which highlight the importance of sexual health screenings and counseling on safe sex practices, especially in the MSM community, and additional attention should be paid to repeat presenters for risk compensation that risk behavior counseling by CBOs and considerations for pre-exposure prophylaxis (PrEP) as an alternative intervention tool by ART doctors should be encouraged, despite previously nPEP use may not correlate with increased high-risk behaviors among MSM population.[39,47] PrEP has not been officially promoted across China but it is currently available at some ART clinics in pilot sites. Corresponding guideline suggests HIV-serodiscordant couples, nPEP repeat presenters as well as groups of high-risk behaviors including MSM, intravenous drug users, and individuals not in a mutually monogamous relationship.[35]
4.1. Medication uptake and SEs
A large majority of patients (93.3%) were prescribed nPEP within 48 hours. It is worth mentioning that 7.4% at 0:00 to 6:00 and 26.9% at 18:00 to 0:00 came to CBOs for nPEP counseling, which indicates the flexibility of working time by CBOs just meets the target population's requirement for services. Despite potential benefits, the provision of nPEP remains underutilized because of the cost to patients.[48] In our study, 9 MSM gave up treatment since they could not afford the nPEP cost. Overall, half the participants selected the relatively inexpensive regimen of “TDF/FTC” ($ 286.96). Therefore, we suggest improve healthcare providers’ ability to navigate the systems required to have nPEP medications covered by insurance, which is particularly important to those most willing to use nPEP but with lower or no incomes, for example, student group. To the best of our knowledge, the regimen of E/C/F/TAF, of whom price decreased from $431.88 to $186.96 for a full course of nPEP since January 2020, had been covered by insurance, owing to drug negotiation between the National Healthcare Security Administration and manufacturers, quite inspiring news for domestic clients. A prospective trial found E/C/F/TAF was well-tolerated when used as an nPEP regimen.[19]
Our analysis revealed that 18 participants were with documented SEs and 3 of them discontinued treatments, mainly presented as mild gastrointestinal, neurologic disorders, and musculoskeletal pain but were well coped with, no serious adverse events occurred. It may remind us that such kind of SEs is common in ARVs, which can be tolerated by most nPEP users. A meta-analysis by Ford et al showed that SEs could lead to treatment interruption or non-compliance, thereby affecting the efficacy of nPEP.[21] Their findings indicated a total of 1033 participants from 64% of the studies had terminated nPEP due to SEs. A systematic review in Nigeria also found 23.8% of the patients could not finish treatment induced by SEs.[49] Treatment completion was associated with SEs in our study. All these suggest ongoing adherence education, medication guidance, and psychological supports are essential in the course of nPEP for avoiding non-compliance.
4.2. Adherence to nPEP and retention in follow-up
Our study achieved quite encouraging results on medication adherence, with an nPEP completion rate of 93.6%, higher than similar researches, as seen in findings from Belgium (60%–66.4%), America (64%), and Canada (49%).[27,50–52] Our analysis by the multi-variate model highlighted that SEs were important considerations affecting nPEP compliance. In general, the HIV-testing follow-up of our research also demonstrated a higher rate (91.9%). The study aforementioned in Belgium found 41.1% failed to attend their follow-up schedule,[50] the same as other similar studies, the follow-up rates just ranged from 30% to 60%.[18,26,53,54] The efficacy of nPEP greatly relies on the compliance of patients to the regimen prescribed. In addition, ongoing follow-up consultations in the process of nPEP can bring about advantages beyond monitoring SEs and increasing adherence. Follow-up is of paramount importance as it is the key not only to offer an opportunity for confirming the results of nPEP protection but a chance for more counseling on subsequent risk behaviors. Furthermore, follow-up visits are considered as an occasion for discussing PrEP which might be the optimum therapy option for a subgroup of clients consulting for nPEP.
Our good outcomes in adherence and retention in care could be ascribed to nPEP publicities ahead of the recruitment as well as the “one-to-one” follow-up model by CBOs. Efforts contributed to publicizing nPEP knowledge by Nanning Yitongxing Healthcare Center and Liuzhou Hongying Working Group were particularly appreciated. An nPEP feuilleton through the WeChat public account (wwwnnchcn) of the Healthcare Center was established aiming at community publicity and advocacy; besides, nPEP information through QQ, Weibo, Blued (a strong social gay APP connecting gay communities around the globe) was conveyed, which helped MSM correctly grasp nPEP, urging them to complete the treatment. On the other hand, our lower drop-out rate would be inseparable from an LGBT-friendly environment amid the research. Despite the criminalization of homosexuality in China is not proactively enforced, discrimination against MSM hinders them to receive HIV-related service. However, MSM CBOs show their unique and irreplaceable strengths in regard to LGBT-based HIV prevention: Firstly, as a supplement to CDC and medical institutions, CBOs are regarded as a crucial bridge between HIV high-risk groups and authorities in health. Secondly, CBOs’ flexible working hours and diversified serving manners can satisfy the variable needs of target groups. Thirdly, most important CBOs share a common subculture with the LGBT community, which effectively alleviates stigma and discrimination against the homosexual population, thereby a trust patient–prescriber relationship being created and better reach out to the hidden groups.[55,56] CBOs engagement in this MSM-oriented nPEP highlights such advantages. On the contrary, nPEP implemented independently by the Department of STI Control in Singapore indicated MSM has significantly associated with LTFU, hence correspondingly affected adherence.[26] Taken together, potential models fitting the LGBT group ought to be explored just as a similar study suggests a “one-size-fits-all” model for nPEP is probably not effective for marginalized populations.[28]
4.3. HIV seroconversions
In this research, follow-up HIV assessments at week-4 to week-6 after exposure showed no seroconversions. One nPEP recipient was found subsequently seroconverted to HIV at 3-month after exposure due to ongoing high-risk behaviors, not ascribed as nPEP failure, as observed in other similar studies.[51,57] There is something noticeable that 46 participants’ source contact had been confirmed as HIV positive, and 44 nPEP users were tested as negative during the repeating HIV serology, except for 2 not complying with the follow-up appointment. All again testify that nPEP, one of several biomedical HIV prevention strategies, is truly effective in real-world settings. From an epidemiological perspective, the provision of nPEP at the same time could help new HIV cases identification, and our results show that 5 HIV-infected MSM were discovered, including 4 at baseline and 1 during the service, which is in agreement with findings from a Cameroon review.[58]
4.4. Other laboratory testing
Since nPEP regimens may pose an inhibitory effect on the hepatitis B virus (HBV), recipients need to be tested for liver and kidney function, HBV, etc.[34,59] However, our research findings demonstrated 82.3% had tests for CBC, renal, and liver function, and only 70.1%, 47.6%, respectively, received tests on HBV and hepatitis C virus. Data showed more disappointedly for the follow-up assessment at week-4 to week-6 after exposure, merely 55.4% had tests for CBC, renal, and liver function, in spite of obtaining $14.49 for transportation subsidy with the presentation of test reports. To our understanding, this part had not been underscored before nPEP as well as counseling in the service. Although there was no liver and kidney damage caused by ARVs reported in our research, it does not mean there is no risk, which reminds the Chinese nPEP guideline makers should make much account of such tests in the future.
4.5. Limitations
There were several crucial limitations in this study. On the one hand, our research was confined to participants’ self-report to assess nPEP use, instead of using validated clinical records, including data on source contact and HIV status, medication adherence, and side effects self-reported by patients in the process of consultation, subjected to self-reporting bias. On the other hand, our study showed that side effect was an essential element associated with adherence to nPEP. However, we could not rule out the existence of unmeasured confounders, for instance, education level and income failed to be captured as socio-demographic factors. Additionally, the study was well laid out at the beginning with strong support by both domestic and international cooperative projects. Hence, real conditions should be deliberated when the study findings are extrapolated to other settings in China.
5. Conclusions
Through partnerships with CBOs, our pilot study on nPEP aiming at MSM group from September 2017 to December 2019 in two cities of Southwestern China revealed three important findings. First of all, CBOs’ engagement in HIV nPEP, especially the “one-to-one” follow-up supports by peer educators partly ensure medication compliance and follow-up retention. This collaborative model would be encouraged to other places where conditions permitted, in particular China where the “China AIDS Fund for Non-Governmental Organizations” has been officially launched since 2015. Second, adequate publicities on nPEP knowledge could be conducive to the efficacy of post-exposure prophylaxis. The role of CBOs should be highlighted in publicity and advocacy. Third, from the perspective of providers, tailored interventions are needed to address the subsequent high-risk behaviors among MSM.
Acknowledgments
The authors would like to thank all staff members from U.S. CDC Global AIDS Program, China Office, Guangxi CDC, Nanning and Liuzhou CDCs, Nanning the Fourth People's Hospital, Liuzhou People's Hospital, and Guangxi Longtan Hospital, in particular the peer educators from Nanning Yitongxing Healthcare Center and Liuzhou Hongying Working Group for involving in the research. We thank all our participants for their time. Besides, we would like to deliver thanks to QGH from Guangxi Medical University for assistance with the statistical analysis.
Author contributions
GHL, YFW, QYZ, SJL, and RJL conceived and designed the study. YFW conducted data processing and statistical analysis as well as wrote the manuscript. GHL revised the manuscript. We further confirm that the order of authors listed in the manuscript has been approved by all of us. All authors read and approved the final manuscript.
Conceptualization: Yufei Wu, Qiuying Zhu, Shujia Liang, Rongjian Li, Guanghua Lan.
Data curation: Yufei Wu, Yuejiao Zhou.
Formal analysis: Yufei Wu.
Funding acquisition: Guanghua Lan.
Investigation: Guanghua Lan, Yufei Wu, Qiuying Zhu, Nengxiu Liang.
Methodology: Yufei Wu.
Project administration: Guanghua Lan.
Software: Chunying Li.
Supervision: Yufei Wu, Guanghua Lan.
Validation: Guanghua Lan.
Writing – original draft: Yufei Wu.
Writing – review & editing: Guanghua Lan, Yufei Wu.
Footnotes
Abbreviations: AIDS = acquired immune deficiency syndrome, ART = antiretroviral therapy, ARVs = antiretrovirals, CBC = complete blood count, CBO = community-based organization, CDC = Center for Disease Control and Prevention, HBV = hepatitis B virus, HIV = human immunodeficiency virus, IDS = infectious disease specialist, LGBT = lesbian, gay, bisexual, and transgender, LTFU = loss to follow-up, MSM = men who have sex with men, nPEP = non-occupational post-exposure prophylaxis, PrEP = pre-exposure prophylaxis, SEs = side effects, STIs = sexually transmitted infections, UAI = unprotected anal intercourse.
How to cite this article: Wu Y, Zhu Q, Zhou Y, Liang S, Li R, Liang N, Li C, Lan G. Implementation of HIV non-occupational post-exposure prophylaxis for men who have sex with men in 2 cities of Southwestern China. Medicine. 2021;100:43(e27563).
This study was supported by the Technical Collaboration with the People's Republic of China on Innovative Approach on AIDS between U.S. CDC (5U2GGH001153) and Project of Guangxi Natural Science Foundation (2017GXNSFAA198370). The sponsors had no role in the present protocol.
All procedures performed in this study were in accordance with the ethical standards of the Ethics Review Committee of Guangxi Institutional Review Board (IRB No: GW-2017-0012) and with the 1964 Helsinki declaration and its later amendments. All participants gave written informed consent before involving in the research.
The authors have no conflicts of interest to disclose.
The datasets generated during and/or analyzed during the present study are available from the corresponding author on reasonable request.
HIV = human immunodeficiency virus, MSM = men who have sex with men, nPEP = non-occupational post-exposure prophylaxis.
ART = antiretroviral therapy, ARVs = antiretrovirals, CBO = community-based organization, HIV = human immunodeficiency virus, MSM = men who have sex with men, nPEP = non-occupational post-exposure prophylaxis.
ART = antiretroviral therapy, ARVs = antiretrovirals, HIV = human immunodeficiency virus, MSM = men who have sex with men, nPEP = non-occupational post-exposure prophylaxis, SEs = side effects.
Missing value, 2 could not be confirmed whether finished the 28-day course or not.
HIV = human immunodeficiency virus, MSM = men who have sex with men, nPEP = non-occupational post-exposure prophylaxis, SEs = side effects.
Fisher exact test and χ2 test.
nPEP = non-occupational post-exposure prophylaxis, SEs = side effects.
References
- [1].Bureau of Disease Prevention and Control, National Health Commission of the People's Republic of China. New progress in AIDS prevention and control in China in 2019. Chin J AIDS STD 2019;12:1205. [Google Scholar]
- [2].Wang Y, Huang KS. An overview of global and China AIDS population on its size, spatial distribution and mortality characteristics. Popul Soc 2018;4:78–88. [Google Scholar]
- [3].Zhang DP, Lu HY, Zhuang MH, et al. Enhancing HIV testing and treatment among men who have sex with men in China: a pilot model with two-rapid tests, single blood draw session, and intensified case management in six cities in 2013. PLoS One 2016;11:e0166812. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [4].Tang SY, Tang WM, Meyers K, Chan P, Chen Z, Tucker JD. HIV and syphilis among men who have sex with men and transgender individuals in China: a scoping review. Lancet 2016;388:S74. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [5].NCAIDS, NCSTD, China CDC. Update on the AIDS /STD epidemic in China in December 2017. Chin J AIDS STD 2018;2:111. [Google Scholar]
- [6].National Health and Family Planning Commission of the People's Republic of China. China AIDS Response Progress Report. 2015;Beijing, China: Chinese Health and Family Planning Commission, http://www.unaids.org/sites/default/files/country/documents/CHN_narrative_report_2015.pdf [Google Scholar]
- [7].Chow EP, Wilson DP, Zhang J, Jing J, Zhang L. Human immunodeficiency virus prevalence is increasing among men who have sex with men in China: findings from a review and meta-analysis. Sex Transm Dis 2011;9:845–57. [DOI] [PubMed] [Google Scholar]
- [8].Beyrer C, Razak MH, Lisam K, Chen J, Lui W, Yu XF. Overland heroin trafficking routes and HIV-1 spread in south and south-east Asia. AIDS 2000;1:75–83. [DOI] [PubMed] [Google Scholar]
- [9].Chen J, Liu W, Nancy LY. Molecular-epidemiological analysis of HIV-1 initial prevalence in Guangxi, China. Zhonghua Liu Xing Bing Xue Za Zhi 1999;2:74–7. [PubMed] [Google Scholar]
- [10].Li ML, Li RJ, Shen ZY, et al. Spatial distribution of HIV, HCV, and coinfections among drug users in the southwestern border areas of China (2004–2014): a cohort study of a national methadone maintenance treatment program. BMC Public Health 2017;1:759. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [11].Ge XM, Yang WM, Zhu QY, et al. Epidemiological characteristics of HIV/AIDS in Guangxi Zhuang Autonomous Region, 2010–2017. Chin J Epidemiol 2019;3:315–21. [DOI] [PubMed] [Google Scholar]
- [12].Zhou YJ, Li XM, Zhang C, et al. Rates of HIV, syphilis, and HCV infections among different demographic groups of female sex workers in Guangxi China: evidence from 2010 national sentinel surveillance data. AIDS Care 2013;11:1433–41. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [13].Wang XF, Lan GH, Shen ZY, et al. HIV and syphilis prevalence trends among men who have sex with men in Guangxi, China: yearly cross-sectional surveys, 2008–2012. BMC Infect Dis 2014;14:367. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [14].Guangxi Center for Disease Control and Prevention. HIV/AIDS Prevention and Treatment Information System. 2018. [Google Scholar]
- [15].Guangxi Center for Disease Control and Prevention. 2010–2018 HIV Sentinel Surveillance Results. [Google Scholar]
- [16].Saag MS, Benson CA, Gandhi RT, et al. Antiretroviral drugs for treatment and prevention of HIV infection in adults: 2016 recommendations of the International Antiviral Society-USA Panel. JAMA 2016;2:191–210. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [17].Cresswell F, Waters L, Briggs E, et al. UK guideline for the use of HIV Post-Exposure Prophylaxis Following Sexual Exposure, 2015. Int J STD AIDS 2016;9:713–38. [DOI] [PubMed] [Google Scholar]
- [18].McDougal SJ, Alexander J, Dhanireddy S, Harrington RD, Stekler JD. Non-occupational post-exposure prophylaxis for HIV: 10-year retrospective analysis in Seattle, Washington. PLoS One 2014;8:e105030. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [19].Gantner P, Hessamfar M, Souala MF, et al. Elvitegravir–Cobicistat–Emtricitabine–Tenofovir Alafenamide single-tablet regimen for human immunodeficiency virus postexposure prophylaxis. Clin Infect Dis 2020;5:943–6. [DOI] [PubMed] [Google Scholar]
- [20].Scannell M, Kim T, Guthrie BJ. A meta-analysis of HIV post-exposure prophylaxis among sexually assaulted patients in the United States. J Assoc Nurses AIDS Care 2018;1:60–9. [DOI] [PubMed] [Google Scholar]
- [21].Ford N, Irvine C, Shubber Z, et al. Adherence to HIV postexposure prophylaxis: a systematic review and meta-analysis. AIDS 2014;18:2721–7. [DOI] [PubMed] [Google Scholar]
- [22].Mitchell JW, Sophus AI, Petroll AE. HIV-negative partnered men's willingness to use non-occupational post-exposure prophylaxis and associated factors in a U.S. sample of HIV-negative and HIV-discordant male couples. LGBT Health 2016;2:146–52. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [23].Wong K, Hughes CA, Plitt S, et al. HIV non-occupational postexposure prophylaxis in a Canadian province: treatment completion and follow-up testing. Int J STD AIDS 2010;9:617–21. [DOI] [PubMed] [Google Scholar]
- [24].Minas B, Laing S, Jordan H, Mak DB. Improved awareness and appropriate use of non-occupational post-exposure prophylaxis (nPEP) for HIV prevention following a multi-modal communication strategy. BMC Public Health 2012;12:906. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [25].Thomas R, Galanakis C, Vézina S, et al. Adherence to post-exposure prophylaxis (PEP) and incidence of HIV seroconversion in a major North American cohort. PLoS One 2015;11:e0142534. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [26].Teo AKJ, Tai BC, Chio MT, La HH. A mixed methods study of non-occupational post-exposure prophylaxis at an STI clinic in Singapore: five-year retrospective analysis and providers’ perspectives. PLoS One 2018;8:e0202267. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [27].Malinverni S, Libois A, Gennotte AF, La Morté C, Mols P. Prescription of non-occupational post-exposure HIV prophylaxis by emergency physicians: an analysis on accuracy of prescription and compliance. PLoS One 2016;4:e0153021. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [28].Bogoch II, Scully EP, Zachary KC, et al. Patient attrition between the emergency department and clinic among individuals presenting for HIV nonoccupational postexposure prophylaxis. Clin Infect Dis 2014;11:1618–24. [DOI] [PubMed] [Google Scholar]
- [29].Zeng Z, Li Z, Lan GH, Liu H, Xu J, Yin WY. Qualitative study on the demand for non-occupational post-exposure prophylaxis among MSM in Guangxi Zhuang Autonomous Region. Chin J Dis Control Prev 2018;12:1274–7. [Google Scholar]
- [30].Li JZ, Zhu YW, Ren QY, et al. Investigation on the demand for non-occupational post-exposure prophylaxis among men who have sex with men in Jinan. Chin J AIDS STD 2020;1:51–3. [Google Scholar]
- [31].Lu TY, Mao X, Peng EL, et al. Bibliometric analysis on research hotspots on HIV post-exposure prophylaxis related articles in the world, 2000–2017. Chin J Epidemiol 2018;39:1501–6. (in Chinese). [DOI] [PubMed] [Google Scholar]
- [32].Qvist T, Cowan SA, Graugaard C, Helleberg M. High linkage to care in a community-based rapid HIV testing and counseling project among men who have sex with men in Copenhagen. Sex Transm Dis 2014;3:209–14. [DOI] [PubMed] [Google Scholar]
- [33].Stahlman S, Beyrer C, Sullivan PS, Mayer KH, Baral SD. Engagement of gay men and other men who have sex with men (MSM) in the response to HIV: a critical step in achieving an AIDS-free generation. AIDS Behav 2016;(Suppl 3): 330–40. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [34].Ford N, Mayer KH. World Health Organization Postexposure Prophylaxis Guideline Development Group. World Health Organization Guidelines on Postexposure Prophylaxis for HIV: recommendations for a public health approach. Clin Infect Dis 2015;(Suppl 3): S161–4. [DOI] [PubMed] [Google Scholar]
- [35].Tan DHS, Hull MW, Yoong D, et al. Canadian guideline on HIV pre-exposure prophylaxis and non-occupational post-exposure prophylaxis. CMAJ 2017;189:E1448–58. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [36].O’Donnell S, Tan DHS, Hull MW. New Canadian guideline provides evidence-based approach to non-occupational HIV prophylaxis. CJEM 2019;1:21–5. [DOI] [PubMed] [Google Scholar]
- [37].Updated guidelines for antiretroviral postexposure prophylaxis after sexual, injection drug use, or other nonoccupational exposure to HIV – United States, 2016. MMWR Morb Mortal Wkly Rep 2016;17:458. [DOI] [PubMed] [Google Scholar]
- [38].Qi TK, Lu HZ. Interpretation for Canadian guideline on HIV pre-exposure prophylaxis and non-occupational post-exposure prophylaxis. World Clin Drugs 2018;11:727–31. [Google Scholar]
- [39].Koyama A, Middlebrooks L, Bullock A. Updates on HIV non-occupational post-exposure prophylaxis. Curr Opin Pediatr 2019;4:454–61. [DOI] [PubMed] [Google Scholar]
- [40].AIDS and Hepatitis C Professional Group, Society of Infectious Diseases, Chinese Medical Association; Chinese Center for Disease Control and Prevention. Chinese guidelines for diagnosis and treatment of HIV/AIDS (2018). Inter J Epidemiol Infect Dis 2018;6:361–78. [Google Scholar]
- [41].Chio MTW, Tan HH. A retrospective audit of postexposure prophylaxis following sexual exposure seen at the Department of STI Control Clinic. Dermatol Bull 2010;21:27–8. [Google Scholar]
- [42].Gulholm T, Jamani S, Poynten IM, Templeton DJ. Non-occupational HIV post-exposure prophylaxis at a Sydney metropolitan sexual health clinic. Sex Health 2013;10:438–41. [DOI] [PubMed] [Google Scholar]
- [43].Oldenburg CE, Barnighausen T, Harling G, Mimiaga MJ, Mayer KH. Adherence to post-exposure prophylaxis for non-forcible sexual exposure to HIV: a systematic review and meta-analysis. AIDS Behav 2014;18:217–25. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [44].Bryant J, Baxter L, Hird S. Non-occupational postexposure prophylaxis for HIV: a systematic review. Health Technol Assess 2009;13:iii.ix-x, 1-60. [DOI] [PubMed] [Google Scholar]
- [45].Patel P, Borkowf CB, Brooks JT, Lasry A, Lansky A, Mermin J. Estimating per-act HIV transmission risk: a systematic review. AIDS 2014;10:1509–19. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [46].Armishaw J, Hoy JF, Watson KM, Wright EJ, Price BG, Pierce AB. Non-occupational post-exposure prophylaxis in Victoria, Australia: responding to high rates of re-presentation and low rates of follow-up. Int J STD AIDS 2011;12:714–8. [DOI] [PubMed] [Google Scholar]
- [47].Donnell D, Mimiaga MJ, Mayer K, Chesney M, Koblin B, Coates T. Use of non-occupational post-exposure prophylaxis does not lead to an increase in high risk sex behaviors in men who have sex with men participating in the EXPLORE trial. AIDS Behav 2010;5:1182–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [48].Mitchell JW, Sophus AI, Petroll AE. HIV-negative partnered men's willingness to use non-occupational post-exposure prophylaxis and associated factors in a U.S. sample of HIV-negative and HIV-discordant male couples. LGBT Health 2016;2:146–52. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [49].Iloanusi SH, Mgbere OO, Abughosh SM, Essien EJ. HIV non-occupational post exposure prophylaxis in Nigeria: a systematic review of research evidence and practice. Int J MCH AIDS 2019;2:101–19. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [50].Malinverni S, Gennotte AF, Schuster M, De Wit S, Mols P, Libois A. Adherence to HIV post-exposure prophylaxis: a multivariate regression analysis of a 5-year prospective cohort. J Infect 2018;1:78–85. [DOI] [PubMed] [Google Scholar]
- [51].Beymer MR, Weiss RE, Bolan RK, et al. Differentiating nonoccupational postexposure prophylaxis seroconverts and nonseroconverters in a community-based clinic in Los Angeles, California. Open Forum Infect Dis 2017;2:ofx061. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [52].Wong K, Hughes CA, Plitt S, et al. HIV non-occupational post-exposure prophylaxis in a Canadian province: treatment completion and follow-up testing. Int J STD AIDS 2010;9:617–21. [DOI] [PubMed] [Google Scholar]
- [53].Gantner P, Treger M, De Miscault C, et al. Predictors of standard follow-up completion after sexual exposure to HIV: five-year retrospective analysis in a French HIV-Infection Care Center. PLoS One 2015;12:e0145440. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [54].Farrugia Parsons B, Fisher K, Cordery D, Cloudwell D. Counselling improves follow-up HIV testing at week 6 for HIV post-exposure prophylaxis recipients. Sex Health 2013;3:288–9. [DOI] [PubMed] [Google Scholar]
- [55].Zhang G, Wang P, Sha S, et al. Community based organizations on application and approval of the projects supported by China AIDS Fund for Non-Governmental Organizations in 2015. Chin J AIDS STD 2017;7:660–8. [Google Scholar]
- [56].Xue H, Wu JM, Xia XL, et al. Involvement of non-governmental organizations in HIV/AIDS control and prevention in China, 2012–2014. Chin J Public Health 2018;3:428–31. [Google Scholar]
- [57].Chomchey N, Woratanarat T, Hiransuthikul N, et al. Factors associated with intention to take non-occupational HIV post-exposure prophylaxis among Thai men who have sex with men. J Virus Erad 2017;3:128–39. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [58].Kouanfack C, Meli H, Cumber SN, et al. Non-occupational HIV post-exposure prophylaxis: a 10-year retrospective review of data following sexual exposure from Yaounde Central Hospital, Cameroon. Int J MCH AIDS 2019;2:138–45. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [59].Jain S, Mayer KH. Practical guidance for nonoccupational postexposure prophylaxis to prevent HIV infection: an editorial review. AIDS 2014;11:1545–54. [DOI] [PMC free article] [PubMed] [Google Scholar]

