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Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America logoLink to Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America
letter
. 2022 Jul 27;75(11):2045–2046. doi: 10.1093/cid/ciac618

Pharyngeal Chlamydia trachomatis in Men Who Have Sex With Men in a Human Immunodeficiency Virus (HIV) Pre-exposure Prophylaxis Program in Hanoi, Vietnam

Hao T M Bui 1, Paul C Adamson 2,, Giang M Le 3, Jeffrey D Klausner 4,2
PMCID: PMC10200314  PMID: 35883257

To the Editor—We read with great interest the report by Evers et al [1], exploring the anatomical site distribution and risk factors for pharyngeal Chlamydia trachomatis infections in a large sample of men who have sex with men (MSM) in The Netherlands. The investigators reported a 10.6% prevalence of C. trachomatis overall, but a low prevalence of pharyngeal infections (1.2%). Compared with rectal and urogenital sites, pharyngeal C. trachomatis infections comprised the lowest prevalence by anatomic site.

We would like to share findings of an ongoing study screening for C. trachomatis and Neisseria gonorrhoeae among MSM enrolled in a human immunodeficiency virus (HIV) pre-exposure prophylaxis (PrEP) program in Hanoi, Vietnam. PrEP has been available in Vietnam since 2019 [2]. The Sexual Health Promotion Clinic is the largest PrEP program in Hanoi, providing PrEP for 2695 individuals cumulatively [3]. Our study provides quarterly screening for C. trachomatis and N. gonorrhoeae at 3 anatomic sites using nucleic acid amplification testing, as recommended by the Vietnam national PrEP guidelines [4].

Thus far, 218 study participants have enrolled; all are MSM with a median age of 24.0 years (interquartile range: 21.5–28.0 years) (Table 1). Overall, the prevalence of C. trachomatis at any anatomic site was 23% (50/218), with rectal infections comprising 68% (34/50) and urogenital infections comprising 20% (10/50). Chlamydia trachomatis was detected in 6.9% (15/218) of pharyngeal specimens. The prevalence of pharyngeal-only C. trachomatis was 4.1% (9/218). Pharyngeal and rectal infections occurred concurrently in 12% (6/50), but there were no concurrent pharyngeal and urogenital infections. The prevalence of pharyngeal C. trachomatis was 9.1% (5/55) among those reporting pharyngeal symptoms in the past week compared with 6.1% (10/163; P = .45) among those without.

Table 1.

Demographic, Behavioral, and Clinical Characteristics of 218 Men Who Have Sex With Men in an HIV PrEP Program in Hanoi, Vietnam

Chlamydia trachomatis Infections
All Participants (N = 218) Overall (n = 50) Pharyngeal (n = 15) Pharyngeal-Only (n = 9)
Median [IQR] age, years 24.0 [21.5–28.0] 24.0 [21.5–28.0] 23.9 [20.9–29.1] 23.9 [20.9–29.1]
Age
 16–24 years 117 (53.7) 24 (48.0) 6 (40) 2 (22.2)
 25–34 years 85 (39) 20 (40.0) 5 (33.3) 4 (44.4)
 ≥35 years 16 (7.3) 6 (12.0) 4 (26.7) 3 (33.3)
Number of male partners in the past month, median [IQR] 1 [1–2] 2 [1–3] 2 [1–3] 2 [1–2]
Oral sex in the past week 124 (56.9) 36 (72.0) 11 (73.3) 6 (66.7)
Deep kissing in the past week 119 (54.6) 32 (64.0) 11 (73.3) 6 (66.7)
Pharyngeal symptoms in the past week 55 (25.2) 13 (26.0) 5 (33.3) 3 (33.3)
Genital symptoms in the past week 35 (16.1) 6 (12.0) 1 (6.7) 0 (0)
Rectal symptoms in the past week 33 (15.1) 8 (16.0) 4 (26.7) 1 (11.1)
Genital C. trachomatis 10 (6.9) 10 (20.0) 0 (0) 0 (0)
Rectal C. trachomatis 34 (15.6) 34 (68.0) 6 (40.0) 0 (0)
Pharyngeal C. trachomatis 15 (6.7) 15 (30.0) 15 (100) 9 (100)

Data are presented as n (%) unless otherwise indicated. Abbreviations: HIV, human immunodeficiency virus; IQR, interquartile range; PrEP, pre-exposure prophylaxis.

The prevalence of both pharyngeal and pharyngeal-only C. trachomatis infections within our study population of MSM on PrEP in Vietnam was higher than the Evers et al estimates among MSM in The Netherlands. Similar to the findings here, we recently reported a C. trachomatis prevalence of 28.5% overall, 6.3% for pharyngeal and 5.2% for pharyngeal-only C. trachomatis, among HIV-uninfected MSM in Hanoi [5]. Evers et al report pharyngeal and pharyngeal-only C. trachomatis infections were the lowest prevalence sites, but we found a higher prevalence of pharyngeal infections compared with urogenital infections. We also found most pharyngeal infections were asymptomatic. The differences in prevalence are likely explained by the different study populations and settings, but access to screening might play a role, as most of our study population was receiving screening for the first time.

Screening for pharyngeal C. trachomatis for MSM on PrEP continues to be recommended by many national guidelines [6, 7]. However, as Evers et al note, spontaneous clearance of infections, infrequent symptoms, and rare development of complications limit the individual and public health impact of screening. Additionally, there are costs to screening, which are particularly important in resource-limited settings, and potential harms to overtreatment such as adverse effects and increased antimicrobial resistance due to more antibiotic consumption [8]. Additional research on clinical outcomes and cost-effectiveness is needed to demonstrate the clinical and public health benefit of pharyngeal screening for C. trachomatis.

Contributor Information

Hao T M Bui, Center for Training and Research on Substance Abuse–HIV (CREATA-H), Hanoi Medical University, Hanoi, Vietnam.

Paul C Adamson, Division of Infectious Diseases, David Geffen School of Medicine at UCLA, Los Angeles, California, USA.

Giang M Le, Center for Training and Research on Substance Abuse–HIV (CREATA-H), Hanoi Medical University, Hanoi, Vietnam.

Jeffrey D Klausner, Population and Public Health Sciences, Keck School of Medicine at USC, Los Angeles, California, USA.

Notes

Ethics statement. The study was approved by the Institutional Review Board of Hanoi Medical University.

Financial support. This work was supported by the US National Institute of Allergy and Infectious Diseases (R21 AI157817 to G. M. L and J. D. K.) and the Fogarty International Center (K01TW012170 to P. C. A). All authors report a no charge donation of study materials from Abbott Molecular.

References

  • 1. Evers YJ, Dukers-Muijrers NHTM, van Liere GAFS, et al. Pharyngeal Chlamydia trachomatis in men who have sex with men (MSM) in The Netherlands: a large retrospective cohort study. Clin Infect Dis 2022; 74:1480–4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2. PEPFAR - U.S . President's Emergency Plan for AIDS Relief. Country Operational Plan Vietnam COP 2018 Strategic Direction Summary, 2018. Available at: https://www.aidsdatahub.org/resource/vietnam-2018-country-operationalplan-strategic-direction-summary. Accessed 17 June 2022.
  • 3. Sexual Health Promotion Clinic at Hanoi Medical University Vietnam . Monthly report of PrEP progress at SHP Clinc as May 2022, 2022. Unpublished data. Accessed 17 June 2022
  • 4. Vietnam Authority of HIV/AIDS Prevention and Control (VAAC) . Guidline for Provision of Pre-Exposure Prophylaxis (PrEP) Services (document number 133 issued on 12 March 2020). Vietnam Ministry of Health. In: Hanoi, Vietnam. 2020.
  • 5. Adamson PC, Bhatia R, Tran KDC, et al. Prevalence, anatomic distribution, and correlates of Chlamydia trachomatis and Neisseria gonorrhoeae infections among a cohort of men who have sex with men in Hanoi, Vietnam. Sex Transm Dis 2022; 49:504–10. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6. The Australasian Society for HIV Viral Hepatitis and Sexual Health Medicine . National PrEP Guideline Update. Prevent HIV by prescribing PrEP. Sydney, Australia, 2021.
  • 7. Centers for Disease Control and Prevention . Preexposure prophylaxis for the prevention of HIV infection in the United States—2021 update: a clinical practice guideline. Atlanta, GA: US Public Health Service, 2021.
  • 8. Wi TE, Ndowa FJ, Ferreyra C, et al. Diagnosing sexually transmitted infections in resource-constrained settings: challenges and ways forward. J Int AIDS Soc 2019; 22(Suppl 6):e25343. [DOI] [PMC free article] [PubMed] [Google Scholar]

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