Abstract
We conducted secondary data analysis using a biobehavioral survey dataset of 1538 MSM from Zimbabwe. Survey participants were screened for the four symptoms suggestive of tuberculosis infection using the WHO TB screening algorithm. Results: All participants experienced at least one symptom suggestive of tuberculosis. 40% of HIV-positive MSM reported having had a cough in the last month and 13% of them experienced unexpected weight loss. The prevalence of experiencing any of the four TB symptoms amongst HIV-positive MSM was 23%.
Contribution
There is an urgent need for active TB case finding and treatment amongst HIV-positive MSM in Zimbabwe. Clinicians will need to ensure that MSM who need TB testing receive it timeously.
Keywords: HIV, Tuberculosis symptoms, Case finding, MSM
Background
Despite being both preventable and treatable, TB remains an important public health problem in all countries and age groups [1]. Globally and in sub-Saharan Africa, tuberculosis is a major cause of mortality and morbidity [2, 3]. Being HIV-positive without viral load suppression is a predisposing factor for TB infection, amongst MSM. TB prevalence surveys in resource-poor countries consistently show a high burden of patients with TB disease who remain undiagnosed and are thus infectious to others [4]. Improving international case detection for TB also contributes to achieving health-related global goals [5]. HIV prevalence is declining in Zimbabwe but remains one of the highest in sub-Saharan Africa at 11.6% among the general population [6] and is higher at 23.4% among men who have sex with men (MSM) [7].
Eliciting of symptoms is an essential step in the diagnosis and care of presumptive MSM tuberculosis patients [8]. MSM are among the critical populations identified to be at higher risk of tuberculosis infection and disease [9]. However, there is limited TB data among MSM [10, 11].
Methods
Data from our study on HIV and STI biobehavioral surveys (BBS) among MSM in Zimbabwe [7] was used to determine the prevalence of tuberculosis (TB) symptoms amongst HIV-positive MSM. Data were collected from 1538 individual MSM in the Zimbabwe cities of Harare and Bulawayo.
The study was a cross-sectional BBS using respondent-driven sampling (RDS). RDS is a peer-referral sampling methodology designed for data collection among hard-to-reach populations. Consenting participants completed a questionnaire on sociodemographics, sexual identity and history, sexual behaviour, mental health, alcohol and drug use, HIV testing services, stigma and violence, social cohesion, health services and TB. As part of the study, participants were screened for the four symptoms suggestive of tuberculosis infection using the WHO TB screening algorithm, and to our knowledge, this is the first and only BBS in Zimbabwe to have done so. After being tested for HIV, participants were also screened for tuberculosis (TB) symptoms. Participants who screened positive for TB symptoms were offered the option of being driven that day to a designated MSM-friendly referral healthcare facility that offers MSM-friendly HIV and other related services. Additionally, a peer escort to accompany them was provided. If the participant declined, they were given a referral card for the clinic that offers MSM-friendly HIV and related services. STATA statistical package version 17 was used for statistical analysis. The study received ethical clearance from the national institutional review board, the Medical Research Council of Zimbabwe # (MRCZ/A/2156).
Results
In terms of demographics, the HIV-positive MSM were older than the negative, with Mean (Standard deviations) of 31.8 (9.2) and 26.4 (7.9) years respectively, p = 0.001. The majority (> 96%) were Black Africans, who had primarily attained (> 70%) secondary education. Close to 40% were unemployed, see Table 1. All participants experienced at least one symptom suggestive of tuberculosis, with prevalences of 7%, 4%, 7%, and 1% for persistent cough, night sweats, unexpected weight loss and fever respectively. Having had a cough in the last month was higher among HIV-positive MSMs compared to those not affected with HIV, 40% vs. 5%, p = 0.001. The same was the case with experiencing unexpected weight loss, 13% vs. 6%, p = 0.001 and experiencing a fever in the last month, 3% vs. 1%, p = 0.037. The prevalence of experiencing any of the four TB symptoms was 13%, and this prevalence was higher among the HIV-positive MSM compared to those who are not infected with HIV, 23% vs. 11%, p = 0.001. Three per cent reported that they had been exposed to a person with TB in the last 12 months.
Table 1.
Baseline demographics and comparison of prevalence of TB symptoms among HIV Positive and HIV-negative MSM
| Variable | HIV Positive | HIV negative | P-Value |
|---|---|---|---|
| Demographics | |||
| Age in years | |||
| Mean (Standard Deviation) | 31.8 (9.2) | 26.4 (7.9) | 0.001 |
| Ethnic Group | |||
|
Black African Other races |
327 (96.2) 13 (3.8) |
1,151 (98.3) 20 (1.7) |
0.035 |
| Education Level | |||
|
None None and Primary Secondary Tertiary Vocational |
57 (4.9) 827 (70.6) 226 (19.3) 61 (5.2) |
25 (7.4) 245 (72.1) 55 (16.2) 15 (4.4) |
0.222 |
| Employment Status | |||
|
Self-employed Employed full time Employed part-time Full-time student Retired Unemployed and unemployed |
103 (30.3) 59 (17.4) 35 (10.3) 20 (5.9) 123 (36.2) |
262 (22.4) 149 (12.7) 123 (10.5) 184 (15.7) 453 (38.7) |
0.001 |
| TB Symptoms | |||
| In the last month, have you had a cough | |||
| Prevalence | 44/ 340 (40%) | 62/1171 (5%) | 0.001 |
| In the last month, have you had night sweats? | |||
| Prevalence | 17/340 (5%) | 37/1171 (3%) | 0.108 |
| In the last month, have you had any unplanned weight loss? | |||
| Prevalence | 43/340 (13%) | 67/1171 (6%) | 0.001 |
| In the last month, have you had a fever or a “hot body”? | |||
| Prevalence | 9/340 (3%) | 13/1171 (1%) | 0.037 |
| Experienced at least one of the four TB symptoms | |||
| Prevalence | 77/340 (23%) | 125/1171 (11%) | 0.001 |
| In the past 12 months, have you been exposed to someone with TB? | |||
| Prevalence | 14/340 (4%) | 39/1171 (3%) | 0.487 |
Discussions
A systematic review by Divala and others [8] shows that invariably, tuberculosis symptom screening is a critical entry point for the diagnosis of the disease [12–15]. Additionally, there is a need for more accurate screening tools, that remain accessible and low-cost for countries with high tuberculosis burden.
Some individuals wait for the spontaneous resolution of TB symptoms, and most do not seek healthcare help [15]. The biological and epidemiological interconnectedness of TB and HIV has generated a new form of stigma, TB–HIV stigma, which sometimes makes people afraid to go for TB symptoms as this would be perceived to be HIV-related TB.
We note that there is limited information on TB among critical populations such as MSM, and the findings in this letter are crucial for understanding TB symptoms among MSM. There is a need for ongoing campaigns to encourage people to seek healthcare help when experiencing TB symptoms so that we do not have infectious patients who remain undiagnosed and are thus contagious to others. Targeted TB screening is warranted, especially among key populations, resulting in a greater yield of identifying TB cases, which aligns with the International Standards for Tuberculosis Care.
Tuberculosis symptom screening has limitations. However, there is a need to increase the frequency of when it is offered to MSM to enhance the opportunity of identifying those individuals in need of further investigations and treatment. Additionally, in Zimbabwe MSM experience considerable amounts of stigma and discrimination at most health facilities due to cultural imperatives as noted in the formative survey which was part of the BBS survey [7]. For Zimbabwe to ensure its health for all targets are met timeously there is a need to ensure that no group is left behind, including MSM and other key populations. A key intervention by the Zimbabwe Ministry of Health will be to train its healthcare workers in the provision of key population-friendly services and non-discriminatory behaviour.
Non-governmental organisations in Zimbabwe provide principally HIV-related services to MSM in secluded locals to avoid harassment from the police and security forces [7]. It will be also key to provide tuberculosis-related screening to those MSM using such services. Those individuals who screen positive for tuberculosis should immediately be provided with tuberculosis diagnostic tests and those testing positive should be immediately linked to care.
Acknowledgements
The authors would like to thank all individuals who took part in the survey.
Abbreviations
- BBS
Biobehavioral Survey
- HIV
Human Immunodeficiency Virus
- MSM
Men who have Sex with Men
- RDS
Respondent Driven Sampling
- TB
Tuberculosis
Author contributions
GMus conceived the brief communication. GMus & MM carried out the statistical analysis. GMus & MM wrote the first draft of the brief communication. All authors (MM, IC, TD, BM, CS, DM, OM, EM, RB, GM, and GMus) contributed to the writing of the brief communication. All authors (MM, IC, TD, BM, CS, DM, EM, RB, GM) read and approved the final brief communication.
Funding
The study was not funded.
Declarations
Competing interests
The authors declare no competing interests.
Footnotes
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Change history
4/29/2024
A Correction to this paper has been published: 10.1186/s12981-024-00617-4
References
- 1.World Health Organization Global Tuberculosis Report. 2021. Geneva, Switzerland: WHO; 2021.
- 2.World Health Organization Global Health Estimates. 2016: deaths by cause, age, sex, by country and by region. Geneva, Switzerland: WHO; 2018.
- 3.Corbett EL, Marston B, Churchyard GJ, De Cock KM. Tuberculosis in sub-saharan Africa: opportunities, challenges and change in the era of antiretroviral treatment. Lancet. 2006;367:926–37. doi: 10.1016/S0140-6736(06)68383-9. [DOI] [PubMed] [Google Scholar]
- 4.Borgdorff MW, Nagelkerke NJ, Dye C, Nunn P. Gender and tuberculosis: a comparison of prevalence surveys with notification data to explore sex differences in case detection. Int J Tuberculosis Lung Disease. 2000;4:123–32. [PubMed] [Google Scholar]
- 5.Kemp JR, Gillian M, Simwaka BN, Salaniponi FM, Squire BS. Can Malawi’s poor afford free tuberculosis services? Patient and household costs associated with a tuberculosis diagnosis in Lilongwe. Bull World Health Organ. 2007;85:580–5. doi: 10.2471/BLT.06.033167. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Ministry of Health and Child Care (MoHCC). Zimbabwe Population-based HIV Impact Assessment (ZIMPHIA 2020): Final Report. Harare. 2021.
- 7.HIV and STI Biobehavioral Survey among Men Who Have Sex with Men . Transgender women, and Genderqueer individuals in Zimbabwe - Final Report. New York: ICAP at Columbia University; 2020. [Google Scholar]
- 8.Divala TH, Lewis J, Bulterys MA, Lutje V, Corbett EL, Schumacher SG, MacPherson P. Missed opportunities for diagnosis and treatment in patients with TB symptoms: a systematic review. Public Health Action. 2022;12(1):10–7. doi: 10.5588/pha.21.0022. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.UNAIDS. HIV prevention among key populations. 2016.
- 10.Xin HN, Li XW, Zhang L, Li Z, Zhang HR, Yang Y. Tuberculosis infection testing in HIV-positive men who have sex with men from Xi’an China. Epidemiol Infect. 2017;145(3):498–502. doi: 10.1017/S0950268816002703. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.WHO. UNAIDS CDC, FHI 360 . Biobehavioral survey guidelines for populations at risk for HIV. Geneva: World Health Organisation; 2017. [Google Scholar]
- 12.Storla DG, Yimer S, Bjune GA. A systematic review of delay in the diagnosis and treatment of tuberculosis. BMC Public Health. 2008;8(1):15. doi: 10.1186/1471-2458-8-15. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Kranzer K, Afnan-Holmes H, Tomlin K, Golub JE, Shapiro AE, Schaap A, Corbett EL, Lönnroth K, Glynn JR. The benefits to communities and individuals of screening for active tuberculosis disease: a systematic review. Int J Tuberc Lung Dis. 2013;17(4):432–46. doi: 10.5588/ijtld.12.0743. [DOI] [PubMed] [Google Scholar]
- 14.Yoon C, Dowdy DW, Esmail H, MacPherson P, Schumacher SG. Screening for tuberculosis: time to move beyond symptoms. Lancet Respir Med. 2019;7(3):202–4. doi: 10.1016/S2213-2600(19)30039-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Willie B, Hakim AJ, Badman SG, Weikum D, Narokobi R, Coy K, Gabuzzi J, Pekon S, Gene S, Amos A, Kupul M, Hou P, Dala NM, Whiley DM, Wapling J, Kaldor KM, Vallely AJ, Kelly-Hanku A. High prevalence of pulmonary tuberculosis among female sex workers, men who have sex with men, and transgender women in Papua New Guinea. Trop Med Health. 2021;49:4. doi: 10.1186/s41182-020-00293-w. [DOI] [PMC free article] [PubMed] [Google Scholar]
