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. 2015 Jan 25;6(1):19–21. doi: 10.5588/pha.15.0064

Coverage of clinic-based TB screening in South Africa may be low in key risk groups

N McCreesh 1,, I Faghmous 1, C Looker 1, P J Dodd 1,2, I D Plumb 1, K Shanaube 3, M Muyoyeta 3,4, P Godfrey-Faussett 5, H Ayles 3,5, R G White 1
PMCID: PMC4809721  PMID: 27051606

Abstract

The South African Ministry of Health has proposed screening all clinic attendees for tuberculosis (TB). Amongst other factors, male sex and bar attendance are associated with higher TB risk. We show that 45% of adults surveyed in Western Cape attended a clinic within 6 months, and therefore potentially a relatively high proportion of the population could be reached through clinic-based screening. However, fewer than 20% of all men aged 18–25 years, or men aged 26–45 who attend bars, attended a clinic. The population-level impact of clinic-based screening may be reduced by low coverage among key risk groups.

Keywords: tuberculosis, screening, South Africa, primary health care


South Africa has one of the highest tuberculosis (TB) burdens in the world, with an estimated disease prevalence in 2013 of 715 per 100 000 population.1 Disease incidence has been falling since 2008,2 but the decline is slow, and new approaches are needed to accelerate the rate of decline. As part of its ‘90s’ strategy, on World TB Day 2015, the South African Ministry of Health proposed implementing screening of all health centre attendees for TB disease (unpublished speech given by Minister of Health A. Motsoaledi). This is a potentially more cost-effective approach than community-based screening programmes, as it is plausible that the prevalence of TB will be higher in clinic attendees than in the wider community, and the costs of reaching clinic attendees are likely to be lower than more active community-based screening programmes. Its population-level impact will be lower, however, if screening coverage is low among population subgroups that are at higher risk of developing TB disease. We investigated clinic attendance in adults in Western Cape, and in particular among two key risk groups: (young) men and people who visit bars.

STUDY POPULATION, DESIGN AND METHODS

The study sampling frame consisted of adults living in eight communities in Western Cape, South Africa, who were enrolled in the final Zambia/South Africa TB and acquired immune-deficiency syndrome Reduction (ZAMSTAR) prevalence survey.3 Four sampling enumeration areas (SEAs) from each ZAMSTAR community were selected proportional to size, and 40 people were sampled at random from each SEA, stratified by sex and age. A full description of the sampling method is given elsewhere.4

Respondents were interviewed in their own homes using a structured questionnaire.4 The main purpose of the questionnaire was to collect data on contact and activity patterns relevant to Mycobacterium tuberculosis transmission. Respondents were also asked if they had visited a health care facility for any reason in the last 6 months.

Logistic regression was used to examine associations between a number of variables and clinic attendance. Estimates were adjusted for age and sex and weighted to account for the stratified sampling design.

Ethical approval was obtained from the University of Stellenbosch Health Research Ethics Committee, Stellenbosch, South Africa (N04/10/173), the University of Zambia Biomedical Research Ethics Committee, Lusaka, Zambia (007-10-04), and the London School of Hygiene & Tropical Medicine Ethics Committee, London, UK (A211 3008).

RESULTS

A total of 1272 adults living in Western Cape were interviewed. Results are presented for the 1271 adults who provided information on clinic attendance.

Overall, 55% (95% confidence interval [CI] 48–61) of women and 29% (95%CI 23–34) of men reported visiting a clinic in the past 6 months (Table 1). Adjusting for sex, the odds of having visited a clinic increased with age (P = 0.001), with people aged 18–25 years having 0.47 (95%CI 0.31–0.70) times the odds compared to people aged >45 years. People who reported attending bars had 0.45 (95%CI 0.33–0.60) times the odds of clinic attendance compared to people who reported never attending bars.

TABLE 1.

Association between sex, age and bar attendance and clinic attendance within the previous 6 months

graphic file with name i2220-8372-6-1-19-t01.jpg

Reported clinic attendance in the past 6 months was >50% for women in all age groups who never attended bars and for women aged >45 years who attended bars (Table 2). Reported attendance was <20% for all men aged 18–25 and for men aged 26–45 who attended bars.

TABLE 2.

Proportion of people reporting clinic attendance in past 6 months by sex, age and bar attendance

graphic file with name i2220-8372-6-1-19-t02.jpg

DISCUSSION

We demonstrate that a clinic-based screening approach in Western Cape could achieve a potentially relatively high overall level of population coverage, with 45% of adults reporting visiting a clinic in the last 6 months. In line with other studies from South Africa, we show that clinic attendance is lower among men than women,5,6 and is lower in younger than older adults.5 Coverage may be substantially lower than average in some population groups, in particular men aged 18–25 and men aged 26–45 who visit bars. Fewer than 20% of men in these groups may be reached by clinic-based screening programmes in any 6-month period. This is of particular concern, as these demographic groups are at increased risk of contracting TB,7,8 and passive case detection may be particularly inadequate in people who consume alcohol,9 potentially reducing the wider impact of clinic-based TB screening programmes.

We present data on clinic visits in the last 6 months. Coverage will be higher over longer time periods, as a higher proportion of the population will visit a clinic in 12 months, for example, than in 6 months. For people who visit clinics less frequently, however, time between screenings will be longer, reducing the average impact of screening on the time between the onset of infectiousness and diagnosis. Coverage will also be lower if not all clinics screen 100% of attendees.

The main limitation of our approach is that data on both clinic and bar attendance were collected for similar time periods. This means that some of the observed inverse association between bar and clinic attendance may have resulted from illness that caused individuals to both attend a clinic and to stop attending bars, rather than a genuine reluctance or inability to attend clinics in people who visit bars. This may have biased the association upwards, but is unlikely to be responsible for more than a small proportion of the large observed difference in clinic attendance.

A second limitation of our findings is that only communities with a clinic could be selected for inclusion in the original ZAMSTAR study. Clinic usage has been shown to decrease in South Africa as distance to the nearest clinic increases.10 Coverage may therefore be lower in communities with poorer access to health care, reducing overall coverage.

Clinic-based TB screening programmes have the potential to reach nearly half the adult population over a 6-month period in Western Cape, and may be a cost-effective way to reduce the prevalence of TB. Their effectiveness may be reduced by poor coverage in certain risk groups, however, and we recommend that clinic-based screening should be supplemented by case-finding programmes targeting key risk groups.

Acknowledgments

The authors would like to acknowledge the ZAMSTAR study team and R Dunbar, K Eames, J Edmunds, A Crampin and I Kleinschmidt, all of whom contributed advice in the design and analysis of the social contact survey. We would like to thank the Ministry of Health, District Health Management teams and the communities where the studies were undertaken for their help and advice.

NM was supported by the UK Medical Research Council (MR/J005088/1), London, UK. RGW, PJD, CL and IP were supported by the Consortium to Respond Effectively to the AIDS TB Epidemic funded by the Bill and Melinda Gates Foundation (19790.01), Seattle, WA, USA. RGW was also supported by the Bill and Melinda Gates Foundation (OPP1084276) and the UK Medical Research Council (G0802414, MR/J005088/1).

Footnotes

Conflicts of interest: none declared.

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