Abstract

BackgroundSouth Africa has one of the highest tuberculosis incidence rates. Biologic disease-modifying anti-rheumatic drugs are associated with an increased risk of tuberculosis. The objective of this study was to describe the tuberculosis disease incidence rate among public sector patients receiving biologic therapies in the Western Cape Province.MethodsA retrospective, descriptive analysis was undertaken using routine health data collated by the Provincial Health Data Centre from January 2007 (first use of biologic therapy in the Western Cape) to September 2018.ResultsWe identified 609 patients treated with tumour necrosis factor-alpha (TNF-α) or non-TNF-α biologic therapies. Thirty-seven (37) patients developed tuberculosis after biologic therapy exposure, of whom the majority (78%) had an immune mediated inflammatory disease and the remainder (22%) a haematologic malignancy. The incidence rate of tuberculosis per 100,000 person-years was 2227 overall [95% confidence interval (CI): 1591, 3037]. Patients treated with TNF-α inhibitors and non-TNF-α inhibitors had estimated incidence rates of 2819 [95% CI: 1669, 4480] and 1825 [95% CI: 1131, 2797], respectively (p = 0.10).ConclusionPatients exposed to both TNF-α and non-TNF-α biologic therapies may have a higher incidence of tuberculosis disease compared to the background risk of 681 cases per 100,000 per year in the Western Cape.

Highlights

  • South Africa has one of the highest tuberculosis incidence rates

  • This study describes the incidence rate and time to TB onset among public sector patients receiving biologic therapies in this high-TB burden setting in the Western Cape

  • Significant differences were observed between age groups, where patients with an immune mediated inflammatory disease (IMID) were younger than patients with a haematologic malignancy

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Summary

Introduction

South Africa has one of the highest tuberculosis incidence rates. Biologic disease-modifying antirheumatic drugs are associated with an increased risk of tuberculosis. The use of biologic therapy is limited by the risk of opportunistic infections, in particular tuberculosis (TB) disease [1, 6,7,8,9,10,11,12,13], because it suppresses the immune response of the patient to pathogens Patients receiving biologic therapies may have an additional risk for developing TB due to their underlying disease (inflammatory condition or haematological malignancy) or its treatment including synthetic disease modifying anti-rheumatic drugs (DMARDs) and corticosteroid exposure [13, 18]

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