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Published on: August 16, 2021
Tuberculosis in pediatric patients treated with anti-TNFα drugs: a cohort study
Joan Calzada-Hernández1, Jordi Anton-López2, Rosa Bou-Torrent3
1Pediatric Rheumatology Unit, Pediatrics Department, Hospital Sant Joan de Déu, Universitat de Barcelona, Esplugues, Spain. jcalzada@hsjdbcn.org.
Insights
Latent tuberculosis infection (LTBI) screening in children before anti-TNFα therapy is crucial. Combining tuberculin skin test (TST) and interferon-gamma release assay (IGRA) is recommended, with no routine retesting needed if asymptomatic.
Area of Science:
- Pediatric Rheumatology
- Infectious Disease Epidemiology
- Immunology
Background:
- Anti-TNFα therapy increases tuberculosis (TB) risk in adults, but pediatric data are limited.
- Optimal latent tuberculosis infection (LTBI) screening strategies in children on anti-TNFα agents remain debated.
- This study assesses LTBI prevalence and outcomes in pediatric patients undergoing anti-TNFα treatment.
Purpose of the Study:
- To determine the prevalence of latent tuberculosis infection (LTBI) in children and adolescents before initiating anti-TNFα therapy.
- To evaluate the long-term safety and efficacy of anti-TNFα treatment in this cohort regarding TB incidence.
- To provide recommendations for LTBI screening in pediatric populations receiving anti-TNFα agents.
Main Methods:
- A cohort observational study was conducted in pediatric patients receiving anti-TNFα agents.
- Initial LTBI screening used tuberculin skin test (TST) and/or QuantiFERON Gold-In Tube test (QTF-G).
- Patients were monitored every six months for TB symptoms; repeat testing was only performed if symptoms arose or after known TB contact.
Main Results:
- The study included 221 pediatric patients (261 treatments) with various rheumatic, inflammatory bowel, and eye diseases.
- LTBI prevalence was 1.4% (3/221), with QTF-G detecting all cases, including those negative on TST.
- No incident cases of active TB disease were observed during a median follow-up of 2.3 years (641 patient-years).
Conclusions:
- The LTBI prevalence in this pediatric cohort was comparable to general population screening.
- Initial screening for LTBI in children prior to anti-TNFα therapy should include both TST and IGRA.
- Systematic repetition of LTBI tests is unnecessary in asymptomatic children without known TB contact during anti-TNFα treatment.
Background:
Adult patients receiving anti-TNFα drugs are at increased risk of tuberculosis (TB), but studies in pediatric populations are limited, and the best strategy for latent tuberculosis infection (LTBI) screening in this population remains controversial. We describe the prevalence of LTBI prior to anti-TNFα therapy and the long-term follow-up after biological treatment initiation in a cohort of children and adolescents.
Methods:
Cohort observational study in children and adolescents receiving anti-TNFα agents in a tertiary-care pediatric hospital. LTBI was ruled out prior to the implementation of anti-TNFα drugs by tuberculin skin test (TST), and, from March 2012 on, QuantiFERON Gold-In Tube test (QTF-G). During anti-TNFα treatment, patients were evaluated every 6 months for TB with history and physical examination. TST/QTF-G were not repeated unless signs or symptoms consistent with TB arose or there was proven TB contact.
Results:
The final cohort consisted of 221 patients (56.1% female; 261 treatments), of whom 51.7%/30.0%/17.3% were treated with etanercept/adalimumab/infliximab, respectively, for a variety of rheumatic diseases (75.6%), inflammatory bowel disease (20.8%), and inflammatory eye diseases (3.6%). The median (IQR) age at diagnosis of the primary condition was 6.8 years (2.7-11.0) and the duration of the disease before implementing the anti-TNFα agent was 1.8 years (0.6-4.2). LTBI was diagnosed in 3 adolescent girls (prevalence rate: 1.4%; 95% CI: 0.4-4.2) affected with juvenile idiopathic arthritis: TST tested positive in only 1, while QTF-G was positive in all cases (including 2 patients already on etanercept). They all received antiTB chemoprophylaxis and were later (re)treated with etanercept for 24-29 months, without incidences. No incident cases of TB disease were observed during the follow-up period under anti-TNFα treatment of 641 patients-year, with a median (IQR) time per patient of 2.3 years (1.4-4.3).
Conclusions:
In our study, the prevalence of LTBI (1.4%) was similar to that reported in population screening studies in Spain; no incident cases of TB disease were observed. In low-burden TB settings, initial screening for TB in children prior to anti-TNFα treatment should include both TST and an IGRA test, but systematic repetition of LTBI immunodiagnostic tests seems unnecessary in the absence of symptoms or known TB contact.
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