1. Impact of systematic early tuberculosis detection using Xpert MTB/RIF Ultra in children with severe pneumonia in high tuberculosis burden countries (TB-Speed pneumonia): a stepped wedge cluster randomized trial
- Author
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Mao Tan Eang, Laurence Borand, Maryline Bonnet, Sylvain Godreuil, Olivier Marcy, Raoul Moh, Jean-Voisin Taguebue, Sandra Mavale, Juliet Mwanga-Amumpere, Manon Lounnas, James A Seddon, Veronica Mulenga, Celso Khosa, Eric Wobudeya, Hélène Font, Aurélia Vessière, Chishala Chabala, Laurence Adonis-Koffi, Delphine Gabillard, Christophe Delacourt, Bordeaux population health (BPH), Université de Bordeaux (UB)-Institut de Santé Publique, d'Épidémiologie et de Développement (ISPED)-Institut National de la Santé et de la Recherche Médicale (INSERM), University of Zambia [Lusaka] (UNZA), Maputo Central Hospital, Ministry of Health [Mozambique], Centre Hospitalier Universitaire [Treichville] (CHU), Epicentre Ouganda [Mbarara] [Médecins Sans Frontières], Epicentre [Paris] [Médecins Sans Frontières], National Center for Tuberculosis and Leprosy Control [Phnom Penh, Cambodia] (CENAT), CHU Necker - Enfants Malades [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Stellenbosch University, Imperial College London, Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier), Maladies infectieuses et vecteurs : écologie, génétique, évolution et contrôle (MIVEGEC), Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD [France-Sud]), Bugema University [Kampala], Recherches Translationnelles sur le VIH et les maladies infectieuses endémiques et émergentes (TransVIHMI), and Institut de Recherche pour le Développement (IRD)-Université de Yaoundé I-Université Cheikh Anta Diop [Dakar, Sénégal] (UCAD)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Montpellier (UM)
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Pediatrics ,Nasopharyngeal aspirate ,Aftercare ,030204 cardiovascular system & hematology ,law.invention ,Study Protocol ,0302 clinical medicine ,Randomized controlled trial ,law ,Clinical endpoint ,Uganda ,030212 general & internal medicine ,Cluster randomised controlled trial ,Cameroon ,Child ,Children ,Mozambique ,Cause of death ,lcsh:RJ1-570 ,Diagnostic Trial ,Patient Discharge ,3. Good health ,Stool ,Child, Preschool ,Cambodia ,Life Sciences & Biomedicine ,medicine.medical_specialty ,Tuberculosis ,Zambia ,Disease cluster ,Xpert MTB ,Sensitivity and Specificity ,03 medical and health sciences ,RIF ultra ,medicine ,Humans ,Xpert ,Science & Technology ,business.industry ,lcsh:Pediatrics ,Mycobacterium tuberculosis ,Pneumonia ,medicine.disease ,Xpert MTB/RIF ultra ,Pediatrics, Perinatology and Child Health ,MTB ,1114 Paediatrics and Reproductive Medicine ,[SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie ,business - Abstract
Background In high tuberculosis (TB) burden settings, there is growing evidence that TB is common in children with pneumonia, the leading cause of death in children under 5 years worldwide. The current WHO standard of care (SOC) for young children with pneumonia considers a diagnosis of TB only if the child has a history of prolonged symptoms or fails to respond to antibiotic treatments. As a result, many children with TB-associated severe pneumonia are currently missed or diagnosed too late. We therefore propose a diagnostic trial to assess the impact on mortality of adding the systematic early detection of TB using Xpert MTB/RIF Ultra (Ultra) performed on nasopharyngeal aspirates (NPA) and stool samples to the WHO SOC for children with severe pneumonia, followed by immediate initiation of anti-TB treatment in children testing positive on any of the samples. Methods TB-Speed Pneumonia is a pragmatic stepped-wedge cluster randomized controlled trial conducted in six countries with high TB incidence rate (Côte d’Ivoire, Cameroon, Uganda, Mozambique, Zambia and Cambodia). We will enrol 3780 children under 5 years presenting with WHO-defined severe pneumonia across 15 hospitals over 18 months. All hospitals will start managing children using the WHO SOC for severe pneumonia; one hospital will be randomly selected to switch to the intervention every 5 weeks. The intervention consists of the WHO SOC plus rapid TB detection on the day of admission using Ultra performed on 1 nasopharyngeal aspirate and 1 stool sample. All children will be followed for 3 months, with systematic trial visits at day 3, discharge, 2 weeks post-discharge, and week 12. The primary endpoint is all-cause mortality 12 weeks after inclusion. Qualitative and health economic evaluations are embedded in the trial. Discussion In addition to testing the main hypothesis that molecular detection and early treatment will reduce TB mortality in children, the strength of such pragmatic research is that it provides some evidence regarding the feasibility of the intervention as part of routine care. Should this intervention be successful, safe and well tolerated, it could be systematically implemented at district hospital level where children with severe pneumonia are referred. Trial registration ClinicalTrials.gov, NCT03831906. Registered 6 February 2019.
- Published
- 2021
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