Publications des scientifiques de l'IRD

Gunasekera K. S., Marcy Olivier, Munoz J., Lopez-Varela E., Sekadde M. P., Franke M. F., Bonnet Maryline, Ahmed S., Amanullah F., Anwar A., Augusto O., Aurilio R. B., Banu S., Batool I., Brands A., Cain K. P., Carratala-Castro L., Caws M., Click E. S., Cranmer L. M., Garcia-Basteiro A. L., Hesseling A. C., Huynh J., Kabir S., Lecca L., Mandalakas A., Mavhunga F., Myint A., Myo K., Nampijja D., Nicol M. P., Orikiriza P., Palmer M., Sant'Anna C. C., Siddiqui S. A., Smith J. P., Song R., Thuong N. T. T., Ung V., van der Zalm M. M., Verkuijl S., Viney K., Walters E. G., Warren J. L., Zar H. J., Marais B., Graham S. M., Debray T. P. A., Cohen T., Seddon J. A. (2023). Development of treatment-decision algorithms for children evaluated for pulmonary tuberculosis: an individual participant data meta-analysis. Lancet Child and Adolescent Health, 7 (5), p. 336-346. ISSN 2352-4642.

Titre du document
Development of treatment-decision algorithms for children evaluated for pulmonary tuberculosis: an individual participant data meta-analysis
Année de publication
2023
Type de document
Article référencé dans le Web of Science WOS:000982299000001
Auteurs
Gunasekera K. S., Marcy Olivier, Munoz J., Lopez-Varela E., Sekadde M. P., Franke M. F., Bonnet Maryline, Ahmed S., Amanullah F., Anwar A., Augusto O., Aurilio R. B., Banu S., Batool I., Brands A., Cain K. P., Carratala-Castro L., Caws M., Click E. S., Cranmer L. M., Garcia-Basteiro A. L., Hesseling A. C., Huynh J., Kabir S., Lecca L., Mandalakas A., Mavhunga F., Myint A., Myo K., Nampijja D., Nicol M. P., Orikiriza P., Palmer M., Sant'Anna C. C., Siddiqui S. A., Smith J. P., Song R., Thuong N. T. T., Ung V., van der Zalm M. M., Verkuijl S., Viney K., Walters E. G., Warren J. L., Zar H. J., Marais B., Graham S. M., Debray T. P. A., Cohen T., Seddon J. A.
Source
Lancet Child and Adolescent Health, 2023, 7 (5), p. 336-346 ISSN 2352-4642
Background Many children with pulmonary tuberculosis remain undiagnosed and untreated with related high morbidity and mortality. Recent advances in childhood tuberculosis algorithm development have incorporated prediction modelling, but studies so far have been small and localised, with limited generalisability. We aimed to evaluate the performance of currently used diagnostic algorithms and to use prediction modelling to develop evidence-based algorithms to assist in tuberculosis treatment decision making for children presenting to primary health-care centres.Methods For this meta-analysis, we identified individual participant data from a WHO public call for data on the management of tuberculosis in children and adolescents and referral from childhood tuberculosis experts. We included studies that prospectively recruited consecutive participants younger than 10 years attending health-care centres in countries with a high tuberculosis incidence for clinical evaluation of pulmonary tuberculosis. We collated individual participant data including clinical, bacteriological, and radiological information and a standardised reference classification of pulmonary tuberculosis. Using this dataset, we first retrospectively evaluated the performance of several existing treatment-decision algorithms. We then used the data to develop two multivariable prediction models that included features used in clinical evaluation of pulmonary tuberculosis-one with chest x-ray features and one without-and we investigated each model's generalisability using internal-external cross-validation. The parameter coefficient estimates of the two models were scaled into two scoring systems to classify tuberculosis with a prespecified sensitivity target. The two scoring systems were used to develop two pragmatic, treatment-decision algorithms for use in primary health-care settings.Findings Of 4718 children from 13 studies from 12 countries, 1811 (38 center dot 4%) were classified as having pulmonary tuberculosis: 541 (29 center dot 9%) bacteriologically confirmed and 1270 (70 center dot 1%) unconfirmed. Existing treatment-decision algorithms had highly variable diagnostic performance. The scoring system derived from the prediction model that included clinical features and features from chest x-ray had a combined sensitivity of 0 center dot 86 [95% CI 0 center dot 68-0 center dot 94] and specificity of 0 center dot 37 [0 center dot 15-0 center dot 66] against a composite reference standard. The scoring system derived from the model that included only clinical features had a combined sensitivity of 0 center dot 84 [95% CI 0 center dot 66-0 center dot 93] and specificity of 0 center dot 30 [0 center dot 13-0 center dot 56] against a composite reference standard. The scoring system from each model was placed after triage steps, including assessment of illness acuity and risk of poor tuberculosis-related outcomes, to develop treatment-decision algorithms.Interpretation We adopted an evidence-based approach to develop pragmatic algorithms to guide tuberculosis treatment decisions in children, irrespective of the resources locally available. This approach will empower health workers in primary health-care settings with high tuberculosis incidence and limited resources to initiate tuberculosis treatment in children to improve access to care and reduce tuberculosis-related mortality. These algorithms have been included in the operational handbook accompanying the latest WHO guidelines on the management of tuberculosis in children and adolescents. Future prospective evaluation of algorithms, including those developed in this work, is necessary to investigate clinical performance.Funding WHO, US National Institutes of Health.
Plan de classement
Santé : généralités [050]
Description Géographique
MOZAMBIQUE ; KENYA ; AFRIQUE DU SUD ; BRESIL ; OUGANDA ; BURKINA FASO ; CAMBODGE ; CAMEROUN ; VIET NAM ; PAKISTAN ; MYANMAR ; BANGLADESH
Localisation
Fonds IRD [F B010087789]
Identifiant IRD
fdi:010087789
Contact