<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>73</volume><submitter>Chabala C</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>In children with severe acute malnutrition (SAM) tuberculosis is common, challenging to diagnose, and often fatal. We developed tuberculosis treatment decision algorithms (TDAs) for children under the age of 5 years with SAM.&lt;h4>Methods&lt;/h4>In this prospective diagnostic study, we enrolled and followed up children aged &lt;60 months hospitalised with SAM at three tertiary hospitals in Zambia and Uganda from 4 November 2019 to 20 June 2022. We included children aged 2-59 months with SAM as defined by WHO and hospitalised following the WHO clinical criteria. We excluded children with current or history of antituberculosis treatment within the preceding 3 months. They underwent tuberculosis symptom screening, clinical assessment, chest X-ray, abdominal ultrasound, Xpert MTB/RI</pubmed_abstract><journal>EClinicalMedicine</journal><pagination>102688</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11245985</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Development of tuberculosis treatment decision algorithms in children below 5 years hospitalised with severe acute malnutrition in Zambia and Uganda: a prospective diagnostic cohort study.</pubmed_title><pmcid>PMC11245985</pmcid><pubmed_authors>Mwango E</pubmed_authors><pubmed_authors>Occelli E</pubmed_authors><pubmed_authors>Razafimanantsoa M</pubmed_authors><pubmed_authors>Beuscart A</pubmed_authors><pubmed_authors>Chimbini M</pubmed_authors><pubmed_authors>Ngambi M</pubmed_authors><pubmed_authors>Roucher C</pubmed_authors><pubmed_authors>Nangozi J</pubmed_authors><pubmed_authors>Silavwe M</pubmed_authors><pubmed_authors>Ton Nu Nguyet MH</pubmed_authors><pubmed_authors>Poublan J</pubmed_authors><pubmed_authors>Sserunjogi R</pubmed_authors><pubmed_authors>Siasulingana T</pubmed_authors><pubmed_authors>Font H</pubmed_authors><pubmed_authors>Himwaze DA</pubmed_authors><pubmed_authors>Balestre E</pubmed_authors><pubmed_authors>Nduna B</pubmed_authors><pubmed_authors>Businge GB</pubmed_authors><pubmed_authors>Kapula C</pubmed_authors><pubmed_authors>Koskas N</pubmed_authors><pubmed_authors>Serre A</pubmed_authors><pubmed_authors>Kuppers A</pubmed_authors><pubmed_authors>Barungi C</pubmed_authors><pubmed_authors>Chungu C</pubmed_authors><pubmed_authors>Zyambo K</pubmed_authors><pubmed_authors>Graham S</pubmed_authors><pubmed_authors>Inambao M</pubmed_authors><pubmed_authors>Wasswa A</pubmed_authors><pubmed_authors>Esperou H</pubmed_authors><pubmed_authors>Kapasa M</pubmed_authors><pubmed_authors>Kapotwe V</pubmed_authors><pubmed_authors>TB-Speed SAM study group</pubmed_authors><pubmed_authors>Namulinda F</pubmed_authors><pubmed_authors>Aciparu S</pubmed_authors><pubmed_authors>Wobudeya E</pubmed_authors><pubmed_authors>Charpin A</pubmed_authors><pubmed_authors>Pumbwe M</pubmed_authors><pubmed_authors>Kagoya E</pubmed_authors><pubmed_authors>Chakopo M</pubmed_authors><pubmed_authors>Lounnas M</pubmed_authors><pubmed_authors>Chirwa U</pubmed_authors><pubmed_authors>Mumba W</pubmed_authors><pubmed_authors>Kanyama M</pubmed_authors><pubmed_authors>Babirekere E</pubmed_authors><pubmed_authors>Mesnier S</pubmed_authors><pubmed_authors>Nassozi R</pubmed_authors><pubmed_authors>Marcy O</pubmed_authors><pubmed_authors>Badrichani A</pubmed_authors><pubmed_authors>Moono R</pubmed_authors><pubmed_authors>Chilanga M</pubmed_authors><pubmed_authors>Hambulo C</pubmed_authors><pubmed_authors>Mwambazi M</pubmed_authors><pubmed_authors>Bonnet M</pubmed_authors><pubmed_authors>Mankunshe E</pubmed_authors><pubmed_authors>Doreen M</pubmed_authors><pubmed_authors>Zulu S</pubmed_authors><pubmed_authors>Chilonga J</pubmed_authors><pubmed_authors>Chifunda K</pubmed_authors><pubmed_authors>Zimba K</pubmed_authors><pubmed_authors>Habiyambere G</pubmed_authors><pubmed_authors>Mulenga V</pubmed_authors><pubmed_authors>Chola D</pubmed_authors><pubmed_authors>Businge G</pubmed_authors><pubmed_authors>D'Elbee M</pubmed_authors><pubmed_authors>Vessiere A</pubmed_authors><pubmed_authors>Couffin-Cadiergues S</pubmed_authors><pubmed_authors>Ntambi S</pubmed_authors><pubmed_authors>Kasakwa K</pubmed_authors><pubmed_authors>Hellen A</pubmed_authors><pubmed_authors>Sophia C</pubmed_authors><pubmed_authors>Nawakwi G</pubmed_authors><pubmed_authors>Chabala C</pubmed_authors><pubmed_authors>Halende B</pubmed_authors><pubmed_authors>Shankalala P</pubmed_authors><pubmed_authors>Mundundu G</pubmed_authors><pubmed_authors>Hamze B</pubmed_authors></additional><is_claimable>false</is_claimable><name>Development of tuberculosis treatment decision algorithms in children below 5 years hospitalised with severe acute malnutrition in Zambia and Uganda: a prospective diagnostic cohort study.</name><description>&lt;h4>Background&lt;/h4>In children with severe acute malnutrition (SAM) tuberculosis is common, challenging to diagnose, and often fatal. We developed tuberculosis treatment decision algorithms (TDAs) for children under the age of 5 years with SAM.&lt;h4>Methods&lt;/h4>In this prospective diagnostic study, we enrolled and followed up children aged &lt;60 months hospitalised with SAM at three tertiary hospitals in Zambia and Uganda from 4 November 2019 to 20 June 2022. We included children aged 2-59 months with SAM as defined by WHO and hospitalised following the WHO clinical criteria. We excluded children with current or history of antituberculosis treatment within the preceding 3 months. They underwent tuberculosis symptom screening, clinical assessment, chest X-ray, abdominal ultrasound, Xpert MTB/RI</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jul</publication><modification>2026-06-03T00:32:24.796Z</modification><creation>2025-02-19T02:33:39.886Z</creation></dates><accession>S-EPMC11245985</accession><cross_references><pubmed>39007063</pubmed><doi>10.1016/j.eclinm.2024.102688</doi></cross_references></HashMap>