Paediatric tuberculosis – new advances to close persistent gaps
•Children are over-represented among TB deaths; most dying without accessing TB care.•Major gaps persist in TB preventive treatment (TPT) provision and TB case detection.•Reducing the TPT gap requires major upscaling of household contact investigation.•Reducing the TB case detection gap requires acc...
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Published in | International journal of infectious diseases Vol. 113; no. Suppl 1; pp. S63 - S67 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
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Elsevier Ltd
01.12.2021
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Abstract | •Children are over-represented among TB deaths; most dying without accessing TB care.•Major gaps persist in TB preventive treatment (TPT) provision and TB case detection.•Reducing the TPT gap requires major upscaling of household contact investigation.•Reducing the TB case detection gap requires acceptance of some over-treatment.•New approaches are required to improve the accuracy of diagnostic (rule-in and rule-out) tests.
Young children are most vulnerable to develop severe forms of tuberculosis (TB) and are over-represented among TB deaths. Almost all children estimated to have died from TB were never diagnosed or offered TB treatment.
Improved access to TB preventive treatment (TPT) requires major upscaling of household contact investigation with allocation of adequate resources. Symptom-based screening is often discouraged in adults for fear of generating drug resistance, if TB cases are missed. However, the situation in vulnerable young children is different, as they present minimal risk of drug resistance generation. Further, the perceived need for additional diagnostic evaluation presents a major barrier to TPT access and underlies general reluctance to consider pragmatic decentralised models of care.
Widespread roll-out of Xpert MTB/RIF Ultra® represents an opportunity for improved case detection in young children, but attaining full impact will require the use of non-sputum specimens. The new Fujifilm SILVAMP TB LAM® urine assay demonstrated good diagnostic accuracy in HIV-positive and malnourished children, but further validation is required. Given the limited accuracy of all available tests and the excellent tolerance of TB drugs in children, the global community may have to accept some over-treatment if we want to close the persistent case detection gap in young children. |
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AbstractList | Young children are most vulnerable to develop severe forms of tuberculosis (TB) and are overrepresented among TB deaths. Almost all children estimated to have died from TB were never diagnosed or offered TB treatment.
Improved access to TB preventive treatment (TPT) requires major upscaling of household contact investigation with allocation of adequate resources. Symptom-based screening is often discouraged in adults for fear of generating drug resistance, if TB cases are missed. However, the situation in vulnerable young children is different, as they present minimal risk of drug resistance generation. Further, the perceived need for additional diagnostic evaluation presents a major barrier to TPT access and underlies general reluctance to consider pragmatic decentralised models of care.
Widespread roll-out of Xpert MTB/RIF Ultra
®
represents an opportunity for improved case detection in young children, but attaining full impact will require the use of non-sputum specimens. The new Fujifilm SILVAMPTB LAM
®
urine assay demonstrated good diagnostic accuracy in HIV-positive and malnourished children, but further validation is required. Given the limited accuracy of all available tests and the excellent tolerance of TB drugs in children, the global community may have to accept some over-treatment if we want to close the persistent case detection gap in young children. Young children are most vulnerable to develop severe forms of tuberculosis (TB) and are over-represented among TB deaths. Almost all children estimated to have died from TB were never diagnosed or offered TB treatment.Improved access to TB preventive treatment (TPT) requires major upscaling of household contact investigation with allocation of adequate resources. Symptom-based screening is often discouraged in adults for fear of generating drug resistance, if TB cases are missed. However, the situation in vulnerable young children is different, as they present minimal risk of drug resistance generation. Further, the perceived need for additional diagnostic evaluation presents a major barrier to TPT access and underlies general reluctance to consider pragmatic decentralised models of care.Widespread roll-out of Xpert MTB/RIF Ultra® represents an opportunity for improved case detection in young children, but attaining full impact will require the use of non-sputum specimens. The new Fujifilm SILVAMP TB LAM® urine assay demonstrated good diagnostic accuracy in HIV-positive and malnourished children, but further validation is required. Given the limited accuracy of all available tests and the excellent tolerance of TB drugs in children, the global community may have to accept some over-treatment if we want to close the persistent case detection gap in young children. •Children are over-represented among TB deaths; most dying without accessing TB care.•Major gaps persist in TB preventive treatment (TPT) provision and TB case detection.•Reducing the TPT gap requires major upscaling of household contact investigation.•Reducing the TB case detection gap requires acceptance of some over-treatment.•New approaches are required to improve the accuracy of diagnostic (rule-in and rule-out) tests. Young children are most vulnerable to develop severe forms of tuberculosis (TB) and are over-represented among TB deaths. Almost all children estimated to have died from TB were never diagnosed or offered TB treatment. Improved access to TB preventive treatment (TPT) requires major upscaling of household contact investigation with allocation of adequate resources. Symptom-based screening is often discouraged in adults for fear of generating drug resistance, if TB cases are missed. However, the situation in vulnerable young children is different, as they present minimal risk of drug resistance generation. Further, the perceived need for additional diagnostic evaluation presents a major barrier to TPT access and underlies general reluctance to consider pragmatic decentralised models of care. Widespread roll-out of Xpert MTB/RIF Ultra® represents an opportunity for improved case detection in young children, but attaining full impact will require the use of non-sputum specimens. The new Fujifilm SILVAMP TB LAM® urine assay demonstrated good diagnostic accuracy in HIV-positive and malnourished children, but further validation is required. Given the limited accuracy of all available tests and the excellent tolerance of TB drugs in children, the global community may have to accept some over-treatment if we want to close the persistent case detection gap in young children. Young children are most vulnerable to develop severe forms of tuberculosis (TB) and are over-represented among TB deaths. Almost all children estimated to have died from TB were never diagnosed or offered TB treatment. Improved access to TB preventive treatment (TPT) requires major upscaling of household contact investigation with allocation of adequate resources. Symptom-based screening is often discouraged in adults for fear of generating drug resistance, if TB cases are missed. However, the situation in vulnerable young children is different, as they present minimal risk of drug resistance generation. Further, the perceived need for additional diagnostic evaluation presents a major barrier to TPT access and underlies general reluctance to consider pragmatic decentralised models of care. Widespread roll-out of Xpert MTB/RIF Ultra® represents an opportunity for improved case detection in young children, but attaining full impact will require the use of non-sputum specimens. The new Fujifilm SILVAMP TB LAM® urine assay demonstrated good diagnostic accuracy in HIV-positive and malnourished children, but further validation is required. Given the limited accuracy of all available tests and the excellent tolerance of TB drugs in children, the global community may have to accept some over-treatment if we want to close the persistent case detection gap in young children.Young children are most vulnerable to develop severe forms of tuberculosis (TB) and are over-represented among TB deaths. Almost all children estimated to have died from TB were never diagnosed or offered TB treatment. Improved access to TB preventive treatment (TPT) requires major upscaling of household contact investigation with allocation of adequate resources. Symptom-based screening is often discouraged in adults for fear of generating drug resistance, if TB cases are missed. However, the situation in vulnerable young children is different, as they present minimal risk of drug resistance generation. Further, the perceived need for additional diagnostic evaluation presents a major barrier to TPT access and underlies general reluctance to consider pragmatic decentralised models of care. Widespread roll-out of Xpert MTB/RIF Ultra® represents an opportunity for improved case detection in young children, but attaining full impact will require the use of non-sputum specimens. The new Fujifilm SILVAMP TB LAM® urine assay demonstrated good diagnostic accuracy in HIV-positive and malnourished children, but further validation is required. Given the limited accuracy of all available tests and the excellent tolerance of TB drugs in children, the global community may have to accept some over-treatment if we want to close the persistent case detection gap in young children. |
Author | Triasih, Rina Marais, Ben J. Seddon, James A. Amanullah, Farhana Mandalakas, Anna M. Marcy, Olivier Hesseling, Anneke C. Casenghi, Martina Verkuijl, Sabine Graham, Stephen M. |
AuthorAffiliation | b Global TB Programme, World Health Organisation (WHO), Geneva, Switzerland c Elizabeth Glaser Pediatric AIDS Foundation, Geneva, Switzerland h Department of Infectious Diseases, Imperial College London, London, United Kingdom d Department of Paediatrics, Faculty of Medicine, Public Health and Nursing, Universitas Gadjah Mada and Dr. Sardjito Hospital, Yogyakarta, Indonesia g University of Bordeaux, Inserm, French National Research Institute for Sustainable Development, UMR 1219, Bordeaux, France i Centre for International Child Health, University of Melbourne, Melbourne, Australia a The Children’s Hospital at Westmead and the Marie Bashir Institute for Infectious Diseases and Biosecurity, University of Sydney, Sydney, Australia j International Union against Tuberculosis and Lung Disease, Paris, France e Desmond Tutu TB Centre, Department of Paediatrics and Child Health, Stellenbosch University, South Africa k The Indus Hospital, Karachi, Pakistan f Global Tuberculosis Program, Department of Ped |
AuthorAffiliation_xml | – name: b Global TB Programme, World Health Organisation (WHO), Geneva, Switzerland – name: e Desmond Tutu TB Centre, Department of Paediatrics and Child Health, Stellenbosch University, South Africa – name: k The Indus Hospital, Karachi, Pakistan – name: g University of Bordeaux, Inserm, French National Research Institute for Sustainable Development, UMR 1219, Bordeaux, France – name: f Global Tuberculosis Program, Department of Pediatrics, Baylor College of Medicine and Texas Children’s Hospital, Houston, United States – name: a The Children’s Hospital at Westmead and the Marie Bashir Institute for Infectious Diseases and Biosecurity, University of Sydney, Sydney, Australia – name: c Elizabeth Glaser Pediatric AIDS Foundation, Geneva, Switzerland – name: d Department of Paediatrics, Faculty of Medicine, Public Health and Nursing, Universitas Gadjah Mada and Dr. Sardjito Hospital, Yogyakarta, Indonesia – name: h Department of Infectious Diseases, Imperial College London, London, United Kingdom – name: i Centre for International Child Health, University of Melbourne, Melbourne, Australia – name: j International Union against Tuberculosis and Lung Disease, Paris, France |
Author_xml | – sequence: 1 givenname: Ben J. orcidid: 0000-0003-3404-2690 surname: Marais fullname: Marais, Ben J. email: ben.marais@health.nsw.gov.au organization: The Children’s Hospital at Westmead and the Marie Bashir Institute for Infectious Diseases and Biosecurity, University of Sydney, Sydney, Australia – sequence: 2 givenname: Sabine orcidid: 0000-0002-0046-4759 surname: Verkuijl fullname: Verkuijl, Sabine organization: Global TB Programme, World Health Organisation (WHO), Geneva, Switzerland – sequence: 3 givenname: Martina orcidid: 0000-0002-7295-3076 surname: Casenghi fullname: Casenghi, Martina organization: Elizabeth Glaser Pediatric AIDS Foundation, Geneva, Switzerland – sequence: 4 givenname: Rina surname: Triasih fullname: Triasih, Rina organization: Department of Paediatrics, Faculty of Medicine, Public Health and Nursing, Universitas Gadjah Mada and Dr. Sardjito Hospital, Yogyakarta, Indonesia – sequence: 5 givenname: Anneke C. surname: Hesseling fullname: Hesseling, Anneke C. organization: Desmond Tutu TB Centre, Department of Paediatrics and Child Health, Stellenbosch University, South Africa – sequence: 6 givenname: Anna M. surname: Mandalakas fullname: Mandalakas, Anna M. organization: Global Tuberculosis Program, Department of Pediatrics, Baylor College of Medicine and Texas Children’s Hospital, Houston, United States – sequence: 7 givenname: Olivier surname: Marcy fullname: Marcy, Olivier organization: University of Bordeaux, Inserm, French National Research Institute for Sustainable Development, UMR 1219, Bordeaux, France – sequence: 8 givenname: James A. surname: Seddon fullname: Seddon, James A. organization: Desmond Tutu TB Centre, Department of Paediatrics and Child Health, Stellenbosch University, South Africa – sequence: 9 givenname: Stephen M. surname: Graham fullname: Graham, Stephen M. organization: Centre for International Child Health, University of Melbourne, Melbourne, Australia – sequence: 10 givenname: Farhana surname: Amanullah fullname: Amanullah, Farhana organization: The Indus Hospital, Karachi, Pakistan |
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Keywords | case finding childhood prevention tuberculosis gap child Prevention Tuberculosis Child Childhood Case finding Gap |
Language | English |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Sabine VERKUIJL is a staff member of the World Health Organization (WHO). She alone is responsible for the views expressed in this publication and they do not necessarily represent the decisions or policies of WHO. The designations used and the presentation of the material in this publication do not imply the expression of any opinion whatsoever on the part of WHO concerning the legal status of any country, territory, city or area, or of its authorities, nor concerning the delimitation of its frontiers or boundaries. |
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Snippet | •Children are over-represented among TB deaths; most dying without accessing TB care.•Major gaps persist in TB preventive treatment (TPT) provision and TB case... Young children are most vulnerable to develop severe forms of tuberculosis (TB) and are over-represented among TB deaths. Almost all children estimated to have... Young children are most vulnerable to develop severe forms of tuberculosis (TB) and are overrepresented among TB deaths. Almost all children estimated to have... |
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SubjectTerms | Adult case finding Child Child, Preschool childhood gap HIV Seropositivity Human health and pathology Humans Infectious diseases Life Sciences Overtreatment Pediatrics prevention Santé publique et épidémiologie tuberculosis Tuberculosis - diagnosis Tuberculosis - drug therapy Tuberculosis - epidemiology |
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