Upfront Xpert MTB/RIF for diagnosis of pediatric TB-Does it work? Experience from India.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2020
Historique:
received: 26 03 2020
accepted: 27 06 2020
entrez: 7 8 2020
pubmed: 7 8 2020
medline: 30 9 2020
Statut: epublish

Résumé

Diagnosis of TB in pediatric population poses several challenges. A novel initiative was implemented in several major cities of India aimed at providing upfront access to free-of-cost Xpert MTB/RIF to presumptive pediatric TB cases. This paper aims to describe the experience of implementing this large initiative and assess feasibility of the intervention in high TB burden settings. Data were drawn from the pediatric TB project implemented in 10 major cities of India between April 2014 and March 2018. In each city, providers, both public and private, were engaged and linked with a high throughput Xpert MTB/RIF lab (established in that city) through rapid specimen transportation and electronic reporting system. Rates and proportions were estimated to describe the characteristics of this cohort. Of the total 94,415 presumptive pediatric TB cases tested in the project, 6,270 were diagnosed positive for MTB (6.6%) on Xpert MTB/RIF (vs 2% on smear microscopy). Among MTB positives, 545 cases were rifampicin resistant (8.7%). The median duration between collection of specimens and reporting of results was 0 days (same day) and >89% cases were initiated on treatment. Approximately 50% of the specimens tested were non-sputum. The number of providers/facilities engaged under the project increased >10-fold (from 124 in Q2'14 to 1416 in Q1'18). This project, which was one of the largest initiatives globally among pediatric population, demonstrated the feasibility of sustaining rapid and upfront access to free-of-cost Xpert MTB/RIF testing. The project underscores the efficiency of this rapid diagnostic assay in tackling several challenges in pediatric TB diagnosis, identifies opportunities for further interventions as well as brings to light scope for effective engagement with healthcare providers. The findings have facilitated a policy decision by National TB Programme mandating the use of Xpert MTB/RIF as a primary diagnostic tool for TB diagnosis in children, which is being scaled-up.

Sections du résumé

BACKGROUND
Diagnosis of TB in pediatric population poses several challenges. A novel initiative was implemented in several major cities of India aimed at providing upfront access to free-of-cost Xpert MTB/RIF to presumptive pediatric TB cases. This paper aims to describe the experience of implementing this large initiative and assess feasibility of the intervention in high TB burden settings.
METHODS
Data were drawn from the pediatric TB project implemented in 10 major cities of India between April 2014 and March 2018. In each city, providers, both public and private, were engaged and linked with a high throughput Xpert MTB/RIF lab (established in that city) through rapid specimen transportation and electronic reporting system. Rates and proportions were estimated to describe the characteristics of this cohort.
RESULTS
Of the total 94,415 presumptive pediatric TB cases tested in the project, 6,270 were diagnosed positive for MTB (6.6%) on Xpert MTB/RIF (vs 2% on smear microscopy). Among MTB positives, 545 cases were rifampicin resistant (8.7%). The median duration between collection of specimens and reporting of results was 0 days (same day) and >89% cases were initiated on treatment. Approximately 50% of the specimens tested were non-sputum. The number of providers/facilities engaged under the project increased >10-fold (from 124 in Q2'14 to 1416 in Q1'18).
CONCLUSION
This project, which was one of the largest initiatives globally among pediatric population, demonstrated the feasibility of sustaining rapid and upfront access to free-of-cost Xpert MTB/RIF testing. The project underscores the efficiency of this rapid diagnostic assay in tackling several challenges in pediatric TB diagnosis, identifies opportunities for further interventions as well as brings to light scope for effective engagement with healthcare providers. The findings have facilitated a policy decision by National TB Programme mandating the use of Xpert MTB/RIF as a primary diagnostic tool for TB diagnosis in children, which is being scaled-up.

Identifiants

pubmed: 32756559
doi: 10.1371/journal.pone.0236057
pii: PONE-D-20-08697
pmc: PMC7406076
doi:

Substances chimiques

Antibiotics, Antitubercular 0
Rifampin VJT6J7R4TR

Types de publication

Journal Article Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0236057

Subventions

Organisme : World Health Organization
ID : 001
Pays : International

Déclaration de conflit d'intérêts

The authors [AK, DP, NR, SM, RS, SC, SS, CMD, CB] are affiliated with Foundation for Innovative New Diagnostics, a non-profit international organization. However, this does not alter our adherence to PLOS ONE policies on sharing data and materials.

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Auteurs

Aakshi Kalra (A)

Foundation for Innovative New Diagnostics, New Delhi, India.

Debadutta Parija (D)

Foundation for Innovative New Diagnostics, New Delhi, India.

Neeraj Raizada (N)

Foundation for Innovative New Diagnostics, New Delhi, India.

K S Sachdeva (KS)

Central TB Division, Government of India, New Delhi, India.

Raghuram Rao (R)

Central TB Division, Government of India, New Delhi, India.

Soumya Swaminathan (S)

World Health Organization, Geneva, Switzerland.

Ashwani Khanna (A)

State TB office, Govt of National Capital Territory, Delhi, India.

Kamal Kishore Chopra (KK)

New Delhi TB Centre, New Delhi, India.

M Hanif (M)

New Delhi TB Centre, New Delhi, India.

Varinder Singh (V)

Lady Hardinge Medical College and Assoc Kalawati Saran Children's Hospital, New Delhi, India.

K R Umadevi (KR)

National Institute of research in Tuberculosis, Chennai, India.

K N Sheladia (KN)

District TB Centre, Surat Municipal Corporation, Gujarat, India.

Rama Rao (R)

State TB Office, Vijayawada, Andhra Pradesh, India.

N Vasundhara (N)

District TB Centre, Visakhapatnam, Andhra Pradesh, India.

Anil S (A)

State TB Training and Demonstration Centre/Intermediate Reference Laboratory, Bangalore, Karnataka, India.

Nirmala A R (N)

State TB Training and Demonstration Centre/Intermediate Reference Laboratory, Bangalore, Karnataka, India.

Abdul Azeem (A)

State TB Training and Demonstration Centre/Intermediate Reference Laboratory, Bangalore, Karnataka, India.

Vijay Chhajlani (V)

District TB Centre, Indore, Madhya Pradesh, India.

Jyoti Khurana (J)

Intermediate Reference Laboratory, Indore, Madhya Pradesh, India.

N J Das (NJ)

Office of the Jt. Director of Health Services (TB), Directorate of Health Services, Assam, India.

Bandana Choudhury (B)

Intermediate Reference Laboratory, Guwahati, Assam, India.

Sreenivas Achuthan Nair (SA)

Stop TB Partnership, Geneva, Switzerland.

Shalini Mall (S)

Foundation for Innovative New Diagnostics, New Delhi, India.

Rajashree Sen (R)

Foundation for Innovative New Diagnostics, New Delhi, India.

Sarabjit Singh Chadha (SS)

Foundation for Innovative New Diagnostics, New Delhi, India.

Claudia M Denkinger (CM)

Foundation for Innovative New Diagnostics, Geneva, Switzerland.

Catharina Boehme (C)

Foundation for Innovative New Diagnostics, Geneva, Switzerland.

Sanjay Sarin (S)

Foundation for Innovative New Diagnostics, New Delhi, India.

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Classifications MeSH