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Updated: Feb 6, 2026

Diagnosing Pulmonary Tuberculosis with the Xpert MTB/RIF Test
Published on: April 9, 2012
Upfront Xpert MTB/RIF testing on various specimen types for presumptive infant TB cases for early and appropriate
Neeraj Raizada1, Sunil D Khaparde2, Raghuram Rao2
1Foundation for Innovative New Diagnostics, New Delhi, India.
Insights
Rapid Xpert testing for infant tuberculosis (TB) is feasible, enabling same-day diagnosis and prompt treatment. However, high early mortality rates in infants with TB necessitate further research into care pathways.
Area of Science:
- Pediatrics
- Infectious Diseases
- Diagnostics
Background:
- Diagnosing tuberculosis (TB) in infants is difficult due to non-specific symptoms and low-sensitivity diagnostic tools.
- This often delays crucial treatment initiation for young children.
- Upfront use of Xpert/MTB RIF (Xpert) testing offers a rapid, sensitive, and specific diagnostic solution.
Purpose of the Study:
- To assess the feasibility and utility of upfront Xpert testing for diagnosing TB in infants (<2 years).
- To evaluate the application of Xpert testing on non-sputum specimens for infant TB diagnosis.
- To determine the impact of rapid diagnosis on treatment initiation and outcomes.
Main Methods:
- Established high-throughput laboratories in four cities, linked to healthcare providers via rapid transport and electronic reporting.
- Offered free upfront Xpert testing to all presumptive infant TB cases (<2 years) at public and private facilities.
- Utilized non-sputum specimens for a significant proportion of the testing.
Main Results:
- Enrolled 7,994 presumptive infant TB cases, diagnosing 465 (5.8%) cases.
- The majority of specimens (93.9%) were non-sputum, with higher TB positivity in these samples.
- Detected rifampicin resistance in 5.6% of infant TB cases, demonstrating the value of upfront resistance testing.
- Achieved same-day diagnosis and a median two-day turnaround time to treatment initiation.
- Observed an 11.0% case mortality rate, predominantly pre- or early treatment mortality.
Conclusions:
- Upfront Xpert testing is feasible for rapid diagnosis of TB in infants, facilitating timely treatment.
- The detection of rifampicin resistance highlights an added benefit of this rapid diagnostic approach.
- High early mortality rates underscore the need for improved infant TB care pathways despite prompt diagnosis and treatment.
Background:
Diagnosis of tuberculosis (TB) in infants is challenging due to non-specific clinical presentations of the disease in this age-group and low sensitivity of widely available TB diagnostic tools, which in turn delays prompt access to TB treatment. Upfront access to Xpert/MTB RIF (Xpert) testing, a highly sensitive and specific rapid diagnostic tool, could potentially address some of these challenges. Under the current project, we assessed the utility and feasibility of applying upfront Xpert for diagnosis of tuberculosis in infants, including for testing of non-sputum specimens.
Methods:
A high throughput lab was established in each of the four project cities, and linked to various health care providers across the city, through rapid specimen transportation and electronic reporting linkages. Free Xpert testing was offered to all infant (<2 years of age) presumptive TB cases (both pulmonary and extra-pulmonary) seeking care at public and private health facilities.
Results:
A total of 7,994 presumptive infant TB cases were enrolled in the project from April 2014 to October 2016, detecting 465 (5.8%, CI: 5.3-6.4) TB cases. The majority (93.9%; CI: 93.4-94.4) of patient specimens were non-sputum and TB positivity was higher amongst non-sputum specimens. Further, a high proportion (5.6% CI 3.8-8.1) of infant TB cases were found to be rifampicin resistant. Covering large cities with a single lab per city over more than two years, the project demonstrated the feasibility of same-day diagnosis with upfront Xpert testing. This in turn led to prompt treatment initiation, with a two-day median turnaround time to treatment initiation. Case mortality observed in the project cohort of diagnosed TB cases was 11.0% (CI 8.4-14.1), the majority of which was pre- or early treatment mortality, in spite of prompt access to treatment for most diagnosed cases.
Conclusion:
The current project demonstrated the feasibility of applying rapid and upfront Xpert testing for presumptive infant TB cases. Rapid TB diagnosis in turn facilitates prompt and appropriate treatment initiation. Further, levels of rifampicin resistance observed in infants TB cases highlight the additional benefit of upfront resistance testing. However, high rates of early case mortality, in spite of prompt diagnosis and treatment initiation, highlight the need for further research in infant patient pathways for overall improvement in TB care for infant populations.
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