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Recent advances in tuberculosis
1. Dr. Amit Vatkar
MBBS, DCH, DNB Pediatrics
Fellow in Pediatric Neurology, Mumbai
Trained in Neurophysiology & Epilepsy, USA
Contact No. : +91-8767844488
Email: vatkaramit@yahoo.com
RECENT UPDATES IN
CHILDHOOD
TUBERCULOSIS
2. Tuberculosis – the facts
• Most cases occurred in
– Asia (59%) and
– Africa (26%)
WHO report 2011
6. TB disease and infection -
definitions
TB disease
• Detection of M. tuberculosis and/or clinical
symptoms compatible with tuberculosis
Latent infection with M. tuberculosis (LTBI)
• Presence of an immune response in a skin test
or an IFN-γ release assay (IGRA)
• Absence of clinical symptoms
7. Diagnosis of active tuberculosis
• Patient history
• Chest X-ray
• Culture
• Acid-fast bacilli staining
• Nucleic acid amplification testing
19. TUBERCULIN SKIN TEST
• Two preparations of PPD are available - PPD-S
and PPD RT23.
• Two TU PPD RT23 withTween 80 is equivalent to
5 TU of PPD-S.
• Current recommendation is to use 2 TU RT23.
• If it is not available 5 TU is acceptable, but there
a risk of false positivity.
• Cut off for positive result is an induration of 10
mm. In HIV positive patients 5 mm is the cut off.
20. New TB diagnostic tools
Between 2007 and 2010 the WHO has recommended
several new diagnostic tests to improve TB diagnosis:
– Fluorescent microscopy using LED technology—2009
– Liquid culture: MGIT (mycobacterium growth
indicator
tubes) and MODS (microscopic observation drug
susceptibility assay)—2007/2009
– Nucleic Acid Amplification Test (NAAT):
Xpert MTB/RIF—2010
23. Performance of Xpert MTB/RIF vs. other diagnostic modalities
Boehme et., Lancet 2011
24. Liquid culture: MGIT (mycobacterium growth
indicator tubes) and MODS (microscopic
observation
drug susceptibility assay).Advantages
+ Both are a lot faster than solid
media
(2 wks vs. 3-6 wks).
+ MGIT had 81.5% sensitivity and
99.6% specificity in detecting MTB.
+ MGIT results had high concordance
with solid media: 97% for rifampin
and 96% for isoniazid resistance.
+ MODS is close to 98% sensitive and
nearly 99% specific in detecting
rifampin resistance, and 98%
sensitive and 96% specific for
isoniazid resistance.
+ MODS is inexpensive.
Disadvantages
- Both MGIT and MODS require
trained technicians, sample
processing, and biosafety levels
appropriate only for reference
laboratory settings.
- MGIT is costly (@$30,000 per
machine and $5 for a tube).
- MGIT also requires another test
to do rapid speciation to
distinguish between MTB and
non-TB mycobacteria.
- MODS may have standardization
issues that can hamper its
accuracy.
25. Nucleic acid amplification test
(NAAT): Xpert MTB/RIF
Xpert MTB/RIF
Advantages Disadvantages
98% sensitivity
in smear-positive samples
expensive
machinery: currently about
$17,000 for the machine and
$17 per cartridge
specificity is 99%. requires electric
supply and annual calibration
Gives results within 2 hours Does not test resistance to
drugs other than rifampicin
Requires minimal sample
preparation
26.
27. NEONATED OF MOTHER WITH TUBERCULOSIS
• INH prophylaxis (10 mg/kg) for 6 months to all the babies-
diagnosed to have active TB during pregnancy, after delivery
or exposed to any case of active disease after delivery.
• Rule out congenital TB
• practical purpose RNTCP recommends BCG vaccination at
birth even if INH chemoprophylaxis is planned.
• Isolation of baby is indicated only if mother is having a
smear positive MDR TB.
• Isolation may be considered when mother is sick, non
adherent to therapy, received ATT for less than 2 weeks or
suspected to have MDR TB.
• Barrier nursing, using face mask and appropriate cough
hygiene are advised for all the mothers.
28. Recommendation
Xpert MTB/RIF should be used rather than
conventional microscopy and culture as the initial
diagnostic test in children suspected of having
• children suspected of having TB
• MDR TB or HIV-associated TB
• extrapulmonary TB
• TB meningitis