TB in children Flashcards
Exposure of TB in Children
(+) History
(-)PPD, CXR, Ssx, Microbiology
Different Ssx of TB in children
Chronic cough Hemoptysis Weight Loss Non-specific Cervical Lymphadenopathy
Chest Xray findings in TB
Adult: Cavitary Lesions
Pedia: Hilar lymphadenopathy
Typical SSx in adult TB
Chronic cough with hemoptysis
CXR: Upper Lobe Lesions (Apical Gohn’s focus)
Sputum: (+)
Typical Ssx in Pedia TB
Non-specific
Difficulty to obtain sputum
Typical History of pediatric TB patients
Exposure within householf; howwever informations might be hard to illicit due to stigma
PPD
SQ - > 48-72 hours -> induration or erythema
Cut Off Measurement for positive effect
Based on Population
Low Endemicity : >5mm
High Endemicity: >10 mm
Cut off measurement for positive effect based on risk
High Risk: >5mm
Low risk: >8mm
Exposure
(+)Exposure
(-) PPD, CXR, SSx, SPutum
Significant contract with adult
Reasons why children is not included as source of infections
Do not have significantly bacillary load
Their cough is not forceful enough
Cavitary disease is rare are not severe
_____TB is more common in children
Pacuibacillary TB
-low bacillary load
Minimum Distance to be infective
3 ft or 1 meter
Management for exposure of TB
<5 years (specially <2 years): Primary prophylaxis
INFECTION
(+) Exposure, PPD
(-) CXR, SSX, Sputum
NoteL CXR may be normal or reveal presence of granulomatous or calcifications
Group of radiologic/ pathologic findings, not clinical
Primary Complex
Most common way of Transmission of TB
Droplet nuclei
Immunocompetent adult cut off
15 years old
In what years is the greatest risk for progression from infection to disease
2-3 years
Treatment of infection
Secondary Prophylaxis
T or F, PPD testing is routine for adults?
False
Role of PPD in pediatric patients
Know when treatment is most beneficial
DISEASE
(+) Exposure, PPD and any of the following
CXR, SSX, or SPutum AFB
Criteria for Pedia TB
3 out of 5 (Exposure, PPD, CXR, Ssx, Sputum)
Extrapulmonary sites for adults (TB)
15%
Lymphatic (25%)
Pleura (23%)
Meningeal (4%)
Extrapulmonary sites for Pedia
25-30%
Lymphatic 67%
Meningeal 23%
2 ways of Transmission for TB
Droplet nuclei
Direct nuclei
Children are usually infected by?
Untreated adolescent or adult in the household
Interval necessary for source to convert to a smear neagtive state if organisms are fully sensitive
2 weeks
Children or adolescent that should be considered as potentially contagious
“symptomatic adult type pTB”
Role of child in transmission
harbor latent infection
-partially healed but dormant infection can be reactivated as infectious PTB
Other portals of entry of entry may be important for the pediatric TB patient
Ingestion - unpasteurized milk
Contamination of a supeficial skin infection
Congenital infection is rare
Perinatal (Congenital) TB can be acquire via:
Transplacental - umbilical vein
In utero aspiration of amniotic fluid
Ingestion of infected amniotic fluid or secretions
Perinatal (Postnatal) TB can be acquired via
Inhalation of tubercle bacilli
Ingestion of infected breast milk or cow’s milk
Perinatal TB ssx appear during
2 weeks of life:
Loss of appetite Failure to gain weight fever ear/nasal discharge cough pneumonia jaundice hepatosplenomegaly
Lesion on the skin overlying a lymphnode usually in the cervical area
Scrofuloderma
Complications usually occur during___
5 years after acquisition of TB infection in childhood
especially the 1st year
Complications:
Miliary or acute meningeal TB (2-6 months) Endobronchial TB Bone/joint involvement (1 year) Renal Lesions (5-25 years)
Timetable of tb
Wallgren’s timetable
Primary Complex
parenchymal pulmonary focus
Regional lymph nodes
Since about 70% of lung foci are subpleural, localized pleurisy is common
Hallmark of primary TB in the lung
Relatively large size of the regional lymphadenitis vs relatively small size of initial lung focus
usual sequence in primary TB
hilar lymphadenopathy -> focal hyperinflation -> atelactasis of supplied portion: COLLAPSE-CONSOLIDATION or SEGMENTAL TB
Tuberculin skin test
PPD, test for cell mediated immunity againts M.TB
Negative results in PPD…
Incubation period (3 weeks to 3 months)
Temporary desensitization with measles (regained after 1 month)
Influenza and immuniztaion with influenza
Sensitization to tuberculin tends to remain undiminished for life (Immune system is working, even if treated -> will detect antigen from now or forever)
Considerations: LTBI treatment
- infants and children < 5 years of age with LTBI have been
- Risk for progression to disease is high
- Infants and young children are more likely to have life
Optimal dosing of new patients
Daily, but if not possible, weekly
Treatment: LTBI
9 month course of INH as self administered daily therapy
Treatment of TB in children
WHO:
Isoniazid (H) -> 10 mg/kg Max: 300mg/day Rifampicin (R) -> 15mg/kg Max: 600mg/day Pyranazinamide(Z) 35 mg/kg Ethambutol(E) 20mg/kg Streptomycin (S) - IM replaced by ethambutol
Side effect of ethambutol
optic neuritis
Use treatment regimen 2 HRZ 4 HR in the ff:
Children with suspected or confirmed PTB or TB peripheral lymphadenitis
Low HIV prevalence or Low resistance to isoniazid
Children who are HIV negative
Continuation phase of treatment
3x weekly regimens HIV uninfected with well established DOT
Treatment for infants (0-3 months) with suspected or confirmed PTB or TB peripheral lymphadenitis
Standard treatment
Treatment for children with suspected or confirmed TB menigitis
HRZE 2 HR 10, for a total of 12 months
If not penetrative to CNS, 6 month duration
Treatment for children with suspected or confirmed osteoarticular TB
HRZE 2 HR 10 for a total of 12 months
Treatment for Children with proven or suspected PTB or TB meningitis caused by MDR-TB
fluoroquinolone in the context of a well functioning control program and within an appropriate regimen.
Other options:
(6-9 mos): bedaquiline, delamanid
Treatment modality on Exposure
H x 3 mos + repeat PPD (if positive, extend tx for 9 mo)
Treatment modality on Infection
H x 9 months
treatment Modality (extent of disease) Pulmonary
HRZ x 2 mo + HR 4 x months
use 3x weekly regimens during continuation phase is as effective as daily regimen
treatment modality (extra pulmonary)
6 months - non life threatening forms
9 months - bone and joint
12 months - TB meningitis