Tuberculosis in Children
above link takes u to anice article about pediatric pulmonary
TB, from Archieves Diseases in children, Education and Practice issue;
although following article is not derived from above article.
Magnitude of Pediatric tuberculosis:
As the children get infection from adults with chronic
pulmonary tuberculosis; the extent of infection or disease in children is
directly related to prevalence of chronic pulmonary tuberculosis in adults.
Annual rate of infection is 2.1%/year for under 5 year age
group.
Nearly 40 million children are likely to be exposed to the
risk and nearly 3-4 million children under 5 years are estimated to be
infected.
Agent: Mycobacterium Tuberculosis (human type)
Predisposing factors:
- Low socioeconomic group
- Poverty
- Poor ventilation,
- Overcrowding
- Close contact with sputum positive cases
- Unhygienic living conditions
Precipitating factors:
- Infections like measles, whooping cough
- Chronic diarrhea
- Severe malnutrition
- Compromised immune status
Transmission:
Droplet Infection
Incubation period: 4-8 weeks
Evolution and timetable of untreated of untreated primary TB
infection
Wallgreen’s Calender of TB events (modified)
Time scale since infection | Comments | Events |
0-4 weeks | Infection | None |
4-8 weeks | Hypersensitivity / Latent TB, most children get MT | Febrile illness, E nodosum, Phlyctenular conjunctivitis |
2-4 months | Primary focus, nonspecific resistance, greater risk of | Ghons complex with progressive healing in most cases, |
3-12 months | Focus complications | Pleural effusion (75% cases), Cavity, Coin shadow, |
3-9 months | Complications of nodes | Rupture, empyema, bronchopneumonia, consolidation, |
9 – 24 months | Diminished risk of dissemination | Meningitis, military, subcortical tuberculoma rupture, in |
1-3 yrs | Bone, joints, kidneys (>3 yrs) | |
Resistance reduced by early infection, PEM, measles, | ||
Adult type | Childhood |
Tissue has already acquired allergy and immunity by prior | Infection occurs for the first time, tissue has no |
Lowering of immune response/ defense locally in the lungs | T cell response plays a significant role causing disseminated |
No significant hilar or regional lymphadenopathy | Well marked regional lymphadenopathy |
Hematogenous spread is uncommon | Lymphatic and hematogenous spread more common than local |
Cavitatory lesion may be seen | Common with MDR & HIV positive patient |
Chronic pulm. TB is highly infectious | Iary infection is usually noninfectious |
In adults main cause of death and disability is pulm. TB | Main cause of death and disability is non pulmonary TB |
Healing of the lesion is mainly by calcification/ fibrosis | Calcification is more common, fibrosis is unusul |
Pulmonary Pathogenesis of Pediatric TB
Parenchymal Progression
Ghon’s focus = lymphangitis + enlarged Lymph nodes
Primary complex
Healed Primary complex
Pneumonia
Massive pneumonia
Primary cavity
Bronchopneumonia
Pleurisy
Lymphatic progression:
Mediastinal LN
Partial bronchial obstruction
Complete Bronchial obstruction
Obstructive emphysema
Collapse
Collapse consolidation
Synpneumonic effusion
Rupture of bronchus/ fistula
Subcarinal LN causing tracheal splaying
Hematogenous Progression:
Acute military TB
Protracted or disseminated TB
CNS – tuberculoma, TB Meningitis,
Ritchies focus
Dactylitis
Spinal TB (Potts)
TB psteomyelitis
Chronic Pulmonary TB:
Assman’s focus (subapical)
Pulmonary infiltration – cavity
Bronchogenic spread – bronchiectasis
Extensive bilateral fibrocaseous TB
Fibrous phthisis
Investigations:
Family History and family screening
Hematological = Hb ESR
MT test
XR chest
AFB gastric Lavage
USG abdomen – for LN and ileocaecal
Tb
CTscan Brain – tuberculoma and
exudates
LN biopsy
Sputum , CSF , pleural fluid, urine,
blood, culture
Tr Br Lavage
ELISA/ TB PCR Tests
Mantaux Test:
TU PPD with RT 23 or 1: 1000 is used with preferably a dose
of 5 TU, to detect greater number of true positives,
Given intradermally, read after 48-72 hrs
Palpate and measure induration , not erythema
Positive test reaction = 10 mm or more
Mild / + 0-14
mm
Moderate / ++ 15-20
mm
Severe +++ 21-30
mm
Very severe reaction ++++ blisters/ necrosis
or more than 30 mm
Treatment:
General supportive
Dietary
Environmental and psychological counseling
Chemotherapy with AKT
RNTCP
DOT regimen
IAP
Intensive phase + continuation phase
Indian Academy of Pediatrics ( IAP) consensus for TB
management in children
Cases divide in 5 groups
- Group I: 6 HR
- Asymptomatic MT positive < 3 yr age
- Asymptomatic MT positive <5 yr with PEM III IV
- MT positive : recent converter (no sings or healed
lesions) - Child less than 3 yr with family contact history
- Child < 5 yr with PEM III IV and contact
Group II: 2 HRZ + 4 HR
- Primary complex
- Symptomatic MT positive < 3yr, without localization
- Symptomatic MT positive < 5 yr + PEM III IV without
localization - Isolated LN disease
- Pleural effusion
Group III: 2 HRZE + 4 HR
Progressive
pulmonary disease
Multiple TB LN disease
-------- if
nonresolving, can be extended by 3 months
Group IV: 2HRZE + 7 HR
Miliary or
disseminated disease
Cavity
disease or bronchopneumonia
Osteoarticular
disease
Abdominal
pericardial or GU disease
Group V: 2 HRZE + 10 HR
Neuro TB
Dosage
recommendations: mg/kg/ dose/ day
Drug | Daily therapy | Intermittent therapy |
INH | 5 | 15 |
RMP | 10 | 15 |
PZA | 25 | 30 |
EMB | 20 | 30 |
SM | 20 | 30 |
Prednisolone | 1-2 | - |
Prednisolone:
Indicated
in:
Neuro TB,
Miliary TB
Serous TB
Endobronchial
Tb/ segmental lesion
GU TB/
sinus formation
Special cases:
Baby born to TB mother: in IIIrd
trimester
Breast
feeding may be continued
BCG to be
given at birth
If XRChest
normal, give 6 HR
If XRchest
abnormal 2HRZ+7HR
Congenital
TB 2 HRZ + 7 HR
BCG adenitis:
If LN is
small. < 1.5 cm = no treatment required
Increasing
or fluctuant = 6 H
Excision
+/-
Drugs for MDR TB:
1. Ethionamide
2. .Fluroquinolones:
double dose
a. Ciprofloxacxin
b. Ofloxacin
c. Sparfloxacin
d. lamefloxacin
3. Aminoglycosides
a. Kanamycin
b. Amikacin
4. Cycloserine
5. rifamycin
derivatives
a. rifabutin
b. rifapentin
c. rifadine
d. CGP.
FCE etc
For any queries, write to drdoctor@hotmail.com
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Dr Kondekar Santosh venketraman is a MD pediatrician at seth GS medical college and
KEM HOSPITAL MUMBAI INDIA