3. Introduction
Global disease burden: 9 mil cases and 1.5
mil deaths in 2013.
One of the main causes of death worldwide.
HIV and drug resistance TB incidences are
increasing.
02 new anti TB drugs: Bedaquiline &
Delamanid for Rx of drug registant TB.
5. Epidemiology
Global incidence is slowly declining but
disease burden remains the same
Case detection rate is only 64%
3.3 mil were missed to diagnose
Mortality 16 per 100000 population
TB + HIV around 1.1 mil
MDR TB in 3.5% of new cases
6.
7.
8. Key Risk Factors
Under nutrition (26.9%)
Indoor air pollution (22.2%)
Smoking (15.8%)
HIV infection (11%)
Alcohol abuse(9.8%)
Diabetes (7.5%)
11. Clinical Presentation of TB
Fever with Chills
Night sweats
Anorexia
Weight loss
Fatigue
12. Clinical Presentation of TB
Productive, prolonged
cough (duration of 2-3
weeks)
Hemoptysis
Chest pain
Signs may vary based
on HIV status
13. Common Sites of TB Disease
Lungs
Pleura
Central nervous system
Lymphatic system
Genitourinary systems
Bones and joints
Disseminated (miliary TB)
14. Diagnosis of TB
Dx of active TB Dx of latent TB
Sputum smear
microscopy + Chest
Radiograph
Culture: Automated
liquid media/
Traditional solid
media
NAAT: Gene Xpert
Tuberculin skin test
-Mantoux test
-C-TB
IGRAs
-QuantiFERON-TB Gold
-T-SPOT TB test
15. Diagnosis of TB
PTB (Smear-positive) PTB (Smear-negative)
One AFB-positive
smear; patient with at
least one positive
smear result
(irrespective of
quantity of AFBs seen
on microscopy)
Patients with three
negative smear and
radiological findings
Patients with negative
smear results and a
positive culture
Patients who are unable
to produce sputum and
with highly suspicious
radiological and clinical
findings
18. Chest Radiograph
Diagnosis of PTB solely on basis of
CXR not encouraged
May have unusual appearance in
HIV-positive persons
CXR is helpful in HIV+, smear- negative
patients
Cannot confirm diagnosis of TB
Arrow points to cavity in
patient's right upper lobe.
20. Cultures
Culture is indicated for
New and retreatment PTB cases
still smear- positive at end of
intensive phase
Symptomatic contacts of known
MDR cases
Should be requested for ALL
retreatment patients
Relapse
Failure
Return after default
Colonies of M.
tuberculosis
growing on media
21. Diagnosis in Children
1. Patient history
• Contact to PTB+
• Symptoms consistent with TB
• HIV test
2. Clinical Exam
3. TST
4. Bacteriological confirmation
5. Investigations for EPTBGuidance of National Tb Programmes for the Management of TB in Children
WHO/HTM/TB/2006.371
23. Treatment of TB
Drug sensitive cases
INH+RIF+PZA+EMB for 2 months intensive phase
followed by INH+RIF for next 04 months
DOTS was previously widely implemented, but
not recommended by WHO at present
Meta analysis reported no clinical difference
between DOTS and self administered therapy
Adjunctive corticosteroids reduce inflammation
and improves outcome in TB meningitis
24. Treatment of TB cont…
Monitoring of therapy
In smear +ve pulmonary TB, sputum for AFB at 2
& 5 months interval
Median time interval to sputum culture
conversion of smear +ve pulmonary TB is 4-6 wks
Regular monitoring of LFT is not recommended
unless patient has high risk of
hepatotoxicity(Alcohol abuse, viral hepatitis,
pregnancy)
25. Treatment of Drug Resistant TB
INH mono-resistant TB
6 months with RIF+PZA+EMB or 9 months with
RIF+PZA+EMB in first 02 months intensive phase and
RIF+EMB in the continuation phase
26. Treatment of Drug Resistant TB
cont..
MDR TB
At least 4 drugs to which the strain is susceptible
Use a later generation fluoroquinolone plus an
injectable drug(6-8 months or 21-24 months)
Adding a 1st
line drug + additional group 4 drug
Oxazolidinones are used for fluoroquinolone
resistant MDR
Monitoring for adverse effect
Single drug should not be given in a failing
regimen
27. Treatment of Drug Resistant TB
cont..
XDR TB and resistant beyond XDR
Regimens should be based on prevailing patterns
of drug resistance and similar to MDR TB
Differential susceptibility to fluoroquinolones can
occur
Other group 4 or group 5 drugs can be used, but
their efficacy in unclear
28. Prognosis of Post TB Lung Disease
10 year fatality rates of smear +ve cases are 70%
for untreated smear +ve cases & 20% for
untreated smear –ve cases
For cases with HIV co-infection, 83% for smear
+ve and 74% for smear –ve cases
Mortality with treatment is 2.5% for without HIV
and 14% with HIV co-infection.
Post TB bronchiectasis, fibrosis, COPD and
aspergilloma etc
29. Prevention of TB
Close Contacts
WHO Criteria for
investigating contact
Smear +ve pulmonary
TB
MDR TB
Child < 5 yrs
HIV Co-infection
30. Prevention of TB cont…
Preventive therapy
In high burden countries preventive therapy is
only limited to people with HIV and children < 5
yrs with household contact
Isoniazide for 6-12 months for contacts with or
without HIV
Isoniazide for 36 months in HIV contact with
positive or unknown TST status
31. Prevention of TB cont…
Infection Control
WHO recommendations:
Opening windows for natural ventilation, 12 air
change per hour
Wind driven roof or wall turbine/exhaust fan
Personnel protection by properly fitted face
mask like surgical masks should be used in MDR TB
patients and their contacts
Negative pressure isolation rooms
32. Prevention of TB cont…
Vaccines
An ideal effective vaccine is yet to come
BCG can prevent childhood severe forms of
infection but protection wanes by adolescence
Currently 15 vaccine candidates are in clinical
trials
Vaccine development is hindered by poor
understanding of what constitutes protective
immunity
33. TB has killed 1 billion
people in past 02
centuries
Development of widely
available low cost
screening test
Development of effective
vaccine
Political and economic
stability
Improvement of
socioeconomic condition
Public hearth efforts
FROM WHO__ (Is this consistent with Manual) ? Although chest radiographic abnormalities are common in HIV-infected persons without TB, chest x-ray plays an important role in the diagnosis of TB among PLWHA. CXR presentations of TB in HIV patients are now well characterised and should no longer be considered ‘atypical’ for TB in HIV-prevalent settings. CXR plays a significant role in shortening the delay of diagnosis and should be done early in the course of investigation of a TB suspect. CXR can also be an important entry point to diagnosing non-TB chest diseases, which are common among PLWHA. However, the limitations that exist for its wider use such as unavailability at peripheral health facilities and difficulty of interpreting results, even by trained physicians need to be acknowledged and dealt with accordingly. Research is needed to identify innovative ways to enhance the ability of clinicians, including non-physicians, to interpret CXRs accurately, to assess the feasibility and added value of peer reviewing of CXRs and to evaluate novel imaging techniques that might replace conventional radiography.