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WELCOME
Tuberculosis
Presented by
Maj Shahriar Jahan
Trainee In Medicine, 2nd
term
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.
Mycobacterium tuberculosis
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
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%)
Immunopathogenesis of TB
Outcomes of Infection
Clinical Presentation of TB
 Fever with Chills
 Night sweats
 Anorexia
 Weight loss
 Fatigue
Clinical Presentation of TB
Productive, prolonged
cough (duration of 2-3
weeks)
Hemoptysis
Chest pain
Signs may vary based
on HIV status
Common Sites of TB Disease
 Lungs
 Pleura
 Central nervous system
 Lymphatic system
 Genitourinary systems
 Bones and joints
 Disseminated (miliary TB)
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
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
Diagnosis of TB
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.
AFB in sputum smear TB granuloma
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
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
Treatment of TB
Anti
TB
Drugs
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
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)
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
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
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
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
Prevention of TB
Close Contacts
WHO Criteria for
investigating contact
Smear +ve pulmonary
TB
MDR TB
Child < 5 yrs
HIV Co-infection
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
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
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
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
THANK YOUTHANK YOU

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Tuberculosis

  • 2. Tuberculosis Presented by Maj Shahriar Jahan Trainee In Medicine, 2nd term
  • 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
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  • 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
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  • 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.
  • 19. AFB in sputum smear TB granuloma
  • 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
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Editor's Notes

  1. 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.