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Multi drug resistant T.B. (MDR)
 Dr. Gopalrao M.D. Ph.D.
 Professor of Community Medicine
 CAR Medical College




                                    1
Global Fact sheet:
 T.B. Incidence: 8.8 million people
are affected by TB annually world
wide.
 1.4 million deaths occur annually
world wide.
 MDR-TB is defined as disease
having resistance to two or more of
the anti T.B. drugs with or without
resistance to other anti TB drugs
It is a major threat to TB control
program world wide.
                                       2
Countries having problem of MDR T.B.
   Russia
   Peoples Republic of China
   India
   Western Europe
   United states
   United Kingdom
   Germany
   Central Europe
   Lithuania
   Latvia
   Estonia

                                       3
4
Indian Scenario
 Prevalence of MDR T.B. in new smear +ve cases is less than
  3% and 12 to 17% amongst previously treated PTB cases.
• India is the highest TB burden country in the world.
• India is 17th among 22 high burden countries in terms of
   incidence rate
• Accounts for 20% of global burden of TB.
• Every year 1.8 million persons develop TB
• There are point eight million new smear positive cases.
• The annual risk of becoming infected with TB is 1.5 %



                                                               5
Case study from Andhra Pradesh
 Study conducted on 75 MDR T.B. cases.




                                          6
1
               5                9
               3                    14           1
Reported                6                    5
               2
MDR cases                           2
                   10                    5   1
from 18
districts of            5       2
Andhra
Pradesh        2            1       2



                                                     7
8
NO. OF    % OF PATIENTS
                                      PATIENTS
             SOB, Cough, fever           38           50%
                Cough, fever             20           27%
                SOB, cough               6            8%
             Cough, fever, loss          2            3%
Complaints     of appetite
             SOB, cough, fever,          2            3%
              loss of appetite
  among            cough                 2            3%
             SOB, Haemoptysis            1            1%
             Cough, loss of       1              1%
 MDRTB       appetite
             Cough, fever,        1              1%
             haemoptysis
             SOB                  1              1%
 Patients
             SOB, cough,          1              1%
             haemoptysis
             Cough, fever,chest   1              1%
             pain                                                12
Clinical factors promoting resistance
 Delayed diagnosis and isolation
 Inappropriate drug regimen.
       Inadequate initial therapy
       Incomplete course of treatment
       Inappropriate treatment modifications
       Adding single drug to a failing regimen
       Inappropriate use of chemoprophylaxis
   Poor adherence and incomplete Follow up
   Failure to isolate MDR TB patients
   Failure to employ DOT
   Over the counter anti TB
   Faked drugs
Mechanism of Resistance
 TB specific drugs
    INH, PZA, ETH


 Antibiotics with activity against TB
    RIF
    Aminogycosides
    Flouroquinolones
Mechanism of resistance
 INH
    Chromosomally mediated
    Loss of catalase/peroxidase
    Mutation in mycolic acid synthesis
    Regulators of peroxide response
Mechanism of resistance
 Rifampin
    Reduced binding to RNA polymerase
       Clusters of mutations at “Rifampin Resistance Determining
        Region” (RRDR)


   Reduced Cell wall permeability
Treatment of MDR TB
 Factors determining Success
    Culture of MDR TB
    Reliable susceptibility
    Reliable history of previous drug regimens
    Program to assure delivery of prescribed drugs (DOT)
    Correct choice of modified treatment regimen
    Reliable follow up
New Chemotherapeutic Agents
 Not many. Low interest from pharmaceutical industry
 Derivatives of Rifamycin
   Rifabutin: Sensitive subset of Rifampin resistant strains
   Rifapentine: Extended half-life but more mono-resistance to
    rifamycins
   KRM-1648. benzoxazinorifamycin. In vitro and animal models.
 New flouroquinolones
   Gatifloxacin, Moxifloxacin, levofloxacin, sparfloxacin
 Nitroimidazoles
   related to metronidazole. May work better against latent bacilli
 Avoiding pro-drug problems
Chemoprophylaxis
 Determinants of intervention
   Likelihood of infection with MDR TB
       Low
       Intermediate
       High


   Likelihood of developing MDR TB
       Immune suppression
Global TB control targets
                                     2015: 50% reduction in TB prevalence and
                                          death rates by 2015


 2015: Goal 6: Combat HIV/AIDS, malaria and other
        diseases
     Target 8: to have halted by 2015 and begun to reverse
               the incidence…
      Indicator 23:      prevalence and deaths associated with TB
      Indicator 24:      proportion of TB cases detected
                         and cured under DOTS
                              2005: World Health Assembly:
                                   -     To detect at least 70% of infectious TB cases
                                   -     To treat successfully at least 85% of detected
                                   cases
Stop TB Strategy
to reach the 2015 MDGs
22
23
Thank You




            24

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Multi-drug resistant Tuberculosis

  • 1. Multi drug resistant T.B. (MDR)  Dr. Gopalrao M.D. Ph.D.  Professor of Community Medicine  CAR Medical College 1
  • 2. Global Fact sheet:  T.B. Incidence: 8.8 million people are affected by TB annually world wide.  1.4 million deaths occur annually world wide.  MDR-TB is defined as disease having resistance to two or more of the anti T.B. drugs with or without resistance to other anti TB drugs It is a major threat to TB control program world wide. 2
  • 3. Countries having problem of MDR T.B.  Russia  Peoples Republic of China  India  Western Europe  United states  United Kingdom  Germany  Central Europe  Lithuania  Latvia  Estonia 3
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  • 5. Indian Scenario  Prevalence of MDR T.B. in new smear +ve cases is less than 3% and 12 to 17% amongst previously treated PTB cases. • India is the highest TB burden country in the world. • India is 17th among 22 high burden countries in terms of incidence rate • Accounts for 20% of global burden of TB. • Every year 1.8 million persons develop TB • There are point eight million new smear positive cases. • The annual risk of becoming infected with TB is 1.5 % 5
  • 6. Case study from Andhra Pradesh  Study conducted on 75 MDR T.B. cases. 6
  • 7. 1 5 9 3 14 1 Reported 6 5 2 MDR cases 2 10 5 1 from 18 districts of 5 2 Andhra Pradesh 2 1 2 7
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  • 12. NO. OF % OF PATIENTS PATIENTS SOB, Cough, fever 38 50% Cough, fever 20 27% SOB, cough 6 8% Cough, fever, loss 2 3% Complaints of appetite SOB, cough, fever, 2 3% loss of appetite among cough 2 3% SOB, Haemoptysis 1 1% Cough, loss of 1 1% MDRTB appetite Cough, fever, 1 1% haemoptysis SOB 1 1% Patients SOB, cough, 1 1% haemoptysis Cough, fever,chest 1 1% pain 12
  • 13. Clinical factors promoting resistance  Delayed diagnosis and isolation  Inappropriate drug regimen.  Inadequate initial therapy  Incomplete course of treatment  Inappropriate treatment modifications  Adding single drug to a failing regimen  Inappropriate use of chemoprophylaxis  Poor adherence and incomplete Follow up  Failure to isolate MDR TB patients  Failure to employ DOT  Over the counter anti TB  Faked drugs
  • 14. Mechanism of Resistance  TB specific drugs  INH, PZA, ETH  Antibiotics with activity against TB  RIF  Aminogycosides  Flouroquinolones
  • 15. Mechanism of resistance  INH  Chromosomally mediated  Loss of catalase/peroxidase  Mutation in mycolic acid synthesis  Regulators of peroxide response
  • 16. Mechanism of resistance  Rifampin  Reduced binding to RNA polymerase  Clusters of mutations at “Rifampin Resistance Determining Region” (RRDR)  Reduced Cell wall permeability
  • 17. Treatment of MDR TB  Factors determining Success  Culture of MDR TB  Reliable susceptibility  Reliable history of previous drug regimens  Program to assure delivery of prescribed drugs (DOT)  Correct choice of modified treatment regimen  Reliable follow up
  • 18. New Chemotherapeutic Agents  Not many. Low interest from pharmaceutical industry  Derivatives of Rifamycin  Rifabutin: Sensitive subset of Rifampin resistant strains  Rifapentine: Extended half-life but more mono-resistance to rifamycins  KRM-1648. benzoxazinorifamycin. In vitro and animal models.  New flouroquinolones  Gatifloxacin, Moxifloxacin, levofloxacin, sparfloxacin  Nitroimidazoles  related to metronidazole. May work better against latent bacilli  Avoiding pro-drug problems
  • 19. Chemoprophylaxis  Determinants of intervention  Likelihood of infection with MDR TB  Low  Intermediate  High  Likelihood of developing MDR TB  Immune suppression
  • 20. Global TB control targets 2015: 50% reduction in TB prevalence and death rates by 2015 2015: Goal 6: Combat HIV/AIDS, malaria and other diseases Target 8: to have halted by 2015 and begun to reverse the incidence… Indicator 23: prevalence and deaths associated with TB Indicator 24: proportion of TB cases detected and cured under DOTS 2005: World Health Assembly: - To detect at least 70% of infectious TB cases - To treat successfully at least 85% of detected cases
  • 21. Stop TB Strategy to reach the 2015 MDGs
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  • 24. Thank You 24