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Dr. Satti M. Saleh
 Chief of Infectious Diseases Department MGH
  Director of IC Unit Meeqat General hospital
CBAHI IC TEAM Member                     Medical
     Director Meeqat General Hospital
HISTORY
•   * Mycobacterium tuberculosis
    * MoTT•
     * 24/3/1882 (Robert Koch) •
     * 1993 (WHO – International Emergency)•
      * 2000 ( Global partenership    (STOP TB))•
      * DOT strategy•
     * DOTS strategy •
      * 2006 ( THE STOP TB STRATEGY)•
CLINICAL SYNDROMS
Primary TB (1st Exposure)
* Laten TB 
* Reactivation TB 
* Pulmonary TB 
* Extra pulmonary TB 
DIAGNOSIS:
AFB stain
* Culture 
LJmedia 
Bactec 
* Molecular Method      
PCR 
Species determination 
Drug resistant mutation 
Typing 
* Others    
BASIC CONTROL
Detection of cases
* Treatment (DOT)
* INH Prophylaxis for 
high risk
* Contact investigation
* Isolation
Standardized short-course anti-TB
treatment (SCC) given under direct and
    supportive observation (DOT).
1- INH 5mg /kg 
2- RMP 10mg/kg 
3- PZA 20-25mg/kg 
4- ETM 15-25mg/kg 

4 Drugs for 1st 2 months 
1st 2 Drugs for 2nd 4 months 
Isolation
AIRBORNE 
Negative pressure 
HEPA filters 
HEPA mask 
Special mask for patient 
   Pulmonary TB S+A   Till sputum
    Negative
DRUG RESISTANT
TB
Mono resistant (1 drug)
* Poly Resistant ( ~ 1 not 
MDR)
* MDR (INH + RIF) 
* Extensively resistant (XDR –   
all 1st line)
Other drugs
1- Amikacine
2- Kanamycine
3- Thiacetazone
4-Quinilone
5- cycloserine
6-clofazemine
TREATMENT OF LATENT
INFECTION


* Tuberculin test
* PPD +ve
* PPD -ve (2 step testing)
* (Avoid misclassification)
INDICATION
 HIV ≥ 5mm
* Immunosuppressive drugs ≥ 5mm 
* Close contact of TB patient ≥ 5mm 
Fibrotic lesion on CXR ≥ 5mm 
Recently infected 2years ~10mm 
person
* High risk medical conditions 
~10mm
DOTS STRATEGY
 - Detect smear +ve case & reporting
 - Observation of therapy( DOTs )
 - Treatment monitoring ( recording,
reporting assessment) -
  - Short course            (Drug
Supply)
 - Government & non – government
commitment
STOP TB STRATEGY (2006 –
2015)
* DOTs
* TB + HIV 
* Health System support 
* Engage all health care 
provider
* Empower people with TB & 
community
*Enable & promote research 
Standardized recording and
reporting
Helps to keep track of each individual patient   

           and to monitor overall programme
                                 performance
Sustained political and financial
commitment.
TB can be cured and the epidemic reversed if    

      adequate resources and administrative
          support for TB control are provided
Dots

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Dots

  • 1.
  • 2.
  • 3. Dr. Satti M. Saleh Chief of Infectious Diseases Department MGH Director of IC Unit Meeqat General hospital CBAHI IC TEAM Member Medical Director Meeqat General Hospital
  • 4. HISTORY • * Mycobacterium tuberculosis * MoTT• * 24/3/1882 (Robert Koch) • * 1993 (WHO – International Emergency)• * 2000 ( Global partenership (STOP TB))• * DOT strategy• * DOTS strategy • * 2006 ( THE STOP TB STRATEGY)•
  • 5. CLINICAL SYNDROMS Primary TB (1st Exposure) * Laten TB  * Reactivation TB  * Pulmonary TB  * Extra pulmonary TB 
  • 6. DIAGNOSIS: AFB stain * Culture  LJmedia  Bactec  * Molecular Method  PCR  Species determination  Drug resistant mutation  Typing  * Others 
  • 7. BASIC CONTROL Detection of cases * Treatment (DOT) * INH Prophylaxis for  high risk * Contact investigation * Isolation
  • 8. Standardized short-course anti-TB treatment (SCC) given under direct and supportive observation (DOT). 1- INH 5mg /kg  2- RMP 10mg/kg  3- PZA 20-25mg/kg  4- ETM 15-25mg/kg  4 Drugs for 1st 2 months  1st 2 Drugs for 2nd 4 months 
  • 9. Isolation AIRBORNE  Negative pressure  HEPA filters  HEPA mask  Special mask for patient   Pulmonary TB S+A Till sputum Negative
  • 10. DRUG RESISTANT TB Mono resistant (1 drug) * Poly Resistant ( ~ 1 not  MDR) * MDR (INH + RIF)  * Extensively resistant (XDR –  all 1st line)
  • 11. Other drugs 1- Amikacine 2- Kanamycine 3- Thiacetazone 4-Quinilone 5- cycloserine 6-clofazemine
  • 12. TREATMENT OF LATENT INFECTION * Tuberculin test * PPD +ve * PPD -ve (2 step testing) * (Avoid misclassification)
  • 13. INDICATION  HIV ≥ 5mm * Immunosuppressive drugs ≥ 5mm  * Close contact of TB patient ≥ 5mm  Fibrotic lesion on CXR ≥ 5mm  Recently infected 2years ~10mm  person * High risk medical conditions  ~10mm
  • 14. DOTS STRATEGY - Detect smear +ve case & reporting - Observation of therapy( DOTs ) - Treatment monitoring ( recording, reporting assessment) - - Short course (Drug Supply) - Government & non – government commitment
  • 15. STOP TB STRATEGY (2006 – 2015) * DOTs * TB + HIV  * Health System support  * Engage all health care  provider * Empower people with TB &  community *Enable & promote research 
  • 16.
  • 17. Standardized recording and reporting Helps to keep track of each individual patient  and to monitor overall programme performance
  • 18. Sustained political and financial commitment. TB can be cured and the epidemic reversed if  adequate resources and administrative support for TB control are provided