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Dr.Ch.Anjana
Department of general medicine
Katuri medical College and hospital
Untreated one case of TB can cause 10-15 new cases/year
Theme for national TB elimination programme in 2022-
Invest in TB and save lives
 TB notification rate-19.5 lakh
INCIDENCE OF TB:188 cases/lakh
MDR notification-4lakh
XDR notification-1lakh
Case fatality rate-3-20%
Case specific death rate-37 per lakh
EPIDEMIOLOGICAL DETERMINANTS:
Agent factors:
Mycobacterium tuberculosis-obligate aerobe
Facultative intracellular
 Host factors:
Age group-15-45 years
Social factors:
Poverty, malnutrition, overcrowding, unhygienic conditions
PATHOPHYSIOLOGY:
1.Primary TB:
Bacilli first attacks the hilar area
First lesion-Ghon’s focus
If the lymphnode also involved along with Ghon’s focus-
Ghon’s complex
Ghon’s complex calcifies and forms Ranke’s complex
In 95% ,TB infection is healed
2.Progressive primary tb:
TB Bacilli may cause a local inflammatory reaction
Usually seen in low immunity
Symptoms:Fever,chronic cough,pneumonia like
illness,erythema nodosum,phlyctenular conjunctivitis etc
Seen in 1-2% of total primary TB cases
3.Latent tb:
Bacilli is dormant
Seen in 2-4 % of total primary tb cases
Secondary/reactivation TB:
Under stressors,Tb bacilli gets activated and cause
cavitation
This is delayed type -4 hypersensitivity reaction
From cavities to bronchus,TB Bacilli may spread to others
Approximately 40% of Indian population may have
primary TB infection
Chest X-ray
Sputum
Genotypic tests
Culture methods
Molecular tests
Serological tests
Tuberculin skin test
1. CHEST X-RAY
 High sensitivity but poor specific ity
Usually upper lobe disease with infiltrates and cavities
2. SPUTUM:
Most sensitive and specific
Done in designated microscopy centres
2 samples- spot sample and morning sample
Checked within 24 hours
Minimum 5ml of sputum should be collected
Sputum should be expectorated- no.of squamous epithelial
cells should be <10% in expectorated sputum
Turn around time is -24 hours
Types of sputum testing
1.Conventional method:Zeihl Neelsen staining is used
2.LED microscopy: ZN staining is used.Better than
conventional method
3.Fluorescence microscopy:
Auromine -O- Rhodamine stain is used.
Best test
3. GENOTYPIC TESTS
CBNAAT:
Highly specific and good sensitivity
Diagnostic and confirmatory
Biggest advantage-Turn around time is 90 minutes(with in
2 hours)
Rifampicin status also can be known.
Machine is GeneX pert.
TruNAAT:
Indianized version of CBNAAT
Less expensive
Approved by NTEP
Turn around time is 1 hour
LINE PROBE ASSAY:
Resistance pattern can be found
FL LPA-Resistance to Isoniazid can be found
SL LPA-Resistance to fluoroquinolones,second line
injectables/drugs can be found
Drug resistance Target region
Isoniazid Inh A promoter,kat G
Ethionamide Inh A promotor
Fluoroquinolone gyr A,gyr B
Amikacin,kanamycin,
Capriom
rrs, eis promotor
4. CULTURE METHODS:
 Solid media:
Egg based
Lowenstein Jensen media
Takes about 8-10 weeks
 Liquid culture:
Using BACTEC/MGIT method
Kirchner media/Middle brook media
Takes about 1-2 weeks
5. Molecular tests:
BACTEC 460-Tells about C02 emission
MGIT 960-Tells about O2 consumption and metabolism
rate
They are also used for DST.
6. Serological tests:
IGRA test-Interferon gamma release assay
Tells about primary or secondary TB
Not for diagnosis of TB
Used to diagnose latent TB in some countries
Gives information about presence of TB bacilli
Antigen-Antibody test and Quantiferon test:
Gives information about TB infection not disease
7. TUBERCULIN SKIN TEST:
Also known as pirquet test/Montoux test
Uses 1 unit of ppd
Not for diagnosis
Read after 48 hours,within 96 hours
Average time is 72 hours
Wheal/flare raection
>5mm HIV, severe
immunosuppression,close
cotacts of TB,h/0 prior TB
>10mm Recent immigrants,IVDA,<4
yrs, Adolescents with exposure
from high risk groups
>15mm No risk factor
Diagnosis in NTEP
1. Sputum for AFB
2. CXR
3. CBNAAT
4. TruNAAT
5. LPA
6. Liquid culture-Gold standard
Laboratory turn around time:
Solid culture Lowenstein –
Jensen media
3 weeks-SP
4-8 weeks-SN
Automated liquid
culture
BACTEC,MGIT 8-10 days-SP
2-6 weeks-SN
Molecular testing Line probe assay
for detection of
drug resistance
1-3 days
CBNAAT 2 hours
TruNAAT 1 hour for TB
detection and 1
hour for
resistance
detection
1962-National TB control program
1997-Revised national TB control program (RNTCP)
DOTS(Directly observed treatment short course)
was
started
2020-National TB elimination program
End TB(means to reduce TB death and incidence)
Reduction in deaths by 90% by 2025
Reduction in TB incidence rate by 80% by 2025
DEFINITION:
1. Presumptive TB case(TB suspect):
Any person with c/o cough/fever/night sweats for >2 weeks
with or without significant weight loss.
2. Drug sensitive tuberculosis:
Sensitive to Rifampicin and Isoniazid.
3. Drug resistance
H mono drug – only Isoniazid
Multi drug resistance – Resistance to atleast H and R
Polydrug resistance - Any two drugs resistance not
including H and R
XDR TB - Resistance to H and R + Any
fluoroquinolone +Any group A second
line(Bedaquiline,Linezolid
(Previous- any 2nd line injectables)
Pre XDR TB- Resistance to H and R +Any fluoroquinolone
Presumptive MDR-ATT for >1month and default for >1
month or currently on ATT,poor response (no clinical
improvement or sputum positive at 3rd or 5th month of
follow up) or any contact of MDR case
Recurrent TB (Relapse of TB) - cured after ATT .But now
microbiologically confirmed sputum positive
Presumptive TB case
Sputum+NAAT+CXR
Doing sputum test is minimum requirement
If sputum test and NAAT are negative,CXR is normal-
Rule out tb and refer
If suputum is positive – microbiologically confirmed tb
 First line drugs:
Isoniazid,Rifampicin,Pyrazinamide, Ethambutol
Second line drugs:
Regimen Intensive phase Continuation phase
Drug sensitive TB 2 HRZE 4 HRE
H mono/poly drug
regimen TB
6 ZER0
Shorter oral
Bedaquiline
containing
regimen(Shorter
MDR)
4-6 CHOBZEE
Clofazimine,High
dose
Isoniazid,Levofloxacin
,Bedaquiline,
Pyrazinamide,
Ethambutol,
Ethionamide,Bedaqui
line is given for 6
months always
5 C0ZE
Clofazamine
Levofloxacin
Pyrazinamide
Ethambutol
Longer MDR/XDR TB 18-20 L2C2BDQ
Levofloxacin,Linezolid
,Clofazimine,
Cycloserine,Bedaquili
ne
Cinformed absence of resistance to or lack of suspicion of
the ineffectiveness of a drug in the shorter MDR-TB
regimen
No H/O exposure to one or more second line drugs used in
the shorter MDR TB regimen for >1month
R resistant TB
MDR TB with R resistance and single gene mutation H
resistance
 Patients started on TB treatment becomes 50-80% non-infectious
within 48 hours of taking Rifampicin and >95% non-infectious by 2
weeks
5 weight bands for adults
Weight category Intensive
phase(no.of FDC
tablets)
Continuation
phase(no.of FDC
tabs)
25-34 Kg 2 2
35-49 Kg 3 3
50-64 Kg 4 4
65-75 Kg 5 5
> 75 Kg 6 6
 FDC contains
Isoniazid-75mg
Rifampicin-150mg
Pyrazinamide-400mg
Ethionamide-275 mg
 FDC dosage chart for children has 6 weight bands
H-50 mg
R-75mg
Z-150 mg
Ethionamide is given separately
 Bedaquiline –
Week 0-2- 400mg daily
Week 3-24- 200mg 3 times /week
BPaL Regimen:
 Bedaquiline,Pretomanid,Linezolid
 Advocated by WHO
 Taken up by few districts under NTEP
 Given if there is flouroquinolone resistance and there is no exposure
(< 2 weeks exposure to Bedaquiline/Linezolid)
 Dosage-
Pretomanid-200mg once daily for 26 weeks
Bedaquiline – 400mg once daily for the first 2 weeks
200mg three times a week for the next 24 weeks
Linezolid-1200mg once daily for 24 weeks
HIV associated TB
Early intiation of ART during anti TB treatment is
advised
ART should be started within the first 8 weeks of anti-TB
treatment
ART should be started with in 2 weeks Of TB treatment
for profoundly immunocompromised patients with CD4+ T
cell count of <50/mcL
Clinical evaluation:
Height
Weight
Physical examination
Psychiatry evaluation if required
Laboratory based evaluation:
HIV testing following counselling
Liver function tests,RBS,CBP,S.electrolytes,Urine
pregnancy test in women of reproductive age,ECG
 Old regimen:
Isoniazid-300mg *6 months
Newer regimen:
 Drug sensitive TB:
Shorter TPT(TB preventive treatment):3 months of weekly
Rifapentine and Isoniazid
 Drug resistant TB:
R resistant, FQ sensitive-6 months of daily Levofloxacin
H resistant,R sensitive-4 months of Rifampicin
Persons on TPT will be monitored for clinical and laboratory
parameters as below:
 Screening with symptoms(cough,fever,night sweats,weight loss)
 Any side effects
 If any sign or symptom,the person may be referred to the nearby TB
centre and evaluated for active TB/Drug resistant TB
latest pulmonary tuberculosis guidelines.pptx
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latest pulmonary tuberculosis guidelines.pptx

  • 1. Dr.Ch.Anjana Department of general medicine Katuri medical College and hospital
  • 2. Untreated one case of TB can cause 10-15 new cases/year Theme for national TB elimination programme in 2022- Invest in TB and save lives
  • 3.  TB notification rate-19.5 lakh INCIDENCE OF TB:188 cases/lakh MDR notification-4lakh XDR notification-1lakh Case fatality rate-3-20% Case specific death rate-37 per lakh
  • 4. EPIDEMIOLOGICAL DETERMINANTS: Agent factors: Mycobacterium tuberculosis-obligate aerobe Facultative intracellular  Host factors: Age group-15-45 years Social factors: Poverty, malnutrition, overcrowding, unhygienic conditions
  • 5. PATHOPHYSIOLOGY: 1.Primary TB: Bacilli first attacks the hilar area First lesion-Ghon’s focus If the lymphnode also involved along with Ghon’s focus- Ghon’s complex Ghon’s complex calcifies and forms Ranke’s complex In 95% ,TB infection is healed
  • 6. 2.Progressive primary tb: TB Bacilli may cause a local inflammatory reaction Usually seen in low immunity Symptoms:Fever,chronic cough,pneumonia like illness,erythema nodosum,phlyctenular conjunctivitis etc Seen in 1-2% of total primary TB cases 3.Latent tb: Bacilli is dormant Seen in 2-4 % of total primary tb cases
  • 7. Secondary/reactivation TB: Under stressors,Tb bacilli gets activated and cause cavitation This is delayed type -4 hypersensitivity reaction From cavities to bronchus,TB Bacilli may spread to others Approximately 40% of Indian population may have primary TB infection
  • 8. Chest X-ray Sputum Genotypic tests Culture methods Molecular tests Serological tests Tuberculin skin test
  • 9. 1. CHEST X-RAY  High sensitivity but poor specific ity Usually upper lobe disease with infiltrates and cavities
  • 10.
  • 11. 2. SPUTUM: Most sensitive and specific Done in designated microscopy centres 2 samples- spot sample and morning sample Checked within 24 hours Minimum 5ml of sputum should be collected Sputum should be expectorated- no.of squamous epithelial cells should be <10% in expectorated sputum Turn around time is -24 hours
  • 12. Types of sputum testing 1.Conventional method:Zeihl Neelsen staining is used 2.LED microscopy: ZN staining is used.Better than conventional method 3.Fluorescence microscopy: Auromine -O- Rhodamine stain is used. Best test
  • 13. 3. GENOTYPIC TESTS CBNAAT: Highly specific and good sensitivity Diagnostic and confirmatory Biggest advantage-Turn around time is 90 minutes(with in 2 hours) Rifampicin status also can be known. Machine is GeneX pert.
  • 14. TruNAAT: Indianized version of CBNAAT Less expensive Approved by NTEP Turn around time is 1 hour LINE PROBE ASSAY: Resistance pattern can be found FL LPA-Resistance to Isoniazid can be found SL LPA-Resistance to fluoroquinolones,second line injectables/drugs can be found
  • 15. Drug resistance Target region Isoniazid Inh A promoter,kat G Ethionamide Inh A promotor Fluoroquinolone gyr A,gyr B Amikacin,kanamycin, Capriom rrs, eis promotor
  • 16. 4. CULTURE METHODS:  Solid media: Egg based Lowenstein Jensen media Takes about 8-10 weeks  Liquid culture: Using BACTEC/MGIT method Kirchner media/Middle brook media Takes about 1-2 weeks
  • 17. 5. Molecular tests: BACTEC 460-Tells about C02 emission MGIT 960-Tells about O2 consumption and metabolism rate They are also used for DST. 6. Serological tests: IGRA test-Interferon gamma release assay Tells about primary or secondary TB Not for diagnosis of TB Used to diagnose latent TB in some countries Gives information about presence of TB bacilli
  • 18. Antigen-Antibody test and Quantiferon test: Gives information about TB infection not disease 7. TUBERCULIN SKIN TEST: Also known as pirquet test/Montoux test Uses 1 unit of ppd Not for diagnosis Read after 48 hours,within 96 hours Average time is 72 hours Wheal/flare raection
  • 19. >5mm HIV, severe immunosuppression,close cotacts of TB,h/0 prior TB >10mm Recent immigrants,IVDA,<4 yrs, Adolescents with exposure from high risk groups >15mm No risk factor
  • 20. Diagnosis in NTEP 1. Sputum for AFB 2. CXR 3. CBNAAT 4. TruNAAT 5. LPA 6. Liquid culture-Gold standard
  • 21. Laboratory turn around time: Solid culture Lowenstein – Jensen media 3 weeks-SP 4-8 weeks-SN Automated liquid culture BACTEC,MGIT 8-10 days-SP 2-6 weeks-SN Molecular testing Line probe assay for detection of drug resistance 1-3 days CBNAAT 2 hours TruNAAT 1 hour for TB detection and 1 hour for resistance detection
  • 22. 1962-National TB control program 1997-Revised national TB control program (RNTCP) DOTS(Directly observed treatment short course) was started 2020-National TB elimination program
  • 23. End TB(means to reduce TB death and incidence) Reduction in deaths by 90% by 2025 Reduction in TB incidence rate by 80% by 2025
  • 24. DEFINITION: 1. Presumptive TB case(TB suspect): Any person with c/o cough/fever/night sweats for >2 weeks with or without significant weight loss.
  • 25. 2. Drug sensitive tuberculosis: Sensitive to Rifampicin and Isoniazid. 3. Drug resistance H mono drug – only Isoniazid Multi drug resistance – Resistance to atleast H and R Polydrug resistance - Any two drugs resistance not including H and R XDR TB - Resistance to H and R + Any fluoroquinolone +Any group A second line(Bedaquiline,Linezolid (Previous- any 2nd line injectables)
  • 26. Pre XDR TB- Resistance to H and R +Any fluoroquinolone Presumptive MDR-ATT for >1month and default for >1 month or currently on ATT,poor response (no clinical improvement or sputum positive at 3rd or 5th month of follow up) or any contact of MDR case Recurrent TB (Relapse of TB) - cured after ATT .But now microbiologically confirmed sputum positive
  • 27. Presumptive TB case Sputum+NAAT+CXR Doing sputum test is minimum requirement If sputum test and NAAT are negative,CXR is normal- Rule out tb and refer If suputum is positive – microbiologically confirmed tb
  • 28.
  • 29.
  • 30.
  • 31.  First line drugs: Isoniazid,Rifampicin,Pyrazinamide, Ethambutol Second line drugs:
  • 32.
  • 33. Regimen Intensive phase Continuation phase Drug sensitive TB 2 HRZE 4 HRE H mono/poly drug regimen TB 6 ZER0 Shorter oral Bedaquiline containing regimen(Shorter MDR) 4-6 CHOBZEE Clofazimine,High dose Isoniazid,Levofloxacin ,Bedaquiline, Pyrazinamide, Ethambutol, Ethionamide,Bedaqui line is given for 6 months always 5 C0ZE Clofazamine Levofloxacin Pyrazinamide Ethambutol
  • 34. Longer MDR/XDR TB 18-20 L2C2BDQ Levofloxacin,Linezolid ,Clofazimine, Cycloserine,Bedaquili ne
  • 35. Cinformed absence of resistance to or lack of suspicion of the ineffectiveness of a drug in the shorter MDR-TB regimen No H/O exposure to one or more second line drugs used in the shorter MDR TB regimen for >1month R resistant TB MDR TB with R resistance and single gene mutation H resistance
  • 36.  Patients started on TB treatment becomes 50-80% non-infectious within 48 hours of taking Rifampicin and >95% non-infectious by 2 weeks
  • 37. 5 weight bands for adults Weight category Intensive phase(no.of FDC tablets) Continuation phase(no.of FDC tabs) 25-34 Kg 2 2 35-49 Kg 3 3 50-64 Kg 4 4 65-75 Kg 5 5 > 75 Kg 6 6
  • 38.  FDC contains Isoniazid-75mg Rifampicin-150mg Pyrazinamide-400mg Ethionamide-275 mg  FDC dosage chart for children has 6 weight bands H-50 mg R-75mg Z-150 mg Ethionamide is given separately
  • 39.  Bedaquiline – Week 0-2- 400mg daily Week 3-24- 200mg 3 times /week BPaL Regimen:  Bedaquiline,Pretomanid,Linezolid  Advocated by WHO  Taken up by few districts under NTEP  Given if there is flouroquinolone resistance and there is no exposure (< 2 weeks exposure to Bedaquiline/Linezolid)
  • 40.  Dosage- Pretomanid-200mg once daily for 26 weeks Bedaquiline – 400mg once daily for the first 2 weeks 200mg three times a week for the next 24 weeks Linezolid-1200mg once daily for 24 weeks
  • 41.
  • 42. HIV associated TB Early intiation of ART during anti TB treatment is advised ART should be started within the first 8 weeks of anti-TB treatment ART should be started with in 2 weeks Of TB treatment for profoundly immunocompromised patients with CD4+ T cell count of <50/mcL
  • 43. Clinical evaluation: Height Weight Physical examination Psychiatry evaluation if required Laboratory based evaluation: HIV testing following counselling Liver function tests,RBS,CBP,S.electrolytes,Urine pregnancy test in women of reproductive age,ECG
  • 44.
  • 45.
  • 46.
  • 47.  Old regimen: Isoniazid-300mg *6 months Newer regimen:  Drug sensitive TB: Shorter TPT(TB preventive treatment):3 months of weekly Rifapentine and Isoniazid  Drug resistant TB: R resistant, FQ sensitive-6 months of daily Levofloxacin H resistant,R sensitive-4 months of Rifampicin
  • 48. Persons on TPT will be monitored for clinical and laboratory parameters as below:  Screening with symptoms(cough,fever,night sweats,weight loss)  Any side effects  If any sign or symptom,the person may be referred to the nearby TB centre and evaluated for active TB/Drug resistant TB