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TUBERCULOSIS(Part 2)
Dr Ruchi Dua
Associate Professor(MD,DNB)
Department of Pulmonary Medicine
Aiims Rishikesh
MCQ & Revision of Part 1
OBJECTIVES
• What are complications of tuberculosis?
• What are various presentations of EPTB?
• Drug resistant tuberculosis
• DOTS & RNTCP
COMPLICATIONS
COMPLICATIONS
• Local-
• ARDS/respiratory failure
• Bronchiectasis/PTOAD
• aspergilloma
• haemoptysis (symp )
• Pleural -Empyema/pneumo
• Extensive lung destruction
• Rt middle lobe syndrome
• Scar ca
• Systemic-
• shock
• amyloidosis
• disseminated tb-(laryngeal tb)
• Cor-pulmonale
EPTB
• Common sites:LN,PE
• Any site
• Diagnosis:more difficult
LN TB
•LN-site
•painless enlargement
,systemic symptoms<50%
•Matting
•Sinus/fistula
•FNAC/Bx/NAAT/smear/culture
Pleural Effusion
• Pain/dyspnea/cough
• Fever/dec appetite
• Radiology
• Pleural fluid analysis
SKELETAL TB
•Site
•Pain/joint swelling/dec
range of motion.
•Draining sinuses and
abscesses
•Systemic symptoms
•Radiographic changes
m/b nonspecific
CNS TB
• Tuberculous meningitis(MC), intracranial tuberculomas, , cranial
nerve palsies and communicating hydrocephalus , cranial vasculitis
may lead to focal neurologic deficits.
• Malaise, headache, fever, or personality change,A/S,seizures/focal
defects
• CSF –lymphocytic,increased protein,ADA,CB NAAT
Koch’s abdomen
•Site-gut/peritoneum/LN
•pain,nausea/vomitting
•altered bowel habbits
•Distension
•Diagnosis:ascetic fluid
analysis/LN
sampling/radiology
Miliary
• Fever/dec appetite/wt loss/vague-elderly
• Haematogenous
• Fulminant disease -septic shock, ARDS,MOF
• CXR/Liver/spleen BX/BM
• Haematological-anaemia(NCNC),hyponatremia
PRESENTATION(Extra-Pulmonary)
• Genitourinary-infertility, urinary difficulties
• CVS-pericarditis(pain/dyspnea)
CLINICAL CLUES-EPTB
• Ascites -lymphocyte predominance and negative bacterial cultures
• Chronic lymphadenopathy (especially cervical)
• CSF -lymphocytic pleocytosis / elevated protein /low glucose
• Pleural effusion -Exudative / lymphocyte predominance/negative bacterial cultures
• Joint inflammation (monoarticular) with negative bacterial cultures
• Persistent sterile pyuria
• Unexplained pericardial effusion, constrictive pericarditis, or pericardial
calcification/Vertebral osteomyelitis involving the thoracic spine
MANAGEMENT
Principles of chemotherapy
• Variable bacilli population:rapid growers,slow growers,dormant
• Longer duration
• 2 phases of treatment
• Need for multiple drugs to treat(spontaneous resistance)
TREATMENT REGIMENS
Type of TB case Intensive Phase Continuation Phase
New(CAT 1) 2RHEZ 4RHE
Retreatment(CAT 2) 2SHREZ/1RHEZ 5RHE
R;rifampicin,H:isoniazid,E:ethambutal,Z:pyrazinamide,S:streptomyci
n
Intermittent regimens
are being changed to
daily regimens under
RNTCP in India
• New case:CAT 1
• Smear positive
• Smear negative
• EPTB
• Retreatment:CAT 2
• Relapse
• Defaulter
• failure
• CAT 4 :MDR
• CAT 5:XDR
• Definitions
• MDR:R and H
• XDR:R and H,any FQ,any injectables(kanamycin,amikacin,capreomycin)
• Primary & acquired resistance
• Mono/poly drug resistance:DRTB
Drug Resistance:Magnitude
• 3% Primary
• 12% Acquired
• XDR 4-20% of MDR
Dx in drug resistant Tb
• MDR-TB:
• Rapid Molecular Test ( LPA/ CB-NAAT)
• Liquid Culture & DST
• Solid Culture & DST
• XDR-TB:
• Liquid Culture & DST
• Solid Culture & DST
• LPA(Genotypic methods)
Changed to
daily
OLD
Grouping of antiTb drugs(2017 ,RNTCP
guidelines)
FQ Levo/moxi/gati
Injectable agents K/A/C
Other second line drugs Etio/prothio/cycloserine/linezolid
Add on drugs D1:Z/E/H high dose,D2:Bedaquiline/delaminid
D3:PAS,Amoxy-clav,Meropenem,imipenem
cilastatin
RNTCP 2017
DR TB:Principles of Treatment
• MDR:4 second line drugs /not used
• XDR:7 drugs
• Duration:24(MDR),36(XDR)
DOTS plus previously
Second line drugs
• Treatment longer
• Toxic
• Expensive
• Stress:emergence rather than treatment of DRTb
more
Newer ATT
• Bedaquiline
• Delaminid
• protaminid
MCQ
• A pt on ATT C/O burning soles
• A pt on ATT C/O loss of appetite & vomittings
• A pt on ATT C/O dec vision
DOTS & RNTCP
Advantages
• Directly observed
• Standardised treatment
• Free of cost
TB & HIV
• Increased chances of reactivation/relapse
• Atypical presentations
• Higher ADR/drug interactions
• Priorty to treat Tb first and then ART
TB & DM
• Higher risk
• Glycemic control must for cure
• Higher chances of ADR

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535nnn,nhrggfdfhddsgyddyreyrrfeesg5sfgrsfg_tb_2.pptx

  • 1. TUBERCULOSIS(Part 2) Dr Ruchi Dua Associate Professor(MD,DNB) Department of Pulmonary Medicine Aiims Rishikesh
  • 2. MCQ & Revision of Part 1
  • 3. OBJECTIVES • What are complications of tuberculosis? • What are various presentations of EPTB? • Drug resistant tuberculosis • DOTS & RNTCP
  • 5. COMPLICATIONS • Local- • ARDS/respiratory failure • Bronchiectasis/PTOAD • aspergilloma • haemoptysis (symp ) • Pleural -Empyema/pneumo • Extensive lung destruction • Rt middle lobe syndrome • Scar ca
  • 6. • Systemic- • shock • amyloidosis • disseminated tb-(laryngeal tb) • Cor-pulmonale
  • 7. EPTB • Common sites:LN,PE • Any site • Diagnosis:more difficult
  • 8. LN TB •LN-site •painless enlargement ,systemic symptoms<50% •Matting •Sinus/fistula •FNAC/Bx/NAAT/smear/culture
  • 9. Pleural Effusion • Pain/dyspnea/cough • Fever/dec appetite • Radiology • Pleural fluid analysis
  • 10. SKELETAL TB •Site •Pain/joint swelling/dec range of motion. •Draining sinuses and abscesses •Systemic symptoms •Radiographic changes m/b nonspecific
  • 11. CNS TB • Tuberculous meningitis(MC), intracranial tuberculomas, , cranial nerve palsies and communicating hydrocephalus , cranial vasculitis may lead to focal neurologic deficits. • Malaise, headache, fever, or personality change,A/S,seizures/focal defects • CSF –lymphocytic,increased protein,ADA,CB NAAT
  • 12. Koch’s abdomen •Site-gut/peritoneum/LN •pain,nausea/vomitting •altered bowel habbits •Distension •Diagnosis:ascetic fluid analysis/LN sampling/radiology
  • 13. Miliary • Fever/dec appetite/wt loss/vague-elderly • Haematogenous • Fulminant disease -septic shock, ARDS,MOF • CXR/Liver/spleen BX/BM • Haematological-anaemia(NCNC),hyponatremia
  • 14. PRESENTATION(Extra-Pulmonary) • Genitourinary-infertility, urinary difficulties • CVS-pericarditis(pain/dyspnea)
  • 15. CLINICAL CLUES-EPTB • Ascites -lymphocyte predominance and negative bacterial cultures • Chronic lymphadenopathy (especially cervical) • CSF -lymphocytic pleocytosis / elevated protein /low glucose • Pleural effusion -Exudative / lymphocyte predominance/negative bacterial cultures • Joint inflammation (monoarticular) with negative bacterial cultures • Persistent sterile pyuria • Unexplained pericardial effusion, constrictive pericarditis, or pericardial calcification/Vertebral osteomyelitis involving the thoracic spine
  • 17. Principles of chemotherapy • Variable bacilli population:rapid growers,slow growers,dormant • Longer duration • 2 phases of treatment • Need for multiple drugs to treat(spontaneous resistance)
  • 18. TREATMENT REGIMENS Type of TB case Intensive Phase Continuation Phase New(CAT 1) 2RHEZ 4RHE Retreatment(CAT 2) 2SHREZ/1RHEZ 5RHE R;rifampicin,H:isoniazid,E:ethambutal,Z:pyrazinamide,S:streptomyci n Intermittent regimens are being changed to daily regimens under RNTCP in India
  • 19. • New case:CAT 1 • Smear positive • Smear negative • EPTB • Retreatment:CAT 2 • Relapse • Defaulter • failure
  • 20. • CAT 4 :MDR • CAT 5:XDR • Definitions • MDR:R and H • XDR:R and H,any FQ,any injectables(kanamycin,amikacin,capreomycin) • Primary & acquired resistance • Mono/poly drug resistance:DRTB
  • 21. Drug Resistance:Magnitude • 3% Primary • 12% Acquired • XDR 4-20% of MDR
  • 22. Dx in drug resistant Tb • MDR-TB: • Rapid Molecular Test ( LPA/ CB-NAAT) • Liquid Culture & DST • Solid Culture & DST • XDR-TB: • Liquid Culture & DST • Solid Culture & DST • LPA(Genotypic methods)
  • 24.
  • 25. OLD
  • 26. Grouping of antiTb drugs(2017 ,RNTCP guidelines) FQ Levo/moxi/gati Injectable agents K/A/C Other second line drugs Etio/prothio/cycloserine/linezolid Add on drugs D1:Z/E/H high dose,D2:Bedaquiline/delaminid D3:PAS,Amoxy-clav,Meropenem,imipenem cilastatin
  • 28.
  • 29. DR TB:Principles of Treatment • MDR:4 second line drugs /not used • XDR:7 drugs • Duration:24(MDR),36(XDR) DOTS plus previously
  • 30. Second line drugs • Treatment longer • Toxic • Expensive • Stress:emergence rather than treatment of DRTb more
  • 31. Newer ATT • Bedaquiline • Delaminid • protaminid
  • 32. MCQ • A pt on ATT C/O burning soles • A pt on ATT C/O loss of appetite & vomittings • A pt on ATT C/O dec vision
  • 34. Advantages • Directly observed • Standardised treatment • Free of cost
  • 35. TB & HIV • Increased chances of reactivation/relapse • Atypical presentations • Higher ADR/drug interactions • Priorty to treat Tb first and then ART
  • 36. TB & DM • Higher risk • Glycemic control must for cure • Higher chances of ADR