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Tuberculosis
Qom university of medical science
Aliakbar Mohammadi
extern
The biggest cause of death among infectious
disease
1/3 of people worldwide are infected
1.5 to 2 million people die every year
resistence
Importance
Mycobacterium tuberculosis
Mycobacterium bovis
Mycobacterium africanum
...
ETIOLOGIC AGENT
Infectious: No clinical sign or symptom
Disease: signs and symptoms
Infection VS disease
M. tuberculosis is most commonly transmitted from
a person with infectious pulmonary TB by droplet
nuclei.
Those with culture-negative pulmonary TB and
extrapulmonary TB are essentially noninfectious.
Source of infection
the risk of developing disease after being infected
depends largely on endogenous factors.
Disease
About one-third of patients died within 1 year after
diagnosis.
More than 50% died within 5 years.
The 5-year mortality rate among sputum smear–
positive cases was 65%.
 Of the survivors at 5 years, ~60% had undergone
spontaneous remission.
NATURAL HISTORY OF DISEASE
PATHOGENESIS AND IMMUNITY
In fact, cases of active TB are often accompanied
by strongly positive skin-test reactions. There is also
evidence of reinfection with a new strain of M.
tuberculosis in patients previously treated for active
disease. This evidence underscores the fact that
previous latent or active TB may not confer fully
protective immunity.
Pulmonary
Extrapulmonary
Both
CLINICAL MANIFESTATIONS
Primary
Postprimary (adult-type, secondary).
PULMONARY TB
Soon after the initial infection with tubercle bacilli
 May be asymptomatic
Fever
pleuritic chest pain
often seen in children
middle and lower lung zones
hilar or paratracheal lymphadenopathy
erythema nodosum on the legs
Primary Disease
In the majority of cases, the lesion heals
Spontaneously
In young children and persons with impaired
immunitymay progress rapidly to clinical illness
Pleural effusion
Necrosis and cavitation in primary site
Enlarged lymph nodes may compress bronchi
obstruction
Pneumonia
Disseminated or miliary disease
Tuberculous meningitis
Reactivation
Re-infection
Postprimary (Adult-Type) Disease
Apical and posterior segments of the upper lobes
Superior segments of the lower lobes
Infiltrates to extensive cavitary disease
Pneumonia
Symptoms and signs are often nonspecific and,
consisting mainly of diurnal fever and night sweats
due to defervescence, weight loss, anorexia,
general malaise, and weakness.
Postprimary (Adult-Type) Disease
In up to 90% of cases cough eventually develops
often initially nonproductive and limited to the
morning and subsequently accompanied by the
production of purulent sputum.
Hemoptysis (in 20–30%)
Pleuritic chest pain
Dyspnea
Physical findings are of limited use in pulmonary
TB.
Rales
Rhonchi
mild anemia leukocytosis, and thrombocytosis with
a slightly elevated erythrocyte sedimentation rate
and/or C-reactive protein level.
lymph nodes
Pleura
genitourinary tract
Bones and joints
Meninges
Peritoneum
Pericardium
EXTRAPULMONARY TB
painless swelling of the lymph nodes
commonly at posterior cervical and supraclavicular
sites
Associated pulmonary disease is present in fewer
than 50% of cases
The diagnosis is established by fine-needle
aspiration biopsy (with a yield of up to 80%) or
surgical excision biopsy.
Lymph Node TB (Tuberculous
Lymphadenitis)
~20% of extrapulmonary cases
The effusion may be small, remain unnoticed, and
resolve spontaneously or may be sufficiently large
to cause symptoms such as fever, pleuritic chest
pain, and dyspnea.
dullness to percussion and absence of breath
sounds.
Pleural TB
Determination of the pleural concentration of
adenosine deaminase (ADA) may be a useful
screening test, and TB may be excluded if the
value is very low.
Hoarseness
Dysphonia
Dysphagia
Chronic productive cough
Acid-fast smear
Biopsy
TB of the Upper Airways
~10–15% of all extrapulmonary cases
Urinary frequency
Dysuria
Nocturia
Hematuria
Flank or abdominal pain
Culture of three morning urine specimens yields a
definitive diagnosis in nearly 90% of cases.
Genitourinary TB
~10% of extrapulmonary cases
Weight-bearing joints
Aspiration of the abscess or bone biopsy confirms
the tuberculous etiology
Skeletal TB
The key to the diagnosis of TB remains a high
index of suspicion.
AFB MICROSCOPY
low sensitivity (40–60%)
inexpensive
two or three sputum specimens, preferably
collected early in the morning, should be
submitted to the laboratory.
DIAGNOSIS
MYCOBACTERIAL CULTURE
Definitive diagnosis
2–3 weeks
DRUG SUSCEPTIBILITY TESTING
to isoniazid and rifampin
RADIOGRAPHIC PROCEDURES
chest radiographic
CT scan
Tuberculin Skin Testing
lack of mycobacterial species specificity
False-positive reactions may be caused by
infections with nontuberculous mycobacteria and
by BCG vaccination.
limited value in the diagnosis of active TB
DIAGNOSIS OF LATENT M.
TUBERCULOSIS INFECTION
 to prevent morbidity and death by curing TB while
preventing the emergence of drug resistance
to interrupt transmission by rendering patients
noninfectious.
TREATMENT
Four major drugs are considered first-line agents
for the treatment of TB: isoniazid, rifampin,
pyrazinamide, and ethambutol
DRUGS
(1) the fluoroquinolone antibiotics;
(2) the injectable aminoglycosides kanamycin,
amikacin, and streptomycin;
(3) the injectable polypeptide capreomycin and the
oral agents
(4) Ethionamide and prothionamide
(5) cycloserine and terizidone (therizidone),
(6) PAS (para-aminosalicylic acid)
SECONED LINE
Standard short-course regimens are divided into an
initial, or bactericidal, phase and a continuation, or
sterilizing, phase.
The treatment regimen of choice for virtually all
forms of drug-susceptible TB in adults consists of a
2-month initial (or intensive) phase of isoniazid,
rifampin, pyrazinamide, and ethambutol followed
by a 4-month continuation phase of isoniazid and
rifampin
REGIMS
Harrisons-Principles-of-Internal-Medicine,-19th-
Edition
REFERENCE
Thanks FoR YOUR ATTENTION

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Tuberculosis

  • 1. Tuberculosis Qom university of medical science Aliakbar Mohammadi extern
  • 2. The biggest cause of death among infectious disease 1/3 of people worldwide are infected 1.5 to 2 million people die every year resistence Importance
  • 3.
  • 4.
  • 6. Infectious: No clinical sign or symptom Disease: signs and symptoms Infection VS disease
  • 7. M. tuberculosis is most commonly transmitted from a person with infectious pulmonary TB by droplet nuclei. Those with culture-negative pulmonary TB and extrapulmonary TB are essentially noninfectious. Source of infection
  • 8.
  • 9. the risk of developing disease after being infected depends largely on endogenous factors. Disease
  • 10.
  • 11. About one-third of patients died within 1 year after diagnosis. More than 50% died within 5 years. The 5-year mortality rate among sputum smear– positive cases was 65%.  Of the survivors at 5 years, ~60% had undergone spontaneous remission. NATURAL HISTORY OF DISEASE
  • 13. In fact, cases of active TB are often accompanied by strongly positive skin-test reactions. There is also evidence of reinfection with a new strain of M. tuberculosis in patients previously treated for active disease. This evidence underscores the fact that previous latent or active TB may not confer fully protective immunity.
  • 16. Soon after the initial infection with tubercle bacilli  May be asymptomatic Fever pleuritic chest pain often seen in children middle and lower lung zones hilar or paratracheal lymphadenopathy erythema nodosum on the legs Primary Disease
  • 17. In the majority of cases, the lesion heals Spontaneously In young children and persons with impaired immunitymay progress rapidly to clinical illness Pleural effusion Necrosis and cavitation in primary site Enlarged lymph nodes may compress bronchi obstruction
  • 18. Pneumonia Disseminated or miliary disease Tuberculous meningitis
  • 19.
  • 20.
  • 22. Apical and posterior segments of the upper lobes Superior segments of the lower lobes Infiltrates to extensive cavitary disease Pneumonia Symptoms and signs are often nonspecific and, consisting mainly of diurnal fever and night sweats due to defervescence, weight loss, anorexia, general malaise, and weakness. Postprimary (Adult-Type) Disease
  • 23. In up to 90% of cases cough eventually develops often initially nonproductive and limited to the morning and subsequently accompanied by the production of purulent sputum. Hemoptysis (in 20–30%) Pleuritic chest pain Dyspnea
  • 24. Physical findings are of limited use in pulmonary TB. Rales Rhonchi mild anemia leukocytosis, and thrombocytosis with a slightly elevated erythrocyte sedimentation rate and/or C-reactive protein level.
  • 25. lymph nodes Pleura genitourinary tract Bones and joints Meninges Peritoneum Pericardium EXTRAPULMONARY TB
  • 26. painless swelling of the lymph nodes commonly at posterior cervical and supraclavicular sites Associated pulmonary disease is present in fewer than 50% of cases The diagnosis is established by fine-needle aspiration biopsy (with a yield of up to 80%) or surgical excision biopsy. Lymph Node TB (Tuberculous Lymphadenitis)
  • 27. ~20% of extrapulmonary cases The effusion may be small, remain unnoticed, and resolve spontaneously or may be sufficiently large to cause symptoms such as fever, pleuritic chest pain, and dyspnea. dullness to percussion and absence of breath sounds. Pleural TB
  • 28. Determination of the pleural concentration of adenosine deaminase (ADA) may be a useful screening test, and TB may be excluded if the value is very low.
  • 30. ~10–15% of all extrapulmonary cases Urinary frequency Dysuria Nocturia Hematuria Flank or abdominal pain Culture of three morning urine specimens yields a definitive diagnosis in nearly 90% of cases. Genitourinary TB
  • 31. ~10% of extrapulmonary cases Weight-bearing joints Aspiration of the abscess or bone biopsy confirms the tuberculous etiology Skeletal TB
  • 32. The key to the diagnosis of TB remains a high index of suspicion. AFB MICROSCOPY low sensitivity (40–60%) inexpensive two or three sputum specimens, preferably collected early in the morning, should be submitted to the laboratory. DIAGNOSIS
  • 33. MYCOBACTERIAL CULTURE Definitive diagnosis 2–3 weeks DRUG SUSCEPTIBILITY TESTING to isoniazid and rifampin RADIOGRAPHIC PROCEDURES
  • 35. Tuberculin Skin Testing lack of mycobacterial species specificity False-positive reactions may be caused by infections with nontuberculous mycobacteria and by BCG vaccination. limited value in the diagnosis of active TB DIAGNOSIS OF LATENT M. TUBERCULOSIS INFECTION
  • 36.  to prevent morbidity and death by curing TB while preventing the emergence of drug resistance to interrupt transmission by rendering patients noninfectious. TREATMENT
  • 37. Four major drugs are considered first-line agents for the treatment of TB: isoniazid, rifampin, pyrazinamide, and ethambutol DRUGS
  • 38. (1) the fluoroquinolone antibiotics; (2) the injectable aminoglycosides kanamycin, amikacin, and streptomycin; (3) the injectable polypeptide capreomycin and the oral agents (4) Ethionamide and prothionamide (5) cycloserine and terizidone (therizidone), (6) PAS (para-aminosalicylic acid) SECONED LINE
  • 39. Standard short-course regimens are divided into an initial, or bactericidal, phase and a continuation, or sterilizing, phase. The treatment regimen of choice for virtually all forms of drug-susceptible TB in adults consists of a 2-month initial (or intensive) phase of isoniazid, rifampin, pyrazinamide, and ethambutol followed by a 4-month continuation phase of isoniazid and rifampin REGIMS
  • 41. Thanks FoR YOUR ATTENTION