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1

 

 

PULMONARY TB

 

ETIOLOGY

 

M. tuberculosis, is the most important cause of tuberculosis disease in 

 

humans. 

bacilli are non-spore-forming, nonmotile, weakly gram-positive curved 

 

rods  obligate aerobes that grow in synthetic media containing glycerol as 

 

the carbon source and ammonium salts as the nitrogen source 

 

(Loewenstein-Jensen culture media).

A hallmark of all mycobacteria is acid fastness 

 

-

 

Growth 3–6 wk

 ,

 

drug susceptibility testing 4 wk

 .

 

-

 

Growth can be detected in 1–3 wk in selective liquid medium 

using radiolabeled nutrients (the BACTEC radiometric system

.)

 

-

rapid test by nucleic acid amplification (NAA) tests(PCR

.)

 

 

EPIDEMIOLOGY

 

Latent tuberculosis infection (LTBI) :-occurs after the inhalation of infective 
droplet nuclei containing M. tuberculosis. A reactive tuberculin skin test 

and the absence of clinical and radiographic manifestations

 

 .

 

 

tuberculosis ( disease):-  occurs when clinical or radiographic changes 
become apparent. Untreated  LTBI  40% → tuberculosis

 

 

 

 


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2

 

 

Transmission

 

person to person,  airborne mucus droplet nuclei, particles 1–5 μm in diameter that 
contain M.TB

  

 

 

 

The chance of transmission increases

1-patient has an acid-fast smear of sputum

 

 

-

extensive upper lobe infiltrate or cavity

 

2-

 

-

3-copious production of thin sputum

 

 

-

4-severe and forceful cough

 

 

-

Environmental factors( poor air circulation

)

5-

 

 

Most adults no longer transmit the organism within 2 weeks after 
adequate chemotherapy

 

person to person,  airborne mucus droplet nuclei, particles 1–5 μm in 
diameter that contain M.TB

  

 

The chance of transmission increases

:

-

 

 

 

-

patient has an acid-fast smear of sputum

.

 

 

-

extensive upper lobe infiltrate or cavity

 .

 

-

copious production of thin sputum

.

 

 

-

severe and forceful cough

.

 

 

-

Environmental factors( poor air circulation

.)

 

Most adults no longer transmit the organism within 2 weeks after 
adequate chemotherapy

 

 

 


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3

 

 

 

PATHOGENESIS

 

The primary complex of tuberculosis includes

 

 

local infection and the regional lymph nodes

 

 .

 

The lung is the portal of entry in >98% of cases

 .

 

The tubercle bacilli multiply initially within alveoli and alveolar ducts

 ..

 

The tissue reaction in the lung parenchyma and

 

 

lymph nodes intensifies over the next 2–12 wk as

 

 

the organisms grow in number and tissue

 

 

hypersensitivity develops

 

Immunity

 

tubercle bacilli replicate

 

 

Cell-mediated immunity develops 2–12 wk after infection, along with 

tissue hypersensitivity

.

 

mycobacterial antigen load

;

 

cell-mediated immunity, which enhances intracellular killing& tissue 
hypersensitivity which promotes extracellular killing

 

.

 

heals completely by fibrosis or calcification  Occasionally

:

-

  

 

focal pneumonitis and pleuritis, cavity , collapse-consolidation or 
segmental lesion

 

 

 


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4

 

 

 

Pregnancy and the Newborn

  

 

  

 

Congenital tuberculosis is rare

 .

 

A- lesion in the placenta through the umbilical vein

 .

 

B- aspiration or ingestion of infected amniotic fluid

 .

 

C- the most common route of infection for the neonate is postnatal airborne 
transmission from an adult with infectious pulmonary tuberculosis

 

The Mantoux tuberculin skin test

 

-

is the intradermal injection of 0.1 mL(5 tuberculin units) of purified 

protein derivative (PPD

.)

 

-

 

induce induration through local vasodilatation, edema, fibrin deposition, 

and recruitment of other inflammatory cells to the area

 .

 

-

The amount of induration should be measured by a trained person 48–72 

hr after administration

  .

 

-

Tuberculin sensitivity develops 3 wk to 3 mo—most often in 4–8 wk—

after inhalation of organisms

.

 

Y interferon

 

CLINICAL MANIFESTATIONS AND DIAGNOSIS

 

Tuberculosis infection   :- no signs or symptoms, Occasionally,  low-grade 

fever and mild cough

.

 

Primary Pulmonary Disease

 

The primary complex includes the parenchymal pulmonary focus and the 

regional lymph nodes

 .

 

About 70% of lung foci are subpleural, and localized pleurisy is common

 


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5

 

 

The usual sequence is hilar lymphadenopathy, focal hyperinflation, and 
then atelectasis.  collapse-consolidation or segmental TB . endobronchial 
tuberculosis . lobar pneumonia , thin-walled primary tuberculosis cavity

 

>

55

 %

of infants and children have  no physical finding

 .

 

 

Nonproductive cough and mild dyspnea ,  fever

,

 

 

night sweats, anorexia, decreased activity

 

 ,

 

failure-to-thrive

 .

 

 

Occasionally residual calcification of the primary

 

 

focus or regional lymph nodes

.

 

The appearance of calcification ( least 6–12 mo

)

 

Diagnosis

 

isolation of M. tuberculosis (for culture and smear staining

:)

-

 

  

-

Sputum specimens

 

   

-

Induce sputum with a jet nebulizer and chest          percussion followed 

by nasopharyngeal              suctioning (1 mo

 .)

 

  

-

in young children is the early morning gastric acid obtained before the 

child has arisen

.

 

 

3

 

consecutive morning gastric aspirates yield the organisms in <50% of 
cases

 

Negative cultures never exclude the diagnosis of tuberculosis in a child

.

 

positive tuberculin skin test +abnormal chest

 

 

radiograph consistent with tuberculosis + history of

 

 

contact→TB

.

 


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6

 

 

 

Miliary tuberculosis

 

usually complicates the primary infection,2–6 mo

 .

 

most common in infants & young children

,

 

 

malnourished or immunosuppressed patients

.

 

Lesions are  more numerous in the lungs, spleen

,

 

 

liver, and bone marrow than other tissues

.

 

Fever, wt loss, anorexia, Lymphadenopathy

,

 

 

hepatosplenomegali, Resp. feature late

.

 

 

 

. Biopsy of the liver or bone marrow with appropriate 

Diagnosis
bacteriologic and histologic examinations more often yields an 

early diagnosis

.

 

CXR  miliary pattern 2-3 mm nodules

 

 

Perinatal TB

 

2nd-3rd week

 

-

fever, resp. distress, poor feeding

 

-

FTT

.

 

Lymphadenopathy, hepatosplenomegali

 

-

CXR  hilar& mediastinal  LN, lung infilterate

.

 

DD congenital infection

.

 


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7

 

 

Treatment

 

The standard therapy of intrathoracic tuberculosis is a

 

 

6

 

mo : isoniazid and rifampin + pyrazinamide in

 

 

the 1st 2 mo .100%

 

 

Nine month regimens of isoniazid and rifampin

.

 

INH resistance recommend adding a 4th drug—usually streptomycin, ethambutol, or 

ethionamide—to the initial regimen

.

 

DOT directly observed therapy

 

 

intermittent (twice weekly) administration of drugs after an initial period as short as 

2 wk of daily therapy is as effective in children as daily therapy for the entire course

.

 

LATENT TUBERCULOSIS INFECTION

 

 

9 mo of isoniazid, once a day

 

If daily therapy is not possible, DOT twice a week can be used for 9 mo

 

rifampin, once a day

 

Supportive Care

.

 

 

adequately treated

 .

 

Adequate nutrition

 

Prevention

 

BCG is 50% effective in preventing pulmonary tuberculosis

.

 

The protective effect for disseminated and meningeal tuberculosis is 
slightly higher, with BCG preventing 50–80% of cases

 

 




رفعت المحاضرة من قبل: Mohammed Musa
المشاهدات: لقد قام عضوان و 97 زائراً بقراءة هذه المحاضرة








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