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    Diagnosis of Pulmonary

    Tuberculosis

    Presenter: 4A Ri

    Sep. 29,2008

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    Why diagnosis important?

    Diagnosis of tuberculosis in most cases clinical diagnosis based upon the clinical presentation

    (hx & PE)

    In 15-20% of pt with suspected TB lab confirmation never obtained

    Early diagnosis and initiation of effectivetherapy

    reducing morbidity and mortality from TB

    minimize the spread of infection

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    Outline

    Screening for prior infection

    Tuberculin skin test

    Diagnosis of pulmonary TB Medical history

    Physical examination

    Chest radiograph

    Bacteriologic exam

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    Screening for prior infectionTuberculin skin test

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    Screening for prior infection

    Whom to screen High prevalence and high risk population

    (HIV)

    How to screen Mantoux tuberculin test (ie, purified protein

    derivative or PPD, tuberculin skin test)

    How to interpret Determine maximum diameter of indurationby palpation

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    Mantoux Tuberculin Test

    Preferred method of testing for TBinfection in adults and children

    Tuberculin skin testing useful for Examining person who is not ill but may be

    infected

    Determining how many people in group are

    infected

    Examining person who has symptoms of TB

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    Mantoux test

    Inject intradermally0.1 ml of 5TU PPDtuberculin

    Produce wheal 6 mmto 10 mm in diameter

    Represent DTH

    (delayed typehypersensitivity)

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    Reading ofMantoux test

    Read reaction 48-72hours after injection

    Measure onlyinduration

    Record reaction inmm

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    Classifying the tuberculin reaction

    >5 mm is classified as positive in

    HIV-positive persons

    Recent contacts of TB case Persons with fibroticchanges on CXR

    consistent with old healed TB

    Patients with organ transplants and other

    immunosuppressed patients

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    Classifying the tuberculin reaction

    >10 mm is classified as positive in Recent arrivals from high-prevalence

    countries

    Injection drug users Residents and employees of high-risk settings

    Mycobacteriology laboratory personnel

    Persons with clinicalconditions that placethem at high risk

    Children

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    Classifying the tuberculin reaction

    >15 mm is classified as positive in

    Persons with no known risk factors for TB

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    Factors may affect TST

    False negative Faulty application

    Anergy

    Acute TB (2-10 wks to convert) Very youngage (< 6 months old)

    Live-virus vaccination

    Overwhelming TB disease

    False positive BCG vaccination (usually

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    Boosting

    Some people with LTBI may havenegative skin test reaction when tested

    years after infection Initial skin test may stimulate (boost)ability to react to tuberculin

    Positive reactions to subsequent tests maybe misinterpreted as a new infection

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    Two-Step Testing

    Use two-step testing for initial skin testingof adults who will be retested within 1-3weeks

    If first test (+), consider the person infected

    If first test (-), give second test 1-3 weeks later

    If second test (+), consider person infected

    If second test (-), consider person uninfected

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    Screening for prior infection

    5020 80% TST

    ,TST

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    Diagnosis of Pulmonary TB

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    Diagnosis of disease

    Medical history

    Physical examination Chest radiograph

    Bacteriologic exam

    AFS Culture

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    Medical History

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    Medical History

    Symptoms of disease

    History of TB exposure, infection, or

    disease Past TB treatment

    Demographic risk factors for TB

    Medicalconditions that increase risk forTB disease

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    Medical History

    High prevalence population

    More likely to be exposed to and infected withbacillus

    Immigrant from high prevalence area

    Resident or worker in jail

    Long term care facility

    Close contact to pt with active TB

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    Medical History

    High risk population More likely to progress from infection to active TB

    HIV (+) or other immunodeficiency

    CRF DM

    IVDA

    Alcoholics

    Malnourished

    Malignancy

    Gastrectomy

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    Ph

    ysical Examination

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    Physical Examination

    Productive, prolonged cough duration of ~3 weeks

    Chest pain

    Hemoptysis Fever/Chills

    Night sweats

    Appetite loss

    Weight loss

    Easily fatigued

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    Chest radiograp

    hy

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    Chest radiography

    Classical radiograph appearance Infiltration

    Cavitation

    Fibrosis with traction Enlargement of hilar and mediastinallymph node

    In reactivaiton TB

    Classically fibrocavitary apical disease

    Primary TB Middle or lower lobe consolidation

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    Chest radiography

    Abnormalities oftenseen in apical orposterior segments of

    upper lobe orsuperior segments oflower lobe

    May have unusualappearance in HIV-positive persons

    Cannot confirmdiagnosis of TB!!

    cavity in patients RULclassic" for adult-type, reactivation tuberculosis

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    Classic adult TB CXR

    PA view

    diffuse parenchymaldisease with multiplecavities and bullaformation on the left

    Sputum smear waspositive for AFB

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    Chest radiography

    No chest X-ray pattern is absolutelytypical of TB

    10-15% of culture-positive TB patients notdiagnosed by X-ray

    40% of patients diagnosed as having TBon the basis of x-ray alone do not haveactive TB

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    0

    20

    40

    60

    80

    100

    Diagnosed by X-

    ray alone

    Actual cases

    X

    -ray-based evaluation causesover-diagnosis of TB

    NTI, Ind J Tuberc, 1974

    Over-

    diagnosis

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    Bacteriologic Exam

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    Specimen Collection

    Obtain 3 sputum specimens for smearexamination and culture

    Persons unable to cough up sputum induce sputum bronchoscopy

    gastricaspiration

    Follow infection control precautionsduring specimen collection

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    Three Specimens

    Three specimens optimal

    Spot specimen on first visit; sputum containergiven to patient

    Early morningcollection by patient on nextday

    Spot specimen during second visit

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    Three sputum smears are optimal

    81%

    93%

    100%

    0%

    50%

    100%

    First Second ThirdCumulativePositivity

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    Number of sputum samples required

    overall diagnostic yield for sputumexamination related to

    the quantity of sputum (at least 5 mL)

    the quality of sputum

    multiple samples obtained at different timesto the laboratory for processing

    3 samples obtained at least eight hours apart withat least one sample obtained in the early morning

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    Number of sputum samples required

    several studies have suggested that only twosamples may be sufficient to capture themajority of cases:

    R

    etrospective study Nelson, SM, Deike,MA, Cartwright, CP. Value of examining multiple sputumspecimens in the diagnosis of pulmonary tuberculosis. J ClinMicrobiol 1998; 36:467.

    overall, 92 percent of cases would have beendetected with two specimens

    Craft, DW, Jones, MC, Blanchet, CN, et al. Value of examining three acid-fact bacillus

    sputum smears for the removal of patients suspected of having tuberculosis from the"airborn precautions"category. J Clin Microbiol 2000; 38:4285.

    a third sputum smear was of no additionalvalue

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    Smear Examination

    Strongly consider TB in patients withsmears containingacid-fast bacilli (AFB)

    Results should be available within 24hours of specimen collection

    Presumptive diagnosis of TB

    Not specific for M. tuberculosis

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    AFB Smear

    Sensitivity: 40-70%

    Specificity: 90%

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    Reporting on AFBMicroscopy

    Number ofbacilli seen Result reported

    None per 100 oil immersion fields Negative

    1-9 per 100 oil immersion fields Scanty, reportexact number

    10-99 per 100 oil imm

    ersion fields 1+

    1-10 per oil immersion field 2+

    > 10 per oil immersion field 3+

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    Proportion of patients with pulmonary

    TB who have positive AFB smears

    0

    10

    20

    30

    40

    50

    60

    70 HIVNegative

    Early HIV

    Late HIV

    AFB positivity in

    TB patients

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    Open tuberculosis

    A tuberculous ulceration or other form of

    tuberculosis in wh

    ich

    tubercle bacilli arepresent in the excretions or secretions.

    Pulmonary tuberculosis, especially withcavitation.

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    Cultures

    Colonies of

    M. tuberculosisgrowing on media

    Gold standard for TB diagnosisUse to confirm diagnosis of TBCulture all specimens, even if smear negativeResults in 4 to 14 days when liquid mediumsystems used

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    Cultures

    Sensitivity: 80-85%

    Specificity: 98%

    Times needed: Solid medium

    4-8 wks

    Liquid medium

    2 wks

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    AFB smear vs. Cultures

    AFB smear

    ml5000-10000

    Rapid diagnosis

    Cultures

    ml10-100

    More sensitive

    Allows drug susceptivity test

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    98%

    70%

    0

    20

    40

    60

    80

    100

    AFB Microscopy X-ray

    Microscopy is more objective

    and reliable than X-ray

    Inter-observer

    agreement

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    50%

    98%

    0

    20

    40

    60

    80

    100

    AFB Microscopy X-ray

    M

    icroscopy is a more specific test th

    anX-ray for TB diagnosis

    Specificity

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    Diagnosis of Pulmonary TBCough 3 weeks

    AFB X 3

    Broad-spectrum antibiotic 10-14 days

    If symptoms persist, repeat AFB smears, X-ray

    If consistent with TB

    Anti-TB Treatment

    If 1 positive,

    X-ray andevaluation

    If 2/3 positive:Anti-TB Rx

    Ifnegative:

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    Diagnosis of pulmonary TB

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    Recommended DiagnosticApproach

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    Take HomeMessage

    Non-specific symptoms

    Often over diagnosis

    AFB smear

    Rapid diagnosis, presumptive diagnosis

    Culture

    Gold standard, more sensitive

    TB

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    Source

    UpToDate, Diagnosis of pulmonarytuberculosis, 2008, John Bernardo,MD

    ,

    ,Taiwan Guidelines on TB Diagnosis &Treatment, Edition 3,

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    Th

    anks for your attention!