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Diagnosis of Community Acquired Pneumonia

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Title: Diagnosis of Community Acquired Pneumonia


1
Diagnosis of Community Acquired Pneumonia
  • Eva ampachová
  • Virology
  • Hospital Ceské Budejovice

2
Characteristic symptoms of CAP
  • Bacterial
  • acute onset, high fever, cough with expectoration
    (purulent), high level of CRP, typical clinical
    findings and X-ray
  • Atypical
  • slower onset, fever (often without cough),
    expectoration scarce or none, low to moderate CRP
    level, unspecific clinical findings, X-ray
    reveals pneumonia

3
Community Acquired Pneumonia (CAP)
  • Bacterial
  • Pneumococcus, Haemophillus, Moraxella, Gram
    negative rods, others
  • Atypical
  • Mycoplasma, Chlamydia, Legionella, viruses

4
Agents causing atypical pneumonia
  • Mycoplasma pneumoniae
  • Chlamydia pneumoniae
  • Legionella sp.
  • Viruses

5
Mycoplasma pneumoniae
  • Outbreaks every 4-5 years
  • Sporadic cases can be detected
  • Predominantly in children and young adults

6
Diagnostic of Mycoplasma pneumoniae
  • Direct detection of microorganism
  • Culture
  • Antigen detection
  • DNA detection (PCR)
  • Antibody detection

7
Direct detection of microrganism
  • Culture
  • Slow, less sensitive
  • Antigen detection
  • Not widely used, less sensitive
  • DNA detection (PCR)
  • Promising
  • The main problem is a valid sample

8
Antibody detection
  • Complement binding reaction (CBR)
  • Fourfold increase of antibody titre
  • Best sensitivity and specificity
  • Enzyme immunoassay (EIA)
  • IgG, IgA, IgM classes
  • Differences in results depending on manufacturer
    of a test

9
Comparison of EIA tests
  • Five kits from different manufacturers
  • All sera tested in IgG, IgA, IgM classes
  • Panel of CBR seroconversion and CBR negative
    sera

10
Results
  • Sensitivity
  • IgA 68-97, IgM 87-97
  • Specificity
  • IgA 76-100, IgM 60-99
  • PPV
  • IgA 91-99, IgM 90-99
  • NPV
  • IgA 50-90, IgM 78-91

11
Pitfalls in EIA testing
  • High sensitivity was combined with low
    specificity and vice versa
  • No manufacturer had excelent quality of tests for
    both IgA and IgM
  • Correct diagnosis from the first sample could be
    done in approx. 40 of cases,

12
Conclusion (Mycoplasma)
  • It is essential to choose carefully not only
    manufacturer but also the test used.
  • No approach is free of charge. You pay for high
    sensitivity with low specificity
  • First sample testing leads to diagnosis in 40 of
    cases

13
Chlamydia pneumoniae
  • Occurs more frequently in older patients, can
    cause complications in patients with other
    diseases
  • Outbreaks occur locally, with no typical
    periodicity
  • Most cases are sporadic

14
Diagnostic of Chlamydia pneumoniae
  • Direct detection of microorganism
  • Culture
  • Antigen detection
  • DNA detection
  • Detecton of antibodies

15
Direct detection of microorganism
  • Culture
  • difficult
  • Antigen detection
  • low sensitivity and specificity
  • DNA detection
  • Promising
  • The main problem is valid sample

16
Antibody testing
  • EIA
  • Mostly genus specific, less sensitive in early
    stage of infection, Ab detected long time after
    resolution of the disease
  • Imunofluorescent test (MIF)
  • golden standard, time and labour-consuming
  • Immunoblott
  • Confirmaton method

17
Immunoblott results in detection of acute
infection
  • Panel of 43 sera from patients with clinical and
    microbiological markers of acute Chlamydia
    pneumoniae infection
  • Concordant results (MIF and IB) 63
  • Negative or borderline IgA in IB 21
  • IB negative, MIF positive 16
  • Results of reconvalescent blood sample proved the
    diagnosis
  • Infants with C. trachomatis respiratory tract
    infection (6) 100

18
Immunoblott in detection of chronic Chlamydia
infection
  • Tested on panel of 80 sera with several month
    persistence of IgG and IgA MIF antibodies to
    Chlamydia pneumoniae
  • IB positive IgG and IgA 31
  • IB positive IgG only 51
  • IB negative 18

19
Antibodies are not disease. To treat antibody
levels without corresponding illness is a serious
mistake. It leads to impropper use of antibiotics
and it is one of the causes of increasing ATB
resistance.
20
Conclusion (Chlamydia)
  • IB is a confirmatory method
  • IB is less sensitive than MIF (can be negative in
    early phases of acute infection)
  • Interpretation of the results should be based on
    laboratory and clinical data and on patients
    history
  • So caled persistent infection is diagnostic
    problem. Only long term survey of patient and
    repeated testing may help

21
Conclusions
  • Diagnosis of Chlamydia pneumoniae and Mycoplasma
    pneumoniae is based mainly on antibody testing
  • Culture and PCR have their limits (valid sample)
  • Carefull choice of tests and interpretation of
    the results with reasonable knowledge of clinical
    data seems to be essential
  • Without interpretation the results might be
    misleading
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