Pulmonology focuses on diagnosing and treating lung and airway conditions such as asthma, COPD, and pneumonia, as well as overall respiratory health.

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Influenza: Diagnosis and Evaluation

Accurate and timely diagnosis of influenza is critical for initiating appropriate antiviral therapy, implementing infection control measures, and preventing the inappropriate use of antibiotics. While a clinical diagnosis based on symptoms and local epidemiological data is often sufficient during the peak of an outbreak, laboratory confirmation is essential for high-risk patients, hospitalized individuals, and cases with atypical presentations. At Liv Hospital, we employ a tiered diagnostic approach that balances speed, accuracy, and clinical utility to ensure optimal patient outcomes.

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Clinical Diagnosis and Physical Examination

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The initial evaluation begins with a thorough clinical assessment. The “influenza-like illness” (ILI) definition—fever of at least 37.8°C accompanied by cough or sore throat—is a standard screening tool. However, sensitivity varies.

  • Physical Findings: Examination typically reveals a fever, flushed face, and hot, moist skin. The eyes may be watery and red. Examination of the pharynx often shows hyperemia but usually without exudates. Auscultation of the chest is largely clear in uncomplicated cases, although rhonchi or scattered wheezes may be heard.
  • Limitations: Clinical diagnosis is difficult because many other respiratory viruses, such as RSV, adenovirus, and parainfluenza, can mimic the flu. Therefore, reliance on symptoms alone can lead to misdiagnosis, particularly outside of the peak flu season.
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Rapid Influenza Diagnostic Tests (RIDTs)

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These are antigen detection assays that can provide results in less than 15 minutes. They work by detecting the viral nucleoprotein antigen.

  • Utility: Their main advantage is speed, enabling immediate decisions on antiviral treatment in an outpatient setting.
  • Accuracy Concerns: RIDTs have high specificity but relatively low sensitivity (50-70 percent). This means a positive result is reliable, but a negative result does not rule out influenza. False negatives are common. Therefore, in a high-prevalence setting, a negative RIDT in a symptomatic patient should not preclude treatment if clinical suspicion is high.

Molecular Assays: The Gold Standard

Reverse Transcription Polymerase Chain Reaction (RT-PCR) and other molecular assays are the most sensitive and specific diagnostic tools available.

  • Mechanism: These tests detect the viral genetic material (RNA) in respiratory specimens. They can distinguish between influenza A and B and identify specific subtypes (e.g., H1N1 vs. H3N2).
  • Advantages: They are far more sensitive than antigen tests and are less likely to produce false-negative results. While historically slower, rapid molecular assays now allow for results in under an hour with high accuracy. Liv Hospital utilizes these advanced molecular platforms for definitive diagnosis, particularly for hospitalized patients.
PULMONOLOGY

Immunofluorescence Assays

Direct and indirect immunofluorescence assays involve staining respiratory epithelial cells from a nasopharyngeal specimen with fluorescently labeled antibodies.

  • Procedure: Cells are viewed under a fluorescence microscope. If viral antigens are present, they will glow.
  • Speed and Sensitivity: These tests yield results in a few hours and have an intermediate sensitivity between RIDTs and viral culture. They require specialized equipment and trained personnel to interpret the slides.

Viral Culture

Viral culture was traditionally the gold standard but has largely been replaced by molecular methods for routine diagnosis due to the time required.

  • Methodology: The virus is grown in cell cultures or embryonated eggs.
  • Importance: While too slow for immediate patient management (taking 3 to 10 days), viral culture remains vital for public health surveillance. It enables complete antigenic characterization of the virus, which is essential for assessing the match between circulating strains and the vaccine and for monitoring the emergence of antiviral resistance.

Serological Testing

Serology involves testing blood samples for antibodies to the influenza virus.

  • Diagnosis: It usually requires paired serum samples, one collected during the acute phase and one collected weeks later during the convalescent phase. A fourfold rise in antibody titer indicates recent infection.
  • Clinical Use: Due to delays in results, serology is primarily used for retrospective diagnosis in research studies or epidemiological investigations rather than for acute patient care.

Radiological Evaluation

Imaging is not indicated for uncomplicated influenza but is crucial when complications are suspected.

  • Chest Radiography: A chest X-ray is the first-line imaging modality for patients with hypoxia, severe breathlessness, or abnormal lung sounds. In primary viral pneumonia, bilateral interstitial infiltrates may be seen. In secondary bacterial pneumonia, lobar consolidation is more common.
  • Computed Tomography (CT): CT scans may be used in complex cases to evaluate the extent of lung involvement, detect abscesses, or rule out pulmonary embolism in patients with severe respiratory failure.

Laboratory Biomarkers

Routine blood tests can provide supportive information but are non-specific.

  • Complete Blood Count: Leukopenia (low white blood cell count) is a common finding in the early phase of viral infection. Later, leukocytosis (high white count) may suggest a secondary bacterial infection.
  • Inflammatory Markers: C-reactive protein (CRP) and procalcitonin levels can help distinguish between viral and bacterial etiologies. Procalcitonin is typically lower in pure viral infections and elevated in bacterial superinfection, aiding in antibiotic stewardship decisions.

Evaluating Complications

Diagnosis extends beyond identifying the virus to assessing organ function.

  • Pulse Oximetry and Arterial Blood Gas: Essential for evaluating oxygenation status and ventilation in patients with respiratory distress.
  • Cardiac Enzymes and ECG: Used to evaluate patients for myocarditis or exacerbation of underlying ischemic heart disease.
  • Renal Function Tests: Important for patients with severe dehydration or rhabdomyolysis.

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Assoc. Prof. MD. Engin Aynacı Assoc. Prof. MD. Engin Aynacı Pulmonology Overview and Definition
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FREQUENTLY ASKED QUESTIONS

How accurate are the rapid flu tests?

Rapid tests are good at confirming the flu if positive, but they miss many cases; a negative result does not prove you do not have the flu.

The nasopharyngeal swab collects cells from the back of the nose where the virus replicates, providing the best sample for accurate testing.

No, blood tests for flu antibodies take weeks to show results; diagnosis for immediate treatment relies on swabs of the respiratory tract.

An X-ray is needed if there are signs of pneumonia, such as difficulty breathing, low oxygen levels, or chest pain, to check for fluid or infection in the lungs.

RT-PCR (molecular testing) is the most reliable method, as it detects viral genetic material with very high sensitivity and specificity.

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