I. Introduction & Definition

  • Definition: A diagnostic procedure performed during flexible bronchoscopy where saline is instilled into a subsegment of the lung and aspirated back to sample the alveolar and distal airway milieu.
  • Concept: Often referred to as a “Liquid Biopsy” of the lower respiratory tract.
  • Site: usually performed in the Right Middle Lobe (RML) or Lingula (highest yield due to anatomy), or the most affected area radiologically.

II. Indications

1. Diagnostic Indications

  • Non-resolving Pneumonia: To identify resistant bacteria, fungi (Aspergillus), or Pneumocystis jirovecii (PCP).
  • Immunocompromised Host: Evaluation of opportunistic infections.
  • Interstitial Lung Disease (ILD): To determine cellularity (lymphocytic vs. neutrophilic) or identify hemorrhage.
  • Aspiration Syndromes: Detection of lipid-laden macrophages.
  • Pulmonary Hemorrhage: Diagnosis of Diffuse Alveolar Hemorrhage (DAH).

2. Therapeutic Indications

  • Pulmonary Alveolar Proteinosis (PAP): Whole lung lavage to wash out surfactant protein accumulation.
  • Mucus Plugging: To dislodge tenacious plugs (e.g., in severe Asthma or Cystic Fibrosis).

III. Procedure (Technique)

  1. Wedging: The bronchoscope tip is wedged into a segmental or subsegmental bronchus.
  2. Instillation: Sterile non-bacteriostatic saline is instilled.
    • Dose: 1 ml/kg per aliquot (usually 3 aliquots).
  3. Aspiration: Gentle suction is applied to retrieve the fluid (effluent).
    • Adequacy: >40% recovery of instilled volume is considered adequate.

IV. Analysis and Interpretation

The fluid is sent for Microscopy, Culture, Cytology, and PCR.

1. Normal Pediatric BAL Profile

  • Macrophages: 80–90% (Predominant cell type).
  • Lymphocytes: <10%.
  • Neutrophils: <3%.
  • Eosinophils: <1%.

2. Abnormal Patterns

FindingDifferential Diagnosis
Neutrophilia (>50%)Bacterial pneumonia, Aspiration, Cystic Fibrosis.
Lymphocytosis (>15%)Hypersensitivity Pneumonitis, Sarcoidosis, Viral infection, TB.
Eosinophilia (>5%)Asthma, ABPA, Parasitic infection, Drug reaction.
Hemosiderin-laden MacrophagesDiffuse Alveolar Hemorrhage (DAH), Idiopathic Pulmonary Hemosiderosis.
Lipid-laden MacrophagesChronic Aspiration (sensitive but non-specific).
Milky/Opaque FluidPulmonary Alveolar Proteinosis (PAP).
Silver Stain (+)Pneumocystis jirovecii Pneumonia (PCP).

V. Complications

  • Transient Fever: Most common (10–30% of cases) due to cytokine release.
  • Hypoxemia: Transient drop in SpO2 during and immediately after the procedure.
  • Bronchospasm.
  • Bleeding: Usually minor/self-limiting.