Bronchoalveolar Lavage in Interstitial Lung Diseases to Characterization of Specific Inflammatory Cellular Infiltrate in Different Interstitial Lung Diseases

Maha Ahmed Abd EL Gawad Mohammed Okasha

Status: Not yet enrolling

Conditions: Interstitial Lung Diseases

Treatments: Procedure: bronchoscopy

Study type: Observational

Funder types: Other

Identifiers

NCT07208201

BAL in ILD

Details and patient eligibility

About

Interstitial lung disease (ILD) represents a various group of disorders characterized by inflammation and fibrosis within the lung parenchyma.[1] ILD refers to a group of diffuse parenchymal lung disorders, including a spectrum of conditions such as idiopathic pulmonary fibrosis (IPF), sarcoidosis, and connective tissue disease-associated ILD (CTD-ILD) characterized by inflammation and fibrosis of the interstitium.

ILD results in Impaired lung function and, in severe cases, respiratory failure.[1] Diagnosing ILD is a complex task due to the heterogeneous nature of these disorders.

Distinguishing between different ILD subtypes and identifying disease progression present ongoing challenges in clinical practice. .[2] BAL emerges as a key investigative tool , allowing for the collection of bronchoalveolar fluid.

The cellular and molecular composition of BAL fluid provides valuable insights into the underlying pathology, aiding in the differential diagnosis of ILD subtypes.

The gold standard in BAL analysis is cytological examination by microscopy.[3] Flow cytometry is an updated method of BAL analysis which can provide quicker and more objective results and, with the appropriate design of antibody panels, accurately quantify the main leukocyte subsets.

Several studies have described the usefulness of flowcytometry for the discrimination of sarcoidosis from other lymphocytic pathologies or even to perform leukocyte subset counting in diverse ILDs.[4][5]

Both microscopic and flowcytometric examination of BAL in ILD are complementary tools that provide comprehensive information about the cellular landscape of the lower respiratory tract ,conclusive for:

Accurate diagnosis

Primary aim:

Characterization of specific inflammatory cellular infiltrate in different interstitial lung diseases.

- Secondary aims:

1. Correlation between clinical ,radiological and inflammatory cellular pattern as regards BAL findings of different interstitial lung diseases
2. Assessment of impact on outcome, prognosis and survival of the disease as regards management modification after BAL characterization

Enrollment: 66 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Age ≥ 18 years
• Clinical suspicion of ILD based on symptoms, clinical examination, and radiological findings or newly diagnosed cases .
• HRCT findings consistent with ILD
• Willingness to undergo bronchoscopy with BAL and provide informed consent

Exclusion criteria

• Hemodynamic instability or ICU admission at time of evaluation
• Oxygen saturation < 88% on room air or < 92% on oxygen therapy
• Absolute contraindications to bronchoscopy (e.g., uncorrected bleeding diathesis, recent myocardial infarction)
• Associated chronic chest diseases other than ILD (COPD. bronchial asthma and lung cancer )
• Known active pulmonary infection or recent antibiotic treatment (< 2 weeks)
• Pregnancy