What Is Bronchoalveolar Lavage and How Is It Done?

Bronchoalveolar lavage (BAL) is a diagnostic procedure used in pulmonary medicine to sample the cellular and non-cellular components of the lower respiratory tract, including the air sacs and small airways. The technique involves inserting a flexible tube, called a bronchoscope, into the lung airways. A sterile saline solution is gently introduced and immediately suctioned back out to collect a fluid sample for laboratory analysis. This procedure provides insights into inflammatory, infectious, and malignant processes occurring deep within the lungs, offering information unavailable through simple sputum samples or imaging alone.

Clinical Situations Requiring BAL

A physician typically orders BAL when less invasive diagnostic methods, such as chest X-rays or blood tests, fail to provide a clear diagnosis for persistent lung symptoms. It is a crucial tool for investigating diffuse interstitial lung diseases (ILDs), which cause scarring of the lung tissue. BAL can differentiate between types of ILD, such as hypersensitivity pneumonitis and sarcoidosis, by analyzing inflammatory cell patterns in the fluid. The procedure is particularly valuable for identifying deep lung infections, especially in immunocompromised patients undergoing chemotherapy or organ transplantation. BAL can detect opportunistic pathogens like Pneumocystis jirovecii pneumonia, mycobacteria, and certain viruses.

Executing the Lavage Procedure

The BAL procedure begins with the patient receiving local anesthesia to the nose and throat, often combined with moderate sedation to ensure comfort and suppress the cough reflex. A flexible bronchoscope, a thin tube equipped with a light and camera, is gently inserted through the mouth or nose and navigated down the windpipe into the bronchial tree. The physician monitors the scope’s progress on a video screen to visualize the airways and identify the specific lung segment for sampling.

Once the bronchoscope reaches the target airway, it is “wedged” into a smaller bronchus, sealing off the area. This allows sampling of the distal air sacs, or alveoli. A sterile, warmed normal saline solution (typically 100 to 240 milliliters total) is instilled through the bronchoscope in several small aliquots. The fluid is left in place for a few seconds to “wash” the alveolar surfaces, collecting cells and other components.

Immediately following instillation, the fluid is gently suctioned back into sterile collection traps for laboratory processing. Typically, 40 to 70 percent of the instilled fluid volume is recovered, with the first aliquot often having a lower return. The recovered fluid, now called bronchoalveolar lavage fluid, or BALF, contains a representative sample of the environment deep within the lung tissue.

Laboratory Analysis of the Fluid

Once the BAL fluid reaches the laboratory, it undergoes a detailed analysis, starting with a total cell count and a differential cell count. The differential count categorizes the various cell types present, primarily alveolar macrophages, lymphocytes, neutrophils, and eosinophils. In a healthy non-smoker, alveolar macrophages make up the vast majority of the cells, usually 80 to 90 percent.

Changes in the percentages of these cells are highly informative for diagnosing interstitial lung diseases. For instance, a significant increase in lymphocytes, especially above 25%, strongly suggests conditions like sarcoidosis or hypersensitivity pneumonitis. Conversely, a high percentage of neutrophils, greater than 3%, can point toward inflammatory conditions like usual interstitial pneumonia or acute lung injury. An eosinophil count exceeding 25% is virtually diagnostic for acute eosinophilic pneumonia.

Beyond cell analysis, the laboratory performs microbiological studies, including cultures for common bacteria, fungi, and mycobacteria like tuberculosis. Special stains and molecular tests are also conducted to identify specific findings, such as lipid-laden macrophages indicative of aspiration or specific proteins associated with pulmonary alveolar proteinosis. The combination of cell patterns and infectious agent identification provides the physician with a comprehensive diagnostic profile.

Patient Preparation and Recovery

Proper preparation for BAL is important to maximize safety and diagnostic yield. Patients are required to fast for six to eight hours before the procedure to minimize the risk of aspiration during sedation. Patients must also temporarily stop taking certain medications, particularly blood thinners, which could increase the risk of minor bleeding.

During the procedure, the patient’s heart rate, blood pressure, and oxygen saturation are continuously monitored. The procedure is generally well-tolerated, and most patients are observed for two to four hours afterward while the effects of the sedation wear off. A common side effect is a temporary sore throat from the bronchoscope and a mild cough, which usually resolves within a day.

Some patients may experience a transient low-grade fever, occurring in up to 30% of cases, which is self-limiting and resolves within 24 hours. Because a small amount of fluid remains in the lungs, there may be a temporary decrease in lung function, and supplemental oxygen is often administered. Patients are advised to seek medical attention if they experience persistent fever, chest pain, or shortness of breath.