bal fluid analysis
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PPT on Bal fluid analysisTRANSCRIPT
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Broncho-Alveolar Broncho-Alveolar Lavage Fluid Lavage Fluid
AnalysisAnalysis
By Dr Uttam Kumar DasBy Dr Uttam Kumar DasPGT Dept of Pathology
BSMC Bankura05.03.2014
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Introduction:BAL is performed with the FOB in a wedge position within the selected broncho-pulmonary segment.
The total instilled volume of normal saline should be from 100-300ml, repeated 2 to 6 times with 20-50ml saline each.
To obtain an adequate specimen 40-60 mL (usually 40-70% recovery of the total instillate) must be drawn back.
Aspirates and washings provide information on the status of the respiratory tract in small bronchi beyond reach of the bronchoscopic brush.
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Area That Is Lavaged Procedures were usually performed in the
right middle lobe or lingula
But lavage can be done in the most affected areas of the lung
(In evaluating BAL in patients with Pneumocystis jiroveciipneumonia, it was found that lavage in the upper lobeshad a higher yield than the traditional right middle lobeor lingula)
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Handling of Aspirated Fluid At the time of the lavage cells should be
stored in silicone-coated or similar containers
Cell counts should probably be made on unfiltered, unwashed, and unconcentrated
samples (If concentration is performed, the method should be specified)
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Centrifugation to concentrate proteins and cells can lead to loss of cells
Washing the cells can change the differential count considerably
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Satisfactory Sample1. A total of 2×106 cells is considered a minimum
requirement
2. Furthermore, more than 10 macrophages should be present in a high-powered microscopic field
3. Degenerative changes should cover less than 20% of the specimen area on the slide
4. If the number of squamous epithelial cells, bronchial cells, RBCs, or inflammatory cells exceeds that of macrophages, the specimen is considered unsatisfactory
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The Storage of Fluid Cells stored at 4< C can be analyzed up to 24
hours after the procedure without significant changes in the count and differentials
Certain proteins may be temperature sensitive and the samples may need to be stored at -80< C
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Correcting for Bronchoalveolar Lavage Dilution Instilled fluid is mixed with the endogenous fluid
in the alveoli
Alveolar space is also in contact with a vascular space-So water and solutes can transfer into the alveolar space
This process leads to the uncertainty of any measurement of the concentration of any material in the alveolar space
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Solution
One method has been to report per mL ofaspirated fluid.
Using this correction method has allowed clinicians to quantitate the number of bacteria in the alveolar space and to therefore diagnose bacterial pneumonia
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Unsatisfactory BAL specimen that shows squamous epithelial cells (large cells) and degenerating columnar epithelial cells (arrow)
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Steps in Handling Cellular Population of Bronchoalveolar Lavage Fluid
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Cellular Staining
Papanicolaou Stain: -Detect Cancer & Infection -Not good at differentiating between
inflammatory cells
Toluidine blue staining: -Mast cells are better seen
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Wright-Giemsa stain: -Good at differentiating between inflammatory
cells
Diff-Quik (modification of the Wright-Giemsa stain): -Is a rapid method allowing staining of the slide
within a few minutes
Limitations: -The cells must be adequately adhered to the slide
prior to fixation -Some cells are underestimated by these
techniques
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Oil red O stain: -In fat embolism
Fat and Lipid stain (e.g. Sudan III): -Lipoid pneumonia (aspiration) Lipid-laden alveolar macrophage index >
100 (Sensitivity of 100%, Specificity 57%)
Periodic acid-Schiff (PAS): -Pulmonary alveolar proteinosis
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Other stains
KOH preparation: Fungal
Auramine-rhodamine or Ziehl-Neelson: Mycobacterial
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Modified acid fast stain (Kinyoun): Nocardia Silver methenamine: Pneumocystis jirovecii
pneumonia, fungal Direct fluorescent antibody testing (DFA) for
Legionella
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Number of Cells Counted
De Brauwer et al determined that between 300 and 500 cells counted provided a good representation of the number of nucleated cells for a BAL sample
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Different cell types in respiratory tract Upper respiratory tract Ciliated pseudostratified columnar cells Squamous cells
Trachea and bronchi Peudostratified Ciliated columnar cells Goblet cells
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Terminal bronchioles Low columnar or cuboidal-may be ciliated
Club cells (Clara cells)-nonciliated, secretory cuboidal cells
Alveoli Type I pneumocytes-simple squamous alveolar cells
Type-II pneumocytes-great alveolar cells
Dust Cell-in the alveoli
Alveolar macrophages- in the connective tissue of alveolar walls or interalveolar
septa
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General indications for BAL:
-Non-resolving pneumonia
- Diffuse lung infiltrates (interstitial
and/or alveolar)
- Infiltrates in an immunocompromised
host
- Suspected alveolar hemorrhage
- Quantitative cultures for VAP
- Exclusion of diagnosable conditions by
BAL
- Research
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Gross examination-
Pulmonary alveolar proteinosis
-Opaque or translucent brownish or sandy colored fluid
-Sediments out into two layers if left to sit
Alveolar hemorrhage
-Sequentially more hemorrhagic with each aliquot
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Amorphous, predominantly acellular debris (pulmonary alveolar proteinosis)
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Papanicolaou stain- foamy proteinaceous alveolar cast
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Alveolar macrophages
Normal >80%
Decreased in
Sarcoidosis (to 55% or less)
Cell count and differential count
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Predominance of alveolar macrophages in BAL from a normal subject
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This photomicrograph shows an asbestos body under higher magnification, surrounded by alveolar macrophages
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Neutrophils (Normal <3%): Nonspecific, but suggests active alveolitis
Increased in: ARDS Connective tissue disorders Idiopathic pulmonary fibrosis Infection Pneumoconiosis Wegener's granulomatosis
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BAL neutrophil predomnance with intracellular bacteria
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Eosinophils (Normal <1-2%) Low to Moderate Eosinophilia (5-20%):
Drug induced lung disease Minocycline Nitrofurantoin Penicillin
Infections Parasitic Mycobacterial Fungal
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Bronchial Asthma
Malignancies (infrequently)
Other interstitial pneumonias occasionally (BOOP or COP, IPF/UIP, ILD associated with Connective tissue disorders, Sarcoidosis)
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BAL eosinophilia
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Moderate to Marked Eosinophilia (>20%):
Allergic bronchopulmonary aspergillosis
Acute eosinophilic pneumonia
Churg-Strauss syndrome
Chronic eosinophilic pneumonia
Idiopathic hypereosinophilic syndrome
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Lymphocytes (Normal <15%) Normal CD4/CD8 (0.9-2.5:1): Tuberculosis Malignancies
Low CD4/CD8: Hypersensitivity Pneumonitis Silicosis Drug-induced lung disease HIV infection BOOP (COP)
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Elevated CD4/CD8: Active sarcoidosis (>4:1 up to 10:1)AsbestosisBerylliosisCrohn's diseaseConnective tissue disordersSometimes in normal persons (inc. with
age)
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BAL Lymphocytosis
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Erythrocytes
◦ Elevated erythrocyte count - early sign of
alveolar hemorrhage (first several hours)
◦ Phagocytosed erythrocytes - alveolar
hemorrhage within 48 hrs
◦ Hemosiderin laden macrophages - alveolar
hemorrhage > 48hrs
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Foamy macrophages: Non specific finding May be seen in amiodarone use
Malignancies (sensitivity ranges from 35% to 70%) ◦ Lymphangitic carcinomatosis ◦ Lymphoma ◦ Bronchoalveolar carcinoma and other primary lung
malignancies◦ Extrapulmonary malignancies
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Hemosiderin Laden Macrophages: 20% is highly specific and sensitive for alveolar
hemorrhage
Langerhans cells >5% suggestive of Pulmonary Langerhans cell
histiocytosis
Cytomegalic cells Viral pneumonias (cytomegalovirus, herpes)
Sulfur granules: Actinomycetes
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Microbiology
Cultures
Polymerase chain reaction (PCR) TB and
others
Quantitative or semi-quantitative
cultures VAP
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GMS BAL fluid showing round to cup shaped cysts of Pneumocystis
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Pap-stained BAL fluid demonstrating large, retractile yeast forms of Blastomyces dermatiditis (400X)
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Pap-stained BAL fluid showing variably-sized, round yeast forms of Cryptococcus neoformans (1000X)
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Wright-stained BAL fluid demonstrating intracellular yeast forms of Histoplasma capsulatum
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Wright-stained BAL fluid demonstrating oblong, budding yeast forms with pseudohyphae (1000X)
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Complications/Adverse events:
No complications in up to 95%
Cough
Transient fever (2.5%)
Transient chills and myalgias
Transient infiltrates in most (resolves in 24 hours)
Bronchospasm (<1%)
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Transient fall of lung function
Transient decrease in baseline PaO2
In patients with already severely compromised respiratory status, the loss of lung function may necessitate the need for Mechanical Ventilation
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Pulmonary alveolar microlithiasis
Calcospherites can be demonstrated in BAL fluid
(one of the tiny round bodies formed during calcification by chemical union of calcium particles and albuminous matter of cells)
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Thank You