BAL-ILD CALCULATOR
Patient Data
Age:
Fibrosis:
BAL Data (%)
Lymphocytes:
CD4:
CD8:
Ratio 4/8:
Neutrophils
Eosinophils:
Languerhans:
Macrophages:
Sum:

Results should be interpreted in the clinical and analytical context of the patient.

Leukocyte content
Pathology probability (%)
Lymphocyte predominance:
Macrophage predominance:
Neutrophil predominance:
Eosinophil predominance:
Languerhans predominance:
If lymphocyte predominance
Sarcoidosis probability:
HP probability:
LIP/COP probability:
If neutrophil predominance
Infectious probability:
Other neutrophilic:
Survival prognosis
L/N Risk:
Score:
75P-OS:

Diagnostic Utility of Bronchoalveolar Lavage Flow Cytometric Leukocyte Profiling in Interstitial Lung Disease and Infection

Erika M. Novoa-Bolivar, José A. Ros, Sonia Pérez-Fernández, José A. Campillo, Ruth López-Hernández, Rosana González-López, Inmaculada Ruiz-Lorente, Almudena Otálora-Alcaraz, Cristina Ortuño-Hernández, Lourdes Gimeno, Diana Ceballos-Francisco, Manuel Muro, Elena Solana-Martínez, Pablo Martínez-Camblor, Alfredo Minguela*.

Biomolecules 2025, 15(4), 597, https://doi.org/10.3390/biom15040597

Predictive Value of Flow Cytometry Quantification of BAL Lymphocytes and Neutrophils in ILD

Erika M. Novoa-Bolivar, José A. Ros, Sonia Pérez-Fernández, José A. Campillo, Ruth López-Hernández, Rosana González-López, Almudena Otálora-Alcaraz, Cristina Ortuño-Hernández, Lourdes Gimeno, Inmaculada Ruiz-Lorente, Diana Ceballos-Francisco, Manuel Muro, Elena Solana, Pablo Martínez-Camblor, Alfredo Minguela*.

Cells 2024, 13(24), 2066, https://doi.org/10.3390/cells13242066
Series of cases used for the calculations in this web
Cell-predominant pathologies (N) Man (%) Age
BAL-control 112 53.3% 53.5±16.6
Sarcoidosis 82 48.20% 55.6±14.8
Hypersensitivity pneumonitis (HP) 48 49.0% 50,4±17.6
Organized cryptogenic pneumonia (COP) 44 46.50% 62.3±17.4
Lymphocytic interstitial pneumonia (LIP) 37 69.20% 53.2±15.9
Desquamative interstitial pneumonitis (DIP) 35 52.8% 54.4±20.8
Nonspecific interstitial pneumonia (NSIP) 156 48.1% 59.3±15.5
Pneumoconioses 27 96.3% 56.5±16.0
Unclassifiable-ILD (U-ILD) 80 60.0% 61.3±12.4
Usual interstitial pneumonia (UIP = IPF) 145 71.70% 65.8±12.3
Respiratory bronchiolitis ILD (RB-ILD) 25 40.0% 53.3±22.8
Acute interstitial pneumonia (AIP) 26 56.0% 57.5±21.9
Pulmonary infection 231 59.0% 62.1±15.6
Eosinophilic-ILD 17 80.0% 48.4±22.7
Pulm. Langerhans c. histiocytosis (PLCH) 9 66.7% 36.7±15.8
IMIB IMIB-Arrixaca