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Lights Criteria for Exudative Effusions

Lights Criteria for Exudative Effusions

Distinguishes exudative from transudative pleural effusions using protein and LDH comparisons

Lights Criteria for Exudative Effusions

Lights Criteria for Exudative Effusions

Distinguishes exudative from transudative pleural effusions using protein and LDH comparisons

Instructions

Light’s Criteria help differentiate between transudative and exudative pleural effusions. It requires measuring pleural fluid and serum protein, lactate dehydrogenase (LDH), and comparing their ratios. An effusion is classified as exudative if it meets one or more of the criteria. The tool is quick, widely used, and provides critical diagnostic guidance in patients with pleural effusion.

Overview
When to use
Why use
Evidences

Interpretation

Criteria

Exudative if ANY of the following are met

Pleural fluid protein / Serum protein > 0.5

Yes

Pleural fluid LDH / Serum LDH > 0.6

Yes

Pleural fluid LDH > 2/3 upper limit of normal serum LDH

Yes

 If none are met → Transudative effusion.

Light’s Criteria use pleural fluid and serum protein/LDH relationships to classify pleural effusions as exudates; they are highly sensitive for exudates but can misclassify diuretic‑treated transudates (“pseudoexudates”), where albumin or protein gradients improve specificity
https://pubmed.ncbi.nlm.nih.gov/4642731/

Contemporary reviews estimate 20–30% misclassification of true transudates as exudates in diuretic‑treated heart failure, motivating adjunct use of gradients or NT‑proBNP in suspected cardiac effusions.
https://www.sciencedirect.com/science/article/pii/S0954611123001671

Comparative studies suggest Light’s remains best for detecting exudates, while the serum–effusion albumin gradient (SEAG) >1.2 g/dL or protein gradient >3.1 g/dL best reclassify transudates miscalled exudates by Light’s.
https://pmc.ncbi.nlm.nih.gov/articles/PMC7652193/

Guidelines recommend Light’s Criteria as first‑line to distinguish exudates from transudates, supplemented by SEAG (>1.2 g/dL) or protein gradient (>3.1 g/dL) when clinical suspicion favors a transudate despite “exudate” by Light’s
https://pmc.ncbi.nlm.nih.gov/articles/PMC11093145/

Pleural NT‑proBNP supports cardiac transudates; cholesterol ≥55 mg/dL is a proposed single‑marker exudate discriminator with variable adoption; pleural glucose <60 mg/dL suggests specific exudative etiologies (parapneumonic, malignancy, rheumatoid, TB).
https://pmc.ncbi.nlm.nih.gov/articles/PMC10415955/

Overview
When to use
Why use
Evidences

Pleural effusion, the accumulation of fluid between the lung and chest wall, can arise from multiple causes, including heart failure, infection, malignancy, and liver disease. Determining whether an effusion is transudative or exudative is essential because it guides diagnostic evaluation and subsequent management.

Light’s Criteria, introduced in 1972, remain the most widely accepted and validated method for this purpose. They classify an effusion as exudative when there is evidence of increased capillary permeability or impaired lymphatic drainage, typically due to conditions like pneumonia, tuberculosis, pulmonary embolism, or cancer. In contrast, transudative effusions are usually linked to systemic processes such as heart failure, cirrhosis, or nephrotic syndrome, where fluid accumulates without direct pleural disease.

The criteria compare pleural fluid protein and LDH to serum values. If the ratios exceed certain thresholds, the effusion is considered exudative. This approach provides a sensitive method for detecting pleural pathology, though it may occasionally misclassify effusions, especially in patients on diuretics. In such cases, additional tools such as serum-effusion albumin gradient or clinical context are used.

Overview
When to use
Why use
Evidences

Interpretation

Criteria

Exudative if ANY of the following are met

Pleural fluid protein / Serum protein > 0.5

Yes

Pleural fluid LDH / Serum LDH > 0.6

Yes

Pleural fluid LDH > 2/3 upper limit of normal serum LDH

Yes

 If none are met → Transudative effusion.

Light’s Criteria use pleural fluid and serum protein/LDH relationships to classify pleural effusions as exudates; they are highly sensitive for exudates but can misclassify diuretic‑treated transudates (“pseudoexudates”), where albumin or protein gradients improve specificity
https://pubmed.ncbi.nlm.nih.gov/4642731/

Contemporary reviews estimate 20–30% misclassification of true transudates as exudates in diuretic‑treated heart failure, motivating adjunct use of gradients or NT‑proBNP in suspected cardiac effusions.
https://www.sciencedirect.com/science/article/pii/S0954611123001671

Comparative studies suggest Light’s remains best for detecting exudates, while the serum–effusion albumin gradient (SEAG) >1.2 g/dL or protein gradient >3.1 g/dL best reclassify transudates miscalled exudates by Light’s.
https://pmc.ncbi.nlm.nih.gov/articles/PMC7652193/

Guidelines recommend Light’s Criteria as first‑line to distinguish exudates from transudates, supplemented by SEAG (>1.2 g/dL) or protein gradient (>3.1 g/dL) when clinical suspicion favors a transudate despite “exudate” by Light’s
https://pmc.ncbi.nlm.nih.gov/articles/PMC11093145/

Pleural NT‑proBNP supports cardiac transudates; cholesterol ≥55 mg/dL is a proposed single‑marker exudate discriminator with variable adoption; pleural glucose <60 mg/dL suggests specific exudative etiologies (parapneumonic, malignancy, rheumatoid, TB).
https://pmc.ncbi.nlm.nih.gov/articles/PMC10415955/

Frequently Asked Questions

Features and Services FAQs

Discover the full range of features and services we offer and how to use them.

What is the main purpose of Light’s Criteria?+
Can Light’s Criteria misclassify effusions?+
What is the next step if criteria suggest exudate?+
Are transudative effusions always benign?+
Do Light’s Criteria replace cytology or microbiology?+
Is LDH a reliable marker across all labs?+

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