Light's Criteria

Updated: Feb 02, 2026
  • Author: Swarup Sri Varaday, MD, FRCA, FCARSI; Chief Editor: Meda Raghavendra (Raghu), MD  more...
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Light's Criteria

In the realm of clinical medicine, efficient and accurate diagnosis of pleural effusions serves as the cornerstone for timely interventions and improved patient outcomes. Light's criteria, established by Richard Light in 1972, [1]  have been pivotal in recognizing the nature of pleural effusions, aiding in the differentiation between transudative and exudative origins. [2, 3, 4, 5]  This review aims to provide clinicians with a comprehensive understanding of Light's criteria, their clinical significance, limitations, and contemporary applications in managing pleural effusions. 

Transudative vs exudative pleural effusion

Transudative effusion occurs when fluid permeates the pleural cavity via intact pulmonary vessels, often in association with conditions such as congestive heart failure (CHF). [2, 3] Exudative effusion occurs when fluid escapes into the pleural space through lesions in blood and lymph vessels due to inflammation.

Causes of transudative effusions are commonly linked to increased hydrostatic pressure (eg, in CHF) or decreased oncotic pressure (eg, in cirrhosis or nephrotic syndrome). [2] Exudative effusions can result from infections (eg, pneumonia or tuberculosis), various malignancies (eg, lung or breast cancer), pulmonary embolism, or pancreatitis. Occasional exceptions also exist, in which processes that typically cause exudative effusions cause transudative effusions. (See Table 1 below.) 

Table 1. Causes of Pleural Effusions: Transudative, Exudative, and Exceptions (Open Table in a new window)

Effusion Type

Causes

Exudative 

Abdominal fluid: Abscess in tissues near lung, ascites, Meigs syndrome, pancreatitis

 

Connective-tissue disease: Churg-Strauss disease, lupus, rheumatoid arthritis, Wegener granulomatosis

 

Endocrine: Hypothyroidism, ovarian hyperstimulation

 

Iatrogenic: Drug-induced, esophageal perforation, feeding tube in lung

 

Infectious: Abscess in tissues near lung, bacterial pneumonia, fungal disease, parasites, tuberculosis

 

Inflammatory: Acute respiratory distress syndrome, asbestosis, pancreatitis, radiation, sarcoidosis, uremia

 

Lymphatic abnormalities: Chylothorax, malignancy, lymphangiectasia

 

Malignancy: Carcinoma, lymphoma, leukemia, mesothelioma, paraproteinemia

Transudative 

Atelectasis: Due to increased negative intrapleural pressure

 

Cerebrospinal fluid leak into pleural space: Thoracic spine injury, ventriculoperitoneal shunt dysfunction

 

Heart failure

 

Hepatic hydrothorax

 

Hypoalbuminemia

 

Iatrogenic: Misplaced catheter into lung

 

Nephrotic syndrome

 

Peritoneal dialysis

 

Urinothorax: Due to obstructive uropathy

Exceptions* Amyloidosis
  Chylothorax
  Constrictive pericarditis
  Hypothyroid pleural effusion
  Malignancy
  Pulmonary embolism
  Sarcoidosis
  Superior vena cava obstruction
  Trapped lung

*Processes that typically cause exudative effusions but occasionally cause transudative effusions.

Parameters measured

Light's criteria encompass the following three parameters:

  • Pleural fluid protein level
  • Serum–to–pleural fluid ratio
  • Pleural fluid lactate dehydrogenase (LDH) level

These criteria serve as a fundamental screening tool for differentiating transudative from exudative pleural effusions, enabling an initial categorization that directs subsequent diagnostic evaluation. (See Table 2 below.) At least one criterion must be satisfied to categorize an effusion as exudative.

Table 2. Light's Criteria for Differentiating Transudative and Exudative Pleural Effusions (Open Table in a new window)

Criterion 

Transudate 

Exudate 

Pleural fluid protein (g/dL) 

< 2.5 

≥ 3 

Serum–to–pleural fluid ratio 

< 0.5 

> 0.5 

Pleural fluid lactate dehydrogenase (LDH) (%) 

< 60% of upper limit of normal serum LDH 

≥ 60% of upper limit of normal serum LDH 

Clinical application and diagnostic utility

In clinical settings, application of Light's criteria facilitates rapid decision-making regarding patient management. Transudative effusions, often associated with systemic conditions such as CHF or cirrhosis, [2] may necessitate optimization of primary disease management. Conversely, exudative effusions, frequently linked to infections, malignancies, or inflammatory conditions, may prompt urgent interventions or specific targeted therapy.

Light's criteria are the most sensitive test for exudates, [6, 7, 8]  but they are less specific than some other criteria (see Table 3 below). This means that some patients may be misidentified as having an exudative pleural effusion according to Light's criteria when they actually have a transudative pleural effusion. 

Table 3. Sensitivity and Specificity of Various Tests for Identifying Exudative Pleural Effusions  (Open Table in a new window)

Test 

Sensitivity (%) 

Specificity (%) 

Light’s criteria 

98 

83 

Pleural fluid protein–to–serum protein ratio >0.5 

85 

84 

Pleural fluid lactate dehdrogenase (LDH)–to–serum LDH ratio >0.6 

90 

82 

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

82 

89 

Pleural fluid cholesterol >60 mg/dL 

54 

92 

Pleural fluid cholesterol level >43 mg/dL 

75 

80 

Pleural fluid–to–serum cholesterol ratio >0.3 

89 

81 

Serum/pleural fluid albumin level ≤1.2 g/dL 

87 

92 

In a study comparing seven different LDH- and cholesterol-based approaches to differentiating exudates from transudates, Cha et al found that the only one with diagnostic accuracy comparable to that of Light's criteria was Lépine's criteria: pleural fluid LDH greater than 0.6 the upper limit of normal serum LDH and pleural fluid cholesterol greater than 40 mg/dL (1.04 mmol/L). [9]

Challenges and limitations

Despite its clinical utility, Light's criteria have inherent limitations. Atypical presentations, comorbidities, or certain clinical scenarios may challenge the straightforward application of these criteria. Additionally, there are instances in which overlap between transudative and exudative classifications can occur, mandating additional investigations or clinical judgment for accurate diagnosis. 

The evolving landscape of diagnostic tools and technologies has supplemented Light's criteria with adjunctive methods such as advanced imaging techniques, molecular diagnostics, and biomarker analyses. [10, 11, 5, 8]  Integrating these contemporary approaches with Light's criteria enhances diagnostic accuracy and aids in comprehensive patient management. (See Table 4 below.)

Table 4. Investigations Complementary to Light's Criteria in Evaluation of Pleural Effusions  (Open Table in a new window)

Investigation 

Contribution to Evaluation 

Clinical Impact 

Advanced imaging 

Identifies loculations, pleural thickening, or underlying pathology 

Provides detailed anatomic insights 

 

Differentiates between benign and malignant pleural diseases 

Guides targeted interventions and management strategies 

Molecular diagnosis 

Identifies specific genetic or molecular markers indicative of certain conditions 

Enhances precision in diagnosing causes

 

Facilitates early detection of infectious or malignant etiologies 

Aids in initiating prompt and targeted treatments 

Biomarker analysis 

Measures specific biomarkers (eg, proinflammatory cytokines, tumor markers) 

Offers insights into disease activity and severity 

 

Assists in prognostication and in monitoring of treatment responses 

Guides therapeutic decisions and patient counseling 

Thoracoscopy 

Provides direct visualization and biopsy of pleural abnormalities 

Facilitates histopathologic confirmation of suspected diagnoses 

 

Enables targeted tissue sampling for definitive diagnosis 

Assists in guiding specific treatment interventions 

Light's criteria remain a fundamental clinical tool for swiftly characterizing pleural effusions. They are indispensable, but their application requires thorough understanding, careful consideration of limitations, and appropriate complementary use of adjunctive diagnostic methods for a holistic approach to patient care in clinical settings.

Ongoing research into refining and enhancing diagnostic algorithms, incorporating novel biomarkers, and evaluating the impact of personalized medicine on pleural effusion management holds promise for further improving diagnostic accuracy and patient outcomes in clinical care. 

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