Related Experiment Video
Updated: May 16, 2026

07:45
Severe Burn Injury in a Swine Model for Clinical Dressing Assessment
Published on: November 6, 2018
Plasma chromogranin A after severe burn trauma
Andreas E Lindahl1, Aili Low, Mats Stridsberg
1Department of Surgical Sciences, Uppsala University, Uppsala, Sweden.
Neuropeptides
|December 5, 2012
Summary
Plasma chromogranin A (P-CgA) levels indicate neuroendocrine activation and predict organ dysfunction in burn patients. Higher P-CgA release correlates with increased injury severity and organ dysfunction following major burns.
Area of Science:
- Trauma and Burn Care
- Neuroendocrinology
- Critical Care Medicine
Background:
- Plasma chromogranin A (P-CgA) is a marker of sympathetic stress, predicting mortality in medical intensive care.
- The magnitude of P-CgA release may reflect stress load and injury severity in burn patients.
Purpose of the Study:
- To investigate the relationship between plasma chromogranin A (P-CgA) levels and injury severity in burn intensive care patients.
- To determine if P-CgA can predict organ dysfunction after major burn injuries.
Main Methods:
- Fifty-one burn patients with >10% burn area were studied.
- Plasma chromogranin A (P-CgA) was measured twice daily for seven days post-injury.
- Organ dysfunction was assessed using SOFA scores at day 7; P-CgA measures (24h value, mean, max, AUC) were correlated with SOFA scores.
Main Results:
- P-CgA variability differed between patient groups, with high variability linked to deeper injuries and older age.
- All P-CgA measures correlated with SOFA scores, but not total burn size.
- Age, burn size, and P-CgA levels (at 24h, mean, or max) independently predicted organ dysfunction. Age, burn area, and P-CgA at 24h best predicted organ dysfunction (AUC 0.91).
Conclusions:
- Neuroendocrine activation, indicated by plasma chromogranin A (P-CgA), is independently associated with organ dysfunction after major burn injuries.
- P-CgA serves as a valuable marker for assessing injury severity and predicting outcomes in burn patients.
Related Concept Videos
Burn Injuries
Burn injuries occur when the skin and underlying tissues are damaged due to exposure to heat, electricity, chemicals, radiation, or friction. They can vary in severity, from minor superficial burns to severe deep burns that can be life-threatening.
The damage results in the death of skin cells, which can lead to a massive loss of fluid. Dehydration, electrolyte imbalance, and renal and circulatory failure follow, which can be fatal. Burn patients are treated with intravenous fluids to offset...
The damage results in the death of skin cells, which can lead to a massive loss of fluid. Dehydration, electrolyte imbalance, and renal and circulatory failure follow, which can be fatal. Burn patients are treated with intravenous fluids to offset...
Blood Studies for Cardiovascular System I: Cardiac Biomarkers
Cardiac biomarkers are enzymes, proteins, and hormones released into the blood when cardiac cells are injured. They are powerful tools for triaging.
The essential diagnostic tools for detecting myocardial necrosis and monitoring individuals suspected of having acute coronary syndrome (ACS) include:
Troponins
Troponins, particularly cardiac troponins I and T, are the most precise and sensitive markers of myocardial injury. They are detectable within 4-6 hours of myocardial injury and remain...
The essential diagnostic tools for detecting myocardial necrosis and monitoring individuals suspected of having acute coronary syndrome (ACS) include:
Troponins
Troponins, particularly cardiac troponins I and T, are the most precise and sensitive markers of myocardial injury. They are detectable within 4-6 hours of myocardial injury and remain...
Acute Pancreatitis II: Pathophysiology
The pathophysiology of acute pancreatitis centers on injury to pancreatic acinar cells, which initiates a cascade of harmful intracellular events.This injury leads to premature activation of trypsinogen to trypsin in the pancreas. Trypsin then activates other digestive enzymes, such as chymotrypsin, elastase, and phospholipase A2, which begin breaking down pancreatic tissue. The resulting autodigestion causes local inflammation, tissue swelling, hemorrhage, and fat necrosis.Injured acinar cells...

