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Noninvasive markers for esophageal varices in children with cirrhosis
Parisa Rahmani1, Fatemeh Farahmand1, Ghobad Heidari2
1Pediatric Gastroenterology and Hepatology Research Center, Tehran University of Medical Sciences, Tehran, Iran.
Insights
Noninvasive markers like platelet count and APRI can help identify children with high-risk esophageal varices (EV), potentially reducing the need for invasive endoscopy. This aids in diagnosing EV in pediatric liver cirrhosis patients.
Area of Science:
- Pediatric Gastroenterology
- Hepatology
- Diagnostic Imaging
Background:
- Esophageal varices (EV) diagnosis relies on invasive procedures like esophagogastroduodenoscopy (EGD).
- There's a need for noninvasive, cost-effective methods to diagnose EV in children with liver cirrhosis.
Purpose of the Study:
- To identify noninvasive markers for diagnosing esophageal varices in pediatric liver cirrhosis patients.
Main Methods:
- Cross-sectional study of 98 children with liver cirrhosis.
- Evaluation of spleen size, platelet count, liver function tests, and risk scores before endoscopy.
- Endoscopic assessment for EV presence, severity, and red signs.
Main Results:
- Esophageal varices were found in 43.9% of subjects.
- Univariate analysis showed significant differences in spleen size, platelet count, INR, APRI, platelet count to spleen size ratio, and risk score between patients with and without EV.
- Logistic regression revealed no independent association between these parameters and EV presence.
Conclusions:
- Platelet count, risk score, platelet count to spleen size ratio, and APRI show potential for identifying high-risk EV patients.
- These noninvasive markers may decrease the reliance on invasive EGD for EV diagnosis in children.
Background:
The diagnosis of esophageal varices (EV) is based on the findings of esophagogastroduodenoscopy (EGD), biopsy, and serum markers. Thus, noninvasive cost-effective tests through which high-risk EV children can be diagnosed are needed.
Purpose:
This cross-sectional study aimed to identify the noninvasive markers for EV in children with liver cirrhosis.
Methods:
A total of 98 children with liver cirrhosis were evaluated in this study. The spleen size, platelet count, serum albumin, liver function test results, and risk scores were evaluated prior to endoscopy. The endoscopic investigations aimed to identify the presence of EV and red signs, and determine varices sizes.
Results:
Endoscopy revealed varices in 43 subjects (43.9%). The spleen size, platelet count, international normalized ratio, aspartate aminotransferase to platelet ratio index (APRI), platelet count to spleen size ratio, and risk score differed significantly between patients with and without EV on univariate analysis; however, the logistic regression analysis showed no differences, indicating that none of these parameters were independently associated with the presence of EV.
Conclusion:
Platelet count, risk score, platelet count to spleen size, and APRI can be useful tools for the identification of highrisk patients with EV and might reduce the need for invasive methods like EGD.
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