2020Journal of Sheikh Zayed Medical CollegeOpen access

Predictive role of Natural Anticoagulants in Prognosis of Chronic Liver Disease in Pediatric Age Group

Sana Ajmal, Hina Sehar, Saleha Zafar, Saima Farhan, Nisar Ahmad, Muhammad Atif Riza

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Abstract

Background: In asymptomatic peadiatric patients, cirrhosis is considered to be compensated, with or without gastroesophageal varices, it may be decompensated. Both Antithrombin III, Protein C and D dimers are sensitive markers of liver disease. Objective: To determine the frequency of compensated and decompensated cirrhosis in cirrhotic peadiatric patients and compare the status of protein C, Antithrombin lll deficiency and D-dimer in both groups. Methodology: In this cross sectional study, 80 peadiatric patients suspected to have cirrhosis were included, from November, 2015 to April, 2016, by non-probability convenience sampling. Variables included were; compensated and decompensated chronic liver disease, Antithrombin III, D dimer and Protein C, as natural anticoagulents. Data was analyzed by SPSS 13. Results: Out of 80 patients, 70 (87.5%) were in the compensated phase of cirrhosis. Mean Antithrombin III showed significant reduction in patients with decompensated cirrhosis (50.0±4.05%) when compared with patients with compensated liver disease (84.52 ±15.36%). Mean Protein C level exhibited also significant reduction in the decompensated patient groups (40±4.7%) when compared with the compensated group of patients (77.92±6.67%). The mean D-dimer levels showed significantly higher levels only in patients with signs of decompensated cirrhosis (840±11.85μg/L) when compared with compensated disease (629±6.29). Conclusion: Our study concluded that the natural anticoagulants Antithrombin III, Protein C and D dimer, reflect hepatocellular impairment in both compensated as well as decompensated peadiatric patients of cirrhosis. However, these are markedly decreased in decompensated disease except for D dimer. Key words: Cirrhosis, Anti-thrombin III, Protein C, Protein S, D-dimer.

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Background: In asymptomatic peadiatric patients, cirrhosis is considered to be compensated, with or without gastroesophageal varices, it may be decompensated. Both Antithrombin III, Protein C and D dimers are sensitive markers of liver disease. Objective: To determine the frequency of compensated and decompensated cirrhosis in cirrhotic peadiatric patients and compare the status of protein C, Antithrombin lll deficiency and D-dimer in both groups. Methodology: In this cross sectional study, 80 peadiatric patients suspected to have cirrhosis were included, from November, 2015 to April, 2016, by non-probability convenience sampling. Variables included were; compensated and decompensated chronic liver disease, Antithrombin III, D dimer and Protein C, as natural anticoagulents. Data was analyzed by SPSS 13. Results: Out of 80 patients, 70 (87.5%) were in the compensated phase of cirrhosis. Mean Antithrombin III showed significant reduction in patients with decompensated cirrhosis (50.0±4.05%) when compared with patients with compensated liver disease (84.52 ±15.36%). Mean Protein C level exhibited also significant reduction in the decompensated patient groups (40±4.7%) when compared with the compensated group of patients (77.92±6.67%). The mean D-dimer levels showed significantly higher levels only in patients with signs of decompensated cirrhosis (840±11.85μg/L) when compared with compensated disease (629±6.29). Conclusion: Our study concluded that the natural anticoagulants Antithrombin III, Protein C and D dimer, reflect hepatocellular impairment in both compensated as well as decompensated peadiatric patients of cirrhosis. However, these are markedly decreased in decompensated disease except for D dimer. Key words: Cirrhosis, Anti-thrombin III, Protein C, Protein S, D-dimer.

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Available abstract

Background: In asymptomatic peadiatric patients, cirrhosis is considered to be compensated, with or without gastroesophageal varices, it may be decompensated. Both Antithrombin III, Protein C and D dimers are sensitive markers of liver disease. Objective: To determine the frequency of compensated and decompensated cirrhosis in cirrhotic peadiatric patients and compare the status of protein C, Antithrombin lll deficiency and D-dimer in both groups. Methodology: In this cross sectional study, 80 peadiatric patients suspected to have cirrhosis were included, from November, 2015 to April, 2016, by non-probability convenience sampling. Variables included were; compensated and decompensated chronic liver disease, Antithrombin III, D dimer and Protein C, as natural anticoagulents. Data was analyzed by SPSS 13. Results: Out of 80 patients, 70 (87.5%) were in the compensated phase of cirrhosis. Mean Antithrombin III showed significant reduction in patients with decompensated cirrhosis (50.0±4.05%) when compared with patients with compensated liver disease (84.52 ±15.36%). Mean Protein C level exhibited also significant reduction in the decompensated patient groups (40±4.7%) when compared with the compensated group of patients (77.92±6.67%). The mean D-dimer levels showed significantly higher levels only in patients with signs of decompensated cirrhosis (840±11.85μg/L) when compared with compensated disease (629±6.29). Conclusion: Our study concluded that the natural anticoagulants Antithrombin III, Protein C and D dimer, reflect hepatocellular impairment in both compensated as well as decompensated peadiatric patients of cirrhosis. However, these are markedly decreased in decompensated disease except for D dimer. Key words: Cirrhosis, Anti-thrombin III, Protein C, Protein S, D-dimer.

Key concepts: Cirrhosis, Medicine, Gastroenterology, Internal medicine, Antithrombin, D-dimer, Liver disease, Asymptomatic

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