The association between plasminogen activator inhibitor type-1 and clinical outcome in paediatric sepsis
Antonius H Pudjiadi1, Kania Adhyanisitha, Hardiono D Pusponegoro
1Department of Child-Health, Cipto Mangunkusumo Hospital-Faculty of Medicine Universitas Indonesia, Jakarta, Indonesia.
Insights
Plasminogen activator inhibitor type-1 (PAI-1) levels decreased significantly in pediatric sepsis survivors without overt disseminated intravascular coagulation (DIC). PAI-1 levels did not change significantly in non-survivors or those with overt DIC, indicating its complex role in sepsis outcomes.
Area of Science:
- Pediatric critical care medicine
- Hematology
- Infectious diseases
Background:
- Plasminogen activator inhibitor type-1 (PAI-1) is an acute phase protein crucial for inhibiting fibrinolysis.
- Elevated PAI-1 levels are associated with poorer outcomes in sepsis and sepsis-induced disseminated intravascular coagulation (DIC).
- Understanding PAI-1 dynamics in pediatric sepsis is vital for predicting clinical outcomes.
Purpose of the Study:
- To investigate the relationship between plasma PAI-1 levels and clinical outcomes in children diagnosed with sepsis.
- To analyze PAI-1 level changes over time in relation to DIC status and survival.
Main Methods:
- A prospective study involving 35 children with sepsis.
- Plasma PAI-1 levels were measured on day 1 and day 4 of admission.
- Coagulation profiles were assessed on day 4, and patients were followed for 28 days for survival outcomes.
Main Results:
- PAI-1 levels significantly decreased from day 1 to day 4 in non-overt DIC patients (95.25 ± 46.57 vs. 60.36 ± 37.31 ng/ml, P ≤ 0.001).
- Survivors showed a statistically significant decrease in PAI-1 from day 1 to day 4 (82.47 ± 44.43 vs. 58.39 ± 32.98 ng/ml, P = 0.021).
- No significant PAI-1 level changes were observed between day 1 and day 4 in overt DIC patients or non-survivors. PAI-1 positively correlated with DIC score (r = 0.606, P ≤ 0.001).
Conclusions:
- PAI-1 levels decrease over time in pediatric sepsis survivors, particularly those without overt DIC.
- The lack of significant PAI-1 reduction in overt DIC and non-survivors suggests a different pathophysiological role in severe sepsis.
- PAI-1 levels and their dynamic changes may serve as potential biomarkers for sepsis severity and outcome prediction in children.
Abstract:
: Acute phase protein plasminogen activator inhibitor type-1 (PAI-1) is a key element in fibrinolysis inhibition in sepsis-induced disseminated intravascular coagulation (DIC). Elevated PAI-1 level is related to worse outcome in sepsis. The aim of this study was to investigate the relationship between plasma PAI-1 level and clinical outcome in children with sepsis. A total of 35 children with sepsis were enrolled into this prospective study. Plasma PAI-1 was measured on day-1 and day-4. Systemic coagulation profile was measured on day-4. Individuals were followed up until 28 days. The mean PAI-1 from day-1 to day-4 in overt DIC children was not statistically significant. Contrarily, among nonovert DIC individuals, there was a significant difference (P ≤ 0.001) in PAI-1 levels on day-1 compared with day-4 were 95.25 ± 46.57 vs. 60.36 ± 37.31 ng/ml, respectively. Among survivors, mean PAI-1 level on day-1 was statistically higher than PAI-1 level on day-4 (82.47 ± 44.43 vs. 58.39 ± 32.98 ng/ml), P = 0.021. There was no significant difference between PAI-1 levels on day-1 compared with day-4 in nonsurvivors. PAI-1 was correlated to DIC score with r = 0.606 (P ≤ 0.001). PAI-1 levels significantly decreased on day-4 compared with day-1 among nonovert DIC individuals, and not in overt DIC individuals. Changes in PAI-1 levels in nonsurvivors did not differ. PAI-1 level was positively correlated with DIC score.
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