scholarly journals Hypoglycemia and lactic acidosis outperform King’s College criteria for predicting death or transplant in acetaminophen toxic patients

2018 ◽  
Vol 56 (7) ◽  
pp. 622-625 ◽  
Author(s):  
Michael Levine ◽  
Samuel J. Stellpflug ◽  
Anthony F. Pizon ◽  
David A. Peak ◽  
Janna Villano ◽  
...  
2018 ◽  
Vol 56 (10) ◽  
pp. 908-909
Author(s):  
Jeremy Brice Bitton ◽  
Josh Jiaxing Wang ◽  
Winnie Teng ◽  
Eric Villeneuve ◽  
Sophie Gosselin

2021 ◽  
Vol 50 (1) ◽  
pp. 761-761
Author(s):  
Sagar Dave ◽  
Guinevere Johnson ◽  
William Teeter ◽  
Thomas Scalea ◽  
Christopher Kolokythas ◽  
...  

2017 ◽  
Vol 2 ◽  
pp. 73-73
Author(s):  
Ahmed Kayal ◽  
Vladimir Marquez-Azalgara ◽  
Siegfried R. Erb ◽  
Charles H. Scudamore ◽  
Eric M. Yoshida

2022 ◽  
Vol 11 (2) ◽  
pp. 432
Author(s):  
Tudor Lucian Pop ◽  
Cornel Olimpiu Aldea ◽  
Dan Delean ◽  
Bogdan Bulata ◽  
Dora Boghiţoiu ◽  
...  

Objectives: In children, acute liver failure (ALF) is a severe condition with high mortality. As some patients need liver transplantation (LT), it is essential to predict the fatal evolution and to refer them early for LT if needed. Our study aimed to evaluate the prognostic criteria and scores for assessing the outcome in children with ALF. Methods: Data of 161 children with ALF (54.66% female, mean age 7.66 ± 6.18 years) were analyzed based on final evolution (32.91% with fatal evolution or LT) and etiology. We calculated on the first day of hospitalization the PELD score (109 children), MELD, and MELD-Na score (52 children), and King’s College Criteria (KCC) for all patients. The Nazer prognostic index and Wilson index for predicting mortality were calculated for nine patients with ALF in Wilson’s disease (WD). Results: PELD, MELD, and MELD-Na scores were significantly higher in patients with fatal evolution (21.04 ± 13.28 vs. 13.99 ± 10.07, p = 0.0023; 36.20 ± 19.51 vs. 20.08 ± 8.57, p < 0.0001; and 33.07 ± 8.29 vs. 20.08 ± 8.47, p < 0.0001, respectively). Moreover, age, bilirubin, albumin, INR, and hemoglobin significantly differed in children with fatal evolution. Function to etiology, PELD, MELD, MELD-Na, and KCC accurately predicted fatal evolution in toxic ALF (25.33 vs. 9.90, p = 0.0032; 37.29 vs. 18.79, p < 0.0001; 34.29 vs. 19.24, p = 0.0002, respectively; with positive predicting value 100%, negative predicting value 88.52%, and accuracy 89.23% for King’s College criteria). The Wilson index for predicting mortality had an excellent predictive strength (100% sensibility and specificity), better than the Nazer prognostic index. Conclusions: Prognostic scores may be used to predict the fatal evolution of ALF in children in correlation with other parameters or criteria. Early estimation of the outcome of ALF is essential, mainly in countries where emergency LT is problematic, as the transfer to a specialized center could be delayed, affecting survival chances.


2015 ◽  
Author(s):  
Sean Rhyee ◽  
Katherine Boyle

Acetaminophen is the most common toxic ingestion in the United States, causing 400 deaths per year. Poisoning occurs both intentionally and unintentionally, with suicidal intent, overuse for treatment of pain, and ingestion of multiple medications containing acetaminophen all contributing. Aspirin poisoning remains a concern even though its popularity as an analgesic and antipyretic has decreased over time. Among nonaspirin nonsteroidal antiinflammatory drugs (NSAIDs), ibuprofen and naproxen are the most commonly encountered in overdose, likely due to their easy availability as over-the-counter medications. This review covers the principles of toxicity, immediate stabilization, diagnosis and definitive therapy, and disposition and outcomes related to acetaminophen, aspirin, and ibuprofen and other NSAIDs. Tables describe N-acetylcysteine dosing, King’s College criteria for acetaminophen-induced liver failure, and indications for hemodialysis in aspirin poisoning. Figures include a pie chart showing acetaminophen metabolization, the Rumack-Matthew nomogram, and a graph showing frequency of hepatotoxicity in patients receiving N-acetylcysteine. This review contains 3 highly rendered figures, 3 tables, and 97 references.


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