Literature DB >> 25950372

Extracorporeal treatment for valproic acid poisoning: systematic review and recommendations from the EXTRIP workgroup.

Marc Ghannoum1, Martin Laliberté, Thomas D Nolin, Robert MacTier, Valery Lavergne, Robert S Hoffman, Sophie Gosselin.   

Abstract

BACKGROUND: The EXtracorporeal TReatments In Poisoning (EXTRIP) workgroup presents its systematic review and clinical recommendations on the use of extracorporeal treatment (ECTR) in valproic acid (VPA) poisoning.
METHODS: The lead authors reviewed all of the articles from a systematic literature search, extracted the data, summarized the key findings, and proposed structured voting statements following a predetermined format. A two-round modified Delphi method was chosen to reach a consensus on voting statements and the RAND/UCLA Appropriateness Method was used to quantify disagreement. Anonymous votes were compiled, returned, and discussed in person. A second vote was conducted to determine the final workgroup recommendations.
RESULTS: The latest literature search conducted in November 2014 retrieved a total of 79 articles for final qualitative analysis, including one observational study, one uncontrolled cohort study with aggregate analysis, 70 case reports and case series, and 7 pharmacokinetic studies, yielding a very low quality of evidence for all recommendations. Clinical data were reported for 82 overdose patients while pharmaco/toxicokinetic grading was performed in 55 patients. The workgroup concluded that VPA is moderately dialyzable (level of evidence = B) and made the following recommendations: ECTR is recommended in severe VPA poisoning (1D); recommendations for ECTR include a VPA concentration > 1300 mg/L (9000 μmol/L)(1D), the presence of cerebral edema (1D) or shock (1D); suggestions for ECTR include a VPA concentration > 900 mg/L (6250 μmol/L)(2D), coma or respiratory depression requiring mechanical ventilation (2D), acute hyperammonemia (2D), or pH ≤ 7.10 (2D). Cessation of ECTR is indicated when clinical improvement is apparent (1D) or the serum VPA concentration is between 50 and 100 mg/L (350-700 μmol/L)(2D). Intermittent hemodialysis is the preferred ECTR in VPA poisoning (1D). If hemodialysis is not available, then intermittent hemoperfusion (1D) or continuous renal replacement therapy (2D) is an acceptable alternative.
CONCLUSIONS: VPA is moderately dialyzable in the setting of overdose. ECTR is indicated for VPA poisoning if at least one of the above criteria is present. Intermittent hemodialysis is the preferred ECTR modality in VPA poisoning.

Entities:  

Keywords:  Anticonvulsant; Extracoporeal treatments; Poisoning; Recommendations; Valproic acid

Mesh:

Substances:

Year:  2015        PMID: 25950372     DOI: 10.3109/15563650.2015.1035441

Source DB:  PubMed          Journal:  Clin Toxicol (Phila)        ISSN: 1556-3650            Impact factor:   4.467


  15 in total

1.  Novel Mechanisms of Valproate Hepatotoxicity: Impaired Mrp2 Trafficking and Hepatocyte Depolarization.

Authors:  Dong Fu; Panli Cardona; Henry Ho; Paul B Watkins; Kim L R Brouwer
Journal:  Toxicol Sci       Date:  2019-07-31       Impact factor: 4.849

2.  Renal replacement therapy in the management of intoxications in children: recommendations from the Pediatric Continuous Renal Replacement Therapy (PCRRT) workgroup.

Authors:  Rupesh Raina; Manpreet K Grewal; Martha Blackford; Jordan M Symons; Michael J G Somers; Christoph Licht; Rajit K Basu; Sidharth Kumar Sethi; Deepa Chand; Gaurav Kapur; Mignon McCulloch; Arvind Bagga; Vinod Krishnappa; Hui-Kim Yap; Marcelo de Sousa Tavares; Timothy E Bunchman; Michelle Bestic; Bradley A Warady; Maria Díaz-González de Ferris
Journal:  Pediatr Nephrol       Date:  2019-08-24       Impact factor: 3.714

Review 3.  Extracorporeal Removal of Poisons and Toxins.

Authors:  Joshua David King; Moritz H Kern; Bernard G Jaar
Journal:  Clin J Am Soc Nephrol       Date:  2019-08-22       Impact factor: 8.237

Review 4.  Antiepileptic Drug Removal by Continuous Renal Replacement Therapy: A Review of the Literature.

Authors:  Sherif Hanafy Mahmoud
Journal:  Clin Drug Investig       Date:  2017-01       Impact factor: 2.859

5.  Amitriptyline accumulation in tissues after coated activated charcoal hemoperfusion-a randomized controlled animal poisoning model.

Authors:  Tejs Jansen; Lotte C G Hoegberg; Thomas Eriksen; Kim P Dalhoff; Bo Belhage; Sys S Johansen
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  2019-06-11       Impact factor: 3.000

6.  Valproate-Induced Hyperammonemic Encephalopathy Following Accidental Ingestion in a Toddler.

Authors:  Moftah Alhagamhmad; Aisha Elarwah; Alia Alhassony; Shirin Alougly; Hamza Milad; Aziza Dehoam; Suliman Elbrgathy; Nuri Shembesh; Emhemed Mousa; Abdulhamid ElShiky
Journal:  J Pediatr Pharmacol Ther       Date:  2021-02-15

7.  Rapid Rescue From Hyperammonemic Coma After Valproic Acid Poisoning: Dual Therapy With Continuous Renal Replacement Therapy and L-Carnitine Supplementation.

Authors:  Shyam Kiran Gandam Venkata; Kenneth Guillotte; BreeAnna Murphy; Sai Sruthi Bhuram; Sudeep Chakravarthy Bhuram
Journal:  Cureus       Date:  2021-06-27

Review 8.  The Role of RRT in Hyperammonemic Patients.

Authors:  Shruti Gupta; Andrew Z Fenves; Robert Hootkins
Journal:  Clin J Am Soc Nephrol       Date:  2016-05-19       Impact factor: 8.237

Review 9.  The Role of Renal Replacement Therapy in the Management of Pharmacologic Poisonings.

Authors:  Aibek E Mirrakhimov; Aram Barbaryan; Adam Gray; Taha Ayach
Journal:  Int J Nephrol       Date:  2016-11-30

10.  All guns blazing: management and survival of massive valproic acid overdose - case report and literature review.

Authors:  Shaikha Al Jawder; Eiman AlJishi; Shaikhah Al-Otaibi; Mohammed S Al-Shahrani
Journal:  Open Access Emerg Med       Date:  2018-01-25
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