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Extracorporeal treatment for carbamazepine poisoning: Systematic review and recommendations from the EXTRIP workgroup
Context. The Extracorporeal Treatments in Poisoning (EXTRIP) workgroup was created to provide evidence and consensus-based recommendations on the use of extracorporeal treatments (ECTRs) in poisoning. Objectives. To perform a systematic review and provide clinical recommendations for ECTR in carbama...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Taylor & Francis
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4782683/ https://www.ncbi.nlm.nih.gov/pubmed/25355482 http://dx.doi.org/10.3109/15563650.2014.973572 |
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author | Ghannoum, Marc Yates, Christopher Galvao, Tais F. Sowinski, Kevin M. Vo, Thi Hai Vân Coogan, Andrew Gosselin, Sophie Lavergne, Valery Nolin, Thomas D. Hoffman, Robert S. |
author_facet | Ghannoum, Marc Yates, Christopher Galvao, Tais F. Sowinski, Kevin M. Vo, Thi Hai Vân Coogan, Andrew Gosselin, Sophie Lavergne, Valery Nolin, Thomas D. Hoffman, Robert S. |
author_sort | Ghannoum, Marc |
collection | PubMed |
description | Context. The Extracorporeal Treatments in Poisoning (EXTRIP) workgroup was created to provide evidence and consensus-based recommendations on the use of extracorporeal treatments (ECTRs) in poisoning. Objectives. To perform a systematic review and provide clinical recommendations for ECTR in carbamazepine poisoning. Methods. After a systematic literature search, the subgroup extracted the data and summarized the findings following a pre-determined format. The entire workgroup voted via a two-round modified Delphi method to reach a consensus on voting statements, using a RAND/UCLA Appropriateness Method to quantify disagreement. Anonymous votes were compiled, returned, and discussed in person. A second vote determined the final recommendations. Results. Seventy-four articles met inclusion criteria. Articles included case reports, case series, descriptive cohorts, pharmacokinetic studies, and in-vitro studies; two poor-quality observational studies were identified, yielding a very low quality of evidence for all recommendations. Data on 173 patients, including 6 fatalities, were reviewed. The workgroup concluded that carbamazepine is moderately dialyzable and made the following recommendations: ECTR is suggested in severe carbamazepine poisoning (2D). ECTR is recommended if multiple seizures occur and are refractory to treatment (1D), or if life-threatening dysrhythmias occur (1D). ECTR is suggested if prolonged coma or respiratory depression requiring mechanical ventilation are present (2D) or if significant toxicity persists, particularly when carbamazepine concentrations rise or remain elevated, despite using multiple-dose activated charcoal (MDAC) and supportive measures (2D). ECTR should be continued until clinical improvement is apparent (1D) or the serum carbamazepine concentration is below 10 mg/L (42 the μ in μmol/L looks weird.) (2D). Intermittent hemodialysis is the preferred ECTR (1D), but both intermittent hemoperfusion (1D) or continuous renal replacement therapies (3D) are alternatives if hemodialysis is not available. MDAC therapy should be continued during ECTR (1D). Conclusion. Despite the low quality of the available clinical evidence and the high protein binding capacity of carbamazepine, the workgroup suggested extracorporeal removal in cases of severe carbamazepine poisoning. |
format | Online Article Text |
id | pubmed-4782683 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-47826832016-03-23 Extracorporeal treatment for carbamazepine poisoning: Systematic review and recommendations from the EXTRIP workgroup Ghannoum, Marc Yates, Christopher Galvao, Tais F. Sowinski, Kevin M. Vo, Thi Hai Vân Coogan, Andrew Gosselin, Sophie Lavergne, Valery Nolin, Thomas D. Hoffman, Robert S. Clin Toxicol (Phila) Review Article Context. The Extracorporeal Treatments in Poisoning (EXTRIP) workgroup was created to provide evidence and consensus-based recommendations on the use of extracorporeal treatments (ECTRs) in poisoning. Objectives. To perform a systematic review and provide clinical recommendations for ECTR in carbamazepine poisoning. Methods. After a systematic literature search, the subgroup extracted the data and summarized the findings following a pre-determined format. The entire workgroup voted via a two-round modified Delphi method to reach a consensus on voting statements, using a RAND/UCLA Appropriateness Method to quantify disagreement. Anonymous votes were compiled, returned, and discussed in person. A second vote determined the final recommendations. Results. Seventy-four articles met inclusion criteria. Articles included case reports, case series, descriptive cohorts, pharmacokinetic studies, and in-vitro studies; two poor-quality observational studies were identified, yielding a very low quality of evidence for all recommendations. Data on 173 patients, including 6 fatalities, were reviewed. The workgroup concluded that carbamazepine is moderately dialyzable and made the following recommendations: ECTR is suggested in severe carbamazepine poisoning (2D). ECTR is recommended if multiple seizures occur and are refractory to treatment (1D), or if life-threatening dysrhythmias occur (1D). ECTR is suggested if prolonged coma or respiratory depression requiring mechanical ventilation are present (2D) or if significant toxicity persists, particularly when carbamazepine concentrations rise or remain elevated, despite using multiple-dose activated charcoal (MDAC) and supportive measures (2D). ECTR should be continued until clinical improvement is apparent (1D) or the serum carbamazepine concentration is below 10 mg/L (42 the μ in μmol/L looks weird.) (2D). Intermittent hemodialysis is the preferred ECTR (1D), but both intermittent hemoperfusion (1D) or continuous renal replacement therapies (3D) are alternatives if hemodialysis is not available. MDAC therapy should be continued during ECTR (1D). Conclusion. Despite the low quality of the available clinical evidence and the high protein binding capacity of carbamazepine, the workgroup suggested extracorporeal removal in cases of severe carbamazepine poisoning. Taylor & Francis 2014-12-01 2014-10-30 /pmc/articles/PMC4782683/ /pubmed/25355482 http://dx.doi.org/10.3109/15563650.2014.973572 Text en © 2014 The Author(s). Published by Taylor & Francis. http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted. |
spellingShingle | Review Article Ghannoum, Marc Yates, Christopher Galvao, Tais F. Sowinski, Kevin M. Vo, Thi Hai Vân Coogan, Andrew Gosselin, Sophie Lavergne, Valery Nolin, Thomas D. Hoffman, Robert S. Extracorporeal treatment for carbamazepine poisoning: Systematic review and recommendations from the EXTRIP workgroup |
title | Extracorporeal treatment for carbamazepine poisoning: Systematic review and recommendations from the EXTRIP workgroup |
title_full | Extracorporeal treatment for carbamazepine poisoning: Systematic review and recommendations from the EXTRIP workgroup |
title_fullStr | Extracorporeal treatment for carbamazepine poisoning: Systematic review and recommendations from the EXTRIP workgroup |
title_full_unstemmed | Extracorporeal treatment for carbamazepine poisoning: Systematic review and recommendations from the EXTRIP workgroup |
title_short | Extracorporeal treatment for carbamazepine poisoning: Systematic review and recommendations from the EXTRIP workgroup |
title_sort | extracorporeal treatment for carbamazepine poisoning: systematic review and recommendations from the extrip workgroup |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4782683/ https://www.ncbi.nlm.nih.gov/pubmed/25355482 http://dx.doi.org/10.3109/15563650.2014.973572 |
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