The effectiveness of patient-tailored treatment for acute organophosphate poisoning

Background: To determine a new pralidoxime (PAM) treatment guideline based on the severity of acute organophosphate intoxication patients, APACHE II score, and dynamic changes in serum butyrylcholinesterase (BuChE) activity. Methods: This is a randomization trial. All patients received supportive ca...

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Main Authors: Chih-Chuan Lin, Dong-Zong Hung, Hsien-Yi Chen, Kuang-Hung Hsu
Format: Article
Language:English
Published: Elsevier 2016-12-01
Series:Biomedical Journal
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2319417016303067
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author Chih-Chuan Lin
Dong-Zong Hung
Hsien-Yi Chen
Kuang-Hung Hsu
author_facet Chih-Chuan Lin
Dong-Zong Hung
Hsien-Yi Chen
Kuang-Hung Hsu
author_sort Chih-Chuan Lin
collection DOAJ
description Background: To determine a new pralidoxime (PAM) treatment guideline based on the severity of acute organophosphate intoxication patients, APACHE II score, and dynamic changes in serum butyrylcholinesterase (BuChE) activity. Methods: This is a randomization trial. All patients received supportive care measurements and atropinization. Each enrolled patient was treated with 2 gm PAM intravenously as the loading dose. The control group was treated according to the WHO's recommended PAM regimen, and the experimental group was treated according to their APACHE II scores and dynamic changes in BuChE activity. If a patient's APACHE II score was ≧26 or there was no elevation in BuChE activity at the 12th hour when compared to the 6th, doses of 1 g/h PAM (i.e., doubled WHO's recommended PAM regimen) were given. The levels of the serum BuChE and red blood cells acetylcholinesterase and the serum PAM levels were also measured. Results: Forty-six organophosphate poisoning patients were enrolled in this study. There were 24 patients in the control group and 22 patients in the experimental group. The hazard ratio of death in the control group to that of the experimental group was 111.51 (95% CI: 1.17–1.613.45; p = 0.04). The RBC acetylcholinesterase level was elevated in the experimental group but was not in the control group. The experimental group did not exhibit a higher PAM blood level than did the control group. Conclusion: The use of PAM can be guided by patient severity. Thus, may help to improve the outcomes of organophosphate poisoning patients.
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spelling doaj.art-18e7190ecb0e4718b04c9e026c15aaba2022-12-22T02:08:28ZengElsevierBiomedical Journal2319-41702016-12-0139639139910.1016/j.bj.2016.11.001The effectiveness of patient-tailored treatment for acute organophosphate poisoningChih-Chuan Lin0Dong-Zong Hung1Hsien-Yi Chen2Kuang-Hung Hsu3Department of Emergency Medicine, Chang Gung Memorial Hospital at Linkou, Chang Gung University College of Medicine, Taoyuan, TaiwanDepartment of Emergency Medicine, Toxicology Center, China Medical University Hospital, Taichung, TaiwanDepartment of Emergency Medicine, Chang Gung Memorial Hospital at Linkou, Chang Gung University College of Medicine, Taoyuan, TaiwanLaboratory for Epidemiology, Department of Health Care Management, and Healthy Aging Research Center, Chang Gung University, Taoyuan, TaiwanBackground: To determine a new pralidoxime (PAM) treatment guideline based on the severity of acute organophosphate intoxication patients, APACHE II score, and dynamic changes in serum butyrylcholinesterase (BuChE) activity. Methods: This is a randomization trial. All patients received supportive care measurements and atropinization. Each enrolled patient was treated with 2 gm PAM intravenously as the loading dose. The control group was treated according to the WHO's recommended PAM regimen, and the experimental group was treated according to their APACHE II scores and dynamic changes in BuChE activity. If a patient's APACHE II score was ≧26 or there was no elevation in BuChE activity at the 12th hour when compared to the 6th, doses of 1 g/h PAM (i.e., doubled WHO's recommended PAM regimen) were given. The levels of the serum BuChE and red blood cells acetylcholinesterase and the serum PAM levels were also measured. Results: Forty-six organophosphate poisoning patients were enrolled in this study. There were 24 patients in the control group and 22 patients in the experimental group. The hazard ratio of death in the control group to that of the experimental group was 111.51 (95% CI: 1.17–1.613.45; p = 0.04). The RBC acetylcholinesterase level was elevated in the experimental group but was not in the control group. The experimental group did not exhibit a higher PAM blood level than did the control group. Conclusion: The use of PAM can be guided by patient severity. Thus, may help to improve the outcomes of organophosphate poisoning patients.http://www.sciencedirect.com/science/article/pii/S2319417016303067OrganophosphatePoisoning severityPAM dose
spellingShingle Chih-Chuan Lin
Dong-Zong Hung
Hsien-Yi Chen
Kuang-Hung Hsu
The effectiveness of patient-tailored treatment for acute organophosphate poisoning
Biomedical Journal
Organophosphate
Poisoning severity
PAM dose
title The effectiveness of patient-tailored treatment for acute organophosphate poisoning
title_full The effectiveness of patient-tailored treatment for acute organophosphate poisoning
title_fullStr The effectiveness of patient-tailored treatment for acute organophosphate poisoning
title_full_unstemmed The effectiveness of patient-tailored treatment for acute organophosphate poisoning
title_short The effectiveness of patient-tailored treatment for acute organophosphate poisoning
title_sort effectiveness of patient tailored treatment for acute organophosphate poisoning
topic Organophosphate
Poisoning severity
PAM dose
url http://www.sciencedirect.com/science/article/pii/S2319417016303067
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