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本文引用的文献

1
Propylene glycol accumulation in critically ill patients receiving continuous intravenous lorazepam infusions.危重症患者持续静脉输注劳拉西泮时丙二醇的蓄积。
Ann Pharmacother. 2009 Dec;43(12):1964-71. doi: 10.1345/aph.1M313. Epub 2009 Nov 17.
2
Exposure to the pharmaceutical excipients benzyl alcohol and propylene glycol among critically ill neonates.危重新生儿接触药用辅料苯甲醇和丙二醇的情况。
Pediatr Crit Care Med. 2009 Mar;10(2):256-9. doi: 10.1097/PCC.0b013e31819a383c.
3
Determination of a lorazepam dose threshold for using the osmol gap to monitor for propylene glycol toxicity.确定使用渗透压间隙监测丙二醇毒性时劳拉西泮的剂量阈值。
Pharmacotherapy. 2008 Aug;28(8):984-91. doi: 10.1592/phco.28.8.984.
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A prospective evaluation of propylene glycol clearance and accumulation during continuous-infusion lorazepam in critically ill patients.对危重症患者持续输注劳拉西泮期间丙二醇清除率及蓄积情况的前瞻性评估。
J Intensive Care Med. 2008 May-Jun;23(3):184-94. doi: 10.1177/0885066608315808.
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Recognition, treatment, and prevention of propylene glycol toxicity.丙二醇毒性的识别、治疗与预防。
Semin Dial. 2007 May-Jun;20(3):217-9. doi: 10.1111/j.1525-139X.2007.00280.x.
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Osmol gap as a surrogate marker for serum propylene glycol concentrations in patients receiving lorazepam for sedation.渗透压间隙作为接受劳拉西泮镇静治疗患者血清丙二醇浓度的替代标志物。
Pharmacotherapy. 2006 Jan;26(1):23-33. doi: 10.1592/phco.2006.26.1.23.
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Propylene glycol toxicity: a severe iatrogenic illness in ICU patients receiving IV benzodiazepines: a case series and prospective, observational pilot study.丙二醇毒性:接受静脉注射苯二氮䓬类药物的重症监护病房患者中的一种严重医源性疾病:病例系列及前瞻性观察性初步研究
Chest. 2005 Sep;128(3):1674-81. doi: 10.1378/chest.128.3.1674.
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Relationship of continuous infusion lorazepam to serum propylene glycol concentration in critically ill adults.危重症成年患者中持续输注劳拉西泮与血清丙二醇浓度的关系。
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Propylene glycol-associated renal toxicity from lorazepam infusion.劳拉西泮静脉输注所致丙二醇相关性肾毒性。
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Agitation by sedation.
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儿童丙二醇中毒

Propylene glycol toxicity in children.

作者信息

Lim Terri Y, Poole Robert L, Pageler Natalie M

机构信息

Departments of Pharmacy, Lucile Packard Children's Hospital Stanford, Palo Alto, California.

Division of Critical Care Medicine, Department of Pediatrics, Stanford University Medical School, Stanford, California ; Clinical Informatics, Lucile Packard Children's Hospital Stanford, Palo Alto, California.

出版信息

J Pediatr Pharmacol Ther. 2014 Oct-Dec;19(4):277-82. doi: 10.5863/1551-6776-19.4.277.

DOI:10.5863/1551-6776-19.4.277
PMID:25762872
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4341412/
Abstract

Propylene glycol (PG) is a commonly used solvent for oral, intravenous, and topical pharmaceutical agents. Although PG is generally considered safe, when used in high doses or for prolonged periods, PG toxicity can occur. Reported adverse effects from PG include central nervous system (CNS) toxicity, hyperosmolarity, hemolysis, cardiac arrhythmia, seizures, agitation, and lactic acidosis. Patients at risk for toxicity include infants, those with renal or hepatic insuficiency, epilepsy, and burn patients receiving extensive dermal applications of PG containing products. Laboratory monitoring of PG levels, osmolarity, lactate, pyruvate, bicarbonate, creatinine, and anion gap can assist practitioners in making the diagnosis of PG toxicity. Numerous studies and case reports have been published on PG toxicity in adults. However, very few have been reported in pediatric patient populations. A review of the literature is presented.

摘要

丙二醇(PG)是口服、静脉注射和局部用药常用的溶剂。尽管PG通常被认为是安全的,但在高剂量或长期使用时,可能会发生PG毒性。PG报告的不良反应包括中枢神经系统(CNS)毒性、高渗性、溶血、心律失常、癫痫发作、躁动和乳酸酸中毒。毒性风险患者包括婴儿、肾或肝功能不全者、癫痫患者以及接受含PG产品广泛皮肤应用的烧伤患者。对PG水平、渗透压、乳酸、丙酮酸、碳酸氢盐、肌酐和阴离子间隙进行实验室监测有助于医生诊断PG毒性。关于成人PG毒性已发表了大量研究和病例报告。然而,儿科患者群体中的报告却非常少。本文对相关文献进行了综述。