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化疗药物外渗:预防与治疗

Extravasation of chemotherapeutic agents: prevention and treatment.

作者信息

Goolsby Tiffany V, Lombardo Fredric A

机构信息

Division of Clinical and Administrative Pharmacy Sciences, Howard University College of Pharmacy, Washington, DC 20059, USA.

出版信息

Semin Oncol. 2006 Feb;33(1):139-43. doi: 10.1053/j.seminoncol.2005.11.007.

Abstract

Most chemotherapeutic agents can cause varying degrees of local tissue injuries when extravasated. The medical treatment of extravasation is based on proper maintenance of the intravenous (IV) line and application of cold or warm compresses, plus the use of antidotes when available. Antidotes for extravasation that have been shown to be useful are sodium thiosulfate for nitrogen mustard, dimethylsulfoxide for anthracyclines and mitomycin, and hyaluronidase for the vinca alkaloids. New treatments include dexrazoxane, sargramostim, and hyperbaric oxygen for doxorubicin extravasations. Tissue damage secondary to drug infiltration occurs as a result of one of two major mechanisms: (1) the drug is absorbed by local cells in the tissue and binds to critical structures (eg, DNA, microtubules), causing cell death; and (2) the drug does not bind to cellular DNA. Damage to immediately adjacent tissue is more readily neutralized than is damage to surrounding tissue.

摘要

大多数化疗药物外渗时可导致不同程度的局部组织损伤。外渗的医学处理基于正确维护静脉输液通路、应用冷敷或热敷,以及在有可用解毒剂时使用解毒剂。已证明有用的外渗解毒剂有:用于氮芥的硫代硫酸钠、用于蒽环类药物和丝裂霉素的二甲亚砜,以及用于长春花生物碱的透明质酸酶。新的治疗方法包括用于阿霉素外渗的右丙亚胺、沙格司亭和高压氧。药物浸润继发的组织损伤是由两种主要机制之一引起的:(1)药物被组织中的局部细胞吸收并与关键结构(如DNA、微管)结合,导致细胞死亡;(2)药物不与细胞DNA结合。紧邻组织的损伤比周围组织的损伤更容易被中和。

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