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本文引用的文献

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Exposure of hospital pharmacists and nurses to antineoplastic agents.医院药剂师和护士对抗肿瘤药物的接触。
J Occup Med. 1993 Jan;35(1):57-60.
2
The comparative pharmacology of cyclophosphamide and ifosfamide.环磷酰胺与异环磷酰胺的比较药理学
Semin Oncol. 1982 Dec;9(4 Suppl 1):2-7.
3
Acute nonlymphocytic leukemia after therapy with alkylating agents for ovarian cancer: a study of five randomized clinical trials.卵巢癌接受烷化剂治疗后发生的急性非淋巴细胞白血病:五项随机临床试验的研究
N Engl J Med. 1982 Dec 2;307(23):1416-21. doi: 10.1056/NEJM198212023072302.
4
The efficiency of protective gloves used in the handling of cytotoxic drugs.处理细胞毒性药物时使用的防护手套的效率。
Cancer Chemother Pharmacol. 1984;12(3):151-3. doi: 10.1007/BF00256536.
5
Permeability of latex and polyvinyl chloride gloves to 20 antineoplastic drugs.乳胶和聚氯乙烯手套对20种抗肿瘤药物的通透性
Am J Hosp Pharm. 1984 Dec;41(12):2618-23.
6
Occupational exposure to cyclophosphamide.职业性接触环磷酰胺。
Lancet. 1984 Jan 28;1(8370):186-8. doi: 10.1016/s0140-6736(84)92111-1.
7
Urinary thioether excretion in nurses handling cytotoxic drugs.接触细胞毒性药物的护士的尿硫醚排泄情况。
Lancet. 1982 Aug 21;2(8295):443-4. doi: 10.1016/s0140-6736(82)90474-3.
8
A study of occupational exposure to antineoplastic drugs and fetal loss in nurses.一项关于护士职业接触抗肿瘤药物与胎儿流产的研究。
N Engl J Med. 1985 Nov 7;313(19):1173-8. doi: 10.1056/NEJM198511073131901.
9
Risk of acute nonlymphocytic leukemia and preleukemia in patients treated with cyclophosphamide for non-Hodgkin's lymphomas. Comparison with results obtained in patients treated for Hodgkin's disease and ovarian carcinoma with other alkylating agents.接受环磷酰胺治疗的非霍奇金淋巴瘤患者发生急性非淋巴细胞白血病和白血病前期的风险。与接受其他烷化剂治疗的霍奇金病和卵巢癌患者的结果比较。
Ann Intern Med. 1985 Aug;103(2):195-200. doi: 10.7326/0003-4819-103-2-195.
10
Spontaneous abortions and malformations in the offspring of nurses exposed to anaesthetic gases, cytostatic drugs, and other potential hazards in hospitals, based on registered information of outcome.基于结局的登记信息,对在医院接触麻醉气体、细胞毒性药物及其他潜在危害的护士所生育后代的自然流产和畸形情况进行研究。
J Epidemiol Community Health. 1985 Jun;39(2):141-7. doi: 10.1136/jech.39.2.141.

对职业接触细胞毒性药物的医院工作人员尿液中环磷酰胺和异环磷酰胺的生物监测。

Biological monitoring of cyclophosphamide and ifosfamide in urine of hospital personnel occupationally exposed to cytostatic drugs.

作者信息

Ensslin A S, Stoll Y, Pethran A, Pfaller A, Römmelt H, Fruhmann G

机构信息

Institut und Poliklinik für Arbeitsmedizin, Universität München, Germany.

出版信息

Occup Environ Med. 1994 Apr;51(4):229-33. doi: 10.1136/oem.51.4.229.

DOI:10.1136/oem.51.4.229
PMID:8199663
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1127952/
Abstract

The occupational exposure of 21 nurses and pharmacy personnel from eight hospitals to cyclophosphamide and ifosfamide was determined by quantifying the amount of the drugs handled and by measuring the urinary excretion of the unmetabolised substances. Preparing antineoplastic drugs for intravenous treatment was the major task of all study participants. Twenty four hour urine was collected on days when cyclophosphamide and/or ifosfamide were mixed, on average 3900 mg cyclophosphamide and/or 5900 mg ifosfamide. The analyses were performed by gas chromatography with electron capture, detection limit 2.5 micrograms/24 hour urine. Despite standard safety precautions, including a vertical laminar air flow safety cabinet and gloves, cyclophosphamide was detected in 12 of 31 and ifosfamide in four of 21 urine samples on days when the drugs were handled. Excretion of cyclophosphamide ranged from 3.5 to 38 micrograms/24 h (mean 11.4 micrograms/24 h) urine, ifosfamide from 5 to 12.7 micrograms/24 h (mean 9 micrograms/24 h) urine. Based on an excretion rate of 11.3% unmetabolised cyclophosphamide, the average amount excreted corresponded to an uptake of 101 micrograms cyclophosphamide. For ifosfamide the mean quantity incorporated was 20 micrograms assuming that 45% of the drug was excreted. Pertaining to the doses handled, the uptake of cyclophosphamide and ifosfamide was estimated to be approximately 0.0025% and 0.0004% respectively. Despite time-consuming purification procedures, gas chromatographic analysis is a suitable method for monitoring personnel occupationally exposed to cyclophosphamide and ifosfamide and is a major contribution to the evaluation of potential health risks of exposed personnel.

摘要

通过对21名来自8家医院的护士和药剂人员处理的环磷酰胺和异环磷酰胺的量进行定量,并测量未代谢物质的尿排泄量,来确定他们的职业暴露情况。为静脉治疗配制抗肿瘤药物是所有研究参与者的主要任务。在环磷酰胺和/或异环磷酰胺混合的日子里收集24小时尿液,平均混合3900毫克环磷酰胺和/或5900毫克异环磷酰胺。分析采用带有电子捕获的气相色谱法,检测限为2.5微克/24小时尿液。尽管采取了标准的安全防护措施,包括垂直层流空气安全柜和手套,但在处理这些药物的日子里,31份尿液样本中有12份检测到环磷酰胺,21份尿液样本中有4份检测到异环磷酰胺。环磷酰胺的排泄量为3.5至38微克/24小时(平均11.4微克/24小时)尿液,异环磷酰胺为5至12.7微克/24小时(平均9微克/24小时)尿液。根据未代谢环磷酰胺11.3%的排泄率,平均排泄量相当于摄入了101微克环磷酰胺。对于异环磷酰胺,假设45%的药物被排泄,则平均摄入量为20微克。就处理的剂量而言,环磷酰胺和异环磷酰胺的摄入量估计分别约为0.0025%和0.0004%。尽管净化程序耗时,但气相色谱分析是监测职业接触环磷酰胺和异环磷酰胺人员的合适方法,对评估接触人员的潜在健康风险有重要作用。