Antineoplastic drug contamination in the urine of Canadian healthcare workers

被引:59
作者
Hon, Chun-Yip [1 ,2 ]
Teschke, Kay [1 ]
Shen, Hui [1 ]
Demers, Paul A. [3 ,4 ]
Venners, Scott [5 ]
机构
[1] Univ British Columbia, Sch Populat & Publ Hlth, Vancouver, BC V5Z 1M9, Canada
[2] Ryerson Univ, Sch Occupat & Publ Hlth, Toronto, ON, Canada
[3] Canc Care Ontario, Occupat Canc Res Ctr, Toronto, ON, Canada
[4] Univ Toronto, Dalla Lana Sch Publ Hlth, Toronto, ON, Canada
[5] Simon Fraser Univ, Fac Hlth Sci, Burnaby, BC V5A 1S6, Canada
关键词
Antineoplastic drugs; Urinary concentration; Healthcare workers; Hospital medication system; Risk assessment; OCCUPATIONAL-EXPOSURE; CYCLOPHOSPHAMIDE EXCRETION; PHARMACY TECHNICIANS; HOSPITAL PERSONNEL; DERMAL EXPOSURE; AGENTS; TRENDS;
D O I
10.1007/s00420-015-1026-1
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Purpose The purpose of this study was to quantify the urine concentration of non-metabolized cyclophosphamide (CP), a commonly administered antineoplastic drug, among potentially exposed Canadian healthcare workers and to identify factors associated with the drug concentration levels. Methods Participants were asked to provide two sets of 24-h urine samples (at two different sampling events), and the level of CP was quantified using high-performance liquid chromatography-tandem mass spectrometry. In addition to demographic information, participants were surveyed regarding their frequency of handling of antineoplastic drugs, safe drug handling training, and known contact with CP on their work shift. Descriptive and inferential statistical analyses were performed. A backward stepwise linear mixed effect model was conducted to identify the factors associated with urine concentration levels. Results We collected 201 urine samples, and 55 % (n = 111) had levels greater than the LOD of 0.05 ng/mL. The mean urinary CP concentration was 0.156 ng/mL, the geometric mean was 0.067 ng/mL, the geometric standard deviation was 3.18, the 75th percentile was 0.129 ng/mL, and the range was < LOD to 2.37 ng/mL. All eight job categories evaluated had some urinary concentrations in excess of the LOD with unit clerks having the highest average level. Workers who worked in the drug administration unit, but were not responsible for administering the drugs to patients, i.e., volunteers, oncologists, ward aides, and dieticians, had the largest proportion of samples exceeding the LOD. We did not find any correlation between the urinary concentration levels and known contact with CP during the work shift. Two factors were found to be significantly associated with urinary CP concentration: (1) Workers who had a duty to handle antineoplastic drugs had higher concentration levels, and (2) workers who had not received safe drug handling training had higher levels of CP in their urine compared with those who had. Conclusions The presence of non-metabolized CP in urine confirms that, despite the existence of control measures, a broad range of healthcare workers are at risk of exposure to antineoplastic drugs. A review of the effectiveness of interventions to reduce exposure is warranted and should apply to all healthcare workers involved in some capacity with the hospital medication system. This study identified two factors that are related to the urine CP concentration levels which can serve as an impetus for reducing exposure.
引用
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页码:933 / 941
页数:9
相关论文
共 34 条
[1]  
[Anonymous], 2004, PREVENTING OCCUPATIO
[2]   Proposal for the assessment of quantitative dermal exposure limits in occupational environments: Part 1. Development of a concept to derive a quantitative dermal occupational exposure limit [J].
Bos, PMJ ;
Brouwer, DH ;
Stevenson, H ;
Boogaard, PJ ;
de Kort, WLAM ;
van Hemmen, JJ .
OCCUPATIONAL AND ENVIRONMENTAL MEDICINE, 1998, 55 (12) :795-804
[3]   Urinary cyclophosphamide excretion and micronuclei frequencies in peripheral lymphocytes and in exfoliated buccal epithelial cells of nurses handling antineoplastics [J].
Burgaz, S ;
Karahalil, B ;
Bayrak, P ;
Taskin, L ;
Yavuzaslan, F ;
Bökesoy, I ;
Anzion, RBM ;
Bos, RP ;
Platin, N .
MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 1999, 439 (01) :97-104
[4]   Preventing occupational exposures to antineoplastic drugs in health care settings [J].
Connor, Thomas H. ;
McDiarmid, Melissa A. .
CA-A CANCER JOURNAL FOR CLINICIANS, 2006, 56 (06) :354-365
[5]   Evaluation of Antineoplastic Drug Exposure of Health Care Workers at Three University-Based US Cancer Centers [J].
Connor, Thomas H. ;
DeBord, Gayle ;
Pretty, Jack R. ;
Oliver, Marc S. ;
Roth, Tracy S. ;
Lees, Peter S. J. ;
Krieg, Edward F., Jr. ;
Rogers, Bonnie ;
Escalante, Carmen P. ;
Toennis, Christine A. ;
Clark, John C. ;
Johnson, Belinda C. ;
McDiarmid, Melissa A. .
JOURNAL OF OCCUPATIONAL AND ENVIRONMENTAL MEDICINE, 2010, 52 (10) :1019-1027
[6]   Clinical pharmacokinetics of cyclophosphamide [J].
de Jonge, ME ;
Huitema, ADR ;
Rodenhuis, S ;
Beijnen, JH .
CLINICAL PHARMACOKINETICS, 2005, 44 (11) :1135-1164
[7]  
Dranitsaris George, 2005, J Oncol Pharm Pract, V11, P69, DOI 10.1191/1078155205jp155oa
[8]  
Favier B, 2003, B CANCER, V90, P905
[9]   Dermal exposure to cyclophosphamide in hospitals during preparation, nursing and cleaning activities [J].
Fransman, W ;
Vermeulen, R ;
Kromhout, H .
INTERNATIONAL ARCHIVES OF OCCUPATIONAL AND ENVIRONMENTAL HEALTH, 2005, 78 (05) :403-412
[10]   An Accurate Substitution Method for Analyzing Censored Data [J].
Ganser, Gary H. ;
Hewett, Paul .
JOURNAL OF OCCUPATIONAL AND ENVIRONMENTAL HYGIENE, 2010, 7 (04) :233-244