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本文引用的文献

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Rapid identification of laboratory contamination with Mycobacterium tuberculosis using variable number tandem repeat analysis.使用可变数目串联重复序列分析快速鉴定结核分枝杆菌的实验室污染情况。
J Clin Microbiol. 2001 Jan;39(1):69-74. doi: 10.1128/JCM.39.1.69-74.2001.
2
Review of false-positive cultures for Mycobacterium tuberculosis and recommendations for avoiding unnecessary treatment.结核分枝杆菌培养假阳性的综述及避免不必要治疗的建议。
Clin Infect Dis. 2000 Dec;31(6):1390-5. doi: 10.1086/317504. Epub 2000 Nov 17.
3
Transmission of Mycobacterium tuberculosis from medical waste.结核分枝杆菌通过医疗废物传播。
JAMA. 2000 Oct 4;284(13):1683-8. doi: 10.1001/jama.284.13.1683.
4
Misdiagnoses of tuberculosis resulting from laboratory cross-contamination of Mycobacterium tuberculosis cultures--New Jersey, 1998.
MMWR Morb Mortal Wkly Rep. 2000 May 19;49(19):413-6.
5
Isolation and stigma: the experience of patients with active tuberculosis.隔离与污名化:活动性肺结核患者的经历
J Community Health Nurs. 1999 Winter;16(4):233-41. doi: 10.1207/S15327655JCHN1604_3.
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Pharmacokinetic factors in the modern drug treatment of tuberculosis.结核病现代药物治疗中的药代动力学因素
Clin Pharmacokinet. 1999 Aug;37(2):127-46. doi: 10.2165/00003088-199937020-00003.
7
Mycobactericidal activity of selected disinfectants using a quantitative suspension test.采用定量悬液试验检测选定消毒剂的杀分枝杆菌活性。
J Hosp Infect. 1999 Feb;41(2):111-21. doi: 10.1016/s0195-6701(99)90048-8.
8
Computer analysis of IS6110 RFLP patterns of Mycobacterium tuberculosis.结核分枝杆菌IS6110限制性片段长度多态性模式的计算机分析
Methods Mol Biol. 1998;101:395-422. doi: 10.1385/0-89603-471-2:395.
9
Utility of molecular epidemiology of tuberculosis.结核病分子流行病学的效用
Eur Respir J. 1998 Apr;11(4):795-7. doi: 10.1183/09031936.98.11040795.
10
Investigation of cross contamination in a Mycobacterium tuberculosis laboratory using IS6110 DNA fingerprinting.使用IS6110 DNA指纹技术对结核分枝杆菌实验室中的交叉污染进行调查。
Int J Tuberc Lung Dis. 1998 May;2(5):425-9.

荷兰44家实验室中结核分枝杆菌培养假阳性情况(1993年至2000年):发生率、危险因素及后果

False-positive mycobacterium tuberculosis cultures in 44 laboratories in The Netherlands (1993 to 2000): incidence, risk factors, and consequences.

作者信息

de Boer Annette S, Blommerde Barbara, de Haas Petra E W, Sebek Maruschka M G G, Lambregts-van Weezenbeek Kitty S B, Dessens Mirjam, van Soolingen Dick

机构信息

Center for Infectious Diseases Epidemiology, The Hague, The Netherlands.

出版信息

J Clin Microbiol. 2002 Nov;40(11):4004-9. doi: 10.1128/JCM.40.11.4004-4009.2002.

DOI:10.1128/JCM.40.11.4004-4009.2002
PMID:12409366
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC139647/
Abstract

False-positive Mycobacterium tuberculosis cultures are a benchmark for the quality of laboratory processes and patient care. We studied the incidence of false-positive cultures, risk factors, and consequences for patients during the period from 1993 to 2000 in 44 peripheral laboratories in The Netherlands. The national reference laboratory tested 8,889 M. tuberculosis isolates submitted by these laboratories. By definition, a culture was false positive (i) if the DNA fingerprint of the isolate was identical to that of an isolate from another patient processed within 7 days in the same laboratory, (ii) if the isolate was taken from a patient without clinical signs of tuberculosis, and/or (iii) if the false-positive test result was confirmed by the peripheral laboratory and/or the public health tuberculosis officer. We identified 213 false-positive cultures (2.4%). The overall incidence of false-positive cultures decreased over the years, from 3.9% in 1993 to 1.1% in 2000. Laboratories with false-positive cultures more often processed less than 3,000 samples per year (P < 0.05). Among 110 patients for whom a false-positive culture was identified from 1995 to 1999, we found that for 36% of the patients an official tuberculosis notification had been provided to the appropriate public health services, 31% of the patients were treated, 14% of the patients were hospitalized, and a contact investigation had been initiated for 16% of the patients. The application of DNA fingerprinting to identify false-positive M. tuberculosis cultures and the provision of feedback to peripheral laboratories are useful instruments to improve the quality of laboratory processes and the quality of medical care.

摘要

结核分枝杆菌培养假阳性是实验室操作流程和患者护理质量的一个基准。我们研究了1993年至2000年期间荷兰44家外围实验室中假阳性培养物的发生率、危险因素及对患者的影响。国家参考实验室检测了这些实验室提交的8889株结核分枝杆菌分离株。根据定义,若分离株的DNA指纹与同一实验室7天内处理的另一患者的分离株相同,或分离株取自无结核病临床症状的患者,和/或若外围实验室及/或公共卫生结核病官员确认检测结果为假阳性,则该培养物为假阳性。我们识别出213例假阳性培养物(2.4%)。多年来假阳性培养物的总体发生率有所下降,从1993年的3.9%降至2000年的1.1%。有假阳性培养物的实验室每年处理的样本往往少于3000份(P<0.05)。在1995年至1999年期间识别出假阳性培养物的110例患者中,我们发现36%的患者已向适当的公共卫生服务机构进行了官方结核病通报,31%的患者接受了治疗,14%的患者住院,16%的患者已启动接触者调查。应用DNA指纹识别结核分枝杆菌培养假阳性并向外围实验室提供反馈是提高实验室操作流程质量和医疗护理质量的有用手段。