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MMWR Morb Mortal Wkly Rep. 2013 Dec 13;62(49):1014-5.

本文引用的文献

1
Updated guidelines for using Interferon Gamma Release Assays to detect Mycobacterium tuberculosis infection - United States, 2010.更新的使用干扰素γ释放试验来检测结核分枝杆菌感染的指南-美国,2010 年。
MMWR Recomm Rep. 2010 Jun 25;59(RR-5):1-25.
2
Guidelines for preventing the transmission of Mycobacterium tuberculosis in health-care settings, 2005.《2005年医疗机构内预防结核分枝杆菌传播指南》
MMWR Recomm Rep. 2005 Dec 30;54(RR-17):1-141.
3
Treatment of tuberculosis.结核病的治疗。
MMWR Recomm Rep. 2003 Jun 20;52(RR-11):1-77.
4
Targeted tuberculin testing and treatment of latent tuberculosis infection. American Thoracic Society.潜伏性结核感染的靶向结核菌素检测与治疗。美国胸科学会。
MMWR Recomm Rep. 2000 Jun 9;49(RR-6):1-51.
5
Diagnostic Standards and Classification of Tuberculosis in Adults and Children. This official statement of the American Thoracic Society and the Centers for Disease Control and Prevention was adopted by the ATS Board of Directors, July 1999. This statement was endorsed by the Council of the Infectious Disease Society of America, September 1999.《成人及儿童结核病诊断标准与分类》。本美国胸科学会和疾病控制与预防中心的官方声明于1999年7月由美国胸科学会董事会通过。本声明于1999年9月得到美国传染病学会理事会的认可。
Am J Respir Crit Care Med. 2000 Apr;161(4 Pt 1):1376-95. doi: 10.1164/ajrccm.161.4.16141.

全国纯化蛋白衍生物结核菌素制品短缺。

National shortage of purified-protein derivative tuberculin products.

出版信息

MMWR Morb Mortal Wkly Rep. 2013 Apr 26;62(16):312.

PMID:23615675
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4604962/
Abstract

Tubersol, a product of Sanofi Pasteur Limited, is in short supply nationwide until at least the end of May 2013. Tubersol is one of two purified-protein derivative (PPD) tuberculin products licensed by the Food and Drug Administration (FDA). The manufacturer has notified CDC that 50-dose vials of Tubersol will remain unavailable until the end of May 2013 and that supplies of 10-dose vials are still being reestablished: the product is available only by contacting Sanofi directly (at https://www.vaccineshoppe.com/index.cfm? or telephone, 800-822-2463). JHP Pharmaceuticals, LLC, the manufacturer of Aplisol, the other PPD tuberculin product licensed by FDA, has notified FDA that the product is available in restricted quantity. Acute local shortages of Aplisol also have been reported to CDC by TB control officials, as health-care providers switch from Tubersol to Aplisol. The shortages of Aplisol probably will diminish as Tubersol supplies are restored to their preshortage availability in the normal distribution networks. This report advises public health officials, clinicians, and workers in occupational health and infection control about how to adapt to the shortage.

摘要

Tubersol,由赛诺菲巴斯德有限公司生产,在全国范围内的供应短缺至少持续到 2013 年 5 月底。Tubersol 是美国食品和药物管理局(FDA)批准的两种纯化蛋白衍生物(PPD)结核菌素产品之一。制造商已通知疾病预防控制中心,50 剂量瓶的 Tubersol 将在 2013 年 5 月底之前无法供应,而 10 剂量瓶的供应仍在重新建立中:只能通过直接联系赛诺菲(在 https://www.vaccineshoppe.com/index.cfm?或电话,800-822-2463)获得该产品。Aplisol 的制造商 JHP 制药有限责任公司已通知 FDA,该产品的供应数量有限。由于医疗保健提供者从 Tubersol 转向 Aplisol,结核病控制官员也向疾病预防控制中心报告了 Aplisol 的急性局部短缺情况。随着 Tubersol 供应恢复到正常分销网络的短缺前水平,Aplisol 的短缺情况可能会减少。本报告就如何应对短缺问题向公共卫生官员、临床医生以及职业健康和感染控制工作者提供建议。