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Opportunities for Cytotechnologists in a Changing Environment

机译:在不断变化的环境中为细胞技术人员提供的机会

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The profession of cytotechnology revolved primarily around the Papanicolaou (Pap) test until the advent of the human papillomavirus (HPV) test, automated screening technologies, and advances in molecular diagnostics. In 2012, new cervical cancer screening guidelines were implemented by the American Cancer Society, the American Society for Colposcopy and Cervical Pathology, and the American Society for Clinical Pathology (ASCP). These guidelines set forth the following parameters: 1. Initiate Pap test screening at age 21 years, 2. Initiate cotesting with the HPV test at age 30 years. 3. Lengthen the screening interval between Pap tests: every 3 years for a negative Pap test alone and every 5 years for both negative Pap and HPV tests. 4. Stop Pap test screening at age 65 years based on 3 negative Pap tests or negative HPV test or after hysterectomy for benign disease, The change in the screening intervals alone will affect the laboratory's volume of Pap tests. Many laboratories, especially those in private hospitals and academic medical centers, have already noticed a decrease in their numbers of Pap tests. If the HPV test receives approval from the US Food and Drug Administration for primary screening in which the Pap test will be used as a triage tool for a positive HPV test, the Pap test volume will decrease even more.
机译:细胞技术专业一直围绕着Papanicolaou(Pap)测试,直到人类乳头瘤病毒(HPV)测试,自动筛选技术以及分子诊断技术的发展。 2012年,美国癌症学会,美国阴道镜和宫颈病理学会以及美国临床病理学会(ASCP)实施了新的宫颈癌筛查指南。这些准则规定了以下参数:1.在21岁时开始进行Pap测试筛查; 2.在30岁时开始与HPV测试进行共同测试。 3.延长子宫颈抹片检查之间的筛查间隔:单独进行阴性子宫颈抹片检查每3年一次,对子宫颈抹片检查和HPV阴性检查每5年一次。 4.根据3项Pap阴性或HPV阴性或子宫切除术后的良性疾病,在65岁时停止Pap筛查。仅筛查间隔的变化将影响实验室的Pap筛查量。许多实验室,尤其是私家医院和学术医学中心的实验室,已经注意到其巴氏试验的数量有所减少。如果HPV检测获得美国食品和药物管理局的初步筛查批准,其中Pap检测将被用作HPV检测阳性的分类工具,则Pap检测量将减少更多。

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