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美国的人乳头瘤病毒疫苗接种实践:初级保健提供者是否利用性行为史和宫颈癌筛查结果来推荐 HPV 疫苗?

Human papillomavirus vaccine practices in the USA: do primary care providers use sexual history and cervical cancer screening results to make HPV vaccine recommendations?

机构信息

Health Services and Economics Branch, Applied Research Program, Division of Cancer Control and Population Sciences, National Cancer Institute, Executive Plaza North, Room 4017, 6130 Executive Boulevard, MSC 7344, Bethesda, MD 20892-7344, USA.

出版信息

Sex Transm Infect. 2012 Oct;88(6):433-5. doi: 10.1136/sextrans-2011-050437. Epub 2012 Apr 21.

DOI:10.1136/sextrans-2011-050437
PMID:22522751
Abstract

OBJECTIVES

Guidelines recommend against the use of Papanicolaou (Pap) or human papillomavirus (HPV) testing when determining eligibility for the HPV vaccine. Optimally, the HPV vaccine should be administered before sexual initiation. Guidelines recommend that age-eligible women with past exposure to HPV should still be vaccinated. Little is known about how primary care providers (PCPs) use sexual history and HPV and Pap tests in their HPV vaccine recommendations.

METHODS

Data from the 2007 Cervical Cancer Screening Supplement (CCSS) administered with the National Ambulatory Medical Care Survey (NAMCS) and the National Hospital Ambulatory Medical Care Survey (NHAMCS) were used to assess HPV vaccination recommendations. The CCSS investigates cervical cancer screening practices, HPV testing and HPV vaccine recommendations among PCPs. A summary measure of compliance with guidelines was defined as rarely or never using the number of sexual partners and HPV tests and Pap tests to determine vaccine receipt. A total of 421 PCPs completed the CCSS in 2007.

RESULTS

Among NAMCS and NHAMCS providers who recommend the HPV vaccine, only 53% (95% CI 42% to 63%) reported making guideline-consistent recommendations. The majority reported sometimes to always recommending the HPV vaccine to women with a history of an abnormal Pap result (85%; 95% CI 75% to 91%) and a positive HPV test (79%; 95% CI 70% to 86%).

CONCLUSIONS

A large proportion of providers report practices that are inconsistent with guidelines. Providers may also be recommending the vaccine to women who may receive little benefit from the vaccine. Provider and system-level efforts to improve guideline-consistent practices are needed.

摘要

目的

指南建议在确定 HPV 疫苗接种资格时不使用巴氏涂片(Pap)或人乳头瘤病毒(HPV)检测。最佳情况下,HPV 疫苗应在性活动开始前接种。指南建议,曾接触过 HPV 的适龄女性仍应接种疫苗。关于初级保健提供者(PCP)如何在 HPV 疫苗推荐中使用性行为史、HPV 和 Pap 检测,知之甚少。

方法

使用 2007 年宫颈癌筛查补充调查(CCSS)的数据,该调查与国家门诊医疗调查(NAMCS)和国家医院门诊医疗调查(NHAMCS)一起进行,以评估 HPV 疫苗接种推荐情况。CCSS 调查了 PCP 进行宫颈癌筛查的实践、HPV 检测和 HPV 疫苗推荐情况。将遵守指南的综合指标定义为很少或从不使用性伴侣数量以及 HPV 检测和巴氏涂片检测来确定疫苗接种。共有 421 名 PCP 于 2007 年完成了 CCSS。

结果

在 NAMCS 和 NHAMCS 中,建议接种 HPV 疫苗的提供者中,只有 53%(95%CI,42%至 63%)报告了符合指南的建议。大多数人报告有时会向有异常 Pap 结果史(85%;95%CI,75%至 91%)和 HPV 检测阳性史(79%;95%CI,70%至 86%)的女性建议接种 HPV 疫苗。

结论

很大比例的提供者报告的做法与指南不一致。提供者也可能向可能从疫苗中获益甚少的女性推荐疫苗。需要在提供者和系统层面做出努力,以改善符合指南的做法。

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