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在管理式医疗宫颈癌筛查项目中增加人乳头瘤病毒检测的成本效益

Cost-effectiveness of adding human papilloma virus testing to a managed care cervical cancer screening program.

作者信息

Lonky Neal M, Hunter Mark I, Sadeghi Mashod, Edwards Gary, Bajamundi Kathy, Monk Bradley J

机构信息

Department of Obstetrics and Gynecology, Kaiser Permanente Medical Center, Anaheim, CA, USA.

出版信息

J Low Genit Tract Dis. 2007 Oct;11(4):258-64. doi: 10.1097/LGT.0b013e318057f319.

Abstract

OBJECTIVE

The purpose of this study was to demonstrate a methodology for auditing the impact of HCII testing on the direct cost of cervical cancer cytological screening, where the test is collected in all women screened and processed routinely in women age 30 years and older.

MATERIALS AND METHODS

After a policy change to screen all patients 30 years or older with both Pap smears and high-risk human papillomavirus (HR-HPV), as well as cocollection of HR-HPV in women younger than 30 years, all cytological, HPV, and histological data pertaining to cervical screening was collected retrospectively during a 2-month period. We documented the direct costs of performing these tests and estimated the necessary compliance rate for balanced cost-effectiveness.

RESULTS

During the 2-month period, 8,300 women were screened with both Pap smear and HPV cocollection. Of the 'nonnormal' cytological findings, 5% of patients showed either atypical squamous cells (3.5%) or squamous intraepithelial abnormalities (1.5%). An additional 427 (5%) patients had the finding of positive HR-HPV with normal cytology. Six of these patients opted for immediate colposcopy, 2 of which were found to have cervical intraepithelial neoplasia 2. In women age 30 years and older, 900 patients per 1,000 screened would be eligible for a 2-year screening interval based on negative cytology and negative HR-HPV. Based on the direct costs associated with this cohort, no more than 164 women could request screening at an interval shorter than 3 years for the total costs of such a program to equal that of one without HR-HPV cocollection.

CONCLUSIONS

By adding HCII collection to the Pap smear for our entire screening cohort, we intended to reduce the number of tests performed, which was impacted by its age distribution. Our findings indicate that at least 736 of the 900 double-negative patients (82%) would have to be screened at no less than 3 years for such a screening paradigm to be cost-effective in managing women 30 years and older.

摘要

目的

本研究的目的是展示一种方法,用于审核高危型人乳头瘤病毒(HCII)检测对宫颈癌细胞学筛查直接成本的影响,该检测应用于所有接受筛查的女性,并对30岁及以上女性进行常规检测。

材料与方法

在政策改变为对所有30岁及以上患者同时进行巴氏涂片和高危型人乳头瘤病毒(HR-HPV)检测,以及对30岁以下女性同时采集HR-HPV样本后,回顾性收集了2个月期间所有与宫颈筛查相关的细胞学、HPV和组织学数据。我们记录了进行这些检测的直接成本,并估计了实现成本效益平衡所需的依从率。

结果

在这2个月期间,8300名女性同时接受了巴氏涂片和HPV联合检测。在“非正常”细胞学检查结果中,5%的患者显示非典型鳞状细胞(3.5%)或鳞状上皮内异常(1.5%)。另外427名(5%)患者HR-HPV检测呈阳性但细胞学检查正常。其中6名患者选择立即进行阴道镜检查,其中2名被发现患有宫颈上皮内瘤变2级。在30岁及以上的女性中,每1000名接受筛查的患者中有900名基于细胞学检查阴性和HR-HPV检测阴性符合2年筛查间隔的条件。根据该队列的直接成本,为使此类项目的总成本与不进行HR-HPV联合检测的项目相等,间隔短于3年要求筛查的女性人数不得超过164名。

结论

通过在整个筛查队列中对巴氏涂片增加HCII样本采集,我们旨在减少检测次数,检测次数受其年龄分布影响。我们的研究结果表明,为使这种筛查模式在管理30岁及以上女性时具有成本效益,900名双阴性患者中至少736名(82%)必须至少每3年筛查一次。

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