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针对低级别鳞状上皮内病变或人乳头瘤病毒DNA阳性意义不明确的非典型鳞状细胞转诊的女性进行的阴道镜检查后管理策略:一项为期两年的前瞻性研究。

Postcolposcopy management strategies for women referred with low-grade squamous intraepithelial lesions or human papillomavirus DNA-positive atypical squamous cells of undetermined significance: a two-year prospective study.

作者信息

Guido Richard, Schiffman Mark, Solomon Diane, Burke Louis

机构信息

Magee-Womens Hospital of the University of Pittsburgh Health Care System, PA, USA.

出版信息

Am J Obstet Gynecol. 2003 Jun;188(6):1401-5. doi: 10.1067/mob.2003.456.

Abstract

OBJECTIVE

This study was undertaken to compare postcolposcopy management strategies for women referred for low-grade squamous intraepithelial lesions (LSIL) or oncogenic human papillomavirus (HPV) DNA-positive atypical squamous cells of undetermined significance (ASCUS), with cervical intraepithelial neoplasia (CIN) grade 1 or less found at initial colposcopy.

STUDY DESIGN

A 2-year prospective follow-up of 1539 women was designed to assess the percentage sensitivity of different postcolposcopy management strategies to detect subsequent CIN grade 2 or 3 and percentage referral to repeat colposcopy.

RESULTS

HPV testing at 12 months was sensitive (92.2%) for detection of CIN grade 2 or 3 with a referral rate to repeat colposcopy of 55.0%. Repeat semiannual cytology with referral to colposcopy at an ASCUS threshold demonstrated similar sensitivity (88.0%) but with a higher rate of referral to colposcopy (63.6%). Combining cytology and HPV testing did not increase sensitivity and hurt specificity. Baseline viral load and colposcopic impression were not helpful.

CONCLUSION

The most efficient test for identifying women with CIN grade 2 or 3 after colposcopy might be an HPV test alone at 12 months.

摘要

目的

本研究旨在比较针对因低度鳞状上皮内病变(LSIL)或致癌性人乳头瘤病毒(HPV)DNA阳性意义不明确的非典型鳞状细胞(ASCUS)而转诊、初次阴道镜检查发现宫颈上皮内瘤变(CIN)1级或更低级别的女性,阴道镜检查后的管理策略。

研究设计

对1539名女性进行为期2年的前瞻性随访,以评估不同阴道镜检查后管理策略检测后续CIN 2级或3级的敏感度百分比以及转诊至重复阴道镜检查的百分比。

结果

12个月时进行HPV检测对检测CIN 2级或3级的敏感度为92.2%,转诊至重复阴道镜检查的比例为55.0%。以ASCUS为阈值进行半年一次的重复细胞学检查并转诊至阴道镜检查,显示出相似的敏感度(88.0%),但转诊至阴道镜检查的比例更高(63.6%)。将细胞学检查和HPV检测相结合并未提高敏感度且损害了特异性。基线病毒载量和阴道镜印象并无帮助。

结论

阴道镜检查后识别CIN 2级或3级女性的最有效检测方法可能是仅在12个月时进行HPV检测。

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