Evidence map›Paper›PMID 27418345›Full record

ArticleJournal of general internal medicine2016

Cost-Effectiveness of Primary HPV Testing, Cytology and Co-testing as Cervical Cancer Screening for Women Above Age 30 Years.

Xian Wen Jin, Laura Lipold, Julie Foucher, Andrea Sikon, Jennifer Brainard, Jerome Belinson, Sarah Schramm, Kelly Nottingham, Bo Hu, Michael B Rothberg

Abstract read
In one paragraph

Article in Journal of general internal medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 2 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

32 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Accuracy of cytological examination of Tao brush endometrial sampling in diagnosing endometrial premalignancy and malignancy.International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics · 2022
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  14. Canadian family physician Medecin de famille canadien · 2022
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  18. Cotesting in Cervical Cancer Screening.American journal of clinical pathology · 2021
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Xian Wen JinDepartment of Internal Medicine, Cleveland Clinic, Cleveland, OH, USA. jinx@ccf.org.
Laura LipoldDepartment of Family Medicine, Cleveland Clinic, Cleveland, OH, USA.
Julie FoucherCleveland Clinic Lerner College of Medicine, Cleveland Clinic, Cleveland, OH, USA.
Andrea SikonDepartment of Internal Medicine, Cleveland Clinic, Cleveland, OH, USA.
Jennifer BrainardDepartment of Pathology, Cleveland Clinic, Cleveland, OH, USA.
Jerome BelinsonDepartment of Obstetrics and Gynecology, Cleveland Clinic, Cleveland, OH, USA.
Sarah SchrammMedicine Institute Center for Value Based Care Research, Cleveland Clinic, Cleveland, OH, USA.
Kelly NottinghamMedicine Institute Center for Value Based Care Research, Cleveland Clinic, Cleveland, OH, USA.
Bo HuDepartment of Quantitative Health Science, Cleveland Clinic, Cleveland, OH, USA.
Michael B RothbergDepartment of Internal Medicine, Cleveland Clinic, Cleveland, OH, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCervical cancer screening guidelines for women aged ≥30 years allow for co-testing or primary cytology testing. Our objective was to determine the test characteristics and costs associated with Cytology, HPV and Co-testing screening strategies. MAIN

methodsRetrospective cohort study of women undergoing cervical cancer screening with both cytology and HPV (Hybrid Capture 2) testing from 2004 to 2010 in an integrated health system. The electronic health record was used to identify women aged ≥30 years who had co-testing. Unsatisfactory or unavailable test results and incorrectly ordered tests were excluded. The main outcome was biopsy-proven cervical intraepithelial neoplasia grade 3 or higher (CIN3+). KEY

resultsThe final cohort consisted of 99,549 women. Subjects were mostly white (78.4 %), married (70.7 %), never smokers (61.3 %) and with private insurance (86.1 %). Overall, 5121 (5.1 %) tested positive for HPV and 6115 (6.1 %) had cytology ≥ ASCUS; 1681 had both and underwent colposcopy and 310 (0.3 %) had CIN3+. Sensitivity for CIN3+ was 91.9 % for Primary Cytology, 99.4 % for Co-testing, and 94.8 % for Primary HPV; specificity was 97.3 % for Co-testing and Primary Cytology and 97.9 % for Primary HPV. Over a 3-year screening interval, Primary HPV detected more cases of CIN3+ and was less expensive than Primary Cytology. Co-testing detected 14 more cases of CIN3+ than Primary HPV, but required an additional 100,277 cytology tests and 566 colposcopies at an added cost of $2.38 million, or $170,096 per additional case detected.

conclusionsPrimary HPV was more effective and less expensive than Primary Cytology. Primary HPV screening appears to represent a cost-effective alternative to Co-testing.

Indexed as

PapillomaviridaeAdultAge FactorsCohort StudiesCost-Benefit AnalysisCytological TechniquesEarly Detection of CancerFemaleHuman Papillomavirus DNA TestsHumansMiddle AgedRetrospective StudiesUterine Cervical NeoplasmsVaginal Smears

Identifiers

PMID27418345
PMCPMC5071282

What OpenQuestion holds

Textmetadata
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.