BMJ 2001;322:893-894 ( 14 April )

Papers

Human papillomavirus testing and the management of women with mildly abnormal cervical smears: an observational study

Editorial by Manos

Gemma Rebello, consultant cytopathologist aNick Hallam, consultant virologist bGeorge Smart, consultant gynaecologist aDavid Farquharson, patient services director, reproductive medicine aJane McCafferty, colposcopy sister a

a Colposcopy Clinic, Royal Infirmary of Edinburgh, Lothian University Hospitals NHS Trust, Edinburgh EH3 9YW, b Regional Clinical Virology Laboratory, City Hospital, Lothian University Hospitals NHS Trust, Edinburgh EH10 5SB

Correspondence to: N Hallam

The first 150 words of the full text of this article appear below.

Following publication of a report in Health Technology Assessment the NHS is running a pilot scheme screening women for human papillomavirus if they have a mildly dyskaryotic or borderline smear.1 How reliable is testing for human papillomavirus as a marker for high grade disease in those with mildly abnormal smears?


    Participants, methods, and results

Three hundred and thirty three consecutive new patients (aged 17 to 61 years, median 30 years) referred for colposcopy with persistent borderline or mildly dyskaryotic smears and who consented to the study were tested for human papillomavirus (high risk types only) with the Digene Hybrid Capture assay HC II (Abbott Laboratories, Maidenhead), by using cervical brush specimens placed in Digene transport medium, and were treated by large loop excision of the transformation zone.

The table summarises test performance, and table A on the BMJ 's website presents results by age, smear history, and test cut off.2 Subjects aged under 30 years (166) were more . . . [Full text of this article]


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Rapid Responses:

Read all Rapid Responses

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