Abstract

ObjectiveTo determine if electrical impedance spectroscopy (EIS) improves the diagnostic accuracy of colposcopy when used as an adjunct.DesignProspective, comparative, multi-centre clinical study.SettingThree colposcopy clinics: two in England and one in Ireland.PopulationWomen referred with abnormal cytology.MethodsIn phase 1, EIS was assessed against colposcopic impression and histopathology of the biopsies taken. In phase 2, a probability index and cut-off value for the detection of high-grade cervical intraepithelial neoplasia (HG–CIN, i.e. grade CIN2+) was derived to indicate sites for biopsy. EIS data collection and analyses were performed in real time and blinded to the clinician. The phase-2 data were analysed using different cut-off values to assess performance of EIS as an adjunct.Main outcome measureHistologically confirmed HG–CIN (CIN2+).ResultsA total of 474 women were recruited: 214 were eligible for analysis in phase 1, and 215 were eligible in phase 2. The average age was 33.2 years (median age 30.3 years, range 20–64 years) and 48.5% (208/429) had high-grade cytology. Using the cut-off from phase 1 the accuracy of colposcopic impression to detect HG–CIN when using EIS as an adjunct at the time of examination improved the positive predictive value (PPV) from 78.1% (95% CI 67.5–86.4) to 91.5%. Specificity was also increased from 83.5% (95% CI 75.2–89.9) to 95.4%, but sensitivity was significantly reduced from 73.6% (95% CI 63.0–82.5) to 62.1%, and the negative predictive value (NPV) was unchanged. The positive likelihood ratio for colposcopic impression alone was 4.46. This increased to 13.5 when EIS was used as an adjunct. The overall accuracy of colposcopy when used with EIS as an adjunct was assessed by varying the cut-off applied to a combined test index. Using a cut-off set to give the same sensitivity as colposcopy in phase 2, EIS increased the PPV to detect HG–CIN from 53.5% (95% CI 45.0–61.8) to 67%, and specificity increased from 38.5% (95% CI 29.4–48.3) to 65.1%. NPV was not significantly increased. Alternatively, applying a cut-off to give the same specificity as colposcopy alone increased EIS sensitivity from 88.5% (95% CI 79.9–94.4) to 96.6%, and NPV from 80.8% (95% CI 67.5–90.4) to 93.3%. PPV was not significantly increased. The receiver operator characteristic (ROC) to detect HG–CIN had an area under the curve (AUC) of 0.887 (95% CI 0.840–0.934).ConclusionsEIS used as an adjunct to colposcopy improves colposcopic performance. The addition of EIS could lead to more appropriate patient management with lower intervention rates.

Highlights

  • The ability to identify correctly those who have, and those who do not have, disease is pivotal to the success of any screening programme

  • Prevention of cervical cancer depends on colposcopic detection and treatment of high-grade cervical intraepithelial neoplasia (HG–CIN, i.e. CIN2+) in women referred with abnormal cytology

  • In phase 2 we evaluated the performance of colposcopy with and without Electrical impedance spectroscopy (EIS), where the disease reference standard was defined as histologically confirmed HG–CIN in any biopsy suggested either by the colposcopist or by EIS, where the EIS measurement exceeded the median for HG–CIN derived from phase 1

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Summary

Introduction

The ability to identify correctly those who have, and those who do not have, disease is pivotal to the success of any screening programme. Prevention of cervical cancer depends on colposcopic detection and treatment of high-grade cervical intraepithelial neoplasia (HG–CIN, i.e. CIN2+) in women referred with abnormal cytology. Accuracy of detection of high-grade cervical intraepithelial neoplasia training.[1,2] Low colposcopic performance can result in failure to detect disease (inadequate sensitivity), or unnecessary treatment in the absence of disease (inadequate specificity). The models used a numerical analysis method often applied to the solution of physics field problems. This finite element modelling (FEM) involves modelling the tissue as elements (voxels) at the subcellular level, and including the features such as nuclear size and cell arrangements found in both normal and abnormal cervical epithelia.[3,4,5,6]

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