Literature DB >> 34976288

Increased Uniformity in Diagnostic Accuracy of Pigmented Lesions Using Electrical Impedance Spectroscopy Information.

Graham Litchman1,2,3, Rebeca Teplitz1,2,3, Ryan M Svoboda1,2,3, James Q Del Rosso1,2,3.   

Abstract

BACKGROUND: Novel non-invasive technologies augment information available to a clinician to enhance diagnosis. Electrical impedance spectroscopy (EIS) is a highly sensitive technology used before biopsy to differentiate equivocal lesions through differences in electrical resistance of benign versus malignant cells. A recent study of an EIS device approved by the United States Food and Drug Administration supported this device's impact on clinical management among dermatology residents. The device provides an EIS score, which increases with greater likelihood of malignancy.
OBJECTIVE: We investigated whether the addition of an EIS score improved uniformity and diagnostic accuracy of pigmented lesions.
METHODS: A post-hoc analysis of previously collected data from a survey of 164 dermatology residents was performed. Residents were asked to determine whether they would biopsy a lesion based on clinical morphology alone versus clinical morphology with an EIS score. A total of 45 lesions were assessed (including 17 malignant and 28 benign lesions). Subjects were grouped by percent correct pre-EIS score biopsy decisions and divided into quartiles.
RESULTS: With clinical assessment alone, the mean correct decisions to biopsy was 59.9%. With the addition of EIS score, the mean increased to 71.0%. All quartiles significantly increased their correct biopsy decisions with EIS (P<0.001), but the lowest scoring quartiles improved more than the highest scoring quartiles.
CONCLUSION: The data from the EIS device were designed to be integrated into the biopsy decision as an additional piece of information in the diagnostic pathway. The study findings are consistent with this objective. In addition to clinical judgment, the use of the EIS score most increased the lowest-scoring residents, but all were improved after integrating the EIS score. EIS information improved homogeneity of ability and diagnostic accuracy.
Copyright © 2021. Matrix Medical Communications. All rights reserved.

Entities:  

Keywords:  Electrical impedance spectroscopy; melanoma; noninvasive technology

Year:  2021        PMID: 34976288      PMCID: PMC8711612     

Source DB:  PubMed          Journal:  J Clin Aesthet Dermatol        ISSN: 1941-2789


  5 in total

1.  Assessment of clinician accuracy for diagnosing melanoma on the basis of electrical impedance spectroscopy score plus morphology versus lesion morphology alone.

Authors:  Ryan M Svoboda; Giselle Prado; Rachel S Mirsky; Darrell S Rigel
Journal:  J Am Acad Dermatol       Date:  2018-09-15       Impact factor: 11.527

2.  Mortality burden and prognosis of thin melanomas overall and by subcategory of thickness, SEER registry data, 1992-2013.

Authors:  Shoshana M Landow; Annie Gjelsvik; Martin A Weinstock
Journal:  J Am Acad Dermatol       Date:  2016-11-22       Impact factor: 11.527

3.  Age-Specific Incidence of Melanoma in the United States.

Authors:  Kelly G Paulson; Deepti Gupta; Teresa S Kim; Joshua R Veatch; David R Byrd; Shailender Bhatia; Katherine Wojcik; Aude G Chapuis; John A Thompson; Margaret M Madeleine; Jennifer M Gardner
Journal:  JAMA Dermatol       Date:  2020-01-01       Impact factor: 10.282

4.  Accuracy of Skin Cancer Diagnosis by Physician Assistants Compared With Dermatologists in a Large Health Care System.

Authors:  Alyce M Anderson; Martha Matsumoto; Melissa I Saul; Aaron M Secrest; Laura K Ferris
Journal:  JAMA Dermatol       Date:  2018-05-01       Impact factor: 10.282

5.  Clinical performance of the Nevisense system in cutaneous melanoma detection: an international, multicentre, prospective and blinded clinical trial on efficacy and safety.

Authors:  J Malvehy; A Hauschild; C Curiel-Lewandrowski; P Mohr; R Hofmann-Wellenhof; R Motley; C Berking; D Grossman; J Paoli; C Loquai; J Olah; U Reinhold; H Wenger; T Dirschka; S Davis; C Henderson; H Rabinovitz; J Welzel; D Schadendorf; U Birgersson
Journal:  Br J Dermatol       Date:  2014-10-19       Impact factor: 9.302

  5 in total

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