Number needed to biopsy ratio and diagnostic accuracy for melanoma detection.


Journal

Journal of the American Academy of Dermatology
ISSN: 1097-6787
Titre abrégé: J Am Acad Dermatol
Pays: United States
ID NLM: 7907132

Informations de publication

Date de publication:
Sep 2020
Historique:
received: 13 12 2019
revised: 03 04 2020
accepted: 20 04 2020
pubmed: 4 5 2020
medline: 26 2 2021
entrez: 4 5 2020
Statut: ppublish

Résumé

The number needed to biopsy (NNB) ratio for melanoma diagnosis is calculated by dividing the total number of biopsies by the number of biopsied melanomas. It is the inverse of positive predictive value (PPV), which is calculated by dividing the number of biopsied melanomas by the total number of biopsies. NNB is increasingly used as a metric to compare the diagnostic accuracy of health care practitioners. To investigate the association of NNB with the standard statistical measures of sensitivity and specificity. We extracted published diagnostic accuracy data from 5 cross-sectional skin cancer reader studies (median [min-max] readers/study was 29 [8-511]). Because NNB is a ratio, we converted it to PPV. Four studies showed no association and 1 showed a negative association between PPV and sensitivity. All 5 studies showed a positive association between PPV and specificity. Reader study data. An individual health care practitioner with a lower NNB is likely to have a higher specificity than one with a higher NNB, assuming they practice under similar conditions; no conclusions can be made about their relative sensitivities. We advocate for additional research to define quality metrics for melanoma detection and caution when interpreting NNB.

Sections du résumé

BACKGROUND BACKGROUND
The number needed to biopsy (NNB) ratio for melanoma diagnosis is calculated by dividing the total number of biopsies by the number of biopsied melanomas. It is the inverse of positive predictive value (PPV), which is calculated by dividing the number of biopsied melanomas by the total number of biopsies. NNB is increasingly used as a metric to compare the diagnostic accuracy of health care practitioners.
OBJECTIVE OBJECTIVE
To investigate the association of NNB with the standard statistical measures of sensitivity and specificity.
METHODS METHODS
We extracted published diagnostic accuracy data from 5 cross-sectional skin cancer reader studies (median [min-max] readers/study was 29 [8-511]). Because NNB is a ratio, we converted it to PPV.
RESULTS RESULTS
Four studies showed no association and 1 showed a negative association between PPV and sensitivity. All 5 studies showed a positive association between PPV and specificity.
LIMITATIONS CONCLUSIONS
Reader study data.
CONCLUSIONS CONCLUSIONS
An individual health care practitioner with a lower NNB is likely to have a higher specificity than one with a higher NNB, assuming they practice under similar conditions; no conclusions can be made about their relative sensitivities. We advocate for additional research to define quality metrics for melanoma detection and caution when interpreting NNB.

Identifiants

pubmed: 32360723
pii: S0190-9622(20)30725-8
doi: 10.1016/j.jaad.2020.04.109
pmc: PMC7484328
mid: NIHMS1609160
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

780-787

Subventions

Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States

Informations de copyright

Copyright © 2020 American Academy of Dermatology, Inc. Published by Elsevier Inc. All rights reserved.

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Auteurs

Michael A Marchetti (MA)

Dermatology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York. Electronic address: marchetm@mskcc.org.

Ashley Yu (A)

Dermatology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.

Japbani Nanda (J)

Dermatology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.

Philipp Tschandl (P)

Department of Dermatology, Medical University of Vienna, Vienna, Austria.

Harald Kittler (H)

Department of Dermatology, Medical University of Vienna, Vienna, Austria.

Ashfaq A Marghoob (AA)

Dermatology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.

Allan C Halpern (AC)

Dermatology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.

Stephen W Dusza (SW)

Dermatology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.

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Classifications MeSH