Association of Second-Opinion Strategies in the Histopathologic Diagnosis of Cutaneous Melanocytic Lesions With Diagnostic Accuracy and Population-Level Costs.


Journal

JAMA dermatology
ISSN: 2168-6084
Titre abrégé: JAMA Dermatol
Pays: United States
ID NLM: 101589530

Informations de publication

Date de publication:
01 Sep 2021
Historique:
pubmed: 3 6 2021
medline: 26 3 2022
entrez: 2 6 2021
Statut: ppublish

Résumé

Diagnostic variation among pathologists interpreting cutaneous melanocytic lesions could lead to suboptimal care. To estimate the potential association of second-opinion strategies in the histopathologic diagnosis of cutaneous melanocytic lesions with diagnostic accuracy and 1-year population-level costs in the US. Decision analysis with 1-year time horizon including melanocytic lesion diagnoses available from US pathologists participating in the Melanoma Pathology Study (M-Path) and from the study panel of reference pathologists who classified cases using the MPATH-Dx classification tool. M-Path data collection occurred from July 2013 through March 2015; analyses for the present study were performed between April 2015 and January 2021. Various second-opinion strategies for interpretation of melanocytic cutaneous lesions. Estimated accuracy of pathologists' diagnoses, defined as concordance with the reference panel diagnoses, and 1-year postbiopsy medical costs under various second-opinion strategies. Expected percentage of concordant diagnoses, including percentages of overinterpretation and underinterpretation, and 1-year costs of medical care per 100 000 in the US population. Decision-analytic model parameters were based on diagnostic interpretations for 240 cases by 187 pathologists compared with reference panel diagnoses. Without second opinions, 83.2% of diagnoses in the US were estimated to be accurate-ie, concordant with the reference diagnosis; with overinterpretation (8.0%) or underinterpretation (8.8%), and 16 850 misclassified diagnoses per 100 000 biopsies. Accuracy increased under all second-opinion strategies. Accuracy (87.4% concordance with 3.6% overinterpretation and 9.1% underinterpretation) and cost (an increase of more than $10 million per 100 000 biopsies per year) were highest when second opinions were universal (eg, performed on all biopsies), relative to no second opinions. A selective second-opinion strategy based on pathologists' desire or institutional requirements for a second opinion was most accurate (86.5% concordance; 4.4% overinterpretation; 9.1% underinterpretation) and would reduce costs by more than $1.9 million per 100 000 skin biopsies relative to no second opinions. Improvements in diagnostic accuracy with all second-opinion strategies were associated with reductions in overinterpretation but not underinterpretation. In this decision-analytic model, selective second-opinion strategies for interpretation of melanocytic skin lesions showed the potential to improve diagnostic accuracy and decrease costs relative to no second opinions or universal second opinions.

Identifiants

pubmed: 34076664
pii: 2780646
doi: 10.1001/jamadermatol.2021.1779
pmc: PMC8173465
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

1102-1106

Subventions

Organisme : NCI NIH HHS
ID : R01 CA201376
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA023108
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA225585
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA151306
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA200690
Pays : United States

Auteurs

Anna N A Tosteson (ANA)

The Dartmouth Institute for Health Policy and Clinical Practice, Lebanon, New Hampshire.
Norris Cotton Cancer Center, Lebanon, New Hampshire.

Stephanie Tapp (S)

The Dartmouth Institute for Health Policy and Clinical Practice, Lebanon, New Hampshire.

Linda J Titus (LJ)

The Dartmouth Institute for Health Policy and Clinical Practice, Lebanon, New Hampshire.
Norris Cotton Cancer Center, Lebanon, New Hampshire.

Heidi D Nelson (HD)

Oregon Health & Science University, Portland.

Gary M Longton (GM)

Program in Biostatistics, Fred Hutchinson Cancer Research Center, Seattle, Washington.

Mackenzie Bronson (M)

The Dartmouth Institute for Health Policy and Clinical Practice, Lebanon, New Hampshire.

Margaret Pepe (M)

Program in Biostatistics, Fred Hutchinson Cancer Research Center, Seattle, Washington.

Patricia A Carney (PA)

Oregon Health & Science University, Portland.

Tracy Onega (T)

The Dartmouth Institute for Health Policy and Clinical Practice, Lebanon, New Hampshire.
Department of Population Health Sciences, University of Utah, Salt Lake City.

Michael W Piepkorn (MW)

Division of Dermatology, University of Washington School of Medicine, Seattle.
Dermatopathology Northwest, Bellevue, Washington.

Stevan R Knezevich (SR)

Pathology Associates, Clovis, California.

Raymond Barnhill (R)

Departments of Pathology and Translational Research, Institut Curie, Paris, France.
Paris Sciences and Letters Research University, Paris, France.

Martin A Weinstock (MA)

Department of Dermatology, Brown University, Providence, Rhode Island.

David E Elder (DE)

Department of Pathology and Laboratory Medicine, Hospital of the University of Pennsylvania, Philadelphia.

Joann G Elmore (JG)

David Geffen School of Medicine, Department of Medicine, University of California, Los Angeles.

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Classifications MeSH