Nonparametric Limits of Agreement in Method Comparison Studies: A Simulation Study on Extreme Quantile Estimation.

Bland–Altman analysis agreement coverage limits of agreement method comparison quantile estimation repeatability reproducibility

Journal

International journal of environmental research and public health
ISSN: 1660-4601
Titre abrégé: Int J Environ Res Public Health
Pays: Switzerland
ID NLM: 101238455

Informations de publication

Date de publication:
11 11 2020
Historique:
received: 28 09 2020
revised: 06 11 2020
accepted: 09 11 2020
entrez: 14 11 2020
pubmed: 15 11 2020
medline: 28 1 2021
Statut: epublish

Résumé

Bland-Altman limits of agreement and the underlying plot are a well-established means in method comparison studies on quantitative outcomes. Normally distributed paired differences, a constant bias, and variance homogeneity across the measurement range are implicit assumptions to this end. Whenever these assumptions are not fully met and cannot be remedied by an appropriate transformation of the data or the application of a regression approach, the 2.5% and 97.5% quantiles of the differences have to be estimated nonparametrically. Earlier, a simple Sample Quantile (SQ) estimator (a weighted average of the observations closest to the target quantile), the Harrell-Davis estimator (HD), and estimators of the Sfakianakis-Verginis type (SV) outperformed 10 other quantile estimators in terms of mean coverage for the next observation in a simulation study, based on sample sizes between 30 and 150. Here, we investigate the variability of the coverage probability of these three and another three promising nonparametric quantile estimators with n=50(50)200,250(250)1000. The SQ estimator outperformed the HD and SV estimators for n=50 and was slightly better for n=100, whereas the SQ, HD, and SV estimators performed identically well for n≥150. The similarity of the boxplots for the SQ estimator across both distributions and sample sizes was striking.

Identifiants

pubmed: 33187125
pii: ijerph17228330
doi: 10.3390/ijerph17228330
pmc: PMC7698333
pii:
doi:

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Références

Ann Clin Biochem. 2019 Mar;56(2):198-203
pubmed: 30259759
Optom Vis Sci. 2015 Mar;92(3):e71-80
pubmed: 25650900
Clin Exp Pharmacol Physiol. 2010 Feb;37(2):143-9
pubmed: 19719745
Stat Methods Med Res. 1999 Jun;8(2):135-60
pubmed: 10501650
J Magn Reson Imaging. 2018 Aug;48(2):507-513
pubmed: 29517830
Br J Math Stat Psychol. 2020 Nov;73(3):506-521
pubmed: 31944263
Anesth Analg. 2017 Sep;125(3):1075
pubmed: 28759494
Int J Biostat. 2016 Nov 1;12(2):
pubmed: 27838682
Lancet. 1986 Feb 8;1(8476):307-10
pubmed: 2868172
Stat Methods Med Res. 2018 May;27(5):1559-1574
pubmed: 27587594
Br J Anaesth. 2016 Mar;116(3):430-1
pubmed: 26865136
Diagnostics (Basel). 2020 May 22;10(5):
pubmed: 32456091
Comput Biol Med. 2018 Sep 1;100:247-252
pubmed: 30056297
Scand J Clin Lab Invest. 2020 Sep;80(5):408-411
pubmed: 32362172
Br J Anaesth. 2016 Nov;117(5):569-575
pubmed: 27799171
BMC Med Res Methodol. 2018 May 22;18(1):45
pubmed: 29788915

Auteurs

Oke Gerke (O)

Department of Nuclear Medicine, Odense University Hospital, 5000 Odense C, Denmark.
Department of Clinical Research, University of Southern Denmark, 5000 Odense C, Denmark.

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