Objective: To evaluate, across multiple sample sizes, the degree that data-driven methods result in (1) optimal cutoffs different from population optimal cutoff and (2) bias in accuracy estimates.Study design and setting: A total of 1,000 samples of sample size 100, 200, 500 and 1,000 each were randomly drawn to simulate studies of different sample sizes from a database (n = 13,255) synthesized to assess Edinburgh Postnatal Depression Scale (EPDS) screening accuracy. Optimal cutoffs were selected by maximizing Youden's J (sensitivity+specificity-1). Optimal cutoffs and accuracy estimates in simulated samples were compared to population values.Results: Optimal cutoffs in simulated samples ranged from >= 5 to >= 17 for n = 100, >= 6 to >= 16 for n = 200, >= 6 to >= 14 for n = 500, and >= 8 to >= 13 for n = 1,000. Percentage of simulated samples identifying the population optimal cutoff (>= 11) was 30% for n = 100, 35% for n = 200, 53% for n = 500, and 71% for n = 1,000. Mean overestimation of sensitivity and underestimation of specificity were 6.5 percentage point (pp) and -1.3 pp for n = 100, 4.2 pp and -1.1 pp for n = 200, 1.8 pp and -1.0 pp for n = 500, and 1.4 pp and -1.0 pp for n = 1,000.Conclusions: Small accuracy studies may identify inaccurate optimal cutoff and overstate accuracy estimates with data-driven methods. (C) 2021 Elsevier Inc. All rights reserved.

Data-driven methods distort optimal cutoffs and accuracy estimates of depression screening tools: a simulation study using individual participant data / Bhandari, P.M., Levis, B., Neupane, D., Patten, S.B., Shrier, I., Thombs, B.D., Benedetti, A., Sun, Y., He, C., Rice, D.B., Krishnan, A., Wu, Y., Azar, M., Sanchez, T.A., Chiovitti, M.J., Saadat, N., Riehm, K.E., Imran, M., Negeri, Z., Boruff, J.T., et al.. - In: JOURNAL OF CLINICAL EPIDEMIOLOGY. - ISSN 0895-4356. - 137:(2021), pp. 137-147. [10.1016/j.jclinepi.2021.03.031]

Data-driven methods distort optimal cutoffs and accuracy estimates of depression screening tools: a simulation study using individual participant data

Sun Y.;Tonelli M.;Aceti F.;Fernandes M.;Meuti V.;
2021

Abstract

Objective: To evaluate, across multiple sample sizes, the degree that data-driven methods result in (1) optimal cutoffs different from population optimal cutoff and (2) bias in accuracy estimates.Study design and setting: A total of 1,000 samples of sample size 100, 200, 500 and 1,000 each were randomly drawn to simulate studies of different sample sizes from a database (n = 13,255) synthesized to assess Edinburgh Postnatal Depression Scale (EPDS) screening accuracy. Optimal cutoffs were selected by maximizing Youden's J (sensitivity+specificity-1). Optimal cutoffs and accuracy estimates in simulated samples were compared to population values.Results: Optimal cutoffs in simulated samples ranged from >= 5 to >= 17 for n = 100, >= 6 to >= 16 for n = 200, >= 6 to >= 14 for n = 500, and >= 8 to >= 13 for n = 1,000. Percentage of simulated samples identifying the population optimal cutoff (>= 11) was 30% for n = 100, 35% for n = 200, 53% for n = 500, and 71% for n = 1,000. Mean overestimation of sensitivity and underestimation of specificity were 6.5 percentage point (pp) and -1.3 pp for n = 100, 4.2 pp and -1.1 pp for n = 200, 1.8 pp and -1.0 pp for n = 500, and 1.4 pp and -1.0 pp for n = 1,000.Conclusions: Small accuracy studies may identify inaccurate optimal cutoff and overstate accuracy estimates with data-driven methods. (C) 2021 Elsevier Inc. All rights reserved.
2021
Accuracy estimates; Bias; Cherry-picking; Data-driven methods; Depression; Optimal cutoff
01 Pubblicazione su rivista::01a Articolo in rivista
Data-driven methods distort optimal cutoffs and accuracy estimates of depression screening tools: a simulation study using individual participant data / Bhandari, P.M., Levis, B., Neupane, D., Patten, S.B., Shrier, I., Thombs, B.D., Benedetti, A., Sun, Y., He, C., Rice, D.B., Krishnan, A., Wu, Y., Azar, M., Sanchez, T.A., Chiovitti, M.J., Saadat, N., Riehm, K.E., Imran, M., Negeri, Z., Boruff, J.T., et al.. - In: JOURNAL OF CLINICAL EPIDEMIOLOGY. - ISSN 0895-4356. - 137:(2021), pp. 137-147. [10.1016/j.jclinepi.2021.03.031]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1681764
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