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Determining reference ranges and sample sizes in parallel-group studies
BACKGROUND AND OBJECTIVES: Reference ranges are widely used to locate the major range of the target probability distribution. When future measurements fall outside the reference range, they are classified as atypical and require further investigation. The fundamental principles and statistical prope...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9710766/ https://www.ncbi.nlm.nih.gov/pubmed/36449490 http://dx.doi.org/10.1371/journal.pone.0278447 |
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author | Shieh, Gwowen |
author_facet | Shieh, Gwowen |
author_sort | Shieh, Gwowen |
collection | PubMed |
description | BACKGROUND AND OBJECTIVES: Reference ranges are widely used to locate the major range of the target probability distribution. When future measurements fall outside the reference range, they are classified as atypical and require further investigation. The fundamental principles and statistical properties of reference ranges are closely related to those of tolerance interval procedures. Existing investigations of reference ranges and tolerance intervals mainly devoted to the primitive cases of one- and paired-sample designs. Although reference ranges hold considerable promise for parallel group designs, the corresponding methodological and computational issues for determining reference limits and sample sizes have not been adequately addressed. METHODS: This paper describes a complete collection of one- and two-sided reference ranges for assessing measurement differences in parallel-group studies that assume variance homogeneity. RESULTS: The problem of sample size determination for precise reference ranges is also examined under the expected half-width and assurance probability considerations. Unlike the current methods, the suggested sample size criteria explicitly accommodate desired interval width in precise interval estimation. CONCLUSIONS: Theoretical examinations and empirical assessments are presented to validate the usefulness of the proposed reference range and sample size procedures. To enhance the usages of the recommended techniques in practical applications, computer programs are developed for efficient calculation and exact analysis. A real data example regarding tablet absorption rate and extent is presented to illustrate the suggested assessments between two drug formulations. |
format | Online Article Text |
id | pubmed-9710766 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-97107662022-12-01 Determining reference ranges and sample sizes in parallel-group studies Shieh, Gwowen PLoS One Research Article BACKGROUND AND OBJECTIVES: Reference ranges are widely used to locate the major range of the target probability distribution. When future measurements fall outside the reference range, they are classified as atypical and require further investigation. The fundamental principles and statistical properties of reference ranges are closely related to those of tolerance interval procedures. Existing investigations of reference ranges and tolerance intervals mainly devoted to the primitive cases of one- and paired-sample designs. Although reference ranges hold considerable promise for parallel group designs, the corresponding methodological and computational issues for determining reference limits and sample sizes have not been adequately addressed. METHODS: This paper describes a complete collection of one- and two-sided reference ranges for assessing measurement differences in parallel-group studies that assume variance homogeneity. RESULTS: The problem of sample size determination for precise reference ranges is also examined under the expected half-width and assurance probability considerations. Unlike the current methods, the suggested sample size criteria explicitly accommodate desired interval width in precise interval estimation. CONCLUSIONS: Theoretical examinations and empirical assessments are presented to validate the usefulness of the proposed reference range and sample size procedures. To enhance the usages of the recommended techniques in practical applications, computer programs are developed for efficient calculation and exact analysis. A real data example regarding tablet absorption rate and extent is presented to illustrate the suggested assessments between two drug formulations. Public Library of Science 2022-11-30 /pmc/articles/PMC9710766/ /pubmed/36449490 http://dx.doi.org/10.1371/journal.pone.0278447 Text en © 2022 Gwowen Shieh https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Shieh, Gwowen Determining reference ranges and sample sizes in parallel-group studies |
title | Determining reference ranges and sample sizes in parallel-group studies |
title_full | Determining reference ranges and sample sizes in parallel-group studies |
title_fullStr | Determining reference ranges and sample sizes in parallel-group studies |
title_full_unstemmed | Determining reference ranges and sample sizes in parallel-group studies |
title_short | Determining reference ranges and sample sizes in parallel-group studies |
title_sort | determining reference ranges and sample sizes in parallel-group studies |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9710766/ https://www.ncbi.nlm.nih.gov/pubmed/36449490 http://dx.doi.org/10.1371/journal.pone.0278447 |
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