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The effectiveness of split tablet dosing versus alternate-day dosing of warfarin: a randomized control trial
Due to large dosage variation, a variety of warfarin prescription regimens are utilized for specific doses such as tablet splitting, or pill strength alternating. The clinical comparison between the two is lacking. We hypothesize that both approaches result in different times in therapeutic range. W...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8674310/ https://www.ncbi.nlm.nih.gov/pubmed/34912021 http://dx.doi.org/10.1038/s41598-021-03606-z |
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author | Kaewsaengeak, Chanyapat Pienputtarapong, Usanee Tocharoenchok, Teerapong |
author_facet | Kaewsaengeak, Chanyapat Pienputtarapong, Usanee Tocharoenchok, Teerapong |
author_sort | Kaewsaengeak, Chanyapat |
collection | PubMed |
description | Due to large dosage variation, a variety of warfarin prescription regimens are utilized for specific doses such as tablet splitting, or pill strength alternating. The clinical comparison between the two is lacking. We hypothesize that both approaches result in different times in therapeutic range. We randomized patients with specific warfarin dosage and stable INR for 6 months or longer to receive the whole tablet, alternate-day dosing or the split tablet, same daily-dosing regimen without initial dose change and followed them every 6 weeks for 6 months. The primary outcome was a time in therapeutic range of 2.0–3.0. The secondary outcomes included dosage, compliance, INR, anticoagulant-related events. A total of 66 patients were enrolled, 32 randomly assigned to the split tablet regimen (group S) and 34 to the alternate-day regimen (group A) with two withdrawers. The mean age was 58.6 ± 8.5 years. All baseline characteristics of both groups were similar. The average time in therapeutic range was 72.8 ± 25.4% in group S and 74.9 ± 22.0% in group A (p = 0.72). There were no significant differences in warfarin dosage, compliance, INR and, complications between the two groups. Both warfarin prescription methods, the split tablet and the alternate-day had comparable time in the therapeutic range. |
format | Online Article Text |
id | pubmed-8674310 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-86743102021-12-16 The effectiveness of split tablet dosing versus alternate-day dosing of warfarin: a randomized control trial Kaewsaengeak, Chanyapat Pienputtarapong, Usanee Tocharoenchok, Teerapong Sci Rep Article Due to large dosage variation, a variety of warfarin prescription regimens are utilized for specific doses such as tablet splitting, or pill strength alternating. The clinical comparison between the two is lacking. We hypothesize that both approaches result in different times in therapeutic range. We randomized patients with specific warfarin dosage and stable INR for 6 months or longer to receive the whole tablet, alternate-day dosing or the split tablet, same daily-dosing regimen without initial dose change and followed them every 6 weeks for 6 months. The primary outcome was a time in therapeutic range of 2.0–3.0. The secondary outcomes included dosage, compliance, INR, anticoagulant-related events. A total of 66 patients were enrolled, 32 randomly assigned to the split tablet regimen (group S) and 34 to the alternate-day regimen (group A) with two withdrawers. The mean age was 58.6 ± 8.5 years. All baseline characteristics of both groups were similar. The average time in therapeutic range was 72.8 ± 25.4% in group S and 74.9 ± 22.0% in group A (p = 0.72). There were no significant differences in warfarin dosage, compliance, INR and, complications between the two groups. Both warfarin prescription methods, the split tablet and the alternate-day had comparable time in the therapeutic range. Nature Publishing Group UK 2021-12-15 /pmc/articles/PMC8674310/ /pubmed/34912021 http://dx.doi.org/10.1038/s41598-021-03606-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Kaewsaengeak, Chanyapat Pienputtarapong, Usanee Tocharoenchok, Teerapong The effectiveness of split tablet dosing versus alternate-day dosing of warfarin: a randomized control trial |
title | The effectiveness of split tablet dosing versus alternate-day dosing of warfarin: a randomized control trial |
title_full | The effectiveness of split tablet dosing versus alternate-day dosing of warfarin: a randomized control trial |
title_fullStr | The effectiveness of split tablet dosing versus alternate-day dosing of warfarin: a randomized control trial |
title_full_unstemmed | The effectiveness of split tablet dosing versus alternate-day dosing of warfarin: a randomized control trial |
title_short | The effectiveness of split tablet dosing versus alternate-day dosing of warfarin: a randomized control trial |
title_sort | effectiveness of split tablet dosing versus alternate-day dosing of warfarin: a randomized control trial |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8674310/ https://www.ncbi.nlm.nih.gov/pubmed/34912021 http://dx.doi.org/10.1038/s41598-021-03606-z |
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