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Dosage individualization proposed for anti-gout medications among the patients with gout
BACKGROUND: The conventional one-size-fits-all approach has been criticized for almost all drugs used especially for chronic diseases, including gout. The present study was aimed to explore the need of individualization and optimization of the dose of anti-gout medications among gout patients. METHO...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8448378/ https://www.ncbi.nlm.nih.gov/pubmed/34534233 http://dx.doi.org/10.1371/journal.pone.0257082 |
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author | Sapkota, Binaya Chaudhary, Suraj Gurung, Prakash Humagain, Anisha Sapkota, Sujan |
author_facet | Sapkota, Binaya Chaudhary, Suraj Gurung, Prakash Humagain, Anisha Sapkota, Sujan |
author_sort | Sapkota, Binaya |
collection | PubMed |
description | BACKGROUND: The conventional one-size-fits-all approach has been criticized for almost all drugs used especially for chronic diseases, including gout. The present study was aimed to explore the need of individualization and optimization of the dose of anti-gout medications among gout patients. METHODS: Cross-sectional study was carried out among 384 randomly selected new gout patients visiting two gout treatment centers at Lalitpur Metropolitan City, Nepal and who were taking antigout medications. Patients not taking anti-gout medications and not showing willingness to participate were excluded. The eGFR was calculated with the CKD Epidemiology Collaboration (CKD-EPI) creatinine equation (2009). Doses to be individualized were decided based on the Renal Drug Handbook and verified with the BNF 80. Data were analyzed via R 4.0.3 by applying the multinomial logistic regression to analyze statistical significance of risk with various predictors, and considering a p-value <0.05 statistically significant. Comorbidities were coded as per the ICD-11 coding and medicines were coded according to the WHO Guidelines for ATC classification and DDD assignment 2020. RESULTS: The high risk of progression to CKD increased in the age range 54–63 and ≥84 years by 17.77 and 43.02 times, respectively. Also, high risk increased by 29.83 and 20.2 times for the overweight and the obese respectively. Aceclofenac 100mg was prescribed for maximum patients (30.5%). Need of dose individualization was realized in 30 patients, with maximum (7) in case of etoricoxib 90mg. Various glucocorticoids were prescribed for 36.9% patients, out of whom 3.8%required dose individualization and 15.9% patients with xanthine oxidase inhibitors, out of whom 1.3% required dose individualization. CONCLUSION: Thirty cases required dose individualization, which was although minimal but could have meaningful impact on the clinical success of the individual patient. Based on the recommendation on dose individualization, those patients could be optimized on their therapy on future follow ups. |
format | Online Article Text |
id | pubmed-8448378 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-84483782021-09-18 Dosage individualization proposed for anti-gout medications among the patients with gout Sapkota, Binaya Chaudhary, Suraj Gurung, Prakash Humagain, Anisha Sapkota, Sujan PLoS One Research Article BACKGROUND: The conventional one-size-fits-all approach has been criticized for almost all drugs used especially for chronic diseases, including gout. The present study was aimed to explore the need of individualization and optimization of the dose of anti-gout medications among gout patients. METHODS: Cross-sectional study was carried out among 384 randomly selected new gout patients visiting two gout treatment centers at Lalitpur Metropolitan City, Nepal and who were taking antigout medications. Patients not taking anti-gout medications and not showing willingness to participate were excluded. The eGFR was calculated with the CKD Epidemiology Collaboration (CKD-EPI) creatinine equation (2009). Doses to be individualized were decided based on the Renal Drug Handbook and verified with the BNF 80. Data were analyzed via R 4.0.3 by applying the multinomial logistic regression to analyze statistical significance of risk with various predictors, and considering a p-value <0.05 statistically significant. Comorbidities were coded as per the ICD-11 coding and medicines were coded according to the WHO Guidelines for ATC classification and DDD assignment 2020. RESULTS: The high risk of progression to CKD increased in the age range 54–63 and ≥84 years by 17.77 and 43.02 times, respectively. Also, high risk increased by 29.83 and 20.2 times for the overweight and the obese respectively. Aceclofenac 100mg was prescribed for maximum patients (30.5%). Need of dose individualization was realized in 30 patients, with maximum (7) in case of etoricoxib 90mg. Various glucocorticoids were prescribed for 36.9% patients, out of whom 3.8%required dose individualization and 15.9% patients with xanthine oxidase inhibitors, out of whom 1.3% required dose individualization. CONCLUSION: Thirty cases required dose individualization, which was although minimal but could have meaningful impact on the clinical success of the individual patient. Based on the recommendation on dose individualization, those patients could be optimized on their therapy on future follow ups. Public Library of Science 2021-09-17 /pmc/articles/PMC8448378/ /pubmed/34534233 http://dx.doi.org/10.1371/journal.pone.0257082 Text en © 2021 Sapkota et al 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 Sapkota, Binaya Chaudhary, Suraj Gurung, Prakash Humagain, Anisha Sapkota, Sujan Dosage individualization proposed for anti-gout medications among the patients with gout |
title | Dosage individualization proposed for anti-gout medications among the patients with gout |
title_full | Dosage individualization proposed for anti-gout medications among the patients with gout |
title_fullStr | Dosage individualization proposed for anti-gout medications among the patients with gout |
title_full_unstemmed | Dosage individualization proposed for anti-gout medications among the patients with gout |
title_short | Dosage individualization proposed for anti-gout medications among the patients with gout |
title_sort | dosage individualization proposed for anti-gout medications among the patients with gout |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8448378/ https://www.ncbi.nlm.nih.gov/pubmed/34534233 http://dx.doi.org/10.1371/journal.pone.0257082 |
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