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Impact of air temperature and drug concentration on liquid emission from elastomeric pumps
BACKGROUND: Elastomeric pumps (EPs) are devices that allow quantitative and continuous drug administration without the need for electronic control, and they are used by being filled with anticancer agents. Although the package inserts of several manufacturers that provide EPs describe the relationsh...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7783981/ https://www.ncbi.nlm.nih.gov/pubmed/33397508 http://dx.doi.org/10.1186/s40780-020-00185-5 |
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author | Abe, Tomoya Matsuzaka, Kazumasa Nakayama, Toshiaki Otsuka, Masanobu Sagara, Atsunobu Sato, Fumiaki Yumoto, Tetsuro |
author_facet | Abe, Tomoya Matsuzaka, Kazumasa Nakayama, Toshiaki Otsuka, Masanobu Sagara, Atsunobu Sato, Fumiaki Yumoto, Tetsuro |
author_sort | Abe, Tomoya |
collection | PubMed |
description | BACKGROUND: Elastomeric pumps (EPs) are devices that allow quantitative and continuous drug administration without the need for electronic control, and they are used by being filled with anticancer agents. Although the package inserts of several manufacturers that provide EPs describe the relationship between the flow rate per unit time and temperature, the solution is only saline solution or 5% glucose solution, and data on anticancer drugs have not been published. In this study, we focused on 5-fluorouracil (5-FU), a drug frequently used in cancer chemotherapy, and examined the effect of changes in standard of EPs and temperature on drug emission. METHODS: We evaluated the EP data of patients treated with Baxter Infusor® LV5 and SV2.5 in terms of emission rate, relationship between 5-FU prescription amount and emission rate, and relationship between emission rate and monthly air temperature in LV5 and SV2.5. The number of EPs sampled in the study was N = 5708 (n = 2988 for LV5 and n = 2720 for SV2.5). RESULTS: In LV5, the emission rate varied from 88 to 97% (median 94.0%), whereas in SV2.5, the emission rate was observed as 97 to 98% (median 97.4%). The 5-FU prescription amount and the emission rate were not correlated in LV5 and SV2.5, respectively (LV5; y = − 0.0015x + 97.305, R(2) = 0.0226, SV2.5; y = − 0.001x + 100.25, R(2) = 0.0466). LV5 showed a higher emission rate in the months with higher air temperature and a lower emission rate in the month with lower air temperature. In addition, LV5 showed a significant reduction in emission rate compared with SV2.5 in all months (P < 0.001). CONCLUSIONS: In this study, we clarified that air temperature is an important factor that affects the drug emission of EPs. Therefore, it is necessary to examine the conditions for total fluid volume suitable for the air temperature in each region and to provide sufficient information to patients. |
format | Online Article Text |
id | pubmed-7783981 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-77839812021-01-05 Impact of air temperature and drug concentration on liquid emission from elastomeric pumps Abe, Tomoya Matsuzaka, Kazumasa Nakayama, Toshiaki Otsuka, Masanobu Sagara, Atsunobu Sato, Fumiaki Yumoto, Tetsuro J Pharm Health Care Sci Research Article BACKGROUND: Elastomeric pumps (EPs) are devices that allow quantitative and continuous drug administration without the need for electronic control, and they are used by being filled with anticancer agents. Although the package inserts of several manufacturers that provide EPs describe the relationship between the flow rate per unit time and temperature, the solution is only saline solution or 5% glucose solution, and data on anticancer drugs have not been published. In this study, we focused on 5-fluorouracil (5-FU), a drug frequently used in cancer chemotherapy, and examined the effect of changes in standard of EPs and temperature on drug emission. METHODS: We evaluated the EP data of patients treated with Baxter Infusor® LV5 and SV2.5 in terms of emission rate, relationship between 5-FU prescription amount and emission rate, and relationship between emission rate and monthly air temperature in LV5 and SV2.5. The number of EPs sampled in the study was N = 5708 (n = 2988 for LV5 and n = 2720 for SV2.5). RESULTS: In LV5, the emission rate varied from 88 to 97% (median 94.0%), whereas in SV2.5, the emission rate was observed as 97 to 98% (median 97.4%). The 5-FU prescription amount and the emission rate were not correlated in LV5 and SV2.5, respectively (LV5; y = − 0.0015x + 97.305, R(2) = 0.0226, SV2.5; y = − 0.001x + 100.25, R(2) = 0.0466). LV5 showed a higher emission rate in the months with higher air temperature and a lower emission rate in the month with lower air temperature. In addition, LV5 showed a significant reduction in emission rate compared with SV2.5 in all months (P < 0.001). CONCLUSIONS: In this study, we clarified that air temperature is an important factor that affects the drug emission of EPs. Therefore, it is necessary to examine the conditions for total fluid volume suitable for the air temperature in each region and to provide sufficient information to patients. BioMed Central 2021-01-05 /pmc/articles/PMC7783981/ /pubmed/33397508 http://dx.doi.org/10.1186/s40780-020-00185-5 Text en © The Author(s) 2021 Open AccessThis 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Abe, Tomoya Matsuzaka, Kazumasa Nakayama, Toshiaki Otsuka, Masanobu Sagara, Atsunobu Sato, Fumiaki Yumoto, Tetsuro Impact of air temperature and drug concentration on liquid emission from elastomeric pumps |
title | Impact of air temperature and drug concentration on liquid emission from elastomeric pumps |
title_full | Impact of air temperature and drug concentration on liquid emission from elastomeric pumps |
title_fullStr | Impact of air temperature and drug concentration on liquid emission from elastomeric pumps |
title_full_unstemmed | Impact of air temperature and drug concentration on liquid emission from elastomeric pumps |
title_short | Impact of air temperature and drug concentration on liquid emission from elastomeric pumps |
title_sort | impact of air temperature and drug concentration on liquid emission from elastomeric pumps |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7783981/ https://www.ncbi.nlm.nih.gov/pubmed/33397508 http://dx.doi.org/10.1186/s40780-020-00185-5 |
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