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Validation of a novel automated system, Fluispotter®, for serial sampling of dried blood spots
Repeated blood sampling is required in certain clinical and research settings, which is currently performed by drawing blood from venous catheters requiring manual handling of each sample at the time of collection. A novel body-worn device for repeated serial samples, Fluispotter®, with automated ex...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bioscientifica Ltd
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10305485/ https://www.ncbi.nlm.nih.gov/pubmed/36939600 http://dx.doi.org/10.1530/EC-23-0087 |
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author | Krogh, Jesper Plomgaard, Peter Frikke-Schmidt, Ruth Velschow, Sten Johannesen, Jesper Hilsted, Linda Maria Schrøder, Malene Feldt-Rasmussen, Ulla |
author_facet | Krogh, Jesper Plomgaard, Peter Frikke-Schmidt, Ruth Velschow, Sten Johannesen, Jesper Hilsted, Linda Maria Schrøder, Malene Feldt-Rasmussen, Ulla |
author_sort | Krogh, Jesper |
collection | PubMed |
description | Repeated blood sampling is required in certain clinical and research settings, which is currently performed by drawing blood from venous catheters requiring manual handling of each sample at the time of collection. A novel body-worn device for repeated serial samples, Fluispotter®, with automated extraction, collection, and storage of up to 20 venous dried blood spot samples over the course of 20 h may overcome problems with current methods for serial sampling. The purpose of this study was to assess the performance and safety of Fluispotter for the first time in healthy subjects. Fluispotter consists of a cartridge with tubing, a reservoir for flushing solution, pumps and filterpaper, and a multi-lumen catheter placed in the brachial vein. We recruited healthy subjects for testing in an in-hospital setting. Fluispotter was attached by an anesthesiologist to 22 healthy subjects of which 9/22 (40.9%) participants had all 20 samples taken, which was lower than the goal of complete sampling in 80% of the subjects (P = 0.02). The main reason for sample failure was clogging of blood flow which was observed in 11/22 (50%) of the participants. No serious adverse events occurred, and the participants rated the pain from the insertion and the removal of catheter as very low. A cortisol profile showed nadir values at midnight and highest values at 05:00 h. Although full sampling was not successful in all participants, the Fluispotter technology proved safe and highly acceptable to the participants producing the expected cortisol profile without the requirement of staff during sample collection. |
format | Online Article Text |
id | pubmed-10305485 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Bioscientifica Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-103054852023-06-29 Validation of a novel automated system, Fluispotter®, for serial sampling of dried blood spots Krogh, Jesper Plomgaard, Peter Frikke-Schmidt, Ruth Velschow, Sten Johannesen, Jesper Hilsted, Linda Maria Schrøder, Malene Feldt-Rasmussen, Ulla Endocr Connect Research Repeated blood sampling is required in certain clinical and research settings, which is currently performed by drawing blood from venous catheters requiring manual handling of each sample at the time of collection. A novel body-worn device for repeated serial samples, Fluispotter®, with automated extraction, collection, and storage of up to 20 venous dried blood spot samples over the course of 20 h may overcome problems with current methods for serial sampling. The purpose of this study was to assess the performance and safety of Fluispotter for the first time in healthy subjects. Fluispotter consists of a cartridge with tubing, a reservoir for flushing solution, pumps and filterpaper, and a multi-lumen catheter placed in the brachial vein. We recruited healthy subjects for testing in an in-hospital setting. Fluispotter was attached by an anesthesiologist to 22 healthy subjects of which 9/22 (40.9%) participants had all 20 samples taken, which was lower than the goal of complete sampling in 80% of the subjects (P = 0.02). The main reason for sample failure was clogging of blood flow which was observed in 11/22 (50%) of the participants. No serious adverse events occurred, and the participants rated the pain from the insertion and the removal of catheter as very low. A cortisol profile showed nadir values at midnight and highest values at 05:00 h. Although full sampling was not successful in all participants, the Fluispotter technology proved safe and highly acceptable to the participants producing the expected cortisol profile without the requirement of staff during sample collection. Bioscientifica Ltd 2023-03-20 /pmc/articles/PMC10305485/ /pubmed/36939600 http://dx.doi.org/10.1530/EC-23-0087 Text en © the author(s) https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. (https://creativecommons.org/licenses/by-nc/4.0/) |
spellingShingle | Research Krogh, Jesper Plomgaard, Peter Frikke-Schmidt, Ruth Velschow, Sten Johannesen, Jesper Hilsted, Linda Maria Schrøder, Malene Feldt-Rasmussen, Ulla Validation of a novel automated system, Fluispotter®, for serial sampling of dried blood spots |
title | Validation of a novel automated system, Fluispotter®, for serial sampling of dried blood spots |
title_full | Validation of a novel automated system, Fluispotter®, for serial sampling of dried blood spots |
title_fullStr | Validation of a novel automated system, Fluispotter®, for serial sampling of dried blood spots |
title_full_unstemmed | Validation of a novel automated system, Fluispotter®, for serial sampling of dried blood spots |
title_short | Validation of a novel automated system, Fluispotter®, for serial sampling of dried blood spots |
title_sort | validation of a novel automated system, fluispotter®, for serial sampling of dried blood spots |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10305485/ https://www.ncbi.nlm.nih.gov/pubmed/36939600 http://dx.doi.org/10.1530/EC-23-0087 |
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