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Developing a trigger tool to monitor adverse events during haemodialysis in children: a pilot project
ABSTRACT: BACKGROUND: We developed a paediatric haemodialysis trigger tool (pHTT) for application per haemodialysis (HD) session in children receiving intermittent in-centre HD and systematically monitored adverse events. METHODS: Single-centre quality improvement study performed over two 8-week cyc...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9925574/ https://www.ncbi.nlm.nih.gov/pubmed/35913566 http://dx.doi.org/10.1007/s00467-022-05673-4 |
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author | Balasubramanian, Ramnath Folwell, Rachel Wheatley, Arran Ramsey, Heidi Barton, Carmen Reid, Christopher J. D. Sinha, Manish D. |
author_facet | Balasubramanian, Ramnath Folwell, Rachel Wheatley, Arran Ramsey, Heidi Barton, Carmen Reid, Christopher J. D. Sinha, Manish D. |
author_sort | Balasubramanian, Ramnath |
collection | PubMed |
description | ABSTRACT: BACKGROUND: We developed a paediatric haemodialysis trigger tool (pHTT) for application per haemodialysis (HD) session in children receiving intermittent in-centre HD and systematically monitored adverse events. METHODS: Single-centre quality improvement study performed over two 8-week cycles. Data collected prospectively using a ‘per-dialysis session’ pHTT tool including 54 triggers across six domains, adapted from a recently described haemodialysis trigger tool (HTT) for adults. Each trigger was evaluated for level of harm following assessment by two authors. Following a period of training, HD nurses completed the HTT at the end of each dialysis session. RESULTS: There were 241 triggers over 182 dialysis sessions, with 139 triggers in 91 HD sessions for 15 children, age range 28–205 months, over an 8-week period (first cycle) and 102 triggers in 91 HD sessions for 13 children, age range 28–205 months, over a further 8-week period (second cycle). After interventions informed by the pHTT, the harm rate per session was significantly reduced from 1.03 (94/91) to 0.32 (29/91), P < 0.001. There was a significant difference between the distribution of triggers by harm category (P < 0.001) and between the proportion of triggers across the various domains of the pHTT (P = 0.004) between the two cycles. No triggers were evaluated as causing permanent harm. CONCLUSIONS: This pilot study demonstrates potential benefits of a bedside tool to monitor adverse events during haemodialysis in children. Thus, following interventions informed by the pHTT, the harm rate per session was significantly reduced. Under standard patient safety systems, the vast majority of triggers identified by the pHTT would remain unreported and perhaps lead to missed opportunities to improve patient safety. We propose the use of a paediatric HTT as part of standard care by centres providing HD to children in the future. GRAPHICAL ABSTRACT: A higher resolution version of the Graphical abstract is available as Supplementary information [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00467-022-05673-4. |
format | Online Article Text |
id | pubmed-9925574 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-99255742023-02-15 Developing a trigger tool to monitor adverse events during haemodialysis in children: a pilot project Balasubramanian, Ramnath Folwell, Rachel Wheatley, Arran Ramsey, Heidi Barton, Carmen Reid, Christopher J. D. Sinha, Manish D. Pediatr Nephrol Original Article ABSTRACT: BACKGROUND: We developed a paediatric haemodialysis trigger tool (pHTT) for application per haemodialysis (HD) session in children receiving intermittent in-centre HD and systematically monitored adverse events. METHODS: Single-centre quality improvement study performed over two 8-week cycles. Data collected prospectively using a ‘per-dialysis session’ pHTT tool including 54 triggers across six domains, adapted from a recently described haemodialysis trigger tool (HTT) for adults. Each trigger was evaluated for level of harm following assessment by two authors. Following a period of training, HD nurses completed the HTT at the end of each dialysis session. RESULTS: There were 241 triggers over 182 dialysis sessions, with 139 triggers in 91 HD sessions for 15 children, age range 28–205 months, over an 8-week period (first cycle) and 102 triggers in 91 HD sessions for 13 children, age range 28–205 months, over a further 8-week period (second cycle). After interventions informed by the pHTT, the harm rate per session was significantly reduced from 1.03 (94/91) to 0.32 (29/91), P < 0.001. There was a significant difference between the distribution of triggers by harm category (P < 0.001) and between the proportion of triggers across the various domains of the pHTT (P = 0.004) between the two cycles. No triggers were evaluated as causing permanent harm. CONCLUSIONS: This pilot study demonstrates potential benefits of a bedside tool to monitor adverse events during haemodialysis in children. Thus, following interventions informed by the pHTT, the harm rate per session was significantly reduced. Under standard patient safety systems, the vast majority of triggers identified by the pHTT would remain unreported and perhaps lead to missed opportunities to improve patient safety. We propose the use of a paediatric HTT as part of standard care by centres providing HD to children in the future. GRAPHICAL ABSTRACT: A higher resolution version of the Graphical abstract is available as Supplementary information [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00467-022-05673-4. Springer Berlin Heidelberg 2022-08-01 2023 /pmc/articles/PMC9925574/ /pubmed/35913566 http://dx.doi.org/10.1007/s00467-022-05673-4 Text en © Crown 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Balasubramanian, Ramnath Folwell, Rachel Wheatley, Arran Ramsey, Heidi Barton, Carmen Reid, Christopher J. D. Sinha, Manish D. Developing a trigger tool to monitor adverse events during haemodialysis in children: a pilot project |
title | Developing a trigger tool to monitor adverse events during haemodialysis in children: a pilot project |
title_full | Developing a trigger tool to monitor adverse events during haemodialysis in children: a pilot project |
title_fullStr | Developing a trigger tool to monitor adverse events during haemodialysis in children: a pilot project |
title_full_unstemmed | Developing a trigger tool to monitor adverse events during haemodialysis in children: a pilot project |
title_short | Developing a trigger tool to monitor adverse events during haemodialysis in children: a pilot project |
title_sort | developing a trigger tool to monitor adverse events during haemodialysis in children: a pilot project |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9925574/ https://www.ncbi.nlm.nih.gov/pubmed/35913566 http://dx.doi.org/10.1007/s00467-022-05673-4 |
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