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Remotely supervised ultrasound‐guided peripheral intravenous cannulation training: A prospective cohort study examining success rates and patient experience
INTRODUCTION: Ultrasound‐guided peripheral intravenous cannulation (USGPIVC) benefits patients with difficult intravenous access (DIVA) through visualising otherwise non‐visible and non‐palpable veins. Supervised live‐case training is an important component of learning this skill, but supervisor ava...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9644440/ https://www.ncbi.nlm.nih.gov/pubmed/36405792 http://dx.doi.org/10.1002/ajum.12318 |
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author | Peters, Nathan Thomas, Joel Woods, Christine Rickard, Claire Marsh, Nicole |
author_facet | Peters, Nathan Thomas, Joel Woods, Christine Rickard, Claire Marsh, Nicole |
author_sort | Peters, Nathan |
collection | PubMed |
description | INTRODUCTION: Ultrasound‐guided peripheral intravenous cannulation (USGPIVC) benefits patients with difficult intravenous access (DIVA) through visualising otherwise non‐visible and non‐palpable veins. Supervised live‐case training is an important component of learning this skill, but supervisor availability can present a barrier limiting or delaying staff completing their training. AIMS: The aim of this study was to determine the first‐attempt success rate of newly trained USGPIVC inserters using remote supervision and timely written feedback based on app‐based screen recordings taken during insertion. Secondary aims were overall procedural success, and inserter and patient experiences. METHODS: This study is an observational cohort study carried out between October and December 2021. Fourteen newly trained junior medical officers (JMOs) were eligible to utilise USGPIVC on a minimum of five consenting patients while simultaneously recording the ultrasound screen during insertion to capture their technique. Feedback was generated following expert review of these recordings against a standardised feedback tool. RESULTS: Average first‐attempt success was 71% (n = 72) in the 102 patients recruited. The average time for JMOs to receive feedback was 30 h, and 13 JMOs (93%) felt well supported and completed the remote training pathway. The majority of patients were female (n = 59; 58%), were aged 41–80 years (n = 75; 74%) and had ≥2 risk factors for DIVA (n = 57; 56%). CONCLUSIONS: First‐attempt success rates were similar when comparing remote supervision used in this study to direct supervision used by other studies.This finding supports incorporating remote supervision into training guidelines for USGPIVC as an alternative method of supervision, particularly when supervisor availability is limited. |
format | Online Article Text |
id | pubmed-9644440 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-96444402023-09-16 Remotely supervised ultrasound‐guided peripheral intravenous cannulation training: A prospective cohort study examining success rates and patient experience Peters, Nathan Thomas, Joel Woods, Christine Rickard, Claire Marsh, Nicole Australas J Ultrasound Med Original Articles INTRODUCTION: Ultrasound‐guided peripheral intravenous cannulation (USGPIVC) benefits patients with difficult intravenous access (DIVA) through visualising otherwise non‐visible and non‐palpable veins. Supervised live‐case training is an important component of learning this skill, but supervisor availability can present a barrier limiting or delaying staff completing their training. AIMS: The aim of this study was to determine the first‐attempt success rate of newly trained USGPIVC inserters using remote supervision and timely written feedback based on app‐based screen recordings taken during insertion. Secondary aims were overall procedural success, and inserter and patient experiences. METHODS: This study is an observational cohort study carried out between October and December 2021. Fourteen newly trained junior medical officers (JMOs) were eligible to utilise USGPIVC on a minimum of five consenting patients while simultaneously recording the ultrasound screen during insertion to capture their technique. Feedback was generated following expert review of these recordings against a standardised feedback tool. RESULTS: Average first‐attempt success was 71% (n = 72) in the 102 patients recruited. The average time for JMOs to receive feedback was 30 h, and 13 JMOs (93%) felt well supported and completed the remote training pathway. The majority of patients were female (n = 59; 58%), were aged 41–80 years (n = 75; 74%) and had ≥2 risk factors for DIVA (n = 57; 56%). CONCLUSIONS: First‐attempt success rates were similar when comparing remote supervision used in this study to direct supervision used by other studies.This finding supports incorporating remote supervision into training guidelines for USGPIVC as an alternative method of supervision, particularly when supervisor availability is limited. John Wiley and Sons Inc. 2022-09-16 /pmc/articles/PMC9644440/ /pubmed/36405792 http://dx.doi.org/10.1002/ajum.12318 Text en © 2022 The Authors. Australasian Journal of Ultrasound in Medicine published by John Wiley & Sons Australia, Ltd on behalf of Australasian Society for Ultrasound in Medicine. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Peters, Nathan Thomas, Joel Woods, Christine Rickard, Claire Marsh, Nicole Remotely supervised ultrasound‐guided peripheral intravenous cannulation training: A prospective cohort study examining success rates and patient experience |
title | Remotely supervised ultrasound‐guided peripheral intravenous cannulation training: A prospective cohort study examining success rates and patient experience |
title_full | Remotely supervised ultrasound‐guided peripheral intravenous cannulation training: A prospective cohort study examining success rates and patient experience |
title_fullStr | Remotely supervised ultrasound‐guided peripheral intravenous cannulation training: A prospective cohort study examining success rates and patient experience |
title_full_unstemmed | Remotely supervised ultrasound‐guided peripheral intravenous cannulation training: A prospective cohort study examining success rates and patient experience |
title_short | Remotely supervised ultrasound‐guided peripheral intravenous cannulation training: A prospective cohort study examining success rates and patient experience |
title_sort | remotely supervised ultrasound‐guided peripheral intravenous cannulation training: a prospective cohort study examining success rates and patient experience |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9644440/ https://www.ncbi.nlm.nih.gov/pubmed/36405792 http://dx.doi.org/10.1002/ajum.12318 |
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