The University of Southampton
University of Southampton Institutional Repository

Whole blood thiamine, intravenous thiamine supplementation and delirium occurrence in the intensive care unit: retrospective cohort analyses

Whole blood thiamine, intravenous thiamine supplementation and delirium occurrence in the intensive care unit: retrospective cohort analyses
Whole blood thiamine, intravenous thiamine supplementation and delirium occurrence in the intensive care unit: retrospective cohort analyses
Background: thiamine di-phosphate is an essential cofactor in glucose metabolism, glutamate transformation and acetylcholinesterase activity, pathways associated with delirium occurrence. We hypothesised that a deficiency in whole blood thiamine and intravenous thiamine supplementation could impact delirium occurrence.

Aim: to establish whether a deficiency in whole blood thiamine and/or intravenous thiamine supplementation within 72 hours of intensive care admission is associated with delirium occurrence.

Method: the first dataset was secondary analysis of a previous study in an intensive care unit in the Netherlands, reported in 2017. The second dataset contained consecutive intensive care admissions 2 years before (period 1: October 2014 to October 2016) and after (period 2: April 2017 to April 2019) routine thiamine supplementation was introduced within 72 hours of admission. Delirium was defined as a positive Confusion Assessment Method-Intensive Care Unit score(s) in 24 hours.

Results: analysis of the first dataset (n=57) using logistic regression showed no relationship between delirium and sepsis or whole blood thiamine, but a significant association with age (p=0.014). In the second dataset (n=3074), 15.1% received IV thiamine in period 1 and 62.6% during period 2. Hierarchical regression analysis reported reduction in delirium occurrence in the second period; this did not reach statistical significance, OR =0.81 (95% CI: 0.652 – 1.002); p=0.052.

Conclusion: no relationship was detected between whole blood thiamine and delirium occurrence on admission, at 24 and 48 hours. It remains unclear whether routine intravenous thiamine supplementation during intensive care admission impacts delirium occurrence. Further prospective randomised clinical trials are needed.
2210-7703
Mumin, Muhammad
b3856b32-9d40-4f10-b99c-b433494cc447
McKenzie, Cathrine
ec344dee-5777-49c5-970e-6326e82c9f8c
Page, Valerie
e58b8256-7de3-484c-a7cc-fe0879d0b2d0
Aitken, Leanne
6007b9b8-bf47-4c08-b4b0-cf5d6642374e
Grocott, Mike
1e87b741-513e-4a22-be13-0f7bb344e8c2
Cunningham, Emma
2c96a4ca-3dcf-458b-8e12-4ec939ca2af0
Hanks, Fraser
ec1a4378-37f9-450a-aee8-b61715e4561a
Hadfield, Daniel
5f905810-e943-4fab-85ea-cb4594c557de
Slooter, A.J.C.
48c57a09-be42-45ee-9410-44e2acc1db08
van Dellen, Edwin
e17b963d-5ae8-4b2a-887c-1c86a42ee590
McAuley, D.F.
b91a3af4-a15e-434f-ad50-b2681fc5aa00
Spronk, Peter E.
3826029e-5d71-45d4-9e6b-983a0f5b8f2b
Mumin, Muhammad
b3856b32-9d40-4f10-b99c-b433494cc447
McKenzie, Cathrine
ec344dee-5777-49c5-970e-6326e82c9f8c
Page, Valerie
e58b8256-7de3-484c-a7cc-fe0879d0b2d0
Aitken, Leanne
6007b9b8-bf47-4c08-b4b0-cf5d6642374e
Grocott, Mike
1e87b741-513e-4a22-be13-0f7bb344e8c2
Cunningham, Emma
2c96a4ca-3dcf-458b-8e12-4ec939ca2af0
Hanks, Fraser
ec1a4378-37f9-450a-aee8-b61715e4561a
Hadfield, Daniel
5f905810-e943-4fab-85ea-cb4594c557de
Slooter, A.J.C.
48c57a09-be42-45ee-9410-44e2acc1db08
van Dellen, Edwin
e17b963d-5ae8-4b2a-887c-1c86a42ee590
McAuley, D.F.
b91a3af4-a15e-434f-ad50-b2681fc5aa00
Spronk, Peter E.
3826029e-5d71-45d4-9e6b-983a0f5b8f2b

Mumin, Muhammad, McKenzie, Cathrine, Page, Valerie, Aitken, Leanne, Grocott, Mike, Cunningham, Emma, Hanks, Fraser, Hadfield, Daniel, Slooter, A.J.C., van Dellen, Edwin, McAuley, D.F. and Spronk, Peter E. (2023) Whole blood thiamine, intravenous thiamine supplementation and delirium occurrence in the intensive care unit: retrospective cohort analyses. International journal of clinical pharmacy. (doi:10.1007/s11096-023-01690-x). (In Press)

Record type: Article

Abstract

Background: thiamine di-phosphate is an essential cofactor in glucose metabolism, glutamate transformation and acetylcholinesterase activity, pathways associated with delirium occurrence. We hypothesised that a deficiency in whole blood thiamine and intravenous thiamine supplementation could impact delirium occurrence.

Aim: to establish whether a deficiency in whole blood thiamine and/or intravenous thiamine supplementation within 72 hours of intensive care admission is associated with delirium occurrence.

Method: the first dataset was secondary analysis of a previous study in an intensive care unit in the Netherlands, reported in 2017. The second dataset contained consecutive intensive care admissions 2 years before (period 1: October 2014 to October 2016) and after (period 2: April 2017 to April 2019) routine thiamine supplementation was introduced within 72 hours of admission. Delirium was defined as a positive Confusion Assessment Method-Intensive Care Unit score(s) in 24 hours.

Results: analysis of the first dataset (n=57) using logistic regression showed no relationship between delirium and sepsis or whole blood thiamine, but a significant association with age (p=0.014). In the second dataset (n=3074), 15.1% received IV thiamine in period 1 and 62.6% during period 2. Hierarchical regression analysis reported reduction in delirium occurrence in the second period; this did not reach statistical significance, OR =0.81 (95% CI: 0.652 – 1.002); p=0.052.

Conclusion: no relationship was detected between whole blood thiamine and delirium occurrence on admission, at 24 and 48 hours. It remains unclear whether routine intravenous thiamine supplementation during intensive care admission impacts delirium occurrence. Further prospective randomised clinical trials are needed.

Text
Manuscript_delirium_IJCP_Re_Submission_v3_FINAL_10.12 - Accepted Manuscript
Restricted to Repository staff only until 27 December 2024.
Available under License Other.
Request a copy

More information

Accepted/In Press date: 27 December 2023

Identifiers

Local EPrints ID: 485907
URI: http://eprints.soton.ac.uk/id/eprint/485907
ISSN: 2210-7703
PURE UUID: d94695e3-24b4-4222-b4f3-ac02df74d7d6
ORCID for Cathrine McKenzie: ORCID iD orcid.org/0000-0002-5190-9711
ORCID for Mike Grocott: ORCID iD orcid.org/0000-0002-9484-7581

Catalogue record

Date deposited: 04 Jan 2024 02:06
Last modified: 18 Mar 2024 04:17

Export record

Altmetrics

Contributors

Author: Muhammad Mumin
Author: Cathrine McKenzie ORCID iD
Author: Valerie Page
Author: Leanne Aitken
Author: Mike Grocott ORCID iD
Author: Emma Cunningham
Author: Fraser Hanks
Author: Daniel Hadfield
Author: A.J.C. Slooter
Author: Edwin van Dellen
Author: D.F. McAuley
Author: Peter E. Spronk

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×