Mumin Muhammad A, McKenzie Cathrine A, Page Valerie J, Hadfield Daniel, Aitken Leanne M, Hanks Fraser, Cunningham Emma, Blackwood Bronagh, Van Dellen Edwin, Slooter Arjen J C, Grocott Michael P W, McAuley Daniel F, Spronk Peter E
King's College Hospital NHS Foundation Trust, Denmark Hill, London, SE5 9RS, UK.
Institute of Pharmaceutical Sciences, Kings College London, London, UK.
Int J Clin Pharm. 2024 Jun;46(3):631-638. doi: 10.1007/s11096-023-01690-x. Epub 2024 Feb 8.
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.
To establish whether a deficiency in whole blood thiamine and/or intravenous thiamine supplementation within 72 h of intensive care admission is associated with delirium occurrence.
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 h of admission. Delirium was defined as a positive Confusion Assessment Method-Intensive Care Unit score(s) in 24 h.
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.
No relationship was detected between whole blood thiamine and delirium occurrence on admission, at 24 and 48 h. It remains unclear whether routine intravenous thiamine supplementation during intensive care admission impacts delirium occurrence. Further prospective randomised clinical trials are needed.
硫胺二磷酸是葡萄糖代谢、谷氨酸转化和乙酰胆碱酯酶活性中的一种必需辅因子,这些途径与谵妄的发生相关。我们推测全血硫胺素缺乏和静脉补充硫胺素可能会影响谵妄的发生。
确定重症监护病房入院72小时内全血硫胺素缺乏和/或静脉补充硫胺素是否与谵妄的发生有关。
第一个数据集是对荷兰一家重症监护病房先前一项研究的二次分析,该研究于2017年报道。第二个数据集包含在入院72小时内引入常规硫胺素补充之前(第1阶段:2014年10月至2016年10月)和之后(第2阶段:2017年4月至2019年4月)的连续重症监护病房入院病例。谵妄定义为24小时内意识模糊评估方法-重症监护病房评分为阳性。
使用逻辑回归对第一个数据集(n = 57)进行分析,结果显示谵妄与败血症或全血硫胺素之间无关联,但与年龄有显著相关性(p = 0.014)。在第二个数据集(n = 3074)中,第1阶段有15.1%的患者接受静脉硫胺素治疗,第2阶段为62.6%。分层回归分析报告称,第二阶段谵妄的发生率有所降低;但未达到统计学意义,OR = 0.81(95%CI 0.652 - 1.002);p = 0.052。
在入院时、24小时和48小时,未检测到全血硫胺素与谵妄发生之间的关系。目前尚不清楚重症监护病房入院期间常规静脉补充硫胺素是否会影响谵妄的发生。需要进一步进行前瞻性随机临床试验。