The Effect of Dexmedetomidine on the Mini-Cog Score and High-Mobility Group Box 1 Levels in Elderly Patients with Postoperative Neurocognitive Disorders Undergoing Orthopedic Surgery.
Seung Hee YooMi Jin JueYu-Hee KimSooyoung ChoWon-Joong KimKye-Min KimJong In HanHeeseung LeePublished in: Journal of clinical medicine (2023)
Dexmedetomidine prevents postoperative cognitive dysfunction by inhibiting high-mobility group box 1 (HMGB1), which acts as an inflammatory marker. This study investigated the HMGB1 levels and the cognitive function using a Mini-Cog© score in elderly patients undergoing orthopedic surgery with dexmedetomidine infusion. In total, 128 patients aged ≥ 65 years were analyzed. The patients received saline in the control group and dexmedetomidine in the dexmedetomidine group until the end of surgery. Blood sampling and the Mini-Cog© test were performed before the surgery and on postoperative days 1 and 3. The primary outcomes were the effect of dexmedetomidine on the HMGB1 levels and the Mini-Cog© score in terms of postoperative cognitive function. The Mini-Cog© score over time differed significantly between the groups ( p = 0.008), with an increase in the dexmedetomidine group. The postoperative HMGB1 levels increased over time in both groups; however, there was no significant difference between the groups ( p = 0.969). The probability of perioperative neurocognitive disorders decreased by 0.48 times as the Mini-Cog© score on postoperative day 3 increased by 1 point. Intraoperative dexmedetomidine has shown an increase in the postoperative Mini-Cog© score. Thus, the Mini-Cog© score is a potential tool for evaluating cognitive function in elderly patients.
Keyphrases
- patients undergoing
- cardiac surgery
- minimally invasive
- coronary artery bypass
- end stage renal disease
- newly diagnosed
- ejection fraction
- chronic kidney disease
- surgical site infection
- low dose
- transcription factor
- acute kidney injury
- bipolar disorder
- metabolic syndrome
- risk assessment
- adipose tissue
- acute coronary syndrome
- mouse model
- patient reported outcomes
- insulin resistance
- skeletal muscle
- weight loss
- human health
- glycemic control