Association between sleep duration on the night before surgery and postoperative cognitive function: a prospective cohort study (Preprint)

2021 ◽  
Author(s):  
Ayasa Takamino ◽  
Masakazu Kotoda ◽  
Yosuke Nakadate ◽  
Sohei Hishiyama ◽  
Tetsuya Iijima ◽  
...  

BACKGROUND As the world is rapidly aging, and the number of elderly patients who undergo surgery is rising, postoperative cognitive dysfunction (POCD) among those patients has become an increasing healthcare problem. Although understanding risk factors and mechanisms underlying the pathogenesis of POCD is critically important from a preventative viewpoint, such knowledge and evidence are lacking. A growing body of evidence suggest an association between cognitive function and sleep duration. The emergence of up-to-date wearable sleep trackers allows researchers to investigate sleep duration without disturbing the patients’ sleep. OBJECTIVE This study investigated the association between sleep duration on the night before surgery and postoperative cognitive function using a wearable sleep tracker. METHODS In this 6-month prospective cohort study, we analyzed data from 194 patients aged ≥65 years who underwent elective non-cardiac and non-cranial surgery under general anesthesia. According to the sleep duration on the night before surgery, patients were categorized into following four groups: <5 h, 5–7 h, 7–9 h, and >9 h. Perioperative cognitive function and domains were assessed using a neuropsychological test battery, and the incidence and prevalence of POCD over 6 months after surgery were analyzed using the multiple logistic regression analysis. RESULTS During the 6-month follow-up period, 41 patients (21%) developed POCD. The incidence of POCD was significantly elevated for the patients with sleep duration less than 5 h (vs. 7–9 h; adjusted odds ratio, 2.67; 95% CI, 1.01–7.04; P <.05). The association between sleep duration and prevalence of POCD was limited to the early postoperative period (at 1 week and 1 month). Among the cognitive domains assessed, attentional function was significantly impaired in patients with a sleep duration of less than 5 h. [vs. 7–9 h at 1 week; 4/37 (10.8%) vs. 0/73 (0%); P <.05]. CONCLUSIONS Sleep duration less than 5 h on the night before surgery was significantly associated with worse attentional function after surgery and higher incidence of POCD. The present results indicate that sleep deprivation on the night before surgery may have a temporary but significantly negative influence on the patient’s postoperative cognitive function and is a potential target for preventing POCD. CLINICALTRIAL N/A

2021 ◽  
pp. 1-8
Author(s):  
Xiao Liu ◽  
Ayiguli Abudukeremu ◽  
Yuan Jiang ◽  
Zhengyu Cao ◽  
Maoxiong Wu ◽  
...  

Background: Several kinds of motor dysfunction can predict future cognitive impairment in elderly individuals. However, the ability of the fine motor index (FINEA) and gross motor index (GROSSA) to predict the risk of cognitive impairment has not been assessed. Objective: We investigated the associations between FINEA/GROSSA and cognitive impairment. Methods: The data of 4,745 participants from The Irish Longitudinal Study on Ageing (TILDA) were analyzed. Cognitive function was assessed using the Mini-Mental State Examination (MMSE). We first assessed the correlation between the FINEA GROSSA and MMSE in a cross-sectional study. Then, we further investigated the predictive role of the incidence of cognitive impairment in a prospective cohort study. Results: We found that both FINEA and GROSSA were negatively correlated with MMSE in both the unadjusted (FINEA: B = –1.00, 95%confidence intervals (CI): –1.17, –0.83, t = –11.53, p <  0.001; GROSSA: B = –0.85, 95%CI: –0.94, –0.76, t = –18.29, p <  0.001) and adjusted (FINEA: B = –0.63, 95%CI: –0.79, –0.47, t = –7.77, p <  0.001; GROSSA: B = –0.57, 95%CI: –0.66, –0.48, t = –12.61, p <  0.001) analyses in a cross-sectional study. In a prospective cohort study, both high FINEA and high GROSSA were associated with an increased incidence of cognitive function impairment (FINEA: adjusted odds ratios (OR) = 2.35, 95%CI: 1.05, 5.23, p = 0.036; GROSSA adjusted OR = 3.00, 95%CI: 1.49, 6.03, p = 0.002) after 2 years of follow-up. Conclusion: Higher FINEA and GROSSA scores were both associated with an increased incidence of cognitive impairment. FINEA or GROSSA might be a simple tool for identifying patients with cognitive impairment.


2018 ◽  
Vol 46 (12) ◽  
pp. e1121-e1127 ◽  
Author(s):  
Stine Estrup ◽  
Cilia K. W. Kjer ◽  
Frederik Vilhelmsen ◽  
Lone M. Poulsen ◽  
Ismail Gøgenur ◽  
...  

SLEEP ◽  
2019 ◽  
Vol 42 (Supplement_1) ◽  
pp. A322-A323
Author(s):  
Bao-Peng Liu ◽  
Zhen-Zhen Liu ◽  
Ze-Ying Wang ◽  
Di An ◽  
Yan-Xin Wei ◽  
...  

2018 ◽  
Vol 8 (1) ◽  
Author(s):  
Xiaoxue Liu ◽  
Qiaofeng Song ◽  
Wanning Hu ◽  
Xiaochen Han ◽  
Jianhui Gan ◽  
...  

BMJ Open ◽  
2020 ◽  
Vol 10 (1) ◽  
pp. e034657 ◽  
Author(s):  
Qianyu Cui ◽  
Dexiang Wang ◽  
Min Zeng ◽  
Jia Dong ◽  
Hailong Jin ◽  
...  

IntroductionThe incidence of covert stroke and cognitive dysfunction has gradually increased due to an ageing population. Recently, a prospective cohort study reported perioperative covert stroke was associated with an increased risk of postoperative cognitive dysfunction (POCD) 1 year after non-cardiac surgery. However, the mechanism remains unclear.Methods and analysisThis is a prospective observational trial aiming to investigate the cumulative incidence of perioperative covert stroke and test the hypothesis that perioperative covert stroke associates with POCD in elderly patients undergoing non-cardiac and non-neurological surgery. Data on risk factors, brain MRI, cognitive function evaluation and serum immune-inflammatory cytokines will be collected and analysed.Ethics and disseminationEthical approval has been granted by the Medical Ethics Committee of Beijing Tiantan Hospital, Capital Medical University (reference number: KY2017-027-02). The results of this study will be disseminated through presentations at scientific conferences and publication in scientific journals.Trial registration numberNCT03081429.


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