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Background:
Systematic Review

Preoperative Risk Factors Associated with Increased Incidence of Postoperative Delirium: Systematic Review of Qualified Clinical Studies

1
School of Medicine, University of Crete, 71003 Crete, Greece
2
Department of Anesthesiology, Critical Care and Pain Medicine, Policlinico Umberto I Teaching Hospital, Sapienza University of Rome, 00185 Rome, Italy
*
Author to whom correspondence should be addressed.
Geriatrics 2023, 8(1), 24; https://doi.org/10.3390/geriatrics8010024
Submission received: 30 September 2022 / Revised: 20 December 2022 / Accepted: 30 January 2023 / Published: 7 February 2023
(This article belongs to the Special Issue Advancing the Care of Delirium and Comorbid Dementia)

Abstract

:
Postoperative delirium (POD) is an acute alteration of mental state, characterized by reduced awareness and attention, occurring up to five postoperative days after recovery from anesthesia. Several original studies and reviews have identified possible perioperative POD risk factors; however, there is no comprehensive review of the preoperative risk factors in patients diagnosed with POD using only validated diagnostic scales. The aim of this systematic review was to report the preoperative risk factors associated with an increased incidence of POD in patients undergoing non-cardiac and non-brain surgery. The reviewed studies included original research papers that used at least one validated diagnostic scale to identify POD occurrence for more than 24 h. A total of 6475 references were retrieved from the database search, with only 260 of them being suitable for further review. Out of the 260 reviewed studies, only 165 that used a validated POD scale reported one or more preoperative risk factors. Forty-one risk factors were identified, with various levels of statistical significance. The extracted risk factors could serve as a preoperative POD risk assessment workup. Future studies dedicated to the further evaluation of the specific preoperative risk factors’ contributions to POD could help with the development of a weighted screening tool.

1. Introduction

Postoperative delirium (POD) is an acute alteration of mental state, characterized by reduced awareness and attention, occurring up to five postoperative days after recovery from anesthesia [1,2,3]. This neuropsychiatric disturbance seems to have an incidence ranging from 11% to 51% in older adults [4,5]. POD severely affects the postoperative recovery of patients, prolonging their hospital stay and increasing healthcare costs [6]. Furthermore, several studies suggest that POD is a ‘neurotoxic’ event possibly correlated with long-term effects such as postoperative cognitive dysfunction [4]. In 2017, the European Society of Anesthesiologists delivered dedicated guidelines that reported the need for routine monitoring using validated scales [7].
Multiple pathophysiological mechanisms underlying this phenomenon have been presented in the literature, with acetylcholine deficiency being one of the most established theories [8]. The central anticholinergic properties of anesthetic drugs, together with surgical stress, were considered to be the main contributors to POD’s pathogenesis [9]. However, several other possible risk factors have been suggested in the literature. These factors can be categorized as either modifiable or non-modifiable, and they can be detected before surgical procedures (pre-operative), during (intra-operative), or after them (postoperative) [10,11,12]. Several original studies and reviews have listed possible POD risk factors to be screened preoperatively. Some articles reported increased statistical association, while others calculated the odds ratio [13,14]. Interestingly, some articles claimed to report significant risk factors, although this significance was not verified in the statistical analyses. Such factors include sleep disruption at home, obstructive sleep apnea, total intravenous versus inhaled anesthesia, and general versus locoregional anesthesia [15,16,17,18,19,20]. The use of a risk stratification work-up that includes factors not clearly associated with POD can be substantially misleading and result in inappropriate patient selection or prescription of unnecessary drugs.
The available literature lacks a comprehensive report of the preoperative risk factors associated with an increased risk of POD based on a systematic review (SR) of clinical studies using only validated diagnostic scales. The aim of this SR is to report the preoperative risk factors associated with an increased incidence of POD in patients undergoing non-cardiac and non-brain surgery. The reviewed studies include original research studies that use at least one validated diagnostic scale to identify POD occurrence.

2. Methods

A systematic literature search was performed by assessing 6 databases in accordance with the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) statement recommendations [21]. This SR was registered in the International Prospective Register of Systematic Reviews (PROSPERO registration number: CRD42021246906). It selectively included original studies that accomplished the postoperative monitoring of patients undergoing non-cardiac or non-brain procedures for longer than 24 h using validated scales [22]. In order to launch the related literature search, the following keywords were used: postoperative, delirium, confusion, post-anesthesia, and anesthesia recovery. Moreover, specific search strings were used in 6 scientific databases (Appendix A). A total of 6475 references were retrieved. The suitable studies included randomized clinical trials (RCTs), retrospective and prospective studies, case-control studies, and cohort studies. The other criteria included a population older than 18 years old, POD as the primary subject of the study, and English as the main manuscript language. Studies that did not include an original dataset (meta-analyses, reviews, commentaries, editorials, etc.), case-series presenting less than 5 cases, protocols of trials registered online, and reports published as abstracts were excluded. Of the reviewed studies, 260, which were published between 1987 and March 2021, were considered eligible (Figure 1).
The selected studies were thoroughly reviewed in order to identify those that reported preoperative risk factors associated with an increased incidence of POD. Apart from the preoperative risk factor extraction, the POD monitoring scale used was also recorded. As a secondary endpoint, the extracted POD risk factors are presented in a clinical record form (Table 1) that can serve as a literature-generated work-up for standardized preoperative risk stratification.
All the randomized studies that reported POD risk factors were evaluated using the Cochrane Collaboration’s risk of bias tool [23,24]. The risk of bias was assessed independently during the data extraction process.

3. Results

In 165 out of the 260 reviewed studies, one or more preoperative risk factors have been associated with an increased risk of POD. The types of POD monitoring scales used in the 165 studies are described. A total of 41 risk factors are identified and categorized into 7 groups: demographics, laboratory testing, comorbidities, cumulative scores, chronic therapies, habits, and type of surgery. Within each of these groups, individual risk factors are listed, reporting first those supported by the largest number of studies. For each variable, the lowest value associated with the statistical evidence, that is, with an increased incidence of POD, is reported as a threshold, and the odds ratio (OR) value or range indicated by all the relevant studies is mentioned.

3.1. Types of Scales Used

A single POD diagnostic scale is used in 110/165 (66.6%) studies, 48/165 (18.5%) used 2 diagnostic scales, and 3 or more scales are used in 7/165 (4.2%). The most frequently used diagnostic scale is the Confusion Assessment Method (CAM), which is included in 158/165 (95.7%); the Diagnostic and Statistical Manual of Mental Disorders (DSM) in 58/165 (35.1%); the CAM-Intensive Care Unit (ICU) in 38/165 (23.0%); the Delirium Rating Scale (DSR) in 20/165 (12.1%); the Delirium Observation Screening in 13/165 (7.8%); the Nursing Delirium Screening Scale (Nu-DESC) in 11/165 (6.6%); the Memorial Delirium Assessment Scale (MDAS) in 9/165 (5.4%); the International Classification of Disease (ICD) in 5/165 (3.0%); the Neelon and Champagne Confusion Scale (NEECHAM) in 5/165 (3.0%); the Delirium Symptom Interview (DSI) in 3/165 (1.8%); and the 4AT in 1/165 (0.6%).

3.2. Demographics

The included demographic risk factors are age, gender, and educational level. Advanced age is consistently and extensively reported as a POD risk factor in 88/165 (53.3%) of the studies selected as suitable for the present SR [25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66,67,68,69,70,71,72,73,74,75,76,77,78,79,80,81,82,83,84,85,86,87,88,89,90,91,92,93,94,95,96,97,98,99,100,101,102,103,104,105,106,107,108,109,110,111,112]. A higher incidence of POD is described in patients aged ≥60 years in 7/165 (4.24%) studies [44,45,108,109,110,111,112]. With increasing age, the POD risk becomes increasingly pronounced: patients aged 60–79 have an OR of 1.06–1.27 [54,55,56,57,58,59,60,61,62,63,64,65,66,67,68,73,101], while those aged ≥80 years old have an OR of 1.07–2.67 [27,103]. Gender, which is evaluated in 29/165 (17.5%) of the selected studies, is a possible predictive risk factor for POD [25,37,45,46,47,48,49,50,52,53,55,59,60,62,63,64,65,66,67,68,69,70,74,100,110,113,114,115,116]. In 24 studies [37,45,46,48,49,50,52,55,59,60,62,63,64,65,66,67,68,69,70,110,113,114,115,116], which recorded data from 7900 patients (5152 were male and 2748 female), reported no differences in the POD incidence between male and female patients. In 3 studies, female gender was associated with a higher risk of POD (up to an OR of 11.02) [25,47,53]. In 2 studies, male gender was associated with a higher risk of POD (up to an OR to 5.78) [74,100]. Educational level is considered a possible predictive risk factor for POD, as reported in 10/165 (6.0%) of the studies [26,50,54,55,61,62,65,70,100,117]. Patients with a lower educational level (<8 years) tend to have a high risk of POD [p = 0.001, OR = 3.27 (1.43–7.44)] [50,117].

3.3. Laboratory Testing

Among the laboratory testing risk factors are the plasma concentration of albumin, sodium, total bilirubin, blood glucose, calcium, hemoglobin, and pro-inflammatory markers (CRP, TNF-a, IL-6, C-reactive protein/albumin ratio). In total, 9/165 (5.45%) articles mention albumin as a possible POD risk factor [30,33,76,96,98,105,107,118,119]. Preoperative laboratory testing demonstrates that albumin is lower in patients with POD [33,118] and could possibly predict a higher risk when values are below 3.9 g/dL [119] (p < 0.002). The CRP levels are described as a possible preoperative risk factor in 5/165 (3.03%) studies [75,76,116,120,121]. Pre-operative C-reactive protein (CRP) is significantly higher (7.0 ± 15.2 mg/L, p < 0.017) in patients with delirium, and values above 7 mg/L are especially considered predictive of POD [116]. The hemoglobin levels are considered to be a possible risk factor for POD in 4/165 (2.42%) studies. In a total of 214 patients, a relevant hemoglobin level above 13.16 g/dL is associated with POD (p < 0.006) [76,98,107,122]. In 3/165 (1.81%) studies, blood glucose is demonstrated to be a possible risk factor for POD [76,99,107]. A blood glucose level >8.4 mmol/L is considered a predictive risk factor (p < 0.001, OR = 1.142) [99]. Another inflammatory marker, IL-6, is found in 3/165 (1.81%) studies to serve as a possible predictive marker for POD [98,121,123]. In one study, where 55/272 (20.2%) patients developed POD, higher levels of serum IL-6 are identified in the POD group preoperatively, further supporting that correlation (>17.9 pg/mL) (p < 0.0036, OR = 1.51). The sodium levels are found in 2/165 (1.21%) studies to be a possible high-risk factor of POD [74,107]. Values <135 mEq/L or >146 mEq/L are considered potential predictors of POD. In a study of 228 patients, 57 of whom (25%) developed POD, a sodium serum level between 136 and 145 mEq/L is revealed in 46/57 (80%) delirious patients. In 8/57 (14%) patients with POD, a serum sodium value over 145 mEq/L during the preoperative period is analyzed and found to be a sizeable risk factor in comparison to the non-POD group. In 3/57 (5.2%) patients with POD, a sodium serum level <136 mEq/L is identified to be highly associated with POD when compared to the non-POD group (p < 0.05) [107]. TNF-a is revealed in 2/165 (1.21%) studies to be a possible and considerable POD risk factor. A total of 79 patients who developed POD are demonstrated to have a higher TNF-a level (>8.2 nmol/L) than the non-POD patients (p < 0.018, OR = 1.43) [98,121]. Bilirubin is identified in one study as a potential risk factor, with 120/572 patients developing POD when the total bilirubin level is >18.00 µmol/L and the direct bilirubin is >5.1 µmol/L (p < 0.001, OR = 1.077) [76]. Serum calcium is found in one study to be a predictive factor for POD. Some 120/572 (20.9%) POD-positive patients have a serum calcium value <2.18 mmol/L, and hypocalcemia is revealed to be a predictive risk factor for POD (p < 0.004) [76]. The C-reactive protein/albumin ratio (CAR) is revealed to be a possible POD risk factor. In a study of 272 patients in which preoperative blood tests were conducted, the 55 patients who developed POD exhibit a higher CAR (>2.90), thus making it a relevant predictor (p < 0.001, OR = 3.04) [98].

3.4. Cumulative Indicators

Among the tested cumulative indicators found to be associated with an increased risk of POD are the MMSE score, ASA score, BMI, Charlson Comorbidity Index score, APACHE II, mini-cog score, Barthel Index, GDS, and CES-D fatigue status. The Mini Mental Scale Exam (MMSE), a diagnostic scale concerning cognitive function, is found to be a predictor of POD in 25/165 studies (15.1%) [20,35,41,42,48,50,51,54,60,62,63,65,66,70,71,74,86,97,98,105,109,114,116,124,125]. In particular, 145/450 (32.22%) patients with POD are demonstrated to have a lower level of MMSE (<17) compared to 47 patients without any POD event (p < 0.001) [35,86]. The American Society of Anesthesiology (ASA) physical status score is considered in 22/165 (13.33%) studies to be POD predictor [41,44,47,48,51,53,54,59,60,61,62,67,68,69,70,73,78,88,100,104,112,126]. In particular, 51/411 (12.4%) patients with POD are demonstrated to preoperatively have an ASA score below 2 and 32/411 (7.78%) patients to have an ASA score above 2 (OR = 2.21, p < 0.001) [88,112]. The Body Mass Index (BMI) is considered in 18/165 (10.9%) studies to be a predictor of POD [45,46,48,50,51,53,55,62,67,68,69,74,109,114,115,125,127,128]. In particular, 176/1061 (16.58%) patients with POD are demonstrated to have a BMI < 20 preoperatively (p < 0.05) [74,114]. The Charlson Comorbidity Index score (CCI) estimates the 10-year survival rates by examining several comorbidities, and it is considered in 8/165 (4.8%) studies to be a predictor of POD [30,51,72,74,83,85,86,109]. A higher CCI score (CCI ≥ 2) seems to be identified as a risk factor for POD development. The APACHE II score, a mortality index for ICU patients, is considered in 6/165 (3.6%) studies to be a predictor of POD [52,56,64,94,113,129], with 2 of the studies [94,129] identifying statistically significant correlation with POD development. The mini-cog score is a fast cognitive impairment screening test that can detect people with dementia. Scores ≤2 are considered to indicate impairment and to be a possible predictor of POD, as shown in 2/165 (1.2%) studies [30,130]. The Barthel Index for Activities of Daily Living is considered in 2/165 (1.2%) [30,74] studies to be a predictor of POD. Patients presenting with POD have lower Barthel Index values at a statistically significant level in both studies. The Geriatric Depression Scale (GDS) is considered in 3/165 (1.8%) studies to be a predictor of POD. An increased GDS score is associated with POD development in all three studies [46,74,114]. The CES-D fatigue status [78] is considered in 1/165 (0.6%) study to be a predictor of POD, with 30% of patients presenting with POD having a positive CES-D status preoperatively (p < 0.05).

3.5. Comorbidities

Various comorbidities are associated with an increased POD incidence. These include diabetes, cardiovascular conditions (coronary and vascular disease, arterial hypertension), cerebral conditions (depression, sensory impairment, history of stroke, cerebral vascular disease, sleep disorders), lung conditions (respiratory disease and pulmonary hypertension), and renal conditions.
Diabetes is considered in 12/165 (7.2%) [31,39,45,46,54,57,65,95,98,107,114,131] studies to be a potential predictor of POD. Only in 4/165 (2.4%) studies [31,39,95,131] is diabetes identified as a statistically significant risk factor (OR = 2.98). The remaining eight studies identified no or insignificant correlation between diabetes and POD.
Cardiovascular: Coronary and vascular disease is considered in 8/165 (4.8%) [26,31,45,57,95,98,114,132] studies to be a risk factor for POD development. Three of the studies identified statistically significant correlation between cardiovascular disease and POD development. Hypertension is considered in 8/165 (4.8%) [31,39,45,57,95,98,114,132] studies to be a potential risk factor for POD. Only in two studies (1.2%) [39,98] do researchers find statistically significant correlation between hypertension and POD development.
Cerebral: Depression is mentioned in one study 1/165 (0.6%) to be a risk factor for POD development at a statistically significant level (p < 0.001) [39]. Sensory impairment is considered in 2/165 (1.2%) [31,133] studies to be a potential risk factor for POD development. In one study [31], all types of sensory impairment are included, while the other focuses on hearing impairment [133]. Sensory deprivation is associated with an increased incidence of POD [134]. A history of stroke is identified as a potential risk factor for POD development in 5/165 (3%) studies [57,76,100,135,136]. Three of the studies suggest statistically significant correlation between prior strokes and POD (OR = 5.618) [76,100,135]. Cerebral vascular disease is highly correlated in two studies as a potential risk factor for POD development. A total of 99/462 (21.4%) patients with cerebrovascular disease developed delirium postoperatively [95,114]. Sleeping disorders are identified in 4/165 studies to be a potential risk factor for POD development [137,138,139,140]. The existence of obstructive sleep apnea syndrome is especially correlated with an increased incidence of POD (up to sixfold) in certain patient groups [137,138,139].
Renal failure is considered in two studies to be a potential risk factor for POD development. Only one study suggests that renal failure is associated at a statistically significant level with POD development (OR = 1.4) [39].
Lung conditions: Respiratory disease is considered in 3/165 (1.8%) studies to be a potential risk factor for POD [31,45,95]. However, only one study identifies statistically significant correlation [45]. Pulmonary hypertension is suggested in one study 1/165 to be a risk factor for POD (p < 0.001, OR = 1.8) [39].

3.6. Chronic Therapies

Among the chronic therapies, the following are included as risk factors: benzodiazepines [37,45,135,141], psychoactive drugs [135], B-blockers [98], and anticholinergics [104]. Benzodiazepine use is identified as a statistically significant risk factor in 4/165 (2.4%) studies (OR = 1.48–4.99) [37,45,135,141]. Psychoactive drugs are identified in one study to be a significant risk factor for POD development [135]. Treatment with beta-blockers is considered to be a risk factor for POD development in 1 study (p = 0.025) [98]. Anticholinergic drugs are considered to be a risk factor for POD development in 2/165 studies (1.2%) [104,142]. A special scale regarding the central anticholinergic effects of some drugs that was developed is known as the Anticholinergic Drug Scale (ADS). The ADS score is associated at a statistically significant level with POD development [104].

3.7. Habits

Among the habits considered to be possible risk factors are smoking [33,45,55,77,84,98,143], alcohol [25,31,33,39,45,55,57,77,84,132,133,144], and drug abuse [39]. Smoking is considered to be a potential risk factor for POD development in 7/165 studies [33,45,55,77,84,98,143]. Only one study identifies statistically significant correlation (p = 0.04) [55], with the rest of the studies finding no correlation [33,45,77,84,98,143]. Alcohol abuse is considered a predictor of POD development in 10/165 (6%) [25,31,33,39,45,55,77,84,132,133] studies. However, there is a big variance among the studies regarding the cut-off limit of the definition above. A total of 6 studies identify statistically significant correlation between alcohol abuse and POD development (OR = 2.3) [25,33,39,55,132,133], while 4 studies identify no correlation [31,45,77,84]. Drug abuse is considered a risk factor for POD development in a single study (p < 0.001) [39].

3.8. Type of Surgery

The type of surgery and indication criteria (elective or emergency) are strong predictors of POD. Intrathoracic and intra-abdominal [145,146] operations are associated with a higher incidence of POD compared to all the other surgical sites [107,144,145,146,147]. In the high-risk operations for POD, peripheral vascular procedures, urological procedures [OR = 4.03], spinal procedures [OR = 3.70], and orthopedic procedures [OR = 6.23] are included. [117,144]. Out of the orthopedic procedures, almost 1/3 patients undergoing total knee replacement and 1/4 patients undergoing hip arthroplasty develop POD [148]. Emergency surgeries are correlated with a high incidence of POD compared to elective ones, with up to 51% of patients admitted in an emergency setting developing POD [133]. As far as common surgical procedures are concerned, current clinical evidence regarding delirium is conflicting, with some observational studies reporting a lower risk of delirium with minimally invasive surgery, while others report no difference [53,149,150].

3.9. Risk of Bias Assessment

All the randomized studies that report at least one risk factor included in the current study were evaluated for bias using the Cochrane Collaboration’s risk of bias tool. The overall assessment suggests an intermediate quality of data, attributed mainly to the limited reporting regarding the blinding of data (Figure 2).

4. Discussion

In this SR of clinical studies published online up to March 2021, only validated POD scales were used in adult patients undergoing non-cardiac or non-brain surgeries. Several preoperative risk factors associated with an increased incidence of postoperative delirium were identified. A large variety of diagnostic scales were used throughout the selected studies. The presented risk factors were categorized into seven groups: demographics (age, gender, educational level); laboratory testing (albumin, bilirubin, glucose, hemoglobin, CRP, TNF, IL-6, sodium); comorbidities (metabolic, cardiovascular, cerebral, lung, renal); cumulative indicators (MMSE score, ASA score, BMI, CCI score, APACHE II, mini-cog score, Barthel Index, GDS, CES-D fatigue status); chronic therapies (psychoactive drugs, beta-blockers, benzodiazepines); habits (smoking, alcohol abuse, drug abuse); and type of surgery and setting (intrathoracic, intraabdominal, peripheral vascular, orthopedic, urological, ambulatory, and emergency). Several studies in the field identified individual or lists of risk factors associated with POD development, although a specific preoperative risk assessment for POD is not sufficiently addressed yet, as a large number of them listed POD risk factors in the introduction or in the discussion part that were not supported by specific evidence [151,152,153,154,155,156,157,158,159,160,161,162,163,164,165,166,167,168,169,170,171,172,173,174,175,176,177,178,179,180,181,182,183,184].
This SR was conducted in accordance with the PRISMA guidelines [21], and it was based on using the literature search strategy proposed by the ESA task force on POD [7]. However, this approach may have restricted the studies we finally assessed due to the possible mismatch between the searched keywords and published data, as extracted by the algorithm used by the scientific library databases. It is of note that despite the large number of papers extracted, only 260 out of the 6475 (4%) fulfilled the criteria and used a validated diagnostic scale. The bias assessment suggested the intermediate level quality of the data overall. However, due to the high heterogeneity of study types included, it was not possible to perform a reliable quality assessment of all the studies using a single tool. This could be a limitation of our study. Finally, the selective inclusion of only original studies may have hindered us from identifying other potential POD contributors that have not been sufficiently studied yet or showed poor correlation due to the limited population size. These characteristics are, at the same time, possibly a limitation and quality criterion of the present SR.
In the present study, it is clear that among the variables associated with an increased incidence of POD, some have strong predictive value, as listed in Table 1. These variables should become part of every preoperative assessment and be reported with a specific focus on the evaluation of the POD risk. Interestingly, pain, which had been theorized to be a risk factor for POD and measured using the visual analogue pain scale (VAS), was tested in 3/165 (1.8%) studies but not found to be statistically significant in any of them [51,65,68]. The same applies for liver disease, where none of the studies identified statistically significant correlation with POD, with the exception of hepatic encephalopathy [45,185]. Dyslipidemia was evaluated in 4/165 (2.4%) studies to be a risk factor for POD [68,95,98,114], with no statistically significant correlation being identified, suggesting that other comorbidities that such patients have could be contributors to POD’s development. In a recent review by our study group, perioperative risk factors were identified [186]. This difference is attributed to the search criteria used during the literature screening, as well as to the fact that we only focused on preoperative risk factors but in a much wider timeline of published studies. We found some risk factors that are similar to those identified in the perioperative-focused research, as expected. However, there are some minor but substantial differences between the previous study and the current review. Despite the fact that the other research presents a similar subject, the evidence collected relies on independent processes (literature search, study selection, data extraction).
One of the study’s limitations is the great variance in the group characteristics in the reviewed studies, which did not permit us to perform a weighted analysis of the impacts of individual risk factors. Despite this, the use of a standardized data extraction form warrants the presentation of risk factors that are statistically associated with an increased incidence of POD, thereby mitigating the confounding impact of individual, procedural, or environmental-related characteristics.

5. Conclusions

The present SR provides a reliable and validated list of the preoperative risk factors associated with an increased risk of POD. Creating a screening tool using these risk factors should become a standard of care, and patients presenting an increased risk should be purposely treated throughout their hospitalization. Future studies should evaluate how to accurately identify high-risk patients and effectively minimize POD’s occurrence, as well as how to assess the influence of concurring risk factors on the perioperative clinical course.

Author Contributions

Conceptualization, V.K., L.M., M.S. and F.B.; methodology V.K., L.M. and F.B.; software, V.K., L.M., M.S. and F.B.; validation V.K., L.M., M.S. and F.B.; formal analysis, V.K., L.M. and F.B.; investigation, V.K., L.M., M.S. and F.B.; resources, F.B.; data curation, V.K and F.B.; writing—original draft preparation, V.K., L.M. and F.B.; writing—review and editing V.K., L.M., M.S. and F.B.; visualization, V.K. and F.B.; supervision, F.B.; project administration, F.B. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Data is contained within the article.

Conflicts of Interest

The authors declare no conflict of interest.

Appendix A. Full List of Literature Search Strings

  • PubMed: (delirium OR delirious OR confusion OR disorientation OR bewilderment) AND (postoperative OR “postoperative” OR post intervention OR “post intervention” OR “post-surgical” OR postsurgical OR “post-surgery” OR post surgery OR “anesthesia recovery” OR “anesthesia recovery” OR “anesthesia recovery period”[- Mesh] OR post anesthesia OR “post anesthesia” OR “post anesthesia”)
  • EMBASE: (((‘delirium’/exp OR delirium OR delirious OR ‘confusion’/exp OR confusion OR ‘disorientation’/exp OR disorientation OR bewilderment) AND (‘postoperative complication’/exp OR postoperative OR ‘post-operative’ OR ‘postoperative period’/exp OR post-intervention OR ‘post intervention’ OR ‘post-surgical’ OR postsurgical OR ‘post-surgery’ OR post-surgery OR ‘anesthesia recovery’/exp OR ‘anesthesia recovery’ OR ‘anesthesia recovery’/exp OR ‘anesthesia recovery’ OR post anesthesia OR ‘post anesthesia’ OR ‘post anesthesia’)) OR ‘postoperative delirium’/exp) AND ([cochrane review]/lim OR [systematic review]/lim OR [meta-analysis]/lim OR [randomized controlled trial]/lim OR ‘observational study’ OR ‘case study’)
  • CINAHL: (delirium OR delirious OR confusion OR disorientation OR bewilderment) AND (postoperative OR “postoperative” OR post intervention OR “post intervention” OR “post-surgical” OR postsurgical OR “post-surgery” OR post-surgery OR “anesthesia recovery” OR “anesthesia recovery” OR post anesthesia OR “post anesthesia” OR “post anesthesia”) Limiters—Publication Type: Case Study, MetaAnalysis, Randomized Controlled Trial, Systematic Review OR ((delirium OR delirious OR confusion OR disorientation OR bewilderment) AND (postoperative OR “postoperative” OR post intervention OR “post intervention” OR “post-surgical” OR postsurgical OR “post-surgery” OR post-surgery OR “anesthesia recovery” OR “anesthesia recovery” OR post anesthesia OR “post anesthesia” OR “post anesthesia”)) AND (observational study OR observational research) OR (MH “delirium” OR MH “confusion+”) AND ((MH “postoperative complications”) OR (MH “postoperative period”)) Limiters—Publication Type: Case Study, MetaAnalysis, Randomized Controlled Trial, Systematic Review OR (MH “delirium” OR MH “confusion+”) AND ((MH “postoperative complications”) OR (MH “postoperative period”)) AND ((observational study OR observational research))
  • COCHRANE: #1 ((delirium OR delirious OR confusion OR disorientation OR bewilderment) AND (postoperative OR “postoperative” OR post intervention OR “post intervention” OR “post-surgical” OR postsurgical OR “post-surgery” OR post-surgery OR “anesthesia recovery” OR “anesthesia recovery” OR post anesthesia OR “post anesthesia” OR “post anesthesia”)):ti,ab,kw 1829 #2 MeSH descriptor: [Delirium] explode all trees 765 #3 MeSH descriptor: [Confusion] explode all trees 899 #4 #2 OR #3 899 #5 MeSH descriptor: [Postoperative Period] explode all trees 5872 #6 MeSH descriptor: [Postoperative Complications] explode all trees 39635 #7 MeSH descriptor: [Anesthesia Recovery Period] explode all trees 2031 #8 #5 OR #6 OR #7 43861 #9 #4 AND #8 326 #10 #1 OR #9 1853
  • SCOPUS: TITLE-ABS (delirium OR delirious OR confusion OR disorientation OR bewilderment) AND TITLE-ABS (postoperative OR {post-operative} OR post intervention OR {post intervention} OR {post-surgical} OR postsurgical OR {post-surgery} OR post-surgery OR {anesthesia recovery} OR {anesthesia recovery} OR post anesthesia OR {post anesthesia} OR {post anesthesia}) AND TITLE-ABS ({systematic review} OR {case series} OR {randomized controlled trial} OR rct OR {meta-analysis} OR metanalysis OR {observational study})
  • WEB OF SCIENCE: TITLE-ABS (delirium OR delirious OR confusion OR disorientation OR bewilderment) AND TITLE-ABS (postoperative OR {post-operative} OR post intervention OR {post intervention} OR {post-surgical} OR postsurgical OR {post-surgery} OR post-surgery OR {anesthesia recovery} OR {anesthesia recovery} OR post anesthesia OR {post anesthesia} OR {post anesthesia}) AND TITLE-ABS ({systematic review} OR {case series} OR {randomized controlled trial} OR rct OR {meta-analysis} OR metanalysis OR {observational study})

References

  1. ICD-10 Version:2016. Available online: https://icd.who.int/browse10/2016/en#/F05.8 (accessed on 21 June 2022).
  2. American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders (Dsm-5), 5th ed.; Psychiatric Pub Inc.: Washington, DC, USA, 2013. [Google Scholar]
  3. Fadayomi, A.B.; Ibala, R.; Bilotta, F.; Westover, M.B.; Akeju, O. A Systematic Review and Meta-Analysis Examining the Impact of Sleep Disturbance on Postoperative Delirium. Crit. Care Med. 2018, 46, E1204–E1212. [Google Scholar] [CrossRef] [PubMed]
  4. Daiello, L.A.; Racine, A.M.; Yun Gou, R.; Marcantonio, E.R.; Xie, Z.; Kunze, L.J.; Vlassakov, K.V.; Inouye, S.K.; Jones, R.N.; Alsop, D.; et al. Postoperative Delirium and Postoperative Cognitive Dysfunction: Overlap and Divergence. Anesthesiology 2019, 131, 477–491. [Google Scholar] [CrossRef] [PubMed]
  5. Wittmann, M.; Kirfel, A.; Jossen, D.; Mayr, A.; Menzenbach, J. The Impact of Perioperative and Predisposing Risk Factors on the Development of Postoperative Delirium and a Possible Gender Difference. Geriatrics 2022, 7, 65. [Google Scholar] [CrossRef] [PubMed]
  6. Inouye, S.K.; Westendorp, R.G.J.; Saczynski, J.S. Delirium in Elderly People. Lancet 2014, 383, 911–922. [Google Scholar] [CrossRef]
  7. Aldecoa, C.; Bettelli, G.; Bilotta, F.; Sanders, R.D.; Audisio, R.; Borozdina, A.; Cherubini, A.; Jones, C.; Kehlet, H.; Maclullich, A.; et al. European Society of Anaesthesiology Evidence-Based and Consensus-Based Guideline on Postoperative Delirium. Eur. J. Anaesthesiol. 2017, 34, 192–214. [Google Scholar] [CrossRef]
  8. Hála, M. Pathophysiology of Postoperative Delirium: Systemic Inflammation as a Response to Surgical Trauma Causes Diffuse Microcirculatory Impairment. Med. Hypotheses 2007, 68, 194–196. [Google Scholar] [CrossRef]
  9. Steiner, L.A. Postoperative Delirium. Part 1: Pathophysiology and Risk Factors. Eur. J. Anaesthesiol. 2011, 28, 628–636. [Google Scholar] [CrossRef]
  10. Hermanides, J.; Qeva, E.; Preckel, B.; Bilotta, F. Perioperative Hyperglycemia and Neurocognitive Outcome after Surgery: A Systematic Review. Minerva Anestesiol. 2018, 84, 1178–1188. [Google Scholar] [CrossRef]
  11. Borozdina, A.; Qeva, E.; Cinicola, M.; Bilotta, F. Perioperative Cognitive Evaluation. Curr. Opin. Anaesthesiol. 2018, 31, 756–761. [Google Scholar] [CrossRef]
  12. Falegnami, A.; Patriarca, R.; Costantino, F.; di Gravio, G.; Bilotta, F. Surveying Work-as-Done in Post-Operative Delirium Risk Factors Collection and Diagnosis Monitoring. Appl. Ergon. 2021, 92, 3347. [Google Scholar] [CrossRef]
  13. Viderman, D.; Brotfain, E.; Bilotta, F.; Zhumadilov, A. Risk Factors and Mechanisms of Postoperative Delirium After Intracranial Neurosurgical Procedures. Asian J. Anesthesiol. 2020, 58, 5–13. [Google Scholar] [CrossRef]
  14. Delp, S.; Mei, W.; Spies, C.D.; Neuner, B.; Aldecoa, C.; Bettelli, G.; Bilotta, F.; Sanders, R.D.; Kramer, S.; Weiss, B. Clinical Practice in the Management of Postoperative Delirium by Chinese Anesthesiologists: A Cross-Sectional Survey Designed by the European Society of Anaesthesiology. J. Int. Med. Res. 2020, 48, 7207. [Google Scholar] [CrossRef]
  15. Nishikawa, K.; Nakayama, M.; Omote, K.; Namiki, A. Recovery Characteristics and Post-Operative Delirium after Long-Duration Laparoscope-Assisted Surgery in Elderly Patients: Propofol-Based vs. Sevoflurane-Based Anesthesia. Acta Anaesthesiol. Scand. 2004, 48, 162–168. [Google Scholar] [CrossRef]
  16. Bilotta, F.; Giordano, G.; Pugliese, F. Preoperative Stratification for Postoperative Delirium: Obstructive Sleep Apnea Is a Predictor, the STOP-BANG Is Not? J. Thorac. Dis. 2019, 11, S202–S206. [Google Scholar] [CrossRef]
  17. Litaker, D.; Locala, J.; Franco, K.; Bronson, D.L.; Tannous, Z. Preoperative Risk Factors for Postoperative Delirium. Gen. Hosp. Psychiatry 2001, 23, 84–89. [Google Scholar] [CrossRef]
  18. Shah, S.; Weed, H.G.; He, X.; Agrawal, A.; Ozer, E.; Schuller, D.E. Alcohol-Related Predictors of Delirium after Major Head and Neck Cancer Surgery. Arch. Otolaryngol. Head Neck Surg. 2012, 138, 266–271. [Google Scholar] [CrossRef]
  19. Cotoia, A.; Mirabella, L.; Beck, R.; Matrella, P.; Assenzo, V.; Hazot, T.C.; Cinnella, G.; Liu, N.; Dambrosio, M. Effects of Closed-Loop Intravenous Anesthesia Guided by Bispectral Index in Adult Patients on Emergence Delirium: A Randomized Controlled Study. Minerva Anestesiol. 2018, 84, 437–446. [Google Scholar] [CrossRef]
  20. Todd, O.M.; Gelrich, L.; MacLullich, A.M.; Driessen, M.; Thomas, C.; Kreisel, S.H. Sleep Disruption at Home As an Independent Risk Factor for Postoperative Delirium. J. Am. Geriatr. Soc. 2017, 65, 949–957. [Google Scholar] [CrossRef]
  21. Page, M.J.; McKenzie, J.E.; Bossuyt, P.M.; Boutron, I.; Hoffmann, T.C.; Mulrow, C.D.; Shamseer, L.; Tetzlaff, J.M.; Akl, E.A.; Brennan, S.E.; et al. The PRISMA 2020 Statement: An Updated Guideline for Reporting Systematic Reviews. BMJ 2021, 372, n71. [Google Scholar] [CrossRef]
  22. Bilotta, F.; Russo, G.; Trombi, M.; Verrengia, M.; Sangermano, C.; Sportelli, A.; Foti, L.; Villa, G.; Romagnoli, S. Comprehensive Analysis of Clinical Evidence on Postoperative Delirium: Literature Search and Screening of Original Studies That Used Validated Diagnostic Scales. PROSPERO 2021, CRD42021246906. Available online: https://www.crd.york.ac.uk/prospero/display_record.php?RecordID=246906 (accessed on 21 June 2022).
  23. Resources|Cochrane Bias. Available online: https://methods.cochrane.org/bias/resources (accessed on 21 June 2022).
  24. Higgins, J.P.T.; Altman, D.G.; Gøtzsche, P.C.; Jüni, P.; Moher, D.; Oxman, A.D.; Savović, J.; Schulz, K.F.; Weeks, L.; Sterne, J.A.C. The Cochrane Collaboration’s Tool for Assessing Risk of Bias in Randomised Trials. BMJ 2011, 343, D5928. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  25. Williams-Russo, P.; Urquhart, B.L.; Sharrock, N.E.; Charlson, M.E. Post-Operative Delirium: Predictors and Prognosis in Elderly Orthopedic Patients. J. Am. Geriatr. Soc. 1992, 40, 759–767. [Google Scholar] [CrossRef] [PubMed]
  26. Papaioannou, A.; Fraidakis, O.; Michaloudis, D.; Balalis, C.; Askitopoulou, H. The Impact of the Type of Anaesthesia on Cognitive Status and Delirium during the First Postoperative Days in Elderly Patients. Eur. J. Anaesthesiol. 2005, 22, 492–499. [Google Scholar] [CrossRef] [PubMed]
  27. Freter, S.H.; Dunbar, M.J.; MacLeod, H.; Morrison, M.; MacKnight, C.; Rockwood, K. Predicting Post-Operative Delirium in Elective Orthopaedic Patients: The Delirium Elderly At-Risk (DEAR) Instrument. Age Ageing 2005, 34, 169–171. [Google Scholar] [CrossRef]
  28. Schrader, S.L.P.; Wellik, K.E.; Demaerschalk, B.M.; Caselli, R.J.; Woodruff, B.K.; Wingerchuk, D.M. Adjunctive Haloperidol Prophylaxis Reduces Postoperative Delirium Severity and Duration in At-Risk Elderly Patients. Neurologist 2008, 14, 134–137. [Google Scholar] [CrossRef]
  29. da Cunha, P.T.S.; Artifon, A.N.; Lima, D.P.; Marques, W.V.; Rahal, M.A.; Ribeiro, R.R.; Kitadai, F.T. Hip Fractures in the Elderly: Surgical Treatment Timing and Its Correlation with Delirium and Infection. Acta Ortop. Bras. 2008, 16, 173–176. [Google Scholar] [CrossRef]
  30. Robinson, T.N.; Raeburn, C.D.; Angles, E.M.; Moss, M. Low Tryptophan Levels Are Associated with Postoperative Delirium in the Elderly. Am. J. Surg. 2008, 196, 670–674. [Google Scholar] [CrossRef]
  31. Gao, R.; Yang, Z.Z.; Li, M.; Shi, Z.C.; Fu, Q. Probable Risk Factors for Postoperative Delirium in Patients Undergoing Spinal Surgery. Eur. Spine J. 2008, 17, 1531. [Google Scholar] [CrossRef]
  32. Tognoni, P.; Simonato, A.; Robutti, N.; Pisani, M.; Cataldi, A.; Monacelli, F.; Carmignani, G.; Odetti, P. Preoperative Risk Factors for Postoperative Delirium (POD) after Urological Surgery in the Elderly. Arch Gerontol. Geriatr. 2011, 52, 21. [Google Scholar] [CrossRef]
  33. Patti, R.; Saitta, M.; Cusumano, G.; Termine, G.; di Vita, G. Risk Factors for Postoperative Delirium after Colorectal Surgery for Carcinoma. Eur. J. Oncol. Nurs. 2011, 15, 519–523. [Google Scholar] [CrossRef]
  34. Mangnall, L.T.; Gallagher, R.; Stein-Parbury, J. Postoperative Delirium After Colorectal Surgery in Older Patients. Am. J. Crit. Care 2011, 20, 45–55. [Google Scholar] [CrossRef] [Green Version]
  35. Lee, H.J.; Hwang, D.S.; Wang, S.K.; Chee, I.S.; Baeg, S.; Kim, J.L. Early Assessment of Delirium in Elderly Patients after Hip Surgery. Psychiatry Investig. 2011, 8, 340–347. [Google Scholar] [CrossRef]
  36. Jankowski, C.J.; Trenerry, M.R.; Cook, D.J.; Buenvenida, S.L.; Stevens, S.R.; Schroeder, D.R.; Warner, D.O. Cognitive and Functional Predictors and Sequelae of Postoperative Delirium in Elderly Patients Undergoing Elective Joint Arthroplasty. Anesth. Analg. 2011, 112, 1186–1193. [Google Scholar] [CrossRef]
  37. Do, T.D.; Lemogne, C.; Journois, D.; Safran, D.; Consoli, S.M. Low Social Support Is Associated with an Increased Risk of Postoperative Delirium. J. Clin. Anesth. 2012, 24, 126–132. [Google Scholar] [CrossRef]
  38. Jia, Y.; Jin, G.; Guo, S.; Gu, B.; Jin, Z.; Gao, X.; Li, Z. Fast-Track Surgery Decreases the Incidence of Postoperative Delirium and Other Complications in Elderly Patients with Colorectal Carcinoma. Langenbecks Arch. Surg. 2014, 399, 77–84. [Google Scholar] [CrossRef]
  39. Fineberg, S.J.; Nandyala, S.V.; Marquez-Lara, A.; Oglesby, M.; Patel, A.A.; Singh, K. Incidence and Risk Factors for Postoperative Delirium after Lumbar Spine Surgery. Spine 2013, 38, 1790–1796. [Google Scholar] [CrossRef]
  40. Large, M.C.; Reichard, C.; Williams, J.T.B.; Chang, C.; Prasad, S.; Leung, Y.; Dubeau, C.; Bales, G.T.; Steinberg, G.D. Incidence, Risk Factors, and Complications of Postoperative Delirium in Elderly Patients Undergoing Radical Cystectomy. Urology 2013, 81, 123–129. [Google Scholar] [CrossRef]
  41. Wu, Y.; Wang, J.; Wu, A.S.; Yue, Y. Do Fluctuations in Endogenous Melatonin Levels Predict the Occurrence of Postoperative Cognitive Dysfunction (POCD)? Int. J. Neurosci. 2014, 124, 787–791. [Google Scholar] [CrossRef]
  42. Deiner, S.; Lin, H.M.; Bodansky, D.; Silverstein, J.; Sano, M. Do Stress Markers and Anesthetic Technique Predict Delirium in the Elderly? Dement. Geriatr. Cogn. Disord. 2014, 38, 366–374. [Google Scholar] [CrossRef]
  43. de Jonghe, A.; van Munster, B.C.; Goslings, J.C.; Kloen, P.; van Rees, C.; Wolvius, R.; van Velde, R.; Levi, M.; de Haan, R.J.; de Rooij, S.E.; et al. Effect of Melatonin on Incidence of Delirium among Patients with Hip Fracture: A Multicentre, Double-Blind Randomized Controlled Trial. CMAJ 2014, 186, E547–E556. [Google Scholar] [CrossRef]
  44. Saporito, A.; Sturini, E. Incidence of Postoperative Delirium Is High Even in a Population without Known Risk Factors. J. Anesth. 2014, 28, 198–201. [Google Scholar] [CrossRef] [PubMed]
  45. Chen, Y.L.; Lin, H.C.; Lin, K.H.; Lin, L.S.; Hsieh, C.E.; Ko, C.J.; Hung, Y.J.; Lin, P.Y. Low Hemoglobin Level Is Associated with the Development of Delirium after Hepatectomy for Hepatocellular Carcinoma Patients. PLoS ONE 2015, 10, e0119199. [Google Scholar] [CrossRef] [PubMed]
  46. Tai, S.; Xu, L.; Zhang, L.; Fan, S.; Liang, C. Preoperative Risk Factors of Postoperative Delirium after Transurethral Prostatectomy for Benign Prostatic Hyperplasia. Int. J. Clin. Exp. Med. 2015, 8, 4569–4574. [Google Scholar] [CrossRef] [PubMed]
  47. Gottschalk, A.; Hubbs, J.; Vikani, A.R.; Gottschalk, L.B.; Sieber, F.E. The Impact of Incident Postoperative Delirium on Survival of Elderly Patients After Surgery for Hip Fracture Repair. Anesth. Analg. 2015, 121, 1336–1343. [Google Scholar] [CrossRef] [PubMed]
  48. Wang, R.; Chen, J.; Wu, G. Variable Lung Protective Mechanical Ventilation Decreases Incidence of Postoperative Delirium and Cognitive Dysfunction during Open Abdominal Surgery. Int. J. Clin. Exp. Med. 2015, 8, 21208–21214. [Google Scholar]
  49. Raats, J.W.; van Eijsden, W.A.; Crolla, R.M.P.H.; Steyerberg, E.W.; van der Laan, L. Risk Factors and Outcomes for Postoperative Delirium after Major Surgery in Elderly Patients. PLoS ONE 2015, 10, 0136071. [Google Scholar] [CrossRef]
  50. Kratz, T.; Heinrich, M.; Schlauß, E.; Diefenbacher, A. Preventing Postoperative Delirium. Dtsch. Arztebl. Int. 2015, 112, 0289. [Google Scholar] [CrossRef]
  51. Liang, C.K.; Chu, C.L.; Chou, M.Y.; Lin, Y.T.; Lu, T.; Hsu, C.J.; Lam, H.C.; Chen, L.K. Developing a Prediction Model for Post-Operative Delirium and Long-Term Outcomes Among Older Patients Receiving Elective Orthopedic Surgery: A Prospective Cohort Study in Taiwan. Rejuvenation Res. 2015, 18, 347–355. [Google Scholar] [CrossRef]
  52. Mohammadi, M.; Ahmadi, M.; Khalili, H.; Cheraghchi, H.; Arbabi, M. Cyproheptadine for the Prevention of Postoperative Delirium: A Pilot Study. Ann. Pharmacother. 2016, 50, 180–187. [Google Scholar] [CrossRef]
  53. Jeong, D.M.; Kim, J.A.; Ahn, H.J.; Yang, M.; Heo, B.Y.; Lee, S.H. Decreased Incidence of Postoperative Delirium in Robot-Assisted Thoracoscopic Esophagectomy Compared with Open Transthoracic Esophagectomy. Surg. Laparosc. Endosc. Percutan. Tech. 2016, 26, 516–522. [Google Scholar] [CrossRef]
  54. Brown, C.H.; LaFlam, A.; Max, L.; Wyrobek, J.; Neufeld, K.J.; Kebaish, K.M.; Cohen, D.B.; Walston, J.D.; Hogue, C.W.; Riley, L.H. Delirium After Spine Surgery in Older Adults: Incidence, Risk Factors, and Outcomes. J. Am. Geriatr. Soc. 2016, 64, 2101–2108. [Google Scholar] [CrossRef] [PubMed]
  55. Kim, M.Y.; Park, U.J.; Kim, H.T.; Cho, W.H. DELirium Prediction Based on Hospital Information (Delphi) in General Surgery Patients. Medicine 2016, 95, 3072. [Google Scholar] [CrossRef] [PubMed]
  56. Su, X.; Meng, Z.T.; Wu, X.H.; Cui, F.; Li, H.L.; Wang, D.X.; Zhu, X.; Zhu, S.N.; Maze, M.; Ma, D. Dexmedetomidine for Prevention of Delirium in Elderly Patients after Non-Cardiac Surgery: A Randomised, Double-Blind, Placebo-Controlled Trial. Lancet 2016, 388, 1893–1902. [Google Scholar] [CrossRef]
  57. Liu, Y.; Ma, L.; Gao, M.; Guo, W.; Ma, Y. Dexmedetomidine Reduces Postoperative Delirium after Joint Replacement in Elderly Patients with Mild Cognitive Impairment. Aging Clin. Exp. Res. 2016, 28, 729–736. [Google Scholar] [CrossRef] [PubMed]
  58. Winter, A.; Steurer, M.P.; Dullenkopf, A. Postoperative Delirium Assessed by Post Anesthesia Care Unit Staff Utilizing the Nursing Delirium Screening Scale: A Prospective Observational Study of 1000 Patients in a Single Swiss Institution. BMC Anesthesiol. 2015, 15, 184. [Google Scholar] [CrossRef] [PubMed]
  59. Moerman, S.; Vochteloo, A.J.H.; Tuinebreijer, W.E.; Maier, A.B.; Mathijssen, N.M.C.; Nelissen, R.G.H.H. Factors Associated with the Course of Health-Related Quality of Life after a Hip Fracture. Arch. Orthop. Trauma Surg. 2016, 136, 935–943. [Google Scholar] [CrossRef]
  60. Stukenberg, S.; Franck, M.; Spies, C.D.; Neuner, B.; Myers, I.; Radtke, F.M. How Can Postoperative Delirium Be Predicted in Advance? A Secondary Analysis Comparing Three Methods of Early Assessment in Elderly Patients. Minerva Anestesiol. 2016, 82, 751–759. [Google Scholar]
  61. Zhang, Z.Y.; Gao, D.P.; Yang, J.J.; Sun, X.R.; Zhang, H.; Hu, J.; Fang, Z.Y.; Yang, J.J.; Ji, M.H. Impact of Length of Red Blood Cells Transfusion on Postoperative Delirium in Elderly Patients Undergoing Hip Fracture Surgery: A Cohort Study. Injury 2016, 47, 408–412. [Google Scholar] [CrossRef]
  62. Guo, Y.; Sun, L.; Li, L.; Jia, P.; Zhang, J.; Jiang, H.; Jiang, W. Impact of Multicomponent, Nonpharmacologic Interventions on Perioperative Cortisol and Melatonin Levels and Postoperative Delirium in Elderly Oral Cancer Patients. Arch. Gerontol. Geriatr. 2016, 62, 112–117. [Google Scholar] [CrossRef]
  63. De Castro, S.M.; Ünlü, Ç.; Tuynman, J.B.; Honig, A.; van Wagensveld, B.A.; Steller, E.P.; Vrouenraets, B.C. Incidence and Risk Factors of Delirium in the Elderly General Surgical Patient. Am. J. Surg. 2014, 208, 26–32. [Google Scholar] [CrossRef]
  64. Watne, L.O.; Idland, A.V.; Fekkes, D.; Raeder, J.; Frihagen, F.; Ranhoff, A.H.; Chaudhry, F.A.; Engedal, K.; Wyller, T.B.; Hassel, B. Increased CSF Levels of Aromatic Amino Acids in Hip Fracture Patients with Delirium Suggests Higher Monoaminergic Activity. BMC Geriatr. 2016, 16, 149. [Google Scholar] [CrossRef]
  65. van Grootven, B.; Detroyer, E.; Devriendt, E.; Sermon, A.; Deschodt, M.; Flamaing, J.; Dubois, C.; Milisen, K. Is Preoperative State Anxiety a Risk Factor for Postoperative Delirium among Elderly Hip Fracture Patients? Geriatr. Gerontol. Int. 2016, 16, 948–955. [Google Scholar] [CrossRef]
  66. Hempenius, L.; Slaets, J.P.J.; van Asselt, D.; de Bock, T.H.; Wiggers, T.; van Leeuwen, B.L. Long Term Outcomes of a Geriatric Liaison Intervention in Frail Elderly Cancer Patients. PLoS ONE 2016, 11, e0143364. [Google Scholar] [CrossRef] [Green Version]
  67. Franck, M.; Nerlich, K.; Neuner, B.; Schlattmann, P.; Brockhaus, W.R.; Spies, C.D.; Radtke, F.M. No Convincing Association between Post-Operative Delirium and Post-Operative Cognitive Dysfunction: A Secondary Analysis. Acta Anaesthesiol. Scand. 2016, 60, 1404–1414. [Google Scholar] [CrossRef]
  68. Pinho, C.; Cruz, S.; Santos, A.; Abelha, F.J. Postoperative Delirium: Age and Low Functional Reserve as Independent Risk Factors. J. Clin. Anesth. 2016, 33, 507–513. [Google Scholar] [CrossRef]
  69. Zheng, Y.B.; Ruan, G.M.; Fu, J.X.; Su, Z.L.; Cheng, P.; Lu, J.Z. Postoperative Plasma 8-Iso-Prostaglandin F2α Levels Are Associated with Delirium and Cognitive Dysfunction in Elderly Patients after Hip Fracture Surgery. Clin. Chim. Acta 2016, 455, 149–153. [Google Scholar] [CrossRef]
  70. Sun, L.; Jia, P.; Zhang, J.; Zhang, X.; Zhang, Y.; Jiang, H.; Jiang, W.; Guo, Y. Production of Inflammatory Cytokines, Cortisol, and Aβ1-40 in Elderly Oral Cancer Patients with Postoperative Delirium. Neuropsychiatr. Dis. Treat. 2016, 12, 2789–2795. [Google Scholar] [CrossRef]
  71. Sugano, N.; Aoyama, T.; Sato, T.; Kamiya, M.; Amano, S.; Yamamoto, N.; Nagashima, T.; Ishikawa, Y.; Masudo, K.; Taguri, M.; et al. Randomized Phase II Study of TJ-54 (Yokukansan) for Postoperative Delirium in Gastrointestinal and Lung Malignancy Patients. Mol. Clin. Oncol. 2017, 7, 569–573. [Google Scholar] [CrossRef]
  72. van der Zanden, V.; Beishuizen, S.J.; Scholtens, R.M.; de Jonghe, A.; de Rooij, S.E.; van Munster, B.C. The Effects of Blood Transfusion on Delirium Incidence. J. Am. Med. Dir. Assoc. 2016, 17, 748–753. [Google Scholar] [CrossRef]
  73. Tei, M.; Wakasugi, M.; Kishi, K.; Tanemura, M.; Akamatsu, H. Incidence and Risk Factors of Postoperative Delirium in Elderly Patients Who Underwent Laparoscopic Surgery for Colorectal Cancer. Int. J. Colorectal. Dis. 2016, 31, 67–73. [Google Scholar] [CrossRef]
  74. Chu, C.S.; Liang, C.K.; Chou, M.Y.; Lin, Y.T.; Hsu, C.J.; Chou, P.H.; Chu, C.L. Short-Form Mini Nutritional Assessment as a Useful Method of Predicting the Development of Postoperative Delirium in Elderly Patients Undergoing Orthopedic Surgery. Gen. Hosp. Psychiatry 2016, 38, 15–20. [Google Scholar] [CrossRef] [PubMed]
  75. Neerland, B.E.; Hall, R.J.; Seljeflot, I.; Frihagen, F.; MacLullich, A.M.J.; Ræder, J.; Wyller, T.B.; Watne, L.O. Associations Between Delirium and Preoperative Cerebrospinal Fluid C-Reactive Protein, Interleukin-6, and Interleukin-6 Receptor in Individuals with Acute Hip Fracture. J. Am. Geriatr. Soc. 2016, 64, 1456–1463. [Google Scholar] [CrossRef] [PubMed]
  76. Guo, Y.; Jia, P.; Zhang, J.; Wang, X.; Jiang, H.; Jiang, W. Prevalence and Risk Factors of Postoperative Delirium in Elderly Hip Fracture Patients. J. Int. Med. Res. 2016, 44, 317–327. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  77. Xue, P.; Wu, Z.; Wang, K.; Tu, C.; Wang, X. Incidence and Risk Factors of Postoperative Delirium in Elderly Patients Undergoing Transurethral Resection of Prostate: A Prospective Cohort Study. Neuropsychiatr. Dis. Treat. 2016, 12, 137. [Google Scholar] [CrossRef] [PubMed]
  78. Sato, T.; Hatakeyama, S.; Okamoto, T.; Yamamoto, H.; Hosogoe, S.; Tobisawa, Y.; Yoneyama, T.; Hashiba, E.; Yoneyama, T.; Hashimoto, Y.; et al. Slow Gait Speed and Rapid Renal Function Decline Are Risk Factors for Postoperative Delirium after Urological Surgery. PLoS ONE 2016, 11, 0153961. [Google Scholar] [CrossRef]
  79. El-Gabalawy, R.; Patel, R.; Kilborn, K.; Blaney, C.; Hoban, C.; Ryner, L.; Funk, D.; Legaspi, R.; Fisher, J.A.; Duffin, J.; et al. A Novel Stress-Diathesis Model to Predict Risk of Post-Operative Delirium: Implications for Intra-Operative Management. Front. Aging Neurosci. 2017, 9, 274. [Google Scholar] [CrossRef]
  80. Mazzola, P.; Ward, L.; Zazzetta, S.; Broggini, V.; Anzuini, A.; Valcarcel, B.; Brathwaite, J.S.; Pasinetti, G.M.; Bellelli, G.; Annoni, G. Association Between Preoperative Malnutrition and Postoperative Delirium After Hip Fracture Surgery in Older Adults. J. Am. Geriatr. Soc. 2017, 65, 1222–1228. [Google Scholar] [CrossRef]
  81. Petersen, P.B.; Jørgensen, C.C.; Kehlet, H.; Madsen, F.; Hansen, T.B.; Husted, H.; Laursen, M.B.; Hansen, L.T.; Kjærsgaard-Andersen, P.; Solgaard, S. Delirium after Fast-Track Hip and Knee Arthroplasty—A Cohort Study of 6331 Elderly Patients. Acta Anaesthesiol. Scand. 2017, 61, 767–772. [Google Scholar] [CrossRef]
  82. Xin, X.; Xin, F.; Chen, X.; Zhang, Q.; Li, Y.; Huo, S.; Chang, C.; Wang, Q. Hypertonic Saline for Prevention of Delirium in Geriatric Patients Who Underwent Hip Surgery. J. Neuroinflamm. 2017, 14, 1–9. [Google Scholar] [CrossRef]
  83. Cunningham, E.L.; Mawhinney, T.; Beverland, D.; O’Brien, S.; Mcauley, D.F.; Cairns, R.; Passmore, P.; McGuinness, B. Observational Cohort Study Examining Apolipoprotein E Status and Preoperative Neuropsychological Performance as Predictors of Post-Operative Delirium in an Older Elective Arthroplasty Population. Age Ageing 2017, 46, 779–786. [Google Scholar] [CrossRef]
  84. Bhattacharya, B.; Maung, A.; Barre, K.; Maerz, L.; Rodriguez-Davalos, M.I.; Schilsky, M.; Mulligan, D.C.; Davis, K.A. Postoperative Delirium Is Associated with Increased Intensive Care Unit and Hospital Length of Stays after Liver Transplantation. J. Surg. Res. 2017, 207, 223–228. [Google Scholar] [CrossRef]
  85. Wu, X.M.; Xu, W.C.; Yu, Y.J.; Han, L.; Zhang, J.; Yang, L.J. Postoperative Serum Thioredoxin Concentrations Correlate with Delirium and Cognitive Dysfunction after Hip Fracture Surgery in Elderly Patients. Clin. Chim. Acta 2017, 466, 93–97. [Google Scholar] [CrossRef]
  86. Beishuizen, S.J.E.; Scholtens, R.M.; van Munster, B.C.; de Rooij, S.E. Unraveling the Relationship between Delirium, Brain Damage, and Subsequent Cognitive Decline in a Cohort of Individuals Undergoing Surgery for Hip Fracture. J. Am. Geriatr. Soc. 2017, 65, 130–136. [Google Scholar] [CrossRef]
  87. Elsamadicy, A.A.; Adogwa, O.; Lydon, E.; Sergesketter, A.; Kaakati, R.; Mehta, A.I.; Vasquez, R.A.; Cheng, J.; Bagley, C.A.; Karikari, I.O. Depression as an Independent Predictor of Postoperative Delirium in Spine Deformity Patients Undergoing Elective Spine Surgery. J. Neurosurg. Spine 2017, 27, 209–214. [Google Scholar] [CrossRef]
  88. Xiang, D.; Xing, H.; Tai, H.; Xie, G. Preoperative C-Reactive Protein as a Risk Factor for Postoperative Delirium in Elderly Patients Undergoing Laparoscopic Surgery for Colon Carcinoma. Biomed. Res. Int. 2017, 2017, 5635640. [Google Scholar] [CrossRef]
  89. Wang, L.; Seok, S.; Kim, S.; Kim, K.; Lee, S.; Lee, K. The Risk Factors of Postoperative Delirium after Total Knee Arthroplasty. J. Knee Surg. 2017, 30, 600–605. [Google Scholar] [CrossRef]
  90. Mosk, C.A.; van Vugt, J.L.A.; de Jonge, H.; Witjes, C.D.M.; Buettner, S.; Ijzermans, J.N.M.; van der Laan, L. Low Skeletal Muscle Mass as a Risk Factor for Postoperative Delirium in Elderly Patients Undergoing Colorectal Cancer Surgery. Clin. Interv. Aging 2018, 13, 2097. [Google Scholar] [CrossRef]
  91. Tahir, M.; Malik, S.S.; Ahmed, U.; Kozdryk, J.; Naqvi, S.H.; Malik, A. Risk Factors for Onset of Delirium after Neck of Femur Fracture Surgery: A Prospective Observational Study. SICOT J. 2018, 4, 2018018. [Google Scholar] [CrossRef]
  92. Susano, M.J.; Scheetz, S.D.; Grasfield, R.H.; Cheung, D.; Xu, X.; Kang, J.D.; Smith, T.R.; Lu, Y.; Groff, M.W.; Chi, J.H.; et al. Retrospective Analysis of Perioperative Variables Associated with Postoperative Delirium and Other Adverse Outcomes in Older Patients After Spine Surgery. J. Neurosurg. Anesthesiol. 2019, 31, 385–391. [Google Scholar] [CrossRef]
  93. Gutierrez, R.; Egaña, J.I.; Saez, I.; Reyes, F.; Briceño, C.; Venegas, M.; Lavado, I.; Penna, A. Intraoperative Low Alpha Power in the Electroencephalogram Is Associated with Postoperative Subsyndromal Delirium. Front. Syst. Neurosci. 2019, 13, 56. [Google Scholar] [CrossRef]
  94. Zhao, B.; Ni, Y.; Tian, X. Low Plasma Cholinesterase Activity Is Associated With Postoperative Delirium After Noncardiac Surgery in Elderly Patients: AProspective Observational Study. Psychosomatics 2019, 60, 190–196. [Google Scholar] [CrossRef] [PubMed]
  95. Tao, L.; Xiaodong, X.; Qiang, M.; Jiao, L.; Xu, Z. Prediction of Postoperative Delirium by Comprehensive Geriatric Assessment among Elderly Patients with Hip Fracture. Ir. J. Med. Sci. 2019, 188, 1311–1315. [Google Scholar] [CrossRef] [PubMed]
  96. Oe, S.; Togawa, D.; Yamato, Y.; Hasegawa, T.; Yoshida, G.; Kobayashi, S.; Yasuda, T.; Banno, T.; Arima, H.; Mihara, Y.; et al. Preoperative Age and Prognostic Nutritional Index Are Useful Factors for Evaluating Postoperative Delirium Among Patients With Adult Spinal Deformity. Spine 2019, 44, 472–478. [Google Scholar] [CrossRef] [PubMed]
  97. Wada, S.; Inoguchi, H.; Sadahiro, R.; Matsuoka, Y.J.; Uchitomi, Y.; Sato, T.; Shimada, K.; Yoshimoto, S.; Daiko, H.; Shimizu, K. Preoperative Anxiety as a Predictor of Delirium in Cancer Patients: A Prospective Observational Cohort Study. World J. Surg. 2019, 43, 134–142. [Google Scholar] [CrossRef]
  98. Peng, J.; Wu, G.; Chen, J.; Chen, H. Preoperative C-Reactive Protein/Albumin Ratio, a Risk Factor for Postoperative Delirium in Elderly Patients After Total Joint Arthroplasty. J. Arthroplasty 2019, 34, 2601–2605. [Google Scholar] [CrossRef]
  99. Li, Q.H.; Yu, L.; Yu, Z.W.; Fan, X.L.; Yao, W.X.; Ji, C.; Deng, F.; Luo, X.Z.; Sun, J.L. Relation of Postoperative Serum S100A12 Levels to Delirium and Cognitive Dysfunction Occurring after Hip Fracture Surgery in Elderly Patients. Brain Behav. 2019, 9, e01176. [Google Scholar] [CrossRef]
  100. Wang, Y.; Yu, H.; Qiao, H.; Li, C.; Chen, K.; Shen, X. Risk Factors and Incidence of Postoperative Delirium in Patients Undergoing Laryngectomy. Otolaryngol. Head Neck Surg. 2019, 161, 807–813. [Google Scholar] [CrossRef]
  101. Roijers, J.P.; Hopmans, C.J.; Janssen, T.L.; Mulder, P.G.H.; Buimer, M.G.; Ho, G.H.; de Groot, H.G.W.; Veen, E.J.; van der Laan, L. The Role of Delirium and Other Risk Factors on Mortality in Elderly Patients with Critical Limb Ischemia Undergoing Major Lower Limb Amputation. Ann. Vasc. Surg. 2019, 60, 270–278.e2. [Google Scholar] [CrossRef]
  102. Shim, E.J.; Noh, H.L.; Lee, K.M.; Hwang, H.; Son, K.L.; Jung, D.; Kim, W.H.; Kong, S.H.; Suh, Y.S.; Lee, H.J.; et al. Trajectory of Severity of Postoperative Delirium Symptoms and Its Prospective Association with Cognitive Function in Patients with Gastric Cancer: Results from a Prospective Observational Study. Support Care Cancer 2019, 27, 2999–3006. [Google Scholar] [CrossRef]
  103. de Jong, L.; van Rijckevorsel, V.A.J.I.M.; Raats, J.W.; Klem, T.M.A.L.; Kuijper, T.M.; Roukema, G.R. Delirium after Hip Hemiarthroplasty for Proximal Femoral Fractures in Elderly Patients: Risk Factors and Clinical Outcomes. Clin. Interv. Aging 2019, 14, 427–435. [Google Scholar] [CrossRef]
  104. Mueller, A.; Spies, C.D.; Eckardt, R.; Weiss, B.; Pohrt, A.; Wernecke, K.D.; Schmidt, M. Anticholinergic Burden of Long-Term Medication Is an Independent Risk Factor for the Development of Postoperative Delirium: A Clinical Trial. J. Clin. Anesth. 2020, 61, 109632. [Google Scholar] [CrossRef]
  105. Yuan, Y.; Li, Z.; Yang, N.; Han, Y.; Ji, X.; Han, D.; Wang, X.; Li, Y.; Liu, T.; Yuan, F.; et al. Exosome α-Synuclein Release in Plasma May Be Associated with Postoperative Delirium in Hip Fracture Patients. Front. Aging Neurosci. 2020, 12, 67. [Google Scholar] [CrossRef]
  106. Lu, G.W.; Chou, Y.E.; Jin, W.L.; Su, X.B. Usefulness of Postoperative Serum Translocator Protein as a Predictive Marker for Delirium after Breast Cancer Surgery in Elderly Women. J. Int. Med. Res. 2020, 48, 1–10. [Google Scholar] [CrossRef]
  107. Wu, J.; Gao, S.; Zhang, S.; Yu, Y.; Liu, S.; Zhang, Z.; Mei, W. Perioperative Risk Factors for Recovery Room Delirium after Elective Non-Cardiovascular Surgery under General Anaesthesia. Perioper. Med. 2021, 10, 1–12. [Google Scholar] [CrossRef]
  108. Flikweert, E.R.; Izaks, G.J.; Knobben, B.A.S.; Stevens, M.; Wendt, K. The Development of a Comprehensive Multidisciplinary Care Pathway for Patients with a Hip Fracture: Design and Results of a Clinical Trial. BMC Musculoskelet. Disord. 2014, 15, 188. [Google Scholar] [CrossRef]
  109. Anbar, R.; Beloosesky, Y.; Cohen, J.; Madar, Z.; Weiss, A.; Theilla, M.; Koren Hakim, T.; Frishman, S.; Singer, P. Tight Calorie Control in Geriatric Patients Following Hip Fracture Decreases Complications: A Randomized, Controlled Study. Clin. Nutr. 2014, 33, 23–28. [Google Scholar] [CrossRef]
  110. Wang, N.Y.; Hirao, A.; Sieber, F. Association between Intraoperative Blood Pressure and Postoperative Delirium in Elderly Hip Fracture Patients. PLoS ONE 2015, 10, e0123892. [Google Scholar] [CrossRef]
  111. Yang, X.; Li, Z.; Gao, C.; Liu, R. Effect of Dexmedetomidine on Preventing Agitation and Delirium after Microvascular Free Flap Surgery: A Randomized, Double-Blind, Control Study. J. Oral Maxillofac. Surg. 2015, 73, 1065–1072. [Google Scholar] [CrossRef]
  112. Hempenius, L.; Slaets, J.P.J.; van Asselt, D.Z.B.; Schukking, J.; de Bock, G.H.; Wiggers, T.; van Leeuwen, B.L. Interventions to Prevent Postoperative Delirium in Elderly Cancer Patients Should Be Targeted at Those Undergoing Nonsuperficial Surgery with Special Attention to the Cognitive Impaired Patients. Eur. J. Surg. Oncol. 2015, 41, 28–33. [Google Scholar] [CrossRef]
  113. Hall, R.J.; Watne, L.O.; Idland, A.V.; Raeder, J.; Frihagen, F.; MacLullich, A.M.J.; Staff, A.C.; Wyller, T.B.; Fekkes, D. Cerebrospinal Fluid Levels of Neopterin Are Elevated in Delirium after Hip Fracture. J. Neuroinflamm. 2016, 13, 1–9. [Google Scholar] [CrossRef]
  114. Maekawa, Y.; Sugimoto, K.; Yamasaki, M.; Takeya, Y.; Yamamoto, K.; Ohishi, M.; Ogihara, T.; Shintani, A.; Doki, Y.; Mori, M.; et al. Comprehensive Geriatric Assessment Is a Useful Predictive Tool for Postoperative Delirium after Gastrointestinal Surgery in Old-Old Adults. Geriatr. Gerontol. Int. 2016, 16, 1036–1042. [Google Scholar] [CrossRef] [PubMed]
  115. Tanaka, P.; Goodman, S.; Sommer, B.R.; Maloney, W.; Huddleston, J.; Lemmens, H.J. The Effect of Desflurane versus Propofol Anesthesia on Postoperative Delirium in Elderly Obese Patients Undergoing Total Knee Replacement: A Randomized, Controlled, Double-Blinded Clinical Trial. J. Clin. Anesth. 2017, 39, 17–22. [Google Scholar] [CrossRef] [PubMed]
  116. Pan, Z.; Huang, K.; Huang, W.; Kim, K.H.; Wu, H.; Yu, Y.; Kim, K.N.; Yi, S.; Shin, D.A.; Vora, D.; et al. The Risk Factors Associated with Delirium after Lumbar Spine Surgery in Elderly Patients. Quant. Imaging Med. Surg. 2019, 9, 700. [Google Scholar] [CrossRef] [PubMed]
  117. Deiner, S.; Luo, X.; Lin, H.M.; Sessler, D.I.; Saager, L.; Sieber, F.E.; Lee, H.B.; Sano, M. Intraoperative Infusion of Dexmedetomidine for Prevention of Postoperative Delirium and Cognitive Dysfunction in Elderly Patients Undergoing Major Elective Noncardiac Surgery: A Randomized Clinical Trial. JAMA Surg. 2017, 152, e171505. [Google Scholar] [CrossRef] [PubMed]
  118. Ganai, S.; Lee, K.F.; Merrill, A.; Lee, M.H.; Bellantonio, S.; Brennan, M.; Lindenauer, P. Adverse Outcomes of Geriatric Patients Undergoing Abdominal Surgery Who Are at High Risk for Delirium. Arch. Surg. 2007, 142, 1072–1078. [Google Scholar] [CrossRef]
  119. Lee, J.K.; Park, Y.S. Delirium after Spinal Surgery in Korean Population. Spine 2010, 35, 1729–1732. [Google Scholar] [CrossRef]
  120. Vasunilashorn, S.M.; Dillon, S.T.; Inouye, S.K.; Ngo, L.H.; Fong, T.G.; Jones, R.N.; Travison, T.G.; Schmitt, E.M.; Alsop, D.C.; Freedman, S.D.; et al. High C-Reactive Protein Predicts Delirium Incidence, Duration, and Feature Severity After Major Noncardiac Surgery. J. Am. Geriatr. Soc. 2017, 65, e109–e116. [Google Scholar] [CrossRef]
  121. Jin, L.; Yao, R.; Heng, L.; Pang, B.; Sun, F.G.; Shen, Y.; Zhong, J.F.; Zhao, P.P.; Wu, C.Y.; Li, B.P. Ultrasound-Guided Continuous Thoracic Paravertebral Block Alleviates Postoperative Delirium in Elderly Patients Undergoing Esophagectomy: A Randomized Controlled Trial. Medicine 2020, 99, e19896. [Google Scholar] [CrossRef]
  122. Cerejeira, J.; Batista, P.; Nogueira, V.; Vaz-Serra, A.; Mukaetova-Ladinska, E.B. The Stress Response to Surgery and Postoperative Delirium: Evidence of Hypothalamic-Pituitary-Adrenal Axis Hyperresponsiveness and Decreased Suppression of the GH/IGF-1 Axis. J. Geriatr. Psychiatry Neurol. 2013, 26, 185–194. [Google Scholar] [CrossRef]
  123. Lee, C.; Lee, C.H.; Lee, G.; Lee, M.; Hwang, J. The Effect of the Timing and Dose of Dexmedetomidine on Postoperative Delirium in Elderly Patients after Laparoscopic Major Non-Cardiac Surgery: A Double Blind Randomized Controlled Study. J. Clin. Anesth. 2018, 47, 27–32. [Google Scholar] [CrossRef]
  124. Fukata, S.; Kawabata, Y.; Fujisiro, K.; Katagawa, Y.; Kuroiwa, K.; Akiyama, H.; Terabe, Y.; Ando, M.; Kawamura, T.; Hattori, H. Haloperidol Prophylaxis Does Not Prevent Postoperative Delirium in Elderly Patients: A Randomized, Open-Label Prospective Trial. Surg. Today 2014, 44, 2305–2313. [Google Scholar] [CrossRef]
  125. Monacelli, F.; Signori, A.; Prefumo, M.; Giannotti, C.; Nencioni, A.; Romairone, E.; Scabini, S.; Odetti, P. Delirium, Frailty, and Fast-Track Surgery in Oncogeriatrics: Is There a Link? Dement. Geriatr. Cogn. Disord. Extra 2018, 8, 33–41. [Google Scholar] [CrossRef]
  126. Youn, Y.C.; Shin, H.W.; Choi, B.S.; Kim, S.Y.; Lee, J.Y.; Ha, Y.C. Rivastigmine Patch Reduces the Incidence of Postoperative Delirium in Older Patients with Cognitive Impairment. Int. J. Geriatr. Psychiatry 2017, 32, 1079–1084. [Google Scholar] [CrossRef]
  127. Punjasawadwong, Y.; Pipanmekaporn, T.; Wongpakaran, N. Abstract PR164. Anesth. Analg. 2016, 123, 211. [Google Scholar] [CrossRef]
  128. Xu, W.B.; Hu, Q.H.; Wu, C.N.; Fan, Z.K.; Song, Z.F. Serum Soluble Fibrinogen-like Protein 2 Concentration Predicts Delirium after Acute Pancreatitis. Brain Behav. 2019, 9, e01261. [Google Scholar] [CrossRef]
  129. Fuchita, M.; Khan, S.H.; Perkins, A.J.; Gao, S.; Wang, S.; Kesler, K.A.; Khan, B.A. Perioperative Risk Factors for Postoperative Delirium in Patients Undergoing Esophagectomy. Ann. Thorac. Surg. 2019, 108, 190–195. [Google Scholar] [CrossRef]
  130. Culley, D.J.; Flaherty, D.; Fahey, M.C.; Rudolph, J.L.; Javedan, H.; Huang, C.C.; Wright, J.; Bader, A.M.; Hyman, B.T.; Blacker, D.; et al. Poor Performance on a Preoperative Cognitive Screening Test Predicts Postoperative Complications in Older Orthopedic Surgical Patients. Anesthesiology 2017, 127, 765–774. [Google Scholar] [CrossRef]
  131. Deng, Y.; Wang, R.; Li, S.; Zhu, X.; Wang, T.; Wu, J.; Zhang, J. Methylene Blue Reduces Incidence of Early Postoperative Cognitive Disorders in Elderly Patients Undergoing Major Non-Cardiac Surgery: An Open-Label Randomized Controlled Clinical Trial. J. Clin. Anesth. 2021, 68, 110108. [Google Scholar] [CrossRef]
  132. Liu, P.; Li, Y.W.; Wang, X.S.; Zou, X.; Zhang, D.Z.; Wang, D.X.; Li, S.Z. High Serum Interleukin-6 Level Is Associated with Increased Risk of Delirium in Elderly Patients after Noncardiac Surgery: A Prospective Cohort Study. Chin. Med. J. 2013, 126, 3621–3627. [Google Scholar] [CrossRef]
  133. Park, E.A.; Kim, M.Y. Postoperative Delirium Is Associated with Negative Outcomes and Long-Term Mortality in Elderly Koreans: A Retrospective Observational Study. Medicina 2019, 55, 618. [Google Scholar] [CrossRef]
  134. Rudolph, J.L.; Marcantonio, E.R. Postoperative Delirium: Acute Change with Long-Term Implications. Anesth. Analg. 2011, 112, 1202. [Google Scholar] [CrossRef] [PubMed]
  135. Onuma, H.; Inose, H.; Yoshii, T.; Hirai, T.; Yuasa, M.; Kawabata, S.; Okawa, A. Preoperative Risk Factors for Delirium in Patients Aged ≥75 Years Undergoing Spinal Surgery: A Retrospective Study. J. Int. Med. Res. 2020, 48, 1–12. [Google Scholar] [CrossRef] [PubMed]
  136. Ballweg, T.; White, M.; Parker, M.; Casey, C.; Bo, A.; Farahbakhsh, Z.; Kayser, A.; Blair, A.; Lindroth, H.; Pearce, R.A.; et al. Association between Plasma Tau and Postoperative Delirium Incidence and Severity: A Prospective Observational Study. Br. J. Anaesth. 2021, 126, 458–466. [Google Scholar] [CrossRef] [PubMed]
  137. Flink, B.J.; Rivelli, S.K.; Cox, E.A.; White, W.D.; Falcone, G.; Vail, T.P.; Young, C.C.; Bolognesi, M.P.; Krystal, A.D.; Trzepacz, P.T.; et al. Obstructive Sleep Apnea and Incidence of Postoperative Delirium after Elective Knee Replacement in the Nondemented Elderly. Anesthesiology 2012, 116, 788–796. [Google Scholar] [CrossRef] [PubMed]
  138. Gupta, R.M.; Parvizi, J.; Hanssen, A.D.; Gay, P.C. Postoperative Complications in Patients with Obstructive Sleep Apnea Syndrome Undergoing Hip or Knee Replacement: A Case-Control Study. Mayo Clin. Proc. 2001, 76, 897–905. [Google Scholar] [CrossRef]
  139. Roggenbach, J.; Klamann, M.; von Haken, R.; Bruckner, T.; Karck, M.; Hofer, S. Sleep-Disordered Breathing Is a Risk Factor for Delirium after Cardiac Surgery: A Prospective Cohort Study. Crit. Care 2014, 18, 1–10. [Google Scholar] [CrossRef]
  140. Kudoh, A.; Katagai, H.; Takazawa, T. Anesthesia with Ketamine, Propofol, and Fentanyl Decreases the Frequency of Postoperative Psychosis Emergence and Confusion in Schizophrenic Patients. J. Clin. Anesth. 2002, 14, 107–110. [Google Scholar] [CrossRef]
  141. Chaiwat, O.; Chanidnuan, M.; Pancharoen, W.; Vijitmala, K.; Danpornprasert, P.; Toadithep, P.; Thanakiattiwibun, C. Postoperative Delirium in Critically Ill Surgical Patients: Incidence, Risk Factors, and Predictive Scores. BMC Anesthesiol. 2019, 19, 1–10. [Google Scholar] [CrossRef]
  142. Berggren, D.; Gustafson, Y.; Eriksson, B.; Bucht, G.; Hansson, L.I.; Reiz, S.; Winblad, B. Postoperative Confusion after Anesthesia in Elderly Patients with Femoral Neck Fractures. Anesth. Analg. 1987, 66, 497–504. [Google Scholar] [CrossRef]
  143. Seo, J.S.; Park, S.W.; Lee, Y.S.; Chung, C.; Kim, Y.B. Risk Factors for Delirium after Spine Surgery in Elderly Patients. J. Korean Neurosurg. Soc. 2014, 56, 28–33. [Google Scholar] [CrossRef]
  144. Lynch, E.P.; Lazor, M.A.; Gellis, J.E.; Orav, J.; Goldman, L.; Marcantonio, E.R. The Impact of Postoperative Pain on the Development of Postoperative Delirium. Anesth. Analg. 1998, 86, 781–785. [Google Scholar] [CrossRef]
  145. Zhang, Y.; He, S.T.; Nie, B.; Li, X.Y.; Wang, D.X. Emergence Delirium Is Associated with Increased Postoperative Delirium in Elderly: A Prospective Observational Study. J. Anesth. 2020, 34, 675–687. [Google Scholar] [CrossRef]
  146. Radtke, F.M.; Franck, M.; MacGuill, M.; Seeling, M.; Lütz, A.; Westhoff, S.; Neumann, U.; Wernecke, K.D.; Spies, C.D. Duration of Fluid Fasting and Choice of Analgesic Are Modifiable Factors for Early Postoperative Delirium. Eur. J. Anaesthesiol. 2010, 27, 411–416. [Google Scholar] [CrossRef]
  147. Knaak, C.; Brockhaus, W.R.; Spies, C.; Borchers, F.; Piper, S.K.; Radtke, F.M.; Lachmann, G. Presurgical Cognitive Impairment Is Associated with Postoperative Delirium and Postoperative Cognitive Dysfunction. Minerva Anestesiol. 2020, 86, 394–403. [Google Scholar] [CrossRef]
  148. Contín, A.M.; Perez-Jara, J.; Alonso-Contín, A.; Enguix, A.; Ramos, F. Postoperative Delirium after Elective Orthopedic Surgery. Int. J. Geriatr. Psychiatry 2005, 20, 595–597. [Google Scholar] [CrossRef]
  149. Shin, Y.H.; Kim, D.K.; Jeong, H.J. Impact of Surgical Approach on Postoperative Delirium in Elderly Patients Undergoing Gastrectomy: Laparoscopic versus Open Approaches. Korean J. Anesthesiol. 2015, 68, 379. [Google Scholar] [CrossRef]
  150. Tan, C.B.; Ng, J.; Jeganathan, R.; Kawai, F.; Pan, C.X.; Pollock, S.; Turner, J.; Cohen, S.; Chorost, M. Cognitive Changes after Surgery in the Elderly: Does Minimally Invasive Surgery Influence the Incidence of Postoperative Cognitive Changes Compared to Open Colon Surgery? Dement. Geriatr. Cogn. Disord 2015, 39, 125–131. [Google Scholar] [CrossRef]
  151. Humeidan, M.L.; Reyes, J.P.C.; Mavarez-Martinez, A.; Roeth, C.; Nguyen, C.M.; Sheridan, E.; Zuleta-Alarcon, A.; Otey, A.; Abdel-Rasoul, M.; Bergese, S.D. Effect of Cognitive Prehabilitation on the Incidence of Postoperative Delirium Among Older Adults Undergoing Major Noncardiac Surgery: The Neurobics Randomized Clinical Trial. JAMA Surg. 2021, 156, 1. [Google Scholar] [CrossRef]
  152. Melegari, G.; Albertini, G.; Romani, A.; Malaguti, S.; Traccitto, F.; Giuliani, E.; Cavallini, G.M.; Bertellini, E.; Barbieri, A. Why Should You Stay One Night? Prospective Observational Study of Enhanced Recovery in Elderly Patients. Aging Clin. Exp. Res. 2021, 33, 1955–1961. [Google Scholar] [CrossRef]
  153. Windmann, V.; Spies, C.; Knaak, C.; Wollersheim, T.; Piper, S.K.; Vorderwülbecke, G.; Kurpanik, M.; Kuenz, S.; Lachmann, G. Intraoperative Hyperglycemia Increases the Incidence of Postoperative Delirium. Minerva Anestesiol. 2019, 85, 1201–1210. [Google Scholar] [CrossRef]
  154. Vlisides, P.E.; Das, A.R.; Thompson, A.M.; Kunkler, B.; Zierau, M.; Cantley, M.J.; McKinney, A.M.; Giordani, B. Home-Based Cognitive Prehabilitation in Older Surgical Patients: A Feasibility Study. J. Neurosurg. Anesthesiol. 2019, 31, 212–217. [Google Scholar] [CrossRef] [PubMed]
  155. Coburn, M.; Sanders, R.D.; Maze, M.; Rossaint, R.; Belda, J.; Borghi, B.; Rosencher, N.; Arnold, G.; Albaladejo, P.; Capdevila, X.; et al. The Hip Fracture Surgery in Elderly Patients (HIPELD) Study: Protocol for a Randomized, Multicenter Controlled Trial Evaluating the Effect of Xenon on Postoperative Delirium in Older Patients Undergoing Hip Fracture Surgery. Trials 2012, 13, 180. [Google Scholar] [CrossRef] [PubMed]
  156. Morino, T.; Hino, M.; Yamaoka, S.; Misaki, H.; Ogata, T.; Imai, H.; Miura, H. Risk Factors for Delirium after Spine Surgery: An Age-Matched Analysis. Asian. Spine J. 2018, 12, 703. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  157. Adogwa, O.; Elsamadicy, A.A.; Vuong, V.D.; Fialkoff, J.; Cheng, J.; Karikari, I.O.; Bagley, C.A. Association between Baseline Cognitive Impairment and Postoperative Delirium in Elderly Patients Undergoing Surgery for Adult Spinal Deformity. J. Neurosurg Spine. 2018, 28, 103–108. [Google Scholar] [CrossRef] [PubMed]
  158. Clemmesen, C.G.; Lunn, T.H.; Kristensen, M.T.; Palm, H.; Foss, N.B. Effect of a Single Pre-Operative 125 Mg Dose of Methylprednisolone on Postoperative Delirium in Hip Fracture Patients; a Randomised, Double-Blind, Placebo-Controlled Trial. Anaesthesia 2018, 73, 1353–1360. [Google Scholar] [CrossRef]
  159. Sieber, F.; Neufeld, K.J.; Gottschalk, A.; Bigelow, G.E.; Oh, E.S.; Rosenberg, P.B.; Mears, S.C.; Stewart, K.J.; Ouanes, J.P.P.; Jaberi, M.; et al. Depth of Sedation as an Interventional Target to Reduce Postoperative Delirium: Mortality and Functional Outcomes of the Strategy to Reduce the Incidence of Postoperative Delirium in Elderly Patients Randomised Clinical Trial. Brit J. Anaesth. 2019, 122, 480. [Google Scholar] [CrossRef]
  160. Hassel, B.; Mariussen, E.; Idland, A.V.; Dahl, G.T.; Ræder, J.; Frihagen, F.; Berg, J.P.; Chaudhry, F.A.; Wyller, T.B.; Watne, L.O. CSF Sodium at Toxic Levels Precedes Delirium in Hip Fracture Patients. Neurotoxicology 2018, 69, 11–16. [Google Scholar] [CrossRef]
  161. Racine, A.M.; Fong, T.G.; Gou, Y.; Travison, T.G.; Tommet, D.; Erickson, K.; Jones, R.N.; Dickerson, B.C.; Metzger, E.; Marcantonio, E.R.; et al. Clinical Outcomes in Older Surgical Patients with Mild Cognitive Impairment. Alzheimers Dement. 2018, 14, 590. [Google Scholar] [CrossRef]
  162. Mu, D.L.; Zhang, D.Z.; Wang, D.X.; Wang, G.; Li, C.J.; Meng, Z.T.; Li, Y.W.; Liu, C.; Li, X.Y. Parecoxib Supplementation to Morphine Analgesia Decreases Incidence of Delirium in Elderly Patients After Hip or Knee Replacement Surgery: A Randomized Controlled Trial. Anesth. Analg. 2017, 124, 1992–2000. [Google Scholar] [CrossRef]
  163. Nadler, J.W.; Evans, J.L.; Fang, E.; Preud’Homme, X.A.; Daughtry, R.L.; Chapman, J.B.; Bolognesi, M.P.; Attarian, D.E.; Wellman, S.S.; Krystal, A.D. A Randomised Trial of Peri-Operative Positive Airway Pressure for Postoperative Delirium in Patients at Risk for Obstructive Sleep Apnoea after Regional Anaesthesia with Sedation or General Anaesthesia for Joint Arthroplasty. Anaesthesia 2017, 72, 729–736. [Google Scholar] [CrossRef]
  164. Westhoff, D.; Witlox, J.; Koenderman, L.; Kalisvaart, K.J.; de Jonghe, J.F.M.; van Stijn, M.F.M.; Houdijk, A.P.J.; Hoogland, I.C.M.; MacLullich, A.M.J.; van Westerloo, D.J.; et al. Preoperative Cerebrospinal Fluid Cytokine Levels and the Risk of Postoperative Delirium in Elderly Hip Fracture Patients. J. Neuroinflamm. 2013, 10, 122. [Google Scholar] [CrossRef]
  165. Witlox, J.; Slor, C.J.; Jansen, R.W.M.M.; Kalisvaart, K.J.; van Stijn, M.F.M.; Houdijk, A.P.J.; Eikelenboom, P.; van Gool, W.A.; de Jonghe, J.F.M. The Neuropsychological Sequelae of Delirium in Elderly Patients with Hip Fracture Three Months after Hospital Discharge. Int. Psychogeriatr. 2013, 25, 1521–1531. [Google Scholar] [CrossRef]
  166. Mézière, A.; Paillaud, E.; Belmin, J.; Pariel, S.; Herbaud, S.; Canouï-Poitrine, F.; le Thuaut, A.; Marty, J.; Plaud, B. Delirium in Older People after Proximal Femoral Fracture Repair: Role of a Preoperative Screening Cognitive Test. Ann. Fr. Anesth Reanim. 2013, 32, e91–e96. [Google Scholar] [CrossRef]
  167. Lundström, M.; Olofsson, B.; Stenvall, M.; Karlsson, S.; Nyberg, L.; Englund, U.; Borssén, B.; Svensson, O.; Gustafson, Y. Postoperative Delirium in Old Patients with Femoral Neck Fracture: A Randomized Intervention Study. Aging Clin. Exp. Res. 2007, 19, 178–186. [Google Scholar] [CrossRef]
  168. Leung, J.M.; Sands, L.P.; Rico, M.; Petersen, K.L.; Rowbotham, M.C.; Dahl, J.B.; Ames, C.; Chou, D.; Weinstein, P. Pilot Clinical Trial of Gabapentin to Decrease Postoperative Delirium in Older Patients. Neurology 2006, 67, 1251–1253. [Google Scholar] [CrossRef]
  169. Kalisvaart, K.J.; de Jonghe, J.F.M.; Bogaards, M.J.; Vreeswijk, R.; Egberts, T.C.G.; Burger, B.J.; Eikelenboom, P.; van Gool, W.A. Haloperidol Prophylaxis for Elderly Hip-Surgery Patients at Risk for Delirium: A Randomized Placebo-Controlled Study. J. Am. Geriatr. Soc. 2005, 53, 1658–1666. [Google Scholar] [CrossRef]
  170. Kudoh, A.; Katagai, H.; Takase, H.; Takazawa, T. Effect of Preoperative Discontinuation of Antipsychotics in Schizophrenic Patients on Outcome during and after Anaesthesia. Eur. J. Anaesth. 2004, 21, 414–416. [Google Scholar] [CrossRef]
  171. Kudoh, A.; Takase, H.; Takazawa, T. A Comparison of Anesthetic Quality in Propofol-Spinal Anesthesia and Propofol-Fentanyl Anesthesia for Total Knee Arthroplasty in Elderly Patients. J. Clin. Anesth. 2004, 16, 405–410. [Google Scholar] [CrossRef]
  172. Kudoh, A.; Katagai, H.; Takazawa, T. Antidepressant Treatment for Chronic Depressed Patients Should Not Be Discontinued Prior to Anesthesia. Can. J. Anaesth. 2002, 49, 132–136. [Google Scholar] [CrossRef]
  173. Aizawa, K.I.; Kanai, T.; Saikawa, Y.; Takabayashi, T.; Kawano, Y.; Miyazawa, N.; Yamamoto, T. A Novel Approach to the Prevention of Postoperative Delirium in the Elderly after Gastrointestinal Surgery. Surg. Today 2002, 32, 310–314. [Google Scholar] [CrossRef]
  174. Marcantonio, E.R.; Flacker, J.M.; John Wright, R.; Resnick, N.M. Reducing Delirium after Hip Fracture: A Randomized Trial. J. Am. Geriatr. Soc. 2001, 49, 516–522. [Google Scholar] [CrossRef] [PubMed]
  175. Milisen, K.; Foreman, M.D.; Abraham, I.L.; de Geest, S.; Godderis, J.; Vandermeulen, E.; Fischler, B.; Delooz, H.H.; Spiessens, B.; Broos, P.L.O. A Nurse-Led Interdisciplinary Intervention Program for Delirium in Elderly Hip-Fracture Patients. J. Am. Geriatr. Soc. 2001, 49, 523–532. [Google Scholar] [CrossRef] [PubMed]
  176. Kaneko, T.; Cai, J.; Ishikura, T.; Kobayashi, M.; Naka, T.; Kaibara, N. Prophylactic Consecutive Administration of Haloperidol Can Reduce the Occurrence of Postoperative Delirium in Gastrointestinal Surgery. Yonago Acta. Med. 1999, 42, 179–184. [Google Scholar]
  177. Dimartini, A.F.; Trzepacz, P.T.; Pajer, K.A.; Faett, D.; Fung, J. Neuropsychiatric Side Effects of FK506 vs. Cyclosporine A: First-Week Postoperative Findings. Psychosomatics 1997, 38, 565–569. [Google Scholar] [CrossRef]
  178. Oh, E.S.; Leoutsakos, J.M.; Rosenberg, P.B.; Pletnikova, A.M.; Khanuja, H.S.; Sterling, R.S.; Oni, J.K.; Sieber, F.E.; Fedarko, N.S.; Akhlaghi, N.; et al. Effects of Ramelteon on the Prevention of Postoperative Delirium in Older Patients Undergoing Orthopedic Surgery: The RECOVER Randomized Controlled Trial. Am. J. Geriatr. Psychiatry 2021, 29, 90–100. [Google Scholar] [CrossRef]
  179. Oh, T.K.; Park, H.Y.; Shin, H.J.; Jeon, Y.T.; Do, S.H.; Hwang, J.W. The Role of Perioperative Statin Use in the Prevention of Delirium After Total Knee Replacement Under Spinal Anesthesia. J. Arthroplast. 2018, 33, 3666–3671. [Google Scholar] [CrossRef]
  180. Kin, K.; Yasuhara, T.; Tomita, Y.; Umakoshi, M.; Morimoto, J.; Date, I. SF-36 Scores Predict Postoperative Delirium after Surgery for Cervical Spondylotic Myelopathy. J. Neurosurg. Spine. 2019, 30, 777–782. [Google Scholar] [CrossRef]
  181. Chevillon, C.; Hellyar, M.; Madani, C.; Kerr, K.; Kim, S.C. Preoperative Education on Postoperative Delirium, Anxiety, and Knowledge in Pulmonary Thromboendarterectomy Patients. Am. J. Crit. Care 2015, 24, 164–171. [Google Scholar] [CrossRef]
  182. Hempenius, L.; Slaets, J.P.J.; van Asselt, D.; de Bock, G.H.; Wiggers, T.; van Leeuwen, B.L. Outcomes of a Geriatric Liaison Intervention to Prevent the Development of Postoperative Delirium in Frail Elderly Cancer Patients: Report on a Multicentre, Randomized, Controlled Trial. PLoS ONE 2013, 8, e64834. [Google Scholar] [CrossRef]
  183. Cerejeira, J.M.S.; Nogueira, V.; Luís, P.; Vaz-Serra, A.; Mukaetova-Ladinska, E.B. The Cholinergic System and Inflammation: Common Pathways in Delirium Pathophysiology. J. Am. Geriatr. Soc. 2012, 60, 669–675. [Google Scholar] [CrossRef]
  184. Lee, H.; Ju, J.W.; Oh, S.Y.; Kim, J.; Jung, C.W.; Ryu, H.G. Impact of Timing and Duration of Postoperative Delirium: A Retrospective Observational Study. Surgery 2018, 164, 137–143. [Google Scholar] [CrossRef]
  185. Lee, H.; Yang, S.M.; Chung, J.; Oh, H.W.; Yi, N.J.; Suh, K.S.; Oh, S.Y.; Ryu, H.G. Effect of Perioperative Low-Dose Dexmedetomidine on Postoperative Delirium After Living-Donor Liver Transplantation: A Randomized Controlled Trial. Transplant. Proc. 2020, 52, 239–245. [Google Scholar] [CrossRef]
  186. Mevorach, L.; Forookhi, A.; Farcomeni, A.; Romagnoli, S.; Bilotta, F. Perioperative Risk Factors Associated with Increased Incidence of Postoperative Delirium: Systematic Review, Meta-Analysis, and Grading of Recommendations Assessment, Development, and Evaluation System Report of Clinical Literature. Br. J. Anaesth. 2022, 130, e254–e262. [Google Scholar] [CrossRef]
Figure 1. PRISMA flow diagram.
Figure 1. PRISMA flow diagram.
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Figure 2. Risk of bias assessment of randomized studies [25,26,43,48,52,55,57,62,66,71,82,109,111,115,117,121,123,124,126,131].
Figure 2. Risk of bias assessment of randomized studies [25,26,43,48,52,55,57,62,66,71,82,109,111,115,117,121,123,124,126,131].
Geriatrics 08 00024 g002aGeriatrics 08 00024 g002b
Table 1. Clinical record table including the risk factors correlated with POD development at a statistically significant level (cited in ≥2 studies).
Table 1. Clinical record table including the risk factors correlated with POD development at a statistically significant level (cited in ≥2 studies).
Risk Factor
Demographics
Age≥60
Gender *Female
Education<8 years
Laboratory #
Albumin<3.9 g/dL
CRP>7 mg/L
Hemoglobin>13.16 g/dL
Glucose>8.4 mmol/L
TNF-a>8.2 nmol/L
IL-6>17.9 pg/mL
Cumulative scores
MMSE<17
CCI≥2
Mini–Cog≤2
Comorbidities
DiabetesYes
StrokeYes
Chronic therapies
BenzodiazepinesYes
Habits
Alcohol abuseYes
Surgery
Emergency Yes
Intrathoracic, intrabdominal, Orthopedic, spinal, peripheral vascularYes
Minimally invasive *Yes
* Variables associated with controversial evidence # Variables associated with limited evidence. CRP = C-Reactive Protein, MMSE = Mini Mental State Examination, CCI = Charlson Comorbidity Index.
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Karageorgos, V.; Mevorach, L.; Silvetti, M.; Bilotta, F. Preoperative Risk Factors Associated with Increased Incidence of Postoperative Delirium: Systematic Review of Qualified Clinical Studies. Geriatrics 2023, 8, 24. https://doi.org/10.3390/geriatrics8010024

AMA Style

Karageorgos V, Mevorach L, Silvetti M, Bilotta F. Preoperative Risk Factors Associated with Increased Incidence of Postoperative Delirium: Systematic Review of Qualified Clinical Studies. Geriatrics. 2023; 8(1):24. https://doi.org/10.3390/geriatrics8010024

Chicago/Turabian Style

Karageorgos, Vlasios, Lior Mevorach, Melissa Silvetti, and Federico Bilotta. 2023. "Preoperative Risk Factors Associated with Increased Incidence of Postoperative Delirium: Systematic Review of Qualified Clinical Studies" Geriatrics 8, no. 1: 24. https://doi.org/10.3390/geriatrics8010024

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