Prevalence and Risk Factors of Delirium Among Stroke Patients
LihongXian1
YujieLi2
HuanYan3
SiminLi3
HuanhuanZhu2
FengyinZhang2
JuanLi4✉Email
1Affiliated Hospital of Guizhou Medical UniversityNo. 28, Beijing Road, Yunyan District550004Guiyang CityGuizhou ProvinceChina
2School of NursingGuizhou University of Chinese MedicineNo. 50, Shi Dong Road, Nanming DistrictGuiyang CityGuizhou ProvinceChina
3Zunyi Medical UniversityNo.1 Road, Campus, Xinpu New District563000Zunyi CityGuizhou ProvinceChina
4Nursing Department of Guizhou Provincial People’s Hospital83 Zhongshan East Road, Nanming District550002Guiyang CityGuizhou ProvinceChina
Lihong Xian1, Yujie Li2, Huan Yan3, Simin Li3, Huanhuan Zhu2, Fengyin Zhang2, Juan Li4,*
1Affiliated Hospital of Guizhou Medical University, No. 28, Beijing Road, Yunyan District, Guiyang City, 550004, Guizhou Province, China.
2School of Nursing, Guizhou University of Chinese Medicine, No. 50, Shi Dong Road, Nanming District, Guiyang City, Guizhou Province, China.
3Zunyi Medical University, No.1 Road, Campus, Xinpu New District, Zunyi City,563000,Guizhou Province, China.
4Nursing Department of Guizhou Provincial People's Hospital, 83 Zhongshan East Road, Nanming District, Guiyang City, 550002, Guizhou Province, China.
Lihong Xian and Juan Li contributed equally to this paper.
Corresponding author: Juan Li, Nursing Department of Guizhou Provincial People's Hospital, 83 Zhongshan East Road, Nanming District, Guiyang City, 550002, Guizhou Province, China.
Email: 694807055@qq.com
A
Abstract
Background
Delirium is a common but often underdiagnosed neuropsychiatric syndrome among hospitalized patients, particularly in those with acute neurological conditions such as stroke. Post-stroke delirium (PSD) is associated with prolonged hospital stays, increased mortality, and poorer functional outcomes. While previous studies have explored various risk factors for PSD, findings remain inconsistent across populations and clinical settings. This study aims to investigate the prevalence of delirium among stroke patients and to analyze its risk factors.
Methods
A
From October 2023 to July 2024, a total of 281 stroke patients from the Neurology and Neurosurgery Departments of Guizhou Provincial People's Hospital were selected using a convenience sampling method. The Confusion Assessment Method for the ICU (CAM-ICU) was used for delirium diagnosis.
Results
The overall prevalence of post-stroke delirium (PSD) was 20.28% (57/281). Stroke type, smoking, alcohol consumption, NIHSS score, WBC count, and the presence of physical restraints were identified as risk factors for PSD, while hemoglobin (Hb) served as a protective factor.
Conclusions
The prevalence of PSD in this study was relatively high. Nursing staff should consider these factors in stroke patient care and take proactive preventive measures to reduce the occurrence of PSD.
A
Clinical Trial Registration: Not applicable.
Keywords:
stroke
delirium
post-stroke delirium
prevalence
risk factors
A
A
1. Introduction
Stroke, also known as cerebrovascular accident, is a type of cerebrovascular disease primarily characterized by intracerebral hemorrhage or ischemia. Its main types include ischemic stroke and hemorrhagic stroke. Stroke is known for its high incidence, high disability rate, and high mortality rate,[1] significantly increasing the care burden on healthcare providers. Although the global age-standardized mortality rate of stroke has declined in recent years, the age-standardized prevalence continues to rise markedly.[2] Delirium is a common complication among stroke patients, with clinical manifestations that include altered levels of consciousness, changes in orientation, memory, thought, or behavior. It can rapidly develop into a fluctuating state in a short time, leading to adverse outcomes such as prolonged hospitalization, impaired mobility, long-term cognitive decline, increased risk of dementia, and even death.[3, 4] Currently, studies focusing on post-stroke delirium (PSD) remain limited. Existing evidence shows that nurses often lack adequate knowledge of delirium, and confidence in its recognition and management remains insufficient, contributing to underdiagnosis and misdiagnosis of PSD.[5]
Although international clinical guidelines advocate for early and proactive identification of risk factors and symptoms in high-risk stroke survivors,[6, 7] the detection of delirium in acute care settings is still suboptimal.[8] Furthermore, due to the lack of specific nursing guidelines for stroke detection and management, clinical attention to PSD remains inadequate.[9] Delirium management in nursing is a multifaceted process that involves both pharmacological and non-pharmacological interventions.[10] Early and rapid identification of delirium is crucial for initiating timely interventions, preventing related complications, and mitigating functional decline.[11]
Therefore, this study aims to assess the prevalence of delirium among stroke patients using the Confusion Assessment Method for the ICU (CAM-ICU), and to explore its influencing factors from multiple dimensions, including clinical characteristics and laboratory indicators. Identifying these risk factors can assist nursing staff in early detection and provide a reference for developing targeted PSD prevention and management strategies, ultimately aiming to reduce its prevalence.
2. Materials and Methods
2.1 Participants
From October 2023 to July 2024, 281 stroke inpatients were enrolled from the Neurology and Neurosurgery Departments of Guizhou Provincial People's Hospital using convenience sampling. Inclusion criteria: (1) Diagnosed with ischemic or hemorrhagic stroke (Chinese Stroke Guidelines, 2018/2019)[12, 13]; (2) Age ≥ 18; (3) Hospitalization > 24 hours; (4) Glasgow Coma Scale (GCS) score > 8; (5) Provided informed consent. Exclusion Criteria: (1) Patients who had experienced delirium prior to hospital admission; (2) patients with a history of psychiatric disorders or dementia; (3) patients with severe visual, auditory, and/or speech impairments that prevented effective communication. According to the sampling principle proposed by Wang Jialiang,[14] the required sample size should be 5 to 10 times the number of questionnaire items. Considering a potential 10% rate of invalid responses, and given that the questionnaire included 34 items, the final targeted sample size was set at 300.
A
All procedures were performed in compliance with relevant laws and institutional guidelines and have been approved by the Ethics Committee of Guizhou Provincial People's Hospital (Approval No.: Ethics-Research−2024−055).
2.2 Study Tools
2.2.1 General Information Questionnaire
The general information questionnaire was developed by the researchers based on literature review and expert consultation in nursing, tailored to the objectives of this study. It consists of three main sections: (1)Basic patient information: including name, age, gender, ethnicity, marital status, place of residence, educational level, smoking history, and alcohol consumption history; (2)Clinical data: including types of chronic comorbidities, history of stroke, hearing impairment, visual impairment, stroke type, Barthel Index score, NIHSS score,[15] presence of infection, and physical restraint; (3) Laboratory indicators: including hemoglobin level, white blood cell count, and platelet count.
2.2.2 Glasgow Coma Scale (GCS)
The Glasgow Coma Scale (GCS) was developed in 1974 by Graham Teasdale and Bryan Jennett at the University of Glasgow to assess a patient’s level of consciousness and degree of coma.[16] The scale consists of three components: eye-opening response (4 points), verbal response (5 points), and motor response (6 points), with a total score ranging from 3 to 15. Higher scores indicate closer to normal consciousness, whereas lower scores reflect more severe impairment.
In this study, the GCS was used primarily to screen eligible participants with scores greater than 8.
2.2.3 Confusion Assessment Method for the ICU (CAM-ICU)
The CAM-ICU was developed by Ely et al.[17] as a modification of the original Confusion Assessment Method (CAM) specifically for use in ICU patients. It is known for its simplicity, high accuracy, and time efficiency.
A
CAM-ICU is widely recommended by clinical guidelines and authoritative literature, and is commonly used by nurses in patients with trauma, neurological conditions, or undergoing surgery. The CAM-ICU evaluates four key features: ① Acute onset or fluctuating course;② Inattention; ③ Altered level of consciousness; ④ Disorganized thinking. A diagnosis of delirium is confirmed when both features ① and ② are present, along with either feature ③ or ④.
2.2.4 Method of Data Collection
Data were collected using standardized paper-based questionnaires. All participants were screened strictly according to the inclusion and exclusion criteria. Prior to the investigation, members of the research team received uniform training. Patients were informed of the study’s purpose and significance, and written informed consent was obtained before distributing the questionnaires. During data collection, researchers used standardized instructions to explain the questionnaires. Upon completion, each questionnaire was reviewed immediately for completeness and collected on the spot. A total of 281 valid questionnaires were returned, yielding a response rate of 93.67%.
2.2.5 Statistical Analysis
All data were analyzed using SPSS version 26.0. Continuous variables with normal distribution were expressed as mean ± standard deviation, while those with non-normal distribution were described using median and interquartile range (IQR). Categorical variables were reported as frequency and percentage.
Univariate analysis of categorical variables was performed using the chi-square test. Based on the results of normality testing, continuous variables were analyzed using either the independent samples t-test or the Mann–Whitney U test for non-parametric comparisons. Binary logistic regression analysis was conducted to identify independent risk factors. A P-value < 0.05 was considered statistically significant.
3. Results
3.1 General Characteristics and Univariate Analysis of PSD
The 281 patients ranged in age from 21 to 92 years (mean = 60.18 ± 14.13), with 184 males (65.48%) and 97 females (34.52%). Univariate analysis using the chi-square test indicated that stroke type, smoking, alcohol consumption, Barthel Index (BI), infection, and physical restraint were significantly associated with PSD (P < 0.05). See Table 1. Normality tests were conducted for NIHSS scores, Hb, WBC, and PLT levels, and all variables were found to deviate significantly from normal distribution (P < 0.001). See Table 2.
Table 1
Univariate Analysis of Delirium in Stroke Patients (N = 281)
Variable
Non-PSD
(n = 224, 79.72%)
PSD
(n = 57, 20.28%)
χ²
P-value
Stroke type
  
5.26
0.022 *
– Ischemic
77 (34.37%)
10 (17.54%)
  
– Hemorrhagic
147 (65.63%)
47 (82.46%)
  
Age group
  
0.113a
0.945
– < 60 years
106 (47.32%)
28 (49.12%)
  
– 60–74 years
76 (33.93%)
18 (31.58%)
  
– ≥ 75 years
42 (18.75%)
11 (19.30%)
  
Gender
  
3.714b
0.054
– Male
140 (62.50%)
44 (77.19%)
  
– Female
84 (37.50%)
13 (22.81%)
  
Education level
  
4.372a
0.112
– Low
86 (38.39%)
15 (26.32%)
  
– Medium
85 (37.95%)
30 (52.63%)
  
– High
53 (23.66%)
12 (21.05%)
  
Marital status
  
0.478a
0.924
– Widowed
17 (7.59%)
3 (5.26%)
  
– Married
199 (88.84%)
52 (91.24%)
  
– Single
3 (1.34%)
1 (1.75%)
  
– Divorced
5 (2.23%)
1 (1.75%)
  
Chronic diseases
  
2.303a
0.316
– None
89 (39.73%)
23 (40.35%)
  
– 1–2 conditions
126 (56.25%)
29 (50.88%)
  
– ≥3 conditions
9 (4.02%)
5 (8.77%)
  
Ethnicity
  
0.516b
0.472
– Han
194 (86.61%)
52 (91.23%)
  
– Minority
30 (13.39%)
5 (8.77%)
  
Residence
  
0.184b
0.668
– Rural
88 (39.29%)
20 (35.09%)
  
– Urban
136 (60.71%)
37 (64.91%)
  
Smoking
  
20.439b
< 0.001 ***
– Yes
84 (37.50%)
41 (71.93%)
  
– No
140 (62.50%)
16 (28.07%)
  
Alcohol use
  
21.271b
< 0.001 ***
– Yes
79 (35.27%)
40 (70.18%)
  
– No
145 (64.73%)
17 (29.82%)
  
Stroke history
  
0.138b
0.71
– Yes
25 (11.16%)
8 (14.04%)
  
– No
199 (88.84%)
49 (85.96%)
  
Hearing impairment
  
0.693b
0.405
– Yes
14 (6.25%)
6 (10.53%)
  
– No
210 (93.75%)
51 (89.47%)
  
Visual impairment
  
1.543b
0.214
– Yes
14 (6.25%)
6 (10.53%)
  
– No
210 (93.75%)
51 (89.47%)
  
Barthel Index
  
11.644a
0.009 **
– ≤40
102 (45.53%)
40 (70.18%)
  
– 41–60
18 (8.04%)
4 (7.02%)
  
– 61–99
83 (37.05%)
10 (17.54%)
  
– 100
21 (9.38%)
3 (5.26%)
  
Infection
  
7.781b
0.005 **
– Yes
1 (0.45%)
4 (7.02%)
  
– No
223 (99.55%)
53 (92.98%)
  
Restraint
  
15.083b
< 0.001 ***
– Yes
1 (0.45%)
6 (10.53%)
  
– No
223 (99.55%)
51 (89.47%)
  
Notes: *P < 0.05; **P < 0.01; ***P < 0.001; a Fisher’s exact test; b multiple-response items
Table 2
Normality Test for Continuous Variables (N = 281)
Name
Sample size
Mean
SD
Skewness
Kurtosis
K- S Test(p)
S- W Test(p)
NIHSS
281
3.612
2.248
2.058
14.134
0.000***
0.000***
Hb
281
130.690
25.279
0.107
0.644
0.000***
0.028*
WBC
281
4.582
1.068
2.062
12.695
0.000***
0.000***
PLT
281
213.765
81.464
1.716
5.701
0.000***
0.000***
3.2 Multivariate Analysis of PSD
Variables with statistical significance in univariate analysis—including stroke type, smoking, alcohol consumption, BI score, infection, restraint, NIHSS score, Hb, and WBC—were included in a binary logistic regression model, with PSD as the dependent variable. Results showed that stroke type, smoking, alcohol use, infection, restraint, NIHSS score, Hb, and WBC were significant predictors of PSD. See Table 3.
Table 3
Binary Logistic Regression Analysis of Risk Factors for PSD (N = 281)
Independent variable
β
SE
Wald
P
OR
95%CI
Lower
Upper
Constant
-2.234
4.025
0.308
0.579
0.107
-10.122
5.654
Smoking
1.219
0.487
6.271
0.012*
3.385
0.265
2.174
Alcohol use
1.062
0.496
4.585
0.032*
2.892
0.090
2.034
Stroke type
1.546
1.298
1.418
0.234
4.690
-0.999
4.090
Barthel Index (BI)
-0.197
0.226
0.765
0.382
0.821
-0.639
0.245
Infection
2.075
1.494
1.928
0.165
7.965
-0.854
5.004
Restraint
4.233
1.493
8.044
0.005**
68.950
1.308
7.159
NIHSS Score
0.205
0.084
5.992
0.014*
1.228
0.041
0.369
Hb
-0.052
0.010
25.889
0.000***
0.949
-0.073
-0.032
WBC
0.816
0.218
14.049
0.000***
2.261
0.389
1.242
4. Discussion
4.1 Notable Prevalence of Post-Stroke Delirium (PSD)
This study revealed a PSD prevalence of 20.28%, which is slightly lower than the 27.07% reported by Pasinska et al.[18] and the 25.0% indicated in a recent meta-analysis by Ye et al.,[19] yet higher than the 10.7% found in a prospective observational study by Nydahl et al.[20] in Germany. The differences may be attributed to variations in study populations, assessment tools, and socioeconomic contexts across countries and regions.
Previous studies have shown that up to two-thirds of ICU nurses have limited knowledge of delirium, increasing the risk of misdiagnosis or missed diagnosis.[21] Many healthcare professionals also feel inadequately trained to assess and manage delirium effectively.[22] Therefore, nursing administrators should strengthen education and training related to PSD to reduce its incidence and alleviate the clinical and financial burden on stroke patients.
4.2 Risk Factors for PSD
The results of this study indicate a significant association between stroke type and the occurrence of post-stroke delirium (PSD), with patients experiencing hemorrhagic stroke being at a higher risk of developing delirium than those with ischemic stroke. This finding is consistent with the results reported by Ye et al.[19] The underlying reason may be that hemorrhagic stroke involves intracerebral bleeding due to vascular rupture, which causes damage to brain parenchyma and dysfunction of neural cells, thereby increasing the likelihood of delirium.[23]
To reduce the incidence of PSD, community healthcare providers should strengthen education and health management for the general population to help prevent hemorrhagic stroke, thereby indirectly decreasing the risk of PSD.
This study also found that the incidence of delirium was higher in male patients than in females. This may be attributed to two factors. First, estrogen levels in women are generally higher than in men. Estrogen has been shown to effectively suppress the release of peripheral and central proinflammatory cytokines and to help protect the blood–brain barrier from damage to a certain extent.[24] Second, unhealthy lifestyle habits such as long-term smoking and alcohol consumption are more prevalent in men. When such behaviors are abruptly stopped, neurotransmitter levels in the brain—such as dopamine and serotonin—may undergo drastic changes, disrupting neural signal transmission and triggering delirium.[25]
A
Moreover, multivariate analysis showed that smoking, alcohol use, physical restraint, higher NIHSS scores at admission, and elevated WBC levels had significant positive associations with PSD, while hemoglobin (Hb) was a significant protective factor. Smoking and alcohol consumption have been confirmed in multiple studies as independent risk factors for delirium.[26, 27] Psychotropic substances in tobacco and alcohol can impair the metabolic function of brain cells, reduce intercellular communication, and hinder information processing, thereby triggering delirium.[28]
This study identified physical restraint as a risk factor for delirium. The use of restraints may intensify patient agitation and contribute to reduced physical and cognitive function.[29] Some studies suggest that while combining physical restraints with sedative medications may enhance immobilization, both interventions are independently associated with an increased risk of delirium.[30] Therefore, healthcare providers are advised to carefully evaluate treatment plans, avoiding medications and nursing practices that may precipitate delirium.
NIHSS score was also identified as a risk factor for PSD. The higher the score, the greater the risk of delirium, likely due to the extent of neurological impairment. This finding is consistent with results reported by Mansutti et al.[31] It is recommended that nurses closely monitor male patients with high NIHSS scores and a history of smoking or alcohol use, ensuring early identification of risk factors and timely implementation of preventive management strategies.
Hb was found to be a protective factor against delirium in this study, consistent with findings by Kijima et al.[32] The brain relies heavily on oxygen and glucose for its metabolic processes, which occur at a high rate and require adequate oxygen supply. Low Hb levels impair the body's ability to deliver oxygen, potentially lowering blood oxygen saturation and triggering delirium.
In recent years, the concept of prehabilitation through nutrition and exercise has been introduced in nursing, aiming to enhance immunity, improve circulation, and boost antioxidant capacity by optimizing patients’ nutritional and physical status prior to treatment.[33] This approach has shown promise in reducing postoperative complications.[34] Given the close relationship between a patient’s nutritional status and nursing education and dietary management, healthcare professionals should assess nutritional conditions during patient care and provide timely support and guidance to families. This may help prevent Hb reduction caused by malnutrition and reduce the risk of delirium.
A
Additionally, elevated WBC was identified as a risk factor for PSD. Studies have shown that inflammatory cytokines such as interleukin−1 and interleukin−6 may induce delirium by activating endothelial cells, impairing cerebral blood flow, increasing blood–brain barrier permeability, and altering neurotransmission.[35, 3637] Nurses play a vital role in hospital infection control and can help reduce the incidence of delirium through effective infection prevention strategies. In a study by Korean researchers Song, Lee, and Jung,[38] infection control was incorporated as part of a delirium prevention protocol, showing significant outcomes.
In future practice, it is recommended that nurses adopt a comprehensive approach to delirium prevention and management by considering all potential risk factors and implementing coordinated interventions. Further studies exploring PSD risk factors may expand on the present findings by increasing the sample size and incorporating additional serum biomarkers. This will allow for an in-depth exploration of the underlying mechanisms of PSD and enable clinical staff to rapidly identify high-risk individuals and initiate targeted early interventions to prevent disease onset.
5. Conclusion
This study investigated the prevalence and associated risk factors of delirium among stroke patients, revealing a PSD (post-stroke delirium) prevalence rate of 20.28%. Patients with hemorrhagic stroke were found to be at a higher risk of developing delirium compared to those with ischemic stroke. Smoking, alcohol consumption, elevated NIHSS scores, increased white blood cell (WBC) count, and the use of physical restraints were identified as significant risk factors for PSD, while hemoglobin (Hb) served as a protective factor.
As a single-center study, although it included nearly 10 months of inpatient data from the neurology and neurosurgery departments, it did not analyze the prevalence of PSD among stroke patients in the emergency department. Therefore, the sample size was relatively limited. Future research may expand the sample size and include additional hospital departments based on the current study to identify more potential risk factors associated with PSD. This would support clinical healthcare providers in developing early and targeted prevention and management strategies for delirium in stroke patients.
Meanwhile, it is recommended that nursing administrators enhance the training and supervision of clinical nursing staff on PSD-related knowledge. By equipping nurses with a comprehensive understanding of delirium assessment and prevention strategies, the incidence of PSD can be effectively reduced—thereby alleviating the clinical and financial burden on stroke patients and improving their overall quality of life.
List of abbreviations
Post
stroke delirium (PSD)
Confusion Assessment Method for the ICU (CAM
ICU)
hemoglobin (Hb)
Glasgow Coma Scale (GCS)
interquartile range (IQR)
NIHSS score(NIH Stroke Scale)
Declarations
Ethics approval and consent to participate
A
This study was approved by the Ethics Committee of Guizhou Provincial People's Hospital (Approval No.: Ethics-Research-2024-055).Patients were informed of the study’s purpose and significance, and written informed consent was obtained before distributing the questionnaires.
A
The study was conducted in accordance with the principles of the Declaration of Helsinki.
Conflict of interest disclosure
The authors declare no conflicts of interest.
Consent for publication
Not applicable.
A
Data Availability
The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.
The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.
Competing interests
The authors declare that they have no competing interests.
A
Funding
This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.
A
Author Contribution
Lihong Xian: Conceptualization, Methodology, Writing - original draft.Yujie Li: Data curation, Formal analysis, Visualization. Huan Yan: Software, Data curation, Writing - review &amp; editing. Project administration, Methodology, Formal analysis. Simin Li: Investigation, Resources, Validation. Huanhuan Zhu: Investigation, Visualization, Writing - review &amp; editing. Fengyin Zhang: Resources, Validation, Supervision. Juan Li : Conceptualization, Supervision, Writing - review &amp; editing. All authors read and approved the final manuscript.
Acknowledgements
The authors would like to thank all the medical and nursing staff from the Neurology and Neurosurgery Departments of Guizhou Provincial People’s Hospital for their support and collaboration during the data collection process. Special appreciation is also extended to the patients and their families who participated in this study.
References
1.
Collaborators GBDS. Global, regional, and national burden of stroke, 1990–2016: A systematic analysis for the global burden of disease study 2016. Lancet Neurol. 2019;18:439–58. https://doi.org/10.1016/S1474-4422(19)30034-1.
2.
Sun J, Qiao Y, Zhao M, Magnussen CG, Xi B. Global, regional, and national burden of cardiovascular diseases in youths and young adults aged 15–39 years in 204 countries/territories, 1990–2019: A systematic analysis of global burden of disease study 2019. BMC Med. 2023;21:222. https://doi.org/10.1186/s12916-023-02925-4.
3.
Dros J, Kowalska K, Pasinska P, Szyper-Maciejowska A, Gorzkowska A, Klimkowicz-Mrowiec A. Delirium post-stroke-influence on post-stroke dementia (research study-part of the propolis study). J Clin Med. 2020;9. https://doi.org/10.3390/jcm9072165.
4.
Gong X, Jin S, Zhou Y, Lai L, Wang W. Impact of delirium on acute stroke outcomes: A systematic review and meta-analysis. Neurol Sci. 2024;45:1897–911. https://doi.org/10.1007/s10072-023-07287-6.
5.
Wong EK, Lee JY, Surendran AS, et al. Nursing perspectives on the confusion assessment method: A qualitative focus group study. Age Ageing. 2018;47:880–6. https://doi.org/10.1093/ageing/afy107.
6.
Delirium clinical care standard. Australian Commission on Safety and Quality in Health Care; 2021.
7.
Rieck KM, Pagali S, Miller DM. Delirium in hospitalized older adults. Hosp Pract (1995). 2020;48:3–16. https://doi.org/10.1080/21548331.2019.1709359.
8.
Marcantonio ER. Delirium in hospitalized older adults. N Engl J Med. 2018;378:96–7. https://doi.org/10.1056/NEJMc1714932.
9.
Powers WJ, Rabinstein AA, Ackerson T, et al. 2018 guidelines for the early management of patients with acute ischemic stroke: A guideline for healthcare professionals from the american heart association/american stroke association. Stroke. 2018;49:e46–110. https://doi.org/10.1161/STR.0000000000000158.
10.
Eckstein C, Burkhardt H. Multicomponent, nonpharmacological delirium interventions for older inpatients: A scoping review. Z Gerontol Geriatr. 2019;52:229–42. https://doi.org/10.1007/s00391-019-01627-y.
11.
Alvarez-Perez FJ, Paiva F. Prevalence and risk factors for delirium in acute stroke patients. A retrospective 5-years clinical series. J Stroke Cerebrovasc Dis. 2017;26:567–73. https://doi.org/10.1016/j.jstrokecerebrovasdis.2016.11.120.
12.
Chinese guidelines for diagnosis and treatment of acute ischemic stroke 2018. Chinese Journal of Neurology: Neurology Branch of Chinese Medical Association & Cerebrovascular Disease Group of Neurology Branch of Chinese Medical Association; 2018. pp. 666–82.
13.
Chinese guidelines for diagnosis and treatment of acute intracerebral hemorrhage 2019. Chinese Journal of Neurology: Neurology Branch of the Chinese Medical Association, & Cerebrovascular Disease Group of the Neurology Branch of the Chinese Medical Association. 2019. pp. 994–1005.
14.
Wang J. Clinical epidemiology: Clinical research design, measurement and evaluation. 4th ed. Shanghai Science and Technology; 2014.
15.
Brott T, Adams HJ, Olinger CP, et al. Measurements of acute cerebral infarction: a clinical examination scale. Stroke. 1989;20(7):864–70. https://doi:10.1161/01.str.20.7.864.
16.
Teasdale G, Jennett B. Assessment of coma and impaired consciousness. A practical scale. Lancet. 1974;2:81–4. https://doi.org/10.1016/s0140-6736(74)91639-0.
17.
Ely EW, Margolin R, Francis J, et al. Evaluation of delirium in critically ill patients: Validation of the confusion assessment method for the intensive care unit (cam-icu). Crit Care Med. 2001;29:1370–9. https://doi.org/10.1097/00003246-200107000-00012.
18.
Pasinska P, Kowalska K, Klimiec E, et al. Poststroke delirium clinical motor subtypes: The prospective observational polish study (propolis). J Neuropsychiatry Clin Neurosci. 2019;31:104–11. https://doi.org/10.1176/appi.neuropsych.18040073.
19.
Ye F, Ho MH, Lee JJ. Prevalence of post-stroke delirium in acute settings: A systematic review and meta-analysis. Int J Nurs Stud. 2024;154:104750. https://doi.org/10.1016/j.ijnurstu.2024.104750.
20.
Nydahl P, Bartoszek G, Binder A, et al. Prevalence for delirium in stroke patients: A prospective controlled study. Brain Behav. 2017;7:e00748. https://doi.org/10.1002/brb3.748.
21.
Mohd Yosli HN, Hong W, Kazura K, et al. Knowledge, attitude, perception and current practices of health personnel in managing post-stroke delirium in a new stroke centre in malaysia. Malays J Med Sci. 2023;30:157–74. https://doi.org/10.21315/mjms2023.30.4.14.
22.
Herrera E, Rutherford W, Plume T, Fields W, Mollon D. Evaluation of education and patient screening for delirium among patients with stroke: Knowledge, confidence, and patient outcomes. J Contin Educ Nurs. 2023;54:61–70. https://doi.org/10.3928/00220124-20230113-05.
23.
Yinhu T, Huimin X, Yan L, Yao H, Xue Y, Yang W. Meta-analysis of the incidence of post stroke delirium. Nurs J Chin People’S Liberation Army. 2024;41:81–4. https://doi.org/10.3969/j.issn.2097G1826.2024.06.020.
24.
Maldonado JR. Delirium pathophysiology: An updated hypothesis of the etiology of acute brain failure. Int J Geriatr Psychiatry. 2018;33:1428–57. https://doi.org/10.1002/gps.4823.
25.
Suzuki S, Brown CM, Dela Cruz CD, Yang E, Bridwell DA, Wise PM. Timing of estrogen therapy after ovariectomy dictates the efficacy of its neuroprotective and antiinflammatory actions. Proc Natl Acad Sci U S A. 2007;104:6013–8. https://doi.org/10.1073/pnas.0610394104.
26.
Mansutti I, Saiani L, Morandini M, Palese A. Post-stroke delirium risk factors, signs and symptoms of onset and outcomes as perceived by expert nurses: A focus group study. J Stroke Cerebrovasc Dis. 2020;29:105013. https://doi.org/10.1016/j.jstrokecerebrovasdis.2020.105013.
27.
Zhao J, Liang G, Hong K, et al. Risk factors for postoperative delirium following total hip or knee arthroplasty: A meta-analysis. Front Psychol. 2022;13:993136. https://doi.org/10.3389/fpsyg.2022.993136.
28.
Zaal IJ, Devlin JW, Peelen LM, Slooter AJ. A systematic review of risk factors for delirium in the icu. Crit Care Med. 2015;43:40–7. https://doi.org/10.1097/CCM.0000000000000625.
29.
Wang J, Ji Y, Wang N, et al. Establishment and validation of a delirium prediction model for neurosurgery patients in intensive care. Int J Nurs Pract. 2020;26:e12818. https://doi.org/10.1111/ijn.12818.
30.
Desai S, Chau T, George L. Intensive care unit delirium. Crit Care Nurs Q. 2013;36:370–89. https://doi.org/10.1097/CNQ.0b013e3182a10e8e.
31.
Mansutti I, Saiani L, Cargnelutti D, et al. Delirium prevalence, risk factors and outcomes among patients with acute stroke: A multi-centre observational study. J Vasc Nurs. 2022;40:172–80. https://doi.org/10.1016/j.jvn.2022.09.003.
32.
Kijima E, Kayama T, Saito M, et al. Pre-operative hemoglobin level and use of sedative-hypnotics are independent risk factors for post-operative delirium following total knee arthroplasty. BMC Musculoskelet Disord. 2020;21:279. https://doi.org/10.1186/s12891-020-03206-4.
33.
Arends J, Bachmann P, Baracos V, et al. Espen guidelines on nutrition in cancer patients. Clin Nutr. 2017;36:11–48. https://doi.org/10.1016/j.clnu.2016.07.015.
34.
Whittle J, Wischmeyer PE, Grocott MPW, Miller TE. Surgical prehabilitation: Nutrition and exercise. Anesthesiol Clin. 2018;36:567–80. https://doi.org/10.1016/j.anclin.2018.07.013.
35.
Broadhurst C, Wilson K. Immunology of delirium: New opportunities for treatment and research. Br J Psychiatry. 2001;179:288–9. https://doi.org/10.1192/bjp.179.4.288.
36.
Kowalska K, Klimiec E, Weglarczyk K, et al. Reduced ex vivo release of pro-inflammatory cytokines and elevated plasma interleukin-6 are inflammatory signatures of post-stroke delirium. J Neuroinflammation. 2018;15:111. https://doi.org/10.1186/s12974-018-1156-y.
37.
Trzepacz PT, Bourne R, Zhang S. Designing clinical trials for the treatment of delirium. J Psychosom Res. 2008;65:299–307. https://doi.org/10.1016/j.jpsychores.2008.06.001.
38.
Song J, Lee M, Jung D. The effects of delirium prevention guidelines on elderly stroke patients. Clin Nurs Res. 2018;27:967–83. https://doi.org/10.1177/1054773817721400.
Table
Abstract
Background: Delirium is a common but often underdiagnosed neuropsychiatric syndrome among hospitalized patients, particularly in those with acute neurological conditions such as stroke. Post-stroke delirium (PSD) is associated with prolonged hospital stays, increased mortality, and poorer functional outcomes. While previous studies have explored various risk factors for PSD, findings remain inconsistent across populations and clinical settings. This study aims to investigate the prevalence of delirium among stroke patients and to analyze its risk factors. Methods: From October 2023 to July 2024, a total of 281 stroke patients from the Neurology and Neurosurgery Departments of Guizhou Provincial People's Hospital were selected using a convenience sampling method. The Confusion Assessment Method for the ICU (CAM-ICU) was used for delirium diagnosis. Results: The overall prevalence of post-stroke delirium (PSD) was 20.28% (57/281). Stroke type, smoking, alcohol consumption, NIHSS score, WBC count, and the presence of physical restraints were identified as risk factors for PSD, while hemoglobin (Hb) served as a protective factor. Conclusions: The prevalence of PSD in this study was relatively high. Nursing staff should consider these factors in stroke patient care and take proactive preventive measures to reduce the occurrence of PSD. Clinical Trial Registration: Not applicable.
Total words in MS: 3149
Total words in Title: 9
Total words in Abstract: 191
Total Keyword count: 5
Total Images in MS: 0
Total Tables in MS: 3
Total Reference count: 38