lin han

Prof. Dr. lin han

orcid

Research Focus & Metrics

Academic Career Length

8Years (2019-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 November 2020 in International Journal of Nursing Studies
Verified
Journal Article
Closed access
YMYuxia Ma
Yuxia Ma
BHBo He
Bo He
MJMengyao Jiang
Mengyao Jiang
YYYanlin Yang
Yanlin Yang
CWChenxia Wang
Chenxia Wang
LHlin han
lin han

4 March 2019 in The Journal of nutrition, health and aging
Verified
Journal Article
Open access
PDF file
BHB. He
B. He
YMY. Ma
Y. Ma
CWC. Wang
C. Wang
MJM. Jiang
M. Jiang
CGC. Geng
C. Geng
LHlin han
lin han
To systematically assess the prevalence of frailty, including prefrailty, stratified prevalence according to frailty criteria, gender, age, and region, and the risk factors for frailty in China.

25 February 2021 in Nursing Open
Verified
Journal Article
Open access
PDF file
CHCan Huang
Can Huang
YMYuxia Ma
Yuxia Ma
CWChenxia Wang
Chenxia Wang
MJMengyao Jiang
Mengyao Jiang
LFLoretta Yuet Foon
Loretta Yuet Foon
LHlin han
lin han
Aim: Pressure injuries are common adverse events in clinical practice, affecting the well‐being of patients and causing considerable financial burden to healthcare systems. It is therefore essential to use reliable assessment tools to identify pressure injuries for early prevention. The Braden Scale is a widely used tool to assess pressure injury risk, but the literature is currently lacking in determining its accuracy. This study aimed to evaluate the accuracy of the Braden Scale in assessing pressure injury risk.Design: Systematic review and meta‐analysis.Methods: Articles published between 1973–2020 from periodicals indexed in the PubMed, EMBASE, CINAHL, Web of Science and the Cochrane Library were selected. Two reviewers independently selected the relevant studies for inclusion. Data were analysed by the STATA 15.0 and the RevMan 5.3 software.Results: In total, 60 studies involving 49,326 individuals were eligible for this meta‐analysis. The pooled SEN, SPE, PLR, NLR, DOR and AUC were 0.78 (95% CI: 0.74 to 0.82), 0.72 (95% CI: 0.66 to 0.78), 2.80 (95% CI: 2.30 to 3.50), 0.30 (95% CI: 0.26 to 0.35), 9.00 (95% CI: 7.00 to 13.00) and 0.82 (95% CI: 0.79 to 0.85), respectively. Subgroup analyses indicated that the AUC was higher for prospective design (0.84, 95% CI: 0.81 to 0.87), mean age <60 years (0.87, 95% CI: 0.84 to 0.90), hospital (0.82, 95% CI: 0.79 to 0.86) and Caucasian population (0.86, 95% CI: 0.82 to 0.88). In addition, 18 was found to be the optimal cut‐off value.Conclusion: The evidence indicated that the Braden Scale had a moderate predictive validity. It was more suitable for mean age <60 years, hospitalized patients and the Caucasian population, and the cut‐off value of 18 might be used for the risk assessment of pressure injuries in clinical practice. However, due to the different cut‐off values used among included studies, the results had a significant heterogeneity. Future studies should explore the optimal cut‐off value in the same clinical environment.

7 April 2022 in Frontiers in Aging Neuroscience
Verified
Journal Article
Open access
YCYanru Chen
Yanru Chen
XQXiaoling Qian
Xiaoling Qian
YZYuanyuan Zhang
Yuanyuan Zhang
WSWenli Su
Wenli Su
YHYanan Huang
Yanan Huang
YMYuxia Ma
Yuxia Ma
Background and Purpose: Alzheimer’s disease (AD) is a devastating neurodegenerative disorder with no cure, and available treatments are only able to postpone the progression of the disease. Mild cognitive impairment (MCI) is considered to be a transitional stage preceding AD. Therefore, prediction models for conversion from MCI to AD are desperately required. These will allow early treatment of patients with MCI before they develop AD. This study performed a systematic review and meta-analysis to summarize the reported risk prediction models and identify the most prevalent factors for conversion from MCI to AD.Methods: We systematically reviewed the studies from the databases of PubMed, CINAHL Plus, Web of Science, Embase, and Cochrane Library, which were searched through September 2021. Two reviewers independently identified eligible articles and extracted the data. We used the Critical Appraisal and Data Extraction for Systematic Reviews of Prediction Modeling Studies (CHARMS) checklist for the risk of bias assessment.Results: In total, 18 articles describing the prediction models for conversion from MCI to AD were identified. The dementia conversion rate of elderly patients with MCI ranged from 14.49 to 87%. Models in 12 studies were developed using the data from the Alzheimer’s Disease Neuroimaging Initiative (ADNI). C-index/area under the receiver operating characteristic curve (AUC) of development models were 0.67–0.98, and the validation models were 0.62–0.96. MRI, apolipoprotein E genotype 4 (APOE4), older age, Mini-Mental State Examination (MMSE) score, and Alzheimer’s Disease Assessment Scale cognitive (ADAS-cog) score were the most common and strongest predictors included in the models.Conclusion: In this systematic review, many prediction models have been developed and have good predictive performance, but the lack of external validation of models limited the extensive application in the general population. In clinical practice, it is recommended that medical professionals adopt a comprehensive forecasting method rather than a single predictive factor to screen patients with a high risk of MCI. Future research should pay attention to the improvement, calibration, and validation of existing models while considering new variables, new methods, and differences in risk profiles across populations.

13 January 2022 in European Journal of Clinical Nutrition
Verified
Journal Article
Closed access
PDF file
YRYue Ruan
Yue Ruan
LCLian Chen
Lian Chen
DSDongli She
Dongli She
YCYuehuan Chung
Yuehuan Chung
LGLong Ge
Long Ge
LHlin han
lin han

15 August 2022 in Journal of Neurology
Verified
Journal Article
Closed access
PDF file
XWXinyu Wang
Xinyu Wang
YHYanan Huang
Yanan Huang
YCYanru Chen
Yanru Chen
TYTingting Yang
Tingting Yang
WSWenli Su
Wenli Su
YMYuxia Ma
Yuxia Ma