820 results on '"GE Long"'
Search Results
352. Targeted agents for patients with advanced/metastatic pancreatic cancer: A protocol for systematic review and network meta-analysis.
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Baoshan Di, Bei Pan, Long Ge, Jichun Ma, Yiting Wu, Tiankang Guo, Di, Baoshan, Pan, Bei, Ge, Long, Ma, Jichun, Wu, Yiting, and Guo, Tiankang
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- 2018
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353. Chinese herbal injections for unstable angina pectoris: A protocol for systematic review and network meta-analyses.
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Fengwen Yang, Jiahan Zou, Xuemei Li, Long Ge, Jinhui Tian, Myeong Soo Lee, Junhua Zhang, Yang, Fengwen, Zou, Jiahan, Li, Xuemei, Ge, Long, Tian, Jinhui, Lee, Myeong Soo, and Zhang, Junhua
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- 2018
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354. Chinese herbal injections for heart failure: A protocol for systematic review and network meta-analyses.
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Fengwen Yang, Jiahan Zou, Long Ge, Jinhui Tian, Myeong Soo Lee, Ji Hee Jun, Junhua Zhang, Yang, Fengwen, Zou, Jiahan, Ge, Long, Tian, Jinhui, Lee, Myeong Soo, Jun, Ji Hee, and Zhang, Junhua
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- 2018
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355. The evaluation research on livable city based on multiplication model and AHP
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Yan, Feng-ying, primary, Yuan, Guo-dong, additional, Ge, Long, additional, and Li, Huai-gang, additional
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- 2011
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356. Studies on the Kunming’s flue-cured tobacco smoking and carbohydrate-related in different sub-climatic zones
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HAN, Ding-guo, primary, YI, Ke, additional, WANG, Xiang, additional, GE, Long, additional, YANG, Xiao-an, additional, TANG, Guo-qing, additional, and LU, Xiang-yang, additional
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- 2011
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357. Operation Integrity Evaluations for Deepwater Drilling Riser System
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Ge, Long, primary, Bhalla, Kenneth, additional, and Stahl, Matthew, additional
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- 2010
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358. Evaluation of Comparative Efficacy and Safety of Surgical Approaches for Total Hip Arthroplasty: A Systematic Review and Network Meta-analysis.
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Yan, Lei, Ge, Long, Dong, Shengjie, Saluja, Kiran, Li, Dijun, Reddy, K. Srikanth, Wang, Qi, Yao, Liang, Li, Jiao Jiao, Roza da Costa, Bruno, Xing, Dan, and Wang, Bin
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- 2023
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359. Improved Active Queue Management Algorithm for High Performance Networks
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Ge, Long, primary, Sun, Jinsheng, additional, and Wang, Zhiquan, additional
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- 2009
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360. F-ECN: A Loss Discrimination Based on Fuzzy Logic Control
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Yang, Xinhao, primary, Ge, Long, additional, and Wang, Zhiquan, additional
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- 2009
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361. Risk of incident diabetes after COVID-19 infection: A systematic review and meta-analysis.
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Lai, Honghao, Yang, Manli, Sun, Mingyao, Pan, Bei, Wang, Quan, Wang, Jing, Tian, Jinhui, Ding, Guowu, Yang, Kehu, Song, Xuping, and Ge, Long
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TYPE 2 diabetes ,COVID-19 ,TYPE 1 diabetes ,DIABETES ,POST-acute COVID-19 syndrome - Abstract
COVID-19 might be a risk factor for various chronic diseases. However, the association between COVID-19 and the risk of incident diabetes remains unclear. We aimed to meta-analyze evidence on the relative risk of incident diabetes in patients with COVID-19. In this systematic review and meta-analysis, the Embase, PubMed, CENTRAL, and Web of Science databases were searched from December 2019 to June 8, 2022. We included cohort studies that provided data on the number, proportion, or relative risk of diabetes after confirming the COVID-19 diagnosis. Two reviewers independently screened studies for eligibility, extracted data, and assessed risk of bias. We used a random-effects meta-analysis to pool the relative risk with corresponding 95 % confidence intervals. Prespecified subgroup and meta-regression analyses were conducted to explore the potential influencing factors. We converted the relative risk to the absolute risk difference to present the evidence. This study was registered in advance (PROSPERO CRD42022337841). Ten articles involving 11 retrospective cohorts with a total of 47.1 million participants proved eligible. We found a 64 % greater risk (RR = 1.64, 95%CI: 1.51 to 1.79) of diabetes in patients with COVID-19 compared with non-COVID-19 controls, which could increase the number of diabetes events by 701 (558 more to 865 more) per 10,000 persons. We detected significant subgroup effects for type of diabetes and sex. Type 2 diabetes has a higher relative risk than type 1. Moreover, men may be at a higher risk of overall diabetes than women. Sensitivity analysis confirmed the robustness of the results. No evidence was found for publication bias. COVID-19 is strongly associated with the risk of incident diabetes, including both type 1 and type 2 diabetes. We should be aware of the risk of developing diabetes after COVID-19 and prepare for the associated health problems, given the large and growing number of people infected with COVID-19. However, the body of evidence still needs to be strengthened. [Display omitted] • Eleven cohorts involving 47.1 million participants were included. • A 64 % greater risk of diabetes was found in patients with COVID-19. • A significant association was found for both type 1 diabetes and type 2 diabetes. • Subgroup analysis and sensitivity analyses proved the robustness. [ABSTRACT FROM AUTHOR]
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- 2022
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362. Crosstalk noise analysis for distributed parameter high-speed interconnect lines based on the transfer function
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Ji, Xiaopeng, primary, Ge, Long, additional, Han, Xiaodong, additional, and Wang, Zhiquan, additional
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- 2008
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363. Wire-Sizing for Interconnect Performance Optimization Considering High Inductance Effects
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Ji, Xiaopeng, primary, Ge, Long, additional, Han, Xiaodong, additional, and Wang, Zhiquan, additional
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- 2008
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364. Effect of Aidi injection plus chemotherapy on gastric carcinoma: a Meta-analysis of randomized controlled trials.
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Wang Jiancheng, Ge Long, Zhao Ye, Li Jinlong, Zhang Pan, Mao Lei, and Yang Kehu
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- 2015
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365. Self-assembly synthesis and electrochemical performance of Li1.5Mn0.75Ni0.15Co0.10O2+δ microspheres with multilayer shells.
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Yu, Ruizhi, Wang, Xianyou, Wang, Di, Ge, Long, Shu, Hongbo, and Yang, Xiukang
- Abstract
Novel Li
1.5 Mn0.75 Ni0.15 Co0.10 O2+δ microspheres with hierarchical multilayer shells were rationally designed and successfully prepared through a layer-by-layer self-assembly deposit with a co-precipitation process. The microsphere with multilayer shells consists of a Li1.5 Mn0.75 Ni0.25 O2+δ inner core and hierarchical multilayer shells. The structure and electrochemical properties of the spherical Li1.5 Mn0.75 Ni0.15 Co0.10 O2+δ cathode material with multilayer shells are evaluated and compared to those of the conventional Li1.5 Mn0.75 Ni0.15 Co0.10 O2+δ cathode material with the same chemical composition as the multilayer spherical cathode material. The results show that the spherical cathode material with multilayer shells delivers a high discharge capacity of 257.8 mA h g−1 at a rate of 0.1 C with an outstanding capacity retention of 96.1% after 100 cycles at 0.5 C between 2.0 and 4.6 V. Especially, the spherical cathode material with multilayer shells exhibits an improved rate capability with a capacity of 102.7 mA h g−1 even at a high discharge rate of 10 C, and it is apparently superior to the conventional Li1.5 Mn0.75 Ni0.15 Co0.10 O2+δ cathode material (64.9 mA h g−1 ). Thus, the reasonable design for function and structure of cathode materials will be significant for improving the lithium ion battery performance. [ABSTRACT FROM AUTHOR]- Published
- 2015
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366. Modeling of Electrodynamic Suspension Systems
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Kim, Nam Ho, primary and Ge, Long, additional
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- 2006
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367. Material Property Identification and Sensitivity Analysis Using Indentation and FEM
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Ge, Long, primary, Kim, Nam Ho, additional, Bourne, Gerald R., additional, and Sawyer, W. Gregory, additional
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- 2006
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368. F-6-2-2 Crashworthiness Simulation and Structural Optimization of Commercial Vehicle
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Jin, Xian long, primary, Zhang, Xiao yun, additional, Ge, Long, additional, Li, Yu xuan, additional, and Wang, Hai liang, additional
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- 2002
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369. An umbrella review of meta-analyses on diagnostic accuracy of C-reactive protein.
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Yang, Qiuyu, Li, Mengting, Cao, Xiao, Lu, Yao, Tian, Chen, Sun, Mingyao, Lai, Honghao, Tian, Jinhui, Li, Jiang, and Ge, Long
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Background: Multiple studies and meta-analyses have reported the diagnostic value of C-reactive protein (CRP) in several diseases. However, the precision, and influence of potential bias regarding the diagnostic values of existing evidence may have implications for clinical practice.Methods: We performed an umbrella review of diagnostic test accuracy studies of CRP for diseases by searching PubMed, Embase, China National Knowledge Infrastructure, and WanFang databases up to March 7, 2021. Five independent reviewers evaluated eligibility, extracted data, and assessed methodological quality. We descriptively analyzed the diagnostic accuracy of CRP for multiple diseases, heterogeneity between studies, and publication bias.Results: Seventy-four meta-analyses were included, with 13 diseases classified according to the International Classification of Diseases-11 (ICD-11). The methodological quality of the included meta-analyses was mostly low, with only 16 meta-analyses rated as moderate or high, including seven diseases classified by ICD-11. CRP had a relatively greater diagnostic accuracy for two of these diseases. For postoperative infectious complications after bariatric surgery, sensitivity and specificity were 0.81 (0.34-1) and 0.91 (0.73-1), respectively. For anastomotic leakage after colorectal surgery, sensitivity and specificity were 0.95 (0.75-0.99) and 0.95 (0.75-0.99), respectively.Conclusions: The diagnostic accuracy of CRP for multiple diseases has been extensively studied; however, most studies have low methodological quality. Evidence indicates that CRP has a relatively greater diagnostic accuracy for inflammation and infection diseases, especially for postoperative infectious complications after bariatric surgery and anastomotic leakage after colorectal surgery. [ABSTRACT FROM AUTHOR]- Published
- 2022
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370. Facile synthesis and performances of nanosized Li[sub 2]TiO[sub 3]-based shell encapsulated LiMn[sub 1/3]Ni1/3 Co1/3O[sub 2] microspheres.
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Yang, Xiukang, Yu, Ruizhi, Ge, Long, Wang, Di, Zhao, Qinglan, Wang, Xianyou, Bai, Yansong, Yuan, Hao, and Shu, Hongbo
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LiMn[sub 1/3]Ni[sub 1/3]Co[sub 1/3]O[sub 2] microspheres covered by a nanosized Li[sub 2]TiO[sub 3]-based shell are prepared by a facile synthesis method. First, a controllable TiO[sub 2] nano-layer is grown on the surface of a spherical Mn[sub 1/3] Ni[sub 1/3]Co[sub 1/3]CO[sub 3] precursor, and then the resultant TiO[sub 2]@LiMn[sub 1/3]Ni[sub 1/3]Co[sub 1/3]O[sub 2] hybrid is synchronously transformed in situ into a hierarchical Li[sub 2]TiO[sub 3]@LiMn[sub 1/3]Ni[sub 1/3]Co[sub 1/3]O[sub 2] microsphere through a solid-phase reaction. It has been found that the hierarchical Li[sub 2]TiO[sub 3]@LiMn[sub 1/3]Ni[sub 1/3]Co[sub 1/3]O[sub 2] microspheres exhibit a good rate capability with a discharge capacity of 92.3 mA h g[sup -1] even at higher rates of 20 C between 3.0 and 4.3 V. Besides, they possess excellent cyclic stability especially at high rates, with a capacity retention of 90.3% after 500 cycles at a 20 C rate. The enhanced electrochemical performance of the hierarchical Li[sub 2]TiO[sub 3]@LiMn[sub 1/3]Ni[sub 1/3]Co[sub 1/3]O[sub 2] at high rates is attributed to the stable and fast Li[sup +]-conductor characteristic of the nanosized Li[sub 2]TiO[sub 3]-based shell. Thus, the Li[sub 2]TiO[sub 3]@LiMn[sub 1/3]Ni[sub 1/3]Co[sub 1/3]O[sub 2] microspheres will be a promising cathode material for lithium-ion batteries with high power density and excellent cycling performance. [ABSTRACT FROM AUTHOR]
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- 2014
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371. Benefits and harms of drug treatment for type 2 diabetes: systematic review and network meta-analysis of randomised controlled trials
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Shi, Qingyang, Nong, Kailei, Vandvik, Per Olav, Guyatt, Gordon H, Schnell, Oliver, Rydén, Lars, Marx, Nikolaus, Brosius, Frank C, Mustafa, Reem A, Agarwal, Arnav, Zou, Xinyu, Mao, Yunhe, Asadollahifar, Aminreza, Chowdhury, Saifur Rahman, Zhai, Chunjuan, Gupta, Sana, Gao, Ya, Lima, João Pedro, Numata, Kenji, Qiao, Zhi, Fan, Qinlin, Yang, Qinbo, Jin, Yinghui, Ge, Long, Yang, Qiuyu, Zhu, Hongfei, Yang, Fan, Chen, Zhe, Lu, Xi, He, Siyu, Chen, Xiangyang, Lyu, Xiafei, An, Xingxing, Chen, Yaolong, Hao, Qiukui, Standl, Eberhard, Siemieniuk, Reed, Agoritsas, Thomas, Tian, Haoming, and Li, Sheyu
- Abstract
ObjectiveTo compare the benefits and harms of drug treatments for adults with type 2 diabetes, adding non-steroidal mineralocorticoid receptor antagonists (including finerenone) and tirzepatide (a dual glucose dependent insulinotropic polypeptide (GIP)/glucagon-like peptide-1 (GLP-1) receptor agonist) to previously existing treatment options.DesignSystematic review and network meta-analysis.Data sourcesOvid Medline, Embase, and Cochrane Central up to 14 October 2022.Eligibility criteria for selecting studiesEligible randomised controlled trials compared drugs of interest in adults with type 2 diabetes. Eligible trials had a follow-up of 24 weeks or longer. Trials systematically comparing combinations of more than one drug treatment class with no drug, subgroup analyses of randomised controlled trials, and non-English language studies were deemed ineligible. Certainty of evidence was assessed following the GRADE (grading of recommendations, assessment, development and evaluation) approach.ResultsThe analysis identified 816 trials with 471 038 patients, together evaluating 13 different drug classes; all subsequent estimates refer to the comparison with standard treatments. Sodium glucose cotransporter-2 (SGLT-2) inhibitors (odds ratio 0.88, 95% confidence interval 0.83 to 0.94; high certainty) and GLP-1 receptor agonists (0.88, 0.82 to 0.93; high certainty) reduce all cause death; non-steroidal mineralocorticoid receptor antagonists, so far tested only with finerenone in patients with chronic kidney disease, probably reduce mortality (0.89, 0.79 to 1.00; moderate certainty); other drugs may not. The study confirmed the benefits of SGLT-2 inhibitors and GLP-1 receptor agonists in reducing cardiovascular death, non-fatal myocardial infarction, admission to hospital for heart failure, and end stage kidney disease. Finerenone probably reduces admissions to hospital for heart failure and end stage kidney disease, and possibly cardiovascular death. Only GLP-1 receptor agonists reduce non-fatal stroke; SGLT-2 inhibitors are superior to other drugs in reducing end stage kidney disease. GLP-1 receptor agonists and probably SGLT-2 inhibitors and tirzepatide improve quality of life. Reported harms were largely specific to drug class (eg, genital infections with SGLT-2 inhibitors, severe gastrointestinal adverse events with tirzepatide and GLP-1 receptor agonists, hyperkalaemia leading to admission to hospital with finerenone). Tirzepatide probably results in the largest reduction in body weight (mean difference −8.57 kg; moderate certainty). Basal insulin (mean difference 2.15 kg; moderate certainty) and thiazolidinediones (mean difference 2.81 kg; moderate certainty) probably result in the largest increases in body weight. Absolute benefits of SGLT-2 inhibitors, GLP-1 receptor agonists, and finerenone vary in people with type 2 diabetes, depending on baseline risks for cardiovascular and kidney outcomes (https://matchit.magicevidence.org/230125dist-diabetes).ConclusionsThis network meta-analysis extends knowledge beyond confirming the substantial benefits with the use of SGLT-2 inhibitors and GLP-1 receptor agonists in reducing adverse cardiovascular and kidney outcomes and death by adding information on finerenone and tirzepatide. These findings highlight the need for continuous assessment of scientific progress to introduce cutting edge updates in clinical practice guidelines for people with type 2 diabetes.Systematic review registrationPROSPERO CRD42022325948.
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- 2023
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372. Comparison of seven popular structured dietary programmes and risk of mortality and major cardiovascular events in patients at increased cardiovascular risk: systematic review and network meta-analysis
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Karam, Giorgio, Agarwal, Arnav, Sadeghirad, Behnam, Jalink, Matthew, Hitchcock, Christine L, Ge, Long, Kiflen, Ruhi, Ahmed, Waleed, Zea, Adriana M, Milenkovic, Jovana, Chedrawe, Matthew AJ, Rabassa, Montserrat, El Dib, Regina, Goldenberg, Joshua Z, Guyatt, Gordon H, Boyce, Erin, and Johnston, Bradley C
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ObjectiveTo determine the relative efficacy of structured named diet and health behaviour programmes (dietary programmes) for prevention of mortality and major cardiovascular events in patients at increased risk of cardiovascular disease.DesignSystematic review and network meta-analysis of randomised controlled trials.Data sourcesAMED (Allied and Complementary Medicine Database), CENTRAL (Cochrane Central Register of Controlled Trials), Embase, Medline, CINAHL (Cumulative Index to Nursing and Allied Health Literature), and ClinicalTrials.gov were searched up to September 2021.Study selectionRandomised trials of patients at increased risk of cardiovascular disease that compared dietary programmes with minimal intervention (eg, healthy diet brochure) or alternative programmes with at least nine months of follow-up and reporting on mortality or major cardiovascular events (such as stroke or non-fatal myocardial infarction). In addition to dietary intervention, dietary programmes could also include exercise, behavioural support, and other secondary interventions such as drug treatment.Outcomes and measuresAll cause mortality, cardiovascular mortality, and individual cardiovascular events (stroke, non-fatal myocardial infarction, and unplanned cardiovascular interventions).Review methodsPairs of reviewers independently extracted data and assessed risk of bias. A random effects network meta-analysis was performed using a frequentist approach and grading of recommendations assessment, development and evaluation (GRADE) methods to determine the certainty of evidence for each outcome.Results40 eligible trials were identified with 35 548 participants across seven named dietary programmes (low fat, 18 studies; Mediterranean, 12; very low fat, 6; modified fat, 4; combined low fat and low sodium, 3; Ornish, 3; Pritikin, 1). At last reported follow-up, based on moderate certainty evidence, Mediterranean dietary programmes proved superior to minimal intervention for the prevention of all cause mortality (odds ratio 0.72, 95% confidence interval 0.56 to 0.92; patients at intermediate risk: risk difference 17 fewer per 1000 followed over five years), cardiovascular mortality (0.55, 0.39 to 0.78; 13 fewer per 1000), stroke (0.65, 0.46 to 0.93; 7 fewer per 1000), and non-fatal myocardial infarction (0.48, 0.36 to 0.65; 17 fewer per 1000). Based on moderate certainty evidence, low fat programmes proved superior to minimal intervention for prevention of all cause mortality (0.84, 0.74 to 0.95; 9 fewer per 1000) and non-fatal myocardial infarction (0.77, 0.61 to 0.96; 7 fewer per 1000). The absolute effects for both dietary programmes were more pronounced for patients at high risk. There were no convincing differences between Mediterranean and low fat programmes for mortality or non-fatal myocardial infarction. The five remaining dietary programmes generally had little or no benefit compared with minimal intervention typically based on low to moderate certainty evidence.ConclusionsModerate certainty evidence shows that programmes promoting Mediterranean and low fat diets, with or without physical activity or other interventions, reduce all cause mortality and non-fatal myocardial infarction in patients with increased cardiovascular risk. Mediterranean programmes are also likely to reduce stroke risk. Generally, other named dietary programmes were not superior to minimal intervention.Systematic review registrationPROSPERO CRD42016047939
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- 2023
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373. Geometry and Temperature Dependence of meso-Aryl Rotation in Strained Metalloporphyrins: Adjustable Turnstile Molecules.
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Zaichun Zhou, Xi Zhang, Qiuhua Liu, Ziqiang Yan, Chengjin Lv, and Ge Long
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- 2013
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374. Dynamic modeling of electromagnetic suspension system.
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Kim, Nam H and Ge, Long
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DYNAMIC models , *ELECTROMAGNETISM , *MAGNETIC suspension , *STABILITY (Mechanics) , *ROLLING friction - Abstract
Characteristics of magnetic-levitation systems are studied using dynamic models that include motion-dependent lift, drag, slip, and roll motions. The contact constraint between the vehicle and the track is modeled using a compliant contact model, and inelastic restitution is modeled using damping. Unknown numerical parameters are identified using an optimization technique and experimental data. The numerical tests are focused on the damping characteristics, stability in lifting and slip motions, the lifting efficiency, and the contact behavior with the track. It turns out that the suspension system does not have any inherent damping in the lifting direction. However, a stable behavior is observed in the traveling direction. The model also shows that the system has a strong concentric force that stabilizes the vehicle in the slip motion as well as in the rolling motion. [ABSTRACT FROM AUTHOR]
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- 2013
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375. Toward better translation of clinical research evidence into rapid recommendations for traditional Chinese medicine interventions: A methodological framework
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Li, Qianrui, Luo, Xiaochao, Li, Ling, Ma, Bin, Yao, Minghong, Liu, Jiali, Ge, Long, Chen, Xiaofan, Wu, Xi, Deng, Hongyong, Zhou, Xu, Wen, Zehuai, Li, Guowei, and Sun, Xin
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Rapid recommendation is a novel methodological framework for developing clinical practice guidelines and this framework shares the basic features of classical guidelines but differs from classical clinical practice guidelines in its `rapid’ development process (typically within 90 days) with an aim of translating practice-changing studies to recommendations. A recent global innovation of guideline development methodology is the proposal of a rapid recommendation framework for Traditional Chinese Medicine (TCM), which has the potential to add value to the translation of evidence to practice for TCM interventions. Up to now, more than 180 rapid recommendations have been published, but none of them is pertaining to TCM interventions. Due to the nature of multi-dimensional evidence sources for TCM interventions, including classical randomized controlled trials and real world evidence, a more sophisticated methodological approach to synthesize and evaluate the totality of evidence about effects of TCM interventions is required. Therefore, appropriate modification to the rapid recommendation framework is necessary. In the efforts to respond to these needs, we have proposed a specific approach to developing rapid recommendations for TCM interventions the Multi-dimensional Evidence Synthesis, Evaluation and Recommendations for TCM interventions (MESERT).
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- 2022
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376. Large Language Models in Traditional Chinese Medicine: A Scoping Review.
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Ren, Yaxuan, Luo, Xufei, Wang, Ye, Li, Haodong, Zhang, Hairong, Li, Zeming, Lai, Honghao, Li, Xuanlin, Ge, Long, ESTILL, Janne, Zhang, Lu, Yang, Shu, Chen, Yaolong, Wen, Chengping, and Bian, Zhaoxiang
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LANGUAGE models , *CHINESE medicine , *HERBAL medicine , *MEDICAL language , *DATA protection - Abstract
ABSTRACT Background Methods Results Conclusion The application of large language models (LLMs) in medicine has received increasing attention, showing significant potential in teaching, research, and clinical practice, especially in knowledge extraction, management, and understanding. However, the use of LLMs in Traditional Chinese Medicine (TCM) has not been thoroughly studied. This study aims to provide a comprehensive overview of the status and challenges of LLM applications in TCM.A systematic search of five electronic databases and Google Scholar was conducted between November 2022 and April 2024, using the Arksey and O'Malley five‐stage framework to identify relevant studies. Data from eligible studies were comprehensively extracted and organized to describe LLM applications in TCM and assess their performance accuracy.A total of 29 studies were identified: 24 peer‐reviewed articles, 1 review, and 4 preprints. Two core application areas were found: the extraction, management, and understanding of TCM knowledge, and assisted diagnosis and treatment. LLMs developed specifically for TCM achieved 70% accuracy in the TCM Practitioner Exam, while general‐purpose Chinese LLMs achieved 60% accuracy. Common international LLMs did not pass the exam. Models like EpidemicCHAT and MedChatZH, trained on customized TCM corpora, outperformed general LLMs in TCM consultation.Despite their potential, LLMs in TCM face challenges such as data quality and security issues, the specificity and complexity of TCM data, and the nonquantitative nature of TCM diagnosis and treatment. Future efforts should focus on interdisciplinary talent cultivation, enhanced data standardization and protection, and exploring LLM potential in multimodal interaction and intelligent diagnosis and treatment. [ABSTRACT FROM AUTHOR]
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- 2024
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377. Systematic review/meta‐analysis on the role of CB1R regulation in sleep‐wake cycle in rats.
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Xue, Jianjun, Xu, Ziqing, Zhang, Jie, Hou, Huaijing, Ge, Long, and Yang, Kehu
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CANNABINOID receptors , *RAPID eye movement sleep , *SLEEP latency , *SOMNOLOGY , *EYE movements - Abstract
Objective: A systematic review/meta‐analysis was conducted to investigate the effect of cannabinoid type‐1 receptor (CB1R) regulation on the sleep‐wake cycle of rats and to provide new ideas and evidence‐based basis for clinical research on the treatment of sleep disorders. Methods: We searched Cochrane Library, PubMed, Web of Science, Embase, Chinese Biomedicine Literature Database (CBM), China National Knowledge Infrastructure, WanFang, and VIP databases for relevant papers, about the effects of CB1R agonists/antagonists on sleep‐wake cycle in rats, from inception to November 2023. Two reviewers performed study screening, data extraction, and risk of bias assessment using the SYRCLE's risk of bias tool. Meta‐analysis was performed using RevMan 5.3 software. Heterogeneity test was performed on the included studies (Test standard α = 0.1). I2 value was used to evaluate the heterogeneity. Forest plot was drawn, and p ≤ 0.05 indicates statistically significant difference. Results: A total of 16 trials involving 484 experimental rats were included. The methodological quality evaluation results showed that the overall quality of the included studies was low. The results of the meta‐analysis showed that single administration of CB1R agonists could shorten the wakefulness (W) time in the first 6 h (h) (standardized mean difference (SMD) = –2.52, 95% confidence interval (CI) (–3.83, –1.22), p = 0.0002) and 24 h (SMD = –0.84, 95% CI (–1.31, –0.36), p = 0.0005) after administration, prolong nonrapid eye movement sleep (NREM) time (SMD = 1.75, 95% CI (0.54, 2.95), p = 0.005) and rapid eye movement sleep (REM) time (SMD = 1.76, 95% CI (0.26, 3.26), p = 0.02), and increase REM frequency after administration (SMD = 1.67, 95% CI (0.98, 2.35), p < 0.00001), these results were all statistically different. There were no significant differences in sleep latency and average duration of REM. Single administration of CB1R antagonists prolonged the first 6 h W time after administration (SMD = 1.36, 95%CI (0.29, 2.43), p = 0.01), shortened the first 6 h NREM time (SMD = –1.73, 95% CI (–2.88, –0.57), p = 0.003) and REM time (SMD = –2.07, 95% CI (–3.17, –0.96), p = 0.0003) after administration, and increased the frequency of W after administration (SMD = 3.57, 95% CI (1.42, 5.72), p = 0.001). There was no statistical difference in the average duration of W. REM time and REM frequency increased after continuous CB1R agonist withdrawal. Conclusions: According to the existing evidence, CB1R played a pivotal role in regulating the sleep‐wake cycle in rats. CB1R agonists tended to reduce W time, increase NREM and REM sleep times, boost REM frequency, and promote sleep. Conversely, CB1R antagonists could increase the duration and frequency of W, shorten NREM and REM sleep times, and promote W. [ABSTRACT FROM AUTHOR]
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- 2024
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378. Impact of sodium intake on blood pressure, mortality and major cardiovascular events: an umbrella review of systematic reviews and meta-analyses.
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Yang, Qiuyu, Vernooij, Robin W. M., Zhu, Hongfei, Nesrallah, Gihad, Bai, Chunyang, Wang, Qi, Li, Ying, Xia, Danni, Bała, Małgorzata M., Warzecha, Sylwia, Sun, Mingyao, Jayedi, Ahmad, Shab-Bidar, Sakineh, Pan, Bei, Tian, Jinhui, Yang, Kehu, Ge, Long, and Johnston, Bradley C.
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SYSTOLIC blood pressure , *MORTALITY , *SODIUM , *BLOOD pressure , *CERTAINTY , *UMBRELLAS - Abstract
AbstractA plethora of systematic reviews with meta-analyses (SRMAs) evaluating sodium intake on cardiovascular health have been published. However, the quality of the SRMAs, that report absolute estimates of effect for major cardiovascular events and the corresponding certainty of the evidence has not been explicitly summarized. We conducted an umbrella review to assess the strength and validity of associations between lower sodium intake and cardiovascular outcomes. We used a modified, more stringent, version of the AMSTAR 2 instrument and the GRADE approach to assess SRMA methodological quality and evidence certainty, respectively. Across three cardiovascular risk strata, we computed the absolute risk reduction (ARR) for binary outcomes. We included 56 SRMAs. In various cardiovascular risk populations, moderate to high certainty evidence suggested that lower sodium intake reduced systolic blood pressure (BP) by −8.69 to −2.00 mmHg, and had concordant but smaller effects on diastolic BP. Salt substitutes conferred a small but important reduction in all-cause and cardiovascular mortality [ARR 12 fewer per 1000; 9 fewer per 1000; respectively], and had little to no effect on the risk of stroke [ARR 1 fewer per 1000]. Moderate to high certainty evidence suggested that lower sodium intake is probably beneficial for the prevention of major cardiovascular events, especially in low cardiovascular risk populations. [ABSTRACT FROM AUTHOR]
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- 2024
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379. Guidelines for the Diagnosis and Treatment of Lumbar Spinal Stenosis with Integrated Traditional Chinese Medicine and Western Medicine (2023)
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WEI Xu, XU Weiguo, LI Luguang, QIN Xiaokuan, GE Long, YANG Kexin, GAO Jinghua, ZHU Liguo
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spinal stenosis ,lumbar spinal stenosis ,integrated traditional chinese medicine & western medicine ,diagnostic and treatment guideline ,Medicine - Abstract
Lumbar spinal stenosis is one of the most common causes of low back and leg pain. However, there is a lack of evidence-based guidelines for the treatment of lumbar spinal stenosis with integrated traditional Chinese medicine and western medicine. To standardize the diagnosis and treatment of lumbar spinal stenosis with a combination of traditional Chinese medicine and western medicine, this guideline strictly followed the relevant guiding principles for the development of guidelines both domestically and internationally. A multidisciplinary working group was established. We adopted the GRADE approach to grade the quality of evidence and the strength of recommendation. Finally recommendations on the treatment of lumbar spinal stenosis with integrated traditional Chinese medicine and western medicine were formed, aiming to standardize clinical practice. This guideline is for patients with all degrees of lumbar spinal stenosis.
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- 2024
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380. Research on Evaluation Index System of Scientific and Technological Achievements in Traditional Chinese Medicine Clinical Research
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LAI Honghao, GUO Jihua, YOU Liangzhen, WANG Jiabo, LIU Cunzhi, LIU Yue, LIU Baoli, SUN Xin, LI Hui, YANG Zhongqi, JI Guang, ZHAO Linhua, ZHAO Hui, SHANG Hongcai, ZENG Fang, WEI Xu, ZHANG Xiaoxiao, GE Long
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zhong yi yao biao zhun hua ,traditional chinese medicine ,evaluation indexes ,scientific and technological achievements ,categorical evaluation ,Medicine - Abstract
Background The effective evaluation of scientific and technological achievements in traditional Chinese medicine (TCM) is of great significance in promoting the innovative development of TCM. Previous evaluations of scientific and technological achievements in TCM often used a generalized evaluation method, leading to problems such as inappropriate indicators and limited dimensions, which is not conducive to reflecting the multiple values of achievements in a scientific and comprehensive way. Consequently, there is an urgent need to establish categorized and multi-dimensional evaluation index system for the evaluation of scientific and technological achievements in TCM in the new period. Objective To establish a scientific, categorized, reliable and comprehensive evaluation index system that reflects the principles of TCM and highlights its unique advantages aiming at the scientific and technological achievements in TCM, in accordance with the contemporary requirements for scientific and technological evaluation in China. Methods This study began in November 2022 and was completed in May 2023. A preliminary index framework was developed through literature review and focus group discussions. Delphi expert consultation was then conducted over two rounds to determine the evaluation indexes and points. The hierarchical analysis method was used to calculate the weight of each index. Results The final evaluation index system of scientific and technological achievements in TCM clinical research comprised 10 threshold indicators, 4 primary indicators, 17 secondary indicators, and 17 evaluation points. After testing, the positive coefficient of experts in both rounds of Delphi method implementation was 100%, the authority coefficient was 0.94 and 0.93, respectively. The Kendall's W consistency test for each level of indicators yielded two-tailed significance (P
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- 2024
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381. Ontology of clinical practice guidelines for Integrated Traditional Chinese and Western Medicine.
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Wang, Yongbo, Ren, Xiangying, Gao, Kuang, Chen, Mukun, Huang, Qiao, Yan, Siyu, Zhu, Yan, Sun, Xin, Chen, Yaolong, Ge, Long, Gu, Jinguang, Gao, Feng, Hu, Wenbin, Hong, Liang, Zhao, Chen, Shang, Hongcai, and Jin, Yinghui
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CHINESE medicine , *KNOWLEDGE representation (Information theory) , *MODULAR design , *CLINICAL medicine , *ONTOLOGY - Abstract
Objective: Clinical practice guidelines (CPGs) for Integrated Traditional Chinese and Western Medicine (TCM and WM) are important medical documents used to assist medical decision‐making and are of great significance for standardizing clinical pathways. However, due to the constraints of text format, it is difficult for Integrated TCM and WM CPGs to play a real role in medical practice. In addition, how to standardize the structure and semantic relationships between Integrated TCM and WM CPG knowledge, and realize the construction of computable, sharable and reliable CPGs, remains an urgent issue to be addressed. Therefore, we are proposing an ontology of CPGs for Integrated TCM and WM. Methods: We first initialized domain concepts and relationships to ensure the accuracy of the ontology knowledge structure. We then screened CPGs that meet the standards for Integrated TCM and WM, analyzed and classified the contents, and extracted the common structures. Based on the seven‐step ontology construction method combined with inference‐complement, referring to the representation methods and hierarchical relationships of terms and concepts in MeSH, ICD‐10, SNOMED‐CT, and other ontologies and terminology sets, we formed the concept structure and semantic relationship tables for the ontology. We also achieved the matching and mapping between the ontology and reference ontologies and term sets. Next, we defined the aspects and constraints of properties, selected multiple Integrated TCM and WM CPGs as instances to populate, and used ontology reasoning tools and formulated defined inference rules to reason and extend the ontology. Finally, we evaluated the performance of the ontology. Results: The content of the Integrated TCM and WM CPGs is divided into nine parts: basic information, background, development method, clinical question, recommendation, evidence, conclusion, result, and reason for recommendations. The Integrated TCM and WM CPG ontology has 152 classes and defines 90 object properties and 114 data properties, with a maximum classification depth of 4 layers. The terms of disease, drug and examination item names in the ontology have been standardized. Conclusions: This study proposes an Integrated TCM and WM CPG ontology. The ontology adopts a modular design, which has both sharing and scaling ability, and can express rich guideline knowledge. It provides important support for the semantic processing and computational application of guideline documents. [ABSTRACT FROM AUTHOR]
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- 2024
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382. The complete chloroplast genome sequence of Hydrocotyle sibthorpioides (Apiales: araliaceae).
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Ge, Long, Shen, Liqun, Chen, Qinyi, Li, Ximin, and Zhang, Lin
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HYDROCOTYLE ,ARALIACEAE ,CHLOROPLAST DNA ,NUCLEOTIDE sequencing ,MEDICINAL plants - Abstract
Hydrocotyle sibthorpioides Lam. is a widespread and important Chinese medicinal plant. In this study, we have sequenced the complete chloroplast genome of H. sibthorpioides, which is 152,880 bp in length with large (LSC 84,064 bp) and small (SSC 18,690 bp) single-copy regions separated by a pair of inverted repeats (IRs 25,063 bp) and contains 113 unique genes with 17 genes duplicated in the IR making a total of 130 genes. The phylogenetic analysis strongly supports the position of H. sibthorpioides and indicates it belongs to the Araliaceae family, potential to facilitate a better understanding of population and phylogenetic studies in Apiales. [ABSTRACT FROM AUTHOR]
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- 2017
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383. Antibody and cellular therapies for treatment of covid-19: a living systematic review and network meta-analysis
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Siemieniuk, Reed AC, Bartoszko, Jessica J, Díaz Martinez, Juan Pablo, Kum, Elena, Qasim, Anila, Zeraatkar, Dena, Izcovich, Ariel, Mangala, Sophia, Ge, Long, Han, Mi Ah, Agoritsas, Thomas, Arnold, Donald, Ávila, Camila, Chu, Derek K, Couban, Rachel, Cusano, Ellen, Darzi, Andrea J, Devji, Tahira, Foroutan, Farid, Ghadimi, Maryam, Khamis, Assem, Lamontagne, Francois, Loeb, Mark, Miroshnychenko, Anna, Motaghi, Sharhzad, Murthy, Srinivas, Mustafa, Reem A, Rada, Gabriel, Rochwerg, Bram, Switzer, Charlotte, Vandvik, Per O, Vernooij, Robin WM, Wang, Ying, Yao, Liang, Guyatt, Gordon H, and Brignardello-Petersen, Romina
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ObjectiveTo evaluate the efficacy and safety of antiviral antibody therapies and blood products for the treatment of novel coronavirus disease 2019 (covid-19).DesignLiving systematic review and network meta-analysis, with pairwise meta-analysis for outcomes with insufficient data.Data sourcesWHO covid-19 database, a comprehensive multilingual source of global covid-19 literature, and six Chinese databases (up to 21 July 2021).Study selectionTrials randomising people with suspected, probable, or confirmed covid-19 to antiviral antibody therapies, blood products, or standard care or placebo. Paired reviewers determined eligibility of trials independently and in duplicate.MethodsAfter duplicate data abstraction, we performed random effects bayesian meta-analysis, including network meta-analysis for outcomes with sufficient data. We assessed risk of bias using a modification of the Cochrane risk of bias 2.0 tool. The certainty of the evidence was assessed using the grading of recommendations assessment, development, and evaluation (GRADE) approach. We meta-analysed interventions with ≥100 patients randomised or ≥20 events per treatment arm.ResultsAs of 21 July 2021, we identified 47 trials evaluating convalescent plasma (21 trials), intravenous immunoglobulin (IVIg) (5 trials), umbilical cord mesenchymal stem cells (5 trials), bamlanivimab (4 trials), casirivimab-imdevimab (4 trials), bamlanivimab-etesevimab (2 trials), control plasma (2 trials), peripheral blood non-haematopoietic enriched stem cells (2 trials), sotrovimab (1 trial), anti-SARS-CoV-2 IVIg (1 trial), therapeutic plasma exchange (1 trial), XAV-19 polyclonal antibody (1 trial), CT-P59 monoclonal antibody (1 trial) and INM005 polyclonal antibody (1 trial) for the treatment of covid-19. Patients with non-severe disease randomised to antiviral monoclonal antibodies had lower risk of hospitalisation than those who received placebo: casirivimab-imdevimab (odds ratio (OR) 0.29 (95% CI 0.17 to 0.47); risk difference (RD) −4.2%; moderate certainty), bamlanivimab (OR 0.24 (0.06 to 0.86); RD −4.1%; low certainty), bamlanivimab-etesevimab (OR 0.31 (0.11 to 0.81); RD −3.8%; low certainty), and sotrovimab (OR 0.17 (0.04 to 0.57); RD −4.8%; low certainty). They did not have an important impact on any other outcome. There was no notable difference between monoclonal antibodies. No other intervention had any meaningful effect on any outcome in patients with non-severe covid-19. No intervention, including antiviral antibodies, had an important impact on any outcome in patients with severe or critical covid-19, except casirivimab-imdevimab, which may reduce mortality in patients who are seronegative.ConclusionIn patients with non-severe covid-19, casirivimab-imdevimab probably reduces hospitalisation; bamlanivimab-etesevimab, bamlanivimab, and sotrovimab may reduce hospitalisation. Convalescent plasma, IVIg, and other antibody and cellular interventions may not confer any meaningful benefit.Systematic review registrationThis review was not registered. The protocol established a priori is included as a data supplement.FundingThis study was supported by the Canadian Institutes of Health Research (grant CIHR- IRSC:0579001321).Readers’ noteThis article is a living systematic review that will be updated to reflect emerging evidence. Interim updates and additional study data will be posted on our website (www.covid19lnma.com).
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- 2021
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384. Prophylaxis against covid-19: living systematic review and network meta-analysis
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Bartoszko, Jessica J, Siemieniuk, Reed A C, Kum, Elena, Qasim, Anila, Zeraatkar, Dena, Ge, Long, Han, Mi Ah, Sadeghirad, Behnam, Agarwal, Arnav, Agoritsas, Thomas, Chu, Derek K, Couban, Rachel, Darzi, Andrea J, Devji, Tahira, Ghadimi, Maryam, Honarmand, Kimia, Izcovich, Ariel, Khamis, Assem, Lamontagne, Francois, Loeb, Mark, Marcucci, Maura, McLeod, Shelley L, Motaghi, Sharhzad, Murthy, Srinivas, Mustafa, Reem A, Neary, John D, Pardo-Hernandez, Hector, Rada, Gabriel, Rochwerg, Bram, Switzer, Charlotte, Tendal, Britta, Thabane, Lehana, Vandvik, Per O, Vernooij, Robin W M, Viteri-García, Andrés, Wang, Ying, Yao, Liang, Ye, Zhikang, Guyatt, Gordon H, and Brignardello-Petersen, Romina
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ObjectiveTo determine and compare the effects of drug prophylaxis on SARS-CoV-2 infection and covid-19.DesignLiving systematic review and network meta-analysis.Data sourcesWorld Health Organization covid-19 database, a comprehensive multilingual source of global covid-19 literature to 25 March 2021, and six additional Chinese databases to 20 February 2021.Study selectionRandomised trials of people at risk of covid-19 who were assigned to receive prophylaxis or no prophylaxis (standard care or placebo). Pairs of reviewers independently screened potentially eligible articles.MethodsRandom effects bayesian network meta-analysis was performed after duplicate data abstraction. Included studies were assessed for risk of bias using a modification of the Cochrane risk of bias 2.0 tool, and certainty of evidence was assessed using the grading of recommendations assessment, development, and evaluation (GRADE) approach.ResultsThe first iteration of this living network meta-analysis includes nine randomised trials—six of hydroxychloroquine (n=6059 participants), one of ivermectin combined with iota-carrageenan (n=234), and two of ivermectin alone (n=540), all compared with standard care or placebo. Two trials (one of ramipril and one of bromhexine hydrochloride) did not meet the sample size requirements for network meta-analysis. Hydroxychloroquine has trivial to no effect on admission to hospital (risk difference 1 fewer per 1000 participants, 95% credible interval 3 fewer to 4 more; high certainty evidence) or mortality (1 fewer per 1000, 2 fewer to 3 more; high certainty). Hydroxychloroquine probably does not reduce the risk of laboratory confirmed SARS-CoV-2 infection (2 more per 1000, 18 fewer to 28 more; moderate certainty), probably increases adverse effects leading to drug discontinuation (19 more per 1000, 1 fewer to 70 more; moderate certainty), and may have trivial to no effect on suspected, probable, or laboratory confirmed SARS-CoV-2 infection (15 fewer per 1000, 64 fewer to 41 more; low certainty). Owing to serious risk of bias and very serious imprecision, and thus very low certainty of evidence, the effects of ivermectin combined with iota-carrageenan on laboratory confirmed covid-19 (52 fewer per 1000, 58 fewer to 37 fewer), ivermectin alone on laboratory confirmed infection (50 fewer per 1000, 59 fewer to 16 fewer) and suspected, probable, or laboratory confirmed infection (159 fewer per 1000, 165 fewer to 144 fewer) remain very uncertain.ConclusionsHydroxychloroquine prophylaxis has trivial to no effect on hospital admission and mortality, probably increases adverse effects, and probably does not reduce the risk of SARS-CoV-2 infection. Because of serious risk of bias and very serious imprecision, it is highly uncertain whether ivermectin combined with iota-carrageenan and ivermectin alone reduce the risk of SARS-CoV-2 infection.Systematic review registrationThis review was not registered. The protocol established a priori is included as a supplement.Readers’ noteThis article is a living systematic review that will be updated to reflect emerging evidence. Updates may occur for up to two years from the date of original publication.
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- 2021
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385. Janus Kinase Inhibitors and Risk of Venous Thromboembolism: A Systematic Review and Meta-analysis
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Bilal, Jawad, Riaz, Irbaz Bin, Naqvi, Syed Arsalan Ahmed, Bhattacharjee, Sandipan, Obert, Michelle R., Sadiq, Maryam, Abd El Aziz, Mohammad A., Nooman, Yahya, Prokop, Lary J., Ge, Long, Murad, Mohammad H., Bryce, Alan H., McBane, Robert D., and Kwoh, C. Kent
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To assess the risk of venous thromboembolism (VTE) in patients treated with Janus kinase (JAK) inhibitors in clinical trials.
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- 2021
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386. An efficient scheme for SDN state consistency verification in cloud computing environment.
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Wang, Xiaoyan, Chen, Xingshu, Wang, Yitong, and Ge, Long
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CLOUD computing ,SOFTWARE-defined networking ,VIRTUAL networks - Abstract
Summary: Software‐defined networking (SDN) decouples the control and data planes to simplify network management and function deployment. SDN provides a solution for managing large‐scale virtual networks in the cloud environment. However, in the process of SDN network update, various attacks can lead to network state inconsistency. In this paper, a comprehensive and efficient verification scheme is proposed to defend the security threats and guarantee the network state consistency in the cloud environment. The scheme verifies the consistency of network update from two stages of network update request and response. Firstly, the flow path model and the security space are abstracted to quickly verify whether the network request is allowed. Then, a novel forwarding path probing and verification method is designed to validate the actual forwarding path and locate the abnormal path in real time. With the two‐stage verification, the scheme can prevent the spread of illegal flow rules and ensure the correct delivery and execution of flow rules. Finally, we carry out a series of experiments in OpenStack. The results show that the proposed scheme can detect security threats and label the abnormal forwarding path in real time to ensure the network state consistency, while introducing negligible performance overhead. [ABSTRACT FROM AUTHOR]
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- 2020
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387. Insomnia and risk of mortality from all-cause, cardiovascular disease, and cancer: Systematic review and meta-analysis of prospective cohort studies.
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Ge, Long, Guyatt, Gordon, Tian, Jinhui, Pan, Bei, Chang, Yaping, Chen, Yajing, Li, Huijuan, Zhang, Junmei, Li, Yahong, Ling, Juan, and Yang, Kehu
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Growing evidence indicates that insomnia may be associated with mortality. However, these findings have been inconsistent. We systematically searched MEDLINE and EMBASE to identify prospective cohort studies that assessed the association between insomnia disorder/individual insomnia symptoms and the risk of mortality among adults aged ≥18 yrs. We addressed this association using summary hazard ratios (HRs) and 95% confidence intervals (CIs) calculated using random-effects meta-analysis, and the GRADE approach to rate the certainty of evidence. Twenty-nine cohorts including 1,598,628 individuals (55.3% men; mean age 63.7 yrs old) with a median follow-up duration of 10.5 yrs proved eligible. Difficulty falling asleep (DFA) and non-restorative sleep (NRS) were associated with an increased risk of all-cause mortality (DFA: HR = 1.13, 95%CI 1.03 to 1.23, p = 0.009, moderate certainty; NRS: HR = 1.23, 95%CI 1.07 to 1.42, p = 0.003, high certainty) and cardiovascular disease mortality (DFA: 1.20, 95%CI: 1.01, 1.43; p = 0.04, moderate certainty; NRS: HR = 1.48, 95%CI 1.06 to 2.06, p = 0.02, moderate certainty). Convincing associations between DFA and all-cause mortality were restricted to the mid to older-aged population (moderate credibility). Insomnia disorder, difficulty maintaining sleep, and early morning awakening proved to be unassociated with all-cause and cardiovascular disease mortality. No insomnia symptoms proved to be associated with cancer-related mortality. [ABSTRACT FROM AUTHOR]
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- 2019
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388. How is AMSTAR applied by authors – a call for better reporting
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Pieper, Dawid, Koensgen, Nadja, Breuing, Jessica, Ge, Long, and Wegewitz, Uta
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610 Medical sciences ,Medicine ,3. Good health - Abstract
Background: The Assessment of Multiple Systematic Reviews (AMSTAR) tool has become the most widely used tool for investigating the methodological quality of systematic reviews (SR). Originally, AMSTAR was developed for SRs of RCTs for evaluating treatment interventions. Its applicability to SRs of other[for full text, please go to the a.m. URL], Brücken bauen – von der Evidenz zum Patientenwohl; 19. Jahrestagung des Deutschen Netzwerks Evidenzbasierte Medizin
389. Tenecteplase versus alteplase for acute ischemic stroke: a systematic review and meta-analysis of randomized and non-randomized studies.
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Ma, Yu, Xiang, Hunong, Busse, Jason W., Yao, Minghong, Guo, Jian, Ge, Long, Li, Bo, Luo, Xiaochao, Mei, Fan, Liu, Jiali, Wang, Yuning, Liu, Yanmei, Li, Wentao, Zou, Kang, Li, Ling, and Sun, Xin
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ISCHEMIC stroke , *ALTEPLASE , *INTRACRANIAL hemorrhage , *FIBRINOLYTIC agents , *BAYESIAN analysis - Abstract
Objective: Alteplase is the current standard of care for acute ischemic stroke. Tenecteplase is a newer fibrinolytic agent with preferable administration and lower costs; however, its comparative effectiveness to alteplase remains uncertain. We set out to perform a systematic review and meta-analysis to establish the benefits and harms of tenecteplase versus alteplase for acute ischemic stroke. Methods: We searched PubMed, Embase, Cochrane Central Register of Controlled Trials (CENTRAL), and ClinicalTrials.gov from inception to April 2023 for randomized and non-randomized studies that compared tenecteplase versus alteplase for acute ischemic stroke. Paired reviewers independently assessed risk of bias and extracted data. We performed both conventional meta-analyses and Bayesian network meta-analyses (NMA) with random-effects models and used the GRADE approach to evaluate the certainty of evidence. Our primary efficacy outcome was excellent functional outcome at 3 months, defined as a score of 0–1 on the modified Rankin Scale. Our primary safety outcomes were symptomatic intracranial hemorrhage and all-cause mortality. Results: Thirty-six studies were eligible for review, including 12 randomized (n = 5533) and 24 non-randomized studies (n = 44,956). Moderate certainty evidence showed that there was no difference between tenecteplase and alteplase in increasing the proportion of patients achieving excellent functional outcome at 3 months (odds ratio [OR], 1.10; 95% CI 0.98–1.23; risk difference [RD] 2.4%, 95% CI − 0.5 to 5.2), while moderate certainty evidence from NMA suggested that 0.25 mg/kg tenecteplase significantly improved excellent functional outcome at 3 months (OR, 1.16; 95% credible interval 1.02–1.32). Moderate certainty evidence showed that, compared to alteplase, tenecteplase may make little to no difference in the prevalence of symptomatic intracranial hemorrhage (OR, 1.12; 95% CI 0.79–1.59; RD 0.3%, 95% CI − 0.5 to 1.4), and probably reduces all-cause mortality (adjusted odds ratio [aOR], 0.44; 95% CI 0.30–0.64; RD − 4.6%; 95% CI − 5.8 to − 2.9). Conclusions: Moderate certainty evidence suggested that there was little to no difference between tenecteplase and alteplase in increasing the proportion of patients achieving excellent functional outcome at 3 months and the risk of symptomatic intracranial hemorrhage, while compared to alteplase, tenecteplase probably reduce all-cause mortality. Administration of 0.25 mg/kg tenecteplase after acute ischemic stroke is suggestive of increasing the proportion of patients that achieve excellent functional outcome at 3 months. [ABSTRACT FROM AUTHOR]
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- 2024
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390. Efficacy and safety of gastrointestinal bleeding prophylaxis in critically ill patients: systematic review and network meta-analysis
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Wang, Ying, Ye, Zhikang, Ge, Long, Siemieniuk, Reed A C, Wang, Xin, Wang, Yingkai, Hou, Liangying, Ma, Zhuo, Agoritsas, Thomas, Vandvik, Per Olav, Perner, Anders, Møller, Morten H, Guyatt, Gordon H, and Liu, Lihong
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ObjectiveTo determine, in critically ill patients, the relative impact of proton pump inhibitors (PPIs), histamine-2 receptor antagonists (H2RAs), sucralfate, or no gastrointestinal bleeding prophylaxis (or stress ulcer prophylaxis) on outcomes important to patients.DesignSystematic review and network meta-analysis.Data sourcesMedline, PubMed, Embase, Cochrane Central Register of Controlled Trials, trial registers, and grey literature up to March 2019.Eligibility criteria for selecting studies and methodsWe included randomised controlled trials that compared gastrointestinal bleeding prophylaxis with PPIs, H2RAs, or sucralfate versus one another or placebo or no prophylaxis in adult critically ill patients. Two reviewers independently screened studies for eligibility, extracted data, and assessed risk of bias. A parallel guideline committee (BMJRapid Recommendation) provided critical oversight of the systematic review, including identifying outcomes important to patients. We performed random-effects pairwise and network meta-analyses and used GRADE to assess certainty of evidence for each outcome. When results differed between low risk and high risk of bias studies, we used the former as best estimates.ResultsSeventy two trials including 12 660 patients proved eligible. For patients at highest risk (>8%) or high risk (4-8%) of bleeding, both PPIs and H2RAs probably reduce clinically important gastrointestinal bleeding compared with placebo or no prophylaxis (odds ratio for PPIs 0.61 (95% confidence interval 0.42 to 0.89), 3.3% fewer for highest risk and 2.3% fewer for high risk patients, moderate certainty; odds ratio for H2RAs 0.46 (0.27 to 0.79), 4.6% fewer for highest risk and 3.1% fewer for high risk patients, moderate certainty). Both may increase the risk of pneumonia compared with no prophylaxis (odds ratio for PPIs 1.39 (0.98 to 2.10), 5.0% more, low certainty; odds ratio for H2RAs 1.26 (0.89 to 1.85), 3.4% more, low certainty). It is likely that neither affect mortality (PPIs 1.06 (0.90 to 1.28), 1.3% more, moderate certainty; H2RAs 0.96 (0.79 to 1.19), 0.9% fewer, moderate certainty). Otherwise, results provided no support for any affect on mortality, Clostridium difficileinfection, length of intensive care stay, length of hospital stay, or duration of mechanical ventilation (varying certainty of evidence).ConclusionsFor higher risk critically ill patients, PPIs and H2RAs likely result in important reductions in gastrointestinal bleeding compared with no prophylaxis; for patients at low risk, the reduction in bleeding may be unimportant. Both PPIs and H2RAs may result in important increases in pneumonia. Variable quality evidence suggested no important effects of interventions on mortality or other in-hospital morbidity outcomes.Systematic review registrationPROSPERO CRD42019126656.
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- 2020
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391. A living WHO guideline on drugs for covid-19
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Lamontagne, Francois, Agoritsas, Thomas, Macdonald, Helen, Leo, Yee-Sin, Diaz, Janet, Agarwal, Arnav, Appiah, John Adabie, Arabi, Yaseen, Blumberg, Lucille, Calfee, Carolyn S, Cao, Bin, Cecconi, Maurizio, Cooke, Graham, Dunning, Jake, Geduld, Heike, Gee, Patrick, Manai, Hela, Hui, David S, Kanda, Seema, Kawano-Dourado, Leticia, Kim, Yae-Jean, Kissoon, Niranjan, Kwizera, Arthur, Laake, Jon Henrik, Machado, Flavia R, Qadir, Nida, Sarin, Rohit, Shen, Yinzhong, Zeng, Linan, Brignardello-Petersen, Romina, Lytvyn, Lyubov, Siemieniuk, Reed, Zeraatkar, Dena, Bartoszko, Jessica, Ge, Long, Maguire, Brittany, Rochwerg, Bram, Guyatt, Gordon, and Vandvik, Per Olav
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Clinical questionWhat is the role of drug interventions in the treatment and prevention of covid-19?RecommendationsThe first version on this living guidance focuses on corticosteroids. It contains a strong recommendation for systemic corticosteroids in patients with severe and critical covid-19, and a weak or conditional recommendation against systemic corticosteroids in patients with non-severe covid-19. Corticosteroids are inexpensive and are on the World Health Organisation list of essential medicines.Howthis guideline was createdThis guideline reflects an innovative collaboration between the WHO and the MAGIC Evidence Ecosystem Foundation, driven by an urgent need for global collaboration to provide trustworthy and living covid-19 guidance. A standing international panel of content experts, patients, clinicians, and methodologists, free from relevant conflicts of interest, produce recommendations for clinical practice. The panel follows standards, methods, processes, and platforms for trustworthy guideline development using the GRADE approach. We apply an individual patient perspective while considering contextual factors (that is, resources, feasibility, acceptability, equity) for countries and healthcare systems.The evidenceA living systematic review and network meta-analysis, supported by a prospective meta-analysis, with data from eight randomised trials (7184 participants) found that systemic corticosteroids probably reduce 28 day mortality in patients with critical covid-19 (moderate certainty evidence; 87 fewer deaths per 1000 patients (95% confidence interval 124 fewer to 41 fewer)), and also in those with severe disease (moderate certainty evidence; 67 fewer deaths per 1000 patients (100 fewer to 27 fewer)). In contrast, systemic corticosteroids may increase the risk of death in patients without severe covid-19 (low certainty evidence; absolute effect estimate 39 more per 1000 patients, (12 fewer to 107 more)). Systemic corticosteroids probably reduce the need for invasive mechanical ventilation, and harms are likely to be minor (indirect evidence).Understanding the recommendationsThe panel made a strong recommendation for use of corticosteroids in severe and critical covid-19 because there is a lower risk of death among people treated with systemic corticosteroids (moderate certainty evidence), and they believe that all or almost all fully informed patients with severe and critical covid-19 would choose this treatment. In contrast, the panel concluded that patients with non-severe covid-19 would decline this treatment because they would be unlikely to benefit and may be harmed. Moreover, taking both a public health and a patient perspective, the panel warned that indiscriminate use of any therapy for covid-19 would potentially rapidly deplete global resources and deprive patients who may benefit from it most as potentially lifesaving therapy.UpdatesThis is a living guideline. Work is under way to evaluate other interventions. New recommendations will be published as updates to this guideline.Readers noteThis is version 1 of the living guideline, published on 4 September (BMJ2020;370:m3379) version 1. Updates will be labelled as version 2, 3 etc. When citing this article, please cite the version number.SubmittedAugust 28AcceptedAugust 31
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- 2020
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392. Drug treatments for covid-19: living systematic review and network meta-analysis
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Siemieniuk, Reed AC, Bartoszko, Jessica J, Ge, Long, Zeraatkar, Dena, Izcovich, Ariel, Pardo-Hernandez, Hector, Rochwerg, Bram, Lamontagne, Francois, Han, Mi Ah, Kum, Elena, Liu, Qin, Agarwal, Arnav, Agoritsas, Thomas, Alexander, Paul, Chu, Derek K, Couban, Rachel, Darzi, Andrea, Devji, Tahira, Fang, Bo, Fang, Carmen, Flottorp, Signe Agnes, Foroutan, Farid, Heels-Ansdell, Diane, Honarmand, Kimia, Hou, Liangying, Hou, Xiaorong, Ibrahim, Quazi, Loeb, Mark, Marcucci, Maura, McLeod, Shelley L, Motaghi, Sharhzad, Murthy, Srinivas, Mustafa, Reem A, Neary, John D, Qasim, Anila, Rada, Gabriel, Riaz, Irbaz Bin, Sadeghirad, Behnam, Sekercioglu, Nigar, Sheng, Lulu, Switzer, Charlotte, Tendal, Britta, Thabane, Lehana, Tomlinson, George, Turner, Tari, Vandvik, Per O, Vernooij, Robin WM, Viteri-García, Andrés, Wang, Ying, Yao, Liang, Ye, Zhikang, Guyatt, Gordon H, and Brignardello-Petersen, Romina
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ObjectiveTo compare the effects of treatments for coronavirus disease 2019 (covid-19).DesignLiving systematic review and network meta-analysis.Data sourcesUS Centers for Disease Control and Prevention COVID-19 Research Articles Downloadable Database, which includes 25 electronic databases and six additional Chinese databases to 20 July 2020.Study selectionRandomised clinical trials in which people with suspected, probable, or confirmed covid-19 were randomised to drug treatment or to standard care or placebo. Pairs of reviewers independently screened potentially eligible articles.MethodsAfter duplicate data abstraction, a bayesian random effects network meta-analysis was conducted. Risk of bias of the included studies was assessed using a modification of the Cochrane risk of bias 2.0 tool, and the certainty of the evidence using the grading of recommendations assessment, development and evaluation (GRADE) approach. For each outcome, interventions were classified in groups from the most to the least beneficial or harmful following GRADE guidance.Results23 randomised controlled trials were included in the analysis performed on 26 June 2020. The certainty of the evidence for most comparisons was very low because of risk of bias (lack of blinding) and serious imprecision. Glucocorticoids were the only intervention with evidence for a reduction in death compared with standard care (risk difference 37 fewer per 1000 patients, 95% credible interval 63 fewer to 11 fewer, moderate certainty) and mechanical ventilation (31 fewer per 1000 patients, 47 fewer to 9 fewer, moderate certainty). These estimates are based on direct evidence; network estimates for glucocorticoids compared with standard care were less precise because of network heterogeneity. Three drugs might reduce symptom duration compared with standard care: hydroxychloroquine (mean difference −4.5 days, low certainty), remdesivir (−2.6 days, moderate certainty), and lopinavir-ritonavir (−1.2 days, low certainty). Hydroxychloroquine might increase the risk of adverse events compared with the other interventions, and remdesivir probably does not substantially increase the risk of adverse effects leading to drug discontinuation. No other interventions included enough patients to meaningfully interpret adverse effects leading to drug discontinuation.ConclusionGlucocorticoids probably reduce mortality and mechanical ventilation in patients with covid-19 compared with standard care. The effectiveness of most interventions is uncertain because most of the randomised controlled trials so far have been small and have important study limitations.Systematic review registrationThis review was not registered. The protocol is included as a supplement.Readers’ noteThis article is a living systematic review that will be updated to reflect emerging evidence. Updates may occur for up to two years from the date of original publication.
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- 2020
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393. Efficacy and safety of Tanreqing injection for cough caused by acute trachea-bronchitis disease: A systematic review and meta-analysis of randomized controlled trials.
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Ma, Ning, Pan, Bei, Ge, Long, Li, Mengting, Zhu, Hongfei, Deng, Xiyuan, Li, Dan, Wang, Xiaoman, Wu, Lei, Xiao, Jingmin, Lai, Honghao, Tian, Jinhui, Niu, Junqiang, and Yang, Kehu
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DRUG efficacy , *ONLINE information services , *HERBAL medicine , *INJECTIONS , *META-analysis , *MEDICAL information storage & retrieval systems , *CONFIDENCE intervals , *SYSTEMATIC reviews , *BRONCHITIS , *TREATMENT effectiveness , *VITAL capacity (Respiration) , *COUGH , *DESCRIPTIVE statistics , *FORCED expiratory volume , *MEDLINE , *DRUG side effects , *CHINESE medicine , *PATIENT safety , *DRUG administration , *DRUG dosage , *EVALUATION - Abstract
Tanreqing injection (TRQI) is an intravenous herbal preparation derived from 5 types of traditional Chinese medicines including Scutellariae Radix, Lonicerae Japonicae Flos, Forsythiae Fructus, bear bile powder and goral horn, incorporating baicalin, chlorogenic acid, ursodeoxycholic acid, and goose deoxycholic acid and other compounds known for anti-inflammatory properties, is widely used in China to treat cough caused by acute trachea-bronchitis disease (ATB). To investigate the clinical efficacy and safety of Tanreqing injection (TRQI) with and without Western medicine (WM) for cough caused by acute trachea-bronchitis (ATB). We systematically searched eight databases, including CENTRAL, Embase, PubMed, Science Direct, Wiley, China National Knowledge Infrastructure, Chinese Biomedical Literature Database and WanFang, from inception to August 2023 for randomized clinical trials (RCTs) on TRQI for cough caused by ATB. The critical outcomes of interest were time to symptom disappearance, including time for cough symptom to disappear and time to improve cough and sputum production. Important outcomes included symptom disappearance rate, adverse events (AEs) and lung function. We carried out random-effects meta-analysis using Review Manager 5.4 and assessed the certainty of evidence utilizing the Grading of Recommendations Assessment, Development and Evaluation (GRADE) approach. A total of 2872 citations were identified by our search, of which 26 eligible RCTs enrolled 2731 participants. Low to moderate certainty evidence showed that when compared with WM, TRQI plus WM treatment was associated with a favorable effect on the time for cough symptom to disappear (MD -2.21 d, 95% CI −2.64 to −1.78), time to improve cough and sputum production (MD −0.68 d, 95% CI −0.83 to −0.53), symptom disappearance rate (RR 1.37, 95% CI 1.20 to 1.55), forced vital capacity, and forced expiratory volume in 1 s (MD 0.38 L, 95% CI 0.26 to 0.50; MD 2.92%, 95% CI 1.29 to 4.56, respectively). In terms of AEs, there was no association between TRQI plus WM and WM (RR 0.55, 95% CI 0.14 to 2.21; low-certainty evidence). Very low certainty evidence showed that TRQI alone was associated with reduced time to improve cough and sputum (MD -0.14 d, 95% CI −0.26 to −0.02) and increased symptom disappearance rate (RR 1.89, 95% CI 1.24 to 2.88; low certainty evidence) compared to WM. The overall efficacy of TRQI or WM for ATB cough is better than that of WM, and TRQI also effectively improve symptoms in patients with similar adverse events. However, due to the lack of methodological rigor of included studies, the present findings should be interpreted with caution. We advocate better high-quality and convincing clinical studies to be performed to prove the effectiveness and safety of TRQIs. [Display omitted] • This study was in accordance with PRISMA to ensure higher reporting quality. • The study used the GRADE approach to rate the certainty of evidence, which is an easy-to-understand approach for clinician. • Our study showed that the overall efficacy of Tanreqing injection or with western medicine for ATB cough is better than western medicine. [ABSTRACT FROM AUTHOR]
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- 2024
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394. Pharmacotherapy for adults with overweight and obesity: a systematic review and network meta-analysis of randomised controlled trials.
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Shi, Qingyang, Wang, Yang, Hao, Qiukui, Vandvik, Per Olav, Guyatt, Gordon, Li, Jing, Chen, Zhe, Xu, Shishi, Shen, Yanjiao, Ge, Long, Sun, Feng, Li, Ling, Yu, Jiajie, Nong, Kailei, Zou, Xinyu, Zhu, Siyi, Wang, Cong, Zhang, Shengzhao, Qiao, Zhi, and Jian, Zhongyu
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RANDOMIZED controlled trials , *DRUG therapy , *WEIGHT loss , *GLUCAGON-like peptide-1 agonists , *OBESITY - Abstract
Pharmacotherapy provides an option for adults with overweight and obesity to reduce their bodyweight if lifestyle modifications fail. We summarised the latest evidence for the benefits and harms of weight-lowering drugs. This systematic review and network meta-analysis included searches of PubMed, Embase, and Cochrane Library (CENTRAL) from inception to March 23, 2021, for randomised controlled trials of weight-lowering drugs in adults with overweight and obesity. We performed frequentist random-effect network meta-analyses to summarise the evidence and applied the Grading of Recommendations Assessment, Development, and Evaluation frameworks to rate the certainty of evidence, calculate the absolute effects, categorise interventions, and present the findings. The study was registered with PROSPERO, CRD 42021245678. 14 605 citations were identified by our search, of which 132 eligible trials enrolled 48 209 participants. All drugs lowered bodyweight compared with lifestyle modification alone; all subsequent numbers refer to comparisons with lifestyle modification. High to moderate certainty evidence established phentermine–topiramate as the most effective in lowering weight (odds ratio [OR] of ≥5% weight reduction 8·02, 95% CI 5·24 to 12·27; mean difference [MD] of percentage bodyweight change −7·98, 95% CI −9·27 to −6·69) followed by GLP-1 receptor agonists (OR 6·33, 95% CI 5·00 to 8·00; MD −5·79, 95% CI −6·34 to −5·25). Naltrexone–bupropion (OR 2·69, 95% CI 2·10 to 3·44), phentermine–topiramate (2·40, 1·68 to 3·44), GLP-1 receptor agonists (2·22, 1·74 to 2·84), and orlistat (1·71, 1·42 to 2·05) were associated with increased adverse events leading to drug discontinuation. In a post-hoc analysis, semaglutide, a GLP-1 receptor agonist, showed substantially larger benefits than other drugs with a similar risk of adverse events as other drugs for both likelihood of weight loss of 5% or more (OR 9·82, 95% CI 7·09 to 13·61) and percentage bodyweight change (MD −11·40, 95% CI −12·51 to −10·29). In adults with overweight and obesity, phentermine–topiramate and GLP-1 receptor agonists proved the best drugs in reducing weight; of the GLP-1 agonists, semaglutide might be the most effective. 1.3.5 Project for Disciplines of Excellence, West China Hospital, Sichuan University. [ABSTRACT FROM AUTHOR]
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- 2024
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395. Bacteremia following different oral procedures: Systematic review and meta‐analysis.
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Martins, Carolina C., Lockhart, Peter B., Firmino, Ramon T., Kilmartin, Catherine, Cahill, Thomas J., Dayer, Mark, Occhi‐Alexandre, Ingrid G. P., Lai, Honghao, Ge, Long, and Thornhill, Martin H.
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ORAL surgery , *MEDICAL information storage & retrieval systems , *DENTAL scaling , *DISEASE duration , *RESEARCH funding , *BACTEREMIA , *META-analysis , *ORAL hygiene , *SYSTEMATIC reviews , *MEDLINE , *MEDICAL databases , *TOOTH root planing , *MASTICATION , *DENTAL extraction , *TOOTH care & hygiene , *ACTIVITIES of daily living , *DENTAL prophylaxis - Abstract
To evaluate the timing, duration and incidence of bacteremia following invasive dental procedures (IDPs) or activities of daily living (ADL). Eight databases were searched for randomized (RCTs) and nonrandomized controlled trials (nRCTs) evaluating bacteremia before and after IDPs or ADL in healthy individuals. The risk of bias was assessed by RoB 2.0 and ROBINS‐I. For the meta‐analysis, the primary outcomes were the timing and duration of bacteremia. The secondary outcome was the incidence of bacteremia, measuring the proportion of patients with bacteremia within 5 min after the end of the procedure compared with baseline. We included 64 nRCTs and 25 RCTs. Peak bacteremia occurred within 5 min after the procedure and then decreased over time. Dental extractions showed the highest incidence of bacteremia (62%–66%), followed by scaling and root planing (SRP) (44%–36%) and oral health procedures (OHP) (e.g., dental prophylaxis and dental probing without SRP) (27%–28%). Other ADL (flossing and chewing) (16%) and toothbrushing (8%–26%) resulted in bacteremia as well. The majority of studies had some concerns RCTs or moderate risk of bias nRCTs. Dental extractions, SRP and OHP, are associated with the highest frequency of bacteremia. Toothbrushing, flossing, and chewing also caused bacteremia in lower frequency. [ABSTRACT FROM AUTHOR]
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- 2024
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396. Quality appraisal of clinical practice guidelines addressing massage interventions using the AGREE II instrument.
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Fan, Mingyue, Liu, Aolin, Lu, Taoying, Zhou, Xiaowen, Tian, Chen, Liu, Bingqing, Xie, Qianwen, Cai, Jianxiong, Yin, Lingjia, Ge, Long, and Wu, Darong
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MASSAGE , *INTRACLASS correlation , *CHINESE medicine - Abstract
Objective: The purpose of this study was to systematically evaluate the methodological quality of massage-related clinical practice guidelines (CPGs)/consensus on massage using the Appraisal of Guidelines Research and Evaluation (AGREE II) instrument and to summarize the current status of recommendations in the CPGs. Methods: The Chinese National Knowledge Infrastructure (CNKI), WanFang Data, China Science and Technology Journal Database (VIP), China Biology Medicine disc (CBM), PubMed, Embase, and guideline websites (such as the Chinese Medical Ace Base, the China Association of Chinese Medicine, the World Health Organization, Guideline International Network, National Institute for Health and Care Excellence, Scottish Intercollegiate Guidelines Network) were searched from inception to October 31, 2022. In addition, the reference lists of relevant studies were reviewed to identify domestic and overseas massage CPGs/consensus. The search terms adopted a combination of subject words and free words, mainly including traditional Chinese medicine, complementary therapies, Tuina, massage, manipulation, chiropractic/osteopathic, spinal, acupressure, guideline, and consensus. Two researchers independently completed the eligible records and extracted the data. Before the formal research, calibrations were performed twice on AGREE II, and all reviewers completed the pilot test three times until they understood and reached an agreement on the assessment items. Three researchers appraised the methodological quality of the included guidelines using the AGREE II instrument and calculated the overall intraclass correlation coefficient (ICC) of agreement. Results: The evaluation results showed that among the 49 eligible CPGs/consensus, 4 (8.2%) CPGs/consensus were considered "recommended", 15 (30.6%) CPGs/consensus were considered "recommended with modifications", and 30 (61.2%) CPGs/consensus were considered "not recommended", while the consensus was considered "not recommended". Generally, the scores in the six domains of the guidelines were all higher than the consensus. Evaluation results for the overall quality of 36 CPGs showed that 4 (11%) were "good quality", 15 (42%) were "sufficient quality" and 17 (47%) were "lower quality". The AGREE II quality scores of domains ranged from 0.30 to 0.75 ([ICC = 0.993, 95% CI (0.992, 0.995)]). The domain of scope and purpose (domain 1), with a median score of 0.75 (0.52~0.91), performed best in the guidelines with AGREE II, and stakeholder involvement (domain 2) [median 0.39 (0.31~0.56)] and application (domain 5) [median 0.30 (0.17~0.47] obtained lower scores. The consensus score of domain 1 was better at 26.0 (21.6~44.8), followed by rigor of development (domain 3) with a score of 18.0 (10.0~28.9). A total of 119 massage-related recommendations were extracted from 49 guidelines/consensuses, including "in favor" (102, 85.7%), "against" (9, 7.6%), and "did not make recommendations" (8, 6.7%). Conclusion: The overall quality of the included guidelines was low, and most of the guidelines were not "recommended". In future guideline updates, the existing evidence should be used, the professional composition of members of the expert group should be enriched, and patients' values and preferences should be fully considered. It is necessary to clearly propose recognizable recommendations and strengthen the rigor and standardization of guideline formulation. Thus, clear standard guidelines can be formulated to better guide clinical practice. [ABSTRACT FROM AUTHOR]
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- 2024
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397. The effects of exercise on insomnia disorders: An umbrella review and network meta-analysis.
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Tian, Chen, Wei, Yuanyuan, Xu, Meng, Liu, Jianing, Tong, Bo, Ning, Jinling, Wang, Yong, Wang, Yiyun, Estill, Janne, and Ge, Long
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SLEEP latency , *SLEEP duration , *SLEEP quality , *INSOMNIA , *AEROBIC exercises - Abstract
To summarize the evidence of various exercise modalities on population with insomnia disorders. PubMed, Embase, Cochrane Library, and Web of Science were searched for eligible studies published from inception to October 2022 and updated on September 2023. Systematic reviews with meta-analyses and randomized controlled trials designed to investigate the effect of various exercise modalities on population with insomnia were eligible. A total of 4 SRs with (very) low methodological quality and 1034 participants in 10 network meta-analyses explored the association between different types and intensity exercise modalities with insomnia disorders. Various exercise modalities could significantly improve total sleep time and sleep quality and alleviate insomnia severity. Compared to passive control, moderate aerobic exercise, moderate aerobic exercise combined with light intensity strength and mind-body exercise can improve sleep efficiency and reduce wake after sleep onset by objectively measured. Moderate intensity strength, light intensity strength and mind-body exercise can improve sleep efficiency subjectively measured; mind-body exercise can reduce sleep onset latency and wake time after sleep onset, and increase total sleep time; moderate aerobic exercise can reduce sleep onset latency. Moderate intensity strength, light intensity strength, mind body exercise and moderate aerobic exercise combined with light intensity strength can the severity of insomnia and improv sleep quality. Exercise had a positive effect on relief insomnia and improve sleep quality. Moderate aerobic exercise, mind-body exercise and moderate aerobic exercise combined with light intensity strength play an important role in improving the sleep quality in people with insomnia disorders. • Exercise has a positive effect on relieving the insomnia disorders. • Effect of various intensities, types of exercise in improving insomnia are different. • Exercise can alleviate the severity of insomnia and improve sleep quality. • The evidence on the effect of exercise on insomnia is low in quantity and quality. • In the future, more high-quality studies are needed. [ABSTRACT FROM AUTHOR]
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- 2024
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398. Interpretation of Update on Consolidated Framework for Implementation Research (CFIR 2.0)
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HUANG Jiajie, LAI Honghao, SUN Mingyao, LIU Jianing, ZHAO Weilong, TANG Wenjing, YANG Shuihua, PAN Bei, TIAN Jinhui, MA Xiaoting, GE Long
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implementation science ,consolidated framework for implementation research ,evidence-based practice ,interpretation ,Medicine - Abstract
The Consolidated Framework for Implementation Research (CFIR) is a commonly used theoretical framework in the field of implementation science, which helps researchers identify potential and actual influencing factors of the progress and effectiveness of implementation. CFIR was firstly proposed in 2009 with a 13-year history of development. In 2022, the CFIR development team updated CFIR based on user feedback, adding 21 constructs and 19 subconstructs to the original framework structure, adjusting some of the constructs and redefining certain concepts, resulted in CFIR 2.0 which is more practical and general. This paper aims to provide a reference for domestic researchers to understand and use CFIR 2.0 by reviewing and introducing the development background, origin, and update content of CFIR.
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- 2023
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399. White rice consumption and risk of cardiometabolic and cancer outcomes: A systematic review and dose-response meta-analysis of prospective cohort studies.
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Lai, Honghao, Sun, Mingyao, Liu, Yafei, Zhu, Hongfei, Li, Mengting, Pan, Bei, Wang, Qi, Yang, Qiuyu, Cao, Xiao, Tian, Chen, Lu, Yao, Song, Xuping, Ding, Guowu, Tian, Jinhui, Yang, Kehu, and Ge, Long
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DISEASE risk factors , *TYPE 2 diabetes , *CANCER prognosis , *RICE , *CARDIOVASCULAR diseases risk factors , *BROWN rice - Abstract
White rice is the food more than half of the world's population depends on. White rice intake can significantly increase the glycemic load of consumers and bring some adverse health effects. However, the quality of evidence implicating white rice in adverse health outcomes remains unclear. To evaluate the association between white rice consumption and the risk of cardiometabolic and cancer outcomes, a systematic review and dose-response meta-analysis of the relevant publications were performed. Twenty-three articles including 28 unique prospective cohorts with 1,527,198 participants proved eligible after a comprehensive search in four databases. For the risk of type 2 diabetes mellitus (T2DM), the pooled RR was 1.18 (16 more per 1000 persons) for comparing the highest with the lowest category of white rice intake, with moderate certainty evidence. Females presented a higher risk (23 more per 1000 persons) in subgroup analysis. And every additional 150 grams of white rice intake per day was associated with a 6% greater risk of T2DM (5 more per 1000 persons) with a linear positive trend. We found no significant associations between white rice intake and risk of cardiovascular diseases (CVD), CVD mortality, cancer, and metabolic syndrome. In conclusion, moderate certainty evidence demonstrated that white rice intake was associated with T2DM risk, with a linear positive trend. However, low to very low certainty of evidence suggested that no substantial associations were found between white rice intake and other cardiometabolic and cancer outcomes. More cohorts are needed to strength the evidence body. [ABSTRACT FROM AUTHOR]
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- 2023
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400. Molnupiravir for the treatment of non-severe COVID-19: a systematic review and meta-analysis of 14 randomized trials with 34 570 patients–authors' response.
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Sun, Mingyao, Lai, Honghao, Zhang, Zhigang, and Ge, Long
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COVID-19 treatment , *MOLNUPIRAVIR , *SEQUENTIAL analysis , *ARTIFICIAL respiration , *MORTALITY - Abstract
A systematic review and meta-analysis of 14 randomized trials with 34,570 patients was conducted to evaluate the efficacy of molnupiravir for the treatment of non-severe COVID-19. The results showed that molnupiravir was associated with a reduction in the risk of hospitalization, risk of mechanical ventilation, and time to symptom resolution. The review also found that molnupiravir was most effective in non-severe patients, particularly those at highest risk of hospitalization. However, no significant differences were found in adverse events, all-cause mortality, rate and time to viral clearance, or duration of hospitalization. The authors acknowledge the limitations of their review and emphasize the need for more large-sample studies to clarify the true efficacy of molnupiravir. They also express the importance of exploring other drugs that have the potential to treat COVID-19 and improve important outcomes such as mortality and viral clearance. [Extracted from the article]
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- 2023
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