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Diagnosis and management of endometrial hyperplasia: A UK national audit of adherence to national guidance 2012–2020

Author summary Why was this study done? New national guidance was introduced in the United Kingdom with recommendations for the care and surveillance of people with endometrial hyperplasia (EH). Comparing patterns of care with these recommendations has identified opportunities for improvement. What did the researchers do and find? After the guidance, medical treatment of non-atypical hyperplasia increased and more patients achieved histological regression, avoiding hysterectomy. Surveillance of hyperplasia for those who do not undergo hysterectomy could be improved. A greater proportion of women with atypia diagnosed in 2020 commenced medical management and fewer underwent hysterectomy; the impact of the pandemic on care must be considered as a contributory factor towards this. What do these findings mean? This work has identified where the care of patients with EH diverged from recommended guidance. Clinicians may use these findings to review their local care pathways and qu ....

United Kingdom , Green Top , United States , City Of , Royal College Of Obstetricians , Stata Corp , Clinical Research Training Fellowship , British Society For Gynaecological Endoscopy , World Health Organisation , American College Of Obstetricians , Centre For Reproductive Health , Society Of Obstetricians , Research Collaborative In Obstetrics , Health Research Authority , Group Authors , Green Top Guide , United Kingdom Wide , Edinburgh Usher Institute , Population Health Sciences , Creative Commons Attribution License , Health Research , Research Training Fellowship , Reproductive Health , British Society , American College , Gynaecological Endoscopy ,

Comparative effectiveness of GLP-1 receptor agonists on glycaemic control, body weight, and lipid profile for type 2 diabetes: systematic review and network meta-analysis

Objective To evaluate the comparative efficacy and safety of glucagon-like peptide-1 receptor agonists (GLP-1RAs) on glycaemic control, body weight, and lipid profile in adults with type 2 diabetes.

Design Systematic review and network meta-analysis.

Data sources PubMed, Web of Science, Cochrane Central Register of Controlled Trials (CENTRAL), and Embase from database inception to 19 August 2023.

Eligibility criteria for selecting studies Eligible randomised controlled trials enrolled adults with type 2 diabetes who received GLP-1RA treatments and compared effects with placebo or any GLP-1RA drug, with a follow-up duration of at least 12 weeks. Trials with a crossover design, non-inferiority studies comparing GLP-1RA and other drug classes without a placebo group, using withdrawn drugs, and non-English studies were deemed ineligible.

Results 76 eligible trials involving 15 GLP-1RA drugs and 39 246 participants were included in this network meta-analysis; a ....

United States , Chong Zhi Wang , Delong Li , Haiqiang Yao , Manqi Zhang , Yuqi Wu , Drug Administration , Cinema Confidence In Network Meta , National Natural Science Foundation Of China , Stata Corp , European Association For The Study Of Diabetes , University Of Chinese Medicine Talent Research , American Diabetes Association , Research Funds For The Central Universities , Zhi Wang , Cochrane Central Register , Controlled Trials , European Association , Clarivate Analytics , Webplot Digitizer , Network Meta Analysis , National Natural Science Foundation , Fundamental Research Funds , Central Universities , Beijing University , Open Access ,

Vitamin D supplementation and major cardiovascular events: D-Health randomised controlled trial

Objective To investigate whether supplementing older adults with monthly doses of vitamin D alters the incidence of major cardiovascular events.

Design Randomised, double blind, placebo controlled trial of monthly vitamin D (the D-Health Trial). Computer generated permuted block randomisation was used to allocate treatments.

Setting Australia from 2014 to 2020.

Participants 21 315 participants aged 60-84 years at enrolment. Exclusion criteria were self-reported hypercalcaemia, hyperparathyroidism, kidney stones, osteomalacia, sarcoidosis, taking >500 IU/day supplemental vitamin D, or unable to give consent because of language or cognitive impairment.

Intervention 60 000 IU/month vitamin D3 (n=10 662) or placebo (n=10 653) taken orally for up to five years. 16 882 participants completed the intervention period: placebo 8270 (77.6%); vitamin D 8552 (80.2%).

Main outcome measures The main outcome for this analysis was the occurrence of a maj ....

Northern Territory , United States , North Carolina , Davidc Whiteman , Penelopem Webb , Brucek Armstrong , Rachele Neale , Mary Waterhouse , Peterr Ebeling , Sabbirt Rahman , Alisonj Venn , Duarte Romero , Catherine Baxter , Michaelg Kimlin , Donalds Mcleod , Gunter Hartel , Queensland Health , Research Council , Women Health Initiative Trial , University Of Western Australia , Stata Corp , National Collaborative Research Infrastructure Strategy , National Health , R Foundation For Statistical Computing , Bridie Thompson , D Health Trial ,

Semi-field evaluation of the space spray efficacy of Fludora Co-Max EW against wild insecticide-resistant Aedes aegypti and Culex quinquefasciatus mosquito populations from Abidjan, Côte d'Ivoire | Parasites & Vectors

Space spraying of insecticides is still an important means of controlling Aedes and Culex mosquitoes and arboviral diseases. This study evaluated the space spray efficacy of Fludora Co-Max EW, (water-based insecticide space spray combining flupyradifurone and transfluthrin with film forming aqueous spray technology (FFAST)), against wild insecticide-resistant Aedes aegypti and Culex quinquefasciatus mosquitoes from Abidjan, Côte d’Ivoire, compared with K-Othrine EC (deltamethrin-only product), in small-scale field trials. Wild Ae. aegypti and Cx. quinquefasciatus mosquito larvae were collected in Abidjan, Côte d’Ivoire from August to December 2020. Mosquito larvae were reared in the laboratory until the adult stage. Fludora Co-Max EW and K-Othrine EC were tested against emerged adult females (F0 generation) using ultra-low volume cold fogging (ULV) and thermal fogging (TF) delivery technology, both outdoors and indoors in Agboville, Côte d’Ivoi ....

Coted Ivoire , United Kingdom , United States , Baden Wüberg , Swingtec Gmb , Bayer Ag , Stata Corp , Microsoft Corp , Omicron Group , Fludora Co Max , Swingtec Gmbh , East Windsor , For Fuldora Co Max , Wilkw Test , College Station ,