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Total 2707 results found since Jan 2013.
Pro-Con Debate: Consideration of Race, Ethnicity, and Gender Is Detrimental to Successful Mentorship
Anesth Analg. 2023 Oct 1;137(4):747-753. doi: 10.1213/ANE.0000000000006502. Epub 2023 Sep 5.ABSTRACTAnesthesiology remains a specialty with low representation of women or members of racial and ethnic groups considered underrepresented in medicine (UiM). In the United States, women account for 33% of anesthesiology residents, while physicians identifying as Black, African American, Latinx, American Indian, or Alaska Native account for approximately 10%. Underrepresentation of these groups is even more pronounced in academic anesthesiology, especially at the senior ranks and roles, such as department chairs. Leaders in the f...
Source: Anesthesia and Analgesia - September 15, 2023 Category: Anesthesiology Authors: Alicia B Barclay Kenneth Moran Dmitry Tumin Kimberley R Nichols Source Type: research
Enhancing Healthcare Through Industry-Specific Large Language Models
The following is a guest article by Tisson Mathew, Founder and CEO at SkyPoint AI
Why Large Language Models Trained on Industry Context are Essential for Effective Generative AI in the Healthcare Space
Ask ChatGPT an important but complicated healthcare-related question, and you might very well get a wrong—and potentially dangerous—answer. Navigating the complexities of medical data, regulations, and patient care can place demands on generative AI technologies that can’t be fulfilled. But there is a way to take full advantage of the power of GenAI — with industry-specific LLMs that are securely supplied wit...
Source: EMR and HIPAA - September 13, 2023 Category: Information Technology Authors: Guest Author Tags: AI/Machine Learning C-Suite Leadership Health IT Company Healthcare IT Hospital - Health System AI Companion DataStax EMR Generative AI Healthcare AI Healthcare AI Ethics Healthcare ChatGPT Healthcare LLMs Large Language Models Source Type: blogs
A retrospective study on newborn screening for metabolic disorders
Bioinformation. 2022 Dec 31;18(12):1122-1125. doi: 10.6026/973206300181122. eCollection 2022.ABSTRACTThe process of testing newborn infants for hormonal, genetic, metabolic, and other disorders is known as newborn screening (NSB). Newborn screening is essential for detecting, diagnosing, and treating disorders that could save serious consequences for a newborn's health. Congenital Hypothyroidism (CH), Cystic Fibrosis (CF), Glucose-6-phosphate dehydrogenase (G6PD) deficiency, and Profound Biotinidase deficiency (BD) are common disorders in India. A retrospective analysis of the results of NBS by Cord blood spots was perform...
Source: Bioinformation - September 13, 2023 Category: Bioinformatics Authors: Karam Chandrajit Singh Prabhkiran Dhillon Thushara Thulaseedharan Source Type: research
Infections due to Salmonella sp. in children with chronic granulomatous disease: Our experience from North India
Clin Immunol. 2023 Sep 11:109769. doi: 10.1016/j.clim.2023.109769. Online ahead of print.ABSTRACTInfections with non-typhoidal Salmonella sp. have been documented in children with chronic granulomatous disease (CGD), but the prevalence of salmonella infection in children with CGD in underdeveloped countries is unknown. We assessed the clinical profiles of CGD patients diagnosed at our tertiary care centre in north India and had Salmonella sp.infections. We found three patients with Salmonella sp. bloodstream infections (2-proven, 1-probable) among the 99 CGD patients. After receiving cotrimoxazole prophylaxis following a C...
Source: Clinical Immunology - September 13, 2023 Category: Allergy & Immunology Authors: Suprit Basu Pandiarajan Vignesh K Prithiviraj Pallavi L Nadig Aravind Sekar Amit Rawat Source Type: research
A retrospective study on newborn screening for metabolic disorders
Bioinformation. 2022 Dec 31;18(12):1122-1125. doi: 10.6026/973206300181122. eCollection 2022.ABSTRACTThe process of testing newborn infants for hormonal, genetic, metabolic, and other disorders is known as newborn screening (NSB). Newborn screening is essential for detecting, diagnosing, and treating disorders that could save serious consequences for a newborn's health. Congenital Hypothyroidism (CH), Cystic Fibrosis (CF), Glucose-6-phosphate dehydrogenase (G6PD) deficiency, and Profound Biotinidase deficiency (BD) are common disorders in India. A retrospective analysis of the results of NBS by Cord blood spots was perform...
Source: Bioinformation - September 13, 2023 Category: Bioinformatics Authors: Karam Chandrajit Singh Prabhkiran Dhillon Thushara Thulaseedharan Source Type: research
Mutation spectrum and enzyme profiling of G6PD deficiency in neonates of north India: a prospective study
J Genet. 2023;102:40.ABSTRACTGlucose-6-phosphate dehydrogenase (G6PD) deficiency is a common X-linked disorder with well-established clinical and allelic heterogeneity and ethnic disparity. With ~390,000 annual births with G6PD deficiency in India, it emerges as the most predictable and preventable inbornmetabolic error. Disease prevalence and mutation spectrum have been reasonably reported fromcentral, western and southern parts of India and are mostly retrospective studies.Although prevalence data fromnorth India is available, there is paucity of data on the mutation spectrum and genotype-phenotype correlation (GxP). Thu...
Source: Journal of Genetics - September 7, 2023 Category: Genetics & Stem Cells Authors: Upasana Bhattacharyya Preeti Deswal Sunil Kumar Polipalli Diksha Sharma Manpreet Kaur Serb-Nbs Initiative Group Seema Kapoor B K Thelma Source Type: research
