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2.
Acad Med ; 94(6): 819-825, 2019 06.
Article in English | MEDLINE | ID: mdl-30801270

ABSTRACT

Medical educators have not reached widespread agreement on core content for a U.S. medical school curriculum. As a first step toward addressing this, five U.S. medical schools formed the Robert Wood Johnson Foundation Reimagining Medical Education collaborative to define, create, implement, and freely share core content for a foundational medical school course on microbiology and immunology. This proof-of-concept project involved delivery of core content to preclinical medical students through online videos and class-time interactions between students and facilitators. A flexible, modular design allowed four of the medical schools to successfully implement the content modules in diverse curricular settings. Compared with the prior year, student satisfaction ratings after implementation were comparable or showed a statistically significant improvement. Students who took this course at a time point in their training similar to when the USMLE Step 1 reference group took Step 1 earned equivalent scores on National Board of Medical Examiners-Customized Assessment Services microbiology exam items. Exam scores for three schools ranged from 0.82 to 0.84, compared with 0.81 for the national reference group; exam scores were 0.70 at the fourth school, where students took the exam in their first quarter, two years earlier than the reference group. This project demonstrates that core content for a foundational medical school course can be defined, created, and used by multiple medical schools without compromising student satisfaction or knowledge. This project offers one approach to collaboratively defining core content and designing curricular resources for preclinical medical school education that can be shared.


Subject(s)
Curriculum/trends , Education, Medical, Undergraduate/legislation & jurisprudence , Interdisciplinary Placement/methods , Schools, Medical/legislation & jurisprudence , Allergy and Immunology/education , Educational Measurement/methods , Humans , Interdisciplinary Placement/trends , Microbiology/education , Personal Satisfaction , Schools, Medical/standards , Students, Medical/statistics & numerical data , United States/epidemiology , Videotape Recording/methods
3.
J Palliat Med ; 18(4): 338-49, 2015 Apr.
Article in English | MEDLINE | ID: mdl-25549065

ABSTRACT

BACKGROUND: Recent focus on palliative and end-of-life care has led medical schools worldwide to enhance their palliative care curricula. OBJECTIVE: The objective of the study was to describe recent curricular innovations in palliative care for medical students, evaluate the quality of studies in the field, and inform future research and curricular design. METHODS: The authors searched Medline, Scopus, and Educational Resource Information Center (ERIC) for English-language articles published between 2007 and 2013 describing a palliative care curriculum for medical students. Characteristics of the curricula were extracted, and methodological quality was assessed using the Medical Education Research Study Quality Instrument (MERSQI). RESULTS: The sample described 48 curricula in 12 countries. Faculty were usually interdisciplinary. Palliative care topics included patient assessment, communication, pain and symptom management, psychosocial and spiritual needs, bioethics and the law, role in the health care system, interdisciplinary teamwork, and self-care. Thirty-nine articles included quantitative evaluation, with a mean MERSQI score of 9.9 (on a scale of 5 to 18). The domain most likely to receive a high score was data analysis (mean 2.51 out of 3), while the domains most likely to receive low scores were validity of instrument (mean 1.05) and outcomes (mean 1.31). CONCLUSIONS: Recent innovations in palliative care education for medical students represent varied settings, learner levels, instructors, educational modalities, and palliative care topics. Future curricula should continue to incorporate interdisciplinary faculty. Studies could be improved by integrating longitudinal curricula and longer-term outcomes; collaborating across institutions; using validated measures; and assessing higher-level outcomes including skills, behaviors, and impact on patient care.


Subject(s)
Education, Medical, Undergraduate/standards , Palliative Care/standards , Terminal Care/standards , Curriculum/standards , Curriculum/trends , Databases, Bibliographic , Education, Medical, Undergraduate/trends , Humans , Internationality , Palliative Care/methods , Palliative Care/trends , Terminal Care/methods , Terminal Care/trends
4.
Diabetes ; 63(2): 688-700, 2014 Feb.
Article in English | MEDLINE | ID: mdl-24186867

ABSTRACT

Maternal obesity and gestational diabetes mellitus (GDM) are associated with obesity and diabetes risk in offspring. We tested whether maternal insulin resistance, which frequently coexists with GDM and obesity, could independently contribute to dysregulation of offspring metabolism. Female mice haploinsufficient for insulin receptor substrate-1 (IRS1-het) are hyperinsulinemic and insulin resistant during pregnancy, despite normal plasma glucose and body weight, and thus serve as a model of isolated maternal insulin resistance. Wild-type (WT) offspring of IRS1-het dams insulin resistance-exposed [IR-exposed] were compared with WT offspring of WT dams. Despite no differences in adiposity, male IR-exposed pups were glucose intolerant (P = 0.04) and hyperinsulinemic (1.3-fold increase, P = 0.02) by 1 month of age and developed progressive fasting hyperglycemia. Moreover, male IR-exposed pups challenged with high-fat diet exhibited insulin resistance. Liver lipidomic analysis of 3-week-old IR-exposed males revealed increases in the 16:1n7 fraction of several lipid classes, suggesting increased Scd1 activity. By 6 months of age, IR-exposed males had increased lipid accumulation in liver as well as increased plasma refed fatty acids, consistent with disrupted lipid metabolism. Our results indicate that isolated maternal insulin resistance, even in the absence of hyperglycemia or obesity, can promote metabolic perturbations in male offspring.


Subject(s)
Dyslipidemias/etiology , Glucose Intolerance/etiology , Hyperinsulinism/etiology , Insulin Resistance/physiology , Aging , Animals , Blood Glucose , Body Weight , Female , Gene Expression Regulation , Haplotypes , Insulin Receptor Substrate Proteins/genetics , Insulin Receptor Substrate Proteins/metabolism , Male , Mice , Pregnancy , Pregnancy Complications/metabolism , Prenatal Exposure Delayed Effects
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