Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 7 de 7
Filter
1.
Acad Med ; 91(7): 898-9, 2016 07.
Article in English | MEDLINE | ID: mdl-27351818
2.
Child Maltreat ; 21(2): 113-24, 2016 05.
Article in English | MEDLINE | ID: mdl-26928410

ABSTRACT

Exposure to childhood trauma is a major public health concern and is especially prevalent among children in the child welfare system (CWS). State and tribal CWSs are increasingly focusing efforts on identifying and serving children exposed to trauma through the creation of trauma-informed systems. This evaluation of a statewide initiative in Connecticut describes the strategies used to create a trauma-informed CWS, including workforce development, trauma screening, policy change, and improved access to evidence-based trauma-focused treatments during the initial 2-year implementation period. Changes in system readiness and capacity to deliver trauma-informed care were evaluated using stratified random samples of child welfare staff who completed a comprehensive assessment prior to (N = 223) and 2 years following implementation (N = 231). Results indicated significant improvements in trauma-informed knowledge, practice, and collaboration across nearly all child welfare domains assessed, suggesting system-wide improvements in readiness and capacity to provide trauma-informed care. Variability across domains was observed, and frontline staff reported greater improvements than supervisors/managers in some domains. Lessons learned and recommendations for implementation and evaluation of trauma-informed care in child welfare and other child-serving systems are discussed.


Subject(s)
Child Abuse/therapy , Child Health Services/organization & administration , Child Welfare , Social Work/organization & administration , Wounds and Injuries/psychology , Wounds and Injuries/therapy , Child , Child Abuse/psychology , Connecticut , Health Plan Implementation , Humans
5.
Acad Med ; 82(5): 479-85, 2007 May.
Article in English | MEDLINE | ID: mdl-17457072

ABSTRACT

The popularity of problem-based learning (PBL) reflects medical educators' recognition that case study can enhance the preclinical medical school curriculum. However, the PBL method itself has features, particularly its reliance on small-group work with tutor-facilitators, that are expensive to implement and that limit the potential educational value of case study. The author systematically analyzes specific aspects of the PBL methodology and concludes that the PBL approach misuses the faculty, tends to compromise the authenticity of cases, and results in an unnecessarily varied and impoverished educational experience for students. Approaches to case study with different assumptions need to be devised. A model is proposed that shifts the goal of case study from development of problem-solving skills to development of ideas that allow meaningful engagement in sophisticated discussions of medicine. In this model, the method shifts from self-directed learning to independent study guided by the expertise of the faculty. One possible approach to case study based on this model is briefly described. It consists of reading published cases from the medical literature, with analysis and discussion of the cases led by faculty experts in large-group format. The approach immerses students in an authentic, state-of-the-art discussion of medicine and is easily incorporated into any curriculum structure at limited cost. The author argues that, contrary to the claims of proponents, the glass is "mostly empty" for PBL and that we can generate the higher-level discussion that case study merits only by moving away from PBL's extraneous assumptions.


Subject(s)
Education, Medical, Undergraduate/methods , Faculty, Medical , Models, Educational , Problem-Based Learning/methods , Adult , Group Processes , Humans , Professional Role , Program Evaluation , Schools, Medical , Students, Medical/psychology , Time Factors
6.
J Nephrol ; 15(6): 713-5, 2002.
Article in English | MEDLINE | ID: mdl-12495290

ABSTRACT

We report the first documented case of X-linked chronic granulomatous disease (CGD) in association with IgA nephropathy in a 22 year old male with multiple soft tissue abscesses. The case highlights the potential role of staphylococcal infections in the pathogenesis of IgA nephropathy and suggests the hypothesis that the neutrophil defect in CGD predisposes to such infections which may trigger IgA immune complex formation.


Subject(s)
Glomerulonephritis, IGA/complications , Glomerulonephritis, IGA/pathology , Granulomatous Disease, Chronic/complications , Granulomatous Disease, Chronic/pathology , Adult , Biopsy, Needle , Follow-Up Studies , Glomerulonephritis, IGA/diagnosis , Granulomatous Disease, Chronic/diagnosis , Humans , Immunohistochemistry , Male , Risk Assessment , Severity of Illness Index
7.
Ren Fail ; 24(3): 249-58, 2002 May.
Article in English | MEDLINE | ID: mdl-12166692

ABSTRACT

Isolated perfusion of the rat kidney causes hypoxic damage in the cells of the thick ascending limb of the loop of Henle. The cell damage is driven by active solute transport, which generates an imbalance of oxygen supply and demand. This injury is paradoxically prevented by adding the mitochondrial electron transport inhibitors rotenone or antimycin to the perfusion media. The present study shows that rotenone and antimycin decrease production of hydrogen peroxide in the thick ascending limb during perfusion. The findings support the hypothesis that the injury in this model is dependent on mitochondrial electron flow and suggest that mitochondrial electron flow, driven by the work of active solute transport in the presence of limited oxygen availability, may result in the generation of toxic oxygen metabolites.


Subject(s)
Hypoxia/metabolism , Kidney Diseases/metabolism , Loop of Henle/injuries , Loop of Henle/metabolism , Oxygen/metabolism , Amitrole/pharmacology , Animals , Catalase/drug effects , Cell Membrane/drug effects , Cell Membrane/enzymology , Chemotherapy, Cancer, Regional Perfusion , Disease Models, Animal , Dose-Response Relationship, Drug , Electron Transport/physiology , Enzyme Inhibitors/pharmacology , Epithelial Cells/drug effects , Epithelial Cells/ultrastructure , Mitochondria/drug effects , Mitochondria/metabolism , Rats , Rotenone/pharmacology , Uncoupling Agents/pharmacology
SELECTION OF CITATIONS
SEARCH DETAIL
...