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1.
Ann Anat ; 225: 42-47, 2019 Sep.
Article in English | MEDLINE | ID: mdl-30930197

ABSTRACT

The growing influence and importance of internationalization in higher education, especially in medical education, inspired anatomists at Columbia University New York, USA and at the Martin Luther University Halle-Wittenberg, Germany, to start a novel international preclinical collaboration project. As part of the anatomy dissection course a group of volunteer medical students from Halle dissected selected areas of the human body with the help of an English, illustrated, iPad-run dissection script (American Dissector). Meanwhile the rest of the students worked with a traditional German text-based dissector. Additionally, participating German students were matched with US students, with whom they connected via video-conferencing and discussed subjects like differences between their health care systems, structure and content of the anatomy course and the differences in their medical education systems. Questionnaires were sent for feedback and checklists confirmed dissection findings. Results indicated that the American Dissector was successfully shared internationally. The majority (62%) found it easier to find structures using the American Dissector compared to the standard dissector and also 62% needed the atlas two times less when using the American Dissector. Furthermore, students enjoyed their interaction with their international peers and the vast majority (77%) wished there were more interactions like this in the medical curriculum. This publication describes an approach to embed internationalization in the preclinical medical curriculum based in the gross anatomy course in a German Medical school, located in East Germany. Considering its history as a former German Democratic Republic faculty this is a meaningful step towardglobalization of medical education in this part of Germany.


Subject(s)
Anatomy/education , Internationality , Schools, Medical/organization & administration , Students, Medical/classification , Checklist , Computers , Computers, Handheld , Dissection/education , Female , Germany , Germany, East , Humans , Intersectoral Collaboration , Language , Male , Manuals as Topic , New York City , Pilot Projects , Surveys and Questionnaires , Videoconferencing , Young Adult
2.
Bone Marrow Transplant ; 48(1): 46-9, 2013 Jan.
Article in English | MEDLINE | ID: mdl-22609886

ABSTRACT

Cyclosporine (CsA) and MTX are commonly used for GVHD prophylaxis in pediatric allo-SCT. Mucositis and hepatic toxicity frequently restrict the delivery of the fourth dose of MTX. Folinic acid (FA) may ameliorate MTX toxicity. We conducted a retrospective chart review of all pediatric patients who received CsA and MTX for GVHD prophylaxis from January 2000 to July 2010. Patients treated before July 2007 (N=29) did not receive FA and those treated from July 2007 onward did receive FA (N=18). Patients who received FA were significantly more likely to receive day +11 MTX (odds ratio (OR) 10.42, 95% confidence interval (CI): 1.21-262.27) but there was no significant difference in Grade III-IV GVHD between the two groups (OR 1.15, 95% CI: 0.08-18.14). FA did not impact relapse-free survival (RFS) (P=0.82). Increased likelihood of receiving day +11 MTX suggests that FA ameliorates MTX toxicity, such as severe mucositis. FA administration for MTX GVHD prophylaxis should be studied in a prospective, randomized fashion.


Subject(s)
Folic Acid Antagonists/adverse effects , Graft vs Host Disease/prevention & control , Immunosuppressive Agents/adverse effects , Leucovorin/therapeutic use , Methotrexate/adverse effects , Stem Cell Transplantation/adverse effects , Vitamin B Complex/therapeutic use , Adolescent , Chemical and Drug Induced Liver Injury/prevention & control , Child , Child, Preschool , Cyclosporine/adverse effects , Cyclosporine/therapeutic use , Drug Monitoring , Drug Therapy, Combination/adverse effects , Female , Folic Acid Antagonists/administration & dosage , Folic Acid Antagonists/therapeutic use , Graft vs Host Disease/etiology , Graft vs Host Disease/physiopathology , Humans , Immunosuppressive Agents/administration & dosage , Immunosuppressive Agents/therapeutic use , Infant , Male , Methotrexate/administration & dosage , Methotrexate/therapeutic use , Mucositis/chemically induced , Mucositis/physiopathology , Mucositis/prevention & control , Retrospective Studies , Severity of Illness Index , Survival Analysis , Transplantation, Homologous
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