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1.
Am J Pharm Educ ; 74(10): 190, 2010 Dec 15.
Article in English | MEDLINE | ID: mdl-21436931

ABSTRACT

OBJECTIVES: To determine pharmacy students' perceptions of a required research project in a doctor of pharmacy curriculum. METHODS: A survey instrument was administered to senior pharmacy students to determine their perceptions of the project advisor and overall project experience and their postgraduation employment plans. RESULTS: Two-hundred twenty-nine (81.5%) students completed a survey instrument. The majority agreed or strongly agreed that the project provided a valuable learning experience (88.2%), provided a competitive advantage for postgraduate job opportunities (73.2%), and should be a continued graduation requirement (74.2%). Respondents with plans for a residency or fellowship were more likely than those entering a community or hospital/institutional pharmacy to agree that completion of the project made them more qualified or marketable and should be continued as a graduation requirement (p < 0.05). CONCLUSIONS: A required research project was perceived by pharmacy students to be a beneficial experience. Students pursuing residency or fellowship were more likely to feel the project was beneficial than students entering the workforce.


Subject(s)
Biomedical Research/methods , Curriculum , Perception , Students, Pharmacy/psychology , Health Surveys/methods , Humans , Problem-Based Learning/methods
2.
Pharmacotherapy ; 29(2): 227-35, 2009 Feb.
Article in English | MEDLINE | ID: mdl-19170591

ABSTRACT

Multiple sclerosis is a chronic inflammatory and demyelinating disease of the central nervous system and the leading cause of neurologic disability in young adults. Established therapies, such as interferon and glatiramer, have only partial effects, and they offer limited or no effect on the progression of multiple sclerosis. The etiology of multiple sclerosis is unclear; however, the disease is presumed to be a T-cell-mediated autoimmune disease influenced by genetic and environmental factors. Therefore, targeting of lymphocytes may be a promising means of therapy for multiple sclerosis. Daclizumab is a humanized monoclonal antibody approved for use in preventing renal allograft rejection. The agent is under investigation in phase II trials for the treatment of multiple sclerosis and has demonstrated positive clinical outcomes, including decreased relapse rates. Adverse events included urinary tract infections, respiratory tract infections, paresthesias, mild leukopenia, transient elevations in liver enzyme and bilirubin levels, rash, postinfusion reactions (fever), lymphadenopathy, transient thrombocytopenia, and nausea. Daclizumab may be an alternative or add-on therapy when conventional immunomodulators fail or when existing approved therapies cannot be used. Besides ongoing phase II trials, additional phase II or III trials are required to determine the extended benefits of the agent, as well as clinical outcomes.


Subject(s)
Antibodies, Monoclonal/administration & dosage , Immunoglobulin G/administration & dosage , Immunosuppressive Agents/administration & dosage , Multiple Sclerosis/drug therapy , Antibodies, Monoclonal/adverse effects , Antibodies, Monoclonal/pharmacokinetics , Antibodies, Monoclonal, Humanized , Clinical Trials as Topic , Daclizumab , Drug Delivery Systems , Drug Therapy, Combination , Humans , Immunoglobulin G/adverse effects , Immunosuppressive Agents/adverse effects , Immunosuppressive Agents/pharmacokinetics , Lymphocytes/drug effects , Lymphocytes/metabolism , Magnetic Resonance Imaging , Multiple Sclerosis/physiopathology
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