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1.
J Med Educ Curric Dev ; 7: 2382120520980473, 2020.
Article in English | MEDLINE | ID: mdl-33354625

ABSTRACT

There are many methods to assess resident competency. In this report the author describes an experience that strongly suggests the superiority of direct observation compared to other methods. Literature comparing direct observation to other methods is cited. In addition ways to create time for direct observation and how to promote wider use of direct observation are discussed.

2.
Am J Med Sci ; 353(2): 116-118, 2017 Feb.
Article in English | MEDLINE | ID: mdl-28183410

ABSTRACT

The promotion of change and growth within medical education is oftentimes the result of a complex mix of societal, cultural and economic forces. Graduate medical education in internal medicine is not immune to these forces. Several entities and organizations can be identified as having a major influence on internal medicine training and graduate medical education as a whole. We have reviewed how this is effectively accomplished through these entities and organizations. The result is a constantly changing and dynamic landscape for internal medicine training.


Subject(s)
Education, Medical, Graduate , Internal Medicine/education , Politics , Humans
5.
Ann Intern Med ; 144(12): 920-6, 2006 Jun 20.
Article in English | MEDLINE | ID: mdl-16785480

ABSTRACT

There has been considerable change in the practice of internal medicine in the past quarter century, including the rise of specialization, increasing time pressure, the hospitalist movement, and the rapidly changing responsibilities of internists in inpatient and outpatient settings. Training programs have not adequately responded to these trends, and there is a consensus that the residency education system urgently needs redesign.


Subject(s)
Internal Medicine/education , Internship and Residency , Models, Educational , Ambulatory Care , Curriculum , Education, Medical, Graduate/economics , Faculty, Medical/standards , Financing, Organized , Hospitals, Teaching/economics , Hospitals, Teaching/standards , Humans , Inpatients , Internship and Residency/economics , Internship and Residency/standards , Quality of Health Care , United States
6.
Am J Hematol ; 71(3): 184-90, 2002 Nov.
Article in English | MEDLINE | ID: mdl-12410573

ABSTRACT

We studied 28 patients with accelerated phase chronic myelogenous leukemia (CML) who were enrolled on the Novartis expanded access study 114. Diagnosis of accelerated phase CML was based on karyotypic evolution (n = 9) and hematologic criteria (n = 18). All patients were begun on 600 mg/day of imatinib mesylate. Dose reductions to 400 mg/day and then 300 mg/day were prescribed for an absolute neutrophil count (ANC) of <0.5/microl or a platelet count of <20,000/microl. Twenty-seven of the 28 patients continued treatment for a median of 34 weeks. Eleven patients developed thrombocytopenia following an average of 8.4 +/- 1.4 weeks of therapy. The onset of thrombocytopenia was associated with disease progression in one patient and a decline in bone marrow megakaryocytes in the other 10. Nine patients recovered to a platelet count of >20,000/microl after an average of 19.7 +/- 1.8 weeks. Patients who developed thrombocytopenia had a longer duration of disease (9.39 vs. 4.35 years; P < 0.01) and were more likely to be diagnosed with accelerated phase CML by hematologic criteria. Hematologic responses in patients with and without thrombocytopenia were comparable; however, 31.3% of patients without thrombocytopenia had a complete cytogenetic response compared to none of those with thrombocytopenia. Grade III-IV thrombocytopenia is common in accelerated phase CML and may be a marker for the inability to achieve cytogenetic response using single agent imatinib mesylate.


Subject(s)
Antineoplastic Agents/adverse effects , Leukemia, Myeloid, Accelerated Phase/drug therapy , Piperazines/adverse effects , Pyrimidines/adverse effects , Thrombocytopenia/chemically induced , Thrombocytopenia/physiopathology , Antineoplastic Agents/administration & dosage , Antineoplastic Agents/therapeutic use , Benzamides , Cell Count , Cytogenetic Analysis , Disease Progression , Dose-Response Relationship, Drug , Humans , Imatinib Mesylate , Leukemia, Myeloid, Accelerated Phase/pathology , Leukemia, Myeloid, Accelerated Phase/physiopathology , Megakaryocytes/pathology , Piperazines/administration & dosage , Piperazines/therapeutic use , Pyrimidines/administration & dosage , Pyrimidines/therapeutic use , Time Factors
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