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4.
J Community Hosp Intern Med Perspect ; 10(5): 381-385, 2020 Sep 03.
Article in English | MEDLINE | ID: mdl-33235666

ABSTRACT

BACKGROUND: The scoring rubric on the USMLE Step 1 examination will be changing to pass/fail in January 2022. This study elicits internal medicine resident perspectives on USMLE pass/fail scoring at the national level. OBJECTIVE: To assess internal medicine resident opinions regarding USMLE pass/fail scoring and examine how variables such as gender, scores on USMLE 1 and 2, PGY status and type of medical school are associated with these results. METHODS: In the fall of 2019, the authors surveyed current internal medicine residents via an on-line tool distributed through their program directors. Respondents indicated their Step 1 and Step 2 Clinical Knowledge scores from five categorical ranges. Questions on medical school type, year of training year, and gender were included. The results were analyzed utilizing Pearson Chi-square testing and multivariable logistic regression. RESULTS: 4012 residents responded, reflecting 13% of internal medicine residents currently training in the USA. Fifty-five percent of respondents disagreed/strongly disagreed with pass/fail scoring and 34% agreed/strongly agreed. Group-based differences were significant for gender, PGY level, Step 1 score, and medical school type; a higher percentage of males, those training at the PGY1 level, and graduates of international medical schools (IMGs) disagreed with pass/fail reporting. In addition, high scorers on Step 1 were more likely to disagree with pass/fail reporting than low scoring residents. CONCLUSION: Our results suggest that a majority of internal medicine residents, currently training in the USA prefer that USMLE numerical scoring is retained and not changed to pass/fail.

5.
Am J Med ; 133(10): 1223-1226.e6, 2020 10.
Article in English | MEDLINE | ID: mdl-32659220

ABSTRACT

This statement was released in June 2020 by the Alliance for Academic Internal Medicine to provide guidance for the 2020-2021 residency application cycle in light of the COVID-19 pandemic. While many of the recommendations are specific to this cycle, others, such as the Department Summary Letter of Evaluation, are meant to be an enduring change to the internal medicine residency application process. AAIM realizes that some schools may not yet have the tools or resources to implement the template fully this cycle and look toward collaboration within the internal medicine education community to facilitate adoption in the cycles to come.


Subject(s)
Coronavirus Infections , Correspondence as Topic , Internal Medicine/organization & administration , Internship and Residency/organization & administration , Job Application , Pandemics , Pneumonia, Viral , COVID-19 , Humans
6.
Indian J Exp Biol ; 52(8): 814-9, 2014 Aug.
Article in English | MEDLINE | ID: mdl-25141545

ABSTRACT

Acute dose of organophosphorus pesticide Triazophos (O,O-diethyl O-1-phenyl-1H-1,2,4-triazol-3-yl phosphorothioate; Tz) administered orally affects oxidative stress parameters and the histo-architecture of liver, kidney and brain tissues. The results indicate a dose dependent induction of oxidative stress as evident by increased malondialdehyde level and decreased antioxidant defense including glutathione and superoxide dismutase activity in rat liver, kidney and brain. AChE activity was found significantly decreased in the Tz treated groups as compared to the vehicle control (DMSO) group. Histopathological examination of liver, kidney and brain in Tz treated rats revealed medullary congestion and hydropic degeneration of hepatocytes in liver and medullary congestion in kidney. However, no significant histopathological changes were observed in brain tissues.


Subject(s)
Organothiophosphates/toxicity , Oxidative Stress/drug effects , Pesticides/toxicity , Triazoles/toxicity , Animals , Antioxidants/metabolism , Brain/drug effects , Glutathione/metabolism , Kidney/drug effects , Lipid Peroxidation/drug effects , Liver/drug effects , Malondialdehyde/metabolism , Rats
7.
J Grad Med Educ ; 6(4): 680-5, 2014 Dec.
Article in English | MEDLINE | ID: mdl-26140118

ABSTRACT

BACKGROUND: Rater errors, such as halo/reverse halo, range restriction, and leniency errors, are frequently cited as threats to the validity of resident assessment by faculty. OBJECTIVE: We studied whether participation in faculty development on the use of a new Milestone-based assessment tool reduced rater error for participants compared to individuals who did not participate. METHODS: We reviewed evaluations of resident Milestones completed by faculty at the end of rotations between July 2012 and June 2013. The 2 Milestones in each competency with the greatest number of ratings were selected for analysis. RESULTS: A total of 412 evaluations were analyzed, including 217 completed by faculty who participated in the development activity, and 240 completed by nonparticipant faculty. All evaluations that contained identical scores for all Milestones (16%) were completed by nonparticipant faculty (χ(2)  =  37.498, P < .001). Faculty who had participated in development assigned a wider range of scores and lower minimum scores to residents, and provided the highest ratings for residents less frequently (P < .001) than nonparticipants. CONCLUSIONS: Faculty who participated in education about the Milestones demonstrated significantly less halo, range restriction, and leniency errors than faculty members who did not participate. These findings support a recommendation to develop a cadre of "core faculty" by training them in the use of Milestone assessment tools, and making them responsible for a significant portion of resident assessments.

8.
Toxicol Int ; 20(1): 1-5, 2013 Jan.
Article in English | MEDLINE | ID: mdl-23833430

ABSTRACT

The present study was designed to determine the lethal dose 50 (LD50) of combination of cypermethrin, a pyrethroid, and endosulfan, an organochlorine compound in Wistar rats. LD50 is the amount (dose) of a chemical, calculated as per the concentration of chemicals that produces death in 50% of a population of test animals to which it is administered by any of a variety of methods. A single oral dose of combination of cypermethrin and endosulfan were dissolved in dimethyl sulfoxide (DMSO) in a ratio of 1:1 and administered orally at the concentration of 165 mg/kg body weight (b.w), 330 mg/kg b.w, 660 mg/kg b.w, and 1320 mg/kg b.w to experimental animals. LD50 was calculated according to the method described by Miller and Tainter (1994) and was observed as 691.83 mg/kg b.w for this combination. Single dose of test article at 165 mg/kg b.w did not reveal any toxic signs or behavioral alterations, hence considered as No observed Adverse Effect level (NOAEL).

9.
Toxicol Int ; 20(1): 61-7, 2013 Jan.
Article in English | MEDLINE | ID: mdl-23833440

ABSTRACT

BACKGROUND: Endosulfan, a neurotoxic organochlorine insecticide and cypermethrin, a synthetic pyrethroid insecticide used to control pests in domestic, industrial, and agricultural situations. MATERIALS AND METHODS: The present study was carried out to investigate the acute oral toxicity, behavioral and histopathological changes of combination of endosulfan and cypermethrin in albino rats. According to Miller and Tainter analysis method, at 48 h, LD50 value of combination of endosulfan and cypermethrin (ratio 1:1) in rats was found to be 691.83 mg/kg bw by oral gavage. RESULTS: When combination of both these pesticides was administered orally at concentration of 103.72 mg/kg bw, 172.95 mg/kg bw and 207.50 mg/kg bw, respectively, as a single dose, no significant changes in behavior of rats was observed, neither in dosed nor in control group of rats. Combination of endosulfan- and cypermethrin-treated rats showed mild histopathological changes in liver and kidney in group IV (207.50 mg/kg BW) as compared to the control. However, no significant changes were observed in brain and small intestine at either dose of combination of endosulfan and cypermethrin with respect to control. CONCLUSION: Thus, the present study, first of its kind in India, demonstrated the oral toxicity, behavioral, and histo-architectual alterations after induction of combination of endosulfan and cypermethrin at acute doses in Wistar rats.

11.
Am J Gastroenterol ; 101(11): 2659-62, 2006 Nov.
Article in English | MEDLINE | ID: mdl-16952289

ABSTRACT

Over the counter (OTC) medicines are commonly used in the United States despite a lack of scientific evidence for clinical utility and toxicity associated with their use. A case of jaundice and IgA nephropathy as a consequence of use of a muscle enhancing OTC supplement that was advertised as innocuous with no hormonal activity is described. IgA nephropathy has not been described previously in association with the use of testosterone. The case highlights that, besides adulteration, the misrepresentation of chemicals present in OTC medications and supplements can create confusion and a false sense of security with their use.


Subject(s)
Dietary Supplements/adverse effects , Glomerulonephritis, IGA/chemically induced , Jaundice, Obstructive/chemically induced , Pyridines/adverse effects , Toluidines/adverse effects , Adult , Humans , Male , Testosterone/adverse effects
12.
Crit Care Clin ; 18(4): 767-80, 2002 Oct.
Article in English | MEDLINE | ID: mdl-12418440

ABSTRACT

Acute arthritis in critically ill patients may be caused by local or systemic infection, by a flare of chronic joint disease such as rheumatoid or crystal-associated arthritis, or by less common entities such as hemarthrosis. Diagnosis requires analysis of synovial fluid, and appropriate treatment is based on its findings. Prompt diagnosis and treatment are usually necessary to prevent the significant morbidity associated with these conditions.


Subject(s)
Arthritis/therapy , Critical Care/methods , Arthritis/diagnosis , Arthritis/physiopathology , Arthritis, Infectious/diagnosis , Arthritis, Infectious/physiopathology , Arthritis, Infectious/therapy , Chondrocalcinosis/diagnosis , Chondrocalcinosis/drug therapy , Chondrocalcinosis/physiopathology , Gout/diagnosis , Gout/drug therapy , Gout/physiopathology , Hemarthrosis/diagnosis , Hemarthrosis/physiopathology , Hemarthrosis/therapy , Humans , Risk Factors
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