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1.
Am J Pharm Educ ; 78(6): 116, 2014 Aug 15.
Artigo em Inglês | MEDLINE | ID: mdl-25147388

RESUMO

OBJECTIVES: To determine a measurable definition of academic entitlement, measure academic entitlement in graduating doctor of pharmacy (PharmD) students, and compare the academic performance between students identified as more or less academically entitled. METHODS: Graduating students at a private health sciences institution were asked to complete an electronic survey instrument that included demographic data, academic performance, and 2 validated academic entitlement instruments. RESULTS: One hundred forty-one of 243 students completed the survey instrument. Fourteen (10%) students scored greater than the median total points possible on 1 or both of the academic entitlement instruments and were categorized as more academically entitled. Less academically entitled students required fewer reassessments and less remediation than more academically entitled students. The highest scoring academic entitlement items related to student perception of what professors should do for them. CONCLUSION: Graduating pharmacy students with lower levels of academic entitlement were more academically successful than more academically entitled students. Moving from an expert opinion approach to evidence-based decision-making in the area of academic entitlement will allow pharmacy educators to identify interventions that will decrease academic entitlement and increase academic success in pharmacy students.


Assuntos
Educação em Farmácia/normas , Escolaridade , Estudantes de Farmácia/psicologia , Coleta de Dados , Avaliação Educacional , Humanos
2.
Pharmacotherapy ; 33(4): 375-82, 2013 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-23553808

RESUMO

STUDY OBJECTIVE: To determine whether pharmacologic prophylaxis for venous thromboembolism (VTE) was associated with a decrease in the incidence of VTE or an increased incidence of bleeding in patients with chronic liver disease (CLD). DESIGN: Single-center, retrospective cohort analysis. SETTING: University medical center. PATIENTS: A total of 1581 adults with CLD hospitalized over a 3-year period for longer than 24 hours. MEASUREMENTS AND MAIN RESULTS: Medical records were reviewed for the primary outcome of VTE and documented episodes of bleeding during hospitalization and were divided into two groups based on receipt of pharmacologic VTE prophylaxis. During the 1581 hospitalizations, 392 (24.7%) patients received pharmacologic VTE prophylaxis. The incidence of VTE in the prophylaxis group was 0.5% compared with 1.8% in patients without prophylaxis (p=0.05). Documented bleeding rates were lower in the prophylaxis group (2.0% vs 10.3%, p<0.001). Multivariate logistic regression identified active malignancy (odds ratio [OR] 8.76, 95% confidence interval [CI], 2.56-29.58), trauma or surgery during hospitalization (OR 10.29, 95% CI 1.18-89.51), and history of VTE (OR 26.48, 95% CI 6.93-101.16) as risk factors of VTE. Use of pharmacologic VTE prophylaxis was protective against VTE (OR 0.34, 95% CI 0.04-0.88). CONCLUSION: Pharmacologic VTE prophylaxis was associated with a decreased incidence of VTE in patients with CLD without an increased rate of bleeding and should be routinely considered on admission to the hospital. Patients with CLD and active malignancy, trauma or surgery during hospitalization, or history of VTE appear to be at highest risk of VTE and thus warrant pharmacologic prophylaxis. Prospective studies must validate these findings.


Assuntos
Anticoagulantes/uso terapêutico , Hepatopatias/complicações , Tromboembolia Venosa/complicações , Tromboembolia Venosa/prevenção & controle , Anticoagulantes/efeitos adversos , Doença Crônica , Estudos de Coortes , Feminino , Hemorragia/induzido quimicamente , Hospitalização , Humanos , Incidência , Hepatopatias/tratamento farmacológico , Masculino , Pessoa de Meia-Idade , Nevada , Estudos Retrospectivos , Fatores de Risco
4.
Am J Pharm Educ ; 75(2): 33, 2011 Mar 10.
Artigo em Inglês | MEDLINE | ID: mdl-21519422

RESUMO

OBJECTIVE: To implement and assess the effectiveness of card games to teach pharmacotherapeutic topics to pharmacy students and to determine the relationship between students' assessment scores and their learning styles. DESIGN: Two card games, Cardiology Go Fish and Infectious Diseases Gin Rummy, were created and taught to pharmacy students enrolled in an advanced pharmacy practice experience (APPE). Students were required to play each game for 1 hour, 3 times over a 6-week period. ASSESSMENT: Forty-five students completed a 90-question assessment administered prior to and after the 6-week period in which the games were played. Students' cardiology and infectious diseases assessment scores improved significantly as compared with scores on pharmacy practice questions, 19.2% vs. 5.1%, (p < 0.001) and 10.3% vs. 5.1% (p = 0.006), respectively. Students learned from participating in the games regardless of their learning preference as determined by the VARK (visual, aural, read/write, kinesthetic) questionnaire; however, the cardiology assessment scores of students with a preference for kinetic learning improved the most. CONCLUSIONS: Incorporating innovative learning tools such as card games into the curriculum of APPEs can enhance the educational experience of pharmacy students.


Assuntos
Educação em Farmácia/métodos , Jogos e Brinquedos , Aprendizagem Baseada em Problemas/métodos , Estudantes de Farmácia , Adulto , Currículo , Avaliação Educacional , Feminino , Humanos , Masculino , Materiais de Ensino , Adulto Jovem
5.
Pharm. pract. (Granada, Internet) ; 9(1): 31-36, ene.-mar. 2011. tab, ilus
Artigo em Inglês | IBECS | ID: ibc-86124

RESUMO

Objectives: The purpose of this study is to determine the percentage of patients admitted for acute myocardial infarction currently prescribed a statin, with low-density lipoprotein (LDL) <100 mg/dL, and high-density lipoprotein (HDL) <50 mg/dL for men and <55 mg/dL for women and evaluate their medication management with a focus on niacin initiation. Methods: This was a retrospective study from 12/07 to 12/09, conducted at a private, community hospital. Inclusion criteria required patients to have an acute myocaridal infarction (AMI) ICD-9 code, troponin >=0.2 ng/dL and lipid panel performed within 96 hours of troponin. Patients with a triglyceride level > 400 mg/dL were excluded. The residual risk population consisted of patients currently taking a statin with LDL <100 mg/dL and HDL <50/55 mg/dL. Patients were excluded from the residual risk population if they were on niacin, had an allergy to or previously failed niacin therapy, or expired within 72 hours. Results: A total of 553 patients experiencing an AMI had lipid panels available for evaluation. The mean LDL was 97.3 +/- 36.0 mg/dL, mean HDL was 33.5 +/- 11.1 mg/dL, and mean triglycerides were 133.1 +/- 71.3 mg/dL. The majority of patients (n=521, 94.2%) had an HDL < 50 or 55 mg/dL respective of gender. Ninety-two (80.0%) residual risk patients had no change in their home lipid medications post AMI. Fifteen (13.0%) residual risk patients had their dose of statin medication increased. Seven (6.1%) residual risk patients were initiated on niacin. Conclusions: The study results confirm an existence of a residual risk population with nearly 25% of AMI patients meeting the criteria. The results also confirm a low incidence of medication intervention in the residual risk population post AMI (20.0%) regarding lipid therapy, including the initiation of niacin in only 6.1% of patients (AU)


Objetivos: El propósito de este estudio es determinar el porcentaje de pacientes ingresados por un infarto agudo de miocardio que tienen actualmente prescrita una estatina, con lipoproteínas de baja densidad (LDL) <100mg/dL, y lipoproteínas de alta densidad (HDL) <50 mg/dL para hombres y <55 mg/dL para mujeres, y evaluar el manejo de su medicación centrándose en la iniciación a niacina. Métodos: Este fue un estudio retrospectivo de 12/07 a 12/09, realizado en un hospital comunitario privado. Los criterios de inclusión requerían que los pacientes tuviesen un código CIE-9 de infarto agudo de miocardio (IAM), troponina >=0.2 ng/dL y un panel lipídico realizado en las 96 horas de la troponina. Los pacientes con nivel de triglicéridos >400 mg/dL fueron excluidos. La población de riesgo residual consistió en pacientes que tomaban actualmente estatinas con LDL<100 mg/dL y HDL<50/55 mg/dL. Se excluía a los pacientes de la población de riesgo residual si estaban con niacina, tenían alergia o fallo previo a la niacina, o fallecieron en las 72 horas. Resultados: Un total de 553 pacientes que sufrieron un IAM tenían un perfil lipídico disponible para evaluación. La media de LDL fue de 97,3 (DE=36,0) mg/dL, la media de HDL fue de 33,5 (DE=11,1) mg/dL, y la media de triglicéridos fue de 133,1 (DE=71,3) mg/dL. La mayoría de los pacientes (n=521, 94.2%) tenían HDL<50 o 55 mg/dL, respectivamente del su género. 92 (80,0%) pacientes de riesgo residual no tuvo cambios en su medicación domiciliaria de lípidos después del IAM. A 15 (13,0%) pacientes de riesgo residual se le aumentó la dosis de estatinas. En 7 (6,1) pacientes de riesgo residual se inició la niacina. Conclusiones: Los resultados del estudio confirman la existencia de una población de riesgo residual de cerca del 25% de pacientes con IAM que satisface los criterios. Los resultados también confirman la baja incidencia de intervención en la población de riesgo residual post-IAM (20,0%) en relación al tratamiento para los lípidos, incluyendo la iniciación de niacina en sólo el 6,1% de los pacientes (AU)


Assuntos
Humanos , Masculino , Feminino , Hiperlipidemias/complicações , Hiperlipidemias/tratamento farmacológico , Hiperlipidemias/metabolismo , Infarto do Miocárdio/induzido quimicamente , Infarto do Miocárdio/complicações , Infarto do Miocárdio/tratamento farmacológico , Lipoproteínas/uso terapêutico , Niacina/uso terapêutico , /metabolismo , /uso terapêutico , Niacina/metabolismo , Niacina/farmacocinética , Estudos Retrospectivos
6.
Pharm Pract (Granada) ; 9(1): 31-6, 2011 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-25132887

RESUMO

OBJECTIVES: The purpose of this study is to determine the percentage of patients admitted for acute myocardial infarction currently prescribed a statin, with low-density lipoprotein (LDL) <100 mg/dL, and high-density lipoprotein (HDL) <50 mg/dL for men and <55 mg/dL for women and evaluate their medication management with a focus on niacin initiation. METHODS: This was a retrospective study from 12/07 to 12/09, conducted at a private, community hospital. Inclusion criteria required patients to have an acute myocaridal infarction (AMI) ICD-9 code, troponin ≥0.2 ng/dL and lipid panel performed within 96 hours of troponin. Patients with a triglyceride level > 400 mg/dL were excluded. The residual risk population consisted of patients currently taking a statin with LDL <100 mg/dL and HDL <50/55 mg/dL. Patients were excluded from the residual risk population if they were on niacin, had an allergy to or previously failed niacin therapy, or expired within 72 hours. RESULTS: A total of 553 patients experiencing an AMI had lipid panels available for evaluation. The mean LDL was 97.3 ± 36.0 mg/dL, mean HDL was 33.5 ± 11.1 mg/dL, and mean triglycerides were 133.1 ± 71.3 mg/dL. The majority of patients (n=521, 94.2%) had an HDL < 50 or 55 mg/dL respective of gender. Ninety-two (80.0%) residual risk patients had no change in their home lipid medications post AMI. Fifteen (13.0%) residual risk patients had their dose of statin medication increased. Seven (6.1%) residual risk patients were initiated on niacin. CONCLUSIONS: The study results confirm an existence of a residual risk population with nearly 25% of AMI patients meeting the criteria. The results also confirm a low incidence of medication intervention in the residual risk population post AMI (20.0%) regarding lipid therapy, including the initiation of niacin in only 6.1% of patients.

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