20 results match your criteria: "MCPHS University School of Pharmacy[Affiliation]"

Introduction: To address the needs of the community, social accountability (SA) needs to be integrated in health education, especially pharmacy education. This is part one of a two-part commentary that focuses specifically on partnership, competency, and leadership as it relates to SA within pharmacy education.

Commentary: Here the need for partnership in SA, competency of SA in pharmacy education, and leadership in SA is discussed.

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Aim: To assess the association of mental health burden with diabetes-related self-care behaviors and healthcare utilization among older adults.

Method: This cross-sectional 2019 Behavioral Risk Factor Surveillance System (BRFSS) study included ≥ 65 years old adults with self-reported diabetes. Three groups were used based on the number of days in the past month affected by mental health: 0 days (no burden), 1-13 days (occasional burden), and 14-30 days (frequent burden).

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Due to worldwide increases in obesity and average maternal age, the incidence of gestational diabetes mellitus (GDM) is increasing. The primary treatment of GDM is medical nutrition therapy but approximately 15-30% of individuals need pharmacotherapy to reach blood glucose goals to minimize the adverse consequences of hyperglycaemia. In the past, regular and neutral protamine Hagedorn insulin were the mainstays of pharmacological treatment for GDM due to their well-established safety; however, because they are administered as injections and require strict timing of doses and meals to minimize hypoglycaemia, alternatives are often sought.

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Background And Purpose: To describe a large-scale, cultural sensitivity-focused interprofessional book club activity that is required in the first-professional year of an accelerated pharmacy curriculum.

Educational Activity And Setting: An interprofessional book club activity, focusing on the need for cultural sensitivity in health care, is conducted annually for students in the acupuncture, pharmacy, physical therapy, physician assistant, and sonography programs. Each year over 400 students are required to attend and are assigned to interprofessional groups to discuss guided questions pertaining to the book written by Anne Fadiman, The Spirit Catches You and You Fall Down: A Hmong Child, Her American Doctors, and the Collision of Two Cultures.

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Introduction: Medication-related harm represents a significant issue for patient safety and quality of care. One strategy to avoid preventable adverse drug events is to utilize patient-specific factors such as pharmacogenomics (PGx) to individualize therapy.

Objective: We measured the number of patients enrolled in a health-system biobank with actionable PGx results who received relevant medications and assessed the incidence of adverse drug events (ADEs) that might have been prevented had the PGx results been used to inform prescribing.

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Proton pump inhibitors (PPIs) are widely used for acid suppression in the treatment and prevention of many conditions, including gastroesophageal reflux disease, gastric and duodenal ulcers, erosive esophagitis, Helicobacter pylori infection, and pathological hypersecretory conditions. Most PPIs are metabolized primarily by cytochrome P450 2C19 (CYP2C19) into inactive metabolites, and CYP2C19 genotype has been linked to PPI exposure, efficacy, and adverse effects. We summarize the evidence from the literature and provide therapeutic recommendations for PPI prescribing based on CYP2C19 genotype (updates at www.

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The 2018-2019 Research and Graduate Affairs Committee (RGAC) was charged with critically evaluating the leadership development support necessary for pharmacy researchers, including postdoctoral trainees, to develop the skills needed to build and sustain successful research programs and analyzing how well those needs are being met by existing programs both within AACP and at other organizations. The RGAC identified a set of skills that could reasonably be expected to provide the necessary foundation to successfully lead a research team and mapped these skills to the six domains of graduate education in the pharmaceutical sciences established by the 2016-2017 RGAC (Table 1). In addition, the RGAC identified competency in team science and the bench-to-bedside-to-beyond translational spectrum as being critical elements of research leadership.

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The objective of this review is to summarize the pharmacology, efficacy, and safety of cerliponase alfa for the treatment of late infantile neuronal ceroid lipofuscinosis type 2 (CLN2). Cerliponase alfa is recombinant human tripeptidyl peptidase 1 enzyme replacement therapy. A phase 1/2 trial established the efficacy and safety of cerliponase alfa for treatment of neuronal ceroid lipofuscinosis type 2.

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Translating CYP2D6 genotype to metabolizer phenotype is not standardized across clinical laboratories offering pharmacogenetic (PGx) testing and PGx clinical practice guidelines, such as the Clinical Pharmacogenetics Implementation Consortium (CPIC) and the Dutch Pharmacogenetics Working Group (DPWG). The genotype to phenotype translation discordance between laboratories and guidelines can cause discordant cytochrome P450 2D6 (CYP2D6) phenotype assignments and, thus lead to inconsistent therapeutic recommendations and confusion among patients and clinicians. A modified-Delphi method was used to obtain consensus for a uniform system for translating CYP2D6 genotype to phenotype among a panel of international CYP2D6 experts.

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In 2009, the Clinical Pharmacogenetics Implementation Consortium (CPIC, www.cpicpgx.org), a shared project between Pharmacogenomics Knowledge Base (PharmGKB, http://www.

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The use of online resources by patients for their daily health needs has escalated with the proliferation of mobile devices and mobile apps. While healthcare professionals can help their patients access quality online resources and tools, they may not have received the education and training to do this effectively. To meet this educational need, a daylong workshop was developed at a health sciences university that aimed to increase awareness of students in various health disciplines of mobile health-related apps and federally sponsored websites that provide patient-friendly medical information.

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Objective: To compare and contrast experiential education perceptions of pharmacy residency program directors (RPDs) and doctor of pharmacy students in their last year of the curriculum for residency application considerations.

Methods: The New England Regional Departments of Experiential Education (NERDEE) consortium developed a 17-question survey to assess residency factors, including those related to experiential education. The survey was dispersed to advanced pharmacy practice experience (APPE) students from six colleges/schools of pharmacy and RPDs nationwide.

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Background: Patient satisfaction in outpatient phlebotomy settings typically depends on wait time and venipuncture experience, and many patients equate their experiences with their overall satisfaction with the hospital.

Methods: We compared patient service times and preanalytical errors pre- and postimplementation of an integrated electronic health record (EHR)-laboratory information system (LIS) and electronic specimen collection module. We also measured patient wait time and assessed patient satisfaction using a 5-question survey.

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Development of an algorithm to assess appropriateness of overriding alerts for nonformulary medications in a computerized prescriber-order-entry system.

Am J Health Syst Pharm

January 2016

Qoua L. Her, Pharm.D., M.S., M.Sc., is Pharmacy Informatics and Outcomes Research Fellow, MCPHS University School of Pharmacy-Boston and Division of General Internal Medicine and Primary Care, Brigham and Women's Hospital (BWH), Boston, MA. Diane L. Seger, B.S.Pharm., is Senior Pharmaco-Informatics Specialist, Clinical and Quality Analysis, Information Systems, Partners HealthCare System, Inc., Wellesley, MA. Mary G. Amato, Pharm.D., M.P.H., is Associate Professor of Pharmacy Practice, MCPHS University, Boston. Patrick E. Beeler, M.D., is Postdoctoral Research Fellow, Division of General Internal Medicine and Primary Care, BWH, and Research Fellow, Harvard Medical School, Boston. Olivia Dalleur, M.Pharm., Ph.D., is Research Associate in Medicine, Division of General Internal Medicine and Primary Care, BWH, and Assistant Professor in Clinical Pharmacy, Louvain Drug Research Institute, Clinical Pharmacy Research Group, Cliniques, Universitaires Saint-Luc, Université catholique de Louvain, Brussels, Belgium. Sarah P. Slight, M.Pharm., Ph.D., P.G.Dip., is Senior Lecturer/Associate Professor of Pharmacy Practice, Wolfson Research Institute, School of Medicine, Pharmacy and Health, Durham University, Queen's Campus, Stockton-on-Tees, England, and Visiting Research Scholar, Division of General Internal Medicine and Primary Care, BWH. Patricia C. Dykes, Ph.D., RN, FACMI, is Program Director, Center for Patient Safety, Research and Practice, BWH. David W. Bates, M.D., M.Sc., is Senior Vice President for Quality and Safety and Chief Quality Officer, Division of General Internal Medicine and Primary Care, BWH.

Purpose: An algorithm for assessing the appropriateness of physician overrides of clinical decision support alerts triggered by nonformulary medication (NFM) requests is described.

Methods: Data on a random sample of 5000 NFM alert overrides at Brigham and Women's Hospital over a four-year period (2009-12) were extracted from the hospital's computerized prescriber-order-entry (CPOE) system. Through an iterative process, a scheme for categorizing the reasons given by prescribers for alert overrides was developed.

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Alzheimer's disease (AD) is a progressive neurodegenerative condition primarily affecting individuals 65 years of age and older. There are few therapies available, and the disease is eventually fatal. Although the molecular mechanisms responsible for the development of AD remain unknown, a strong correlation between insulin dysfunction in type 2 diabetes mellitus and AD has recently been established.

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Sterile product compounding using an i.v. compounding workflow management system at a pediatric hospital.

Am J Health Syst Pharm

August 2014

Thomas T. Moniz, Pharm.D., is Informatics Pharmacist, Department of Pharmacy, Boston Children's Hospital, Boston, MA. Stephen Chu, Pharm.D., is Clinical Pediatric Pharmacist, Department of Pharmacy, Boston Children's Hospital, and Adjunct Professor, MCPHS University School of Pharmacy-Boston. Crystal Tom, Pharm.D., BCPS, is General Pediatrics Pharmacist Team Lead, Department of Pharmacy, Boston Children's Hospital, and Adjunct Professor, Bouvé College of Health Sciences School of Pharmacy, Northeastern University, Boston, and MCPHS University School of Pharmacy-Boston. Peter Lutz, Pharm.D., is Associate Director of Pharmacy, Department of Pharmacy, Boston Children's Hospital, and Adjunct Professor, Bouvé College of Health Sciences School of Pharmacy, Northeastern University, and MCPHS University School of Pharmacy-Boston. Alana Arnold, Pharm.D., BCPS, AQ-ID, is Associate Director of Pharmacy, Boston Children's Hospital, and Adjunct Professor, Bouvé College of Health Sciences School of Pharmacy, Northeastern University, and MCPHS University School of Pharmacy-Boston. Kathleen M. Gura, Pharm.D., BCNSP, FASHP, FPPAG, is Team Leader, Surgical Program, and Clinical Pharmacy Specialist in Gastroenterology/Nutrition, Boston Children's Hospital, and Adjunct Professor, Bouvé College of Health Sciences School of Pharmacy, Northeastern University, and MCPHS University School of Pharmacy-Boston. Al Patterson, Pharm.D., is Director of Pharmacy, Boston Children's Hospital, and Adjunct Professor, Bouvé College of Health Sciences School of Pharmacy, Northeastern University, and MCPHS University School of Pharmacy-Boston.

Article Synopsis
  • The study highlights the benefits of an automated intravenous (i.v.) compounding workflow management system in improving patient safety at a pediatric hospital.
  • Over a 13-month evaluation period, this system detected errors in 0.68% of the 425,683 medication doses prepared, with significant numbers requiring rework or destruction due to compounding mistakes.
  • Approximately 23% of the errors identified were not detectable by the previous verification methods, with some posing risks for adverse drug events, although most errors were related to imaging issues that were not clinically significant.
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