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Updated Sep. 2, 2010
 
 
 
Improving the Safety of IV Drug Delivery: Interpreting Current Standards To Improve Practices
Various recommendations are available to help health systems improve their intravenous (IV) drug delivery processes. One of the more significant guidelines came out of the Second Consensus Development Conference on the Safety of Intravenous Drug Delivery Systems, held in August 2008, which reflects the standards put forth in the United States Pharmacopoeia (USP) Chapter <797> guidelines and the Joint Commission’s medication management standards.

To request a free hard copy of this Bench to Bedside article, please email your full name, mailing address, and institution to pharmacypracticenews@mcmahonmed.com
NOVEMBER, 2009
Clinical Use of Desirudin, a New Subcutaneously Administered Direct Thrombin Inhibitor
Thrombin is a serine protease that plays a pivotal role in the coagulation process. It is produced via stepwise activation of proenzymes following vascular injury. Once formed, thrombin converts soluble fibrinogen to insoluble fibrin. It also stimulates platelets and enhances production of additional thrombin, facilitating blood clot stabilization. Higher thrombin concentrations are associated with denser, more rigid clots.

To request a free hard copy of this Bench to Bedside article, please email your full name, mailing address, and institution to pharmacypracticenews@mcmahonmed.com
NOVEMBER, 2009
Implementing the Recommendations of the Consensus Development Conference: The Road to Compliance
New standards for the preparation of IV drugs presented at recent meetings— including the Consensus Development Conference and the American Society of Health-System Pharmacists—constitute a paradigm shift from “traditional” inpatient practice because they place a greater emphasis on safety concerns.

To request a free hard copy of this Bench to Bedside article, please email your full name, mailing address, and institution to pharmacypracticenews@mcmahonmed.com
OCTOBER, 2009
Improving the Safety of IV Drug Delivery
In 2000, Bates et al published a consensus document with the goal of helping health systems balance cost, quality, efficiency, and safety of IV drug delivery systems in relation to the medication-use process as a whole. The expert panel concluded that manufacturer-prepared, point-of-care (POC)–activated, and pharmacy- based IV admixture programs were superior to other types of products for IV drug delivery (IV push, volume control chambers, and augmented IV push systems).

To request a free hard copy of this Bench to Bedside article, please email your full name, mailing address, and institution to pharmacypracticenews@mcmahonmed.com
SEPTEMBER, 2009
Medication Safety and Quality Part 4: Measurement and Reporting
The 1999 Institute of Medicine (IOM) Report, To Err is Human, was instrumental in exposing the public to the reality of errors occurring in the health care field and highlighted the need to focus on medication and patient safety.
JUNE, 2009
Medication Safety and Quality Part 3: Managing High-Alert Medications
The Institute of Medicine has estimated that at least 1.5 million preventable adverse drug events occur annually in the United States. Winterstein and colleagues have identified that inappropriate use of anticoagulants, overdoses of opiates, and inappropriate dosing and monitoring of insulin account for at least 50% of all preventable adverse drug events.
APRIL, 2009
Development of Guidance for Establishing Bioequivalence for Nonabsorbed Antibiotics: A Pathway Fraught With Challenges
Non-Absorbed Locally Acting drugs: Implications of Imminent Guidances Office of Generic Drugs recently issued draft guidance on methods to establish bioequivalence of generic and branded agents such as oral non-absorbed antibiotics. If equivalence is not proven then the implications to patient and Society for certain antibiotics are significant.
FEBRUARY, 2009
Medication Safety and Quality Part 2: Education and Professional Development
The advancement of medication safety and quality initiatives has led to a greater need for education and professional development programs. In addition to the internal assessment of medicationuse safety, health care organizations are increasingly adopting national patient safety practices and standards to optimize patient care. In doing so, medication safety and quality competencies, in addition to the clinical and operational training obtained through traditional educational experiences, are needed.
FEBRUARY, 2009
Medication Safety and Quality Part 1: Building a Medication Safety Team in a Health System
Patient safety is a top priority for all major health care organizations, government agencies, and health care payers. The grassroots movement for patient safety was highlighted in the Institute of Medicine (IOM) report entitled “To Err Is Human,” which suggested that between 44,000 and 98,000 people die each year as a result of medical misadventures, ranking medical errors among the top 10 causes of death in the United States.
DECEMBER, 2008
INVEGA® (paliperidone): An Important Agent for the Treatment of Patients With Schizophrenia
Schizophrenia—a biological disease that manifests as a collection of related problems in behavior, thoughts, and feelings—affects with an estimated lifetime prevelence between 0.5% and 1%. The symptoms of schizophrenia, which can fluctuate in severity and duration over a person’s lifetime, can be clustered into groups of related indicators designated as positive, negative, cognitive, and affective. Positive symptoms include hallucinations, delusions, and other types of thought disorders. Negative symptoms include alogia, avolition, and flat affect.
NOVEMBER, 2008
Reformulated ZOSYN: USP <788> Compliance and Expanded Compatibility
Zosyn® (piperacillin/tazobactam) is an intravenous antibiotic combination product of piperacillin (a semisynthetic penicillin) and tazobactam (a ß-lactamase inhibitor). It is indicated for the treatment of patients with moderate to severe infections caused by piperacillin-resistant, piperacillin/tazobactam-susceptible strains of indicated organisms.
DECEMBER, 2007
Two Hospitals Successfully Balance Custom and Premix Solutions
The first two parts of this educational series provided a detailed account of the benefits of using manufactured, premix drug and parenteral nutrition (PN) solutions. The articles focused on reasons why most hospitals and health systems already rely on premix intravenous (I.V.) drug infusions and why an increasing number of facilities have begun to adopt premix PN.
MARCH, 2007

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