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2.
Am J Health Syst Pharm ; 77(23): 1986-1993, 2020 11 16.
Article in English | MEDLINE | ID: mdl-32417878

ABSTRACT

PURPOSE: This report describes a health-system pharmacy's response to a natural disaster while staff members simultaneously prepared for the coronavirus disease 2019 (COVID-19) pandemic. By detailing our experience, we hope to help other institutions that are current facing or could encounter similar crises. SUMMARY: In early March 2020, a tornado destroyed the health system's warehouse for storage of most clinical supplies, including personal protective equipment and fluids. The pharmacy purchasing team collaborated with suppliers and manufacturers to recover losses and establish alternative storage areas. Days later, the pharmacy department was forced to address the impending COVID-19 pandemic. Key elements of the COVID-19 response included reducing the potential for virus exposure for patients and staff; overcoming challenges in sourcing of staff, personal protective equipment, and medications; and changing care delivery practices to maintain high-quality patient care while maximizing social distancing. The pharmacy department also created distance learning opportunities for 70 pharmacy students on rotations. After an initial plan, ongoing needs include adjustment in patient care activities if significant staff losses occur, when and how to resume clinical activities, and how to best utilize the resources accumulated. Elements of practice changes implemented to reduce COVID-19 threats to patients and pharmacy personnel have proven beneficial and will be further evaluated for potential continuation. CONCLUSION: The pharmacy department's efforts to respond to a natural disaster and unprecedented pandemic have proven successful to this point and have illuminated several lessons, including the necessity of cohesive department communication, staff flexibility, prioritization of teamwork, and external collaboration.


Subject(s)
COVID-19/epidemiology , Community Health Planning/methods , Drug Storage/methods , Pharmacy Service, Hospital/methods , Pharmacy Service, Hospital/supply & distribution , Tornadoes , COVID-19/therapy , Humans , Interprofessional Relations , Natural Disasters/prevention & control , Pandemics/prevention & control , Patient Care Team , Tornadoes/prevention & control
3.
Am J Health Syst Pharm ; 67(1): 27-37, 2010 Jan 01.
Article in English | MEDLINE | ID: mdl-20044366

ABSTRACT

PURPOSE: The effectiveness and tolerability of switching patients' therapy from brand-name to generic clozapine are reviewed. SUMMARY: Clozapine is the most effective treatment for patients with refractory psychotic disorders and is also effective for reducing suicidal and violent behavior in this same population. Generic versions of clozapine are widely used. However, possible differences in pharmacokinetic profiles between branded and generic clozapine, and the potential risks of medication changes in severely ill but stable patients, may result in apprehension about converting from branded to generic clozapine. Articles, abstracts, and clinical presentations that compared clinical outcomes between Clozaril (Novartis Pharmaceuticals, East Hanover, NJ) and generic forms of clozapine in patients with primary psychotic disorders, bipolar disorder, or related conditions were identified via a computerized search of the medical literature. Thirteen relevant reports, mostly uncontrolled observational studies or chart reviews, described the effects of switching from brand-name to generic clozapine in 966 patients. The majority of patients tolerated conversion without worsening of symptoms or adverse effects, increased intensive service utilization, or medication adjustment. Clinical deterioration was described in a case review and in one randomized, controlled study. CONCLUSION: Available literature supports the effectiveness and safety of generic clozapine formulations in patients who previously were stable during treatment with brand-name clozapine. The risk of poor outcome after conversion to a generic clozapine formulation appears to be low but difficult to predict. Patients should be closely monitored during the first one to three months after conversion from one formulation to another.


Subject(s)
Antipsychotic Agents/therapeutic use , Clozapine/therapeutic use , Drugs, Generic/therapeutic use , Psychotic Disorders/drug therapy , Antipsychotic Agents/adverse effects , Antipsychotic Agents/pharmacokinetics , Clozapine/adverse effects , Clozapine/pharmacokinetics , Drugs, Generic/adverse effects , Drugs, Generic/pharmacokinetics , Humans , Therapeutic Equivalency
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