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1.
Journal of the American Pharmacists Association : JAPhA ; 2022.
Article in English | EuropePMC | ID: covidwho-2046722

ABSTRACT

Background The University of Kentucky HealthCare Anticoagulation Clinic at the Gill Heart and Vascular Institute in Lexington, Kentucky designed and implemented a drive-up clinic for warfarin management with the goal to minimize person-to-person exposure during the coronavirus disease 2019 (COVID-19) pandemic. Objective The purpose of this study is to evaluate the effect on warfarin management in a pharmacist-led anticoagulation service when transitioned from an in-person clinic to a drive-up clinic during the COVID-19 pandemic. Methods This is a retrospective observational cohort study of 68 patients seen in the University of Kentucky HealthCare Anticoagulation Clinic on warfarin therapy for any indication. Patients were included if they had scheduled visits at least three times in the period 6 months prior to, during, and following the initiation of the drive-up clinic. The primary outcome is the difference in time in therapeutic range (TTR) prior to and during the drive-up clinic. Results The difference between the mean TTR in period 1 (69.1% ± 23.2%) and period 2 (69.6% ± 19.2%) was not significant (p=0.882). The mean TTR in period 3 (70.5% ± 20.8%) did not differ significantly from either period 1 (p=0.688) or period 2 (p=0.746). Safety outcomes including reported bleeding events and emergency department visits or hospital admissions for bleeding or thrombotic events were consistently low across each period. Conclusion The results of this study illustrate a drive-up clinic for warfarin management may be a reasonable alternative approach to providing care for outpatient anticoagulant management and may support non-traditional clinic models for long-term management of anticoagulation and other chronic disease states.

2.
Ann Pharmacother ; 56(4): 387-392, 2022 Apr.
Article in English | MEDLINE | ID: covidwho-1331907

ABSTRACT

BACKGROUND: Extracorporeal membrane oxygenation (ECMO) is a potential option for the management of severe acute respiratory failure secondary to COVID-19. Conflicting the use of this therapy is the known coagulopathy within COVID-19, leading to an incidence of venous thrombotic events of 25% to 49%. To date, limited guidance is available on optimal anticoagulation strategies in this population. OBJECTIVE: The purpose of this study was to evaluate the utilization of a pharmacist-driven bivalirudin dosing protocol for anticoagulation in the setting of ECMO for COVID-19-associated respiratory failure. METHODS: This was a single-center retrospective chart review over a 9-month period of patients receiving bivalirudin while on ECMO. All patients with acute respiratory failure requiring ECMO with a positive SARS-CoV-2 polymerase chain reaction were included. Bivalirudin was dosed via aPTT monitoring after a starting dose of 0.2 or 0.3 mg/kg/h. RESULTS: There were 33 patients included in this study, all receiving mechanical ventilation. The most common starting dose of bivalirudin was 0.2 mg/kg/h, with an average time to therapeutic range of 20 hours. Compared to previous reports, rates of bleeding were low at 15.1%, and 6.1% of patients developed a new venous thromboembolic event while on ECMO. ECMO survival was 51.5%, with an ICU mortality rate of 48.5%. CONCLUSION AND RELEVANCE: In the first published report of its use within this population, bivalirudin was found to be a viable choice for anticoagulation in those patients on ECMO for severe respiratory failure secondary to COVID-19.


Subject(s)
COVID-19 , Extracorporeal Membrane Oxygenation , Respiratory Insufficiency , Anticoagulants/adverse effects , COVID-19/complications , COVID-19/therapy , Extracorporeal Membrane Oxygenation/adverse effects , Extracorporeal Membrane Oxygenation/methods , Hirudins , Humans , Peptide Fragments , Recombinant Proteins , Respiratory Insufficiency/therapy , Retrospective Studies , SARS-CoV-2
3.
Chest ; 158(6): 2590-2601, 2020 12.
Article in English | MEDLINE | ID: covidwho-898607

ABSTRACT

The coexistence of coronavirus disease 2019 (COVID-19) and pulmonary embolism (PE), two life-threatening illnesses, in the same patient presents a unique challenge. Guidelines have delineated how best to diagnose and manage patients with PE. However, the unique aspects of COVID-19 confound both the diagnosis and treatment of PE, and therefore require modification of established algorithms. Important considerations include adjustment of diagnostic modalities, incorporation of the prothrombotic contribution of COVID-19, management of two critical cardiorespiratory illnesses in the same patient, and protecting patients and health-care workers while providing optimal care. The benefits of a team-based approach for decision-making and coordination of care, such as that offered by pulmonary embolism response teams (PERTs), have become more evident in this crisis. The importance of careful follow-up care also is underscored for patients with these two diseases with long-term effects. This position paper from the PERT Consortium specifically addresses issues related to the diagnosis and management of PE in patients with COVID-19.


Subject(s)
Aftercare , Anticoagulants/therapeutic use , COVID-19/complications , Extracorporeal Membrane Oxygenation , Hospitalization , Patient Care Team/organization & administration , Pulmonary Embolism/therapy , Thrombolytic Therapy/methods , Ambulatory Care , COVID-19/metabolism , Computed Tomography Angiography , Echocardiography , Fibrin Fibrinogen Degradation Products/metabolism , Humans , Lower Extremity , Point-of-Care Systems , Practice Guidelines as Topic , Pulmonary Embolism/complications , Pulmonary Embolism/diagnosis , Pulmonary Embolism/metabolism , Referral and Consultation , Risk Assessment , Ultrasonography
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