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1.
J Am Coll Clin Pharm ; 3(8): 1471-1479, 2020 Dec.
Article in English | MEDLINE | ID: covidwho-1898812

ABSTRACT

Beginning in March 2020, New York City began the fight against coronavirus disease 2019. Health care workers were faced with a disease that led to significant morbidity and mortality with no proven therapies. As hospitals became inundated with patients and underwent rapid expansion of capacity, resources such as drugs, protective and medical equipment, and hospital staff became limited. Pharmacists played a critical role in the management of clinical care and drug delivery during the pandemic. As members of the department of pharmacy within NewYork-Presbyterian Hospital, we describe our experiences and processes to overcome challenges faced during the pandemic. Strict inventory management through the use of daily usage reports, frequent communication, and minimization of waste was critical for the management of drug shortages. The creation of guidelines, protocols, and restrictions were not only used to mitigate drug shortages, but also helped educate health care providers and guided medication use. Managing technology through setting up new automatic dispensing cabinets to address hospital expansions and modifying the electronic order entry system to include new protocols and drug shortage information were also vital. Additional key pharmacist functions included provision of investigational drug service support and training of pharmacists, prescribers, nurses, and respiratory therapists to educate and standardize medication use. Through implementation of operational and clinical processes, pharmacists managed critical drug inventory and guided patient treatment. As the pandemic continues, pharmacists will remain vital members of the multidisciplinary team dedicated to the fight against the virus.

2.
Critical Care Medicine ; 50:113-113, 2022.
Article in English | Academic Search Complete | ID: covidwho-1599261

ABSTRACT

The median propofol dose upon suspicion of possible PRIS was 20 mcg/kg/min (range, 20-50 mcg/kg/min) and providers decreased the dose in six (75%) patients at that time. B Introduction: b Propofol-related infusion syndrome (PRIS) is a rare and potentially devastating complication associated with prolonged high doses of propofol. Secondary outcomes included propofol dose and duration upon suspicion of PRIS, characterization of PRIS presentation, and mortality. [Extracted from the article] Copyright of Critical Care Medicine is the property of Lippincott Williams & Wilkins and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full . (Copyright applies to all s.)

3.
Pharmacotherapy ; 42(1): 71-90, 2022 01.
Article in English | MEDLINE | ID: covidwho-1469536

ABSTRACT

Data regarding the use of corticosteroids for treatment of acute respiratory distress syndrome (ARDS) are conflicting. As the coronavirus disease 2019 (COVID-19) pandemic progresses, more literature supporting the use of corticosteroids for COVID-19 and non-COVID-19 ARDS have emerged. Glucocorticoids are proposed to attenuate the inflammatory response and prevent progression to the fibroproliferative phase of ARDS through their multiple mechanisms and anti-inflammatory properties. The purpose of this systematic review was to comprehensively evaluate the literature surrounding corticosteroid use in ARDS (non-COVID-19 and COVID-19) in addition to a narrative review of clinical considerations of corticosteroid use in these patient populations. OVID Medline and EMBASE were searched. Randomized controlled trials evaluating the use of corticosteroids for COVID-19 and non-COVID-19 ARDS in adult patients on mortality outcomes were included. Risk of bias was assessed with the Risk of Bias 2.0 tool. There were 388 studies identified, 15 of which met the inclusion criteria that included a total of 8877 patients. The studies included in our review reported a mortality benefit in 6/15 (40%) studies with benefit being seen at varying time points of mortality follow-up (ICU survival, hospital, and 28 and 60 days) in the COVID-19 and non-COVID-19 ARDS studies. The two non-COVID19 trials assessing lung injury score improvements found that corticosteroids led to significant improvements with corticosteroid use. The number of mechanical ventilation-free days significantly were found to be increased with the use of corticosteroids in all four studies that assessed this outcome. Corticosteroids are associated with improvements in mortality and ventilator-free days in critically ill patients with both COVID-19 and non-COVID-19 ARDS, and evidence suggests their use should be encouraged in these settings. However, due to substantial differences in the corticosteroid regimens utilized in these trials, questions still remain regarding the optimal corticosteroid agent, dose, and duration in patients with ARDS.


Subject(s)
Adrenal Cortex Hormones , COVID-19 Drug Treatment , Respiratory Distress Syndrome , Adrenal Cortex Hormones/therapeutic use , Adult , Humans , Respiratory Distress Syndrome/drug therapy
6.
Community Ment Health J ; 57(7): 1252-1254, 2021 10.
Article in English | MEDLINE | ID: covidwho-1303329

ABSTRACT

This report describes the development, implementation and outcomes of a "COVID-19 Anxiety Hotline," designed to address the community's mental health crisis provoked by the coronavirus pandemic. The service was specifically designed using survey data regarding the effects of the COVID-19 pandemic on its staff and community members. Callers had around-the-clock direct access to mental healthcare providers at no cost. Quantitative analysis showed that nearly three out of four callers experienced new onset anxiety and insomnia driven by fear of exposure, and had difficulty accessing mental health care. In addition to immediate support, referral to tele-mental health care was provided to 86% of callers. Qualitative analysis indicates the effectiveness of immediate support and appropriate referrals using a tele-health platform. Our report indicates that the service was utilized by the general population, by health care workers, and rapidly provided referrals to individuals with limited access to mental health care during the pandemic.


Subject(s)
COVID-19 , Pandemics , Health Personnel , Hotlines , Humans , Mental Health , New York/epidemiology , SARS-CoV-2
8.
Ann Pharmacother ; 56(1): 5-15, 2022 01.
Article in English | MEDLINE | ID: covidwho-1228971

ABSTRACT

BACKGROUND: Propofol is commonly used to achieve ventilator synchrony in critically ill patients with coronavirus disease 2019 (COVID-19), yet its safety in this patient population is unknown. OBJECTIVE: To evaluate the safety, in particular the incidence of hypertriglyceridemia, of continuous infusion propofol in patients with COVID-19. METHODS: This was a retrospective study at 1 academic medical center and 1 affiliated teaching hospital in New York City. Adult, critically ill patients with COVID-19 who received continuous infusion propofol were included. Patients who received propofol for <12 hours, were transferred from an outside hospital while on mechanical ventilation, or did not have a triglyceride concentration obtained during the infusion were excluded. RESULTS: A total of 252 patients were included. Hypertriglyceridemia (serum triglyceride concentration ≥ 400 mg/dL) occurred in 38.9% of patients after a median cumulative dose of 4307 mg (interquartile range [IQR], 2448-9431 mg). The median time to triglyceride elevation was 3.8 days (IQR, 1.9-9.1 days). In the multivariable regression analysis, obese patients had a significantly greater odds of hypertriglyceridemia (odds ratio = 1.87; 95% CI = 1.10, 3.21). There was no occurrence of acute pancreatitis. The incidence of possible propofol-related infusion syndrome was 3.2%. CONCLUSION AND RELEVANCE: Hypertriglyceridemia occurred frequently in patients with COVID-19 who received propofol but did not lead to acute pancreatitis. Elevated triglyceride concentrations occurred more often and at lower cumulative doses than previously reported in patients without COVID-19. Application of these data may aid in optimal monitoring for serious adverse effects of propofol in patients with COVID-19.


Subject(s)
COVID-19 , Pancreatitis , Propofol , Acute Disease , Adult , Humans , Intensive Care Units , Propofol/adverse effects , Respiration, Artificial , Retrospective Studies , SARS-CoV-2
9.
Aerospace America ; 59(3):57, 2021.
Article in English | ProQuest Central | ID: covidwho-1187328

ABSTRACT

In a year where everything seems a little (or a lot) different, FIRST Lego League was no exception. Teams and organizers had to figure out how to run a competition with the new Covid-19 restrictions. Some school teams never actually met each other face to face throughout the entire season. For the tournaments, everything moved to a remote, online environment while trying to recreate as much of the experience as possible. Still, an amazing 120 teams choose to compete in Virginia/Washington DC, participating in 8 regional tournaments that were run from 23 Jan to 7 Feb. The top 64 of those teams also competed in the VA-DC FLL Championship tournament on 27 Feb. Whether it was finding new ways to utilize outdoor space to spending more time in sports to just getting up and dancing, teams challenged themselves to tackle this real-world problem as a part of their Innovation Project.

10.
Pharmacotherapy ; 40(12): 1180-1191, 2020 12.
Article in English | MEDLINE | ID: covidwho-866159

ABSTRACT

Evidence-based management of analgesia and sedation in COVID-19-associated acute respiratory distress syndrome remains limited. Non-guideline recommended analgesic and sedative medication regimens and deeper sedation targets have been employed for patients with COVID-19 due to exaggerated analgesia and sedation requirements with extended durations of mechanical ventilation. This, coupled with a desire to minimize nurse entry into COVID-19 patient rooms, marked obesity, altered end-organ function, and evolving medication shortages, presents numerous short- and long-term challenges. Alternative analgesic and sedative agents and regimens may pose safety risks and require judicious bedside management for appropriate use. The purpose of this commentary is to provide considerations and solutions for designing safe and effective analgesia and sedation strategies for adult patients with considerable ventilator dyssynchrony and sedation requirements, such as COVID-19.


Subject(s)
Analgesics/therapeutic use , COVID-19 Drug Treatment , COVID-19/complications , Evidence-Based Medicine/methods , Hypnotics and Sedatives/therapeutic use , Respiration, Artificial/methods , Humans , SARS-CoV-2
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