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Critical Care Medicine ; 50:123-123, 2022.
Article in English | Academic Search Complete | ID: covidwho-1597929

ABSTRACT

B Introduction: b Continuous infusion sedative and analgesic medications are frequently used in the management of mechanically ventilated patients with acute respiratory distress syndrome (ARDS) due to coronavirus disease 2019 (COVID-19). There were no differences in duration of mechanical ventilation, ICU length of stay, and symptoms of withdrawal and pain. B Methods: b A single-center, retrospective study was conducted in mechanically ventilated adult patients with ARDS due to COVID-19 infection who received >=7 days of continuous infusion opioid and/or benzodiazepine. [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.)

2.
J Thromb Thrombolysis ; 51(4): 966-970, 2021 May.
Article in English | MEDLINE | ID: covidwho-834030

ABSTRACT

Coronavirus disease 2019 (COVID-19) appears to be associated with increased arterial and venous thromboembolic disease. These presumed abnormalities in hemostasis have been associated with filter clotting during continuous renal replacement therapy (CRRT). We aimed to characterize the burden of CRRT filter clotting in COVID-19 infection and to describe a CRRT anticoagulation protocol that used anti-factor Xa levels for systemic heparin dosing. Multi-center study of consecutive patients with COVID-19 receiving CRRT. Primary outcome was CRRT filter loss. Sixty-five patients were analyzed, including 17 using an anti-factor Xa protocol to guide systemic heparin dosing. Fifty-four out of 65 patients (83%) lost at least one filter. Median first filter survival time was 6.5 [2.5, 33.5] h. There was no difference in first or second filter loss between the anti-Xa protocol and standard of care anticoagulation groups, however fewer patients lost their third filter in the protocolized group (55% vs. 93%) resulting in a longer median third filter survival time (24 [15.1, 54.2] vs. 17.3 [9.5, 35.1] h, p = 0.04). The rate of CRRT filter loss is high in COVID-19 infection. An anticoagulation protocol using systemic unfractionated heparin, dosed by anti-factor Xa levels is reasonable approach to anticoagulation in this population.


Subject(s)
Biomarkers, Pharmacological/analysis , COVID-19 , Continuous Renal Replacement Therapy , Critical Illness/therapy , Drug Monitoring/methods , Heparin , Micropore Filters/adverse effects , Anticoagulants/administration & dosage , Anticoagulants/adverse effects , Blood Coagulation/drug effects , COVID-19/blood , COVID-19/physiopathology , COVID-19/therapy , Clinical Protocols , Continuous Renal Replacement Therapy/adverse effects , Continuous Renal Replacement Therapy/methods , Dose-Response Relationship, Drug , Equipment Failure Analysis , Factor Xa/analysis , Female , Heparin/administration & dosage , Heparin/adverse effects , Humans , Male , Middle Aged , SARS-CoV-2
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