key: cord-0747077-d7h9gdfd
authors: Reeder, Jacob A.; Reynolds, Tessa R.; Gilbert, Brian W.
title: Successful Use of Aspirin, Apixaban, and Viscoelastography in a Patient with Severe COVID Disease and Allergy to Porcine Products
date: 2021-01-29
journal: Hosp Pharm
DOI: 10.1177/0018578721990898
sha: 9d378e63014c3242b86a006ce757174049e3e367
doc_id: 747077
cord_uid: d7h9gdfd

Coagulation abnormalities are frequently described in patients with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Common thromboprophylaxis and anticoagulation treatment strategies include the use of heparinoid therapy. We describe a 57-year-old woman with an allergy to porcine products that was started on apixaban for anticoagulation therapy given her allergy profile and need for venous thromboembolism prophylaxis. Apixaban and aspirin therapy were optimized with the support of serial viscoelastography and platelet function assays. Our patient experienced respiratory failure requiring intubation for 7 days but was successfully weaned to room air, tolerated a regular diet, and ultimately discharged to home after a 17-day hospital course. Here we report the safe and successful use of aspirin, apixaban, and viscoelastography for COVID-19-associated coagulopathy.

The World Health Organization has characterized the corona virus disease 2019 (COVID19) as a global pandemic in early March of 2020. The virus responsible for this disease has been defined as severe acute respiratory syndrome (SARS) coronavirus 2 (SARSCoV2). SARSCoV2 targets the respiratory epithelium, causing acute lung injury with potential for respiratory failure. 1 While much is still unknown about the downstream complications of this disease, an ini tial coagulopathy has been characterized by increased level of clotting factors, enhanced platelet activation, and sup pressed fibrinolyisis for those with severe illness. 1, 2 Exact definitions differ between consensus groups and societies, but the laboratory findings in COVID19associated coagu lopathy can include: elevated ddimer, elevated prothrombin time (PT) and international normalized ratio (INR), and increased platelet count and fibrinogen. Though these are surrogate markers, the abnormalities noted in these lab val ues have correlated with a significant increase in thrombo embolic complications. 3 Notably, Klok et al. reported an incidence of venous thromboembolism (VTE) in 27% of patients receiving standard thromboprophylaxis, while others have evaluated empiric full dose anticoagulation regardless of clot presence. 4 The formation of VTE during COVID, even in patients receiving prophylactic or full doses of anticoagulation, have been described which has prompted many to initiate antiplatelet regimens in addition to antico agulation. However, the addition of concomitant antiplatelet regimens with full dose anticoagulation may increase the patients risk for bleeding making monitoring of coagulopa thy imperative. Thromboelastography (TEG) can measure whole blood clot formation and breakdown and is ideal for critically ill patients. 5 Critically ill patients are already at an increased risk for VTE for numerous reasons, and COVID 19 potentiates that risk. 4, 6 The importance of recognizing this risk is imperative to mitigating morbidity and mortality in these patients. 3

A 57yearold woman presented to our emergency depart ment with an 8day history of cough, myalgia, dysgeusia, and endorsed increasing shortness of breath. Her past medi cal history included arthritis, type II diabetes mellitus, hyperlipidemia, hypertension, obesity, and coronary artery disease requiring stent placement. Of note, the patient's allergy history included pork and porcine products. Upon initial evaluation, she was found to be febrile (100.4°F), tachycardic with a heart rate of 102 beats per minute, and an oxygen saturation of 54% on room air. Empiric antimicro bial treatment was started, and intravenous fluid administra tion was withheld for high suspicion of COVID19 disease. Chest Xray findings revealed diffuse increased interstitial and airspace opacities through the lungs. A nasopharyngeal swab resulted positive for SARSCoV2 via a polymerase chain reaction. Her initial baseline inflammatory labs included: Creactive protein >190 mg/L, ferritin 306 ng/ mL, lactate dehydrogenase 669 units/L, and a ddimer 1087 ng/mL. Other significant findings included: white blood cell count 11 100/uL, red blood cell count 3.95/µL, hemoglobin 10.8 g/dL, hematocrit 34.1%, and platelet count of 397 000/uL. Chemical venous thromboembolism prophylaxis was warranted; however, our patient had a significant allergy to pork and porcine products. Due to her allergy profile, hepa rinoids were avoided. The decision was made to start a direct oral anticoagulant (DOAC), apixaban 5 mg by mouth twice daily and resume her home regimen of aspirin 81 mg by mouth daily. Since the patient was started on full antico agulation with apixaban, the decision was made to hold her clopidogrel due to the concern for increased bleeding risk. She was also started on 6 mg of dexamethasone by mouth once daily. Over the next 24 hours, the patient required increasing respiratory support to maintain oxygen saturation with bilevel positive airway pressure noninvasive ventila tion. The following day, her ddimer increased to 2287 ng/ mL and a viscoelastic test (TEG ® ) was performed to assist with coagulopathy identification. We also wanted to ensure a therapeutic effect with apixaban given the significant drugdrug interaction with dexamethasone being a pglyco protein inducer. The initial TEG ® resulted with a shortened K time and increased maximum amplitude reflecting a hypercoagulable state. Given these objective findings and clinical course of the patient, the decision was made to increase the apixaban to 10 mg by mouth twice daily (BID). Overnight, the patient required intubation for refractory hypoxemia. Daily TEG ® labs were performed to assess the patient's response and assist in pharmacologic management, including dose titration of apixaban and aspirin which are included in Table 1 . On day 3, the TEG ® resulted with an increase in the maximum amplitude from 80 to 82 mm suggesting an increase in platelet activity or quantity. Concomitantly, an increasing ddimer and thrombocytosis was also present. Therefore, the decision was made to increase her dose of aspirin from 81 to 325 mg daily, while maintaining the apixaban dose at 10 mg BID. A platelet func tion assay was drawn the next day to provide a more sensi tive measure of platelet reactivity. Our patients assay resulted 450 aspirin reaction units (ARU). A result of <550 ARU sig nifies aspirin induced platelet dysfunction. After 7 days of apixaban 10 mg twice daily and a decreasing ddimer, the dose was decreased to 5 mg twice daily. Our patient was extubated on day 9 of hospital stay and transferred out of the intensive care unit on day 11. She was successfully weaned to room air, tolerated a regular diet, and ultimately discharged to home after a 17day hospital course.

Evidence for the most appropriate treatment in COVID19 positive patients is constantly evolving. A guidance docu ment for the management of this patient population is avail able through the National Institute of Health (NIH), however, nearly all the recommendations regarding antithrombotic therapy are based on expert opinion. 7 Although some guid ance is provided for COVID19 positive patients transition ing from warfarin to a DOAC in the outpatient setting, limited direction has been provided when initiating DOACs for the use of confirmed or suspected VTE in the inpatient setting. 7 The NIH document states, patients with COVID19 who experience a thromboembolic event or who are highly suspected to have thromboembolic disease at a time when imaging is not possible, should be managed with therapeutic doses of anticoagulant therapy as per the standard of care for patients without COVID19. 7 In our patient, apixaban was chosen for chemical VTE prophylaxis based on allergy history limiting the use of hepa rinoid products. Additional agents that could be used in this setting include other DOACs, direct thrombin inhibitors, or fondaparinux. The initial dosing regimen of 5 mg twice daily was selected given the need for pharmacologic VTE prophy laxis and was only escalated to 10 mg twice daily once a high suspicion for thromboembolic disease was appreciated via TEG ® . No radiographic imaging was performed to confirm the presence of thromboembolism. Our patient remained on aspirin monotherapy and apixaban 5 mg by mouth twice daily for 2 wk post discharge.

A study performed by Cui et al. reported a sensitivity of 85% and specificity of 88.5% for venous thromboembolism in COVID19 positive patients with a ddimer >1.5 mg/L. 8 Although the ddimer is a nonspecific acute phase reactant, in the setting of a positive COVID19 diagnosis, providers should consider utilizing a similar threshold to guide anti coagulation initiation or escalation. An additional tool that can be used to quantify the presence of coagulopathy is thromboelastography. 5 Our facility utilizes the TEG ® 5000 Thromboelastograph ® Hemostasis Analyzer System. This allows clinicians to identify coagulopathy via whole blood rather than through individual conventional testing. With the help of TEG ® , we were able to optimize pharmacologic ther apy to treat our patients' specific hypercoagulable profile.

The apixaban package insert (PI) describes avoiding concomitant use of pglycoprotein inducers as this reduces drug levels in the blood. 9 Medications included in the PI to avoid include carbamazepine, rifampin, and St Johns wort. 9 While dexamethasone is not listed, the theoretical concern for a decrease in serum concentrations remains. An ongoing study in multiple myeloma patients is investigating this exact drugdrug interaction, and although this is a select patient population, in vivo data such as antiXa levels and plasma apixaban levels are being collected. Until further data are collected and published describing this drugdrug interaction, TEG ® can aid clinicians with quantifying the significance.

Although there remains a paucity of evidence for anti coagulation practices in severe COVID19 disease, several randomized controlled trials are ongoing evaluating multiple thromboprophylaxis strategies. Moving forward, our group will continue to use thromboelastography as an adjunct to conventional coagulation parameters to guide anticoagula tion decisions and consider apixaban as an appropriate alter native to heparinoids.

This is the first case report to our knowledge highlighting the safe and successful use of aspirin and apixaban for COVID19associated coagulopathy in a patient with aller gies to porcine containing products.

Written informed consent for patient information to be published was provided by the patient.

The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

The author(s) received no financial support for the research, author ship, and/or publication of this article.

COVID19 and its implications for thrombosis and anticoagulation

Coagulopathy of coronavirus disease 2019

Anticoagulant treatment is associated with decreased mortality in severe coro navirus disease 2019 patients with coagulopathy

Incidence of thrombotic complications in critically ill ICU patients with COVID19

Tracing the lines: a review of viscoelastography for emergency medicine clinicians

Deep vein thrombosis among intensive care unit patients; an epidemiologic study

Coronavirus disease 2019 (COVID19) treatment guidelines. National Institutes of Health

Prevalence of venous thromboembolism in patients with severe novel coronavirus pneumonia

Eliquis (apixaban)

Jacob A. Reeder https://orcid.org/0000000196668950Brian W. Gilbert https://orcid.org/0000000213857500