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Hematology Consultations during the COVID-19 Pandemic at a University Medical Center

Background Patients with coronavirus disease 2019 (COVID-19) frequently have hematologic derangements prompting specialty consultation. Management of such derangements remain complicated by a nascent evidence base. Our primary objective was to identify the main reasons for hematology consultation in...

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Autores principales: Choi, Daniel C, Seshadri, Madhav, De Sancho, Maria T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Hematology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8330223/
http://dx.doi.org/10.1182/blood-2020-143134
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author Choi, Daniel C
Seshadri, Madhav
De Sancho, Maria T
author_facet Choi, Daniel C
Seshadri, Madhav
De Sancho, Maria T
author_sort Choi, Daniel C
collection PubMed
description Background Patients with coronavirus disease 2019 (COVID-19) frequently have hematologic derangements prompting specialty consultation. Management of such derangements remain complicated by a nascent evidence base. Our primary objective was to identify the main reasons for hematology consultation in patients with COVID-19 at a university medical center in New York City during the initial peak of the pandemic in 2020. We sought to determine the hematologic parameters that may affect patient outcomes and to provide recommendations to improve clinical practice. Methods We completed an observational study of consecutive hematology consultations requested between March 16 and April 27, 2020, for adult patients with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection admitted to a university medical center. Diagnosis of SARS-CoV-2 infection was confirmed via reverse transcriptase polymerase chain reaction of nasopharyngeal swabs. Using the electronic medical record, we collected demographic information, reasons for consultation, laboratory parameters relevant to hematology, diagnoses, recommendations, and outcomes. Descriptive statistics and Wilcoxon rank sum tests were used for data analysis. Results A total of 74 hematology consultations for unique patients were completed during the 6-week study period. The most frequent reason for consultation was for anticoagulation recommendations in the setting of suspected or confirmed acute thrombosis (46%), followed by requests for management advice regarding cytopenias (24%) and other laboratory abnormalities including elevated D-dimer and thrombocytosis (22%). As shown in Table 1, the observed rate of acute thrombosis (35 events in 31 patients, 41% of study population) did not fully account for the observed rate of therapeutic anticoagulation use (55 patients, 74% of study population). Only 5 of 25 patients without diagnosed thrombosis who received therapeutic anticoagulation during admission had a confirmed prior indication for anticoagulation such as atrial fibrillation or venous thromboembolism (VTE). Objectively documented VTE (15 events in 15 patients) was the most common type of thrombosis, followed by thrombotic occlusion of continuous renal replacement (CRRT) circuits (14 events in 14 patients). Two cases of cutaneous thrombosis were also observed, identified on biopsies of retiform purpuric lesions. Unfractionated heparin was the most frequently utilized parenteral agent for therapeutic anticoagulation. Interestingly, a significant number of patients received argatroban (22 patients), despite a comparably low rate of evaluation for heparin-induced thrombocytopenia (10 patients tested). Occluded CRRT circuits accounted for the majority of argatroban use (12 patients), followed by thrombocytopenia (10 patients), including 3 of the 4 patients without thrombosis who received argatroban. Patients objectively diagnosed with acute thromboses had higher levels of D-dimer (median 1166 ng/mL) and ferritin (1420 ng/mL) at initial admission relative to patients without thromboses (median 792 ng/mL and 918 ng/mL, respectively). Notable differences in peak D-dimer (median 7756 ng/mL vs 3399 ng/mL) and fibrinogen nadir (258 mg/dL vs 454 mg/dL) were also observed. Statistical analysis via Wilcoxon rank sum test (p-values reported) corroborated the presence of differences in the distribution of laboratory values between the two groups. Acute thrombosis was also associated with a lower rate of hospital discharge and a higher rate of mortality during the study period (Table 1). Conclusions Hematologic consultation patterns during the peak of the COVID-19 pandemic in New York City were characterized by frequent requests for assistance with anticoagulation management, further corroborated by a high incidence of acute thrombotic events. The early suspicion of thrombosis and laboratory derangements on hospital admission appeared to drive widespread use of empiric anticoagulation. Atypical events like CRRT circuit occlusions and concurrent hematologic abnormalities like thrombocytopenia likely underlie the notable use of argatroban in this cohort. These observations underscore the importance of prospective randomized controlled studies to address anticoagulation strategies and routine hematologic laboratory monitoring in hospitalized patients with COVID-19. [Figure: see text] DISCLOSURES: De Sancho:Sanofi Genzyme:Membership on an entity's Board of Directors or advisory committees;Apellis Pharmaceuticals:Membership on an entity's Board of Directors or advisory committees;Bio Products Laboratory:Membership on an entity's Board of Directors or advisory committees.
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spelling pubmed-83302232021-08-03 Hematology Consultations during the COVID-19 Pandemic at a University Medical Center Choi, Daniel C Seshadri, Madhav De Sancho, Maria T Blood 331.Pathophysiology of Thrombosis Background Patients with coronavirus disease 2019 (COVID-19) frequently have hematologic derangements prompting specialty consultation. Management of such derangements remain complicated by a nascent evidence base. Our primary objective was to identify the main reasons for hematology consultation in patients with COVID-19 at a university medical center in New York City during the initial peak of the pandemic in 2020. We sought to determine the hematologic parameters that may affect patient outcomes and to provide recommendations to improve clinical practice. Methods We completed an observational study of consecutive hematology consultations requested between March 16 and April 27, 2020, for adult patients with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection admitted to a university medical center. Diagnosis of SARS-CoV-2 infection was confirmed via reverse transcriptase polymerase chain reaction of nasopharyngeal swabs. Using the electronic medical record, we collected demographic information, reasons for consultation, laboratory parameters relevant to hematology, diagnoses, recommendations, and outcomes. Descriptive statistics and Wilcoxon rank sum tests were used for data analysis. Results A total of 74 hematology consultations for unique patients were completed during the 6-week study period. The most frequent reason for consultation was for anticoagulation recommendations in the setting of suspected or confirmed acute thrombosis (46%), followed by requests for management advice regarding cytopenias (24%) and other laboratory abnormalities including elevated D-dimer and thrombocytosis (22%). As shown in Table 1, the observed rate of acute thrombosis (35 events in 31 patients, 41% of study population) did not fully account for the observed rate of therapeutic anticoagulation use (55 patients, 74% of study population). Only 5 of 25 patients without diagnosed thrombosis who received therapeutic anticoagulation during admission had a confirmed prior indication for anticoagulation such as atrial fibrillation or venous thromboembolism (VTE). Objectively documented VTE (15 events in 15 patients) was the most common type of thrombosis, followed by thrombotic occlusion of continuous renal replacement (CRRT) circuits (14 events in 14 patients). Two cases of cutaneous thrombosis were also observed, identified on biopsies of retiform purpuric lesions. Unfractionated heparin was the most frequently utilized parenteral agent for therapeutic anticoagulation. Interestingly, a significant number of patients received argatroban (22 patients), despite a comparably low rate of evaluation for heparin-induced thrombocytopenia (10 patients tested). Occluded CRRT circuits accounted for the majority of argatroban use (12 patients), followed by thrombocytopenia (10 patients), including 3 of the 4 patients without thrombosis who received argatroban. Patients objectively diagnosed with acute thromboses had higher levels of D-dimer (median 1166 ng/mL) and ferritin (1420 ng/mL) at initial admission relative to patients without thromboses (median 792 ng/mL and 918 ng/mL, respectively). Notable differences in peak D-dimer (median 7756 ng/mL vs 3399 ng/mL) and fibrinogen nadir (258 mg/dL vs 454 mg/dL) were also observed. Statistical analysis via Wilcoxon rank sum test (p-values reported) corroborated the presence of differences in the distribution of laboratory values between the two groups. Acute thrombosis was also associated with a lower rate of hospital discharge and a higher rate of mortality during the study period (Table 1). Conclusions Hematologic consultation patterns during the peak of the COVID-19 pandemic in New York City were characterized by frequent requests for assistance with anticoagulation management, further corroborated by a high incidence of acute thrombotic events. The early suspicion of thrombosis and laboratory derangements on hospital admission appeared to drive widespread use of empiric anticoagulation. Atypical events like CRRT circuit occlusions and concurrent hematologic abnormalities like thrombocytopenia likely underlie the notable use of argatroban in this cohort. These observations underscore the importance of prospective randomized controlled studies to address anticoagulation strategies and routine hematologic laboratory monitoring in hospitalized patients with COVID-19. [Figure: see text] DISCLOSURES: De Sancho:Sanofi Genzyme:Membership on an entity's Board of Directors or advisory committees;Apellis Pharmaceuticals:Membership on an entity's Board of Directors or advisory committees;Bio Products Laboratory:Membership on an entity's Board of Directors or advisory committees. American Society of Hematology 2020-11-05 2021-08-03 /pmc/articles/PMC8330223/ http://dx.doi.org/10.1182/blood-2020-143134 Text en Copyright © 2020 American Society of Hematology. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle 331.Pathophysiology of Thrombosis
Choi, Daniel C
Seshadri, Madhav
De Sancho, Maria T
Hematology Consultations during the COVID-19 Pandemic at a University Medical Center
title Hematology Consultations during the COVID-19 Pandemic at a University Medical Center
title_full Hematology Consultations during the COVID-19 Pandemic at a University Medical Center
title_fullStr Hematology Consultations during the COVID-19 Pandemic at a University Medical Center
title_full_unstemmed Hematology Consultations during the COVID-19 Pandemic at a University Medical Center
title_short Hematology Consultations during the COVID-19 Pandemic at a University Medical Center
title_sort hematology consultations during the covid-19 pandemic at a university medical center
topic 331.Pathophysiology of Thrombosis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8330223/
http://dx.doi.org/10.1182/blood-2020-143134
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