October 2021: COVID-19 Related Laboratory Coagulation Findings

Speaker

Katrien Devreese, MD, PhD
Professor in Hematology/Coagulation
Ghent University (Belgium

COVID-19 Related Laboratory Coagulation Findings

The high rate of thromboembolism in COVID-19 patients goes along with derangements in coagulation laboratory parameters. Hemostasis testing has an important role in diagnosed COVID-19 patients. Elevated D-dimer levels were found to be a crucial laboratory marker in the risk assessment of thrombosis in COVID-19 patients. The diagnostic approach also includes prothrombin time, platelet count, and fibrinogen. Other markers (activated partial thromboplastin time (aPTT), fibrinolysis parameters, coagulation factors, natural anticoagulants, antiphospholipid antibodies, and parameters obtained by thromboelastography or thrombin generation assays) have been described as being deranged, and may help understand the pathophysiology of thrombosis in COVID-19. For monitoring the heparin anticoagulant therapy, the anti-Xa assay is suggested, because the severe acute phase reaction (high fibrinogen and high factor VIII) shortens the aPTT. Recently, the post-COVID-19 vaccination immune thrombotic thrombocytopenia has been described. Although this is a rare phenomenon, awareness is important with a proper diagnostic approach.

Learning objectives

  • To review the blood coagulation mechanisms involved in COVID-19 infection and define the derangement in laboratory parameters
  • How to monitor anticoagulation therapy in inflammatory patients
  • Highlight interpretation of laboratory tests in overlapping syndromes as antiphospholipid syndrome and heparin-induced thrombocytopenia, and post-vaccine immune thrombotic thrombocytopenia

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Answers to Questions from Live Webinar

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Answers to Questions from Live Webinar

Below is a list of questions received from the live webinar attendees. Click on any question to reveal the speaker's response.

NEW QUESTION/ANSWER

It is common to see necrosis in cHL, hard to put a number on it offhand.

NEW QUESTION/ANSWER

Classic in the 2017 WHO

NEW QUESTION/ANSWER

It can be expressed in both CHL and ALCL so it may not be reliable.

NEW QUESTION/ANSWER

CD15, CD30, CD20, PAX5, OCT2, BOB1 and CD45 can be helpful.

NEW QUESTION/ANSWER

I have never seen this.

NEW QUESTION/ANSWER

No, there is no clinical role for this at present.

NEW QUESTION/ANSWER

This would be highly unusual

NEW QUESTION/ANSWER

I don’t have any experience with J chain but is usually negative in RS-cells. MUM1 is typically positive but not specific.

NEW QUESTION/ANSWER

No

NEW QUESTION/ANSWER

Yes. J-chain and MEF2B have been reported to be useful as well. PMID: 28851661

NEW QUESTION/ANSWER

I don’t think it is particularly helpful, some cases of cHL may have rearranged IGH

NEW QUESTION/ANSWER

No

NEW QUESTION/ANSWER

I don’t find it that helpful

NEW QUESTION/ANSWER

There has been some data to suggest it is prognostic.

NEW QUESTION/ANSWER

It does not appear to commonly result in loss of CD30 expression in follow-up biopsy but I don’t believe this has been extensively studied.

NEW QUESTION/ANSWER

Yes, for T-cell lymphomas including cutaneous T-cell lymphomas it is reasonable to report the % positive tumor cells because some trials that resulted in the approval of brentuximab used specific cutoffs.