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Serial markers of coagulation and inflammation and the occurrence of clinical pulmonary thromboembolism in mechanically ventilated patients with SARS-CoV-2 infection; the prospective Maastricht intensive care COVID cohort.
Mulder, Mark M G; Brandts, LIoyd; Brüggemann, Renée A G; Koelmann, Marcel; Streng, Alexander S; Olie, Renske H; Gietema, Hester A; Spronk, Henri M H; van der Horst, Iwan C C; Sels, Jan-Willem E M; Wildberger, Joachim E; van Kuijk, Sander M J; Schnabel, Ronny M; Ten Cate, Hugo; Henskens, Yvonne M C; van Bussel, Bas C T.
Affiliation
  • Mulder MMG; Department of Intensive Care Medicine, Maastricht University Medical Centre+, Maastricht, The Netherlands. mark.mulder@mumc.nl.
  • Brandts L; Department of Clinical Epidemiology and Medical Technology Assessment, Maastricht University Medical Centre+, Maastricht, The Netherlands.
  • Brüggemann RAG; Department of Internal Medicine, Maastricht University Medical Centre+, Maastricht, The Netherlands.
  • Koelmann M; Department of Intensive Care Medicine, Maastricht University Medical Centre+, Maastricht, The Netherlands.
  • Streng AS; Department of Clinical Chemistry, Central Diagnostic Laboratory, Maastricht University Medical Centre+, Maastricht, The Netherlands.
  • Olie RH; Department of Internal Medicine, Maastricht University Medical Centre+, Maastricht, The Netherlands.
  • Gietema HA; Thrombosis Expert Centre Maastricht and Department of Internal Medicine, Section Vascular Medicine, Maastricht University Medical Centre+, Maastricht, The Netherlands.
  • Spronk HMH; Cardiovascular Research Institute Maastricht (CARIM), Maastricht University, Maastricht, The Netherlands.
  • van der Horst ICC; Department of Radiology and Nuclear Medicine, Maastricht University Medical Centre+, Maastricht, The Netherlands.
  • Sels JEM; GROW School of Oncology and Developmental Biology, Maastricht University, Maastricht, The Netherlands.
  • Wildberger JE; Thrombosis Expert Centre Maastricht and Department of Internal Medicine, Section Vascular Medicine, Maastricht University Medical Centre+, Maastricht, The Netherlands.
  • van Kuijk SMJ; Cardiovascular Research Institute Maastricht (CARIM), Maastricht University, Maastricht, The Netherlands.
  • Schnabel RM; Department of Intensive Care Medicine, Maastricht University Medical Centre+, Maastricht, The Netherlands.
  • Ten Cate H; Cardiovascular Research Institute Maastricht (CARIM), Maastricht University, Maastricht, The Netherlands.
  • Henskens YMC; Department of Intensive Care Medicine, Maastricht University Medical Centre+, Maastricht, The Netherlands.
  • van Bussel BCT; Department of Cardiology, Maastricht University Medical Centre+, Maastricht, The Netherlands.
Thromb J ; 19(1): 35, 2021 May 31.
Article in En | MEDLINE | ID: mdl-34059058
BACKGROUND: The incidence of pulmonary thromboembolism is high in SARS-CoV-2 patients admitted to the Intensive Care. Elevated biomarkers of coagulation (fibrinogen and D-dimer) and inflammation (c-reactive protein (CRP) and ferritin) are associated with poor outcome in SARS-CoV-2. Whether the time-course of fibrinogen, D-dimer, CRP and ferritin is associated with the occurrence of pulmonary thromboembolism in SARS-CoV-2 patients is unknown. We hypothesise that patients on mechanical ventilation with SARS-CoV-2 infection and clinical pulmonary thromboembolism have lower concentrations of fibrinogen and higher D-dimer, CRP, and ferritin concentrations over time compared to patients without a clinical pulmonary thromboembolism. METHODS: In a prospective study, fibrinogen, D-dimer, CRP and ferritin were measured daily. Clinical suspected pulmonary thromboembolism was either confirmed or excluded based on computed tomography pulmonary angiography (CTPA) or by transthoracic ultrasound (TTU) (i.e., right-sided cardiac thrombus). In addition, patients who received therapy with recombinant tissue plasminogen activator were included when clinical instability in suspected pulmonary thromboembolism did not allow CTPA. Serial data were analysed using a mixed-effects linear regression model, and models were adjusted for known risk factors (age, sex, APACHE-II score, body mass index), biomarkers of coagulation and inflammation, and anticoagulants. RESULTS: Thirty-one patients were considered to suffer from pulmonary thromboembolism ((positive CTPA (n = 27), TTU positive (n = 1), therapy with recombinant tissue plasminogen activator (n = 3)), and eight patients with negative CTPA were included. After adjustment for known risk factors and anticoagulants, patients with, compared to those without, clinical pulmonary thromboembolism had lower average fibrinogen concentration of - 0.9 g/L (95% CI: - 1.6 - - 0.1) and lower average ferritin concentration of - 1045 µg/L (95% CI: - 1983 - - 106) over time. D-dimer and CRP average concentration did not significantly differ, 561 µg/L (- 6212-7334) and 27 mg/L (- 32-86) respectively. Ferritin lost statistical significance, both in sensitivity analysis and after adjustment for fibrinogen and D-dimer. CONCLUSION: Lower average concentrations of fibrinogen over time were associated with the presence of clinical pulmonary thromboembolism in patients at the Intensive Care, whereas D-dimer, CRP and ferritin were not. Lower concentrations over time may indicate the consumption of fibrinogen related to thrombus formation in the pulmonary vessels.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Language: En Journal: Thromb J Year: 2021 Document type: Article Affiliation country: Netherlands Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Language: En Journal: Thromb J Year: 2021 Document type: Article Affiliation country: Netherlands Country of publication: United kingdom