1. Activated factor XI-antithrombin complex presenting as an independent predictor of 30-days mortality in out-of-hospital cardiac arrest patients
- Author
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Rene van Oerle, Reidun Aarsetøy, Henri M. H. Spronk, H. Staines, Dennis W.T. Nilsen, Hugo ten Cate, Hildegunn Aarsetøy, Interne Geneeskunde, MUMC+: HVC Trombosezorg (8), MUMC+: MA Alg Interne Geneeskunde (9), MUMC+: HVC Pieken Trombose (9), RS: Carim - B04 Clinical thrombosis and Haemostasis, and MUMC+: DA CDL Analytisch cluster 1K (9)
- Subjects
medicine.medical_specialty ,Resuscitation ,medicine.medical_treatment ,INHIBITION ,030204 cardiovascular system & hematology ,Antithrombins ,Factor XIa ,03 medical and health sciences ,0302 clinical medicine ,AMERICAN-HEART-ASSOCIATION ,Factor XIa-antithrombin complex ,Internal medicine ,medicine ,Coagulopathy ,Humans ,Cardiopulmonary resuscitation ,Asystole ,Coagulation activation ,RISK ,COAGULOPATHY ,Out-of-hospital cardiac arrest ,Thrombin-antithrombin complex ,RESUSCITATION ,STATEMENT ,business.industry ,Proportional hazards model ,Antithrombin ,Factor IXa-antithrombin complex ,Hematology ,Prognosis ,medicine.disease ,Cardiopulmonary Resuscitation ,COAGULATION-FACTOR XI ,Quartile ,INTERNATIONAL LIAISON COMMITTEE ,030220 oncology & carcinogenesis ,Ventricular fibrillation ,SURVIVAL ,Cardiology ,business ,CARDIOPULMONARY ,medicine.drug - Abstract
BACKGROUND: Cardiac arrest and cardiopulmonary resuscitation (CPR) are associated with activated coagulation and microvascular fibrin deposition with subsequent multiorgan failure and adverse outcome.OBJECTIVES: Activated Factor XI-antithrombin (FXIa-AT) complex, activated Factor IX-antithrombin (FIXa-AT) complex and thrombin-antithrombin (TAT) complex were measured as markers of coagulation activation, and evaluated as independent prognostic indicators in out-of-hospital cardiac arrest (OHCA) patients.METHODS: From February 2007 until December 2010 blood samples were collected in close approximation to CPR from patients with OHCA of assumed cardiac origin. Follow-up samples in survivors were drawn 8-12 h and 24-48 h after hospital admission. All measurements were determined by ELISA.RESULTS: Thirty-seven patients presented with asystole and 77 with ventricular fibrillation as first recorded heart rhythm. At 30-days follow-up, 70 patients (61.4%) had died. All patients had elevated levels of FXIa-AT complex, FIXa-AT complex and TAT. Initial levels were significantly higher in non-survivors compared to 30-days survivors. A significant increase in risk of 30-days all-cause mortality was observed through increasing quartiles of all three biomarkers in univariate Cox regression analysis. Compared to the lowest quartile (Q1), only FXIa-AT complex levels in Q3 (HR 3.17, p = 0.011) and Q2 (HR 3.02, p = 0.016) were independently associated with all-cause mortality in the multivariable analysis. FIXa-AT complex and TAT-complex did not behave as independent predictors.CONCLUSIONS: Complexes of FXIa-AT were independently associated with 30-days survival in OHCA-patients.CLINICAL TRIAL REGISTRATION: ClinicalTrials. gov, NCT02886273.
- Published
- 2021
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