PMID- 32703545 OWN - NLM STAT- MEDLINE DCOM- 20201102 LR - 20201102 IS - 1535-7732 (Electronic) IS - 1051-0443 (Linking) VI - 31 IP - 8 DP - 2020 Aug TI - Evaluation of Fibrinogen Levels during Catheter-Directed Thrombolysis for Acute Pulmonary Embolism. PG - 1281-1289 LID - S1051-0443(20)30434-6 [pii] LID - 10.1016/j.jvir.2020.04.032 [doi] AB - PURPOSE: To evaluate the effect of catheter-directed thrombolysis (CDT) with tissue plasminogen activator (tPA) on plasma fibrinogen levels (PFLs) in the setting of acute pulmonary embolism (PE) and the relationship between PFL and hemorrhagic complications. MATERIALS AND METHODS: A retrospective review of CDT procedures between 2009 and 2019 identified 147 CDT procedures for massive or submassive PE (55.8% males; age, 56.5 +/- 14.8 years; 90.5% submassive). All patients received therapeutic anticoagulation during CDT with unfractionated heparin (UFH) (69.4%) or low-molecular-weight heparin (LMWH, 30.6%) infusion. CDT was performed with ultrasound-accelerated thrombolysis (USAT) catheters (n = 98), conventional catheter-directed thrombolysis (CCDT) catheters (n = 34), or a combination of both (n = 15). RESULTS: There was a decrease (P = .007) of 15.1 +/- 69.4 mg/dl from the initial PFL (376.1 +/- 122.7 mg/dl) to the final PFL (361 +/- 118.7 mg/dl), which was measured after a mean of 24.1 +/- 11.7 hours with a mean tPA dose of 28.3 +/- 14.2 mg. The fibrinogen nadir was 327.6 +/- 107.1 mg/dl measured 13.4 +/- 10.3 hours after initiation of thrombolysis. Of patients with hemorrhagic complications (n = 6), initial, final, and nadir PFL were not significantly lower (P = .053, P = .081, and P = .086, respectively) than the remainder of the cohort. No significant difference was noted in initial and final PFL between the LMWH and UFH groups (P = .2 and P = .1, respectively) or between the CCDT and USAT groups (P = .5 and P = .9, respectively). The UFH group had a lower nadir PFL than the LMWH group (P = .03). CONCLUSIONS: Despite a significant drop in PFL during CDT for acute PE, this was not associated with hemorrhagic complications. These findings were not affected by the choice of anticoagulant or catheter delivery system. CI - Copyright (c) 2020 SIR. Published by Elsevier Inc. All rights reserved. FAU - Graif, Assaf AU - Graif A AD - Department of Vascular and Interventional Radiology, Christiana Care Health System, 4755 Ogletown Stanton Rd, Ste 1e20, Newark, DE, 19713. Electronic address: Agraif@christianacare.org. FAU - Grilli, Christopher J AU - Grilli CJ AD - Department of Vascular and Interventional Radiology, Christiana Care Health System, 4755 Ogletown Stanton Rd, Ste 1e20, Newark, DE, 19713. FAU - Kimbiris, George AU - Kimbiris G AD - Department of Vascular and Interventional Radiology, Christiana Care Health System, 4755 Ogletown Stanton Rd, Ste 1e20, Newark, DE, 19713. FAU - Paik, Helen H AU - Paik HH AD - Department of Vascular and Interventional Radiology, Christiana Care Health System, 4755 Ogletown Stanton Rd, Ste 1e20, Newark, DE, 19713. FAU - Leung, Daniel A AU - Leung DA AD - Department of Vascular and Interventional Radiology, Christiana Care Health System, 4755 Ogletown Stanton Rd, Ste 1e20, Newark, DE, 19713. LA - eng PT - Journal Article DEP - 20200720 PL - United States TA - J Vasc Interv Radiol JT - Journal of vascular and interventional radiology : JVIR JID - 9203369 RN - 0 (Anticoagulants) RN - 0 (Biomarkers) RN - 0 (Fibrinolytic Agents) RN - 9001-32-5 (Fibrinogen) RN - EC 3.4.21.68 (Tissue Plasminogen Activator) SB - IM CIN - J Vasc Interv Radiol. 2020 Aug;31(8):1290-1291. PMID: 32624342 MH - Acute Disease MH - Adult MH - Aged MH - Anticoagulants/administration & dosage MH - Biomarkers/blood MH - Female MH - Fibrinogen/*metabolism MH - Fibrinolytic Agents/*administration & dosage/adverse effects MH - Hemorrhage/blood/chemically induced MH - Humans MH - Male MH - Middle Aged MH - Pulmonary Embolism/blood/diagnostic imaging/*drug therapy MH - Retrospective Studies MH - Risk Factors MH - *Thrombolytic Therapy/adverse effects MH - Time Factors MH - Tissue Plasminogen Activator/*administration & dosage/adverse effects MH - Treatment Outcome EDAT- 2020/07/25 06:00 MHDA- 2020/11/03 06:00 CRDT- 2020/07/25 06:00 PHST- 2020/01/17 00:00 [received] PHST- 2020/04/08 00:00 [revised] PHST- 2020/04/09 00:00 [accepted] PHST- 2020/07/25 06:00 [pubmed] PHST- 2020/11/03 06:00 [medline] PHST- 2020/07/25 06:00 [entrez] AID - S1051-0443(20)30434-6 [pii] AID - 10.1016/j.jvir.2020.04.032 [doi] PST - ppublish SO - J Vasc Interv Radiol. 2020 Aug;31(8):1281-1289. doi: 10.1016/j.jvir.2020.04.032. Epub 2020 Jul 20.