Prophylactic fresh frozen plasma versus prothrombin complex concentrate for preprocedural management of the coagulopathy of liver disease: A systematic review.
blood coagulation factors
hemorrhage
international normalized ratio
liver diseases
prothrombin time
Journal
Research and practice in thrombosis and haemostasis
ISSN: 2475-0379
Titre abrégé: Res Pract Thromb Haemost
Pays: United States
ID NLM: 101703775
Informations de publication
Date de publication:
May 2022
May 2022
Historique:
received:
20
08
2021
revised:
19
03
2022
accepted:
04
04
2022
entrez:
7
10
2022
pubmed:
8
10
2022
medline:
8
10
2022
Statut:
epublish
Résumé
The optimal prophylactic preprocedural management of patients with coagulopathy due to liver disease is not known. Our objective was to compare the efficacy and safety of fresh frozen plasma (FFP) with prothrombin complex concentrate (PCC) in the preprocedural management of patients with coagulopathy of liver disease. We conducted a systematic review to examine published evidence regarding treatment with FFP or PCC in adults with coagulopathy of liver disease undergoing an invasive procedure. Direct comparisons and single-arm studies were eligible. Efficacy outcomes included major bleeding, mortality, and correction of prothrombin time (PT) and/or international normalized ratio (INR). Safety outcomes included thrombosis and transfusion-related complications. A total of 95 articles were identified for full-text review. Nine studies were eligible and included in the review. No randomized trials comparing FFP versus PCC were identified. Only two studies directly compared FFP versus PCC. In these studies, PCC appeared to result in higher rates of correction of PT/INR, but bleeding outcomes were not different. In the single-arm studies, bleeding events appeared low overall. Volume overload was the most common recorded adverse event in patients receiving FFP. Thromboembolic events occurred rarely, but exclusively in the PCC group. Due to heterogeneity in study definitions and bias, meta-analysis was not possible. Our study found no evidence to favor a specific product over another. Insufficient data exist on the effects of FFP versus PCC administration before invasive procedures in patients with coagulopathy of liver disease to make conclusions with respect to relative efficacy or safety.
Sections du résumé
Background
UNASSIGNED
The optimal prophylactic preprocedural management of patients with coagulopathy due to liver disease is not known.
Objectives
UNASSIGNED
Our objective was to compare the efficacy and safety of fresh frozen plasma (FFP) with prothrombin complex concentrate (PCC) in the preprocedural management of patients with coagulopathy of liver disease.
Methods
UNASSIGNED
We conducted a systematic review to examine published evidence regarding treatment with FFP or PCC in adults with coagulopathy of liver disease undergoing an invasive procedure. Direct comparisons and single-arm studies were eligible. Efficacy outcomes included major bleeding, mortality, and correction of prothrombin time (PT) and/or international normalized ratio (INR). Safety outcomes included thrombosis and transfusion-related complications.
Results
UNASSIGNED
A total of 95 articles were identified for full-text review. Nine studies were eligible and included in the review. No randomized trials comparing FFP versus PCC were identified. Only two studies directly compared FFP versus PCC. In these studies, PCC appeared to result in higher rates of correction of PT/INR, but bleeding outcomes were not different. In the single-arm studies, bleeding events appeared low overall. Volume overload was the most common recorded adverse event in patients receiving FFP. Thromboembolic events occurred rarely, but exclusively in the PCC group. Due to heterogeneity in study definitions and bias, meta-analysis was not possible. Our study found no evidence to favor a specific product over another.
Conclusions
UNASSIGNED
Insufficient data exist on the effects of FFP versus PCC administration before invasive procedures in patients with coagulopathy of liver disease to make conclusions with respect to relative efficacy or safety.
Identifiants
pubmed: 36204546
doi: 10.1002/rth2.12724
pii: S2475-0379(22)01220-1
pmc: PMC9124952
doi:
Types de publication
Journal Article
Langues
eng
Pagination
e12724Informations de copyright
© 2022 The Authors. Research and Practice in Thrombosis and Haemostasis published by Wiley Periodicals LLC on behalf of International Society on Thrombosis and Haemostasis (ISTH).
Déclaration de conflit d'intérêts
AC has served as a consultant for Synergy; has received royalties from UpToDate; and his institution has received research support on his behalf from Alexion, Bayer, Novartis, Novo Nordisk, Pfizer, Sanofi, and Spark. AMP receives research funding from Novo Nordisk and Sanofi Genzyme. In the past 24 months, MC has served as a consultant for Precision Biologicals, Hemostasis Reference Laboratory, and Syneos Health; and has prepared educational materials and/or participated in educational sessions for Pfizer, CSL Behring, and Diagnostica Stago. MC receives royalties from UpToDate and has relationships with various not‐for‐profit entities, including the American Society of Hematology.
Références
Anesthesiology. 2008 Nov;109(5):918-26
pubmed: 18946305
PLoS Med. 2009 Jul 21;6(7):e1000097
pubmed: 19621072
Semin Hematol. 1991 Jul;28(3 Suppl 6):3-5
pubmed: 1780767
Br J Neurosurg. 2000 Oct;14(5):458-61
pubmed: 11198768
Lancet. 2015 May 23;385(9982):2077-87
pubmed: 25728933
Eur J Gastroenterol Hepatol. 2003 Jan;15(1):15-20
pubmed: 12544689
BMJ. 2016 Oct 12;355:i4919
pubmed: 27733354
Dig Dis Sci. 2022 Feb 5;:
pubmed: 35122595
Pharmacotherapy. 2016 Oct;36(10):1047-1054
pubmed: 27547916
Gut. 1975 Aug;16(8):621-5
pubmed: 1102399
J Trauma Acute Care Surg. 2013 Dec;75(6):947-53
pubmed: 24256665
N Engl J Med. 2010 Mar 4;362(9):823-32
pubmed: 20200386
Intensive Care Med. 2007 Apr;33(4):721-5
pubmed: 17260127
Lancet Haematol. 2017 Jun;4(6):e258-e271
pubmed: 28457980
Thromb Haemost. 2017 Jan 5;117(1):139-148
pubmed: 27761574
Circulation. 2013 Sep 10;128(11):1234-43
pubmed: 23935011
Hepatology. 2014 Oct;60(4):1442
pubmed: 24452495
Transfusion. 2006 Aug;46(8):1279-85
pubmed: 16934060
Transfusion. 2012 Aug;52(8):1673-86; quiz 1673
pubmed: 22257164
Thromb Haemost. 2018 Aug;118(8):1491-1506
pubmed: 30060258
Transfusion. 1999 Nov-Dec;39(11-12):1227-34
pubmed: 10604250
World J Hepatol. 2020 Nov 27;12(11):1115-1127
pubmed: 33312434
Iran Red Crescent Med J. 2013 Dec;15(12):e12260
pubmed: 24693388
Anesth Analg. 2017 Aug;125(2):609-615
pubmed: 28537975
Saudi J Gastroenterol. 2018 Jul-Aug;24(4):220-227
pubmed: 29956689
Indian J Gastroenterol. 2015 Sep;34(5):359-64
pubmed: 26487399
N Engl J Med. 2011 Jul 14;365(2):147-56
pubmed: 21751907
Best Pract Res Clin Haematol. 2006;19(1):97-112
pubmed: 16377544
J Oral Maxillofac Surg. 2017 Jan;75(1):28-34
pubmed: 27677683
Transfus Med Rev. 2007 Jan;21(1):37-48
pubmed: 17174219
Thromb Haemost. 2016 Oct 28;116(5):879-890
pubmed: 27488143
BMC Surg. 2013 Jul 01;13:22
pubmed: 23815798
Am J Gastroenterol. 2020 Jan;115(1):18-40
pubmed: 31895720
Transfusion. 2014 Oct;54(10 Pt 2):2760-8
pubmed: 24827116
Hepatology. 2021 Jan;73(1):366-413
pubmed: 33219529
J Thromb Haemost. 2021 Mar;19(3):664-676
pubmed: 33219597
Aliment Pharmacol Ther. 2020 Oct;52(8):1298-1310
pubmed: 33105981