Assessment of haemostasis and impact of fibrinogen supplementation on clot properties using global haemostasis assays in patients on chronic dialysis.

end-stage renal disease haemodialysis haemostasis hyperfibrinolysis impedance aggregometry point-of-care coagulation management thromboelastometry fibrinogen

Journal

Anaesthesiology intensive therapy
ISSN: 1731-2531
Titre abrégé: Anaesthesiol Intensive Ther
Pays: Poland
ID NLM: 101472620

Informations de publication

Date de publication:
2020
Historique:
entrez: 9 11 2020
pubmed: 10 11 2020
medline: 13 10 2021
Statut: ppublish

Résumé

Multifactorial haemostasis disorders are typical of patients with end-stage renal disease (ESRD) on chronic haemodialysis (HD). Thromboelastometry and impedance aggregometry allow for a comprehensive assessment of clot formation, lysis, and platelet (PLT) function. This study aims to determine the haemostatic profile in a group of patients with ESRD on chronic, interrupted dialysis, especially in terms of PLT function and the impact of A total of 22 patients on chronic HD and 22 healthy controls (HC) were enrolled in the prospective study with a control group. Global haemostasis assays (GHA) were used to describe the haemostasis profile and to assess the effect of fibrinogen concentrate supplementation on improving clot quality. Despite the lack of considerable differences in the number of PLTs, there was a significantly lower potential of PLT aggregation in the HD group (922 ±163 AU*min). A higher concentration of fibrinogen was also observed in this group which presented considerably higher maximum clot firmness (MCF) FIBTEM (22 ±5.3 mm). Clotting time (CT) EXTEM was also prolonged (72 ±23 s). No hyperfibrinolysis was reported. In vitro fibrinogen concentrate supplementation resulted in significant improvement in MCF FIBTEM (30 mm vs. 22 mm; P < 0.001). However, it also led to a deterioration in PLT aggregation as assessed by TRAPtest. The haemostasis profile of ESRD patients demonstrates a limited potential of PLT aggregation, with no improvement after fibrinogen addition.

Identifiants

pubmed: 33165877
pii: 42321
doi: 10.5114/ait.2020.100568
pmc: PMC10183789
pii:
doi:

Substances chimiques

Fibrinogen 9001-32-5

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

274-280

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Auteurs

Jan Pluta (J)

I Department of Anaesthesiology and Intensive Care, Medical University of Warsaw, Warsaw, Poland.

Barbara Nicińska (B)

I Department of Anaesthesiology and Intensive Care, Medical University of Warsaw, Warsaw, Poland.

Magdalena Durlik (M)

Department of Transplantation Medicine and Nephrology, Medical University of Warsaw, Warsaw, Poland.

Janusz Trzebicki (J)

I Department of Anaesthesiology and Intensive Care, Medical University of Warsaw, Warsaw, Poland.

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