MedPath

Impact of Balanced Crystalloid and Colloid Infusion on Haemostasis in Healthy Male Volunteers

Not Applicable
Conditions
Perioperative Hemorrhage
Dilutional Coagulopathy
Interventions
Diagnostic Test: Standard laboratory coagulation tests and rotational thromboelastometry measurements
Registration Number
NCT05148650
Lead Sponsor
Medical University of Silesia
Brief Summary

The project focuses on perioperative bleeding that requires transfusion of blood products and supplementation of intravascular volume with crystalloids and colloids. The implemented fluid therapy affects coagulation and fibrinolysis, depending on the type of fluid used in an intravenous infusion. Massive haemorrhage significantly impacts the perioperative period and postoperative quality of life and requires individualized therapy, rending the ongoing project relevant from the perspective of the patients.

Detailed Description

Perioperative bleeding is a complication that significantly affects postoperative morbidity and quality of life and increases the patient's risk of death. Massive hemorrhage requires individualized therapy, preferably based on international recommendations. It is necessary to transfuse blood and blood products (red blood cells, freshly frozen plasma, platelets, concentrates of coagulation factors) with simultaneous rational supplementation of the intravascular space using crystalloids and colloids. Usually, these are large volumes that are infused over a short time. Proceedings in the operating room and the intensive care unit environment should stabilize the patient's general condition with the lowest possible risk of complications.

However, it has been shown that transfusions are not free from side effects. Transfusions may result not only from "classic" post-transfusion complications (allergic reactions, haemolytic reactions, infections, electrolyte disturbances) but also from iatrogenically generated disorders in the circulatory system (fluid overload), respiratory ( acute lung injury), and hemostasis (risk of hypercoagulability). It is also known that uncontrolled and unbalanced fluid therapy per se may additionally affect the haemodynamic state, haemostasis, and the immune system.

Thromboelastometry (thromboelastography) is becoming the standard of perioperative haemostasis monitoring. It has been documented that it provides more reliable data than standard laboratory tests, such as fibrinogen concentration, activated clotting time (ACT), kaolin-kephalin (aPTT), prothrombin (PT), or INR index. The test can be performed as the so-called point-of-care test (POC), which reduces the waiting time for the result and facilitates goal-directed therapy.

Little is known about the effects of fluid infusion on physiological haemostasis in healthy subjects who do not have a prior bleeding disorder and who are infused with fluids similarly to resuscitation in massive bleeding. Only singular studies in international literature attempted to answer this vital question. Still, the regular progress in the field of fluid therapy makes the obtained data less and less valuable in clinical practice.

Recruitment & Eligibility

Status
UNKNOWN
Sex
Male
Target Recruitment
25
Inclusion Criteria
  • Healthy male volunteers aged 18-30 years
  • The American Society of Anaesthesiologists Physical Status (ASA PS) I risk class
  • Must be able to give informed consent
Exclusion Criteria
  • Female sex
  • Blood type O
  • A positive history of any acute diseases in the last four weeks
  • Chronic diseases
  • Any diagnosed haemostatic disorders
  • History of anticoagulation
  • Any known bleeding diathesis
  • Any pharmacotherapy in the previous week
  • Participants were informed about the prohibition of drinking alcohol, excessive exercise, and stress on the day before blood sampling

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Crystalloid infusionStandard laboratory coagulation tests and rotational thromboelastometry measurementsIntravenous (IV) transfusions were performed of a 20ml/kg of a balanced crystalloid solution (Optilyte®, Fresenius Kabi). The infusions were performed through an intravenous cannula (18G) inserted into a vein in the antecubital fossa on the non-dominant limb at 1000 ml/h
Colloid infusionStandard laboratory coagulation tests and rotational thromboelastometry measurementsIntravenous (IV) transfusions were performed of a 20ml/kg of gelatin 26,500 Da (Geloplasma®, Fresenius Kabi). The infusions were performed through an intravenous cannula (18G) inserted into a vein in the antecubital fossa on the non-dominant limb at 1000 ml/h
Primary Outcome Measures
NameTimeMethod
Rotational thromboelastometry (ROTEM) viscoelastic point-of-care coagulation measurements before and after synthetic colloid infusion60 minutes

EXTEM, INTEM, FIBTEM assays:

* A10: clot firmness amplitude measured after 10 minutes (mm)

* A20: clot firmness amplitude measured after 20minutes (mm)

* AA: alpha angle (\*)

* CFT: clot forming time (s)

* CT: clotting time (s)

* MCE: maximum clot elasticity

* MCF: maximum clot firmness (mm)

* ML: maximum lysis (%)

Standard laboratory tests reporting coagulation status before and after synthetic colloid infusion60 minutes

* fibrinogen concentration (mg/dl)

* APTT: activated partial thromboplastin time (s)

* PT: prothrombin time (s)

* INR: international normalized ratio

* PLT: platelet count (10\^3/ul)

* MPV: mean platelet volume (fl)

* PDW: platelet distribution width (fl)

* P-LCR: platelet-large cell ratio (%)

Standard laboratory tests reporting coagulation status before and after balanced crystalloid infusion60 minutes

* fibrinogen concentration (mg/dl)

* APTT: activated partial thromboplastin time (s)

* PT: prothrombin time (s)

* INR: international normalized ratio

* PLT: platelet count (10\^3/ul)

* MPV: mean platelet volume (fl)

* PDW: platelet distribution width (fl)

* P-LCR: platelet-large cell ratio (%)

Standard laboratory tests reporting fibrinolysis status before and after balanced crystalloid infusion60 minutes

- D-dimer concentration (ug/ml)

Rotational thromboelastometry (ROTEM) viscoelastic point-of-care coagulation measurements before and after balanced crystalloid infusion60 minutes

EXTEM, INTEM, FIBTEM assays:

* A10: clot firmness amplitude measured after 10 minutes (mm)

* A20: clot firmness amplitude measured after 20minutes (mm)

* AA: alpha angle (\*)

* CFT: clot forming time (s)

* CT: clotting time (s)

* MCE: maximum clot elasticity

* MCF: maximum clot firmness (mm)

* ML: maximum lysis (%)

Standard laboratory tests reporting fibrinolysis status before and after synthetic colloid infusion60 minutes

- D-dimer concentration (ug/ml)

Secondary Outcome Measures
NameTimeMethod
Safety outcomes after crystalloid and colloid infusion28 days

Assessment of safety and potential of adverse events after fluid infusion

Trial Locations

Locations (1)

Department of Anaesthesiology and Intensive Care, Faculty of Medical Sciences in Katowice, Medical University of Silesia in Katowice

🇵🇱

Katowice, Silesia, Poland

© Copyright 2025. All Rights Reserved by MedPath