DDAVP Effect by TEG6 in Cardiac Surgery

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorLondon Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's

About this trial

Cardiopulmonary bypass (CPB) is a process that uses a pump that temporarily takes over the function of the heart and lungs during cardiac surgery to maintain blood circulation and oxygenation. Using CPB during cardiac surgery can result in complications with blood clotting. Blood clotting is achieved when molecules in the blood, called platelets, are able to form together with the help of other clotting factors to form a clot. A drug called desmopressin (DDAVP) is used to help blood clot properly by increasing the amount of clotting factors in the blood. Several studies have shown that desmopressin has the ability to reduce the amount of blood transfusions needed for cardiac surgery patients in the postoperative period. At LHSC desmopressin is frequently requested by Cardiac Surgeons and Anesthesiologists to stop bleeding and promote blood clotting where required. A test called TEG6s platelet mapping is a blood test used to help manage the use of blood products by being able to provide information on platelet function and blood clotting activity. At the moment, there is a lack of information regarding the use of TEG6s platelet mapping to analyze the effect of desmopressin on blood clotting in cardiac surgery patients after CPB. The purpose of this study is to investigate the dose-related effects of desmopressin on platelet function in patients undergoing cardiac surgery with CPB. By using TEG6s platelet mapping, this study aims to observe dynamic changes in platelet function following desmopressin administration at various time points in the perioperative and postoperative periods.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age 18 years and above

Undergoing elective cardiac surgery with cardiopulmonary bypass

Able to provide informed consent

Disqualifiers

Hyponatremia

Allergy to desmopressin or its components

History of coronary artery disease with thrombosis

Recent history of thromboembolic events (Stroke/TIA/DVTs)

Trial population

This is a prospective, observational, single centre study being conducted at London Health Sciences Centre (LHSC) with adults undergoing elective cardiac surgery with cardiopulmonary bypass to investigate the dose-related effects of desmopressin on platelet function in patients undergoing cardiac surgery.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Desmopressin after protamine reversal

    Drug

    Desmopressin will be given to participants at a dose of 0.3mcg/kg after protamine reversal at the end of cardiopulmonary bypass (CPB). Platelet function will be assessed by TEG (Thromboelastography) platelet mapping at the following points: 1. T1 TEG6s: after arterial line insertion before skin incision. 2. T2 TEG6s: after protamine (baseline function after CPB) 3. T3 TEG6s: 30 minutes after desmopressin 4. T4 TEG6s: 6 hours after (intensive care unit) ICU admission 5. T5 TEG6s: 24hours after ICU admission

Treatment groups

100 Participants
are divided into 1 treatment group
Group A: Desmopressin after protamine reversal1 intervention

Trial outcomes

Primary outcomes

1

Change in platelet function due to desmopressin administration after cardiopulmonary bypass

This will be measured by TEG6s platelet mapping.

Time frame
After arterial line insertion - 24 hours after admission to the intensive care unit

Secondary outcomes

1

Impact of desmopressin on transfusion products required

This will be measured by recording the amount of blood products required for transfusion.

Time frame
After arterial line insertion - 24 hours after admission to the intensive care unit
2

Impact of desmopressin on chest drainage

This will be measured by recording the fluid drained from the chest of participants

Time frame
After arterial line insertion - 24 hours after admission to the intensive care unit

Other outcomes

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