Myocardial Injury, Perioperative/Postoperative Complications
Conditions
Brief summary
The primary aim of this study is to compare mean arterial pressure (MAP) and cardiac index (CI) based intraoperative hemodynamic management in terms of postoperative high sensitive troponin elevation. The hypothesis of the study is that there will be at least 5ng/L difference between the two groups in terms of troponin elevation occurring in the postoperative period. When power analysis was performed with this primary output, it was calculated that while alpha was 0.05 beta 0.2, 42 patients in each group, a total of 84 patients were required.
Detailed description
Fluid therapy will be started as 2-4 ml/kg/h, according to the clinician's decision for the patient. Afterwards, patients will be managed hemodynamically with one of the MAP and CI algorithms. Targeted fluid therapy will be administered in accordance with the following definitions of normal and algorithms for both groups. Normal definitions: MAP: Baseline MAP +/- 20% and MAP\>65mmHg Baseline MAP: MAP average in the ward at rest the day before surgery CI: Baseline CI +/- 20% and CI \> 2.2 L/m2/min Baseline CI: CI calculated by MostCare monitor before the anesthesia induction starts Low MAP intervention If PPV\>14, apply 500ml crystalloid If PPV\>9 and any additional finding regarding hypovolemia, apply 500ml crystalloid If PPV\<10, start/titrate noradrenaline infusion Low CI intervention If PPV\>9, apply mini fluid challenge (MFC). If MFC is positive, apply 500ml crystalloid. If MFC is negative, evaluate MAP. If MAP is elevated start/titrate remifentanil. If MAP is not elevated start/titrate dopamine/dobutamine in accordance with SVRI
Interventions
OTHERMean arterial pressure based management
Mean arterial pressure group: Low MAP will be intervened in accordance with the protocol as described in the arm
OTHERCardiac index based management
Cardiac index group: Low CI will be intervened in accordance with the protocol as described in the arm. Additionally, if MAP is lower than target MAP along with a normal CI, this will be intervened with noradrenalin infusion/titration
Sponsors
Istanbul Saglik Bilimleri University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)
Eligibility
Sex/Gender
ALL
Age
45 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Patients who will undergo pancreatic-hepatic surgery 2. Patients over 65 years of age or patients over 45 years of age and with at least one of the following comorbidities: coronary artery disease, Congestive heart failure, moderate to severe heart valve disease, peripheral artery disease Moderate to Severe Pulmonary hypertension, cerebrovascular accident older than 1 month, History of pulmonary embolism more than 1 month old, Diabetes Mellitus, Hypertension
Exclusion criteria
1. Presence of atrial fibrillation, sepsis, pulmonary embolism 2. Presence of pulmonary embolism, acute coronary syndrome and cerebrovascular accident in the last month 3. Static respiratory system compliance \< 35ml/cmH2O 4. Patients with preoperative high sensitive Troponin T value \>65ng/liter 5. glomerular filtration rate \< 60 ml/min
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Postoperative high sensitive troponin change | three days | difference between the mean high sensitive troponin elevation between the groups will be evaluated. high sensitive troponin T will be measured one day before the surgery, and daily after the surgery for three days |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| postoperative myocardial injury incidence | three days | high-sensitivity troponin T elevation by at least 5 ng/L from the preoperative concentration to at least 20 ng/L |
| 90-days mortality | 90 days | comparison of mortality frequency on the 90th day of the surgery |
Countries
Turkey (Türkiye)
Outcome results
None listed