Effect Levosimendan Administration on Postoperative NT-proBNP in Cardiac Risk Patients

  • STATUS
    Recruiting
  • End date
    Mar 31, 2023
  • participants needed
    230
  • sponsor
    Medical University of Vienna
Updated on 29 January 2021

Summary

This is a prospective randomised trial investigating the effect of a preemptive administration of levosimendan on postoperative cardiac NT-proBNP concentrations.

Description

Major cardiovascular complications occur in about 3 % of all patients undergoing noncardiac surgery and are even higher in patients with increased preoperative risk factors. N-terminal pro brain natriuretic peptide (NT-proBNP) increases in over two third of patients undergoing surgery and is a strong predictor for perioperative myocardial complications. Levosimendan is a positive inotropic Ca2+ sensitizer and significantly reduces postoperative BNP concentration in cardiac surgery. The evidence in the non-cardiac surgery setting, however, is weak. Therefore, we will test our primary hypothesis that the perioperative administration of levosimendan significantly will reduce postoperative NT-proBNP concentrations in patients undergoing moderate- to high-risk non-cardiac surgery. We will also test the secondary hypotheses that levosimendan will reduce postoperative maximum troponin T (maxTnT) concentration, the incidence of myocardial injury after noncardiac surgery (MINS), myocardial infarction and death within 30 days and one year after surgery.

Details
Condition Cardiovascular Risk Factor
Treatment Placebo, Levosimendan
Clinical Study IdentifierNCT04329624
SponsorMedical University of Vienna
Last Modified on29 January 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Is your age between 65 yrs and 85 yrs?
Gender: Male or Female
Do you have any of these conditions: Do you have Cardiovascular Risk Factor??
All patients need to meet all of the following criteria for inclusion (1-4)
Undergoing major surgery planned for more than 2 hours
65 years of age and 85 years of age
Provide written informed consent AND
Fulfill 2 of the following criteria (A-E)
NT-proBNP 200 ng/L
History of coronary artery disease defined as 1 of the following 7 criteria (I to VII)
I) History of angina
II) History of myocardial infarction or acute coronary syndrome
III) History of a segmental cardiac wall motion abnormality on echocardiography/radionuclide imaging
IV) History of positive myocardial stress test (echocardiographic or radionuclide)
V) History of a coronary artery stenosis > 50%
VI) ECG with pathological Q waves in any two contiguous leads
VII) History of previous artery revascularizations
History of permanent/paroxysmal atrial fibrillation diagnosed by physician/specialist
History of peripheral arterial disease as defined by a physician/specialist diagnosis of a current, or prior history of any 1 of the following 5criteria (I-V)
I) Intermittent claudication
II) Stenosis 70 % detected by angiography or doppler
III) Stenosis 70% detected by angiography or doppler AND requiring medical treatment e.g. ASA or other platelet inhibitor
IV) History of stroke or TIA - diagnosed by physician or CT/MRI
V) Diagnosed cerebral arteriovascular disease (cAVK) diagnosed by a physician/specialist
Any 3 of 10 of the following risk criteria (i - x)
i. History of congestive heart failure defined as a physician diagnosis of a current or prior episode of congestive heart failure OR prior radiographic evidence of vascular redistribution, interstitial pulmonary edema, or frank alveolar pulmonary edema
ii. History of a transient ischemic attack
iii. Diabetes and currently taking an oral hypoglycemic agent or insulin
iv. History of hypertension
v. Hyperlipidemia and currently taking a lipid lowering agent
vi. Documented chronic kidney disease diagnosed by physician/specialist and creatinine clearance > 30 ml/min
vii. History of smoking within 2 years of surgery
viii. Diastolic dysfunction ( grade 1) documented by echocardiography
ix. Age 70 years
x. Preoperative Troponin T (5th generation) 25ng/dL

Exclusion Criteria

Previous adverse response and/or allergy to levosimendan B) ICU Patients undergoing surgery C) Preoperative Sepsis/SIRS needing ICU treatment D) Preoperative hemodynamically instable patients, who requirevasopressor or inotropic support E) Renal or liver transplantation F) History of severe heart failure (e.g. LVEF < 30%) G) Patients undergoing surgery for pheochromocytoma H) Liver cirrhosis I) Pulmonary hypertension (mPAP > 25 mmHg)
Severe Renal Failure defines as creatinine clearance 30ml/min
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