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Clinical Trials/NCT04014647
NCT04014647
Suspended
Not Applicable

Peri-operative Measurement of NT-proBNP to Predict Outcomes in Patients Undergoing Elective Vascular Surgery

Julie Dawson1 site in 1 country200 target enrollmentSeptember 5, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Vascular Surgical Procedure
Sponsor
Julie Dawson
Enrollment
200
Locations
1
Primary Endpoint
NT-proBNP blood test measured on the day of (pre-) vascular surgery
Status
Suspended
Last Updated
2 years ago

Overview

Brief Summary

The team is investigating whether N-terminal pro B-type natriuretic peptide (NT-proBNP) and other cardiac markers are useful for predicting outcomes for patients undergoing vascular surgery. By measuring NT-proBNP before and after surgery, the investigators may be able to determine which patients are at risk of an adverse outcome, such as a heart attack or death.

Detailed Description

Almost 1 in 5 patients who have elective major vascular surgery experience death or a myocardial infarction (MI) at 18 months post-surgery. Research has shown that peri-operative interventions may improve outcomes for high-risk patients. Cardiac bio-markers may be used to identify these high-risk patients, in particular pre- and post-operative NT-proBNP. Mahla found that by comparing surgery outcomes with NT-proBNP concentrations peri-operatively, high-risk patients could be identified and subsequent therapeutic decisions could be made to minimise adverse outcomes. Van Kimmenade evaluated patients with acute heart failure and found that galectin-3 (Gal-3) was the best predictor of 60-day mortality compared with NT-proBNP and apelin (another cardiac marker), whereas NT-proBNP was the most useful for diagnosing HF. The authors also found that the combination of both markers (Gal-3 and NT-proBNP) have an even higher predictive value for outcome. The predictive role of troponin I (cTnI) has been observed in a paper by Bursi et al. (2005) where patients undergoing elective major vascular surgery were stratified using the American College of Cardiology/American Heart Association (ACC/AHA) guidelines and followed up over a period of 24 months. Patients in every group with an elevated post-operative cTnI (≥100ng/L) were at greater risk of either MI or death. The successful identification of high-risk patients can go on to have interventional risk-reducing pharmacological, therapeutic, diagnostic, or observational measures. Prevention of cardiovascular events, particular for an aging population, can have positive impact on both the patient and society as a whole as it may result in patients maintaining their independence, avoiding major illness, avoiding nursing home care and living longer.

Registry
clinicaltrials.gov
Start Date
September 5, 2019
End Date
September 1, 2025
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor Investigator
Principal Investigator

Julie Dawson

Research Services Manager

Norfolk and Norwich University Hospitals NHS Foundation Trust

Eligibility Criteria

Inclusion Criteria

  • Patients who are equal to or over 18 years old
  • Patients scheduled to undergo elective surgery for the following procedures:
  • Infrainguinal arterial reconstruction
  • Aortic aneurysm
  • Aorto-bifemoral bypass / or aortic endarterectomy
  • Femoro-popliteal bypass
  • Femoro-distal bypass
  • Femoral endarterectomy
  • Femoro-femoral crossover
  • Axillo-femoral bypass

Exclusion Criteria

  • Patients undergoing emergency surgery
  • Those who are unable or unwilling to give informed consent
  • Patients with unstable coronary syndromes (acute or recent MI with evidence of important ischemic risk by clinical symptoms or stress testing or unstable or severe angina pectoris)
  • Patients with decompensated heart failure (new onset shortness of breath and rales together with echocardiographic evidence of cardiac dysfunction or deterioration of chronic heart failure despite heart failure therapy)
  • Patients with chronic atrial fibrillation

Outcomes

Primary Outcomes

NT-proBNP blood test measured on the day of (pre-) vascular surgery

Time Frame: 4 days

NT-proBNP blood test measured on the day of (pre-) vascular surgery

NT-proBNP blood test measured on the day 4 after (post-) vascular surgery

Time Frame: 4 days

NT-proBNP blood test measured on the day 4 after (post-) vascular surgery

Change in NT-proBNP peri-operatively

Time Frame: 4 days

Change in NT-proBNP peri-operatively

Secondary Outcomes

  • Pre-, post-, and peri-operative troponin I(4 days)
  • Pre-, post-, and peri-operative galectin-3(4 days)
  • Pre-, post-, and peri-operative CRP(4 days)
  • Pre-, post-, and peri-operative creatinine(4 days)

Study Sites (1)

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