INSIGHT: Perioperative Inflammatory Response Assessment in High-risk Patients Undergoing Noncardiac Surgery

Sponsor
Medical University of Vienna (Other)
Overall Status
Recruiting
CT.gov ID
NCT04753307
Collaborator
Medical University of Graz (Other)
1,400
1
36.4
38.5

Study Details

Study Description

Brief Summary

Postoperative cardiovascular complications are common after noncardiac surgery. The association between perioperative inflammation and the occurrence of cardiovascular complications after surgery is still unknown. Therefore, we will evaluate as our primary aim the association between patients with increased postoperative inflammation, assessed with C-reactive protein measurements, and the occurrence of major cardiovascular complications after noncardiac surgery. We will further evaluate the influence of perioperative inflammation on the occurrence of postoperative acute kidney injury. We will also evaluate the association between inflammation and the influence on Days-At-Home within 30 days. Furthermore, we will evaluate the association between increased inflammatory biomarkers and postoperative N-terminal pro brain natriuretic peptide (NT-proBNP) concentration.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Laboratory measurements

Study Design

Study Type:
Observational
Anticipated Enrollment :
1400 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Perioperative Inflammatory Response Assessment in High-risk Patients Undergoing Noncardiac Surgery - a Prospective Non-interventional Observational Study
Actual Study Start Date :
Jan 19, 2021
Anticipated Primary Completion Date :
Jan 31, 2023
Anticipated Study Completion Date :
Jan 31, 2024

Arms and Interventions

Arm Intervention/Treatment
Patients at least 45 years at-risk for cardiovascular complications

Diagnostic Test: Laboratory measurements
Inflammatory and cardiac biomarkers will be measured before surgery, and on the first, second, third and fifth postoperative day

Outcome Measures

Primary Outcome Measures

  1. Composite of cardiovascular complications [within 30 days after surgery and one year after surgery]

    The primary aim of the study is to investigate the influence of the maximum C-reactive protein value (over the first 3 days after surgery) on the incidence of major cardiovascular complications within 30 days after surgery. The composite binary endpoint is defined as myocardial infarction, myocardial injury after noncardiac surgery, new onset of atrial fibrillation, stroke or death.

Secondary Outcome Measures

  1. C-reactive protein [within 30 days after surgery]

    Secondary goals of the study are to investigate the influence of the C-reactive protein on day 5 on the incidence of cardiovascular complications within 30 days after surgery (combined binary endpoint).

  2. Acute Kidney Injury - C-reactive proteint [within 5 days after surgery]

    We will evaluate the influence C-reactive protein on the occurrence of postoperative acute kidney injury.

  3. Acute Kidney Injury - Interleukin 6 [within 5 days after surgery]

    We will evaluate the influence of Interleukin 6 on the occurrence of postoperative acute kidney injury.

  4. Acute Kidney Injury - Procalcitonin [within 5 days after surgery]

    We will evaluate the influence of Procalcitonin on the occurrence of postoperative acute kidney injury.

  5. Acute Kidney Injury - Copeptin [within 5 days after surgery]

    We will evaluate the influence of Copeptin on the occurrence of postoperative acute kidney injury.

  6. Days at home within 30 days (DAH 30) [within 30 days after surgery]

    We will evaluate the correlation between perioperative inflammation (C-reactive protein, Interleukin 6, Procalcitonin, Copeptin) and the number of days patient spend at home after surgery within 30 days (DAH30). Outcomes measure: Hospital discharge data will be used to calculate hospital length of stay. DAH30 will be calculated using mortality and hospitalization data from the date of the index surgery (day 0). For example, if a patient will die on day 2 after surgery, they were assigned 0 DAH30. If a patient will be discharged from hospital at day 6 after surgery but will be readmitted for 4 days before the second hospital discharge, we will assign 20 DAH30. If a patient will die within 30 days after surgery, irrespective of whether they will spend time at home, DAH30 will be scored as 0.

  7. NT-proBNP [within 5 days after surgery]

    We will evaluate the correlation of each of the following inflammatory parameters including C-reactive protein, Interleukin 6, Procalcitonin, Copeptin on postoperative NT-proBNP concentration. NT-proBNP will be measured before surgery, and on the first, second and third postoperative day.

  8. Interleukin 6 [within 30 days after surgery]

    We investigate the influence of the Interleukin 6 ,measured within the first five days after surgery, on the incidence of cardiovascular complications within 30 days after surgery (combined binary endpoint).

  9. Copeptin [within 30 days after surgery]

    We investigate the influence of the copeptin ,measured within the first five days after surgery, on the incidence of cardiovascular complications within 30 days after surgery (combined binary endpoint).

  10. Procalcitonin [within 30 days after surgery]

    We investigate the influence of the procalcitonin ,measured within the first five days after surgery, on the incidence of cardiovascular complications within 30 days after surgery (combined binary endpoint).

Other Outcome Measures

  1. Atrial fibrillation (AF) evaluation [within 5 days after surgery]

    To evaluate the incidence of asymptomatic atrial fibrillation (AF) and symptomatic AF. Asymptomatic AF will be defined as irregular pulse without any clinical symptoms. Symptomatic AF will be defined as irregular pulse with one of the symptoms including racing heart, fluttering or palpitations; fatigue, shortness of breath; and lightheadedness.

  2. SARS-Cov-2 - Inflammation [within first 5 days after surgery]

    We will evaluate the effect of having a perioperative or previous infection with Severe Acute Respiratory Syndrome Corona Virus 2 (SARS-CoV-2) on postoperative inflammatory parameters including C-reactive protein, Copeptin, Interleukin 6 and Procalcitonin.

  3. SARS-Cov-2 - Cardiovascular Complications [One year after surgery]

    We will evaluate the effect of having a perioperative or previous infection with SARS-CoV-2 on the incidence of our composite outcome including myocardial myocardial infarction, myocardial njury after noncardiac surgery, new onset of atrial fibrillation, stroke or death. We will evaluate the outcome one year after surgery via a telephone interview.

  4. SARS-Cov-2 One Year Follow-Up [One year after surgery]

    We will evaluate the effect of a perioprative or previous SARS-Cov-2 infection on the neurocognitive function one year after surgery. Therefore, we will perform the telphone Montreal Cognitive Assessment (MoCA) before surgery and one year after surgery.

Eligibility Criteria

Criteria

Ages Eligible for Study:
45 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
All patients need to meet all of the following criteria for inclusion (1-4):
  1. Surgery planned for more than two hours

  2. ≥ 45 years of age

  3. Provide written informed consent AND

  4. Fulfill ≥ 1 of the following criteria (A-K)

Inclusion Criteria:
  • NT-proBNP ≥ 200 ng/L

  • Troponin T > 25 ng/L

  • History of coronary artery disease

  • History of peripheral artery disease (PAD)

  • 75 years or older

  • History of transient ischemic attack (TIA) or stroke

  • Current smoking or cessation of smoking within 2 years

  • Diabetes or currently taking anti-diabetic drug

  • Hyperlipidemia

  • History of hypertension or currently taking an antihypertensive drug

  • Atrial fibrillation

Exclusion Criteria:
  • Patients on immune-suppressive therapy

  • ICU patients undergoing surgery

  • Preoperative Sepsis/systemic inflammatory syndrome (SIRS) needing ICU treatment

  • Preoperative hemodynamically instable patients, who require vasopressor or inotropic support

  • History of severe heart failure (defined as left ventricular ejection fraction (LVEF) < 30%)

  • Liver cirrhosis

  • Chronic inflammatory bowel diseases (CIBD)

  • Severe rheumatic diseases requiring immunosuppressive treatment

Contacts and Locations

Locations

Site City State Country Postal Code
1 Medical University of Vienna Vienna Austria 1090

Sponsors and Collaborators

  • Medical University of Vienna
  • Medical University of Graz

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Barbara Kabon, PD Dr. med. univ., Medical University of Vienna
ClinicalTrials.gov Identifier:
NCT04753307
Other Study ID Numbers:
  • INSIGHT
First Posted:
Feb 15, 2021
Last Update Posted:
Feb 18, 2021
Last Verified:
Feb 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 18, 2021