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

Perioperative Inflammatory Response Assessment in High-risk Patients Undergoing Noncardiac Surgery - a Prospective Non-interventional Observational Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04753307
Acronym
INSIGHT
Enrollment
1400
Registered
2021-02-15
Start date
2021-01-19
Completion date
2025-01-31
Last updated
2023-08-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative Complications, Cardiovascular Complication, Myocardial Ischemia, Inflammation

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.

Interventions

Inflammatory and cardiac biomarkers will be measured before surgery, and on the first, second, third and fifth postoperative day

Sponsors

Medical University of Graz
CollaboratorOTHER
Medical University of Vienna
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
45 Years to No maximum
Healthy volunteers
No

Inclusion criteria

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

Design outcomes

Primary

MeasureTime frameDescription
Composite of cardiovascular complicationswithin 30 days after surgery and one year after surgeryThe 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

MeasureTime frameDescription
Acute Kidney Injury - Procalcitoninwithin 5 days after surgeryWe will evaluate the influence of Procalcitonin on the occurrence of postoperative acute kidney injury.
NT-proBNPwithin 5 days after surgeryWe 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.
Interleukin 6within 30 days after surgeryWe 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).
Copeptinwithin 30 days after surgeryWe 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).
Procalcitoninwithin 30 days after surgeryWe 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).
C-reactive proteinwithin 30 days after surgerySecondary 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).
Acute Kidney Injury - C-reactive proteintwithin 5 days after surgeryWe will evaluate the influence C-reactive protein on the occurrence of postoperative acute kidney injury.
Acute Kidney Injury - Interleukin 6within 5 days after surgeryWe will evaluate the influence of Interleukin 6 on the occurrence of postoperative acute kidney injury.
Acute Kidney Injury - Copeptinwithin 5 days after surgeryWe will evaluate the influence of Copeptin on the occurrence of postoperative acute kidney injury.
Days at home within 30 days (DAH 30)within 30 days after surgeryWe 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.

Other

MeasureTime frameDescription
SARS-Cov-2 - Cardiovascular ComplicationsOne year after surgeryWe 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.
SARS-Cov-2 One Year Follow-UpOne year after surgeryWe 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.
SARS-Cov-2 - Inflammationwithin first 5 days after surgeryWe 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.
Atrial fibrillation (AF) evaluationwithin 5 days after surgeryTo 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.

Countries

Austria

Contacts

Primary ContactChristian Reiterer, MD
christian.reiterer@meduniwien.ac.at004340400
Backup ContactBarbara Kabon, MD
barbara.kabon@meduniwien.ac.at004340400

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 9, 2026