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Steroids In caRdiac Surgery Trial (SIRS Trial)

Primary Purpose

Cardiac Surgical Procedures, Cardiopulmonary Bypass, Systemic Inflammatory Response Syndrome

Status
Unknown status
Phase
Phase 4
Locations
Canada
Study Type
Interventional
Intervention
Methylprednisolone
Placebo
Sponsored by
Population Health Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cardiac Surgical Procedures focused on measuring Cardiac Surgical Procedures, Cardiopulmonary Bypass, Systemic inflammatory Response Syndrome, Steroid, Myocardial Infarction, Randomized Clinical Trial

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Age greater than 18 years
  2. Require CPB for any cardiac surgical procedure (such as CABG, Valve, Aorta, or combined procedures)
  3. Must have a EuroSCORE ≥ 6
  4. Provide written informed consent

NOTE: For participating sites in India, China and Hong Kong, the following eligibility criteria will be applied:

  1. Age greater than 18 years
  2. Require CPB for any cardiac surgical procedure (such as CABG, Valve, Aorta, or combined procedures)
  3. Must have at least one of the following:

    1. EuroSCORE greater than or equal to 4 and undergoing valvular surgery
    2. EuroSCORE greater than or equal to 6 and undergoing any other cardiac surgery procedure (i.e. CABG, Aorta)
  4. Provide written informed consent

Exclusion Criteria:

  1. Use of systemic corticosteroids
  2. History of bacterial or fungal infection in last 30 days
  3. Allergy/intolerance to corticosteroids
  4. Will receive Aprotinin
  5. Previous participation in study

Sites / Locations

  • Hamilton General Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Treatment

Placebo

Arm Description

500 mg of methylprednisolone divided into two intravenous doses of 250 mg each, one during anesthetic induction and the other on CPB initiation

500 mg of matching placebo (normal saline solution) divided into two intravenous doses of 250 mg each, one during anesthetic induction and the other on CPB initiation

Outcomes

Primary Outcome Measures

Mortality at 30 days
Composite
Incidence of the composite outcome of death, myocardial infarction, stroke, renal failure (KDIGO Stage III acute kidney injury, 2012 Kidney Disease Improving Global Outcomes (KDIGO) guidelines), or respiratory failure within 30 days

Secondary Outcome Measures

MI or Mortality at 30 days
Composite of death or significant myocardial infarction within 30 days post-randomization
Mortality at 6 months
All-cause mortality at 6 months post-randomization
Atrial Fibrillation
New onset atrial fibrillation within 30 days post-randomization
Transfusion Requirements
Transfusion requirements within first 24 hours post-operative
Chest Tube Output
Chest tube output within first 24 hours post-operative
ICU and Hospital Length of Stay
Length of ICU stay and hospital stay
Infection
Infection within 30 days post-randomization
Delirium
Delirium at day 3 post-operative
Wound Complication
Wound complication within 30 days post-randomization
GI Hemorrhage
GI hemorrhage or GI perforation within 30 days post-randomization
Insulin Use
Post-operative insulin use within the first 24 hours after surgery
Peak Blood Glucose
Peak blood glucose within the first 24 hours after surgery

Full Information

First Posted
January 26, 2007
Last Updated
July 31, 2014
Sponsor
Population Health Research Institute
Collaborators
Canadian Institutes of Health Research (CIHR)
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1. Study Identification

Unique Protocol Identification Number
NCT00427388
Brief Title
Steroids In caRdiac Surgery Trial (SIRS Trial)
Official Title
Phase IV Study of Perioperative Steroid's Effects on Death or MI in High-Risk Patients Undergoing Cardiac Surgery Requiring Cardiopulmonary Bypass
Study Type
Interventional

2. Study Status

Record Verification Date
July 2014
Overall Recruitment Status
Unknown status
Study Start Date
June 2007 (undefined)
Primary Completion Date
February 2014 (Actual)
Study Completion Date
August 2014 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Population Health Research Institute
Collaborators
Canadian Institutes of Health Research (CIHR)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
SIRS trial is a large simple study in which high-risk patients undergoing cardiac surgery requiring the use of cardiopulmonary bypass (CPB) are randomly allocated to receive a pulse dose of Methylprednisolone or a matching placebo. Cardiopulmonary bypass initiates a systemic inflammatory response that facilitates development of post-operative complications. SIRS will confirm or deny the potential clinical benefits of suppressing this response through the use of systemic steroids. Specifically, does 250 mg of intravenous Methylprednisolone given twice, once on anesthetic induction and again on CPB initiation, result in improved early survival and less myocardial infarction in high-risk cardiac surgery patients requiring CPB?
Detailed Description
Cardiopulmonary bypass (CPB) is a commonly performed surgical procedure with over 500,000 per year in North America. CPB initiates a systemic inflammatory response characterized by both cell and protein activation. Platelets, neutrophils, monocytes, macrophages, coagulation, fibrinolytic, and kallikrein cascades all take part in what results in increased endothelial permeability, vascular, and parenchymal damage. These inflammatory pathways facilitate development of post-operative complications including thrombosis, myocardial injury and infarction, respiratory failure, renal and neurological dysfunction, bleeding disorders, altered liver function and ultimately, multiple organ failure. In an attempt to minimize the deleterious effects of CPB, investigators have tested a variety of strategies in cardiac surgery ranging from the complete avoidance of CPB, to the use of biocompatible circuits and pharmacologic agents to abrogate the systemic response. Investigators have consistently demonstrated the efficacy of steroids as the most potent anti-inflammatory agent for use during CPB. In fact, from the available evidence, the 2004 AHA guidelines for coronary artery bypass grafting (CABG) "support liberal prophylactic use in patients undergoing extracorporeal circulation". However, the trials that do exist within this literature are focused on biochemical endpoints and are insufficiently powered to make conclusions on hard clinical endpoints. Our pilot RCT, SIRS I, demonstrated the efficacy of a low dose steroid protocol in the suppression of this inflammatory cascade. We hypothesize that this low dose protocol will yield clinical benefit while avoiding the potential adverse effects of steroids which are known to be dose dependent. The primary aim of the SIRS trial is to determine if perioperative pulse dose Methylprednisolone results in improved early survival and less myocardial infarction in cardiac surgery requiring CPB. Additional secondary aims of the SIRS trial are to determine the effect of steroids on other clinical outcomes including length of stay, new onset atrial fibrillation, transfusion requirements, infectious, wound, and gastrointestinal complications. The design of the SIRS trial is a prospective multicentre international double-blind placebo controlled randomized clinical trial. The sample size of 7500 patients will have 80% to 90% power to detect a 20-30% RRR for the primary outcome with an α=0.05 (two-sided), anticipating a 6% rate of death in the control arm. Our aim is to have 85 international centers participate which, recruiting at 5 patients per month, would complete recruitment in 36 months. This will be a large trial with a simple design and objective outcomes. A sub-group of patients will be enrolled in a renal sub-study. This sub-study will determine if the risk of acute kidney injury is lower in patients treated with intravenous steroid versus placebo, if steroids lead to better preservation of kidney function six months after cardiac surgery, and whether the impact of steroid exposure differs in patients with and without pre-operative chronic kidney disease.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cardiac Surgical Procedures, Cardiopulmonary Bypass, Systemic Inflammatory Response Syndrome
Keywords
Cardiac Surgical Procedures, Cardiopulmonary Bypass, Systemic inflammatory Response Syndrome, Steroid, Myocardial Infarction, Randomized Clinical Trial

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
7507 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Treatment
Arm Type
Experimental
Arm Description
500 mg of methylprednisolone divided into two intravenous doses of 250 mg each, one during anesthetic induction and the other on CPB initiation
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
500 mg of matching placebo (normal saline solution) divided into two intravenous doses of 250 mg each, one during anesthetic induction and the other on CPB initiation
Intervention Type
Drug
Intervention Name(s)
Methylprednisolone
Intervention Description
Given by IV in 2 doses (250 mg each dose for a total of 500 mg)
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
Given in 2 IV doses (approximately 4 ml of 0.9% normal saline solution in each dose)
Primary Outcome Measure Information:
Title
Mortality at 30 days
Time Frame
30 days post-randomization
Title
Composite
Description
Incidence of the composite outcome of death, myocardial infarction, stroke, renal failure (KDIGO Stage III acute kidney injury, 2012 Kidney Disease Improving Global Outcomes (KDIGO) guidelines), or respiratory failure within 30 days
Time Frame
30 days post-randomization
Secondary Outcome Measure Information:
Title
MI or Mortality at 30 days
Description
Composite of death or significant myocardial infarction within 30 days post-randomization
Time Frame
30 days post-randomization
Title
Mortality at 6 months
Description
All-cause mortality at 6 months post-randomization
Time Frame
6 months post-randomization
Title
Atrial Fibrillation
Description
New onset atrial fibrillation within 30 days post-randomization
Time Frame
30 days post-randomization
Title
Transfusion Requirements
Description
Transfusion requirements within first 24 hours post-operative
Time Frame
24 hours post-surgery
Title
Chest Tube Output
Description
Chest tube output within first 24 hours post-operative
Time Frame
24 hours post-surgery
Title
ICU and Hospital Length of Stay
Description
Length of ICU stay and hospital stay
Time Frame
Hospital Discharge
Title
Infection
Description
Infection within 30 days post-randomization
Time Frame
30 days post-randomization
Title
Delirium
Description
Delirium at day 3 post-operative
Time Frame
3 days post-surgery
Title
Wound Complication
Description
Wound complication within 30 days post-randomization
Time Frame
30 days post-randomization
Title
GI Hemorrhage
Description
GI hemorrhage or GI perforation within 30 days post-randomization
Time Frame
30 days post-randomization
Title
Insulin Use
Description
Post-operative insulin use within the first 24 hours after surgery
Time Frame
24 hours post-surgery
Title
Peak Blood Glucose
Description
Peak blood glucose within the first 24 hours after surgery
Time Frame
24 hours post-surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age greater than 18 years Require CPB for any cardiac surgical procedure (such as CABG, Valve, Aorta, or combined procedures) Must have a EuroSCORE ≥ 6 Provide written informed consent NOTE: For participating sites in India, China and Hong Kong, the following eligibility criteria will be applied: Age greater than 18 years Require CPB for any cardiac surgical procedure (such as CABG, Valve, Aorta, or combined procedures) Must have at least one of the following: EuroSCORE greater than or equal to 4 and undergoing valvular surgery EuroSCORE greater than or equal to 6 and undergoing any other cardiac surgery procedure (i.e. CABG, Aorta) Provide written informed consent Exclusion Criteria: Use of systemic corticosteroids History of bacterial or fungal infection in last 30 days Allergy/intolerance to corticosteroids Will receive Aprotinin Previous participation in study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Salim Yusuf, MD, DPhil
Organizational Affiliation
PHRI
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Kevin Teoh, MD, MSc
Organizational Affiliation
McMaster University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Richard P Whitlock, MD, MSc
Organizational Affiliation
McMaster University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hamilton General Hospital
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8L 2X2
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
16566943
Citation
Whitlock RP, Young E, Noora J, Farrokhyar F, Blackall M, Teoh KH. Pulse low dose steroids attenuate post-cardiopulmonary bypass SIRS; SIRS I. J Surg Res. 2006 May 15;132(2):188-94. doi: 10.1016/j.jss.2006.02.013. Epub 2006 Mar 29.
Results Reference
background
PubMed Identifier
15868539
Citation
Whitlock RP, Rubens FD, Young E, Teoh KH. Pro: Steroids should be used for cardiopulmonary bypass. J Cardiothorac Vasc Anesth. 2005 Apr;19(2):250-4. doi: 10.1053/j.jvca.2005.02.010. No abstract available.
Results Reference
background
PubMed Identifier
24766975
Citation
Whitlock R, Teoh K, Vincent J, Devereaux PJ, Lamy A, Paparella D, Zuo Y, Sessler DI, Shah P, Villar JC, Karthikeyan G, Urrutia G, Alvezum A, Zhang X, Abbasi SH, Zheng H, Quantz M, Yared JP, Yu H, Noiseux N, Yusuf S. Rationale and design of the steroids in cardiac surgery trial. Am Heart J. 2014 May;167(5):660-5. doi: 10.1016/j.ahj.2014.01.018. Epub 2014 Mar 1.
Results Reference
background
PubMed Identifier
24598306
Citation
Garg AX, Vincent J, Cuerden M, Parikh C, Devereaux PJ, Teoh K, Yusuf S, Hildebrand A, Lamy A, Zuo Y, Sessler DI, Shah P, Abbasi SH, Quantz M, Yared JP, Noiseux N, Tagarakis G, Rochon A, Pogue J, Walsh M, Chan MT, Lamontagne F, Salehiomran A, Whitlock R; SIRS Investigators. Steroids In caRdiac Surgery (SIRS) trial: acute kidney injury substudy protocol of an international randomised controlled trial. BMJ Open. 2014 Mar 5;4(3):e004842. doi: 10.1136/bmjopen-2014-004842.
Results Reference
background
PubMed Identifier
30833491
Citation
Garg AX, Chan MTV, Cuerden MS, Devereaux PJ, Abbasi SH, Hildebrand A, Lamontagne F, Lamy A, Noiseux N, Parikh CR, Perkovic V, Quantz M, Rochon A, Royse A, Sessler DI, Shah PJ, Sontrop JM, Tagarakis GI, Teoh KH, Vincent J, Walsh M, Yared JP, Yusuf S, Whitlock RP; SIRS Investigators. Effect of methylprednisolone on acute kidney injury in patients undergoing cardiac surgery with a cardiopulmonary bypass pump: a randomized controlled trial. CMAJ. 2019 Mar 4;191(9):E247-E256. doi: 10.1503/cmaj.181644.
Results Reference
derived
PubMed Identifier
28666990
Citation
Theriault S, Whitlock R, Raman K, Vincent J, Yusuf S, Pare G. Gene Expression Profiles for the Identification of Prevalent Atrial Fibrillation. J Am Heart Assoc. 2017 Jun 30;6(7):e006057. doi: 10.1161/JAHA.117.006057.
Results Reference
derived
PubMed Identifier
26460660
Citation
Whitlock RP, Devereaux PJ, Teoh KH, Lamy A, Vincent J, Pogue J, Paparella D, Sessler DI, Karthikeyan G, Villar JC, Zuo Y, Avezum A, Quantz M, Tagarakis GI, Shah PJ, Abbasi SH, Zheng H, Pettit S, Chrolavicius S, Yusuf S; SIRS Investigators. Methylprednisolone in patients undergoing cardiopulmonary bypass (SIRS): a randomised, double-blind, placebo-controlled trial. Lancet. 2015 Sep 26;386(10000):1243-1253. doi: 10.1016/S0140-6736(15)00273-1.
Results Reference
derived

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Steroids In caRdiac Surgery Trial (SIRS Trial)

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