MET: REevaluation for Perioperative cArdIac Risk (MET-REPAIR)

Sponsor
European Society of Anaesthesiology (Other)
Overall Status
Unknown status
CT.gov ID
NCT03016936
Collaborator
(none)
15,000
1
46
326.1

Study Details

Study Description

Brief Summary

Multicentre international prospective cohort study designed to answer the question: "In patients undergoing elevated risk noncardiac surgery, are METs estimated by questionnaire associated with perioperative major adverse cardiovascular events or cardiovascular mortality?" If so:

  1. What is the optimal cut-off for METs estimated by questionnaire to predict perioperative major adverse cardiovascular events or cardiovascular mortality?

  2. How does the optimal cut-off compare with the currently guideline-endorsed 4-MET cut-off?

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    In spite of scarce and non-conclusive evidence on the prognostic value of self-reported functional capacity for perioperative cardiovascular events, the estimation of cardiovascular functional capacity in metabolic equivalents (METs) based on a questionnaire represent the core question in the preoperative cardiac risk assessment in patients undergoing elevated risk noncardiac surgery endorsed by ESA, the ESC, and the ACC/AHA. MET-REPAIR will examine the ability of MET estimated using a questionnaire to predict perioperative cardiovascular events correcting for preoperative risk factors, (e.g. comorbidity and type of surgery) and calculate the effect on risk stratification (net reclassification improvement) by the addition of METs estimated by questionnaire to established risk scores, such as the Revised Cardiac Risk Score (Lee-index) and the NSQIP MICA . Further, investigators will address alternative approaches to functional capacity estimation (1. ability to climb stairs; 2. self-assessed functional capacity compared to peers; 3. Daily/weekly physical activity) and their predictive value for perioperative cardiovascular events.

    The association between elevated natriuretic peptides prior to noncardiac surgery and perioperative cardiovascular events is well established. However, a direct comparison of the predictive ability of biomarkers vs. self-reported MET is lacking. Therefore, in a substudy (NTproBNP substudy), investigators will evaluate in how far the addition of NTproBNP improve prediction of perioperative cardiovascular events and cardiovascular mortality when added to clinical data and estimated METs.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    15000 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    MET: REevaluation for Perioperative cArdIac Risk (MET-REPAIR) Observational Multicentre Study
    Actual Study Start Date :
    Aug 1, 2017
    Anticipated Primary Completion Date :
    Dec 1, 2019
    Anticipated Study Completion Date :
    Jun 1, 2021

    Arms and Interventions

    Arm Intervention/Treatment
    Subgroup for NTproBNP Substudy

    Planned subgroup analyses in patients undergoing vascular, orthopaedic, thoracic surgery, and in patients aged 65 years or older with a RCRI <2 and NSQIP- MICA <1%

    Outcome Measures

    Primary Outcome Measures

    1. Composite of intra or postoperative inhospital cardiovascular mortality, nonfatal cardiac arrest, acute myocardial infarction, stroke and congestive heart failure requiring transfer to a higher care unit or prolonging stay on ICU/intermediate care (≥24h) [within 24 hours after surgery]

      Composite of intra- or postoperative inhospital cardiovascular mortality, nonfatal cardiac arrest, acute myocardial infarction, stroke, and congestive heart failure requiring transfer to a higher unit of care or prolonging stay on ICU/intermediate care (≥24h).

    Secondary Outcome Measures

    1. composite of intra- or postoperative inhospital cardiovascular mortality, nonfatal cardiac arrest, acute myocardial infarction, stroke, and congestive heart failure requiring transfer to a higher unit of care or prolonging stay on ICU/IMC (≥24h) [at 30days after surgery or on discharge]

      composite of intra- or postoperative inhospital cardiovascular mortality, nonfatal cardiac arrest, acute myocardial infarction, stroke, and congestive heart failure requiring transfer to a higher unit of care or prolonging stay on ICU/intermediate care (≥24h)

    2. Inhospital all-cause mortality [at 30days after surgery]

    3. complications ≥ 3 in Clavien Dindo Classification [From date of surgery until up to day 30 after surgery or until discharge if occurred before day 30 and no follow-up call is carried out.]

    4. length of In hospital stay (days), length of ICU stay (days in the ICU) [from date of surgery until discharge or until day 30 after surgery, whichever occurs first. .]

    5. myocardial injury after noncardiac surgery (MINS) [From date of surgery until up to day 30 after surgery or until discharge if occurred before day 30 and no follow-up call is carried out.]

      Only applicable for patients from centres routinely implementing a perioperative troponin screening

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    45 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Planned as Inpatients after surgery

    • 45 years of age or older AND undergoing elective elevated-risk noncardiac surgery as defined by either a Revised Cardiac Risk Index ≥ 2 [9] OR NSQIP MICA>1% [10]

    • 65 years of age or older and undergoing intermediate or high-risk procedures [3]

    • Signed Written informed consent

    Exclusion Criteria:
    • Non-elective surgery, i.e. planned to occur ≤ 72 hours after diagnosis of the acute condition that makes the procedure necessary

    • Acute coronary syndrome or uncontrolled congestive heart failure within the last 30 days of planned day of surgery

    • Stroke within the last 7 days of planned day of surgery

    • Outpatients

    • Patients unable to perform ambulation due to congenital or longstanding illnesses/states (e.g. paraplegics, polio, etc; but explicitly not patients with fractures, needing hip replacement, etc.)

    • Unable to consent or unwilling to participate

    • Previous enrolment in MET REPAIR (in case of repeated surgery)

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Universitätsklinikum Düsseldorf Düsseldorf Germany

    Sponsors and Collaborators

    • European Society of Anaesthesiology

    Investigators

    • Study Chair: Giovanna Lurati Buse, PD Dr., University Hospital, Düsseldorf, Germany

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    European Society of Anaesthesiology
    ClinicalTrials.gov Identifier:
    NCT03016936
    Other Study ID Numbers:
    • MET-REPAIR
    First Posted:
    Jan 11, 2017
    Last Update Posted:
    Jan 15, 2019
    Last Verified:
    Jan 1, 2019
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    Keywords provided by European Society of Anaesthesiology

    Study Results

    No Results Posted as of Jan 15, 2019