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Clinical Trials/NCT03501927
NCT03501927
Terminated
Not Applicable

The Effects of Pre-operative Point-of-Care Focused Cardiac Ultrasound on Patient Outcome - a Prospective, Randomized, Clinical Study (PreOPFOCUS)

Aarhus University Hospital1 site in 1 country337 target enrollmentMay 7, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cardiopulmonary Disease
Sponsor
Aarhus University Hospital
Enrollment
337
Locations
1
Primary Endpoint
Proportion of patients admitted to hospital ≥ 10 days or dead within 30 days
Status
Terminated
Last Updated
5 years ago

Overview

Brief Summary

Mortality and morbidity remain high after non-cardiac surgery. Known risk factors include age, high ASA grade and emergency surgery. Point-of-care focused cardiac ultrasound may elucidate pathology and potential hemodynamic compromise unknown to handling physicians. This study aims to investigate the effects of focused cardiac ultrasound in high-risk patients undergoing non-cardiac surgery with respect to clinical endpoints.

Detailed Description

In non-cardiac surgery major risk factors for morbidity and mortality include ASA classification, age, acute surgery and pre-existing cardiopulmonary disease. These risk factors are sometimes readily available and, along with the type of surgery, allow anaesthesiologists to tailor anaesthetic drugs, fluid therapy and monitoring to the individual patient need. However, cardiopulmonary disease may be occult or masked by other patient-related incapacities. Hence, identification of cardiopulmonary disease is an important priority during the pre-operative anaesthesia evaluation. Routine pre-operative anaesthesia evaluation includes screening with auscultation, blood tests and often electrocardiography. However, these exams are insensitive for detecting cardiopulmonary diseases that may be life threatening during anaesthesia, including ischaemia, heart valve disease and left ventricular hypertrophy. Point-of-care focused cardiac ultrasound (FOCUS) is claimed to be an effective method for filling out this obvious gap in rapid diagnostic capability, as FOCUS can detect both structural and functional cardiac disease as well as pleural effusion. FOCUS performed by anaesthesiologists can identify unknown pathologies in surgical patients and identification of these enables prediction of perioperative morbidity. Although pre-operative FOCUS has been shown to alter anaesthetic patient management, it remains unclear whether the application of FOCUS actually impacts patient outcome. This study aims to clarify whether pre-operative FOCUS changes clinical outcomes in high-risk patients undergoing acute, non-cardiac surgery. The hypothesis of the study is that pre-operative FOCUS reduces the fraction of patients admitted to hospital for more than 10 days or are dead within 30 days after high risk, non-cardiac surgery.

Registry
clinicaltrials.gov
Start Date
May 7, 2018
End Date
September 1, 2020
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Aarhus University Hospital
Responsible Party
Principal Investigator
Principal Investigator

Jan Pallesen

Principal Investigator

Randers Regional Hospital

Eligibility Criteria

Inclusion Criteria

  • Patients scheduled for emergency (\< 6 hours) or urgent surgery (\< 24 hours)15
  • General or neuro-axial anaesthesia planned at the first anesthetic visit
  • ASA classification 3 or
  • Age ≥ 65 years

Exclusion Criteria

  • Previous surgery performed during current hospital admission (including transfers from other hospitals than Randers Regional Hospital/Hospital of Southern Jutland)
  • Low risk surgery or expected surgery time \< 30 minutes or endoscopies.
  • Lack of consent from patient or proxy (in case of patient mental incapacity)
  • Previous participation in the study. Pre-operative FOCUS not possible for logistical reasons or due to requirement for immediate surgery
  • Drop-out Criteria:
  • Patients who refuse participation after formal inclusion will drop out.
  • Patients converted from a primary anaesthetic plan of general/neuro-axial anaesthesia to regional anaesthesia will not drop-out. -

Outcomes

Primary Outcomes

Proportion of patients admitted to hospital ≥ 10 days or dead within 30 days

Time Frame: 30 days after surgery

Secondary Outcomes

  • Re-admissions to hospital(Up to 90 days after surgery)
  • Intensive care treatment(Up to 90 days after surgery)
  • Postoperative ventilator treatment(Up to 90 days after surgery)
  • Development of acute kidney injury(Within 7 days of surgery)
  • Volume(From FOCUS to the start of anaesthesia)
  • Stroke(From start of anaesthesia to 30 days after surgery)
  • Perioperative myocardial damage(From the day before surgery to the day following surgery)
  • Death ≤ 30 days & ≤ 90 days(Up to 90 days after surgery)
  • Admittance to the post-operative care unit(Up to 1 day after surgery)
  • Surgery cancellations due to preoperative FOCUS(Before start of anaeshesia)
  • Changes in anesthetic practice(From start of anaesthesia to start of surgery)
  • Echocardiography(From FOCUS to start of surgery)
  • Anaesthesia type(From FOCUS to the start of anaesthesia)
  • Myocardial infarction(From start of anaesthesia to 30 days after surgery)
  • New onset cardiac arrhythmia(From start of anaesthesia to 30 days after surgery)
  • Length of stay(Up to 90 days after surgery)
  • Accumulated intra- and postoperative infusion of norepinephrine, epinephrine, phenylephrine, ephedrine, dobutamine, dopamine and other vasoactive drugs.(From start of anaesthesia til end of anaesthesia)
  • Accumulated fluid balance(From start of anaesthesia til end of anaesthesia)
  • Surgery postponements due to preoperative FOCUS(Within 7 days of preoperative anaesthetic visit)
  • Surgery changes(From FOCUS to the start of surgery)
  • Anaesthetic monitoring(From start of anaesthesia to end of anaesthesia)
  • Anesthesia time(From start of anaesthesia to end of anaesthesia)
  • Surgery time(From start of surgery to end of surgery)
  • Anastomotic breakdown(From start of anaesthesia to 30 days after surgery)
  • Cardiogenic pulmonary oedema(From start of anaesthesia to 30 days after surgery)
  • Postoperative haemorrhage(From end of anaesthesia to 30 days after surgery)
  • Infektion, source unknown(From end of anaesthesia to 30 days after surgery)
  • Non-fatal cardiac arrest(From start of anaesthesia to 30 days after surgery)
  • Pulmonary embolism(From start of anaesthesia to 30 days after surgery)
  • Gastrointestinal bleed(From start of anaesthesia to 30 days after surgery)
  • Surgical site infection(From end of anaesthesia to 30 days after surgery)
  • Urinary tract infection(From end of anaesthesia to 30 days after surgery)
  • Pneumonia(From start of anaesthesia to 30 days after surgery)

Study Sites (1)

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