Improving Outcomes After Time Sensitive Prehospital Interventions: Rescu Epistry

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

WITHDRAWN

Study Classification

OBSERVATIONAL

Study Start Date

2015-01-31

Study Completion Date

2040-12-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Rescu Epistry includes data points pertaining to prehospital and in-hospital clinical treatments and responses to therapy, survival to discharge and functional outcome data for all cases.

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Out-of Hospital Resuscitation Study

NCT00196248

Ventricular Fibrillation Asystoly Resuscitation

UNKNOWN

REASON 1 Trial: Sonography in Cardiac Arrest

NCT01446471

Cardiac Arrest Pulseless Electrical Activity Asystole

COMPLETED

AI to Improve Data From Danish Cardiac Arrest Registry

NCT05308303

Out-Of-Hospital Cardiac Arrest Trauma Drug Overdose +3 more

UNKNOWN

eFast Diagnosis Performance in Guiding First Aid Resuscitation

NCT03699670

eFast Diagnosis Performance in Guiding First Aid Resuscitation and Hemostasis

COMPLETED

Washington Study of Hemofiltration After Out-of-Hospital Cardiac Arrest

NCT01509040

Cardiac Arrest

COMPLETED PHASE1/PHASE2

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

The prehospital component of health care begins with a call to 911 and ends on arrival to the Emergency Department (ED). In Ontario, prehospital care is provided by a system which includes 22 dispatch centres, 218 Fire and 72 Emergency Medical Services (EMS) who respond to over 1 million 911 calls a year. The prehospital setting is a chaotic, unpredictable environment in which to deliver care and currently there is no data on whether or not this system of care makes a difference in patient outcomes. The question: are the right patients, receiving the right care and making it to the right institutions cannot readily be answered. Outcome-based information to guide future EMS care has been hampered by the lack of comprehensive prehospital data resources that include meaningful patient outcomes.

Why target cardiac arrest, trauma, acute stroke, and sepsis? Ischaemic heart disease is the leading cause of death worldwide, and second leading cause of death in Canada; over 240,000 deaths from heart disease annually. The mean age of cardiac arrest patients is around 65 years of age and this demographic is increasing over time with the population older than 65 expected to double within the next 25 years such that by 2041 about 1 in 4 Canadians will be 65 or older.

Trauma is the number one cause of death and disability in people younger than 40 and confirmed for Canada as well for those under the age of 45. Trauma statistics are biased by the fact that the only data we have comes from the trauma centres and this means a trauma victim must survive long enough to make it to a trauma centre to be counted.

Stroke is the second leading cause of death worldwide, and the leading cause of chronic disability. Stroke is most frequently caused by an interruption of blood supply to portions of the brain due to occlusion of a major brain artery. Stroke statistics have the same bias as trauma statistics. The current registries for trauma and stroke (national and provincial) are administrative data sets containing only patients that are treated at a stroke or trauma centre and miss all those that are treated and released from community centres that are located close enough to a stroke or trauma centre to be subject to a community bypass strategy or referral. Nor do these data sets capture the important prehospital data on the event and time sensitive interventions provided in the prehospital setting.

Sepsis is a clinical syndrome that results from dysregulation of the inflammatory response to severe infection. As sepsis progresses to septic shock it is marked by severe organ dysfunction, coagulopathy, and eventually circulatory collapse and death. The mortality associated with sepsis syndrome ranges from 20 to 50% with increased mortality in patients diagnosed with severe sepsis and septic shock. The average prehospital care interval exceeded 45 minutes, highlighting that there is great potential for early treatment to be delivered by paramedics.

There are no existing registries in Ontario that routinely track prehospital processes of care and outcomes for patients with sepsis who are transported by EMS. Collecting these data is essential to planning any interventions to improve prehospital identification and management of patients with sepsis.

Why the focus on time sensitive interventions? Cardiac arrest, stroke, trauma and sepsis all involve resuscitation and time sensitive intervention. For every one minute delay in defibrillation in a cardiac arrest the survival rate falls 7-10%. For every minute delay in treating a stroke, the average patient loses 2 million brain cells, 13.8 billion synapses, and 12 km of axonal fibres. The mean times for those to reach a trauma centre after stabilization at a local hospital are long at 6.7 hours in Ontario well beyond the 'golden hour' in trauma where the survival is greatest. Similarly, despite widespread acknowledgement of the importance of early recognition and treatment of sepsis, many patients fail to receive appropriate therapy during the first 6 hours after presentation to hospital.

As a result, our society is burdened with staggering socioeconomic costs due to the lack of focus on improving how we care for patients with these time sensitive, life-threatening illnesses. The practical realities of our Canadian geography suggest that a substantial proportion of potential patients do not live close enough to specialized centres of care and receive prehospital care and transport to the closest hospital instead. Rescu Epistry is designed to report on outcomes from these life-threatening illnesses which may benefit from prehospital time sensitive interventions and system optimization initiatives ensuring the right patient gets to the right institute in the right time interval where appropriate care has the greatest chance to be the most effective.

How is Rescu Epistry innovative?

Rescu Epistry has the proven functional and technological ability to expand to other communities in Ontario and to include other provinces in Canada and to collaborate with international investigators who have similar infrastructure and comparable variables. The expansion to other communities has four advantages:

1. It tracks and reports inequalities in access to care that currently exists in Canada for cardiac arrest, trauma and participating regions through targeted interventions and
2. timely reporting of operation and clinical outcomes
3. it provides a real-world comparison to evaluate using observational data the transfer of science into practice (effectiveness or generalizability)
4. it allows our participating services to collaborate easily in trials and studies which may be regional, national or international in scope.

Rescu Epistry is unique from any other administrative research quality dataset as it represents a sentinel event in a patient's life that triggers the creation of a new record and a cascade of data collection that follows from multiple community partners like the 911 operator to a multidisciplinary team in the hospital and in the community. This provides a window of opportunity to not only improve care but also optimize the system of care and measure performance benchmark to ensure science informs and changes practice.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Cardiac Arrest Sepsis Trauma Stroke

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Cardiac arrest

Ischaemic heart disease is the leading cause of death worldwide. However, this is a registry and no interventions are taking place

This is a registry and no interventions are taking place.

Intervention Type OTHER

Trauma

Worldwide, trauma is the number one cause of death and disability in people younger than 40 and confirmed for Canada as well for those under the age of 45. However, this is a registry and no interventions are taking place

This is a registry and no interventions are taking place.

Intervention Type OTHER

Sepsis

Sepsis is a clinical syndrome that results from dysregulation of the inflammatory response to severe infection. However, this is a registry and no interventions are taking place

This is a registry and no interventions are taking place.

Intervention Type OTHER

Stroke

Stroke is the second leading cause of death worldwide, and the leading cause of chronic disability. However, this is a registry and no interventions are taking place

This is a registry and no interventions are taking place.

Intervention Type OTHER

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

This is a registry and no interventions are taking place.

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

Cardiac Arrest Eligibility

1. Individuals of all ages who experience cardiac arrest outside the hospital, with evaluation by organized EMS personnel and:

* Attempts at external defibrillation (by lay responders or emergency personnel), or chest compressions by organized EMS personnel (treated cohort)
* Were pulseless but did not receive attempts to defibrillate or CPR by EMS personnel (untreated cohort - obviously dead by legislative definition)

Traumatic Injury Eligibility
2. Individuals of all ages who experience a traumatic injury outside the hospital, with evaluation by organized EMS personnel and:

* Systolic blood pressure ≤ 90 mmHg or
* Glasgow Coma Scale score ≤12 or
* Respiratory rate \<10 or \>29 breaths per minute or
* Field intubation/advanced airway procedure

Stroke Eligibility
3. individuals of all ages who experience stroke outside the hospital, with evaluation by organized EMS personnel and new onset of signs and symptoms suggestive of an acute stroke

* Unilateral arm/leg weakness or drift or
* Slurred speech or inappropriate words or mute or
* Unilateral facial droop

Sepsis Eligibility

1. Potentially Septic: Individuals of all ages who present with

* Presence of Fever: Temperature \>38°C (tympanic membrane)
* Paramedic suspects possible infection: i.e. suspected pneumonia, urinary tract infection, abdominal pain or distension, meningitis, cellulitis, septic arthritis, infected wound (minimal data set )
2. Severe Sepsis: Individuals of all ages who also present with:

* Presence of Fever: Temperature \>38°C (tympanic membrane)
* Paramedic suspects possible infection: e.g. suspected pneumonia, urinary tract infection, abdominal pain or distension, meningitis, cellulitis, septic arthritis, infected wound; Presence of any one of: (1) respiratory rate \> 22/min or intubated for respiratory support; (2) acute confusion or reduced level of consciousness; (3) presence of hypotension: SBP\<=100mmHg (comprehensive data set)

Eligible Sex

ALL

Accepts Healthy Volunteers

No