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Neuroprognostication Bias: A Collaboration to Reduce the Impact of Self-fulfilling Prophecy in Cardiac ARrEst

Addressing an Inherent Bias in Neuroprognostication: A Collaboration to Reduce the Impact of Self-fulfilling Prophecy in Cardiac ARrEst

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03261089
Acronym
SPARE
Enrollment
600
Registered
2017-08-24
Start date
2017-08-02
Completion date
2027-08-31
Last updated
2025-12-24

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

Conditions

Cardiac Arrest

Keywords

cardiac arrest, neuroprognostication, coma

Brief summary

Cardiovascular disease remains the leading cause of death in the United States. Mortality rates of cardiac arrest range from 60-85%, and approximately 80% of survivors are initially comatose. Of those who survive, 50% are left with a permanent neurological disability, and only 10% are able to resume their former lifestyle. Early prognosis of comatose patients after cardiac arrest is critical for management of these patients, yet predicting outcome for these patients remains quite challenging. The primary study objective of SPARE is to assess the value of using a systematic, multi-modal approach for neuroprognostication in the unconscious post-cardiac arrest population. We hypothesize that prognostication using this approach will be significantly improved compared to historical controls. This approach will be novel because: All patients who are unconscious at least 24 hours post-cardiac arrest, whereas previous studies on neurologic outcome tended to have restrictive inclusion criteria, such as no pre-existing neurologic impairment (e.g. dementia or prior cerebrovascular injury), or included an unduly restrictive population, such as patients with a strictly comatose state. The prognostic modalities used to assess patients will be applied at specific time points that will maximize their utility. Patients' families and clinicians will be encouraged to provide adequate time to allow for a delayed recovery, especially in cases of uncertain outcome, thus minimizing the self-fulfilling prophesy bias of early withdrawal of life-sustaining therapies (WLST). This will be particularly pertinent in the comparison of US and Brazil/Italy patients, as the Brazilian and Italian populations are not commonly exposed to premature WLST (as can be the case in the US), one of the major sources of biases in prognostication studies of cardiac arrest due to the self-fulfilling prophecy.

Detailed description

SPARE is a multi-center, international, prospective registry designed to evaluate the use of a multi-modality approach to neuroprognostication after cardiac arrest. Subjects will be evaluated with standard, accepted, and widely available assessment modalities, including clinical examination, neurophysiologic (electroencephalography and evoked potentials (per site standard of care), serum biomarkers (per site standard of care), and neuroimaging testing. The purpose of this study is to collect data from a prospective large-scale cohort involving cardiac arrest survivors, and the clinical characteristics and prognostic features that affect their neurologic outcome. The ultimate goal is to derive a prediction model for neuroprognostication in cardiac arrest, using multiple clinical modalities that are already clinically in use, but in a standardized fashion. We hypothesize that by using a multimodal approach combining clinical assessment tools obtained at standardized time points, we will improve the accuracy of neuroprognostication in initially unconscious cardiac arrest survivors. The US and non-US populations will be compared, as the non-US population is less exposed to early WLST, thus eliminating the self-fulfilling prophecy bias that has plagued all CA studies to date. Outcomes will be assessed at discharge, at 3 months post-arrest, 6 months, and annually up to 5 years afterwards. The primary outcome will be the proportion of subjects with good versus poor outcome, with a dichotomized approach of the modified Rankin Scale (mRS): good outcome defined as mRS scores of 0-3, and poor outcome as mRS scores of 4-6. Secondary outcome measures include overall scores on the Cerebral Performance Category Scale (CPC), Cerebral Performance Category - Extended (CPC-E), and Montreal Cognitive Assessment (MOCA) (or Telephone Montreal Cognitive Assessment (T-MOCA)).

Interventions

None listed

Sponsors

University of Florida
CollaboratorOTHER
Hospital Israelita Albert Einstein
CollaboratorOTHER
Faculty of Medicine of Ribeirão Preto (FMRP-USP)
CollaboratorOTHER
University of Sao Paulo General Hospital
CollaboratorOTHER
Yale University
CollaboratorOTHER
University of Pennsylvania
CollaboratorOTHER
University of California, San Francisco
CollaboratorOTHER
D'Or Institute for Research and Education
CollaboratorOTHER
National Institute of Neurological Disorders and Stroke (NINDS)
CollaboratorNIH
Boston Medical Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 89 Years
Healthy volunteers
No

Inclusion criteria

* Initially unconscious following cardiac arrest from any non-perfusing rhythm (i.e., ventricular tachycardia, ventricular fibrillation, pulseless electrical activity, asystole) * Sustained return of spontaneous circulation (ROSC) as defined by maintained spontaneous circulation for at least 20 minutes after cardiopulmonary resuscitation.

Exclusion criteria

\- Isolated respiratory arrest without concomitant or ensuing cardiac arrest

Design outcomes

Primary

MeasureTime frameDescription
modified Rankin Score (mRS)14 days, 3 months post-arrest, 6 months, and annually up to 5 years afterwardsA 7-point scale that measures the level of disability or impairment. mRS 0-3 is considered a good outcome while mRS is considered a poor outcome

Secondary

MeasureTime frameDescription
Cerebral Performance Category Scale (CPC)14 days, 3 months post-arrest, 6 months, and annually up to 5 years afterwardsA scale from 1-5 assessing brain function and used to gauge neurological recovery. CPC 1 or 2 is considered good outcome while CPC 3-5 is considered poor outcome
Cerebral Performance Category- Extended (CPC-E)14 days, 3 months post-arrest, 6 months, and annually up to 5 years afterwardsAn advanced multi-domain tool used to assess the detailed neurological and functional recovery.
Montreal Cognitive Assessment (MOCA)14 days, 3 months post-arrest, 6 months, and annually up to 5 years afterwardsA Screening tool for cognitive impairment. Score from 0-30
Short Form 3614 days, 3 months post-arrest, 6 months, and annually up to 5 years afterwardsA 36 item patient reported survey used to measure health status and quality of life.
Glasgow Outcome Scale-Extended (GOS-E)14 days, 3 months post-arrest, 6 months, and annually up to 5 years afterwardsAn 8-point scale used to measure global disability and functional outcome

Countries

Brazil, United States

Contacts

Primary ContactDavid M Greer, MD MA
dgreer@bu.edu(617) 638-5102
Backup ContactRebecca Stafford, BA
Rebecca.Stafford@bmc.org617-414-2422

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026