EEG and SEP Evaluation for Good and Poor Neurological Prognosis After Cardiac Arrest (ProNeCA)

Azienda Ospedaliero-Universitaria Careggi

Status: Completed

Conditions: Neurological Prognosis Cardiac Arrest

Treatments: Diagnostic Test: Neurophysiological Prognosis; Diagnostic Test: Multimodal Prognosis for poor early neurological outcome

Study type: Observational

Funder types: Other

Identifiers

NCT03849911

AOU Careggi

Details and patient eligibility

About

Hypoxic-Ischemic-encephalopathy (HIE) is a severe and frequent neurological complication of successful cardiopulmonary-resuscitation after cardiac arrest (CA). Prognosticating neurological outcomes in patients with HIE is challenging and recent guidelines suggest a multimodal approach. Only few studies have analyzed the prognostic power of the association between instrumental tests and, in addition, most of them were monocentric, retrospective and evaluating only poor outcome.

Full description

Post-anoxic encephalopathy is a severe and frequent neurological complication of successful cardiopulmonary resuscitation and it is usually responsible for coma onset in patients surviving a CA. A reliable early assessment of the neurological prognosis is an important research goal because it could address CA patient management within intensive care units (ICUs).

However, prognosticating neurological outcomes in patients with HIE is challenging and recent guidelines suggest a multimodal approach. Only few studies have analyzed the prognostic power of the association between instrumental tests and, in addition, most of them were monocentric, retrospective and evaluating only poor outcome.

Thus, the investigators designed a multicenter prospective cohort study to assessing the prognostic power of the association of electroencephalogram(EEG) and somatosensory evoked potentials(SEPs) for the prediction of both poor and good neurological outcomes at different times after CA.

The principal aim of this study will be to evaluate the prognostic power of EEG performed in comatose patients within the first 12h after CA for good outcome prediction (cerebral performance categories CPC 1-2-3) and to evaluate its prognostic power for the poor outcome prediction (CPC 4-5) when performed at 24 and 72h after CA.

Moreover, the investigators will aim to evaluate if the combination of EEG and SEPs will allow to correctly identify a greater number of patients with both poor and good outcomes (when performed within the first 12h) and with poor outcomes (when performed after 72h) compared with the use of only a single test. In addition, the investigators will evaluate if the concordance of EEG/SEP patterns will increase the prognostic reliability obtained with a single test.

Finally, the investigators will aim to confirm if the prognostic power of the bilaterally absent(AA) SEP pattern for poor outcome prediction will be reliable at any time of recording after CA, and if other SEP pathological patterns will assume an analogous ominous prognostic significance.

ADDENDUM: after the conclusion of the enrollment we investigated the availability of brain CT data obtained within the first 24 hours after CA. In 7 over 13 centers, including the coordinator center (AOU Careggi, Florence) early brain CT data were available.

Enrollment: 400 patients

Sex: All

Ages: 18 to 90 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• male and female patients between 18 and 90 years of age and
• comatose patients surviving after CA with a Glasgow Coma Scale (GCS) <9

Exclusion criteria

• patients with surgical or traumatic causes of CA,
• patients showing contemporary presence of other neurological diseases (i.e. traumatic brain injury or brain infarction),
• patients with previous severe neurological diseases,
• patients with remote pathological anamnesis showing severe diseases with life expectancy less than 6 months,
• patients with previous severe disability,
• contemporary presence of confounding factors that hamper clinical evaluation (in particular the consciousness state)
• patients with contemporary absence of cortical response N20/P25 and lemniscal wave P14