Data acquisition and analysis

MV Marlous M. L. H. Verhulst
IV Iris M. Visser
HK Hanneke M. Keijzer
NK Nicole L. M. de Kruijf
EP Erwin J. G. Peters
TW Thom Wilbers
RP Roel V. Peelen
JH Jeannette Hofmeijer
MB Michiel J. Blans
ask Ask a question
Favorite

Continuous EEG recordings were started in all patients as soon as possible after arrival at the ICU, always within 24 h after cardiac arrest, and continued for at least 3 days or until a patient’s decease or awakening, as part of standard care. Twenty-one electrodes were placed on the scalp according to the international 10–20 system. EEG recordings were performed using a Nihon Kohden system (VCM Medical, The Netherlands) from the study start to March 2021 and a BrainRT system (OSG, Belgium) from April 2021 onwards. Two reviewers (MV, HK) independently classified anonymized EEG epochs at 6, 12, 24, 36, 48, and 72 h after cardiac arrest blinded to the timing of the epoch, a patient’s clinical status, medication, and outcome. In case of disagreement, consensus was obtained by the consultation of a third reviewer (JH). EEG patterns were classified as suppressed with or without superimposed synchronous activity, continuous, or other patterns [4].

SSEP recordings were performed off-sedation using a Nicolet EDX system (Natus Medical Inc., USA) as part of standard care at the treating physician’s request, generally between 48 and 72 h in patients who remained comatose after restoration of normothermia. Bilaterally absence of N20 responses was considered predictive of poor neurological outcome.

PLR were tested daily by treating physicians and categorized as present or bilaterally absent. Bilaterally absent PLR > 72 h after cardiac arrest was considered predictive of poor neurological outcome.

ONSD was measured daily by trained personnel in the first 3 days after cardiac arrest, or until decease or awakening. Three consecutive measurements per eye were performed each day using an Affiniti 70C ultrasound system (Philips, The Netherlands). A linear probe with a frequency range of 3–12 MHz was used. Sterile ultrasound gel was placed on the probe and a sterile probe cover was placed over it, preventing ultrasound gel from touching the eye. The probe was placed transversally on the superior lateral part of the upper eyelid, angled caudally and medially with the head of the patient 30° elevated. No pressure was put on the eye. The field was reduced to a depth of 4 cm. The ONSD was measured 3 mm behind the retina [21] at the transition from the hyperechoic retrobulbar fat to the hypoechoic line, in the presence of hyperechoic striped bands, or at the transition from the hyperechoic retrobulbar fat to the hypoechoic region of the optic nerve, in absence of striped bands. These marker placements both correspond to the outer edges of the dura mater [22] (Fig. 1). The mean of three binocular ONSD measurements per day was used for further analysis.

Examples of ultrasound images of the ONSD for a patient with good neurological outcome (left, ONSD = 5.01 mm) and a patient with poor neurological outcome (right, ONSD = 8.10 mm). The eyeball and optic nerve including its sheath are delineated in blue. The red horizontal line indicates the ONSD

Do you have any questions about this protocol?

Post your question to gather feedback from the community. We will also invite the authors of this article to respond.

post Post a Question
0 Q&A