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The association between early impairment in cerebral autoregulation and outcome in a pediatric swine model of cardiac arrest
Journal article   Open access   Peer reviewed

The association between early impairment in cerebral autoregulation and outcome in a pediatric swine model of cardiac arrest

Matthew P. Kirschen, Ryan W. Morgan, Tanmay Majmudar, William P. Landis, Tiffany Ko, Ramani Balu, Sriram Balasubramanian, Alexis Topjian, Robert M. Sutton, Robert A. Berg, …
Resuscitation plus, v 4, 100051
01 Dec 2020
PMID: 34223325
url
https://doi.org/10.1016/j.resplu.2020.100051View
Published, Version of Record (VoR)CC BY-NC-ND V4.0 Open

Abstract

Critical Care Medicine Emergency Medicine General & Internal Medicine Life Sciences & Biomedicine Science & Technology
Aims: Evaluate cerebral autoregulation (CAR) by intracranial pressure reactivity index (PRx) and cerebral blood flow reactivity index (CBFx) during the first four hours following return of spontaneous circulation (ROSC) in a porcine model of pediatric cardiac arrest. Determine whether impaired CAR is associated with neurologic outcome. Methods: Four-week-old swine underwent seven minutes of asphyxia followed by ventricular fibrillation induction and hemodynamic-directed CPR. Those achieving ROSC had arterial blood pressure, intracranial pressure (ICP), and microvascular cerebral blood flow (CBF) monitored for 4h. Animals were assigned an 8-h post-ROSC swine cerebral performance category score (1= normal; 2-4=abnormal neurologic function). In this secondary analytic study, we calculated PRx and CBFx using a continuous, moving correlation coefficient between mean arterial pressure (MAP) and ICP, and between MAP and CBF, respectively. Burden of impaired CAR was the area under the PRx or CBFx curve using a threshold of 0.3 and normalized as percentage of monitoring duration. Results: Among 23 animals, median PRx was 0.14 [0.06,0.25] and CBFx was 0.36 [0.05,0.44]. Median burden of impaired CAR was 21% [18,27] with PRx and 30% [17,40] with CBFx. Neurologically abnormal animals (n= 10) did not differ from normal animals (n=13) in post-ROSC MAP (63 vs. 61 mmHg, p=0.74), ICP (15 vs. 14mmHg, p= 0.78) or CBF (274 vs. 397 Perfusion Units, p= 0.12). CBFx burden was greater among abnormal than normal animals (45% vs. 24%, p=0.001), but PRx burden was not (25% vs. 20%, p=0.38). Conclusion: CAR is impaired early after ROSC. A greater burden of CAR impairment measured by CBFx was associated with abnormal neurologic outcome.

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Collaboration types
Domestic collaboration
Web of Science research areas
Critical Care Medicine
Emergency Medicine
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