Abstract
Aim
To describe the cerebral blood flow velocity pattern and investigate cerebral autoregulation
using transcranial Doppler ultrasonography (TCD) following a global hypoxic-ischaemic
(HI) event in children.
Methods
This was a prospective, observational study in a quaternary-level paediatric intensive
care unit. Intubated children, newborn to 17 years admitted to the PICU following
HI injury (asphyxia, drowning, cardiac arrest) were eligible for inclusion. TCD was
performed daily until post-injury day 8, discharge, or death, whichever occurred earliest.
Results
Twenty-six patients were enrolled. Median age was 3 years (0.33, 11.75), initial pH
6.95, and initial lactate 5.4. Median post-resuscitation Glasgow Coma Score was 3T.
Across the entire cohort, cerebral blood flow velocity (CBFV) was near normal on day
1. Flow velocity increased to a maximum median value of 1.4 standard deviations above
normal on day 3 and slowly downtrended back to baseline by the end of the study period.
Median Paediatric Extended Version of the Glasgow Outcome Score was 4 at three months.
No patient in the favourable outcome group had extreme CBFV on day one, and only one
patient in the favourable group had extreme CBFV on PID 2. In contrast, 38% of patients
in the unfavourable group had extreme CBFV on PID 1 (p=.039 compared to frequency
in favourable group), and 55% had extreme CBFV on PID 2 (p = .023 compared to frequency
in favourable group). No patient had consistently intact cerebral autoregulation throughout
the study period.
Conclusions
Following a HI event, patients with favourable neurologic outcomes had flow velocity
near normal whereas unfavourable outcomes had more extreme flow velocity. Intermittently
intact cerebral autoregulation was more frequently seen in those with favourable neurologic
outcomes though return to the autoregulatory baseline appears delayed.
Keywords
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Article info
Publication history
Published online: February 13, 2018
Accepted:
February 5,
2018
Received in revised form:
October 27,
2017
Received:
August 6,
2017
Identification
Copyright
© 2018 Elsevier B.V. All rights reserved.