Institutional members access full text with Ovid®

Share this article on:

Age-Specific Cerebral Perfusion Pressure Thresholds and Survival in Children and Adolescents With Severe Traumatic Brain Injury*

Allen, Baxter B. MD1; Chiu, Ya-lin MS2; Gerber, Linda M. PhD3; Ghajar, Jamshid MD, PhD3,4; Greenfield, Jeffrey P. MD, PhD5

Pediatric Critical Care Medicine: January 2014 - Volume 15 - Issue 1 - p 62–70
doi: 10.1097/PCC.0b013e3182a556ea
Neurocritical Care

Objectives: Evidence-based traumatic brain injury guidelines support cerebral perfusion pressure thresholds for adults at a class 2 level, but evidence is lacking in younger patients. The purpose of this study is to identify the impact of age-specific cerebral perfusion pressure thresholds on short-term survival among patients with severe traumatic brain injury.

Design: Institutional review board-approved, prospective, observational cohort study.

Setting: Level I or II trauma centers in New York State.

Patients: Data on all patients with a postresuscitation Glasgow Coma Score less than 9 were added in the Brain Trauma Foundation prospective New York State TBI-trac database.

Measurements and Main Results: We calculated the survival rates and relative risks of mortality for patients with severe traumatic brain injury based on predefined age-specific cerebral perfusion pressure thresholds. A higher threshold and a lower threshold were defined for each age group: 60 and 50 mm Hg for 12 years old or older, 50 and 35 mm Hg for 6–11 years, and 40 and 30 mm Hg for 0–5 years. Patients were stratified into age groups of 0–11, 12–17, and 18 years old or older. Three exclusive groups of CPP-L (events below low cerebral perfusion pressure threshold), CPP-B (events between high and low cerebral perfusion pressure thresholds), and CPP-H (events above high cerebral perfusion pressure threshold) were defined. As an internal control, we evaluated the associations between cerebral perfusion pressure events and events of hypotension and elevated intracranial pressure. Survival was significantly higher in 0–11 and 18 years old or older age groups for patients with CPP-H events compared with those with CPP-L events. There was a significant decrease in survival with prolonged exposure to CPP-B events for the 0–11 and 18 years old and older age groups when compared with the patients with CPP-H events (p = 0.0001 and p = 0.042, respectively). There was also a significant decrease in survival with prolonged exposure to CPP-L events in all age groups compared with the patients with CPP-H events (p< 0.0001 for 0- to 11-yr olds, p = 0.0240 for 12- to 17-yr olds, and p < 0.0001 for 18-yr old and older age groups). The 12- to 17-year olds had a significantly higher likelihood of survival compared with adults with prolonged exposure to CPP-L events (< 50 mm Hg). CPP-L events were significantly related to systemic hypotension for the 12- to 17-year-old group (p = 0.004) and the 18-year-old and older group (p < 0.0001). CPP-B events were significantly related to systemic hypotension in the 0- to 11-year-old group (p = 0.014). CPP-B and CPP-L events were significantly related to elevated intracranial pressure in all age groups.

Conclusions: Our data provide new evidence that cerebral perfusion pressure targets should be age specific. Furthermore, cerebral perfusion pressure goals above 50 or 60 mm Hg in adults, above 50 mm Hg in 6- to 17-year olds, and above 40 mm Hg in 0- to 5-year olds seem to be appropriate targets for treatment-based studies. Systemic hypotension had an inconsistent relationship to events of low cerebral perfusion pressure, whereas elevated intracranial pressure was significantly related to all low cerebral perfusion pressure events across all age groups. This may impart a clinically important difference in care, highlighting the necessity of controlling intracranial pressure at all times, while targeting systolic blood pressure in specific instances.

1Department of Neurology, Weill Cornell Medical College, New York, NY.

2Department of Public Health, Weill Cornell Medical College, New York, NY.

3Department of Surgery, Jamaica Hospital Medical Center, New York, NY.

4Brain Trauma Foundation, New York, NY.

5Department of Neurological Surgery, Weill Cornell Medical College, New York, NY.

* See also p. 86.

Supplemental digital content is available for this article. Direct URL citations appear in the printed text and are provided in the HTML and PDF versions of this article on the journal’s website (http://journals.lww.com/pccmjournal).

Supported, in part, by the New York State Department of Health to the Brain Trauma Foundation. Supported, in part, by funds from the Clinical Translational Science Center (CTSC), National Center for Advancing Translational Sciences (NCATS) grant #UL1-TR000457-06.

Dr. Jamshid Ghajar is President of the Brain Trauma Foundation, which received grant money for part of this research from the New York State Department of Health. The remaining authors have disclosed that they do not have any potential conflicts of interest.

Presented, in part, at the American Association of Neurological Surgeons Annual Meeting, Denver, CO, April 13, 2011.

For information regarding this article, E-mail: bba2003@nyp.org

©2014The Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies