4.5 Review

Cerebral Perfusion Pressure Targets Individualized to Pressure-Reactivity Index in Moderate to Severe Traumatic Brain Injury: A Systematic Review

期刊

JOURNAL OF NEUROTRAUMA
卷 34, 期 5, 页码 963-970

出版社

MARY ANN LIEBERT, INC
DOI: 10.1089/neu.2016.4450

关键词

cerebral blood flow autoregulation; therapeutic approaches for the treatment of central nervous system injury; TBI; vascular reactivity

资金

  1. European Union [602150-2]
  2. National Institute for Health Research (UK)
  3. Academy of Medical Sciences (AMS) [AMS-CSF4-Newcombe] Funding Source: researchfish
  4. National Institute for Health Research [ACF-2009-14-007, NF-SI-0512-10090] Funding Source: researchfish

向作者/读者索取更多资源

Traumatic brain injury (TBI) frequently triggers a disruption of cerebral autoregulation. The cerebral perfusion pressure (CPP) at which autoregulation is optimal (CPPopt) varies between individuals, and can be calculated based on fluctuations between arterial blood pressure and intracranial pressure. This review assesses the effect of individualizing CPP targets to pressure reactivity index (a measure of autoregulation) in patients with TBI. Cochrane Central Register of Controlled Trials, MEDLINE (R), Embase, and Cumulative Index of Nursing and Allied Health Literature were searched in March 2015 for studies assessing the effect of targeting CPPopt in TBI. We included all studies that assessed the impact of targeting CPPopt on outcomes including mortality, neurological outcome, and physiological changes. Risk of bias was assessed using the RTI Item Bank and evidence quality was considered using the Grading of Recommendations Assessment, Development, and Evaluation (GRADE) criteria. Eight cohort studies (based on six distinct data sets) assessing the association between CPPopt and mortality, Glasgow Outcome Scale and physiological measures in TBI were included. The quality of evidence was deemed very low based on the GRADE criteria. Although the data suggest an association between variation from CPPopt and poor clinical outcome at 6 months, the quality of evidence prevents firm conclusions, particularly regarding causality, from being drawn. Available data suggest that targeting CPPopt might represent a technique to improve outcomes following TBI, but currently there is insufficient high-quality data to support a recommendation for use in clinical practice. Further prospective, randomized controlled studies should be undertaken to clarify its role in the acute management of TBI.

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