Arterial Oxygenation in Traumatic Brain Injury-Relation to Cerebral Energy Metabolism, Autoregulation, and Clinical Outcome

被引:22
作者
Wettervik, Teodor Svedung [1 ]
Engquist, Henrik [2 ]
Howells, Timothy [1 ]
Lenell, Samuel [1 ]
Rostami, Elham [1 ]
Hillered, Lars [1 ]
Enblad, Per [1 ]
Lewen, Anders [1 ]
机构
[1] Uppsala Univ, Sect Neurosurg, Dept Neurosci, SE-75185 Uppsala, Sweden
[2] Uppsala Univ, Dept Surg Sci Anesthesia & Intens Care, Uppsala, Sweden
基金
瑞典研究理事会;
关键词
autoregulation; energy metabolism; hyperoxia; neurointensive care; traumatic brain injury; SEVERE HEAD-INJURY; BLOOD-FLOW; TISSUE OXYGEN; PRESSURE REACTIVITY; PERFUSION-PRESSURE; INTRACEREBRAL MICRODIALYSIS; NORMOBARIC HYPEROXIA; NEUROINTENSIVE CARE; INSPIRED OXYGEN; MANAGEMENT;
D O I
10.1177/0885066620944097
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Background: Ischemic and hypoxic secondary brain insults are common and detrimental in traumatic brain injury (TBI). Treatment aims to maintain an adequate cerebral blood flow with sufficient arterial oxygen content. It has been suggested that arterial hyperoxia may be beneficial to the injured brain to compensate for cerebral ischemia, overcome diffusion barriers, and improve mitochondrial function. In this study, we investigated the relation between arterial oxygen levels and cerebral energy metabolism, pressure autoregulation, and clinical outcome. Methods: This retrospective study was based on 115 patients with severe TBI treated in the neurointensive care unit, Uppsala university hospital, Sweden, 2008 to 2018. Data from cerebral microdialysis (MD), arterial blood gases, hemodynamics, and intracranial pressure were analyzed the first 10 days post-injury. The first day post-injury was studied in particular. Results: Arterial oxygen levels were higher and with greater variability on the first day post-injury, whereas it was more stable the following 9 days. Normal-to-high mean pO(2)was significantly associated with better pressure autoregulation/lower pressure reactivity index (P= .02) and lower cerebral MD-lactate (P= .04) on day 1. Patients with limited cerebral energy metabolic substrate supply (MD-pyruvate below 120 mu M) and metabolic disturbances with MD-lactate-/pyruvate ratio (LPR) above 25 had significantly lower arterial oxygen levels than those with limited MD-pyruvate supply and normal MD-LPR (P= .001) this day. Arterial oxygenation was not associated with clinical outcome. Conclusions: Maintaining a pO(2)above 12 kPa and higher may improve oxidative cerebral energy metabolism and pressure autoregulation, particularly in cases of limited energy substrate supply in the early phase of TBI. Evaluating the cerebral energy metabolic profile could yield a better patient selection for hyperoxic treatment in future trials.
引用
收藏
页码:1075 / 1083
页数:9
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