Figaji Anthony A, Zwane Eugene, Thompson Crispin, Fieggen A Graham, Argent Andrew C, Le Roux Peter D, Peter Jonathan C
Divisions of Neurosurgery, School of Child and Adolescent Health, University of Cape Town, Red Cross Children's Hospital, Cape Town, South Africa.
Childs Nerv Syst. 2009 Oct;25(10):1335-43. doi: 10.1007/s00381-009-0821-y. Epub 2009 Feb 13.
Brain tissue oxygen tension (PbtO(2)) monitoring is used increasingly in adult severe traumatic brain injury (TBI) management. Several factors are known to influence PbtO(2) in adults, but the variables that affect PbtO(2) in pediatric TBI are not well described. This study examines the relationships between PbtO(2) and (1) physiological markers of potential secondary insults commonly used in pediatric TBI, in particular intracranial pressure (ICP), cerebral perfusion pressure (CPP), and systemic hypoxia, and (2) other clinical factors and treatment received that may influence PbtO(2).
In this prospective observational study, 52 children (mean age, 6.5 +/- 3.4 years; range, 9 months to 14 years old) with severe TBI and a median post-resuscitation Glasgow Coma Score (GCS) of 5 were managed with continuous PbtO(2) monitoring. The relationships between PbtO(2) parameters (Pbt)(2)(low), PbtO(2) < 5, PbtO(2) < 10, and mPbtAO(2)(24)) and clinical, physiological, and treatment factors were explored using time-linked data and Spearman's correlation coefficients.
No clinical, physiological, or treatment variable was significantly associated with all PbtO(2) parameters, but individual associations were found with initial GCS (PbtO(2) < 5, p = 0.0113), admission Pediatric Trauma Score (PbtO(2) < 10, 0.0175), mICP > 20 (mPbtO(2)(24), p = 0.0377), CPP(low) (PbtO(2)(low), p = 0.0065), CPP < 40 (PbtO(2)(low), p = 0.0269; PbtO(2) < 5, p = 0.0212), P(a)O(2) < 60 (mPbtO(2)(24), p = 0.0037), S(a)O(2) < 90 (PbtO(2)(low), p = 0.0438), and use of inotropes during ICU care (PbtO(2)(low), p = 0.0276; PbtO(2) < 10, p = 0.0277; p = mPbtO(2)(24)).
Delivery of oxygen to the brain is important to limit secondary neuronal injury after severe TBI. Our data show that PbtO(2) is poorly predicted by clinical and physiological factors commonly measured in the pediatric ICU. Multimodality monitoring may be needed to detect all secondary cerebral insults in pediatric TBI.
脑组织氧分压(PbtO₂)监测在成人重型创伤性脑损伤(TBI)管理中的应用越来越广泛。已知有几个因素会影响成人的PbtO₂,但影响小儿TBI中PbtO₂的变量尚未得到充分描述。本研究探讨了PbtO₂与(1)小儿TBI中常用的潜在继发性损伤的生理指标之间的关系,特别是颅内压(ICP)、脑灌注压(CPP)和全身性缺氧,以及(2)其他可能影响PbtO₂的临床因素和所接受的治疗。
在这项前瞻性观察研究中,对52例重度TBI儿童(平均年龄6.5±3.4岁;范围9个月至14岁)进行了连续PbtO₂监测,复苏后格拉斯哥昏迷评分(GCS)中位数为5分。使用时间关联数据和Spearman相关系数探讨了PbtO₂参数(Pbt₂(低)、PbtO₂<5、PbtO₂<l0和mPbtAO₂(24))与临床、生理和治疗因素之间的关系。
没有临床、生理或治疗变量与所有PbtO₂参数显著相关,但发现个别关联与初始GCS(PbtO₂<5,p = 0.0113)、入院小儿创伤评分(PbtO₂<10,0.0175)、mICP>20(mPbtO₂(24),p = 0.0377)、CPP(低)(PbtO₂(低),p = 0.0065)、CPP<40(PbtO₂(低),p = 0.0269;PbtO₂<5,p = 0.0212)、P(a)O₂<60(mPbtO₂(24),p = 0.0037)、S(a)O₂<90(PbtO₂(低),p = 0.0438)以及ICU护理期间使用血管活性药物(PbtO₂(低),p = 0.?276;PbtO₂<10,p = 0.0277;p = mPbtO₂(24))有关。
向脑输送氧气对于限制重度TBI后的继发性神经元损伤很重要。我们的数据表明,小儿ICU中常用的临床和生理因素对PbtO₂的预测效果不佳。可能需要多模式监测来检测小儿TBI中的所有继发性脑损伤。