Cuny E, Richer E, Castel J P
Clinique Universitaire de Neurochirurgie, Hôpital Pellegrin, Bordeaux, France.
Brain Inj. 2001 Oct;15(10):917-25. doi: 10.1080/02699050110065277.
In the initial phase of severe head injury, dysautonomic abnormalities are frequent. Within the framework of a prospective study, evaluating the efficacy of continuous intrathecal Baclofen therapy (CIBT) on hypertonia during the initial recovery phase of severe head injury, the authors report on the preliminary results of this treatment on paroxysmal dysautonomia about four patients. Continuous intrathecal Baclofen infusion was first delivered, for a test period, continuously for 6 days. If a relapse of dysautonomia occurred at the end of the test period, an implantation of a continuous intrathecal infusion pump delivering Baclofen was performed. Results were assessed with four continuous variables; duration (days), dose of Baclofen per day (microg/d), number of dysautonomic paroxysmal episodes per day, and initial recovery evaluated by a scale of the first initial stages of head injury coma recovery. For three patients: (1) the number of dysautonomic paroxysmal episodes per day and the doses of Baclofen during the follow-up period were correlated (p = 0.02, p < 0.001, p = 0.008, respectively, distribution-free test of Spearman), (2) during the test period and the relapse after the test period, the number of paroxysmal episodes and the Baclofen dose are correlated to p < 0.05, p = 0.03, p = 0.04, respectively (distribution-free test of Spearman). The second statistical test was used to prove that Baclofen doses and number of paroxysmal dysautonomic episodes are correlated independently of the duration of follow-up. The fourth patient improved with CIBT without any recurrence at the end of the treatment test period. For the four patients, recovery score increased during the overall follow-up. In the authors' experience CIBT is very efficient to control paroxysmal dysautonomia during the initial recovery phase in severe head injury, and seems to facilitate recovery.
在重度颅脑损伤的初始阶段,自主神经功能异常很常见。在一项前瞻性研究的框架内,评估持续鞘内注射巴氯芬疗法(CIBT)对重度颅脑损伤初始恢复阶段高肌张力的疗效,作者报告了该疗法对约4例患者阵发性自主神经功能异常的初步结果。首先进行持续鞘内巴氯芬输注,为期6天,作为试验期。如果在试验期结束时自主神经功能异常复发,则植入持续鞘内输注泵给予巴氯芬。结果通过四个连续变量进行评估:持续时间(天)、每日巴氯芬剂量(微克/天)、每日自主神经功能异常阵发性发作次数,以及通过颅脑损伤昏迷恢复初始阶段的量表评估初始恢复情况。对于3例患者:(1)随访期间每日自主神经功能异常阵发性发作次数与巴氯芬剂量相关(分别为p = 0.02、p < 0.001、p = 0.008,Spearman非参数检验),(2)在试验期及试验期后的复发期,阵发性发作次数与巴氯芬剂量分别相关,p < 0.05、p = 0.03、p = 0.04(Spearman非参数检验)。第二次统计检验用于证明巴氯芬剂量与自主神经功能异常阵发性发作次数的相关性与随访持续时间无关。第4例患者在治疗试验期结束时经CIBT治疗后病情改善且无任何复发。对于这4例患者,在整个随访期间恢复评分增加。根据作者的经验,CIBT在重度颅脑损伤初始恢复阶段控制阵发性自主神经功能异常非常有效,且似乎有助于恢复。