Pozzi Marco, Avantaggiato Paolo, Pastore Valentina, Carnovale Carla, Clementi Emilio, Strazzer Sandra
Scientific Institute IRCCS Eugenio Medea, 23842 Bosisio Parini, Italy.
Unit of Clinical Pharmacology, Department of Biomedical and Clinical Sciences L. Sacco, "Luigi Sacco" University Hospital, Università di Milano, 20157 Milan, Italy.
Brain Sci. 2021 Jul 19;11(7):949. doi: 10.3390/brainsci11070949.
Carbamazepine and oxcarbazepine are used for behavioral disorders following organic diseases. After severe acquired brain injury, patients may develop frontal symptoms. In our neurological rehabilitation routine, oxcarbazepine is used for better safety over carbamazepine, although its efficacy is not clarified. We aimed to improve knowledge on this use of oxcarbazepine, by probing clinical factors associated with response. We retrospectively examined the clinical records of our patients, collecting clinical variables and outcomes of efficacy, both clinician-rated and caregiver/self-rated. We described the distribution of clinical variables and examined their associations via logistic regressions. Patients in our cohort were predominantly pediatric, with frontal lobe damage and irritable/reactive. With an oxcarbazepine median dose of 975 mg, almost half of patients improved. We found several clinical factors associated with clinician-rated efficacy: absence of frontal damage and absence of irritability/reactivity symptoms; clinical factors associated with caregivers/patients-rated efficacy were: higher DRS score at baseline and higher patient age. In this retrospective study, we observed that oxcarbazepine was differentially efficacious in patients with specific characteristics. Our study could not examine drug therapy separately from neuropsychological therapy, nor the influence of dose. Our associative results should be verified experimentally, also assessing causality and establishing dose-related efficacy and safety.
卡马西平和奥卡西平用于治疗器质性疾病后的行为障碍。严重的后天性脑损伤后,患者可能会出现额叶症状。在我们的神经康复常规治疗中,使用奥卡西平是因为其安全性优于卡马西平,尽管其疗效尚不明确。我们旨在通过探究与反应相关的临床因素,提高对奥卡西平这种用途的认识。我们回顾性检查了患者的临床记录,收集了临床变量以及临床医生评定和照料者/自我评定的疗效结果。我们描述了临床变量的分布情况,并通过逻辑回归分析了它们之间的关联。我们队列中的患者主要是儿童,存在额叶损伤且易激惹/反应性强。奥卡西平的中位剂量为975毫克,几乎一半的患者病情有所改善。我们发现了几个与临床医生评定疗效相关的临床因素:无额叶损伤和无易激惹/反应性症状;与照料者/患者评定疗效相关的临床因素有:基线时DRS评分较高和患者年龄较大。在这项回顾性研究中,我们观察到奥卡西平对具有特定特征的患者疗效存在差异。我们的研究无法将药物治疗与神经心理治疗分开考察,也无法考察剂量的影响。我们的相关性结果应通过实验进行验证,同时评估因果关系并确定剂量相关的疗效和安全性。