Cheng B-C, Chang W-N, Chang C-S, Chee C-Y, Huang C-R, Chen J-B, Chang C-J, Hung P-L, Wang K-W, Chang H-W, Lu C-H
Department of Medicine, Chang Gung Memorial Hospital-Kaohsiung, Kaohsiung, Taiwan.
Eur J Neurol. 2003 Nov;10(6):655-62. doi: 10.1046/j.1468-1331.2003.00683.x.
To determine the clinical features, prognostic factors, and therapeutic results of Guillain-Barré syndrome (GBS) in order to improve the therapeutic strategy for this disease. We retrospectively reviewed the electrodiagnostic study and medical records of patients with GBS admitted to Chang Gung Memorial Hospital, Kaohsiung, between January 1986 and December 2000. Outcomes and prognosis were followed-up after 1 year. Ninety-six patients were enrolled in this study. According to the clinical and electrophysiological findings, 77 patients were acute inflammatory demyelinating polyradiculoneuropathy, seven were Miller Fisher syndrome, and six were axonal forms, and six were unclassified. At a follow-up of 1 year, 61 patients (64%) recovered, 30 (31%) had residua and five (5%) died. Amongst these 30 had residua, including unassisted gait in 19, assisted gait in four, and wheel/bed bound in seven. According to the statistical analysis, disabilities at the nadir (P < 0.0001) and at admission (P = 0.014) were significant prognostic factors. Variables used for the stepwise logistic regression, and the results revealed that after analysis for all the above variables, only disability at the nadir (P < 0.0001) was independently associated with the treatment failure rate. Our study revealed 27% of cases in need of respiratory support during hospitalization, and 5% of hospital-treated patients die from the complications. Furthermore, 31% had residua at a follow-up of 1 year or more. If prognostic factors are considered, disability at the nadir during hospitalization demonstrates consistently poor therapeutic outcomes. Therefore, early diagnosis, choice of appropriate treatment, and preventing complications during acute stages are essential to maximize the potential for survival.
为确定吉兰 - 巴雷综合征(GBS)的临床特征、预后因素及治疗效果,以改进该病的治疗策略。我们回顾性分析了1986年1月至2000年12月间入住高雄长庚纪念医院的GBS患者的电诊断研究及病历资料。随访1年后观察结局及预后情况。本研究共纳入96例患者。根据临床及电生理检查结果,77例为急性炎症性脱髓鞘性多发性神经根神经病,7例为米勒 - 费希尔综合征,6例为轴索性,6例未分类。随访1年时,61例(64%)恢复,30例(31%)有后遗症,5例(5%)死亡。在这30例有后遗症的患者中,19例需无辅助行走,4例需辅助行走,7例需轮椅/卧床。经统计分析,最低点时的残疾程度(P < 0.0001)及入院时的残疾程度(P = 0.014)是显著的预后因素。用于逐步逻辑回归分析的变量及结果显示,对上述所有变量进行分析后,仅最低点时的残疾程度(P < 0.0001)与治疗失败率独立相关。我们的研究显示,27%的病例住院期间需要呼吸支持,5%的住院治疗患者死于并发症。此外,随访1年及以上时有31%的患者有后遗症。若考虑预后因素,住院期间最低点时的残疾程度始终显示治疗效果不佳。因此,早期诊断、选择合适的治疗方法以及预防急性期并发症对于最大限度提高生存潜力至关重要。