Neurological Intensive Care Unit, Montreal Neurological Institute and Hospital McGill University, Montreal, Quebec, Canada,
Neurocrit Care. 2013 Oct;19(2):199-205. doi: 10.1007/s12028-013-9853-y.
To assess the safety and effectiveness of lumbar drains as adjuvant therapy in severe bacterial meningitis, and compare it to standard treatment.
A retrospective cohort study of all patients above the age of 18 years with bacterial meningitis and altered mental status admitted to the Montreal Neurological Hospital Intensive Care Unit from January 2000 to December 2010.
Thirty-seven patients were identified using clinical and cerebrospinal fluid criteria. Patients were divided into lumbar drain (LD) (n = 11) and conventional therapy (no LD) (n = 26) groups.
Outcomes were assessed using meningitis-related mortality and the Glasgow Outcome Scale (GOS) at 1 and 3 months.
All patients received broad-spectrum antibiotic therapy, 84% received steroids. There was no significant difference in mean age, type of bacteria, or time from arrival in ER to initiation of therapy. There was significantly less co-morbidity (24% healthy vs. 18.1%) and coma (GCS < 8 34.6 vs. 54.5%) in the conventional therapy group, as well as a longer duration of symptoms prior to admission (mean 1.34 ± 1.24 vs. 2.19 ± 2.34 days). The mean opening pressure was high in all patients (20-55 cm H2O in the LD and 12-60 cm H2O in the no LD). Mean time from arrival in ER to insertion of the lumbar drain was 37 h. Lumbar drains were set for a maximum drainage of 10 cc/h and an ICP below 10 mmHg. Despite greater clinical severity, the LD group had 0% mortality and 91% of the patients achieved a GOS of 4-5. The non-LD group had 15.4% mortality and only 60% achieved a GOS of 4-5. No adverse events were associated with LD therapy.
In this study, the use of lumbar drainage in adult patients with severe bacterial meningitis was safe, and likely contributed to the low mortality and morbidity.
评估腰椎引流作为辅助治疗严重细菌性脑膜炎的安全性和有效性,并将其与标准治疗进行比较。
对 2000 年 1 月至 2010 年 12 月期间在蒙特利尔神经学医院重症监护病房因细菌性脑膜炎和意识改变而入院的年龄大于 18 岁的所有患者进行回顾性队列研究。
根据临床和脑脊液标准,共确定 37 例患者。患者分为腰椎引流(LD)组(n = 11)和常规治疗(无 LD)组(n = 26)。
使用与脑膜炎相关的死亡率和格拉斯哥结局量表(GOS)在 1 个月和 3 个月时评估结果。
所有患者均接受广谱抗生素治疗,84%接受类固醇治疗。LD 组和常规治疗组之间的平均年龄、细菌类型或从急诊室到达至开始治疗的时间均无显著差异。常规治疗组的合并症(24%健康患者 vs. 18.1%)和昏迷(GCS < 8,34.6% vs. 54.5%)发生率显著较低,且入院前症状持续时间较长(LD 组平均 1.34 ± 1.24 天 vs. 2.19 ± 2.34 天)。所有患者的平均颅内压均较高(LD 组为 20-55cmH2O,常规治疗组为 12-60cmH2O)。从急诊室到达至插入腰椎引流的平均时间为 37 小时。腰椎引流的最大引流速度为 10cc/h,颅内压低于 10mmHg。尽管临床严重程度较高,但 LD 组的死亡率为 0%,91%的患者达到 GOS 4-5 级。常规治疗组的死亡率为 15.4%,只有 60%的患者达到 GOS 4-5 级。LD 治疗无不良事件。
在这项研究中,腰椎引流在成人严重细菌性脑膜炎患者中的应用是安全的,可能有助于降低死亡率和发病率。