Zwagerman Nathan T, Wang Eric W, Shin Samuel S, Chang Yue-Fang, Fernandez-Miranda Juan C, Snyderman Carl H, Gardner Paul A
Departments of1Neurological Surgery and.
2Otolaryngology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
J Neurosurg. 2018 Oct 19;131(4):1172-1178. doi: 10.3171/2018.4.JNS172447. Print 2019 Oct 1.
Based on a null hypothesis that the use of short-term lumbar drainage (LD) after endoscopic endonasal surgery (EES) for intradural pathology does not prevent postoperative CSF leaks, a trial was conducted to assess the effect of postoperative LD on postoperative CSF leak following standard reconstruction.
A prospective, randomized controlled trial of lumbar drain placement after endoscopic endonasal skull base surgery was performed from February 2011 to March 2015. All patients had 3-month follow-up data. Surgeons were blinded to which patients would or would not receive the drain until after closure was completed. An a priori power analysis calculation assuming 80% of power, 5% postoperative CSF leak rate in the no-LD group, and 16% in the LD group determined a planned sample size of 186 patients. A routine data and safety check was performed with every 50 patients being recruited to ensure the efficacy of randomization and safety. These interim tests were run by a statistician who was not blinded to the arms they were evaluating. This study accrued 230 consecutive adult patients with skull base pathology who were eligible for endoscopic endonasal resection. Inclusion criteria (high-flow leak) were dural defect greater than 1 cm2 (mandatory), extensive arachnoid dissection, and/or dissection into a ventricle or cistern. Sixty patients were excluded because they did not meet the inclusion criteria. One hundred seventy patients were randomized to either receive or not receive a lumbar drain.
One hundred seventy patients were randomized, with a mean age of 51.6 years (range 19-86 years) and 38% were male. The mean BMI for the entire cohort was 28.1 kg/m2. The experimental cohort with postoperative LD had an 8.2% rate of CSF leak compared to a 21.2% rate in the control group (odds ratio 3.0, 95% confidence interval 1.2-7.6, p = 0.017). In 106 patients in whom defect size was measured intraoperatively, a larger defect was associated with postoperative CSF leak (6.2 vs 2.9 cm2, p = 0.03). No significant difference was identified in BMI between those with (mean 28.4 ± 4.3 kg/m2) and without (mean 28.1 ± 5.6 kg/m2) postoperative CSF leak (p = 0.79). Furthermore, when patients were grouped based on BMI < 25, 25-29.9, and > 30 kg/m2, no difference was noted in the rates of CSF fistula (p = 0.97).
Among patients undergoing intradural EES judged to be at high risk for CSF leak as defined by the study's inclusion criteria, perioperative LD used in the context of vascularized nasoseptal flap closure significantly reduced the rate of postoperative CSF leaks.Clinical trial registration no.: NCT03163134 (clinicaltrials.gov).
基于一项无效假设,即在内镜鼻内手术(EES)治疗硬膜内病变后使用短期腰椎引流(LD)不能预防术后脑脊液漏,进行了一项试验以评估术后LD对标准重建术后脑脊液漏的影响。
2011年2月至2015年3月,在内镜鼻内颅底手术后进行了一项关于腰椎引流管放置的前瞻性随机对照试验。所有患者均有3个月的随访数据。在伤口缝合完成后,外科医生才知道哪些患者会或不会接受引流。一项先验效能分析计算假设效能为80%,无LD组术后脑脊液漏率为5%,LD组为16%,确定计划样本量为186例患者。每招募50例患者进行一次常规数据和安全性检查,以确保随机化的有效性和安全性。这些中期试验由一名对所评估的分组不盲的统计学家进行。本研究纳入了230例连续的有颅底病变且适合内镜鼻内切除的成年患者。纳入标准(高流量漏)为硬膜缺损大于1 cm²(必需)、广泛的蛛网膜剥离和/或剥离进入脑室或脑池。60例患者因不符合纳入标准而被排除。170例患者被随机分为接受或不接受腰椎引流。
170例患者被随机分组,平均年龄51.6岁(范围19 - 86岁),38%为男性。整个队列的平均BMI为28.1 kg/m²。术后使用LD的试验组脑脊液漏率为8.2%,而对照组为21.2%(优势比3.0,95%置信区间1.2 - 7.6,p = 0.017)。在术中测量缺损大小的106例患者中,较大的缺损与术后脑脊液漏相关(6.2 vs 2.9 cm²,p = 0.03)。有术后脑脊液漏的患者(平均28. + 4.3 kg/m²)和无术后脑脊液漏的患者(平均28.1 + 5.6 kg/m²)之间的BMI无显著差异(p = 0.79)。此外,当患者按BMI < 25、25 - 29.9和> 30 kg/m²分组时,脑脊液瘘的发生率无差异(p = 0.97)。
在根据研究纳入标准判断为脑脊液漏高风险的硬膜内EES患者中,在带血管蒂鼻中隔瓣封闭的情况下使用围手术期LD可显著降低术后脑脊液漏的发生率。临床试验注册号:NCT03163134(clinicaltrials.gov)。