腰腹膜分流联合Ommaya储液器使脑室内化疗在颅内压升高的情况下持续治疗脑膜轻脑膜转移。

Byungjun Woo, Ho-Shin Gwak, Ji-Woong Kwon, Sang-Hoon Shin, Heon Yoo
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引用次数: 1

摘要

背景:脑脊液(CSF)化疗治疗轻脑膜转移(LM)可以通过Ommaya蓄水池在脑室内进行。然而,脑积水合并LM可干扰化疗药物的分布,脑室-腹膜分流可阻止药物分布到脑室外CSF空间。本研究探讨了腰腹膜(LP)分流与Ommaya储液器结合的可行性,以控制颅内压并允许脑室内化疗。方法:我们确定了16例LM患者,他们同时或依次接受了Ommaya储液器和LP分流术,随后接受了脑室内化疗。通过评估1)注射后0、6和12小时采集的脑脊液样本中脑室内注射药物的分布,以及2)与程序和药物给药相关的不良事件,来评估这种联合脑室化疗的可行性。结果:在LP分流器插入后的中位随访期间,患者接受了中位7轮(范围1-37)脑室化疗。获得了6例患者的药代动力学数据。Ommaya水库的基线甲氨蝶呤(MTX)水平从339.9µM到1523.5µM不等。从LP分流液中采集的脑脊液显示其消除半衰期(t1/2)为2.63 h, 12 h时MTX浓度与基线时的平均比值为0.05±0.05,保证了药物从脑室到椎管的分布。9例患者(56%)因导管移位、故障或感染接受了翻修手术。在这些患者中,发生了脑室化疗引起的脑脊液感染(n=3),但在我们开始采用完全无菌技术后,后来的病例没有发生感染。结论:LP分流联合Ommaya储液器插入是LM患者既能控制颅内压又能继续脑室化疗的可行选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Lumboperitoneal Shunt Combined With Ommaya Reservoir Enables Continued Intraventricular Chemotherapy for Leptomeningeal Metastasis With Increased Intracranial Pressure.

Lumboperitoneal Shunt Combined With Ommaya Reservoir Enables Continued Intraventricular Chemotherapy for Leptomeningeal Metastasis With Increased Intracranial Pressure.

Lumboperitoneal Shunt Combined With Ommaya Reservoir Enables Continued Intraventricular Chemotherapy for Leptomeningeal Metastasis With Increased Intracranial Pressure.

Lumboperitoneal Shunt Combined With Ommaya Reservoir Enables Continued Intraventricular Chemotherapy for Leptomeningeal Metastasis With Increased Intracranial Pressure.

Background: Intra-cerebrospinal fluid (CSF) chemotherapy for leptomeningeal metastasis (LM) can be delivered intraventricularly via an Ommaya reservoir. However, hydrocephalus associated with LM can interfere with chemotherapeutic drug distribution, and ventriculoperitoneal shunts can prevent drug distribution to the extra-ventricular CSF space. This study examined the feasibility of combining a lumboperitoneal (LP) shunt with an Ommaya reservoir to both control intracranial pressure and allow for intraventricular chemotherapy.

Methods: We identified 16 patients with LM who received both an Ommaya reservoir and an LP shunt, either concurrently or sequentially, and subsequently received intraventricular chemotherapy. The feasibility of this combination for intraventricular chemotherapy was evaluated by assessing 1) the distribution of intraventricularly injected drugs in CSF samples collected 0, 6, and 12 h post-injection and 2) adverse events associated with the procedure and drug administration.

Results: Patients received a median of seven rounds (range 1-37) of intraventricular chemotherapy during a median follow-up period of 5.2 months after LP shunt insertion. Pharmacokinetic data were obtained from six patients. Baseline methotrexate (MTX) levels from Ommaya reservoirs varied from 339.9 µM to 1,523.5 µM. CSF sampled from LP shunt reservoirs revealed an elimination half-life (t1/2) of 2.63 h, and the mean ratio of MTX concentration at 12 h to that at baseline was 0.05±0.05, ensuring drug distribution from the ventricle to the spinal canal. Nine patients (56%) underwent revision surgery due to catheter migration, malfunction, or infection. Among these patients, CSF infections attributable to intraventricular chemotherapy (n=3) occurred, but no infections occurred in later cases after we began to employ a complete aseptic technique.

Conclusion: LP shunt combined with Ommaya reservoir insertion is a feasible option for achieving both intracranial pressure control and the continuation of intraventricular chemotherapy in patients with LM.

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