Department of Neurosurgery, Heidelberg University Hospital, Im Neuenheimer Feld 400, 69120, Heidelberg, Germany.
Christoph Miethke GmbH & Co. KG, Potsdam, Germany.
Acta Neurochir (Wien). 2023 Dec;165(12):4031-4044. doi: 10.1007/s00701-023-05751-y. Epub 2023 Aug 29.
In pediatric hydrocephalus (HC) treatment, programmable gravitational valves offer greater flexibility to manage overdrainage during children's growth. However, it remains unclear whether these devices provide better outcomes rather than their precursors. The study assessed the benefit from programmability of gravitational valve, i.e., programmable-SHUNTASSISTANT (proSA®) vs. SHUNTASSISTANT® (SA®).
Clinical records and imaging of pediatric patients with hydrocephalus of non-tumoral etiology treated with fixed (SA®) or programmable (proSA®) gravitational valves between January 2006 and January 2022 were analyzed in a retrospective single-center study. Valve survival was compared in relation to age and etiology. Lately explanted valves received biomechanical analysis.
A total of 391 gravitational valves (254 SA® and 137 proSA®) were inserted in 244 patients (n = 134 males). One hundred thirty-three SA® (52.4%) and 67 proSA® (48.9%) were explanted during a follow-up of 81.1 ± 46.3 months. Valve survival rate at 1 and 5 years with proSA® was 87.6% and 60.6% compared to 81.9% and 58.7% with SA®, with mean survival time 56.4 ± 35.01 and 51.4 ± 43.0 months, respectively (P = 0.245). Age < 2 years at implantation correlated with significantly lower valve survival rates (P < 0.001), while HC etiology showed no significant impact. Overdrainage alone accounted for more SA® revisions (39.8% vs. 3.1%, P < 0.001), while dysfunctions of the adjustment system represented the first cause of valve replacement in proSA® cohort (45.3%). The biomechanical analysis performed on 41 proSA® and 31 SA® showed deposits on the valve's internal surface in 97.6% and 90.3% of cases.
Our comparative study between proSA® and SA® valves in pediatric HC demonstrated that both valves showed similar survival rates, regardless of etiology but only with young age at implantation. The programmability may be beneficial in preventing sequelae of chronic overdrainage but does not reduce need for valve revision and proSA® valve should be considered in selected cases in growing children older than 2 years.
在儿科脑积水(HC)治疗中,可编程重力阀在儿童生长期间提供了更大的灵活性来管理过度引流。然而,目前尚不清楚这些设备是否比它们的前身提供了更好的效果。本研究评估了重力阀可编程性的益处,即可编程-SHUNTASSISTANT(proSA®)与 SHUNTASSISTANT®(SA®)相比。
回顾性分析了 2006 年 1 月至 2022 年 1 月期间采用固定(SA®)或可编程(proSA®)重力阀治疗非肿瘤性病因脑积水的儿科患者的临床记录和影像学资料。比较了与年龄和病因有关的阀门存活率。最近,对已取出的阀门进行了生物力学分析。
共植入 391 个重力阀(254 个 SA®和 137 个 proSA®),治疗 244 名患者(n=134 名男性)。133 个 SA®(52.4%)和 67 个 proSA®(48.9%)在 81.1±46.3 个月的随访中被取出。proSA®的 1 年和 5 年的阀门存活率分别为 87.6%和 60.6%,而 SA®的分别为 81.9%和 58.7%,平均生存时间分别为 56.4±35.01 个月和 51.4±43.0 个月(P=0.245)。植入时年龄<2 岁与显著较低的阀门存活率相关(P<0.001),而 HC 病因无显著影响。单纯过度引流导致更多的 SA®修订(39.8% vs. 3.1%,P<0.001),而调节系统的功能障碍是 proSA®组阀门更换的首要原因(45.3%)。对 41 个 proSA®和 31 个 SA®进行的生物力学分析显示,97.6%和 90.3%的病例中阀内表面有沉积物。
我们在儿科 HC 中对 proSA®和 SA®阀门进行的比较研究表明,两种阀门的存活率相似,与病因无关,但仅与植入时的年龄较小有关。编程功能可能有助于预防慢性过度引流的后遗症,但不能减少阀门更换的需求,在 2 岁以上生长中的儿童中,应考虑在特定情况下使用 proSA®阀门。