Kutscher Anja, Nestler Ulf, Bernhard Matthias K, Merkenschlager Andreas, Thome Ulrich, Kiess Wieland, Schob Stefan, Meixensberger Juergen, Preuss Matthias
Department of Neurosurgery.
Division of Neuropediatrics.
J Neurosurg Pediatr. 2015 Dec;16(6):621-5. doi: 10.3171/2015.4.PEDS15106. Epub 2015 Sep 4.
Congenital hydrocephalus has a major impact on the lives of patients and their relatives, as well as their long-term neurological development and social integration. The aim of this study was to assess the self-reported health-related quality of life (HRQOL) of patients after reaching adulthood.
A total of 31 patients who required CSF shunt treatment for congenital hydrocephalus within the 1st year of life (between 1963 and 1987) agreed to undergo a structured SF-36 self-assessment. An age-matched German standard cohort was used as control. Additional parameters of surgical, social, and global neurological outcome were analyzed. The mean patient age was 35 years (range 26-51 years, 13 females and 18 males). Hydrocephalus etiologies were posthemorrhagic hydrocephalus (n = 9), postinfectious hydrocephalus (n = 5), aqueductal stenosis (n = 10), myelomeningocele (n = 2), and unknown cause (n = 5).
The mean modified Rankin Scale score was 1.6 (range 0-4). Hydrocephalic patients achieved lower scores for the SF-36 items physical functioning (70.5 vs. 93.5, p < 0.05), physical role functioning (74.2 vs. 88.3, p < 0.05), and general health perceptions (64.5 vs. 72.3, p < 0.05). Emotional, social role functioning, and mental health items did not differ between the groups. Assessment of vitality and pain resulted in a trend to worse values. Whereas the Physical Component Summary score was lower (46.1 vs. 54.3, p < 0.05), the Mental Component Summary score was not significantly different (50.2 vs. 48.7, p = 0.3). There was neither a statistically significant difference between subgroups of different etiologies nor an association with the number of subsequent hydrocephalus-related surgeries.
Adult HRQOL for patients with congenital hydrocephalus appears to be similar to that for healthy con with regard to mental health and social functioning aspects. Physical impairment is a predominant factor of compro quality of life.
先天性脑积水对患者及其亲属的生活、长期神经发育和社会融入都有重大影响。本研究的目的是评估成年后患者自我报告的健康相关生活质量(HRQOL)。
共有31例在1岁以内(1963年至1987年)因先天性脑积水需要脑脊液分流治疗的患者同意接受结构化的SF - 36自我评估。以年龄匹配的德国标准队列作为对照。分析了手术、社会和整体神经学结果的其他参数。患者平均年龄为35岁(范围26 - 51岁,女性13例,男性18例)。脑积水病因包括出血后脑积水(n = 9)、感染后脑积水(n = 5)、导水管狭窄(n = 10)、脊髓脊膜膨出(n = 2)和病因不明(n = 5)。
改良Rankin量表平均评分为1.6(范围0 - 4)。脑积水患者在SF - 36项目中的身体功能(70.5对93.5,p < 0.05)、身体角色功能(74.2对88.3,p < 0.05)和总体健康感知(64.5对72.3,p < 0.05)得分较低。两组在情感、社会角色功能和心理健康项目上无差异。活力和疼痛评估结果显示有变差的趋势。身体成分总结得分较低(46.1对54.3,p < 0.05),而心理成分总结得分无显著差异(50.2对48.7,p = 0.3)。不同病因亚组之间既无统计学显著差异,也与随后与脑积水相关的手术次数无关。
先天性脑积水患者成年后的健康相关生活质量在心理健康和社会功能方面似乎与健康对照者相似。身体损伤是生活质量下降的主要因素。