Lang D A, Neil-Dwyer G, Garfield J
Department of Neurosurgery, Wessex Neurological Centre, Southampton University Hospitals, United Kingdom.
J Neurosurg. 1999 Sep;91(3):359-63. doi: 10.3171/jns.1999.91.3.0359.
The goals of this study were twofold: 1) to determine outcome, including quality of life, in patients who have undergone surgery for petroclival meningioma in which a standard skull base approach was used; and 2) to assess the impact of the patients' surgical treatment on their caregivers.
Seventeen patients (13 women and four men ranging in age from 29 to 63 years) who underwent a transpetrosal approach for a petroclival meningioma during a 5-year period were prospectively included in this study. Pre- and postoperative data including adverse events were noted. The patients were assessed at 3, 6, and 12 months postoperatively, and annually thereafter, and they completed a postoperative SF-36 questionnaire. In addition, each patient's caregiver was interviewed to determine the effect of the patient's illness on the caregiver's life and responsibilities. Twenty-two operations were performed. A new permanent neurological deficit developed in five patients and in eight a temporary deficit or exacerbation of existing deficits occurred. Two patients underwent surgery to create a facial-hypoglossal nerve communication; five required a temporary percutaneous gastrostomy and/or tracheostomy; three required a shunt; and one underwent successful squint surgery. At 1 year postoperatively 13 patients had made a good or moderate recovery, three were severely disabled, and one had died--outcomes in keeping with other studies. By contrast, responses to the SF-36 questionnaire showed that, in all eight of its categories, between 43% and 75% of surviving patients were functioning below accepted norms. Fifty-six percent of caregivers experienced a major change in lifestyle and 38% experienced a major change with respect to their work.
After transpetrosal excision of a petroclival meningioma, the quality of life for the patient is worse than that indicated in surgeons' reported results. The impact on the patient's caregiver is profound-a burden perhaps not fully appreciated by the surgeon.
本研究有两个目标:1)确定采用标准颅底入路手术治疗岩斜区脑膜瘤患者的预后,包括生活质量;2)评估患者手术治疗对其照料者的影响。
前瞻性纳入17例在5年期间接受经岩骨入路治疗岩斜区脑膜瘤的患者(13例女性和4例男性,年龄29至63岁)。记录术前和术后数据,包括不良事件。患者在术后3、6和12个月以及此后每年接受评估,并完成术后SF-36问卷。此外,对每位患者的照料者进行访谈,以确定患者疾病对照料者生活和责任的影响。共进行了22次手术。5例患者出现了新的永久性神经功能缺损,8例出现了暂时性缺损或现有缺损加重。2例患者接受了面神经舌下神经吻合手术;5例需要临时经皮胃造口术和/或气管切开术;3例需要分流术;1例斜视手术成功。术后1年,13例患者恢复良好或中等,3例严重残疾,1例死亡——结果与其他研究一致。相比之下,SF-36问卷的回复显示,在所有八个类别中,43%至75%的存活患者功能低于公认标准。56%的照料者生活方式发生了重大变化;38%的照料者工作方面发生了重大变化。
经岩骨切除岩斜区脑膜瘤后,患者的生活质量比外科医生报告的结果所示的要差。对患者照料者的影响深远——这一负担可能未被外科医生充分认识到。