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1.
J Neurosurg ; : 1-8, 2022 Feb 18.
Article En | MEDLINE | ID: mdl-35180698

OBJECTIVE: The growth characteristics of vestibular schwannomas (VSs) under surveillance can be studied using a Bayesian method of growth risk stratification by time after surveillance onset, allowing dynamic evaluations of growth risks. There is no consensus on the optimum surveillance strategy in terms of frequency and duration, particularly for long-term growth risks. In this study, the long-term conditional probability of new VS growth was reported for patients after 5 years of demonstrated nongrowth. This allowed modeling of long-term VS growth risks, the creation of an evidence-based surveillance protocol, and the proposal of a cost-benefit analysis decision aid. METHODS: The authors performed an international multicenter retrospective analysis of prospectively collected databases from five tertiary care referral skull base units. Patients diagnosed with sporadic unilateral VS between 1990 and 2010 who had a minimum of 10 years of surveillance MRI showing VS nongrowth in the first 5 years of follow-up were included in the analysis. Conditional probabilities of growth were calculated according to Bayes' theorem, and nonlinear regression analyses allowed modeling of growth. A cost-benefit analysis was also performed. RESULTS: A total of 354 patients were included in the study. Across the surveillance period from 6 to 10 years postdiagnosis, a total of 12 tumors were seen to grow (3.4%). There was no significant difference in long-term growth risk for intracanalicular versus extracanalicular VSs (p = 0.41). At 6 years, the residual conditional probability of growth from this point onward was seen to be 2.28% (95% CI 0.70%-5.44%); at 7 years, 1.35% (95% CI 0.25%-4.10%); at 8 years, 0.80% (95% CI 0.07%-3.25%); at 9 years, 0.47% (95% CI 0.01%-2.71%); and at 10 years, 0.28% (95% CI 0.00%-2.37%). Modeling determined that the remaining lifetime risk of growth would be less than 1% at 7 years 7 months, less than 0.5% at 8 years 11 months, and less than 0.25% at 10 years 4 months. CONCLUSIONS: This multicenter study evaluates the conditional probability of VS growth in patients with long-term VS surveillance (6-10 years). On the basis of these growth risks, the authors posited a surveillance protocol with imaging at 6 months (t = 0.5), annually for 3 years (t = 1.5, 2.5, 3.5), twice at 2-year intervals (t = 5.5, 7.5), and a final scan after 3 years (t = 10.5). This can be used to better inform patients of their risk of growth at particular points along their surveillance timeline, balancing the risk of missing late growth with the costs of repeated imaging. A cost-benefit analysis decision aid was also proposed to allow units to make their own decisions regarding the cessation of surveillance.

2.
J Neurosurg ; 103(3): 439-43, 2005 Sep.
Article En | MEDLINE | ID: mdl-16235674

OBJECT: The aim of this study was to evaluate the quality of clinical studies appearing in neurosurgical journals during three decades. METHODS: Clinical studies published in 1982, 1992, and 2002 in Neurosurgery, Journal of Neurosurgery (JNS), and British Journal of Neurosurgery (BJN) were evaluated. The feature study types were categorized as follows: Type 1, prospective randomized controlled trials (PRCTs); Type 2, other prospective studies; Type 3, retrospective case-controlled and cross-sectional studies; and Type 4, case reports. Among a total of 786 articles, the following study types were identified: Type 1, eight (1%); Type 2, 46 (6%); Type 3, 81 (10%); and Type 4, 651 (83%). Overall, the proportion of study types did not differ among journals. Between 1982 and 2002, increases in the proportion of study Types 1 (0 compared with 2%, respectively), 2 (4 compared with 10%, respectively), and 3 (5 compared with 13%, respectively) and decreases in the proportion of study Type 4 (92 compared with 75%, respectively; p < 0.001) were apparent only in JNS and Neurosurgery (p < 0.01). Between 1982 and 2002, the median number of patients (two compared with 14, respectively) and the mean number of authors per study (3.4 compared with 4.8, respectively) increased (p < 0.001). The JNS had a greater mean number of authors per study than the other journals (p < 0.001). CONCLUSIONS: During the three decades evaluated, case reports remained the predominant study design in these prominent neurosurgical journals, notwithstanding the modest increases in study Types 1 and 2 and the associated escalations in author and patient numbers in the same period.


Clinical Trials as Topic/standards , Neurosurgery/standards , Publishing/standards , Case-Control Studies , Humans , Neurosurgery/trends , Publishing/trends , Quality Control , Research Design , Retrospective Studies
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