Use of Rituximab and Risk of Re-hospitalization for Children with Neuromyelitis Optica Spectrum Disorder.

Sabrina Gmuca, Rui Xiao, Pamela F Weiss, Amy T Waldman, Jeffrey S Gerber
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引用次数: 3

Abstract

Background: Treatment algorithms for neuromyelitis optica spectrum disorder (NMOSD) vary, and sparse data exist regarding the impact of initial treatments on disease course. We aimed to determine whether administration of rituximab during first hospitalization reduces 1-year readmission rates.

Methods: We conducted a retrospective cohort study of subjects with NMOSD using the Pediatric Health Information System database from 2005-2015. Subjects were ages 1 to 21 years who received glucocorticoids and an ICD-9-CM code indicating neuromyelitis optica (NMO) during first hospitalization. All subjects had at least 12 months of continuous enrollment. The primary exposure was ≥1 rituximab dose during first hospitalization. We tested for the association of rituximab use with all-cause re-hospitalization, the primary outcome, using survival analysis. Re-hospitalization was considered if a hospital admission occurred > 30 days after initial discharge with exclusion of admissions with re-dosing of rituximab and data were censored at 12 months. Secondary outcomes included time to and median duration of re-hospitalization using 25th percentiles of survival time and the Wilcoxon-rank sum test, respectively.

Results: Of 180 subjects who met inclusion criteria, 71.7% were female and the median age was 13 years (IQR: 10, 15). 52 subjects (28.9%) received rituximab during first hospitalization, and there was an increasing trend in rituximab use over time (p<0.01). Overall, 36.7% of children were readmitted and time to readmission was a median of 365 days (IQR: 138, 365). Rituximab exposure was not associated with re-hospitalization (adjusted HR: 0.71: 95% CI: 0.38, 1.34) nor a reduced time to re-hospitalization. Median duration of re-hospitalization was 2 days shorter in the rituximab exposed group (p=0.02). Receipt of physical therapy, a surrogate marker for neurologic impairment, during first hospitalization was associated with re-admission within 12 months (adjusted HR: 4.81; 95% CI: 1.14, 20.29).

Conclusions: Among children with NMOSD, first-line administration of rituximab was not associated with risk of or time to re-hospitalization. Rituximab use was found to be associated with a shorter duration of re-hospitalization. Need for physical therapy during first hospitalization was independently associated with an increased risk of re-admission.

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使用利妥昔单抗与儿童视谱障碍神经脊髓炎再次住院的风险
背景:神经脊髓炎视谱障碍(NMOSD)的治疗方法各不相同,关于初始治疗对病程影响的数据很少。我们的目的是确定首次住院时使用利妥昔单抗是否能降低1年的再入院率。方法:我们利用2005-2015年儿科健康信息系统数据库对NMOSD患者进行回顾性队列研究。受试者年龄在1至21岁之间,首次住院期间接受糖皮质激素治疗,并接受ICD-9-CM编码,提示视神经脊髓炎(NMO)。所有受试者至少连续入组12个月。首次住院时的主要暴露剂量为≥1利妥昔单抗剂量。我们使用生存分析测试了使用利妥昔单抗与全因再住院(主要结局)的关联。如果首次出院后> 30天入院,则考虑再次住院,排除再次给药利妥昔单抗的入院,并在12个月时审查数据。次要结局包括再住院时间和中位住院时间,分别采用生存时间的第25百分位和wilcoxon秩和检验。结果:符合纳入标准的180例受试者中,71.7%为女性,中位年龄为13岁(IQR: 10,15)。52例(28.9%)患者在首次住院时接受了利妥昔单抗治疗,并且随着时间的推移,利妥昔单抗的使用呈增加趋势(结论:在NMOSD患儿中,一线给予利妥昔单抗与再次住院的风险和时间无关。发现使用利妥昔单抗与较短的再住院时间相关。首次住院期间需要物理治疗与再入院风险增加独立相关。
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