Department of Pharmaceutical Outcomes and Policy, College of Pharmacy, University of Florida, Gainesville, Florida 32610-0494, USA.
Pediatr Pulmonol. 2013 Sep;48(9):874-84. doi: 10.1002/ppul.22711. Epub 2012 Nov 8.
Evidence on the effectiveness of respiratory syncytial virus (RSV) immunoprophylaxis with palivizumab in children with cystic fibrosis (CF) is lacking.
We utilized Medicaid Extract files from 27 states from 1999 to 2006 linked to the National Cystic Fibrosis Registry to establish a cohort of children 0-2 years with CF diagnosis. Eligible children entered the cohort after CF diagnosis and after RSV season onset, and were followed until season end, second birthday, death, or hospitalizations for reasons other then the study outcome. Two outcomes were examined: hospitalization for RSV infections (RSV-ha), or hospitalization for acute respiratory infections (ARI-ha). Palivizumab exposure was defined based on pharmacy or procedure claims as current (claim date plus 30 days), former (day 31-60 after a claim), and no exposure (days before the first or >60 days after any claim). Both outcomes were examined in a Cox regression model, adjusting for RSV risk factors and CF severity via exposure propensity score.
The matched cohort included 1,974 infants (2,875 infant seasons), who experienced 32 RSV-ha and 212 ARI-ha (3.9 and 26.2/1,000 season months, respectively). Compared to periods of no use, the adjusted hazard ratio for current use was 0.57 (95% confidence interval [CI]: 0.20-1.60) for RSV-related hospitalization and 0.85 (95% CI: 0.59-1.21) for ARI-related hospitalization. Each month of increasing age reduced the ARI-ha by 5.8%.
RSV hospitalization incidence was low suggesting either little contribution of the virus to respiratory infections in patients with CF or lack of RSV testing. Unadjusted and adjusted RSV-hospitalization incidence rates suggested potentially positive effects of palivizumab, but results were inconclusive due to small event rates. Hospitalizations for acute respiratory illness with possible RSV contribution showed no association with palivizumab use, suggesting limited overall effect of palivizumab. Younger age greatly increased infection risk.
缺乏关于帕利珠单抗预防呼吸道合胞病毒(RSV)在囊性纤维化(CF)儿童中的有效性的证据。
我们利用了 1999 年至 2006 年来自 27 个州的医疗补助提取文件,这些文件与国家囊性纤维化登记处相关联,以建立一个 0-2 岁 CF 诊断儿童的队列。符合条件的儿童在 CF 诊断后和 RSV 季节开始后进入队列,并随访至季节结束、两岁生日、死亡或因研究结果以外的其他原因住院。我们检查了两个结果:因 RSV 感染而住院(RSV-ha),或因急性呼吸道感染而住院(ARI-ha)。帕利珠单抗的暴露情况是根据药房或程序索赔来定义的,分别为当前(索赔日期加 30 天)、前(索赔后第 31-60 天)和无暴露(首次索赔前或任何索赔后>60 天)。我们在 Cox 回归模型中检查了这两个结果,通过暴露倾向评分调整了 RSV 危险因素和 CF 严重程度。
匹配的队列包括 1974 名婴儿(2875 个婴儿季节),他们经历了 32 次 RSV-ha 和 212 次 ARI-ha(分别为每 1000 个季节月 3.9 和 26.2/1000 个季节月)。与无使用期相比,当前使用的调整后的危险比分别为 0.57(95%置信区间[CI]:0.20-1.60)和 0.85(95%CI:0.59-1.21),用于 RSV 相关住院和 ARI 相关住院。年龄每增加一个月,ARI-ha 减少 5.8%。
RSV 住院发生率较低,这表明病毒对 CF 患者的呼吸道感染贡献较小,或者缺乏 RSV 检测。未调整和调整后的 RSV 住院发生率表明帕利珠单抗可能具有积极作用,但由于事件发生率较低,结果不确定。急性呼吸道疾病伴可能 RSV 贡献的住院与帕利珠单抗使用无关,表明帕利珠单抗的总体效果有限。年龄较小大大增加了感染风险。