首页> 外文期刊>Pediatric Pulmonology >Beyond randomized controlled trials: a 'real life' experience of respiratory syncytial virus infection prevention in infancy with and without palivizumab.
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Beyond randomized controlled trials: a 'real life' experience of respiratory syncytial virus infection prevention in infancy with and without palivizumab.

机译:除了随机对照试验之外,在有或没有帕利珠单抗的婴儿期预防呼吸道合胞病毒感染的“现实生活”经历。

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A population-based study of the impact of palivizumab on confirmed Respiratory Syncytial Virus (RSV) hospitalizations over a 7-year period within and between two similar health regions . Clinicians in Calgary implemented palivizumab prophylaxis for high-risk infants during the last four RSV seasons; clinicians in Edmonton did not. The two cities are part of a unified health care system and similar sociodemographics. Infants <36 weeks (wk) of gestational age (GA) were identified. RSV prophylaxis data and RSV-hospitalizations for high-risk infants eligible for prophylaxis were reviewed, as well as that of moderate-risk infants (33-35 weeks GA) for whom RSV prophylaxis was not given a high priority in the recommendations published by the Canadian Paediatric Society (CPS). Prevalence of RSV hospitalization before and after palivizumab was determined (1995-1998 and 1999-2002, respectively). There were 411 high-risk infants eligible for palivizumab prior to its provision (Pre) and 496 during the prophylaxis program (Post) in Calgary. There were 401 Pre and 425 Post in Edmonton, where no such prophylaxis program was implemented. In Calgary where palivizumab was offered (Post), RSV hospitalization was significantly reduced: 7.3% Pre versus 3.0% Post (OR, 2.53, 95% CI, 1.34, 4.76). No reduction was observed in Edmonton where palivizumab was not offered: 5.0% Pre versus 7.1% Post (OR, 1.45, 95% CI, 0.81, 2.59; P = 0.212). RSV hospitalizations did not change for moderate-risk infants not receiving palivizumab in Calgary (OR, 1.26, 95% CI, 0.75, 2.12; P = 0.389). An RSV prevention program with palivizumab for high-risk infants reduced RSV hospitalizations, providing "real life" evidence of the benefits of this prophylaxis strategy. Further research is required to determine if specific sub-sets of moderate-risk infants would also benefit from an RSV prophylaxis program with palivizumab.
机译:一项基于人群的帕利珠单抗对已确认的呼吸道合胞病毒(RSV)住院治疗的影响(在两个相似的健康区域之内和之间),历时7年。在过去的四个RSV季节中,卡尔加里的临床医生对高危婴儿实施了帕利珠单抗预防;埃德蒙顿的临床医生没有。这两个城市是统一医疗体系和类似社会人口统计学的一部分。确定婴儿的孕周(GA)<36周(wk)。审查了符合条件的高危婴儿的RSV预防数据和RSV住院治疗,以及由RSV公布的建议中未将RSV预防作为高优先级的中危婴儿(GA 33-35周)加拿大儿科协会(CPS)。确定了帕利珠单抗之前和之后的RSV住院率(分别为1995-1998和1999-2002)。在卡尔加里,有411名高风险婴儿在接受帕利珠单抗治疗前(服药前)和496位在预防计划(后)服药期间入药。埃德蒙顿有401个Pre和425个Post,没有实施这种预防程序。在提供帕利珠单抗(Post)的卡尔加里(Calgary),RSV的住院率显着降低:Pre分别为7.3%和Post的3.0%(OR,2.53、95%CI,1.34、4.76)。在未提供帕利珠单抗的埃德蒙顿中未观察到减少:前者为5.0%,后者为7.1%(OR,1.45、95%CI,0.81、2.59; P = 0.212)。没有在卡尔加里接受帕利珠单抗的中度危险婴儿的RSV住院治疗没有改变(OR,1.26,95%CI,0.75,2.12; P = 0.389)。帕利珠单抗为高危婴儿制定的RSV预防计划减少了RSV的住院治疗,为这种预防策略的益处提供了“现实生活”证据。需要进一步的研究来确定中危婴儿的特定亚型是否也将从帕利珠单抗的RSV预防计划中受益。

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