Claydon Jennifer, Popescu Constantin R, Shaiba Lana, Christopherson Cheryl, Human Derek, Taylor Richard, Solimano Alfonso, Lavoie Pascal M
Children's & Women's Health Centre of British Columbia (Claydon, Popescu, Christopherson, Human, Solimano, Lavoie); Divisions of Neonatology (Popescu, Shaiba, Solimano, Lavoie) and Cardiology (Human), Department of Pediatrics, University of British Columbia; British Columbia Children's Hospital Research Institute (Popescu, Human, Lavoie), Vancouver, BC; Victoria General Hospital (Taylor), Victoria, BC; University of Toronto (Shaiba), Toronto, Ont.
CMAJ Open. 2019 Feb 18;7(1):E88-E93. doi: 10.9778/cmajo.20180167. Print 2019 Jan-Mar.
It has been hypothesized that 4 doses of palivizumab, a neutralizing monoclonal antibody against respiratory syncytial virus (RSV), administered during a fixed-date RSV season may reduce hospital admissions comparably to the standard 5-dose schedule. We report outcomes in children with congenital heart disease approved to receive this 4-dose palivizumab schedule in British Columbia.
We performed a population-based descriptive cohort analysis of all 406 approved palivizumab courses over 4 seasons (2012/13 to 2015/16) in 325 children with hemodynamically significant congenital heart disease enrolled in the British Columbia RSV Immunoprophylaxis Program. The primary outcome was in-season hospital admission for potential RSV-related lower respiratory tract infection (LRTI). Secondary outcomes include timing of admission in relation to dosing. Analysis was by intention-to-treat.
Of the 406 approved palivizumab courses, 391 were administered. In 33 cases (8.4%), an additional dose was given immediately after cardiac bypass surgery. There were 17 RSV-confirmed hospital admissions (median age of children 5.9 mo [interquartile range 4-10 mo]) and 8 admissions in which the child was not tested for RSV, for a maximum of 25 potential RSV-related admissions (6.2 per 100 approvals [95% confidence interval 4.0-9.0]). Twenty-four (96%) of the 25 admissions occurred within the 4-dose palivizumab dosing period, and the remaining admission occurred 52 days after the fourth dose. Sixty-four (72%) of 89 admissions were RSV-negative; the baseline clinical characteristics of these children were not different from those of children with RSV-confirmed admissions.
In infants with hemodynamically significant congenital heart disease, a 4-dose fixed-date palivizumab schedule over a 6-month season provided seasonal protection comparable to that in a clinical trial involving a standard 5-dose schedule. Because RSV was responsible for only 19% of admissions for LRTI in our cohort, it is critical to continue to emphasize other preventive measures, including family education toward proper hand hygiene, breast-feeding and limiting infectious exposures in children at high risk.
有假设认为,在固定日期的呼吸道合胞病毒(RSV)流行季给予4剂帕利珠单抗(一种抗RSV的中和单克隆抗体),与标准的5剂给药方案相比,可能会同等程度地减少住院率。我们报告了在不列颠哥伦比亚省被批准接受这种4剂帕利珠单抗给药方案的先天性心脏病患儿的治疗结果。
我们对参加不列颠哥伦比亚省RSV免疫预防项目的325例有血流动力学意义的先天性心脏病患儿在4个季节(2012/13至2015/16)内的所有406个被批准的帕利珠单抗疗程进行了基于人群的描述性队列分析。主要结局是因潜在的RSV相关下呼吸道感染(LRTI)导致的流行季住院。次要结局包括与给药相关的住院时间。分析采用意向性治疗。
在406个被批准的帕利珠单抗疗程中,391个进行了给药。在33例(8.4%)中,在心脏搭桥手术后立即给予了额外一剂。有17例确诊为RSV的住院病例(患儿中位年龄5.9个月[四分位间距4 - 10个月]),8例未对患儿进行RSV检测的住院病例,最多有25例潜在的RSV相关住院病例(每100次批准中有6.2例[95%置信区间4.0 - 9.0])。25例住院病例中有24例(96%)发生在4剂帕利珠单抗给药期内,其余1例住院发生在第四剂给药后52天。89例住院病例中有64例(72%)RSV检测呈阴性;这些患儿的基线临床特征与确诊为RSV的住院患儿无差异。
在有血流动力学意义的先天性心脏病婴儿中,在6个月的流行季采用4剂固定日期的帕利珠单抗给药方案提供的季节性保护与涉及标准5剂给药方案的临床试验相当。由于在我们的队列中RSV仅导致19%的LRTI住院病例,继续强调其他预防措施至关重要,包括对高危儿童进行适当手部卫生、母乳喂养和限制感染暴露的家庭教育。