Goldstein Mitchell, Fergie Jaime, Krilov Leonard R
Department of Pediatrics, Loma Linda University Children's Hospital, Loma Linda, CA, USA.
Department of Infectious Diseases, Driscoll Children's Hospital, Corpus Christi, TX, USA.
Infect Dis Ther. 2021 Mar;10(Suppl 1):17-26. doi: 10.1007/s40121-020-00388-1. Epub 2021 Mar 3.
Despite being a leading cause of hospitalization due to lower respiratory tract infections, the treatment of respiratory syncytial virus (RSV) infection is primarily supportive. Palivizumab is the only licensed immunoprophylaxis (IP) available for preventing severe RSV infection in high-risk populations including ≤ 35 weeks' gestational age (wGA) infants and children with chronic lung disease of prematurity or congenital heart disease. The American Academy of Pediatrics (AAP) has published its IP recommendations since the approval of palivizumab. In 2014, the AAP stopped recommending RSV IP in 29-34 wGA infants without comorbidities and stated that RSV hospitalization (RSVH) risk in otherwise healthy ≥ 29 wGA infants and term infants was similar. Since then, experts in the field have debated the appropriateness of the 2014 policy change, and several real-world evidence studies at the national and regional levels in the US have examined the impact of the AAP policy on 29-34 wGA infants. Overall, these studies showed a significant decline in RSV IP use and a concurrent increase in RSVH risk among 29-34 wGA infants relative to term infants in the seasons after the 2014 policy change. A similar decrease in IP use and increase in RSVH risk was also observed among < 29 wGA infants relative to term infants after the 2014 policy change. This decrease could be an unintended consequence as < 29 wGA infants are an in-policy population recommended to receive RSV IP. According to the National Perinatal Association, strong evidence exists to support the use of RSV IP in all ≤ 32 wGA and 32-35 wGA infants with risk factors such as attending day care, having ≥ 1 school-aged siblings, twin or greater multiple gestation, younger age, and exposure to parental smoking. Until new preventive and treatment options become available, palivizumab can help prevent and mitigate RSV disease burden among high-risk preterm infants.
尽管呼吸道合胞病毒(RSV)感染是导致下呼吸道感染住院的主要原因,但对其治疗主要是支持性的。帕利珠单抗是唯一可用于预防高危人群(包括胎龄≤35周的婴儿以及患有早产儿慢性肺病或先天性心脏病的儿童)发生严重RSV感染的获批免疫预防药物。自帕利珠单抗获批以来,美国儿科学会(AAP)已发布其免疫预防建议。2014年,AAP不再建议对无合并症的29 - 34周胎龄婴儿进行RSV免疫预防,并指出在其他方面健康的≥29周胎龄婴儿和足月儿中,RSV住院(RSVH)风险相似。从那时起,该领域的专家一直在争论2014年政策变化的合理性,美国国内和地区层面的多项真实世界证据研究考察了AAP政策对29 - 34周胎龄婴儿的影响。总体而言,这些研究表明,在2014年政策变化后的季节中,相对于足月儿,29 - 34周胎龄婴儿的RSV免疫预防药物使用显著下降,同时RSVH风险上升。在2014年政策变化后,相对于足月儿,<29周胎龄婴儿中也观察到免疫预防药物使用类似的减少和RSVH风险的增加。这种减少可能是一个意外后果,因为<29周胎龄婴儿是建议接受RSV免疫预防的符合政策人群。根据全国围产期协会的说法,有强有力的证据支持对所有≤32周胎龄以及有诸如上日托、有≥1名学龄兄弟姐妹、双胎或多胎妊娠、年龄较小以及接触父母吸烟等风险因素的32 - 35周胎龄婴儿使用RSV免疫预防药物。在新的预防和治疗选择出现之前,帕利珠单抗有助于预防和减轻高危早产儿的RSV疾病负担。