Live vaccines following intravenous immunoglobulin for Kawasaki disease: Are we vaccinating appropriately?

被引:0
|
作者
Cardenas-Brown, Cassandra [1 ,10 ]
Lucas, Ryan D. [2 ,4 ]
Buttery, Jim [7 ,8 ,9 ]
Britton, Philip N. [3 ,4 ,5 ]
Wood, Nicholas [2 ,4 ,5 ]
Singh-Grewal, Davinder [1 ,4 ,6 ]
Burgner, David [7 ,8 ]
机构
[1] Sydney Childrens Hosp Network Randwick & Westmead, Dept Rheumatol, Sydney, NSW, Australia
[2] Sydney Childrens Hosp Network Randwick & Westmead, Dept Gen Med, Sydney, NSW, Australia
[3] Sydney Childrens Hosp Network Randwick & Westmead, Dept Infect Dis, Sydney, NSW, Australia
[4] Univ Sydney, Fac Med & Hlth, Discipline Child & Adolescent Hlth, Sydney, NSW, Australia
[5] Natl Ctr Immunisat Res & Surveillance, Sydney, NSW, Australia
[6] Univ New South Wales, Fac Med, Sch Womens & Childrens Hlth, Sydney, NSW, Australia
[7] Murdoch Childrens Res Inst, Infect & Immun Theme, Melbourne, Vic, Australia
[8] Univ Melbourne, Melbourne Med Sch, Dept Paediat, Melbourne, Vic, Australia
[9] Melbourne Childrens Campus, Ctr Hlth Analyt, Melbourne, Vic, Australia
[10] Childrens Hosp Westmead, Hawksbury Rd & Hainsworth St, Westmead, NSW 2145, Australia
关键词
immunisation; intravenous immunoglobulin; Kawasaki disease; IMMUNE GLOBULIN; MEASLES; DIAGNOSIS;
D O I
10.1111/jpc.16484
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Aim Australian and New Zealand guidelines recommend that live vaccines be postponed for 11 months after treatment of Kawasaki disease (KD) with intravenous immunoglobulin (IVIG). We aimed to describe patterns of live-vaccine administration after KD treatment, focusing on the measles-mumps-rubella/measles-mumps-rubella-varicella (MMR/MMRV) vaccines, and to compare real-world practice with current recommendations.Methods We combined data from inpatient Electronic Health Records and the Australian Immunisation Register for all children who received IVIG for the treatment of KD under the age of 5 years at two Australian tertiary children's hospitals over a 12-year period. Children who received IVIG <11 months before a scheduled MMR/MMRV were deemed 'at risk' of breaching the guidelines, and those whose subsequent vaccination occurred <11 months after the IVIG were deemed to have 'breached' the guidelines.Results Of those at risk, three-quarters (76%) breached the guidelines for their first MMR/MMRV. Findings were similar (50%-80%) for the second MMR/MMRV dose.Conclusions The majority of Australian children treated for KD with IVIG may not be optimally protected by MMRV vaccination. Immunisation systems should address this avoidable risk.
引用
收藏
页码:1217 / 1222
页数:6
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