Long-term hearing and neurodevelopmental outcomes following Kawasaki disease: A population-based cohort study

被引:10
作者
Robinson, Cal [1 ,2 ]
Lao, Francis [3 ]
Chanchlani, Rahul [4 ,5 ,6 ]
Gayowsky, Anastasia [6 ]
Darling, Elizabeth [7 ]
Batthish, Michelle [8 ]
机构
[1] McMaster Univ, Dept Pediat, Hamilton, ON, Canada
[2] Hosp Sick Children, Dept Paediat, Div Nephrol, Toronto, ON, Canada
[3] McMaster Univ, Michael G DeGroote Sch Med, Hamilton, ON, Canada
[4] McMaster Univ, Dept Pediat, Div Nephrol, Hamilton, ON, Canada
[5] McMaster Univ, Dept Hlth Res Methods Evidence & Impact, Hamilton, ON, Canada
[6] ICES McMaster, Hamilton, ON, Canada
[7] McMaster Univ, McMaster Midwifery Res Ctr, Hamilton, ON, Canada
[8] McMaster Univ, Dept Pediat, Div Rheumatol, Hamilton, ON, Canada
关键词
Kawasaki disease; Children; Hearing loss; Development; Attention-deficit hyperactivity disorder; CHILDREN; HEALTH; EPIDEMIOLOGY; SURVEILLANCE; PREVALENCE; DISORDERS; STATEMENT; CANADA;
D O I
10.1016/j.braindev.2021.03.001
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Kawasaki disease (KD) incidence is increasing in Ontario. Cardiovascular sequelae following KD are well-described. However, there are limited data on non-cardiovascular outcomes. Objectives: To determine the risk of hearing loss, anxiety, developmental disorders, intellectual disabilities and attention-deficit/hyperactivity disorder (ADHD) among KD survivors vs. non-exposed children. Methods: We included all Ontario children (<= 18 yr) surviving hospitalization with a KD diagnosis between 1995 and 2018, using population-based health administrative databases. We excluded children with prior KD diagnoses and non-residents. KD cases were matched with 100 non-exposed children by age, sex and year. Follow-up continued until death or March 2019. We calculated the prevalence, incidence and adjusted hazard ratios (aHR [95%CI]) of outcomes between 0-1 yr, 1-5 yr, 5-10 yr and >10 yr follow-up. Results: Among 4597 KD survivors, 364 (7.9%) were diagnosed with hearing loss, 1213 (26.4%) anxiety disorders, 398 (8.7%) developmental disorders, 51 (1.1%) intellectual disability and 21 (0.5%) ADHD, during median 11 year follow-up. Compared to 459,700 non-exposed children, KD survivors were not at increased risk of hearing loss after adjustment for potential confounders. KD survivors were at increased risk of anxiety disorders between 0-1 yr (aHR 1.75 [1.46-2.10]), 1-5 yr (aHR 1.13 [1.01-1.28]), 510 yr (aHR 1.14 [1.03-1.28]) and >10 yr (aHR 1.11 [1.02-1.22]); developmental disorders between 0-1 yr (aHR 1.49 [1.28-1.74]) and 1-5 yr (aHR 1.19 [1.02-1.40]); intellectual disabilities >10 yr (aHR 2.36 [1.36-4.10]); and ADHD >10 yr (aHR 2.01 [1.14-3.57]). Conclusions: KD survivors are at increased risk of being diagnosed with anxiety disorders sooner, being diagnosed with developmental disorders between 0 and 5 yr and being diagnosed with intellectual disabilities or ADHD >10 yr after KD diagnosis. This may justify enhanced developmental and audiological surveillance of KD survivors. (C) 2021 The Japanese Society of Child Neurology. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:735 / 744
页数:10
相关论文
共 34 条
[1]  
AMANO S, 1980, ACTA PATHOL JAPON, V30, P365
[2]  
[Anonymous], 2015, DEV DISABILITIES CAN
[3]   Physical and psychosocial health in children who have had Kawasaki disease [J].
Baker, AL ;
Gauvreau, K ;
Newburger, JW ;
Sundel, RP ;
Fulton, DR ;
Jenkins, KJ .
PEDIATRICS, 2003, 111 (03) :579-583
[4]   The epidemiology and global burden of autism spectrum disorders [J].
Baxter, A. J. ;
Brugha, T. S. ;
Erskine, H. E. ;
Scheurer, R. W. ;
Vos, T. ;
Scott, J. G. .
PSYCHOLOGICAL MEDICINE, 2015, 45 (03) :601-613
[5]   The REporting of studies Conducted using Observational Routinely-collected health Data (RECORD) Statement [J].
Benchimol, Eric I. ;
Smeeth, Liam ;
Guttmann, Astrid ;
Harron, Katie ;
Moher, David ;
Petersen, Irene ;
Sorensen, Henrik T. ;
von Elm, Erik ;
Langan, Sinead M. .
PLOS MEDICINE, 2015, 12 (10)
[6]   Passive surveillance for Kawasaki disease in San Diego county [J].
Bronstein, DE ;
Besser, RE ;
Burns, JC .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 1997, 16 (11) :1015-1018
[7]   Behaviour sequelae following acute Kawasaki disease [J].
Carlton-Conway D. ;
Ahluwalia R. ;
Henry L. ;
Michie C. ;
Wood L. ;
Tulloh R. .
BMC Pediatrics, 5 (1)
[8]  
CIHI, NAT AMB CAR REP SYST
[9]   Dissecting Kawasaki disease: a state-of-the-art review [J].
Dietz, S. M. ;
van Stijn, D. ;
Burgner, D. ;
Levin, M. ;
Kuipers, I. M. ;
Hutten, B. A. ;
Kuijpers, T. W. .
EUROPEAN JOURNAL OF PEDIATRICS, 2017, 176 (08) :995-1009
[10]   Psychiatric Adverse Effects of Pediatric Corticosteroid Use [J].
Drozdowicz, Linda B. ;
Bostwick, J. Michael .
MAYO CLINIC PROCEEDINGS, 2014, 89 (06) :817-834