Epidemiological and clinical characteristics of severe hand-foot-and-mouth disease (HFMD) among children: a 6-year population-based study.
Adolescent
Animals
Child
Child, Preschool
China
/ epidemiology
Cough
/ epidemiology
Enterovirus Infections
/ epidemiology
Female
Foot-and-Mouth Disease
/ epidemiology
Hand, Foot and Mouth Disease
/ epidemiology
Humans
Incidence
Infant
Male
Research Design
Respiratory Sounds
Risk Factors
Seasons
Vomiting
/ epidemiology
Children
Epidemiological characteristics
Hand-foot-and-mouth disease (HFMD)
Risk factors
Journal
BMC public health
ISSN: 1471-2458
Titre abrégé: BMC Public Health
Pays: England
ID NLM: 100968562
Informations de publication
Date de publication:
27 May 2020
27 May 2020
Historique:
received:
11
03
2020
accepted:
19
05
2020
entrez:
29
5
2020
pubmed:
29
5
2020
medline:
28
10
2020
Statut:
epublish
Résumé
Hand-foot-and-mouth disease (HFMD) is considered to be self-limited, however, severe HFMD is a deadly threat for children worldwide, therefore, it is essential to define the clinical and epidemiologic characteristics of children with severe HFMD and identify the risk factors of death. Between 2013 and 2018, children who diagnosed with severe HFMD from Chongqing, China were enrolled in this population-based study. A total of 459 severe HFMD children cases were identified during the study period, including 415 survivors and 44 fatal cases. Demographic, geographical, epidemiological and clinical data of the cases were acquired and analyzed. Risk factors of the death because of severe HFMD children included female, aged 1 ~ 3 years, enterovirus 71 infection, falling ill in winter, more than one children in home, being taken care of by grandparents, the caregivers' education not more than 9 years, having fever more than 3 days, consciousness disorders, general weakness, vomiting, general weakness, abnormal pupillary light reflex, repeated cough, tachypnea, moist rales, white frothy sputum, pink frothy sputum, and cyanosis on lips or the whole body, tachycardia, arrhythmia, cold limbs, pale complexion, weakened pulse. (all p < 0.05). Spatial-temporal analysis detected high-value clusters, the most likely cluster located at rural countries in the northern parts of Chongqing, from January, 2015 to July, 2017. (p < 0.01). Besides, some urban districts were also found high incidence of severe HFMD cases according to the incidence maps. The detection of clinical risk factors and the temporal, spatial and socio-demographic distribution epidemiological characteristics of severe HFMD contribute to the timely diagnosis and intervention, the results of this study can be the reference of further clinical and public health practice.
Sections du résumé
BACKGROUND
BACKGROUND
Hand-foot-and-mouth disease (HFMD) is considered to be self-limited, however, severe HFMD is a deadly threat for children worldwide, therefore, it is essential to define the clinical and epidemiologic characteristics of children with severe HFMD and identify the risk factors of death.
METHODS
METHODS
Between 2013 and 2018, children who diagnosed with severe HFMD from Chongqing, China were enrolled in this population-based study. A total of 459 severe HFMD children cases were identified during the study period, including 415 survivors and 44 fatal cases. Demographic, geographical, epidemiological and clinical data of the cases were acquired and analyzed.
RESULTS
RESULTS
Risk factors of the death because of severe HFMD children included female, aged 1 ~ 3 years, enterovirus 71 infection, falling ill in winter, more than one children in home, being taken care of by grandparents, the caregivers' education not more than 9 years, having fever more than 3 days, consciousness disorders, general weakness, vomiting, general weakness, abnormal pupillary light reflex, repeated cough, tachypnea, moist rales, white frothy sputum, pink frothy sputum, and cyanosis on lips or the whole body, tachycardia, arrhythmia, cold limbs, pale complexion, weakened pulse. (all p < 0.05). Spatial-temporal analysis detected high-value clusters, the most likely cluster located at rural countries in the northern parts of Chongqing, from January, 2015 to July, 2017. (p < 0.01). Besides, some urban districts were also found high incidence of severe HFMD cases according to the incidence maps.
CONCLUSIONS
CONCLUSIONS
The detection of clinical risk factors and the temporal, spatial and socio-demographic distribution epidemiological characteristics of severe HFMD contribute to the timely diagnosis and intervention, the results of this study can be the reference of further clinical and public health practice.
Identifiants
pubmed: 32460823
doi: 10.1186/s12889-020-08961-6
pii: 10.1186/s12889-020-08961-6
pmc: PMC7254654
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
801Subventions
Organisme : Chongqing Yuzhong District Science and Technology Bureau
ID : 20190116
Références
Zhonghua Liu Xing Bing Xue Za Zhi. 2014 Mar;35(3):271-5
pubmed: 24831625
J Epidemiol. 2019 Sep 5;29(9):354-362
pubmed: 30416163
J Epidemiol Community Health. 2014 Jun;68(6):500-2
pubmed: 24652348
J Virol. 2009 Jul;83(13):6477-83
pubmed: 19386699
Emerg Infect Dis. 2003 Jan;9(1):78-85
pubmed: 12533285
Indian Pediatr. 2018 Feb 15;55(2):137-139
pubmed: 29242411
Clin Microbiol Infect. 2012 May;18(5):E110-8
pubmed: 22404077
Sci Rep. 2017 Aug 21;7(1):8900
pubmed: 28827733
Arch Dis Child. 2004 Apr;89(4):368-73
pubmed: 15033850
Nat Med. 2009 Jul;15(7):728-9
pubmed: 19584857
Mod Pathol. 2000 Nov;13(11):1200-5
pubmed: 11106077
J Virol Methods. 2016 May;231:44-7
pubmed: 26912234
Epidemiol Infect. 2014 Apr;142(4):776-88
pubmed: 23809877
J Pediatr. 1998 Dec;133(6):795-8
pubmed: 9842048
Int J Environ Res Public Health. 2018 Feb 05;15(2):
pubmed: 29401726
PLoS Med. 2016 Feb 16;13(2):e1001958
pubmed: 26882540
Arch Virol. 2014 Sep;159(9):2451-5
pubmed: 24719197
BMC Infect Dis. 2015 Oct 31;15:486
pubmed: 26520791
Emerg Microbes Infect. 2018 Mar 21;7(1):37
pubmed: 29559626
Pediatrics. 2002 Jun;109(6):e88
pubmed: 12042582
Int J Infect Dis. 2017 Nov;64:15-19
pubmed: 28882666
Lancet Infect Dis. 2010 Nov;10(11):778-90
pubmed: 20961813
J Infect. 2018 Nov;77(5):448-454
pubmed: 30149028
Clin Infect Dis. 2000 Sep;31(3):678-83
pubmed: 11017815
Clin Dev Immunol. 2012;2012:876241
pubmed: 22956971
N Engl J Med. 2010 Apr 8;362(14):e49
pubmed: 20375401
Emerg Microbes Infect. 2017 Jul 12;6(7):e62
pubmed: 28698666
Sci Rep. 2019 Aug 12;9(1):11662
pubmed: 31406192
World J Pediatr. 2018 Oct;14(5):437-447
pubmed: 30280313
Lancet Neurol. 2010 Nov;9(11):1097-105
pubmed: 20965438
MMWR Morb Mortal Wkly Rep. 2015 Jul 31;64(29):805
pubmed: 26225481
Brain Pathol. 2015 Sep;25(5):614-24
pubmed: 26276025
Eur J Clin Microbiol Infect Dis. 2018 Mar;37(3):391-398
pubmed: 29411190
Virol J. 2012 Jan 09;9:8
pubmed: 22230340
Lancet Infect Dis. 2014 Apr;14(4):308-318
pubmed: 24485991
Lancet. 1999 Nov 13;354(9191):1682-6
pubmed: 10568570
Rev Med Virol. 2007 Nov-Dec;17(6):371-9
pubmed: 17487831
Virol J. 2015 Jun 03;12:83
pubmed: 26036928
Emerg Infect Dis. 2016 Nov;22(11):1884-1893
pubmed: 27767012
Jpn J Infect Dis. 2017 Nov 22;70(6):604-608
pubmed: 28890503
Rev Med Virol. 2015 Mar;25(2):115-28
pubmed: 25704797
Am J Trop Med Hyg. 2007 Jul;77(1):188-91
pubmed: 17620652
MMWR Morb Mortal Wkly Rep. 2015 Sep 04;64(34):940-3
pubmed: 26334674
Lancet. 2012 Jul 21;380(9838):206
pubmed: 22826834
Pediatr Infect Dis J. 2014 Sep;33(9):966-70
pubmed: 24577041