Objective To test the hypothesis that measles infection increases the incidence of non-measles infectious diseases over a prolonged period of time. Design A population-based matched cohort study. Data sources This study examined children aged 1-15 years in The Health Improvement Network UK general practice medical records database. Participants included 2228 patients diagnosed with measles between 1990 and 2014, which were matched on age, sex, general practitioner practice and calendar year with 19930 children without measles. All controls had received at least one measles vaccination. Children with a history of immune-compromising conditions or with immune-suppressive treatment were excluded. Primary outcome measures Incidence rate ratio (IRR) of infections, anti-infective prescriptions and all-cause hospitalisations following measles in predetermined periods using multivariate analysis to adjust for confounding variables. Results In children with measles, the incidence rate for non-measles infectious disease was significantly increased in each time period assessed up to 5 years postmeasles: 43% in the first month (IRR: 1.43; 95%CI 1.22 to 1.68), 22% from month one to the first year (IRR: 1.22; 95%CI 1.14 to 1.31), 10% from year 1 to 2.5 years (IRR: 1.10; 95%CI 1.02 to 1.19) and 15% (IRR: 1.15; 95%CI 1.06 to 1.25) in years 2.5 to 5 years of follow-up. Children with measles were more than three times as likely to receive an anti-infective prescription in the first month and 15%-24%more likely between the first month and 5 years. The rate of hospitalisation in children with measles was increased only in the month following diagnosis but not thereafter (IRR: 2.83; 95%CI 1.72 to 4.67). Conclusion Following measles, children had increased rates of diagnosed infections, requiring increased prescribing of antimicrobial therapies. This population-based matched cohort study supports the hypothesis that measles has a prolonged impact on host resistance to non-measles infectious diseases.
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Univ London, Sch Pharm, Ctr Paediat Pharm Res, London WC1H 9JP, England
UCL, Inst Child Hlth, London, England
Guys & St Thomas NHS Fdn Trust, Evelina Childrens Hosp, London, EnglandUniv London, Sch Pharm, Ctr Paediat Pharm Res, London WC1H 9JP, England
Ackers, Ruth
Besag, Frank M. C.
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Univ London, Sch Pharm, Ctr Paediat Pharm Res, London WC1H 9JP, England
UCL, Inst Child Hlth, London, England
SEPT S Essex Partnership NHS Trust, Twinwoods Hlth Resource Ctr, Bedford, EnglandUniv London, Sch Pharm, Ctr Paediat Pharm Res, London WC1H 9JP, England
Besag, Frank M. C.
Hughes, Elaine
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Kings Coll Hosp London, Dept Paediat, London, EnglandUniv London, Sch Pharm, Ctr Paediat Pharm Res, London WC1H 9JP, England
Hughes, Elaine
Squier, Waney
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John Radcliffe Hosp, Dept Neuropathol, Oxford OX3 9DU, EnglandUniv London, Sch Pharm, Ctr Paediat Pharm Res, London WC1H 9JP, England
Squier, Waney
Murray, Macey L.
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Univ London, Sch Pharm, Ctr Paediat Pharm Res, London WC1H 9JP, England
UCL, Inst Child Hlth, London, EnglandUniv London, Sch Pharm, Ctr Paediat Pharm Res, London WC1H 9JP, England
Murray, Macey L.
Wong, Ian C. K.
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Univ London, Sch Pharm, Ctr Paediat Pharm Res, London WC1H 9JP, England
UCL, Inst Child Hlth, London, England
Univ Hong Kong, Li Ka Shing Fac Med, Dept Pharmacol & Pharm, Hong Kong, Hong Kong, Peoples R ChinaUniv London, Sch Pharm, Ctr Paediat Pharm Res, London WC1H 9JP, England