Hemolytic uremic syndrome caused by Shiga toxin-producing Escherichia coli in children: incidence, risk factors, and clinical outcome

dc.contributor.authorElisa Ylinen
dc.contributor.authorSaara Salmenlinna
dc.contributor.authorJani Halkilahti
dc.contributor.authorTimo Jahnukainen
dc.contributor.authorLinda Korhonen
dc.contributor.authorTiia Virkkala
dc.contributor.authorRuska Rimhanen-Finne
dc.contributor.authorMatti Nuutinen
dc.contributor.authorJanne Kataja
dc.contributor.authorPekka Arikoski
dc.contributor.authorLaura Linkosalo
dc.contributor.authorXiangning Bai
dc.contributor.authorAndreas Matussek
dc.contributor.authorHannu Jalanko
dc.contributor.authorHarri Saxén
dc.contributor.organizationfi=kliininen laitos|en=Department of Clinical Medicine|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organization-code1.2.246.10.2458963.20.61334543354
dc.converis.publication-id47401252
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/47401252
dc.date.accessioned2022-10-28T13:12:36Z
dc.date.available2022-10-28T13:12:36Z
dc.description.abstract<p><strong>Background</strong> Hemolytic uremic syndrome (HUS) is a multisystemic disease. In a nationwide study, we characterized the incidence, clinical course, and prognosis of HUS caused by Shiga toxin (Stx)-producing Escherichia coli (STEC) strains with emphasis on risk factors, disease severity, and long-term outcome. </p><p><strong>Methods</strong> The data on pediatric HUS patients from 2000 to 2016 were collected from the medical records. STEC isolates from fecal cultures of HUS and non-HUS patients were collected from the same time period and characterized by whole genome sequencing analysis. </p><p><strong>Results</strong> Fifty-eight out of 262 culture-positive cases developed verified (n = 58, 22%) STEC-HUS. Another 29 cases had probable STEC-HUS, the annual incidence of STEC-HUS being 0.5 per 100,000 children. Eleven different serogroups were detected, O157 being the most common (n = 37, 66%). Age under 3 years (OR 2.4), stx2 (OR 9.7), and stx2a (OR 16.6) were found to be risk factors for HUS. Fifty-five patients (63%) needed dialysis. Twenty-nine patients (33%) developed major neurological symptoms. Complete renal recovery was observed in 57 patients after a median 4.0 years of follow-up. Age under 3 years, leukocyte count over 20 x 10(9)/L, and need for dialysis were predictive factors for poor renal outcome. </p><p><strong>Conclusions</strong> Age under 3 years, stx2, and stx2a were risk factors for HUS in STEC-positive children. However, serogroup or stx types did not predict the renal outcome or major CNS symptoms.</p>
dc.format.pagerange1759
dc.identifier.eissn1432-198X
dc.identifier.jour-issn0931-041X
dc.identifier.olddbid180494
dc.identifier.oldhandle10024/163588
dc.identifier.urihttps://www.utupub.fi/handle/11111/38629
dc.identifier.urlhttps://link.springer.com/article/10.1007/s00467-020-04560-0
dc.identifier.urnURN:NBN:fi-fe2021042821796
dc.language.isoen
dc.okm.affiliatedauthorKataja, Janne
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3123 Gynaecology and paediatricsen_GB
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherSPRINGER
dc.publisher.countryGermanyen_GB
dc.publisher.countrySaksafi_FI
dc.publisher.country-codeDE
dc.relation.doi10.1007/s00467-020-04560-0
dc.relation.ispartofjournalPediatric Nephrology
dc.relation.issue9
dc.relation.volume35
dc.source.identifierhttps://www.utupub.fi/handle/10024/163588
dc.titleHemolytic uremic syndrome caused by Shiga toxin-producing Escherichia coli in children: incidence, risk factors, and clinical outcome
dc.year.issued2020

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