Please use this identifier to cite or link to this item: https://dora.health.qld.gov.au/qldresearchjspui/handle/1/1475
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dc.contributor.authorCook, Aislinnen_US
dc.contributor.authorHsia, Yingfenen_US
dc.contributor.authorRussell, Nealen_US
dc.contributor.authorSharland, Mikeen_US
dc.contributor.authorCheung, Kamanen_US
dc.contributor.authorGrimwood, Keithen_US
dc.contributor.authorCross, Jacken_US
dc.contributor.authorCotrim da Cunha, Deniseen_US
dc.contributor.authorMagalhães, Gloria Reginaen_US
dc.contributor.authorRenk, Hannaen_US
dc.contributor.authorHindocha, Avnien_US
dc.contributor.authorMcMaster, Paddyen_US
dc.contributor.authorOkomo, Uduaken_US
dc.contributor.authorDarboe, Saffiatouen_US
dc.contributor.authorAlvarez-Uria, Gerardoen_US
dc.contributor.authorJinka, Dasaratha Ren_US
dc.contributor.authorMurki, Srinivasen_US
dc.contributor.authorKandraju, Hemasreeen_US
dc.contributor.authorDharmapalan, Dhanyaen_US
dc.contributor.authorEsposito, Susannaen_US
dc.contributor.authorBianchini, Soniaen_US
dc.contributor.authorFukuoka, Kahoruen_US
dc.contributor.authorAizawa, Yutaen_US
dc.contributor.authorJimenez-Juarez, Rodolfo Norbertoen_US
dc.contributor.authorOjeda-Diezbarroso, Karlaen_US
dc.contributor.authorPirš, Matejaen_US
dc.contributor.authorRožič, Mojcaen_US
dc.contributor.authorAnugulruengkitt, Suvapornen_US
dc.contributor.authorJantarabenjakul, Watsamonen_US
dc.contributor.authorCheng, Ching-Lanen_US
dc.contributor.authorJian, Bai-Xiuen_US
dc.contributor.authorSpyridakis, Evangelosen_US
dc.contributor.authorZaoutis, Theoklisen_US
dc.contributor.authorBielicki, Juliaen_US
dc.date.accessioned2021-08-25T03:30:00Z-
dc.date.available2021-08-25T03:30:00Z-
dc.date.issued2021-02-
dc.identifier.citationCook A, Hsia Y, Russell N, Sharland M, Cheung K, Grimwood K, Cross J, Cotrim da Cunha D, Magalhães GR, Renk H, Hindocha A, McMaster P, Okomo U, Darboe S, Alvarez-Uria G, Jinka DR, Murki S, Kandraju H, Dharmapalan D, Esposito S, Bianchini S, Fukuoka K, Aizawa Y, Jimenez-Juarez RN, Ojeda-Diezbarroso K, Pirš M, Rožič M, Anugulruengkitt S, Jantarabenjakul W, Cheng CL, Jian BX, Spyridakis E, Zaoutis T, Bielicki J. Association of Empiric Antibiotic Regimen Discordance With 30-Day Mortality in Neonatal and Pediatric Bloodstream Infection-A Global Retrospective Cohort Study. Pediatr Infect Dis J. 2021 Feb 1;40(2):137-143. doi: 10.1097/INF.0000000000002910en_US
dc.identifier.urihttp://dora.health.qld.gov.au/qldresearchjspui/handle/1/1475-
dc.description.abstractWhile there have been studies in adults reporting discordant empiric antibiotic treatment associated with poor outcomes, this area is relatively unexplored in children and neonates despite evidence of increasing resistance to recommended first-line treatment regimens. Patient characteristics, antibiotic treatment, microbiology, and 30-day all-cause outcome from children <18 years with blood-culture-confirmed bacterial bloodstream infections (BSI) were collected anonymously using REDCap™ through the Global Antibiotic Prescribing and Resistance in Neonates and Children network from February 2016 to February 2017. Concordance of early empiric antibiotic treatment was determined using European Committee on Antimicrobial Susceptibility Testing interpretive guidelines. The relationship between concordance of empiric regimen and 30-day mortality was investigated using multivariable regression. Four hundred fifty-two children with blood-culture-positive BSI receiving early empiric antibiotics were reported by 25 hospitals in 19 countries. Sixty percent (273/452) were under the age of 2 years. S. aureus, E. coli, and Klebsiella spp. were the most common isolates, and there were 158 unique empiric regimens prescribed. Fifteen percent (69/452) of patients received a discordant regimen, and 7.7% (35/452) died. Six percent (23/383) of patients with concordant regimen died compared with 17.4% (12/69) of patients with discordant regimen. Adjusting for age, sex, presence of comorbidity, unit type, hospital-acquired infections, and Gram stain, the odds of 30-day mortality were 2.9 (95% confidence interval: 1.2-7.0; P = 0.015) for patients receiving discordant early empiric antibiotics. Odds of mortality in confirmed pediatric BSI are nearly 3-fold higher for patients receiving a discordant early empiric antibiotic regimen. The impact of improved concordance of early empiric treatment on mortality, particularly in critically ill patients, needs further evaluation.en_US
dc.language.isoenen_US
dc.publisherLippincott Williams & Wilkinsen_US
dc.relation.ispartofThe Pediatric infectious disease journalen_US
dc.subjectantibioticsen_US
dc.subjectAnti-Bacterial Agentsen_US
dc.subjectBacterial Infectionsen_US
dc.subjectChildrenen_US
dc.titleAssociation of Empiric Antibiotic Regimen Discordance With 30-Day Mortality in Neonatal and Pediatric Bloodstream Infection-A Global Retrospective Cohort Studyen_US
dc.typeArticleen_US
dc.identifier.doi10.1097/inf.0000000000002910-
item.languageiso639-1en-
item.openairetypeArticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
Appears in Sites:Gold Coast Health Publications
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