Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/49749
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dc.contributor.authorKotagiri P.-
dc.contributor.authorRyan J.-
dc.contributor.authorToussaint N.D.-
dc.date.accessioned2023-05-18T03:22:02Z-
dc.date.available2023-05-18T03:22:02Z-
dc.date.copyright2016-
dc.date.issued2023-05-02en
dc.identifier.citationJournal of the American Society of Nephrology. Conference: Kidney Week 2016. Chicago, IL United States. 27 (pp 281A), 2016. Date of Publication: November 2016.-
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/49749-
dc.description.abstractBackground: Urinary tract infections (UTI) are the commonest infectious complication in kidney transplant recipients (KTRs). Effects on graft function are unclear. No recommendations exist regarding treatment of asymptomatic bacteriuria but concern that immunosuppression and denervation of the graft masks symptoms often prompts treatment. We aimed to identify potential risk factors for UTIs, microbiological profile and role of treatment of asymptomatic bacteriuria, and effects on graft outcomes. Method(s): Retrospective analysis of UTIs in KTRs transplanted between Jan 2012 and Dec 2013 in two Australian tertiary transplant centres where patients are routinely commenced on prophylactic sulfamethoxazole/trimethoprim. Clinical and microbiological data was analysed for the first year following transplantation. Result(s): 276 KTRs were evaluated, 67% male, mean age of 51yrs. 158 recipients (57%) had no bacteriuria in the first year post-transplant, 75 (27%) had only asymptomatic bacteriuria, 21 (8%) had symptomatic UTIs and 22 (8%) with UTIs developed either pyelonephritis or urosepsis. Most frequent pathogens identified were Enterococcus Faecalis and Escherichia Coli, and 36% were multi-drug resistant. Female gender was a risk factor for infection (p=0.002) and presence of a ureteric JJ stent significantly increased the risk of asymptomatic bacteriuria and symptomatic UTIs (p=0.003). Diabetes, age and prior transplantation did not increase risk. Presence of infection was not associated with increased rejection or adverse longer-term outcomes with similar renal function at 12 months. For all episodes of bacteriuria in our cohort (n=420), cases of untreated asymptomatic bacteriuria (n=185) followed by symptomatic UTI with the same organism were significantly higher (p=0.002) compared to cases of treated asymptomatic bacteriuria (n=139). Conclusion(s): Treatment of asymptomatic bacteriuria in the first year post-transplant may be beneficial to prevent subsequent episodes of symptomatic UTIs.-
dc.publisherWolters Kluwer Health-
dc.relation.ispartofJournal of the American Society of Nephrology-
dc.subject.meshasymptomatic bacteriuria-
dc.subject.meshcohort analysis-
dc.subject.meshconference abstract-
dc.subject.meshcontrolled study-
dc.subject.meshdiabetes mellitus-
dc.subject.meshdouble J stent-
dc.subject.meshEnterococcus faecalis-
dc.subject.meshEscherichia coli-
dc.subject.meshgender-
dc.subject.meshtissue-
dc.subject.meshinfectious agent-
dc.subject.meshkidney function-
dc.subject.meshkidney graft-
dc.subject.meshkidney transplantation-
dc.subject.meshmajor clinical study-
dc.subject.meshmiddle aged-
dc.subject.meshmulticenter study-
dc.subject.meshnon-
dc.subject.meshoutcome assessment-
dc.subject.meshpatient history of transplantation-
dc.subject.meshprevention-
dc.subject.meshpyelonephritis-
dc.subject.meshretrospective study-
dc.subject.meshrisk factor-
dc.subject.meshsurgery-
dc.subject.meshurinary tract infection-
dc.subject.meshurosepsis-
dc.subject.meshcotrimoxazole-
dc.titleUrinary Tract Infections in the First Year Post Kidney Transplantation.-
dc.typeConference Abstract-
dc.description.conferencenameKidney Week 2016-
dc.description.conferencelocationChicago, IL, United States-
dc.type.studyortrialObservational study (cohort, case-control, cross sectional, or survey)-
local.date.conferencestart2016-11-15-
dc.identifier.institution(Kotagiri, Toussaint) Royal Melbourne Hospital, Parkville, Australia-
dc.identifier.institution(Ryan) Monash Health, Clayton, Australia-
dc.identifier.institution(Toussaint) Univ of Melbourne, Australia-
local.date.conferenceend2016-11-20-
dc.identifier.affiliationmh(Ryan) Monash Health, Clayton, Australia-
item.openairetypeConference Abstract-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
crisitem.author.deptNephrology-
Appears in Collections:Conference Abstracts
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