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Therapeutic outcome of spinal implant infections caused by Staphylococcus aureus A retrospective observational study

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dc.contributor.authorCho, Oh-Hyun-
dc.contributor.authorBae, In-Gyu-
dc.contributor.authorMoon, Song Mi-
dc.contributor.authorPark, Seong Yeon-
dc.contributor.authorKwak, Yee Gyung-
dc.contributor.authorKim, Baek-Nam-
dc.contributor.authorYu, Shi Nae-
dc.contributor.authorJeon, Min Hyok-
dc.contributor.authorKim, Tark-
dc.contributor.authorChoo, Eun Ju-
dc.contributor.authorLee, Eun Jung-
dc.contributor.authorKim, Tae Hyong-
dc.contributor.authorChoi, Seong-Ho-
dc.contributor.authorChung, Jin-Won-
dc.contributor.authorKang, Kyung-Chung-
dc.contributor.authorLee, Jung Hee-
dc.contributor.authorLee, Yu-Mi-
dc.contributor.authorLee, Mi Suk-
dc.contributor.authorPark, Ki-Ho-
dc.date.available2020-02-27T09:41:02Z-
dc.date.created2020-02-06-
dc.date.issued2018-10-
dc.identifier.issn0025-7974-
dc.identifier.urihttps://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/3275-
dc.description.abstractSpinal implant infection is a rare but significant complication of spinal fusion surgery, and the most common pathogen is Staphylococcus aureus. It is difficult to treat due to this pathogen's biofilm-forming ability and antibiotic resistance. We evaluated the therapeutic outcome of treatments for S aureus spinal implant infections. We retrospectively reviewed all patients with S aureus spinal implant infections at 11 tertiary-care hospitals over a 9-year period. Parameters predictive of treatment failure and recurrence were analyzed by Cox regression. Of the 102 patients with infections, 76 (75%) were caused by methicillin-resistant S aureus (MRSA) and 51 (50%) were late-onset infections. In all, 83 (81%) patients were managed by debridement, antibiotics, and implant retention (DAIR) and 19 (19%) had their implants removed. The median duration of all antibiotic therapies was 52 days. During a median follow-up period of 32 months, treatment failure occurred in 37 (36%) cases. The median time to treatment failure was 113 days, being <1 year in 30 (81%) patients. DAIR (adjusted hazard ratio [aHR], 6.27; P=.01) and MRSA infection (aHR, 4.07; P=.009) were independently associated with treatment failure. Rifampin-based combination treatments exhibited independent protective effects on recurrence (aHR, 0.23; P=.02). In conclusion, among patients with S aureus spinal implant infections, MRSA and DAIR were independent risk factors for treatment failure, and these risk factors were present in the majority of patients. In this difficult-to-treat population, the overall treatment failure rate was 36%; rifampin may improve the outcomes of patients with S aureus spinal implant infections.-
dc.language영어-
dc.language.isoen-
dc.publisherLIPPINCOTT WILLIAMS & WILKINS-
dc.relation.isPartOfMEDICINE-
dc.subjectHEMATOGENOUS VERTEBRAL OSTEOMYELITIS-
dc.subjectPROSTHETIC JOINT INFECTIONS-
dc.subjectRISK-FACTORS-
dc.subjectANTIBIOTIC-TREATMENT-
dc.subjectRESISTANT-
dc.subjectCOMBINATION-
dc.subjectVANCOMYCIN-
dc.subjectMANAGEMENT-
dc.subjectRIFAMPICIN-
dc.subjectFUSION-
dc.titleTherapeutic outcome of spinal implant infections caused by Staphylococcus aureus A retrospective observational study-
dc.typeArticle-
dc.type.rimsART-
dc.description.journalClass1-
dc.identifier.wosid000452230500051-
dc.identifier.doi10.1097/MD.0000000000012629-
dc.identifier.bibliographicCitationMEDICINE, v.97, no.40-
dc.identifier.scopusid2-s2.0-85054449616-
dc.citation.titleMEDICINE-
dc.citation.volume97-
dc.citation.number40-
dc.contributor.affiliatedAuthorMoon, Song Mi-
dc.type.docTypeArticle-
dc.subject.keywordAuthorinstrumentation-
dc.subject.keywordAuthoroutcome-
dc.subject.keywordAuthorrifampin-
dc.subject.keywordAuthorspondylitis-
dc.subject.keywordAuthortreatment-
dc.subject.keywordAuthorvertebral osteomyelitis-
dc.subject.keywordPlusHEMATOGENOUS VERTEBRAL OSTEOMYELITIS-
dc.subject.keywordPlusPROSTHETIC JOINT INFECTIONS-
dc.subject.keywordPlusRISK-FACTORS-
dc.subject.keywordPlusANTIBIOTIC-TREATMENT-
dc.subject.keywordPlusRESISTANT-
dc.subject.keywordPlusCOMBINATION-
dc.subject.keywordPlusVANCOMYCIN-
dc.subject.keywordPlusMANAGEMENT-
dc.subject.keywordPlusRIFAMPICIN-
dc.subject.keywordPlusFUSION-
dc.relation.journalResearchAreaGeneral & Internal Medicine-
dc.relation.journalWebOfScienceCategoryMedicine, General & Internal-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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