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An increase in red blood cell distribution width from baseline predicts mortality in patients with severe sepsis or septic shock.

DC Field Value Language
dc.contributor.author강신욱-
dc.contributor.author김영삼-
dc.contributor.author김은진-
dc.contributor.author김찬호-
dc.contributor.author박정탁-
dc.contributor.author오형중-
dc.contributor.author유태현-
dc.contributor.author최준용-
dc.contributor.author한승혁-
dc.contributor.author한재현-
dc.contributor.author한지숙-
dc.date.accessioned2014-12-18T09:44:07Z-
dc.date.available2014-12-18T09:44:07Z-
dc.date.issued2013-
dc.identifier.issn1364-8535-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/88727-
dc.description.abstractINTRODUCTION: A potential independent association was recently demonstrated between high red blood cell distribution width (RDW) and the risk of all-cause mortality in critically ill patients, although the mechanism underlying this relationship remains unclear. Little is known about the impact changes in RDW may have on survival in critically ill patients. Therefore, we investigated the prognostic significance of changes in RDW during hospital stay in patients with severe sepsis or septic shock. METHODS: We prospectively enrolled 329 patients who were admitted to the emergency department (ED) and received a standardized resuscitation algorithm (early-goal directed therapy) for severe sepsis or septic shock. The relationship between the changes in RDW during the first 72 hours after ED admission and all-cause mortality (28-day and 90-day) were analyzed by categorizing the patients into four groups according to baseline RDW value and ΔRDW72hr-adm (RDW at 72 hours - RDW at baseline). RESULTS: The 28-day and 90-day mortality rates were 10% and 14.6%, respectively. Patients with increased RDW at baseline and ΔRDW72hr-adm >0.2% exhibited the highest risks of 28-day and 90-day mortality, whereas the patients with normal RDW level at baseline and ΔRDW72hr-adm ≤0.2% (the reference group) had the lowest mortality risks. For 90-day mortality, a significantly higher mortality risk was observed in the patients whose RDW increased within 72 hours of ED admission (normal RDW at baseline and ΔRDW72hr-adm >0.2%), compared to the reference group. These associations remained unaltered even after adjusting for age, sex, Sequential Organ Failure Assessment (SOFA) score, Charlson Comorbidity Index, renal replacement therapy, albumin, hemoglobin, lactate, C-reactive protein and infection sites in multivariable models. CONCLUSIONS: We found that an increase in RDW from baseline during the first 72 hours after hospitalization is significantly associated with adverse clinical outcomes. Therefore, a combination of baseline RDW value and an increase in RDW can be a promising independent prognostic marker in patients with severe sepsis or septic shock.-
dc.description.statementOfResponsibilityopen-
dc.relation.isPartOfCRITICAL CARE-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAged-
dc.subject.MESHCause of Death-
dc.subject.MESHErythrocyte Indices*-
dc.subject.MESHFemale-
dc.subject.MESHHospital Mortality*-
dc.subject.MESHHospitalization-
dc.subject.MESHHumans-
dc.subject.MESHKaplan-Meier Estimate-
dc.subject.MESHLength of Stay-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHPrognosis-
dc.subject.MESHProportional Hazards Models-
dc.subject.MESHProspective Studies-
dc.subject.MESHSepsis/blood*-
dc.subject.MESHSepsis/mortality*-
dc.subject.MESHShock, Septic/blood*-
dc.subject.MESHShock, Septic/mortality*-
dc.subject.MESHTime Factors-
dc.titleAn increase in red blood cell distribution width from baseline predicts mortality in patients with severe sepsis or septic shock.-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학)-
dc.contributor.googleauthorChan Ho Kim-
dc.contributor.googleauthorJung Tak Park-
dc.contributor.googleauthorEun Jin Kim-
dc.contributor.googleauthorJae Hyun Han-
dc.contributor.googleauthorJi Suk Han-
dc.contributor.googleauthorJun Yong Choi-
dc.contributor.googleauthorSeung Hyeok Han-
dc.contributor.googleauthorTae-Hyun Yoo-
dc.contributor.googleauthorYoung Sam Kim-
dc.contributor.googleauthorShin-Wook Kang-
dc.contributor.googleauthorHyung Jung Oh-
dc.identifier.doi10.1186/cc13145-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA00053-
dc.contributor.localIdA00707-
dc.contributor.localIdA01037-
dc.contributor.localIdA01654-
dc.contributor.localIdA02417-
dc.contributor.localIdA02526-
dc.contributor.localIdA04191-
dc.contributor.localIdA04304-
dc.contributor.localIdA04320-
dc.contributor.localIdA04327-
dc.contributor.localIdA00823-
dc.relation.journalcodeJ00652-
dc.identifier.eissn1466-609X-
dc.identifier.pmid24321201-
dc.subject.keywordSeptic Shock-
dc.subject.keywordSevere Sepsis-
dc.subject.keywordRenal Replacement Therapy-
dc.subject.keywordSequential Organ Failure Assessment-
dc.subject.keywordCharlson Comorbidity Index-
dc.contributor.alternativeNameKang, Shin Wook-
dc.contributor.alternativeNameKim, Young Sam-
dc.contributor.alternativeNameKim, Eun Jin-
dc.contributor.alternativeNameKim, Chan Ho-
dc.contributor.alternativeNamePark, Jung Tak-
dc.contributor.alternativeNameOh, Hyung Jung-
dc.contributor.alternativeNameYoo, Tae Hyun-
dc.contributor.alternativeNameChoi, Jun Yong-
dc.contributor.alternativeNameHan, Seung Hyeok-
dc.contributor.alternativeNameHan, Jae Hyun-
dc.contributor.alternativeNameHahn, Jee Sook-
dc.contributor.affiliatedAuthorKang, Shin Wook-
dc.contributor.affiliatedAuthorKim, Young Sam-
dc.contributor.affiliatedAuthorKim, Chan Ho-
dc.contributor.affiliatedAuthorPark, Jung Tak-
dc.contributor.affiliatedAuthorOh, Hyung Jung-
dc.contributor.affiliatedAuthorYoo, Tae Hyun-
dc.contributor.affiliatedAuthorChoi, Jun Yong-
dc.contributor.affiliatedAuthorHan, Seung Hyeok-
dc.contributor.affiliatedAuthorHan, Jae Hyun-
dc.contributor.affiliatedAuthorHahn, Jee Sook-
dc.contributor.affiliatedAuthorKim, Eun Jin-
dc.rights.accessRightsfree-
dc.citation.volume17-
dc.citation.number6-
dc.citation.startPage282-
dc.identifier.bibliographicCitationCRITICAL CARE, Vol.17(6) : 282, 2013-
dc.identifier.rimsid33576-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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