6533b85cfe1ef96bd12bd47a

RESEARCH PRODUCT

Albumin replacement in patients with severe sepsis or septic shock.

Gattinoni LCaironi PPesenti AFumagalli RTognoni GRomero MLatini RMasson SVincent JlSuter PmValsecchi MgSantosuosso ACavana MOrtu AGabini RPerno SAnelli AAmoruso RFerraris SBorelli MMassei RPoli G Riva IPapagni GBortone FMamprin FKeim RBrivio MColageo UMimii EpSangiorgi GSiniscalchi APierucci EGiovannitti AGentile CPascucci FAntonini BZummo UValsecchi RCerisara MTrezzi TDossena ARibola ATamayo LZoppellari RVolta CaMangani VFanfani EChelazzi CBartoli TParrini VOggioni RFedele AMolin ABerri CGuarino AIsetta MBonfiglio MTissino FSilvestri LMilanesi MSbrana GMotta EIannaco ICasadio McPasetti GsPalandini ACascione CPuscio DCellai FBoccalatte DSilvestri SFausto CiLupo VZompanti VIacobone EGattari DRonzoni GBeck EFrancesconi SColombo RRaimondi FCastelli ADe Gasperi ARadrizzani DFerla LeGiudici RBellato VBordone GGavazzeni VLesmo ARipamonti DVesconi SPapoff ARossi ANoto APezzi AZanforlin GKandil HBallotta ABettini FVaghi GmRossi SPessina CCasagrande DTrivellato ACostagli VMoise GFurla MMarelli SCaspani LPanigada MBruzzone PIsgrò SAbbruzzese CTagliabue PSolca MBonazzi MCattaneo ARossi NAndreoni PPasetto AGirardis MBarbieri EPiazza OZagara GBono MGalzerano AGarzilli TDentini NBindi MBiancofiore GMercante WpDisconzi MmTodesco NLunardi SSani ECarli MBracciotti GGori VBraccini PMaggio GBraschi ABottazzi AIotti GNicora BSalati GSalsi PAntonelli MPennisi MaBello GCaccese RD'ambrosio MRocco MSanseverino MGatta ANastasi MCorsi AFacondini FFranchi FMongelli PFerrario MCarulli FDel Curto SSchiappacasse GDalpiaz CArmani SVerderosa IMarzullo ATonetti FDe Piero MeLivigni SFiore GCerutti AErbetta SNapolitano RPastorelli MBona FDebernardi FGallo MSegala VParigi LPerzolla DMarson FChiarandini PCammarano CSermann GDe Lucia SFrigerio ADistaso FFranco RBossi ELaudi CDe Nardin MViolo TLazzari FVestali ADella Mora EPolati EMartini ACristallini STotaro CMilan BDan MRuberti SDanzi V.Antonino GiarratanoSanti Maurizio RaineriAndrea Cortegiani

subject

Malemedicine.medical_specialtyALBUMIN SEPSIS SEVERE SEPSIS SEPTIC SHOCKSepsiSerum albuminSettore MED/41 - AnestesiologiaAged; Albumins; Female; Humans; Isotonic Solutions; Male; Middle Aged; Rehydration Solutions; Sepsis; Serum Albumin; Shock Septic; Survival Rate; Treatment OutcomeSepsisIntensive careAlbuminsSepsismedicineHumansalbumin replacementSurvival rateSerum AlbuminIsotonic SolutionAgedAged; Albumins; Female; Humans; Isotonic Solutions; Male; Middle Aged; Rehydration Solutions; Sepsis; Serum Albumin; Shock Septic; Survival Rate; Treatment Outcome; Medicine (all)SEPSISbiologybusiness.industrySeptic shockRehydration SolutionSepticMedicine (all)AlbuminSEPTIC SHOCKOrgan dysfunctionAlbuminShockGeneral MedicineMiddle Agedmedicine.diseaseShock SepticSurgerySurvival RateTreatment OutcomeAnesthesiaRelative riskRehydration Solutionsbiology.proteinFemalemedicine.symptomIsotonic SolutionsbusinessHuman

description

BACKGROUND: Although previous studies have suggested the potential advantages of albumin administration in patients with severe sepsis, its efficacy has not been fully established. METHODS: In this multicenter, open-label trial, we randomly assigned 1818 patients with severe sepsis, in 100 intensive care units (ICUs), to receive either 20% albumin and crystalloid solution or crystalloid solution alone. In the albumin group, the target serum albumin concentration was 30 g per liter or more until discharge from the ICU or 28 days after randomization. The primary outcome was death from any cause at 28 days. Secondary outcomes were death from any cause at 90 days, the number of patients with organ dysfunction and the degree of dysfunction, and length of stay in the ICU and the hospital. RESULTS: During the first 7 days, patients in the albumin group, as compared with those in the crystalloid group, had a higher mean arterial pressure (P = 0.03) and lower net fluid balance (P<0.001). The total daily amount of administered fluid did not differ significantly between the two groups (P = 0.10). At 28 days, 285 of 895 patients (31.8%) in the albumin group and 288 of 900 (32.0%) in the crystalloid group had died (relative risk in the albumin group, 1.00; 95% confidence interval [CI], 0.87 to 1.14; P = 0.94). At 90 days, 365 of 888 patients (41.1%) in the albumin group and 389 of 893 (43.6%) in the crystalloid group had died (relative risk, 0.94; 95% CI, 0.85 to 1.05; P = 0.29). No significant differences in other secondary outcomes were observed between the two groups. CONCLUSIONS: In patients with severe sepsis, albumin replacement in addition to crystalloids, as compared with crystalloids alone, did not improve the rate of survival at 28 and 90 days. (Funded by the Italian Medicines Agency; ALBIOS ClinicalTrials.gov number, NCT00707122.) Copyright © 2014 Massachusetts Medical Society. All rights reserved.

10.1056/nejmoa1305727http://hdl.handle.net/11573/612987