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The DOse REsponse Multicentre International Collaborative Initiative (DO‐RE‐MI)

dc.contributor.authorMONTI, G.
dc.contributor.authorHERRERA, M.
dc.contributor.authorKINDGEN‐MILLES, D.
dc.contributor.authorMARINHO, A.
dc.contributor.authorCRUZ, D.
dc.contributor.authorMARIANO, F.
dc.contributor.authorGIGLIOLA, G.
dc.contributor.authorMORETTI, E.
dc.contributor.authorALESSANDRI, E.
dc.contributor.authorROBERT, R.
dc.contributor.authorRONCO, C.
dc.contributor.authorDOSE RESPONSE MULTICENTRE INTERNATIONAL COLLABORATIVE INITIATIVE SCIENTIFIC COMMITTEE
dc.date.accessioned2011-03-16T11:27:43Z
dc.date.available2011-03-16T11:27:43Z
dc.date.issued2007
dc.description.abstractContrib Nephrol. 2007;156:434-43. The DOse REsponse Multicentre International Collaborative Initiative (DO-RE-MI). Monti G, Herrera M, Kindgen-Milles D, Marinho A, Cruz D, Mariano F, Gigliola G, Moretti E, Alessandri E, Robert R, Ronco C; Dose Response Multicentre International Collaborative Initiative Scientific Committee. Department of Anesthesiology and Intensive Care, Hospital Niguarda, Milan, Italy, and Anesthesiology Clinic, University of Düsseldorf, Germany. Gianpaola.monti@ospedaleniguarda.it Abstract BACKGROUND: Current practices for renal replacement therapy (RRT) in ICU remain poorly defined. The observational DOse REsponse Multicentre International collaborative initiative (DO-RE-MI) survey addresses the issue of how the different modes of RRT are currently chosen and performed. The primary endpoint of DO-RE-MI will be the delivered dose versus in ICU, 28-day, and hospital mortality, and the secondary endpoint, the hemodynamic response to RRT. Here, we report the first preliminary descriptive analysis after 1-year recruitment. METHODS: Data from 431 patients in need of RRT with or without acute renal failure (mean age 61.2+15.9) from 25 centers in 5 countries (Spain, Italy, Germany, Portugal, France) were entered in electronic case report forms (CRFs) available via the website acutevision.net. RESULTS: On admission, 51% patients came from surgery, 36% from the emergency department, and 16% from internal medicine. On admission, mean SOFA and SAPS II were 13 and 50, respectively. The first criteria to initiate RRT was the RIFLE in 38% (failure: 70%, injury: 25%, risk: 22%), the second the high urea/creatinine, and the third immunomodulation. A total of 3,010 cumulative CRF were reported: continuous venovenous hemodiafiltration (CVVHDF) 60%, continuous venovenous hemofiltration (CVVH) 15%, intermittent hemodialysis (IHD) 15%, high-volume hemofiltration (HVHF) 7%, continuous venovenous hemodialysis (CVVHD) 1%, and coupled plasma filtration adsorption/CVVD 2%. In 15% of cases, the patient was shifted to another modality. Mean blood flow rates (ml/min) in the different modalities were: 145 (CVVHDF), 200 (CVVH), 215 (IHD), 283 (HVHF), and 150 (CVVHD). Downtime ranged from 8 to 28% of the total treatment time. Clotting of the circuit accounted for 74% of treatment interruptions. CONCLUSIONS: Despite a large variability in the criteria of choice of RRT, CVVHDF remains the most used (49%). Clotting and clinical reasons were the most common causes for RRT downtime. In continuous RRT, a large variability in the delivered dose is observed in the majority of patients and often in the same patient from one day to another. Preliminary analysis suggests that in a large number of cases the delivered dose is far from the 'adequate' 35 ml/h/kg.por
dc.identifier.issn0302-5144
dc.identifier.urihttp://hdl.handle.net/10400.16/558
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherKragerpor
dc.relation.publisherversionhttp://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowFreePage&ArtikelNr=0000102137&Ausgabe=0&ProduktNr=233035&filefp=0000102137fp.pdfpor
dc.titleThe DOse REsponse Multicentre International Collaborative Initiative (DO‐RE‐MI)por
dc.typejournal article
dspace.entity.typePublication
oaire.citation.titleContributions to Nephrologypor
rcaap.rightsrestrictedAccesspor
rcaap.typearticlepor

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