Circulating adrenomedullin estimates survival and reversibility of organ failure in sepsis: the prospective observational multinational Adrenomedullin and Outcome in Sepsis and Septic Shock-1 (AdrenOSS-1) study

Background: Adrenomedullin (ADM) regulates vascular tone and endothelial permeability during sepsis. Levels of circulating biologically active ADM (bio-ADM) show an inverse relationship with blood pressure and a direct relationship with vasopressor requirement. In the present prospective observational multinational Adrenomedullin and Outcome in Sepsis and Septic Shock 1 (, AdrenOSS-1) study, we assessed relationships between circulating bio-ADM during the initial intensive care unit (ICU) stay and short-term outcome in order to eventually design a biomarker-guided randomized controlled trial.... Mehr ...

Verfasser: Mebazaa A.
Geven C.
Hollinger A.
Wittebole X.
Chousterman B. G.
Blet A.
Gayat E.
Hartmann O.
Scigalla P.
Struck J.
Bergmann A.
Antonelli M.
Beishuizen A.
Constantin J. -M.
Damoisel C.
Deye N.
Di Somma S.
Dugernier T.
Francois B.
Gaudry S.
Huberlant V.
Lascarrou J. -B.
Marx G.
Mercier E.
Oueslati H.
Pickkers P.
Sonneville R.
Legrand M.
Laterre P. -F.
Laterre P. F.
Berghe C.
Dujardin M. -F.
Renard S.
Collienne C.
Zapatero D. C.
Vinetti M.
De Schryver N.
Thirifays A.
Mairesse J.
Petre H.
Buelens I.
Henin P.
Trine H.
Laurent Y.
Sebastien L.
Geukens P.
Kehl L.
Vignon P.
Pichon N.
Begot E.
Fedou A. -L.
Chapellas C.
Galy A.
Rodier N.
Baudrillart L.
Nouaille M.
Laleu S.
Mancia C.
Daix T.
Bourzeix P.
Herafa I.
Duchambon A. -A.
Lascarrou J. B.
Fiancette M.
Colin G.
Henry-Lagarrigue M.
Lacherade J. -C.
Lebert C.
Martin-Levevre L.
Vinatier I.
Yehia A.
Bachoumas K.
Joret A.
Reignier J.
Rousseau C.
Maquigneau N.
Alcourt Y.
Zinzonni V. E.
Deschamps A.
Robert A.
Simeon-Vieules V.
Aubrey A.
Mabilat C.
Garot D.
Ehrmann S.
Legras A.
Jouan Y.
Dequin P. F.
Guillon A.
Bodet-Contentin L.
Rouve E.
Salmon C.
Brick L.
Massat S.
Desachy A.
Fally M. A.
Robin L.
Cracco C.
Lafon C.
Calvat S.
Rouleau S.
Schnell D.
Lasocki S.
Fesard P.
Leblanc D.
Bouhours G.
Chassier C.
Conte M.
Gaillard T.
Denou F.
Kerymel M.
Guyon M.
Loiez A.
Lebreton S.
Meziani F.
Allam H.
Chenaf S.
Rahmani H.
Heenen S.
Kummerlen C.
Delabranche X.
Boivin A.
Clere-Jehl R.
Rabouel Y.
Pottecher J.
Bayer S.
Metzger C.
Hecketsweiler S.
Ludes P. O.
Besancenot H.
Dhif N.
Freys G.
Lessinger J. -M.
Launoy A.
Ruimy A.
Meyer A.
Szozot M.
Fournier M. -C.
Abroug S.
Louadah B.
Feliot E.
Voicu S.
Malissin I.
Megarbane B.
Manivet P.
Victori G.
Kelly D. S.
La Foucher B.
Pierre V.
Kerdjana L.
Beeken T.
Goury A.
Garcon P.
Gaugain S.
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Barthelemy R.
Soyer B.
Jacob L.
Bonnet F.
Legall C.
Cupaciu A.
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Bouadma L.
Mourvillier B.
Deiler V.
Magalhaes E.
Neuville M.
Timsit J. -F.
Radjou A.
Dubief E.
Messika J.
La Combe B.
Roux D.
Berquier G.
Laissi M.
Ricard J. -D.
Perbet S.
Delmas J.
Pascal J.
Cayot S.
Guerin R.
Jabaudon M.
Roszyk L.
Rolhion C.
Bourdier J.
Lematte M.
Gouhier C.
Verlhac C.
Godet T.
Radji S.
Caumon E.
Thibault S.
Marx N.
Schuerholz T.
Pezechk J.
Feld F.
Brulls C.
Beeker T.
Simon T. -P.
Deisz R.
Schindler A.
Meier B.
Janisch T.
Hohn A.
Schedler D.
Wetsch W.
Schroder D.
Meier-Hellmann A.
Lucht A.
Henker R.
Rommer M.
Meinig T.
Zacharowski K. D.
Meybohm P.
Lindau S.
Mutlak H.
Kluge S.
Ringeis G.
Fullekrug B.
Singer B.
Nierhaus A.
Bangert K.
De Heer G.
Frings D.
Fuhrmann V.
Muller J.
Schreiber J.
Sensen B.
Siedler S.
Siewecke A.
Soffker G.
Wichmann D.
Kerinn M.
Jaschinski U.
Kreuser I.
Zanquila M.
Kortgen A.
Bloos F.
Gonnert F.
Thomas-Ruddel D.
Haucke A.
Kolanos S.
Kohlberg K. K.
Bloos P.
Schwope K.
Russo V.
Simona S.
Bartoli C.
Navarin S.
Bongiovanni C.
Orru M.
Quatrocchi D.
Zoccoli G.
Varchetta A.
Vallecoccia M. S.
Cutuli S. L.
Digravio V.
Quattrochi D.
D'Arrigo S.
Leone F. E.
Beishuizen B.
Rinket M.
Border N.
Bos-Burgmeijer M.
Braad A.
Papendorp S.
Cornet A.
Vermeijden J.
Trof R. J.
Van Wezel H.
Heunks L.
Hoedemaekers A.
Van Der Hoeven H.
Roovers N.
Hemelaar P.
Dokumenttyp: Artikel
Erscheinungsdatum: 2018
Verlag/Hrsg.: BioMed Central Ltd.
Schlagwörter: Biomarker / Outcome / Sepsis-2 / Sepsis-3 / Adrenomedullin / Aged / Belgium / Chi-Square Distribution / Female / France / Germany / Hospital Mortality / Hospitalization / Human / Intensive Care Unit / Italy / Length of Stay / Male / Middle Aged / Multiple Organ Failure / Netherland / Patient Outcome Assessment / Proportional Hazards Model / Prospective Studie / Sepsi / Survival Analysis
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-26965510
Datenquelle: BASE; Originalkatalog
Powered By: BASE
Link(s) : http://hdl.handle.net/11573/1307718

Background: Adrenomedullin (ADM) regulates vascular tone and endothelial permeability during sepsis. Levels of circulating biologically active ADM (bio-ADM) show an inverse relationship with blood pressure and a direct relationship with vasopressor requirement. In the present prospective observational multinational Adrenomedullin and Outcome in Sepsis and Septic Shock 1 (, AdrenOSS-1) study, we assessed relationships between circulating bio-ADM during the initial intensive care unit (ICU) stay and short-term outcome in order to eventually design a biomarker-guided randomized controlled trial. Methods: AdrenOSS-1 was a prospective observational multinational study. The primary outcome was 28-day mortality. Secondary outcomes included organ failure as defined by Sequential Organ Failure Assessment (SOFA) score, organ support with focus on vasopressor/inotropic use, and need for renal replacement therapy. AdrenOSS-1 included 583 patients admitted to the ICU with sepsis or septic shock. Results: Circulating bio-ADM levels were measured upon admission and at day 2. Median bio-ADM concentration upon admission was 80.5 pg/ml [IQR 41.5-148.1 pg/ml]. Initial SOFA score was 7 [IQR 5-10], and 28-day mortality was 22%. We found marked associations between bio-ADM upon admission and 28-day mortality (unadjusted standardized HR 2.3 [CI 1.9-2.9]; adjusted HR 1.6 [CI 1.1-2.5]) and between bio-ADM levels and SOFA score (p < 0.0001). Need of vasopressor/inotrope, renal replacement therapy, and positive fluid balance were more prevalent in patients with a bio-ADM > 70 pg/ml upon admission than in those with bio-ADM ≤ 70 pg/ml. In patients with bio-ADM > 70 pg/ml upon admission, decrease in bio-ADM below 70 pg/ml at day 2 was associated with recovery of organ function at day 7 and better 28-day outcome (9.5% mortality). By contrast, persistently elevated bio-ADM at day 2 was associated with prolonged organ dysfunction and high 28-day mortality (38.1% mortality, HR 4.9, 95% CI 2.5-9.8). Conclusions: AdrenOSS-1 shows that ...