Prior Exposure to Angiotensin II Receptor Blockers in Patients With Septic Shock to Individualize Mean Arterial Pressure Target? A Post Hoc Analysis of the Sepsis and Mean Arterial Pressure (SEPSISPAM) Trial.


Journal

Critical care medicine
ISSN: 1530-0293
Titre abrégé: Crit Care Med
Pays: United States
ID NLM: 0355501

Informations de publication

Date de publication:
01 04 2021
Historique:
pubmed: 17 2 2021
medline: 24 8 2021
entrez: 16 2 2021
Statut: ppublish

Résumé

Individualizing a target mean arterial pressure is challenging during the initial resuscitation of patients with septic shock. The Sepsis and Mean Arterial Pressure (SEPSISPAM) trial suggested that targeting high mean arterial pressure might reduce the occurrence of acute kidney injury among those included patients with a past history of chronic hypertension. We investigated whether the class of antihypertensive medications used before the ICU stay in chronic hypertensive patients was associated with the severity of acute kidney injury occurring after inclusion, according to mean arterial pressure target. Post hoc analysis of the SEPSISPAM trial. The primary outcome was the occurrence of severe acute kidney injury during the ICU stay defined as kidney disease improving global outcome stage 2 or higher. Secondary outcomes were mortality at day 28 and mortality at day 90. All patients with chronic hypertension included in SEPSISPAM with available antihypertensive medications data in the hospitalization report were included. We analyzed 297 patients. Severe acute kidney injury occurred in 184 patients, without difference according to pre-ICU exposure to antihypertensive medications. Patients with pre-ICU exposure to angiotensin II receptor blockers had significantly less severe acute kidney injury in the high mean arterial pressure target group (adjusted odd ratio 0.24 with 95% CI [0.09-0.66]; p = 0.006). No statistically significant association was found after adjustment for pre-ICU exposure to antihypertensive medications and survival. Our results suggest that patients with septic shock and chronic hypertension treated with angiotensin II receptor blocker may benefit from a high mean arterial pressure target to reduce the risk of acute kidney injury occurrence.

Identifiants

pubmed: 33591012
doi: 10.1097/CCM.0000000000004872
pii: 00003246-202104000-00028
doi:

Substances chimiques

Angiotensin Receptor Antagonists 0
Antihypertensive Agents 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e412-e422

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2021 by the Society of Critical Care Medicine and Wolters Kluwer Health, Inc. All Rights Reserved.

Déclaration de conflit d'intérêts

Dr. Dequin’s institution received funding from Angers University Hospital, the French Ministry of Health, Abionic, Atox Bio, Sphingotec GMBH, Adrenomed, Medspace, Aridis, Merck, Combioxin, GSK, Med-Immune, Genentech INH, Rev-Immune, Faron, Kenta, and Tigenix, and he received support for article research from the French Ministry of Health. Dr. Gonzalez disclosed work for hire. Dr. Teboul received funding from Getinge/Pulsion. Dr. Radermacher’s institution received funding from Deutsche Forschungsgemeinschaft and the German Ministry of Defense. The remaining authors have disclosed that they do not have any potential conflicts of interest.

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Auteurs

Julien Demiselle (J)

Department of Medical Intensive Care, University Hospital of Angers, Angers, France.

Valérie Seegers (V)

Service de Biométrie, Institut de Cancérologie de l'Ouest, Centre Paul Papin, Angers, France.

Marie Lemerle (M)

Department of Medical Intensive Care, University Hospital of Angers, Angers, France.

Ferhat Meziani (F)

Department of Medical Intensive Care, University Hospital of Strasbourg, Nouvel Hôpital Civil, Strasbourg, France.
INSERM (French National Institute of Health and Medical Research), UMR 1260, Regenerative Nanomedicine (RNM), FMTS, Strasbourg, France.

Fabien Grelon (F)

Medical and Surgical Intensive Care Unit, Le Mans Hospital, Le Mans, France.

Bruno Megarbane (B)

Department of Medical and Toxicological Intensive Care, Lariboisière University Hospital, University of Paris, INSERM UMRS-1144, Paris, France.

Nadia Anguel (N)

Department of Medical Intensive Care, Bicêtre University Hospital, AP-HP, Paris-Saclay University, Le Kremlin Bicêtre, France.

Jean-Paul Mira (JP)

Department of Medical Intensive Care, Cochin University Hospital, Paris, France.

Pierre-François Dequin (PF)

Department of Medical Intensive Care, Tours University Hospital, Tours, France.

Soizic Gergaud (S)

Department of Surgical Intensive Care, University Hospital of Angers, Angers, France.

Nicolas Weiss (N)

Department of Medical Intensive Care, Georges Pompidou European Hospital, Paris, France.

François Legay (F)

Department of Medical Intensive Care, Saint Brieuc Hospital, Saint Brieuc, France.

Yves Le Tulzo (Y)

Department of Infectious Diseases and Medical Intensive Care, Rennes University Hospital, Rennes, France.

Marie Conrad (M)

Department of Medical Intensive Care, Nancy University Hospital, Nancy, France.

René Robert (R)

Department of Medical Intensive Care, Université de Poitiers, CHU Poitiers, Poitiers, France.

Frédéric Gonzalez (F)

Department of Medical and Surgical Intensive Care, Avicenne Teaching Hospital, Bobigny, France.

Christophe Guitton (C)

Department of Medical Intensive Care, Nantes University Hospital, Nantes, France.

Fabienne Tamion (F)

Department of Medical Intensive Care, Rouen University Hospital, Rouen, France.

Jean-Marie Tonnelier (JM)

Department of Medical Intensive Care, Brest University Hospital, Brest, France.

Jean-Pierre Bédos (JP)

Department of Medical and Surgical Intensive Care, Versailles Hospital, Versailles, France.

Thierry Van Der Linden (T)

Department of Intensive Care, Saint Philibert hospital, Catholic university of Lille, Lille, France.

Antoine Vieillard-Baron (A)

Department of Medical and Surgical Intensive Care, Boulogne Billancourt University Hospital, Boulogne Billancourt, France.
Inserm U1018, Center for Research in Epidemiology and Population Health (CESP), Faculty of Paris Saclay, Villejuif, France.

Eric Mariotte (E)

Department of Intensive Care, Saint Louis Hospital, Paris, France.

Gaël Pradel (G)

Department of Intensive Care, Avignon Hospital, Avignon, France.

Olivier Lesieur (O)

Department of Medical and Surgical Intensive Care, La Rochelle Saint Louis Hospital, La Rochelle, France.

Jean-Damien Ricard (JD)

Department of Medico-Surgical Intensive Care, Université de Paris, Assistance Publique - Hôpitaux de Paris, Louis Mourier Hospital, Colombes, France.

Fabien Hervé (F)

Department of Medical and Surgical Intensive Care, Quimper Hospital, Quimper, France.

Damien du Cheyron (D)

Department of Medical Intensive Care, Caen University Hospital, Caen, France.

Claude Guerin (C)

Department of Medical Intensive Care, Edouard Herriot Hospital, Lyon, France.

Jean-Louis Teboul (JL)

Department of Medical Intensive Care, Bicêtre University Hospital, AP-HP, Paris-Saclay University, Le Kremlin Bicêtre, France.

Julie Helms (J)

Department of Medical Intensive Care, University Hospital of Strasbourg, Nouvel Hôpital Civil, Strasbourg, France.
ImmunoRhumatologie Moléculaire, INSERM UMR_S1109, LabEx TRANSPLANTEX, Centre de Recherche d'Immunologie et d'Hématologie, Faculté de Médecine, Fédération Hospitalo-Universitaire (FHU) OMICARE, Fédération de Médecine Translationnelle de Strasbourg (FMTS), Université de Strasbourg (UNISTRA), Strasbourg, France.

Peter Radermacher (P)

Institut für Anästhesiologische Pathophysiologie und Verfahrensentwicklung, Universitätsklinikum, Helmholtzstrasse 8-1, Ulm, Germany.

Pierre Asfar (P)

Department of Medical Intensive Care, University Hospital of Angers, Angers, France.

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