Effects of Hemorrhagic Shock and Rhabdomyolysis on Renal Microcirculation, Oxygenation, and Function in a Female Swine Model

Author:

Bergis Benjamin1,Laemmel Elisabeth2,Laitselart Philippe3,Isnard Pierre4,Terzi Fabiola5,Seguret Manon6,Hejl Carine7,Huertas Alice8,Decante Benoit9,Vicaut Eric10,Duranteau Jacques11,Harrois Anatole12,Libert Nicolas13ORCID

Affiliation:

1. 1Department of Anesthesia and Surgical Intensive Care, Bicetre Hospital, Paris-Saclay University, Assistance Publique -Hôpitaux de Paris, Le Kremlin-Bicetre, France; Microcirculation Laboratory, UMR 942, Paris Cité University, Paris, France; UMRS 999, Emerging Team DYNAMIC - Organ Dysfunction and Microcirculation, Paris-Saclay University, Le Kremlin-Bicetre, France.

2. 2Microcirculation Laboratory, UMR 942, Paris Cité University, Paris, France.

3. 3Microcirculation Laboratory, UMR 942, Paris Cité University, Paris, France; Department of Anesthesia and Intensive Care, Percy Military Teaching Hospital, Clamart, France.

4. 4Paris Cité University, INSERM U1151, CNRS UMR 8253, Necker Children Hospital Institute, Department “Growth and Signaling,” Paris, France; Department of Pathology, Necker Children Hospital, Assistance Publique -Hôpitaux de Paris, Paris, France.

5. 5Paris Cité University, INSERM U1151, CNRS UMR 8253, Necker Children Hospital Institute, Department “Growth and Signaling,” Paris, France; Department of Pathology, Necker Children Hospital, Assistance Publique -Hôpitaux de Paris, Paris, France.

6. 6Department of Anesthesia and Surgical Intensive Care, Bicetre Hospital, Paris-Saclay University, Assistance Publique -Hôpitaux de Paris, Le Kremlin-Bicêtre, France; Microcirculation Laboratory, UMR 942, Paris Cité University, Paris, France.

7. 7Department of Biology, Percy Military Teaching Hospital, Clamart, France.

8. 8UMRS 999, Emerging Team DYNAMIC - Organ Dysfunction and Microcirculation, Paris-Saclay University, Le Kremlin-Bicêtre, France.

9. 9Research and Innovation Unit, Marie Lannelongue Hospital, Le Plessis-Robinson, France.

10. 10Microcirculation Laboratory, UMR 942, Paris Cité University, Paris, France; Clinical Research Unit, UMR 942, Paris Cité University, Saint Louis - Lariboisière Hospital, Assistance Publique -Hôpitaux de Paris, Paris, France.

11. 11Department of Anesthesia and Surgical Intensive Care, Bicetre Hospital, Paris-Saclay University, Assistance Publique -Hôpitaux de Paris, Le Kremlin-Bicêtre, France; UMRS 999, emerging team DYNAMIC - Organ dysfunction and microcirculation, Paris-Saclay University, Le Kremlin-Bicetre, France.

12. 12Department of Anesthesia and Surgical Intensive Care, Bicetre Hospital, Paris-Saclay University, Assistance Publique–Hôpitaux de Paris, Le Kremlin-Bicêtre, France; UMRS 999, emerging team DYNAMIC– Organ dysfunction and microcirculation, Paris-Saclay University, Le Kremlin-Bicetre, France.

13. 13UMRS 999, Emerging Team DYNAMIC– Organ Dysfunction and Microcirculation, Paris-Saclay University, Le Kremlin-Bicetre, France; Department of Anesthesia and Intensive Care, Percy Military Teaching Hospital, Clamart, France; French Armed-Forces Biomedical Research Institute (IRBA), Bretigny-sur-Orge, France.

Abstract

Background Hemorrhagic shock (HS) and rhabdomyolysis (RM) are two important risk factors for acute kidney injury after severe trauma; however, the effects of the combination of RM and HS on kidney function are unknown. The purpose of this study was to determine the impact of RM and HS on renal function, oxygenation, perfusion, and morphology in a pig model. Methods Forty-seven female pigs were divided into five groups: sham, RM, HS, HS and moderate RM (RM4/HS), and HS and severe RM (RM8/HS). Rhabdomyolysis was induced by intramuscular injection of glycerol 50% with a moderate dose (4 ml/kg for the RM4/HS group) or a high dose (8 ml/kg for the RM and RM8/HS groups). Among animals with HS, after 90 min of hemorrhage, animals were resuscitated with fluid followed by transfusion of the withdrawn blood. Animals were followed for 48 h. Macro- and microcirculatory parameters measurements were performed. Results RM alone induced a decrease in creatinine clearance at 48 h (19 [0 to 41] vs. 102 [56 to 116] ml/min for RM and sham, respectively; P = 0.0006) without alteration in renal perfusion and oxygenation. Hemorrhagic shock alone impaired temporarily renal microcirculation, function, and oxygenation that were restored with fluid resuscitation. The RM4/HS and RM8/HS groups induced greater impairment of renal microcirculation and function than HS alone at the end of blood spoliation that was not improved by fluid resuscitation. Mortality was increased in the RM8/HS and RM4/HS groups in the first 48 h (73% vs. 56% vs. 9% for the RM8/HS, RM4/HS, and HS groups, respectively). Conclusions The combination of HS and RM induced an early deleterious effect on renal microcirculation, function, and oxygenation with decreased response to resuscitation and transfusion compared with HS or RM alone. Editor’s Perspective What We Already Know about This Topic What This Article Tells Us That Is New

Publisher

Ovid Technologies (Wolters Kluwer Health)

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