The pathophysiological impact of intra-abdominal hypertension in pigs.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2023
Historique:
received: 21 11 2022
accepted: 08 08 2023
medline: 31 8 2023
pubmed: 28 8 2023
entrez: 28 8 2023
Statut: epublish

Résumé

Intra-abdominal hypertension and abdominal compartment syndrome are common with clinically significant consequences. We investigated the pathophysiological effects of raised IAP as part of a more extensive exploratory animal study. The study design included both pneumoperitoneum and mechanical intestinal obstruction models. Forty-nine female swine were divided into six groups: a control group (Cr; n = 5), three pneumoperitoneum groups with IAPs of 20mmHg (Pn20; n = 10), 30mmHg (Pn30; n = 10), 40mmHg (Pn40; n = 10), and two mechanical intestinal occlusion groups with IAPs of 20mmHg (MIO20; n = 9) and 30mmHg (MIO30; n = 5). There were significant changes (p<0.05) noted in all organ systems, most notably systolic blood pressure (SBP) (p<0.001), cardiac index (CI) (p = 0.003), stroke volume index (SVI) (p<0.001), mean pulmonary airway pressure (MPP) (p<0.001), compliance (p<0.001), pO2 (p = 0.003), bicarbonate (p = 0.041), hemoglobin (p = 0.012), lipase (p = 0.041), total bilirubin (p = 0.041), gastric pH (p<0.001), calculated glomerular filtration rate (GFR) (p<0.001), and urine output (p<0.001). SVV increased progressively as the IAP increased with no obvious changes in intravascular volume status. There were no significant differences between the models regarding their impact on cardiovascular, respiratory, renal and gastrointestinal systems. However, significant differences were noted between the two models at 30mmHg, with MIO30 showing worse metabolic and hematological parameters, and Pn30 and Pn40 showing a more rapid rise in creatinine. This study identified and quantified the impact of intra-abdominal hypertension at different pressures on several organ systems and highlighted the significance of even short-lived elevations. Two models of intra-abdominal pressure were used, with a mechanical obstruction model showing more rapid changes in metabolic and haematological changes. These may represent different underlying cellular and vascular pathophysiological processes, but this remains unclear.

Sections du résumé

BACKGROUND
Intra-abdominal hypertension and abdominal compartment syndrome are common with clinically significant consequences. We investigated the pathophysiological effects of raised IAP as part of a more extensive exploratory animal study. The study design included both pneumoperitoneum and mechanical intestinal obstruction models.
METHODS
Forty-nine female swine were divided into six groups: a control group (Cr; n = 5), three pneumoperitoneum groups with IAPs of 20mmHg (Pn20; n = 10), 30mmHg (Pn30; n = 10), 40mmHg (Pn40; n = 10), and two mechanical intestinal occlusion groups with IAPs of 20mmHg (MIO20; n = 9) and 30mmHg (MIO30; n = 5).
RESULTS
There were significant changes (p<0.05) noted in all organ systems, most notably systolic blood pressure (SBP) (p<0.001), cardiac index (CI) (p = 0.003), stroke volume index (SVI) (p<0.001), mean pulmonary airway pressure (MPP) (p<0.001), compliance (p<0.001), pO2 (p = 0.003), bicarbonate (p = 0.041), hemoglobin (p = 0.012), lipase (p = 0.041), total bilirubin (p = 0.041), gastric pH (p<0.001), calculated glomerular filtration rate (GFR) (p<0.001), and urine output (p<0.001). SVV increased progressively as the IAP increased with no obvious changes in intravascular volume status. There were no significant differences between the models regarding their impact on cardiovascular, respiratory, renal and gastrointestinal systems. However, significant differences were noted between the two models at 30mmHg, with MIO30 showing worse metabolic and hematological parameters, and Pn30 and Pn40 showing a more rapid rise in creatinine.
CONCLUSIONS
This study identified and quantified the impact of intra-abdominal hypertension at different pressures on several organ systems and highlighted the significance of even short-lived elevations. Two models of intra-abdominal pressure were used, with a mechanical obstruction model showing more rapid changes in metabolic and haematological changes. These may represent different underlying cellular and vascular pathophysiological processes, but this remains unclear.

Identifiants

pubmed: 37639437
doi: 10.1371/journal.pone.0290451
pii: PONE-D-22-32095
pmc: PMC10461824
doi:

Substances chimiques

Bicarbonates 0
Bilirubin RFM9X3LJ49

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0290451

Informations de copyright

Copyright: © 2023 Wise et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Déclaration de conflit d'intérêts

Robert Wise: Dr. Wise declares that he has no financial or personal relationships that may have inappropriately influenced him in writing this paper. He is currently a member of the WSACS. Reitze Rodseth: Prof. Rodseth declares that he has no financial or personal relationships that may have inappropriately influenced him in writing this paper. He is supported in part by the National Research Foundation of South Africa. Ester Párraga-Ros: Prof. Párraga-Ros declares that she has no financial or personal relationships that may have inappropriately influenced him in writing this paper. Rafael Latorre: Prof. Latorre declares that he has no financial or personal relationships that may have inappropriately influenced him in writing this paper. Octavio López Albors: Prof. Lopez Albors declares that he has no financial or personal relationships that may have inappropriately influenced him in writing this paper. Laura Correa-Martín: Prof. Correa-Martín declares that he has no financial or personal relationships that may have inappropriately influenced him in writing this paper. Francisco M. Sánchez-Margallo: Prof. Sánchez-Margallo declares that he has no financial or personal relationships that may have inappropriately influenced him in writing this paper. Irma Eugenia Candanosa-Aranda: Prof. Candanosa-Aranda declares that he has no financial or personal relationships that may have inappropriately influenced him in writing this paper. Jan Poelaert: Prof. Poelaert declares that he has no financial or personal relationships that may have inappropriately influenced him in writing this paper. Gregorio Castellanos: Prof. Castellanos declares that he has no financial or personal relationships that may have inappropriately influenced him in writing this paper. Manu L. N. G. Malbrain: MLNGM is Professor of Critical Care Research at the 1st Department of Anaesthesiology and Intensive Therapy, Medical University of Lublin, Poland. He is co-founder, past-President and current Treasurer of WSACS (The Abdominal Compartment Society, http://www.wsacs.org). He is member of the medical advisory Board of Pulsion Medical Systems (part of Getinge group, Solna, Sweden), Serenno Medical, Potrero Medical, Sentinel Medical Technologies and Baxter. He consults for BBraun, Becton Dickinson, ConvaTec, Spiegelberg, and Holtech Medical, and received speaker’s fees from PeerVoice. He holds stock options for Serenno and Potrero. He is co-founder and President of the International Fluid Academy (IFA). The IFA (http://www.fluidacademy.org) is integrated within the not-for-profit charitable organization iMERiT, International Medical Education and Research Initiative, under Belgian law.

Références

Eur J Anaesthesiol. 2014 Jul;31(7):371-80
pubmed: 24625464
J Crit Care. 2015 Jun;30(3):584-8
pubmed: 25703956
Afr Health Sci. 2011 Sep;11(3):427-32
pubmed: 22275934
Acta Anaesthesiol Scand. 2002 May;46(5):552-60
pubmed: 12027850
J Am Soc Nephrol. 2011 Apr;22(4):615-21
pubmed: 21310818
Intensive Care Med. 2013 Sep;39(9):1653-5
pubmed: 23812340
Br J Haematol. 1982 Mar;50(3):509-19
pubmed: 7066203
Crit Care Res Pract. 2012;2012:763181
pubmed: 22454767
Am J Kidney Dis. 2011 Jan;57(1):159-69
pubmed: 21184922
J Appl Physiol (1985). 2000 Oct;89(4):1317-21
pubmed: 11007564
Arterioscler Thromb Vasc Biol. 2011 May;31(5):1215-8
pubmed: 21330610
PLoS One. 2016 Feb 05;11(2):e0148058
pubmed: 26849559
Lancet. 1991 Dec 7;338(8780):1409-11
pubmed: 1683417
Turk J Med Sci. 2014;44(3):360-4
pubmed: 25558633
Ann Intensive Care. 2020 Oct 1;10(1):130
pubmed: 33001288
Adv Chronic Kidney Dis. 2016 May;23(3):160-6
pubmed: 27113692
BMC Emerg Med. 2017 Mar 23;17(1):10
pubmed: 28330440
Crit Care Resusc. 2005 Dec;7(4):298-302
pubmed: 16539585
Chin J Traumatol. 2015;18(6):352-6
pubmed: 26917027
Ann Intensive Care. 2020 May 24;10(1):64
pubmed: 32449147
Joint Bone Spine. 2008 May;75(3):291-4
pubmed: 18403245
Lancet. 1992 Jan 25;339(8787):250-1
pubmed: 1346212
Int J Surg. 2015 Jul;19:67-71
pubmed: 25980395
Crit Care Med. 2009 Feb;37(2):650-8
pubmed: 19114894
Anaesthesiol Intensive Ther. 2014 Nov-Dec;46(5):433-50
pubmed: 25432560
Am J Respir Crit Care Med. 1997 Oct;156(4 Pt 1):1082-91
pubmed: 9351606
Intensive Care Med. 2008 Dec;34(12):2218-25
pubmed: 18607565
Crit Care. 2012 Oct 26;16(5):R208
pubmed: 23098278
Crit Care Med. 2012 Jun;40(6):1879-86
pubmed: 22488004
Ann Intensive Care. 2021 May 17;11(1):79
pubmed: 33999276
Thromb Res. 2007;120(1):11-3
pubmed: 17046049
J Clin Pathol. 1983 Jun;36(6):693-6
pubmed: 6343437
Crit Care Med. 2019 Apr;47(4):535-542
pubmed: 30608280
Intensive Care Med. 2013 Jul;39(7):1190-206
pubmed: 23673399
Platelets. 2009 Jun;20(4):277-81
pubmed: 19459134
Crit Care. 2016 Mar 16;20:67
pubmed: 26983963
Crit Care Med. 2008 Jun;36(6):1823-31
pubmed: 18520642
Exp Clin Cardiol. 2004 Winter;9(4):243-7
pubmed: 19641715
J Appl Physiol (1985). 1991 Jun;70(6):2611-8
pubmed: 1885456
Eur J Intern Med. 2011 Dec;22(6):e95-8
pubmed: 22075321
Crit Care. 2015 Mar 28;19:126
pubmed: 25888382
Ann Intensive Care. 2019 Apr 25;9(1):52
pubmed: 31025221
Intensive Care Med. 2004 Mar;30(3):357-71
pubmed: 14730376
Crit Care. 2011;15(1):R33
pubmed: 21247472
Crit Care. 2010;14(4):R128
pubmed: 20598125
Am J Respir Crit Care Med. 2004 Feb 15;169(4):534-41
pubmed: 14670801
Br J Anaesth. 2010 Nov;105(5):691-7
pubmed: 20693177
Clujul Med. 2015;88(2):188-95
pubmed: 26528070
Ann Intensive Care. 2012 Jul 5;2 Suppl 1:S3
pubmed: 22873419
J Trauma. 2009 Mar;66(3):713-9
pubmed: 19276743
Crit Care. 2013 Oct 21;17(5):R249
pubmed: 24144138
Biosci Trends. 2015 Apr;9(2):129-33
pubmed: 25971699
J Appl Physiol (1985). 1992 Feb;72(2):575-82
pubmed: 1559935
Anaesth Intensive Care. 2012 Jan;40(1):79-89
pubmed: 22313065

Auteurs

Robert Wise (R)

Faculty Medicine and Pharmacy, Vrije Universiteit Brussel (VUB), Brussels, Belgium.
Discipline of Anaesthesiology, and Critical Care, Nelson R Mandela School of Medicine, University of KwaZulu-Natal, Durban, South Africa.
Adult Intensive Care Unit, John Radcliffe Hospital, Oxford University Hospitals Trust, Oxford, United Kingdom.

Reitze Rodseth (R)

Discipline of Anaesthesiology, and Critical Care, Nelson R Mandela School of Medicine, University of KwaZulu-Natal, Durban, South Africa.

Ester Párraga-Ros (E)

Department of Anatomy and Comparative Pathology, Veterinary Faculty, University of Murcia, Murcia, Spain.

Rafael Latorre (R)

Department of Anatomy and Comparative Pathology, Veterinary Faculty, University of Murcia, Murcia, Spain.

Octavio López Albors (O)

Department of Anatomy and Comparative Pathology, Veterinary Faculty, University of Murcia, Murcia, Spain.

Laura Correa-Martín (L)

Laparoscopy Department Jesus Uson Minimally Invasive Surgery Centre, Caceres, Spain.

Francisco M Sánchez-Margallo (F)

Laparoscopy Department Jesus Uson Minimally Invasive Surgery Centre, Caceres, Spain.

Irma Eugenia Candanosa-Aranda (I)

Highlands Teaching and Research Farm, Faculty of Veterinary Medicine, National Autonomous University of Mexico, Queretaro. Mexico.

Jan Poelaert (J)

Faculty Medicine and Pharmacy, Vrije Universiteit Brussel (VUB), Brussels, Belgium.

Gregorio Castellanos (G)

Department of General Surgery, Virgen de la Arrixaca General University Hospital, Murcia, Spain.

Manu L N G Malbrain (M)

First Department of Anaesthesiology and Intensive Care Medicine, Medical University of Lublin, Lublin, Poland.
Medical Director (CMO), Medical Data Management, Medaman, Geel, Belgium.
International Fluid Academy, Lovenjoel, Belgium.

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