Impact of perioperative inflammation on days alive and at home after surgery.

days alive and at home delirium hospital readmission inflammation mortality surgery

Journal

BJA open
ISSN: 2772-6096
Titre abrégé: BJA Open
Pays: England
ID NLM: 9918419157906676

Informations de publication

Date de publication:
Jun 2022
Historique:
received: 20 12 2021
accepted: 01 03 2022
medline: 14 4 2022
pubmed: 14 4 2022
entrez: 17 8 2023
Statut: epublish

Résumé

Perioperative inflammation is associated with perioperative complications, including delirium, that are associated with a reduced number of postoperative days alive and at home at 90 days (DAH90). We tested whether inflammation was associated with DAH90 even when adjusting for perioperative factors, and whether inflammation independently was associated with DAH90 when adjusting for delirium. We conducted a prospective cohort study of major, non-intracranial surgical patients who were older than 65 yr ( Before adjusting for delirium, a postoperative day 1 increased IL-8 was associated with fewer DAH90 at the 0.75 quantile (β=-0.082; 95% confidence interval [CI], -0.19 to -0.006) after adjusting for demographic (age and sex) and perioperative factors (cardiovascular surgery, National Surgical Quality Improvement Program risk of death, and operative time). IL-10 was similarly associated with DAH90 at the 0.5 (β=-0.026; 95% CI, -0.19 to -0.001) and 0.75 (β= -0.035; 95% CI, -0.07 to -0.006) quantiles. Neither cytokine was significantly associated with DAH90 once delirium and baseline Trail Making Test B were added to the models. Perioperative inflammation predicts DAH90, but when delirium is added to the model inflammation loses significance as a predictor, whereas delirium is significant. Targeting perioperative inflammation may reduce delirium and moderate hospital readmission and mortality. NCT03124303.

Sections du résumé

Background UNASSIGNED
Perioperative inflammation is associated with perioperative complications, including delirium, that are associated with a reduced number of postoperative days alive and at home at 90 days (DAH90). We tested whether inflammation was associated with DAH90 even when adjusting for perioperative factors, and whether inflammation independently was associated with DAH90 when adjusting for delirium.
Methods UNASSIGNED
We conducted a prospective cohort study of major, non-intracranial surgical patients who were older than 65 yr (
Results UNASSIGNED
Before adjusting for delirium, a postoperative day 1 increased IL-8 was associated with fewer DAH90 at the 0.75 quantile (β=-0.082; 95% confidence interval [CI], -0.19 to -0.006) after adjusting for demographic (age and sex) and perioperative factors (cardiovascular surgery, National Surgical Quality Improvement Program risk of death, and operative time). IL-10 was similarly associated with DAH90 at the 0.5 (β=-0.026; 95% CI, -0.19 to -0.001) and 0.75 (β= -0.035; 95% CI, -0.07 to -0.006) quantiles. Neither cytokine was significantly associated with DAH90 once delirium and baseline Trail Making Test B were added to the models.
Conclusions UNASSIGNED
Perioperative inflammation predicts DAH90, but when delirium is added to the model inflammation loses significance as a predictor, whereas delirium is significant. Targeting perioperative inflammation may reduce delirium and moderate hospital readmission and mortality.
Clinical trial registration UNASSIGNED
NCT03124303.

Identifiants

pubmed: 37588271
doi: 10.1016/j.bjao.2022.100006
pii: S2772-6096(22)00005-3
pmc: PMC10430844
doi:

Banques de données

ClinicalTrials.gov
['NCT03124303']

Types de publication

Journal Article

Langues

eng

Pagination

100006

Informations de copyright

© 2022 The Authors.

Références

Br J Anaesth. 2021 Dec;127(6):e205-e207
pubmed: 34598782
Anesthesiology. 2019 Jul;131(1):84-93
pubmed: 31094760
Br J Anaesth. 2021 May;126(5):996-1008
pubmed: 33648701
Br J Anaesth. 2019 Dec;123(6):777-794
pubmed: 31668347
BMC Geriatr. 2019 Oct 16;19(1):272
pubmed: 31619178
Br J Anaesth. 2022 Mar;128(3):e229-e231
pubmed: 35090723
Anaesthesia. 2020 Jan;75 Suppl 1:e143-e150
pubmed: 31903564
J Am Soc Nephrol. 2015 Dec;26(12):2947-51
pubmed: 25952257
Ann Thorac Surg. 2022 Mar;113(3):1000-1007
pubmed: 33774004
J Neurosci. 2013 Sep 18;33(38):15248-58
pubmed: 24048854
Brain. 2019 Jan 1;143(1):47-54
pubmed: 31802104
EClinicalMedicine. 2019 Apr 27;11:18-26
pubmed: 31317130
BMJ. 2011 Jul 20;343:d4331
pubmed: 21775401
Br J Anaesth. 2020 Jul;125(1):55-66
pubmed: 32499013
J Vasc Surg. 2007 Jan;45(1):2-9; discussion 9
pubmed: 17123769
JAMA. 2017 Sep 26;318(12):1161-1174
pubmed: 28973626
Br J Anaesth. 2021 Apr;126(4):791-798
pubmed: 33158499
Br J Anaesth. 2018 Aug;121(2):384-397
pubmed: 30032877
Br J Anaesth. 2021 Feb;126(2):458-466
pubmed: 33228978
Br J Anaesth. 2021 Nov;127(5):e168-e170
pubmed: 34489090
JAMA. 2012 Nov 7;308(17):1761-7
pubmed: 23117776

Auteurs

David Kunkel (D)

Department of Anesthesiology, University of Wisconsin, Madison, WI, USA.

Margaret Parker (M)

Department of Anesthesiology, University of Wisconsin, Madison, WI, USA.

Cameron Casey (C)

Department of Anesthesiology, University of Wisconsin, Madison, WI, USA.

Bryan Krause (B)

Department of Anesthesiology, University of Wisconsin, Madison, WI, USA.

Jennifer Taylor (J)

Faculty of Medicine and Health, University of Sydney, Sydney, Australia.
Department of Anaesthetics, Royal Prince Alfred Hospital, Sydney Local Health District, Camperdown, NSW, Australia.

Robert A Pearce (RA)

Department of Anesthesiology, University of Wisconsin, Madison, WI, USA.

Richard Lennertz (R)

Department of Anesthesiology, University of Wisconsin, Madison, WI, USA.

Robert D Sanders (RD)

Faculty of Medicine and Health, University of Sydney, Sydney, Australia.
Department of Anaesthetics, Royal Prince Alfred Hospital, Sydney Local Health District, Camperdown, NSW, Australia.

Classifications MeSH