A comparison of intraoperative goal-directed intravenous administration of crystalloid versus colloid solutions on the postoperative maximum N-terminal pro brain natriuretic peptide in patients undergoing moderate- to high-risk noncardiac surgery.


Journal

BMC anesthesiology
ISSN: 1471-2253
Titre abrégé: BMC Anesthesiol
Pays: England
ID NLM: 100968535

Informations de publication

Date de publication:
04 08 2020
Historique:
received: 21 03 2020
accepted: 22 07 2020
entrez: 6 8 2020
pubmed: 6 8 2020
medline: 24 9 2021
Statut: epublish

Résumé

N-terminal pro brain natriuretic peptide (NT-proBNP) and troponin T are released during myocardial wall stress and/or ischemia and are strong predictors for postoperative cardiovascular complications. However, the relative effects of goal-directed, intravenous administration of crystalloid compared to colloid solutions on NT-proBNP and troponin T, especially in relatively healthy patients undergoing moderate- to high-risk noncardiac surgery, remains unclear. Thus, we evaluated in this sub-study the effect of a goal-directed crystalloid versus a goal-directed colloid fluid regimen on postoperative maximum NT-proBNP concentration. We further evaluated the incidence of myocardial injury after noncardiac surgery (MINS) between both study groups. Thirty patients were randomly assigned to receive additional intravenous fluid boluses of 6% hydroxyethyl starch 130/0.4 and 30 patients to receive lactated Ringer's solution. Intraoperative fluid management was guided by oesophageal Doppler-according to a previously published algorithm. The primary outcome were differences in postoperative maximum NT-proBNP (maxNT-proBNP) between both groups. As our secondary outcome we evaluated the incidence of MINS between both study groups. We defined maxNT-proBNP as the maximum value measured within 2 h after surgery and on the first and second postoperative day. In total 56 patients were analysed. There was no significant difference in postoperative maximum NT-proBNP between the colloid group (258.7 ng/L (IQR 199.4 to 782.1)) and the crystalloid group (440.3 ng/L (IQR 177.9 to 691.2)) during the first 2 postoperative days (P = 0.29). Five patients in the colloid group and 7 patients in the crystalloid group developed MINS (P = 0.75). Based on this relatively small study goal-directed colloid administration did not decrease postoperative maxNT-proBNP concentration as compared to goal-directed crystalloid administration. ClinicalTrials.gov ( NCT01195883 ) Registered on 6th September 2010.

Sections du résumé

BACKGROUND
N-terminal pro brain natriuretic peptide (NT-proBNP) and troponin T are released during myocardial wall stress and/or ischemia and are strong predictors for postoperative cardiovascular complications. However, the relative effects of goal-directed, intravenous administration of crystalloid compared to colloid solutions on NT-proBNP and troponin T, especially in relatively healthy patients undergoing moderate- to high-risk noncardiac surgery, remains unclear. Thus, we evaluated in this sub-study the effect of a goal-directed crystalloid versus a goal-directed colloid fluid regimen on postoperative maximum NT-proBNP concentration. We further evaluated the incidence of myocardial injury after noncardiac surgery (MINS) between both study groups.
METHODS
Thirty patients were randomly assigned to receive additional intravenous fluid boluses of 6% hydroxyethyl starch 130/0.4 and 30 patients to receive lactated Ringer's solution. Intraoperative fluid management was guided by oesophageal Doppler-according to a previously published algorithm. The primary outcome were differences in postoperative maximum NT-proBNP (maxNT-proBNP) between both groups. As our secondary outcome we evaluated the incidence of MINS between both study groups. We defined maxNT-proBNP as the maximum value measured within 2 h after surgery and on the first and second postoperative day.
RESULTS
In total 56 patients were analysed. There was no significant difference in postoperative maximum NT-proBNP between the colloid group (258.7 ng/L (IQR 199.4 to 782.1)) and the crystalloid group (440.3 ng/L (IQR 177.9 to 691.2)) during the first 2 postoperative days (P = 0.29). Five patients in the colloid group and 7 patients in the crystalloid group developed MINS (P = 0.75).
CONCLUSIONS
Based on this relatively small study goal-directed colloid administration did not decrease postoperative maxNT-proBNP concentration as compared to goal-directed crystalloid administration.
TRIAL REGISTRATION
ClinicalTrials.gov ( NCT01195883 ) Registered on 6th September 2010.

Identifiants

pubmed: 32753064
doi: 10.1186/s12871-020-01104-9
pii: 10.1186/s12871-020-01104-9
pmc: PMC7405415
doi:

Substances chimiques

Colloids 0
Crystalloid Solutions 0
Hydroxyethyl Starch Derivatives 0
Peptide Fragments 0
Ringer's Lactate 0
Troponin T 0
pro-brain natriuretic peptide (1-76) 0
Natriuretic Peptide, Brain 114471-18-0

Banques de données

ClinicalTrials.gov
['NCT01195883']
EudraCT
['2005–004602-86']

Types de publication

Comparative Study Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

192

Références

Eur Heart J. 2007 Jul;28(14):1678-82
pubmed: 17569679
Anesthesiology. 2017 Jan;126(1):47-65
pubmed: 27792044
BMJ. 1997 Oct 11;315(7113):909-12
pubmed: 9361539
Br J Anaesth. 2014 Feb;112(2):281-9
pubmed: 24056586
Anesthesiology. 2019 May;130(5):728-744
pubmed: 30882476
Br J Surg. 2006 Sep;93(9):1069-76
pubmed: 16888706
Circulation. 1996 Jun 1;93(11):1946-50
pubmed: 8640966
Anaesthesia. 2018 Oct;73(10):1223-1228
pubmed: 30144029
Anesth Analg. 2015 Feb;120(2):389-402
pubmed: 25565318
Anesthesiology. 2013 Aug;119(2):270-83
pubmed: 23528538
Crit Care. 2013 Mar 05;17(2):209
pubmed: 23672779
Am J Hosp Pharm. 1983 Jun;40(6):1016-9
pubmed: 6869387
Br J Anaesth. 2018 Apr;120(4):734-744
pubmed: 29576114
Br J Anaesth. 2002 Oct;89(4):622-32
pubmed: 12393365
J Am Coll Cardiol. 2014 Jan 21;63(2):170-80
pubmed: 24076282
Anesthesiology. 2018 Jan;128(1):55-66
pubmed: 29068831
Anesthesiology. 2014 Mar;120(3):564-78
pubmed: 24534856
J Am Coll Cardiol. 2009 Oct 20;54(17):1599-606
pubmed: 19833258
Can J Cardiol. 2017 Jan;33(1):17-32
pubmed: 27865641
Anesthesiology. 2019 Apr;130(4):550-559
pubmed: 30875354
Am J Physiol Heart Circ Physiol. 2011 Jul;301(1):H12-20
pubmed: 21551272
Anaesthesia. 2009 Feb;64(2):165-78
pubmed: 19143695
Anesthesiology. 2002 Oct;97(4):820-6
pubmed: 12357146
JAMA. 2017 Apr 25;317(16):1642-1651
pubmed: 28444280
Anesthesiology. 2018 Feb;128(2):317-327
pubmed: 29189290
JAMA. 2012 Jun 6;307(21):2295-304
pubmed: 22706835
Crit Care Med. 1990 Jul;18(7):728-33
pubmed: 2364713
J Am Coll Surg. 2012 May;214(5):778-87
pubmed: 22440057

Auteurs

Christian Reiterer (C)

Department of Anaesthesia, Intensive Care Medicine and Pain Medicine, Medical University of Vienna, Spitalgasse 23, 1090, Vienna, Austria.

Barbara Kabon (B)

Department of Anaesthesia, Intensive Care Medicine and Pain Medicine, Medical University of Vienna, Spitalgasse 23, 1090, Vienna, Austria. barbara.kabon@meduniwien.ac.at.

Alexander Taschner (A)

Department of Anaesthesia, Intensive Care Medicine and Pain Medicine, Medical University of Vienna, Spitalgasse 23, 1090, Vienna, Austria.

Oliver Zotti (O)

Department of Anaesthesia, Intensive Care Medicine and Pain Medicine, Medical University of Vienna, Spitalgasse 23, 1090, Vienna, Austria.

Andrea Kurz (A)

Department of Outcomes Research and General Anaesthesiology, Anaesthesiology Institute, Cleveland Clinic, Cleveland, OH, USA.

Edith Fleischmann (E)

Department of Anaesthesia, Intensive Care Medicine and Pain Medicine, Medical University of Vienna, Spitalgasse 23, 1090, Vienna, Austria.

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Classifications MeSH