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Impact of mild hypercapnia in critically ill patients with metabolic acidosis

  • Ary Serpa Neto
  • , Ahmad Nasser
  • , Prashanti Marella
  • , Tomoko Fujii
  • , Kazunari Takahashi
  • , Kevin Laupland
  • , Alexis Tabah
  • , Antony G. Attokaran
  • , Aashish Kumar
  • , James McCullough
  • , Kiran Shekar
  • , Peter Garrett
  • , Sebastiaan Blank
  • , Siva Senthuran
  • , Stephen Luke
  • , Mairead McNamara
  • , Rinaldo Bellomo
  • , Kyle White*
  • *Corresponding author for this work
  • Monash University
  • Austin Health
  • University of Melbourne
  • Queen Elizabeth II Jubilee Hospital
  • University of Queensland
  • Caboolture Hospital
  • The Jikei University School of Medicine
  • Queensland University of Technology
  • Royal Brisbane and Women's Hospital
  • Queensland Health
  • Rockhampton Hospital
  • Logan Hospital
  • Griffith University Queensland
  • Sunshine Coast University Hospital
  • James Cook University Queensland
  • Townsville University Hospital
  • Princess Alexandra Hospital

Research output: Contribution to journal › Article › Academic › peer-review

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Abstract

Purpose: Clinical trials focusing on critically ill patients with metabolic acidosis, a common exclusion criterion is the presence of a PaCO2 > 45 mmHg. The aim of this study was to assess the impact of mild hypercapnia on patient characteristics, severity, and clinical outcomes in critically ill patients with metabolic acidosis. Material and methods: Multicentre, retrospective, observational study conducted in 12 intensive care units (ICUs) in Queensland, Australia. Patients with metabolic acidosis and concurrent vasopressor requirement were included and the exposure of interest was the PaCO2 level at the time of meeting the eligibility criteria divided in two groups: PaCO2 ≤ 45 mmHg and PaCO2 46–50 mmHg. Primary clinical outcome was major adverse kidney events within 30 days (MAKE30). Results: We studied 5601 patients, with 3605 (64.4 %) in the PaCO2 ≤ 45 mmHg group and 1996 (35.6 %) in the PaCO2 46–50 mmHg group. The incidence of MAKE30 was lower in the PaCO2 46–50 mmHg group (29 % vs. 34 %; OR, 0.79 [95 %CI, 0.69 to 0.90]; p < 0.001) as was the use of renal replacement therapy, and the incidence of acute kidney injury. After adjustment for confounders, no outcome was different between the groups. The maximum fall of pH associated with an increase of 1 mmHg of PaCO2 in the PaCO2 46–50 mmHg group was 0.006. Conclusion: In patients with metabolic acidosis, after adjustment for potential confounders, mild hypercapnia does not increase the MAKE-30 rate and does not have a major impact on pH.

Original languageEnglish
Article number154936
JournalJournal of critical care
Volume85
DOIs
Publication statusPublished - 1 Feb 2025
Externally publishedYes

Keywords

  • Metabolic acidosis
  • clinical trials
  • hypercapnia
  • mortality

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