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 , on behalf of the Queensland Critical Care Research Network (QCCRN) and the SODa-BIC investigators
{"title":"代谢性酸中毒重症患者轻度高碳酸血症的影响。","authors":"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 , on behalf of the Queensland Critical Care Research Network (QCCRN) and the SODa-BIC investigators","doi":"10.1016/j.jcrc.2024.154936","DOIUrl":null,"url":null,"abstract":"<div><h3>Purpose</h3><div>Clinical trials focusing on critically ill patients with metabolic acidosis, a common exclusion criterion is the presence of a PaCO<sub>2</sub> > 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.</div></div><div><h3>Material and methods</h3><div>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 PaCO<sub>2</sub> level at the time of meeting the eligibility criteria divided in two groups: PaCO<sub>2</sub> ≤ 45 mmHg and PaCO<sub>2</sub> 46–50 mmHg. Primary clinical outcome was major adverse kidney events within 30 days (MAKE30).</div></div><div><h3>Results</h3><div>We studied 5601 patients, with 3605 (64.4 %) in the PaCO<sub>2</sub> ≤ 45 mmHg group and 1996 (35.6 %) in the PaCO<sub>2</sub> 46–50 mmHg group. The incidence of MAKE30 was lower in the PaCO<sub>2</sub> 46–50 mmHg group (29 % vs. 34 %; OR, 0.79 [95 %CI, 0.69 to 0.90]; <em>p</em> < 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 PaCO<sub>2</sub> in the PaCO<sub>2</sub> 46–50 mmHg group was 0.006.</div></div><div><h3>Conclusion</h3><div>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.</div></div>","PeriodicalId":15451,"journal":{"name":"Journal of critical care","volume":"85 ","pages":"Article 154936"},"PeriodicalIF":3.2000,"publicationDate":"2024-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Impact of mild hypercapnia in critically ill patients with metabolic acidosis\",\"authors\":\"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 , on behalf of the Queensland Critical Care Research Network (QCCRN) and the SODa-BIC investigators\",\"doi\":\"10.1016/j.jcrc.2024.154936\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Purpose</h3><div>Clinical trials focusing on critically ill patients with metabolic acidosis, a common exclusion criterion is the presence of a PaCO<sub>2</sub> > 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.</div></div><div><h3>Material and methods</h3><div>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 PaCO<sub>2</sub> level at the time of meeting the eligibility criteria divided in two groups: PaCO<sub>2</sub> ≤ 45 mmHg and PaCO<sub>2</sub> 46–50 mmHg. Primary clinical outcome was major adverse kidney events within 30 days (MAKE30).</div></div><div><h3>Results</h3><div>We studied 5601 patients, with 3605 (64.4 %) in the PaCO<sub>2</sub> ≤ 45 mmHg group and 1996 (35.6 %) in the PaCO<sub>2</sub> 46–50 mmHg group. The incidence of MAKE30 was lower in the PaCO<sub>2</sub> 46–50 mmHg group (29 % vs. 34 %; OR, 0.79 [95 %CI, 0.69 to 0.90]; <em>p</em> < 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 PaCO<sub>2</sub> in the PaCO<sub>2</sub> 46–50 mmHg group was 0.006.</div></div><div><h3>Conclusion</h3><div>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.</div></div>\",\"PeriodicalId\":15451,\"journal\":{\"name\":\"Journal of critical care\",\"volume\":\"85 \",\"pages\":\"Article 154936\"},\"PeriodicalIF\":3.2000,\"publicationDate\":\"2024-10-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of critical care\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0883944124004234\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CRITICAL CARE MEDICINE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of critical care","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0883944124004234","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CRITICAL CARE MEDICINE","Score":null,"Total":0}
Impact of mild hypercapnia in critically ill patients with metabolic acidosis
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.
期刊介绍:
The Journal of Critical Care, the official publication of the World Federation of Societies of Intensive and Critical Care Medicine (WFSICCM), is a leading international, peer-reviewed journal providing original research, review articles, tutorials, and invited articles for physicians and allied health professionals involved in treating the critically ill. The Journal aims to improve patient care by furthering understanding of health systems research and its integration into clinical practice.
The Journal will include articles which discuss:
All aspects of health services research in critical care
System based practice in anesthesiology, perioperative and critical care medicine
The interface between anesthesiology, critical care medicine and pain
Integrating intraoperative management in preparation for postoperative critical care management and recovery
Optimizing patient management, i.e., exploring the interface between evidence-based principles or clinical insight into management and care of complex patients
The team approach in the OR and ICU
System-based research
Medical ethics
Technology in medicine
Seminars discussing current, state of the art, and sometimes controversial topics in anesthesiology, critical care medicine, and professional education
Residency Education.