Timing of invasive mechanical ventilation in patients with sepsis: the impact of excluding non-intubated patients

IF 8.8 1区 医学 Q1 CRITICAL CARE MEDICINE Critical Care Pub Date : 2024-12-18 DOI:10.1186/s13054-024-05208-3
Yun Ji, Libin Li
{"title":"Timing of invasive mechanical ventilation in patients with sepsis: the impact of excluding non-intubated patients","authors":"Yun Ji, Libin Li","doi":"10.1186/s13054-024-05208-3","DOIUrl":null,"url":null,"abstract":"<p>Dear Editor,</p><p>Early initiation of invasive mechanical ventilation (IMV) may represent a potentially beneficial approach for sepsis patients [1]. A recent study by Kim et al. [2], published in <i>Critical Care</i>, provides evidence supporting this approach, reporting that earlier IMV initiation (on the first day of ICU admission) may be associated with lower mortality.</p><p>However, in their study, 2,363 patients who never required IMV during their ICU stay were excluded from the analysis. While this approach focuses on patients who received IMV, it may inadvertently select a population with more severe illness for comparison, potentially introducing bias into the results. In clinical practice, a subset of sepsis patients may benefit from a wait-and-see strategy, where intubation is avoided through the use of non-invasive ventilation or other supportive measures, potentially reducing the risks associated with IMV. Excluding these patients from the analysis may have influenced the reported outcomes and the perceived benefits of early IMV.</p><p>To better illustrate this issue, we conducted an analysis of sepsis patients using the Medical Information Mart for Intensive Care (MIMIC)-IV database [3] (refer to Additional file 1: Supplemental methods). Among 24,518 ICU patients with sepsis, 12,654 received IMV on the first day of ICU admission (early IMV group). Of the remaining 11,864 patients (non-early IMV group), 1,217 eventually required IMV later during their ICU stay (delayed IMV group), while the rest did not receive IMV during their ICU stay (Additional file 1: Fig. S1).</p><p>First, we compared the early IMV group and the non-early IMV group. Propensity score matching (PSM) improved the balance of baseline characteristics between the two groups, achieving an absolute standardized mean difference (SMD) &lt; 0.10 (Additional file 1: Table S1). After matching, the 90-day mortality rate was 23.3% (1,413/6,067) in the early IMV group and 28.5% (1,731/6,067) in the non-early IMV group. The Kaplan–Meier curve for 90-day mortality in the matched cohort is shown in Fig. 1A. Early IMV was associated with lower 90-day mortality in both univariable analysis (hazard ratio [HR], 0.79; 95% confidence interval (CI), 0.74–0.85; <i>P</i> &lt; 0.001) and multivariable analysis (HR, 0.77; 95% CI, 0.72–0.83; <i>P</i> &lt; 0.001).</p><figure><figcaption><b data-test=\"figure-caption-text\">Fig. 1</b></figcaption><picture><source srcset=\"//media.springernature.com/lw685/springer-static/image/art%3A10.1186%2Fs13054-024-05208-3/MediaObjects/13054_2024_5208_Fig1_HTML.png?as=webp\" type=\"image/webp\"/><img alt=\"figure 1\" aria-describedby=\"Fig1\" height=\"1097\" loading=\"lazy\" src=\"//media.springernature.com/lw685/springer-static/image/art%3A10.1186%2Fs13054-024-05208-3/MediaObjects/13054_2024_5208_Fig1_HTML.png\" width=\"685\"/></picture><p>Kaplan–Meier curves for 90-day mortality based on the timing of IMV in the matched cohort. <b>A</b> Comparison between the early IMV group and the non-early IMV group (including patients who did not receive IMV during their ICU stay). The multivariable Cox proportional hazards model was adjusted for weight, mean arterial pressure, temperature, and GCS, which were identified as statistically significant in the univariable analysis (<i>P</i> &lt; 0.05) (Table S1). <b>B</b> Comparison between the early IMV group and the delayed IMV group (excluding patients who did not receive IMV during their ICU stay). The multivariable Cox proportional hazards model was adjusted for temperature and GCS, which were identified as statistically significant in the univariable analysis (<i>P</i> &lt; 0.05) (Table S2). CI, confidence interval; GCS, Glasgow coma scale; IMV, invasive mechanical ventilation</p><span>Full size image</span><svg aria-hidden=\"true\" focusable=\"false\" height=\"16\" role=\"img\" width=\"16\"><use xlink:href=\"#icon-eds-i-chevron-right-small\" xmlns:xlink=\"http://www.w3.org/1999/xlink\"></use></svg></figure><p>Next, we compared the early IMV group and the delayed IMV group. Similarly, PSM improved the balance of baseline characteristics between the two groups (absolute SMD &lt; 0.10; Additional file 1: Table S2). After matching, the 90-day mortality rate was 27.1% (302/1,116) in the early IMV group and 45.3% (505/1,116) in the delayed IMV group. The Kaplan–Meier curve for 90-day mortality in the matched cohort is shown in Fig. 1B. Early IMV was associated with significantly lower 90-day mortality in both univariable analysis (HR, 0.53; 95% CI, 0.46–0.61;<i> P</i> &lt; 0.001) and multivariable analysis (HR, 0.52; 95% CI, 0.45–0.60; <i>P</i> &lt; 0.001).</p><p>Our findings demonstrate that early IMV is associated with lower mortality, aligning with the results reported by Kim et al. [2]. However, as shown in Fig. 1, the exclusion of patients who never received IMV during their ICU stay may lead to an overestimation of the mortality benefits associated with early IMV. Thus, we believe that including the 2,363 patients who did not receive IMV during their ICU stay could provide a more comprehensive understanding of the mortality benefits associated with early IMV and potentially refine the findings of Kim et al.’s study [2].</p><p>The datasets presented in the current study are available in the MIMIC-IV database (https://mimic.mit.edu/).</p><dl><dt style=\"min-width:50px;\"><dfn>CI:</dfn></dt><dd>\n<p>Confidence interval</p>\n</dd><dt style=\"min-width:50px;\"><dfn>HR:</dfn></dt><dd>\n<p>Hazard ratio</p>\n</dd><dt style=\"min-width:50px;\"><dfn>ICU:</dfn></dt><dd>\n<p>Intensive care unit</p>\n</dd><dt style=\"min-width:50px;\"><dfn>MIMIC:</dfn></dt><dd>\n<p>Medical information mart for intensive care</p>\n</dd><dt style=\"min-width:50px;\"><dfn>IMV:</dfn></dt><dd>\n<p>Invasive mechanical ventilation</p>\n</dd><dt style=\"min-width:50px;\"><dfn>PSM:</dfn></dt><dd>\n<p>Propensity score matching</p>\n</dd><dt style=\"min-width:50px;\"><dfn>SMD:</dfn></dt><dd>\n<p>Standardized mean difference</p>\n</dd></dl><ol data-track-component=\"outbound reference\" data-track-context=\"references section\"><li data-counter=\"1.\"><p>Lee KG, Roca O, Casey JD, Semler MW, Roman-Sarita G, Yarnell CJ, Goligher EC. When to intubate in acute hypoxaemic respiratory failure? Options and opportunities for evidence-informed decision making in the intensive care unit. Lancet Respir Med. 2024;12(8):642–54.</p><p>Article PubMed Google Scholar </p></li><li data-counter=\"2.\"><p>Kim G, Oh DK, Lee SY, Park MH, Lim CM. Impact of the timing of invasive mechanical ventilation in patients with sepsis: a multicenter cohort study. Crit Care. 2024;28(1):297.</p><p>Article PubMed PubMed Central Google Scholar </p></li><li data-counter=\"3.\"><p>Johnson AEW, Bulgarelli L, Shen L, Gayles A, Shammout A, Horng S, Pollard TJ, Hao S, Moody B, Gow B, et al. MIMIC-IV, a freely accessible electronic health record dataset. Sci Data. 2023;10(1):1.</p><p>Article CAS PubMed PubMed Central Google Scholar </p></li></ol><p>Download references<svg aria-hidden=\"true\" focusable=\"false\" height=\"16\" role=\"img\" width=\"16\"><use xlink:href=\"#icon-eds-i-download-medium\" xmlns:xlink=\"http://www.w3.org/1999/xlink\"></use></svg></p><p>Not applicable.</p><p>This work was supported by Natural Science Foundation of Zhejiang Province (grant No. LQ22H150001).</p><h3>Authors and Affiliations</h3><ol><li><p>Department of Surgical Intensive Care Unit, the Second Affiliated Hospital, School of Medicine, Zhejiang University, 88 Jiefang Road, Hangzhou, Zhejiang, China</p><p>Yun Ji &amp; Libin Li</p></li></ol><span>Authors</span><ol><li><span>Yun Ji</span>View author publications<p>You can also search for this author in <span>PubMed<span> </span>Google Scholar</span></p></li><li><span>Libin Li</span>View author publications<p>You can also search for this author in <span>PubMed<span> </span>Google Scholar</span></p></li></ol><h3>Contributions</h3><p>YJ extracted the data and performed the statistical analyses. YJ and LL participated in the discussion and wrote the manuscript.</p><h3>Corresponding author</h3><p>Correspondence to Yun Ji.</p><h3>Ethics approval and consent to participate</h3>\n<p>The establishment of this database was approved by the Massachusetts Institute of Technology (Cambridge, MA) and Beth Israel Deaconess Medical Center (Boston, MA) and consent was obtained for the original data collection. Therefore, the ethical approval statement and the need for informed consent were waived for this manuscript.</p>\n<h3>Consent for publication</h3>\n<p>Not applicable.</p>\n<h3>Competing interests</h3>\n<p>The authors declare no competing interests.</p><h3>Publisher's Note</h3><p>Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.</p><h3>Additional file1 (DOCX 192 KB)</h3><p><b>Open Access</b> This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.</p>\n<p>Reprints and permissions</p><img alt=\"Check for updates. 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Timing of invasive mechanical ventilation in patients with sepsis: the impact of excluding non-intubated patients. <i>Crit Care</i> <b>28</b>, 415 (2024). https://doi.org/10.1186/s13054-024-05208-3</p><p>Download citation<svg aria-hidden=\"true\" focusable=\"false\" height=\"16\" role=\"img\" width=\"16\"><use xlink:href=\"#icon-eds-i-download-medium\" xmlns:xlink=\"http://www.w3.org/1999/xlink\"></use></svg></p><ul data-test=\"publication-history\"><li><p>Received<span>: </span><span><time datetime=\"2024-12-01\">01 December 2024</time></span></p></li><li><p>Accepted<span>: </span><span><time datetime=\"2024-12-06\">06 December 2024</time></span></p></li><li><p>Published<span>: </span><span><time datetime=\"2024-12-18\">18 December 2024</time></span></p></li><li><p>DOI</abbr><span>: </span><span>https://doi.org/10.1186/s13054-024-05208-3</span></p></li></ul><h3>Share this article</h3><p>Anyone you share the following link with will be able to read this content:</p><button data-track=\"click\" data-track-action=\"get shareable link\" data-track-external=\"\" data-track-label=\"button\" type=\"button\">Get shareable link</button><p>Sorry, a shareable link is not currently available for this article.</p><p data-track=\"click\" data-track-action=\"select share url\" data-track-label=\"button\"></p><button data-track=\"click\" data-track-action=\"copy share url\" data-track-external=\"\" data-track-label=\"button\" type=\"button\">Copy to clipboard</button><p> Provided by the Springer Nature SharedIt content-sharing initiative </p>","PeriodicalId":10811,"journal":{"name":"Critical Care","volume":"22 1","pages":""},"PeriodicalIF":8.8000,"publicationDate":"2024-12-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Critical Care","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1186/s13054-024-05208-3","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CRITICAL CARE MEDICINE","Score":null,"Total":0}
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Abstract

Dear Editor,

Early initiation of invasive mechanical ventilation (IMV) may represent a potentially beneficial approach for sepsis patients [1]. A recent study by Kim et al. [2], published in Critical Care, provides evidence supporting this approach, reporting that earlier IMV initiation (on the first day of ICU admission) may be associated with lower mortality.

However, in their study, 2,363 patients who never required IMV during their ICU stay were excluded from the analysis. While this approach focuses on patients who received IMV, it may inadvertently select a population with more severe illness for comparison, potentially introducing bias into the results. In clinical practice, a subset of sepsis patients may benefit from a wait-and-see strategy, where intubation is avoided through the use of non-invasive ventilation or other supportive measures, potentially reducing the risks associated with IMV. Excluding these patients from the analysis may have influenced the reported outcomes and the perceived benefits of early IMV.

To better illustrate this issue, we conducted an analysis of sepsis patients using the Medical Information Mart for Intensive Care (MIMIC)-IV database [3] (refer to Additional file 1: Supplemental methods). Among 24,518 ICU patients with sepsis, 12,654 received IMV on the first day of ICU admission (early IMV group). Of the remaining 11,864 patients (non-early IMV group), 1,217 eventually required IMV later during their ICU stay (delayed IMV group), while the rest did not receive IMV during their ICU stay (Additional file 1: Fig. S1).

First, we compared the early IMV group and the non-early IMV group. Propensity score matching (PSM) improved the balance of baseline characteristics between the two groups, achieving an absolute standardized mean difference (SMD) < 0.10 (Additional file 1: Table S1). After matching, the 90-day mortality rate was 23.3% (1,413/6,067) in the early IMV group and 28.5% (1,731/6,067) in the non-early IMV group. The Kaplan–Meier curve for 90-day mortality in the matched cohort is shown in Fig. 1A. Early IMV was associated with lower 90-day mortality in both univariable analysis (hazard ratio [HR], 0.79; 95% confidence interval (CI), 0.74–0.85; P < 0.001) and multivariable analysis (HR, 0.77; 95% CI, 0.72–0.83; P < 0.001).

Fig. 1
Abstract Image

Kaplan–Meier curves for 90-day mortality based on the timing of IMV in the matched cohort. A Comparison between the early IMV group and the non-early IMV group (including patients who did not receive IMV during their ICU stay). The multivariable Cox proportional hazards model was adjusted for weight, mean arterial pressure, temperature, and GCS, which were identified as statistically significant in the univariable analysis (P < 0.05) (Table S1). B Comparison between the early IMV group and the delayed IMV group (excluding patients who did not receive IMV during their ICU stay). The multivariable Cox proportional hazards model was adjusted for temperature and GCS, which were identified as statistically significant in the univariable analysis (P < 0.05) (Table S2). CI, confidence interval; GCS, Glasgow coma scale; IMV, invasive mechanical ventilation

Full size image

Next, we compared the early IMV group and the delayed IMV group. Similarly, PSM improved the balance of baseline characteristics between the two groups (absolute SMD < 0.10; Additional file 1: Table S2). After matching, the 90-day mortality rate was 27.1% (302/1,116) in the early IMV group and 45.3% (505/1,116) in the delayed IMV group. The Kaplan–Meier curve for 90-day mortality in the matched cohort is shown in Fig. 1B. Early IMV was associated with significantly lower 90-day mortality in both univariable analysis (HR, 0.53; 95% CI, 0.46–0.61; P < 0.001) and multivariable analysis (HR, 0.52; 95% CI, 0.45–0.60; P < 0.001).

Our findings demonstrate that early IMV is associated with lower mortality, aligning with the results reported by Kim et al. [2]. However, as shown in Fig. 1, the exclusion of patients who never received IMV during their ICU stay may lead to an overestimation of the mortality benefits associated with early IMV. Thus, we believe that including the 2,363 patients who did not receive IMV during their ICU stay could provide a more comprehensive understanding of the mortality benefits associated with early IMV and potentially refine the findings of Kim et al.’s study [2].

The datasets presented in the current study are available in the MIMIC-IV database (https://mimic.mit.edu/).

CI:

Confidence interval

HR:

Hazard ratio

ICU:

Intensive care unit

MIMIC:

Medical information mart for intensive care

IMV:

Invasive mechanical ventilation

PSM:

Propensity score matching

SMD:

Standardized mean difference

  1. Lee KG, Roca O, Casey JD, Semler MW, Roman-Sarita G, Yarnell CJ, Goligher EC. When to intubate in acute hypoxaemic respiratory failure? Options and opportunities for evidence-informed decision making in the intensive care unit. Lancet Respir Med. 2024;12(8):642–54.

    Article PubMed Google Scholar

  2. Kim G, Oh DK, Lee SY, Park MH, Lim CM. Impact of the timing of invasive mechanical ventilation in patients with sepsis: a multicenter cohort study. Crit Care. 2024;28(1):297.

    Article PubMed PubMed Central Google Scholar

  3. Johnson AEW, Bulgarelli L, Shen L, Gayles A, Shammout A, Horng S, Pollard TJ, Hao S, Moody B, Gow B, et al. MIMIC-IV, a freely accessible electronic health record dataset. Sci Data. 2023;10(1):1.

    Article CAS PubMed PubMed Central Google Scholar

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Not applicable.

This work was supported by Natural Science Foundation of Zhejiang Province (grant No. LQ22H150001).

Authors and Affiliations

  1. Department of Surgical Intensive Care Unit, the Second Affiliated Hospital, School of Medicine, Zhejiang University, 88 Jiefang Road, Hangzhou, Zhejiang, China

    Yun Ji & Libin Li

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Contributions

YJ extracted the data and performed the statistical analyses. YJ and LL participated in the discussion and wrote the manuscript.

Corresponding author

Correspondence to Yun Ji.

Ethics approval and consent to participate

The establishment of this database was approved by the Massachusetts Institute of Technology (Cambridge, MA) and Beth Israel Deaconess Medical Center (Boston, MA) and consent was obtained for the original data collection. Therefore, the ethical approval statement and the need for informed consent were waived for this manuscript.

Consent for publication

Not applicable.

Competing interests

The authors declare no competing interests.

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Ji, Y., Li, L. Timing of invasive mechanical ventilation in patients with sepsis: the impact of excluding non-intubated patients. Crit Care 28, 415 (2024). https://doi.org/10.1186/s13054-024-05208-3

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脓毒症患者有创机械通气的时机:排除非插管患者的影响
亲爱的编辑,早期启动有创机械通气(IMV)可能是对脓毒症患者有益的方法[1]。Kim 等人最近在《重症监护》(Critical Care)杂志上发表的一项研究[2]提供了支持这种方法的证据,报告称较早启动 IMV(在入住 ICU 的第一天)可能与较低的死亡率有关。然而,在他们的研究中,2363 名在入住 ICU 期间从未需要 IMV 的患者被排除在分析之外。虽然这种方法侧重于接受 IMV 的患者,但可能会无意中选择病情更严重的人群进行比较,从而可能给结果带来偏差。在临床实践中,一部分脓毒症患者可能会从观望策略中获益,即通过使用无创通气或其他支持性措施避免插管,从而降低与 IMV 相关的风险。为了更好地说明这一问题,我们使用重症监护医学信息市场(MIMIC)-IV 数据库[3]对脓毒症患者进行了分析(参见附加文件 1:补充方法)。在 24,518 名 ICU 败血症患者中,12,654 人在入住 ICU 的第一天就接受了 IMV(早期 IMV 组)。在剩余的 11864 名患者(非早期 IMV 组)中,有 1217 名患者在入住 ICU 后最终需要接受 IMV(延迟 IMV 组),其余患者在入住 ICU 期间没有接受 IMV(附加文件 1:图 S1)。首先,我们比较了早期 IMV 组和非早期 IMV 组。倾向评分匹配(PSM)改善了两组间基线特征的平衡,绝对标准化均值差异(SMD)为 0.10(附加文件 1:表 S1)。匹配后,早期 IMV 组的 90 天死亡率为 23.3%(1,413/6,067),非早期 IMV 组为 28.5%(1,731/6,067)。配对队列的 90 天死亡率 Kaplan-Meier 曲线见图 1A。在单变量分析(危险比 [HR],0.79;95% 置信区间 (CI),0.74-0.85;P &lt;0.001)和多变量分析(HR,0.77;95% CI,0.72-0.83;P &lt;0.001)中,早期 IMV 与较低的 90 天死亡率相关。A 早期IMV组与非早期IMV组(包括在ICU住院期间未接受IMV的患者)之间的比较。多变量 Cox 比例危险模型对体重、平均动脉压、体温和 GCS 进行了调整,这些因素在单变量分析中具有统计学意义(P &lt; 0.05)(表 S1)。B 早期 IMV 组与延迟 IMV 组的比较(不包括在重症监护病房住院期间未接受 IMV 的患者)。多变量 Cox 比例危险模型对体温和 GCS 进行了调整,这两项指标在单变量分析中具有统计学意义(P &lt; 0.05)(表 S2)。CI,置信区间;GCS,格拉斯哥昏迷量表;IMV,有创机械通气全尺寸图片接下来,我们比较了早期 IMV 组和延迟 IMV 组。同样,PSM 改善了两组之间基线特征的平衡(绝对 SMD &lt; 0.10;附加文件 1:表 S2)。匹配后,早期 IMV 组的 90 天死亡率为 27.1%(302/1,116),延迟 IMV 组为 45.3%(505/1,116)。配对队列中 90 天死亡率的 Kaplan-Meier 曲线见图 1B。在单变量分析(HR,0.53;95% CI,0.46-0.61;P &lt;0.001)和多变量分析(HR,0.52;95% CI,0.45-0.60;P &lt;0.001)中,早期 IMV 与 90 天死亡率显著降低相关。然而,如图 1 所示,将在 ICU 住院期间从未接受过 IMV 的患者排除在外可能会导致高估与早期 IMV 相关的死亡率益处。因此,我们认为将 2363 名在重症监护室住院期间未接受 IMV 的患者包括在内,可以更全面地了解与早期 IMV 相关的死亡率获益,并有可能完善 Kim 等人的研究结果[2].本研究中提供的数据集可在 MIMIC-IV 数据库(https://mimic.mit.edu/)。CI:置信区间HR:危险比ICU:重症监护病房MIMIC:重症监护医学信息集市IMV:有创机械通气PSM:倾向评分匹配SMD:标准化均值差异Lee KG, Roca O, Casey JD, Semler MW, Roman-Sarita G, Yarnell CJ, Goligher EC.急性低氧血症呼吸衰竭何时插管?重症监护室循证决策的选择与机遇。Lancet Respir Med.2024;12(8):642-54. Article PubMed Google Scholar Kim G, Oh DK, Lee SY, Park MH, Lim CM.有创机械通气时机对脓毒症患者的影响:一项多中心队列研究。Crit Care.2024;28(1):297.Article PubMed PubMed Central Google Scholar Johnson AEW, Bulgarelli L, Shen L, Gayles A, Shammout A, Horng S, Pollard TJ, Hao S, Moody B, Gow B, et al. MIMIC-IV, a free accessible electronic health record dataset.Sci Data.2023;10(1):1.Article CAS PubMed PubMed Central Google Scholar Download referencesNot applicable.本研究得到浙江省自然科学基金资助(批准号:LQ22H150001)。作者及单位浙江省杭州市解放路88号浙江大学医学院附属第二医院外科重症监护室季云&amp; 李利斌作者季云查看作者发表的论文您也可以在PubMed Google Scholar中搜索该作者李利斌查看作者发表的论文您也可以在PubMed Google Scholar中搜索该作者ContributionsYJ提取了数据并进行了统计分析。伦理批准和参与同意该数据库的建立得到了麻省理工学院(马萨诸塞州剑桥市)和贝斯以色列女执事医疗中心(马萨诸塞州波士顿市)的批准,并获得了原始数据收集的同意。出版同意书不适用。利益冲突作者声明不存在利益冲突。出版商注释施普林格-自然公司在出版地图和机构隶属关系的管辖权声明方面保持中立。附加文件1 (DOCX 192 KB)开放存取本文采用知识共享署名-非商业性-禁止衍生 4.0 国际许可协议进行许可,该协议允许以任何媒介或格式进行任何非商业性使用、共享、分发和复制,只要您适当注明原作者和来源,提供知识共享许可协议的链接,并说明您是否修改了许可材料。根据本许可协议,您无权分享源自本文或本文部分内容的改编材料。本文中的图片或其他第三方材料均包含在文章的知识共享许可协议中,除非在材料的信用栏中另有说明。如果材料未包含在文章的知识共享许可协议中,且您打算使用的材料不符合法律规定或超出了许可使用范围,则您需要直接获得版权所有者的许可。如需查看该许可的副本,请访问 http://creativecommons.org/licenses/by-nc-nd/4.0/.Reprints and permissionsCite this articleJi, Y., Li, L. Timing of invasive mechanical ventilation in patients with sepsis: the impact of excluding nonintubated patients.https://doi.org/10.1186/s13054-024-05208-3Download citationReceived:01 December 2024Accepted:06 December 2024Published: 18 December 2024DOI: https://doi.org/10.1186/s13054-024-05208-3Share this articleAnyone you share the following link with will be able to read this content:Get shareable linkSorry, a shareable link is not currently available for this article.Copy to clipboard Provided by the Springer Nature SharedIt content-sharing initiative.
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Critical Care
Critical Care 医学-危重病医学
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3.30%
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1.5 months
期刊介绍: Critical Care is an esteemed international medical journal that undergoes a rigorous peer-review process to maintain its high quality standards. Its primary objective is to enhance the healthcare services offered to critically ill patients. To achieve this, the journal focuses on gathering, exchanging, disseminating, and endorsing evidence-based information that is highly relevant to intensivists. By doing so, Critical Care seeks to provide a thorough and inclusive examination of the intensive care field.
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