This study investigates the use of computational frameworks for sepsis. We consider two dimensions for investigation – early diagnosis of sepsis (EDS) and mortality prediction rate for sepsis patients (MPS). We concentrate on the clinical parameters on which sepsis diagnosis and prognosis are currently done, including customized treatment plans based on historical data of the patient. We identify the most notable literature that uses computational models to address EDS and MPS based on those clinical parameters. In addition to the review of the computational models built upon the clinical parameters, we also provide details regarding the popular publicly available data sources. We provide brief reviews for each model in terms of prior art and present an analysis of their results, as claimed by the respective authors. With respect to the use of machine learning models, we have provided avenues for model analysis in terms of model selection, model validation, model interpretation, and model comparison. We further present the challenges and limitations of the use of computational models, providing future research directions. This study intends to serve as a benchmark for first-hand impressions on the use of computational models for EDS and MPS of sepsis, along with the details regarding which model has been the most promising to date. We have provided details regarding all the ML models that have been used to date for EDS and MPS of sepsis.
{"title":"Investigating computational models for diagnosis and prognosis of sepsis based on clinical parameters: Opportunities, challenges, and future research directions","authors":"Jyotirmoy Gupta , Amit Kumar Majumder , Diganta Sengupta , Mahamuda Sultana , Suman Bhattacharya","doi":"10.1016/j.jointm.2024.04.006","DOIUrl":"10.1016/j.jointm.2024.04.006","url":null,"abstract":"<div><p>This study investigates the use of computational frameworks for sepsis. We consider two dimensions for investigation – early diagnosis of sepsis (EDS) and mortality prediction rate for sepsis patients (MPS). We concentrate on the clinical parameters on which sepsis diagnosis and prognosis are currently done, including customized treatment plans based on historical data of the patient. We identify the most notable literature that uses computational models to address EDS and MPS based on those clinical parameters. In addition to the review of the computational models built upon the clinical parameters, we also provide details regarding the popular publicly available data sources. We provide brief reviews for each model in terms of prior art and present an analysis of their results, as claimed by the respective authors. With respect to the use of machine learning models, we have provided avenues for model analysis in terms of model selection, model validation, model interpretation, and model comparison. We further present the challenges and limitations of the use of computational models, providing future research directions. This study intends to serve as a benchmark for first-hand impressions on the use of computational models for EDS and MPS of sepsis, along with the details regarding which model has been the most promising to date. We have provided details regarding all the ML models that have been used to date for EDS and MPS of sepsis.</p></div>","PeriodicalId":73799,"journal":{"name":"Journal of intensive medicine","volume":"4 4","pages":"Pages 468-477"},"PeriodicalIF":0.0,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2667100X24000744/pdfft?md5=25f1779e49c9e98ed44a5c02345f8a85&pid=1-s2.0-S2667100X24000744-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141699597","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-07-01Epub Date: 2024-04-10DOI: 10.1016/j.jointm.2023.12.009
Sebastian Ocrospoma , Marcos I. Restrepo
The global population is aging at an unprecedented rate, resulting in a growing and vulnerable elderly population in need of efficient comprehensive healthcare services that include long-term care and skilled nursing facilities. In this context, severe aspiration pneumonia, a condition that carries substantial morbidity, mortality, and financial burden, especially among elderly patients requiring admission to the intensive care unit, has attracted greater concern. Aspiration pneumonia is defined as a pulmonary infection related to aspiration or dysphagia in etiology. Prior episodes of coughing on food or liquid intake, a history of relevant underlying conditions, abnormalities on videofluoroscopy or water swallowing, and gravity-dependent shadow distribution on chest imaging are among the clues that suggest aspiration. Patients with aspiration pneumonia tend to be elderly, frail, and suffering from more comorbidities than those without this condition. Here, we comprehensively address the epidemiology, clinical characteristics, diagnosis, treatment, prevention, and prognosis of severe aspiration community-acquired pneumonia in the elderly to optimize care of this high-risk demographic, enhance outcomes, and minimize the healthcare costs associated with this illness. Emphasizing preventive measures and effective management strategies is vital in ensuring the well-being of our aging population.
{"title":"Severe aspiration pneumonia in the elderly","authors":"Sebastian Ocrospoma , Marcos I. Restrepo","doi":"10.1016/j.jointm.2023.12.009","DOIUrl":"10.1016/j.jointm.2023.12.009","url":null,"abstract":"<div><p>The global population is aging at an unprecedented rate, resulting in a growing and vulnerable elderly population in need of efficient comprehensive healthcare services that include long-term care and skilled nursing facilities. In this context, severe aspiration pneumonia, a condition that carries substantial morbidity, mortality, and financial burden, especially among elderly patients requiring admission to the intensive care unit, has attracted greater concern. Aspiration pneumonia is defined as a pulmonary infection related to aspiration or dysphagia in etiology. Prior episodes of coughing on food or liquid intake, a history of relevant underlying conditions, abnormalities on videofluoroscopy or water swallowing, and gravity-dependent shadow distribution on chest imaging are among the clues that suggest aspiration. Patients with aspiration pneumonia tend to be elderly, frail, and suffering from more comorbidities than those without this condition. Here, we comprehensively address the epidemiology, clinical characteristics, diagnosis, treatment, prevention, and prognosis of severe aspiration community-acquired pneumonia in the elderly to optimize care of this high-risk demographic, enhance outcomes, and minimize the healthcare costs associated with this illness. Emphasizing preventive measures and effective management strategies is vital in ensuring the well-being of our aging population.</p></div>","PeriodicalId":73799,"journal":{"name":"Journal of intensive medicine","volume":"4 3","pages":"Pages 307-317"},"PeriodicalIF":0.0,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2667100X24000173/pdfft?md5=b2c35ed3a2e7b84c59cce380d1992e47&pid=1-s2.0-S2667100X24000173-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140784757","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-07-01Epub Date: 2024-02-29DOI: 10.1016/j.jointm.2023.12.007
Claire Roger
Effective treatment of sepsis not only demands prompt administration of appropriate antimicrobials but also requires precise dosing to enhance the likelihood of patient survival. Adequate dosing refers to the administration of doses that yield therapeutic drug concentrations at the infection site. This ensures a favorable clinical and microbiological response while avoiding antibiotic-related toxicity. Therapeutic drug monitoring (TDM) is the recommended approach for attaining these goals. However, TDM is not universally available in all intensive care units (ICUs) and for all antimicrobial agents. In the absence of TDM, healthcare practitioners need to rely on several factors to make informed dosing decisions. These include the patient's clinical condition, causative pathogen, impact of organ dysfunction (requiring extracorporeal therapies), and physicochemical properties of the antimicrobials. In this context, the pharmacokinetics of antimicrobials vary considerably between different critically ill patients and within the same patient over the course of ICU stay. This variability underscores the need for individualized dosing. This review aimed to describe the main pathophysiological changes observed in critically ill patients and their impact on antimicrobial drug dosing decisions. It also aimed to provide essential practical recommendations that may aid clinicians in optimizing antimicrobial therapy among critically ill patients.
{"title":"Understanding antimicrobial pharmacokinetics in critically ill patients to optimize antimicrobial therapy: A narrative review","authors":"Claire Roger","doi":"10.1016/j.jointm.2023.12.007","DOIUrl":"10.1016/j.jointm.2023.12.007","url":null,"abstract":"<div><p>Effective treatment of sepsis not only demands prompt administration of appropriate antimicrobials but also requires precise dosing to enhance the likelihood of patient survival. Adequate dosing refers to the administration of doses that yield therapeutic drug concentrations at the infection site. This ensures a favorable clinical and microbiological response while avoiding antibiotic-related toxicity. Therapeutic drug monitoring (TDM) is the recommended approach for attaining these goals. However, TDM is not universally available in all intensive care units (ICUs) and for all antimicrobial agents. In the absence of TDM, healthcare practitioners need to rely on several factors to make informed dosing decisions. These include the patient's clinical condition, causative pathogen, impact of organ dysfunction (requiring extracorporeal therapies), and physicochemical properties of the antimicrobials. In this context, the pharmacokinetics of antimicrobials vary considerably between different critically ill patients and within the same patient over the course of ICU stay. This variability underscores the need for individualized dosing. This review aimed to describe the main pathophysiological changes observed in critically ill patients and their impact on antimicrobial drug dosing decisions. It also aimed to provide essential practical recommendations that may aid clinicians in optimizing antimicrobial therapy among critically ill patients.</p></div>","PeriodicalId":73799,"journal":{"name":"Journal of intensive medicine","volume":"4 3","pages":"Pages 287-298"},"PeriodicalIF":0.0,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2667100X24000094/pdfft?md5=f2c846ee17691e22dd7a2eb034c01622&pid=1-s2.0-S2667100X24000094-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140470002","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
<div><h3>Background</h3><p>To evaluate the effect of recombinant human thrombopoietin (rhTPO) on clinical prognosis by exploring changes in endothelial cell injury markers and inflammatory factors in patients with sepsis after treatment with rhTPO.</p></div><div><h3>Methods</h3><p>This retrospective observational study involved patients with sepsis (diagnosed according to Sepsis 3.0) admitted to Shanghai General Hospital intensive care unit from January 1, 2019 to December 31, 2022. Patients were divided into two groups (control and rhTPO) according to whether they received rhTPO. Baseline information, clinical data, prognosis, and survival status of the patients, as well as inflammatory factors and immune function indicators were collected. The main monitoring indicators were endothelial cell-specific molecule (ESM-1), human heparin-binding protein (HBP), and CD31; secondary monitoring indicators were interleukin (IL)-6, tumor necrosis factor (TNF)-α, extravascular lung water index, platelet, antithrombin III, fibrinogen, and international normalized ratio. We used intraperitoneal injection of lipopolysaccharide (LPS) to establish a mouse model of sepsis. Mice were randomly divided into four groups: normal saline, LPS, LPS + rhTPO, and LPS + rhTPO + LY294002. Plasma indicators in mice were measured by enzyme-linked immunosorbent assay.</p></div><div><h3>Results</h3><p>A total of 84 patients were included in the study. After 7 days of treatment, ESM-1 decreased more significantly in the rhTPO group than in the control group compared with day 1 (median=38.6 [interquartile range, IQR: 7.2 to 67.8] pg/mL <em>vs.</em> median=23.0 [IQR: −15.7 to 51.5] pg/mL, <em>P</em>=0.008). HBP and CD31 also decreased significantly in the rhTPO group compared with the control group (median=59.6 [IQR: −1.9 to 91.9] pg/mL <em>vs.</em> median=2.4 [IQR: −23.2 to 43.2] pg/mL; median=2.4 [IQR: 0.4 to 3.5] pg/mL <em>vs.</em> median=−0.6 [IQR: −2.2 to 0.8] pg/mL, <em>P</em> <0.001). Inflammatory markers IL-6 and TNF-α decreased more significantly in the rhTPO group than in the control group compared with day 1 (median=46.0 [IQR: 15.8 to 99.1] pg/mL <em>vs.</em> median=31.2 [IQR: 19.7 to 171.0] pg/mL, <em>P</em> <0.001; median=17.2 [IQR: 6.4 to 23.2] pg/mL <em>vs.</em> median=0.0 [IQR: 0.0 to 13.8] pg/mL, <em>P</em>=0.010). LPS + rhTPO-treated mice showed significantly lower vascular von Willebrand factor (<em>P</em>=0.003), vascular endothelial growth factor (<em>P</em>=0.002), IL-6 (<em>P</em> <0.001), and TNF-α (<em>P</em> <0.001) than mice in the LPS group. Endothelial cell damage factors vascular von Willebrand factor (<em>P</em>=0.012), vascular endothelial growth factor (<em>P</em>=0.001), IL-6 (<em>P</em> <0.001), and TNF-α (<em>P</em>=0.001) were significantly elevated by inhibiting the PI3K/Akt pathway.</p></div><div><h3>Conclusion</h3><p>rhTPO alleviates endothelial injury and inflammatory indices in sepsis, and may regulate septic endothelial cell
背景通过探讨脓毒症患者接受rhTPO治疗后血管内皮细胞损伤标志物和炎症因子的变化,评估重组人血小板生成素(rhTPO)对临床预后的影响。方法这项回顾性观察研究涉及2019年1月1日至2022年12月31日期间上海总医院重症监护室收治的脓毒症患者(根据脓毒症3.0标准诊断)。根据患者是否接受rhTPO治疗,将其分为两组(对照组和rhTPO组)。收集患者的基线信息、临床数据、预后和生存状况,以及炎症因子和免疫功能指标。主要监测指标为内皮细胞特异性分子(ESM-1)、人肝素结合蛋白(HBP)和CD31;次要监测指标为白细胞介素(IL)-6、肿瘤坏死因子(TNF)-α、血管外肺水指数、血小板、抗凝血酶Ⅲ、纤维蛋白原和国际标准化比值。我们采用腹腔注射脂多糖(LPS)的方法建立了败血症小鼠模型。小鼠被随机分为四组:正常生理盐水组、LPS 组、LPS + rhTPO 组和 LPS + rhTPO + LY294002 组。小鼠血浆指标通过酶联免疫吸附试验测定。治疗 7 天后,与第 1 天相比,rhTPO 组的 ESM-1 降幅比对照组更明显(中位数=38.6 [四分位距:7.2 至 67.8] pg/mL vs. 中位数=23.0 [四分位距:-15.7 至 51.5] pg/mL,P=0.008)。与对照组相比,rhTPO 组的 HBP 和 CD31 也显著下降(中位数=59.6 [IQR: -1.9 to 91.9] pg/mL vs. 中位数=2.4 [IQR: -23.2 to 43.2] pg/mL;中位数=2.4 [IQR: 0.4 to 3.5] pg/mL vs. 中位数=-0.6 [IQR: -2.2 to 0.8] pg/mL,P <0.001)。与第 1 天相比,rhTPO 组炎症指标 IL-6 和 TNF-α 的下降幅度比对照组更大(中位数=46.0 [IQR: 15.中位数=31.2 [IQR: 19.7 to 171.0] pg/mL, P <0.001;中位数=17.2 [IQR: 6.4 to 23.2] pg/mL vs. 中位数=0.0 [IQR: 0.0 to 13.8] pg/mL, P=0.010)。经 LPS + rhTPO 处理的小鼠的血管冯-威廉因子(P=0.003)、血管内皮生长因子(P=0.002)、IL-6(P <0.001)和 TNF-α (P <0.001)均明显低于 LPS 组小鼠。内皮细胞损伤因子血管冯-威廉因子(P=0.012)、血管内皮生长因子(P=0.001)、IL-6(P <0.001)和TNF-α(P=0.001)在抑制PI3K/Akt通路后显著升高。
{"title":"Recombinant human thrombopoietin in alleviating endothelial cell injury in sepsis","authors":"Yun Xie, Hui Lv, Daonan Chen, Peijie Huang, Shaohong Wu, Hongchao Shi, Qi Zhao, Ruilan Wang","doi":"10.1016/j.jointm.2023.12.006","DOIUrl":"10.1016/j.jointm.2023.12.006","url":null,"abstract":"<div><h3>Background</h3><p>To evaluate the effect of recombinant human thrombopoietin (rhTPO) on clinical prognosis by exploring changes in endothelial cell injury markers and inflammatory factors in patients with sepsis after treatment with rhTPO.</p></div><div><h3>Methods</h3><p>This retrospective observational study involved patients with sepsis (diagnosed according to Sepsis 3.0) admitted to Shanghai General Hospital intensive care unit from January 1, 2019 to December 31, 2022. Patients were divided into two groups (control and rhTPO) according to whether they received rhTPO. Baseline information, clinical data, prognosis, and survival status of the patients, as well as inflammatory factors and immune function indicators were collected. The main monitoring indicators were endothelial cell-specific molecule (ESM-1), human heparin-binding protein (HBP), and CD31; secondary monitoring indicators were interleukin (IL)-6, tumor necrosis factor (TNF)-α, extravascular lung water index, platelet, antithrombin III, fibrinogen, and international normalized ratio. We used intraperitoneal injection of lipopolysaccharide (LPS) to establish a mouse model of sepsis. Mice were randomly divided into four groups: normal saline, LPS, LPS + rhTPO, and LPS + rhTPO + LY294002. Plasma indicators in mice were measured by enzyme-linked immunosorbent assay.</p></div><div><h3>Results</h3><p>A total of 84 patients were included in the study. After 7 days of treatment, ESM-1 decreased more significantly in the rhTPO group than in the control group compared with day 1 (median=38.6 [interquartile range, IQR: 7.2 to 67.8] pg/mL <em>vs.</em> median=23.0 [IQR: −15.7 to 51.5] pg/mL, <em>P</em>=0.008). HBP and CD31 also decreased significantly in the rhTPO group compared with the control group (median=59.6 [IQR: −1.9 to 91.9] pg/mL <em>vs.</em> median=2.4 [IQR: −23.2 to 43.2] pg/mL; median=2.4 [IQR: 0.4 to 3.5] pg/mL <em>vs.</em> median=−0.6 [IQR: −2.2 to 0.8] pg/mL, <em>P</em> <0.001). Inflammatory markers IL-6 and TNF-α decreased more significantly in the rhTPO group than in the control group compared with day 1 (median=46.0 [IQR: 15.8 to 99.1] pg/mL <em>vs.</em> median=31.2 [IQR: 19.7 to 171.0] pg/mL, <em>P</em> <0.001; median=17.2 [IQR: 6.4 to 23.2] pg/mL <em>vs.</em> median=0.0 [IQR: 0.0 to 13.8] pg/mL, <em>P</em>=0.010). LPS + rhTPO-treated mice showed significantly lower vascular von Willebrand factor (<em>P</em>=0.003), vascular endothelial growth factor (<em>P</em>=0.002), IL-6 (<em>P</em> <0.001), and TNF-α (<em>P</em> <0.001) than mice in the LPS group. Endothelial cell damage factors vascular von Willebrand factor (<em>P</em>=0.012), vascular endothelial growth factor (<em>P</em>=0.001), IL-6 (<em>P</em> <0.001), and TNF-α (<em>P</em>=0.001) were significantly elevated by inhibiting the PI3K/Akt pathway.</p></div><div><h3>Conclusion</h3><p>rhTPO alleviates endothelial injury and inflammatory indices in sepsis, and may regulate septic endothelial cell","PeriodicalId":73799,"journal":{"name":"Journal of intensive medicine","volume":"4 3","pages":"Pages 384-392"},"PeriodicalIF":0.0,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2667100X24000082/pdfft?md5=0d5c0ad6b53ef35c58b4152fa3f88aae&pid=1-s2.0-S2667100X24000082-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140760516","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-07-01Epub Date: 2024-02-27DOI: 10.1016/j.jointm.2024.01.001
Jean-Marc Cavaillon , Benjamin G. Chousterman , Tomasz Skirecki
Acute infections cause local and systemic disorders which can lead in the most severe forms to multi-organ failure and eventually to death. The host response to infection encompasses a large spectrum of reactions with a concomitant activation of the so-called inflammatory response aimed at fighting the infectious agent and removing damaged tissues or cells, and the anti-inflammatory response aimed at controlling inflammation and initiating the healing process. Fine-tuning at the local and systemic levels is key to preventing local and remote injury due to immune system activation. Thus, during bacterial sepsis and Coronavirus disease 2019 (COVID-19), concomitant systemic and compartmentalized pro-inflammatory and compensatory anti-inflammatory responses are occurring. Immune cells (e.g., macrophages, neutrophils, natural killer cells, and T-lymphocytes), as well as endothelial cells, differ from one compartment to another and contribute to specific organ responses to sterile and microbial insult. Furthermore, tissue-specific microbiota influences the local and systemic response. A better understanding of the tissue-specific immune status, the organ immunity crosstalk, and the role of specific mediators during sepsis and COVID-19 can foster the development of more accurate biomarkers for better diagnosis and prognosis and help to define appropriate host-targeted treatments and vaccines in the context of precision medicine.
{"title":"Compartmentalization of the inflammatory response during bacterial sepsis and severe COVID-19","authors":"Jean-Marc Cavaillon , Benjamin G. Chousterman , Tomasz Skirecki","doi":"10.1016/j.jointm.2024.01.001","DOIUrl":"10.1016/j.jointm.2024.01.001","url":null,"abstract":"<div><p>Acute infections cause local and systemic disorders which can lead in the most severe forms to multi-organ failure and eventually to death. The host response to infection encompasses a large spectrum of reactions with a concomitant activation of the so-called inflammatory response aimed at fighting the infectious agent and removing damaged tissues or cells, and the anti-inflammatory response aimed at controlling inflammation and initiating the healing process. Fine-tuning at the local and systemic levels is key to preventing local and remote injury due to immune system activation. Thus, during bacterial sepsis and Coronavirus disease 2019 (COVID-19), concomitant systemic and compartmentalized pro-inflammatory and compensatory anti-inflammatory responses are occurring. Immune cells (e.g., macrophages, neutrophils, natural killer cells, and T-lymphocytes), as well as endothelial cells, differ from one compartment to another and contribute to specific organ responses to sterile and microbial insult. Furthermore, tissue-specific microbiota influences the local and systemic response. A better understanding of the tissue-specific immune status, the organ immunity crosstalk, and the role of specific mediators during sepsis and COVID-19 can foster the development of more accurate biomarkers for better diagnosis and prognosis and help to define appropriate host-targeted treatments and vaccines in the context of precision medicine.</p></div>","PeriodicalId":73799,"journal":{"name":"Journal of intensive medicine","volume":"4 3","pages":"Pages 326-340"},"PeriodicalIF":0.0,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2667100X24000045/pdfft?md5=7590daf6861ffd42ec236c1e4825825f&pid=1-s2.0-S2667100X24000045-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140469726","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-07-01Epub Date: 2023-12-06DOI: 10.1016/j.jointm.2023.10.003
Qinglin Li , Guanggang Li , Dawei Li , Yan Chen , Feihu Zhou
<div><h3>Background</h3><p>Emerging evidence suggests that minimal acute kidney injury (stage 1 AKI) is associated with increased hospital mortality rates. However, for those who do not meet the AKI diagnostic criteria, whether a small increase in serum creatinine (SCr) levels is associated with an increased mortality rate in elderly patients is not known. Therefore, we aimed to investigate small elevations in SCr of <26.5 µmol/L within 48 h after invasive mechanical ventilation (MV) on the short-term mortality of critically ill patients in the geriatric population.</p></div><div><h3>Methods</h3><p>We conducted a retrospective, observational, multicenter cohort study enrolling consecutive elderly patients (≥75 years) who received invasive MV from January 2008 to December 2020. Recursive partitioning was used to calculate the ratio of SCr rise from baseline within 48 h after MV and divided into six groups, (1) <10%, (2) 10%–<20%, (3) 20%–<30%, (4) 30%–<40%, (5) 40%–<50%, and (6) ≥50%, where the reference interval was defined as the ratio <10% based on an analysis, which confirmed that the lowest mortality risk was found in this range. Clinical data and laboratory data were noted. Their general conditions and clinical characteristics were compared between the six groups. Prognostic survival factors were identified using Cox regression analysis. Kaplan–Meier survival analysis was employed for the accumulative survival rate.</p></div><div><h3>Results</h3><p>A total of 1292 patients (1171 men) with a median age of 89 (interquartile range: 85–92) with MV were suitable for further analysis. In all, 376 patients had any stage of early AKI, and 916 patients had no AKI. Among 916 non-AKI patients, 349 patients were in the ratio <10%, 291 in the 10%–<20% group, 169 in the 20%–<30% group, 68 in the 30%–<40% group, 25 in the 40%–<50% group, and 14 in the ≥50% group. The 28-day mortality rates in the six groups from the lowest (<10%) to the highest (≥50%) were 8.0%, 16.8%, 28.4%, 54.4%, 80.0%, and 85.7%, respectively. In the multivariable-adjusted analysis, patients with a ratio of 10%–<20% (hazard ratio [HR]=2.244; 95% confidence interval [CI]: 1.410 to 3.572; <em>P</em>=0.001), 20%–<30% (HR=3.822; 95% CI: 2.433 to 6.194; <em>P <</em>0.001), 30%–<40% (HR=10.472; 95% CI: 6.379 to 17.190; <em>P <</em>0.001), 40%–<50% (HR=13.887; 95% CI: 7.624 to 25.292; <em>P <</em>0.001), and ≥50% (HR=13.618; 95% CI: 6.832 to 27.144; <em>P <</em>0.001) had relatively higher 28-day mortality rates. The 90-day mortality rates in the six strata were 30.1%, 35.1%, 45.0%, 60.3%, 80.0%, and 85.7%, respectively. Significant interactions were also observed between the ratio and 90-day mortality: patients with a ratio of 10%–<20% (HR=1.322; 95% CI: 1.006 to 1.738; <em>P</em>=0.045), 20%–<30% (HR=1.823; 95% CI: 1.356 to 2.452; <em>P <</em>0.001), 30%–<40% (HR=3.751; 95% CI: 2.601 to 5.410; <em>P <</em>0.001),
{"title":"Early and minimal changes in serum creatinine can predict prognosis in elderly patients receiving invasive mechanical ventilation: A retrospective observational study","authors":"Qinglin Li , Guanggang Li , Dawei Li , Yan Chen , Feihu Zhou","doi":"10.1016/j.jointm.2023.10.003","DOIUrl":"10.1016/j.jointm.2023.10.003","url":null,"abstract":"<div><h3>Background</h3><p>Emerging evidence suggests that minimal acute kidney injury (stage 1 AKI) is associated with increased hospital mortality rates. However, for those who do not meet the AKI diagnostic criteria, whether a small increase in serum creatinine (SCr) levels is associated with an increased mortality rate in elderly patients is not known. Therefore, we aimed to investigate small elevations in SCr of <26.5 µmol/L within 48 h after invasive mechanical ventilation (MV) on the short-term mortality of critically ill patients in the geriatric population.</p></div><div><h3>Methods</h3><p>We conducted a retrospective, observational, multicenter cohort study enrolling consecutive elderly patients (≥75 years) who received invasive MV from January 2008 to December 2020. Recursive partitioning was used to calculate the ratio of SCr rise from baseline within 48 h after MV and divided into six groups, (1) <10%, (2) 10%–<20%, (3) 20%–<30%, (4) 30%–<40%, (5) 40%–<50%, and (6) ≥50%, where the reference interval was defined as the ratio <10% based on an analysis, which confirmed that the lowest mortality risk was found in this range. Clinical data and laboratory data were noted. Their general conditions and clinical characteristics were compared between the six groups. Prognostic survival factors were identified using Cox regression analysis. Kaplan–Meier survival analysis was employed for the accumulative survival rate.</p></div><div><h3>Results</h3><p>A total of 1292 patients (1171 men) with a median age of 89 (interquartile range: 85–92) with MV were suitable for further analysis. In all, 376 patients had any stage of early AKI, and 916 patients had no AKI. Among 916 non-AKI patients, 349 patients were in the ratio <10%, 291 in the 10%–<20% group, 169 in the 20%–<30% group, 68 in the 30%–<40% group, 25 in the 40%–<50% group, and 14 in the ≥50% group. The 28-day mortality rates in the six groups from the lowest (<10%) to the highest (≥50%) were 8.0%, 16.8%, 28.4%, 54.4%, 80.0%, and 85.7%, respectively. In the multivariable-adjusted analysis, patients with a ratio of 10%–<20% (hazard ratio [HR]=2.244; 95% confidence interval [CI]: 1.410 to 3.572; <em>P</em>=0.001), 20%–<30% (HR=3.822; 95% CI: 2.433 to 6.194; <em>P <</em>0.001), 30%–<40% (HR=10.472; 95% CI: 6.379 to 17.190; <em>P <</em>0.001), 40%–<50% (HR=13.887; 95% CI: 7.624 to 25.292; <em>P <</em>0.001), and ≥50% (HR=13.618; 95% CI: 6.832 to 27.144; <em>P <</em>0.001) had relatively higher 28-day mortality rates. The 90-day mortality rates in the six strata were 30.1%, 35.1%, 45.0%, 60.3%, 80.0%, and 85.7%, respectively. Significant interactions were also observed between the ratio and 90-day mortality: patients with a ratio of 10%–<20% (HR=1.322; 95% CI: 1.006 to 1.738; <em>P</em>=0.045), 20%–<30% (HR=1.823; 95% CI: 1.356 to 2.452; <em>P <</em>0.001), 30%–<40% (HR=3.751; 95% CI: 2.601 to 5.410; <em>P <</em>0.001), ","PeriodicalId":73799,"journal":{"name":"Journal of intensive medicine","volume":"4 3","pages":"Pages 368-375"},"PeriodicalIF":0.0,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2667100X2300083X/pdfft?md5=2b80a592cf6a98cf850ff92e4197091c&pid=1-s2.0-S2667100X2300083X-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138617300","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Sepsis is a life-threatening organ dysfunction, and septic cardiomyopathy (SCM) may complicate the course of the disease. Infection with multidrug-resistant (MDR) pathogens has been linked with worse outcomes. This study aims to evaluate SCM in patients with infections caused by different antimicrobial-resistant phenotypes.
Method
This retrospective study included patients with sepsis/septic shock, hospitalized, and intubated in the intensive care unit of the University Hospital of Larissa between January 2022 and September 2023 with echocardiographic data during the first two days after infection onset. The patients were divided into two groups: non-MDR-SCM group and MDR-SCM group. The cardiac function was compared between the two groups.
Result
A total of 62 patients were included in the study. Forty-four patients comprised the MDR-SCM and 18 the non-MDR-SCM group. Twenty-six patients (41.9%) presented with left ventricular (LV) systolic dysfunction, and ≤35% right ventricular fractional area change (RVFAC) was present in 56.4%. LV systolic function was more severely impaired in the non-MDR-SCM group (left ventricular ejection fraction, 35.8% ±4.9% vs. 45.6%±2.4%, P=0.049; LV outflow tract velocity time integral, [10.1±1.4] cm vs. [15.3±0.74] cm, P=0.001; LV-Strain, –9.02%±0.9% vs. –14.02%±0.7%, P=0.001). The MDR-SCM group presented with more severe right ventricular (RV) dilatation (right ventricular end-diastolic area/left ventricular end-diastolic area, 0.81±0.03 vs. 0.7±0.05, P=0.042) and worse RV systolic function (RVFAC, 32.3%±1.9% vs. 39.6%±2.7%, P=0.035; tricuspid annular plane systolic excursion, [15.9±0.9] mm vs. [18.1±0.9] mm, P=0.165; systolic tissue Doppler velocity measured at the lateral tricuspid annulus, [9.9±0.5] cm/s vs. [13.1±0.8] cm/s, P=0.002; RV-strain, –11.1%±0.7% vs. –15.1%±0.9%, P=0.002).
Conclusion
SCM related to MDR infection presents with RV systolic dysfunction predominance, while non-MDR-SCM is mainly depicted with LV systolic dysfunction impairment.
背景败血症是一种危及生命的器官功能障碍,而败血症性心肌病(SCM)可能会使病程复杂化。耐多药(MDR)病原体感染与更差的预后有关。这项回顾性研究纳入了 2022 年 1 月至 2023 年 9 月期间在拉里萨大学医院重症监护室住院并插管的脓毒症/脓毒性休克患者,他们在感染发生后的头两天都接受了超声心动图检查。患者被分为两组:非 MDR-SCM 组和 MDR-SCM 组。研究共纳入 62 名患者。研究共纳入 62 例患者,其中 44 例为 MDR-SCM 组,18 例为非 MDR-SCM 组。26名患者(41.9%)出现左心室收缩功能障碍,56.4%的患者右心室折返面积(RVFAC)变化≤35%。非 MDR-SCM 组的左心室收缩功能受损更严重(左心室射血分数,35.8%±4.9% vs. 45.6%±2.4%,P=0.049;左心室流出道速度时间积分,[10.1±1.4] cm vs. [15.3±0.74] cm,P=0.001;左心室应变,-9.02%±0.9% vs. -14.02%±0.7%,P=0.001)。MDR-SCM 组的右心室(RV)扩张更为严重(右心室舒张末期面积/左心室舒张末期面积,0.81±0.03 vs. 0.7±0.05,P=0.042)。05,P=0.042)和更差的 RV 收缩功能(RVFAC,32.3%±1.9% vs. 39.6%±2.7%,P=0.035;三尖瓣环平面收缩期偏移,[15.9±0.9] mm vs. [18.1±0.9] mm,P=0.结论与 MDR 感染相关的 SCM 主要表现为 RV 收缩功能障碍,而非 MDR-SCM 主要表现为 LV 收缩功能障碍。
{"title":"Septic cardiomyopathy phenotype in the critically ill may depend on antimicrobial resistance","authors":"Vasiliki Tsolaki , Kyriaki Parisi , George E. Zakynthinos , Efrosini Gerovasileiou , Nikitas Karavidas , Vassileios Vazgiourakis , Epaminondas Zakynthinos , Demosthenes Makris","doi":"10.1016/j.jointm.2023.11.009","DOIUrl":"10.1016/j.jointm.2023.11.009","url":null,"abstract":"<div><h3>Background</h3><p>Sepsis is a life-threatening organ dysfunction, and septic cardiomyopathy (SCM) may complicate the course of the disease. Infection with multidrug-resistant (MDR) pathogens has been linked with worse outcomes. This study aims to evaluate SCM in patients with infections caused by different antimicrobial-resistant phenotypes.</p></div><div><h3>Method</h3><p>This retrospective study included patients with sepsis/septic shock, hospitalized, and intubated in the intensive care unit of the University Hospital of Larissa between January 2022 and September 2023 with echocardiographic data during the first two days after infection onset. The patients were divided into two groups: non-MDR-SCM group and MDR-SCM group. The cardiac function was compared between the two groups.</p></div><div><h3>Result</h3><p>A total of 62 patients were included in the study. Forty-four patients comprised the MDR-SCM and 18 the non-MDR-SCM group. Twenty-six patients (41.9%) presented with left ventricular (LV) systolic dysfunction, and ≤35% right ventricular fractional area change (RVFAC) was present in 56.4%. LV systolic function was more severely impaired in the non-MDR-SCM group (left ventricular ejection fraction, 35.8% ±4.9% <em>vs</em>. 45.6%±2.4%, <em>P</em>=0.049; LV outflow tract velocity time integral, [10.1±1.4] cm <em>vs</em>. [15.3±0.74] cm, <em>P</em>=0.001; LV-Strain, –9.02%±0.9% <em>vs</em>. –14.02%±0.7%, <em>P</em>=0.001). The MDR-SCM group presented with more severe right ventricular (RV) dilatation (right ventricular end-diastolic area/left ventricular end-diastolic area, 0.81±0.03 <em>vs.</em> 0.7±0.05, <em>P</em>=0.042) and worse RV systolic function (RVFAC, 32.3%±1.9% <em>vs</em>. 39.6%±2.7%, <em>P</em>=0.035; tricuspid annular plane systolic excursion, [15.9±0.9] mm <em>vs</em>. [18.1±0.9] mm, <em>P</em>=0.165; systolic tissue Doppler velocity measured at the lateral tricuspid annulus, [9.9±0.5] cm/s <em>vs</em>. [13.1±0.8] cm/s, <em>P</em>=0.002; RV-strain, –11.1%±0.7% <em>vs</em>. –15.1%±0.9%, <em>P</em>=0.002).</p></div><div><h3>Conclusion</h3><p>SCM related to MDR infection presents with RV systolic dysfunction predominance, while non-MDR-SCM is mainly depicted with LV systolic dysfunction impairment.</p></div>","PeriodicalId":73799,"journal":{"name":"Journal of intensive medicine","volume":"4 3","pages":"Pages 355-361"},"PeriodicalIF":0.0,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2667100X24000100/pdfft?md5=7cd85d81d6c78960d1e103c5c4495df7&pid=1-s2.0-S2667100X24000100-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140764610","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-07-01Epub Date: 2024-02-27DOI: 10.1016/j.jointm.2024.01.002
Jan J. De Waele
Source control is defined as the physical measures undertaken to eliminate the source of infection and control ongoing contamination, as well as restore anatomy and function at the site of infection. It is a key component of the management of patients with sepsis and septic shock and one of the main determinants of the outcome of infections that require source control. While not all infections may require source control, it should be considered in every patient presenting with sepsis; it is applicable and necessary in numerous infections, not only those occurring in the abdominal cavity. Although the biological rationale is clear, several aspects of source control remain under debate. The timing of source control may impact outcome; early source control is particularly relevant for patients with abdominal infections or necrotizing skin and soft tissue infections, as well as for those with more severe disease. Percutaneous procedures are increasingly used for source control; nevertheless, surgery—tailored to the patient and infection—remains a valid option for source control. For outcome optimization, adequate source control is more important than the strategy used. It should be acknowledged that source control interventions may often fail, posing a challenge in this setting. Thus, an individualized, multidisciplinary approach tailored to the infection and patient is preferable.
{"title":"Importance of timely and adequate source control in sepsis and septic shock","authors":"Jan J. De Waele","doi":"10.1016/j.jointm.2024.01.002","DOIUrl":"10.1016/j.jointm.2024.01.002","url":null,"abstract":"<div><p>Source control is defined as the physical measures undertaken to eliminate the source of infection and control ongoing contamination, as well as restore anatomy and function at the site of infection. It is a key component of the management of patients with sepsis and septic shock and one of the main determinants of the outcome of infections that require source control. While not all infections may require source control, it should be considered in every patient presenting with sepsis; it is applicable and necessary in numerous infections, not only those occurring in the abdominal cavity. Although the biological rationale is clear, several aspects of source control remain under debate. The timing of source control may impact outcome; early source control is particularly relevant for patients with abdominal infections or necrotizing skin and soft tissue infections, as well as for those with more severe disease. Percutaneous procedures are increasingly used for source control; nevertheless, surgery—tailored to the patient and infection—remains a valid option for source control. For outcome optimization, adequate source control is more important than the strategy used. It should be acknowledged that source control interventions may often fail, posing a challenge in this setting. Thus, an individualized, multidisciplinary approach tailored to the infection and patient is preferable.</p></div>","PeriodicalId":73799,"journal":{"name":"Journal of intensive medicine","volume":"4 3","pages":"Pages 281-286"},"PeriodicalIF":0.0,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2667100X24000070/pdfft?md5=ffbb1b073bf9cca19274d820812937bb&pid=1-s2.0-S2667100X24000070-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140465223","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-07-01Epub Date: 2024-03-02DOI: 10.1016/j.jointm.2024.01.003
Junfeng Wang, Mingxia Ji
Background
Early evaluation of prognosis in cardiogenic shock (CS) is crucial for tailored treatment selection. Both lactate clearance and lactate levels are considered useful prognostic biomarkers in patients with CS. However, there is yet no literature comparing the 6-hour lactate clearance rate (Δ6Lac) with lactate levels measured at admission (L1) and after 6 h (L2) to predict 30-day mortality in CS.
Methods
In this observational cohort study, 95 patients with CS were treated at Department of Intensive Care Unit, Yiwu Central Hospital between January 2020 and December 2022. Of these, 88 patients met the eligibility criteria. The lactate levels were measured after admission (L1) as the baseline lactate value, and were measured after 6 h (L2) following admission. The primary endpoint of the study was survival rate at 30 days. A receiver operating characteristic curve was used for data analysis. Univariate and multivariate Cox regression analyses were performed based on Δ6Lac. Kaplan–Meier (KM) survival curves were generated to compare the 30-day survival rates among L1, L2, and Δ6Lac.
Results
The Δ6Lac model showed the highest area under the curve value (0.839), followed by the L2 (0.805) and L1 (0.668) models. The Δ6Lac model showed a sensitivity of 84.2% and specificity of 75.4%. The L1 and L2 models had sensitivities of 57.9% each and specificities of 89.9% and 98.6%, respectively. The cut-off values for Δ6Lac, L1, and L2 were 18.2%, 6.7 mmol/L, and 6.1 mmol/L, respectively. Univariate Cox regression analysis revealed a significant association between Δ6Lac and 30-day mortality. After adjusting for five models in multivariate Cox regression, Δ6Lac remained a significant risk factor for 30-day mortality in patients with CS. In our fifth multivariate Cox regression model, Δ6Lac remained a risk factor associated with 30-day mortality (hazard ratio [HR]=5.14, 95% confidence interval [CI]: 1.48 to 17.89, P=0.010) as well as L2 (HR=8.42, 95% CI: 1.26 to 56.22, P=0.028). The KM survival curve analysis revealed that L1 >6.7 mmol/L (HR=8.08, 95% CI: 3.23 to 20.20, P <0.001), L2 >6.1 mmol/L (HR=25.97, 95% CI: 9.76 to 69.15, P <0.001), and Δ6Lac ≤18.2% (HR=8.92, 95% CI: 2.95 to 26.95, P <0.001) were associated with a higher risk of 30-day mortality.
Conclusions
Δ6Lac is a better predictor for 30-day mortality in CS than lactate levels at admission. It has a predictive value equivalent to that of lactate level at 6 h after admission, making it an important surrogate indicator for evaluating the suitability as well as poor prognosis after CS treatment. We found that a cut-off value of 18.2% for Δ6Lac provided the most accurate assessment of early prognosis in CS.
{"title":"The 6-hour lactate clearance rate in predicting 30-day mortality in cardiogenic shock","authors":"Junfeng Wang, Mingxia Ji","doi":"10.1016/j.jointm.2024.01.003","DOIUrl":"10.1016/j.jointm.2024.01.003","url":null,"abstract":"<div><h3>Background</h3><p>Early evaluation of prognosis in cardiogenic shock (CS) is crucial for tailored treatment selection. Both lactate clearance and lactate levels are considered useful prognostic biomarkers in patients with CS. However, there is yet no literature comparing the 6-hour lactate clearance rate (Δ6Lac) with lactate levels measured at admission (L1) and after 6 h (L2) to predict 30-day mortality in CS.</p></div><div><h3>Methods</h3><p>In this observational cohort study, 95 patients with CS were treated at Department of Intensive Care Unit, Yiwu Central Hospital between January 2020 and December 2022. Of these, 88 patients met the eligibility criteria. The lactate levels were measured after admission (L1) as the baseline lactate value, and were measured after 6 h (L2) following admission. The primary endpoint of the study was survival rate at 30 days. A receiver operating characteristic curve was used for data analysis. Univariate and multivariate Cox regression analyses were performed based on Δ6Lac. Kaplan–Meier (KM) survival curves were generated to compare the 30-day survival rates among L1, L2, and Δ6Lac.</p></div><div><h3>Results</h3><p>The Δ6Lac model showed the highest area under the curve value (0.839), followed by the L2 (0.805) and L1 (0.668) models. The Δ6Lac model showed a sensitivity of 84.2% and specificity of 75.4%. The L1 and L2 models had sensitivities of 57.9% each and specificities of 89.9% and 98.6%, respectively. The cut-off values for Δ6Lac, L1, and L2 were 18.2%, 6.7 mmol/L, and 6.1 mmol/L, respectively. Univariate Cox regression analysis revealed a significant association between Δ6Lac and 30-day mortality. After adjusting for five models in multivariate Cox regression, Δ6Lac remained a significant risk factor for 30-day mortality in patients with CS. In our fifth multivariate Cox regression model, Δ6Lac remained a risk factor associated with 30-day mortality (hazard ratio [HR]=5.14, 95% confidence interval [CI]: 1.48 to 17.89, <em>P</em>=0.010) as well as L2 (HR=8.42, 95% CI: 1.26 to 56.22, <em>P</em>=0.028). The KM survival curve analysis revealed that L1 >6.7 mmol/L (HR=8.08, 95% CI: 3.23 to 20.20, <em>P</em> <0.001), L2 >6.1 mmol/L (HR=25.97, 95% CI: 9.76 to 69.15, <em>P</em> <0.001), and Δ6Lac ≤18.2% (HR=8.92, 95% CI: 2.95 to 26.95, <em>P</em> <0.001) were associated with a higher risk of 30-day mortality.</p></div><div><h3>Conclusions</h3><p>Δ6Lac is a better predictor for 30-day mortality in CS than lactate levels at admission. It has a predictive value equivalent to that of lactate level at 6 h after admission, making it an important surrogate indicator for evaluating the suitability as well as poor prognosis after CS treatment. We found that a cut-off value of 18.2% for Δ6Lac provided the most accurate assessment of early prognosis in CS.</p></div>","PeriodicalId":73799,"journal":{"name":"Journal of intensive medicine","volume":"4 3","pages":"Pages 393-399"},"PeriodicalIF":0.0,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2667100X24000112/pdfft?md5=bd8b5539076cac8494a1d18d7fe70aaa&pid=1-s2.0-S2667100X24000112-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140087757","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-07-01Epub Date: 2023-12-27DOI: 10.1016/j.jointm.2023.11.005
Sebastian Berger , Pascale Grzonka , Simon A. Amacher , Sabina Hunziker , Anja I. Frei , Raoul Sutter
Physical restraints are widely used and accepted as protective measures during treatment in intensive care unit (ICU). This review of the literature summarizes the adverse events and outcomes associated with physical restraint use, and the risk factors associated with their use during treatment in the ICU. The PubMed, Scopus, and Google Scholar databases were screened using predefined search terms to identify studies pertaining to adverse events and/or outcomes associated with physical restraint use, and the factors associated with their use in adult patients admitted to the ICU. A total of 24 articles (including 6126 patients) that were published between 2006 and 2022 were identified. The described adverse events associated with physical restraint use included skin injuries, subsequent delirium, neurofunctional impairment, and a higher rate of post-traumatic stress disorder. Subsequent delirium was the most frequent adverse event to be reported. No alternative measures to physical restraints were discussed, and only one study reported a standardized protocol for their use. Although physical restraint use has been reported to be associated with adverse events (including neurofunctional impairment) in the literature, the available evidence is limited. Although causality cannot be confirmed, a definite association appears to exist. Our findings suggest that it is essential to improve awareness regarding their adverse impact and optimize approaches for their detection, management, and prevention using protocols or checklists.
{"title":"Adverse events related to physical restraint use in intensive care units: A review of the literature","authors":"Sebastian Berger , Pascale Grzonka , Simon A. Amacher , Sabina Hunziker , Anja I. Frei , Raoul Sutter","doi":"10.1016/j.jointm.2023.11.005","DOIUrl":"https://doi.org/10.1016/j.jointm.2023.11.005","url":null,"abstract":"<div><p>Physical restraints are widely used and accepted as protective measures during treatment in intensive care unit (ICU). This review of the literature summarizes the adverse events and outcomes associated with physical restraint use, and the risk factors associated with their use during treatment in the ICU. The PubMed, Scopus, and Google Scholar databases were screened using predefined search terms to identify studies pertaining to adverse events and/or outcomes associated with physical restraint use, and the factors associated with their use in adult patients admitted to the ICU. A total of 24 articles (including 6126 patients) that were published between 2006 and 2022 were identified. The described adverse events associated with physical restraint use included skin injuries, subsequent delirium, neurofunctional impairment, and a higher rate of post-traumatic stress disorder. Subsequent delirium was the most frequent adverse event to be reported. No alternative measures to physical restraints were discussed, and only one study reported a standardized protocol for their use. Although physical restraint use has been reported to be associated with adverse events (including neurofunctional impairment) in the literature, the available evidence is limited. Although causality cannot be confirmed, a definite association appears to exist. Our findings suggest that it is essential to improve awareness regarding their adverse impact and optimize approaches for their detection, management, and prevention using protocols or checklists.</p></div>","PeriodicalId":73799,"journal":{"name":"Journal of intensive medicine","volume":"4 3","pages":"Pages 318-325"},"PeriodicalIF":0.0,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2667100X23000920/pdfft?md5=7fc5b4b8e0c73afdfdef7e254fa76cae&pid=1-s2.0-S2667100X23000920-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141424195","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}