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Search Results (415)

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10 pages, 231 KiB  
Article
Efficacy of Adjunct Hemoperfusion Compared to Standard Medical Therapy on 28-Day Mortality in Leptospirosis Patients with Renal Failure and Shock: A Single-Center Randomized Controlled Trial
by Danice Romagne Leano, Romina Danguilan, Mel-Hatra Arakama, Vince Apelin, Paolo Pinkerton Alamillo and Eric Chua
Trop. Med. Infect. Dis. 2024, 9(9), 206; https://doi.org/10.3390/tropicalmed9090206 - 9 Sep 2024
Viewed by 292
Abstract
Hemoperfusion is a novel adjunct therapy that targets the dysregulated inflammatory events in severe sepsis. Previous studies have reported conflicting results on its efficacy and safety. This study was designed to assess the efficacy and safety of hemoperfusion among leptospirosis patients in septic [...] Read more.
Hemoperfusion is a novel adjunct therapy that targets the dysregulated inflammatory events in severe sepsis. Previous studies have reported conflicting results on its efficacy and safety. This study was designed to assess the efficacy and safety of hemoperfusion among leptospirosis patients in septic shock and renal failure in terms of improvement in 28-day mortality, SOFA score, level of inflammatory markers, hemodynamics, and renal and pulmonary function. A total of 37 severe leptospirosis patients were enrolled and randomized into either standard medical therapy (SMT) alone, n = 20, or with hemoperfusion (HP), n = 17. Vital signs, urine output, vasopressor dose, PaO2/FiO2 (P/F) ratio, and biochemical parameters of patients from each treatment arm were compared. The hemoperfusion group showed a 36.84% (p = 0.017) risk reduction in 28-day mortality. Levels of procalcitonin, IL6, and lactate significantly decreased from baseline to day 7 in both groups. Statistically significant improvements in serum creatinine (p = 0.04) and PF ratio (p = 0.045) were observed in the hemoperfusion cohort. Intention-to-treat and per-protocol approaches showed that hemoperfusion increased the survival rate and decreased the mortality risk. This benefit for survival persisted even when patients were also receiving extracorporeal membrane oxygenation (ECMO), showing that hemoperfusion’s benefits are independent of ECMO use. Hemoperfusion is a safe and effective adjunct therapy for managing severe sepsis. It promotes earlier renal and pulmonary function recovery and improves the survival of septic shock patients. Full article
15 pages, 1738 KiB  
Article
Kinetics of the Lactate to Albumin Ratio in New Onset Sepsis: Prognostic Implications
by Irene Karampela, Dimitris Kounatidis, Natalia G. Vallianou, Fotis Panagopoulos, Dimitrios Tsilingiris and Maria Dalamaga
Diagnostics 2024, 14(17), 1988; https://doi.org/10.3390/diagnostics14171988 - 8 Sep 2024
Viewed by 411
Abstract
The lactate to albumin ratio (LAR) has been associated with the severity and outcome of critical illness and sepsis. However, there are no studies on the kinetics of the LAR during the early phase of sepsis. Therefore, we aimed to investigate the LAR [...] Read more.
The lactate to albumin ratio (LAR) has been associated with the severity and outcome of critical illness and sepsis. However, there are no studies on the kinetics of the LAR during the early phase of sepsis. Therefore, we aimed to investigate the LAR and its kinetics in critically ill patients with new onset sepsis regarding the severity and outcome of sepsis. We prospectively enrolled 102 patients with sepsis or septic shock within 48 h from diagnosis. LARs were recorded at inclusion in the study and one week later. Patients were followed for 28 days. LAR was significantly lower one week after enrollment compared to baseline in all patients (p < 0.001). LARs were significantly higher in patients with septic shock and in nonsurvivors compared to patients with sepsis and survivors, respectively, both at inclusion (p < 0.001, p < 0.001) and at one week later (p < 0.001, p < 0.001). LARs at baseline were positively associated with the severity of sepsis (APACHE II: r = 0.29, p = 0.003; SOFA: r = 0.33, p < 0.001) and inflammatory biomarkers, such as C-reactive protein (r = 0.29, p < 0.1), procalcitonin (r = 0.47, p < 0.001), interleukin 6 (r = 0.28, p = 0.005) interleukin 10 (r = 0.3, p = 0.002) and suPAR (r = 0.28, p = 0.004). In addition, a higher LAR, but not its kinetics, was an independent predictor of 28-day mortality (at inclusion: HR 2.27, 95% C.I. 1.01–5.09, p = 0.04; one week later: HR: 4.29, 95% C.I. 1.71–10.78, p = 0.002). In conclusion, the LAR may be a valuable prognostic indicator in critically ill patients with sepsis at admission and one week later. Full article
(This article belongs to the Section Pathology and Molecular Diagnostics)
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<p>Lactate to albumin ratio upon inclusion in the study and one week after in 102 patients.</p>
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<p>Lactate to albumin ratio upon inclusion in the study and one week later in patients with sepsis (<span class="html-italic">n</span> = 60) and septic shock (<span class="html-italic">n</span> = 42).</p>
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<p>Lactate to albumin ratio upon inclusion in the study and one week later in survivors (<span class="html-italic">n</span> = 72) and nonsurvivors (<span class="html-italic">n</span> = 30).</p>
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<p>Lactate to albumin ratio upon inclusion in the study is significantly associated with APACHE II (r = 0.29, <span class="html-italic">p</span> = 0.003) and SOFA (r = 0.33, <span class="html-italic">p</span> &lt; 0.001) scores. In blue: correlation of LAR with SOFA score. In orange: correlation of LAR with APACHE score.</p>
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<p>The area under the Receiver Operating Characteristic curve (AUROC) distinguishing survivors from nonsurvivors in 102 patients with sepsis. (<b>A</b>) <b>At inclusion:</b> LAR, AUROC &gt; 0.706; CRP, AUROC &gt; 0.705; procalcitonin, AUROC &gt; 0.628. (<b>B</b>) <b>One week after inclusion:</b> LAR, AUROC &gt; 0.750; CRP, AUROC &gt; 0.497; procalcitonin, AUROC &gt; 0.653. (<b>C</b>) LAR kinetics expressed as LAR difference, AUROC &gt; 0.51, and LAR percentage change from baseline, AUROC &gt; 0.48.</p>
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<p>The area under the Receiver Operating Characteristic curve (AUROC) distinguishing survivors from nonsurvivors in 102 patients with sepsis. (<b>A</b>) <b>At inclusion:</b> LAR, AUROC &gt; 0.706; CRP, AUROC &gt; 0.705; procalcitonin, AUROC &gt; 0.628. (<b>B</b>) <b>One week after inclusion:</b> LAR, AUROC &gt; 0.750; CRP, AUROC &gt; 0.497; procalcitonin, AUROC &gt; 0.653. (<b>C</b>) LAR kinetics expressed as LAR difference, AUROC &gt; 0.51, and LAR percentage change from baseline, AUROC &gt; 0.48.</p>
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<p>(<b>A</b>) Kaplan–Meier estimates of mortality in 102 septic patients based on LARs at inclusion cutoff values obtained via ROC analysis (log-rank test: 9.904, <span class="html-italic">p</span> = 0.002). (<b>B</b>) Kaplan–Meier estimates of mortality in 102 septic patients based on LAR one week after inclusion cutoff values obtained via ROC analysis (log-rank test: 30.57, <span class="html-italic">p</span> &lt; 0.001).</p>
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12 pages, 482 KiB  
Article
Predicting Mortality in Sepsis: The Role of Dynamic Biomarker Changes and Clinical Scores—A Retrospective Cohort Study
by Norberth-Istvan Varga, Adela-Teodora Benea, Madalina-Ianca Suba, Adrian Vasile Bota, Cecilia Roberta Avram, Casiana Boru, Tiberiu Liviu Dragomir, Mirandolina Prisca, Tanasescu Sonia, Monica Susan and Florin George Horhat
Diagnostics 2024, 14(17), 1973; https://doi.org/10.3390/diagnostics14171973 - 6 Sep 2024
Viewed by 295
Abstract
Background: The prognostic value of baseline inflammatory markers in sepsis remains controversial, with conflicting evidence regarding their association with mortality. The dynamic changes in these markers over time might offer additional insights into disease progression and patient outcomes. Methods: This retrospective observational study [...] Read more.
Background: The prognostic value of baseline inflammatory markers in sepsis remains controversial, with conflicting evidence regarding their association with mortality. The dynamic changes in these markers over time might offer additional insights into disease progression and patient outcomes. Methods: This retrospective observational study included 138 patients with severe infections. The inflammatory biomarkers procalcitonin (PCT), C-reactive protein (CRP), and lactate (LAC) were measured at three time points: upon hospital admission (baseline), approximately 24–48 h after admission (second measurement; M2), and 48–72 h after admission (third measurement; M3). The primary outcome was 30-day mortality. A Mann–Whitney U test was used to compare the biomarker levels between the survivors and non-survivors. A Spearman’s correlation was used to assess the relationships between the baseline parameters. A logistic regression and a receiver operating characteristic (ROC) curve analysis were employed to evaluate the prognostic value of the baseline markers and their dynamic changes. Results: The baseline LAC and SOFA score were significantly associated with 30-day mortality. The percentage decrease in PCT, CRP, and LAC from the baseline to M3 emerged as strong predictors of survival, with the ROC curve analysis demonstrating superior discriminatory ability compared to the baseline values. CRP_Delta exhibited the highest AUC (0.903), followed by PCT_Delta (0.843) and LAC_Delta (0.703). Conclusions: The dynamic changes in these inflammatory biomarkers, particularly PCT, CRP, and LAC, offer valuable prognostic information beyond their baseline levels in predicting 30-day mortality in severe infections. These findings highlight the importance of monitoring biomarker trends for early risk stratification and potential treatment guidance. Full article
(This article belongs to the Special Issue New Diagnostic and Testing Strategies for Infectious Diseases)
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<p>ROC curves of the baseline variables and their corresponding percentage of change within the 72 h timeframe (third measurement).</p>
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22 pages, 7510 KiB  
Systematic Review
Evaluation of Population Pharmacokinetic Models of Micafungin: Implications for Dosing Regimen Optimization in Critically Ill Patients
by Xiping Li, Xiaoqin Liu, Juehui Mao, Dong Liu and Zheng Jiao
Pharmaceutics 2024, 16(9), 1145; https://doi.org/10.3390/pharmaceutics16091145 - 29 Aug 2024
Viewed by 333
Abstract
Micafungin (MFG) is a widely used echinocandin antifungal agent for treating invasive candidiasis, particularly in critically ill patients. However, its pharmacokinetics can be highly variable in this population. This systematic review aims to summarize population pharmacokinetic models and provide recommendations for its use [...] Read more.
Micafungin (MFG) is a widely used echinocandin antifungal agent for treating invasive candidiasis, particularly in critically ill patients. However, its pharmacokinetics can be highly variable in this population. This systematic review aims to summarize population pharmacokinetic models and provide recommendations for its use in intensive care unit (ICU) patients. Monte Carlo simulations were implemented to compare pharmacokinetic parameters and probability of target attainment (PTA) against various Candida species. A total of 16 studies were included, of which 6 studies were conducted in adult ICU patients. The key covariates were body size, liver function, and sepsis-related organ failure assessment score (SOFA) score. The median MFG clearance in adult ICU patients was 30–51% higher than in adult non-ICU patients. For infections with C. albican with MIC below 0.016 mg/L, micafungin dosages of 100 and 150 mg/d were recommended for adult non-ICU and ICU patients, respectively. For C. tropicalis and C. glabrata, 200 and 250 mg/d were recommended, respectively. However, for C. krusei and C. parapsilosis, none of the tested dosage regimens achieved assumed PTA criteria within MIC ranges of 0.125–0.25 mg/L and 0.125–2 mg/L, respectively. Therefore, MFG dosage regimens in ICU and non-ICU patients should be tailored based on the Candida spp. and their respective MIC values. Full article
(This article belongs to the Special Issue Optimizing Drug Safety and Efficacy: Pharmacokinetic Modeling)
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<p>PRISMA flow diagram for identifying population pharmacokinetics studies of MFG.</p>
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<p>Risk bias map of the included population pharmacokinetics studies.</p>
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<p>Simulated concentration–time profiles of MFG over 24 h at steady state in 70-kg adult patients administered with multiple doses of 100 mg MFG once daily [<a href="#B8-pharmaceutics-16-01145" class="html-bibr">8</a>,<a href="#B11-pharmaceutics-16-01145" class="html-bibr">11</a>,<a href="#B12-pharmaceutics-16-01145" class="html-bibr">12</a>,<a href="#B16-pharmaceutics-16-01145" class="html-bibr">16</a>,<a href="#B17-pharmaceutics-16-01145" class="html-bibr">17</a>,<a href="#B27-pharmaceutics-16-01145" class="html-bibr">27</a>,<a href="#B28-pharmaceutics-16-01145" class="html-bibr">28</a>,<a href="#B29-pharmaceutics-16-01145" class="html-bibr">29</a>,<a href="#B30-pharmaceutics-16-01145" class="html-bibr">30</a>,<a href="#B31-pharmaceutics-16-01145" class="html-bibr">31</a>,<a href="#B32-pharmaceutics-16-01145" class="html-bibr">32</a>,<a href="#B33-pharmaceutics-16-01145" class="html-bibr">33</a>]. The solid purple lines represent the median of the simulated concentration–time profiles and the light blue shadows represent the 5th–95th percentiles of the concentration–time profiles. MFG, micafungin.</p>
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<p>Distribution of the BW-adjusted CL of micafungin at steady state for various typical populations [<a href="#B8-pharmaceutics-16-01145" class="html-bibr">8</a>,<a href="#B11-pharmaceutics-16-01145" class="html-bibr">11</a>,<a href="#B12-pharmaceutics-16-01145" class="html-bibr">12</a>,<a href="#B16-pharmaceutics-16-01145" class="html-bibr">16</a>,<a href="#B17-pharmaceutics-16-01145" class="html-bibr">17</a>,<a href="#B18-pharmaceutics-16-01145" class="html-bibr">18</a>,<a href="#B19-pharmaceutics-16-01145" class="html-bibr">19</a>,<a href="#B20-pharmaceutics-16-01145" class="html-bibr">20</a>,<a href="#B21-pharmaceutics-16-01145" class="html-bibr">21</a>,<a href="#B27-pharmaceutics-16-01145" class="html-bibr">27</a>,<a href="#B28-pharmaceutics-16-01145" class="html-bibr">28</a>,<a href="#B29-pharmaceutics-16-01145" class="html-bibr">29</a>,<a href="#B30-pharmaceutics-16-01145" class="html-bibr">30</a>,<a href="#B31-pharmaceutics-16-01145" class="html-bibr">31</a>,<a href="#B32-pharmaceutics-16-01145" class="html-bibr">32</a>,<a href="#B33-pharmaceutics-16-01145" class="html-bibr">33</a>]. The SOFA scores were set to 7 for ICU patients with SOFA &lt; 10 and 11 for ICU patients with SOFA ≥ 10. The vertical dashed lines in each panel represented the median values of CL per body weight from all patients within each group.</p>
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<p>The effect of covariates on CL of micafungin in included studies [<a href="#B8-pharmaceutics-16-01145" class="html-bibr">8</a>,<a href="#B12-pharmaceutics-16-01145" class="html-bibr">12</a>,<a href="#B16-pharmaceutics-16-01145" class="html-bibr">16</a>,<a href="#B18-pharmaceutics-16-01145" class="html-bibr">18</a>,<a href="#B19-pharmaceutics-16-01145" class="html-bibr">19</a>,<a href="#B20-pharmaceutics-16-01145" class="html-bibr">20</a>,<a href="#B27-pharmaceutics-16-01145" class="html-bibr">27</a>,<a href="#B28-pharmaceutics-16-01145" class="html-bibr">28</a>,<a href="#B29-pharmaceutics-16-01145" class="html-bibr">29</a>,<a href="#B30-pharmaceutics-16-01145" class="html-bibr">30</a>,<a href="#B31-pharmaceutics-16-01145" class="html-bibr">31</a>]. * BW was transformed to equivalent FFM; ** For binary covariates, SOFA, 0 for SOFA ≥ 10 and 1 for SOFA &lt; 10; TBIL, 0 for TBIL ≥ 68.4 μmol/L and 1 for TBIL &lt; 68.4 μmol/L; ALB, 0 for ALB ≤ 25 (g/L) and ALB &gt; 25 (g/L); BW, body weight; FFM, free-fat mass; ALT, alanine amino transferase; AST, aspartate aminotransferase; PLT, platelet count; TBILI, total bilirubin; ALB, albumin; SOFA, sepsis-related organ failure assessment score.</p>
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<p>The PTA of micafungin for ICU adults or non-ICU adults against <span class="html-italic">Candida</span> spp. over 24 h at steady state [<a href="#B8-pharmaceutics-16-01145" class="html-bibr">8</a>,<a href="#B11-pharmaceutics-16-01145" class="html-bibr">11</a>,<a href="#B12-pharmaceutics-16-01145" class="html-bibr">12</a>,<a href="#B16-pharmaceutics-16-01145" class="html-bibr">16</a>,<a href="#B17-pharmaceutics-16-01145" class="html-bibr">17</a>,<a href="#B27-pharmaceutics-16-01145" class="html-bibr">27</a>,<a href="#B28-pharmaceutics-16-01145" class="html-bibr">28</a>,<a href="#B29-pharmaceutics-16-01145" class="html-bibr">29</a>,<a href="#B30-pharmaceutics-16-01145" class="html-bibr">30</a>,<a href="#B31-pharmaceutics-16-01145" class="html-bibr">31</a>,<a href="#B32-pharmaceutics-16-01145" class="html-bibr">32</a>,<a href="#B33-pharmaceutics-16-01145" class="html-bibr">33</a>]. The MIC breakpoints for <span class="html-italic">C. albicans</span> (blue), <span class="html-italic">C. glabrata</span> (purple), <span class="html-italic">C. krusei</span> (black), <span class="html-italic">C. tropicalis</span> (orange), and <span class="html-italic">C. parapsilosis</span> (green) are marked vertically with dashed lines in each panel, respectively. A PTA of 90% is highlighted horizontally with black dashed lines. All patients were administered intravenously with 100 mg MFG once daily for 7 days. The SOFA score in the ICU group was set to 11.</p>
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15 pages, 4828 KiB  
Article
An Integrated Approach Based on Clinical Data Combined with Metabolites and Biomarkers for the Assessment of Post-Operative Complications after Cardiac Surgery
by Peter Meinarovich, Alisa Pautova, Evgenii Zuev, Ekaterina Sorokina, Ekaterina Chernevskaya and Natalia Beloborodova
J. Clin. Med. 2024, 13(17), 5054; https://doi.org/10.3390/jcm13175054 - 26 Aug 2024
Viewed by 460
Abstract
Background: Early diagnosis of post-operative complications is an urgent task, allowing timely prescribing of appropriate therapy and reducing the cost of patient treatment. The purpose of this study was to determine whether an integrated approach based on clinical data, along with metabolites and [...] Read more.
Background: Early diagnosis of post-operative complications is an urgent task, allowing timely prescribing of appropriate therapy and reducing the cost of patient treatment. The purpose of this study was to determine whether an integrated approach based on clinical data, along with metabolites and biomarkers, had greater predictive value than the models built on fewer data in the early diagnosis of post-operative complications after cardiac surgery. Methods: The study included patients (n = 62) admitted for planned cardiac surgery (coronary artery bypass grafting with cardiopulmonary bypass) with (n = 26) or without (n = 36) post-operative complications. Clinical and laboratory data on the first day after surgery were analyzed. Additionally, patients’ blood samples were collected before and on the first day after surgery to determine biomarkers and metabolites. Results: Multivariate PLS-DA models, predicting the presence or absence of post-operative complications, were built using clinical data, concentrations of metabolites and biomarkers, and the entire data set (ROC-AUC = 0.80, 0.71, and 0.85, respectively). For comparison, we built univariate models using the EuroScore2 and SOFA scales, concentrations of lactate, the dynamic changes of 4-hydroxyphenyllactic acid, and the sum of three sepsis-associated metabolites (ROC-AUC = 0.54, 0.79, 0.62, 0.58, and 0.70, respectively). Conclusions: The proposed complex model using the entire dataset had the best characteristics, which confirms the expediency of searching for new predictive models based on a variety of factors. Full article
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<p>Study design summary (CABG—coronary artery bypass grafting).</p>
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<p>Resulting pipeline for building multivariate predictive models.</p>
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<p>VIP scores for PLS analysis. The blue line marks the threshold of importance (VIP score &gt; 1.0).</p>
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<p>Classification results of the final model fit on all data: scatter plot (<b>a</b>) and confusion matrix (<b>b</b>). Blue points (0) correspond to patients without complications (<span class="html-italic">n</span> = 36), orange points (1) correspond to patients with complications (<span class="html-italic">n</span> = 26) in (<b>a</b>).</p>
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<p>ROC curves for three multivariate models based on all data (<b>a</b>), clinical data (<b>b</b>), metabolites and biomarkers (<b>c</b>); and five univariate models based on SOFA (<b>d</b>), lactate (<b>e</b>), ΔΣ3AMM (<b>f</b>), Δp-HPhLA (<b>g</b>), and EuroScore2 (<b>h</b>). Blue lines explain means of true positive rate/false positive rate co-ordinates. Other lines show different cross-validation splits. Grey zone demonstrates 95% CI.</p>
Full article ">Figure 5 Cont.
<p>ROC curves for three multivariate models based on all data (<b>a</b>), clinical data (<b>b</b>), metabolites and biomarkers (<b>c</b>); and five univariate models based on SOFA (<b>d</b>), lactate (<b>e</b>), ΔΣ3AMM (<b>f</b>), Δp-HPhLA (<b>g</b>), and EuroScore2 (<b>h</b>). Blue lines explain means of true positive rate/false positive rate co-ordinates. Other lines show different cross-validation splits. Grey zone demonstrates 95% CI.</p>
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25 pages, 19272 KiB  
Article
6DoF Object Pose and Focal Length Estimation from Single RGB Images in Uncontrolled Environments
by Mayura Manawadu and Soon-Yong Park
Sensors 2024, 24(17), 5474; https://doi.org/10.3390/s24175474 - 23 Aug 2024
Viewed by 710
Abstract
Accurate 6DoF (degrees of freedom) pose and focal length estimation are important in extended reality (XR) applications, enabling precise object alignment and projection scaling, thereby enhancing user experiences. This study focuses on improving 6DoF pose estimation using single RGB images of unknown camera [...] Read more.
Accurate 6DoF (degrees of freedom) pose and focal length estimation are important in extended reality (XR) applications, enabling precise object alignment and projection scaling, thereby enhancing user experiences. This study focuses on improving 6DoF pose estimation using single RGB images of unknown camera metadata. Estimating the 6DoF pose and focal length from an uncontrolled RGB image, obtained from the internet, is challenging because it often lacks crucial metadata. Existing methods such as FocalPose and Focalpose++ have made progress in this domain but still face challenges due to the projection scale ambiguity between the translation of an object along the z-axis (tz) and the camera’s focal length. To overcome this, we propose a two-stage strategy that decouples the projection scaling ambiguity in the estimation of z-axis translation and focal length. In the first stage, tz is set arbitrarily, and we predict all the other pose parameters and focal length relative to the fixed tz. In the second stage, we predict the true value of tz while scaling the focal length based on the tz update. The proposed two-stage method reduces projection scale ambiguity in RGB images and improves pose estimation accuracy. The iterative update rules constrained to the first stage and tailored loss functions including Huber loss in the second stage enhance the accuracy in both 6DoF pose and focal length estimation. Experimental results using benchmark datasets show significant improvements in terms of median rotation and translation errors, as well as better projection accuracy compared to the existing state-of-the-art methods. In an evaluation across the Pix3D datasets (chair, sofa, table, and bed), the proposed two-stage method improves projection accuracy by approximately 7.19%. Additionally, the incorporation of Huber loss resulted in a significant reduction in translation and focal length errors by 20.27% and 6.65%, respectively, in comparison to the Focalpose++ method. Full article
(This article belongs to the Special Issue Computer Vision and Virtual Reality: Technologies and Applications)
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<p>Projection of an object onto the image plane of a pinhole camera using perspective projection.</p>
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<p>Initial position and orientation of the real-world chair and the image plane based on ground truth values.</p>
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<p>Change of the projection scale of the image after setting <math display="inline"><semantics> <msub> <mi>t</mi> <mi>z</mi> </msub> </semantics></math> to an arbitrary value.</p>
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<p>Obtaining the same projection size of the chair by re-scaling the focal length relative to the adjustment of <math display="inline"><semantics> <msub> <mi>t</mi> <mi>z</mi> </msub> </semantics></math>.</p>
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<p>Two-stage approach for predicting the 6DoF pose estimation and focal length from a single uncontrolled RGB image.</p>
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<p>Comparison of the outputs from the proposed method with Focalpose [<a href="#B13-sensors-24-05474" class="html-bibr">13</a>] and Focalpose++ [<a href="#B14-sensors-24-05474" class="html-bibr">14</a>] using Pix3D dataset. Subfigures (<b>a</b>–<b>t</b>) represents different classes of chair, sofa, bed and table of Pix3D Dataset. Metadata of these images are not available during the inference time.</p>
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<p>(<b>a</b>) Input single RGB image, (<b>b</b>) prediction from Focalpose [<a href="#B13-sensors-24-05474" class="html-bibr">13</a>], (<b>c</b>) prediction from the proposed work (Stage II output), (<b>d</b>) outputs by employing multiple refiner iterations to Stage II of the proposed approach. The green-colored contours represent the predicted pose during each iteration in the refiner of Stage II, and the red colored contour represent the ground truth.</p>
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<p>Distribution of <math display="inline"><semantics> <msub> <mi>t</mi> <mi>z</mi> </msub> </semantics></math> across different classes in Pix3D dataset.</p>
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16 pages, 2497 KiB  
Article
Exploring Ventilator-Associated Pneumonia: Microbial Clues and Biomarker Insights from a Retrospective Study
by Ahmed M. Gouda, Ashraf E. Sileem, Hanan M. Elnahas, Ahmed E. Tawfik, Refaat A. Eid, Ayed A. Shati, Saleh M. Al-Qahtani, Samy A. Dawood, Mohammed A. Alshehri, Mohamed Eissa, Mohamed A. Soltan, Ahmed E. Noreldin, Amir Helmy Elwishahy and Essamedin M. Negm
Medicina 2024, 60(8), 1346; https://doi.org/10.3390/medicina60081346 - 19 Aug 2024
Viewed by 1056
Abstract
Background and Objectives: Ventilator-associated pneumonia (VAP) is a common complication in critically ill patients receiving mechanical ventilation. The incidence rates of VAP vary, and it poses significant challenges due to microbial resistance and the potential for adverse outcomes. This study aims to [...] Read more.
Background and Objectives: Ventilator-associated pneumonia (VAP) is a common complication in critically ill patients receiving mechanical ventilation. The incidence rates of VAP vary, and it poses significant challenges due to microbial resistance and the potential for adverse outcomes. This study aims to explore the microbial profile of VAP and evaluate the utility of biomarkers and illness severity scores in predicting survival. Materials and Methods: A retrospective cohort study was conducted involving 130 patients diagnosed with VAP. Microbial analysis of bronchoalveolar lavage (BAL) fluid, as well as measurements of C-reactive protein (CRP) and procalcitonin (PCT) levels, were performed. Sequential Organ Failure Assessment (SOFA) and Acute Physiology and Chronic Health Evaluation II (APACHE II) scores were calculated to assess illness severity. Statistical analyses were conducted to determine correlations and associations. Results: The study revealed that Klebsiella pneumoniae (K. pneumoniae) (50.7%) and Pseudomonas aeruginosa (P. aeruginosa) (27.69%) were the most identified microorganisms in VAP cases. SOFA (p-value < 0.0001) and APACHE II (p-value < 0.0001) scores were effective in assessing the severity of illness and predicting mortality in VAP patients. Additionally, our investigation highlighted the prognostic potential of CRP levels (odds ratio [OR]: 0.980, 95% confidence interval [CI] 0.968 to 0.992, p = 0.001). Elevated levels of CRP were associated with reduced survival probabilities in VAP patients. Conclusion: This study highlights the microbial profile of VAP and the importance of biomarkers and illness severity scores in predicting survival. Conclusions: The findings emphasize the need for appropriate management strategies to combat microbial resistance and improve outcomes in VAP patients. Full article
(This article belongs to the Section Pulmonology)
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<p>Study flow diagram.</p>
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<p>A pie chart representing the microbiological profile of VAP Patients.</p>
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<p>Bar charts showing the comparative scores between the “died” and “recovered” groups of VAP Patients. (<b>a</b>) WBC count, (<b>b</b>) platelet count, (<b>c</b>) CRP, (<b>d</b>) procalcitonin, (<b>e</b>) SOFA, and (<b>f</b>) APACHE II Scores. * <span class="html-italic">p</span>-value &lt; 0.001.</p>
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<p>Antibiotic susceptibility profiles of <span class="html-italic">E. coli</span>, <span class="html-italic">A. baumanii</span>, <span class="html-italic">K. pneumoniae</span>, and <span class="html-italic">P. aeruginosa.</span> Abbreviations: AMP/PEN (ampicillin/penicillin), CFZ (cefazolin), FEP (cefepime), CRO (ceftriaxone), AMP/SUL (ampicillin/sulbactam), F (nitrofurantoin), PIP/TAZ (piperacillin/tazobactam), CIP (ciprofloxacin), ATM (aztreonam), TOB (tobramycin), CAZ (ceftazidime), SXT (sulfa-trimethoprim), MEP (meropenem), IMP (imipenem), ERT (ertapenem), GEN (gentamycin), AK (amikacin), LEV (levofloxacin), FOS (Fosfomycin), TIG (tigecycline), COL (colistin).</p>
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<p>Antibiotic susceptibility of Gram-positive MRSA. Abbreviations: NAF/OX (nafcillin/oxacillin), E (erythromycin), CLINDA (clindamycin), SXT (sulfa trimethoprim), TET (tetracycline), GEN/pen (gentamycin/penicillin), MOXIFLOX (moxifloxacin), VAN (vancomycin), LZD (linezolid).</p>
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<p>Correlations between APACHE II and SOFA scores and multiple laboratory values in VAP patients. (<b>a</b>,<b>b</b>) correlation between SOFA score and CRP and Procalcitonin. (<b>c</b>,<b>d</b>) correlation between APACHE II and CRP and Procalcitonin. (<b>e</b>,<b>f</b>) correlation of SOFA score and APACHE II with WBCs count, respectively. (<b>g</b>,<b>h</b>) correlation of SOFA score and APACHE II with platelets count, respectively.</p>
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13 pages, 865 KiB  
Article
The Respiratory Adjusted Shock Index at Admission Is a Valuable Predictor of In-Hospital Outcomes for Elderly Emergency Patients with Medical Diseases at a Japanese Community General Hospital
by Taiki Hori, Ken-ichi Aihara, Takeshi Watanabe, Kaori Inaba, Keisuke Inaba, Yousuke Kaneko, Saki Kawata, Keisuke Kawahito, Hiroki Kita, Kazuma Shimizu, Minae Hosoki, Kensuke Mori, Teruyoshi Kageji, Hideyuki Uraoka and Shingen Nakamura
J. Clin. Med. 2024, 13(16), 4866; https://doi.org/10.3390/jcm13164866 - 18 Aug 2024
Viewed by 585
Abstract
Background: The respiratory adjusted shock index (RASI) is a risk score whose usefulness in patients with sepsis and trauma has previously been reported. However, its relevance in elderly emergency patients with medical diseases is yet to be clarified. This study assessed the [...] Read more.
Background: The respiratory adjusted shock index (RASI) is a risk score whose usefulness in patients with sepsis and trauma has previously been reported. However, its relevance in elderly emergency patients with medical diseases is yet to be clarified. This study assessed the usefulness of the RASI, which can be evaluated without requiring special equipment, to provide objective and rapid emergency responses. Methods: In this retrospective study, we recruited patients with medical diseases, aged 65 years or older, who were transported to the emergency room from Tokushima Prefectural Kaifu Hospital and underwent arterial blood gas testing from 1 January 2022 to 31 December 2023. We investigated the association of the RASI with other indices, including the lactate level, National Early Warning Score 2 (NEWS2), Shock Index (SI), Sequential Organ Failure Assessment (SOFA) score, quick SOFA (qSOFA) score, and systemic inflammatory response syndrome (SIRS). Results: In this study, we included 260 patients (mean age, 86 years), of whom 234 were admitted to the hospital; 27 and 49 patients died within 7 and 30 days of admission, respectively. The RASI was positively correlated with the lactate level, NEWS2, SI, and increase in the SOFA score (p < 0.001). The RASI was higher in patients with a SIRS or qSOFA score ≥ 2 than in those without (p < 0.001). It predicted death within 7 and 30 days of admission with an area under the curve (AUC) of 0.80 (95% confidence interval [CI]: 0.73–0.87), sensitivity of 96.3%, and specificity of 53.6% when the cutoff value was set to 1.58 and with an AUC of 0.73 (95% CI: 0.66–0.81), sensitivity of 69.4%, and specificity of 70.6% when the cutoff value was set to 1.83, respectively. Conclusions: The RASI is a simple indicator that can be used for predicting in-hospital outcomes in elderly emergency patients with medical diseases. Larger prospective studies based on this study are needed. Full article
(This article belongs to the Special Issue Geriatric Emergency Medicine: Clinical Advances and Trends)
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<p>Association of RASI with lactate, NEWS2, Shock Index, ΔSOFA score, and SIRS criteria. (<b>a</b>) Association between RASI and lactate. (<b>b</b>) Association between RASI and NEWS2. (<b>c</b>) Association between RASI and Shock Index. (<b>d</b>) Association between RASI and ΔSOFA score. (<b>e</b>) Comparison of RASI in patients with qSOFA scores of ≥2 or &lt;2. (<b>f</b>) Comparison of RASI in patients with or without SIRS. Abbreviations: RASI: respiratory adjusted shock index; NEWS2: National Early Warning Score 2; SOFA: Sequential Organ Failure Assessment; qSOFA: quick Sequential Organ Failure Assessment; SIRS: systemic inflammatory response syndrome.</p>
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<p>Comparison of RASI between individuals who died and those who did not die within 7 and 30 days. Comparison of RASI in patients who died within 7 (<b>a</b>) and 30 days (<b>b</b>) after admission. Abbreviation: RASI: respiratory adjusted shock index.</p>
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<p>Predictive capacities of RASI, lactate, NEWS2, Shock Index, ΔSOFA score, qSOFA score, and SIRS criteria for death within 7 and 30 days. Predictive capacities for death within 7 days (<b>a</b>) and 30 days (<b>b</b>) were evaluated using decision curve analysis. Abbreviations: RASI: respiratory adjusted shock index; NEWS2: National Early Warning Score 2; SOFA: Sequential Organ Failure Assessment; qSOFA: quick Sequential Organ Failure Assessment; SIRS: systemic inflammatory response syndrome.</p>
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11 pages, 471 KiB  
Article
Rotational Thromboelastometric Profile in Early Sepsis: A Prospective Cohort Study
by Piotr F. Czempik and Agnieszka Wiórek
Biomedicines 2024, 12(8), 1880; https://doi.org/10.3390/biomedicines12081880 - 17 Aug 2024
Viewed by 511
Abstract
Background: Coagulation abnormalities are common in sepsis patients and are associated with increased mortality. This study aimed to assess the hemostatic profile of sepsis patients using rotational thromboelastometry (ROTEM) and to find the ROTEM parameters best predicting short-term mortality. Methods: We conducted a [...] Read more.
Background: Coagulation abnormalities are common in sepsis patients and are associated with increased mortality. This study aimed to assess the hemostatic profile of sepsis patients using rotational thromboelastometry (ROTEM) and to find the ROTEM parameters best predicting short-term mortality. Methods: We conducted a prospective analysis of consecutive sepsis patients hospitalized in the intensive care unit. The inclusion criteria were diagnosis of sepsis or septic shock and pro-calcitonin concentration >0.5 ng mL−1. Clinical, standard laboratory, and ROTEM analyses were performed. Results: The study group comprised 38 (49%) males and 40 (51%) females. Median Sequential Organ Failure Assessment (SOFA) score was 8 (interquartile range IQR 5–11) points. The most common primary sites of infection were pneumonia (n = 27/35%), intra-abdominal (n = 27/35%), urinary tract infection (n=20/26%), and others (n = 4/6%). The following parameters evaluating fibrinogen function were outside the reference range: clotting time (CT), clot amplitude (A) at 10 and 20 min, and maximal clot firmness (MCF). Out of 78 patients, 28 (36%) died in the intensive care unit. Significant differences between survivors and non-survivors of sepsis were present for the ROTEM parameters assessing fibrinolytic activity. Conclusions: ROTEM in the early phase of sepsis reveals increased coagulation mediated through the function of fibrinogen. Non-survivors showed slightly lower fibrinolytic activity than survivors; however, it was still within test reference values. The highest predicting value was obtained by a model incorporating, among others, extrinsic coagulation pathway fibrinolytic parameters. Full article
(This article belongs to the Special Issue Sepsis: Pathophysiology and Early Diagnostics)
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<p>The study flow chart. <sup>1</sup> Procalcytonin. <sup>2</sup> Low-molecular-weight heparin. <sup>3</sup> Unfractionated heparin. <sup>4</sup> Prothrombin complex concentrate.</p>
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11 pages, 427 KiB  
Article
Evaluating the Utility of Clinical Scores APACHE, CURB, SOFA, and NEWS2 at Admission and 5-Days after Symptom Onset in Predicting Severe COVID-19 in Patients with Diabetes
by Radu Ion, Jaya Shankar Sai Kumar Kimidi, Chaitanya Kalapala, Oktrian FNU, Varshika Ramakrishnan Chandrababu, Omprakash Reddy Desireddygari, Mirela Loredana Grigras, Ovidiu Rosca, Felix Bratosin, Flavius Cioca, Romulus Timar and Rodica Anamaria Negrean
J. Pers. Med. 2024, 14(8), 868; https://doi.org/10.3390/jpm14080868 - 16 Aug 2024
Viewed by 459
Abstract
The elevated risk of severe COVID-19 outcomes in patients with diabetes underscores the need for effective predictive tools. This study aimed to assess the predictive accuracy of APACHE II, CURB-65, SOFA, and NEWS2 scores at critical time points in diabetic patients diagnosed with [...] Read more.
The elevated risk of severe COVID-19 outcomes in patients with diabetes underscores the need for effective predictive tools. This study aimed to assess the predictive accuracy of APACHE II, CURB-65, SOFA, and NEWS2 scores at critical time points in diabetic patients diagnosed with COVID-19, aiming to guide early and potentially life-saving interventions. In a prospective cohort study conducted from January 2021 to December 2023, adult patients with type 1 or type 2 diabetes and confirmed SARS-CoV-2 infection were evaluated. Clinical scores were calculated at admission and five days post-symptom onset, with data analyzed using receiver operating characteristic (ROC) curves and logistic regression to determine areas under the curve (AUC) and hazard ratios (HR) for severe outcomes. Among the 141 diabetic patients studied, ROC analysis revealed high AUC values for SOFA (0.771 at admission, 0.873 at day five) and NEWS2 (0.892 at admission, 0.729 at day five), indicating strong predictive accuracy for these scores. The APACHE II score’s AUC improved from 0.698 at admission to 0.806 on day five, reflecting worsening patient conditions. Regression analysis showed significant HRs associated with exceeding threshold scores: The SOFA score HR at day five was 3.07 (95% CI: 2.29–4.12, p < 0.001), indicating a threefold risk of severe outcomes. Similarly, the APACHE II score showed an HR of 2.96 (95% CI: 2.21–3.96, p < 0.001) at day five, highlighting its utility in predicting severe disease progression. The SOFA and NEWS2 scores demonstrated excellent early predictive accuracy for severe COVID-19 outcomes in diabetic patients, with significant AUC and HR findings. Continuous score monitoring, especially of APACHE II and SOFA, is crucial for managing and potentially mitigating severe complications in this vulnerable population. These tools can effectively assist in the timely escalation of care, thus potentially reducing morbidity and mortality among diabetic patients during the COVID-19 pandemic. Full article
(This article belongs to the Special Issue Novel Diagnostics and Therapies for Infectious Disease)
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<p>Forest plot analysis of risk of COVID-19 development in patients with diabetes.</p>
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12 pages, 635 KiB  
Article
Can We Improve Mortality Prediction in Patients with Sepsis in the Emergency Department?
by Sonia Luka, Adela Golea, Ștefan Cristian Vesa, Crina-Elena Leahu, Raluca Zăgănescu and Daniela Ionescu
Medicina 2024, 60(8), 1333; https://doi.org/10.3390/medicina60081333 - 16 Aug 2024
Viewed by 801
Abstract
Background and Objectives: Sepsis represents a global health challenge and requires advanced diagnostic and prognostic approaches due to its elevated rate of morbidity and fatality. Our study aimed to assess the value of a novel set of six biomarkers combined with severity [...] Read more.
Background and Objectives: Sepsis represents a global health challenge and requires advanced diagnostic and prognostic approaches due to its elevated rate of morbidity and fatality. Our study aimed to assess the value of a novel set of six biomarkers combined with severity scores in predicting 28 day mortality among patients presenting with sepsis in the Emergency Department (ED). Materials and Methods: This single-center, observational, prospective cohort included sixty-seven consecutive patients with septic shock and sepsis enrolled from November 2020 to December 2022, categorized into survival and non-survival groups based on outcomes. The following were assessed: procalcitonin (PCT), soluble Triggering Receptor Expressed on Myeloid Cells-1 (sTREM-1), the soluble form of the urokinase plasminogen activator receptor (suPAR), high-sensitivity C-reactive protein (hs-CRP), interleukin-6 (IL-6), and azurocidin 1 (AZU1), alongside clinical scores such as the Quick Sequential Organ Failure Assessment (qSOFA), Systemic Inflammatory Response Syndrome (SIRS), the Sequential Organ Failure Assessment (SOFA), the Acute Physiology and Chronic Health Evaluation II (APACHE II), the Simplified Acute Physiology Score II and III (SAPS II/III), the National Early Warning Score (NEWS), Mortality in Emergency Department Sepsis (MEDS), the Charlson Comorbidity Index (CCI), and the Glasgow Coma Scale (GCS). The ability of each biomarker and clinical score and their combinations to predict 28 day mortality were evaluated. Results: The overall mortality was 49.25%. Mechanical ventilation was associated with a higher mortality rate. The levels of IL-6 were significantly higher in the non-survival group and had higher AUC values compared to the other biomarkers. The GCS, SOFA, APACHEII, and SAPS II/III showed superior predictive ability. Combining IL-6 with suPAR, AZU1, and clinical scores SOFA, APACHE II, and SAPS II enhanced prediction accuracy compared with individual biomarkers. Conclusion: In our study, IL-6 and SAPS II/III were the most accurate predictors of 28 day mortality for sepsis patients in the ED. Full article
(This article belongs to the Special Issue Emergency Medicine and Emergency Room Medical Concerns)
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<p>Flowchart of the patients included in the study.</p>
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14 pages, 3474 KiB  
Article
A Real-World Data Observational Analysis of the Impact of Liposomal Amphotericin B on Renal Function Using Machine Learning in Critically Ill Patients
by Ignasi Sacanella, Erika Esteve-Pitarch, Jessica Guevara-Chaux, Julen Berrueta, Alejandro García-Martínez, Josep Gómez, Cecilia Casarino, Florencia Alés, Laura Canadell, Ignacio Martín-Loeches, Santiago Grau, Francisco Javier Candel, María Bodí and Alejandro Rodríguez
Antibiotics 2024, 13(8), 760; https://doi.org/10.3390/antibiotics13080760 - 12 Aug 2024
Viewed by 599
Abstract
Background: Liposomal amphotericin B (L-AmB) has become the mainstay of treatment for severe invasive fungal infections. However, the potential for renal toxicity must be considered. Aims: To evaluate the incidence of acute kidney injury (AKI) in critically ill patients receiving L-AmB for more [...] Read more.
Background: Liposomal amphotericin B (L-AmB) has become the mainstay of treatment for severe invasive fungal infections. However, the potential for renal toxicity must be considered. Aims: To evaluate the incidence of acute kidney injury (AKI) in critically ill patients receiving L-AmB for more than 48 h. Methods: Retrospective, observational, single-center study. Clinical, demographic and laboratory variables were obtained automatically from the electronic medical record. AKI incidence was analyzed in the entire population and in patients with a “low” or “high” risk of AKI based on their creatinine levels at the outset of the study. Factors associated with the development of AKI were studied using random forest models. Results: Finally, 67 patients with a median age of 61 (53–71) years, 67% male, a median SOFA of 4 (3–6.5) and a crude mortality of 34.3% were included. No variations in serum creatinine were observed during the observation period, except for a decrease in the high-risk subgroup. A total of 26.8% (total population), 25% (low risk) and 13% (high risk) of patients developed AKI. Norepinephrine, the SOFA score, furosemide (general model), potassium, C-reactive protein and procalcitonin (low-risk subgroup) were the variables identified by the random forest models as important contributing factors to the development of AKI other than L-AmB administration. Conclusions: The development of AKI is multifactorial and the administration of L-AmB appears to be safe in this group of patients. Full article
(This article belongs to the Special Issue Infection Diagnostics and Antimicrobial Therapy for Critical Patient)
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<p>Flow chart of included patients.</p>
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<p>Contribution of each confounding variable according to the random forest (RF) model for variables associated with the development of AKI with the total dose of L-AmB administered at day 3 (Model 1) or the total duration of L-AmB administration (Model 2). This RF model was applied to the whole population of patients.</p>
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<p>Contribution of each confounding variable according to the random forest (RF) model for variables associated with the development of AKI, considering either the total dose of L-AmB administered on day 3 (model 1) or the total duration of L-AmB administration (model 2). This RF model was applied to patients with a lower risk of AKI. Note: the total duration of L-AmB was not deemed important by the model and thus does not appear in the graph.</p>
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14 pages, 1246 KiB  
Article
Patterns, Outcomes and Economic Burden of Primary vs. Secondary Bloodstream Infections: A Single Center, Cross-Sectional Study
by Ioannis Chandroulis, Georgios Schinas, Anne-Lise de Lastic, Eleni Polyzou, Stamatia Tsoupra, Christos Davoulos, Martha Kolosaka, Vasiliki Niarou, Spyridoula Theodoraki, Dimitrios Ziazias, Foteini Kosmopoulou, Christina-Panagiota Koutsouri, Charalambos Gogos and Karolina Akinosoglou
Pathogens 2024, 13(8), 677; https://doi.org/10.3390/pathogens13080677 - 9 Aug 2024
Viewed by 499
Abstract
Bloodstream infections (BSIs) can be primary or secondary, with significant associated morbidity and mortality. Primary bloodstream infections (BSIs) are defined as infections where no clear infection source is identified, while secondary BSIs originate from a localized infection site. This study aims to compare [...] Read more.
Bloodstream infections (BSIs) can be primary or secondary, with significant associated morbidity and mortality. Primary bloodstream infections (BSIs) are defined as infections where no clear infection source is identified, while secondary BSIs originate from a localized infection site. This study aims to compare patterns, outcomes, and medical costs between primary and secondary BSIs and identify associated factors. Conducted at the University Hospital of Patras, Greece, from May 2016 to May 2018, this single-center retrospective cohort study included 201 patients with confirmed BSIs based on positive blood cultures. Data on patient characteristics, clinical outcomes, hospitalization costs, and laboratory parameters were analyzed using appropriate statistical methods. Primary BSIs occurred in 22.89% (46 patients), while secondary BSIs occurred in 77.11% (155 patients). Primary BSI patients were younger and predominantly nosocomial, whereas secondary BSI was mostly community-acquired. Clinical severity scores (SOFA, APACHE II, SAPS, and qPitt) were significantly higher in primary compared to secondary BSI. The median hospital stay was longer for primary BSI (21 vs. 12 days, p < 0.001). Although not statistically significant, mortality rates were higher in primary BSI (43.24% vs. 26.09%). Total care costs were significantly higher for primary BSI (EUR 4388.3 vs. EUR 2530.25, p = 0.016), driven by longer hospital stays and increased antibiotic costs. This study underscores the distinct clinical and economic challenges of primary versus secondary BSI and emphasizes the need for prompt diagnosis and tailored antimicrobial therapy. Further research should focus on developing specific management guidelines for primary BSI and exploring interventions to reduce BSI burden across healthcare settings. Full article
(This article belongs to the Special Issue Hospital-Acquired Infections and Multidrug-Resistant (MDR) Pathogens)
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<p>Most common pathogens between primary and secondary BSI. (* denotes statistical significance).</p>
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<p>Distribution of length of stay between primary and secondary BSI.</p>
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<p>Mortality rate between primary and secondary BSI.</p>
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<p>Distribution of total costs and antibiotic costs between primary and secondary BSI.</p>
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10 pages, 2110 KiB  
Article
Club Cell Secretory Protein-16 (CC16) as a Prognostic Biomarker for COVID-19 and H1N1 Viral Infections
by Shane Moore, Keerthana Gopichandran, Elizabeth Sevier, Siddhika Gamare, Sultan Almuntashiri, Gustavo Ramírez, Nora Regino, Luis Jiménez-Alvarez, Alfredo Cruz-Lagunas, Tatiana S. Rodriguez-Reyna, Joaquin Zuñiga, Caroline A. Owen, Xiaoyun Wang and Duo Zhang
Diagnostics 2024, 14(16), 1720; https://doi.org/10.3390/diagnostics14161720 - 8 Aug 2024
Viewed by 675
Abstract
Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) and H1N1 viruses are inflammatory lung pathogens that can lead to acute lung injury (ALI) and acute respiratory distress syndrome (ARDS). ALI/ARDS are still life-threatening diseases in critically ill patients with 30–40% mortality in the last [...] Read more.
Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) and H1N1 viruses are inflammatory lung pathogens that can lead to acute lung injury (ALI) and acute respiratory distress syndrome (ARDS). ALI/ARDS are still life-threatening diseases in critically ill patients with 30–40% mortality in the last decade. Currently, there are no laboratory tests for the early diagnosis or prognosis of ALI/ARDS. Club cell secretory protein (CC16) has been investigated as a potential biomarker of lung epithelial damage in various lung diseases. In this study, we evaluated whether plasma CC16 reflects the severity of COVID-19 and H1N1 infections. The plasma CC16 levels showed no significant differences between H1N1 and COVID-19 groups (p = 0.09). Among all subjects, CC16 levels were significantly higher in non-survivors than in survivors (p = 0.001). Upon the area under the receiver operating characteristic (AUROC) analysis, CC16 had an acceptable value to distinguish survivors and non-survivors (p = 0.002). In the COVID-19 group, plasma CC16 levels moderately correlated with the Acute Physiology and Chronic Health Evaluation II (APACHE II) score (r = 0.374, p = 0.003) and Sequential Organ Failure Assessment (SOFA) score (r = 0.474, p < 0.001). In the H1N1 group, a positive correlation was observed between the CC16 levels and hospital length of stay (r = 0.311, p = 0.022). Among all the patients, weak correlations between plasma CC16 levels with the SOFA score (r = 0.328, p < 0.001) and hospital length of stay (r = 0.310, p < 0.001) were observed. Thus, circulating CC16 might reflect the severity of COVID-19 and H1N1 infections. Full article
(This article belongs to the Section Clinical Laboratory Medicine)
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<p>Comparison of plasma CC16 in various groups. (<b>A</b>) COVID-19 (<span class="html-italic">n</span> = 60) versus H1N1 (<span class="html-italic">n</span> = 61). (<b>B</b>) ROC curve to distinguish between COVID-19 and H1N1 based on CC16 level. (<b>C</b>) Survivors (<span class="html-italic">n</span> = 96) vs. non-survivors (<span class="html-italic">n</span> = 25). (<b>D</b>) ROC curve to distinguish between survivors and non-survivors based on CC16 level.</p>
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<p>Correlation analyses between plasma CC16 and the prognostic parameters in COVID-19 patients. Pearson correlation was used to evaluate relationships between (<b>A</b>) CC16 and PaO<sub>2</sub>/FIO<sub>2</sub> (<span class="html-italic">n</span> = 60), (<b>B</b>) CC16 and APACHE III score (<span class="html-italic">n</span> = 60), (<b>C</b>) CC16 and SOFA score (<span class="html-italic">n</span> = 60), and (<b>D</b>) CC16 and hospital length of stay (<span class="html-italic">n</span> = 60).</p>
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<p>Correlation analyses between plasma CC16 and the prognostic parameters in H1N1 patients. Pearson correlation was used to evaluate relationships between (<b>A</b>) CC16 and PaO<sub>2</sub>/FIO<sub>2</sub> (<span class="html-italic">n</span> = 57), (<b>B</b>) CC16 and APACHE III score (<span class="html-italic">n</span> = 43), (<b>C</b>) CC16 and SOFA score (<span class="html-italic">n</span> = 52), and (<b>D</b>) CC16 and hospital length of stay (<span class="html-italic">n</span> = 54).</p>
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<p>Correlation analyses between plasma CC16 and the prognostic parameters in infected patients from COVID-19 and H1N1 groups. Pearson correlation was used to evaluate relationships between (<b>A</b>) CC16 and PaO<sub>2</sub>/FIO<sub>2</sub> (<span class="html-italic">n</span> = 117), (<b>B</b>) CC16 and APACHE III score (<span class="html-italic">n</span> = 103), (<b>C</b>) CC16 and SOFA score (<span class="html-italic">n</span> = 112), and (<b>D</b>) CC16 and hospital length of stay (<span class="html-italic">n</span> = 114).</p>
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10 pages, 895 KiB  
Article
Association between Inflammation-Based Prognostic Markers and Mortality in Patients Admitted to Intensive Care Units
by Ah Ran Oh, Jeong-Am Ryu, Seung Joo Lee, Chung Su Kim and Sangmin Maria Lee
Diagnostics 2024, 14(16), 1709; https://doi.org/10.3390/diagnostics14161709 - 6 Aug 2024
Viewed by 615
Abstract
Background: We compared the prognostic value of the C-reactive protein (CRP)-to-albumin ratio (CAR), neutrophil-to-lymphocyte ratio (NLR), and modified Glasgow prognostic score (mGPS) with the Sequential Organ Failure Assessment (SOFA) score in an intensive care unit (ICUs). Methods: This study used the data of [...] Read more.
Background: We compared the prognostic value of the C-reactive protein (CRP)-to-albumin ratio (CAR), neutrophil-to-lymphocyte ratio (NLR), and modified Glasgow prognostic score (mGPS) with the Sequential Organ Failure Assessment (SOFA) score in an intensive care unit (ICUs). Methods: This study used the data of 53,877 adult patients admitted to an ICU between June 2013 and May 2022. Using the CAR, NLR, and mGPS values, as well as the SOFA score from the ICU, we conducted multivariable logistic regression analysis and used the receiver operating characteristic (ROC) curve to compare the predictive value for 28-day and 1-year mortality. Results: A total of 2419 patients (4.5%) died within 28 days, and 6209 (11.5%) patients died within 1 year. After an adjustment, all predictors were found to be independent risk factors for 28-day mortality (odds ratio [OR] 1.31, 95% confidence interval [CI] 1.29–1.33, p < 0.001 for the SOFA score; OR 1.05, 95% CI 1.03–1.07, p < 0.001 for CAR; OR 1.01, 95% CI 1.00–1.02, p < 0.001 for the NLR; and OR 1.19, 95% CI 1.08–1.30, p < 0.001 for the mGPS). This trend persisted for the 1-year mortality. In ROC curve analysis, the CAR showed better predictability than the NLR and mGPS. Furthermore, the predictive power of the CAR was significantly higher than that of the SOFA score for 1-year mortality. Conclusions: The CAR, NLR, and mGPS values at ICU admission were independent risk factors of mortality after ICU admission. The predictive value of CAR was higher than that of the SOFA score for 1-year mortality. CAR assessment at ICU admission may be a feasible predictor of long-term mortality. Full article
(This article belongs to the Special Issue ICU Disease Diagnosis)
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<p>Patient selection flowchart.</p>
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<p>Receiver operating characteristic curves of the CAR, NLR, and mGPS values and the SOFA score for (<b>A</b>) 28-day mortality and (<b>B</b>) 1-year mortality after ICU admission.</p>
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<p>Receiver operating characteristic curves of CAR and SOFA score according to ICU type for (<b>A</b>) 28-day mortality and (<b>B</b>) 1-year mortality.</p>
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