Pub Date : 2026-03-09eCollection Date: 2026-01-01DOI: 10.1155/ccrp/4492230
Zainab A Almardod, Kishore G Sam, Eman E Younis
Background: Thrombocytopenia is a common hematologic abnormality in the intensive care unit (ICU), affecting approximately 50% of patients. It is associated with increased mortality and bleeding risk. Despite its clinical significance, epidemiological studies on ICU-related thrombocytopenia in Gulf Cooperation Council countries remain limited.
Methods: This prospective observational cohort study was conducted to investigate the prevalence, risk factors, characteristics, and clinical outcomes of thrombocytopenia in the ICU. We included ICU patients admitted for ≥ 24 h, excluding pregnant women and individuals under 18. Thrombocytopenia was defined as a platelet count < 150 × 109/L after ruling out pseudothrombocytopenia. Patients were stratified by thrombocytopenia severity and followed until discharge, death, or 30 days post onset. Risk factors were analyzed using multivariable modified Poisson regression models. The Naranjo probability scale and the 4Ts score were used for causal assessment of drug-induced thrombocytopenia (DIT) and heparin-induced thrombocytopenia (HIT). Primary outcomes included three-month ICU mortality and major bleeding. Kaplan-Meier with log-rank tests assessed time-to-mortality.
Results: The study enrolled 276 patients; 38.8% had thrombocytopenia, including 23.4% with severe thrombocytopenia. The incidence of new-onset thrombocytopenia was 22.5%. DIT was suspected in 15% of cases, including five patients with potential HIT. Shock diagnosis was a significant predictor of new-onset thrombocytopenia (adjusted risk ratio = 2.26, 95% confidence interval: 1.35-3.79). Thrombocytopenic patients had higher Acute Physiology and Chronic Health Evaluation (APACHE) IV scores (p < 0.001) and experienced more major bleeding events (16.8% vs. 8.3%, p = 0.03) and higher mortality rates (27.1% vs. 5.3%, p < 0.001) with reduced time-to-mortality (log-rank p = 0.01). New-onset thrombocytopenia was independently associated with major bleeding and mortality.
Conclusion: Thrombocytopenia is prevalent in the ICU, correlating to disease severity, major bleeding, and mortality. The study's findings underscore the need for timely recognition and effective management of thrombocytopenia to improve patient outcomes.
{"title":"Prevalence, Risk Factors, Characteristics, and Clinical Outcomes of Thrombocytopenia in the Intensive Care Unit: A Prospective Single-Center Cohort Study.","authors":"Zainab A Almardod, Kishore G Sam, Eman E Younis","doi":"10.1155/ccrp/4492230","DOIUrl":"https://doi.org/10.1155/ccrp/4492230","url":null,"abstract":"<p><strong>Background: </strong>Thrombocytopenia is a common hematologic abnormality in the intensive care unit (ICU), affecting approximately 50% of patients. It is associated with increased mortality and bleeding risk. Despite its clinical significance, epidemiological studies on ICU-related thrombocytopenia in Gulf Cooperation Council countries remain limited.</p><p><strong>Methods: </strong>This prospective observational cohort study was conducted to investigate the prevalence, risk factors, characteristics, and clinical outcomes of thrombocytopenia in the ICU. We included ICU patients admitted for ≥ 24 h, excluding pregnant women and individuals under 18. Thrombocytopenia was defined as a platelet count < 150 × 10<sup>9</sup>/L after ruling out pseudothrombocytopenia. Patients were stratified by thrombocytopenia severity and followed until discharge, death, or 30 days post onset. Risk factors were analyzed using multivariable modified Poisson regression models. The Naranjo probability scale and the 4Ts score were used for causal assessment of drug-induced thrombocytopenia (DIT) and heparin-induced thrombocytopenia (HIT). Primary outcomes included three-month ICU mortality and major bleeding. Kaplan-Meier with log-rank tests assessed time-to-mortality.</p><p><strong>Results: </strong>The study enrolled 276 patients; 38.8% had thrombocytopenia, including 23.4% with severe thrombocytopenia. The incidence of new-onset thrombocytopenia was 22.5%. DIT was suspected in 15% of cases, including five patients with potential HIT. Shock diagnosis was a significant predictor of new-onset thrombocytopenia (adjusted risk ratio = 2.26, 95% confidence interval: 1.35-3.79). Thrombocytopenic patients had higher Acute Physiology and Chronic Health Evaluation (APACHE) IV scores (<i>p</i> < 0.001) and experienced more major bleeding events (16.8% vs. 8.3%, <i>p</i> = 0.03) and higher mortality rates (27.1% vs. 5.3%, <i>p</i> < 0.001) with reduced time-to-mortality (log-rank <i>p</i> = 0.01). New-onset thrombocytopenia was independently associated with major bleeding and mortality.</p><p><strong>Conclusion: </strong>Thrombocytopenia is prevalent in the ICU, correlating to disease severity, major bleeding, and mortality. The study's findings underscore the need for timely recognition and effective management of thrombocytopenia to improve patient outcomes.</p>","PeriodicalId":46583,"journal":{"name":"Critical Care Research and Practice","volume":"2026 ","pages":"4492230"},"PeriodicalIF":1.8,"publicationDate":"2026-03-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12968733/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147436606","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 : 2026-02-25eCollection Date: 2026-01-01DOI: 10.1155/ccrp/8835519
Vinay Kumari, Choki Dema, Jyoti Sarin
Objective: To evaluate the effectiveness of multisensory stimulation in enhancing consciousness levels and physiological parameters among critically ill patients in the ICU.
Methods: A quasi-experimental, nonequivalent control group pretest-post-test design was employed. Seventy-one patients with Glasgow Coma scale (GCS) scores below 13 were recruited through convenience sampling. Participants were divided into an experimental group (n = 34), which received multisensory stimulation twice daily for 7 days, and a comparison group (n = 37), which received standard ICU care. Physiological indicators (heart rate, respiration rate, blood pressure, temperature, SpO2, and glucose) and consciousness levels (GCS) were determined before and after the intervention. Data were analyzed using SPSS version 20.0, with statistical significance established at p ≤ 0.05.
Result: Experimental and comparison groups showed significant differences in consciousness from day 4 to 7 with higher GCS scores in the experimental group. Repeated measures ANOVA demonstrated improvement in GCS scores from the evening of day 2 till day 7 (p = 0.05). In contrast, the comparison group experienced a higher incidence of physiological adverse events such as tachycardia and bradycardia.
Conclusion: Multisensory stimulation is a safe and effective method to enhance consciousness in critically ill patients without inducing adverse physiological effects. Early integration of MSS into ICU protocols is recommended. Further research is needed to explore MSS's efficacy across diverse medical conditions.
{"title":"Effect of Auditory and Tactile Stimulation on the Level of Consciousness and Physiological Parameters in ICU Patients With Altered Consciousness.","authors":"Vinay Kumari, Choki Dema, Jyoti Sarin","doi":"10.1155/ccrp/8835519","DOIUrl":"10.1155/ccrp/8835519","url":null,"abstract":"<p><strong>Objective: </strong>To evaluate the effectiveness of multisensory stimulation in enhancing consciousness levels and physiological parameters among critically ill patients in the ICU.</p><p><strong>Methods: </strong>A quasi-experimental, nonequivalent control group pretest-post-test design was employed. Seventy-one patients with Glasgow Coma scale (GCS) scores below 13 were recruited through convenience sampling. Participants were divided into an experimental group (<i>n</i> = 34), which received multisensory stimulation twice daily for 7 days, and a comparison group (<i>n</i> = 37), which received standard ICU care. Physiological indicators (heart rate, respiration rate, blood pressure, temperature, SpO<sub>2</sub>, and glucose) and consciousness levels (GCS) were determined before and after the intervention. Data were analyzed using SPSS version 20.0, with statistical significance established at <i>p</i> ≤ 0.05.</p><p><strong>Result: </strong>Experimental and comparison groups showed significant differences in consciousness from day 4 to 7 with higher GCS scores in the experimental group. Repeated measures ANOVA demonstrated improvement in GCS scores from the evening of day 2 till day 7 (<i>p</i> = 0.05). In contrast, the comparison group experienced a higher incidence of physiological adverse events such as tachycardia and bradycardia.</p><p><strong>Conclusion: </strong>Multisensory stimulation is a safe and effective method to enhance consciousness in critically ill patients without inducing adverse physiological effects. Early integration of MSS into ICU protocols is recommended. Further research is needed to explore MSS's efficacy across diverse medical conditions.</p>","PeriodicalId":46583,"journal":{"name":"Critical Care Research and Practice","volume":"2026 ","pages":"8835519"},"PeriodicalIF":1.8,"publicationDate":"2026-02-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12933182/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147311172","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 : 2026-02-17eCollection Date: 2026-01-01DOI: 10.1155/ccrp/6920702
Tung Phi Nguyen, Thang Trong Khong, Hoai Thi Thu Vu, Nam Ngoc Phuong Nguyen, Phong Van Phan, Hue Thi Le, Tra Thi Hoang, Huyen Thi Nguyen, Loan Thi Phan, Yen Thi Kim Nguyen, Phuong Khanh Nguyen Hoang
Background: Persistent severe acute kidney injury (PS-AKI)-recently standardized as Kidney Disease: Improving Global Outcomes (KDIGO) Stage 3 persisting ≥ 72 h, or renal replacement therapy/death after Stage 3 diagnosis-has emerged as a trajectory-based phenotype complementing conventional KDIGO staging. Evidence in contemporary intensive care unit (ICU) cohorts remains limited.
Methods: We retrospectively studied adults admitted to a tertiary ICU (January 2024-June 2025). Acute kidney injury (AKI) was staged per KDIGO 2012, with trajectories classified as Stage 1 AKI, transient AKI (Stage 2-3 resolving within 48 h), persistent mild-moderate AKI, or PS-AKI. The primary outcome was in-hospital mortality; secondary outcomes included renal recovery. Predictors of PS-AKI were explored using logistic regression and gradient boosting with SHAP attribution.
Results: Among 139 ICU patients with AKI screened, 106 met criteria. Most AKI was community-acquired (97/106, 91.5%). PS-AKI accounted for 23% (24/106) and carried the worst outcomes, with in-hospital mortality 54% and renal recovery 17%. Within Stage 2-3, PS-AKI was associated with substantially worse outcomes than non-PS trajectories (mortality 54% vs 10.8%; adjusted HR for death 2.23, 95% CI 0.69-7.21; adjusted OR for renal recovery 0.07, 95% CI 0.01-0.24). A 72-h landmark analysis showed similar but nonsignificant trends. Inflammatory profiles distinguished PS-AKI, with higher neutrophil-to-lymphocyte ratio (NLR), C-reactive protein (CRP), and lower platelets. The composite NLR-to-platelet ratio (NLR/PLT) was independently associated with PS-AKI (adjusted OR 2.51 per doubling, 95% CI 1.52-4.12; AUC 0.86), while the systemic immune-inflammation index (SII) showed no significant association.
Conclusions: In this predominant community-acquired ICU cohort, PS-AKI was common and strongly associated with poor in-hospital outcomes. The co-occurrence of inflammation and thrombocytopenia, summarized by NLR/PLT, may represent a simple exploratory signal for early-risk appraisal. These findings support further research into trajectory-based AKI phenotypes and the potential utility of inflammation-hematologic markers in predicting persistence.
背景:持续性严重急性肾损伤(PS-AKI)——最近被标准化为肾脏疾病:改善总体预后(KDIGO) 3期持续≥72小时,或肾脏替代治疗/ 3期诊断后死亡——已经成为一种基于轨迹的表型,补充了传统的KDIGO分期。当代重症监护病房(ICU)队列的证据仍然有限。方法:我们回顾性研究了2024年1月至2025年6月入住三级ICU的成年人。根据KDIGO 2012,急性肾损伤(AKI)的分期分为1期AKI、短暂性AKI(2-3期48小时内消退)、持续性轻-中度AKI或PS-AKI。主要结局是住院死亡率;次要结局包括肾脏恢复。采用logistic回归和SHAP归因梯度增强方法对PS-AKI的预测因子进行了探讨。结果:139例ICU AKI患者中,106例符合标准。AKI多为社区获得性(97/106,91.5%)。PS-AKI占23%(24/106),预后最差,住院死亡率54%,肾脏恢复17%。在第2-3阶段,PS-AKI的预后明显差于非ps轨迹(死亡率54% vs 10.8%;死亡校正HR 2.23, 95% CI 0.69-7.21;肾脏恢复校正OR 0.07, 95% CI 0.01-0.24)。72小时的里程碑分析显示了类似但不显著的趋势。炎症特征区分PS-AKI,具有较高的中性粒细胞与淋巴细胞比率(NLR), c反应蛋白(CRP)和较低的血小板。综合NLR/血小板比值(NLR/PLT)与PS-AKI独立相关(调整后的OR为2.51 /倍,95% CI为1.52-4.12;AUC为0.86),而全身免疫炎症指数(SII)无显著相关性。结论:在这个主要的社区获得性ICU队列中,PS-AKI是常见的,并且与不良的住院预后密切相关。NLR/PLT总结的炎症和血小板减少的共同发生可能是早期风险评估的一个简单的探索性信号。这些发现支持进一步研究基于轨迹的AKI表型和炎症-血液学标志物在预测持久性方面的潜在效用。
{"title":"Persistent Severe Acute Kidney Injury Among Critically Ill Patients: Outcomes and Predictive Markers-A Single-Center Retrospective Cohort Study.","authors":"Tung Phi Nguyen, Thang Trong Khong, Hoai Thi Thu Vu, Nam Ngoc Phuong Nguyen, Phong Van Phan, Hue Thi Le, Tra Thi Hoang, Huyen Thi Nguyen, Loan Thi Phan, Yen Thi Kim Nguyen, Phuong Khanh Nguyen Hoang","doi":"10.1155/ccrp/6920702","DOIUrl":"https://doi.org/10.1155/ccrp/6920702","url":null,"abstract":"<p><strong>Background: </strong>Persistent severe acute kidney injury (PS-AKI)-recently standardized as Kidney Disease: Improving Global Outcomes (KDIGO) Stage 3 persisting ≥ 72 h, or renal replacement therapy/death after Stage 3 diagnosis-has emerged as a trajectory-based phenotype complementing conventional KDIGO staging. Evidence in contemporary intensive care unit (ICU) cohorts remains limited.</p><p><strong>Methods: </strong>We retrospectively studied adults admitted to a tertiary ICU (January 2024-June 2025). Acute kidney injury (AKI) was staged per KDIGO 2012, with trajectories classified as Stage 1 AKI, transient AKI (Stage 2-3 resolving within 48 h), persistent mild-moderate AKI, or PS-AKI. The primary outcome was in-hospital mortality; secondary outcomes included renal recovery. Predictors of PS-AKI were explored using logistic regression and gradient boosting with SHAP attribution.</p><p><strong>Results: </strong>Among 139 ICU patients with AKI screened, 106 met criteria. Most AKI was community-acquired (97/106, 91.5%). PS-AKI accounted for 23% (24/106) and carried the worst outcomes, with in-hospital mortality 54% and renal recovery 17%. Within Stage 2-3, PS-AKI was associated with substantially worse outcomes than non-PS trajectories (mortality 54% vs 10.8%; adjusted HR for death 2.23, 95% CI 0.69-7.21; adjusted OR for renal recovery 0.07, 95% CI 0.01-0.24). A 72-h landmark analysis showed similar but nonsignificant trends. Inflammatory profiles distinguished PS-AKI, with higher neutrophil-to-lymphocyte ratio (NLR), C-reactive protein (CRP), and lower platelets. The composite NLR-to-platelet ratio (NLR/PLT) was independently associated with PS-AKI (adjusted OR 2.51 per doubling, 95% CI 1.52-4.12; AUC 0.86), while the systemic immune-inflammation index (SII) showed no significant association.</p><p><strong>Conclusions: </strong>In this predominant community-acquired ICU cohort, PS-AKI was common and strongly associated with poor in-hospital outcomes. The co-occurrence of inflammation and thrombocytopenia, summarized by NLR/PLT, may represent a simple exploratory signal for early-risk appraisal. These findings support further research into trajectory-based AKI phenotypes and the potential utility of inflammation-hematologic markers in predicting persistence.</p>","PeriodicalId":46583,"journal":{"name":"Critical Care Research and Practice","volume":"2026 ","pages":"6920702"},"PeriodicalIF":1.8,"publicationDate":"2026-02-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12910387/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146221010","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 : 2026-01-20eCollection Date: 2026-01-01DOI: 10.1155/ccrp/5382735
Amanda de Oliveira Santos, Matheus Cardoso Santos, Maíra Avila Fontes Trindade, Danielle Alves de Andrade Rebouças, Carlos José Oliveira de Matos, Fernanda Oliveira de Carvalho, Paulo Ricardo Martins-Filho, Érika Ramos Silva
Purpose: Neuromuscular electrical stimulation (NMES) has been increasingly used to preserve or restore neuromuscular function in critically ill patients. However, its effects on inflammatory biomarkers and its safety require to be fully elucidated. This study aimed to analyze the available evidence on the impact of NMES on biological markers in critically ill patients.
Methods: This systematic review followed a preregistered protocol (PROSPERO: CRD42023424413). A comprehensive search was conducted in PubMed, EMBASE, Web of Science, Scopus, PEDro, CENTRAL, and Google Scholar to identify randomized controlled trials (RCTs) comparing NMES with control interventions and reporting outcomes related to biological markers.
Results: Ten RCTs were included in this review. Meta-analyses revealed a significant acute increase in interleukin-10 levels (SMD: 0.60; 95% CI: 0.11 to 1.08; p = 0.02) and a delayed reduction in serum C-reactive protein levels (SMD: -0.74; 95% CI: -1.09 to -0.40; p < 0.0001) following NMES application.
Conclusions: Available evidence suggests that NMES can modulate systemic inflammation in mechanically ventilated critically ill patients, with early anti-inflammatory effects (IL-10 elevation) and subsequent attenuation of inflammation (CRP reduction). These findings support the safety of NMES during active phases of critical illness. Further high-quality RCTs are warranted to standardize stimulation protocols, characterize biomarker dynamics, and elucidate the underlying mechanisms to guide evidence-based clinical use.
{"title":"Impact of Neuromuscular Electrical Stimulation on Biological Markers in Critically Ill Patients: A Systematic Review and Meta-Analysis.","authors":"Amanda de Oliveira Santos, Matheus Cardoso Santos, Maíra Avila Fontes Trindade, Danielle Alves de Andrade Rebouças, Carlos José Oliveira de Matos, Fernanda Oliveira de Carvalho, Paulo Ricardo Martins-Filho, Érika Ramos Silva","doi":"10.1155/ccrp/5382735","DOIUrl":"10.1155/ccrp/5382735","url":null,"abstract":"<p><strong>Purpose: </strong>Neuromuscular electrical stimulation (NMES) has been increasingly used to preserve or restore neuromuscular function in critically ill patients. However, its effects on inflammatory biomarkers and its safety require to be fully elucidated. This study aimed to analyze the available evidence on the impact of NMES on biological markers in critically ill patients.</p><p><strong>Methods: </strong>This systematic review followed a preregistered protocol (PROSPERO: CRD42023424413). A comprehensive search was conducted in PubMed, EMBASE, Web of Science, Scopus, PEDro, CENTRAL, and Google Scholar to identify randomized controlled trials (RCTs) comparing NMES with control interventions and reporting outcomes related to biological markers.</p><p><strong>Results: </strong>Ten RCTs were included in this review. Meta-analyses revealed a significant acute increase in interleukin-10 levels (SMD: 0.60; 95% CI: 0.11 to 1.08; <i>p</i> = 0.02) and a delayed reduction in serum C-reactive protein levels (SMD: -0.74; 95% CI: -1.09 to -0.40; <i>p</i> < 0.0001) following NMES application.</p><p><strong>Conclusions: </strong>Available evidence suggests that NMES can modulate systemic inflammation in mechanically ventilated critically ill patients, with early anti-inflammatory effects (IL-10 elevation) and subsequent attenuation of inflammation (CRP reduction). These findings support the safety of NMES during active phases of critical illness. Further high-quality RCTs are warranted to standardize stimulation protocols, characterize biomarker dynamics, and elucidate the underlying mechanisms to guide evidence-based clinical use.</p>","PeriodicalId":46583,"journal":{"name":"Critical Care Research and Practice","volume":"2026 ","pages":"5382735"},"PeriodicalIF":1.8,"publicationDate":"2026-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12820417/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146031088","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 : 2026-01-12eCollection Date: 2026-01-01DOI: 10.1155/ccrp/6179847
Ayesha Shaukat, Muhammad Ahmed Zahoor, Komal Khan, Aiman Shahid Khan, Rubaisha Saleem, Anupama Ariyasiri, Syed Abdul Aziz Jameel, Shahab Afridi, Syeda Javeria Salman, Noor Naeem, Marib Ashraf, Amamah Rauf Chaudhry, Zobia Ahmad, Muhammad Omar Larik, Muhammad Hasanain, Muhammad Umair Anjum, Aymar Akilimali
Introduction: Neurocritical care patients, including those with traumatic brain injury, subarachnoid hemorrhage, and intracerebral hemorrhage, often develop anemia, compromising brain oxygen delivery and increasing morbidity and mortality. Blood transfusion strategies, either liberal or restrictive, are commonly used to manage anemia in these patients, but the optimal approach remains unclear due to mixed results in existing studies.
Methods: A systematic search of PubMed, Cochrane Library, ScienceDirect, and Google Scholar from inception to December 2024 for randomized controlled trials (RCTs) evaluating restrictive versus liberal transfusion strategies in adult neurocritical care patients. Outcomes included mortality, Glasgow Outcome Scale (GOS), red blood cell (RBC) units transfused, sepsis, intensive care unit (ICU)/hospital length of stay, and secondary complications. The study is registered with PROSPERO (CRD42025635426).
Findings: The analysis included seven RCTs with 1941 patients. The restrictive strategy significantly reduced the number of RBC units transfused per patient (MD: 2.36; 95% CI: 1.08-3.64; p = 0.0003) and was associated with a lower incidence of sepsis (RR: 0.73; 95% CI: 0.56-0.96; p = 0.02). There were no significant differences between restrictive and liberal strategies for ICU (RR 0.74; 95% CI 0.28-1.91; p = 0.53), in-hospital (RR 0.77; 95% CI 0.35-1.68), 30-day (RR 0.91; 95% CI 0.70-1.18), 6-month (RR 0.98; 95% CI 0.67-1.44), or long-term mortality (RR 1.00; 95% CI 0.80-1.24). GOS scores at 6 months showed no significant difference (RR 0.94; 95% CI 0.83-1.07). ICU and hospital length of stay were also comparable between strategies. Secondary outcomes, including stroke, brain hypoxia, intracranial hypertension, and other non-neurological complications, showed no significant differences between the two strategies.
Conclusion: Restrictive transfusion strategies are as effective as liberal strategies in terms of mortality and neurological complications, with additional benefits such as fewer RBC transfusions and lower sepsis rates. These findings support restrictive strategies as a safer approach to managing anemia in neurocritical care, though further research on long-term outcomes is needed.
神经危重症患者,包括外伤性脑损伤、蛛网膜下腔出血和脑出血患者,常发生贫血,影响脑氧输送,增加发病率和死亡率。输血策略,无论是自由输血还是限制性输血,通常用于治疗这些患者的贫血,但由于现有研究的结果不一,最佳方法尚不清楚。方法:系统检索PubMed、Cochrane Library、ScienceDirect和谷歌Scholar从成立到2024年12月的随机对照试验(rct),评估成人神经危重症患者的限制性与自由输血策略。结局包括死亡率、格拉斯哥结局量表(GOS)、输血红细胞(RBC)单位、败血症、重症监护病房(ICU)/住院时间和继发并发症。该研究已在PROSPERO注册(CRD42025635426)。结果:该分析包括7项随机对照试验,共1941例患者。限制性策略显著减少每位患者输血的RBC单位数(MD: 2.36; 95% CI: 1.08-3.64; p = 0.0003),并与较低的脓毒症发生率相关(RR: 0.73; 95% CI: 0.56-0.96; p = 0.02)。限制和自由策略在ICU (RR 0.74; 95% CI 0.28-1.91; p = 0.53)、住院(RR 0.77; 95% CI 0.35-1.68)、30天(RR 0.91; 95% CI 0.70-1.18)、6个月(RR 0.98; 95% CI 0.67-1.44)和长期死亡率(RR 1.00; 95% CI 0.80-1.24)之间无显著差异。6个月GOS评分差异无统计学意义(RR 0.94; 95% CI 0.83-1.07)。ICU和住院时间在两种策略之间也具有可比性。次要结局,包括脑卒中、脑缺氧、颅内高压和其他非神经系统并发症,在两种策略之间没有显着差异。结论:在死亡率和神经系统并发症方面,限制性输血策略与自由输血策略同样有效,并具有减少红细胞输血和降低败血症率等额外益处。这些发现支持限制性策略作为一种更安全的方法来管理神经危重症护理中的贫血,尽管需要进一步的长期结果研究。
{"title":"Liberal Versus Restrictive Blood Transfusion Strategies in Neurocritical Care: A Systematic Review and Meta-Analysis of Randomized Controlled Trials.","authors":"Ayesha Shaukat, Muhammad Ahmed Zahoor, Komal Khan, Aiman Shahid Khan, Rubaisha Saleem, Anupama Ariyasiri, Syed Abdul Aziz Jameel, Shahab Afridi, Syeda Javeria Salman, Noor Naeem, Marib Ashraf, Amamah Rauf Chaudhry, Zobia Ahmad, Muhammad Omar Larik, Muhammad Hasanain, Muhammad Umair Anjum, Aymar Akilimali","doi":"10.1155/ccrp/6179847","DOIUrl":"10.1155/ccrp/6179847","url":null,"abstract":"<p><strong>Introduction: </strong>Neurocritical care patients, including those with traumatic brain injury, subarachnoid hemorrhage, and intracerebral hemorrhage, often develop anemia, compromising brain oxygen delivery and increasing morbidity and mortality. Blood transfusion strategies, either liberal or restrictive, are commonly used to manage anemia in these patients, but the optimal approach remains unclear due to mixed results in existing studies.</p><p><strong>Methods: </strong>A systematic search of PubMed, Cochrane Library, ScienceDirect, and Google Scholar from inception to December 2024 for randomized controlled trials (RCTs) evaluating restrictive versus liberal transfusion strategies in adult neurocritical care patients. Outcomes included mortality, Glasgow Outcome Scale (GOS), red blood cell (RBC) units transfused, sepsis, intensive care unit (ICU)/hospital length of stay, and secondary complications. The study is registered with PROSPERO (CRD42025635426).</p><p><strong>Findings: </strong>The analysis included seven RCTs with 1941 patients. The restrictive strategy significantly reduced the number of RBC units transfused per patient (MD: 2.36; 95% CI: 1.08-3.64; <i>p</i> = 0.0003) and was associated with a lower incidence of sepsis (RR: 0.73; 95% CI: 0.56-0.96; <i>p</i> = 0.02). There were no significant differences between restrictive and liberal strategies for ICU (RR 0.74; 95% CI 0.28-1.91; <i>p</i> = 0.53), in-hospital (RR 0.77; 95% CI 0.35-1.68), 30-day (RR 0.91; 95% CI 0.70-1.18), 6-month (RR 0.98; 95% CI 0.67-1.44), or long-term mortality (RR 1.00; 95% CI 0.80-1.24). GOS scores at 6 months showed no significant difference (RR 0.94; 95% CI 0.83-1.07). ICU and hospital length of stay were also comparable between strategies. Secondary outcomes, including stroke, brain hypoxia, intracranial hypertension, and other non-neurological complications, showed no significant differences between the two strategies.</p><p><strong>Conclusion: </strong>Restrictive transfusion strategies are as effective as liberal strategies in terms of mortality and neurological complications, with additional benefits such as fewer RBC transfusions and lower sepsis rates. These findings support restrictive strategies as a safer approach to managing anemia in neurocritical care, though further research on long-term outcomes is needed.</p>","PeriodicalId":46583,"journal":{"name":"Critical Care Research and Practice","volume":"2026 ","pages":"6179847"},"PeriodicalIF":1.8,"publicationDate":"2026-01-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12793887/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145967473","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}
Aim: To evaluate the current status and explore influencing factors of junior intensive care unit (ICU) nurses' recognition and response capabilities to clinical deterioration.
Design: This cross-sectional study followed the STROBE statement.
Methods: From November 2024 to January 2025, 260 junior ICU nurses from five tertiary hospitals in China were recruited. Data were collected using a validated 25-item questionnaire spanning six dimensions to assess their recognition and response abilities. SPSS was used for statistical analyses, including descriptive statistics, Kruskal-Wallis H/Mann-Whitney U tests, and multiple linear regression to examine differences under sociodemographic and occupational factors.
Results: The total score for recognition and response abilities among 250 junior ICU nurses was 99 (95, 103), with an average item score of 3.96 ± 0.83. Dimension scores ranked from lowest to highest: emergency handling, evaluation, teamwork, disease information analysis, disease information acquisition, and clinical decision-making. Education level, work experience, and participation in disease observation training were identified as significant influencing factors.
Conclusions: Junior ICU nurses in China demonstrate relatively strong overall observation skills but insufficient clinical decision-making abilities. Nursing managers and educators should integrate these factors into training to enhance young nurses' capabilities in recognizing and responding to clinical deterioration, which is crucial for improving critical care outcomes.
Patient or public contribution: Patients and the public were not directly involved in the design, implementation, or reporting of this study. However, the results of the study emphasize the importance of improving primary ICU nurses' clinical decision-making skills and emergency response skills, which may have an impact on patient care.
{"title":"Analysis of Influencing Factors of Junior ICU Nurses' Recognition and Response Abilities to Clinical Deterioration: A Cross-Sectional Study.","authors":"Xueqin Guo, Xianke Wang, Chenzi Xu, Yuhan Wang, Xin Li, Lijuan Xiong, Huan Jin","doi":"10.1155/ccrp/3230912","DOIUrl":"10.1155/ccrp/3230912","url":null,"abstract":"<p><strong>Aim: </strong>To evaluate the current status and explore influencing factors of junior intensive care unit (ICU) nurses' recognition and response capabilities to clinical deterioration.</p><p><strong>Design: </strong>This cross-sectional study followed the STROBE statement.</p><p><strong>Methods: </strong>From November 2024 to January 2025, 260 junior ICU nurses from five tertiary hospitals in China were recruited. Data were collected using a validated 25-item questionnaire spanning six dimensions to assess their recognition and response abilities. SPSS was used for statistical analyses, including descriptive statistics, Kruskal-Wallis H/Mann-Whitney <i>U</i> tests, and multiple linear regression to examine differences under sociodemographic and occupational factors.</p><p><strong>Results: </strong>The total score for recognition and response abilities among 250 junior ICU nurses was 99 (95, 103), with an average item score of 3.96 ± 0.83. Dimension scores ranked from lowest to highest: emergency handling, evaluation, teamwork, disease information analysis, disease information acquisition, and clinical decision-making. Education level, work experience, and participation in disease observation training were identified as significant influencing factors.</p><p><strong>Conclusions: </strong>Junior ICU nurses in China demonstrate relatively strong overall observation skills but insufficient clinical decision-making abilities. Nursing managers and educators should integrate these factors into training to enhance young nurses' capabilities in recognizing and responding to clinical deterioration, which is crucial for improving critical care outcomes.</p><p><strong>Patient or public contribution: </strong>Patients and the public were not directly involved in the design, implementation, or reporting of this study. However, the results of the study emphasize the importance of improving primary ICU nurses' clinical decision-making skills and emergency response skills, which may have an impact on patient care.</p>","PeriodicalId":46583,"journal":{"name":"Critical Care Research and Practice","volume":"2025 ","pages":"3230912"},"PeriodicalIF":1.8,"publicationDate":"2025-12-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12717636/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145805876","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 : 2025-12-15eCollection Date: 2025-01-01DOI: 10.1155/ccrp/4830160
Carlos Valladares, Franklyn Vega Batista, Marc Faltas, Mareya Menteyas, Katherine Chiapaikeo-Poco
Background: Prolonged use of intravenous (IV) vasopressors in critically ill patients is associated with significant complications. Droxidopa, a norepinephrine precursor approved for neurogenic orthostatic hypotension, has gained interest as an off-label agent for facilitating vasopressor weaning in ICU settings. This systematic review aimed to evaluate the efficacy and safety of droxidopa for vasopressor weaning in ICU patients.
Methods: A systematic review was conducted following PRISMA guidelines. Databases searched included PubMed, Embase, Cochrane, and Web of Science through April 2025. Eligible studies reporting primary clinical data on droxidopa use in ICU patients were included. Outcomes included time to IV vasopressor discontinuation, duration of droxidopa use, ICU length of stay (LOS), and ICU mortality, and results were narratively synthesized. The risk of bias was assessed using the ROBINS-I and the JBI checklists.
Results: Seven studies involving 161 ICU patients were included. Five studies reported time to vasopressor discontinuation, ranging from 29 to 120 h. The duration of droxidopa use ranged from 87 to 192 h. Two studies reported ICU LOS, ranging from 18 to 44 days. ICU mortality was inconsistently reported. These findings are primarily drawn from small, retrospective studies and should be interpreted cautiously.
Discussion: Findings suggest that droxidopa may effectively facilitate vasopressor weaning in critically ill patients. However, variations in dosing, patient selection, and outcome reporting limit generalizability. Evidence is drawn primarily from small, retrospective studies, some available only as abstracts.
Conclusion: Available evidence on droxidopa for vasopressor weaning in ICU patients remains limited and heterogeneous, with very low certainty. Further research is warranted. No funding was received for this review, and the review was not prospectively registered.
背景:危重患者长期使用静脉(IV)血管加压药物与显著并发症相关。Droxidopa,一种被批准用于神经源性直立性低血压的去甲肾上腺素前体,作为一种标签外药物,在ICU环境中促进血管加压药物的脱机,已经引起了人们的兴趣。本系统综述旨在评价氯希多巴用于ICU患者血管加压药物脱机的有效性和安全性。方法:按照PRISMA指南进行系统评价。检索的数据库包括PubMed、Embase、Cochrane和Web of Science,截止到2025年4月。纳入了符合条件的研究,报告了ICU患者使用氯西多巴的主要临床数据。结果包括静脉降压药停药时间、氯西多巴使用时间、ICU住院时间(LOS)和ICU死亡率,并对结果进行叙述综合。使用ROBINS-I和JBI检查表评估偏倚风险。结果:纳入7项研究,共161例ICU患者。五项研究报告了血管加压素停药的时间,从29到120小时不等。盐酸卓希多巴用药时间为87 ~ 192 h。两项研究报告了ICU的LOS,时间从18天到44天不等。ICU死亡率报告不一致。这些发现主要来自小型回顾性研究,应谨慎解释。讨论:研究结果表明,氯希多巴可有效促进危重患者的血管加压素脱机。然而,剂量、患者选择和结果报告的变化限制了推广。证据主要来自小型的回顾性研究,有些研究只能作为摘要获得。结论:盐酸卓希多巴用于ICU患者血管加压药物脱机的现有证据仍然有限且不均匀,确定性很低。进一步的研究是有必要的。本综述未收到资助,也未进行前瞻性注册。
{"title":"Droxidopa in Critical Care: A Systematic Review of an Emerging Off-Label Practice.","authors":"Carlos Valladares, Franklyn Vega Batista, Marc Faltas, Mareya Menteyas, Katherine Chiapaikeo-Poco","doi":"10.1155/ccrp/4830160","DOIUrl":"10.1155/ccrp/4830160","url":null,"abstract":"<p><strong>Background: </strong>Prolonged use of intravenous (IV) vasopressors in critically ill patients is associated with significant complications. Droxidopa, a norepinephrine precursor approved for neurogenic orthostatic hypotension, has gained interest as an off-label agent for facilitating vasopressor weaning in ICU settings. This systematic review aimed to evaluate the efficacy and safety of droxidopa for vasopressor weaning in ICU patients.</p><p><strong>Methods: </strong>A systematic review was conducted following PRISMA guidelines. Databases searched included PubMed, Embase, Cochrane, and Web of Science through April 2025. Eligible studies reporting primary clinical data on droxidopa use in ICU patients were included. Outcomes included time to IV vasopressor discontinuation, duration of droxidopa use, ICU length of stay (LOS), and ICU mortality, and results were narratively synthesized. The risk of bias was assessed using the ROBINS-I and the JBI checklists.</p><p><strong>Results: </strong>Seven studies involving 161 ICU patients were included. Five studies reported time to vasopressor discontinuation, ranging from 29 to 120 h. The duration of droxidopa use ranged from 87 to 192 h. Two studies reported ICU LOS, ranging from 18 to 44 days. ICU mortality was inconsistently reported. These findings are primarily drawn from small, retrospective studies and should be interpreted cautiously.</p><p><strong>Discussion: </strong>Findings suggest that droxidopa may effectively facilitate vasopressor weaning in critically ill patients. However, variations in dosing, patient selection, and outcome reporting limit generalizability. Evidence is drawn primarily from small, retrospective studies, some available only as abstracts.</p><p><strong>Conclusion: </strong>Available evidence on droxidopa for vasopressor weaning in ICU patients remains limited and heterogeneous, with very low certainty. Further research is warranted. No funding was received for this review, and the review was not prospectively registered.</p>","PeriodicalId":46583,"journal":{"name":"Critical Care Research and Practice","volume":"2025 ","pages":"4830160"},"PeriodicalIF":1.8,"publicationDate":"2025-12-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12714080/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145805894","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}
Objective: Clinical decision-making is one of the most difficult responsibilities of healthcare personnel in the neonatal intensive care unit (NICU). Meanwhile, nurses in NICU are facing countless challenges to take care of these neonates due to complex clinical conditions, prematurity, low birth weight, and physiological instability of the neonates, making clinical decision-making difficult. Thus, it is essential to identify and investigate the challenges in clinical decision-making for nurses in NICU. The aim of the present study was to explore the challenges that nurses face in clinical decision-making in NICU in southern Iran.
Methods: The present study is a qualitative study with the content analysis in Iran from February 2023 to January 2024. Twenty-one NICU nurses participated in this study. Data were collected from individual, in-depth, and semistructured interviews. The interview questions, according to the opinion of the research team, were designed around the research question: "What are the challenges in clinical decision-making for nurses in NICU?" In order to analyze the data, the researchers used the conventional content analysis method.
Results: The means of the participants' ages and work experience were 36.52 ± 5.71 and 12.45 ± 5.83 years, respectively. Three main themes with nine subthemes were obtained in this study. The main themes were "inadequate clinical competence" (lack of knowledge about caring for neonates, lack of clinical skill and experience, and shortage of nurse practitioners in NICUs); "poor self-efficacy" (poor self-confidence, inefficient stress management, and lack of motivation); and "resistance to change" (physician-centeredness, lack of organizational support, and ambiguities about legal rights).
Conclusion: The findings of the study revealed that lack of knowledge, poor clinical skills, and not having a master's degree in neonatal intensive care adversely affect nurses' self-confidence in providing care and making clinical decisions. Also, the common belief that physicians are superior to nurses in the organizational culture and lack of support for nurses undermines nurses' motivation for enhancing their competence and participating in clinical decision-making. Based on the findings, managers and policy makers, by providing a supportive environment, as well as improving the knowledge and clinical skills of nurses, can encourage them to participate in clinical decision-making.
{"title":"Challenges in Clinical Decision-Making for Nurses in Neonatal Intensive Care Unit (NICU): A Qualitative Study.","authors":"Fateme Mohammadi, Maryam Bahmanyar, Parisa Sabetsarvestani, Mostafa Bijani","doi":"10.1155/ccrp/6686680","DOIUrl":"10.1155/ccrp/6686680","url":null,"abstract":"<p><strong>Objective: </strong>Clinical decision-making is one of the most difficult responsibilities of healthcare personnel in the neonatal intensive care unit (NICU). Meanwhile, nurses in NICU are facing countless challenges to take care of these neonates due to complex clinical conditions, prematurity, low birth weight, and physiological instability of the neonates, making clinical decision-making difficult. Thus, it is essential to identify and investigate the challenges in clinical decision-making for nurses in NICU. The aim of the present study was to explore the challenges that nurses face in clinical decision-making in NICU in southern Iran.</p><p><strong>Methods: </strong>The present study is a qualitative study with the content analysis in Iran from February 2023 to January 2024. Twenty-one NICU nurses participated in this study. Data were collected from individual, in-depth, and semistructured interviews. The interview questions, according to the opinion of the research team, were designed around the research question: \"What are the challenges in clinical decision-making for nurses in NICU?\" In order to analyze the data, the researchers used the conventional content analysis method.</p><p><strong>Results: </strong>The means of the participants' ages and work experience were 36.52 ± 5.71 and 12.45 ± 5.83 years, respectively. Three main themes with nine subthemes were obtained in this study. The main themes were \"inadequate clinical competence\" (lack of knowledge about caring for neonates, lack of clinical skill and experience, and shortage of nurse practitioners in NICUs); \"poor self-efficacy\" (poor self-confidence, inefficient stress management, and lack of motivation); and \"resistance to change\" (physician-centeredness, lack of organizational support, and ambiguities about legal rights).</p><p><strong>Conclusion: </strong>The findings of the study revealed that lack of knowledge, poor clinical skills, and not having a master's degree in neonatal intensive care adversely affect nurses' self-confidence in providing care and making clinical decisions. Also, the common belief that physicians are superior to nurses in the organizational culture and lack of support for nurses undermines nurses' motivation for enhancing their competence and participating in clinical decision-making. Based on the findings, managers and policy makers, by providing a supportive environment, as well as improving the knowledge and clinical skills of nurses, can encourage them to participate in clinical decision-making.</p>","PeriodicalId":46583,"journal":{"name":"Critical Care Research and Practice","volume":"2025 ","pages":"6686680"},"PeriodicalIF":1.8,"publicationDate":"2025-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12638141/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145588742","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 : 2025-10-14eCollection Date: 2025-01-01DOI: 10.1155/ccrp/9058296
Zohair Al-Halees, Mosleh Nazzal Alanazi, Patricia Machado, Mary Jane Maghirang, Emad Hakami, Farouk Mostafa Faris, Michelle Gretchen Lo, Mohamed Laimoud
Background: Venoarterial extracorporeal membrane oxygenation (VA-ECMO) is a life-saving mechanical support in patients with cardiogenic shock. There are great variations in the reported rates of neurological complications and associated mortality. Our aim was to analyze our cohort of adult patients supported with VA-ECMO to identify the incidence, outcomes, and predictors of acute ischemic and hemorrhagic strokes.
Methods: A total of 195 patients between January 2016 and January 2023 were reviewed, 22 (11.3%) ECPR patients were excluded, and 173 (88.7%) patients were analyzed. We divided the patients into stroke and nonstroke groups according to the presence of radiologically confirmed acute ischemic and hemorrhagic strokes.
Results: Thirty-five (20.2%) patients had acute cerebrovascular strokes. 13 (7.5%) patients had intracranial hemorrhage (ICH) while 22 (12.7%) patients had ischemic stroke. The median age was 48 years (IQR: 31, 56), 98 (56.6%) patients were males, and 152 (87.9%) patients had cardiac surgeries. The patients who developed cerebrovascular stroke had higher blood lactate at ECMO initiation (8.9 [5.5, 11.2] versus 5.7 [4.6, 11.9] mmol/L, p = 0.02) and 12 h later (8.7 [4.7, 14.5] versus 5.8 [4.6, 15] mmol/L, p = 0.024) with lesser lactate clearance (LC) at 12 h (6.35 [-51.5, 40.6] versus 14.65% [-43.55, 38.3], p < 001) compared to the patients in the nonstroke group. The stroke group had longer ICU stay (21 vs. 15.5 days, p = 0.03), higher frequency of new hemodialysis (62.9% vs. 46.4%, p = 0.026), and on-ECMO mortality (54.3% vs. 44.9%, p = 0.041) compared with the nonstroke group. The ICH was associated with higher hospital mortality (p = 0.021) compared to the ischemic stroke. Logistic multivariate regression revealed that the initial lactate level (OR: 1.6, 95% CI: 1.2-8.92, p = 0.031), cardiopulmonary bypass time (OR:1.8, 95% CI: 1.32-6.42, p = 0.02), and LC at 12 h (OR: 2.4, 95% CI: 1.91-17.4, p = 0.042) were associated with ischemic stroke. Thrombocytopenia (OR: 3.22, 95% CI: 1.82-7.83, p = 0.001) and low body mass index (OR: 2.1, 95% CI: 1.31-4.6, p = 0.02) were associated with ICH.
Conclusions: Ischemic and hemorrhagic strokes are frequent with VA-ECMO support and associated with worse outcomes, especially the hemorrhagic type. Awareness of the incidence and the factors associated with strokes is crucial in early identification and management.
背景:静脉体外膜氧合(VA-ECMO)是一种挽救心源性休克患者生命的机械支持。在报道的神经系统并发症和相关死亡率方面存在很大差异。我们的目的是分析支持VA-ECMO的成年患者队列,以确定急性缺血性和出血性卒中的发生率、结局和预测因素。方法:回顾性分析2016年1月至2023年1月共195例患者,排除22例(11.3%)ECPR患者,分析173例(88.7%)患者。根据影像学证实的急性缺血性和出血性脑卒中,我们将患者分为脑卒中组和非脑卒中组。结果:急性脑血管卒中35例(20.2%)。颅内出血13例(7.5%),缺血性脑卒中22例(12.7%)。中位年龄48岁(IQR: 31,56),男性98例(56.6%),心脏手术152例(87.9%)。发生脑血管卒中的患者在ECMO开始时(8.9[5.5,11.2]比5.7 [4.6,11.9]mmol/L, p = 0.02)和12小时后(8.7[4.7,14.5]比5.8 [4.6,15]mmol/L, p = 0.024)血乳酸清除率(LC)较低(6.35[-51.5,40.6]比14.65% [-43.55,38.3],p < 001)与非卒中组相比。与非卒中组相比,卒中组ICU住院时间更长(21天对15.5天,p = 0.03),新血液透析频率更高(62.9%对46.4%,p = 0.026), ecmo死亡率更高(54.3%对44.9%,p = 0.041)。与缺血性脑卒中相比,脑出血与更高的住院死亡率相关(p = 0.021)。Logistic多因素回归显示,初始乳酸水平(OR: 1.6, 95% CI: 1.2 ~ 8.92, p = 0.031)、体外循环时间(OR:1.8, 95% CI: 1.32 ~ 6.42, p = 0.02)和12 h LC (OR: 2.4, 95% CI: 1.91 ~ 17.4, p = 0.042)与缺血性卒中相关。血小板减少症(OR: 3.22, 95% CI: 1.82-7.83, p = 0.001)和低体重指数(OR: 2.1, 95% CI: 1.31-4.6, p = 0.02)与脑出血相关。结论:在VA-ECMO支持下,缺血性和出血性卒中发生率较高,且预后较差,尤其是出血性卒中。了解与中风相关的发病率和因素对早期识别和治疗至关重要。
{"title":"Cerebrovascular Strokes During Venoarterial Extracorporeal Membrane Oxygenation.","authors":"Zohair Al-Halees, Mosleh Nazzal Alanazi, Patricia Machado, Mary Jane Maghirang, Emad Hakami, Farouk Mostafa Faris, Michelle Gretchen Lo, Mohamed Laimoud","doi":"10.1155/ccrp/9058296","DOIUrl":"10.1155/ccrp/9058296","url":null,"abstract":"<p><strong>Background: </strong>Venoarterial extracorporeal membrane oxygenation (VA-ECMO) is a life-saving mechanical support in patients with cardiogenic shock. There are great variations in the reported rates of neurological complications and associated mortality. Our aim was to analyze our cohort of adult patients supported with VA-ECMO to identify the incidence, outcomes, and predictors of acute ischemic and hemorrhagic strokes.</p><p><strong>Methods: </strong>A total of 195 patients between January 2016 and January 2023 were reviewed, 22 (11.3%) ECPR patients were excluded, and 173 (88.7%) patients were analyzed. We divided the patients into stroke and nonstroke groups according to the presence of radiologically confirmed acute ischemic and hemorrhagic strokes.</p><p><strong>Results: </strong>Thirty-five (20.2%) patients had acute cerebrovascular strokes. 13 (7.5%) patients had intracranial hemorrhage (ICH) while 22 (12.7%) patients had ischemic stroke. The median age was 48 years (IQR: 31, 56), 98 (56.6%) patients were males, and 152 (87.9%) patients had cardiac surgeries. The patients who developed cerebrovascular stroke had higher blood lactate at ECMO initiation (8.9 [5.5, 11.2] versus 5.7 [4.6, 11.9] mmol/L, <i>p</i> = 0.02) and 12 h later (8.7 [4.7, 14.5] versus 5.8 [4.6, 15] mmol/L, <i>p</i> = 0.024) with lesser lactate clearance (LC) at 12 h (6.35 [-51.5, 40.6] versus 14.65% [-43.55, 38.3], <i>p</i> < 001) compared to the patients in the nonstroke group. The stroke group had longer ICU stay (21 vs. 15.5 days, <i>p</i> = 0.03), higher frequency of new hemodialysis (62.9% vs. 46.4%, <i>p</i> = 0.026), and on-ECMO mortality (54.3% vs. 44.9%, <i>p</i> = 0.041) compared with the nonstroke group. The ICH was associated with higher hospital mortality (<i>p</i> = 0.021) compared to the ischemic stroke. Logistic multivariate regression revealed that the initial lactate level (OR: 1.6, 95% CI: 1.2-8.92, <i>p</i> = 0.031), cardiopulmonary bypass time (OR:1.8, 95% CI: 1.32-6.42, <i>p</i> = 0.02), and LC at 12 h (OR: 2.4, 95% CI: 1.91-17.4, <i>p</i> = 0.042) were associated with ischemic stroke. Thrombocytopenia (OR: 3.22, 95% CI: 1.82-7.83, <i>p</i> = 0.001) and low body mass index (OR: 2.1, 95% CI: 1.31-4.6, <i>p</i> = 0.02) were associated with ICH.</p><p><strong>Conclusions: </strong>Ischemic and hemorrhagic strokes are frequent with VA-ECMO support and associated with worse outcomes, especially the hemorrhagic type. Awareness of the incidence and the factors associated with strokes is crucial in early identification and management.</p>","PeriodicalId":46583,"journal":{"name":"Critical Care Research and Practice","volume":"2025 ","pages":"9058296"},"PeriodicalIF":1.8,"publicationDate":"2025-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12540010/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145349147","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 : 2025-09-16eCollection Date: 2025-01-01DOI: 10.1155/ccrp/9757345
[This corrects the article DOI: 10.1155/ccrp/4660819.].
[这更正了文章DOI: 10.1155/ccrp/4660819.]。
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