Pub Date : 2025-12-09DOI: 10.5492/wjccm.v14.i4.107570
Andrea Loggini, Amber Schwertman, Jonatan Hornik, Karam Dallow, Alejandro Hornik
Background: Administration of thrombolytics for acute ischemic stroke (AIS) via telemedicine has expanded in recent years at institutions without on-site neurology specialists. This helped to improve the care of stroke patients in rural areas. However, it is uncertain if telemedicine-administered thrombolytics is as safe and effective as in-person evaluation by neurology specialists.
Aim: The authors conducted a meta-analysis evaluating stroke metrics, safety and outcomes of telemedicine compared to in-person evaluation by neurologist specialist in AIS patients receiving intravenous thrombolytics.
Methods: PubMed, EMBASE, and Cochrane were searched for randomized clinical trials and observational cohort studies. The Mantel-Haenszel method or inverse variance, as applicable, were applied to calculate an overall effect estimate for each outcome by combining specific risk ratio (RR) or standardized mean difference (SMD). Risk of bias was analyzed using the Newcastle-Ottawa Scale. Primary outcome examined was door-to-needle time (DTN). Secondary outcomes were symptomatic intracranial hemorrhage (sICH), mortality, and mRS ≤ 2.
Results: Eleven retrospective cohort studies involving 2350 patients were included in the analysis. Of those, 34% (n = 794) received thrombolytics via telemedicine. Telemedicine was associated with a significantly longer mean DTN compared to in-person evaluation [SMD: 0.72 minutes; 95% confidence interval (CI) 0.22-1.22; P < 0.01], a similar rate of sICH [3.9% vs 4.2%; Odds ratio (OR): 0.75; 95%CI 0.42-1.37; P = 0.35], similar rate of mortality (13.2% vs 14.7%; OR: 0.87; 95%CI 0.47-1.63; P = 0.67), and comparable rate of favorable short-term functional outcome (46.8% vs 50.7%; OR: 0.79; 95%CI 0.41-1.53; P = 0.48). Risk of bias was low to moderate for each outcome.
Conclusion: The available literature suggests that telemedicine is associated with longer DTN compared to in-person evaluation. This difference in stroke metric does not affect safety or outcome. Further studies are needed to understand and address the underlying factors of the longer DTN time.
背景:近年来,在没有现场神经病学专家的机构中,通过远程医疗对急性缺血性卒中(AIS)进行溶栓治疗已经扩大。这有助于改善农村地区中风患者的护理。然而,尚不确定远程医疗溶栓是否与神经病学专家现场评估一样安全有效。目的:作者进行了一项荟萃分析,比较了接受静脉溶栓治疗的AIS患者中远程医疗的卒中指标、安全性和结果,以及由神经科专家亲自评估的结果。方法:检索PubMed、EMBASE和Cochrane,检索随机临床试验和观察性队列研究。应用Mantel-Haenszel方法或逆方差,结合特定风险比(RR)或标准化平均差(SMD)计算每个结局的总体效应估计。偏倚风险采用纽卡斯尔-渥太华量表进行分析。检查的主要终点是门到针的时间(DTN)。次要结局为症状性颅内出血(siich)、死亡率和mRS≤2。结果:11项回顾性队列研究纳入分析,涉及2350例患者。其中,34% (n = 794)通过远程医疗接受溶栓治疗。与面对面评估相比,远程医疗与较长的平均DTN相关[SMD: 0.72分钟;95%置信区间(CI) 0.22-1.22;P < 0.01], sICH发生率相似[3.9% vs 4.2%;优势比(OR): 0.75;95%可信区间0.42 - -1.37;P = 0.35],相似的死亡率(13.2% vs 14.7%; OR: 0.87; 95%CI 0.47-1.63; P = 0.67),以及相似的短期功能预后良好率(46.8% vs 50.7%; OR: 0.79; 95%CI 0.41-1.53; P = 0.48)。每个结果的偏倚风险为低至中等。结论:现有文献表明,与现场评估相比,远程医疗与更长的DTN相关。这种中风指标的差异不影响安全性或结果。需要进一步的研究来了解和解决DTN时间延长的潜在因素。
{"title":"Stroke metrics, safety, and outcomes of telemedicine-administered thrombolytics for acute ischemic stroke: A meta-analysis.","authors":"Andrea Loggini, Amber Schwertman, Jonatan Hornik, Karam Dallow, Alejandro Hornik","doi":"10.5492/wjccm.v14.i4.107570","DOIUrl":"10.5492/wjccm.v14.i4.107570","url":null,"abstract":"<p><strong>Background: </strong>Administration of thrombolytics for acute ischemic stroke (AIS) <i>via</i> telemedicine has expanded in recent years at institutions without on-site neurology specialists. This helped to improve the care of stroke patients in rural areas. However, it is uncertain if telemedicine-administered thrombolytics is as safe and effective as in-person evaluation by neurology specialists.</p><p><strong>Aim: </strong>The authors conducted a meta-analysis evaluating stroke metrics, safety and outcomes of telemedicine compared to in-person evaluation by neurologist specialist in AIS patients receiving intravenous thrombolytics.</p><p><strong>Methods: </strong>PubMed, EMBASE, and Cochrane were searched for randomized clinical trials and observational cohort studies. The Mantel-Haenszel method or inverse variance, as applicable, were applied to calculate an overall effect estimate for each outcome by combining specific risk ratio (RR) or standardized mean difference (SMD). Risk of bias was analyzed using the Newcastle-Ottawa Scale. Primary outcome examined was door-to-needle time (DTN). Secondary outcomes were symptomatic intracranial hemorrhage (sICH), mortality, and mRS ≤ 2.</p><p><strong>Results: </strong>Eleven retrospective cohort studies involving 2350 patients were included in the analysis. Of those, 34% (<i>n</i> = 794) received thrombolytics <i>via</i> telemedicine. Telemedicine was associated with a significantly longer mean DTN compared to in-person evaluation [SMD: 0.72 minutes; 95% confidence interval (CI) 0.22-1.22; <i>P</i> < 0.01], a similar rate of sICH [3.9% <i>vs</i> 4.2%; Odds ratio (OR): 0.75; 95%CI 0.42-1.37; <i>P</i> = 0.35], similar rate of mortality (13.2% <i>vs</i> 14.7%; OR: 0.87; 95%CI 0.47-1.63; <i>P</i> = 0.67), and comparable rate of favorable short-term functional outcome (46.8% <i>vs</i> 50.7%; OR: 0.79; 95%CI 0.41-1.53; <i>P</i> = 0.48). Risk of bias was low to moderate for each outcome.</p><p><strong>Conclusion: </strong>The available literature suggests that telemedicine is associated with longer DTN compared to in-person evaluation. This difference in stroke metric does not affect safety or outcome. Further studies are needed to understand and address the underlying factors of the longer DTN time.</p>","PeriodicalId":66959,"journal":{"name":"世界危重病急救学杂志(英文版)","volume":"14 4","pages":"107570"},"PeriodicalIF":0.0,"publicationDate":"2025-12-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12687052/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145727431","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 : 2025-12-09DOI: 10.5492/wjccm.v14.i4.108840
Vignesh K Nagesh, Emelyn Martinez, Shruthi Badam, Jevon Lamar Harrison, Marina Basta, Vivek Joseph Varughese, Ghulam R Anwar, Vishal Deshpande, Deepa Francis, Damien Islek, Sai Priyanka Pulipaka, Ruchi Bhuju, Pratiksha Moliya, Bilal Niazi, Sameh Elias
Acute liver failure (ALF) is a rare but life-threatening condition marked by rapid hepatic dysfunction, coagulopathy and encephalopathy in patients without prior liver disease. Common causes include drug-induced liver injury, viral hepatitis, and metabolic or autoimmune disorders. This review provides an updated overview of ALF's etiology, diagnosis, and management. Timely diagnosis and risk stratification using tools like the King's College Criteria and Model for End-Stage Liver Disease score are critical for guiding care. Early identification of etiology allows targeted treatments, such as N-acetylcysteine for acetaminophen toxicity or antivirals for hepatitis. Supportive care in specialized intensive care units, focused on hemodynamics, cerebral edema prevention, and metabolic stabilization, remains the cornerstone of management. Advances in extracorporeal liver support systems, such as molecular adsorbent recirculating systems and plasma exchange, offer promising bridges to recovery or liver transplantation - the definitive treatment for irreversible liver injury. Expanded donor criteria and improved allocation policies have enhanced transplantation access. Despite progress, ALF carries significant morbidity and mortality. Emerging therapies, including stem cell treatments and immunomodulatory agents, show potential to revolutionize care. This review emphasizes the need for a multidisciplinary approach and continued research to improve outcomes and refine therapeutic strategies.
{"title":"Management of acute liver failure-an updated literature review.","authors":"Vignesh K Nagesh, Emelyn Martinez, Shruthi Badam, Jevon Lamar Harrison, Marina Basta, Vivek Joseph Varughese, Ghulam R Anwar, Vishal Deshpande, Deepa Francis, Damien Islek, Sai Priyanka Pulipaka, Ruchi Bhuju, Pratiksha Moliya, Bilal Niazi, Sameh Elias","doi":"10.5492/wjccm.v14.i4.108840","DOIUrl":"10.5492/wjccm.v14.i4.108840","url":null,"abstract":"<p><p>Acute liver failure (ALF) is a rare but life-threatening condition marked by rapid hepatic dysfunction, coagulopathy and encephalopathy in patients without prior liver disease. Common causes include drug-induced liver injury, viral hepatitis, and metabolic or autoimmune disorders. This review provides an updated overview of ALF's etiology, diagnosis, and management. Timely diagnosis and risk stratification using tools like the King's College Criteria and Model for End-Stage Liver Disease score are critical for guiding care. Early identification of etiology allows targeted treatments, such as N-acetylcysteine for acetaminophen toxicity or antivirals for hepatitis. Supportive care in specialized intensive care units, focused on hemodynamics, cerebral edema prevention, and metabolic stabilization, remains the cornerstone of management. Advances in extracorporeal liver support systems, such as molecular adsorbent recirculating systems and plasma exchange, offer promising bridges to recovery or liver transplantation - the definitive treatment for irreversible liver injury. Expanded donor criteria and improved allocation policies have enhanced transplantation access. Despite progress, ALF carries significant morbidity and mortality. Emerging therapies, including stem cell treatments and immunomodulatory agents, show potential to revolutionize care. This review emphasizes the need for a multidisciplinary approach and continued research to improve outcomes and refine therapeutic strategies.</p>","PeriodicalId":66959,"journal":{"name":"世界危重病急救学杂志(英文版)","volume":"14 4","pages":"108840"},"PeriodicalIF":0.0,"publicationDate":"2025-12-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12687055/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145727618","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 : 2025-12-09DOI: 10.5492/wjccm.v14.i4.105600
Mayur S Shah, Vedika V Sharma, Syed J Patel, Abdul S Ansari
Background: Cytokines and inflammatory mediators are the key factors that are involved in the pathology of sepsis. Extracorporeal cytokine hemoadsorption devices offer an innovative clinical support system to alleviate the effects of the cytokine storm associated with sepsis.
Aim: To retrospectively evaluate the efficacy of CytoSorb® therapy as an adjunct to standard care in intensive care unit (ICU) patients with septic shock.
Methods: A retrospective study was designed. Data were obtained for the patients who were treated with the CytoSorb® adsorber for the past 5 years. The effects of therapy were assessed by changes in vasopressor requirements, specifically, norepinephrine and epinephrine. In addition, cytokine levels, such as interleukin (IL)-6 and inflammatory biomarkers including C-reactive protein (CRP), procalcitonin, as well as substances such as serum lactate and lactate dehydrogenase were also evaluated. In addition, mean arterial pressure (MAP) and ventilator requirements were also recorded. The survival outcomes were analyzed based on the length of patients' stay in the ICU, and the severity of illness was assessed using Acute Physiology and Chronic Health Evaluation (APACHE II) and Sepsis-associated Organ Failure Assessment (SOFA) scores recorded at baseline and post-therapy.
Results: Following CytoSorb® therapy, the requirement for vasopressor drugs, particularly norepinephrine, was reduced by 40% and a statistically significant improvement in MAP by 7.8%. Additionally, significant reductions were observed in IL-6 and serum lactate levels by 83% and 52% respectively. Around 56% had a delta lactate score of > 1.5, while 23% patients had a score ranging from 1 to < 1.5, and 16% patients had a score between 0.5 and < 1 and merely 5% patients had a score of ≤ 0.5. Besides, serum levels of creatinine, procalcitonin and CRP were significantly reduced by 17.2%, 41.5% and 53.8% respectively. There was a significant reduction in scores, including APACHE II [to 23 (18-29) from 27 (23-33)], and SOFA [to 12 (10-14) from 13 (11-15)]. Mechanical ventilation was required by 96% patients, with a median duration of 12 days, and the median length of hospital stay in overall patients was 26 days, while the median ICU stay was 18 days.
Conclusion: CytoSorb® therapy seems to be a promising adjunctive approach in the management of septic shock.
{"title":"Retrospective evaluation of efficacy of CytoSorb<sup>®</sup> therapy in septic shock patients in a tertiary care intensive care unit.","authors":"Mayur S Shah, Vedika V Sharma, Syed J Patel, Abdul S Ansari","doi":"10.5492/wjccm.v14.i4.105600","DOIUrl":"10.5492/wjccm.v14.i4.105600","url":null,"abstract":"<p><strong>Background: </strong>Cytokines and inflammatory mediators are the key factors that are involved in the pathology of sepsis. Extracorporeal cytokine hemoadsorption devices offer an innovative clinical support system to alleviate the effects of the cytokine storm associated with sepsis.</p><p><strong>Aim: </strong>To retrospectively evaluate the efficacy of CytoSorb<sup>®</sup> therapy as an adjunct to standard care in intensive care unit (ICU) patients with septic shock.</p><p><strong>Methods: </strong>A retrospective study was designed. Data were obtained for the patients who were treated with the CytoSorb<sup>®</sup> adsorber for the past 5 years. The effects of therapy were assessed by changes in vasopressor requirements, specifically, norepinephrine and epinephrine. In addition, cytokine levels, such as interleukin (IL)-6 and inflammatory biomarkers including C-reactive protein (CRP), procalcitonin, as well as substances such as serum lactate and lactate dehydrogenase were also evaluated. In addition, mean arterial pressure (MAP) and ventilator requirements were also recorded. The survival outcomes were analyzed based on the length of patients' stay in the ICU, and the severity of illness was assessed using Acute Physiology and Chronic Health Evaluation (APACHE II) and Sepsis-associated Organ Failure Assessment (SOFA) scores recorded at baseline and post-therapy.</p><p><strong>Results: </strong>Following CytoSorb<sup>®</sup> therapy, the requirement for vasopressor drugs, particularly norepinephrine, was reduced by 40% and a statistically significant improvement in MAP by 7.8%. Additionally, significant reductions were observed in IL-6 and serum lactate levels by 83% and 52% respectively. Around 56% had a delta lactate score of > 1.5, while 23% patients had a score ranging from 1 to < 1.5, and 16% patients had a score between 0.5 and < 1 and merely 5% patients had a score of ≤ 0.5. Besides, serum levels of creatinine, procalcitonin and CRP were significantly reduced by 17.2%, 41.5% and 53.8% respectively. There was a significant reduction in scores, including APACHE II [to 23 (18-29) from 27 (23-33)], and SOFA [to 12 (10-14) from 13 (11-15)]. Mechanical ventilation was required by 96% patients, with a median duration of 12 days, and the median length of hospital stay in overall patients was 26 days, while the median ICU stay was 18 days.</p><p><strong>Conclusion: </strong>CytoSorb<sup>®</sup> therapy seems to be a promising adjunctive approach in the management of septic shock.</p>","PeriodicalId":66959,"journal":{"name":"世界危重病急救学杂志(英文版)","volume":"14 4","pages":"105600"},"PeriodicalIF":0.0,"publicationDate":"2025-12-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12687050/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145727473","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 : 2025-12-09DOI: 10.5492/wjccm.v14.i4.106027
Mugahid Eltahir, Ibrahim Fawzy, Abdulsalam Saif Ibrahim, Ezzeddin A Ibrahim, Rashid Mazhar, Nabil Abd Elhamid Shallik, Ayman El-Menyar, Ahmed Labib Shehatta
Background: In critical care practice, difficult airway management poses a substantial challenge, necessitating urgent intervention to ensure patient safety and optimize outcomes. Extracorporeal membrane oxygenation (ECMO) is a potential rescue tool in patients with severe airway compromise, although evidence of its efficacy and safety remains limited.
Aim: To review the local experience of using ECMO support in patients with difficult airway management.
Methods: This retrospective case series study includes patients with difficult airway management who required ECMO support at a tertiary hospital in a Middle Eastern country.
Results: Between 2016 and 2023, a total of 13 patients required ECMO support due to challenging airway patency in the operating room. Indications for ECMO encompassed various diagnoses, including tracheal stenosis, external tracheal compression, and subglottic stenosis. Surgical interventions such as tracheal resection and anastomosis often necessitated ECMO support to maintain adequate oxygenation and hemodynamic stability. The duration of ECMO support ranged from standby mode (ECMO implantation is readily available) to several days, with relatively infrequent complications observed. Despite the challenges encountered, most patients survived hospital discharge, highlighting the effectiveness of ECMO in managing difficult airways.
Conclusion: This study underscores the crucial role of ECMO as a life-saving intervention in selected cases of difficult airway management. Further research is warranted to refine the understanding of optimal management strategies and improve outcomes in this challenging patient population.
{"title":"Extracorporeal membrane oxygenation support in patients with difficult airway management: Case series of 13 patients.","authors":"Mugahid Eltahir, Ibrahim Fawzy, Abdulsalam Saif Ibrahim, Ezzeddin A Ibrahim, Rashid Mazhar, Nabil Abd Elhamid Shallik, Ayman El-Menyar, Ahmed Labib Shehatta","doi":"10.5492/wjccm.v14.i4.106027","DOIUrl":"10.5492/wjccm.v14.i4.106027","url":null,"abstract":"<p><strong>Background: </strong>In critical care practice, difficult airway management poses a substantial challenge, necessitating urgent intervention to ensure patient safety and optimize outcomes. Extracorporeal membrane oxygenation (ECMO) is a potential rescue tool in patients with severe airway compromise, although evidence of its efficacy and safety remains limited.</p><p><strong>Aim: </strong>To review the local experience of using ECMO support in patients with difficult airway management.</p><p><strong>Methods: </strong>This retrospective case series study includes patients with difficult airway management who required ECMO support at a tertiary hospital in a Middle Eastern country.</p><p><strong>Results: </strong>Between 2016 and 2023, a total of 13 patients required ECMO support due to challenging airway patency in the operating room. Indications for ECMO encompassed various diagnoses, including tracheal stenosis, external tracheal compression, and subglottic stenosis. Surgical interventions such as tracheal resection and anastomosis often necessitated ECMO support to maintain adequate oxygenation and hemodynamic stability. The duration of ECMO support ranged from standby mode (ECMO implantation is readily available) to several days, with relatively infrequent complications observed. Despite the challenges encountered, most patients survived hospital discharge, highlighting the effectiveness of ECMO in managing difficult airways.</p><p><strong>Conclusion: </strong>This study underscores the crucial role of ECMO as a life-saving intervention in selected cases of difficult airway management. Further research is warranted to refine the understanding of optimal management strategies and improve outcomes in this challenging patient population.</p>","PeriodicalId":66959,"journal":{"name":"世界危重病急救学杂志(英文版)","volume":"14 4","pages":"106027"},"PeriodicalIF":0.0,"publicationDate":"2025-12-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12687051/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145727612","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 : 2025-12-09DOI: 10.5492/wjccm.v14.i4.111164
Flavio Eduardo Nacul, Murilo Borges Bezerra, Brenno Cardoso Gomes, Fábio Barlem Hohmann, Ricardo Esper Treml, Tulio Caldonazo, Arnaldo Alves da Silva, Rogerio H Passos, Neymar Elias de Oliveira, Grazielle Pangratz Bedretchuk, Joao Manoel Silva
Background: Refractory septic shock is a critical and multifaceted condition that continues to pose significant challenges in critical care.
Aim: To systematically review randomized trials on emerging interventions for refractory septic shock, assessing mortality, vasopressor use, intensive care unit (ICU) length of stay, and organ dysfunction.
Methods: A systematic search was conducted in PubMed, EMBASE, Cochrane CENTRAL Library, and Web of Science for studies published between 2000 and 2024. Inclusion criteria encompassed randomized controlled trials (RCT) evaluating innovative therapies for refractory septic shock. Variables of interest: The primary outcome was all-cause mortality among patients treated with novel interventions. Secondary outcomes included length of stay in the ICU, total hospital length of stay, and use of vasoactive drugs. Methodological rigor was assessed using the Cochrane Risk of Bias tool.
Results: From 850 records, 24 RCTs met the inclusion criteria, evaluating therapies such as methylene blue, vasopressin, terlipressin, and combinations of hydrocortisone, vitamin C, and thiamine. Mortality rates ranged from 28.6% to 56.8%. Methylene blue reduced vasopressor dependency in patients requiring high norepinephrine doses by 1.0 vasopressor-free day, and terlipressin improved renal perfusion by 13.1%. Combination therapies enhanced secondary outcomes, including reductions in Sequential Organ Failure Assessment score. However, no single intervention consistently demonstrated significant survival benefits.
Conclusion: Adjunctive therapies for refractory septic shock may improve hemodynamics and organ function, however, they have not been shown to consistently reduce mortality. Larger trials are needed to confirm these findings. Multimodal approaches targeting inflammation are critical.
背景:难治性感染性休克是一种严重的、多方面的疾病,在重症监护中继续构成重大挑战。目的:系统回顾有关难治性脓毒性休克新干预措施的随机试验,评估死亡率、血管加压剂使用、重症监护病房(ICU)住院时间和器官功能障碍。方法:系统检索PubMed、EMBASE、Cochrane CENTRAL Library和Web of Science,检索2000 - 2024年间发表的研究。纳入标准包括评估难治性感染性休克创新疗法的随机对照试验(RCT)。感兴趣的变量:主要结果是接受新型干预治疗的患者的全因死亡率。次要结局包括在ICU的住院时间、总住院时间和血管活性药物的使用。采用Cochrane偏倚风险工具评估方法学严谨性。结果:从850个记录中,24个随机对照试验符合纳入标准,评估了亚甲蓝、抗利尿激素、特利加压素以及氢化可的松、维生素C和硫胺素的联合治疗。死亡率从28.6%到56.8%不等。亚甲蓝降低了需要高剂量去甲肾上腺素的患者对血管加压素的依赖1.0天,特利加压素改善肾灌注13.1%。联合治疗增强了次要结果,包括序贯器官衰竭评估评分的降低。然而,没有单一的干预措施始终显示出显著的生存益处。结论:顽固性脓毒性休克的辅助治疗可以改善血液动力学和器官功能,然而,它们并没有被证明能持续降低死亡率。需要更大规模的试验来证实这些发现。针对炎症的多模式方法至关重要。
{"title":"Current and emerging therapeutic options for refractory septic shock: A systematic review.","authors":"Flavio Eduardo Nacul, Murilo Borges Bezerra, Brenno Cardoso Gomes, Fábio Barlem Hohmann, Ricardo Esper Treml, Tulio Caldonazo, Arnaldo Alves da Silva, Rogerio H Passos, Neymar Elias de Oliveira, Grazielle Pangratz Bedretchuk, Joao Manoel Silva","doi":"10.5492/wjccm.v14.i4.111164","DOIUrl":"10.5492/wjccm.v14.i4.111164","url":null,"abstract":"<p><strong>Background: </strong>Refractory septic shock is a critical and multifaceted condition that continues to pose significant challenges in critical care.</p><p><strong>Aim: </strong>To systematically review randomized trials on emerging interventions for refractory septic shock, assessing mortality, vasopressor use, intensive care unit (ICU) length of stay, and organ dysfunction.</p><p><strong>Methods: </strong>A systematic search was conducted in PubMed, EMBASE, Cochrane CENTRAL Library, and Web of Science for studies published between 2000 and 2024. Inclusion criteria encompassed randomized controlled trials (RCT) evaluating innovative therapies for refractory septic shock. Variables of interest: The primary outcome was all-cause mortality among patients treated with novel interventions. Secondary outcomes included length of stay in the ICU, total hospital length of stay, and use of vasoactive drugs. Methodological rigor was assessed using the Cochrane Risk of Bias tool.</p><p><strong>Results: </strong>From 850 records, 24 RCTs met the inclusion criteria, evaluating therapies such as methylene blue, vasopressin, terlipressin, and combinations of hydrocortisone, vitamin C, and thiamine. Mortality rates ranged from 28.6% to 56.8%. Methylene blue reduced vasopressor dependency in patients requiring high norepinephrine doses by 1.0 vasopressor-free day, and terlipressin improved renal perfusion by 13.1%. Combination therapies enhanced secondary outcomes, including reductions in Sequential Organ Failure Assessment score. However, no single intervention consistently demonstrated significant survival benefits.</p><p><strong>Conclusion: </strong>Adjunctive therapies for refractory septic shock may improve hemodynamics and organ function, however, they have not been shown to consistently reduce mortality. Larger trials are needed to confirm these findings. Multimodal approaches targeting inflammation are critical.</p>","PeriodicalId":66959,"journal":{"name":"世界危重病急救学杂志(英文版)","volume":"14 4","pages":"111164"},"PeriodicalIF":0.0,"publicationDate":"2025-12-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12687076/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145727638","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 : 2025-12-09DOI: 10.5492/wjccm.v14.i4.110669
Dat Minh-Tan Truong, Minh Hoang-Nhat Nguyen, Huy Quang Nguyen, Luan Thanh Vo, Thanh Tat Nguyen
Background: The optic nerve sheath diameter (ONSD) measured by ultrasound has emerged as a significant noninvasive method for detecting elevated intracranial pressure (ICP), guiding timely interventions, and monitoring treatment response. Previous studies have shown that the baseline ONSD at admission is a prognostic indicator of mortality in adult patients with cerebrovascular events, traumatic brain injury, hepatic encephalopathy, and acute stroke. However, pediatric data on the dynamic changes in ONSD remain limited.
Aim: To study the association between within-48 hours admission dynamic ONSD changes and mortality in children with clinically relevant elevated ICP.
Methods: This single-institution prospective study was performed at a tertiary Children's Hospital in Vietnam, between November 2023 and August 2024. The primary outcome was in-hospital mortality rate. ONSD data were measured at admission, 24 hours, and 48 hours post-admission to pediatric intensive care unit (PICU). Linear mixed-effects models accounting for repeated measures within individuals were used to analyze the association between ONSD changes and in-hospital mortality.
Results: A total of 69 PICU-admitted children with clinically relevant raised ICP were enrolled and included in the analysis. The median patient age was 6 years (interquartile range: 1-12), and males accounted for 54% of all patients. The in-hospital mortality rate in children with clinically relevant raised ICP was 23.2%. Traumatic brain injury, sepsis-associated encephalopathy, and septic shock were the main causes of death in this cohort. Linear mixed-effects analysis showed that dynamic variability in ONSD values upon PICU admission and during the first 48 hours later correlated significantly with increased mortality. Nonsurvivors had a 5.3% increase in the mean ONSD at 48 hours compared to baseline levels, while the survivors showed a 5.6% reduction in ONSD.
Conclusion: Serial ultrasound-based ONSD measurements within 48 hours of admission better predicted mortality than baseline data in critically ill children, offering a practical, noninvasive tool for early prognosis in elevated ICP.
{"title":"Optic nerve sheath diameter trajectories and mortality in children with clinically relevant elevated intracranial pressure.","authors":"Dat Minh-Tan Truong, Minh Hoang-Nhat Nguyen, Huy Quang Nguyen, Luan Thanh Vo, Thanh Tat Nguyen","doi":"10.5492/wjccm.v14.i4.110669","DOIUrl":"10.5492/wjccm.v14.i4.110669","url":null,"abstract":"<p><strong>Background: </strong>The optic nerve sheath diameter (ONSD) measured by ultrasound has emerged as a significant noninvasive method for detecting elevated intracranial pressure (ICP), guiding timely interventions, and monitoring treatment response. Previous studies have shown that the baseline ONSD at admission is a prognostic indicator of mortality in adult patients with cerebrovascular events, traumatic brain injury, hepatic encephalopathy, and acute stroke. However, pediatric data on the dynamic changes in ONSD remain limited.</p><p><strong>Aim: </strong>To study the association between within-48 hours admission dynamic ONSD changes and mortality in children with clinically relevant elevated ICP.</p><p><strong>Methods: </strong>This single-institution prospective study was performed at a tertiary Children's Hospital in Vietnam, between November 2023 and August 2024. The primary outcome was in-hospital mortality rate. ONSD data were measured at admission, 24 hours, and 48 hours post-admission to pediatric intensive care unit (PICU). Linear mixed-effects models accounting for repeated measures within individuals were used to analyze the association between ONSD changes and in-hospital mortality.</p><p><strong>Results: </strong>A total of 69 PICU-admitted children with clinically relevant raised ICP were enrolled and included in the analysis. The median patient age was 6 years (interquartile range: 1-12), and males accounted for 54% of all patients. The in-hospital mortality rate in children with clinically relevant raised ICP was 23.2%. Traumatic brain injury, sepsis-associated encephalopathy, and septic shock were the main causes of death in this cohort. Linear mixed-effects analysis showed that dynamic variability in ONSD values upon PICU admission and during the first 48 hours later correlated significantly with increased mortality. Nonsurvivors had a 5.3% increase in the mean ONSD at 48 hours compared to baseline levels, while the survivors showed a 5.6% reduction in ONSD.</p><p><strong>Conclusion: </strong>Serial ultrasound-based ONSD measurements within 48 hours of admission better predicted mortality than baseline data in critically ill children, offering a practical, noninvasive tool for early prognosis in elevated ICP.</p>","PeriodicalId":66959,"journal":{"name":"世界危重病急救学杂志(英文版)","volume":"14 4","pages":"110669"},"PeriodicalIF":0.0,"publicationDate":"2025-12-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12687078/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145727680","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}
Nonthyroidal illness syndrome (NTIS) is a common finding in critically ill patients, characterized by disruptions in the hypothalamus-pituitary-thyroid axis, resulting in altered levels of thyroxine (T4), triiodothyronine (T3), and reverse T3. This condition, often considered to be an adaptive response aimed at conserving energy, can become maladaptive in prolonged critical illness, contributing to poor outcomes in intensive care unit patients. The pathophysiology of NTIS involves cytokine-driven alterations in thyroid hormone (TH) metabolism, impaired hormone transport, and reduced receptor sensitivity, which-collectively-suppress thyroid function. Despite these insights, the therapeutic role of TH replacement in patients with NTIS remains uncertain. Low doses of levothyroxine and T3 have been trialed, particularly in patients with cardiovascular comorbidities, but clinical studies report conflicting results regarding their impact on mortality and overall patient outcomes. While some evidence suggests potential benefits of T3 administration in specific subgroups, such as patients with septic shock or severe coronavirus disease 2019, robust clinical trials have yet to conclusively demonstrate improved survival or recovery. The heterogeneity in NTIS presentation and treatment protocols, as well as the complex nature of TH regulation in critically ill patients, complicates efforts to establish clear guidelines for hormone therapy. Future research should prioritize individualized approaches, optimizing hormone dosing and timing, while aiming to elucidate the long-term effects of such interventions on critically ill patients to improve morbidity and mortality outcomes.
{"title":"Critical illness-implications of non-thyroidal illness syndrome and thyroxine therapy.","authors":"Christos Savvidis, Dimitra Ragia, Efthymia Kallistrou, Eleni Kouroglou, Vasiliki Tsiama, Stella Proikaki, Konstantinos Belis, Ioannis Ilias","doi":"10.5492/wjccm.v14.i3.102577","DOIUrl":"10.5492/wjccm.v14.i3.102577","url":null,"abstract":"<p><p>Nonthyroidal illness syndrome (NTIS) is a common finding in critically ill patients, characterized by disruptions in the hypothalamus-pituitary-thyroid axis, resulting in altered levels of thyroxine (T4), triiodothyronine (T3), and reverse T3. This condition, often considered to be an adaptive response aimed at conserving energy, can become maladaptive in prolonged critical illness, contributing to poor outcomes in intensive care unit patients. The pathophysiology of NTIS involves cytokine-driven alterations in thyroid hormone (TH) metabolism, impaired hormone transport, and reduced receptor sensitivity, which-collectively-suppress thyroid function. Despite these insights, the therapeutic role of TH replacement in patients with NTIS remains uncertain. Low doses of levothyroxine and T3 have been trialed, particularly in patients with cardiovascular comorbidities, but clinical studies report conflicting results regarding their impact on mortality and overall patient outcomes. While some evidence suggests potential benefits of T3 administration in specific subgroups, such as patients with septic shock or severe coronavirus disease 2019, robust clinical trials have yet to conclusively demonstrate improved survival or recovery. The heterogeneity in NTIS presentation and treatment protocols, as well as the complex nature of TH regulation in critically ill patients, complicates efforts to establish clear guidelines for hormone therapy. Future research should prioritize individualized approaches, optimizing hormone dosing and timing, while aiming to elucidate the long-term effects of such interventions on critically ill patients to improve morbidity and mortality outcomes.</p>","PeriodicalId":66959,"journal":{"name":"世界危重病急救学杂志(英文版)","volume":"14 3","pages":"102577"},"PeriodicalIF":0.0,"publicationDate":"2025-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12304970/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144980184","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 : 2025-09-09DOI: 10.5492/wjccm.v14.i3.101327
Matthew Cabrera, Sarika Bharil, Meghan Chin, Seife Yohannes, Paul Clark
<p><strong>Background: </strong>A major cause of mortality in the coronavirus disease 2019 (COVID-19) pandemic was acute respiratory distress syndrome (ARDS). Currently, moderate to severe ARDS induced by COVID-19 (COVID ARDS) and other viral and non-viral etiologies are treated by traditional ARDS protocols that recommend 12-16 hours of prone position ventilation (PPV) with neuromuscular blocking agents (NMBA) and a trial of inhaled vasodilators (IVd) if oxygenation does not improve. However, debate on the efficacy of adjuncts to PPV and low tidal volume ventilation persists and evidence about the benefits of IVd/NMBA in COVID ARDS is sparse. In our multi-center retrospective review, we evaluated the impact of PPV, IVd, and NMBA on outcomes and lung mechanics in COVID ARDS patients with moderate to severe ARDS.</p><p><strong>Aim: </strong>To evaluate the impact of PPV used alone or in combination with pulmonary IVd and/or NMBA in mechanically ventilated patients with moderate to severe ARDS during the COVID-19 pandemic.</p><p><strong>Methods: </strong>A retrospective study at two tertiary academic medical centers compared outcomes between COVID ARDS patients receiving PPV and patients in the supine position. PPV patients were divided based on concurrent use of ARDS adjunct therapies resulting in four subgroups: (1) PPV alone; (2) PPV and IVd; (3) PPV and NMBA; and (4) PPV, IVd, and NMBA. Primary outcomes were hospital and intensive care unit (ICU) length of stay (LOS), mortality, and venovenous extracorporeal membrane oxygenation (VV-ECMO) status. Secondary outcomes included changes in lung mechanics at 24-hour intervals for 7 days.</p><p><strong>Results: </strong>Total 114 patients were included in this study. Baseline respiratory parameters and Sequential Organ Failure Assessment scores were significantly worse in the PPV group. ICU LOS and LOS were significantly longer for patients who were proned, but no mortality benefit or difference in VV-ECMO status was found. Among the subgroups, no difference in primary outcomes were found. In the secondary analysis, PPV was associated with a significant improvement in arterial oxygen partial pressure (PaO<sub>2</sub>)/fractional inspired oxygen (FiO<sub>2</sub>) (P/F) ratio from day 1 to day 4 (<i>P</i> < 0.05) and higher driving pressures day 5 to day 7 (<i>P</i> < 0.05). The combination of PPV and IVd together resulted in improvements in P/F ratio from day 1 to day 7 and plateau pressure on day 4 and day 6 (<i>P</i> < 0.05). PPV with NMBA was not associated with improvements in any of the secondary outcomes. The use of all three rescue therapies together resulted in improvements in lung compliance on day 2 (<i>P</i> < 0.05) but no other improvements.</p><p><strong>Conclusion: </strong>In mechanically ventilated patients diagnosed with moderate to severe COVID ARDS, PPV and PPV with the addition of IVd produced a significant and sustained increase in P/F ratio. The combination of PPV, IVd and NMBA im
{"title":"Impact of proning with and without inhaled pulmonary vasodilators and neuromuscular blocking agents in COVID acute respiratory distress syndrome.","authors":"Matthew Cabrera, Sarika Bharil, Meghan Chin, Seife Yohannes, Paul Clark","doi":"10.5492/wjccm.v14.i3.101327","DOIUrl":"10.5492/wjccm.v14.i3.101327","url":null,"abstract":"<p><strong>Background: </strong>A major cause of mortality in the coronavirus disease 2019 (COVID-19) pandemic was acute respiratory distress syndrome (ARDS). Currently, moderate to severe ARDS induced by COVID-19 (COVID ARDS) and other viral and non-viral etiologies are treated by traditional ARDS protocols that recommend 12-16 hours of prone position ventilation (PPV) with neuromuscular blocking agents (NMBA) and a trial of inhaled vasodilators (IVd) if oxygenation does not improve. However, debate on the efficacy of adjuncts to PPV and low tidal volume ventilation persists and evidence about the benefits of IVd/NMBA in COVID ARDS is sparse. In our multi-center retrospective review, we evaluated the impact of PPV, IVd, and NMBA on outcomes and lung mechanics in COVID ARDS patients with moderate to severe ARDS.</p><p><strong>Aim: </strong>To evaluate the impact of PPV used alone or in combination with pulmonary IVd and/or NMBA in mechanically ventilated patients with moderate to severe ARDS during the COVID-19 pandemic.</p><p><strong>Methods: </strong>A retrospective study at two tertiary academic medical centers compared outcomes between COVID ARDS patients receiving PPV and patients in the supine position. PPV patients were divided based on concurrent use of ARDS adjunct therapies resulting in four subgroups: (1) PPV alone; (2) PPV and IVd; (3) PPV and NMBA; and (4) PPV, IVd, and NMBA. Primary outcomes were hospital and intensive care unit (ICU) length of stay (LOS), mortality, and venovenous extracorporeal membrane oxygenation (VV-ECMO) status. Secondary outcomes included changes in lung mechanics at 24-hour intervals for 7 days.</p><p><strong>Results: </strong>Total 114 patients were included in this study. Baseline respiratory parameters and Sequential Organ Failure Assessment scores were significantly worse in the PPV group. ICU LOS and LOS were significantly longer for patients who were proned, but no mortality benefit or difference in VV-ECMO status was found. Among the subgroups, no difference in primary outcomes were found. In the secondary analysis, PPV was associated with a significant improvement in arterial oxygen partial pressure (PaO<sub>2</sub>)/fractional inspired oxygen (FiO<sub>2</sub>) (P/F) ratio from day 1 to day 4 (<i>P</i> < 0.05) and higher driving pressures day 5 to day 7 (<i>P</i> < 0.05). The combination of PPV and IVd together resulted in improvements in P/F ratio from day 1 to day 7 and plateau pressure on day 4 and day 6 (<i>P</i> < 0.05). PPV with NMBA was not associated with improvements in any of the secondary outcomes. The use of all three rescue therapies together resulted in improvements in lung compliance on day 2 (<i>P</i> < 0.05) but no other improvements.</p><p><strong>Conclusion: </strong>In mechanically ventilated patients diagnosed with moderate to severe COVID ARDS, PPV and PPV with the addition of IVd produced a significant and sustained increase in P/F ratio. The combination of PPV, IVd and NMBA im","PeriodicalId":66959,"journal":{"name":"世界危重病急救学杂志(英文版)","volume":"14 3","pages":"101327"},"PeriodicalIF":0.0,"publicationDate":"2025-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12305004/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144980414","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 : 2025-09-09DOI: 10.5492/wjccm.v14.i3.108272
Maneesh Gaddam, Dedeepya Gullapalli, Zayaan A Adrish, Arnav Y Reddy, Muhammad Adrish
Prediction of weaning success from invasive mechanical ventilation remains a challenge in everyday clinical practice. Several prediction scores have been developed to guide success during spontaneous breathing trials to help with weaning decisions. These scores aim to provide a structured framework to support clinical judgment. However, their effectiveness varies across patient populations, and their predictive accuracy remains inconsistent. In this review, we aim to identify the strengths and limitations of commonly used clinical prediction tools in assessing readiness for ventilator liberation. While scores such as the Rapid Shallow Breathing Index and the Integrative Weaning Index are widely adopted, their sensitivity and specificity often fall short in complex clinical settings. Factors such as underlying disease pathophysiology, patient characteristics, and clinician subjectivity impact score performance and reliability. Moreover, disparities in validation across diverse populations limit generalizability. With growing interest in artificial intelligence (AI) and machine learning, there is potential for enhanced prediction models that integrate multidimensional data and adapt to individual patient profiles. However, current AI approaches face challenges related to interpretability, bias, and ethical implementation. This paper underscores the need for more robust, individualized, and transparent prediction systems and advocates for careful integration of emerging technologies into clinical workflows to optimize weaning success and patient outcomes.
{"title":"Predicting weaning failure from invasive mechanical ventilation: The promise and pitfalls of clinical prediction scores.","authors":"Maneesh Gaddam, Dedeepya Gullapalli, Zayaan A Adrish, Arnav Y Reddy, Muhammad Adrish","doi":"10.5492/wjccm.v14.i3.108272","DOIUrl":"10.5492/wjccm.v14.i3.108272","url":null,"abstract":"<p><p>Prediction of weaning success from invasive mechanical ventilation remains a challenge in everyday clinical practice. Several prediction scores have been developed to guide success during spontaneous breathing trials to help with weaning decisions. These scores aim to provide a structured framework to support clinical judgment. However, their effectiveness varies across patient populations, and their predictive accuracy remains inconsistent. In this review, we aim to identify the strengths and limitations of commonly used clinical prediction tools in assessing readiness for ventilator liberation. While scores such as the Rapid Shallow Breathing Index and the Integrative Weaning Index are widely adopted, their sensitivity and specificity often fall short in complex clinical settings. Factors such as underlying disease pathophysiology, patient characteristics, and clinician subjectivity impact score performance and reliability. Moreover, disparities in validation across diverse populations limit generalizability. With growing interest in artificial intelligence (AI) and machine learning, there is potential for enhanced prediction models that integrate multidimensional data and adapt to individual patient profiles. However, current AI approaches face challenges related to interpretability, bias, and ethical implementation. This paper underscores the need for more robust, individualized, and transparent prediction systems and advocates for careful integration of emerging technologies into clinical workflows to optimize weaning success and patient outcomes.</p>","PeriodicalId":66959,"journal":{"name":"世界危重病急救学杂志(英文版)","volume":"14 3","pages":"108272"},"PeriodicalIF":0.0,"publicationDate":"2025-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12304996/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144980425","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 : 2025-09-09DOI: 10.5492/wjccm.v14.i3.102609
Shreyas S Anegundi, Madhuri S Kurdi, Jagadish G Sutagatti, Kaushik A Theerth
Background: Lung ultrasonography is being increasingly used in mechanically ventilated patients to evaluate the lung aeration during incremental positive end expiratory pressure (PEEP) adjustments and to evaluate the weaning process from mechanical ventilation. The effects of PEEP may vary across different lung pathologies and may not consistently correlate with changes in lung aeration as assessed by lung ultrasound scores (LUSs).
Aim: To assess the role of lung ultrasonography in evaluating lung aeration during the application of PEEP in mechanically ventilated patients with various lung pathologies.
Methods: An observational study was conducted over 18 months in a tertiary care hospital. Patients of both genders, aged between 18-75 years, who had been admitted to the intensive care unit, and required mechanical ventilation, were studied. A standard ventilatory strategy was used and incremental levels of PEEP [5, 10, and 15 cm water (H2O)] were applied. Baseline characteristics, including oxygen saturation (SpO2), LUS, mean arterial pressure (MAP), heart rate (HR), and their changes with incremental PEEP levels, were recorded and analyzed.
Results: In this study, 45.9% of patients required a PEEP of 5 cm H2O to achieve the endpoint of lung aeration (LUS of 0). In addition, 86.5% and 13.5% of patients reached the endpoint of lung aeration at PEEP levels of 10 and 15 cm H2O, respectively. The proportion of patients with higher lung scores decreased significantly with increasing PEEP levels (P < 0.001 for 5 and 10 cm H2O and P = 0.032 for 15 cm H2O). SpO2 increased significantly with higher PEEP levels (P < 0.001), confirming the effectiveness of PEEP in improving oxygenation. The results also revealed a significant increase in HR and a decrease in MAP following the application of higher PEEP levels.
Conclusion: Increasing PEEP levels in mechanically ventilated patients improves lung aeration, which can be effectively assessed using bedside lung ultrasonography.
背景:肺超声越来越多地用于机械通气患者在增量呼气末正压(PEEP)调整期间的肺通气和评估机械通气的脱机过程。PEEP的影响可能因不同的肺部病理而异,并且可能与肺超声评分(LUSs)评估的肺通气量变化不一致。目的:探讨肺动脉正压通气(PEEP)在不同肺病理机械通气患者肺通气中的应用价值。方法:在一家三级医院进行了为期18个月的观察性研究。研究对象为年龄在18-75岁之间、曾入住重症监护室并需要机械通气的男女患者。采用标准的通气策略,并应用增量PEEP[5、10和15 cm水(H2O)]。记录并分析基线特征,包括血氧饱和度(SpO2)、LUS、平均动脉压(MAP)、心率(HR)及其随PEEP升高的变化。结果:在本研究中,45.9%的患者需要5 cm H2O的PEEP才能达到肺通气终点(LUS为0)。此外,86.5%和13.5%的患者分别在PEEP水平为10和15 cm H2O时达到肺通气终点。随着PEEP水平的升高,肺评分较高的患者比例显著降低(5、10 cm H2O P < 0.001, 15 cm H2O P = 0.032)。SpO2随PEEP升高而显著升高(P < 0.001),证实了PEEP改善氧合的有效性。结果还显示,在应用较高的PEEP水平后,HR显著增加,MAP显著降低。结论:机械通气患者PEEP升高可改善肺通气,床边肺超声检查可有效评价其通气效果。
{"title":"Role of lung ultrasound in assessing positive end expiratory pressure induced lung recruitment in patients on mechanical ventilation.","authors":"Shreyas S Anegundi, Madhuri S Kurdi, Jagadish G Sutagatti, Kaushik A Theerth","doi":"10.5492/wjccm.v14.i3.102609","DOIUrl":"10.5492/wjccm.v14.i3.102609","url":null,"abstract":"<p><strong>Background: </strong>Lung ultrasonography is being increasingly used in mechanically ventilated patients to evaluate the lung aeration during incremental positive end expiratory pressure (PEEP) adjustments and to evaluate the weaning process from mechanical ventilation. The effects of PEEP may vary across different lung pathologies and may not consistently correlate with changes in lung aeration as assessed by lung ultrasound scores (LUSs).</p><p><strong>Aim: </strong>To assess the role of lung ultrasonography in evaluating lung aeration during the application of PEEP in mechanically ventilated patients with various lung pathologies.</p><p><strong>Methods: </strong>An observational study was conducted over 18 months in a tertiary care hospital. Patients of both genders, aged between 18-75 years, who had been admitted to the intensive care unit, and required mechanical ventilation, were studied. A standard ventilatory strategy was used and incremental levels of PEEP [5, 10, and 15 cm water (H<sub>2</sub>O)] were applied. Baseline characteristics, including oxygen saturation (SpO<sub>2</sub>), LUS, mean arterial pressure (MAP), heart rate (HR), and their changes with incremental PEEP levels, were recorded and analyzed.</p><p><strong>Results: </strong>In this study, 45.9% of patients required a PEEP of 5 cm H<sub>2</sub>O to achieve the endpoint of lung aeration (LUS of 0). In addition, 86.5% and 13.5% of patients reached the endpoint of lung aeration at PEEP levels of 10 and 15 cm H<sub>2</sub>O, respectively. The proportion of patients with higher lung scores decreased significantly with increasing PEEP levels (<i>P</i> < 0.001 for 5 and 10 cm H<sub>2</sub>O and <i>P</i> = 0.032 for 15 cm H<sub>2</sub>O). SpO<sub>2</sub> increased significantly with higher PEEP levels (<i>P</i> < 0.001), confirming the effectiveness of PEEP in improving oxygenation. The results also revealed a significant increase in HR and a decrease in MAP following the application of higher PEEP levels.</p><p><strong>Conclusion: </strong>Increasing PEEP levels in mechanically ventilated patients improves lung aeration, which can be effectively assessed using bedside lung ultrasonography.</p>","PeriodicalId":66959,"journal":{"name":"世界危重病急救学杂志(英文版)","volume":"14 3","pages":"102609"},"PeriodicalIF":0.0,"publicationDate":"2025-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12304999/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144980443","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}