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Perineural dexamethasone: neurotoxicity or neuroprotection? A systematic review of preclinical evidence. 神经周围地塞米松:神经毒性还是神经保护?临床前证据的系统回顾。
IF 3.1 Pub Date : 2025-08-06 DOI: 10.1186/s44158-025-00271-w
Alessandro De Cassai, Domenico Pietro Santonastaso, Francesco Coppolino, Cristiano D'Errico, Gabriele Melegari, Burhan Dost, Giulia Aviani Fulvio, Annalisa Boscolo, Rafael Boscolo-Berto, Paolo Navalesi

Background: Perineural dexamethasone is widely used as an adjuvant to local anesthetics in regional anesthesia to prolong analgesia. However, concerns persist regarding its potential neurotoxic effects, particularly when administered perineurally. This systematic review aims to synthesize preclinical evidence evaluating the neurotoxicity or neuroprotective properties of perineural dexamethasone.

Methods: A systematic search of PubMed, CENTRAL, Scopus, and Embase was conducted through May 22, 2025. Eligible studies included in vivo or in vitro preclinical models assessing the neurotoxic or neuroprotective effects of perineural dexamethasone compared to control conditions. Risk of bias was assessed using the SYRCLE tool for in vivo studies and a narrative evaluation for in vitro studies. A total of 14 studies (11 in vivo, 3 in vitro) met inclusion criteria.

Results: In vitro studies showed that dexamethasone alone was not neurotoxic at clinically relevant doses but could enhance cytotoxicity when combined with local anesthetics at higher concentrations. In vivo models generally demonstrated no significant long-term nerve inflammation, degeneration or demyelination, with some early protective effects observed in perineural dexamethasone groups. However, all in vivo studies were rated at high risk of bias. In nerve injury models, dexamethasone reduced apoptotic and inflammatory markers when administered immediately post-injury, with limited effect when delayed.

Conclusions: Preclinical evidence supports the general safety of low-dose, preservative-free perineural dexamethasone. Nonetheless, high-dose use, additives, and application in patients with neuropathies may pose risks. Given the high risk of bias in existing studies and minimal added benefit over systemic administration, clinical caution is advised.

背景:神经周围地塞米松作为局麻药的辅助剂在区域麻醉中广泛应用,以延长镇痛时间。然而,对其潜在的神经毒性作用的关注仍然存在,特别是在神经周围给药时。本系统综述旨在综合评价神经周围地塞米松的神经毒性或神经保护作用的临床前证据。方法:系统检索PubMed, CENTRAL, Scopus和Embase,截止到2025年5月22日。符合条件的研究包括体内或体外临床前模型,评估与对照组相比,神经周围地塞米松的神经毒性或神经保护作用。使用体内研究的sycle工具和体外研究的叙述性评估来评估偏倚风险。共有14项研究(11项体内研究,3项体外研究)符合纳入标准。结果:体外研究显示,单独地塞米松在临床相关剂量下无神经毒性,但与高浓度局麻药联用可增强细胞毒性。体内模型一般未显示出明显的长期神经炎症、退行性变或脱髓鞘,神经周地塞米松组在早期观察到一些保护作用。然而,所有的体内研究都被评为高偏倚风险。在神经损伤模型中,损伤后立即给予地塞米松可降低细胞凋亡和炎症标志物,延迟给予地塞米松作用有限。结论:临床前证据支持低剂量、不含防腐剂的神经周围地塞米松的一般安全性。尽管如此,在神经病患者中大剂量使用、添加物和应用可能会带来风险。鉴于现有研究的高偏倚风险和与全身给药相比的最小附加益处,建议临床谨慎。
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引用次数: 0
Fascial plane blocks in the era of modern regional anesthesia: shaping the future of pain management. 筋膜平面阻滞在现代区域麻醉时代:塑造疼痛管理的未来。
IF 3.1 Pub Date : 2025-07-25 DOI: 10.1186/s44158-025-00269-4
Burhan Dost
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引用次数: 0
Enhancing epidural analgesia access during labor: a pilot study on the use of translated informational materials. 加强分娩时硬膜外镇痛:一项关于使用翻译信息材料的试点研究。
IF 3.1 Pub Date : 2025-07-24 DOI: 10.1186/s44158-025-00266-7
Fabrizia Calabrese, Paolo Mele, Marta Stella, Alessandro De Cassai, Roberto Tozzi, Paolo Navalesi
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引用次数: 0
Standardizing thoracic segmental spinal anesthesia: an encouraging initiative that warrants methodological rigor. Comment on "A bundle for thoracic segmental spinal anesthesia: it is time to move forward!" 标准化胸段性脊髓麻醉:一项令人鼓舞的举措,保证了方法的严谨性。评论“胸椎节段性脊髓麻醉捆绑:是时候向前迈进了!”
IF 3.1 Pub Date : 2025-07-23 DOI: 10.1186/s44158-025-00267-6
Carmine Pullano
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引用次数: 0
PENG block in elderly patients with hip fracture: less is more? A prospective observational monocentric study. 彭阻滞治疗老年髋部骨折:少即是多?一项前瞻性单中心观察研究。
Pub Date : 2025-07-18 DOI: 10.1186/s44158-025-00265-8
Valerio Donatiello, Aniello Alfieri, Maria Civita Mazza, Pietro Buonavolontà, Antonio Scalvenzi, Elena Prisco, Vincenzo Maffei, Cono Alberto Lanza, Francesco Coppolino, Maria Caterina Pace, Pasquale Sansone, Maria Beatrice Passavanti

Background: Proximal femur fractures in the elderly are a common and serious condition with high morbidity and mortality. Effective postoperative pain control reduces complications, hospital stay, and opioid use. The PEricapsular Nerve Group (PENG) block is a regional anesthesia technique offering motor-sparing analgesia, facilitating spinal anesthesia and early rehabilitation. However, higher local anesthetic (LA) doses may increase the risk of systemic toxicity, particularly in frail, sarcopenic patients. This study evaluates the analgesic efficacy and safety of two ropivacaine concentrations (0.375% vs 0.25%) in PENG blocks.

Methods: This prospective observational monocentric study included 217 patients (aged 65-100) undergoing surgery for osteoporotic proximal femur fractures. Patients received a 20-mL PENG block with either 0.375% or 0.25% ropivacaine prior to spinal anesthesia. Postoperative analgesia included paracetamol and ketorolac, with intramuscular morphine available as rescue. The primary endpoint was the proportion of patients requiring morphine; secondary outcomes included time to first rescue dose. Statistical analyses included chi-square testing, Kaplan-Meier estimates, and non-inferiority analysis (Δ = 0.05).

Results: The proportion of patients requiring rescue morphine was 23% in the 0.375% group and 25% in the 0.25% group (p = 0.87). Non-inferiority was demonstrated, with a difference of - 0.019 (95% CI: - 0.0344 to - 0.0036). No significant differences were observed in time to first rescue dose.

Conclusion: PENG block with 0.25% ropivacaine provides non-inferior analgesia compared to 0.375%, supporting its use in elderly patients to reduce opioid reliance and minimize the risk of local anesthetic systemic toxicity.

Trial registration: Not applicable.

背景:老年人股骨近端骨折是一种常见且严重的疾病,发病率和死亡率都很高。有效的术后疼痛控制可减少并发症、住院时间和阿片类药物的使用。囊外神经阻滞是一种区域麻醉技术,提供运动保留镇痛,促进脊髓麻醉和早期康复。然而,较高的局部麻醉(LA)剂量可能会增加全身毒性的风险,特别是在虚弱的肌肉减少患者中。本研究评估了两种罗哌卡因浓度(0.375% vs 0.25%)在PENG阻滞中的镇痛效果和安全性。方法:本前瞻性单中心观察研究纳入217例(65-100岁)股骨近端骨质疏松性骨折手术患者。患者在脊髓麻醉前接受含0.375%或0.25%罗哌卡因的20ml PENG阻滞。术后镇痛包括扑热息痛、酮咯酸,肌注吗啡抢救。主要终点是需要吗啡的患者比例;次要结局包括到第一次抢救剂量的时间。统计分析包括卡方检验、Kaplan-Meier估计和非劣效性分析(Δ = 0.05)。结果:0.375%组和0.25%组患者需要吗啡救助的比例分别为23%和25% (p = 0.87)。非劣效性证明,差异为- 0.019 (95% CI: - 0.0344至- 0.0036)。与首次抢救剂量相比,时间上无显著差异。结论:与0.375%罗哌卡因相比,0.25%罗哌卡因的PENG阻滞可提供非亚效镇痛,支持其用于老年患者,以减少对阿片类药物的依赖,并最大限度地降低局麻全身毒性的风险。试验注册:不适用。
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引用次数: 0
Methodological limitations in acceleromyographic monitoring: a reply to Dr. Büyükcavlak. 加速肌图监测的方法学局限性:对b<s:1> yy<e:1> kcavlak博士的答复。
Pub Date : 2025-07-17 DOI: 10.1186/s44158-025-00264-9
Federico Piccioni, Giulio L Rosboch
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引用次数: 0
The central role of the anesthesiologist in operating room management: toward an integrated clinical-organizational-technological paradigm. 麻醉师在手术室管理中的核心作用:迈向临床-组织-技术一体化范式。
Pub Date : 2025-07-14 DOI: 10.1186/s44158-025-00263-w
Valentina Bellini, Simone Priolo, Elena Bignami

Efficiency in the operating room is often considered either in terms of clinical excellence or in terms of performance optimization through managerial approaches. However, these dichotomous models-clinician-centered versus engineer-led-fail to capture the complexity of modern surgical care. This paper therefore proposes a multidisciplinary model in which the anesthetist plays a central role, acting as an integrator of clinical needs and organizational logistics. As new technologies emerge, they should support a comprehensive vision that combines patient-centered care with organizational and technological considerations. This approach should complement, rather than replace, clinical judgment.

手术室的效率通常被认为要么是临床卓越,要么是通过管理方法实现绩效优化。然而,这些以临床医生为中心和以工程师为主导的二分模型未能捕捉到现代外科护理的复杂性。因此,本文提出了一个多学科模型,其中麻醉师发挥核心作用,作为临床需求和组织后勤的整合者。随着新技术的出现,它们应该支持将以患者为中心的护理与组织和技术考虑相结合的综合愿景。这种方法应该补充而不是取代临床判断。
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引用次数: 0
Effect of intravenous and intra-cuff magnesium sulphate on post-extubation tracheal morbidity: a randomised single-blind study. 静脉和袖带内硫酸镁对拔管后气管发病率的影响:一项随机单盲研究。
Pub Date : 2025-07-14 DOI: 10.1186/s44158-025-00246-x
Ebenezer Owusu Darkwa, Naa Martekour Vanderpuye, Beauty Annan, Lorraine Baffour-Awuah, Grace-Imelda Obeng Adjei, Raymond Essuman, George Aryee, Robert Djagbletey

Background: Post-extubation sore throat (PEST), cough, and hoarseness are common complications of tracheal intubation. Several agents and techniques have been postulated to reduce their occurrence.

Aim: This study sought to compare the effects of intravenous and intra-cuff magnesium sulphate on the incidence and severity of PEST, cough and hoarseness of voice.

Materials and methods: This was a randomised single-blind study involving 90 surgical patients requiring endotracheal intubation. Patients were randomised into 3 groups: A (control), B (intra-cuff magnesium sulphate) and C (intravenous magnesium sulphate). Participants in Group A had the endotracheal tube cuff (ETTc) inflated with air to a pressure of 25 cmH2O whilst those in Group B had the ETTc inflated with 2 g of magnesium sulphate solution and the pressure adjusted to 25 cmH2O with top-ups of 0.9% normal saline. Participants in Group C had the ETTc filled with air to a pressure of 25 cmH2O and received 2 g of intravenous magnesium sulphate in 20 ml of 0.9% normal saline perfused over 10 min immediately prior to the induction of general anaesthesia. The occurrence of PEST, cough and hoarseness of voice were recorded at 0, 4, 8, 12 and 24 h after surgery.

Results: The incidence of PEST on swallowing in the intra-cuff magnesium sulphate group compared to the intravenous magnesium sulphate group at 4, 8, and 12 h post-operatively were 51.7% vs 12.5%, 51.7% vs 18.8% and 51.7% vs 21.9% respectively. Compared to intra-cuff magnesium sulphate, intravenous magnesium sulphate significantly reduced the incidence and severity of PEST during swallowing at 4, 8, and 12 h. The incidence of PEST at rest in the intra-cuff magnesium sulphate group compared to the intravenous magnesium sulphate group at 0, 4, 8, 12 and 24 h post-operatively were 13.8% vs 9.4%, 20.7% vs 6.3%, 17.2% vs 6.3%, 13.8% vs 3.1% and 13.8% vs 3.1% respectively. Compared to intra-cuff magnesium sulphate, intravenous magnesium sulphate reduced the incidence of PEST at rest, though this was not statistically significant over first 24 h postoperative period. Intravenous magnesium sulphate had significantly lower PEST severity scores at rest at 12 h only compared to intra-cuff magnesium sulphate. There was no statistically significant difference in the incidence and severity of cough and hoarseness between the study groups.

Conclusion: Intravenous magnesium sulphate given at induction was found to be better compared to intra-cuff magnesium sulphate in lowering the incidence and severity of post-extubation sore throat on swallowing but not at rest. However, it does not significantly reduce the incidence or severity of post-extubation cough or hoarseness.

Trial registration: PACTR202211634990263.

背景:拔管后喉咙痛、咳嗽和声音嘶哑是气管插管常见的并发症。有几种药剂和技术可以减少它们的发生。目的:比较静脉注射硫酸镁和袖带内注射硫酸镁对急性肺损伤发生率和严重程度、咳嗽和声音嘶哑的影响。材料和方法:这是一项随机单盲研究,涉及90例需要气管插管的手术患者。患者随机分为3组:A(对照组),B(袖带内硫酸镁)和C(静脉注射硫酸镁)。A组的参与者用空气将气管内套管(ETTc)充气到25 cmH2O的压力,而B组的参与者则用2g硫酸镁溶液将ETTc充气,并将压力调整到25 cmH2O,并补充0.9%生理盐水。C组参与者在全麻诱导前立即将etc充入气压为25 cmH2O的空气,并在20 ml 0.9%生理盐水中灌注2g硫酸镁,灌注时间超过10分钟。分别于术后0、4、8、12、24 h记录患者的PEST、咳嗽和声音嘶哑的发生情况。结果:与静脉注射硫酸镁组相比,袖带内硫酸镁组术后4、8、12 h吞咽不良反应发生率分别为51.7%、12.5%、51.7%、18.8%、51.7%、21.9%。与袖带内硫酸镁相比,静脉注射硫酸镁可显著降低4、8、12 h吞咽过程中PEST的发生率和严重程度。与静脉注射硫酸镁组相比,术后0、4、8、12、24 h静息时PEST的发生率分别为13.8%比9.4%、20.7%比6.3%、17.2%比6.3%、13.8%比3.1%和13.8%比3.1%。与袖带内硫酸镁相比,静息时静脉注射硫酸镁降低了PEST的发生率,尽管在术后24小时内没有统计学意义。与袖带内硫酸镁相比,静脉注射硫酸镁在休息12小时时的PEST严重程度评分显着降低。两组患者咳嗽和声音嘶哑的发生率和严重程度无统计学差异。结论:诱导时静脉注射硫酸镁比袖带内注射硫酸镁更能降低拔管后吞咽时喉咙痛的发生率和严重程度,而静止时则无此效果。然而,它不能显著降低拔管后咳嗽或声音嘶哑的发生率或严重程度。试验注册:PACTR202211634990263。
{"title":"Effect of intravenous and intra-cuff magnesium sulphate on post-extubation tracheal morbidity: a randomised single-blind study.","authors":"Ebenezer Owusu Darkwa, Naa Martekour Vanderpuye, Beauty Annan, Lorraine Baffour-Awuah, Grace-Imelda Obeng Adjei, Raymond Essuman, George Aryee, Robert Djagbletey","doi":"10.1186/s44158-025-00246-x","DOIUrl":"10.1186/s44158-025-00246-x","url":null,"abstract":"<p><strong>Background: </strong>Post-extubation sore throat (PEST), cough, and hoarseness are common complications of tracheal intubation. Several agents and techniques have been postulated to reduce their occurrence.</p><p><strong>Aim: </strong>This study sought to compare the effects of intravenous and intra-cuff magnesium sulphate on the incidence and severity of PEST, cough and hoarseness of voice.</p><p><strong>Materials and methods: </strong>This was a randomised single-blind study involving 90 surgical patients requiring endotracheal intubation. Patients were randomised into 3 groups: A (control), B (intra-cuff magnesium sulphate) and C (intravenous magnesium sulphate). Participants in Group A had the endotracheal tube cuff (ETTc) inflated with air to a pressure of 25 cmH<sub>2</sub>O whilst those in Group B had the ETTc inflated with 2 g of magnesium sulphate solution and the pressure adjusted to 25 cmH<sub>2</sub>O with top-ups of 0.9% normal saline. Participants in Group C had the ETTc filled with air to a pressure of 25 cmH<sub>2</sub>O and received 2 g of intravenous magnesium sulphate in 20 ml of 0.9% normal saline perfused over 10 min immediately prior to the induction of general anaesthesia. The occurrence of PEST, cough and hoarseness of voice were recorded at 0, 4, 8, 12 and 24 h after surgery.</p><p><strong>Results: </strong>The incidence of PEST on swallowing in the intra-cuff magnesium sulphate group compared to the intravenous magnesium sulphate group at 4, 8, and 12 h post-operatively were 51.7% vs 12.5%, 51.7% vs 18.8% and 51.7% vs 21.9% respectively. Compared to intra-cuff magnesium sulphate, intravenous magnesium sulphate significantly reduced the incidence and severity of PEST during swallowing at 4, 8, and 12 h. The incidence of PEST at rest in the intra-cuff magnesium sulphate group compared to the intravenous magnesium sulphate group at 0, 4, 8, 12 and 24 h post-operatively were 13.8% vs 9.4%, 20.7% vs 6.3%, 17.2% vs 6.3%, 13.8% vs 3.1% and 13.8% vs 3.1% respectively. Compared to intra-cuff magnesium sulphate, intravenous magnesium sulphate reduced the incidence of PEST at rest, though this was not statistically significant over first 24 h postoperative period. Intravenous magnesium sulphate had significantly lower PEST severity scores at rest at 12 h only compared to intra-cuff magnesium sulphate. There was no statistically significant difference in the incidence and severity of cough and hoarseness between the study groups.</p><p><strong>Conclusion: </strong>Intravenous magnesium sulphate given at induction was found to be better compared to intra-cuff magnesium sulphate in lowering the incidence and severity of post-extubation sore throat on swallowing but not at rest. However, it does not significantly reduce the incidence or severity of post-extubation cough or hoarseness.</p><p><strong>Trial registration: </strong>PACTR202211634990263.</p>","PeriodicalId":73597,"journal":{"name":"Journal of Anesthesia, Analgesia and Critical Care (Online)","volume":"5 1","pages":"43"},"PeriodicalIF":0.0,"publicationDate":"2025-07-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12261786/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144638791","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}
引用次数: 0
Critical emergency medicine unit: a new model to mitigate critically ill patient boarding in emergency department. 危重急诊医学单元:减轻急诊科危重病人住院的新模式。
Pub Date : 2025-07-10 DOI: 10.1186/s44158-025-00262-x
Felice Urso, Daniele Catalano, Ileana Suprina Petrovic, Enrico Boero, Paola Berchialla, Luigi Vetrugno, Daniela Silengo

Background: Boarding of critically ill patients in the emergency department (ED) is an emerging problem that increases mortality. We have developed a "CREM Unit (critical emergency medicine unit)" led by an anesthetist-intensivist who manages critical patients directly in the ED. This study aims to assess whether the CREM Unit is an effective model for mitigating the boarding of critical patients in the ED and the impact of this on mortality.

Method: This is a retrospective observational study. We collected all patients assigned to the CREM Unit from January 1, 2019, to December 31, 2021. As our primary endpoints, we calculated ED boarding rate and the impact of boarding time on mortality. As a secondary endpoint, we compared observed 28-day mortality to Simplified Acute Physiology Score (SAPS II) predicted mortality.

Results: Patients managed by the CREM unit were 127 in 2019, 181 in 2020, and 206 in 2021, with a clear upward trend, for a total of 514 patients (p < 0.001). Overall boarding rate was 13.9%, and length of stay in ED was not associated with an increased mortality (p = 0.399). Observed mortality was compared with expected mortality, estimated from the SAPS II score for a group of inpatients (n = 295). Moreover, the median value of SAPS II for inpatients was 54 (40.5-69.0), with an expected mortality of 55.3%, while the observed mortality was 36.8% (95% CI 31.9% to 42.1%, p < 0.0001).

Conclusions: Over the years, the number of patients assigned to the CREM Unit has grown steadily. These data suggest that the CREM Unit cares for a significant number of critically ill patients and could have a well-defined role both in keeping their boarding low and may contribute to reducing its impact on mortality.

背景:急诊科(ED)危重病人的入住是一个增加死亡率的新问题。我们已经开发了一个“CREM单元(重症急诊医学单元)”,由一名麻醉医师领导,他直接管理急诊科的重症患者。本研究旨在评估CREM单元是否是一种有效的模式,以减轻急诊科重症患者的入住情况及其对死亡率的影响。方法:回顾性观察性研究。我们收集了2019年1月1日至2021年12月31日分配到CREM病房的所有患者。作为我们的主要终点,我们计算了急诊科登机率和登机时间对死亡率的影响。作为次要终点,我们比较了观察到的28天死亡率和简化急性生理评分(SAPS II)预测死亡率。结果:CREM单元管理的患者在2019年为127例,2020年为181例,2021年为206例,上升趋势明显,共514例(p结论:多年来,CREM单元的患者数量稳步增长。这些数据表明,CREM病房照顾着数量可观的危重病人,可以在保持低住院率和减少死亡率方面发挥明确的作用。
{"title":"Critical emergency medicine unit: a new model to mitigate critically ill patient boarding in emergency department.","authors":"Felice Urso, Daniele Catalano, Ileana Suprina Petrovic, Enrico Boero, Paola Berchialla, Luigi Vetrugno, Daniela Silengo","doi":"10.1186/s44158-025-00262-x","DOIUrl":"10.1186/s44158-025-00262-x","url":null,"abstract":"<p><strong>Background: </strong>Boarding of critically ill patients in the emergency department (ED) is an emerging problem that increases mortality. We have developed a \"CREM Unit (critical emergency medicine unit)\" led by an anesthetist-intensivist who manages critical patients directly in the ED. This study aims to assess whether the CREM Unit is an effective model for mitigating the boarding of critical patients in the ED and the impact of this on mortality.</p><p><strong>Method: </strong>This is a retrospective observational study. We collected all patients assigned to the CREM Unit from January 1, 2019, to December 31, 2021. As our primary endpoints, we calculated ED boarding rate and the impact of boarding time on mortality. As a secondary endpoint, we compared observed 28-day mortality to Simplified Acute Physiology Score (SAPS II) predicted mortality.</p><p><strong>Results: </strong>Patients managed by the CREM unit were 127 in 2019, 181 in 2020, and 206 in 2021, with a clear upward trend, for a total of 514 patients (p < 0.001). Overall boarding rate was 13.9%, and length of stay in ED was not associated with an increased mortality (p = 0.399). Observed mortality was compared with expected mortality, estimated from the SAPS II score for a group of inpatients (n = 295). Moreover, the median value of SAPS II for inpatients was 54 (40.5-69.0), with an expected mortality of 55.3%, while the observed mortality was 36.8% (95% CI 31.9% to 42.1%, p < 0.0001).</p><p><strong>Conclusions: </strong>Over the years, the number of patients assigned to the CREM Unit has grown steadily. These data suggest that the CREM Unit cares for a significant number of critically ill patients and could have a well-defined role both in keeping their boarding low and may contribute to reducing its impact on mortality.</p>","PeriodicalId":73597,"journal":{"name":"Journal of Anesthesia, Analgesia and Critical Care (Online)","volume":"5 1","pages":"42"},"PeriodicalIF":0.0,"publicationDate":"2025-07-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12247336/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144610529","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}
引用次数: 0
Quality of life after ICU: 1-year follow-up in patients with and without COVID. ICU后生活质量:有和无COVID患者随访1年。
Pub Date : 2025-07-01 DOI: 10.1186/s44158-025-00253-y
M Rauseo, G Ferrara, A Cotoia, F Cardinale, S Padalino, N Latronico, L Mirabella, G Cinnella

Background: The purpose of this study was to perform a 1-year follow-up after ICU discharge and evaluate post-intensive care syndrome (PICS) in both COVID (GroupCov) and NON COVID (GroupNCov) patients.

Methods: All consecutive patients discharged from our Intensive Care Unit (ICU) from June to December 2022 were prospectively screened. Scheduled in-person visits were carried on 3, 6, and 12 months after ICU discharge to evaluate physical, cognitive, and mental health status using different scale evaluations (SF-36, Barthel Index, ISI score, PCL-5 score, MNA-sf score, Fatigue Severity Score, MoCA Test, HADS and GDS) by means of standardized questionnaires.

Results: Eighty patients (50 GroupCov vs 30 GroupNCov) were initially included, but some patients did not attend all follow-up visits. At 1-year follow-up, 60 patients (30 COVID-19 and 30 non-COVID) completed all evaluations. Both groups showed PICS, but GroupCov had a better nutritional status, better outcomes in physical evaluations, and a better perception of Quality of Life (QoL) and mental health status, but a worse cognitive assessment in the MoCA Test. Moreover, heterogeneity analysis showed that GroupNCov patients had the same trend during follow-up, while in GroupCov different trends were observed over time, especially a worse nutritional state, often found in older patients, that was related to a longer hospital stay and worse psychophysical outcomes.

Conclusions: This study shows that PICS in SARS-COV2 patients is not always homogeneous, and that different clusters of psychophysical patterns may develop over time. Although our study was only observational, it seems from our preliminary results that performing a follow-up could be the basis for a secondary prevention and to develop new therapeutic strategies after patients discharge from ICU.

背景:本研究的目的是在ICU出院后进行1年随访,评估COVID (GroupCov)和NON - COVID (GroupNCov)患者的重症监护后综合征(PICS)。方法:对2022年6月至12月从我院重症监护室(ICU)连续出院的所有患者进行前瞻性筛查。在ICU出院后3、6、12个月进行定期访视,采用标准化问卷的不同量表(SF-36、Barthel指数、ISI评分、PCL-5评分、MNA-sf评分、疲劳严重程度评分、MoCA测试、HADS和GDS)评估患者的身体、认知和心理健康状况。结果:最初纳入80例患者(50例GroupCov vs 30例GroupNCov),但一些患者未参加所有随访。随访1年,60例患者(30例COVID-19和30例非COVID-19)完成所有评估。两组均表现出PICS,但GroupCov的营养状况更好,身体评估结果更好,生活质量(QoL)和心理健康状况更好,但MoCA测试的认知评估更差。此外,异质性分析显示,GroupNCov患者在随访期间具有相同的趋势,而GroupCov患者随着时间的推移观察到不同的趋势,特别是老年患者的营养状况更差,这与更长的住院时间和更差的心理生理结果有关。结论:本研究表明,SARS-COV2患者的PICS并不总是均匀的,随着时间的推移,不同的心理物理模式集群可能会发展。虽然我们的研究只是观察性的,但从我们的初步结果来看,进行随访似乎可以作为二级预防的基础,并在患者从ICU出院后制定新的治疗策略。
{"title":"Quality of life after ICU: 1-year follow-up in patients with and without COVID.","authors":"M Rauseo, G Ferrara, A Cotoia, F Cardinale, S Padalino, N Latronico, L Mirabella, G Cinnella","doi":"10.1186/s44158-025-00253-y","DOIUrl":"10.1186/s44158-025-00253-y","url":null,"abstract":"<p><strong>Background: </strong>The purpose of this study was to perform a 1-year follow-up after ICU discharge and evaluate post-intensive care syndrome (PICS) in both COVID (GroupCov) and NON COVID (GroupNCov) patients.</p><p><strong>Methods: </strong>All consecutive patients discharged from our Intensive Care Unit (ICU) from June to December 2022 were prospectively screened. Scheduled in-person visits were carried on 3, 6, and 12 months after ICU discharge to evaluate physical, cognitive, and mental health status using different scale evaluations (SF-36, Barthel Index, ISI score, PCL-5 score, MNA-sf score, Fatigue Severity Score, MoCA Test, HADS and GDS) by means of standardized questionnaires.</p><p><strong>Results: </strong>Eighty patients (50 GroupCov vs 30 GroupNCov) were initially included, but some patients did not attend all follow-up visits. At 1-year follow-up, 60 patients (30 COVID-19 and 30 non-COVID) completed all evaluations. Both groups showed PICS, but GroupCov had a better nutritional status, better outcomes in physical evaluations, and a better perception of Quality of Life (QoL) and mental health status, but a worse cognitive assessment in the MoCA Test. Moreover, heterogeneity analysis showed that GroupNCov patients had the same trend during follow-up, while in GroupCov different trends were observed over time, especially a worse nutritional state, often found in older patients, that was related to a longer hospital stay and worse psychophysical outcomes.</p><p><strong>Conclusions: </strong>This study shows that PICS in SARS-COV2 patients is not always homogeneous, and that different clusters of psychophysical patterns may develop over time. Although our study was only observational, it seems from our preliminary results that performing a follow-up could be the basis for a secondary prevention and to develop new therapeutic strategies after patients discharge from ICU.</p>","PeriodicalId":73597,"journal":{"name":"Journal of Anesthesia, Analgesia and Critical Care (Online)","volume":"5 1","pages":"36"},"PeriodicalIF":0.0,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12211204/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144546389","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}
引用次数: 0
期刊
Journal of Anesthesia, Analgesia and Critical Care (Online)
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