Pub Date : 2025-11-12DOI: 10.1186/s13741-025-00606-9
Gabrielle Barbosa Borgomoni, Fábio Antônio Serra de Lima Júnior, Omar Asdrúbal Vilca Mejia, Fábio Biscegli Jatene
Background: Enhanced Recovery After Surgery (ERAS) in cardiac surgery was designed to improve outcomes, reduce complications, and optimize recovery. Despite these efforts, perioperative anemia, a key modifiable risk factor that affects 20 to 41% of patients, remains under-addressed and is strongly associated with increased transfusion rates, morbidity, and mortality. Patient Blood Management (PBM) has demonstrated efficacy in improving outcomes by optimizing hemoglobin levels, reducing blood loss, and minimizing transfusions, although it is not yet fully integrated into cardiac ERAS pathways.
Main text: ERAS pathways are patient-centered, multidisciplinary, preventive and evidence-based. Although the principles of PBM align with ERAS, detailed PBM targets are often neglected in ERAS-based line of care. In cardiac surgery, the risks associated with anemia and transfusion are substantially higher than in other surgical specialties. However, perioperative interventions might manage anemia, mitigate bleeding risks, and improve tolerance to anemia in this particularly sensitive population. Implementation challenges include the need for institutional culture shifts and multidisciplinary education maintaining clinical awareness to support individualized recovery trajectories.
Conclusion: Integrating PBM into cardiac ERAS-based pathways addresses a critical gap that could lead to improved patient outcomes, reduced complications, lower transfusion rates, and optimized resource utilization. While healthcare progressively focuses on safety, quality, and value-based care, the convergence of ERAS and PBM offers a comprehensive approach to advancing perioperative medicine in cardiac surgery.
{"title":"The imperative integration of patient blood management into ERACS: bridging the gap for optimizing outcomes in cardiac surgery.","authors":"Gabrielle Barbosa Borgomoni, Fábio Antônio Serra de Lima Júnior, Omar Asdrúbal Vilca Mejia, Fábio Biscegli Jatene","doi":"10.1186/s13741-025-00606-9","DOIUrl":"10.1186/s13741-025-00606-9","url":null,"abstract":"<p><strong>Background: </strong>Enhanced Recovery After Surgery (ERAS) in cardiac surgery was designed to improve outcomes, reduce complications, and optimize recovery. Despite these efforts, perioperative anemia, a key modifiable risk factor that affects 20 to 41% of patients, remains under-addressed and is strongly associated with increased transfusion rates, morbidity, and mortality. Patient Blood Management (PBM) has demonstrated efficacy in improving outcomes by optimizing hemoglobin levels, reducing blood loss, and minimizing transfusions, although it is not yet fully integrated into cardiac ERAS pathways.</p><p><strong>Main text: </strong>ERAS pathways are patient-centered, multidisciplinary, preventive and evidence-based. Although the principles of PBM align with ERAS, detailed PBM targets are often neglected in ERAS-based line of care. In cardiac surgery, the risks associated with anemia and transfusion are substantially higher than in other surgical specialties. However, perioperative interventions might manage anemia, mitigate bleeding risks, and improve tolerance to anemia in this particularly sensitive population. Implementation challenges include the need for institutional culture shifts and multidisciplinary education maintaining clinical awareness to support individualized recovery trajectories.</p><p><strong>Conclusion: </strong>Integrating PBM into cardiac ERAS-based pathways addresses a critical gap that could lead to improved patient outcomes, reduced complications, lower transfusion rates, and optimized resource utilization. While healthcare progressively focuses on safety, quality, and value-based care, the convergence of ERAS and PBM offers a comprehensive approach to advancing perioperative medicine in cardiac surgery.</p>","PeriodicalId":19764,"journal":{"name":"Perioperative Medicine","volume":"14 1","pages":"124"},"PeriodicalIF":2.1,"publicationDate":"2025-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12613330/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145506218","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-07DOI: 10.1186/s13741-025-00623-8
Jonathan J Szeto, Hope Kim, Catherine Z Shen, Cody Chapman, Julia Tchou, Caoimhe C Duffy
Background: The OR generates over 30% of a healthcare facility's total waste, with more than 60% classified as regulated medical waste (RMW). Municipal waste (MW) is commonly incorrectly classified as RMW, resulting in unnecessary costs and environmental burden. As such, this pilot study aimed to determine if interventions that provide visual cues for waste classification and improve ergonomics in the operating room (OR) can improve waste sorting accuracy.
Methods: In groups of two to four, participants were tasked with quickly solving tangram puzzles while periodically given simulated medical waste to dispose of into either a MW container or a RMW container. Groups first engaged in a control simulation, followed by an intervention simulation where educational signage and the novel adapted waste bin was placed in the OR. Sorting accuracy was assessed, and participants completed a post-participation survey.
Results: 23 participants took part of this pilot study. The proportion of correctly classified waste increased between control (53%) and intervention (88%) conditions, p < 0.01. Cost (n = 21) and sustainability (n = 20) were highly cited reasons why it might be important to correctly dispose of waste. Participants cited location of the containers (n = 13), time issues or OR stress (n = 10), and confusion in waste classification (n = 13) as barriers to accurate waste sorting.
Conclusion: Participants had significant improvement in OR waste classification accuracy after the implementation of educational signage and a novel adapted bin system. These strategies can be employed to increase waste sorting accuracy in the OR or be used as an educational tool during trainings to improve staff understanding of proper waste disposal.
{"title":"Reducing misclassification of medical waste: nudging stakeholders to reduce waste misclassification in a novel simulated operating room built environment.","authors":"Jonathan J Szeto, Hope Kim, Catherine Z Shen, Cody Chapman, Julia Tchou, Caoimhe C Duffy","doi":"10.1186/s13741-025-00623-8","DOIUrl":"10.1186/s13741-025-00623-8","url":null,"abstract":"<p><strong>Background: </strong>The OR generates over 30% of a healthcare facility's total waste, with more than 60% classified as regulated medical waste (RMW). Municipal waste (MW) is commonly incorrectly classified as RMW, resulting in unnecessary costs and environmental burden. As such, this pilot study aimed to determine if interventions that provide visual cues for waste classification and improve ergonomics in the operating room (OR) can improve waste sorting accuracy.</p><p><strong>Methods: </strong>In groups of two to four, participants were tasked with quickly solving tangram puzzles while periodically given simulated medical waste to dispose of into either a MW container or a RMW container. Groups first engaged in a control simulation, followed by an intervention simulation where educational signage and the novel adapted waste bin was placed in the OR. Sorting accuracy was assessed, and participants completed a post-participation survey.</p><p><strong>Results: </strong>23 participants took part of this pilot study. The proportion of correctly classified waste increased between control (53%) and intervention (88%) conditions, p < 0.01. Cost (n = 21) and sustainability (n = 20) were highly cited reasons why it might be important to correctly dispose of waste. Participants cited location of the containers (n = 13), time issues or OR stress (n = 10), and confusion in waste classification (n = 13) as barriers to accurate waste sorting.</p><p><strong>Conclusion: </strong>Participants had significant improvement in OR waste classification accuracy after the implementation of educational signage and a novel adapted bin system. These strategies can be employed to increase waste sorting accuracy in the OR or be used as an educational tool during trainings to improve staff understanding of proper waste disposal.</p>","PeriodicalId":19764,"journal":{"name":"Perioperative Medicine","volume":"14 1","pages":"123"},"PeriodicalIF":2.1,"publicationDate":"2025-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12595910/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145471618","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: Thoracic paravertebral block (TPVB) with liposomal bupivacaine (LB) is increasingly used for postoperative pain control in patients undergoing thoracic surgery, but relevant data are scarce, and there are few data on LB-TPVB combined with drainage tube patient-controlled analgesia (PCA). The aim of this study is to explore the effect of LB-TPVB combined with drainage-tube PCA on postoperative pain after thoracoscopic lobectomy.
Methods: This is a prospective, multicentre, double-blind, randomized controlled study. Participants will be randomly assigned to the standard bupivacaine (SB) group, SB + drainage-tube PCA (DTA) group, LB group, or LB + DTA group. The primary outcome is the 72-h mean Numerical Rating Scale (NRS) pain score at rest. The target sample size is 228 patients, with 57 patients in each group.
Discussion: Our study hypothesizes that preoperative ultrasound-guided thoracic nerve block combined with drainage tube self-controlled analgesia is more effective in reducing postoperative pain following thoracoscopic lobe resection compared to thoracic nerve block alone. Additionally, liposomal bupivacaine was found to be more effective than standard bupivacaine in this context. These results will have implications for improving postoperative analgesia protocols for patients undergoing thoracoscopic lung surgery.
Trial registration: ClinicalTrials.gov, NCT06165991. Registered 29 November 2023, https://clinicaltrials.gov/study/NCT06165991 .
{"title":"Effect of preoperative thoracic paravertebral block using liposomal bupivacaine combined with drainage-tube patient-controlled analgesia on postoperative pain after thoracoscopic lobectomy: a prospective, multicentre, double-blind, randomized controlled study protocol.","authors":"Yongtao Sun, Na Guo, Tinghao Fang, Yanyan Feng, Peng Liu, Dongfeng Sun, Yongmeng Li, Kexuan Liu, Yiyan Ren, Minghui Li, Qiuyue Liu, Xiaoling Yang, Yongliang Chi, Zhongkai Liu, Li Yuan, Bao Lang, Zaiqi Yang, Nianhai Feng, Peijun You, Wensheng Zhang, Diansan Su, Jianbo Wu","doi":"10.1186/s13741-025-00564-2","DOIUrl":"10.1186/s13741-025-00564-2","url":null,"abstract":"<p><strong>Background: </strong>Thoracic paravertebral block (TPVB) with liposomal bupivacaine (LB) is increasingly used for postoperative pain control in patients undergoing thoracic surgery, but relevant data are scarce, and there are few data on LB-TPVB combined with drainage tube patient-controlled analgesia (PCA). The aim of this study is to explore the effect of LB-TPVB combined with drainage-tube PCA on postoperative pain after thoracoscopic lobectomy.</p><p><strong>Methods: </strong>This is a prospective, multicentre, double-blind, randomized controlled study. Participants will be randomly assigned to the standard bupivacaine (SB) group, SB + drainage-tube PCA (DTA) group, LB group, or LB + DTA group. The primary outcome is the 72-h mean Numerical Rating Scale (NRS) pain score at rest. The target sample size is 228 patients, with 57 patients in each group.</p><p><strong>Discussion: </strong>Our study hypothesizes that preoperative ultrasound-guided thoracic nerve block combined with drainage tube self-controlled analgesia is more effective in reducing postoperative pain following thoracoscopic lobe resection compared to thoracic nerve block alone. Additionally, liposomal bupivacaine was found to be more effective than standard bupivacaine in this context. These results will have implications for improving postoperative analgesia protocols for patients undergoing thoracoscopic lung surgery.</p><p><strong>Trial registration: </strong>ClinicalTrials.gov, NCT06165991. Registered 29 November 2023, https://clinicaltrials.gov/study/NCT06165991 .</p>","PeriodicalId":19764,"journal":{"name":"Perioperative Medicine","volume":"14 1","pages":"122"},"PeriodicalIF":2.1,"publicationDate":"2025-11-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12593884/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145459442","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-05DOI: 10.1186/s13741-025-00619-4
Xiaofen Sun, Mingming Han, Zefeng Fan, Xiang Huang, Fang Kang, Juan Li
Background: High-flow nasal oxygen (HFNO) is increasingly used for preoxygenation and apneic oxygenation; however, its efficacy during anesthesia induction for frame-based stereoelectroencephalography (SEEG) remains uncertain. This study evaluated whether HFNO is non-inferior to facemask ventilation in maintaining oxygenation during anesthesia induction for frame-based SEEG.
Methods: In this randomized, controlled, non-inferiority trial, adult patients with refractory epilepsy undergoing frame-based SEEG were randomized to either the HFNO or facemask group. The primary endpoint was the lowest peripheral oxygen saturation (SpO2). Secondary endpoints included arterial blood gas analyses, hemodynamic measures, airway adjuncts use, first-pass intubation success (FPS), time to secure the airway, anesthesiologist satisfaction, patient comfort, and perioperative complications.
Results: Among 46 patients, the median (interquartile range [IQR]) lowest SpO2 was 98 (97-99) % in the HFNO group vs. 96 (95-98) % in the facemask group, with a median difference of 1% (95 confidence interval [CI], 0-2%), confirming non-inferiority within a 2% margin. Post-intubation partial pressure of oxygen (PaO2) was significantly higher in the HFNO group than that in the facemask group, with median (IQR) of 437.8 (411.1-474.4) mmHg and 400.6 (365.6-435.2) mmHg, respectively. HFNO reduced the airway adjuncts use (0/23 vs. 6/23 patients; p = 0.022), shortened the time to secure the airway (p = 0.015), and improved anesthesiologist satisfaction and patient comfort (both p < 0.0001). Hemodynamic parameters and FPS were similar between groups.
Conclusion: HFNO is non-inferior to facemask ventilation in maintaining oxygenation during anesthesia induction for frame-based SEEG. Moreover, HFNO reduces the need for airway adjuncts, shortens airway securement time, and enhances both patient and anesthesiologist satisfaction.
Trial registration: This study was registered in the Chinese Clinical Trial Registry (ChiCTR2100044239; first registration date: March 12, 2021; https://www.chictr.org.cn/showproj.html?proj=119780 ).
背景:高流量鼻氧(HFNO)越来越多地用于预充氧和窒息氧合;然而,其在基于框架的立体脑电图(SEEG)麻醉诱导中的效果仍不确定。本研究评估HFNO在框架型SEEG麻醉诱导期间维持氧合方面是否优于面罩通气。方法:在这项随机、对照、非效性试验中,接受基于框架的SEEG治疗的成人难治性癫痫患者被随机分为HFNO组和面罩组。主要终点为最低外周氧饱和度(SpO2)。次要终点包括动脉血气分析、血流动力学测量、气道辅助工具的使用、首次插管成功率(FPS)、气道固定时间、麻醉师满意度、患者舒适度和围手术期并发症。结果:46例患者中,HFNO组最低SpO2的中位数(四分位间距[IQR])为98(97-99)%,面罩组最低SpO2的中位数(四分位间距[IQR])为96(95-98)%,中位数差异为1%(95可信区间[CI], 0-2%),证实非劣效性在2%范围内。肺动脉高压组插管后氧分压(PaO2)明显高于面罩组,中位数(IQR)分别为437.8 (411.1 ~ 474.4)mmHg和400.6 (365.6 ~ 435.2)mmHg。HFNO减少了气道辅助工具的使用(0/23 vs. 6/23; p = 0.022),缩短了固定气道的时间(p = 0.015),提高了麻醉师的满意度和患者的舒适度(p均为p结论:HFNO在框架型SEEG麻醉诱导期间维持氧合的效果不低于面罩通气。此外,HFNO减少了对气道辅助工具的需求,缩短了气道固定时间,提高了患者和麻醉师的满意度。试验注册:本研究已在中国临床试验注册中心注册(ChiCTR2100044239,首次注册日期:2021年3月12日;https://www.chictr.org.cn/showproj.html?proj=119780)。
{"title":"Application of high-flow nasal oxygen during anesthesia induction for frame-based stereoelectroencephalography: a randomized controlled non-inferiority trial.","authors":"Xiaofen Sun, Mingming Han, Zefeng Fan, Xiang Huang, Fang Kang, Juan Li","doi":"10.1186/s13741-025-00619-4","DOIUrl":"10.1186/s13741-025-00619-4","url":null,"abstract":"<p><strong>Background: </strong>High-flow nasal oxygen (HFNO) is increasingly used for preoxygenation and apneic oxygenation; however, its efficacy during anesthesia induction for frame-based stereoelectroencephalography (SEEG) remains uncertain. This study evaluated whether HFNO is non-inferior to facemask ventilation in maintaining oxygenation during anesthesia induction for frame-based SEEG.</p><p><strong>Methods: </strong>In this randomized, controlled, non-inferiority trial, adult patients with refractory epilepsy undergoing frame-based SEEG were randomized to either the HFNO or facemask group. The primary endpoint was the lowest peripheral oxygen saturation (SpO<sub>2</sub>). Secondary endpoints included arterial blood gas analyses, hemodynamic measures, airway adjuncts use, first-pass intubation success (FPS), time to secure the airway, anesthesiologist satisfaction, patient comfort, and perioperative complications.</p><p><strong>Results: </strong>Among 46 patients, the median (interquartile range [IQR]) lowest SpO<sub>2</sub> was 98 (97-99) % in the HFNO group vs. 96 (95-98) % in the facemask group, with a median difference of 1% (95 confidence interval [CI], 0-2%), confirming non-inferiority within a 2% margin. Post-intubation partial pressure of oxygen (PaO<sub>2</sub>) was significantly higher in the HFNO group than that in the facemask group, with median (IQR) of 437.8 (411.1-474.4) mmHg and 400.6 (365.6-435.2) mmHg, respectively. HFNO reduced the airway adjuncts use (0/23 vs. 6/23 patients; p = 0.022), shortened the time to secure the airway (p = 0.015), and improved anesthesiologist satisfaction and patient comfort (both p < 0.0001). Hemodynamic parameters and FPS were similar between groups.</p><p><strong>Conclusion: </strong>HFNO is non-inferior to facemask ventilation in maintaining oxygenation during anesthesia induction for frame-based SEEG. Moreover, HFNO reduces the need for airway adjuncts, shortens airway securement time, and enhances both patient and anesthesiologist satisfaction.</p><p><strong>Trial registration: </strong>This study was registered in the Chinese Clinical Trial Registry (ChiCTR2100044239; first registration date: March 12, 2021; https://www.chictr.org.cn/showproj.html?proj=119780 ).</p>","PeriodicalId":19764,"journal":{"name":"Perioperative Medicine","volume":"14 1","pages":"121"},"PeriodicalIF":2.1,"publicationDate":"2025-11-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12590915/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145452715","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-30DOI: 10.1186/s13741-025-00590-0
Michael C Grant, Daniel T Engelman
Background: The Enhanced Recovery After Surgery (ERAS®) Society has overseen the development and publication of more than two dozen specialty-specific guidelines and consensus statements. We conducted an appraisal of existing guidelines to compare and contrast recommendations to identify overarching themes regarding the current role and future direction of those guidelines for clinicians and researchers.
Methods: After deriving a list of potential perioperative interventions associated with an ERAS program, specialty-specific guidelines were evaluated on the basis of their inclusion and the strength of the grade of those elements.
Results: Following appraisal of the existing ERAS guidelines, a list of common interventions emerges, which includes pre-, intra-, and postoperative care elements that are endorsed by the overwhelming majority of surgical specialties. However, this perioperative rubric should be modifiable to include a broader range of potential perioperative elements, where appropriate, based on literature specific to those subspecialty surgeries.
Conclusions: More uniform consensus regarding common care elements is likely to contribute to greater harmony in guidelines development as well as the development of process measures and outcome definitions. Guidelines can thus foster the creation of data repositories, establish program benchmarks, and contribute to future research and knowledge transfer.
{"title":"Enhanced recovery after surgery: overarching themes of the ERAS® Society Guidelines & Consensus Statements for Adult Specialty Surgery.","authors":"Michael C Grant, Daniel T Engelman","doi":"10.1186/s13741-025-00590-0","DOIUrl":"10.1186/s13741-025-00590-0","url":null,"abstract":"<p><strong>Background: </strong>The Enhanced Recovery After Surgery (ERAS®) Society has overseen the development and publication of more than two dozen specialty-specific guidelines and consensus statements. We conducted an appraisal of existing guidelines to compare and contrast recommendations to identify overarching themes regarding the current role and future direction of those guidelines for clinicians and researchers.</p><p><strong>Methods: </strong>After deriving a list of potential perioperative interventions associated with an ERAS program, specialty-specific guidelines were evaluated on the basis of their inclusion and the strength of the grade of those elements.</p><p><strong>Results: </strong>Following appraisal of the existing ERAS guidelines, a list of common interventions emerges, which includes pre-, intra-, and postoperative care elements that are endorsed by the overwhelming majority of surgical specialties. However, this perioperative rubric should be modifiable to include a broader range of potential perioperative elements, where appropriate, based on literature specific to those subspecialty surgeries.</p><p><strong>Conclusions: </strong>More uniform consensus regarding common care elements is likely to contribute to greater harmony in guidelines development as well as the development of process measures and outcome definitions. Guidelines can thus foster the creation of data repositories, establish program benchmarks, and contribute to future research and knowledge transfer.</p>","PeriodicalId":19764,"journal":{"name":"Perioperative Medicine","volume":"14 1","pages":"120"},"PeriodicalIF":2.1,"publicationDate":"2025-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12577217/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145409705","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-29DOI: 10.1186/s13741-025-00607-8
Aram Doo, Jeewoon Joung, Seonghoon Ko
Background: Postoperative delirium (POD) is a frequent and serious complication in older patients undergoing orthopedic surgery. This study aimed to compare the effects of midazolam and dexmedetomidine on the incidence of POD in elderly patients undergoing total knee arthroplasty under spinal anesthesia.
Methods: In this prospective, double-blind, randomized, parallel group comparative trial, a total of 175 patients aged 65 years or older were allocated to receive either midazolam or dexmedetomidine for intraoperative sedation. The primary outcome was the incidence of POD, evaluated using the confusion assessment method for five postoperative days. Secondary outcomes included the quality of sedation, incidence of sedation failure, postoperative analgesic profiles, and complication rates.
Results: The incidence of POD was significantly lower in the dexmedetomidine group compared to the midazolam group (13.9% vs. 27.4%, P = 0.045). In addition, dexmedetomidine was associated with superior sedation quality and a significantly lower rate of sedation failure (P = 0.007 and P = 0.018, respectively). Postoperative pain intensity and complication rates were comparable between the two groups.
Conclusion: Dexmedetomidine significantly reduced the incidence of POD and improved sedation quality compared to midazolam. These findings suggest that dexmedetomidine may be a preferable sedative for elderly patients undergoing total knee arthroplasty under spinal anesthesia.
Trial registration: This study was registered with the WHO International Clinical Trials Registry Platform (Trial number: KCT0006587, Registration date: 16th September 2021).
背景:术后谵妄(POD)是老年骨科手术患者常见且严重的并发症。本研究旨在比较咪达唑仑和右美托咪定对脊柱麻醉下老年全膝关节置换术患者POD发生率的影响。方法:在这项前瞻性、双盲、随机、平行组比较试验中,共175例65岁及以上的患者被分配到咪达唑仑或右美托咪定治疗术中镇静。主要观察指标为术后5天的POD发生率,采用混淆评估法进行评估。次要结局包括镇静质量、镇静失败发生率、术后镇痛情况和并发症发生率。结果:右美托咪定组POD发生率显著低于咪达唑仑组(13.9% vs. 27.4%, P = 0.045)。此外,右美托咪定具有较好的镇静质量和较低的镇静失败率(P = 0.007和P = 0.018)。两组术后疼痛强度和并发症发生率相当。结论:与咪达唑仑相比,右美托咪定可显著降低POD的发生率,改善镇静质量。这些发现提示右美托咪定可能是脊柱麻醉下接受全膝关节置换术的老年患者较好的镇静剂。试验注册:本研究已在WHO国际临床试验注册平台注册(试验号:KCT0006587,注册日期:2021年9月16日)。
{"title":"Comparison of midazolam and dexmedetomidine on postoperative delirium in older patients undergoing total knee replacement under spinal anesthesia.","authors":"Aram Doo, Jeewoon Joung, Seonghoon Ko","doi":"10.1186/s13741-025-00607-8","DOIUrl":"10.1186/s13741-025-00607-8","url":null,"abstract":"<p><strong>Background: </strong>Postoperative delirium (POD) is a frequent and serious complication in older patients undergoing orthopedic surgery. This study aimed to compare the effects of midazolam and dexmedetomidine on the incidence of POD in elderly patients undergoing total knee arthroplasty under spinal anesthesia.</p><p><strong>Methods: </strong>In this prospective, double-blind, randomized, parallel group comparative trial, a total of 175 patients aged 65 years or older were allocated to receive either midazolam or dexmedetomidine for intraoperative sedation. The primary outcome was the incidence of POD, evaluated using the confusion assessment method for five postoperative days. Secondary outcomes included the quality of sedation, incidence of sedation failure, postoperative analgesic profiles, and complication rates.</p><p><strong>Results: </strong>The incidence of POD was significantly lower in the dexmedetomidine group compared to the midazolam group (13.9% vs. 27.4%, P = 0.045). In addition, dexmedetomidine was associated with superior sedation quality and a significantly lower rate of sedation failure (P = 0.007 and P = 0.018, respectively). Postoperative pain intensity and complication rates were comparable between the two groups.</p><p><strong>Conclusion: </strong>Dexmedetomidine significantly reduced the incidence of POD and improved sedation quality compared to midazolam. These findings suggest that dexmedetomidine may be a preferable sedative for elderly patients undergoing total knee arthroplasty under spinal anesthesia.</p><p><strong>Trial registration: </strong>This study was registered with the WHO International Clinical Trials Registry Platform (Trial number: KCT0006587, Registration date: 16th September 2021).</p>","PeriodicalId":19764,"journal":{"name":"Perioperative Medicine","volume":"14 1","pages":"119"},"PeriodicalIF":2.1,"publicationDate":"2025-10-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12574253/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145401566","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-27DOI: 10.1186/s13741-025-00600-1
Yu-Mei Feng, Qian-Yun Pang, Ya-Jun Yang, Hong-Liang Liu
Background: Postoperative ischemic stroke is a severe complication in neurosurgery, while intraoperative hypertension is a frequent event. However, their clinical relationship remains poorly understood.
Methods: This retrospective cohort study analyzed data from patients with brain tumors undergoing craniotomies between January 2017 and December 2023 at Chongqing University Cancer Hospital. Multivariate logistic regression identified risk factors for postoperative stroke. Intraoperative hypertension was defined as a mean arterial pressure (MAP) > 105 mmHg, with indices including peak MAP, duration, and area under the curve (AUC). Restricted cubic spline analysis with three knots (10th, 50th, and 90th percentiles) was performed. The outcome was postoperative in-hospital acute ischemic stroke. The risk of stroke was assessed by quartile categorization of hypertension indices.
Results: A total of 1,786 patients were included in the final analysis. Intraoperative hypertension was identified as a risk factor for postoperative ischemic stroke, alongside age and intraoperative crystalloid infusion rate. Quatile analysis revealed the following risk thresholds of intraoperative hypertension: 1) peak value > 123 mmHg (aOR: 2.118, 95% CI: 1.360-3.297); 2) duration > 5 min (aOR: 1.604, 95% CI: 1.033-2.491); 3) AUC > 530 mmHg*min (aOR: 1.811, 95% CI: 1.165-2.816). Intraoperative hypertension was not significantly associated with postoperative stroke risk.
Conclusion: Intraoperative hypertension is a significant predictor of postoperative ischemic stroke in neurosurgical patients, with peak value, the duration, and AUC all demonstrating independent predictive values. These findings underscore the critical need for vigilant intraoperative blood pressure monitoring and management to mitigate stroke risk in neurosurgical patients.
{"title":"Relationship between intraoperative hypertension and postoperative ischemic stroke in neurosurgery-a retrospective cohort study.","authors":"Yu-Mei Feng, Qian-Yun Pang, Ya-Jun Yang, Hong-Liang Liu","doi":"10.1186/s13741-025-00600-1","DOIUrl":"10.1186/s13741-025-00600-1","url":null,"abstract":"<p><strong>Background: </strong>Postoperative ischemic stroke is a severe complication in neurosurgery, while intraoperative hypertension is a frequent event. However, their clinical relationship remains poorly understood.</p><p><strong>Methods: </strong>This retrospective cohort study analyzed data from patients with brain tumors undergoing craniotomies between January 2017 and December 2023 at Chongqing University Cancer Hospital. Multivariate logistic regression identified risk factors for postoperative stroke. Intraoperative hypertension was defined as a mean arterial pressure (MAP) > 105 mmHg, with indices including peak MAP, duration, and area under the curve (AUC). Restricted cubic spline analysis with three knots (10th, 50th, and 90th percentiles) was performed. The outcome was postoperative in-hospital acute ischemic stroke. The risk of stroke was assessed by quartile categorization of hypertension indices.</p><p><strong>Results: </strong>A total of 1,786 patients were included in the final analysis. Intraoperative hypertension was identified as a risk factor for postoperative ischemic stroke, alongside age and intraoperative crystalloid infusion rate. Quatile analysis revealed the following risk thresholds of intraoperative hypertension: 1) peak value > 123 mmHg (aOR: 2.118, 95% CI: 1.360-3.297); 2) duration > 5 min (aOR: 1.604, 95% CI: 1.033-2.491); 3) AUC > 530 mmHg*min (aOR: 1.811, 95% CI: 1.165-2.816). Intraoperative hypertension was not significantly associated with postoperative stroke risk.</p><p><strong>Conclusion: </strong>Intraoperative hypertension is a significant predictor of postoperative ischemic stroke in neurosurgical patients, with peak value, the duration, and AUC all demonstrating independent predictive values. These findings underscore the critical need for vigilant intraoperative blood pressure monitoring and management to mitigate stroke risk in neurosurgical patients.</p>","PeriodicalId":19764,"journal":{"name":"Perioperative Medicine","volume":"14 1","pages":"118"},"PeriodicalIF":2.1,"publicationDate":"2025-10-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12560383/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145378289","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-27DOI: 10.1186/s13741-025-00602-z
Jie Li, Yaqiong Cao, Kun Zhang, Xin Zhuo, Yanhong Zhu, Jie Chen
<p><strong>Objective: </strong>This study aimed to investigate the impact of failure mode and effects analysis (FMEA)-based proactive nursing combined with individualized functional exercise on hip function in patients undergoing total hip arthroplasty (THA).</p><p><strong>Methods: </strong>This was a prospective, single-center, randomized controlled trial. Using a consecutive sampling approach, 100 patients who underwent THA at the Affiliated Hospital of Xuzhou Medical University between October 2022 and January 2024 were enrolled and randomly assigned (random number table method) to either a control group (n = 50) or an intervention group (n = 50). The control group received routine nursing plus standard functional exercise, whereas the intervention group received FMEA-based proactive nursing combined with individualized functional training in addition to routine care. Both groups were followed continuously for 3 months. The primary outcome was hip function, assessed using the Harris hip score (HHS) before and after the intervention. Secondary outcomes included the time to first ambulation, pain during ambulation, and length of hospital stay. Psychological status (anxiety and depression) and quality of life were evaluated before and after the intervention using the Self-Rating Anxiety Scale (SAS), Self-Rating Depression Scale (SDS), and the Short Form-36 questionnaire (SF-36). Postoperative complications were recorded, and nursing satisfaction at discharge was assessed using the Newcastle Satisfaction with Nursing Scale (NSNS).</p><p><strong>Results: </strong>After nursing care, HHS in both the control and intervention groups were higher than before care. Post-intervention, the intervention group showed significantly higher scores than the control group in function (34.62 ± 2.97 vs 27.94 ± 2.87), range of motion (3.64 ± 0.63 vs 2.28 ± 0.45), pain (28.98 ± 4.29 vs 23.52 ± 3.83), and deformity (2.78 ± 0.55 vs 2.02 ± 0.25) (P < 0.05). Patients in the intervention group ambulated for the first time earlier than those in the control group (29.12 ± 3.29 h vs 42.20 ± 4.16 h), with lower pain scores during activity (4.46 ± 0.86 vs 6.06 ± 1.27) and shorter hospital stays (11.40 ± 1.93 days vs 14.84 ± 2.71 days) (P < 0.05). SF-36 scores in both groups improved after nursing care, with the intervention group demonstrating higher post-care scores in physical function (70.92 ± 6.50 vs 60.06 ± 5.88), mental health (67.88 ± 6.17 vs 58.92 ± 5.71), social function (70.92 ± 6.66 vs 62.84 ± 6.11), and bodily pain (67.82 ± 6.68 vs 59.64 ± 5.24) compared with the control group (P < 0.05). Anxiety and depression scores (SAS and SDS) decreased in both groups after nursing care, with the intervention group showing lower scores than the control group (SAS 39.02 ± 3.66 vs 46.88 ± 4.52; SDS 38.98 ± 3.89 vs 49.58 ± 4.05) (P < 0.05). The incidence of postoperative complications was lower in the intervention group (6.00%) than in the control group (22.00%) (P < 0.05), and n
目的:探讨基于失效模式与效果分析(failure mode and effects analysis, FMEA)的主动护理结合个性化功能锻炼对全髋关节置换术(THA)患者髋关节功能的影响。方法:前瞻性、单中心、随机对照试验。采用连续抽样方法,选取2022年10月至2024年1月在徐州医科大学附属医院行THA手术的100例患者,采用随机数字表法随机分为对照组(n = 50)和干预组(n = 50)。对照组采用常规护理加标准功能锻炼,干预组在常规护理的基础上采用基于fmea的主动护理结合个性化功能训练。两组患者均连续随访3个月。主要结果是髋关节功能,在干预前后使用Harris髋关节评分(HHS)进行评估。次要结局包括第一次活动的时间、活动时的疼痛和住院时间。采用焦虑自评量表(SAS)、抑郁自评量表(SDS)和SF-36简易问卷(SF-36)对干预前后的心理状态(焦虑、抑郁)和生活质量进行评估。记录术后并发症,并采用纽卡斯尔护理满意度量表(NSNS)评估出院时护理满意度。结果:护理后,对照组和干预组的HHS均高于护理前。干预后,干预组在功能评分(34.62±2.97 vs 27.94±2.87)、活动范围评分(3.64±0.63 vs 2.28±0.45)、疼痛评分(28.98±4.29 vs 23.52±3.83)、畸形评分(2.78±0.55 vs 2.02±0.25)均显著高于对照组(P)。基于fmea的主动护理结合个性化功能锻炼,加速康复,改善髋关节功能,减少疼痛和负面情绪,提高生活质量,降低并发症发生率,同时提高患者满意度。
{"title":"Impact of FMEA-based proactive nursing combined with individualized functional exercise on hip function in patients following hip replacement.","authors":"Jie Li, Yaqiong Cao, Kun Zhang, Xin Zhuo, Yanhong Zhu, Jie Chen","doi":"10.1186/s13741-025-00602-z","DOIUrl":"10.1186/s13741-025-00602-z","url":null,"abstract":"<p><strong>Objective: </strong>This study aimed to investigate the impact of failure mode and effects analysis (FMEA)-based proactive nursing combined with individualized functional exercise on hip function in patients undergoing total hip arthroplasty (THA).</p><p><strong>Methods: </strong>This was a prospective, single-center, randomized controlled trial. Using a consecutive sampling approach, 100 patients who underwent THA at the Affiliated Hospital of Xuzhou Medical University between October 2022 and January 2024 were enrolled and randomly assigned (random number table method) to either a control group (n = 50) or an intervention group (n = 50). The control group received routine nursing plus standard functional exercise, whereas the intervention group received FMEA-based proactive nursing combined with individualized functional training in addition to routine care. Both groups were followed continuously for 3 months. The primary outcome was hip function, assessed using the Harris hip score (HHS) before and after the intervention. Secondary outcomes included the time to first ambulation, pain during ambulation, and length of hospital stay. Psychological status (anxiety and depression) and quality of life were evaluated before and after the intervention using the Self-Rating Anxiety Scale (SAS), Self-Rating Depression Scale (SDS), and the Short Form-36 questionnaire (SF-36). Postoperative complications were recorded, and nursing satisfaction at discharge was assessed using the Newcastle Satisfaction with Nursing Scale (NSNS).</p><p><strong>Results: </strong>After nursing care, HHS in both the control and intervention groups were higher than before care. Post-intervention, the intervention group showed significantly higher scores than the control group in function (34.62 ± 2.97 vs 27.94 ± 2.87), range of motion (3.64 ± 0.63 vs 2.28 ± 0.45), pain (28.98 ± 4.29 vs 23.52 ± 3.83), and deformity (2.78 ± 0.55 vs 2.02 ± 0.25) (P < 0.05). Patients in the intervention group ambulated for the first time earlier than those in the control group (29.12 ± 3.29 h vs 42.20 ± 4.16 h), with lower pain scores during activity (4.46 ± 0.86 vs 6.06 ± 1.27) and shorter hospital stays (11.40 ± 1.93 days vs 14.84 ± 2.71 days) (P < 0.05). SF-36 scores in both groups improved after nursing care, with the intervention group demonstrating higher post-care scores in physical function (70.92 ± 6.50 vs 60.06 ± 5.88), mental health (67.88 ± 6.17 vs 58.92 ± 5.71), social function (70.92 ± 6.66 vs 62.84 ± 6.11), and bodily pain (67.82 ± 6.68 vs 59.64 ± 5.24) compared with the control group (P < 0.05). Anxiety and depression scores (SAS and SDS) decreased in both groups after nursing care, with the intervention group showing lower scores than the control group (SAS 39.02 ± 3.66 vs 46.88 ± 4.52; SDS 38.98 ± 3.89 vs 49.58 ± 4.05) (P < 0.05). The incidence of postoperative complications was lower in the intervention group (6.00%) than in the control group (22.00%) (P < 0.05), and n","PeriodicalId":19764,"journal":{"name":"Perioperative Medicine","volume":"14 1","pages":"117"},"PeriodicalIF":2.1,"publicationDate":"2025-10-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12560292/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145378316","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-24DOI: 10.1186/s13741-025-00597-7
Emre Şentürk, Zerrin Sungur, Hayriye Şentürk Çiftçi, Metin İlteray Kıkılı, Mehmet Öner Şanlı, Demet Kıvanç, Emre Sertaç Bingül, Mert Canbaz, Rıfat Burak Ergül, Meltem Savran Karadeniz
Background: Postoperative neurocognitive disorders (PNDs) are highly prevalent among the elderly population. Identifying an ideal biomarker for postoperative delirium (POD) and postoperative cognitive dysfunction (POCD) remains a significant challenge. This study aimed to investigate the relationship between these syndromes and various biomarkers, including S-100β, neuron-specific enolase (NSE), interleukin-6 (IL-6), and high-mobility group box-1 (HMGB-1).
Methods: The study included patients aged 60 years and older who underwent surgery for primary urologic malignancies. POD was evaluated in the recovery room using the Confusion Assessment Method (CAM). POCD was assessed preoperatively and at the first week (POCD1) and third month (POCD3) postoperatively using Addenbrooke's Cognitive Examination-III (ACE-III). Biomarker levels of S-100β, neuron-specific enolase (NSE), interleukin-6 (IL-6), and high-mobility group box-1 (HMGB-1) were measured using enzyme-linked immunosorbent assay (ELISA).
Results: A total of 54 patients completed the study. POD was diagnosed in 12 patients (22.2%), while POCD1 and POCD3 were identified in 17 (31.5%) patients and 12 (22.2%) patients respectively. The mean age of the participants was 73.8 ± 7.1 years. Preoperative levels of NSE were significantly higher in patients with POD compared to those without (p = 0.04). Additionally, preoperative and postoperative IL-6 levels, as well as preoperative and postoperative S-100β levels, were significantly elevated in patients with POCD1 compared to those without (p < 0.01, p = 0.01, p < 0.01, and p = 0.03, respectively). Furthermore, preoperative IL-6 and S-100β levels were higher in patients with POCD3 compared to those without (p = 0.01 and p = 0.03, respectively).
Conclusions: In major urologic oncologic surgeries among geriatric patients, IL-6 and S-100β were found to be associated with both POD and POCD, while NSE was specifically associated with POD.
{"title":"The relation between postoperative cognitive disorders and brain damage biomarkers after major urologic surgery: a prospective cohort study.","authors":"Emre Şentürk, Zerrin Sungur, Hayriye Şentürk Çiftçi, Metin İlteray Kıkılı, Mehmet Öner Şanlı, Demet Kıvanç, Emre Sertaç Bingül, Mert Canbaz, Rıfat Burak Ergül, Meltem Savran Karadeniz","doi":"10.1186/s13741-025-00597-7","DOIUrl":"10.1186/s13741-025-00597-7","url":null,"abstract":"<p><strong>Background: </strong>Postoperative neurocognitive disorders (PNDs) are highly prevalent among the elderly population. Identifying an ideal biomarker for postoperative delirium (POD) and postoperative cognitive dysfunction (POCD) remains a significant challenge. This study aimed to investigate the relationship between these syndromes and various biomarkers, including S-100β, neuron-specific enolase (NSE), interleukin-6 (IL-6), and high-mobility group box-1 (HMGB-1).</p><p><strong>Methods: </strong>The study included patients aged 60 years and older who underwent surgery for primary urologic malignancies. POD was evaluated in the recovery room using the Confusion Assessment Method (CAM). POCD was assessed preoperatively and at the first week (POCD1) and third month (POCD3) postoperatively using Addenbrooke's Cognitive Examination-III (ACE-III). Biomarker levels of S-100β, neuron-specific enolase (NSE), interleukin-6 (IL-6), and high-mobility group box-1 (HMGB-1) were measured using enzyme-linked immunosorbent assay (ELISA).</p><p><strong>Results: </strong>A total of 54 patients completed the study. POD was diagnosed in 12 patients (22.2%), while POCD1 and POCD3 were identified in 17 (31.5%) patients and 12 (22.2%) patients respectively. The mean age of the participants was 73.8 ± 7.1 years. Preoperative levels of NSE were significantly higher in patients with POD compared to those without (p = 0.04). Additionally, preoperative and postoperative IL-6 levels, as well as preoperative and postoperative S-100β levels, were significantly elevated in patients with POCD1 compared to those without (p < 0.01, p = 0.01, p < 0.01, and p = 0.03, respectively). Furthermore, preoperative IL-6 and S-100β levels were higher in patients with POCD3 compared to those without (p = 0.01 and p = 0.03, respectively).</p><p><strong>Conclusions: </strong>In major urologic oncologic surgeries among geriatric patients, IL-6 and S-100β were found to be associated with both POD and POCD, while NSE was specifically associated with POD.</p>","PeriodicalId":19764,"journal":{"name":"Perioperative Medicine","volume":"14 1","pages":"116"},"PeriodicalIF":2.1,"publicationDate":"2025-10-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12676895/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145678348","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-24DOI: 10.1186/s13741-025-00603-y
Leonardo Barbosa Santos, Leopoldo Muniz da Silva, Saullo Q Silveira, Rafael S F Nersessian, Giulia D Matheus, Glenio B Mizubuti, Joaquim Edson Vieira
Introduction: Perioperative bronchoaspiration is a serious complication often associated with inadequate fasting or delayed gastric emptying, including that caused by glucagon-like peptide-1 receptor agonists (GLP-1-RAs). Despite growing semaglutide use worldwide, evidence on the effectiveness of current preventive measures-such as residue-free diets-remains limited.
Case presentation: We report a 61-year-old female with obesity and chronic obstructive pulmonary disease who underwent elective coronary angiography. She had been using weekly semaglutide for weight loss, discontinued six days before the procedure, but did not disclose this during preoperative evaluation. Following institutional guidance, she adhered to a 24-h residue-free diet and 12-h fasting. A protocol breach led to omission of preoperative gastric ultrasound. During anesthesia induction, she experienced large-volume regurgitation requiring urgent airway management. Postoperative chest CT revealed aspiration-related inflammatory changes. She recovered uneventfully and later acknowledged omitting semaglutide use from her medical history because she did not consider it a "medication."
Conclusion: This case demonstrates that even stricter dietary measures than those recommended in current guidelines may not eliminate aspiration risk in GLP-1-RA users. Active screening for GLP-1-RA use, consideration of extended discontinuation intervals, and routine bedside gastric ultrasound should be incorporated into perioperative protocols to enhance patient safety.
{"title":"Perioperative bronchoaspiration in a semaglutide user on a residue-free diet: a case report and insights from a complication.","authors":"Leonardo Barbosa Santos, Leopoldo Muniz da Silva, Saullo Q Silveira, Rafael S F Nersessian, Giulia D Matheus, Glenio B Mizubuti, Joaquim Edson Vieira","doi":"10.1186/s13741-025-00603-y","DOIUrl":"10.1186/s13741-025-00603-y","url":null,"abstract":"<p><strong>Introduction: </strong>Perioperative bronchoaspiration is a serious complication often associated with inadequate fasting or delayed gastric emptying, including that caused by glucagon-like peptide-1 receptor agonists (GLP-1-RAs). Despite growing semaglutide use worldwide, evidence on the effectiveness of current preventive measures-such as residue-free diets-remains limited.</p><p><strong>Case presentation: </strong>We report a 61-year-old female with obesity and chronic obstructive pulmonary disease who underwent elective coronary angiography. She had been using weekly semaglutide for weight loss, discontinued six days before the procedure, but did not disclose this during preoperative evaluation. Following institutional guidance, she adhered to a 24-h residue-free diet and 12-h fasting. A protocol breach led to omission of preoperative gastric ultrasound. During anesthesia induction, she experienced large-volume regurgitation requiring urgent airway management. Postoperative chest CT revealed aspiration-related inflammatory changes. She recovered uneventfully and later acknowledged omitting semaglutide use from her medical history because she did not consider it a \"medication.\"</p><p><strong>Conclusion: </strong>This case demonstrates that even stricter dietary measures than those recommended in current guidelines may not eliminate aspiration risk in GLP-1-RA users. Active screening for GLP-1-RA use, consideration of extended discontinuation intervals, and routine bedside gastric ultrasound should be incorporated into perioperative protocols to enhance patient safety.</p>","PeriodicalId":19764,"journal":{"name":"Perioperative Medicine","volume":"14 1","pages":"115"},"PeriodicalIF":2.1,"publicationDate":"2025-10-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12551300/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145368564","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}