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Comparison of intraoperative intravenous lidocaine infusion and transversus abdominis plane block for postoperative analgesia following laparoscopic cholecystectomy: a randomized controlled trial. 术中静脉输注利多卡因与经腹平面阻滞用于腹腔镜胆囊切除术术后镇痛的比较:一项随机对照试验。
IF 3.2 Pub Date : 2025-05-01 DOI: 10.17085/apm.24159
Haris Sheikh, Shakaib Zafar, Kamran Nawaz, Hameed Ullah

Background: Laparoscopic cholecystectomy has been associated with moderate to severe intensity pain, especially in the early postoperative period. Among pain modalities, the transversus abdominis plane (TAP) block has favorable results and fewer associated adverse effects. Current evidence also reports that intravenous lidocaine infusion is effective in reducing acute postoperative pain and decreases overall opioid requirement. This study aimed to compare intravenous lidocaine infusion and bilateral subcostal TAP block for postoperative analgesia following laparoscopic cholecystectomy.

Methods: Thirty patients were randomly classified into the control, lidocaine, and TAP block groups. Intravenous lidocaine infusion was used in the lidocaine arm intraoperatively, while bilateral subcostal TAP block was placed in the TAP block arm as an intervention. The primary outcome was 24 h average pain score. Secondary outcomes included rescue analgesic consumption, postoperative nausea and vomiting, and patient satisfaction.

Results: Comparative analysis between groups showed that the 24 h mean pain score on the visual analog scale score was significantly decreased in the lidocaine group than the control group (mean difference with 95% confidence interval [CI], 2.47 (1.94, 3.00); P < 0.001). Furthermore, the mean pain score was significantly decreased in the lidocaine group than in the TAP block group (mean difference with 95% CI, 1.14 (0.56, 1.72); P < 0.001).

Conclusions: Intravenous lidocaine infusion is a superior modality for postoperative pain management in laparoscopic cholecystectomy than TAP block or routine management. Lidocaine also helped decrease rescue analgesic consumption and achieved better patient satisfaction.

背景:腹腔镜胆囊切除术与中度至重度疼痛有关,特别是在术后早期。在疼痛方式中,腹横面(TAP)阻滞具有良好的效果和较少的相关副作用。目前的证据还表明,静脉输注利多卡因可有效减轻急性术后疼痛,并减少阿片类药物的总体需求。本研究旨在比较利多卡因静脉输注与双侧肋下TAP阻滞在腹腔镜胆囊切除术后的镇痛效果。方法:30例患者随机分为对照组、利多卡因组和TAP阻断组。术中利多卡因臂采用静脉输注利多卡因,而TAP阻滞臂采用双侧肋下TAP阻滞作为干预。主要结局为24小时平均疼痛评分。次要结局包括抢救镇痛药消耗、术后恶心呕吐和患者满意度。结果:组间比较分析显示,利多卡因组24 h视觉模拟量表平均疼痛评分明显低于对照组(95%可信区间均值[CI], 2.47 (1.94, 3.00);P < 0.001)。此外,利多卡因组的平均疼痛评分明显低于TAP阻断组(平均95% CI为1.14 (0.56,1.72);P < 0.001)。结论:静脉输注利多卡因治疗腹腔镜胆囊切除术术后疼痛优于TAP阻滞或常规治疗。利多卡因也有助于减少抢救镇痛的消耗,获得更好的患者满意度。
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引用次数: 0
Anesthesia for rigid bronchoscopy in an extremely premature un-intubated micropremie - A case report. 极度早产非插管微型早产儿刚性支气管镜麻醉1例报告。
Pub Date : 2025-04-01 Epub Date: 2025-04-30 DOI: 10.17085/apm.24129
Benjamin Weingarten, Mohammad Fardeen Maudarbaccus, Farrukh Munshey

Background: Extremely premature neonates can have neonatal respiratory distress syndrome. Anesthetic challenges can result, especially during rigid bronchoscopy requiring maintenance of spontaneous ventilation.

Case: 1-day old 560 g female, 23-weeks and 6 days gestation was born with labored breathing and intubated at birth. Four attempts, including one with video-laryngoscopy and visualization of the endotracheal tube going through the vocal cords failed to detect end tidal carbon dioxide (EtCO2). She was extubated onto bilevel positive pressure and transferred for urgent rigid bronchoscopy under anesthesia to rule out tracheoesophageal fistula. Intraoperatively, lack of EtCO2 for over 1 min after 2.5 mm ETT placement over a rigid bronchoscope was noted and overcome using sustained high peak inspiratory pressures.

Conclusions: Lack of preoperative surfactant administration in extremely premature neonates may lead to significant atelectasis with inability to detect EtCO2 after intubation.

背景:极早产儿可有新生儿呼吸窘迫综合征。麻醉挑战可能导致,特别是在刚性支气管镜检查需要维持自发通气。病例:1日龄560 g女,孕23周6天,出生时呼吸困难,出生时插管。四次尝试,包括一次视频喉镜和气管内管穿过声带的可视化,未能检测到末潮二氧化碳(EtCO2)。她被拔管至双水平正压,并在麻醉下转移到紧急刚性支气管镜检查以排除气管食管瘘。术中,注意到在刚性支气管镜下放置2.5 mm ETT后,EtCO2缺乏超过1分钟,并使用持续的峰值吸气压力克服。结论:极早产儿术前缺乏表面活性剂可导致明显的肺不张,插管后无法检测EtCO2。
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引用次数: 0
Erratum: Practical guidance for monitored anesthesia care during awake craniotomy. 勘误:清醒开颅术中监测麻醉护理的实用指南。
IF 3.2 Pub Date : 2025-04-01 Epub Date: 2025-03-14 DOI: 10.17085/apm.24183.e1
Kyeong Tae Min
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引用次数: 0
Introduction to burnout and well-being for anesthesiologists in South Korea: narrative and brief review. 韩国麻醉师的倦怠和幸福感介绍:叙述和简要回顾。
Pub Date : 2025-04-01 Epub Date: 2025-04-30 DOI: 10.17085/apm.25244
Jeongrim Lee

Burnout is a widespread occupational issue in the medical field, posing significant risks to both physician health and patient care worldwide. While the COVID-19 pandemic highlighted the impact of systemic factors-such as excessive workloads, administrative burdens, and inefficiencies-in exacerbating physician burnout, discussions about well-being remain limited in South Korea. Given the recent challenges faced by healthcare professionals in Korea, addressing burnout has become urgent to prevent further negative outcomes. Although individual efforts toward wellness are important, they are insufficient without systemic support. Distinguishing between burnout and well-being is crucial for developing targeted interventions. Drawing on global examples, comprehensive strategies-including policy reforms, organizational support, mental health resources, and cultural shifts-are recommended to create a sustainable and supportive environment for anesthesiologists in Korea.

职业倦怠是医学领域一个普遍存在的职业问题,在世界范围内对医生健康和患者护理构成重大风险。虽然COVID-19大流行凸显了系统性因素(如工作量过大、行政负担和效率低下)在加剧医生倦怠方面的影响,但在韩国,关于健康的讨论仍然有限。鉴于韩国医疗保健专业人员最近面临的挑战,解决倦怠问题已成为当务之急,以防止进一步的负面后果。虽然个人对健康的努力很重要,但没有系统的支持是不够的。区分倦怠和幸福对于制定有针对性的干预措施至关重要。借鉴全球的例子,综合战略——包括政策改革、组织支持、心理健康资源和文化转变——被推荐为韩国麻醉师创造一个可持续和支持性的环境。
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引用次数: 0
Analysis of characteristics of patients whose sugammadex claims were denied by the Auto Insurance Claims Review Department of Korean Health Insurance Review & Assessment Service: a retrospective single-center review. 韩国健康保险审查与评估服务部汽车保险索赔审查部拒绝的苏麦卡索赔患者特征分析:回顾性单中心审查。
Pub Date : 2025-04-01 Epub Date: 2024-11-22 DOI: 10.17085/apm.24095
Hwa Song Jong, Ki Tae Jung

Background: Recently, there have been many cases where sugammadex used in traffic accident patients has been deducted from auto insurance claims. This study aims to investigate the characteristics of sugammadex deductions through retrospective analysis.

Methods: We included patients who underwent general anesthesia after traffic accidents at our institution between January 2019 and December 2023. Data for patients for whom sugammadex payments were deducted from the Auto Insurance Claims Review Department of the Korean Health Insurance Review and Assessment Service were obtained from the hospital's insurance department, and electronic medical records were analyzed. The characteristics of neuromuscular blockade (NMB) and its reversal, including administration time and dosage of neuromuscular blockading agent (NMBA) and reversal agent, intraoperative neuromuscular transmission (NMT) monitoring results, and reasons for sugammadex use, were assessed and analyzed.

Results: A total of 251 patients deducted sugammadex payments during the study period. The deduction rate significantly decreased from 88-100% in previous years to 43.4% in 2023. Sugammadex was used to reverse deep NMB (55.1%) and in high-risk patients (23.1%). Sugammadex was mostly used to reverse deep NMB (55.1%) and in high-risk patients (23.1%). NMT monitoring was documented in 81.3% of cases, with 38.9% showing deep NMB and 33.3% showing moderate NMB. Despite improved NMT documentation after 2021, sugammadex payment deductions persisted.

Conclusions: Sugammadex payment deductions occur despite clinical necessity, particularly in deep and moderate NMB cases. Thorough documentation may help reduce these deductions. Collaboration between healthcare providers and policymakers is required to use reversal agents guided by clinical evidence.

背景:最近,发生了多起交通事故患者使用的舒格迈司在汽车保险理赔中被扣除的案例。本研究旨在通过回顾性分析调查舒格迈司扣款的特点:我们纳入了2019年1月至2023年12月期间在我院接受交通事故后全身麻醉的患者。从医院保险部门获得韩国健康保险审查和评估服务处汽车保险索赔审查部扣除苏麦卡度费用的患者数据,并对电子病历进行分析。评估和分析了神经肌肉阻滞(NMB)及其逆转的特征,包括神经肌肉阻滞剂(NMBA)和逆转剂的给药时间和剂量、术中神经肌肉传导(NMT)监测结果以及使用舒马地的原因:结果:在研究期间,共有 251 名患者扣除了舒格迈司费用。扣款率从往年的88%-100%大幅降至2023年的43.4%。舒格迈得主要用于逆转深部 NMB(55.1%)和高风险患者(23.1%)。舒降之主要用于逆转深部 NMB(55.1%)和高风险患者(23.1%)。81.3% 的病例记录了 NMT 监测,其中 38.9% 显示深部 NMB,33.3% 显示中度 NMB。尽管2021年后NMT记录有所改善,但舒格迈司的付款扣减仍然存在:结论:尽管有临床必要性,但仍会发生舒格迈司费用扣减的情况,尤其是在深度和中度 NMB 病例中。详尽的文件记录有助于减少这些扣款。医疗服务提供者和政策制定者之间需要合作,在临床证据的指导下使用逆转剂。
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引用次数: 0
Ultrasound-guided continuous edge of laminar block in thoracotomy. 超声引导下椎板块连续边缘在开胸术中的应用。
Pub Date : 2025-04-01 Epub Date: 2025-04-30 DOI: 10.17085/apm.24156
Poonam Kumari, Amarjeet Kumar, Satish Kumar, Neha Mary Noble, Lakshmi Sinha
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引用次数: 0
Evaluation of a multidisciplinary simulation training curriculum for local anesthetic systemic toxicity management: a quasi-experimental study using the Kirkpatrick model in India. 评估局部麻醉系统毒性管理的多学科模拟培训课程:在印度使用Kirkpatrick模型的准实验研究。
Pub Date : 2025-04-01 Epub Date: 2025-01-08 DOI: 10.17085/apm.24146
Pooja Bihani, Naveen Paliwal, Rishabh Jaju, Vikas Rajpurohit

Background: Local anesthetic systemic toxicity (LAST) is a rare life-threatening complication of regional anesthesia. Simulation-based training offers an effective educational approach to improve the management of infrequent events. This quasi-experimental study assessed the impact of a multidisciplinary simulation-based educational intervention on managing LAST as a real peri-operative team.

Methods: Twelve anesthesia trainees and eight nursing staff members participated in the study. The intervention included pre-course learning materials, cognitive aids, and immersive simulation scenarios. Simulation scenarios were conducted at baseline (O1), one week after a boot camp (O2), and six months later (O3). Participants' reactions to the training were evaluated using a 5-point Likert scale, while knowledge acquisition was measured through pre- and post-test questionnaires. Team-based skills acquisition and retention were assessed using a modified checklist from the simulation team assessment tool. Data were analyzed using paired t-tests, with P < 0.05 considered statistically significant.

Results: All participants rated the LAST curriculum as satisfactory to very satisfactory. Significant improvements in both technical and non-technical skills were observed post-intervention (O2), with checklist scores increasing from an average of 39 (4.2) (95% confidence interval [CI], 34.88; 43.11) at O1 to 83.5 (5.7) (95% CI, 77.91; 89.08) at O2 (mean difference, 44.5; P < 0.001). At six months (O3), skill retention was indicated by an average score of 72 (7.8) (95% CI, 62.36; 77.64).

Conclusions: Multidisciplinary, simulation-based educational interventions remarkably improve knowledge and skills related to LAST management, with effective skill retention observed at six months when implemented by multiprofessional teams in real-world settings.

背景:局麻全身毒性(LAST)是一种罕见的危及生命的区域麻醉并发症。基于模拟的培训提供了一种有效的教育方法来改善对罕见事件的管理。这项准实验研究评估了基于多学科模拟的教育干预对作为一个真正的围手术期团队管理LAST的影响。方法:12名麻醉培训生和8名护理人员参与研究。干预包括课前学习材料、认知辅助工具和沉浸式模拟场景。模拟场景分别在基线(O1)、训练营后一周(O2)和六个月后(O3)进行。参与者对培训的反应使用5分李克特量表进行评估,而知识获取则通过测试前和测试后问卷进行测量。基于团队的技能获取和保留使用来自模拟团队评估工具的修改清单进行评估。数据分析采用配对t检验,P < 0.05认为有统计学意义。结果:所有参与者对LAST课程的评价为满意至非常满意。干预后观察到技术和非技术技能的显着改善(O2),检查表得分从平均39分(4.2分)增加(95%置信区间[CI], 34.88;43.11)为0 ~ 83.5 (5.7)(95% CI, 77.91;89.08) O2组(平均差值44.5;P < 0.001)。在6个月时(3),技能保留的平均得分为72 (7.8)(95% CI, 62.36;77.64)。结论:多学科、基于模拟的教育干预措施显著提高了与LAST管理相关的知识和技能,在现实环境中由多专业团队实施时,在六个月后观察到有效的技能保留。
{"title":"Evaluation of a multidisciplinary simulation training curriculum for local anesthetic systemic toxicity management: a quasi-experimental study using the Kirkpatrick model in India.","authors":"Pooja Bihani, Naveen Paliwal, Rishabh Jaju, Vikas Rajpurohit","doi":"10.17085/apm.24146","DOIUrl":"https://doi.org/10.17085/apm.24146","url":null,"abstract":"<p><strong>Background: </strong>Local anesthetic systemic toxicity (LAST) is a rare life-threatening complication of regional anesthesia. Simulation-based training offers an effective educational approach to improve the management of infrequent events. This quasi-experimental study assessed the impact of a multidisciplinary simulation-based educational intervention on managing LAST as a real peri-operative team.</p><p><strong>Methods: </strong>Twelve anesthesia trainees and eight nursing staff members participated in the study. The intervention included pre-course learning materials, cognitive aids, and immersive simulation scenarios. Simulation scenarios were conducted at baseline (O1), one week after a boot camp (O2), and six months later (O3). Participants' reactions to the training were evaluated using a 5-point Likert scale, while knowledge acquisition was measured through pre- and post-test questionnaires. Team-based skills acquisition and retention were assessed using a modified checklist from the simulation team assessment tool. Data were analyzed using paired t-tests, with P < 0.05 considered statistically significant.</p><p><strong>Results: </strong>All participants rated the LAST curriculum as satisfactory to very satisfactory. Significant improvements in both technical and non-technical skills were observed post-intervention (O2), with checklist scores increasing from an average of 39 (4.2) (95% confidence interval [CI], 34.88; 43.11) at O1 to 83.5 (5.7) (95% CI, 77.91; 89.08) at O2 (mean difference, 44.5; P < 0.001). At six months (O3), skill retention was indicated by an average score of 72 (7.8) (95% CI, 62.36; 77.64).</p><p><strong>Conclusions: </strong>Multidisciplinary, simulation-based educational interventions remarkably improve knowledge and skills related to LAST management, with effective skill retention observed at six months when implemented by multiprofessional teams in real-world settings.</p>","PeriodicalId":101360,"journal":{"name":"Anesthesia and pain medicine","volume":"20 2","pages":"166-174"},"PeriodicalIF":0.0,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12066202/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144035024","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
Transforaminal lumbar epidural injection of dexmedetomidine versus magnesium sulfate combined with dexamethasone for lower limb radicular pain management: a randomized, clinical trial. 经椎间孔腰椎硬膜外注射右美托咪定与硫酸镁联合地塞米松治疗下肢神经根性疼痛:一项随机临床试验
Pub Date : 2025-04-01 Epub Date: 2025-01-02 DOI: 10.17085/apm.24125
Mina Maher Raouf, Gehan Ibrahim Abdelrazek Salem, Fady Adib Abdel Malek, Tamer Youssef Elie Hamawy, Sadik Abdel-Maseeh Sadik, Mohammad Awad Elsaed

Background: Epidural steroid injections are frequently used to treat chronic radicular pain of a discogenic origin; however, their efficacy remains limited. Magnesium sulfate and dexmedetomidine are emerging adjuvants with the potential to enhance the effectiveness and prolong the therapeutic duration of steroid injections.

Methods: In this randomized, double-blind study, 90 patients with unilateral lower limb radiculopathy due to lumbar disc prolapse who did not respond to conservative treatment for 12 weeks were assigned to three groups. The control group received dexamethasone (4 mg), lidocaine 2% (40 mg), and saline. The magnesium group received magnesium sulfate (200 mg) with dexamethasone and lidocaine. The dexmedetomidine group received dexmedetomidine (50 mg), dexamethasone, lidocaine, and saline. Pain intensity was assessed using the visual analog scale at 1 week and 1, 3, and 6 months post-treatment. Secondary outcomes included the Modified Oswestry Disability Index (MODI), analgesic consumption, and procedure-related complications.

Results: Both magnesium and dexmedetomidine significantly reduced pain, disability, and analgesic consumption for up to 3 months. By 6 months, the magnesium group demonstrated significant improvement in pain scores and MODI and a decline in ibuprofen use compared to the control and dexmedetomidine groups.

Conclusions: Magnesium significantly reduced pain intensity, disability, and analgesic consumption over a 6-month observation period.

背景:硬膜外类固醇注射常用于治疗椎间盘源性慢性根性疼痛,但其疗效仍然有限。硫酸镁和右美托咪定是新兴的辅助药物,有可能提高类固醇注射的疗效并延长治疗时间:在这项随机双盲研究中,90名因腰椎间盘突出症而导致单侧下肢根性病变、保守治疗12周无效的患者被分为三组。对照组接受地塞米松(4 毫克)、2% 利多卡因(40 毫克)和生理盐水治疗。镁组接受硫酸镁(200 毫克)、地塞米松和利多卡因。右美托咪定组使用右美托咪定(50 微克)、地塞米松、利多卡因和生理盐水。使用视觉模拟量表评估治疗后 1 周、1、3 和 6 个月的疼痛强度。次要结果包括改良奥斯韦特里残疾指数(MODI)、镇痛药消耗量和手术相关并发症:结果:镁和右美托咪定都能在长达3个月的时间内明显减轻疼痛、残疾和镇痛剂用量。到6个月时,与对照组和右美托咪定组相比,镁组的疼痛评分和MODI明显改善,布洛芬的用量也有所减少:结论:在6个月的观察期内,镁可明显减轻疼痛强度、残疾程度和镇痛剂用量。
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引用次数: 0
Optimizing maternal recovery: insights into enhanced recovery after Cesarean delivery. 优化产妇恢复:提高剖宫产后恢复的见解。
Pub Date : 2025-04-01 Epub Date: 2025-04-30 DOI: 10.17085/apm.25211
Hyo-Seok Na

Enhanced recovery after surgery (ERAS) is an innovative perioperative management approach designed to shorten the recovery time, improve patient safety and quality of care, and enhance overall satisfaction. Successful implementation of ERAS requires active collaboration between healthcare providers and patients to facilitate a timely return to daily activities. The ERAS protocol, originally developed for colorectal surgery, has gradually been expanded and adapted to other major surgeries, and more recently, to Cesarean deliveries. Enhanced recovery after Cesarean delivery (ERAC) presents unique challenges due to its distinct patient population, comprising relatively young women. Its dual focus on maternal recovery and neonatal well-being sets it apart from conventional ERAS protocols. Several components of the ERAC protocol have been adapted from the ERAS recommendations; however, supporting evidence remains limited. This review examines the current ERAC protocol and considers the types of research needed to establish an evidence-based ERAC protocol in the future.

术后增强恢复(ERAS)是一种创新的围手术期管理方法,旨在缩短恢复时间,提高患者安全和护理质量,提高整体满意度。ERAS的成功实施需要医疗保健提供者和患者之间的积极合作,以促进及时恢复日常活动。ERAS方案最初是为结肠直肠手术开发的,现已逐渐扩展并适应于其他主要手术,最近也适用于剖宫产。剖宫产后增强恢复(ERAC)提出了独特的挑战,由于其独特的患者群体,包括相对年轻的妇女。其对产妇康复和新生儿健康的双重关注使其有别于传统的ERAS协议。ERAC协议的几个组成部分是根据ERAC的建议改编的;然而,支持证据仍然有限。本文回顾了目前的ERAC方案,并考虑了未来建立循证ERAC方案所需的研究类型。
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引用次数: 0
Treatment of severe pain in a patient with a cervical spinal cord injury at C5-7 level using an intrathecal targeted drug delivery system - A case report. 鞘内靶向给药系统治疗C5-7节段颈脊髓损伤患者剧烈疼痛1例报告
Pub Date : 2025-04-01 Epub Date: 2025-04-30 DOI: 10.17085/apm.24151
Yeong-Min Yoo, Ji-Eun Jung, Hyun-Jin Kim, Hyeon-Soo Park, Hye-Jin Kim, Gyeong-Jo Byeon

Background: Patients with cervical spinal cord injury (SCI) can experience pain refractory to aggressive multimodal therapies. Here, we report the use of an intrathecal targeted drug delivery (ITDD) system to treat severe pain in patients with cervical SCI.

Case: A 64-year-old male patient underwent spinal cord stimulation (SCS) for severe cervical SCI. We proceeded with the ITDD system, placing the catheter tip at the C6 level. After placement of the ITDD system, the patient was monitored for regular refills of morphine sulfate in the drug delivery reservoir every 6 months. We reduced the oral morphine equivalent dose from nearly 333.8 mg/day to 133.8 mg/day.

Conclusions: The ITDD system may be a useful treatment option for patients with cervical SCI who have failed conventional treatments and do not show improvement with SCS.

背景:颈椎脊髓损伤(SCI)患者可以经历对积极的多模式治疗难以治愈的疼痛。在这里,我们报告使用鞘内靶向给药(ITDD)系统来治疗颈椎脊髓损伤患者的严重疼痛。病例:一名64岁男性患者因严重颈椎损伤接受脊髓刺激(SCS)治疗。我们继续使用ITDD系统,将导管尖端置于C6水平。放置ITDD系统后,监测患者每6个月在给药库中定期补充硫酸吗啡。我们将口服吗啡当量剂量从近333.8 mg/天减少到133.8 mg/天。结论:ITDD系统可能是一种有效的治疗选择,对于那些常规治疗失败且SCS没有改善的颈椎脊髓损伤患者。
{"title":"Treatment of severe pain in a patient with a cervical spinal cord injury at C5-7 level using an intrathecal targeted drug delivery system - A case report.","authors":"Yeong-Min Yoo, Ji-Eun Jung, Hyun-Jin Kim, Hyeon-Soo Park, Hye-Jin Kim, Gyeong-Jo Byeon","doi":"10.17085/apm.24151","DOIUrl":"https://doi.org/10.17085/apm.24151","url":null,"abstract":"<p><strong>Background: </strong>Patients with cervical spinal cord injury (SCI) can experience pain refractory to aggressive multimodal therapies. Here, we report the use of an intrathecal targeted drug delivery (ITDD) system to treat severe pain in patients with cervical SCI.</p><p><strong>Case: </strong>A 64-year-old male patient underwent spinal cord stimulation (SCS) for severe cervical SCI. We proceeded with the ITDD system, placing the catheter tip at the C6 level. After placement of the ITDD system, the patient was monitored for regular refills of morphine sulfate in the drug delivery reservoir every 6 months. We reduced the oral morphine equivalent dose from nearly 333.8 mg/day to 133.8 mg/day.</p><p><strong>Conclusions: </strong>The ITDD system may be a useful treatment option for patients with cervical SCI who have failed conventional treatments and do not show improvement with SCS.</p>","PeriodicalId":101360,"journal":{"name":"Anesthesia and pain medicine","volume":"20 2","pages":"160-165"},"PeriodicalIF":0.0,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12066199/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144059010","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
Anesthesia and pain medicine
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