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Preoperative Administration of Angiotensin-Converting Enzyme Inhibitors or Angiotensin II Receptor Blockers: Do We Have Enough “VISION” to Stop It? 术前应用血管紧张素转换酶抑制剂或血管紧张素受体阻滞剂:我们有足够的“视力”来阻止它吗?
Pub Date : 2017-08-01 DOI: 10.1097/01.sa.0000525653.70599.b4
M. London
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引用次数: 1
Innovative Disruption in the World of Neuromuscular Blockade: What Is the “State of the Art?” 神经肌肉阻断世界的创新中断:什么是“艺术状态?”
Pub Date : 2017-08-01 DOI: 10.1097/01.SA.0000525660.70880.8D
M. Naguib, Ken Johnson
morbidity. The risks associated with NMBA could be almost completely eliminated if adequate neuromuscular function measured by a TOF ratio of greater than 0.90 was obtained before allowing emergence from anesthesia and tracheal extubation. Hence, neuromuscular function assessment with a PNS is mandatory whenever either depolarizing or nondepolarizing NMBAs are used to reduce risk of residual block.
发病如果在麻醉和气管拔管前获得足够的神经肌肉功能(TOF比大于0.90),则与NMBA相关的风险几乎可以完全消除。因此,无论何时使用去极化或非去极化nmba来减少残留阻滞的风险,都必须使用PNS进行神经肌肉功能评估。
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引用次数: 0
Implementing a Statistical Model for Protamine Titration: Effects on Coagulation in Cardiac Surgical Patients 实施鱼精蛋白滴定的统计模型:对心脏手术患者凝血的影响
Pub Date : 2017-08-01 DOI: 10.1097/01.sa.0000525620.39586.68
Oskar Hällgren, S. Svenmarker, M. Appelblad
as tramadol pharmacology will ensure the optimal pain management without adverse effects or toxicity. The possibility of misuse, withdrawal symptoms, and adverse effects are greater in the case of tramadol because of its unique simultaneous opioid agonist action and serotonin and norepinephrine reuptake inhibitory effects, which increases the potential for drug interactions. A more thorough understanding of tramadol's pharmacology and pharmacokinetics including the effect of CYP genetic polymorphisms will ensure more targeted prescribing practices. In addition, both patients and practitioners should be aware of the potential for drug interactions, possibility of addiction, toxicity risks, and risk of withdrawal. Hopefully, increased knowledge in these areas will improve the possibility of making an optimal decision regarding the use of this drug.
由于曲马多药理学将确保最佳的疼痛管理,没有不良反应或毒性。曲马多的滥用、戒断症状和不良反应的可能性更大,因为它独特的同时具有阿片激动剂作用和血清素和去甲肾上腺素再摄取抑制作用,这增加了药物相互作用的可能性。更彻底地了解曲马多的药理学和药代动力学,包括CYP遗传多态性的影响,将确保更有针对性的处方实践。此外,患者和从业人员都应该意识到潜在的药物相互作用,成瘾的可能性,毒性风险和停药的风险。希望在这些领域增加的知识将提高对这种药物的使用做出最佳决定的可能性。
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引用次数: 0
Prospective Double Blind Randomized Placebo-Controlled Clinical Trial of the Pectoral Nerves (Pecs) Block Type II 胸神经阻滞II型的前瞻性双盲随机安慰剂对照临床试验
Pub Date : 2017-08-01 DOI: 10.1097/SA.0000000000000338
B. Versyck, G. Geffen, P. V. Houwe
STUDY OBJECTIVE The aim of this clinical trial was to test the hypothesis whether adding the pectoral nerves (Pecs) block type II to the anesthetic procedure reduces opioid consumption during and after breast surgery. DESIGN A prospective randomized double blind placebo-controlled study. SETTING A secondary hospital. PATIENTS 140 breast cancer stage 1-3 patients undergoing mastectomy or tumorectomy with sentinel node or axillary node dissection. INTERVENTIONS Patients were randomized to receive either a Pecs block with levobupivacaine 0.25% (n=70) or placebo block with saline (n=70). MEASUREMENTS The pain levels were evaluated by Numeric Rating Scale (NRS) pain scores at 15-minute intervals during the post anesthesia care unit stay time (PACU), at 2-hour intervals for the first 24h on the ward and at 4-hour intervals for the next 24h. Intraoperative and postoperative opioid consumption were recorded during the full stay. Patient satisfaction was evaluated upon discharge using a 10-point scale. MAIN RESULTS Intraoperative sufentanil requirements were comparable for the Pecs and placebo group (8.0±3.5μg and 7.8±3.0μg, P=0.730). Patients in the Pecs group experienced significantly less pain than patients in the control group (P=0.048) during their PACU stay. Furthermore, patients in the Pecs group required significant less postoperative opioids (9.16±10.15mg and 14.97±14.38mg morphine equivalent, P=0.037) and required significant fewer postsurgical opioid administration interventions than patients in the control group (P=0.045). Both patient-groups were very satisfied about their management (9.6±0.6 and 9.1±1.8 on a 10-point scale, P=0.211). CONCLUSIONS The Pecs block reduces postsurgical opioid consumption during the PACU stay time for patients undergoing breast surgery.
区域麻醉技术用于乳房手术后急性和持续性疼痛,胸神经阻滞II型(Pecs)是一种易于实施的浅表阻滞技术,在胸大肌和胸小肌之间沉积局麻药。局麻药的这种分布阻断了胸神经、肋臂间神经、III-VI肋间神经和胸长神经。这项前瞻性、随机、双盲、安慰剂对照试验旨在评估Pecs block减少阿片类药物消耗的假设,并且在乳房手术患者中至少与围手术期镇痛药一样好,如果不是更好的话。本研究的主要结局指标是数值评定量表疼痛评分和术中及术后阿片类药物消耗。次要结果测量是患者满意度评分。研究数据包括美国麻醉医师学会生理评分1-3分(年龄18-80岁)的I - III期乳腺癌患者,接受乳房切除术或乳房肿瘤切除术并前哨淋巴结或腋窝淋巴结清扫。患者按1:1的比例随机分为研究组(Pecs组,10ml左布比卡因0.25%)或对照组(安慰剂组,生理盐水)。每组70例。在麻醉后护理单位(PACU)停留时间每隔15分钟记录一次疼痛评分,在病房前24小时每隔2小时记录一次疼痛评分,接下来的24小时每隔4小时记录一次疼痛评分。在整个住院期间记录术中和术后阿片类药物的消耗,并在出院时使用10分制评估患者满意度。使用IBM Statistical Package for Social Science Statistics version 21进行统计分析,P < 0.05认为有统计学意义。PACU住院期间,Pecs组患者疼痛程度低于对照组(P = 0.048)。Pecs组术中舒芬太尼需求量与安慰剂组相当(8.0±3.5 μg和7.8±3.0 μg, P = 0.730)。与对照组相比,Pecs组患者术后所需阿片类药物(9.16±10.15 mg和14.97±14.38 mg, P = 0.037)和术后阿片类药物给药干预明显减少(P = 0.045)。两组患者均对护理非常满意(10分制评分分别为9.6±0.6和9.1±1.8,P = 0.211)。综上所述,在麻醉过程中加入Pecs阻滞可显著减少PACU的疼痛和阿片类药物需求,证实了Pecs阻滞在乳房手术术后镇痛中的有效性。
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引用次数: 93
Raising the Alarm on Brain Attacks in Surgical Patients: Are We Doing Enough to Prevent and Treat Postoperative Strokes? 敲响外科患者脑梗死的警钟:我们在预防和治疗术后中风方面做得足够吗?
Pub Date : 2017-07-01 DOI: 10.1097/01.sa.0000527523.87797.b0
L. Glance, R. Holloway
This editorial provides an overview of the study by Christiansen et al, which demonstrates that a history of acute ischemic stroke within 3 months of emergency noncardiac, nonintracranial surgery significantly increased the risk of a postoperative stroke using data from the Danish National Patient Registry. The incidence of postoperative stroke was reported at 0.1% to 0.7%, with the risk declining as more time elapsed between the ischemic event and surgery. Despite the study limitations, this research by Christiansen et al on vulnerability to stroke after surgery supports the need for further research using different approaches and diverse populations to support the validation of the risk. Awareness of the risk of stroke, new neurologic deficits, and clear procedures with stroke teams and perioperative and surgical teams should be in place to ensure better patient outcomes. When undergoing elective surgery, especially in high-risk patients/ procedures, management must be done in close conjunction with stroke teams and comprehensive stroke centers where neuroendovascular specialists and advanced neuroimaging capabilities are readily available to ensure a better quality of care, as well as a better quality of life postprocedure. As of 2017, across America, there are 121 comprehensive stroke centers. When a specialized center is not readily accessible, a protocol to manage at-risk patients via technology, such as telestroke consultation, must be implemented. Currently, the guidelines for preventing postoperative stroke are provided by the Society for Neuroscience in Anesthesiology and Critical Care consensus statement (supported but not endorsed by the American Society of Anesthesiologists). These guidelines have been minimally disseminated in comparison to the information from theAmerican StrokeAssociation. Because of the potential for severe impact on the life of a patient, surgical patients at risk of postoperative stroke must be managed with as much importance given to preventing a recurrent stroke as with dealing with the medical condition being treated.
这篇社论概述了Christiansen等人的研究,该研究利用丹麦国家患者登记处的数据表明,紧急非心脏、非颅内手术后3个月内的急性缺血性卒中史显著增加了术后卒中的风险。据报道,术后卒中的发生率为0.1% - 0.7%,随着缺血事件和手术之间时间的延长,卒中风险下降。尽管研究存在局限性,但Christiansen等人关于手术后卒中易感性的研究表明,有必要使用不同的方法和不同的人群进行进一步的研究,以支持对风险的验证。卒中风险的认识、新的神经功能缺陷、卒中团队、围手术期和外科团队的明确程序应该到位,以确保更好的患者预后。当接受选择性手术时,特别是高风险患者/手术,必须与中风团队和综合中风中心密切合作,在这些中心,神经血管内专家和先进的神经成像能力随时可用,以确保更好的护理质量,以及手术后更好的生活质量。截至2017年,全美共有121家综合性中风中心。当一个专门的中心不容易到达时,必须实施一项协议,通过技术来管理高危患者,如远程卒中咨询。目前,预防术后卒中的指导方针是由麻醉和重症监护神经科学学会共识声明提供的(美国麻醉医师学会支持但不认可)。与美国中风协会的信息相比,这些指南的传播程度最低。由于可能对患者的生命造成严重影响,手术患者术后卒中风险的管理必须与处理正在治疗的医疗状况一样重视预防卒中复发。
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引用次数: 2
Remifentanil Tolerance and Hyperalgesia: Short-term Gain, Long-term Pain? 瑞芬太尼耐受性和痛觉过敏:短期获益,长期疼痛?
Pub Date : 2017-06-01 DOI: 10.1097/SA.0000000000000313
E. Yu, D. H. Tran, S. W. Lam, M. Irwin
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引用次数: 87
STR-324, a Stable Analog of Opiorphin, Causes Analgesia in Postoperative Pain by Activating Endogenous Opioid Receptor-dependent Pathways Opiorphin的稳定类似物STR-324通过激活内源性阿片受体依赖通路引起术后疼痛的镇痛
Pub Date : 2017-06-01 DOI: 10.1097/01.sa.0000521825.85774.2d
P. Sitbon, A. C. Elstraete, Leila Hamdi, V. Juárez-Pérez, J. Mazoit, D. Benhamou, C. Rougeot
Opiorphin is a natural human peptide with strong analgesic properties. These analgesic effects thought to result in a reduction in enkephalin hydrolysis secondary to the compound inhibition of enkephalinase. The purpose of this study was to demonstrate that opiorphin and its stable analog STR-324 are promising analgesics that may be the solution to the quest for a new class of effective, yet safe, painkillers. Inhibitors of enkephalin breakdown could potentially be a class of longacting painkillers with a better safety profile than direct opioid receptor agonists. Although their efficacy in postoperative pain models has not been established, both opiorphin and STR-324 reduced mechanical hypersensitivity through opioid receptor–mediated mechanisms without adverse cardiorespiratory effects in a rat incisional pain model. The demonstrationwas done via the Brennanmodel of plantar incision–induced hypersensitivity with examination of the postsurgical analgesic response to mechanical and thermal stimuli in rats with 7 days of continuously intravenously infused drugs There were a total of 8 to 10 rats per group (mechanical and thermal). Antinociception caused by opiorphin was compared with that of morphine and STR-324, and the expression of spinal c-Fos and the role of opioid receptor–dependent pathways were specifically targeted. Tests were also conducted to assess any manifestation of adverse respiratory and hemodynamic effects with opiorphin. It was found that intravenously administered opiorphin infusion significantly decreased responses to mechanical stimuli postsurgery from days 1 to 4 at 143to 175-kPa mean ranges compared with 23to 30-kPa mean ranges for vehicle (P < 0.05). During this period, no adverse effects in respiratory rate, oxygen saturation, arterial pressure, or heart rate were induced by opiorphin. STR-324 repeatedly demonstrated inhibition of mechanical and thermal hyperalgesia with a potency similar to that of opiorphin. STR-324 significantly reduced the number of pain-evoked spinal c-Fos immunoreactive nuclei that could be identified after immunostaining. Through the use of mechanistic analyses, it was also demonstrated that the opioid antagonist naloxone reversed the antinociceptive effect of STR-324. In conclusion, a significant antinociceptive effect of intravenous opiorphin and STR-324 was demonstrated in a postoperative
Opiorphin是一种天然的人肽,具有很强的镇痛作用。这些镇痛作用被认为导致脑啡肽水解减少,继发于脑啡肽酶的复合抑制。这项研究的目的是证明opiorphin及其稳定的类似物STR-324是有希望的镇痛药,可能是寻求一种新的有效而安全的止痛药的解决方案。脑啡肽分解抑制剂可能是一类长效止痛药,具有比直接阿片受体激动剂更好的安全性。虽然opiorphin和STR-324在术后疼痛模型中的疗效尚未确定,但在大鼠切口疼痛模型中,opiorphin和STR-324均通过阿片受体介导的机制降低机械超敏反应,且无不良心肺作用。采用布伦南足底切口致超敏反应模型,观察连续静脉注药7 d大鼠术后对机械和热刺激的镇痛反应,每组8 ~ 10只(机械组和热组)。将opiorphin与吗啡和STR-324的抗痫作用进行比较,并特异性研究脊髓c-Fos的表达和阿片受体依赖通路的作用。还进行了测试以评估opiorphin对呼吸和血流动力学的不良影响。结果发现,术后第1 ~ 4天静脉注射opiorphin显著降低机械刺激反应,平均范围为143 ~ 175 kpa,而对照组平均范围为23 ~ 30 kpa (P < 0.05)。在此期间,opiorphin未引起呼吸频率、血氧饱和度、动脉压或心率的不良反应。STR-324反复表现出对机械和热痛觉过敏的抑制作用,其效力与opiorphin相似。STR-324显著减少了免疫染色后可识别的疼痛引起的脊髓c-Fos免疫反应核的数量。通过机制分析,也证明了阿片拮抗剂纳洛酮逆转了STR-324的抗伤害性作用。综上所述,术后静脉注射opiorphin和STR-324具有明显的抗伤害性作用
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引用次数: 2
The effects of maternal presence during anesthesia induction on salivary cortisol levels in children undergoing tonsillectomy and/or adenoidectomy. 麻醉诱导过程中母亲的存在对扁桃体切除术和/或腺样体切除术儿童唾液皮质醇水平的影响。
Pub Date : 2017-06-01 DOI: 10.1097/SA.0000000000000335
H. Ozdogan, S. Çetinalp, G. Kuran, O. Tuğal, Murat Tahiroglu, Ummuhan E. Herdem, Süheyl Haytoğlu
OBJECTIVEAlthough parental presence during anesthesia induction is suggested to diminish operative stress level in children, there have been conflicting results about this strategy. The aim of this study was to evaluate the effects of maternal presence during induction on operative stress level in children who had tonsillectomy and/or adenoidectomy by determining the salivary cortisol levels.DESIGNNon-randomized clinical study.SETTINGPreoperative and postoperative recovery rooms, operating room.PATIENTSThe study included 48 children between the ages of 5-12years who underwent tonsillectomy and/or adenoidectomy.INTERVENTIONSThe patients were divided into 2 groups. The children in group 1 were separated from their mothers at the preparation room. The children in group 2 stayed together with their mothers till the anesthesia induction.MEASUREMENTSState Trait Anxiety Inventory (STAI) was performed to the mothers and children preoperatively. Salivary cortisol levels were evaluated in 4 different time frames: 1) in preparation room, 2) after anesthesia induction, 3) at the 30th minute of operation, and 4) in postoperative recovery room.MAIN RESULTSThere were no statistically significant differences between groups regarding demographic features, and operation or anesthesia times. The child's or mothers' preoperative anxiety scores were not different between the groups. Salivary cortisol levels in group 1 were significantly increased after induction and in recovery room compared to those in group 2 (p: 0.001, and p: 0.02, respectively).CONCLUSIONSWe have determined decreased salivary cortisol levels during anesthesia induction and recovery in the maternal presence revealing diminished stress in these periods. Further studies are warranted to determine the effects of parental presence during anesthesia induction especially on surgical outcomes.
目的:虽然在麻醉诱导过程中父母的存在被认为可以降低儿童手术应激水平,但关于这一策略的结果却相互矛盾。本研究的目的是通过测定唾液皮质醇水平来评估诱导过程中母亲的存在对扁桃体切除术和/或腺样体切除术儿童手术应激水平的影响。设计:非随机临床研究。术前、术后恢复室、手术室。患者:该研究包括48名年龄在5-12岁之间的儿童,他们接受了扁桃体切除术和/或腺样体切除术。干预措施将患者分为两组。第一组的孩子在准备室与他们的母亲分开。第二组患儿与母亲在一起直至麻醉诱导。测量方法术前对母子进行状态-特质焦虑量表(STAI)。在4个不同的时间段评估唾液皮质醇水平:1)准备室,2)麻醉诱导后,3)手术第30分钟,4)术后恢复室。主要结果两组患者人口学特征、手术及麻醉时间差异无统计学意义。儿童或母亲的术前焦虑评分在两组之间没有差异。诱导后和恢复室1组唾液皮质醇水平显著高于2组(p: 0.001和p: 0.02)。结论:在麻醉诱导和产妇在场恢复期间,唾液皮质醇水平下降,表明这些时期的应激减轻。需要进一步的研究来确定父母在场对麻醉诱导的影响,特别是对手术结果的影响。
{"title":"The effects of maternal presence during anesthesia induction on salivary cortisol levels in children undergoing tonsillectomy and/or adenoidectomy.","authors":"H. Ozdogan, S. Çetinalp, G. Kuran, O. Tuğal, Murat Tahiroglu, Ummuhan E. Herdem, Süheyl Haytoğlu","doi":"10.1097/SA.0000000000000335","DOIUrl":"https://doi.org/10.1097/SA.0000000000000335","url":null,"abstract":"OBJECTIVE\u0000Although parental presence during anesthesia induction is suggested to diminish operative stress level in children, there have been conflicting results about this strategy. The aim of this study was to evaluate the effects of maternal presence during induction on operative stress level in children who had tonsillectomy and/or adenoidectomy by determining the salivary cortisol levels.\u0000\u0000\u0000DESIGN\u0000Non-randomized clinical study.\u0000\u0000\u0000SETTING\u0000Preoperative and postoperative recovery rooms, operating room.\u0000\u0000\u0000PATIENTS\u0000The study included 48 children between the ages of 5-12years who underwent tonsillectomy and/or adenoidectomy.\u0000\u0000\u0000INTERVENTIONS\u0000The patients were divided into 2 groups. The children in group 1 were separated from their mothers at the preparation room. The children in group 2 stayed together with their mothers till the anesthesia induction.\u0000\u0000\u0000MEASUREMENTS\u0000State Trait Anxiety Inventory (STAI) was performed to the mothers and children preoperatively. Salivary cortisol levels were evaluated in 4 different time frames: 1) in preparation room, 2) after anesthesia induction, 3) at the 30th minute of operation, and 4) in postoperative recovery room.\u0000\u0000\u0000MAIN RESULTS\u0000There were no statistically significant differences between groups regarding demographic features, and operation or anesthesia times. The child's or mothers' preoperative anxiety scores were not different between the groups. Salivary cortisol levels in group 1 were significantly increased after induction and in recovery room compared to those in group 2 (p: 0.001, and p: 0.02, respectively).\u0000\u0000\u0000CONCLUSIONS\u0000We have determined decreased salivary cortisol levels during anesthesia induction and recovery in the maternal presence revealing diminished stress in these periods. Further studies are warranted to determine the effects of parental presence during anesthesia induction especially on surgical outcomes.","PeriodicalId":22104,"journal":{"name":"Survey of Anesthesiology","volume":"92 7","pages":""},"PeriodicalIF":0.0,"publicationDate":"2017-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91450409","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 18
Preoperative risk stratification of critically ill patients. 危重病人术前风险分层。
Pub Date : 2017-06-01 DOI: 10.1097/SA.0000000000000337
Curtis C Copeland, Andrew Young, Tristan Grogan, Eilon Gabel, Anahat K. Dhillon, Vadim Gudzenko
STUDY OBJECTIVERisk assessment historically emphasized cardiac morbidity and mortality in elective, outpatient, non-cardiac surgery. However, critically ill patients increasingly present for therapeutic interventions. Our study investigated the relationship of American Society of Anesthesiologists (ASA) class, revised cardiac risk index (RCRI), and sequential organ failure assessment (SOFA) score with survival to discharge in critically ill patients with respiratory failure.DESIGNRetrospective cohort analysis over a 21-month period.SETTINGFive adult intensive care units (ICUs) at a single tertiary medical center.PATIENTSThree hundred fifty ICU patients in respiratory failure, who underwent 501 procedures with general anesthesia.MEASUREMENTSDemographic, clinical, and surgical variables were collected from the pre-anesthesia evaluation forms and preoperative ICU charts. The primary outcome was survival to discharge.MAIN RESULTSNinety-six patients (27%) did not survive to discharge. There were significant differences between survivors and non-survivors for ASA (3.7 vs. 3.9, p=0.001), RCRI (1.6 vs. 2.0, p=0.003), and SOFA score (8.1 vs. 11.2, p<0.001). Based on the area under the receiver operating characteristic curve for these relationships, there was only modest discrimination between the groups, ranging from the most useful SOFA (0.68) to less useful RCRI (0.60) and ASA (0.59).CONCLUSIONSThis single center retrospective study quantified a high perioperative risk for critically ill patients with advanced airways: one in four did not survive to discharge. Preoperative ASA score, RCRI, and SOFA score only partially delineated survivors and non-survivors. Given the existing limitations, future research may identify assessment tools more relevant to discriminating survival outcomes for critically ill patients in the perioperative environment.
研究目的风险评估历来强调择期、门诊和非心脏手术的心脏发病率和死亡率。然而,危重患者越来越多地出现治疗干预。本研究探讨了美国麻醉医师学会(ASA)分级、修订心脏危险指数(RCRI)和顺序器官衰竭评估(SOFA)评分与危重呼吸衰竭患者生存至出院的关系。设计:21个月的回顾性队列分析。在一个三级医疗中心设有5个成人重症监护病房(icu)。患者:350例ICU呼吸衰竭患者,在全身麻醉下进行了501次手术。从麻醉前评估表和术前ICU图表中收集人口学、临床和手术变量。主要终点是存活至出院。主要结果96例(27%)患者未存活至出院。幸存者和非幸存者在ASA (3.7 vs. 3.9, p=0.001)、RCRI (1.6 vs. 2.0, p=0.003)和SOFA评分(8.1 vs. 11.2, p<0.001)方面存在显著差异。根据这些关系的受试者工作特征曲线下的面积,两组之间只有适度的区别,从最有用的SOFA(0.68)到不太有用的RCRI(0.60)和ASA(0.59)。结论:这项单中心回顾性研究量化了晚期气道危重患者围手术期的高风险:四分之一的患者无法存活出院。术前ASA评分、RCRI和SOFA评分仅部分描绘了幸存者和非幸存者。考虑到现有的局限性,未来的研究可能会确定评估工具,更相关的是在围手术期环境中区分危重患者的生存结果。
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引用次数: 88
Factors Associated With Blood Transfusion During Intracranial Aneurysm Surgery 颅内动脉瘤手术中输血的相关因素
Pub Date : 2017-06-01 DOI: 10.1097/01.sa.0000521854.89244.42
J. Yee, A. Koht, R. McCarthy, J. Bebawy
This single-center retrospective observational study aimed to identify risk factors associated with intraoperative blood transfusions in patients undergoing intracranial aneurysm surgery. Considering known risks associated with blood product transfusion, several organizations now have guidelines that advise a more restrictive approach to product administration than in the past. In addition, criteria for transfusion in intracranial aneurysm surgery are not well defined. The authors of this study hoped to identify risk factors for transfusion in this particular patient population and in the era of more restrictive transfusion patterns. Data from 470 consecutive patients who underwent intracranial aneurysm surgery at Northwestern Memorial Hospital (Chicago, Ill) between 2006 and 2012 were analyzed retrospectively using a multivariate binary logistic regression analysis. In this cohort, 9.5% (46 of 470) received intraoperative red blood cell (RBC) transfusions, and the median estimated blood loss in patients who had an intraoperative transfusion was 500 mL (interquartile range, 275–1000 mL) The median number of RBC units transfused was 2 (interquartile range, 1–2), and the volume transfused was 750 mL (interquartile range, 375–750 mL). Preoperative risk factors associated with transfusions were highly related to aneurysm rupture (older age [P < 0.001], lower admission hemoglobin level [P < 0.001], preoperative rupture [P < 0.001], and higher HuntHess grade [P < 0.001]). Intraoperative risk factors and independent predictors of RBC transfusion included larger aneurysm size (>10 mm; P = 0.03), intracerebral hematoma evacuation (P = 0.02), and intraventricular hemorrhage (P < 0.001). Of these, this study demonstrated that the most significant risk factors for transfusion included presenting hemoglobin of less than 11.7 g/dL and age older than 52 years. Based on the findings of this study, the authors suggest that patients with a hemoglobin less than 11.7 g/dL and those with hemoglobin between 11.7 and 14 g/dL who are older than 52 years should be cross-matched for RBCs before intracranial aneurysm surgery because they fall within the high-risk category of requiring perioperative blood transfusion.
本单中心回顾性观察性研究旨在确定颅内动脉瘤手术患者术中输血的相关危险因素。考虑到与血液制品输血相关的已知风险,一些组织现在有指导方针,建议对产品管理采取比过去更严格的方法。此外,颅内动脉瘤手术中输血的标准也没有很好的定义。这项研究的作者希望在这个特殊的病人群体和在更严格的输血模式时代确定输血的危险因素。使用多元二元logistic回归分析回顾性分析了2006年至2012年间在西北纪念医院(Chicago, illinois)连续接受颅内动脉瘤手术的470例患者的数据。在该队列中,有9.5%(470人中有46人)接受了术中红细胞(RBC)输注,术中输血患者的估计失血量中位数为500 mL(四分位数范围,275-1000 mL),输注红细胞单位中位数为2(四分位数范围,1-2),输注量中位数为750 mL(四分位数范围,375-750 mL)。术前输血相关危险因素与动脉瘤破裂高度相关(年龄较大[P < 0.001]、入院血红蛋白水平较低[P < 0.001]、术前破裂[P < 0.001]、HuntHess分级较高[P < 0.001])。术中输血的危险因素和独立预测因素包括动脉瘤较大(>10 mm;P = 0.03)、脑内血肿排出(P = 0.02)和脑室内出血(P < 0.001)。其中,本研究表明输血最重要的危险因素包括血红蛋白低于11.7 g/dL和年龄大于52岁。基于本研究结果,作者建议年龄大于52岁的血红蛋白低于11.7 g/dL和血红蛋白在11.7 - 14 g/dL之间的患者在颅内动脉瘤手术前应进行红细胞交叉配型,因为他们属于需要围手术期输血的高危人群。
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引用次数: 1
期刊
Survey of Anesthesiology
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