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Perioperative Stroke Following Implantation of Left Ventricular Assist Device: A Retrospective Cohort Study 植入左心室辅助装置后围手术期卒中:一项回顾性队列研究。
IF 2.3 4区 医学 Q2 ANESTHESIOLOGY Pub Date : 2025-02-01 DOI: 10.1053/j.jvca.2024.11.025
Paul Yen MD , Terri Sun MD, MHSc, FRCPC , Jaycee Farmer MSc , Laura Besola MD , Anson Cheung MD, MSc, FRCSC , Defen Peng PhD , Wynne Chiu MSN, CCN(C) , Jamil Bashir MD, FRCSC , Dean Johnston MD, MHSc, FRCPC , Thalia Field MD, MHSc, FRCPC , Alana Flexman MD, MBA, FRCPC

Objectives

Stroke is common following left ventricular assist device (LVAD) implantation, although comprehensive data on perioperative strokes in this uncommon population is lacking. The current study aim was to characterize the presentation, features, and outcomes of perioperative cerebrovascular ischemia post-LVAD implantation at the authors’ institution.

Design

Single-center retrospective cohort.

Setting

St. Paul's Hospital, Vancouver, British Columbia, Canada.

Participants

Adult patients who received an LVAD between January 1, 2008, and August 31, 2021, were included, and those who died intraoperatively or underwent a concurrent cardiac surgical procedure were excluded.

Interventions

Data on demographics, comorbidities, stroke risk factors and characteristics, management, and outcomes (transplant, explant, death with LVAD in situ) were extracted.

Measurements and Main Results

After exclusions, 172 adult patients who underwent LVAD implantation during the study period were included and analyzed. The rate of perioperative stroke was 12.8% (22/172). Of these, 72.7% (16/22) had a stroke occur within 7 days of surgery, and 86.4% (19/22) had a primarily ischemic (v hemorrhagic) event. A total of 68.2% (15/22) were intubated, sedated, or recently extubated at symptom onset, complicating diagnosis. All were managed supportively or palliated without specific stroke intervention. Patients who experienced a perioperative stroke had a significantly lower cumulative incidence of survival to cardiac transplantation and a significantly higher cumulative incidence of dying with their device in situ.

Conclusions

LVAD patients carry a high risk of perioperative stroke. They experience delayed recognition and diagnosis, limited intervention, and poor outcomes. Frequent neurological assessment and a low threshold for neuroimaging are prudent.
目的:左心室辅助装置(LVAD)植入后卒中是常见的,尽管缺乏这一罕见人群围手术期卒中的综合数据。目前的研究目的是描述作者所在机构lvad植入后围手术期脑血管缺血的表现、特征和结果。设计:单中心回顾性队列。地点:加拿大不列颠哥伦比亚省温哥华圣保罗医院。参与者:纳入2008年1月1日至2021年8月31日期间接受LVAD的成年患者,排除术中死亡或同时接受心脏外科手术的患者。干预措施:提取了人口统计学、合并症、卒中危险因素和特征、管理和结果(移植、外植体、原位LVAD死亡)的数据。测量和主要结果:排除后,172例在研究期间接受LVAD植入的成年患者被纳入并分析。围手术期卒中发生率为12.8%(22/172)。其中,72.7%(16/22)的患者在手术后7天内发生中风,86.4%(19/22)的患者主要发生缺血性(出血性)事件。共有68.2%(15/22)的患者在症状发作时插管、镇静或最近拔管,使诊断复杂化。所有的治疗都是支持性的或缓和的,没有特定的卒中干预。围手术期卒中患者的心脏移植累积生存率明显较低,而心脏移植装置原位死亡的累积发生率明显较高。结论:LVAD患者围手术期卒中风险较高。他们的认识和诊断延迟,干预有限,结果不佳。频繁的神经学评估和较低的神经影像学阈值是谨慎的。
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引用次数: 0
Impella-Assisted Weaning from Cardiopulmonary Bypass After Left-Sided Valvular Surgery: An Echocardiographic Conundrum 左侧瓣膜手术后体外循环的叶轮辅助脱机:一个超声心动图难题。
IF 2.3 4区 医学 Q2 ANESTHESIOLOGY Pub Date : 2025-02-01 DOI: 10.1053/j.jvca.2024.11.029
Jordan Holloway MD, Cassidy Wernke DO, Manoj H. Iyer MD, Bryan Whitson MD, PhD, Michael Essandoh MD
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引用次数: 0
Use of Intraoperative Hemostatic Checklists for Blood Management in Patients Undergoing Cardiac Surgery: A Scoping Review 在心脏手术患者血液管理中使用术中止血检查表:一项范围审查。
IF 2.3 4区 医学 Q2 ANESTHESIOLOGY Pub Date : 2025-02-01 DOI: 10.1053/j.jvca.2024.11.028
Biobelemoye Irabor BScN, MD , Asha Kothari MD , Jonathan Hong MD, PhD , Bronte Chiang MLIS , David Kent MSc , Todd A. Duhamel PhD , Mofiyinfoluwa Lawal BSc, MSc , Mohammad El-Diasty MD, PhD , Rakesh C. Arora MD, PhD

Background

Using intraoperative hemostatic checklists may improve rates of surgical re-exploration and utilization of allogenic blood products in patients undergoing cardiac surgery. In this review, the authors explore the current evidence describing the impact of using intraoperative hemostatic checklists on reducing rates of surgical bleeding and perioperative blood product transfusion in this group of patients.

Methods

Following Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines, electronic information was obtained via sources that included Scopus, MEDLINE, EMBASE, and the Cochrane Library. Specifically, randomized controlled and observational studies reporting on hemostatic checklists in cardiac surgery were assessed for the following inclusion criteria: adult patients undergoing cardiac surgery, use of an intraoperative hemostatic checklist, a comparative study design, and full text available in the English language. All conference abstracts, editorials, and other reviews were excluded.

Results

A total of 3,022 articles were retrieved. Four articles, with 19,946 patients, were ultimately included in this review. These studies showed a significant reduction in bleeding re-exploration rates after implementing an intraoperative hemostatic checklist. In addition, three studies showed lower cost per patient, less blood product transfusion, and reduced intensive care unit stay after using checklists.

Conclusions

These findings suggest that using intraoperative hemostatic checklists may reduce surgical re-exploration rates and improve blood product utilization after cardiac surgery. Large multicenter studies are needed to endorse the utilization of these checklists in routine clinical practice.
背景:术中使用止血检查表可以提高心脏手术患者手术再探查率和异体血液制品的使用率。在这篇综述中,作者探讨了目前的证据,这些证据描述了在这组患者中使用术中止血检查表对降低手术出血和围手术期输血率的影响。方法:根据系统评价和荟萃分析指南的首选报告项目,通过Scopus、MEDLINE、EMBASE和Cochrane Library等来源获得电子信息。具体来说,随机对照和观察性研究报告了心脏手术中止血检查表的纳入标准:接受心脏手术的成年患者、术中止血检查表的使用、比较研究设计和英文全文。所有会议摘要、社论和其他综述均被排除在外。结果:共检索到3022篇文献。四篇文章,19946例患者最终被纳入本综述。这些研究表明,在实施术中止血检查表后,出血再探查率显著降低。此外,三项研究表明,使用清单后,每位患者的费用降低,血液制品输血减少,重症监护病房住院时间缩短。结论:术中使用止血清单可减少心脏手术后手术再探查率,提高血液制品利用率。需要大规模的多中心研究来支持这些检查表在常规临床实践中的应用。
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引用次数: 0
Prognostic Impact of Anemia and Blood Transfusions on Cardiovascular Outcomes in Patients Undergoing Vascular Surgery: A Scoping Review 贫血和输血对血管手术患者心血管预后的影响:范围界定综述。
IF 2.3 4区 医学 Q2 ANESTHESIOLOGY Pub Date : 2025-02-01 DOI: 10.1053/j.jvca.2024.10.033
Fulvio Nisi MD , Luca Ratibondi MD , Mattia Hagger MD , Enrico Giustiniano MD , Federico Piccioni MD , Giovanni Badalamenti MD , Sandro Lepidi MD , Mario D'Oria MD

Objective

Prior studies suggest an association of anemia and blood transfusion with increased morbidity and mortality in patients undergoing cardiac surgery. However, the impact of perioperative anemia and blood transfusion on clinical outcomes in patients undergoing major vascular surgery has been poorly defined yet. The primary objectives of this scoping review were to determine the extent of the evidence base that links anemia and blood transfusions to mortality and cardiovascular outcomes in patients undergoing major vascular surgery, and identify recurring themes or gaps in the literature to guide future research.

Methods

A scoping review of the literature from PubMed, Cochrane, and EMBASE databases was conducted up to December 2023 to identify articles related to the impact of anemia and blood transfusions on postoperative cardiovascular outcomes on patients undergoing vascular surgery. Methodology followed the PRISMA Protocols Extension for Scoping Reviews.

Results

Twenty-two articles met the inclusion criteria, including 15 retrospective and 6 observational prospective studies. Anemia definition varied across studies, mainly based on hemoglobin cut-off levels. An association with older age, coronary artery disease, hypertension, diabetes, and other comorbidities was reported. Particularly in peripheral and endovascular aortic surgery, anemia was linked consistently with higher mortality, major adverse cardiac events, and other postoperative complications, such as respiratory and renal issues, surgical site infections, and longer hospital stays, depending on hemoglobin levels. Anemia itself is an important predictor of transfusions. Transfusions in anemic patients were associated with increased mortality, postoperative complications, and increased need for major amputation.

Conclusions

The weight of the evidence suggests that anemia carries a substantial burden of cardiovascular complications, mortality, and multiorgan complications, resulting in increased health care costs. Peripheral and endovascular aortic surgery are affected deeply by the impact of anemia. Anemia itself stands out as a crucial predictor for requiring transfusions. In turn, the effect of transfusion of blood products is associated with worse outcomes and complications.
目的:先前的研究表明,贫血和输血与心脏手术患者发病率和死亡率的增加有关。然而,围术期贫血和输血对大血管手术患者临床预后的影响尚未明确。本次范围界定综述的主要目的是确定贫血和输血与接受大血管手术患者的死亡率和心血管预后有关的证据基础的程度,并找出文献中反复出现的主题或空白点,以指导未来的研究:对截至 2023 年 12 月的 PubMed、Cochrane 和 EMBASE 数据库中的文献进行了范围界定,以确定贫血和输血对血管手术患者术后心血管预后影响的相关文章。研究方法遵循了范围界定综述的 PRISMA 扩展协议:22篇文章符合纳入标准,其中包括15项回顾性研究和6项前瞻性观察研究。不同研究对贫血的定义各不相同,主要基于血红蛋白的临界水平。据报道,贫血与老年人、冠状动脉疾病、高血压、糖尿病和其他合并症有关。特别是在外周和血管内主动脉手术中,贫血与较高的死亡率、主要心脏不良事件和其他术后并发症(如呼吸系统和肾脏问题、手术部位感染和住院时间延长)有关,具体取决于血红蛋白水平。贫血本身是输血的一个重要预测因素。贫血患者输血与死亡率、术后并发症和大截肢需求增加有关:大量证据表明,贫血会导致心血管并发症、死亡率和多器官并发症,从而增加医疗费用。外周和血管内主动脉手术深受贫血的影响。贫血本身就是需要输血的一个重要预测因素。反过来,输注血液制品的影响与更差的预后和并发症有关。
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引用次数: 0
Venovenous or Venoarterial Extracorporeal Membrane Oxygenation for Pulmonary Hemorrhage? It Depends 肺出血采用静脉还是体外膜肺氧合?这取决于
IF 2.3 4区 医学 Q2 ANESTHESIOLOGY Pub Date : 2025-02-01 DOI: 10.1053/j.jvca.2024.11.026
Jamel Ortoleva MD, FASE, Dominic V. Pisano MD
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引用次数: 0
Swinging of the Pendulum: Should We Pursue Surgical Management Over Minimally Invasive Management of Atrial Fibrillation? 钟摆的摆动:心房颤动的手术治疗应优于微创治疗吗?
IF 2.3 4区 医学 Q2 ANESTHESIOLOGY Pub Date : 2025-02-01 DOI: 10.1053/j.jvca.2024.10.040
Kristin Constantine Trela MD, Mark A. Chaney MD, Richa Dhawan MD, MPH
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引用次数: 0
Expert Consensus on the Management of Pleural Drains After Pulmonary Lobectomy.
IF 2.3 4区 医学 Q2 ANESTHESIOLOGY Pub Date : 2025-01-31 DOI: 10.1053/j.jvca.2025.01.040
Javier H Campos, Lovkesh Arora
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引用次数: 0
Evaluation of Angiotensin II in Patients With Catecholamine-Resistant Vasodilatory Shock Requiring Continuous Renal Replacement Therapy (ANGEL CRRT).
IF 2.3 4区 医学 Q2 ANESTHESIOLOGY Pub Date : 2025-01-31 DOI: 10.1053/j.jvca.2025.01.042
Meaghan A Rettele, Adham M Mohamed, Timothy P Berry, Sydney S Wilson, Julie A Welge, Shelby S Shemanski, Rebecca L Shriver, Shais S Jallu, Michelle M Haines, Aaron J Douglas, Majdi S Hamarshi, Jonathan B Kozinn

Objective: To compare clinical outcomes of patients with catecholamine-resistant vasodilatory shock (CRVS) receiving continuous renal replacement therapy who receive adjunctive angiotensin II (ANGII) to those who do not.

Design: Retrospective cohort analysis.

Setting: Multicenter, single health system consisting of one academic medical center and four community hospitals.

Participants: Critically ill adult patients with CRVS (norepinephrine or equivalent dose ≥0.5 mcg/kg/min).

Interventions: Adjunctive ANGII versus standard-of-care (SOC) vasopressors alone (norepinephrine, epinephrine, vasopressin, phenylephrine, dopamine).

Measurements and main results: The primary outcome was intensive care unit mortality. Secondary outcomes included 30-day mortality, Sequential Organ Failure Assessment (SOFA) score at 72 hours, time to shock resolution, and adverse effects. A multivariate logistic regression was used for the primary analysis. The study included 265 patients, of which 70 received ANGII and 195 received SOC. Intensive care unit and 30-day mortality were lower in patients that received ANGII (61.4% v 75.4%, adjusted odds ratio 0.438, 95% confidence interval: 0.239-0.805, p = 0.008; and 67.1% v 78.5%, adjusted odds ratio 0.479, 95% confidence interval: 0.256-0.898, p = 0.022). Differences in time to shock reversal and SOFA score at 72 hours were not statistically significant. The adverse effects evaluated were not statistically significant, apart from an increase in fungal infections in the ANGII group (17.1% v 7.2%, p = 0.016).

Conclusions: ANGII was associated with lower mortality in patients who received renal replacement therapy compared to SOC. This evaluation reaffirms a subgroup of patients that may benefit from the addition of ANGII.

{"title":"Evaluation of Angiotensin II in Patients With Catecholamine-Resistant Vasodilatory Shock Requiring Continuous Renal Replacement Therapy (ANGEL CRRT).","authors":"Meaghan A Rettele, Adham M Mohamed, Timothy P Berry, Sydney S Wilson, Julie A Welge, Shelby S Shemanski, Rebecca L Shriver, Shais S Jallu, Michelle M Haines, Aaron J Douglas, Majdi S Hamarshi, Jonathan B Kozinn","doi":"10.1053/j.jvca.2025.01.042","DOIUrl":"https://doi.org/10.1053/j.jvca.2025.01.042","url":null,"abstract":"<p><strong>Objective: </strong>To compare clinical outcomes of patients with catecholamine-resistant vasodilatory shock (CRVS) receiving continuous renal replacement therapy who receive adjunctive angiotensin II (ANGII) to those who do not.</p><p><strong>Design: </strong>Retrospective cohort analysis.</p><p><strong>Setting: </strong>Multicenter, single health system consisting of one academic medical center and four community hospitals.</p><p><strong>Participants: </strong>Critically ill adult patients with CRVS (norepinephrine or equivalent dose ≥0.5 mcg/kg/min).</p><p><strong>Interventions: </strong>Adjunctive ANGII versus standard-of-care (SOC) vasopressors alone (norepinephrine, epinephrine, vasopressin, phenylephrine, dopamine).</p><p><strong>Measurements and main results: </strong>The primary outcome was intensive care unit mortality. Secondary outcomes included 30-day mortality, Sequential Organ Failure Assessment (SOFA) score at 72 hours, time to shock resolution, and adverse effects. A multivariate logistic regression was used for the primary analysis. The study included 265 patients, of which 70 received ANGII and 195 received SOC. Intensive care unit and 30-day mortality were lower in patients that received ANGII (61.4% v 75.4%, adjusted odds ratio 0.438, 95% confidence interval: 0.239-0.805, p = 0.008; and 67.1% v 78.5%, adjusted odds ratio 0.479, 95% confidence interval: 0.256-0.898, p = 0.022). Differences in time to shock reversal and SOFA score at 72 hours were not statistically significant. The adverse effects evaluated were not statistically significant, apart from an increase in fungal infections in the ANGII group (17.1% v 7.2%, p = 0.016).</p><p><strong>Conclusions: </strong>ANGII was associated with lower mortality in patients who received renal replacement therapy compared to SOC. This evaluation reaffirms a subgroup of patients that may benefit from the addition of ANGII.</p>","PeriodicalId":15176,"journal":{"name":"Journal of cardiothoracic and vascular anesthesia","volume":" ","pages":""},"PeriodicalIF":2.3,"publicationDate":"2025-01-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143501270","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Application of Alfentanil Combined With Dexmedetomidine for Conscious Sedation of Patients During Transesophageal Echocardiography Examination.
IF 2.3 4区 医学 Q2 ANESTHESIOLOGY Pub Date : 2025-01-30 DOI: 10.1053/j.jvca.2025.01.032
Yushan Huang, Xiang Zhao, Jiagao Wang, Zelong Zhuang, Bin Xiao, RanRan

Objectives: To investigate the efficacy and safety of combining alfentanil with dexmedetomidine for conscious sedation in outpatients undergoing transesophageal echocardiography (TEE).

Design: Prospective, randomized, double-blind clinical trial.

Setting: University-affiliated teaching hospital.

Participants: We recruited 80 patients scheduled to undergo transesophageal echocardiography examinations from May 2023 to July 2023.

Interventions: Eighty patients were randomly assigned into 2 groups, namely, the alfentanil + dexmedetomidine (AD) group (n = 40) and the oropharyngeal topical anesthesia with dyclonine + midazolam + dexmedetomidine (MD) group (n = 40).

Measurements and main results: Suppression of the patient's pharyngeal reflexes was assessed, and the hemodynamic parameters, along with the incidence of intraoperative adverse events, were also documented. The primary outcome was the initial sedation success rate, defined as achieving a pharyngeal reflex grade of less than 3, no excessive sedation (Ramsay sedation scores >4), and no serious adverse effects. This rate was significantly higher in the AD group (85%) compared with the MD group (35%) (p < .001). Compared with the MD group (47.5%), the incidence of hypotension in AD group (25.0%) decreased significantly (p < .05). Although the incidence of respiratory depression in AD group (42.5%) was higher than that in MD group (15.0%) (p < .01), no hypoxia and asphyxia occurred in either group. The recovery time of AD group (626.25 ± 295.80) was significantly shorter than that of MD group (768.33 ± 310.43) (p < .05). No serious complications occurred in either group.

Conclusions: Intravenous alfentanil combined with dexmedetomidine effectively inhibits pharyngeal reflexes and demonstrates a favorable safety profile, with fewer incidents of hypotension but a higher incidence of manageable respiratory depression compared with the MD protocol.

{"title":"Application of Alfentanil Combined With Dexmedetomidine for Conscious Sedation of Patients During Transesophageal Echocardiography Examination.","authors":"Yushan Huang, Xiang Zhao, Jiagao Wang, Zelong Zhuang, Bin Xiao, RanRan","doi":"10.1053/j.jvca.2025.01.032","DOIUrl":"https://doi.org/10.1053/j.jvca.2025.01.032","url":null,"abstract":"<p><strong>Objectives: </strong>To investigate the efficacy and safety of combining alfentanil with dexmedetomidine for conscious sedation in outpatients undergoing transesophageal echocardiography (TEE).</p><p><strong>Design: </strong>Prospective, randomized, double-blind clinical trial.</p><p><strong>Setting: </strong>University-affiliated teaching hospital.</p><p><strong>Participants: </strong>We recruited 80 patients scheduled to undergo transesophageal echocardiography examinations from May 2023 to July 2023.</p><p><strong>Interventions: </strong>Eighty patients were randomly assigned into 2 groups, namely, the alfentanil + dexmedetomidine (AD) group (n = 40) and the oropharyngeal topical anesthesia with dyclonine + midazolam + dexmedetomidine (MD) group (n = 40).</p><p><strong>Measurements and main results: </strong>Suppression of the patient's pharyngeal reflexes was assessed, and the hemodynamic parameters, along with the incidence of intraoperative adverse events, were also documented. The primary outcome was the initial sedation success rate, defined as achieving a pharyngeal reflex grade of less than 3, no excessive sedation (Ramsay sedation scores >4), and no serious adverse effects. This rate was significantly higher in the AD group (85%) compared with the MD group (35%) (p < .001). Compared with the MD group (47.5%), the incidence of hypotension in AD group (25.0%) decreased significantly (p < .05). Although the incidence of respiratory depression in AD group (42.5%) was higher than that in MD group (15.0%) (p < .01), no hypoxia and asphyxia occurred in either group. The recovery time of AD group (626.25 ± 295.80) was significantly shorter than that of MD group (768.33 ± 310.43) (p < .05). No serious complications occurred in either group.</p><p><strong>Conclusions: </strong>Intravenous alfentanil combined with dexmedetomidine effectively inhibits pharyngeal reflexes and demonstrates a favorable safety profile, with fewer incidents of hypotension but a higher incidence of manageable respiratory depression compared with the MD protocol.</p>","PeriodicalId":15176,"journal":{"name":"Journal of cardiothoracic and vascular anesthesia","volume":" ","pages":""},"PeriodicalIF":2.3,"publicationDate":"2025-01-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143449079","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Comparison of Perioperative Outcomes for Transfusion of Hemoconcentrated Bypass Versus Cell Saver Blood in Cardiac Surgical Patients.
IF 2.3 4区 医学 Q2 ANESTHESIOLOGY Pub Date : 2025-01-30 DOI: 10.1053/j.jvca.2025.01.035
Himani V Bhatt, Young Hu, Hung-Mo Lin, Natalia Egorova, Yuxia Ouyang, Matthew A Levin

Objective: Hemoconcentration and cell saver use are blood conservation techniques that are often used in cardiac surgery to salvage the patient's own blood to reduce autologous transfusion. The purpose of this study was to examine the perioperative outcomes including transfusion rates in cardiac surgical patients receiving hemoconcentrated blood versus cell saver blood via retrospective chart review. We hypothesized that hemoconcentration would have better patient outcomes, including reduced transfusion rates, compared to only cell salvage technique.

Design: Single-center, retrospective chart review case-control study SETTING: Cardiac operating room of a tertiary care center PARTICIPANTS: Patients over 18 years old who underwent elective open-heart surgery with cardiopulmonary bypass between January 2015 to January 2018. Patients for emergencies, off-pump cases, transplants, and reoperations and with a need for second bypass were excluded.

Interventions: None.

Measurements and main results: The specific outcomes assessed include perioperative transfusion of packed red blood cells and blood products, intensive care unit (ICU) length of stay, hospital length of stay, and surgical site infections. Patient characteristics such as ejection fraction and comorbidities, pulmonary hypertension, atrial fibrillation history, and coagulation dysfunction were also analyzed. Propensity score matching was done to balance the covariates between the groups. The differences for each outcome outlined above were calculated. Of the 744 observations, 735 were used for analysis after propensity matching. Postoperative ICU red blood cell transfusions recorded a mean difference of -0.37 (95% CI: -0.78, 0.04). Postoperative ICU platelets and fresh frozen plasma recorded mean differences of -0.01 (95% CI: -0.11, 0.09) and -0.08 (95% CI: -0.19, 0.03), respectively. There were no significant differences in outcomes in bivariate- and covariate-adjusted models.

Conclusions: There is no significant difference in postoperative blood transfusion rates in hemoconcentrated versus cell saver blood usage in cardiac surgery patients. Further studies are needed to analyze specific quantities and ratios of hemoconcentrated and cell saver blood used in these patients for a more clinically relevant analysis. This would allow incorporation of hemoconcentration and cell saver techniques into better blood conservation processes and guide overall transfusion strategies to reduce transfusion rates of blood and blood products in cardiac surgical patients.

{"title":"Comparison of Perioperative Outcomes for Transfusion of Hemoconcentrated Bypass Versus Cell Saver Blood in Cardiac Surgical Patients.","authors":"Himani V Bhatt, Young Hu, Hung-Mo Lin, Natalia Egorova, Yuxia Ouyang, Matthew A Levin","doi":"10.1053/j.jvca.2025.01.035","DOIUrl":"https://doi.org/10.1053/j.jvca.2025.01.035","url":null,"abstract":"<p><strong>Objective: </strong>Hemoconcentration and cell saver use are blood conservation techniques that are often used in cardiac surgery to salvage the patient's own blood to reduce autologous transfusion. The purpose of this study was to examine the perioperative outcomes including transfusion rates in cardiac surgical patients receiving hemoconcentrated blood versus cell saver blood via retrospective chart review. We hypothesized that hemoconcentration would have better patient outcomes, including reduced transfusion rates, compared to only cell salvage technique.</p><p><strong>Design: </strong>Single-center, retrospective chart review case-control study SETTING: Cardiac operating room of a tertiary care center PARTICIPANTS: Patients over 18 years old who underwent elective open-heart surgery with cardiopulmonary bypass between January 2015 to January 2018. Patients for emergencies, off-pump cases, transplants, and reoperations and with a need for second bypass were excluded.</p><p><strong>Interventions: </strong>None.</p><p><strong>Measurements and main results: </strong>The specific outcomes assessed include perioperative transfusion of packed red blood cells and blood products, intensive care unit (ICU) length of stay, hospital length of stay, and surgical site infections. Patient characteristics such as ejection fraction and comorbidities, pulmonary hypertension, atrial fibrillation history, and coagulation dysfunction were also analyzed. Propensity score matching was done to balance the covariates between the groups. The differences for each outcome outlined above were calculated. Of the 744 observations, 735 were used for analysis after propensity matching. Postoperative ICU red blood cell transfusions recorded a mean difference of -0.37 (95% CI: -0.78, 0.04). Postoperative ICU platelets and fresh frozen plasma recorded mean differences of -0.01 (95% CI: -0.11, 0.09) and -0.08 (95% CI: -0.19, 0.03), respectively. There were no significant differences in outcomes in bivariate- and covariate-adjusted models.</p><p><strong>Conclusions: </strong>There is no significant difference in postoperative blood transfusion rates in hemoconcentrated versus cell saver blood usage in cardiac surgery patients. Further studies are needed to analyze specific quantities and ratios of hemoconcentrated and cell saver blood used in these patients for a more clinically relevant analysis. This would allow incorporation of hemoconcentration and cell saver techniques into better blood conservation processes and guide overall transfusion strategies to reduce transfusion rates of blood and blood products in cardiac surgical patients.</p>","PeriodicalId":15176,"journal":{"name":"Journal of cardiothoracic and vascular anesthesia","volume":" ","pages":""},"PeriodicalIF":2.3,"publicationDate":"2025-01-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143472463","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Journal of cardiothoracic and vascular anesthesia
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