在儿童和成人脊柱手术中,术中细胞回收用于血液保护:一项最新的系统综述。

IF 1.8 Q3 CLINICAL NEUROLOGY
Spine deformity Pub Date : 2025-09-01 Epub Date: 2025-06-04 DOI:10.1007/s43390-025-01098-9
Grant Feuer, Prerana Katiyar, Justin L Reyes, Caroline Taber, Josephine R Coury, Fthimnir M Hassan, Joseph M Lombardi, Ahmed Shawky Abdelgawaad, Alan H Daniels, Lawrence G Lenke, Zeeshan M Sardar
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引用次数: 0

摘要

目的:本系统综述的目的是确定细胞保留在成人和儿童脊柱手术中的疗效。方法:对四个生物医学数据库进行全面系统的综述,以确定感兴趣的研究文章。来自原始研究的文章被汇编成这篇手稿。脊柱手术在美国和世界各地都变得越来越普遍。因此,脊柱外科医生通常使用多种方法来控制失血,包括术中降压、使用晶体和胶体液体复苏、抗纤溶剂、异体输血和自体输血。同种异体血液是手术期间维持血容量的常用方法,但存在输血反应、免疫抑制和病毒性血源性疾病传播等风险。自体血液制品,如术中细胞保存器或细胞挽救(CS),提供了一种返回患者自身血液的方法。然而,CS在这个时候仍然存在争议。一些研究发现它在避免同种异体输血方面是有效的,而另一些研究发现不使用CS的结果没有什么不同。一些研究甚至发现,接受CS的患者更有可能需要异体输血。本系统综述旨在检查所有可用的文献在脊柱手术中使用CS。结论:目前,CS在脊柱手术中的作用存在争议,研究报告的益处不一。许多文章认为,CS只有在出血量大、手术复杂的情况下才具有经济可行性。此外,关于成本效益的研究缺乏,并且由于地理因素而变得复杂。一项多中心大规模随机临床试验可能会导致一个模型的发展,其中CS的效用可以在一系列脊柱手术中进行评估,并可能导致指导方针的发展,推动CS在脊柱手术中使用的个性化方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intraoperative cell salvage utilization for blood conservation during pediatric and adult spinal surgery: a state-of-the-art systematic review.

Purpose: The purpose of this systematic review was to identify the efficacy of cell salvage in adult and pediatric spinal surgery.

Methods: A comprehensive systematic review of four biomedical databases was conducted to identify study articles of interest. Articles from original studies were compiled for the composition of this manuscript. Spinal surgery is becoming increasingly common in both the United States and around the world. As such, spine surgeons typically make use of many methods to manage blood loss including intra-operative hypotension, use of crystalloid and colloid fluid resuscitation, anti-fibrinolytics, allogenic blood transfusions, and autologous transfusions. Allogenic blood is a common method to maintain blood volume throughout surgery but carries risks including transfusion reactions, immunosuppression, and transmission of viral blood-borne illnesses. Autologous blood products, like intra-operative cell saver or cell salvage (CS), offer a way to return the patient's own blood. However, CS remains controversial at this time. Some studies have found it to be efficacious in avoiding allogenic transfusion, while others have found that the results are no different in those who did not utilize CS. Some studies have even found that those who receive CS are more likely to require allogenic transfusions. This systematic review seeks to examine all the available literature on the use of CS in spinal surgery.

Conclusion: Currently, the role of CS is controversial in spinal surgery with studies reporting variable benefit. Many articles suggest that CS is only financially viable at higher volumes of blood loss and in more complex surgeries. Moreover, research regarding cost-effectiveness is lacking and is complicated by geographic factors. A multi-center large-scale randomized clinical trial could lead to the development of a model wherein the utility of CS could be assessed across a range of spinal surgeries, and could lead to the development of guidelines driving an individualized approach to the use of CS in spine surgery.

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来源期刊
CiteScore
3.20
自引率
18.80%
发文量
167
期刊介绍: Spine Deformity the official journal of the?Scoliosis Research Society is a peer-refereed publication to disseminate knowledge on basic science and clinical research into the?etiology?biomechanics?treatment?methods and outcomes of all types of?spinal deformities. The international members of the Editorial Board provide a worldwide perspective for the journal's area of interest.The?journal?will enhance the mission of the Society which is to foster the optimal care of all patients with?spine?deformities worldwide. Articles published in?Spine Deformity?are Medline indexed in PubMed.? The journal publishes original articles in the form of clinical and basic research. Spine Deformity will only publish studies that have institutional review board (IRB) or similar ethics committee approval for human and animal studies and have strictly observed these guidelines. The minimum follow-up period for follow-up clinical studies is 24 months.
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