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同种异体骨在脊柱手术中的应用:安全吗?

The use of allograft bone in spine surgery: is it safe?

作者信息

Mroz Thomas E, Joyce Michael J, Lieberman Isador H, Steinmetz Michael P, Benzel Edward C, Wang Jeffrey C

机构信息

Neuroscience Institute, Center for Spine Health, Cleveland Clinic, Cleveland, OH 44195, USA.

出版信息

Spine J. 2009 Apr;9(4):303-8. doi: 10.1016/j.spinee.2008.06.452. Epub 2008 Sep 19.

Abstract

BACKGROUND CONTEXT

Allograft bone is commonly used in various spinal surgeries. The large amount of recalled allograft tissue, particularly in recent years, has increased concerns regarding the safety of allograft bone for spinal surgery. An analysis of allograft recall and its safety in spinal surgery has not been reported previously.

PURPOSE

To determine 1) the number and types of allograft recall and the reasons for recall, 2) the types of disease transmission to spine patients, and 3) assess the safety of allograft bone in spinal surgery.

STUDY DESIGN/SETTING: Retrospective review.

METHODS

A retrospective review of all Food and Drug Administration (FDA) data from 1994 to June 2007 was reviewed to determine the amount and types of recalled allograft tissue. The literature and data from the Center for Disease Control were reviewed to determine the number and types of disease transmissions from allograft bone that have occurred to spine surgery patients during the study period.

RESULTS

There were 59,476 musculoskeletal allograft tissue specimens recalled by FDA during the study period, which accounts for 96.5% of all allograft tissue recalled in the United States. Improper donor evaluation, contamination, and recipient infections are the main reasons for allograft recall. There has been one case of human immunodeficiency virus infection transmission to a spine surgery patient in 1988. This is the only reported case of viral transmission. There are no reports of bacterial disease transmission from the use of allograft bone to spine surgery patients.

CONCLUSIONS

The precise number of allografts used in spine surgery annually and the precise incidence of disease transmission to spine surgery patients linked to the use of allograft tissue is unknown. Musculoskeletal allograft tissue accounts for the majority of recalled tissue by FDA. Despite the large number of allograft recalls in this country, there is only one documented case in the literature of disease transmission to a spine surgery patient. There appears to be no overt risk associated with the use of allograft bone in spine surgery. However, as discussed in this article, there are certain aspects regarding the use of allograft bone that should be considered.

摘要

背景信息

同种异体骨常用于各种脊柱手术。大量被召回的同种异体组织,尤其是近年来,增加了人们对脊柱手术中同种异体骨安全性的担忧。此前尚未有关于同种异体骨召回及其在脊柱手术中安全性的分析报告。

目的

确定1)同种异体骨召回的数量和类型以及召回原因,2)疾病传播至脊柱患者的类型,3)评估同种异体骨在脊柱手术中的安全性。

研究设计/地点:回顾性研究。

方法

对1994年至2007年6月期间美国食品药品监督管理局(FDA)的所有数据进行回顾性研究,以确定被召回的同种异体组织的数量和类型。查阅疾病控制中心的文献和数据,以确定研究期间同种异体骨传播至脊柱手术患者的疾病数量和类型。

结果

在研究期间,FDA召回了59476份肌肉骨骼同种异体组织标本,占美国召回的所有同种异体组织的96.5%。供体评估不当、污染和受体感染是同种异体骨召回的主要原因。1988年有1例人类免疫缺陷病毒感染传播给了一名脊柱手术患者。这是唯一报告的病毒传播病例。没有关于使用同种异体骨导致细菌疾病传播至脊柱手术患者的报告。

结论

每年用于脊柱手术的同种异体骨的确切数量以及与使用同种异体组织相关的疾病传播至脊柱手术患者的确切发生率尚不清楚。肌肉骨骼同种异体组织占FDA召回组织的大部分。尽管该国大量召回同种异体骨,但文献中仅有1例记录在案的疾病传播给脊柱手术患者的病例。在脊柱手术中使用同种异体骨似乎没有明显风险。然而,如本文所讨论的,在使用同种异体骨时应考虑某些方面。

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