微创牵引复位器与传统手动牵引治疗胫骨骨折:中国某三级医院的比较研究

IF 2.8 3区 医学 Q1 Pharmacology, Toxicology and Pharmaceutics
Therapeutics and Clinical Risk Management Pub Date : 2022-09-23 eCollection Date: 2022-01-01 DOI:10.2147/TCRM.S379135
Junpu Zha, Guolei Zhang, Xiaoqing Wang, Jie Li, Jun Di, Junfei Guo
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引用次数: 0

摘要

背景:胫骨骨折的闭合复位和髓内钉固定可能不需要骨折台或复位辅助设备,如股骨牵引器,只有手动牵引才能帮助复位过程。本研究旨在描述并进一步研究原始设计的微创牵引复位器(MITR)治疗胫骨骨折的有效性。方法:2018年1月至2021年4月,共纳入119例符合条件的胫骨干骨折患者,并根据复位方法的不同回顾性分为MITR组和常规手动牵引(CMT)组。两组患者的年龄、性别、BMI、居住地、吸烟史、饮酒史、损伤机制、骨折类型、ASA、麻醉方式、手术延迟等基线特征具有可比性(均P > 0.05)。比较手术时间、骨折复位时间、术中出血量、透视时间、术中透视次数、VAS、HSS、骨折愈合时间、并发症。结果:所有患者均完成随访,平均18.5个月(12-42个月)。MITR组手术时间、骨折复位时间、术中出血量、透视时间、透视次数均显著减少(P < 0.05)。术后1个月,MITR组VAS评分(1.8±0.8)低于CMT组(2.6±1.5)。术后6个月,MITR组HHS评分(90.8±2.3)高于CMT组(86.4±3.8)。两组平均骨折愈合时间、骨不连、种植体失败、感染情况比较,差异均无统计学意义(P > 0.05)。结论:与CMT相比,MITR有利于胫骨骨折的微创治疗,且在手术时间、骨折复位时间、术中出血量、透视时间、透视次数、VAS和HSS评分满意等方面具有优势。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Use of a Minimally Invasive Traction Repositor versus Conventional Manual Traction for the Treatment of Tibial Fractures: A Comparative Study from a Tertiary Hospital in China.

Use of a Minimally Invasive Traction Repositor versus Conventional Manual Traction for the Treatment of Tibial Fractures: A Comparative Study from a Tertiary Hospital in China.

Use of a Minimally Invasive Traction Repositor versus Conventional Manual Traction for the Treatment of Tibial Fractures: A Comparative Study from a Tertiary Hospital in China.

Use of a Minimally Invasive Traction Repositor versus Conventional Manual Traction for the Treatment of Tibial Fractures: A Comparative Study from a Tertiary Hospital in China.

Background: Closed reduction and intramedullary nail fixation of tibial fractures may not utilize a fracture table or reduction aids like a femoral distractor, and only manual traction will help aid the reduction process. This study aimed to describe and further investigate the effectiveness of an originally designed minimally invasive traction repositor (MITR) for the treatment of tibial fractures.

Methods: From January 2018 to April 2021, a total of 119 eligible patients with tibial shaft fractures were included and retrospectively assigned to two groups according to different reduction methods: MITR group vs conventional manual traction (CMT) group. The baseline characteristics between the two groups were comparable, including age, gender, BMI, residence, smoking history, drinking history, injury mechanism, fracture type, ASA, method of anesthesia, and surgical delay (all P > 0.05). The operation time, fracture reduction duration, intraoperative blood loss, fluoroscopy time, number of intraoperative fluoroscopies, VAS, HSS, fracture healing time, and complications were compared.

Results: All patients completed the follow-ups with an average of 18.5 months (range 12-42 months). The operation time, fracture reduction duration, intraoperative blood loss, fluoroscopy time, and number of fluoroscopies were significantly decreased in the MITR group (all P < 0.05). At one month postoperatively, the VAS score was statistically lower in the MITR group (1.8±0.8) than in the CMT group (2.6±1.5). At 6 months postoperatively, the HHS score was statistically higher in the MITR group (90.8±2.3) than in the CMT group (86.4±3.8). We observed no statistical difference in the mean fracture healing time, bone nonunion, implant failure, and infection between the two groups (all P > 0.05).

Conclusion: Compared with CMT, MITR facilitates the minimally invasive treatment of tibial fractures and has the advantages of operation time, fracture reduction duration, intraoperative blood loss, fluoroscopy time, number of fluoroscopies, and satisfactory VAS and HSS scores.

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来源期刊
Therapeutics and Clinical Risk Management
Therapeutics and Clinical Risk Management HEALTH CARE SCIENCES & SERVICES-
CiteScore
5.30
自引率
3.60%
发文量
139
审稿时长
16 weeks
期刊介绍: Therapeutics and Clinical Risk Management is an international, peer-reviewed journal of clinical therapeutics and risk management, focusing on concise rapid reporting of clinical studies in all therapeutic areas, outcomes, safety, and programs for the effective, safe, and sustained use of medicines, therapeutic and surgical interventions in all clinical areas. The journal welcomes submissions covering original research, clinical and epidemiological studies, reviews, guidelines, expert opinion and commentary. The journal will consider case reports but only if they make a valuable and original contribution to the literature. As of 18th March 2019, Therapeutics and Clinical Risk Management will no longer consider meta-analyses for publication. The journal does not accept study protocols, animal-based or cell line-based studies.
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