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切开复位钢板内固定与吊带治疗锁骨中段骨折:一项前瞻性随机研究方案。

Open reduction and plate fixation versus sling in treatment of mid-shaft fractures of clavicle: A prospective randomized study protocol.

机构信息

Department of Orthopedics, Yanbian University Hospital, Jilin, 133000.

Department of Radiology, Huizhou Central Municipal Hospital, Guangdong, 516001.

出版信息

Medicine (Baltimore). 2021 Jan 29;100(4):e23910. doi: 10.1097/MD.0000000000023910.

Abstract

BACKGROUND

For this prospective randomized clinical trial, it is implemented for the comparison of the outcomes of open reduction and internal fixation versus the sling treatment for mid-shaft clavicle fractures.

METHODS

We will evaluate the eligible patients diagnosed with the mid-shaft clavicle fractures in our hospital from December 2020 to December 2021. The outcomes acquired were reported in accordance with the guidelines of Consolidated Standards of Reporting Trials (CONSORT). Approval for this prospective randomized clinical trial was obtained from the institution alethics review committee of Wuzhong People's Hospital. The criteria for inclusion included: one third of clavicle fracture with at least 1 axial width displacement (Robinson type 2B2 or 2B1); agreed to take part in our research; over 18 years of age; patients with isolated clavicle fracture. While the criteria for exclusion contained: the medial or lateral segment clavicle fracture; open fracture; injuries related to neurovascular; over 21 days of changes from accident. The primary outcome was described as the evidence of nonunion at 1 year, which was defined as the intact bone bridge without X-ray fracture after more than 6 months. The secondary outcomes included the function of arm, overall health, adverse events, the satisfaction related to appearance, and pain.

CONCLUSIONS

It was hypothesized that in the case of clavicular comminuted mid-shaft fracture, for the open reduction and internal fixation, its nonunion rate was lower and satisfaction rate was higher, although there were a variety of complications.

TRIAL REGISTRATION

This study protocol was registered in Research Registry (researchregistry6295).

摘要

背景

本前瞻性随机临床试验旨在比较切开复位内固定与吊带治疗锁骨中段骨折的疗效。

方法

我们将评估 2020 年 12 月至 2021 年 12 月期间在我院诊断为锁骨中段骨折的合格患者。根据 CONSORT 报告标准报告获得的结果。本前瞻性随机临床试验获得了吴忠市人民医院机构伦理审查委员会的批准。纳入标准包括:至少有 1 个轴向宽度移位的三分之一锁骨骨折(Robinson 2B2 或 2B1 型);同意参加我们的研究;年龄超过 18 岁;单纯锁骨骨折。排除标准包括:锁骨内侧或外侧段骨折;开放性骨折;与神经血管相关的损伤;伤后超过 21 天。主要结局为 1 年时非愈合的证据,定义为 6 个月以上 X 线未见骨折的完整骨桥。次要结局包括手臂功能、总体健康状况、不良事件、与外观相关的满意度和疼痛。

结论

假设在粉碎性锁骨中段骨折的情况下,切开复位内固定的不愈合率较低,满意度较高,尽管存在多种并发症。

试验注册

本研究方案在 Research Registry(researchregistry6295)上注册。

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