24 小时内为抗凝髋部骨折患者提供早期手术护理

IF 2.2 3区 医学 Q3 CRITICAL CARE MEDICINE Injury-International Journal of the Care of the Injured Pub Date : 2024-09-28 DOI:10.1016/j.injury.2024.111924
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引用次数: 0

摘要

导言:髋部骨折的发病率和死亡率仍然很高。尽管国际指南提倡紧急手术治疗,但往往会出现延误,尤其是长期接受抗血栓治疗的患者。我们假设,为抗凝髋部骨折患者提供紧急手术治疗与严重出血并发症无关。材料与方法在 2015 年至 2021 年期间,我们回顾性地查看了 1142 名股骨近端骨折患者在入院后 24 小时内接受治疗的临床记录(平均年龄为 80.4 ± 12.4 岁;女性 761 人,男性 381 人)。队列中包括409例股骨颈骨折和733例转子间骨折,采用关节置换术(297例)、保髋技术(147例)或髓内钉(698例)进行治疗。其中,583 名患者(51.1%)接受了长期抗血栓治疗。主要终点包括输血率和术前与术后血红蛋白(Hb)水平的差异。次要终点是住院死亡率和术后血肿发生率,这些血肿需要进行手术修补。结果平均手术时间为 10.3 小时,使用直接口服抗凝剂 (DOAC) 的患者手术时间有所延迟。总体而言,25.9%(n = 296)的患者需要输血。输血率取决于手术持续时间、术前 Hb 水平和 DOAC 抗凝情况。同样,Hb 差异也与手术时间、术前 Hb 水平和 DOAC 抗凝有关。住院患者死亡率为 5.3%(n = 60)。回归分析表明,死亡率与 ASA 分级 4 级和手术时间有关,但与抗血栓治疗的类型无关。3.1%的患者因术后血肿需要手术翻修,手术时间延长和抗血栓治疗(PAI [OR = 3.7, 95 % CI: 1.1-12.7], DOACs [OR = 3.4, 95 % CI: 1.3-8.8], and VKA [OR = 5.5, 95 % CI: 1.8-17.1], p < 0.结论 由于术后血肿和输血需要是可以控制的情况,我们得出结论,在 24 小时内对接受长期抗血栓治疗的髋部骨折患者立即进行手术治疗是可行的,患者也可能从中获益。
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Early surgical care of the anticoagulated hip fracture patient within 24 hours

Introduction

Hip fractures are still associated with high morbidity and mortality. Despite international guidelines advocating for urgent surgical treatment, delays often occur, particularly for patients on long-term antithrombotic therapy. We hypothesised that urgent surgical care for the anticoagulated hip fracture patient is not associated with severe bleeding complications.

Material and Methods

For the period from 2015 to 2021, we retrospectively reviewed clinical records of 1142 patients with proximal femur fractures treated within 24 h of admission to our trauma centre (mean age 80.4 ± 12.4 years; 761 females, 381 males). The cohort comprised 409 femoral neck and 733 trochanteric fractures, managed with either arthroplasty (n = 297), hip-preserving techniques (n = 147), or intramedullary nailing (n = 698). Of these, 583 patients (51.1 %) were on long-term antithrombotic therapy. The primary endpoints included transfusion rate and the difference in haemoglobin (Hb) levels from pre- to postoperative. Secondary endpoints were in-patient mortality and occurrence of postoperative haematomas requiring surgical revision. A regression analysis was performed.

Results

The mean time to surgery was 10.3 h, with delays observed in patients on direct oral anticoagulants (DOACs). Overall, 25.9 % (n = 296) of the patients required blood transfusions. The transfusion rate was dependent on duration of the surgery, preoperative Hb level, and anticoagulation with DOACs. Similarly, the Hb difference was found to be dependent on the duration of surgery, preoperative Hb level, and anticoagulation with DOACs. In-patient mortality was 5.3 % (n = 60). Regression analysis indicated that mortality was dependent on a high ASA classification of 4 and the time to surgery, but not on the type of antithrombotic therapy. 3.1 % of the patients needed surgical revision due to postoperative haematoma with prolonged duration of surgery and antithrombotic therapy (PAI [OR = 3.7, 95 % CI: 1.1–12.7], DOACs [OR = 3.4, 95 % CI: 1.3–8.8], and VKA [OR = 5.5, 95 % CI: 1.8–17.1], p < 0.05) as independent risk factors.

Conclusion

As postoperative haematoma and the need for transfusion are manageable situations, we conclude that immediate surgical treatment of hip fracture patients on long-term antithrombotic therapy within 24 h is feasible and patients may benefit.
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来源期刊
CiteScore
4.00
自引率
8.00%
发文量
699
审稿时长
96 days
期刊介绍: Injury was founded in 1969 and is an international journal dealing with all aspects of trauma care and accident surgery. Our primary aim is to facilitate the exchange of ideas, techniques and information among all members of the trauma team.
期刊最新文献
Editorial Board Fracture-related infection blood-based biomarkers: Diagnostic strategies The value of current diagnostic techniques in the diagnosis of fracture-related infections: Serum markers, histology, and cultures Antimicrobial resistance: Biofilms, small colony variants, and intracellular bacteria In vivo models of infection: Large animals – Mini review on human-scale one-stage revision in a porcine osteomyelitis model
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