Sabzevari Soheil, Boateng Bernadelle, Lavery Jessica A, Bartelstein Meredith K
Department of Surgery, Orthopaedic Service, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Arch Bone Jt Surg. 2024;12(9):645-651. doi: 10.22038/ABJS.2024.75222.3478.
To investigate whether patients with impending or completed fracture of the proximal femur who were treated with bevacizumab in the six weeks prior to surgery are at higher risk of surgical complications than patients given bevacizumab outside of the six-week period.
We retrospectively reviewed cases of hip fracture treated between 1995 and 2020 at our institution. Patients were included if they were age 18 years or older, underwent hip surgery for impending or completed fracture, and received bevacizumab preoperatively but not postoperatively. Charts were reviewed for demographic, surgical, and postoperative details. A Cox model was applied to assess whether the timing of preoperative bevacizumab administration (≤6 weeks vs. >6 weeks) was associated with the risk of a postoperative complication.
Two of the 23 patients who received bevacizumab ≤6 weeks before surgery experienced complications (deep vein thrombosis [n=1] and intraoperative fracture related to progression of disease [n=1]). Of the 53 patients who received bevacizumab more than six weeks preoperatively, five experienced complications (wound drainage [n=2] and deep vein thrombosis [n=3]). In the Cox model, timing of bevacizumab was not associated with postoperative complications (univariable hazard ratio, 0.92; 95% confidence interval, 0.18-4.73).
In this cohort of patients who underwent surgery for hip fractures, we did not observe an increased risk of postoperative complications among those who received bevacizumab within six weeks of surgery relative to those who received bevacizumab more than six weeks before surgery. The retrospective nature of the study and small sample size are limiting factors in this study.
探讨在手术前六周内接受贝伐单抗治疗的股骨近端即将发生骨折或已完成骨折的患者,与在六周期限之外接受贝伐单抗治疗的患者相比,是否有更高的手术并发症风险。
我们回顾性分析了1995年至2020年在我院接受治疗的髋部骨折病例。纳入标准为年龄18岁及以上、因即将发生或已完成的骨折接受髋部手术、术前接受贝伐单抗治疗但术后未接受治疗的患者。查阅病历以获取人口统计学、手术和术后详细信息。应用Cox模型评估术前贝伐单抗给药时间(≤6周与>6周)是否与术后并发症风险相关。
在术前≤6周接受贝伐单抗治疗的23例患者中,有2例出现并发症(深静脉血栓形成[n = 1]和与疾病进展相关的术中骨折[n = 1])。在术前六周以上接受贝伐单抗治疗的53例患者中,有5例出现并发症(伤口引流[n = 2]和深静脉血栓形成[n = 3])。在Cox模型中,贝伐单抗给药时间与术后并发症无关(单变量风险比,0.92;95%置信区间,0.18 - 4.73)。
在这组接受髋部骨折手术的患者中,我们未观察到在手术六周内接受贝伐单抗治疗的患者相对于在手术六周前以上接受贝伐单抗治疗的患者术后并发症风险增加。本研究的回顾性性质和小样本量是本研究的限制因素。