Jagadeesh Nuthan, Deva Venkatesh, Kapadi Sachindra, Shaw Debbie
Trauma and Orthopaedics, Wrightington, Wigan and Leigh NHS Foundation Trust, Wigan, GBR.
Trauma and Orthopaedics, Royal Infirmary of Edinburgh, Edinburgh, GBR.
Cureus. 2022 Dec 17;14(12):e32637. doi: 10.7759/cureus.32637. eCollection 2022 Dec.
Background Hip fractures cause substantial morbidity and mortality worldwide, and the coronavirus disease 2019 (COVID-19) pandemic has only worsened the global burden. Increased 120-day mortality is well established in the literature among hip fractures with COVID-19. However, the risk factors associated with mortality have been poorly understood. We aimed to determine the risk factors associated with increased 120-day mortality among hip fractures with COVID-19. Methods Seventy patients with hip fractures with confirmed COVID-19 infection between March 2020 and December 2021 were included. Thirty-three patients who died within 120 days of admission were allotted to the non-survivor group and the rest 37 patients were allotted to the survivor group. Various parameters such as demographic variables, Nottingham Hip Fracture Score (NHFS), Charlson Comorbidity Index (CCI), American Society of Anesthesiologists (ASA), Abbreviated Mental Score Test (AMTS), National Early Warning Score (NEWS), fracture type, operation type, and delay in surgery were compared between the groups to determine the risk factors for increased mortality. Multivariate regression analysis was performed to know the independent association with increased mortality. Results A total of 33 patients died within 120 days giving the 120-day mortality rate of 47.1%. Baseline parameters such as ASA, AMTS on admission, NEWS on admission, and type of residence did not significantly affect mortality. The mean NHFS was significantly high in non-survivors (5.38 ± 1.52) compared to survivors (4.40 ± 1.75) (p < 0.001). Similarly, mean CCI was also significantly high in non-survivors (5.58 ± 1.74) compared to survivors (4.76 ± 2.29) (p < 0.001). A total of 70% (seven out of 10) of patients with delayed surgery of more than 36 hours from the admission died within 120 days of admission (p < 0.001). Mortality was significantly higher in patients who underwent internal fixation of fractures like a dynamic hip screw (DHS) or intramedullary (IM) nailing than in those who underwent hemiarthroplasty or total hip arthroplasty (THA). Post-operative parameters such as early mobilization and the multidisciplinary approach to review these patients made no difference to the mortality. Multivariate regression analysis of the parameters that made a significant difference in the mortality showed that delay in surgery and type of surgery (internal fixation) independently increased the mortality among these patients (p < 0.001). However, NHFS and CCI were not independently affecting the mortality among hip fractures with concomitant COVID-19. Conclusion The 120-day mortality rate among patients with hip fractures with concomitant COVID-19 was 47.1%. Delay in surgery of more than 36 hours and patients who underwent internal fixation were independent risk factors associated with increased mortality among these patients.
髋部骨折在全球范围内导致了大量的发病和死亡,而2019年冠状病毒病(COVID-19)大流行只会加剧全球负担。COVID-19相关髋部骨折患者120天死亡率增加在文献中已有充分证实。然而,与死亡率相关的危险因素一直未得到充分了解。我们旨在确定COVID-19相关髋部骨折患者120天死亡率增加的危险因素。方法:纳入2020年3月至2021年12月期间确诊为COVID-19感染的70例髋部骨折患者。将入院后120天内死亡的33例患者分配至非存活组,其余37例患者分配至存活组。比较两组之间的各种参数,如人口统计学变量、诺丁汉髋部骨折评分(NHFS)、查尔森合并症指数(CCI)、美国麻醉医师协会(ASA)、简易精神状态检查表(AMTS)、国家早期预警评分(NEWS)、骨折类型、手术类型和手术延迟情况,以确定死亡率增加的危险因素。进行多变量回归分析以了解与死亡率增加的独立关联。结果:共有33例患者在120天内死亡,120天死亡率为47.1%。基线参数如ASA、入院时的AMTS、入院时的NEWS和居住类型对死亡率没有显著影响。与存活组(4.40±1.75)相比,非存活组的平均NHFS显著更高(5.38±1.52)(p<0.001)。同样,与存活组(4.76±2.29)相比,非存活组的平均CCI也显著更高(5.58±1.74)(p<0.001)。入院后手术延迟超过36小时的患者中有70%(10例中的7例)在入院后120天内死亡(p<0.001)。接受动力髋螺钉(DHS)或髓内(IM)钉等骨折内固定的患者死亡率显著高于接受半髋关节置换术或全髋关节置换术(THA)的患者。术后参数如早期活动和对这些患者的多学科评估方法对死亡率没有影响。对死亡率有显著差异的参数进行多变量回归分析表明,手术延迟和手术类型(内固定)独立增加了这些患者的死亡率(p<0.001)。然而,NHFS和CCI并不是COVID-19合并髋部骨折患者死亡率的独立影响因素。结论:COVID-19合并髋部骨折患者的120天死亡率为47.1%。手术延迟超过36小时和接受内固定手术的患者是这些患者死亡率增加的独立危险因素。