Abstract
Introduction
A novel virus, SARS-CoV-2 has caused a fatal global pandemic which particularly affects the elderly and those with co-morbidities. Hip fractures affect elderly populations, necessitate hospital admissions, and place this group at particular risk from COVID-19 infection. This study investigates the effect of COVID-19 infection on 30-day hip fracture mortality.
Method
Data related to seventy-five adult hip fractures admitted to two units during March and April 2020 was reviewed. The mean age was 83.5 years (range 65-98 years) and most (53, 70.7%) were females. The primary outcome measure was 30-day mortality associated with COVID-19 infection.
Results
The COVID-19 infection rate was 26.7% (20 patients), with a significant difference in the 30-day mortality rate in COVID-19 positive group (10/20, 50%) compared to COVID-19 negative group (4/55, 7.3%), with mean time to death of 19.8 days (95% confidence interval 17.0-22.5). The mean time from admission to surgery was 43.1 hours and 38.3 hours, in COVID-19 positive and COVID-19 negative groups, respectively. All COVID-19 positive patients had shown symptoms of fever and cough, and all ten cases who died were from hypoxia. Seven (35%) cases had radiological lung findings consistent with viral pneumonitis which resulted in mortality (70% of mortality). 30% (n = 6) contracted the COVID-19 infection in the community and 70% (n = 14) developed symptoms after hospital admission.
Conclusion
Hip fractures associated with COVID-19 infection have a high 30-day mortality. COVID-19 testing and chest x-ray for patients presenting with hip fractures, helps in early planning of high-risk surgeries and allows counselling of the patients and family using realistic prognosis.
Keywords: Hip fractures, COVID-19, 30-day mortality
Introduction
Recently, a novel virus, SARS-CoV-2 (COVID-19) originating in China at the end of 2019 has been the cause of a fatal global pandemic. At the time of writing, the death toll from COVID-19 infection in the UK has surpassed 30,000 and represents the highest record of national deaths in Europe.1 The overall estimates of COVID-19 death rate in the UK is 0.66% increasing to 7.8% in the population of over 80 years of age2; higher death rates have been reported in cases with underlying health conditions or those of older age.3,4 The virus spreads mainly via close contact and respiratory droplets that lead to a high transmission rate in groups in close contact such as hospitalised patients.5,6
Fragility hip fractures have an estimated incidence of 70,000 cases per year in the UK and are expected to reach 6.3 million world-wide by the year 2050.7,8 This injury affects elderly populations, necessitates hospital admission, and makes this group particularly prone to COVID-19 infection. Hip fracture itself is associated with increased mortality, and the risk of death tends to cluster in the first 30-days after injury, then decreases thereafter.9 The 30-day mortality rate ranges from 3.5%–10%,10,11 with the National Hip Fracture Database (NHFD) showing a UK 30-day mortality rate of 7%.12 Different predictors and risk factors of hip fractures 30-day mortality have been studied,13,14 however there is no published evidence on the effect of COVID-19 on hip fracture 30-day mortality. The aim of this study is to analyse the effect of COVID-19 infection on hip fracture 30-day mortality.
Methods
We retrospectively reviewed all adult hip fractures admitted to two units, in March 2020 and April 2020. Patients characteristics, the Nottingham Hip Fracture Score, the Charlson comorbidity index, and place of residence were recorded. COVID-19 was diagnosed according to the national and local guidelines using reverse transcriptase polymerase chain reaction (SARS-CoV-2 RdRp RT-PCR) of throat swap samples. All patients had received low molecular weight heparin (Enoxaparin sodium forty milligrams) daily to prevent thromboembolic events and underwent surgery when deemed safe following multi-disciplinary consultant review by orthopaedics, Care of the Elderly, and anaesthetics.
The primary outcome measure was 30-day mortality of hip fractures associated with COVID-19 infection; secondary outcome measures were, risk factors of 30-day mortality, medical complications, surgical complications, radiological appearance and laboratory results relating to diagnosis and treatment of COVID-19.
The hip fractures 30-day mortality associated with COVID-19 infection was assessed, but due to the small sample size, the analysis was limited to descriptive statistics to avoid Type I error.15 Kaplan-Meier test was used to present the trend of Survival and Cumulative hazard between groups. Statistical Package for Social Sciences (SPSS, version 24.0, IBM Co., Armonk, NY, USA) was used.
The study was authorized by the local ethical committee as part of the Clinical Effectivenessand Audit Department (registration number: 852), and was performed in accordance with the ethical standards of the 1964 Declaration of Helsinki as revised in 2000.
Results
Seventy-five patients presented with hip fractures during the study period (Table 1). The mean age was 83.5 years (range 65–98 years), and 53 were females (70.7%); all hip fractures were due to low velocity injury and three (4%) had associated injuries (one wrist and two humeral fractures). Twenty patients had COVID-19 infection (26.7%).
Table 1.
Characteristics of patients presented with hip fractures.
COVID-19 positive patients n = 20 | COVID-19 negative patients n = 55 | |
---|---|---|
Age (mean) | 83.7 years | 83.5 years |
Gender | ||
Female | 13 (65%) | 40 (72.7%) |
Mortality | ||
Yes | 10 (50%) | 4 (7.3%) |
Fracture classification | ||
Intra-capsular | 11 (55%) | 39 (71.9%) |
Extra-capsular | 9 (45%) | 16 (29.1%) |
Time from admission to surgery (mean) | 37.4 hours | 39.8 hours |
Operations | ||
Cemented hemiarthroplasty | 10 (50%) | 36 (65.5%) |
Uncemented hemiarthroplasty | 1 (5%) | 0 (0%) |
Dynamic hip screw | 6 (30%) | 11 (20%) |
Intra-medullary nail | 2 (10%) | 3 (5.5%) |
THR | 0 (0%) | 3 (5.4%) |
Conservative | 1 (5%) | 2 (3.6%) |
Type of anaesthesiaa | ||
Spinal | 8 (40%) | 27 (49.1%) |
General | 11 (55%) | 26 (47.3%) |
Complications | ||
Surgicalb | 1 (5%) | 0 |
Medicalc | 0 | 1 (1.8%) |
Nottingham hip fracture score (mean) | 6 | 5.5 |
Charlson co-morbidity index (mean) | 5.4 | 5.1 |
Place of residence | ||
Own home | 13 (65%) | 38 (69.1%) |
Institution | 7 (35%) | 17 (30.9%) |
THR: total hip replacement.
aThree patients were managed conservatively and did not need anaesthesia.
bPeriprosthetic fracture.
cMyocardial infarction.
There was a significant difference of mortality rate in the COVID-19 positive group (n = 10, 50%) compared to COVID-19 negative group (n = 4, 7.3%), with mean time to death of 19.8 days (95% confidence interval: 17.0–22.5 days, Figure 1). The mean time from admission to surgery was 43.1 hours and 38.3 hours in COVID-19 positive and COVID-19 negative groups, respectively. Six patients (30%) contracted the COVID-19 infection in the community and 14 (70%) developed symptoms after hospital admission 13/14 were tested positive post-operatively with mean time to confirmed infection of 12.6 days.
Figure 1.
The survivorship of hip fractures patients during the first 30-days post injury related to COVID-19 infection.
Two thirds of the cases had intra-capsular hip fracture and cemented hip hemiarthroplasty was the most common operation performed (Table 1); three patients were managed conservatively. The mean Nottingham hip fracture score was 5.6 (range 0–8), and the Charlson comorbidity index had a mean of 5.2 (range 0–9). One patient (1.3%) in the COVID-19 negative group had an acute myocardial infarction post-operatively which was the cause of death. The patient who underwent uncemented hip hemiarthroplasty (1.3%) had a periprosthetic fracture which was managed conservatively. Twenty-four (32%) patients were admitted from their own home and 51 (68%) case came from an institution.
The baseline laboratory results between the two groups are given in (Table 2); c-reactive protein and white cell count were higher in the COVID-19 positive group with a relative lymphopaenia.
Table 2.
Laboratory findings of patients presented with hip fractures.
COVID-19 positive patients n = 13 | COVID-19 negative patients n = 22 | |
---|---|---|
CRP | 46.7 | 33.7 |
WCC | 12.3 | 11.2 |
Lymphocytes count | 0.7 | 1.1 |
Pre-operative haemoglobin g/l | 119.1 | 121.1 |
Post-operative haemoglobin g/l | 100.5 | 102.1 |
Haemoglobin drop post-operative g/l | 18.4 | 18.9 |
CRP: C-reactive protein; WCC: White Cell Count (×109 cells/litre).
All COVID-19 positive cases had shown symptoms of fever and cough and received supplemental oxygen, and all ten who died were hypoxic; all 20 positive patients had undergone chest x-ray or/and chest computerised tomography (CT) to assess lung involvement, which showed seven (35%) cases had radiological lung findings of new pulmonary infiltrates, consistent with viral pneumonitis which resulted in mortality (70% of mortality, Figure 2). None of the ten survivors had features of viral pneumonitis on imaging and 7/20 (35%) received antibacterial therapy.
Figure 2.
Chest X ray: (a) at admission and (b) Eleven days post index procedure showing features of viral pneumonitis.
Discussion
This study presents the first evidence of high (50%) 30-day mortality in fragility hip fractures associated with COVID-19 infection. Recent estimates based on data from China predict an overall case fatality of 6.4% in those aged over 65 years and 13.4% in over 85 years group.2 A population-based study in the UK, including more than 3.8 million subjects, projects an estimate of 4.4% 1-year mortality rate in high risk groups.16 Further findings were an expected death rate of 9.7% in over 85 years of age without co-morbidities, which increases to 21.7% in those over 85 years and have more than three co-morbidities. The average time to death from admission was 19.8 days in our study. Similar findings have been reported from the Chinese mainland with mean time from disease onset to death of 17.8 days.2,17
The COVID-19 virus causes a two-phase immune response.18 The second phase, cytokine release syndrome (CRS) which develops after the first week, causes immune-mediated lung damage and/or multi-organ failure, and leads to death. CRS is mediated by leukocytes other than lymphocytes and this leads to leucocytosis associated with lymphopenia. In our study, COVID-19 positive patients had higher mean leukocyte counts and lower mean lymphocytes count compared to COVID-19 negative patients. Various studies have shown that surgery following trauma acts as a ‘‘second hit’’ and induces a strong proinflammatory response.19,20 We have postulated that in hip fractures associated with COVID-19 infection there are three potential hits, trauma, COVID-19 infection and surgery. Hip fracture surgery may act as a ‘‘third hit’’ that boost the hyper immune state caused by COVID-19 virus which may be a major factor in the increased mortality. A recently published trial involving 6425 patients has shown that the immunosuppressant dexamethasone significantly reduced the death rate in COVID-19 positive patients,21 supporting the theory of a hyperimmune reaction leading to higher mortality rates in COVID-19 patients.
We observed radiological evidence of viral pneumonitis in 35% of patients proven to be COVID-19 positive, all of whom died; interestingly, all COVID-19 positive survivors had normal chest x-rays, suggesting that CXR findings of viral pneumonitis could be an indicator of mortality. The main presenting symptoms in our study were cough and fever. Reports from China found that cough, fever and sore throat were the most common presenting feature of COVID-19 infection.22,23 Mi et al. studied ten patients who died due to COVID-19 associated with orthopaedic fractures, six of them presenting with hip fractures;24 60% of their patients had lymphopenia, similar to our findings.
Limitations
The limitations of this study include its retrospective nature, relatively small sample size, and potential confounders for mortality. To improve the sample size, data has been collected from two different units. Due to small sample size, we have not used statistical tests as it may result in false positive findings. However, our study reported a clinically important difference in the 30-day mortality between COVID-19 positive and COVID-19 negative hip fractures patients. We have postulated a ‘‘third hit’’ theory, however, further research will be needed to assess the immune response before and after surgery in hip fractures associated with COVID-19 infection.
Conclusion
On the basis of our study, hip fractures associated with COVID-19 infection have a high 30-day mortality. Whilst we suggest that mortality is greater in the COVID positive group, the numbers are very small in comparison to other recent published works on the topic in which over 6000 patients are included. Our findings may just be chance but we believe they are suggestive of a higher mortality when set against contemporary practices seen in the fight against the virus. Delayed surgery or conservative treatment can be adopted to avoid the ‘‘third hit’’. We have adopted a protocol of COVID-19 testing and CXR, for all patients presenting with hip fractures in our unit. This helps in risk stratification and early planning of high-risk surgeries and allows counselling of the patients and family using realistic prognosis. This study should open a door for nation-wide studies of COVID-19 virus effect on hip fractures.
Acknowledgements
None.
Contributorship: All the authors participated in the planning and design of the study, interpretation of the results, and preparation of the manuscript.
Declaration of conflicting interests: The author(s) declared no conflict of interest with regards to the research, authorship, and/or publication of this article.
Ethical approval: The study was authorized by the local ethical committee as part of the Clinical Effectiveness and Audit Department (registration number: 852).
Funding: The author(s) received no financial support for the research, authorship, and/or publication of this article.
Guarantor: AF.
Informed consent: Informed consent was not sought for the present study because the data for this study was collected retrospectively and anonymously.
Provenance and peer review: Not commissioned, externally peer reviewed.
ORCID iD
Ahmed Fadulelmola https://orcid.org/0000-0001-8565-3147
References
- 1.Coronavirus (COVID-19) roundup – Office for National Statistics, www.ons.gov.uk/peoplepopulationandcommunity/healthandsocialcare/conditionsanddiseases/articles/coronaviruscovid19roundup/2020-03-26 (accessed 8 May 2020).
- 2.Verity R, Okell LC, Dorigatti I, et al. Estimates of the severity of coronavirus disease 2019: a model-based analysis. Lancet Infect Dis 2020; 20: 669–677. [DOI] [PMC free article] [PubMed]
- 3.World Health Organization, www.who.int/news-room/detail/30-01-2020-statement-on-the-second-meeting-of-the-international-health-regulations-(2005)-emergency-committee-regarding-the-outbreak-of-novel-coronavirus-(2019-ncov) (2020, accessed 29 April 2020).
- 4.Onder G, Rezza G, Brusaferro S. Case-fatality rate and characteristics of patients dying in relation to COVID-19 in Italy. JAMA 2020; 323: 1775–1776. [DOI] [PubMed]
- 5.Shereen M, Khan S, Kazmi A, et al. COVID-19 infection: origin, transmission, and characteristics of human coronaviruses. J Adv Res 2020; 24: 91–98. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Rothe C, Schunk M, Sothmann P, et al. Transmission of 2019-nCoV infection from an asymptomatic contact in Germany. N Engl J Med 2020; 382: 970–971. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Gulleberg B, Johnell O, Kanis JA. Worldwide projections for hip fracture. Oteoprosos Int 1997; 7: 407–413. [DOI] [PubMed] [Google Scholar]
- 8.Parker M, Johansen A. Hip fracture. BMJ 2006; 333: 27–30. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Khan MA, Hossain FS, Ahmed I, et al. Predictors of early mortality after hip fracture surgery. Int Orthop (SICOT) 2013; 37: 2119–2124. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Daugaard CL, Jørgensen HL, Riis T, et al. Is mortality after hip fracture associated with surgical delay or admission during weekends and public holidays? A retrospective study of 38,020 patients. Acta Orthop 2012; 83: 609–613. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Carretta E, Bochicchio V, Rucci P, et al. Hip fracture: effectiveness of early surgery to prevent 30-day mortality. Int Orthop 2011; 35: 419–424. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Nhfd.co.uk, www.nhfd.co.uk/files/2019ReportFiles/NHFD_2019_Annual_Report_v101.pdf (2020, accessed 4 May 2020).
- 13.Tsang C, Boulton C, Burgon V, et al. Predicting 30-day mortality after hip fracture surgery. Bone Joint Res 2017; 6: 550–556. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Karres J, Kieviet N, Eerenberg J-P, et al. Predicting early mortality after hip fracture surgery. J Orthop Trauma 2018; 32: 27–33. [DOI] [PubMed] [Google Scholar]
- 15.Kim H. Statistical notes for clinical researchers: type I and type II errors in statistical decision. Restor Dent Endod 2015; 40: 249–252. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Banerjee A, Pasea L, Harris S, et al. Estimating excess 1-year mortality associated with the COVID-19 pandemic according to underlying conditions and age: a population-based cohort study. Lancet 2020; 395: 1715–1725. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17.World Health Organisation. Report of the WHO-China Joint Mission on coronavirus disease, www.who.int/publications-detail/report-of-the-who-china-joint-mission-oncoronavirus-disease-2019-(COVID-19) (2020, accessed 6 May 2020).
- 18.Shi Y, Wang Y, Shao C, et al. COVID-19 infection: the perspectives on immune responses. Cell Death Differ 2020; 27: 1451–1454. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Tschoeke S, Hellmuth M, Hostmann A, et al. The early second hit in trauma management augments the proinflammatory immune response to multiple injuries. J Trauma 2007; 62: 1396–1404. [DOI] [PubMed] [Google Scholar]
- 20.Moore FA, Moore EE. Concepts in the pathogenesis of postinjury multiple organ failure. Surg Clin North Am 1995; 75: 257–277. [DOI] [PubMed] [Google Scholar]
- 21.Chen N, Zhou M, Dong X, et al. Epidemiological and clinical characteristics of 99 cases of 2019 novel coronavirus pneumonia in Wuhan, China: a descriptive study. Lancet 2020; 395: 507–513. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Recoverytrial.net, www.recoverytrial.net/files/recovery_dexamethasone_statement_160620_final.pdf (2020, accessed 20 June 2020).
- 23.Guan WJ, Ni ZY, Hu Y, et al. Clinical characteristics of coronavirus disease 2019 in China. N Engl J Med 2020; 382: 1708–1720. [DOI] [PMC free article] [PubMed]
- 24.Mi B, Chen L, Xiong Y, et al. Characteristics and early prognosis of COVID-19 infection in fracture patients. J Bone Joint Surg 2020; 102: 750–758. [DOI] [PMC free article] [PubMed] [Google Scholar]