Abstract
Introduction:
It is crucial to be aware of post-COVID-19 non-pulmonary complications. Avascular necrosis (AVN) is one of these complications. It should be noted that the risk of AVN persists in individuals who have recovered from the COVID-19 infection. The current study aims to report several cases of AVN after being infected with SARS-CoV-2.
Materials and methods:
This is a single-centre retrospective case series conducted over a 2-year period (January 2021–December 2022) involving individuals who developed AVN after being infected with COVID-19.
Result:
The study included a total of 17 patients. The mean age of patients was 38.65±6.1 years. Twelve of them were male (70.6%) and five were female (29.4%), with a ratio of 3:1. The mean BMI of the patients was 28.3±2.4 kg/m2. Eleven (64.7%) patients reported administering steroid injections throughout the infection course. The mean interval between COVID-19 infection and presentation to the clinic was 6.53 months. The majority of patients (82.3%) complained of bilateral hip pain. Limping was observed in 47% of the cases. MRI showed AVN in all cases. Bilateral core decompression was performed in five cases (29.4%), total hip replacement in three cases (17.6%), and conservative treatment in nine cases (53%).
Conclusion:
The ongoing pandemic may have many long-term sequelae. There is a risk of developing AVN after COVID-19.
Keywords: Avascular necrosis, Osteonecrosis, post-COVID-19 complications, SARS-CoV-2, Post-COVID-19 syndrome
Introduction
Highlights
It is crucial to be aware of post-COVID-19 non-pulmonary complications.
There is a risk of developing avascular necrosis after COVID-19.
The current study aims to report several cases of avascular necrosis after being infected with SARS-CoV-2.
The COVID-19 emerged as the SARS-CoV-2, which was initially discovered in December 2019 in Wuhan, China. It rapidly expanded and developed into a pandemic illness1,2. SARS-CoV-2 binds more efficiently to the angiotensin-converting enzyme 2 receptor found in human glial cells, neurons, respiratory epithelial cells, and vascular endothelial cells3. Increasing evidence suggests that, while many patients are recovering from COVID-19, it has a negative impact on several human body systems as part of post-COVID-19 syndrome. The cardiopulmonary system appears to account for the majority of post-COVID-19 complications. Myocarditis, arrhythmia, and ischaemia are among the cardiac post-COVID-19 complications, whereas bacterial pneumonia, pneumothorax, and pleural effusion are among the most prevalent pulmonary complications4. It is crucial to be aware of non-pulmonary complications, such as strokes, renal failure, and peripheral arterial disorders5. Avascular necrosis (AVN) is one of these complications that, if ignored, can result in severe outcomes, including bone collapse. AVN was prevalent in SARS and may also be common in COVID-19 infections. It should be noted that the risk of AVN persists in individuals who have recovered from COVID-19 infection, similar to SARS6.
The current study aims to report several cases of symptomatic AVN of the femoral head after being infected with COVID-19.
Materials and methods
Study design
This is a single-centre retrospective case series study of patients who developed AVN after being infected with COVID-19. The ethical approval of the study was obtained from the ethical committee of the College of Medicine, University of Sulaimani. All patients provided written consent for their information to be published. The patients were assessed and treated over the past two years (January 2021–December 2022). The study has been written in line with PROCESS 2020 guidelines7.
All the references have been checked for reliability8.
Participants
The sociodemographic and clinical data including age, sex, BMI, duration of COVID-19 infection, history of hospital or ICU admission, history of injection use, interval from the COVID-19 to the onset of symptoms, presentations, MRI, and management, were obtained from the patients, patients’ family, and patients’ medical records.
Inclusion criteria
All patients with a prior history of COVID-19 who developed AVN were included in the study.
Exclusion criteria
Patients with chronic or autoimmune diseases like rheumatoid arthritis, patients with a history of AVN prior to the COVID-19 infection, patients who lack covid-19 polymerase chain reaction evaluation, chronic alcoholic cases, and patients under chemotherapy for bone cancer.
Result
The study included a total of 17 patients ranging in age from 21 to 60 years old (mean=38.65±6.1 years). Twelve of them were male (70.6%) and five were female (29.4%) with a ratio of 3: 1. The mean BMI of the patients was 28.3±2.4 kg/m2, with the majority falling within the range of 25–30 kg/m2 (47.1%). (Table 1). Eight (47%) patients had a history of hospitalization due to the COVID-19 infection, but none were admitted to the ICU. The mean duration of COVID-19 infection was 25.5 days, with a range of 12–52 days. Eleven (64.7%) patients reported receiving steroid injections during the course of infection, three (17.6%) did not, and three were unsure whether they had received the injections or not. The mean interval between COVID-19 infection and presentation to the clinic was 6.53 months, with a range of 2–13 months. Table 2 shows the demographic data and clinical characteristics of each case. The majority of patients (14, 82.3%) experienced bilateral hip pain, two (11.8%) had left hip pain and one (5.9%) had right hip pain. Limping was observed in eight (47%) of the cases, while the remaining portion (53%) had only pain. MRI revealed Grade 2 femoral head AVN in six sites, Grade 3 in twelve sites, Grade 4 in five sites, and the remaining eight sites were unclassified. Bilateral core decompression (CD) was performed in five cases (29.4%), total hip replacement in three cases (17.6%), and conservative treatment was administered in nine cases (53%) as they refused to undergo operation. Table 3 shows the site, presentation, MRI findings, and treatment plan for each of the patients.
Table 1.
The baseline characteristics of the AVN cases
Variables | No. cases/frequency, n (%) |
---|---|
Demographics | |
Age | |
Third decade | 5 (29.4) |
Fourth decade | 6 (35.3) |
Fifth decade | 2 (11.8) |
Sixth decade | 4 (23.5) |
Mean age± SD (min–max) | 38.65±6.1 (21–60 years) |
Sex | |
Male | 12 (70.6) |
Female | 5 (29.4) |
Anthropometric data | |
BMI | |
Normal | 3 (17.6) |
Overweight | 8 (47.1) |
Obesity | 3 (17.6) |
N/A | 3 (17.6) |
Mean BMI± SD (min–max) | 28.3±2.4 (20.5–39) kg/m2 |
Medical history | |
History of trauma | |
Yes | 8 (47) |
No | 9 (53) |
History of bone disease | |
No | 17 (100) |
Hospital admission during COVID-19 | |
Yes | 8 (47) |
No | 9 (53) |
Duration of hospital admission (day) | |
12 | 1 (5.9) |
15 | 4 (23.5) |
16 | 1 (5.9) |
20 | 2 (11.8) |
21 | 1 (5.9) |
30 | 5 (29.4) |
38 | 1 (5.9) |
52 | 1 (5.9) |
N/A | 1 (5.9) |
Steroid use | |
Yes | 11 (64.7) |
No | 3 (17.6) |
N/A | 3 (17.6) |
Duration of steroid use (day) | |
7 | 3 (27.3) |
5 | 4 (36.4) |
4 | 3 (27.3) |
2 | 1 (9) |
Interval from COVID-19 and onset of symptoms (month) | |
2–6 | 9 (53) |
7–12 | 7 (41.1) |
>12 | 1 (5.9) |
AVN site | |
Bilateral femoral head | 14 (82.3) |
Right femoral head | 1 (5.9) |
Left femoral head | 2 (11.8) |
Presentation | |
Hip pain | 17 (100) |
Thigh Pain | 2 (11.8) |
Limping | 8 (47) |
Inability to walk | 2 (11.8) |
AVN, avascular necrosis; N/A, non-available.
Table 2.
Demographic data and clinical characteristics of each case
No. | Age | Sex | BMI (kg/m2) | History of trauma | History of bone disease | Hospital admission during COVID-19 | Duration of hospital admission (day) | ICU admission | Steroid use | Duration of steroid use (day) | Interval from COVID-19 and onset of symptoms (month) |
---|---|---|---|---|---|---|---|---|---|---|---|
1 | 36 | Male | 29 | Yes | No | Yes | 15 | No | Unknown | Nil | 3 |
2 | 33 | Male | 29 | No | No | No | 15 | No | Yes | 7 | 7 |
3 | 36 | Male | 26 | No | No | No | 15 | No | Yes | 7 | 4 |
4 | 59 | Female | 28.9 | No | No | No | 30 | No | Unknown | Nil | 3 |
5 | 23 | Male | 21 | No | No | No | 16 | No | Yes | 7 | 12 |
6 | 22 | Female | 20.5 | No | No | No | 15 | No | No | Nil | 10 |
7 | 28 | Male | 30 | No | No | No | 20 | No | Unknown | Nil | 10 |
8 | 40 | Male | 33 | Yes | No | Yes | Unknown | No | Yes | 5 | 4 |
9 | 33 | Male | 26.8 | Yes | No | Yes | 20 | No | No | Nil | 10 |
10 | 41 | Female | 39 | Yes | No | Yes | 30 | No | Yes | 5 | 13 |
11 | 60 | Female | 29 | Yes | No | Yes | 30 | No | Yes | 5 | 6 |
12 | 21 | Male | 24.6 | No | No | No | 21 | No | Yes | 5 | 3 |
13 | 27 | Male | 27.7 | No | No | No | 30 | No | Yes | 4 | 2 |
14 | 56 | Male | N/A | Yes | No | Yes | 52 | No | Yes | 4 | 2 |
15 | 42 | Male | 32 | No | No | No | 12 | No | No | Nil | 2 |
16 | 60 | Female | N/A | Yes | No | Yes | 38 | No | Yes | 4 | 9 |
17 | 40 | Male | N/A | Yes | No | Yes | 30 | No | Yes | 2 | 11 |
N/A, non-available.
Table 3.
Affected site, presentation, MRI findings, and treatment plan for each case
No. | Site | Presentation | MRI finding | Treatment |
---|---|---|---|---|
1 | Bilateral | Bilateral hip pain and limping | FHAVN Left side grade 2, right side grade 3 | Bilateral core decompression+plasma injection |
2 | Bilateral | Bilateral hip pain, thigh pain, inability to walk distance and limping | FHAVN Left side grade 4, right side grade 4 | Refused operation, conservative |
3 | Bilateral | Bilateral hip pain and limping | FHAVN Left side grade 4, right side grade 3 | Refused operation, conservative |
4 | Bilateral | Bilateral hip pain, limping and inability to walk | FHAVN Left side grade 3, right side grade 3 | Bilateral THR |
5 | Bilateral | Bilateral hip pain and thigh pain and numbness | Bilateral FHAVN | Bilateral core decompression |
6 | Bilateral | Bilateral hip pain | Bilateral FHAVN | Bilateral core decompression |
7 | Bilateral | Bilateral hip pain | Bilateral FHAVN | Bilateral core decompression |
8 | Bilateral | Bilateral hip pan | Bilateral FHAVN | Conservative |
9 | Bilateral | Bilateral hip pain | FHAVN Left side grade 4, right side grade 4 | Bilateral THR |
10 | Right | Right hip pain | Right side FHAVN grade 2 | Conservative |
11 | Bilateral | Bilateral hip pain | FHAVN Left side grade 2, right side grade 3 | Refused operation, conservative |
12 | Left | Left hip pain on walking | Left side FHAVN grade 3 | Refused operation, conservative |
13 | Bilateral | Bilateral hip pain and limping | FHAVN Left side grade 2, right side grade 2 | Refused operation, conservative |
14 | Bilateral | Bilateral hip pan | FHAVN Left side grade 3, right side grade 3 | Refused operation, conservative |
15 | Left | Left hip pain and limping | Left side FHAVN grade 3 | Refused operation, conservative |
16 | Bilateral | Bilateral hip pain and limping | FHAVN Left side grade 3, right side grade 2 | Bilateral core decompression |
17 | Bilateral | Bilateral hip pain and limping | FHAVN Left side grade 3, right side grade 3 | Bilateral THR |
FHAVN, femoral head avascular necrosis; THR, total hip replacement.
Discussion
AVN is a condition in which the blood supply to the bone is disrupted, leading to bone death and subsequent collapse of the bone structure9. AVN of the hip occurs frequently as a result of trauma, most commonly following a femoral neck fracture or hip dislocation. Several causal links to non-traumatic AVN have been discovered10. In the majority of cases, non-traumatic AVN is associated with the use of alcohol, glucocorticoids, co-existing haematological disorders (such as sickle cell anaemia, thalassaemia, polycythemia, and haemophilia), myeloproliferative disorder, Gaucher disease, and conditions, such as hypercholesterolaemia, pregnancy, chronic renal failure, hyperparathyroidism, and Cushing’s disease. However, in around 30% of patients, the cause of non-traumatic AVN remains unknown, and they are classified as idiopathic. The presence of AVN in twins and family clusters suggests that genetic factors may be involved11. The combination of loss of blood perfusion and elevated intraosseous pressure has been recognized as the primary cause of the necrotic process12. The male-to-female ratio is around 4:1, with an average age of onset in the fifth decade. Bilateral AVN has been documented in more than 50% of cases10. In up to 72% of patients, AVN is characterized by nonspecific symptoms13. The mean age of patients in the current study was 38.65 years, and males made up 70.6% of the patients. Bilateral femoral head was involved in 82.3% of the cases. All of the patients had a negative history of bone disease.
Given that the long-term consequences of COVID-19 are predicted to pose a physical, psychological, and financial burden on patients, caregivers, and healthcare systems, it is critical to remember that there may be complications following recovery, including adverse non-pulmonary complications6,14. AVN is a rare sequela that, if not treated, can result in severe complications, including bone collapse 6.
Many medications that may be effective against COVID-19 have been investigated since the pandemic, including antivirals, angiotensin receptor blockers, chloroquine phosphate, and corticosteroids15. The RECOVERY clinical trial, one of the largest trials on COVID-19 treatments, found that corticosteroids reduced the risk of mortality in hospitalized patients with severe COVID-19 who were on a ventilator or receiving oxygen at a 20% concentration16. Although corticosteroids are life-saving in the treatment of COVID-19, they are also a risk factor for the development of AVN15. Corticosteroid-associated AVN accounts for roughly 10–30% of non-traumatic AVN which makes it the most prevalent aetiology of non-traumatic AVN10. As a result, corticosteroids should be used with caution, with care given to the dose and duration. Tocilizumab, a new medication, may be used instead of corticosteroids to suppress the cytokine storm17. It is also unclear whether the risk of AVN is more closely related to the total dosage, the maximal dose, or the duration of treatment18. According to some studies, AVN development requires a cumulative dosage of 2000 mg of prednisone15. Previous rare case reports have described individuals who developed AVN after being administered low-dose steroid therapy19. A study suggests that a risk classification method for the AVN in COVID-19 patients should be developed: (i) low-risk clients would receive no corticosteroids; (ii) moderate-risk clients would receive corticosteroids for less than 1 week with a cumulative dose of less than 2000 mg; and (iii) high-risk patients would receive corticosteroids for at least 1 week with a cumulative dose of 2000 mg or an intravenous pulse of 80 mg/day for at least 3 days20. In the current study, eleven (64.7%) patients reported receiving steroid treatments during the infection. All eleven patients received a single dosage of steroid injection for different periods like a week (3 cases), 5 days (4 cases), and 4 days or less (4 cases).
There is still uncertainty about the time interval between steroid injection and the onset of AVN symptoms. Zhao et al.21 reported an interval of up to 3 years. McKee et al.22 found a mean period of 16.6 months. Following the COVID-19 diagnosis, Agarwala et al.15 discovered a mean time of 58 days (range 45–67 days) for the development of AVN. According to Agarwala et al.15, the sensitivity to developing AVN is increased owing to the COVID-19 virus, and a lower cumulative dosage of steroids is required. The mean interval from COVID-19 infection to the presentation in the current cases was 6.53 months. Other drugs used to treat COVID-19 infection, such as lopinavir and ritonavir, can also cause osteonecrosis. Some virus-related processes have also been proposed as probable causes, including hypercoagulability caused by SARS-CoV-2 and an increase in bone resorption mediated by the ACE-2 receptor. Despite all of these risk factors, only a few cases of AVN following COVID-19 have been documented23.
Diagnosis of AVN in the early stage (stage I) is critical for preventing the disease’s progression and preventing bone collapse24. Plain radiography, MRI, computer-aided tomography, skeletal scintigraphy, and single-photon emission computed tomography are now available as noninvasive diagnostic techniques for AVN11. X-ray-based radiography detection is insufficient to identify AVN at its onset, and its overall sensitivity for early-stage AVN is only around 41%25. MRI is more useful than X-rays in identifying AVN in its early stages26. If not detected at early stages, this problem progresses to osteoarthritis and, eventually, joint replacement12. All cases of the current study were confirmed to have AVN through MRI study.
There has been a greater emphasis on early treatments for AVN26. A variety of non-surgical and surgical approaches have been described27. In the early stages of AVN, minimal weight-bearing and pharmacological agents, such as lipid-lowering medications, vasodilators, anticoagulants, and bisphosphonates may be beneficial27. Although CD is the most generally approved therapy for early-stage AVN of the femoral head, its usage has been criticized due to its poor effectiveness28. Other surgical approaches include osteotomy and bone graft which may assist in slowing the progression of the disease. If non-surgical and joint-saving techniques fail, arthroplasty may be a viable treatment option29. Because of the predicted long-life expectancy in young patients and the short survival time of arthroplasties, preservation of the femoral head and the hip joint is preferable and is the aim of almost all treatment options27. In the current study, bilateral CD was performed in five cases, three cases were scheduled to undergo total hip replacement, and nine cases received conservative therapy due to patient refusal for surgery.
Following discharge, several follow-up strategies should be implemented for COVID-19 patients according to the varied risks. The MRI is the ideal imaging technique for early diagnosis of AVN of the femoral head18. Bisphosphonates and vitamin E should be prescribed to patients while on corticosteroid therapy. Anticoagulants, vasodilators, and traditional Chinese medicine may also be alternatives30. Physical therapy and combination medication can be utilized to postpone or prevent the collapse of steroid-induced AVN of the femoral head in the early stages of the disease31.
In conclusion, the ongoing pandemic may have many long-term sequelae. There is a risk of developing AVN after COVID-19. Early detection of AVN is critical because the resulting bone collapse can be avoided if early treatment is started.
Ethical approval
Ethical approval for this study (Ethical Committee No: 175) was provided by the Ethical Committee of School of Medicine-University of Sulaimani on 4 January 2021.
Consent
Written informed consent was obtained from the patient for publication and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal on request.
Sources of funding
The research has got no funding.
Author contribution
S.K.A. was a major contributor to the conception of the study, as well as in the literature search for related studies, final approval of the manuscript. M.N.H. and F.H.K. were involved in writing the manuscript, literature review, final approval of the manuscript. M.S., A.M.S. and R.K.A. were involved in the literature review, the design of the study, revision of the manuscript. B.A.A.was involved in critical revision of the manuscript and final approval. R.Q.S. and S.H.M. confirm the authenticity of all the raw data, revision of the manuscript
Conflicts of interest disclosure
The authors declare that they have no conflicts of interest.
Research registration unique identifying number (UIN)
The research was registered in the Research Registry with a registration number ofresearchregistry7468.
Guarantor
Fahmi Hussein Kakamad.
Data availability statement
Not applicable.
Provenance and peer review
Not commissioned, externally peer-reviewed.
Footnotes
Sponsorships or competing interests that may be relevant to content are disclosed at the end of this article.
Published online 25 July 2023
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Associated Data
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Data Availability Statement
Not applicable.