Exploring the Association Between COVID-19 and Avascular Necrosis: A Systematic Review.

Exploring the Association Between COVID-19 and Avascular Necrosis: A Systematic Review.

Publication date: Aug 01, 2025

Avascular necrosis (AVN) has emerged as an extrapulmonary complication associated with COVID-19 and corticosteroids. This review aims to evaluate the association between COVID-19 infection, corticosteroid use, and the development of AVN. We conducted a systematic review following the PRISMA guidelines, searching five databases until May 30, 2024. We included cohort and case series studies involving COVID-19 patients who developed AVN. The risk of bias was assessed using the Newcastle-Ottawa Scale (NOS). A total of 13 studies, comprising nine case series and four cohort studies, were included. These studies involved 795 patients with a mean age of 46. 1 years and a male predominance (66%). The cumulative dose of corticosteroids varied, with an average of 1,462. 9 mg. The duration between COVID-19 infection and initial AVN symptoms ranged from 2 to 62 weeks. The most commonly affected bones were the hip and femoral head. The visual analog scale (VAS) score improved with the treatment, and the cases showed improvements. A significant association was found between COVID-19, corticosteroid use, and AVN development. Clinicians should exercise caution when prescribing corticosteroids and monitor for early signs of AVN. Further research is needed to elucidate the pathophysiological mechanisms and explore alternative treatments to mitigate the risk of AVN.

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Concepts Keywords
Clinicians avascular necrosis
Necrosis corticosteroids
Ottawa covid-19
Weeks osteonecrosis
systematic review

Semantics

Type Source Name
disease MESH COVID-19
disease MESH Necrosis
disease MESH infection
pathway REACTOME Reproduction
drug DRUGBANK Coenzyme M
disease MESH osteonecrosis
disease IDO immune response
disease MESH cytokine storm
disease MESH death
disease MESH acute respiratory distress syndrome
disease MESH complications
disease MESH hypoxemic respiratory failure
disease MESH acute kidney injury
disease MESH syndrome
disease MESH long COVID
disease MESH chest pain
disease MESH cognitive impairment
pathway KEGG Viral replication
disease MESH lung inflammation
disease MESH alcohol abuse
disease MESH chronic pain
disease IDO history
drug DRUGBANK Tacrine
pathway KEGG Coronavirus disease
disease MESH Coronavirus Infection
disease MESH Virus Disease
disease MESH Femur Head Necrosis
disease MESH Legg Calve Perthes Disease
disease MESH mucormycosis
disease IDO site
disease MESH hypertension
disease IDO intervention
disease MESH septic arthritis
disease IDO quality
disease IDO country
disease IDO process
disease IDO blood
disease MESH edema
disease MESH vasculitis
disease IDO nucleic acid
disease MESH abnormalities
disease MESH joint pain
disease IDO susceptibility
disease IDO primary infection
drug DRUGBANK Oxygen
disease MESH diabetes mellitus
drug DRUGBANK Methionine
disease MESH coxarthrosis
disease MESH osteoarthritis
disease MESH hypercoagulability
disease MESH inflammation
disease MESH hypoxia
drug DRUGBANK Ribostamycin
drug DRUGBANK Chloroquine
drug DRUGBANK (S)-Des-Me-Ampa
drug DRUGBANK Diethylstilbestrol
drug DRUGBANK Isosorbide Mononitrate
drug DRUGBANK Dimethyl sulfone
disease MESH morbidity
disease MESH osteomyelitis
disease MESH rheumatoid arthritis
pathway KEGG Rheumatoid arthritis
disease MESH Shock
disease MESH disseminated intravascular coagulation
pathway REACTOME Regulated Necrosis

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