What is osteonecrosis
Osteonecrosis (avascular necrosis, AVN) is the death of a section of bone tissue due to interrupted blood supply. Living bone constantly remodels; when blood flow stops, bone cells die, the structure breaks down, and ordinary loading triggers collapse — sinking of the joint surface.
Typical locations
Femoral head (most common). Femoral condyles (knee osteonecrosis). Humeral head. Talus. Scaphoid. Less often — vertebral body.
Risk groups
Men aged 30–50 — 4× more often than women. Bilateral in 40–80% (especially with systemic causes). Etiology unknown in 30%.
Why it's urgent
From early stage to collapse — often 6–18 months. After head collapse, restoration is impossible. Therefore, on suspicion — immediate MRI and urgent consultation.
Main causes
Glucocorticoids
Prolonged prednisolone or analog use (> 2 g cumulative). The most common non-traumatic cause. Often after COVID-19 courses, systemic disease, transplantation.
Alcohol
Chronic abuse alters fat metabolism and bone microcirculation. Risk is dose-dependent.
Trauma
Femoral neck fractures, hip dislocations, fractures of the talus and scaphoid disrupt end-arterial blood supply. May develop weeks to months after injury.
Hematologic disease
Sickle cell disease, antiphospholipid syndrome, thrombophilias, leukemia — disrupt microcirculation in marrow sinuses.
Decompression sickness
"Caisson disease" in divers and caisson workers. Gas emboli block bone capillaries.
Idiopathic
Unknown cause in 30%. A diagnosis of exclusion after ruling out all known factors.
ARCO stages
Stage 0 and I
Normal X-ray. MRI shows bone marrow edema and "double line." Clinically — load-related pain, possibly asymptomatic. MIBRAR® — maximum efficacy.
Stage II
X-ray shows sclerotic and lucent zones. Head shape preserved. Moderate pain. MIBRAR® — core decompression + BMAC, high efficacy.
Stage III
Subchondral fracture — "crescent sign." Beginning of collapse. Increasing pain. MIBRAR® feasible in early cases, often combined with orthopedic offloading.
Stage IV
Complete head collapse, acetabular changes, secondary arthrosis. Endoprosthesis indicated. MIBRAR® only as part of a comprehensive palliative approach.
Osteonecrosis diagnosis
MRI — method of choice
99% sensitivity at early stages, when X-ray is still normal. Detects bone marrow edema, "double line," first signs of necrosis. Mandatory on any suspicion.
X-ray
Not informative at early stages. Useful for stage II–IV: sclerosis, crescent sign, collapse. X-ray dynamics is a key progression criterion.
Lab screening
Cause identification: coagulation panel (thrombophilia), lipid profile, immune workup, systemic disease tests. Critical for preventing involvement of the second joint.
Osteonecrosis treatment with MIBRAR®
At stages I–III the key task is to restore blood supply and stimulate bone regeneration before collapse occurs. MIBRAR® combines surgical decompression with biologic product delivery.
Core decompression
Through a minimal access, channels are placed into the necrosis zone — intraosseous pressure drops, neoangiogenesis is initiated. 30–45 minute procedure.
BMAC into the necrosis zone
Bone marrow concentrate with mesenchymal and hematopoietic cells is delivered through the channels into the lesion. Stimulates new bone formation.
Orthopedic offloading
The first 6–12 weeks — crutches with partial weight-bearing. Protects the regeneration zone from mechanical disruption.
MRI monitoring
Repeat MRI at 3, 6, 12 months — assessing necrosis regression, ruling out progression. Repeat session if needed.
Osteonecrosis is a time-critical diagnosis
On suspicion — urgent MRI and consultation. Don't wait for collapse.
Urgent consultationFrequently asked questions
Death of bone tissue due to interrupted blood supply. Without treatment — collapse and endoprosthesis.
Steroids, alcohol, trauma, coagulopathies, decompression sickness. 30% — idiopathic.
At I–II — yes. Core decompression + BMAC. At late stages with collapse — prosthesis.
Creating channels in the necrosis zone to lower pressure and stimulate regeneration. In MIBRAR®, augmented with BMAC.
As fast as possible. Early to late progression — 6–18 months. After collapse, restoration is impossible.

