PRP for Chronic Hip Trochanteric Bursitis and Gluteal Tendinopathy
For patients with chronic greater trochanteric pain syndrome (GTPS) and gluteal tendinopathy who have failed conservative management, a single ultrasound-guided leukocyte-rich platelet-rich plasma (LR-PRP) injection provides superior pain relief and functional improvement compared to corticosteroid injection, with benefits sustained at 2 years. 1, 2
Evidence Quality and Guideline Context
The recommendation for PRP in this specific condition diverges from broader osteoarthritis guidelines. The American College of Rheumatology/Arthritis Foundation strongly recommends against PRP for hip osteoarthritis due to lack of standardization and insufficient evidence 3. However, gluteal tendinopathy is a distinct pathology from hip osteoarthritis—it involves tendon degeneration rather than articular cartilage disease 3.
Clinical Algorithm for Treatment Selection
Step 1: Confirm Diagnosis
- Ultrasound or MRI confirmation of gluteus medius/minimus tendinopathy with intratendinous pathology 3, 1
- Exclude full-thickness tendon tears (these patients were excluded from successful trials) 1, 2
- Rule out hip osteoarthritis, which would change the treatment paradigm 3
Step 2: Document Failed Conservative Management
- Minimum 3-6 months of conservative therapy including relative rest, NSAIDs, and eccentric strengthening exercises 3
- Symptoms persisting >4 months predict better response to PRP 1
- Mean symptom duration in successful trials was >14-15 months 1, 2
Step 3: Choose Injection Therapy
For gluteal tendinopathy specifically:
- LR-PRP injection is superior to corticosteroid at 12 weeks and beyond 1, 2
- At 12 weeks: PRP group achieved mean modified Harris Hip Score (mHHS) of 74.05 vs. 67.13 for corticosteroid (p=0.048) 1
- At 24 weeks: PRP maintained superiority (77.60 vs. 65.72, p=0.0003) 2
- At 2 years: PRP group improved to mHHS of 82.59, while corticosteroid benefits were not maintained beyond 24 weeks 2
Step 4: Injection Technique
- Perform under ultrasound guidance 1, 2
- Inject intratendinously into gluteus medius/minimus tendons 1, 2
- Include trochanteric bursa if bursitis is present 4
- Single injection is sufficient (no evidence for multiple injections in this condition) 1, 2
Critical Distinctions from General Guidelines
Why gluteal tendinopathy differs from hip OA:
- The 2020 ACR/AF guidelines against PRP apply to intra-articular hip osteoarthritis, not periarticular tendinopathy 3
- Tendinopathy involves hypovascular tendon degeneration at the osteotendinous junction, not cartilage loss 3
- The pathophysiology of chronic tendinosis may be more responsive to growth factors in PRP than degenerative joint disease 3, 1
Expected Outcomes
Success rates at 12 weeks:
- 64.1% of PRP patients achieved mHHS ≥74 vs. 45.9% with corticosteroid 1
- 82% of PRP patients achieved minimal clinically important difference (MCID >8 points) vs. 56.7% with corticosteroid (p=0.016) 1
Long-term durability:
- PRP benefits continue improving through 2 years 2
- Corticosteroid benefits peak at 6 weeks and decline thereafter 2
Important Caveats
Patient selection matters:
- Evidence strongest for patients with symptoms >4 months 1
- Exclude patients with full-thickness gluteal tendon tears 1, 2
- Mean age in successful trials was 60 years with 9:1 female predominance 1, 2
Standardization concerns:
- Use leukocyte-rich PRP specifically (the formulation studied in positive trials) 1, 2
- The ACR's concern about PRP heterogeneity is valid—preparation methods vary widely 3, 5
- One recent trial using different PRP preparation showed no benefit over placebo, highlighting preparation variability 6
Crossover data supports efficacy:
- 27 patients who failed corticosteroid at 16-24 weeks crossed over to LR-PRP 2
- Their mHHS improved from 59.22 to 77.53 at 2 years post-crossover 2
- This provides additional evidence that PRP works when corticosteroid fails 2
Alternative if PRP Unavailable
If LR-PRP is not available or affordable, corticosteroid injection provides short-term benefit (6-12 weeks) but expect diminishing returns beyond 24 weeks 1, 2. Surgery should be reserved for patients who fail both injection therapies after 3-6 months 3.