Surgical Approaches for Refractory Gluteus Medius Pathology
Contemporary Surgical Approaches for Refractory Gluteus Medius Pathology
Figure 4a-b. Endoscopic partial gluteus maximus tenotomy
Given that this condition involves tendon insertion (enthesis) in an area with poor blood supply, we utilize the intermediate portal to perform transtendinous perforations in the degenerated tendon regions Figure 5. These perforations are directed towards the greater trochanter to encourage the development of new blood vessels and enhance blood flow, ultimately promoting healing of the lesion, indicating that this method has yielded exceptional results in both clinical evaluations and imaging examinations for partial tears of up to 25% of the total thickness, as illustrated in Figures 6a-b.

Figure 5. Endoscopic greater trochanter perforations

Figure 6a-b. Hip MRI scan showing a partial gluteus medius tear (a) and a gluteus minor tear (b)
The selection of an appropriate treatment modality becomes more complex when lesions affect between 25% and 50% of the thickness Figure 7. As previously noted, these lesions are situated medial to the gluteus medius tendon, demonstrating tendon continuity in the most lateral region. Direct repair of this lesion would require the disinsertion of a healthy gluteus medius tendon, which is suboptimal. Cutting one healthy tendon to repair another would, at best, result in scar tissue formation, which would not possess the same functionality as native tissue. Consequently, in this subset of lesions, augmentation with a biological collagen patch is employed, in addition to the technique described for the two previous groups.

Figure 7. Hip MRI scan showing a 30% rupture of the gluteus medius and minor tendons
This patch stimulates tissue regeneration, promoting collagen deposition and enhancing the recovery of the gluteus minimus tendon Figure 8a-b. We have achieved favorable outcomes with this technique, which we published in 2024³⁴⁴. The REGENETEN® bioinductive patch (Smith & Nephew) is a highly porous type 1 collagen implant with oriented fibers that stimulate and guide the body’s natural healing response. It supports new tendon growth by interrupting disease progression and promoting cell and blood vessel migration⁴⁵⁴⁷, ultimately resulting in increased tendon thickness.

Figures 8a-b. Endoscopic placement of a REGENETEN® bioinductive patch over the gluteus medius insertion
Our group conducted a prospective study by incorporating the REGENETEN® patch as a single augmentation technique from 2019 to 2024 with a minimum follow-up of 6 months⁴³. The study population comprised patients who underwent hip surgery for tendinopathy refractory to conservative treatment, defined as failure to respond to NSAIDs, three courses of physiotherapy, and a symptom duration exceeding 6 months. In patients with a symptom duration of less than 6 months, surgical intervention was indicated in the presence of 30% to 50% rupture of the gluteus medius minimus tendon complex. All patients underwent preoperative MRI, which was subsequently compared with imaging performed 6 months postoperatively, demonstrating complete healing of the tendon.
Surgical technique
The procedure is conducted on an outpatient basis for all patients utilizing an anesthetic protocol comprising epidural block with sedation, and prophylactic antibiotics administered 30 minutes prior to the start of the surgical procedure. The patient is positioned in the supine decubitus position, with the ipsilateral leg in the surgical field, facilitating abduction, adduction, internal and external rotations, as well as hip flexion and extension movements.
Subsequently, the portals for surgical access are determined through individualized measurements for each patient. Initially, the width of the femur is outlined with a sterile marker at the level of the most lateral prominence of the greater trochanter, which is projected proximally and distally, in the posterior third of the femur (proximal posterolateral accessory portal (PPLA), and distal posterolateral accessory portal (DPLA). Finally, a posterior accessory portal is utilized at the level of the most lateral portion of the greater trochanter using half of the previously defined measurement⁴².
The initial portal established is the DPLA, which is utilized to access the virtual space between the vastus lateralis and the iliotibial band. This space is distended using normal saline solution (NSS) with epinephrine at a concentration of 1 mg per 3 liters of NSS, maintained at a temperature of 30°C⁴⁸. The PPLA is subsequently established utilizing a guide wire under direct visualization with a 70° optic through the DPLA portal. A bursectomy and resection of fibrous bands are performed to identify the gluteus maximus as a landmark. A partial tenotomy of the proximal portion of the distal insertion of the gluteus maximus, approximately 3 cm in length, is executed, which enhances the working space and reduces pressure in the lateral compartment⁴⁹. The proximal end of the greater trochanter and the gluteus medius tendon are identified, and tendon lesions are examined. Subsequently, the greater trochanter is drilled in the areas of gluteus medius tendon degeneration utilizing a 2.3 mm drill through the PPLA.
In patients previously identified with lesions exceeding 30%, the bio-inductive collagen patch is applied after the perforations through the DPLA, which is secured with resorbable anchors through the PPLA, with the arthroscopic lens positioned in the PPLA. Internal and external rotation maneuvers are executed to facilitate perforations, placement, and fixation of the collagen inductive patch. The stability of the fixation is evaluated by conducting flexion and extension, abduction and adduction movements, and rotational movements.
Complete rupture of the gluteus medius tendon presents a significant challenge for surgeons, as the tendon has been displaced from its anatomical position in the greater trochanter, which is typically sclerotic and is associated with a tendon of poor quality. Poor outcomes have been reported with conventional open surgical treatments in such cases. Consequently, we have developed an endoscopic surgical technique, as described for partial tendon lesions, with the notable distinction that in these cases it is crucial to examine the continuity of the tendon with the bone tissue and assess its adherence or detachment. If the tendon is detached, it must be incised longitudinally to identify the sclerotic zone of the bone at the greater trochanter, which is then removed, typically with a 5.5 mm burr drill, to create a bleeding bed where the tendon can heal. The tendon is subsequently fixed with one or two 5.5 mm titanium anchors loaded with double sutures to close the incision and secure the tendon to the bleeding bed of the greater trochanter Figure 9a-c and 10a-d.

Figures 9a-c. Endoscopic view of a longitudinal incision of the gluteus medius tendon (A), exposure of sclerotic bone beneath the tendon (B), bone bed preparation under tendon (C).

Figures 10a-d. Endoscopic view of a gluteus medius tear repair. Placement of a titanium anchor (A) Anchor in bone with sutures (B). Anchor sutures through tendon closing longitudinal incision/ tear (C). Final suture-anchor construct (D).
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