Abstract
Hip arthroscopy has been proven to effectively treat labral tears in the setting of femoroacetabular impingement. Anchors used for this treatment have constantly evolved and improved to ensure safety and minimal invasion. However, acetabular drilling and anchor placement are technically challenging due to the concavity of the acetabular articular surface, limited angles for anchor insertion, and finite bone availability in the anterior and posterior column. Inadequate technique can result in protruding anchors, which may lead to full-thickness articular cartilage damage, manifesting in pain, mechanical symptoms, and impaired function. This Technical Note demonstrates arthroscopic removal of protruding anchors and management of the iatrogenic grade IV cartilage damage. In this description, the technical pearls and pitfalls of acetabular anchor placement to treat labral pathology are presented along with the aforementioned technique.
Technique Video
The importance of the hip labrum in creating a suction seal effect in the hip joint has been demonstrated in previous studies.1,2 Arthroscopic restoration of labral function has been shown to lead to significantly improved short- to long-term patient-reported outcomes, as well as pain reduction and decreased likelihood of conversion to total hip arthroplasty.3,4 However, hip arthroscopy remains a challenging procedure with a steep learning curve; iatrogenic damage to articular surfaces may be caused during many different steps of the procedure, which may lead to a low survivorship rate.5
Suture anchors, consisting of a metal, polyether-ether ketone, bioabsorbable (poly-L-lactic acid), or all-suture anchors, have vastly evolved over the past 2 decades as a method of fixation of the labrum to the acetabular bone. Careful placement of the anchor should be directed in such a way that the anchors remain close to the acetabular rim without penetrating the articular cartilage. However, suture anchors should not be placed too far from the cartilage in such a way that it causes eversion of the labrum.6,7 While considered safe, there have been reports of complications associated with the use of suture anchors.
A mechanical condition caused by a protruding anchor, known as anchor arthropathy, may lead to mechanical erosion of the acetabular and femoral head articular cartilage, or to anchor fragmentation, leading to loose bodies that may potentially cause further chondral injury.8,9 Ultimately, this condition may lead to progressively worsening pain and limited range of motion and activity for the patient, who is typically unresponsive to nonsurgical treatment and will require a revision arthroscopy. This Technical Note presents arthroscopic treatment to remove protruding anchors and manage chondral injury resulting from anchor arthropathy. This study was performed in accordance with the ethical standards in the 1964 Declaration of Helsinki. This study was carried out in accordance with relevant regulations of the US Health Insurance Portability and Accountability Act (HIPAA). Details that might disclose the identity of the subjects under study have been omitted. This study was approved by the institutional review board (IRB ID: 5276).
Surgical Technique (With Video Illustration)
Indication
Physical examination includes assessment of femoroacetabular impingement syndrome using the lateral, anterior, and posterior impingement tests.10 Views for radiographic evaluation include the supine and upright anteroposterior pelvic, false profile, and modified Dunn 45°.11 Preoperative magnetic resonance arthrogram is performed to determine labral retearing or other extra and intra-articular defects, presence of loose bodies, and protrusion of anchors to the acetabular cartilage (Fig 1). Nonoperative treatment is conducted and includes measures such as physical therapy, activity modification, rest, and anti-inflammatory medications. Revision hip arthroscopy treatment is recommended after 3 months of failed conservative measures and progression of symptoms.
Patient Preparation and Positioning
Under general anesthesia, the patient is placed in the supine position on a post-less traction.12 The feet are protected with extra-padding, and the patient is adequately positioned and secured. The operative leg is positioned in neutral rotation and adduction, whereas the contralateral leg is placed at 30° of abduction. The operative table is then fixed at 10 to 15° of Trendelenburg inclination.
Portal Placement
The anterolateral portal is created using fluoroscopic guidance as previously described at the 12-o’clock position.13 The remaining 3 portals, mid-anterior, distal anterolateral accessory, and posterolateral are created under direct visualization.14 Routine portal placement is shown in Figure 2.
Diagnostic Arthroscopy and Articular Cartilage Assessment
A systematic assessment is performed through a diagnostic arthroscopy to assess the intra-articular cartilage, labrum, and ligamentum teres. Notable procedures performed during the previous surgery are assessed, including the placement and function of suture anchors for labral repair. Acetabular cartilage is assessed with an arthroscopic probe to determine detachment of the chondral surface at the chondrolabral junction, as well as full- and partial-thickness tears in articular cartilage (Fig 3). Outerbridge and acetabular labrum articular disruption classifications are used to grade chondral defects,15,16 which can be caused by protruding anchors in the acetabulum.
Other pathologic conditions, such as retearing of the labrum, residual acetabular overcoverage and femoral cam morphology, intra-articular loose bodies, subspine impingement, acetabular notch osteophytes, and instability, also are treated arthroscopically during the procedure.
Identification and Removal of Protruding Anchors
All unviable and unstable cartilage around the edges of the lesion is removed with the use of an arthroscopic shaver. This exposes the protruding anchors and the resulting iatrogenic cartilage injury (Fig 4 A-D). Treatment options for removal of anchor-induced arthropathy are shown on Table 1. In the presented case, the anchors were mobilized and completely exposed through the defect with the use of an arthroscopic probe, and an alligator grasper was then used to perform an en bloc removal (Fig 5 A and B). A ring curette was used to scrape the loose edges of the cartilage and to create perpendicular borders around the lesion (Video 1). Arthroscopic lavage of the hip to remove debris that could cause synovitis or third body wear is then performed.
Table 1.
No visible cartilage penetration
|
Micro-Drilling
Typically, Outerbridge type III and IV lesions are treated with a micro-drilling procedure.17 Indications and contraindications for this procedure are found in Table 2. To perform this, a micro-drilling pick or a 70° curved drill guide with a flexible drill (Arthrex, Naples, FL) is introduced into the joint from the portal offering a perpendicular trajectory to the lesion (mid-anterior or distal anterolateral accessory portal). The drill bit is assembled to reach the desired depth and set on forward speed to reduce the risk of breakage. It is recommended to begin from the periphery of the defect and work towards the center, placing holes 3 to 4 mm apart to avoid subchondral plate fractures. After drilling, the shaver is used to remove debris that may have accumulated in the joint during drilling. Fluid irrigation is ceased to ensure bleeding from each micro-drilled hole.
Table 2.
Indications | Contraindications |
---|---|
|
|
|
Rehabilitation
Following surgery, rehabilitation includes 2 weeks of bracing with limiting flexion range of motion to 90°. In addition, patients are limited to 20 lbs of weight-bearing on the operative extremity for 6 weeks. Patients begin physical therapy the day after surgery and started with passive range of motion using a stationary bike. They then progress to full strength activity over a 3- to 4-month period.
Discussion
Acetabular anchor placement can lead to iatrogenic complications when repairing or reconstructing the labrum. A misdirected anchor can cause damage by penetrating the articular cartilage during drilling or anchor placement. It may also internally detach a segment of the articular cartilage without piercing entirely through the articular cartilage (bubbling). Furthermore, if the anchor is exposed and becomes free, it may act as a loose body that potentially could cause chondral injury throughout the articular surface. Acetabular cartilage lesions may lead to femoral head lesions, leading to advanced stages of osteoarthritis expeditiously. Pearls to avoid cartilage damage during anchor placement are found in Table 3.
Table 3.
Drill through the DALA portal |
Adequate rim preparation using wand and burr |
Use flexible drill bit |
Visualize articular surface during drilling and anchor placement |
Sound the drilled hole with a flexible wire to palpate distal cortex |
Use small-diameter, suture anchors |
DALA, distal anterolateral accessory.
There are different treatment options to remove anchors, which depend on the type of anchor—hard (threaded or barbed) or soft—and the amount of protrusion. In any case, the goal of the removal is to preserve as much cartilage as possible. Hard, threaded anchors may be removed by a reverse screwing motion in the opposite direction of its insertion. Hard, barbed anchors may be removed through their insertion point using an arthroscopic grasper. If the anchors may not be removed retrogradely, they may be removed through anterograde advancement for its removal in the central compartment. If difficult to remove in either direction, one option is to burr down the exposed surface of the anchor, which carries the risk of compromising the labral fixation or provoking an intra-articular loose implant. Finally, if the anchor is protruding completely, it may be removed en bloc with the use of an arthroscopic grasper; however, this may generate a large chondral defect.18,19 Anchor arthropathy may have devastating effects in the post-operative recovery, as well as the short- to long-term survivorship of the hip joint. While the learning curve in hip arthroscopy may be steep, a careful surgical technique should avoid penetrating anchors at all costs, in the pursuit of the best possible outcome in the patients’ treatment.
Footnotes
The authors report the following potential conflicts of interest or sources of funding: B.G.D. reports grants and other from the American Orthopaedic Association, during the conduct of the study; personal fees from Amplitude, personal fees and nonfinancial support from Arthrex, DJO Global, and Medacta; grants, personal fees, nonfinancial support, and other from Stryker, grants from Breg, personal fees from Orthomedica, grants and nonfinancial support from Medwest Associates, grants from ATI Physical Therapy, personal fees and nonfinancial support from St. Alexius Medical Center, grants from Ossur; and nonfinancial support from Zimmer Biomet, DePuy Synthes Sales, Medtronic, Prime Surgical, and Trice Medical, outside the submitted work. Moreover, B.G.D. has patents issued and receives royalties for the following: method and instrumentation for acetabular labrum reconstruction (8920497), licensed by Arthrex; adjustable multi-component hip orthosis (8708941), licensed by Orthomerica and DJO Global; and knotless suture anchors and methods of suture repair (9737292), licensed by Arthrex. Finally, B.G.D. is a board member of the American Hip Institute Research Foundation, AANA Learning Center Committee, Journal of Hip Preservation Surgery, and Arthroscopy and has had ownership interests in the American Hip Institute, Hinsdale Orthopedic Associates, Hinsdale Orthopedic Imaging, SCD#3, North Shore Surgical Suites, and Munster Specialty Surgery Center. Full ICMJE author disclosure forms are available for this article online, as supplementary material.
This study was performed at the American Hip Institute Research Foundation.
Supplementary Data
References
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