Abstract
OBJECTIVE
Imaging the hip joint with optimized MRI protocol parameters provides the radiologist with the ability to reliably diagnose complex hip abnormalities. The institution of appropriate metal artifact reduction techniques and dedicated sequences can enhance visualization of the periprosthetic bone and soft tissues and allow improved detection of the more frequently encountered total hip arthroplasty–related conditions, such as mechanical loosening, polyethylene wear, and adverse local tissue reactions.
CONCLUSION
Finally, through the use of dynamic contrast-enhanced MRI, abnormal femoral head perfusion, one of the most common complications associated with femoral neck fracture internal fixation, can be detected before the development of femoral head osteonecrosis, subchondral collapse, and secondary osteoarthritis. Thus, through the institution of the techniques described in this review article, the challenges associated with MRI of hip arthroplasty and instrumentation can be overcome, allowing for the diagnosis of common associated complications.
Keywords: arthroplasty, hip, MRI
Accurate evaluation of the hip joint is integral to identifying complex hip abnormalities, aiding in preoperative and pre-arthroscopic procedure planning, and assessing for postoperative complications. Although the anatomic location of the hip off isocenter of the imaging bore, as well as the sphericity of the femoral head and relatively thin femoral head and acetabular dome articular cartilage, present challenges to assessing the hip joint with the use of MRI, the use of proper pulse sequence protocols can overcome these challenges.
Furthermore, approximately 2.5 million Americans currently live with a hip arthroplasty [1], and this number is expected to increase in the coming decades, given the increased life expectancy of the aging population, as well as the movement toward hip replacement in younger patients. Although hip arthroplasty provides patients with pain relief and improved subjective function, it is also associated with several complications that can limit arthroplasty’s life span, for which it is integral for imaging to be able to evaluate. In the past, the use of MRI to assess hip arthroplasty had been limited because of metal-related artifact; however, in recent years, protocols and sequences geared toward reducing such artifacts have rendered MRI instrumental in assessing hip arthroplasty–related complications, such as mechanical loosening, polyethylene wear, and adverse local tissue reactions.
The intent of this article is to outline the techniques that can be used to overcome the challenges associated with MRI of hip arthroplasty, as well as the typical MRI features of common hip arthroplasty–associated complications.
Routine Imaging Technique
Hip MRI is ideally performed on a 1.5- or 3-T magnet. Coronal, sagittal, and axial high-resolution surface coil images should be obtained with a two-part shoulder smaller-FOV wrap or multiple-channel cardiac coil to avoid phase-wrap artifact, which would result from the use of a larger-FOV body coil. Cartilage-sensitive moderate-TE fast spin-echo (FSE) sequences with an effective TE of approximately 34 ms at 1.5 T, or 28 ms at 3 T, should be acquired in an effort to maximize the contrast between the hypointense fibrocartilaginous labrum, isointense articular cartilage, and hyperintense fluid. Larger-FOV coronal fast STIR and axial FSE sequences should also be performed using a body coil. These more global images may show alternate abnormalities that may simulate hip joint pain, such as occult sacral or pubic insufficiency fractures, pelvic soft-tissue masses (e.g., adnexal masses or hernias), or remote marrow infiltration indicative of metastatic disease.
Imaging Techniques Around Orthopedic Hardware
The challenge of arthroplasty imaging is that the magnetic susceptibility generated from the metal prosthesis alters the regional static magnetic field, thereby changing local precessional frequencies [2]. This results in field inhomogeneities that distort regional anatomy and reallocate signal from its proper position to overlie like frequency spins, generating areas of signal pileup around areas of signal loss [3, 4], with resultant misregistration artifacts in both the slice selection and readout directions during signal encoding [2, 5]. Metallic implants also accelerate proton dephasing, which degrades the periprosthetic signal [6]. Magnetic susceptibility and its associated artifact vary according to material, peaking with stainless steel and decreasing from cobalt chromium to titanium, and its associated distortion is greatest closest to the metal arthroplasty [7].
Several modifications to routine hip imaging techniques may be performed to mitigate arthroplasty-related artifacts. Imaging at 1.5 T, as opposed to 3 T, is recommended because susceptibility artifact is proportional to the applied magnetic field strength. In addition, because susceptibility artifact is inversely proportional to the magnetic field frequency-encoding and slice select gradient strengths, increasing the gradient amplitudes will decrease susceptibility artifact. Consequently, using a wider receiver bandwidth and a smaller voxel size, which minimizes variation and dephasing within a single voxel, will increase the frequency-encoding and slice select gradient amplitudes, thereby decreasing distortion and improving spatial resolution [2–4]. Moreover, adjusting the direction of the frequency-encoding gradient to run along the long axis of the arthroplasty will diminish susceptibility artifact even further [6]. In addition, using FSE imaging and its 180° refocusing pulse will reduce signal loss from static field dephasing associated with arthroplasty imaging [5]. Finally, intermediate-weighted imaging will provide the spatial resolution, contrast-to-noise ratio, and fluid sensitivity necessary to accurately depict the periprosthetic bone, synovium, and soft tissues, as well as metallic deposits and adverse local tissue reactions [4] (Table 1).
TABLE 1.
Parameter | Coronal MAVRIC Inversion Recovery (Whole Pelvis) |
Coronal MAVRIC FSE (Whole Pelvis) |
Axial FSE (Whole Pelvis) |
Sagittal FSE (Affected Hip) |
Coronal FSE (Affected Hip) |
Oblique Axial FSE (Affected Hip) |
---|---|---|---|---|---|---|
| ||||||
TR (ms) | 4000 | 4000 | 5500 | 5500 | 4100 | 4000 |
TE (ms) | 24 | 24 | 24 | 24 | ||
Inversion time (ms) | 150 | |||||
Bandwidth (kHz) | 125 | 125 | 125 | 125 | ||
Echo-train length | 24 | 24 | 14 | 21 | 24 | 20 |
Flip angle (°) | 110 | 110 | 160 | 160 | 160 | 160 |
No. of excitations | 3 | 4 | 5 | 4 | ||
FOV (cm) | 36 | 36 | 32 | 26 | 26 | 26 |
Matrix | 256 × 192 | 512 × 256 | 512 × 256 | 512 × 384 | 512 × 352 | 512 × 256 |
Slice/gap (mm) | 5.5 | 3.5 | 5/0 | 2.5/0 | 4/0 | 4/0 |
No phase wrap | No | No | Yes | Yes | Yes | Yes |
Note—Patients were imaged in the supine position, with the feet first. MAVRIC = multiacquisition variable-resonance image combination, FSE = fast spin-echo.
It should be noted that a number of the aforementioned artifact reduction techniques will have downstream imaging effects. For example, a decreased signal-to-noise ratio will result from the use of a wide-readout bandwidth and thinner slices, which can be counterbalanced by increasing the number of excitations; however, this will, in turn, lengthen the scan time. On the other hand, steeper gradients will allow decreased interecho spacing and thus enable an increased echo-train length, making shorter imaging times possible, but at the cost of a decreased signal-to-noise ratio [4, 6].
Arthroplasty imaging fat suppression is more homogeneous when it is achieved through the use of STIR imaging, as opposed to frequency-selective fat suppression. Frequency-selective fat suppression takes advantage of the chemical-shift frequency differences between lipid and water and applies a saturation pulse with the same resonant frequency as fat, followed by a spoiling gradient pulse to null the signal from fat [8]; however, frequency shifts adjacent to metal alter the resonance frequency of fat, hampering frequency-selective fat suppression [5]. Inversion recovery fat suppression, on the other hand, exploits fat’s short T1 relaxation time, which is insensitive to magnetic field nonuniformity. STIR imaging uses a 90° inversion pulse at the null point of fat, thereby saturating the signal generated by adipose tissue [8]. Disadvantages associated with the use of inversion recovery imaging are a diminished signal-to-noise ratio and the inability to perform contrast-enhanced imaging, because enhancing tissue is nulled along with the fat signal as a result of its shortened longitudinal recovery time [5].
In recent years, several dedicated MRI 3D multispectral imaging sequences have been generated to address metal-related artifact, including the multiacquisition variable-resonance image combination (MAVRIC) and section encoding for metal artifact correction (SEMAC) techniques, which reduce both in- and through-plane distortion [5]. MAVRIC combines multiple 3D image datasets obtained at overlapped spectral frequency bins centered about the dominant frequency of hydrogen to create a composite image with minimal artifact [9], whereas SEMAC uses section-selective 3D spin-echo images obtained with view-angle tilting to minimize in-plane displacement and two phase-encoding directions to decrease through-plane distortion [10]. Furthermore, MAVRIC SL, a fusion MAVRIC-SEMAC sequence, merges the high signal-to-noise ratio and resolution associated with the MAVRIC sequence with the slice location selectivity that accompanies the SEMAC sequence. This hybrid sequence can acquire not only proton density– and T1-weighted images but also STIR images, allowing homogeneous fat suppression in the presence of metal [3]. Cross-talk artifacts have presented a challenge when it comes to 3D multispectral imaging, because spectral overlap is necessary to reduce gaps between the aforementioned spectral frequency bins. Flexible longitudinal magnetization contrast has been introduced to address this issue and bestows the operator with the ability to select the TR, echo-train length, and flip angle, followed by an automatic distribution of spectral bins to generate the least cross-talk possible. This technique allows less-restrictive spectral bin compositions, as well as the ability to generate T1-weighted 3D multispectral imaging, which is integral in instances where contrast enhancement is necessary, such as when evaluating for osteonecrosis or osteomyelitis [11]. These 3D multispectral imaging sequences allow better visualization of the bone-prosthesis interface and, consequently, arthroplasty component integration [4] (Fig. 1). In the presence of commonly used ceramic-backed metal implants, generally optimized FSE sequences are adequate to visualize the bone-arthroplasty interface; however, in the presence of cobalt chromium components seen in metal-on-metal or some metal-on-polyethylene devices, the 3D multispectral imaging techniques are essential for adequate visualization.
Optimized MRI around postoperative hardware in the hip also allows detection of complications after femoral neck fracture internal fixation, the most common of which is osteonecrosis of the femoral head (Fig. 2). Osteonecrosis is classically delineated on MRI by serpiginous hypointense signal with or without associated subchondral collapse or secondary osteoarthritis. However, it should be noted that these findings of osteonecrosis represent the later stages of abnormal femoral head blood flow, at a point when they are no longer reversible [6]. Reversible femoral head perfusion abnormalities have historically been assessed via radionuclide bone scintigraphy; however, in recent years, dynamic contrast-enhanced MRI and dynamic gadolinium-enhanced subtraction MRI have been used to gauge femoral head viability and perfusion before the onset of osteonecrosis or osteonecrosis [12]. These techniques have proved to be efficacious in assessing femoral head perfusion after displaced femoral neck fracture [13].
Dynamic contrast-enhanced MRI establishes abnormal femoral head blood flow via comparison of contrast-enhanced signal intensity between the affected hip and unaffected contralateral hip [12]. Unenhanced baseline imaging is obtained, followed by repetitive imaging every few seconds for a few minutes after the contrast bolus injection (Table 2). Subsequently, the signal intensity from a small ROI is collected and recorded against time, allowing signal intensity alterations after IV contrast injection and peak enhancement to be derived [14] (Fig. 3). Three main dynamic contrast enhancement curve patterns have emerged: type A curves show 25–30% decreased signal intensity on the affected side, type B curves show 30–70% reduced signal intensity on the affected side, and type C curves exhibit greater than 70% decreased signal intensity on the affected side. Studies thus far have indicated that the type C curves are at increased risk of progression to subsequent osteonecrosis [12].
TABLE 2.
Parameter | Value |
---|---|
| |
TR (ms) | |
Bandwidth (kHz) | 62.5 |
Echo-train length | |
Flip angle (°) | 12 |
No. of excitations | 1 |
FOV (cm) | 40 |
Matrix | 256 × 128 |
Slice/gap (mm) | 4 |
Note—All images were acquired in the coronal plane using the liver acquisition with volume acceleration technique and a cardiac coil. Patients were imaged in the supine position, with the feet first.
Dynamic gadolinium-enhanced subtraction MRI has been found to be particularly useful when evaluating enhancement within the already hyperintense lipid-rich femoral epiphyseal bone marrow. Subtraction imaging is accomplished by obtaining contrast-enhanced images every minute for 5 minutes after the administration of IV contrast agent and then subtracting absolute pixel values from unenhanced imaging by means of customary MRI software [15].
Imaging of Arthroplasty-Associated Complications
A variety of complications have been identified in patients after hip arthroplasty. Some of the more commonly encountered postoperative abnormalities include mechanical loosening, polyethylene wear, and adverse local tissue reactions.
Periprosthetic osseous resorption leading to mechanical loosening is a well-established complication of total hip arthroplasty. It has been theorized that micromotion between the implant or cement surface and the host bone resulting from mechanical stress leads to synoviocyte dispersal along the implant-bone or cement-bone interface, causing synoviallike fibrous membrane formation and the secretion of osteoclast-stimulating cytokines, ultimately resulting in osseous resorption. A spectrum of arthroplasty integration exists and includes complete implant fixation, limited arthroplasty integration represented by fibrous membrane formation, osseous resorption, and, finally, frank component loosening. Complete osseous integration is represented by normal bone marrow signal intensity flush against the cement or arthroplasty (Fig. 4). A thin rim of intermediate signal intensity around the arthroplasty signifies fibrous membrane formation (Fig. 5), whereas osteolysis is defined by a thicker rind of intermediate signal intensity at the prosthesis-bone or cement-bone interface surrounded by a hypointense rim (Fig. 6). Finally, frank component loosening corresponds to circumferential osteolysis with or without associated altered arthroplasty alignment or subsidence [4]. The implementation of the aforementioned metal artifact reduction techniques and dedicated MRI sequences afford improved visualization of the bone-implant interface and, consequently, hip arthroplasty component integration, which may allow early diagnosis and treatment and result in superior patient outcomes [6].
The most common reason for gradual metal-on-polyethylene and ceramic-on-polyethylene hip arthroplasty failure is polyethylene wear. Wear of the acetabular polyethylene liner releases polymeric debris into the joint, resulting in synovitis, increased osteoclastic and decreased osteoblastic activity, and, eventually, bulky osteolysis and implant loosening. MRI features of polyethylene wear include pseudocapsular distention by a thickened isointense-to-hyperintense synovium associated with intermediate-intensity debris, which often decompresses into the greater trochanteric, iliopsoas, and subiliacus bursae. Ultimately, the intermediate intensity particulate debris creates a cytokine-mediated process of periprosthetic bone resorption in the form of a bulky osteolysis [16] (Fig. 7). Intermediate-weighted MRI sequences are vital to detecting the intermediate-intensity particulate debris associated with polyethylene wear.
Metal arthroplasty–associated complications, including metallosis, aseptic lymphocytic vasculitis–associated lesions, and trunnionosis, have been termed adverse local tissue reactions. These reactions are thought to result from hypersensitivity to metallic debris, metal ions, or corrosion products generated by implant-related wear. Greater wear has been found to be associated with increased edge loading, which may result from a shallow acetabular cup or abnormal acetabular cup inclination [17].
Metallosis is associated with above-average metal implant wear, resulting in elevated levels of blood metal ions and a resultant foreign body reaction. MRI shows hypointense intra- or extracapsular metallic debris, hypointense thickened synovium, hypointense osteolysis, and eventual mechanical loosening without features of aggressive surrounding soft-tissue destruction [4] (Fig. 8).
Aseptic lymphocytic vasculitis–associated lesion describes a type IV hypersensitivity reaction to metal, which is most commonly not associated with a high metal implant wear rate. Histologic evaluation of aseptic lymphocytic vasculitis–associated lesion shows metallic debris, corrosion products, lymphocytic infiltrates, and tissue necrosis [18]. Characteristic MRI features include hyperintense synovitis and debris, cystic or solid soft-tissue deposits, and extensive extracapsular regional soft-tissue damage with dehiscence of the anterior and posterior pseudocapsule and decompression into the adjacent iliopsoas, subiliacus, and greater trochanteric bursae [4] (Fig. 9). Nawabi et al. [19] found that increased synovial thickening (median, 12 mm) and a combination of solid and fluid-based synovitis strongly correlated with moderate-to severe aseptic lymphocytic vasculitis–associated lesions. They also found that solid and fluid-based synovitis, pseudocapsular disruption, and synovial decompression into the surrounding bursae were 90% sensitive and 86% specific for predicting intraoperative tissue damage, which is much more reliable than serum ion levels [19].
Trunnion corrosion, also referred to as trunnionosis, reflects a soft-tissue reaction to metal by-products released from micromotion and mechanical wear at the head-neck or neck-stem junctions of mixed alloy modular metal-on-polyethylene arthroplasties [17, 20, 21]. An adverse local tissue reaction has been found to result in synovitis, debris, soft-tissue destruction, thick-walled fluid collections, and associated medial calcar resorption described at MRI [22] (Fig. 10).
Posterior hip dislocation is a potential postoperative complication after total hip arthroplasty placement through a posterior or posterolateral approach. To mitigate this risk, posterior soft-tissue reconstruction is often performed at the time of surgery to enhance hip joint stability [23]. As such, it is imperative to assess the integrity of the posterior joint capsule and short external rotator muscles. Posterior capsular dehiscence can be appreciated at MRI by a lack of continuity of the posterior pseudocapsule and short external rotators with the greater trochanter, often showing a fluid-filled gap interposed between the two, with or without associated anterior pseudocapsular thickening and hyperintensity. Longitudinal MRI studies indicate that the repairs fail early but that the retracted tendons form scar-in-continuity that aligns with the tendon long axis and prevents instability in most cases [23].
A frequent source of anterior hip pain after hip arthroplasty is iliopsoas tendinopathy, which often results from impingement of the iliopsoas tendon by an overly anteverted acetabular cup, oversized acetabular component, or long iliac fixation screws [24]. MRI features of iliopsoas impingement syndrome include tendinosis, partial-thickness tears, and full-thickness tendon rupture, with or without associated iliopsoas or subiliacus bursitis.
After total hip arthroplasty, lateral hip pain is often related to abductor tendinopathy, which ranges from gluteus medius and minimus tendinosis to partial-thickness longitudinal tears to full-thickness tendon tears, with or without associated greater trochanteric bursitis. Acutely, peritendinous edema may be appreciated within the surrounding soft tissues, whereas in the chronic setting, MRI may show scar formation between the ends of the torn tendon fibers, or to the adjacent pseudocapsule or iliotibial band [4].
Although postoperative infection is a relatively uncommon complication after total hip arthroplasty [25], it often presents a diagnostic dilemma at imaging and frequently requires arthrocentesis to confirm or reject its presence. Several nonspecific MRI features of infection include joint effusion, extracapsular soft-tissue edema, and reactive lymphadenopathy. Findings consistent with a sinus tract, abscess, or osteomyelitis are more specific but less sensitive indications of infection. Finally, a thick lamellated hyperintense synovium composed of multiple layers has been found to be both highly sensitive and specific for infection with high inter- and intraobserver reliability [26].
Conclusion
MRI with refined pulse sequence parameters, metal artifact–reducing techniques, and dedicated sequences allows reliable and reproducible evaluation of the native and postarthroplasty hip joint. It affords identification of aseptic loosening, wear-induced synovitis, and metal arthroplasty–associated complications, which can ultimately lead to arthroplasty failure. In addition, more recent use of dynamic contrast-enhanced MRI allows identification of patients who are at increased risk of developing femoral head osteonecrosis and associated collapse.
Acknowledgments
Supported by grant 1R01 AR064840-01 from the National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health.
H. G. Potter has received research support from GE Healthcare.
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