Cementless tapered wedge stems in patients undergoing primary total hip arthroplasty with Dorr C bone—are complication risks increased?
Introduction
With increases in lifespan, the number of elderly patients undergoing primary total hip arthroplasty (THA) continues to grow (1). THA in this group presents a challenge due to the increased risk of medical and surgical complications (2). The optimal method of femoral fixation in these elderly patients remains controversial due to commonly found compromised proximal femoral bone stock, often classified as Dorr type C bone (Figure 1) (3).
According to the Dorr classification system, proximal femoral bone quality may be classified as type A (thick cortices and narrow intramedullary canal), type B (thinning of posterior cortical wall), or type C (thin cortices and wide intramedullary canal) (3,4). Specifically, with the growing use of cementless tapered femoral stems, the outcomes of these implants in patients with suboptimal bone quality need to be examined.
Cementless tapered femoral stems for primary THA are the standard for the treatment of primary hip osteoarthritis in younger patients, relying on immediate implant stability for success (5). However, cementless THA in the elderly remains controversial for fear of fracture or component subsidence (6). Methylmethacrylate is commonly used for stem fixation in patients with Dorr C bone undergoing definitive treatment of hip osteoarthritis (7). However, the use of cemented femoral stems in general has declined due to challenges in obtaining a consistent and reproducible cement mantle for long-term durable fixation. Additionally, the use of cement can lead to medical complications including pulmonary and cardiac collapse, fat embolism, as well as increased operative time (8-12). Therefore, there has been increased interest in the use of cementless THA in older patients with compromised bone quality (5,13).
Given the controversy concerning femoral fixation in suboptimal bone, the purpose of this multicenter study was to compare: (I) clinical outcomes and (II) complications mainly with respect to fracture and subsidence using a tapered femoral prosthesis in patients with Dorr type C versus A/B bone undergoing primary THA.
Methods
This study was conducted in accordance to the Helsinki declaration and approved by institutional/regional/national ethics/committee/ethics board of The University of Louisville Institutional Review Board (No. 16.1002) and informed consent was taken from all the patients.
Following the various Institutional Review Board approvals, a multicenter review at two different institutions was conducted, including 1,030 patients who underwent primary THA from 2004 to 2015 with a tapered wedge cementless femoral stem. All preoperative hip radiographs were categorized using the Dorr classification system (Figure 1) (3). During this period, 48 patients with Dorr C bone who underwent THA were identified. This cohort included 38 females and 10 males who had a mean age of 69 years (range, 51 to 91 years), a mean body mass index (BMI) of 30.5 kg/m2 (range, 19.8 to 43.4 kg/m2), a mean Charlson Comorbidity Index (CCI) of 1.3 (range, 0 to 9), and a mean follow-up of 50.6 months (range, 24.0 to 85 months). These patients were compared to a matched cohort of 48 patients with Dorr A/B bone, matched for age, sex, and BMI. This cohort included 38 females and 10 males who had a mean age of 70 years (range, 50 to 91 years), a mean BMI of 31.1 kg/m2 (range, 20.7 to 50.2 kg/m2), a mean CCI of 1.9 (range, 0 to 4), and a mean follow-up of 46.9 months (range, 24 to 71 months) (Table 1).
Table 1
Variables | Dorr A/B | Dorr C | P value |
---|---|---|---|
Total patients | 48 | 49 | – |
Mean follow-up (month) | 46.9 | 50.6 | 0.2751 |
Demographics | |||
Mean age, years | 69.9 | 68.7 | 0.5409 |
Females | 38 | 38 | – |
Males | 10 | 10 | – |
Mean BMI, kg/m2 | 31.1 | 30.5 | 0.6329 |
Mean CCI | 1.9 | 1.3 | 0.0455 |
BMI, body mass index; CCI, Charlson Comorbidity Index.
All THAs were performed using hydroxyapatite tapered femoral stems (Stryker Accolade I or IITM, Mahwah, New Jersey) in the lateral decubitus position through either a posterior or direct lateral approach (14). The Accolade ITM TMZF component is a titanium-alloy cementless stem with a PureFix hydroxyapatite coating (15). Compared to the first generation design, the Accolade IITM stem is shorter, has an enhanced proximal fit, and utilizes titanium Ti6Al4V alloy (15,16). Despite these minor design differences, these implants rely on similar fixation principles. All patients were immediately full weight bearing postoperatively and started physical therapy on the day of surgery.
Demographic, clinical, and surgical data were extracted from the institutions’ total joint registries. Clinical outcomes were evaluated using preoperative and postoperative Harris Hip Scores (HHSs) (17). Complications including fracture, dislocation, and infection were recorded.
Postoperative anteroposterior (AP) pelvis and AP and lateral hip X-rays were evaluated for femoral component subsidence or loosening (Figure 2) (18,19).
Subsidence was measured using bony landmarks in the AP radiograph. Magnification differences between time intervals were controlled for by knowing and measuring the size of the implanted femoral head.
Student t-tests were performed to evaluate significant differences in demographic variables (age, BMI, CCI), HHSs, composite revision rates, and subsidence between the two groups. All data analyses were performed using SPSS 22 (IBM Corp., Armonk, NY, USA). A P value of 0.05 was set to determine statistical significance.
Results
Clinical outcomes
There were no significant differences in the postoperative HHS (P=0.2653) or the change in HHS (P=0.9320) between the two cohorts (Table 2).
Table 2
Outcomes | Dorr A/B | Dorr C | P value |
---|---|---|---|
Preoperative HHS (mean) | 44.4 | 49.4 | 0.2192 |
Postoperative HHS (mean) | 84.3 | 81.7 | 0.2653 |
Change in HHS (mean) | 44.4 | 43.9 | 0.9320 |
Intraoperative fractures | 0 | 0 | – |
Postoperative periprosthetic fractures | 1 | 1 | – |
Postoperative dislocation | 0 | 1 | – |
Infections requiring revision | 0 | 1 | – |
Mean one year subsidence (mm) | 1.2 | 1.4 | 0.5164 |
Aseptic loosening of acetabular component | 0 | 2 | – |
Aseptic loosening of femoral component | 0 | 0 | – |
HHS, Harris Hip Score.
In patients with Dorr C bone, pre- and postoperative mean HHSs were 49 points (range, 8 to 85 points) and 82 points (range, 50 to 99 points), respectively, with a mean improvement in HHS of 44 points. The Dorr A/B pre- and postoperative mean HHSs were 44 points (range, 28 to 74 points) and 84 points (range, 68 to 99 points), respectively, with a mean improvement in HHS of 44 points.
Complications
Overall, there were three complications in the Dorr C group and one complication in the Dorr A/B group (Table 2). There were no intraoperative fractures or immediate postoperative fractures in either cohort. In the Dorr C group, one patient dislocated during the first year following the index procedure but did not require a revision surgery. There was one case of postoperative prosthetic infection requiring revision surgery in the Dorr C group. In each group, one patient had a fall more than 1 year postoperatively, sustaining a periprosthetic femur fracture requiring revision. There was no difference in revisions for any reason (P=0.232).
Radiographic outcomes
The mean 1-year subsidence of the Dorr C and A/B groups were 1.4 mm (range, 0 to 6 mm) and 1.2 mm (range, 0 to 5 mm) respectively (P=0.5164). Neither group had signs of postoperative aseptic loosening of the femoral component, but 2 patients in the Dorr C group had aseptic loosening of the acetabular component (Table 2).
Discussion
Although THA initially utilized cemented fixation with excellent results, the use of methylmethacrylate is not without risk, as it is associated with complications including loosening, osteolysis, pulmonary embolism, and cement toxicity (10,11,20,21). The utilization of cemented THA has declined markedly due to the advent of cementless designs, with growing interest in the use of cementless femoral stems in elderly patients given the success of long-term biologic fixation (13). Yet, due to need for immediate and rigid implant fixation with the use of cementless implants, there is a concern for fracture and subsidence in patients with compromised host bone quality, such as those with Dorr C bone (22). In this study, we demonstrated that patients with Dorr C bone undergoing cementless THA achieved similar clinical outcomes, complication rates, and radiographic outcomes to those with Dorr A/B bone.
This study is not without limitations. This is a small consecutive series with only 51 primary THA patients who had Dorr C bone receiving a tapered cementless implant. We expect this proportion to rise given the projected increase in the number of elderly patients undergoing primary THA over the next decade. However, this number is consistent with other series in the literature using cementless femoral implants in Dorr C bone, with a total of 210 cases reported in 4 series (Table 3).
Table 3
Author | Hips (number) | Dorr C hips (number) |
Average age (years) |
Follow-up (years) |
Overall aseptic survivorship (%) |
HHS at last follow-up |
---|---|---|---|---|---|---|
Berend et al. (23) | 96 | 48 | 79 | 5 | 97.96 | 84 |
Hozack et al. (24) | 105 | 5 | 61.2 | 6.1 | 99 | 88.6 |
Meding et al. (13) | 2,321 | 127 | 61 | 5.9 | 99.99 | 93.2 |
McLaughlin et al. (25) | 350 | 68 | 69 | 20 | 98 | 89 |
Lindner et al. | 98 | 49 | 68.7 | 4.2 | 100 | 81.7 |
THA, total hip arthroplasty; HHS, Harris Hip score.
Additionally, this is a short-term study with one-year minimum follow-up, and longer-term follow-up may be necessary to fully evaluate any differences between these two groups. Despite these limitations, we believe the results of this multicenter matched cohort study are valuable in understanding the excellent initial outcomes in patients with poor bone quality following cementless THA.
Many studies have demonstrated excellent radiographic, functional, and clinical outcomes of patients undergoing primary THA utilizing a tapered uncemented femoral component. Kolisek et al. demonstrated a 0.3% femoral component revision rate at 5 years using a tapered cementless femoral implant in 936 patients (26). Pierce et al. reported 5-year aseptic and all-cause survivorship rates of 99.4% and 97.9%, respectively, for the femoral component used in this study (27). However, very few studies have stratified outcomes based on Dorr bone classification (Table 3). For example, Issa et al. demonstrated that a cementless tapered stem system has the ability for stable fixation for all Dorr types due to variation in the medial and lateral dimensions based on the stem size (15). In a study including 127 patients with Dorr C bone, Meding et al. demonstrated no difference in aseptic survivorship, HHSs, or radiographic outcomes between the Dorr type A, B, or C cohorts (13). Similarly, in the present study, no significant difference was found in postoperative HHSs between the Dorr type C and Dorr A/B cohorts.
In patients with Dorr C bone quality, attempting to provide rigid and stable fixation with tapered stems against cortical bone can lead to fracture unless the technique for broaching and stem insertion are performed in a careful manner. The variation in the femoral canal medial and lateral fit in the stem design utilized in this study allowed for excellent fit in all bone types, minimizing the risk of fracture. The present study demonstrated similar rates of intraoperative and postoperative periprosthetic femoral fracture between the Dorr C and the Dorr A/B groups. This is in contrast to the finding by Gromov et al. that Dorr C bone resulted in a five-fold increase in the risk of periprosthetic femur fracture compared to Dorr B bone in a cohort of 1,441 patients (P<0.001) (7). However, not all cementless femoral stems are the same and the type of cementless stem design is a risk factor for fracture (28-30). In the present study, there was 1 dislocation in the Dorr C group (2%) and no dislocations in the Dorr A/B group. Recent studies have shown the incidence of dislocation following primary THA to approach 2%, which is comparable to the rate demonstrated in this study (31). There were similar rates of prosthetic joint infection between the two groups in this study, with one infection in the Dorr C group and no infections in the Dorr A/B group.
In terms of radiographic outcomes, there was no significant difference between Dorr C and A/B groups at one year with respect to subsidence. There were no cases of aseptic loosening of the femoral component in either group. These findings are consistent with the findings of Riley et al. who found 2-year aseptic survivorship of cementless femoral components to be 99% in a cohort of 74 patients aged 80 years or older (5).
With the marked rise of the use of cementless femoral components over the past decade, surgeons may feel inclined to use cementless stems in Dorr C bone due to their comfort level using the same predictable and reproducible surgical technique. This study demonstrates clinical and radiographic success of THA with cementless tapered femoral stems in patients with compromised proximal femoral bone stock. We did not identify an increased risk of complications in the Dorr C group especially with respect to intraoperative fracture or subsidence. With careful surgical technique, cementless tapered wedge stems are a viable alternative to cemented femoral fixation in patients with Dorr C bone undergoing primary THA.
Conclusions
Current generation tapered wedge cementless femoral stems provide stable fixation for patients with Dorr C bone quality without increased complications with respect to fracture or subsidence and can be considered an alternative to cemented stems in patients with compromised bone quality.
Acknowledgments
Funding: None.
Footnote
Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at https://atm.amegroups.com/article/view/10.21037/atm.2019.08.124/coif). RD declares the following outside of the submitted work: Baltimore City Medical Society: board or committee member; Flexion Therapeutics: research support; Orthofix, Inc.: research support; Stryker: research support; tissue Gene: research support; United Orthopedics: research support. MAM declares the following outside of the submitted work: AAOS: board or committee member; American Association of Hip and Knee Surgeons: board or committee member; Cymedica: paid consultant; DJ Orthopaedics: paid consultant; research support; Flexion Therapeutics: paid consultant; Johnson & Johnson: paid consultant; research support; Journal of Arthroplasty: editorial or governing board; Journal of Knee Surgery: editorial or governing board; Knee Society: board or committee member; Medicus Works LLC: publishing royalties, financial or material support; Microport: IP royalties; National Institutes of Health (NIAMS & NICHD): research support; Ongoing Care Solutions: paid consultant; research support; Orthopedics: editorial or governing board; Orthosensor: paid consultant; research support; Pacira: paid consultant; Peerwell: paid consultant; stock or stock options; Performance Dynamics: paid consultant; Pfizer: paid consultant; Skye Biologics: paid consultant; Stryker: IP royalties; paid consultant; research support; Surgical Techniques International: editorial or governing board; TissueGene: paid consultant; research support; Up-to-Date: publishing royalties, financial or material support; USMI: stock or stock options; Wolters Kluwer Health-Lippincott Williams & Wilkins: publishing royalties, financial or material support. ALM declares the following outside of the submitted work: AAOS: board or committee member; Journal of Arthroplasty: editorial or governing board; Stryker: IP royalties; paid consultant; paid presenter or speaker; research support. The other authors have no conflicts of interest to declare.
Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved. This study was conducted in accordance to the Helsinki declaration and approved by institutional/regional/national ethics/committee/ethics board of The University of Louisville Institutional Review Board (No. 16.1002) and informed consent was taken from all the patients.
Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.
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