Abstract
Ankle arthritis often results from post-traumatic, rheumatologic, or structural etiologies, and has historically been surgically managed with tibiotalar joint arthrodesis. Total ankle arthroplasty (TAA) is a promising alternative, particularly for failed ankle fusions. The purpose of this study was to review the current literature on this topic and evaluate outcomes of converted failed ankle fusions to TAA. Conditional variables included functional scores, pain relief, complications, and patient satisfaction. This analysis revealed significant improvements in AOFAS functional scores (mean difference: +35.6) and substantial reductions in VAS pain scores (mean difference:-14.3), with a high patient satisfaction rate of 88%. Complications often seen included: 13% intraoperative fractures, 11% delayed wound healing, 11% symptomatic arthrofibrosis, 10% persistent pain requiring revision or proximal amputation, and 3% tendon injuries. Despite the complexity of the procedure, these results support ankle fusion takedown and conversion to TAA as an effective revision strategy for unsatisfied arthrodesis patients. Further clinical research is needed to refine surgical techniques and implant selection.
Introduction
Ankle arthritis is a complex condition traditionally managed with arthrodesis, often as a result of traumatic, rheumatologic, or structural etiologies. While ankle fusion remains a reliable surgical option for select patients, it is not without drawbacks. Long-term complications include progressive adjacent joint arthrosis, persistent pain, and suboptimal patient-reported outcomes. For end-stage arthritis of adjacent joints, these challenges frequently necessitate additional interventions, highlighting the need for alternative approaches, such as total ankle arthroplasty (TAA). Advancements in total ankle arthroplasty have demonstrated comparable complication rates to arthrodesis, while offering patients an alternative that spares joint motion.
Revision surgeries for failed ankle fusions, such as tibiotalocalcaneal arthrodesis, carry substantial risks, including nonunion and amputation. With this in mind, the process of converting a previously performed ankle fusion to a TAA has emerged as a promising alternative, with well documented functional and clinical outcomes. First described in 2004 by Greisberg, this procedure remains technically demanding, requiring meticulous patient selection and adjunctive techniques to mitigate risks.
Despite its challenges, a systematic review of the current literature reveals encouraging outcomes, including enhanced range of motion and patient satisfaction. The purpose of this study was to provide a comprehensive evaluation of ankle arthrodesis takedown and conversion to TAA. By synthesizing data on patient outcomes, and complication rates, we aim to provide evidence-based insights to guide clinical decision-making and advance treatment strategies for patients with previous ankle fusion.
Methods
A formal systematic review was performed using the Preferred Reporting Items for Systematic reviews and Meta-analysis guidelines. A broad search of online databases google scholar, Cochrane Library, and PubMed was conducted, incorporating the following search terms: ankle replacement OR ankle arthrodesis OR takedown total. Each search term was modified to reflect the different databases. Studies and references of selected articles were screened by the primary author (JK). Any potential articles in question were reviewed by the secondary author (CM) and persistent disagreements were reviewed by the senior author (GB). The earliest documentation of this procedure was performed in July 2004 and thus our search was contained between that time point and July 2024. Articles were included if they discussed the types of implants used, presence of adjacent joint arthrodesis, pre- and intra-operative procedures, post-operative protocols, complications, AOFAS scores, and VAS pain scores. Studies were excluded if they did not explore these outcome measures, were outside of our search timeline, were published in non-peer reviewed journals, in vivo or cadaveric studies, or duplicates. The included studies were assessed for study characteristics and outcomes using a data extraction form. When information was missing it was listed as not recorded.
The primary clinical outcome measures included AOFAS functional scores, VAS pain scores, and patient satisfaction, while secondary outcomes included complications such as intraoperative fractures, flexor hallucis longus tendon injuries, delayed wound healing, symptomatic arthrofibrosis, and treatment failures. For continuous outcomes (AOFAS and VAS scores), effect sizes were calculated using mean differences and their corresponding 95% confidence intervals (CIs). For other measures, effect sizes were estimated by calculating the prevalence of each outcome. Freeman-Tukey transformation was used in estimating the prevalence. Heterogeneity among the studies was evaluated using the I² statistic alongside the chi-square test. A threshold of I² ≥ 50% and a chi-square p-value < 0.05 indicated significant heterogeneity, prompting the use of a random-effects model (DerSimonian–Laird method) to calculate the pooled effect sizes for AOFAS scores, VAS scores, intraoperative fractures, delayed wound healing, and treatment failures. In cases where these criteria were not met, a fixed-effects model was employed for the analysis of satisfaction, tendon injuries (specifically flexor hallucis longus), and symptomatic arthrofibrosis.
Meta-regression analyses were conducted to identify potential sources of heterogeneity, by fitting individual models for sample size, publication year, participant age, follow-up duration, and type of implant (Implants included in this analysis were Hintegra, Agility, Inbone, Salto, Infinity, and STAR). Due to the limited number of studies reporting tendon injuries, regression analysis could not be performed. Subgroup analyses were carried out to assess the moderating effects of these sources on the effect sizes, with continuous measures dichotomized at the mean. Statistical significance was set at p < 0.05. Sensitivity analyses were performed to test the robustness of the findings by sequentially excluding each study and recalculating the pooled estimates. Publication bias was evaluated using funnel plots and Egger’s test. All statistical analyses were conducted using Stata version 18.5, with effect-sizes considered statistically significant at p < 0.05.
Results
AOFAS functional score
AOFAS scores were reported by five studies. ,,,,, The pooled mean difference indicated a significant postoperative improvement, with an average increase of 35.6 points (95% CI: 29.4 to 41.84), ranging from 23.4 to 45 points across the studies ( Fig. 1 ). However, substantial heterogeneity was observed among the studies (I² = 73.2%, p = 0.005), indicating variability in effect sizes.
Mean differences of AOFAS functional scores comparing pre- and post-operative levels.
Meta-regression analysis revealed that publication year was significantly associated with the mean difference in AOFAS scores, with more recent studies showing larger improvements (β = 1.02, p = 0.03; Supplementary Table S1 ). In contrast, sample size, participant age, follow-up duration, and implant type were not significant moderators of effect size ( Supplementary Table S1 ). Publication year accounted for 63.3% of the between-study variance.
After adjusting for publication year in subgroup analyses, studies published before 2010 showed a pooled mean difference of 32.5 points (95% CI: 24.8 to 40.1; I² = 71.5%, p = 0.03), whereas those published after 2010 had a pooled effect size of 40.6 points (95% CI: 31.7 to 49.5; I² = 65%, p = 0.091). Although the effect sizes between the two subgroups did not differ statistically (Q(1) = 1.9, p = 0.172), this suggests a gradual improvement over time.
Sensitivity analyses showed that the pooled mean differences (range: 33.4 to 38.3 points) remained stable when each study was excluded sequentially, indicating that no single study unduly influenced the meta-analysis results ( Fig. S1A ). Furthermore, the funnel plot and Egger’s test (t = −1.33, p = 0.275) confirmed the absence of significant publication bias ( Fig. S2A ).
VAS pain scores
Four studies reported VAS scores. ,,, The pooled effect size indicated that converting failed ankle fusions to total ankle replacement was associated with a significant reduction in pain compared to preoperative levels (mean difference: −14.3 points, 95% CI: −19.0 to −9.6; Fig. 2 ). However, substantial heterogeneity was observed among the studies (I² = 97.9%, p < 0.001).
Mean differences of VAS pain scores comparing pre- and post-operative levels.
Meta-regression analysis identified both follow-up duration and implant type as significant contributors to this variability, with implant type accounting for 59.6% of the between-study variance (Table S1). While the pooled analysis suggested potential publication bias, stratification by follow-up duration and implant type eliminated this bias, as confirmed by funnel plots and Egger’s test (p = 0.083; Fig. S2B ).
Subgroup analyses revealed that the implant type significantly influenced pain reduction. Hintegra implants had a smaller mean difference (−5.5 points; 95% CI: −9.0 to −2.1; I² = 98.2%, p < 0.001), whereas other implants demonstrated a more pronounced effect (−41.1 points; 95% CI: −53.1 to −29.0; I² = 58.2%, p = 0.12), with a significant group difference (p < 0.001; Fig. 2 a). Similarly, follow-up duration influenced outcomes. Studies with an average follow-up of ≤52 months showed a mean difference of −41.1 points (95% CI: −53.1 to −29.0; I² = 58.2%, p = 0.12), while those with >52 months of follow-up showed a smaller mean difference of −5.5 points (95% CI: −9.0 to −2.1; I² = 98.2%, p < 0.001), again with a significant group difference (p < 0.001; Fig. 2 b).
Leave-one-out sensitivity analysis revealed that the overall effect size was influenced by certain individual studies ( Fig. S1B ). For example, omitting Preis et al. altered the mean difference to −28.4 points, which was no longer statistically significant (p = 0.064).
Satisfaction
Five studies assessed patient satisfaction. ,,,, The pooled satisfaction rate was 88% (95% CI: 82% to 93%), with no significant heterogeneity observed among the studies (I² = 0%, p = 0.64; Fig. 3 ).
Prevalence of treatment satisfaction after TAA.
Both the funnel plot and Egger’s test (p = 0.286) showed no evidence of publication bias ( Fig. S2C ). Additionally, sensitivity analysis confirmed that the pooled satisfaction rate was stable, as no single study significantly influenced the overall result ( Fig. S1C ).
Complications
Intra-operative fractures
Seven studies identified intraoperative fracture as a complication of TAA. ,,,,,, The pooled prevalence of intraoperative fractures was 13% (95% CI: 3 to 26%), with substantial heterogeneity (I²= 76.4%, p < 0.001), Fig. 4 . The publication year was found to be a significant source of this heterogeneity, accounting for 100% of between-study variation, with no residual heterogeneity observed (Table S1). Studies published before 2010 reported a higher prevalence (26%, 95% CI: 8% to 49%) compared to those published after 2010 (3%, 95% CI: 0% to 9%), with this difference being statistically significant (p = 0.02), Fig. 4 . Funnel plot and Egger’s test (p = 0.987) indicated no evidence of publication bias ( Fig. S2D ). Sensitivity analysis also revealed that omitting individual studies did not statistically change the pooled estimate ( Fig. S1D ).


