Abstract
Background
It is unclear whether Broström with Internal Brace™ augmentation enables patients with structural cavovarus deformity to achieve satisfactory patient-reported outcomes. Patient Reported Outcomes Measurement Information System (PROMIS) measures of physical function (PF) and pain interference (PI) are validated metrics of orthopaedic foot and ankle clinical outcomes. The Cumberland Ankle Instability Tool (CAIT) is a validated metric of ankle stability. This study aimed to determine whether augmentation results in better PROMIS and CAIT for patients with deformities compared to non-augmented.
Methods
37 patients with cavovarus deformity who underwent lateral ankle ligament reconstruction at a single institution between 2013 and 2024 were retrospectively reviewed. Two investigators independently evaluated all records. Revisions, allografts, nonanatomic reconstructions, flexor digitorum longus transfers, progressive collapsing foot deformities, concomitant hindfoot arthrodesis, associated ankle arthroplasties, and concomitant fractures were excluded. Cavovarus deformity was defined radiographically by an increased talo-first metatarsal angle, or Meary’s angle, (>4° convex upward), elevated calcaneal pitch (>30°), increased first metatarsal-calcaneal angle, or Hibb’s angle, (>45°), and a decreased talocalcaneal angle (<20°). Patients completed surveys containing PROMIS and CAIT. T-tests and Kruskal-Wallis tests assessed associations.
Results
Overall, the mean PROMIS PF and PI in patients with structural deformity were 48.0 ± 8.1 and 51.9 ± 9.8, respectively. Compared to non-augmented Broström, augmentation resulted in significantly higher PF and lower PI for patients with deformities (PF 49.7 ± 7.8 vs. 41.9 ± 6.0, p < 0.01; PI 49.9 ± 7.8 vs. 58.8 ± 6.0, p = 0.04). Postoperative CAIT was not significantly different between augmented and non-augmented (19.1 ± 7.9 vs. 12.8 ± 8.5, respectively p = 0.09).
Conclusions
Augmented Broström may enable patients with structural ankle deformity to achieve improved functional outcomes compared to non-augmented Broström, as augmentation resulted in both statistically and clinically significant improvements in PROMIS PF and PROMIS PI compared to non-augmented.
Level of evidence
III
1
Introduction
Various techniques are utilized to restore ankle function in chronic lateral ankle instability (CLAI), including both anatomic and nonanatomic lateral ligament reconstructions ,, . The traditional strategy is through an anatomic reconstruction of the anterior talofibular ligament (ATFL) and calcaneofibular ligament (CFL), known as the Broström procedure .
Recently, surgeons have augmented the Broström procedure with suture tape, which reinforces the stability and integrity of the repair ,,, . While prior studies indicate that augmentation may improve ankle stability compared to traditional, non-augmented Broström, there is mixed data regarding whether augmentation results in improved functional outcomes ,,,,,,,,,,, . While some studies reveal no significant differences in patient-reported outcomes (PROs) between augmented and non-augmented, others demonstrate that augmentation may improve PROs including return to activity, foot and ankle outcome scores (FAOS), Foot and Ankle Disability Index (FADI), American Orthopaedic Foot and Ankle Society (AOFAS) scores, the Foot and Ankle Ability Measure (FAAM), and the Cumberland Ankle Instability Tool (CAIT) ,,,,,,,,,,, .
Multiple types of suture tape augmentation exist. The Internal Brace™ (Arthrex, Naples, FL) has proven a particularly effective option, as prior studies found that Internal Brace augmentation produces favorable outcomes including return to pre-injury activity level, as well as improved AOFAS, FAAM, and CAIT scores ,, .
Few studies have evaluated outcomes following Broström reconstruction in patients with structural deformities. A majority of studies evaluating PROs after Broström exclude patients with deformities including ankle varus ,,,,,,,,, . It therefore remains unclear to what extent patients with structural deformities benefit from lateral ankle ligament reconstruction procedures.
Patient Reported Outcomes Measurement Information System (PROMIS) computerized adaptive tests (CATs) of physical function (PF) and pain interference (PI) are validated metrics in foot and ankle orthopaedics. Unlike many commonly used legacy instruments including FAAM, Foot Function Index, AOFAS scores, and Visual Analogue Scale, PROMIS consistently exhibits greater responsiveness, decreased floor and ceiling effects, improved time efficiency, and easy-to-interpret t-score–based scoring systems ,,,,, . The Cumberland Ankle Instability Tool (CAIT) is a validated metric of ankle stability .
To our knowledge, no prior studies have compared PROMIS and CAIT between augmented Broström and non-augmented Broström in patients with preoperative structural ankle deformities. This study therefore aimed to determine whether augmentation results in better PROMIS and CAIT for patients with cavovarus deformities compared to non-augmented Broström. We hypothesized that Internal Brace augmentation would improve PROMIS and CAIT for patients with deformities compared to Broström without augmentation.
2
Methods
2.1
Population
127 patients who underwent lateral ankle ligament reconstruction at a single institution between January 2013-January 2024 were retrospectively reviewed. Two investigators independently evaluated all records. Revisions, allografts, nonanatomic reconstructions, flexor digitorum longus transfers, progressive collapsing foot deformities, concomitant hindfoot arthrodesis, associated ankle arthroplasties, and concomitant fractures were excluded. 37 patients with structural ankle deformity (varus deformity, n = 37) were identified. Cavovarus deformity was defined radiographically by an increased talo-first metatarsal angle, or Meary’s angle, (>4° convex upward), elevated calcaneal pitch (>30°), increased first metatarsal-calcaneal angle, or Hibb’s angle, (>45°), and a decreased talocalcaneal angle (<20°). These 37 patients were contacted by email to complete surveys via REDCap containing PROMIS CATs and CAIT, as well as additional questions querying self-reported ability to increase activity postoperatively compared to preoperative baseline . After an initial email, if patients did not complete surveys or declined consent, subsequent email and phone calls were attempted for a total of five attempts. All surgeries were performed by foot and ankle fellowship-trained orthopaedic surgeons (n = 4). Surgeon preference determined the choice of traditional Broström versus augmented. Due to evidence suggesting increased stability with mechanical load in augmentation ,,, , surgeons at our institution often performed augmented procedures for patients with deformities, especially considering many of these patients had poor tissue quality. A greater proportion of patients had Broström with augmentation after 2017 because the authors’ institution began performing more augmented than non-augmented due to evidence suggesting augmentation results in improved stability and response to mechanical load , . Augmentation was performed using Internal Brace suture tape (Arthrex, Naples, FL). While a current gold standard has not yet been established, this study seeks to understand which patients and underlying pathologies may benefit most from augmentation.
Many patients in this cohort underwent concomitant procedures at the time of lateral ankle ligament reconstruction. These include correction of bony deformities (i.e., calcaneal osteotomy) and additional soft tissue procedures (i.e. ligamentous reconstruction, synovectomy, tendon transfer, tendon lengthening, etc.). Additional procedures are outlined in Table 1 .
Table 1
List of additional procedures. Many patients received an additional soft tissue or bony procedure. The number of patients who received which procedure is documented in this table. All 37 patients had a calcaneal osteotomy. Aside from calcaneal osteotomy, there was no significant difference in the frequency of additional procedures between augmented and non-augmented.
| Overall | Augmented | Non-augmented | |
|---|---|---|---|
| N | 37 | 29 (78.4) | 8 (21.6) |
| Any additional procedure excluding calcaneal osteotomy (N, %) | 31 (83.8) | 26 (89.7) | 5 (62.5) |
| Procedure | N (%) of patients who had procedure | ||
| Deltoid Repair | 9 (24.3) | 8 (27.6) | 1 (12.5) |
| Syndesmotic reconstruction and deltoid repair | 4 (10.8) | 4 (13.8) | 0 (0) |
| Calcaneal osteotomy | 37 (24.3) | 29 (24.1) | 8 (25) |
| Gastrocnemius recession | 3 (8.1) | 3 (10.3) | 0 (0) |
| Peroneal synovectomy | 11 (29.7) | 10 (34.5) | 1 (12.5) |
| Peroneal tendon reconstruction | 3 (8.1) | 3 (10.3) | 0 (0) |
| Peroneal tendon transfer | 5 (13.5) | 5 (17.2) | 0 (0) |
| Spring ligament reconstruction | 1 (2.7) | 1 (3.4) | 0 (0) |
| Syndesmotic reconstruction | 6 (16.2) | 5 (17.2) | 1 (12.5) |
| Tendoachilles lengthening | 4 (10.8) | 4 (13.8) | 0 (0) |
2.2
Outcomes
Primary outcomes included PROMIS PF and PROMIS PI. Both measures correspond to age-matched norms for the US general population mean score of 50 ,, . Higher PF designates higher physical function, while higher PI indicates more pain interfering with activity. The minimally clinically important difference (MCID) reported in the literature for PROMIS is a difference of 3–30 for PF and 3–25 for PI . Secondary outcomes included postoperative CAIT scores. Higher scores on CAIT indicate greater ankle stability. The MCID reported in the literature for CAIT is a difference of ≥ 3 . Follow-up duration was defined as time from surgery to time to survey completion.
2.3
Statistical methods
T-tests and Kruskal-Wallis tests were used to assess associations between CLAI etiology and PROMIS, as well as between CLAI etiology and CAIT. This study reached 80 % power to detect minimum effect size of 0.52 (Cohen’s d), corresponding to differences of 4.37 for PF and 4.60 for PI, and 80 % power to detect an effect size of 1.15, corresponding to an actual difference in CAIT of 9.24. Therefore, the study was underpowered to detect differences in CAIT.
3
Results
There was no significant difference in the proportion of patients who received an additional soft tissue procedure between augmented and non-augmented (p = 0.10, Table 1 ). Aside from follow-up duration (3.4 ± 1.5 vs. 6.5 ± 2.5, p < 0.01), baseline characteristics were similar between augmented (n = 29) and non-augmented (n = 8) Broström ( Table 2 ).
Table 2
Patient characteristics.
| Overall | Augmented | Non-Augmented | P-Value | |
|---|---|---|---|---|
| N (%) | 37 | 29 (78.4) | 8 (21.6) | |
| Age | 0.22 | |||
| Mean (SD) | 45 (17) | 46 (18) | 40 (10) | |
| Median (IQR) | 43 (31–57) | 46 (31–59) | 41 (31–47) | |
| 18–29 | 6 (16.2) | 5 (17.2) | 1 (12.5) | |
| 30–40 | 11 (29.7) | 8 (27.6) | 3 (37.5) | |
| 41–52 | 8 (21.6) | 5 (17.2) | 3 (37.5) | |
| 53–64 | 6 (16.2) | 5 (17.2) | 1 (12.5) | |
| 65 + | 6 (16.2) | 6 (20.7) | 0 (0) | |
| BMI | 0.28 | |||
| Mean (SD) | 30.4 (6.9) | 29.7 (6.8) | 32.9 (7.0) | |
| 18.5–24.9 | 13 (35.1) | 11 (37.9) | 2 (25) | |
| 25–29.9 | 7 (18.9) | 7 (24.1) | 0 (0) | |
| 30 + | 17 (45.9) | 11 (37.9) | 6 (75) | |
| Sex | 0.42 | |||
| Female | 21 (56.8) | 15 (51.7) | 6 (75) | |
| Male | 16 (43.2) | 14 (48.3) | 2 (25) | |
| Smoking | 0.67 | |||
| Former | 11 (29.7) | 8 (27.6) | 3 (37.5) | |
| Never | 26 (70.3) | 21 (72.4) | 5 (62.5) | |
| Clinical follow up | < 0.01 | |||
| Mean (SD) | 4.1 (2.1) | 3.4 (1.5) | 6.5 (2.5) | |
| Median (IQR) | 3.8 (2.8–5.3) | 3.3 (2.8–4.3) | 6.75 (5.5–7.8) |
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