Translate this page into:
The revised risk analysis index outperforms the 5-factor modified frailty index in predicting postoperative morbidity after pilon fracture fixation
⁎Corresponding author: Gabriel DeOliveira. gdeoliveira@une.edu
-
Received: ,
Accepted: ,
This article was originally published by Reed Elsevier India Pvt. Ltd. and was migrated to Scientific Scholar after the change of Publisher.
Abstract
Abstract
Pilon fractures often result from high energy mechanisms resulting in long-term morbidity and postoperative complications. While there is extensive literature investigating frailty scales as tools for preoperative risk stratification in orthopedic surgery, there is no literature regarding their use in fixation of pilon fractures. The objective of this study was to compare the predictive ability and discriminative accuracy of the Revised Risk Analysis Index (RAI-rev) and the 5-Item Modified Frailty (mFI-5) in 30-day postoperative outcomes following surgical fixation of pilon fractures.
The ACS-NSQIP database was used to identify patients undergoing surgical fixation of pilon fractures from 2015 to 2020. Multivariate analysis was used to analyze the predictive ability of frailty status for 30-day postoperative outcomes. Discriminatory accuracy of frailty scales was assessed using receiver operating characteristic analysis. Significance was determined by p < 0.05.
This study included 2935 patients, aged 33–59, of which 53 % (1562/2935) were male. The RAI-rev categorized 44.2 % (1296/2935) as normal, 44.6 % (1309/2935) as frail, and 11.2 % (330/2935) as severely frail. The mFI-5 was a significant predictor of major complications, readmission, and CDIV complications for severely frail patients and of eLOS, and NHD in both frail and severely frail patients. The RAI-rev had superior discriminative accuracy for most outcomes with good discriminative ability for NHD compared to mFI-5 (0.79 vs 0.74).
This study demonstrated that compared to RAI-rev, mFI-5 is a significant predictor of postoperative complications after surgical fixation of pilon fractures, but RAI-rev had more accurate predictive ability when compared to mFI-5, most notable for NHD (AUC 0.79 vs 0.74). However, ROC values for both RAI (AUC 0.65–0.79) and mFI-5 (AUC 0.59–0.74) still fell below an AUC of 0.80 indicating that overall frailty is not a strong predictor of outcomes. These findings support the need for further research into preoperative risk assessment in pilon fracture patients.
III – retrospective cohort study.
Keywords
Frailty
Pilon fracture
Trauma
Risk analysis index
5-Item modified frailty index
1 Introduction
Pilon fractures account for 3–10 % of all tibial fractures and are serious injuries that often result in significant morbidity and complications.1 These high energy injuries involve complex fracture patters associated with significant soft tissue damage and a high risk of complications.2 Despite advances in surgical techniques, pilon fracture patients have long recovery periods, high risk of soft-tissue complications, and notable risk of deep tissue infections.3 A thorough understanding of the risk factors as well as the development of predictive models is needed to help improve postoperative outcomes in patients with pilon fractures. Being able to identify these factors would significantly improve patient care and surgical strategies.
Frailty is defined as the decrease in physiological reserve which has emerged as an important consideration in surgical outcomes. It has been linked to an increase in postoperative complications, extended hospital stays and non-home discharge (NHD) across different types of surgical specialties.4 Specifically, through the lens of orthopedics, frailty has been linked to a significantly higher risk of fractures in adults.5 It has been well documented in the literature that quantifying frailty via validated models such as 5-factor modified frailty index (mFI-5) and the Risk Analysis Index-revised (RAI-rev) has been shown to be a predictor for surgical outcomes.6,7 The mFI-5 is a widely used tool for assessing frailty in various surgical populations. The frailty index incorporates five variables including diabetes, congestive heart failure, functional status, chronic obstructive pulmonary disease (COPD), and hypertension. The mFI-5 has been validated in many different surgical contexts with a strong predictive ability for length of stay (LOS), NHD, and postoperative complications.8 Introduced by Hall and colleagues,9 RAI-rev is another frailty tool developed to assess frailty with a focus on preoperative risk prediction. The tool incorporates 11 variables including cognitive decline, residence other than independent living, functional status, unintentional weight loss, poor appetite, renal failure, congestive heart failure, shortness of breath, cancer, age, and sex.9,10 Studies have found that RAI-rev has superior predictive ability for outcomes such as 30-day postoperative morbidity and mortality.11–15 Thus, it has been used increasingly to help improve both preoperative management and optimization of patient care.
Despite the advances, there remains a paucity in the literature that investigates the link between frailty and pilon fractures. The complexity of these fractures, often caused by high-energy trauma, usually involves significant soft tissue damage making them difficult to manage while also exposing the role frailty can play in these scenarios. With the importance of preoperative planning and the high complication rates surrounding this type of injury, our study aims to investigate the role frailty, established by RAI-rev and mFI-5, has in predicting outcomes following surgical fixation of pilon fractures. The ability to reliably quantify the risk of postoperative complications would aid in preoperative planning and be of great benefit to surgeons, and most importantly, patients.
2 Methods
2.1 Data source (2015–2020)
The NSQIP is a national database composed of multiple institutions with over 700 participating variables that are composed of multiple variables involved in pre-, intra-, and postoperative outcomes.15,16 Our study utilized years 2015–2019 using the highly reliable data that is entered by each institution by ACS-trained surgical clinical reviewers.15 This study was performed under a Health Insurance Portability and Accountability Act-compliant Participant Use Data File which is considered exempt from institutional review board approval.
2.2 Patient population and baseline characteristics and outcomes
Patients ages ≥18 years diagnosed with pilon fracture treated with external or internal fixation or arthrodesis were included in the study. We utilized the Current Procedural Terminology (CPT) codes 27,826, 27,827, and 27,828. A total of 2935 patients were extracted from the NSQIP database with exclusion of those that were missing any criteria to calculate RAI-rev score. Baseline study variables included age, sex, body mass index (BMI), elective versus nonelective procedure, LOS, ambulation status, and operative time. Medical comorbidities such as diabetes mellitus, COPD, CHF, dyspnea, hypertension, disseminated cancer (defined as multiple metastases by NSQIP), open wound, steroid use, weight loss (substantial unintentional weight loss >10 %), bleeding disorders, preoperative transfusion, ambulation status, and preoperative sepsis/septic shock/systemic inflammatory response (SIRS), functional dependence (including complete and partial dependence), and smoking status.
2.3 5-Item Modified Frailty index (mFI-5)
The mFI-5 is a shorter version of the modified frailty index originally incorporating 11 factors.8 It consists of the five clinical variables reported within the NSQIP, each with a score of 1 to a maximum score of 5 (Supplementary Table 1). The following mFI-5 frailty cutoffs were used: 0 = Non-frail, 1–2 = Frail, 3–5 = Severely frail.17
2.4 Revised risk analysis index (RAI-rev)
The Risk Analysis Index (RAI) was originally described by Hall et al. as a measure of frailty created and applied to surgical patients identified in the Veterans Affairs Surgical Quality Improvement Program (VASQIP).18 The RAI was then recalibrated using the NSQIP to validate it for use in non-veteran surgical patients, termed the RAI-rev.10 RAI-rev was created in the attempts to make up for the deficits in other frailty assessment tools such as the modified frailty phenotype and increase the ability to assess a broader demographic of patients.10 It is calculated using 11 weighted variables (Supplementary Table 2). The frailty cutoffs used in this study were, ≤12 = normal, 13–22 = frail, and ≥23 = severely frail. The cut-offs used were selected based on their alignment with the frailty distribution observed in the studies cohort. This is an advantage of RAI as its design permits recalibration to optimize its predictive utility across different surgical populations.19
2.5 Population characteristics and preoperative variables
Baseline population characteristics were recorded and included age, sex, race, body mass index (BMI), elective surgery status, and LOS. Comorbidities included: Independent function, diabetes mellitus, COPD, CHF, smoking status, dyspnea, hypertension, disseminated cancer, chronic steroid use, weight loss, and bleeding disorders.
2.6 Outcomes and complications
The primary outcome of this study was NHD within 30 days. Secondary outcomes included eLOS (>3 days), major complications, readmission, and clavien-Dindo IV complications (CDIV) within 30 days. Pooled infection status was composed of superficial surgical site infections (sSSI), deep surgical site infections (dSSI), organ space surgical infections (oSSI), and wound dehiscence (Table 2). Major complications consisted of the complications which are a composite of sSSI, dSSI, oSSI, wound dehiscence, pneumonia, unplanned intubation, ventilator dependent >48 h, PE, renal failure, stroke, cardiac arrest, MI, deep vein thrombosis (DVT), sepsis, and systemic shock. Clavien-Dindo IV (CDIV) complications included sepsis, septic shock, pulmonary embolism (PE), myocardial infarction (MI), cardiac arrest requiring CPR, unplanned intubation, ventilator dependent >48 h, acute renal failure needing dialysis and stroke (Table 2).
2.7 Statistical analysis
All statistical analysis was performed using R Studio (IBM SPSS Statistics, NY). Baseline demographic variables were continuous and reported as median values with an interquartile range (IQR). Pre-operative comorbidities and 30-day outcome variables were reported as incidence. Multivariate analysis was performed and the effect sizes of RAI-rev and mFI-5 on primary outcomes were presented as an odds ratio (OR) with a concurrent 95 % confidence interval (95 % CI). The RAI-rev and mFI-5 variables were used as categorical variables and ORs reflect the effect among frail or severely frail cohorts compared to the non-frail cohort which served as the reference group. Discriminatory accuracy of each frailty model was assessed using Receiver Operating Characteristic (ROC) analysis quantified using continuous RAI-rev and mFI-5 scores to obtain area under the curve (AUC)/C-statistic. The discriminatory accuracy of the frailty models was compared using the DeLong test, and overall significance was indicated by a p-value <0.05.
3 Results
The total patient cohort consisted of 2935 individuals who met the inclusion criteria for this study (Table 1) which was patients ages ≥18 years diagnosed with pilon fracture treated with external or internal fixation or arthrodesis. The median age of the cohort was 46 years (range 33–59), with the majority being White (64.1 %) and males comprising 53.2 % of the population. Among the cohort, 27.8 % were current smokers and 26.5 % had hypertension requiring medication. When examining frailty cohorts, 43.2 % (1296/2935) of patients were in the frail cohort of RAI-rev and 11.2 % (330/2935) in the severely frail cohort. For the mFI-5, 30.1 % (883/2935) were frail, while 1.5 % (43/2935) were categorized as severely frail.
| Variable | Value |
| No. of patients | 2935 |
| Age (years, median) | 46 (33–59) |
| Gender (n, %) | |
| Males | 1562 (53.2) |
| Females | 1373 (46.8) |
| BMI (kg/m2, average) | 28.07 |
| Race, n (%) | |
| White | 1882 (64.1) |
| Black or African American | 289 (9.8) |
| Asian | 47 (1.6) |
| Native Hawaiian/Pacific Island | 10 (0.3) |
| American Indian or Alaska Native | 17 (0.6) |
| Unknown | 689 (23.5) |
| Elective Status | |
| Elective | 1787 (60.9) |
| Non-Elective | 1140 (38.8) |
| Length of Stay (days, median) | 1 (1–3) |
| Operation Time (minutes, median) | 117 (81–170) |
| Mortality (n, %) | 9 (0.3) |
| Reoperation (n, %) | 57 (1.9) |
| Readmission (n, %) | 103 (3.5) |
| mFI-5 Frailty titers (n, %) | |
| Nonfrail (mFI-5 = 0) | 2009 (68.4) |
| Frail (mFI-5 = 1–2) | 883 (30.1) |
| Severely frail (mFI-5 = 3–5) | 43 (1.5) |
| RAI-rev Frailty titers (n, %) | |
| Normal (RAI-rev ≤12) | 1309 (44.6) |
| Frail (RAI-rev = 13–22) | 1296 (43.2) |
| Severely frail (RAI-rev ≥23) | 330 (11.2) |
| Comorbidities and risk factors, n (%) | |
| Diabetes mellitus | |
| Insulin | 142 (4.8) |
| Non-insulin | 156 (5.3) |
| Current smoker | 817 (27.8) |
| Dyspnea | |
| Moderate Exertion | 55 (1.9) |
| At Rest | 8 (0.3) |
| Functional health status | |
| Independent | 2837 (96.7) |
| Partially Dependent | 92 (3.1) |
| Totally Dependent | 6 (0.2) |
| Ventilator dependent | 4 (0.1) |
| History of COPD | 91 (3.1) |
| Ascites | 2 (0.1) |
| History of CHF | 18 (0.6) |
| Hypertension requiring medications | 779 (26.5) |
| Currently on dialysis | 15 (0.5) |
| Disseminated cancer | 10 (0.3) |
| Open wound/wound infection | 152 (5.2) |
| Steroid use | 52 (1.8) |
| >10 % loss body weight within 6 months | 6 (0.2) |
| Bleeding disorders | 118 (4.0) |
| Transfusion ≥1 units in 72 h before surgery | 12 (0.4) |
| Variable, n (%) | Cohort |
| Major Postoperative Complications | 155 (5.3) |
| Superficial SSI | 37 (1.3) |
| Deep Incisional SSI | 17 (0.6) |
| Organ Space SSI | 14 (0.5) |
| Wound Disruption | 19 (0.6) |
| Pneumonia | 13 (0.4) |
| Unplanned Reintubation | 7 (0.2) |
| Pulmonary Embolism | 8 (0.3) |
| Prolonged Intubation (≥48 Hours) | 3 (0.1) |
| Acute Renal Failure | 1 (<0.1) |
| CVA/Stroke with neurologic deficit | 0 (<0.1) |
| Cardiac arrest requiring CPR | 1 (<0.1) |
| Myocardial Infarction | 6 (0.2) |
| DVT/Thrombophlebitis | 11 (0.4) |
| Sepsis | 14 (0.5) |
| Septic Shock | 1 (<0.1) |
| Minor Postoperative Complications | |
| Bleeding Transfusion | 41 (1.4) |
| Urinary Tract Infection (UTI) | 25 (0.9) |
| Progressive Renal Insufficiency | 1 (<0.1) |
| Clavien-Dindo Grade IV | 30 (1.0) |
| Discharge Destination | |
| Home | 2561 (87.3) |
| Nonroutine (Rehab, SNF, Hospice) | 334 (11.4) |
A multivariate analysis was conducted to assess the predictive values of the mFI-5 and RAI-rev for poor postoperative outcomes (Table 3). The analysis was performed while controlling for age, sex, ethnicity/race, BMI, ambulation status, nonelective-surgical status, and total operation time for each cohort. The mFI-5 was a significant predictor for major complications, readmission, and CDIV especially in the severely frail cohort compared to the non-frail reference group with OR 4.30 (95 %CI 1.94–9.50; p < 0.001), 5.18 (95 %CI 2.16–12.43; p < 0.001), and 9.82 (95 %CI 2.47–39.07; p = 0.001), respectively. The mFI-5 was also a significant predictor for eLOS and NHD for both frail and severely frail cohorts compared to the non-frail reference group: eLOS frail: 1.54 (95 %CI 1.22–1.89; p < 0.001), severely frail: 5.80 (95 %CI 2.74–12.29; p < 0.001), NHD frail: 2.49 (95 %CI 1.86–3.33; p < 0.001), and severely frail: 10.23 (95 %CI 4.61–22.70). The RAI-rev was not a significant predictor for any outcome for the frail or severely frail cohort.
| Outcomes | Frailty Indices | p-value | |||
| mFI-5 | p-value | RAI-Rev | |||
| Major Complications | Major Complications | ||||
| Frail | 1.37 (0.92–9.50) | 0.118 | Frail | 0.76 (0.54–1.09) | 0.133 |
| Severely frail | 4.30 (1.94–9.50) | <0.001 a | Severely frail | 1.30 (0.73–2.31) | 0.381 |
| eLOS | eLOS | ||||
| Frail | 1.51 (1.22–1.89) | <0.001 a | Frail | 0.90 (0.48–1.70) | 0.745 |
| Severely frail | 5.80 (2.74–12.29) | <0.001 a | Severely frail | 2.82 (1.81–4.28) | 0.334 |
| NHD | NHD | ||||
| Frail | 2.49 (1.86–3.33) | <0.001 a | Frail | 1.06 (0.62–1.81) | 0.844 |
| Severely frail | 10.23 (4.61–22.70) | <0.001 a | Severely frail | 1.53 (0.68–3.44) | 0.300 |
| Readmission | Readmission | ||||
| Frail | 1.03 (0.64–2.76) | 0.897 | Frail | 1.28 (0.60–2.76) | 0.518 |
| Severely frail | 5.18 (2.16–12.43) | <0.001 a | Severely frail | 2.15 (0.64–7.26) | 0.218 |
| CDIV | CDIV | ||||
| Frail | 2.06 (0.78–5.41) | 0.145 | Frail | 0.33 (0.07–1.65) | 0.178 |
| Severely frail | 9.82 (2.47–39.07) | 0.001 a | Severely frail | 0.530 (0.053–5.39) | 0.588 |
To determine the discriminatory accuracy of mFI-5 and RAI-rev, AUC analysis (Table 4 & Fig. 1) was performed for eLOS, major complications, NHD, readmission, and CDIV. AUC analysis revealed that RAI-rev significantly outperformed mFI-5 for eLOS (RAI-rev 0.658 vs mFI-5 0.621; p = 0.0012), major complications (RAI-rev 0.671 vs mFI-5 0.623; p = 0.0254), NHD (RAI-rev 0.798 vs mFI-5 0.733; p < 0.001), and readmission (RAI 0.656 vs mFI-5 0.597; p = 0.0220).
| Outcomes | Frailty Indices | p-value | |
| mFI-5 | RAI-Rev | ||
| eLOS | 0.621 (0.603–0.638) | 0.658 (0.641–0.676) | 0.0012∗ |
| Major Complication | 0.623 (0.605–0.640) | 0.671 (0 0.654–0.688) | 0.0254∗ |
| NHD | 0.733 (0 0.717–0.749) | 0.798 (0.783–0.812) | <0.0001∗ |
| Readmission | 0.597 (0.579–0.615) | 0.656 (0.638–0.673) | 0.0220∗ |
| CDIV | 0.742 (0.726–0.758) | 0.788 (0.773–0.803) | 0.3990 |

4 Discussion
This longitudinal study of 2935 patients extracted from a multicenter database was used to assess the predictive ability and discriminative accuracy of RAI-rev compared to mFI-5 for postoperative patient morbidity in surgical pilon fractures. Only mFI-5 was found to be a significant positive predictor, indicating that higher frailty scores were associated with increased odds for major complications, eLOS, NHD, readmission, and CDIV complications. However, RAI-rev demonstrated significantly increased discriminative accuracy in predicting eLOS, major complications, readmissions, and most markedly NHD compared to mFI-5, evidenced by higher AUC values in ROC analysis indicating its superior ability to distinguish between patients with and without these outcomes.
Evaluating short-term outcomes, such as non-home discharge, provides valuable clinical insights in the acute trauma setting. In the context of pilon fractures, which often occur due to high-energy mechanisms, accurate short-term risk stratification is crucial for early discharge planning, resource allocation, and multidisciplinary coordination. The improved AUC for RAI-rev in predicting NHD underscores its practical utility in identifying acute physiologic vulnerability, particularly when applied preoperatively to identify patients at risk for early complications and disposition challenges.
The findings from this study underscore the importance of integrating frailty assessments into preoperative risk stratification conversations for complex orthopedic injuries. This is the first study to apply frailty models to patients with pilon fractures and was done using a large, multi-institutional cohort.
The mFI-5 is an abbreviated version of the original mFI-11, developed to function as a comorbidity index that can often independently predict adverse postoperative outcomes.20 The mFI-5 is an older frailty model compared to RAI-rev and in regards to orthopedic surgery, it has been validated as a significant predictor of postoperative morbidity and mortality in elective total joint, shoulder arthroscopy and spine surgeries based on ACS-NSQIP data.20–24 In contrast to the mFI-5, the RAI-rev was designed to be mathematically and conceptually superior to mFI-5 and mFI-11, accounting for and correctly scoring advanced patient age and impairment in activities of daily living.9,10 While there has not been any published literature comparing mFI-5 to RAI-rev in lower extremity orthopedic injuries, RAI-rev has had superior discriminative accuracy compared to mFI-5 based on ROC analysis in neurosurgery and orthopedic spine surgery patients.11,12 Based on a similarly structured retrospective database analysis, the RAI-rev was superior in predicting CDIV, NHD, and reoperation rate in neurosurgical patients.11 Similar to this current study, Conlon et al. showed that the RAI-rev is more accurate than mFI-5 for eLOS, readmission, and NHD in patients undergoing surgical fixation for traumatic spine injuries.12 While the literature supports the utility of RAI-rev for elective procedures, this study adds to its superior accuracy in traumatic, non-elective procedures.11,12
While frailty has been closely associated with aging,23 the cohort in this current study had a median age over a decade younger than similar studies investigating RAI-rev.11,12 Studies that have investigated orthopedic trauma and its relationship to frailty include Rege et al., which by using ACS-NSQIP found that the mFI-5 was a significant predictor of mortality and CDIV complications in their young cohort (<60 years old) who underwent surgical fixation for pelvis, acetabular and lower extremity trauma.24 Similarly, out of a single level 1 trauma center, Phen et al. showed that mFI-5 was a significant predictor of any postoperative complication and mortality in patients less than 65 who underwent surgical fixation for lower extremity trauma.25 Similar to Rege et al. and Phen et al., in this study, mFI-5 was a significant predictor of eLOS, and NHD for all frail cohorts, and of major complications, readmissions and CDIV complications for severely frail patients with pilon fractures.24,25 However, among the studies who investigated frailty in young trauma patients using mFI-5, none compared it to any other frailty model, nor was significance for discriminative accuracy using AUC analysis achieved.24,25 In contrast, this current study compared mFI-5 to the RAI-rev for predictive ability and discriminative accuracy. We displayed that while mFI-5 was a significant positive predictor for postoperative complications, RAI-rev had superior discriminative accuracy in a young, non-elective cohort. It is worth noting that while RAI-rev had superior accuracy for postoperative morbidities, the overall predictive value was low with only NHD demonstrating acceptable discriminative ability, consistent with Conlon et al.12
Other risk factors that have been linked to higher postoperative complication rates in surgical pilon fracture patients include open fractures secondary to high energy trauma,26,27 preoperative comorbidities such as diabetes and hypertension,27–29 active smoking,3 and psychiatric conditions.30,31 When comparing these risk factors to the cohort in this study, 27.8 % of our cohort includes current smokers, and 26.5 % have diagnosed hypertension requiring medication. Interestingly, psychiatric conditions, and diabetes have all been linked to frailty,32–34 with diabetes and hypertension being accounted for by mFI-5.
It is also important to address the clinical utility and applicability of RAI. It has already been effectively integrated into electronic health record systems such as Epic and Cerner, making the ability to collect a preoperative frailty assessment accessible to a wide range of clinicians across a variety of different settings.19 Additionally, while not as concise as the mFI-5, the RAI is practical and can be calculated in as little as 30 s without disrupting workflow, which is especially crucial for large, high volume healthcare systems.19
There are several limitations to this study. Regarding discriminative accuracy, while RAI-rev was superior, the overall AUC predictive values were low with c-statistic falling below 0.80 which has been associated with predictive capacity. C-statistics of 0.70 is the lower limit of what is considered an informative model, and this was only accomplished for NHD, which for RAI-rev was just shy of 0.80 at 0.798. Another limitation is inherent to using a database and involves the potential presence of data inconsistencies and inability to clarify certain details such as differentiating between severity or mechanism of injury. Due to the small cohort size, there was an unequal distribution between mFI-5 and RAI-rev severely frail groups and overall between severely frail and frail. This may have artificially inflated the mFI-5 frail cohort, potentially indicating that frailty has less of a role than perceived in this type of injury and influence the risk for postoperative complications with its relationship with frailty. Additionally, postoperative complications were limited to within 30 days of the operation. Further research should incorporate a database such as the Trauma Quality Improvement Program (TQIP) that allows for differentiation between injury severity. Such a study may hold potential in validating either mFI-5, or in the development of a novel model for predicting postoperative complications in pilon fracture patients.
5 Conclusion
This study is the first to directly investigate the relationship between frailty and postoperative outcomes in pilon fracture patients. Our study demonstrated that while mFI-5 was a significant predictor of most complications, RAI-rev had superior and more acceptable accuracy compared to mFI-5 for predicting NHD in pilon fracture patients. However, due to the inability to distinguish if injuries were due to high or low energy mechanisms, further research using a trauma specific database is required to establish the role of frailty in surgical fixation of traumatic injuries. A simple assessment for comorbidities such as those measured in the mFI-5 could be convenient in these patients, but ultimately, RAI-rev demonstrated a stronger ability in assessing frailty for predicting postoperative complications. This study contributes to the existing literature investigating the role of frailty in younger patients. In the context of pilon fractures, a cohort underrepresented in frailty research, this study builds on existing evidence by demonstrating the complementary strengths of frailty models in a high-risk, complex population.
Consent statement
-This study was performed under a Health Insurance Portability and Accountability Act-compliant Participant Use Data File which is considered exempt from institutional review board approval. Patient/guardian consent not required.
Ethics statement
-This study was performed under a Health Insurance Portability and Accountability Act-compliant Participant Use Data File which is considered exempt from institutional review board approval. Patient/guardian consent not required.
CrediT author statement
Gabriel DeOliveira: Conceptualization, Writing, visualization. Amber Park: Software, formal analysis, writing. Arsalaan Sayyed: Writing. Aruni Areti: Writing. Nithin Gupta: Conceptualization, formal analysis, supervision. Taylor Manes: Conceptualization, supervision. Morgan Turnow: Supervision. Benjamin Taylor: Supervision. Jack W. Weick: supervision.
Funding
There was no funding available to or provided for this project.
References
- Tibial pilon fractures: a review of incidence, diagnosis, treatment, and complications. Acta Orthop Belg. 2011;77:432-440.
- [Google Scholar]
- Complications and soft-tissue coverage after complete articular, open tibial plafond fractures. J Orthop Trauma. 2021;35(10):e371-e376.
- [Google Scholar]
- Risk factors of deep infection in operatively treated pilon fractures (AO/OTA: 43) J Orthop. 2015;12(Suppl 1):S7-S13.
- [Google Scholar]
- The identification of frailty: a systematic literature review. J Am Geriatr Soc. 2011;59(11):2129-2138.
- [Google Scholar]
- Predicting fragility fractures based on frailty and bone mineral density among rural community-dwelling older adults. Eur J Endocrinol. 2024;191(1):75-86.
- [Google Scholar]
- A novel surgical risk predictor combining frailty and hypoalbuminemia - a cohort study of 9.8m patients from the ACS-NSQIP database. Int J Surg 2024
- [Google Scholar]
- Effectiveness of risk analysis index frailty scores as a predictor of adverse outcomes in lower extremity reconstruction. J Reconstr Microsurg 2024
- [Google Scholar]
- New 5-factor modified frailty index using American college of surgeons NSQIP data. J Am Coll Surg. 2017;225(4):444-451.e1.
- [Google Scholar]
- Development and initial validation of the risk analysis Index-revised (RAI-rev) Ann Surg. 2017;265(4):667-674.
- [Google Scholar]
- Recalibration and validation of the risk analysis Index-revised for preoperative frailty assessment. Ann Surg. 2019;270(1):84-91.
- [Google Scholar]
- Superior discrimination of the risk analysis index compared with the 5-item modified frailty index in 30-day outcome prediction after anterior cervical discectomy and fusion. J Neurosurg Spine. 2023;39(4):509-519.
- [Google Scholar]
- Risk analysis index and its recalibrated version predict postoperative outcomes better than 5-Factor modified frailty index in traumatic spinal injury. Neurospine. 2022;19(4):1039-1048.
- [Google Scholar]
- The risk analysis index as a predictor of 30-day mortality for Obese patients undergoing elective total joint arthroplasty. J Orthop 2025
- [Google Scholar]
- Orthopedic frailty risk stratification (OFRS): a systematic review of the frailty indices predicting adverse outcomes in orthopedics. J Orthop Surg Res. 2025;20(1):247.
- [Google Scholar]
- Validation of new readmission data in the American college of surgeons national surgical quality improvement program. J Am Coll Surg. 2013;216(3):420-427.
- [Google Scholar]
- Toward robust information: data quality and inter-rater reliability in the American college of surgeons national surgical quality improvement program. J Am Coll Surg. 2010;210(1):6-16.
- [Google Scholar]
- The 5-Item modified frailty index independently predicts morbidity in patients undergoing instrumented fusion following extradural tumor removal. Spine Surg Relat Res. 2022;7(1):19-25.
- [Google Scholar]
- Development and initial validation of the risk analysis index for measuring frailty in surgical populations. JAMA Surg. 2017;152(2):175-182.
- [Google Scholar]
- Frailty screening using the risk analysis index: a user guide. Joint Comm J Qual Patient Saf. 2025;51(3):178-191.
- [Google Scholar]
- The five-item modified frailty index is predictive of 30-day postoperative complications in patients undergoing spine surgery. Spine. 2021;46(14):939-943.
- [Google Scholar]
- New 5-Factor modified frailty index predicts morbidity and mortality in primary hip and knee arthroplasty. J Arthroplast. 2019;34(1):140-144.
- [Google Scholar]
- The 5-Factor modified frailty index predicts complications, hospital admission and mortality following arthroscopic rotator cuff repair. Arthrosc J Arthrosc Relat Surg. 2020;36(2):383-388.
- [Google Scholar]
- The frailty syndrome: definition and natural history. Clin Geriatr Med. 2011;27(1):1-15.
- [Google Scholar]
- Frailty predicts mortality and complications in chronologically young patients with traumatic orthopaedic injuries. Injury. 2018;49(12):2234-2238.
- [Google Scholar]
- Impact of frailty and malnutrition on outcomes after surgical fixation of lower extremity fractures in young patients. J Orthop Trauma. April 2021;35(4):e126-e133.
- [Google Scholar]
- Risk factors of deep infection in operatively treated pilon fractures (AO/OTA: 43) J Orthop. 2015;12(Suppl 1):S7-S13.
- [Google Scholar]
- Risk factors for infection and subsequent adverse clinical results in the setting of operatively treated pilon fractures. J Orthop Trauma. 2022;36(8):406-412.
- [Google Scholar]
- Outcomes of surgically treated pilon fractures: a comparison of patients with and without diabetes. J Orthop Trauma. December 2023;37(12):650-657.
- [Google Scholar]
- Early complications following the operative treatment of pilon fractures with and without diabetes. Foot Ankle Int. 2009;30(11):1042-1047.
- [Google Scholar]
- Is psychiatric illness associated with worse outcomes following pilon fracture? Iowa Orthop J. 2022;42(1):63-68.
- [Google Scholar]
- Depressive disorders lead to increased complications after pilon fracture surgery. Foot & Ankle Orthopaedics. 2022;7(1)
- [Google Scholar]
- Diabetes and frailty: an emerging issue. Part 1: sarcopaenia and factors affecting lower limb function. Br J Diabetes Vasc Dis. 2012;12(3):110-116.
- [Google Scholar]
- Frailty in individuals with depression, bipolar disorder and anxiety disorders: longitudinal analyses of all-cause mortality. BMC Med. 2022;20(1):274.
- [Google Scholar]
- Inflammation and frailty in the elderly: a systematic review and meta-analysis. Ageing Res Rev. 2016;31:1-8.
- [Google Scholar]

