Frailty Indices and Preoperative Clinical Factors for Predicting Myocardial Injury After Non-Cardiac Surgery (MINS) in High-Risk Geriatric Orthopedic Patients: A Machine-Learning Study
Dilek Kalaycı, Edanur Genç Turan, İmran Ceren, Fadime Bozduman Habip, Özlem Şen, Tuğba Aşkın, Çoşkun UlucaköyBackground/Objectives: Myocardial injury after non-cardiac surgery (MINS) is a common, often asymptomatic complication in geriatric orthopedic patients that increases postoperative mortality. The Revised Cardiac Risk Index (RCRI) may not adequately capture the age-related loss of the physiological reserve. We investigated whether frailty indices (mFI-5, mFI-11) improve machine-learning prediction of preoperative MINS risk, and compared an exploratory perioperative model with ASA and RCRI. Methods: In this single-center retrospective study, 656 patients aged ≥ 65 years who underwent major orthopedic surgery with postoperative ICU monitoring and troponin surveillance were analyzed; MINS occurred in 82 (12.5%). The models were as follows: Model 1 (preoperative baseline), Model 2 (+mFI-5), Model 3 (+mFI-11), and an exploratory perioperative model, Model 4 (+intraoperative vasopressor use and postoperative mechanical ventilation). AUCs on a 30% hold-out set were compared with ASA/RCRI using the paired DeLong test, with Bonferroni adjustment across 15 comparisons. A sensitivity analysis with an identical classifier and predictor set isolated the contribution of the frailty indices. Results: Frailty indices did not provide significant incremental value: adding mFI-5 or mFI-11 changed the AUC only marginally (0.5744 to 0.5828 and 0.5881; all p > 0.5). Preoperative models (hold-out AUC 0.6005–0.6935) did not differ significantly from ASA or RCRI after Bonferroni correction. Model 4, incorporating intra- and postoperative variables, reached an AUC of 0.7584, significantly higher than ASA (adjusted p = 0.002) but not RCRI (adjusted p = 0.268). Conclusions: With the algorithm and predictor set held constant, no incremental value of frailty indices was demonstrable, and no model significantly outperformed RCRI after multiplicity correction. The numerically higher AUC of Model 3 versus Model 2 cannot be attributed to frailty indices, as the models differed in both predictors and algorithm. Power was limited; these findings are hypothesis-generating. Whether frailty indices improve prediction needs to be tested in external cohorts large enough to detect it.