It remains unclear whether screening for advanced fibrosis in the community can identify the subgroup of people with nonalcoholic fatty liver disease (NAFLD) at higher risk for development of liverârelated complications. We aimed to determine the prognostic value of baseline noninvasive fibrosis tests for predicting liverârelated outcomes and mortality in patients with NAFLD from type 2 diabetes (T2D) clinics or primary care. Patients (n = 243) who were screened for NAFLD with advanced fibrosis by using NAFLD fibrosis score (NFS), fibrosis 4 score (FIBâ4), enhanced liver fibrosis (ELF) test, and liver stiffness measurements (LSMs) were followed up for clinical outcomes by review of electronic medical records. During a median followâup of 50 months, decompensated liver disease or primary liver cancer occurred in 6 of 35 (17.1%) patients with baseline LSM > 13 kPa, 1 of 17 (5.9%) patients with LSM 9.5â13 kPa, and in no patients with LSM < 9.5 kPa. No patient with lowârisk NFS developed liver decompensation or liverârelated mortality. Following repeat NFSs at the end of followâup, all patients with a liverârelated complication were in the highârisk NFS category. Patients who developed liverârelated complications were also more likely to have baseline highârisk FIBâ4 scores or ELF test â„9.8 compared to patients who did not develop liver outcomes. Conclusion: Liver fibrosis risk stratification in nonâhepatology settings can identify the subset of patients at risk of liverârelated complications. Although the rate of development of a decompensation event or hepatocellular carcinoma was low (2.1% per year) in our patients with compensated cirrhosis (LSM > 13 kPa), these events are projected to lead to a substantial increase in NAFLDârelated disease burden over the next decade due to the high prevalence of NAFLD in people with obesity and T2D.