Abstract

Introduction: Alcohol related liver disease affects diverse communities with individual and social characteristics that can impact outcomes. The Social Vulnerability Index (SVI) integrates a range of metrics and assigns a score between 0 and 1, where higher scores represent an increased risk of social vulnerability. Vulnerable patients with alcohol related liver disease have been reported to have worse outcomes. We sought to assess the impact of SVI on outcomes of patients hospitalized with alcohol related liver disease with access to social support services. Methods: Hospitalizations for alcohol related liver disease at our institution between March and August 2019 were reviewed. All patients were assigned a low or high SVI score based on their residential census tract. Per our standard practice, patients were screened by multi-disciplinary care coordinators to identify needs for rehabilitation counseling, transplant workup, and care coordination after discharge. Demographics, hepatic decompensation, critical care needs, readmission and mortality were compared. Results: Among 73 patients admitted for alcoholic hepatitis, 32 had a low SVI (mean 0.25) and 42 had a high SVI (mean 0.72). African American patients were more likely to have a higher SVI (35% vs 0%, p=< 0.001). Severity of alcohol hepatitis based on discriminant factor (DF) was similar between high and low SVI patients (mean DF 39.6 vs 42.8, p=0.72). After controlling for race, there was not a significant difference in hepatic decompensation, critical care needs, readmission rate or mortality based on SVI. There were 393 patients admitted for alcoholic cirrhosis including 166 with a low SVI (mean 0.26) and 227 with a high SVI (mean 0.73). Patients that were African American (23.6% vs 5.5%, p=< 0.001) or disabled (41.4% vs 29.5%, p=0.008) had a higher SVI. MELD-Na scores were similar between the high and low SVI patients (mean MELD-Na 21.7 vs 22.9, p=0.47). After controlling for age, race and employment, there was not a significant difference in hepatic decompensation, critical care needs, readmission rate or mortality based on SVI. Conclusion: Most patients admitted for alcohol related liver disease had a high SVI; however, SVI did not impact outcomes in our cohort of patients. This may be a result of extensive care coordination efforts at our institution aimed at reducing barriers for vulnerable patients. These early interventions likely decrease the effect of SVI on outcomes.

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