Table 4.
Psychiatric | Psychometric score improvement (QofL, anxiety, depression, sleep, et cetera) |
Negative toxicology (alcohol, other drugs, nicotine) and rates of discordance with patient reports | |
Reduced alcohol consumption per subjective report and quantitative biomarkers (i.e. PEth) | |
Rates of alcohol treatment engagement, retention, and completion (residential rehabilitation, intensive outpatient, group and/or individual psychotherapy, mutual support group milestones [i.e. AA sobriety coins]) | |
Reduced alcohol cravings (subjective report or validated questionnaire) | |
Rates of regained sobriety and alcohol treatment reengagement after relapse | |
Medical | Improved LFTs (AST, ALT, Tbili, albumin) and MELD scores |
Reduced healthcare utilization (hospital admissions, ER visits) | |
Rates of improved symptoms of decompensated cirrhosis and averted LT evaluations | |
Reduced mortality | |
Expedited LT timetables (i.e. accelerated time-to-listing) | |
Improved LT outcomes (lower rates of de-listing, rates of pre- and post-transplant relapse, graft failure, hospital readmission, post-transplant return-to-function) | |
Other | Patient and family satisfaction scores and feedback for in-person and/or virtual visits |
Clinical and administrative personnel satisfaction scores and feedback regarding teamwork quality and clinical operations | |
Satisfaction scores and feedback from intra- and extramural referring clinicians | |
Cost savings generated from reduced healthcare utilization rates (hospital admissions, ER visits) | |
Patient access and utilization rates (no-shows, cancellations, intra- and extramural referrals, et cetera) | |
Reimbursement and revenue generation |
AA, alcoholics anonymous; ALT, alanine aminotransferase; AST, aspartate aminotransferase; ER, emergency room; LFT, liver function tests; LT, liver transplant; MELD, model for end-stage liver disease; PEth, phosphatidylethanol; QofL, quality of life; Tbili, total bilirubin.