ABIM Tx Hepatology study materials
ABIM Tx Hepatology study resources

ABIM Tx Hepatology study plan

ABIM Tx Hepatology · Give each week a clear focus.

8 weeks · About 7 hours per week

Week 1

Evaluation and selection of liver transplant candidates (indications, contraindications, MELD-based allocation, pretransplant management)

  • List the accepted indications for liver transplantation by disease category (cirrhosis with decompensation, HCC, acute liver failure, metabolic disease) and state the prognostic threshold that triggers referral for each

  • Differentiate absolute from relative contraindications, including active substance use, extrahepatic malignancy, cardiopulmonary disease, and psychosocial barriers, and justify each with a survival or resource argument

  • Calculate MELD 3.0 and MELD-Na by hand for at least 20 synthetic laboratory sets and identify which patients would gain or lose priority

  • Describe the exception-point pathways for HCC, cholangiocarcinoma, and metabolic disease and explain how waiting-list mortality is balanced against post-transplant benefit

  • Construct a pretransplant workup checklist covering cardiac risk stratification, pulmonary evaluation, infection screening, and nutrition assessment

Your checkpoint

A one-page MELD 3.0 calculation and exception-points reference sheet plus 20 solved laboratory vignettes with at least 90% arithmetic accuracy

Week 2

Post-transplant complications (biliary, vascular, infectious, renal, neurologic, and malignancy)

  • Classify biliary complications by mechanism and timing: anastomotic stricture, non-anastomotic stricture, bile leak, choledocholithiasis, and sphincter dysfunction

  • Outline the presentation, duplex findings, and management sequence for hepatic artery thrombosis, portal vein thrombosis, and hepatic artery stenosis

  • Interpret the pattern of liver enzyme derangement (cholestatic versus hepatocellular, early versus late) to localize a complication to biliary, vascular, or parenchymal causes

  • Map the expected timeline of each major complication onto a post-transplant calendar from day 0 through year 5

  • Explain the role of endoscopic retrograde cholangiography versus percutaneous drainage versus surgical revision in biliary salvage

Your checkpoint

A complication-timing table covering at least 12 complications with peak onset window, first-line diagnostic test, and initial management

Week 3

Immunosuppression, acute and chronic rejection, and immunology of liver transplantation

  • Compare the mechanisms of calcineurin inhibitors, mTOR inhibitors, antimetabolites, and corticosteroids, including the specific lymphocyte signaling step each drug interrupts

  • Describe induction strategies (basiliximab, alemtuzumab, thymoglobulin) and select an induction regimen for a patient with renal dysfunction or prior malignancy

  • Distinguish acute cellular rejection from chronic ductopenic rejection on clinical, biochemical, and histologic grounds

  • Apply Banff grading criteria to at least 15 biopsy descriptions and assign a rejection grade with the corresponding treatment escalation

  • Design a maintenance immunosuppression plan with trough targets for the first month, first year, and long term, including a renal-sparing conversion strategy

Your checkpoint

A drug-mechanism and toxicity comparison table plus 15 biopsy vignettes with assigned Banff grades and management plans

Week 4

Post-transplant complications (biliary, vascular, infectious, renal, neurologic, and malignancy) & Immunosuppression, acute and chronic rejection, and immunology of liver transplantation

  • Build a prophylaxis schedule for cytomegalovirus, Pneumocystis jirovecii, hepatitis B, and fungal infection according to donor and recipient serostatus

  • Apply a renal-sparing immunosuppression algorithm to a recipient with rising creatinine and explain the calcineurin inhibitor versus mTOR inhibitor trade-offs

  • Recognize the clinical and imaging features of neurotoxicity, including calcineurin inhibitor tremor and posterior reversible encephalopathy syndrome, and state the immediate management step

  • Identify the risk factors, typical timing, and treatment approach for post-transplant lymphoproliferative disorder and non-melanoma skin cancer

  • Explain how immunosuppression is modified when infection and rejection coexist

Your checkpoint

A 30-question self-assessment covering domains 1, 3, and 4 with a written rationale for every wrong answer, scoring at least 80%

Week 5

Perioperative and immediate postoperative care of the liver transplant recipient

  • Describe the intraoperative hemodynamic phases of liver transplantation and explain the pathophysiology and management of reperfusion syndrome

  • Interpret post-reperfusion coagulopathy, fibrinolysis, and transfusion thresholds using viscoelastic testing principles

  • Differentiate early allograft dysfunction from primary nonfunction and state the criteria and the decision point for retransplantation

  • Outline immediate postoperative ICU priorities: ventilation weaning, fluid and electrolyte management, immunosuppression initiation, and infection surveillance

  • Explain the perioperative considerations for a recipient with portopulmonary hypertension or hepatorenal syndrome

Your checkpoint

A perioperative and first-72-hour management checklist organized by system, with explicit escalation triggers

Week 6

Recurrent and de novo liver disease, histopathology and liver biopsy interpretation, and long-term graft and patient outcomes

  • Construct a table of recurrent diseases (hepatitis C, hepatitis B, autoimmune hepatitis, primary biliary cholangitis, primary sclerosing cholangitis, steatotic liver disease) with typical recurrence timing, diagnostic criteria, and prevention strategy

  • Differentiate recurrent disease from acute rejection and from de novo disease using histologic and serologic features on liver biopsy

  • List the features of de novo autoimmune hepatitis and de novo steatotic disease after transplant and identify the implicated immunosuppression factors

  • Explain the components of the liver biopsy report that predict graft survival, including fibrosis stage, ductopenia, and interface activity

  • Summarize long-term outcome drivers: graft failure, renal failure, cardiovascular events, and malignancy, with approximate risk magnitudes

Your checkpoint

A recurrence-versus-rejection comparison table covering at least 6 diseases with diagnostic discriminators and first-line therapy

Week 7

Evaluation and selection of liver transplant candidates (indications, contraindications, MELD-based allocation, pretransplant management) & Recurrent and de novo liver disease, histopathology and liver biopsy interpretation, and long-term graft and patient outcomes

  • Revisit the weakest two domains identified in the week 4 self-assessment and rewrite the underlying decision rules in your own words

  • Apply selection and recurrence concepts to at least 40 timed vignettes covering donor allocation, exception points, and post-transplant biopsy interpretation

  • Distinguish recurrent disease from rejection on at least 10 paired biopsy scenarios without reference material

  • Analyze missed questions by error type: knowledge gap, misread stem, or faulty reasoning

Your checkpoint

An error log of at least 40 timed vignette questions, with every miss reclassified by error type and a corrected teaching point written for each

Week 8

Evaluation and selection of liver transplant candidates (indications, contraindications, MELD-based allocation, pretransplant management) & Perioperative and immediate postoperative care of the liver transplant recipient & Immunosuppression, acute and chronic rejection, and immunology of liver transplantation & Post-transplant complications (biliary, vascular, infectious, renal, neurologic, and malignancy) & Recurrent and de novo liver disease, histopathology and liver biopsy interpretation, and long-term graft and patient outcomes

  • Complete a 100-question cumulative mock examination under timed conditions and review every item

  • Recite the MELD 3.0 calculation, Banff grading scheme, and immunosuppression trough targets from memory

  • Summarize the top 10 highest-yield management algorithms across all five domains in your own words

  • Identify any remaining content gap and schedule a targeted review before the examination date

Your checkpoint

A 100-question cumulative mock examination with a score of at least 80% and a one-page high-yield summary sheet

Milestones

Week 4: Complete the core of domains 1, 3, and 4; score at least 80% on the 30-question self-assessment and have distinct reference sheets for MELD, complications, immunosuppression, and prophylaxis

Week 4: Demonstrate hand-calculation of MELD 3.0 with at least 90% accuracy and correctly assign Banff grades in at least 12 of 15 biopsy vignettes

Week 6: Complete domain 2 and domain 5 study with the recurrence-versus-rejection table and perioperative checklist both finished and self-quizzed once

Week 8: Achieve at least 80% on the timed 100-question mock and confirm every missed domain has a documented review plan