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GCC Nursing Guide — Liver Transplant
Hepatology / Transplant GCC Context SCOT / UAE Transplant Programme Updated Apr 2026
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Indications for Liver Transplant

Common Indications
  • Cirrhosis Child-Pugh C — end-stage from any cause (viral, alcoholic, NASH/NAFLD, autoimmune)
  • Acute liver failure (ALF) — fulminant hepatic failure, King's College criteria
  • Hepatocellular carcinoma (HCC) — within Milan criteria: single nodule ≤5cm OR ≤3 nodules each ≤3cm, no vascular invasion
  • Metabolic disease — Wilson's disease, haemochromatosis, alpha-1 antitrypsin deficiency, primary oxaluria
  • Polycystic liver disease, primary biliary cholangitis (PBC), primary sclerosing cholangitis (PSC)
Child-Pugh C Criteria (Score 10–15)

Encephalopathy, ascites, bilirubin >51 μmol/L, albumin <28 g/L, INR >2.3 — 1-year survival without transplant <35%.

Contraindications

Absolute Contraindications
  • Extrahepatic malignancy (not curable before transplant)
  • Active alcohol/drug use (typically <6 months sobriety)
  • Severe cardiopulmonary disease (uncompensated heart failure, severe pulmonary hypertension PAP >50 mmHg)
  • Uncontrolled sepsis outside the hepatobiliary system
  • Irreversible neurological disease
  • AIDS (not HIV — HIV is a relative CI in most centres)
Relative Contraindications
  • Age >70 years (centre-dependent)
  • Morbid obesity (BMI >40)
  • Portal vein thrombosis (extensive)
  • Prior complex abdominal surgery
  • Renal failure — consider simultaneous liver-kidney transplant
  • HIV infection (requires centre-specific MDT discussion)
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MELD Score — Waitlist Prioritisation

MELD Formula
MELD = 3.78 × ln(bilirubin) + 11.2 × ln(INR) + 9.57 × ln(creatinine) + 6.43

All values in mg/dL. Minimum value for each variable = 1.0 (to avoid negative log). Maximum creatinine = 4.0 mg/dL (or if on dialysis).

MELD-Na (Hyponatraemia Adjustment)

MELD-Na = MELD + 1.32 × (137 − Na) − [0.033 × MELD × (137 − Na)]

Used when serum Na <137 mmol/L. Hyponatraemia worsens prognosis independently of MELD. Na capped at 125 and 137 for calculation.

UKELD Score

UK equivalent: 5.395 × ln(INR) + 1.485 × ln(creatinine) + 3.13 × ln(bilirubin) − 81.565 × ln(Na) + 435. Score ≥49 required for listing in UK.

MELD & 90-day Mortality
<10<5% mortality — Routine listing
10–19~6% — Monitor closely
20–29~20% — Active review
30–39~52% — Urgent consideration
≥40~71% — Emergency status
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Pre-Transplant Nursing Assessment

Cardiovascular Fitness
  • Cardiopulmonary exercise testing (CPET) — VO₂max >10 mL/kg/min preferred
  • ECG, echocardiogram — exclude significant cardiomyopathy, valvular disease
  • Coronary artery disease screening in NAFLD/diabetic patients — high risk in GCC
  • Portopulmonary hypertension (PoPH) — exclude with right heart catheterisation if suspected
  • Hepatopulmonary syndrome (HPS) — SpO₂ monitoring, bubble contrast echocardiogram
Nutritional Status
  • Malnutrition is near-universal in end-stage liver disease — impacts outcomes significantly
  • Use RFH-NPT (Royal Free Hospital Nutritional Prioritising Tool) or MUST
  • Sarcopenia assessment: CT psoas muscle index, 6-minute walk test
  • Dietary referral: high-calorie, high-protein diet (1.2–1.5 g/kg/day protein)
  • Late-night snacking encouraged to prevent overnight catabolism
  • Zinc, magnesium, B-vitamin deficiencies common — supplement accordingly
Social Support & Substance Use
  • Adequate social support essential — post-transplant medication compliance and follow-up
  • Alcohol history: AUDIT score, minimum 6 months documented abstinence for ALD (varies by centre)
  • Drug screening: urine toxicology, hair follicle testing in some centres
  • Psychiatric assessment: depression, anxiety, personality disorders — impact compliance
  • GCC context: alcohol documentation culturally sensitive — approach with non-judgement

Waiting List Management

Nurses play a central role in monitoring patients on the waiting list — early identification of deterioration is key to timely relisting upgrade.

Monitoring Priorities
  • Regular MELD recalculation (3-monthly minimum, more frequently if ≥20)
  • Ascites control: diuretics (spironolactone + furosemide), paracentesis frequency
  • Hepatic encephalopathy: lactulose/rifaximin adherence, ammonia trends
  • Spontaneous bacterial peritonitis (SBP) prophylaxis: norfloxacin/ciprofloxacin
  • Variceal surveillance: gastroscopy q1–2 years, beta-blocker/banding therapy
  • Renal function: rising creatinine — hepatorenal syndrome risk, triggers MELD upgrade

Hospital upgrade criteria: MELD ≥25, refractory ascites, recurrent SBP, progressive encephalopathy, HRS development — escalate immediately to transplant coordinator.

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Living Donor Liver Transplant (LDLT) & GCC Context

LDLT Overview

LDLT uses a partial hepatectomy from a living donor — right lobe (60–65% of liver) most common for adult recipients. Both donor and recipient livers regenerate. Donor safety is paramount: donor mortality risk ~0.1–0.5% for right hepatectomy.

Split Liver Technique

Deceased donor liver split between two recipients (adult + paediatric). Requires careful surgical planning; left lateral segment to child, right extended lobe to adult.

Donor Assessment
  • Age 18–60, healthy BMI, no significant comorbidity
  • ABO compatibility (or compatible with desensitisation protocol)
  • Liver volumetry — CT: donor must retain ≥30% volume (safe remnant)
  • CT hepatic angiography and cholangiography — anatomical planning
  • Psychological evaluation: voluntary, no coercion
GCC Regional Context
  • NAFLD/NASH is the fastest-growing indication for liver transplant in GCC — driven by obesity, T2DM epidemic
  • SCOT (Saudi Centre for Organ Transplantation) — national transplant coordination body in Saudi Arabia
  • UAE Transplant Programme — based at Sheikh Khalifa Medical City, Abu Dhabi; growing LDLT programme
  • Religious rulings (fatwa) support both deceased and living donor transplantation across GCC
  • LDLT preferred in many GCC centres due to limited deceased donor pool
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ICU Priority on Arrival: Systematic ABCDE assessment. Liver transplant patients arrive ventilated. Establish haemodynamic targets, review drain outputs, confirm graft viability with Doppler — first 72 hours are critical.

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Haemodynamic Goals

MAP Target≥65 mmHg
CVP5–10 cmH₂O (low CVP intraop to reduce blood loss)
Urine Output≥0.5 mL/kg/hr
LactateTrending down — rising lactate = graft dysfunction
VasopressorsNoradrenaline first-line — wean as haemodynamics stabilise
CoagulopathyINR, TEG/ROTEM guided — avoid over-transfusion
Fluid Management

Albumin preferred colloid. Avoid normal saline in large volumes (hyperchloraemic acidosis). Target euvolaemia — avoid fluid overload (hepatic vein congestion impairs graft function).

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Drain Assessment & Monitoring

Jackson-Pratt Drains
  • Serous/sanguinous: expected post-op — decreasing volume over 24–48h is reassuring
  • Bilious (green-yellow): bile leak — measure bilirubin in drain fluid if suspected; >3× serum = bile leak
  • Bright red, large volume: surgical bleeding — urgent surgical review
  • Document drain output hourly for first 24h, then 4-hourly
  • T-tube drain (if placed): records bile output — normal = 300–500 mL/day, reducing over weeks
Respiratory Monitoring
  • Prolonged ventilation common in complex cases — daily extubation readiness assessment
  • Right-sided pleural effusion: hepatic hydrothorax — diuretics, +/- pleural drain
  • Phrenic nerve injury: right hemidiaphragm elevation on CXR
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Early Graft Complications — Emergency Recognition

Primary Non-Function (PNF)
Definition

Catastrophic failure of graft function from first 24–72h. Immediate re-listing required.

Signs
  • Markedly elevated AST/ALT (>2500 U/L)
  • Rising INR, unresponsive coagulopathy
  • No bile output from T-tube
  • Progressive encephalopathy
  • Worsening haemodynamics, rising lactate
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Action: Emergency surgical re-listing. Notify transplant team immediately.

Hepatic Artery Thrombosis (HAT)
Timing

Most common vascular complication. Early HAT: first 72h. Risk increased in LDLT.

Signs
  • Sudden rise in AST/ALT (ischaemic pattern >1000 U/L)
  • Fever, elevated WCC
  • Bile duct ischaemia — biliary complications
  • Absent/reduced hepatic artery flow on Doppler
Nursing Action

Daily Doppler ultrasound first 72h. Report any absent waveform immediately. Surgical thrombectomy/re-anastomosis window is narrow — time-critical.

Bile Leak
Presentation
  • Bilious drain output or peritonitic pain
  • Fever, rising CRP, abdominal pain RUQ
  • May present days–weeks post-op
Diagnosis

Drain bilirubin >3× serum bilirubin confirms bile leak. ERCP/MRCP for localisation. CT abdomen if collection.

Management
  • Small leaks: conservative, drain in situ
  • ERCP + sphincterotomy + stent insertion
  • Large/persistent: surgical re-exploration
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Immediate Post-Op ABCDE Priorities

  1. A — Airway: Confirm ETT position, secure fixation. Plan for extubation within 6–24h if haemodynamically stable and warm.
  2. B — Breathing: Ventilator settings — lung-protective (TV 6 mL/kg IBW). SpO₂ ≥95%. Monitor for right pleural effusion on CXR.
  3. C — Circulation: Arterial line, CVC in situ. MAP ≥65, HR 60–100. Review vasopressor requirement, target weaning by hour 6–12 if stable.
  4. D — Disability: GCS on awakening post-sedation hold. Pupils, pain score (CPOT if intubated). Hepatic encephalopathy grade if extubated.
  5. E — Exposure: Inspect surgical wound, all drain sites. Check drain output colour and volume. Abdominal rigidity. Temperature — hypothermia common post long-op.
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Types of Liver Transplant Rejection

Type Timing Mechanism Presentation Management
Hyperacute Minutes–hours Pre-formed antibodies (ABO incompatibility) Graft failure immediately in theatre; prevented by ABO matching Prevented — ABO matching mandatory. Emergency re-transplant if occurs
Acute Cellular (ACR) 6–30 days T-cell mediated immune attack on bile ducts and portal tracts Fever, RUQ pain, jaundice, elevated AST/ALT/ALP/bilirubin, reduced bile Pulsed methylprednisolone 1g IV ×3 days. Most respond within 48–72h
Chronic Rejection Months–years Ductopenic rejection — progressive bile duct loss Slowly rising bilirubin, ALP/GGT >> AST/ALT, ductopenia on biopsy Tacrolimus optimisation, consider switch to mTOR inhibitor; may need re-transplant
Antibody-Mediated (AMR) Variable Donor-specific antibodies (DSA) targeting vascular endothelium Mixed LFT pattern, microvascular injury on biopsy, positive DSA serology Plasmapheresis, IVIG, rituximab; specialist centre management
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Nursing Signs of Rejection

Report to medical team immediately if ≥2 of these are present post-transplant:

  • Jaundice — new or worsening scleral icterus, yellow skin
  • RUQ pain — hepatic capsule pain from graft swelling
  • Fever ≥38.5°C — inflammatory response (also consider infection)
  • Elevated LFTs — rising trend on daily bloods
  • Reduced bile output — from T-tube or dark/reduced urine
  • Malaise, anorexia — non-specific but combined with above is significant
Gold Standard Diagnosis

Liver biopsy — Banff grading for ACR: Grade I (mild, portal inflammation), Grade II (moderate, perivenular involvement), Grade III (severe, necrosis). Prepare patient for procedure; check platelets and INR first.

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LFT Interpretation for Nurses Post-Transplant

Hepatocellular Pattern (ALT/AST elevated predominantly)
  • ACR (early), ischaemia (HAT/portal vein thrombosis), drug hepatotoxicity
  • ALT > AST typically = hepatocellular; AST > ALT = more severe/alcoholic pattern
Cholestatic Pattern (ALP/GGT elevated predominantly)
  • Bile duct stricture, bile leak, chronic rejection (ductopenic), PSC recurrence
  • GGT elevation alone may indicate drug effect or biliary sludge
Bilirubin — Late Rise
  • Chronic rejection: isolated bilirubin rise, ALP up, late phase
  • Haemolysis (post-transfusion): indirect bilirubin rises — check haematology
  • Synthetic failure: rising bilirubin + INR + falling albumin = late graft failure
ACR Treatment — Nursing Monitoring
  • Methylprednisolone 1g IV over 30 min daily ×3 days
  • Monitor blood glucose hourly during infusion (hyperglycaemia common)
  • BP monitoring — acute fluid retention, hypertension
  • Mood changes — steroid-induced psychiatric effects
  • Observe for 48–72h LFT response; if no improvement, repeat biopsy/rescue therapy
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Standard Triple Immunosuppression Therapy

Tacrolimus (TAC)
Calcineurin Inhibitor — Backbone
  • Mechanism: inhibits calcineurin, blocks IL-2 production, suppresses T-cell activation
  • Route: oral BD (once-daily modified-release preparations available)
  • Trough target: 5–15 ng/mL early (0–3 months), 5–10 ng/mL long-term
  • Key toxicity: nephrotoxicity, neurotoxicity (tremor, headache), hypertension, NODAT
Mycophenolate Mofetil (MMF)
Antimetabolite
  • Mechanism: inhibits inosine monophosphate dehydrogenase — blocks purine synthesis, suppresses lymphocyte proliferation
  • Route: oral BD (500mg–1g BD)
  • Key toxicities: bone marrow suppression (leukopenia, anaemia), GI side effects (diarrhoea, nausea)
  • Monitor: FBC weekly ×4, then monthly
Prednisolone
Corticosteroid
  • High dose initially — tapered and often withdrawn by 3–6 months post-transplant
  • Side effects: hyperglycaemia, hypertension, osteoporosis, weight gain, adrenal suppression
  • Tapering schedule: centre-specific — typically 20mg/day → 5mg/day over 3–6 months
  • Never stop abruptly — risk of adrenal insufficiency and rejection

Tacrolimus — Drug Interactions

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High-risk interaction — Azole antifungals markedly increase tacrolimus levels. Fluconazole, voriconazole, itraconazole inhibit CYP3A4 — can increase tacrolimus levels 3–5 fold. Dose reduction and intensive level monitoring mandatory.

Drugs That INCREASE Tacrolimus Levels (CYP3A4 Inhibitors)
Azole antifungals Diltiazem / Verapamil Macrolide antibiotics Grapefruit juice Omeprazole (mild)
Drugs That DECREASE Tacrolimus Levels (CYP3A4 Inducers)
Rifampicin Phenytoin / Carbamazepine St John's Wort Rifabutin
Monitoring Schedule
Tacrolimus troughDaily (ICU) → 2×/wk → monthly
Renal functioneGFR, creatinine — weekly initially
FBC (MMF monitoring)Weekly ×4, then monthly
Blood glucoseDaily fasting (NODAT screening)
Blood pressureDaily — hypertension common
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Infections in Immunosuppressed Patients

CMV — Most Common Opportunistic Infection
  • Peak risk: 1–6 months post-transplant
  • Presentation: fever, leucopenia, fatigue, GI symptoms; can cause hepatitis, pneumonitis, retinitis
  • Prophylaxis: valganciclovir for 3–6 months (D+/R- highest risk)
  • Surveillance: CMV PCR fortnightly for 3–6 months, then monthly
  • Treatment: valganciclovir (oral) or IV ganciclovir for tissue invasive disease
EBV & PTLD (Post-Transplant Lymphoproliferative Disease)
  • EBV-driven lymphoma in immunosuppressed state — rare but serious
  • Presentation: lymphadenopathy, fever, weight loss, elevated LDH
  • EBV PCR monitoring in high-risk patients (D+/R-)
  • Management: reduce immunosuppression first, rituximab, chemotherapy if lymphoma
PCP & Fungal Prophylaxis
  • PCP (Pneumocystis jirovecii): Co-trimoxazole prophylaxis for 6–12 months post-transplant
  • Fungal: Fluconazole prophylaxis first 1–3 months — monitor tacrolimus levels closely
  • Aspergillus: risk in high-dose steroids, prolonged ICU stay — voriconazole if suspected
  • Candida: oral/oesophageal candidiasis — nystatin, fluconazole

Non-compliance with immunosuppression is the single most common cause of late graft loss. Patient education, blister packs, family involvement, and regular level monitoring are essential strategies.

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Metabolic Complications Post-Transplant

NODAT — New-Onset Diabetes

Affects 20–40% of liver transplant recipients. Driven by tacrolimus (insulin resistance), prednisolone (glucose intolerance), pre-existing risk factors (NASH, obesity in GCC patients).

  • Screen: fasting glucose daily initially; HbA1c at 3/12, 6/12, annually
  • Management: dietary modification, metformin (if eGFR allows), insulin
  • Consider tacrolimus dose reduction / switch to cyclosporine in refractory cases
Hypertension

Affects >60% post-transplant. Caused by CNI vasoconstriction, steroid-related sodium retention.

  • Target BP: <130/80 mmHg (lower in proteinuric renal disease)
  • First-line: calcium channel blockers (amlodipine) — no interaction with tacrolimus
  • Avoid ACEi/ARBs early (hyperkalaemia risk with tacrolimus); useful once stable
Hyperlipidaemia

Steroids and mTOR inhibitors (sirolimus/everolimus) cause dyslipidaemia. Monitor annually.

  • Statins: generally safe — pravastatin preferred (less CYP3A4 interaction with tacrolimus)
  • Lifestyle modification: diet, exercise — important in GCC where metabolic risk is high
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Renal Dysfunction — CNI Nephrotoxicity

Calcineurin inhibitors (tacrolimus, cyclosporine) cause afferent arteriolar vasoconstriction, leading to chronic nephrotoxicity. Up to 20% develop CKD stage 3+ by 5 years.

Nursing Monitoring
  • eGFR and serum creatinine monthly ×12 months, then 3-monthly
  • Urinalysis for proteinuria — microalbuminuria is early marker
  • Nephrology co-management if eGFR <45
Management Strategy
  • Minimise tacrolimus dose to lowest therapeutic level (5–8 ng/mL long-term)
  • Consider conversion to mTOR inhibitors (sirolimus/everolimus) — allow CNI reduction/withdrawal
  • Avoid NSAIDs, contrast nephropathy — hydrate before all contrast studies
  • Simultaneous liver-kidney transplant (SLiKT) if pre-transplant eGFR <30
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Bone Health & Malignancy Surveillance

Osteoporosis
  • Steroids accelerate bone loss — 30–40% of patients develop osteoporosis
  • DEXA scan at transplant listing and 12 months post-transplant
  • Calcium 1000 mg/day + Vitamin D 800 IU/day — all post-transplant patients
  • Bisphosphonates if T-score < -2.5 or osteoporotic fracture
  • Weight-bearing exercise encouraged
HCC Surveillance (Recurrence)
  • 6-monthly liver ultrasound + AFP for patients transplanted for HCC
  • Milan criteria expansion (UCSF criteria) — some centres accept slightly larger tumours
  • AFP rising post-transplant: CT triple-phase liver, chest CT
Skin Cancer — GCC Context

Immunosuppressed patients in the Gulf have dramatically elevated skin cancer risk due to intense UV exposure. Annual dermatology review, high-SPF sunscreen daily, protective clothing and sun avoidance during peak hours (10am–4pm) are essential post-transplant advice for GCC patients.

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Vaccination & Lifestyle

Vaccination in Immunocompromised Patients
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Live vaccines are CONTRAINDICATED post-transplant: MMR, varicella, yellow fever, oral typhoid, live influenza (intranasal). Risk of disseminated live vaccine disease in immunosuppressed state.

Recommended (Inactivated)
Influenza (inactivated) — annual Pneumococcal Hepatitis B Hepatitis A COVID-19 HPV

Ideally complete vaccines before transplant — better immune response when not immunosuppressed.

Lifestyle Guidance
  • Alcohol abstinence — mandatory for ALD recipients. Alcohol testing (urine ethyl glucuronide) at follow-up visits. Relapse rates 10–20% at 5 years
  • Diet: healthy Mediterranean-style diet. Avoid unpasteurised food/soft cheeses (Listeria risk)
  • Exercise: aerobic exercise 150 min/week — improves metabolic outcomes, muscle mass, mental health
  • Avoid contact with soil/compost without gloves (Aspergillus risk)
  • Pet hygiene: avoid cat litter (toxoplasmosis), reptile faeces (Salmonella)
  • Travel: avoid live oral typhoid vaccine; ensure travel insurance covers transplant
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MELD Score Calculator

Calculate MELD Score

MELD Score
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    Rejection Types — Quick Reference Table

    FeatureACRChronicAMR
    Timing6–30 daysMonths–yearsVariable
    Dominant LFTALT/AST + ALP/biliBilirubin + ALPMixed
    MechanismT-cellDuctopenicDSA/antibody
    Biopsy findingPortal inflammation, Banff grade I–IIIBile duct lossMicrovascular injury
    TreatmentPulse methylprednisoloneTacrolimus optimisePlasmapheresis, IVIG
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    Tacrolimus — Quick Reference

    ClassCalcineurin inhibitor (CNI)
    MechanismInhibits calcineurin → blocks IL-2 → T-cell suppression
    Early target (0–3m)5–15 ng/mL trough
    Long-term target5–10 ng/mL trough
    Sampling timeTrough — immediately before dose
    Key toxicityNephrotoxicity, neurotoxicity, NODAT
    Major interactionAzole antifungals (levels ↑↑↑)
    Inducer interactionRifampicin (levels ↓↓)
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    Immunosuppression Side Effects — Exam Table

    DrugKey Side EffectsMonitoringExam Pearls
    Tacrolimus Nephrotoxicity, tremor, headache, NODAT, hypertension, alopecia Trough levels, eGFR, BG, BP Narrow therapeutic index; azoles dramatically raise levels
    Mycophenolate Mofetil Leucopenia, thrombocytopenia, anaemia, GI (diarrhoea, nausea) FBC weekly ×4 then monthly Teratogenic — women of childbearing age need contraception
    Prednisolone NODAT, hypertension, osteoporosis, Cushingoid features, peptic ulcer BG, BP, bone density (DEXA) Never stop abruptly; most centres withdraw by 3–6 months
    Sirolimus/Everolimus (mTOR) Hyperlipidaemia, mouth ulcers, impaired wound healing, pneumonitis Lipids, sirolimus levels, LFTs Avoid early post-transplant — impairs wound healing. Used CNI-sparing
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    DHA / DOH / SCFHS / QCHP High-Yield Exam Questions

    High-Yield MCQ Topics

    Q: What is the MELD score formula?

    A: 3.78×ln(bilirubin mg/dL) + 11.2×ln(INR) + 9.57×ln(creatinine mg/dL) + 6.43

    Remember: minimum value for all inputs = 1.0. Creatinine maximum = 4.0 (or dialysis). Score 6–40+ used for waitlist priority.

    Q: First-line treatment for acute cellular rejection?

    A: Pulsed methylprednisolone 1g IV daily ×3 days

    Gold standard diagnosis is liver biopsy (Banff grading). ACR occurs 6–30 days post-transplant. 80–90% respond to steroid pulse.

    Q: Tacrolimus trough target at 1 year post-transplant?

    A: 5–10 ng/mL (long-term maintenance)

    Early (0–3 months): 5–15 ng/mL. Sample as trough — immediately before morning dose. Levels taken at consistent time.

    Q: Most dangerous drug interaction with tacrolimus?

    A: Azole antifungals (fluconazole, voriconazole) — CYP3A4 inhibition causes 3–5-fold level rise

    Can cause acute tacrolimus toxicity: AKI, neurotoxicity, tremor. Dose reduction + intensive monitoring mandatory when combined.

    Further High-Yield Points

    Q: Milan criteria for HCC transplant listing?

    A: Single nodule ≤5cm OR ≤3 nodules each ≤3cm, no macrovascular invasion, no extrahepatic disease

    5-year survival >70% within Milan criteria. Exceeding criteria = higher recurrence risk. AFP monitoring 6-monthly post-transplant.

    Q: Which vaccines are contraindicated post-transplant?

    A: All live vaccines — MMR, varicella (VZV), yellow fever, oral typhoid, live influenza (FluMist/LAIV)

    Risk: disseminated live vaccine disease. Inactivated influenza, pneumococcal, hepatitis B/A, COVID-19 — all safe and recommended.

    Q: Most common cause of late graft loss?

    A: Non-compliance with immunosuppression

    Also: chronic rejection, recurrence of original disease (HCV pre-DAA era, HCC, NAFLD), chronic CNI nephrotoxicity. Patient education on medication adherence is the single most impactful nursing intervention long-term.

    Q: Hepatic artery thrombosis — nursing action?

    A: Urgent Doppler ultrasound — absent/reduced hepatic artery flow = emergency surgical/radiological intervention

    Daily Doppler monitoring for first 72h post-transplant. Early HAT within 72h requires emergency thrombectomy or re-transplant. Report sudden LFT spike (AST >1000) immediately — could be vascular.