First question
Independent indication?ACS, significant left main, refractory angina or selected prognostic indication.
Solely to lower surgical risk?Routine intervention for stable non-left-main CAD has not improved principal randomized outcomes.
A

Which evidence applies?

population before extrapolation
SettingWhat the evidence supports
Elective vascular surgeryCARP: no survival/postoperative-MI benefit. Longer delay.
Kidney transplantISCHEMIA-CKD/listed subgroup: no routine invasive-strategy benefit for stable moderate/severe ischemia. Immediate transplant evidence limited.
Liver transplantObservational comparisons. Joint coronary-risk, treatment-feasibility and transplant-timing decision.
B

Count the full pathway

benefit must survive the delay
Count benefit across the whole pathwayOriginal decision sequence. Coronary benefit must be weighed against procedural harm, recovery, bleeding and lost surgical or transplant opportunity.1 · Establish indicationSymptoms or prognosisBeyond the plannedsurgery2 · Choose feasible careMedical therapy / PCI /CABGInclude recovery and DAPT3 · Reassess readinessInclude harm whilewaitingName conditions and owner
Original decision sequence. Coronary benefit must be weighed against procedural harm, recovery, bleeding and lost surgical or transplant opportunity.
Playing
  • Selection trap Post-transplant survivors cannot establish benefit for everyone evaluated.
  • Recommendation Treatment indication, candidacy impact and readiness reassessment owner.
Stable CAD before elective vascular surgery: CARP found no routine revascularization benefit.
A

Trial at a glance

defined, selected population

Who / treatment

  • Enrollment 510/5,859 screened (9%), 98% men. Stable CAD, elective AAA/lower-extremity vascular surgery.
  • Intervention 59% PCI, 41% CABG among revascularized. No randomized CABG–PCI comparison. Procedure choice was not the randomized question.

Excluded / limits

  • Exclusions Left-main ≥50%, EF <20%, severe AS, urgent/emergency surgery.
  • Applicability Earlier stent/medical era. Not transplant, ACS or urgent limb salvage. Confidence intervals retain uncertainty.
B

Results

revascularization vs no revascularization
EndpointRevascularization versus no revascularization
Mortality at median 2.7 years22% versus 23%, relative risk 0.98, 95% CI 0.70-1.37, P=0.92
MI within 30 days after vascular surgery12% versus 14%, P=0.37
Median randomization-to-vascular-surgery interval54 versus 18 days, P<0.001
C

Apply the 2024 AHA/ACC guideline

indication beyond the operation
  • ACS Treat, then defer elective surgery.
  • Significant left main ≥50% Revascularization reasonable when hemodynamically significant.
  • Stable non-left-main Do not intervene routinely solely to lower perioperative events.
  • Before another test Specify how anatomy would reveal an independent indication or change the operation.
ISCHEMIA-CKD: medical therapy is the foundation for comparable stable advanced-CKD disease.
A

Strategy trial

777 patients

Entry + comparison

  • Entry eGFR <30 mL/min/1.73 m² or dialysis, stable moderate/severe ischemia.
  • Comparison Initial invasive strategy + medical care versus medical care with angiography for clinical failure. Rescue intervention allowed. Conservative care was active medical treatment.

Important exclusions

  • Disease Refractory angina, recent ACS, EF <35%, NYHA III/IV HF/recent HF admission, known or strongly suspected significant unprotected left-main disease.
  • Imaging / surgery Routine CCTA to exclude unknown left main discouraged for kidney risk. Planned major surgery requiring DAPT interruption excluded.
B

Outcomes and treatment exposure

invasive vs conservative
Outcome or treatment exposureInvasive versus conservative strategy
Estimated 3-year death or nonfatal MI36.4% versus 36.7%, adjusted HR 1.01, 95% CI 0.79-1.29
StrokeHR 3.76, 95% CI 1.52-9.32
Death or initiation of dialysisHR 1.48, 95% CI 1.04-2.11. This safety analysis concerned participants not receiving dialysis at baseline
Cumulative revascularization at 3 years50.2% versus 19.6%
C

What changes practice?

no automatic invasive mandate
  • Ischemic burden alone No demonstrated routine invasive-strategy benefit.
  • Still assess anatomy If it creates an independent indication or changes candidacy. Weigh renal injury, bleeding and delay.
  • Do not extrapolate Not CABG versus PCI, immediate transplant surgery, ACS, refractory symptoms, severe LV dysfunction or significant left-main treatment.
Modern stable-CKD strategy evidence outweighs a small historical transplant trial for comparable patients.
A

ISCHEMIA-CKD listed subgroup

post hoc · 194 candidates
Death/nonfatal MI
27/94 vs 30/100
Invasive vs conservative.
Adjusted effect
HR 0.91
95% CI 0.54–1.54.
Transplanted
51
Treatment-by-list-status interaction P=0.68.
  • Limit Small post hoc subgroup, wide interval and substantial crossover. Absence of significance does not establish equivalence. Immediate transplant-operation benefit remains imprecise.
B

Manske 1992

historical comparator

Population + result

  • Population 26 insulin-dependent diabetic patients with atypical or no chest pain, chronic renal failure, substantial CAD during transplant assessment.
  • Unstable angina, MI or cardiac death 10/13 medical vs 2/13 revascularization, median 8.4 months.

Why not a modern rule?

  • Medical care Calcium-channel blocker + aspirin, not contemporary prevention.
  • Inference Small sample, limited precision/generalizability. No predicted transplant benefit assignable from either trial.
C

Decision before PCI

indication + offer access
  • Assess Symptoms, LV function, anatomy, feasible medical care, independent indication, procedural risk and time away from readiness.
  • Donor pathway Living donation allows scheduling. Deceased-donor offers require an explicit antiplatelet/readiness plan.
No randomized liver-transplant trial establishes benefit from routine prophylactic PCI.
A

Recipient cohort versus evaluation cohort

denominator changes the question

Umadat 2025: post-LT outcomes

  • Population 111 asymptomatic recipients with significant angiographic CAD. 66 PCI, 45 medical. CABG excluded.
  • MACE 52% vs 60% at median 32 months, P=0.40.
  • Unadjusted HR 1.16, 95% CI 0.68–1.96.
  • Composite Death, MI, stroke/TIA, new systolic dysfunction or post-LT coronary intervention.
  • Limit Small single-center cohort selected by reaching transplantation. No demonstrated lower MACE, no equivalence conclusion.

Ginard 2025: evaluation harms

  • Population 912 evaluated → 202 angiography → 18 PCI.
  • Complications 8/202 overall, 4/18 after PCI.
  • Death One acute-on-chronic liver-failure death after DAPT-related bleeding.
  • Limit Captures pretransplant harm. Small PCI sample, disease-based treatment selection.
  • One-month DAPT Used in many PCI patients. Does not establish universal transplant timing.
B

AASLD/AST 2026 decision

individual benefit and feasibility
  • Current guidance Significant asymptomatic CAD: multidisciplinary revascularization assessment before/around LT. Replaces older broad consideration for all significant CAD.
  • Balance Lesion significance, hepatic reserve, portal bleeding, kidneys, DAPT tolerance, delayed listing and declined organs.
  • Endpoint caution Umadat MACE is broader than CARP/ISCHEMIA-CKD endpoints.
Selected recipient survival demonstrates feasibility, not a causal revascularization benefit.
A

Wray 2025

historical cohort, long follow-up
Cohort
604 recipients
Pre-LT angiography, 7 centers, transplantation 1998–2010.
CAD / follow-up
145 obstructive CAD
Mean follow-up 7.3 years.
Comparison with recipients without obstructive CADAdjusted mortality association
Any obstructive CADHR 1.39, 95% CI 1.06-1.82
Severe CAD, >70% stenosisHR 1.63, 95% CI 1.19-2.22
Pretransplant revascularizationHR 1.62, 95% CI 1.18-2.23
B

Read the comparison correctly

against recipients without obstructive CAD

What HR 1.62 cannot show

  • Causal harm Revascularized patients differ from recipients without CAD.
  • Risk eliminated Successful treatment does not remove long-term coronary risk.

Cohort checks

  • Start point Evaluation, listing or transplantation?
  • Comparator Similar anatomy/symptoms? Treatment selected for worse disease?
  • Missing interval Deaths, bleeding, delisting and missed organs before LT?
  • Era Current stents, medical care and selection?
C

Residual risk

complete the whole assessment
  • Beyond coronaries HF, RV/vascular disease, frailty and transplant hemodynamic stress.
  • Outcome horizon Post-LT survival is one part of evaluation-to-transplant survival.
A

Contemporary selected cirrhosis cohort

Jenkins · cardiac surgery with cardiopulmonary bypass
30-day mortality
4.1%
220 patients, median MELD 10.
90-day mortality
12.6%
Operated 2014–2022. Recovery deaths matter.
  • By class at 30 days A: 2.8% (n=143). B: 6.8% (n=73). Only 4 class C patients.
  • Selection Confirmed cirrhosis. Prior/concomitant LT and off-pump operations excluded. Declined patients absent.
B

Historical severity gradient

Jacob · 19 studies · 638 patients
Child-Pugh classDeaths / patientsPooled mortality, 95% CI
A38/4209.0% (6.6-12.2%)
B72/19337.3% (30.8-44.3%)
C13/2552.0% (33.5-70.0%)
  • Endpoint Pooled short-term mortality <30 days, variable component follow-up. Mixed CABG/valve studies through early 2014.
  • Limit Heterogeneous historical data, class C n=25. Not a contemporary risk calculator or an individual CABG estimate. Keep the operation and follow-up horizon attached to each rate.
C

Death and decompensation

Suman · 44 cardiac-surgery patients with CPB · 1992–2002
Child-Pugh class, nMortalityHepatic decompensation
A, 311/31 (3.2%)3/31 (9.7%)
B, 125/12 (41.7%)8/12 (66.7%)
C, 11/11/1
  • By 3 months 7/44 deaths, 12/44 hepatic decompensations. These are not 30-day rates.
  • Class C One patient cannot estimate class-specific risk. Contemporary selected outcomes do not erase advanced-disease risk.
Mortality alone misses hepatic decompensation, renal injury, ventilation and lost transplant opportunity.
A

Broader liver disease, not cirrhosis alone

Pétursson · 285 patients · 2010–2020
Group, nDeath by 30 days / in hospital≥1 complication
Child-Pugh A, 2195.9%37.9%
Early B, MELD <12.7, 345.9%38.2%
Advanced B, MELD ≥12.7, 3218.8%59.4%
  • Advanced B Renal failure 21.9%, prolonged ventilation 46.9%.
  • Selection No class C. Early B younger, frequent endocarditis/tricuspid surgery. Conventional MELD 12.7 derived within this dataset.
  • Inference No universal “safe MELD” for CABG.
B

Other outcome estimates

keep endpoints distinct

2025 cirrhosis meta-analysis

  • Inpatient mortality 11% (95% CI 9–14%).
  • Renal failure 30% (21–39%), not an estimate of new dialysis. Check component definitions.

Individual assessment

  • Hepatic Child-Pugh points, dated MELD/version, ascites/encephalopathy, portal bleeding.
  • Operative Kidney reserve, nutrition/frailty, urgency and complexity. Cardiac-surgery/hepatology adjudication.
  • Versions MELD, MELD-Na and MELD 3.0 cutoffs are not interchangeable. Record the score version used by the study and calculator.
C

Calibration in 220 operated patients

Jenkins: mean prediction vs observation
Model or observed outcome30-day mortality90-day mortality
Mayo model, mean predicted20.9%29.6%
VOCAL-Penn, mean predicted9.0%14.0%
Observed4.1%12.6%
  • Limits Nine 30-day deaths. Mean estimates are not individual corrections or evidence of safety for patients declined surgery.
  • Report Calculator, endpoint and limitations.
CABG decision
IndicationCoronary benefit must be established.
FeasibilityHepatic reserve and transplant rescue require separate assessment.
A

CABG-specific absolute risk

Siraw · US inpatient data · 2016–2020
Cirrhosis
8.6%
In-hospital mortality.
Noncirrhotic liver disease
5.9%
In-hospital mortality.
No chronic liver disease
2.8%
In-hospital mortality.
  • Population 7,945 chronic-liver-disease patients matched to 7,945 without. Cirrhosis n=6,687.
  • Adjusted association Mortality OR 4.21 (95% CI 3.61–4.94). No granular Child-Pugh/MELD severity.
B

Avoiding bypass ≠ established safety

Gopaldas · 1998–2009

Observed association

  • Population 6,448 cirrhotic patients among about 3 million CABG admissions.
  • On-pump Excess mortality/morbidity across severity categories.
  • Off-pump Association concentrated in severe disease, defined administratively. No causal off-pump benefit or advanced-cirrhosis safety claim. Operative selection can explain part of the association.

Clinical boundary

  • Technical Suitability and completeness still matter.
  • AHA 2022 Isolated CABG described as contraindicated at MELD >13 or Child-Pugh B/C.
  • Adjudication Experienced team, especially with decompensation. New mixed-operation cohorts do not validate CABG across class B.
C

Simultaneous cardiac surgery + LT

selected-center feasibility
  • 2026 report 46 selected patients, CABG/valve mix. Actuarial survival 74.2% at 1 year, 50% at 5 years.
  • Limits Single center, nonrandomized, not CABG-specific. No staged-care superiority or broadly validated internal score.
  • Plan Medical care, PCI, staged CABG, selected combined surgery or prohibitive risk. Transplant impact and reassessment owner.
A

Choose treatment after establishing an indication

coronary guideline conditions

CABG when surgically suitable

  • Left main Recommended for significant disease.
  • LV dysfunction Recommended: multivessel CAD, severe LV dysfunction and amenable anatomy.
  • Diabetes Preferred: multivessel disease involving LAD, in a suitable surgical candidate.

PCI consideration

  • Left main Selected anatomy permitting equivalent revascularization.
  • Surgery unsuitable PCI remains an option when revascularization is indicated.
  • Heart Team Symptoms, anatomy, LV function, completeness, harm, DAPT, preference and life expectancy.
Labeled CABG illustration showing an internal mammary artery conduit and a saphenous vein graft connecting to native coronary arteries beyond plaque.
Conduit, inflow and target. Illustrative anatomy, not a prescribed graft plan. Assess distal targets and conduit suitability.
Blausen 0151 CABG 02.png by BruceBlaus / Blausen Medical Communications. Source · CC BY 3.0. Unmodified.
B

Evidence: match population and comparator

no cross-trial CABG–PCI inference
Trial / populationOutcomeClinical lesson
FREEDOM · 1,900 Diabetes, multivessel CAD5-year death/MI/stroke: 26.6% PCI vs 18.7% CABG. Stroke: 2.4% vs 5.2%.CABG benefit, stroke tradeoff. Earlier DES era.
STICHES · 1,212 EF ≤35%, CABG-amenable CADMedian 9.8 years: death 58.9% CABG vs 66.1% medical. HR 0.84 (95% CI 0.73–0.97).Selected ischemic CM: long-term CABG benefit, with recovery/time-to-benefit costs.
REVIVED-BCIS2 · 700 EF ≤35%, extensive CAD, viabilityMedian 41 months: death/HF admission 37.2% PCI vs 38.0% medical. HR 0.99 (95% CI 0.78–1.27).No demonstrated endpoint benefit. Viability alone does not establish prognostic PCI benefit.
C

Transplant boundary

benefit must fit the patient
  • Limits Different questions and populations. No immediate liver/kidney-transplant protection estimate or randomized STICHES–REVIVED comparison.
Dialysis CABG–PCI evidence is observational, with conflicting survival signals.
A

Compare early harm and later outcomes

treatment selection remains

USRDS · Chang 2012

  • Population 21,981 dialysis patients, multivessel CABG versus PCI, 1997–2009.
  • Death CABG HR 0.87 (95% CI 0.84–0.90).
  • Death/MI HR 0.88 (95% CI 0.86–0.91).
  • Limit Administrative data, older PCI era, selection/residual confounding.

Taiwan · Pan 2024

  • Population 1,840 propensity-matched dialysis patients, 2009–2015, CABG versus DES PCI.
  • In-hospital death 12.5% vs 3.3%.
  • Overall mortality HR 1.19 (95% CI 1.05–1.35), favoring PCI, median 2.8 years.
  • Tradeoff More repeat revascularization, ACS and rehospitalization after PCI. Observational population/practice differences.
B

What these cohorts cannot establish

no prophylactic-transplant comparison
  • Confounding Anatomy, frailty, urgency and surgical selection persist despite adjustment. Transplant candidates may have different competing risk.
  • Question Neither tested routine intervention versus medical care before transplantation.
C

Individual comparison

when revascularization is indicated
  • Coronary Anatomy/completeness, diabetes, LV function, conduits, CABG recovery, PCI complexity and DAPT.
  • Transplant Nephrology constraints, expected survival with/without transplant and time away from readiness.
  • Counsel No randomized dialysis-specific CABG superiority established by these cohorts. Shorter PCI recovery alone does not settle treatment.
Two decisions
DAPT durationAbbreviated therapy retains a defined antithrombotic regimen.
Permission to operateDepends on interruption, bleeding, thrombosis and urgency.
A

2024 AHA/ACC surgical timing

planned noncardiac surgery
PCI contextTiming anchor
Balloon angioplasty without stentingDelay elective surgery ≥14 days
DES for ACSIdeally delay elective surgery ≥12 months
DES for chronic coronary diseaseA delay ≥6 months is reasonable for elective surgery
Time-sensitive surgery after DESMay be considered ≥3 months when the harm of delay exceeds cardiac risk
BMS or DES within 30 daysElective surgery requiring antiplatelet interruption is potentially harmful
  • DES rows Assume interruption of ≥1 antiplatelet agent.
  • Early time-sensitive surgery Continue DAPT within 30 days of BMS or <3 months of DES unless bleeding outweighs thrombosis protection.
  • Aspirin Continue low dose after PCI when feasible.
B

MASTER DAPT

4,579 high-bleeding-risk patients

What was tested

  • Entry Event-free first month after a specific contemporary DES.
  • Net events Per-protocol death/MI/stroke/major bleeding: 7.5% abbreviated vs 7.7% standard, noninferior.
  • Bleeding Intention-to-treat major/clinically relevant nonmajor bleeding: 6.5% vs 9.4%.

What was not tested

  • Transplant Routine liver/kidney transplantation at one month with all antiplatelets stopped. Short DAPT is not zero antiplatelet therapy.
  • Stent protection Heparin does not replace antiplatelet protection.
C

Organ-offer plan before PCI

interventional + transplant + anesthesia
No randomized trial establishes a universal CABG-to-transplant waiting interval.
A

Recovery determines readiness

clinical domains, not a validated score

Cardiac + systemic

  • Cardiac Indication/grafts, perioperative MI/stroke, rhythm, residual ischemia, ventricular function/congestion.
  • Systemic Lung/kidney recovery, anemia, infection, wound/sternum, activity, nutrition and rehabilitation.

Treatment + timing

  • Antithrombotics Aspirin, P2Y12 indication, OAC and anesthesia/bleeding plan. CABG does not erase constraints, especially after ACS.
  • Cost of delay Malignancy, limb threat, organ failure and operative urgency.
B

Mallick timing association

US readmissions data · 2016–2020
Source population
1,335,175
Elective cardiac operations. CABG, valve and combined.
Subsequent surgery
20,253
Patients undergoing subsequent noncardiac surgery.
  • Around 100 days Modeled inflection. Later surgery: major adverse events adjusted OR 0.69 (95% CI 0.62–0.76).
  • In-hospital death Adjusted OR 0.66 (95% CI 0.46–0.96).
  • Limits Administrative/observational, not CABG-only or transplant-specific. Composite includes cardiac, neurologic, respiratory, renal and other serious complications.
  • Inference No proof every patient benefits from waiting 100 days. An observational inflection is not a mandatory waiting period.
C

Conclude with conditions

operation or organ offer
A

Resolve the decision

clinical state → indication → feasibility
StabilityACS, unstable symptoms, HF/arrhythmia first. Actual activity and limitations.
Coronary significanceDated anatomy/physiology, left main, LV function and prior treatment.
Independent indicationSymptom or prognostic benefit, with expected time to benefit.
FeasibilityMedical care, PCI, CABG or selected combined options. Renal/hepatic reserve and patient priorities.
B

Consultation fields

fill with verified evidence

Treatment decision

  • Context [ ] Operation/organ, stability, dated anatomy/ischemia and LV function.
  • Treatment [ ] Independent indication or none solely to lower operative risk. Feasible medical care, limitations and chosen option.
  • Benefit/harm [ ] Applicable population/limits, time to benefit, kidneys/liver, bleeding, recovery/DAPT and transplant/surgical delay.

Liver + operative plan

  • Cirrhosis [ ] Child-Pugh points, dated MELD/version, decompensation, 30-/90-day mortality and hepatic complications, with source/limits.
  • Readiness [ ] Proceed / optimize / team pending / prohibitive. Conditions, reassessment owner/date and the evidence needed to change the decision.
  • Offer/operation [ ] Dates, antiplatelets, interruption/restart and harm of waiting.
C

Complete the wider assessment

linked workups