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Reduction of Cardiac Allograft Vasculopathy by PCI: Quantification and Correlation With Outcome After Heart
Madeleine Orban1, Anne Kuehl2, Louis Pechmajou3
1Department of Medicine I, University Hospital, LMU Munich, Germany; German Centre for Cardiovascular Research (DZHK), Partner Site Munich Heart Alliance, Berlin, Germany.
Insights
Risk stratification after percutaneous coronary intervention (PCI) for cardiac allograft vasculopathy (CAV) in heart transplant (HTx) patients can be improved. SYNTAX scores complement the ISHLT classification for better risk assessment and personalized invasive follow-up.
Area of Science:
- Cardiology
- Transplantation Medicine
- Interventional Cardiology
Background:
- Cardiac allograft vasculopathy (CAV) is a major complication after heart transplantation (HTx).
- Percutaneous coronary intervention (PCI) may improve outcomes in severe CAV, but risk stratification post-PCI remains challenging.
- Existing risk models for non-transplanted patients may not fully apply to HTx patients with CAV.
Purpose of the Study:
- To evaluate the prognostic value of the International Society for Heart and Lung Transplantation (ISHLT) CAV classification after PCI.
- To determine if risk-stratification models used for non-transplanted patients are applicable to HTx patients with CAV.
- To assess the utility of SYNTAX scores in risk stratification post-PCI for CAV.
Main Methods:
- A study of 203 HTx patients with CAV, divided into two cohorts: CAV1 without PCI (n=126) and CAV2/3 with PCI (n=77).
- Assessment of ISHLT CAV grades, SYNTAX Score I (SXS-I), and SYNTAX Score II (SXS-II) at baseline and post-PCI (residual rISHLT, rSXS-I, rSXS-II).
- Incomplete revascularization (IR) was defined as rSXS-I > 0.
Main Results:
- SYNTAX Score II predicted mortality in the non-PCI cohort, while both SXS-I and SXS-II predicted mortality in the PCI cohort.
- Post-PCI, incomplete revascularization, high residual ISHLT (rISHLT), and the highest tertile of residual SXS-II were associated with increased 5-year mortality.
- Residual SXS-II and incomplete revascularization were significant predictors of 5-year mortality post-PCI.
Conclusions:
- The ISHLT CAV classification is applicable for risk stratification in HTx patients undergoing PCI.
- SYNTAX scores (SXS-I and SXS-II) can complement the ISHLT classification for enhanced risk stratification.
- These scores aid in individualizing invasive follow-up strategies for HTx patients with CAV post-PCI.
Background:
Percutaneous coronary intervention (PCI) might improve outcome at severe stages of cardiac allograft vasculopathy (CAV) among patients after heart transplantation (HTx). Yet, risk stratification of HTx patients after PCI remains challenging.
Aims:
To assess whether the International Society for Heart and Lung Transplantation (ISHLT) CAV classification remains prognostic after PCI and whether risk-stratification models of non-transplanted patients extend to HTx patients with CAV.
Methods:
At 2 European academic centers, 203 patients were stratified in cohort 1 (ISHLT CAV1, without PCI, n = 126) or cohort 2 (ISHLT CAV2 and 3, with PCI). At first diagnosis of CAV or first PCI, respectively, ISHLT CAV grades, SYNTAX scores I and II (SXS-I, SXS-II) were used to quantify baseline and residual CAV (rISHLT, rSXS-I, rSXS-II). RSXS-I > 0 defined incomplete revascularization (IR).
Results:
SXS-II predicted mortality in cohort 1 (P = 0.004), whereas SXS-I (P = 0.009) and SXS-II (P = 0.002) predicted mortality in cohort 2. Post-PCI, IR (P = 0.004), high rISHLT (P = 0.02) and highest tertile of rSXS-II (P = 0.006) were associated with higher 5-year mortality. In bivariable Cox analysis, baseline SXS-II, IR and rSXS-II remained predictors of 5-year mortality post-PCI. There was a strong inverse relationship between baseline and rSXS-I (r = -0.55; P < 0.001 and r = -0.50; P = 0.003, respectively) regarding the interval to first reintervention.
Conclusion:
People with ISHLT CAV classification could apply for risk stratification after PCI. SYNTAX scores could be complemental for risk stratification and individualization of invasive follow-up of HTx patients with CAV.
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