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Patient-Reported Health Status and Clinical Outcomes After CTO-PCI Versus Optimal Medical Therapy: A 12-Month
Velina Doktorova1,2, Georgi Goranov1,2, Petar Nikolov1,2
1First Department of Internal Diseases, Section of Cardiology, Medical University of Plovdiv, 4000 Plovdiv, Bulgaria.
Insights
Percutaneous coronary intervention for chronic total occlusion (CTO-PCI) plus optimal medical therapy (OMT) significantly improved patient-reported angina frequency compared to OMT alone. CTO-PCI also reduced 12-month cardiovascular rehospitalization rates in selected patients with chronic coronary syndrome.
Area of Science:
- Cardiology
- Interventional Cardiology
- Patient-Reported Outcomes
Background:
- Chronic total coronary occlusion (CTO) significantly impacts quality of life due to angina and functional limitations.
- Optimal medical therapy (OMT) is standard, but CTO percutaneous coronary intervention (CTO-PCI) offers a potential adjunctive treatment.
- Assessing CTO-PCI's clinical value requires evaluating patient-reported outcomes (PROs) and patient-centered endpoints.
Purpose of the Study:
- To evaluate the association between CTO-PCI plus OMT and 12-month patient-reported and clinical outcomes compared to OMT alone.
- To assess the impact of CTO-PCI on Seattle Angina Questionnaire (SAQ) Angina Frequency as a primary PRO.
- To compare cardiovascular rehospitalization and survival rates between the two treatment strategies.
Main Methods:
- A single-center, non-randomized retrospective observational cohort study of 251 patients with chronic coronary syndrome and CTO.
- Patients were assigned to either CTO-PCI + OMT (n=153) or OMT alone (n=98).
- Propensity-score overlap weighting was used for sensitivity analysis to address baseline imbalances and selection bias.
Main Results:
- CTO-PCI + OMT was associated with a significantly greater improvement in SAQ Angina Frequency compared to OMT alone (β = 7.07 points; p < 0.001).
- Cardiovascular rehospitalization occurred in 7.2% of the CTO-PCI + OMT group versus 19.4% in the OMT group (OR = 0.32; p = 0.005).
- Survival rates were similar between groups (92.0% vs. 87.4%), but the study was underpowered for mortality analysis.
Conclusions:
- In selected patients with chronic coronary syndrome and CTO, CTO-PCI + OMT improves disease-specific health status, particularly angina frequency.
- CTO-PCI + OMT demonstrated a reduction in 12-month cardiovascular rehospitalizations, though this finding requires cautious interpretation due to study design limitations.
- CTO-PCI should be considered a patient-centered option for carefully selected symptomatic CTO patients, acknowledging potential residual confounding.
Abstract:
Background/Objectives: Chronic total coronary occlusion (CTO) is frequently associated with persistent angina, functional limitation, and impaired health-related quality of life. Although CTO percutaneous coronary intervention (CTO-PCI) has improved technically, its clinical value is best assessed through patient-reported outcomes (PROs) and patient-centered clinical endpoints. This study evaluated the association between CTO-PCI plus optimal medical therapy (OMT) and 12-month patient-reported and clinical outcomes compared with OMT alone. Methods: This single-center, non-randomized retrospective observational cohort analysis included 251 patients with chronic coronary syndrome and angiographically confirmed CTO. Patients were managed with either a CTO-PCI + OMT strategy (n = 153) or OMT alone (n = 98). The analysis used routinely collected clinical, angiographic, echocardiographic, procedural, and follow-up data, complemented by patient-reported Seattle Angina Questionnaire (SAQ) data obtained after written informed consent. The overall SAQ assessment was considered the primary patient-reported framework, and SAQ Angina Frequency was defined as the principal symptom-specific domain for adjusted comparative analysis. Propensity-score overlap weighting was used as a sensitivity analysis to address measured baseline imbalance and treatment-selection bias. Secondary outcomes included Canadian Cardiovascular Society angina class, left ventricular ejection fraction, cumulative 12-month cardiovascular rehospitalization, and survival. Results: The complete-case SAQ population included 217 patients: 136 in the CTO-PCI + OMT group and 81 in the OMT group. Thirty-four patients lacked complete 12-month SAQ data: 24 died before SAQ reassessment, and 10 were lost to SAQ follow-up. SAQ Angina Frequency improved in both groups, from 70.81 ± 17.97 to 92.35 ± 12.37 in the CTO-PCI + OMT group and from 63.09 ± 20.10 to 83.09 ± 15.14 in the OMT group. In the multivariable ANCOVA model, CTO-PCI + OMT was associated with higher 12-month SAQ Angina Frequency compared with OMT alone (β = 7.07 points; 95% CI, 3.36-10.79; p < 0.001). This finding remained consistent in the propensity-score overlap-weighted sensitivity analysis adjusted for baseline SAQ Angina Frequency (β = 6.55 points; 95% CI, 2.39-10.70; p = 0.002). Cardiovascular rehospitalization was observed in 11 of 153 patients (7.2%) in the CTO-PCI + OMT group and in 19 of 98 patients (19.4%) in the OMT group, corresponding to lower odds of cumulative 12-month rehospitalization (OR = 0.32; 95% CI, 0.15-0.71; p = 0.005). The rehospitalization endpoint was analyzed as a cumulative binary outcome rather than as a time-to-event outcome. Overall survival estimates were 92.0% and 87.4%, respectively, with 12 deaths in each group (log-rank p = 0.225). Because only 24 deaths were recorded, the study was underpowered to evaluate mortality differences. Conclusions: In selected patients with chronic coronary syndrome and CTO, CTO-PCI + OMT was associated with greater improvement in disease-specific health status, particularly SAQ Angina Frequency, compared with OMT alone. CTO-PCI + OMT was also associated with lower cumulative 12-month cardiovascular rehospitalization, although this secondary finding should be interpreted cautiously because of the non-randomized retrospective design, modest event numbers, lack of time-to-event rehospitalization data, and potential expectation- and care-related biases. Survival analyses were underpowered and should not be interpreted as evidence of either prognostic benefit or absence of benefit. These findings support consideration of CTO-PCI as a patient-centered therapeutic option in carefully selected symptomatic patients, while acknowledging residual confounding by indication and the open-label study design.
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