LETTERS FROM READERS
Dynamic Coronary Roadmap in Real Practice

Dynamic Coronary Roadmap en la práctica real

  • JUAN M. PÉREZ ASOREY, 1  ORCID logo 
  • JOAQUÍN PÉREZ ASOREY, 2  ORCID logo 
  • 1  Interventional Cardiologist. Chief Resident, Interventional Cardiology, Favaloro Foundation, Buenos Aires.
  • 2  Cardiologist. Fellowship en Hemodinamia y Cardiología Intervencionista, Fundación Favaloro, Ciudad de Buenos Aires
 
 

AUTHORS' REPLY

Firstly, we would like to thank Dr. Pérez Asorey for his critical reading and constructive feedback on our work, as well as for the conceptual framework he provides on the clinical relevance of contrast-induced nephropathy and the need for strategies to optimize the total volume administered during percutaneous coronary interventions (PCIs).

We agree that the absolute magnitude of the reduction in the contrast agent used must be interpreted in context. In our cohort, the group guided by Dynamic Coronary Roadmap (DCR) showed a significant reduction in total contrast volume (median 120 mL vs. 140 mL). In turn, after adjusting for clinical and procedural variables, the estimated reduction was 37.3 mL per patient (95% CI: 24.3--50.5 mL). We acknowledge that a reduction of this magnitude may seem "incremental" in individual terms; however, we believe that its potential value is expressed in the context of (i) institutional strategies for continuous improvement (reduction of redundant injections, among others) and (ii) higher-risk subgroups, where every mL counts.

We understand that a key point for interpretation is that the DCR group included a significantly higher proportion of complex PCIs (39.6% vs. 17.6%). In other words, DCR was more commonly used in more demanding scenarios, where, in actual practice, contrast consumption is substantially higher. The fact that the reduction persists (and remains after multivariable adjustment) suggests a relevant signal of the tool's operational benefit in more complex anatomies and therapeutic strategies.

Regarding the absence of differences in renal function, we share this cautious interpretation. Although CIN was defined in the protocol as an increase in creatinine within 48--72 hours, the comparison presented was based on changes in creatinine levels measured prior to discharge. Moreover, the study was not powered to detect infrequent clinical outcomes. In this context, we consider it reasonable that a single-center observational study does not show "hard" clinical changes, even with a consistent reduction in contrast media, especially when baseline contrast volumes are already relatively low.

In conclusion, we interpret DCR as a valuable complementary tool within a comprehensive low-contrast PCI strategy, and we agree on the need for future multicenter studies (ideally prospective and regional) focused on populations at higher renal risk, with standardized creatinine measurement in the 48--72 h window and assessment of renal and economic outcomes.

Sincerely yours,

Marcelo A. Abud, Facundo Villa, Ignacio L. Paganini,
Javier Cóggiola, Juan P. De Brahi
San Gerónimo Cardiovascular Institute
Endovascular Therapy Service
 
 

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