Comparison of hyperemic efficacy between central and peripheral venous adenosine infusion for fractional flow reserve measurement

Circ Cardiovasc Interv. 2012 Jun;5(3):401-5. doi: 10.1161/CIRCINTERVENTIONS.111.965392. Epub 2012 May 29.

Abstract

Background: Maximal hyperemia is a prerequisite for the accurate measurement of fractional flow reserve (FFR). Although continuous infusion of adenosine via the femoral vein is considered to be the gold standard, this requires an additional invasive procedure for femoral vein access and is difficult to use during transradial coronary catheterization. We performed this prospective study to evaluate the feasibility and efficacy of peripheral intravenous infusion of adenosine for FFR measurement.

Methods and results: Seventy-one patients were prospectively enrolled, and FFR was measured using a 0.014-inch coronary pressure wire. Hyperemic efficacy of adenosine was compared among intracoronary bolus injection and continuous IV infusion (140 μg/min/kg) via the femoral and via the forearm vein. In 20 patients, hyperemic mean transit time and index of microcirculatory resistance were also measured. Mean FFR after bolus administration of adenosine was 0.81±0.10. As compared with femoral vein infusion (FFR: 0.80±0.10), hyperemic efficacy of forearm vein infusion of adenosine (FFR: 0.80±0.11) was not inferior (P for noninferiority=0.01). The number of functionally significant stenoses (FFR <0.75) was also not different between the 2 methods (femoral vein versus forearm vein; 17 (25.0%) versus 17 (25.0%), P=1.0). Both hyperemic mean transit time and index of microcirculatory resistance were not different between the 2 routes of adenosine infusion. Additional bolus injection of adenosine during IV infusion did not improve the hyperemic efficacy but increased the risk of atrioventricular block.

Conclusions: This study suggests that continuous intravenous infusion of adenosine via the forearm vein is a convenient and effective way to induce steady-state hyperemia for invasive physiological measurements.

Clinical trial registration: URL: http://www.clinicaltrials.gov. Unique identifier: NCT01070420.

Publication types

  • Comparative Study
  • Evaluation Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine / administration & dosage*
  • Adenosine / adverse effects
  • Aged
  • Analysis of Variance
  • Coronary Angiography
  • Coronary Stenosis / diagnosis*
  • Coronary Stenosis / diagnostic imaging
  • Coronary Stenosis / physiopathology
  • Feasibility Studies
  • Female
  • Femoral Vein
  • Forearm / blood supply
  • Fractional Flow Reserve, Myocardial*
  • Humans
  • Hyperemia / physiopathology*
  • Infusions, Intravenous
  • Injections, Intra-Arterial
  • Linear Models
  • Male
  • Microcirculation
  • Middle Aged
  • Predictive Value of Tests
  • Prospective Studies
  • Republic of Korea
  • Severity of Illness Index
  • Vascular Resistance
  • Vasodilator Agents / administration & dosage*
  • Vasodilator Agents / adverse effects

Substances

  • Vasodilator Agents
  • Adenosine

Associated data

  • ClinicalTrials.gov/NCT01070420