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Effects of intravenous caffeine on fractional flow reserve measurements in coronary artery disease
BACKGROUND: Intravenous adenosine is used to minimise the coronary micro-resistance to achieve maximal hyperaemia along with nitrates for optimal fractional flow reserve (FFR) measurements. We hypothesise that caffeine, being a competitive inhibitor of adenosine, would influence adenosine-mediated F...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4189297/ https://www.ncbi.nlm.nih.gov/pubmed/25332801 http://dx.doi.org/10.1136/openhrt-2014-000060 |
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author | Mutha, Vivek Asrar ul Haq, Muhammad Van Gaal, William J |
author_facet | Mutha, Vivek Asrar ul Haq, Muhammad Van Gaal, William J |
author_sort | Mutha, Vivek |
collection | PubMed |
description | BACKGROUND: Intravenous adenosine is used to minimise the coronary micro-resistance to achieve maximal hyperaemia along with nitrates for optimal fractional flow reserve (FFR) measurements. We hypothesise that caffeine, being a competitive inhibitor of adenosine, would influence adenosine-mediated FFR readings. METHODS: Consecutive patients undergoing angiogram and FFR measurements were enrolled after abstaining from caffeine for 24 h. Patients with any contraindications to intravenous adenosine or caffeine were excluded. FFR measurements were taken using nitrates and adenosine pre and post 4 mg/kg intravenous caffeine administration and results were compared. RESULTS: 10 patients were analysed (80% men, age 59.9±9.4, weight 87.5±15.6). Baseline caffeine levels were undetectable in all patients and increased significantly postintravenous caffeine administration (16.4±5.5 μg/mL). Baseline preadenosine FFR values were similar before and after caffeine administration (0.91±0.06 vs 0.91±0.07; p=0.41). Postadenosine FFR readings were 0.79±0.07, which increased non-significantly to 0.82±0.11 postcaffeine (p=0.15). Two significant FFR readings (≤0.8) changed to non-significant after caffeine administration (0.77–0.93 and 0.8–0.91). CONCLUSIONS: Caffeine may affect FFR results in some patients. Larger studies are warranted to clarify the extent and magnitude of caffeine/adenosine interaction particularly due to ubiquitous nature of caffeine and increasing importance of FFR in clinical practice. |
format | Online Article Text |
id | pubmed-4189297 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-41892972014-10-20 Effects of intravenous caffeine on fractional flow reserve measurements in coronary artery disease Mutha, Vivek Asrar ul Haq, Muhammad Van Gaal, William J Open Heart Interventional Cardiology BACKGROUND: Intravenous adenosine is used to minimise the coronary micro-resistance to achieve maximal hyperaemia along with nitrates for optimal fractional flow reserve (FFR) measurements. We hypothesise that caffeine, being a competitive inhibitor of adenosine, would influence adenosine-mediated FFR readings. METHODS: Consecutive patients undergoing angiogram and FFR measurements were enrolled after abstaining from caffeine for 24 h. Patients with any contraindications to intravenous adenosine or caffeine were excluded. FFR measurements were taken using nitrates and adenosine pre and post 4 mg/kg intravenous caffeine administration and results were compared. RESULTS: 10 patients were analysed (80% men, age 59.9±9.4, weight 87.5±15.6). Baseline caffeine levels were undetectable in all patients and increased significantly postintravenous caffeine administration (16.4±5.5 μg/mL). Baseline preadenosine FFR values were similar before and after caffeine administration (0.91±0.06 vs 0.91±0.07; p=0.41). Postadenosine FFR readings were 0.79±0.07, which increased non-significantly to 0.82±0.11 postcaffeine (p=0.15). Two significant FFR readings (≤0.8) changed to non-significant after caffeine administration (0.77–0.93 and 0.8–0.91). CONCLUSIONS: Caffeine may affect FFR results in some patients. Larger studies are warranted to clarify the extent and magnitude of caffeine/adenosine interaction particularly due to ubiquitous nature of caffeine and increasing importance of FFR in clinical practice. BMJ Publishing Group 2014-08-04 /pmc/articles/PMC4189297/ /pubmed/25332801 http://dx.doi.org/10.1136/openhrt-2014-000060 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 3.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Interventional Cardiology Mutha, Vivek Asrar ul Haq, Muhammad Van Gaal, William J Effects of intravenous caffeine on fractional flow reserve measurements in coronary artery disease |
title | Effects of intravenous caffeine on fractional flow reserve measurements in coronary artery disease |
title_full | Effects of intravenous caffeine on fractional flow reserve measurements in coronary artery disease |
title_fullStr | Effects of intravenous caffeine on fractional flow reserve measurements in coronary artery disease |
title_full_unstemmed | Effects of intravenous caffeine on fractional flow reserve measurements in coronary artery disease |
title_short | Effects of intravenous caffeine on fractional flow reserve measurements in coronary artery disease |
title_sort | effects of intravenous caffeine on fractional flow reserve measurements in coronary artery disease |
topic | Interventional Cardiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4189297/ https://www.ncbi.nlm.nih.gov/pubmed/25332801 http://dx.doi.org/10.1136/openhrt-2014-000060 |
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