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Comparing methods of adenosine administration in paroxysmal supraventricular tachycardia: a pilot randomized controlled trial
BACKGROUND: Intravenous adenosine is the recommended treatment for paroxysmal supraventricular tachycardia (PSVT). There is no official recommended method of giving adenosine. We compared the success rates between a standard and alternative method of first dose intravenous adenosine in PSVT. METHODS...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8790832/ https://www.ncbi.nlm.nih.gov/pubmed/35081915 http://dx.doi.org/10.1186/s12872-022-02464-5 |
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author | Daengbubpha, Phruek Wittayachamnankul, Borwon Sutham, Krongkarn Chenthanakij, Boriboon Tangsuwanaruk, Theerapon |
author_facet | Daengbubpha, Phruek Wittayachamnankul, Borwon Sutham, Krongkarn Chenthanakij, Boriboon Tangsuwanaruk, Theerapon |
author_sort | Daengbubpha, Phruek |
collection | PubMed |
description | BACKGROUND: Intravenous adenosine is the recommended treatment for paroxysmal supraventricular tachycardia (PSVT). There is no official recommended method of giving adenosine. We compared the success rates between a standard and alternative method of first dose intravenous adenosine in PSVT. METHODS: A pilot parallel randomized controlled study was conducted in the emergency department of a tertiary care hospital. Eligible patients were stable PSVT adult patients. We used block randomization and divided them into two groups, the standard method (double syringe technique of 6 mg of adenosine), and the alternative method (similar to the standard method, then immediately followed by elevating the arm to 90° perpendicular to a horizontal plane for 10 s). The primary outcome was the success rate of electrocardiogram (ECG) response which demonstrated termination of PSVT (at least two-fold of the RR-interval widening or sinus rhythm conversion). Secondary outcomes were complications within one minute after the injection. RESULTS: We allocated 15 patients in each group and analyzed them as intention-to-treat. The success rate was 86.7% in the alternative group and 80% in the standard group (risk difference 6.7%, 95% confidence interval − 19.9 to 33.2%, P 1.00). Complications within one minute after adenosine injection were also similar in both groups, 14 of 15 patients (93%) in each group had no complications, without significant difference. CONCLUSIONS: No evidence of the difference between alternative and standard methods occurred, in terms of the success rate of ECG response and complications within one minute after adenosine injection. The standard method of adenosine injection is a safe, easy-to-administer, and widely available treatment for PSVT. Trial Registration: TCTR20200609001. |
format | Online Article Text |
id | pubmed-8790832 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-87908322022-01-26 Comparing methods of adenosine administration in paroxysmal supraventricular tachycardia: a pilot randomized controlled trial Daengbubpha, Phruek Wittayachamnankul, Borwon Sutham, Krongkarn Chenthanakij, Boriboon Tangsuwanaruk, Theerapon BMC Cardiovasc Disord Research BACKGROUND: Intravenous adenosine is the recommended treatment for paroxysmal supraventricular tachycardia (PSVT). There is no official recommended method of giving adenosine. We compared the success rates between a standard and alternative method of first dose intravenous adenosine in PSVT. METHODS: A pilot parallel randomized controlled study was conducted in the emergency department of a tertiary care hospital. Eligible patients were stable PSVT adult patients. We used block randomization and divided them into two groups, the standard method (double syringe technique of 6 mg of adenosine), and the alternative method (similar to the standard method, then immediately followed by elevating the arm to 90° perpendicular to a horizontal plane for 10 s). The primary outcome was the success rate of electrocardiogram (ECG) response which demonstrated termination of PSVT (at least two-fold of the RR-interval widening or sinus rhythm conversion). Secondary outcomes were complications within one minute after the injection. RESULTS: We allocated 15 patients in each group and analyzed them as intention-to-treat. The success rate was 86.7% in the alternative group and 80% in the standard group (risk difference 6.7%, 95% confidence interval − 19.9 to 33.2%, P 1.00). Complications within one minute after adenosine injection were also similar in both groups, 14 of 15 patients (93%) in each group had no complications, without significant difference. CONCLUSIONS: No evidence of the difference between alternative and standard methods occurred, in terms of the success rate of ECG response and complications within one minute after adenosine injection. The standard method of adenosine injection is a safe, easy-to-administer, and widely available treatment for PSVT. Trial Registration: TCTR20200609001. BioMed Central 2022-01-26 /pmc/articles/PMC8790832/ /pubmed/35081915 http://dx.doi.org/10.1186/s12872-022-02464-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Daengbubpha, Phruek Wittayachamnankul, Borwon Sutham, Krongkarn Chenthanakij, Boriboon Tangsuwanaruk, Theerapon Comparing methods of adenosine administration in paroxysmal supraventricular tachycardia: a pilot randomized controlled trial |
title | Comparing methods of adenosine administration in paroxysmal supraventricular tachycardia: a pilot randomized controlled trial |
title_full | Comparing methods of adenosine administration in paroxysmal supraventricular tachycardia: a pilot randomized controlled trial |
title_fullStr | Comparing methods of adenosine administration in paroxysmal supraventricular tachycardia: a pilot randomized controlled trial |
title_full_unstemmed | Comparing methods of adenosine administration in paroxysmal supraventricular tachycardia: a pilot randomized controlled trial |
title_short | Comparing methods of adenosine administration in paroxysmal supraventricular tachycardia: a pilot randomized controlled trial |
title_sort | comparing methods of adenosine administration in paroxysmal supraventricular tachycardia: a pilot randomized controlled trial |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8790832/ https://www.ncbi.nlm.nih.gov/pubmed/35081915 http://dx.doi.org/10.1186/s12872-022-02464-5 |
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