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Comparing outcomes of clonidine and captopril in patients with hypertensive urgency: A randomized clinical trial
BACKGROUND: Hypertension (HTN) is the second leading risk factor for death and disability. One fourth of healthcare in Eastern Europe and Central Asia is being spent on blood pressure (BP)-related diseases. An important situation in patients with high BP is hypertensive crisis (BP > 180/120 mmHg)...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Isfahan Cardiovascular Research Center, Isfahan University of Medical Sciences
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9931607/ https://www.ncbi.nlm.nih.gov/pubmed/36818154 http://dx.doi.org/10.48305/arya.v18i1.2146 |
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author | Mirdamadi, Ahmad Abrishamkar, Rana Kargaran, Afrooz |
author_facet | Mirdamadi, Ahmad Abrishamkar, Rana Kargaran, Afrooz |
author_sort | Mirdamadi, Ahmad |
collection | PubMed |
description | BACKGROUND: Hypertension (HTN) is the second leading risk factor for death and disability. One fourth of healthcare in Eastern Europe and Central Asia is being spent on blood pressure (BP)-related diseases. An important situation in patients with high BP is hypertensive crisis (BP > 180/120 mmHg), which is divided to hypertensive emergency and urgency. Therefore, here, we decided to compare the effect of captopril and clonidine in patients with hypertensive urgencies, and their side effects. METHODS: This was a parallel-group randomized clinical trial. Patients, who referred to emergency ward with any symptoms of hypertensive crisis, underwent a careful history taking and clinical examination. Individuals with systolic BP (SBP) ≥ 180 mmHg or diastolic BP (DBP) ≥ 110 mmHg with no evidence of end organ damage were randomly assigned into two interventions, clonidine and captopril. 25% decrease in BP was considered as ideal relief. RESULTS: Regarding the duration of response to treatment drugs, patients who received clonidine relieved significantly faster than those who received captopril (P = 0.016). Moreover, the frequencies of side effects such as headache, dizziness/vertigo, dry mouth, and drowsiness in the clonidine group were significantly lower than captopril group (P < 0.05). CONCLUSION: Patients in clonidine group relieved sooner and experienced fewer side effects. Therefore, this study suggests clonidine as a more effective therapeutic for hypertensive urgency compared with captopril. |
format | Online Article Text |
id | pubmed-9931607 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Isfahan Cardiovascular Research Center, Isfahan University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-99316072023-02-17 Comparing outcomes of clonidine and captopril in patients with hypertensive urgency: A randomized clinical trial Mirdamadi, Ahmad Abrishamkar, Rana Kargaran, Afrooz ARYA Atheroscler Original Article BACKGROUND: Hypertension (HTN) is the second leading risk factor for death and disability. One fourth of healthcare in Eastern Europe and Central Asia is being spent on blood pressure (BP)-related diseases. An important situation in patients with high BP is hypertensive crisis (BP > 180/120 mmHg), which is divided to hypertensive emergency and urgency. Therefore, here, we decided to compare the effect of captopril and clonidine in patients with hypertensive urgencies, and their side effects. METHODS: This was a parallel-group randomized clinical trial. Patients, who referred to emergency ward with any symptoms of hypertensive crisis, underwent a careful history taking and clinical examination. Individuals with systolic BP (SBP) ≥ 180 mmHg or diastolic BP (DBP) ≥ 110 mmHg with no evidence of end organ damage were randomly assigned into two interventions, clonidine and captopril. 25% decrease in BP was considered as ideal relief. RESULTS: Regarding the duration of response to treatment drugs, patients who received clonidine relieved significantly faster than those who received captopril (P = 0.016). Moreover, the frequencies of side effects such as headache, dizziness/vertigo, dry mouth, and drowsiness in the clonidine group were significantly lower than captopril group (P < 0.05). CONCLUSION: Patients in clonidine group relieved sooner and experienced fewer side effects. Therefore, this study suggests clonidine as a more effective therapeutic for hypertensive urgency compared with captopril. Isfahan Cardiovascular Research Center, Isfahan University of Medical Sciences 2022-01 /pmc/articles/PMC9931607/ /pubmed/36818154 http://dx.doi.org/10.48305/arya.v18i1.2146 Text en © 2022 Isfahan Cardiovascular Research Center & Isfahan University of Medical Sciences https://creativecommons.org/licenses/by-nc/3.0/This work is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly. |
spellingShingle | Original Article Mirdamadi, Ahmad Abrishamkar, Rana Kargaran, Afrooz Comparing outcomes of clonidine and captopril in patients with hypertensive urgency: A randomized clinical trial |
title | Comparing outcomes of clonidine and captopril in patients with hypertensive urgency: A randomized clinical trial |
title_full | Comparing outcomes of clonidine and captopril in patients with hypertensive urgency: A randomized clinical trial |
title_fullStr | Comparing outcomes of clonidine and captopril in patients with hypertensive urgency: A randomized clinical trial |
title_full_unstemmed | Comparing outcomes of clonidine and captopril in patients with hypertensive urgency: A randomized clinical trial |
title_short | Comparing outcomes of clonidine and captopril in patients with hypertensive urgency: A randomized clinical trial |
title_sort | comparing outcomes of clonidine and captopril in patients with hypertensive urgency: a randomized clinical trial |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9931607/ https://www.ncbi.nlm.nih.gov/pubmed/36818154 http://dx.doi.org/10.48305/arya.v18i1.2146 |
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