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Blood pressure medication and acute kidney injury after intracerebral haemorrhage: an analysis of the ATACH-II trial
BACKGROUND: Acute blood pressure (BP) reduction is standard of care after acute intracerebral haemorrhage (ICH). More acute BP reduction is associated with acute kidney injury (AKI). It is not known if the choice of antihypertensive medications affects the risk of AKI. METHODS: We analysed data from...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10387642/ https://www.ncbi.nlm.nih.gov/pubmed/37529670 http://dx.doi.org/10.1136/bmjno-2023-000458 |
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author | Naidech, Andrew M Wang, Hanyin Hutch, Meghan Murphy, Julianne Paparello, James Bath, Philip Srivastava, Anand Luo, Yuan |
author_facet | Naidech, Andrew M Wang, Hanyin Hutch, Meghan Murphy, Julianne Paparello, James Bath, Philip Srivastava, Anand Luo, Yuan |
author_sort | Naidech, Andrew M |
collection | PubMed |
description | BACKGROUND: Acute blood pressure (BP) reduction is standard of care after acute intracerebral haemorrhage (ICH). More acute BP reduction is associated with acute kidney injury (AKI). It is not known if the choice of antihypertensive medications affects the risk of AKI. METHODS: We analysed data from the ATACH-II clinical trial. AKI was defined by the Kidney Disease: Improving Global Outcomes criteria. We analysed antihypertensive medication from two sources. The first was a case report form that specified the use of labetalol, diltiazem, urapidil or other. We tested the hypothesis that the secondary medication was associated with AKI with χ(2) test. Second, we tested the hypotheses the dosage of diltiazem was associated with AKI using Mann-Whitney U test. RESULTS: AKI occurred in 109 of 1000 patients (10.9%). A higher proportion of patients with AKI received diltiazem after nicardipine (12 (29%) vs 21 (12%), p=0.03). The 95%ile (90%–99% ile) of administered diltiazem was 18 (0–130) mg in patients with AKI vs 0 (0–30) mg in patients without AKI (p=0.002). There was no apparent confounding by indication for diltiazem use. CONCLUSIONS: The use of diltiazem, and more diltiazem, was associated with AKI in patients with acute ICH. |
format | Online Article Text |
id | pubmed-10387642 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-103876422023-08-01 Blood pressure medication and acute kidney injury after intracerebral haemorrhage: an analysis of the ATACH-II trial Naidech, Andrew M Wang, Hanyin Hutch, Meghan Murphy, Julianne Paparello, James Bath, Philip Srivastava, Anand Luo, Yuan BMJ Neurol Open Original Research BACKGROUND: Acute blood pressure (BP) reduction is standard of care after acute intracerebral haemorrhage (ICH). More acute BP reduction is associated with acute kidney injury (AKI). It is not known if the choice of antihypertensive medications affects the risk of AKI. METHODS: We analysed data from the ATACH-II clinical trial. AKI was defined by the Kidney Disease: Improving Global Outcomes criteria. We analysed antihypertensive medication from two sources. The first was a case report form that specified the use of labetalol, diltiazem, urapidil or other. We tested the hypothesis that the secondary medication was associated with AKI with χ(2) test. Second, we tested the hypotheses the dosage of diltiazem was associated with AKI using Mann-Whitney U test. RESULTS: AKI occurred in 109 of 1000 patients (10.9%). A higher proportion of patients with AKI received diltiazem after nicardipine (12 (29%) vs 21 (12%), p=0.03). The 95%ile (90%–99% ile) of administered diltiazem was 18 (0–130) mg in patients with AKI vs 0 (0–30) mg in patients without AKI (p=0.002). There was no apparent confounding by indication for diltiazem use. CONCLUSIONS: The use of diltiazem, and more diltiazem, was associated with AKI in patients with acute ICH. BMJ Publishing Group 2023-07-28 /pmc/articles/PMC10387642/ /pubmed/37529670 http://dx.doi.org/10.1136/bmjno-2023-000458 Text en © Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) 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, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Original Research Naidech, Andrew M Wang, Hanyin Hutch, Meghan Murphy, Julianne Paparello, James Bath, Philip Srivastava, Anand Luo, Yuan Blood pressure medication and acute kidney injury after intracerebral haemorrhage: an analysis of the ATACH-II trial |
title | Blood pressure medication and acute kidney injury after intracerebral haemorrhage: an analysis of the ATACH-II trial |
title_full | Blood pressure medication and acute kidney injury after intracerebral haemorrhage: an analysis of the ATACH-II trial |
title_fullStr | Blood pressure medication and acute kidney injury after intracerebral haemorrhage: an analysis of the ATACH-II trial |
title_full_unstemmed | Blood pressure medication and acute kidney injury after intracerebral haemorrhage: an analysis of the ATACH-II trial |
title_short | Blood pressure medication and acute kidney injury after intracerebral haemorrhage: an analysis of the ATACH-II trial |
title_sort | blood pressure medication and acute kidney injury after intracerebral haemorrhage: an analysis of the atach-ii trial |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10387642/ https://www.ncbi.nlm.nih.gov/pubmed/37529670 http://dx.doi.org/10.1136/bmjno-2023-000458 |
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