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Cerebral Vasospasm After Subarachnoid Hemorrhage: Respective Short-Term Effects of Induced Arterial Hypertension and its Combination With IV Milrinone: A Proof-of-Concept Study Using Transcranial Doppler Ultrasound

OBJECTIVES: It is unclear whether IV milrinone relaxes spasmed cerebral arteries and therefore reduces cerebral blood mean velocity (V(mean)). In patients treated for cerebral vasospasm, we aimed to assess and delineate the respective impacts of induced hypertension and its combination with IV milri...

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Autores principales: Lakhal, Karim, Fresco, Marion H., Hivert, Antoine, Rozec, Bertrand, Cadiet, Julien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10503695/
https://www.ncbi.nlm.nih.gov/pubmed/37720356
http://dx.doi.org/10.1097/CCE.0000000000000973
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author Lakhal, Karim
Fresco, Marion H.
Hivert, Antoine
Rozec, Bertrand
Cadiet, Julien
author_facet Lakhal, Karim
Fresco, Marion H.
Hivert, Antoine
Rozec, Bertrand
Cadiet, Julien
author_sort Lakhal, Karim
collection PubMed
description OBJECTIVES: It is unclear whether IV milrinone relaxes spasmed cerebral arteries and therefore reduces cerebral blood mean velocity (V(mean)). In patients treated for cerebral vasospasm, we aimed to assess and delineate the respective impacts of induced hypertension and its combination with IV milrinone on cerebral hemodynamics as assessed with transcranial Doppler. DESIGN: Observational proof-of-concept prospective study. SETTING: ICU in a French tertiary care center. PATIENTS: Patients with aneurysmal subarachnoid hemorrhage who received induced hypertension (mean arterial blood pressure [MBP] of 100–120 mm Hg) and IV milrinone (0.5 µg/kg/min) for moderate-to-severe cerebral vasospasm. We excluded patients who underwent invasive angioplasty or milrinone discontinuation within 12 hours after the diagnosis of vasospasm. INTERVENTIONS: None. MEASUREMENTS AND MAIN RESULTS: V(mean) was measured at vasospasm diagnosis (T(DIAGNOSIS)), after the induction of hypertension (T(HTN)), and 1 (T(HTN+MILRINONE_H1)) and 12 hours after the adjunction of IV milrinone (T(HTN+MILRINONE_H12)). Thirteen patients were included. Median V(mean) was significantly lower (p < 0.01) at T(HTN+MILRINONE_H1) (99 [interquartile range (IQR) 89; 134] cm.s(−1)) and T(HTN+MILRINONE_H12) (85 [IQR 73–127] cm/s) than at T(DIAGNOSIS) (136 [IQR 115–164] cm/s) and T(HTN) (148 [IQR 115–183] cm/s), whereas T(DIAGNOSIS) and T(HTN) did not significantly differ. In all patients but one, V(mean) at T(HTN+MILRINONE_H1) was lower than its value at T(DIAGNOSIS) (p = 0.0005). V(mean)-to-MBP and V(mean)-to-cardiac output (CO) ratios (an assessment of V(mean) regardless of the level of MBP [n = 13] or CO [n = 7], respectively) were, respectively, similar at T(DIAGNOSIS) and T(HTN) but were significantly lower after the adjunction of milrinone (p < 0.01). CONCLUSIONS: The induction of arterial hypertension was not associated with a significant decrease in V(mean), whereas the adjunction of IV milrinone was, regardless of the level of MBP or CO. This suggests that IV milrinone may succeed in relaxing spasmed arteries.
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spelling pubmed-105036952023-09-16 Cerebral Vasospasm After Subarachnoid Hemorrhage: Respective Short-Term Effects of Induced Arterial Hypertension and its Combination With IV Milrinone: A Proof-of-Concept Study Using Transcranial Doppler Ultrasound Lakhal, Karim Fresco, Marion H. Hivert, Antoine Rozec, Bertrand Cadiet, Julien Crit Care Explor Brief Report OBJECTIVES: It is unclear whether IV milrinone relaxes spasmed cerebral arteries and therefore reduces cerebral blood mean velocity (V(mean)). In patients treated for cerebral vasospasm, we aimed to assess and delineate the respective impacts of induced hypertension and its combination with IV milrinone on cerebral hemodynamics as assessed with transcranial Doppler. DESIGN: Observational proof-of-concept prospective study. SETTING: ICU in a French tertiary care center. PATIENTS: Patients with aneurysmal subarachnoid hemorrhage who received induced hypertension (mean arterial blood pressure [MBP] of 100–120 mm Hg) and IV milrinone (0.5 µg/kg/min) for moderate-to-severe cerebral vasospasm. We excluded patients who underwent invasive angioplasty or milrinone discontinuation within 12 hours after the diagnosis of vasospasm. INTERVENTIONS: None. MEASUREMENTS AND MAIN RESULTS: V(mean) was measured at vasospasm diagnosis (T(DIAGNOSIS)), after the induction of hypertension (T(HTN)), and 1 (T(HTN+MILRINONE_H1)) and 12 hours after the adjunction of IV milrinone (T(HTN+MILRINONE_H12)). Thirteen patients were included. Median V(mean) was significantly lower (p < 0.01) at T(HTN+MILRINONE_H1) (99 [interquartile range (IQR) 89; 134] cm.s(−1)) and T(HTN+MILRINONE_H12) (85 [IQR 73–127] cm/s) than at T(DIAGNOSIS) (136 [IQR 115–164] cm/s) and T(HTN) (148 [IQR 115–183] cm/s), whereas T(DIAGNOSIS) and T(HTN) did not significantly differ. In all patients but one, V(mean) at T(HTN+MILRINONE_H1) was lower than its value at T(DIAGNOSIS) (p = 0.0005). V(mean)-to-MBP and V(mean)-to-cardiac output (CO) ratios (an assessment of V(mean) regardless of the level of MBP [n = 13] or CO [n = 7], respectively) were, respectively, similar at T(DIAGNOSIS) and T(HTN) but were significantly lower after the adjunction of milrinone (p < 0.01). CONCLUSIONS: The induction of arterial hypertension was not associated with a significant decrease in V(mean), whereas the adjunction of IV milrinone was, regardless of the level of MBP or CO. This suggests that IV milrinone may succeed in relaxing spasmed arteries. Lippincott Williams & Wilkins 2023-09-14 /pmc/articles/PMC10503695/ /pubmed/37720356 http://dx.doi.org/10.1097/CCE.0000000000000973 Text en Copyright © 2023 The Authors. Published by Wolters Kluwer Health, Inc. on behalf of the Society of Critical Care Medicine. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Brief Report
Lakhal, Karim
Fresco, Marion H.
Hivert, Antoine
Rozec, Bertrand
Cadiet, Julien
Cerebral Vasospasm After Subarachnoid Hemorrhage: Respective Short-Term Effects of Induced Arterial Hypertension and its Combination With IV Milrinone: A Proof-of-Concept Study Using Transcranial Doppler Ultrasound
title Cerebral Vasospasm After Subarachnoid Hemorrhage: Respective Short-Term Effects of Induced Arterial Hypertension and its Combination With IV Milrinone: A Proof-of-Concept Study Using Transcranial Doppler Ultrasound
title_full Cerebral Vasospasm After Subarachnoid Hemorrhage: Respective Short-Term Effects of Induced Arterial Hypertension and its Combination With IV Milrinone: A Proof-of-Concept Study Using Transcranial Doppler Ultrasound
title_fullStr Cerebral Vasospasm After Subarachnoid Hemorrhage: Respective Short-Term Effects of Induced Arterial Hypertension and its Combination With IV Milrinone: A Proof-of-Concept Study Using Transcranial Doppler Ultrasound
title_full_unstemmed Cerebral Vasospasm After Subarachnoid Hemorrhage: Respective Short-Term Effects of Induced Arterial Hypertension and its Combination With IV Milrinone: A Proof-of-Concept Study Using Transcranial Doppler Ultrasound
title_short Cerebral Vasospasm After Subarachnoid Hemorrhage: Respective Short-Term Effects of Induced Arterial Hypertension and its Combination With IV Milrinone: A Proof-of-Concept Study Using Transcranial Doppler Ultrasound
title_sort cerebral vasospasm after subarachnoid hemorrhage: respective short-term effects of induced arterial hypertension and its combination with iv milrinone: a proof-of-concept study using transcranial doppler ultrasound
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10503695/
https://www.ncbi.nlm.nih.gov/pubmed/37720356
http://dx.doi.org/10.1097/CCE.0000000000000973
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