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Responsiveness to Vasoconstrictor Therapy in Hepatorenal Syndrome Type 1

KEY POINTS: Raising the mean arterial pressure (MAP) during management of hepatorenal syndrome type 1 (HRS-1) is associated with improvement in kidney function, independently of baseline MAP or model for end-stage liver disease. Raising the MAP by 15 mm Hg or greater leads to greater reduction in se...

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Autores principales: Velez, Juan Carlos Q., Karakala, Nithin, Tayebi, Kasra, Wickman, Terrance J., Mohamed, Muner M. B., Kovacic, Rosemary A., Therapondos, George, Kanduri, Swetha R., Allegretti, Andrew S., Belcher, Justin M., Regner, Kevin R., Wentowski, Cathy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Nephrology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10278824/
https://www.ncbi.nlm.nih.gov/pubmed/36763632
http://dx.doi.org/10.34067/KID.0000000000000068
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author Velez, Juan Carlos Q.
Karakala, Nithin
Tayebi, Kasra
Wickman, Terrance J.
Mohamed, Muner M. B.
Kovacic, Rosemary A.
Therapondos, George
Kanduri, Swetha R.
Allegretti, Andrew S.
Belcher, Justin M.
Regner, Kevin R.
Wentowski, Cathy
author_facet Velez, Juan Carlos Q.
Karakala, Nithin
Tayebi, Kasra
Wickman, Terrance J.
Mohamed, Muner M. B.
Kovacic, Rosemary A.
Therapondos, George
Kanduri, Swetha R.
Allegretti, Andrew S.
Belcher, Justin M.
Regner, Kevin R.
Wentowski, Cathy
author_sort Velez, Juan Carlos Q.
collection PubMed
description KEY POINTS: Raising the mean arterial pressure (MAP) during management of hepatorenal syndrome type 1 (HRS-1) is associated with improvement in kidney function, independently of baseline MAP or model for end-stage liver disease. Raising the MAP by 15 mm Hg or greater leads to greater reduction in serum creatinine in HRS-1. Norepinephrine use confers greater probability of improvement in kidney function in HRS-1 compared with midodrine/octreotide. BACKGROUND: Raising mean arterial pressure (MAP) during treatment of hepatorenal syndrome type 1 (HRS-1) with vasoconstrictors (VCs) is associated with renal recovery. However, the optimal MAP target and factors associated with response to VCs remain unclear. METHODS: Records from hospitalized patients with HRS-1 treated with VCs without shock were reviewed searching for those who achieved ≥5 mm Hg rise in MAP within 48 hours. We examined the relationship between the mean MAP achieved during the first 48–72 hours of VC therapy and the change in serum creatinine (sCr) up to day 14. Endpoints were >30% reduction in sCr without need for dialysis or death by day 14 (primary) or by day 30 (secondary). RESULTS: Seventy-seven patients with HRS-1 treated for 2–10 days with either norepinephrine (n=49) or midodrine/octreotide (n=28) were included. The median age was 52 years (interquartile range [IQR], 46–60), 40% were female, and 48% had alcoholic cirrhosis. At VC initiation, median MAP was 70 mm Hg (IQR, 66–73), and median sCr was 3.8 mg/dl (IQR, 2.6–4.9). When analyzed by tertiles of mean MAP increment (5–9, 10–14, ≥15 mm Hg), there was greater reduction in sCr with greater rise in MAP (ANOVA for trend, P < 0.0001). By multivariate logistic regression analysis, mean MAP rise during the first 48–72 hours (odds ratio [OR], 1.15 [1.02 to 1.299], P=0.025), norepinephrine as VC (OR, 5.46 [1.36 to 21.86], P=0.017), and baseline sCr [OR, 0.63 [0.41 to 0.97], P=0.034) were associated with the primary endpoint, whereas mean MAP rise during the first 48–72 hours (OR, 1.17 [1.04 to 1.33], P=0.012) and baseline sCr (OR, 0.63 [0.39 to 0.98], P=0.043) were associated with the secondary endpoint. CONCLUSIONS: Greater magnitude of rise in MAP with VC therapy in HRS-1, lower baseline sCr, and use of norepinephrine over midodrine/octreotide are associated with kidney recovery. Targeting an increment of MAP ≥15 mm Hg may lead to favorable renal outcomes.
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spelling pubmed-102788242023-08-03 Responsiveness to Vasoconstrictor Therapy in Hepatorenal Syndrome Type 1 Velez, Juan Carlos Q. Karakala, Nithin Tayebi, Kasra Wickman, Terrance J. Mohamed, Muner M. B. Kovacic, Rosemary A. Therapondos, George Kanduri, Swetha R. Allegretti, Andrew S. Belcher, Justin M. Regner, Kevin R. Wentowski, Cathy Kidney360 Original Investigation KEY POINTS: Raising the mean arterial pressure (MAP) during management of hepatorenal syndrome type 1 (HRS-1) is associated with improvement in kidney function, independently of baseline MAP or model for end-stage liver disease. Raising the MAP by 15 mm Hg or greater leads to greater reduction in serum creatinine in HRS-1. Norepinephrine use confers greater probability of improvement in kidney function in HRS-1 compared with midodrine/octreotide. BACKGROUND: Raising mean arterial pressure (MAP) during treatment of hepatorenal syndrome type 1 (HRS-1) with vasoconstrictors (VCs) is associated with renal recovery. However, the optimal MAP target and factors associated with response to VCs remain unclear. METHODS: Records from hospitalized patients with HRS-1 treated with VCs without shock were reviewed searching for those who achieved ≥5 mm Hg rise in MAP within 48 hours. We examined the relationship between the mean MAP achieved during the first 48–72 hours of VC therapy and the change in serum creatinine (sCr) up to day 14. Endpoints were >30% reduction in sCr without need for dialysis or death by day 14 (primary) or by day 30 (secondary). RESULTS: Seventy-seven patients with HRS-1 treated for 2–10 days with either norepinephrine (n=49) or midodrine/octreotide (n=28) were included. The median age was 52 years (interquartile range [IQR], 46–60), 40% were female, and 48% had alcoholic cirrhosis. At VC initiation, median MAP was 70 mm Hg (IQR, 66–73), and median sCr was 3.8 mg/dl (IQR, 2.6–4.9). When analyzed by tertiles of mean MAP increment (5–9, 10–14, ≥15 mm Hg), there was greater reduction in sCr with greater rise in MAP (ANOVA for trend, P < 0.0001). By multivariate logistic regression analysis, mean MAP rise during the first 48–72 hours (odds ratio [OR], 1.15 [1.02 to 1.299], P=0.025), norepinephrine as VC (OR, 5.46 [1.36 to 21.86], P=0.017), and baseline sCr [OR, 0.63 [0.41 to 0.97], P=0.034) were associated with the primary endpoint, whereas mean MAP rise during the first 48–72 hours (OR, 1.17 [1.04 to 1.33], P=0.012) and baseline sCr (OR, 0.63 [0.39 to 0.98], P=0.043) were associated with the secondary endpoint. CONCLUSIONS: Greater magnitude of rise in MAP with VC therapy in HRS-1, lower baseline sCr, and use of norepinephrine over midodrine/octreotide are associated with kidney recovery. Targeting an increment of MAP ≥15 mm Hg may lead to favorable renal outcomes. American Society of Nephrology 2023-02-10 /pmc/articles/PMC10278824/ /pubmed/36763632 http://dx.doi.org/10.34067/KID.0000000000000068 Text en Copyright © 2023 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Society of Nephrology https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Investigation
Velez, Juan Carlos Q.
Karakala, Nithin
Tayebi, Kasra
Wickman, Terrance J.
Mohamed, Muner M. B.
Kovacic, Rosemary A.
Therapondos, George
Kanduri, Swetha R.
Allegretti, Andrew S.
Belcher, Justin M.
Regner, Kevin R.
Wentowski, Cathy
Responsiveness to Vasoconstrictor Therapy in Hepatorenal Syndrome Type 1
title Responsiveness to Vasoconstrictor Therapy in Hepatorenal Syndrome Type 1
title_full Responsiveness to Vasoconstrictor Therapy in Hepatorenal Syndrome Type 1
title_fullStr Responsiveness to Vasoconstrictor Therapy in Hepatorenal Syndrome Type 1
title_full_unstemmed Responsiveness to Vasoconstrictor Therapy in Hepatorenal Syndrome Type 1
title_short Responsiveness to Vasoconstrictor Therapy in Hepatorenal Syndrome Type 1
title_sort responsiveness to vasoconstrictor therapy in hepatorenal syndrome type 1
topic Original Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10278824/
https://www.ncbi.nlm.nih.gov/pubmed/36763632
http://dx.doi.org/10.34067/KID.0000000000000068
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