Responsiveness to Vasoconstrictor Therapy in Hepatorenal Syndrome Type 1

Author:

Velez Juan Carlos Q.123ORCID,Karakala Nithin34ORCID,Tayebi Kasra2,Wickman Terrance J.1,Mohamed Muner M. B.12,Kovacic Rosemary A.1,Therapondos George5ORCID,Kanduri Swetha R.12ORCID,Allegretti Andrew S.36ORCID,Belcher Justin M.378ORCID,Regner Kevin R.39ORCID,Wentowski Cathy10

Affiliation:

1. Department of Nephrology, Ochsner Health, New Orleans, Louisiana

2. Ochsner Clinical School, The University of Queensland, Brisbane, Queensland, Australia

3. HRS-HARMONY Consortium

4. Division of Nephrology, Department of Medicine, University of Arkansas for Medical Sciences, Little Rock, Arkansas

5. Multiorgan Transplant Institute, Ochsner Health, New Orleans, Louisiana

6. Division of Nephrology, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts

7. Division of Nephrology, Department of Medicine, Yale University, New Haven, Connecticut

8. Veterans Affairs Connecticut Healthcare, West Haven, Connecticut

9. Division of Nephrology, Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin

10. Department of Pulmonary and Critical Care Medicine, Ochsner Health, New Orleans, Louisiana

Abstract

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.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Psychiatry and Mental health,Neuropsychology and Physiological Psychology

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