Addition of terlipressin to norepinephrine in septic shock and effect of renal perfusion: a pilot study

Ren Fail. 2022 Dec;44(1):1207-1215. doi: 10.1080/0886022X.2022.2095286.

Abstract

Purpose: Terlipressin improves renal function in patients with septic shock. However, the mechanism remains unclear. Here, we aimed to evaluate the effects of terlipressin on renal perfusion in patients with septic shock.

Materials and methods: This pilot study enrolled patients with septic shock in the intensive care unit of the tertiary hospital from September 2019 to May 2020. We randomly assigned patients to terlipressin and usual care groups using a 1:1 ratio. Terlipressin was intravenously pumped at a rate of 1.3 μg/kg/hour for 24 h. We monitored renal perfusion using renal contrast-enhanced ultrasound (CEUS). The primary outcome was peak sonographic signal intensity (a renal perfusion parameter monitored by CEUS) at 24 h after enrollment.

Results: 22 patients were enrolled in this study with 10 in the terlipressin group and 12 in the usual care group. The baseline characteristics of patients between the two groups were comparable. The peak sonographic signal intensity at 24 h after enrollment in the terlipressin group (60.5 ± 8.6 dB) was significantly higher than that in the usual care group (52.4 ± 7.0 dB; mean difference, 7.1 dB; 95% CI, 0.4-13.9; adjusted p = .04). Patients in the terlipressin group had a lower time to peak, heart rates, norepinephrine dose, and a higher stroke volume at 24 h after enrollment. No significant difference in the urine output within 24 h and incidence of acute kidney injury within 28 days was found between the two groups.

Conclusions: Terlipressin improves renal perfusion, increases stroke volume, and decreases norepinephrine dose and heart rates in patients with septic shock.

Keywords: Sepsis; acute kidney injury; renal contrast-enhanced ultrasound; renal perfusion; terlipressin.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Humans
  • Norepinephrine* / therapeutic use
  • Pilot Projects
  • Renal Circulation* / drug effects
  • Shock, Septic* / drug therapy
  • Terlipressin* / therapeutic use
  • Treatment Outcome

Substances

  • Terlipressin
  • Norepinephrine

Grants and funding

This work was supported by the [National Natural Science Foundation of China] under Grant [number 81971812 and 82102300]; [Natural Science Foundation of Jiangsu Province] under Grant [number BK20191264 and BK20200367]; and [Science Foundation of the Commission of Health of Jiangsu Province] under Grant [number ZDB2020009].