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The Effect of Norepinephrine on Cardiac Output in Patients Undergoing Liver Transplant .

Cairo University (CU) logo

Cairo University (CU)

Status

Completed

Conditions

Liver Transplantation

Treatments

Drug: Noradrenaline

Study type

Interventional

Funder types

Other

Identifiers

NCT04376281
MD.241-2019

Details and patient eligibility

About

Early administration of NE in liver transplant recipient might enhance cardiac output through an increase in cardiac preload .

Full description

The derangement of circulatory blood volume in patients with liver cirrhosis makes intraoperative fluid management during liver transplant is challenging . Cirrhotic patients not only have large blood volume but abnormal blood volume distribution, with a substantial fraction of this volume in the splanchnic circulation (. These hemodynamic changes render volume loading in these patients has little impact on CO because a large proportion of infused fluid is shifted to the splanchnic system . In addition, patients with liver cirrhosis is similar to septic patients who have increased total vascular compliance which may cause pooling of blood in venous pool. Several studies in patients with sepsis found that use of low dose vasopressor may convert unstressed blood volume (i.e the amount of blood not causing pressure on the vessels) to stressed volume (i.e additional blood causing a distending pressure on the vascular walls and reflects the effective circulating volume) . However, no previous studies tested the effect of using norepinephrine (NE) on venous return and cardiac preload in patients undergoing liver transplant. An obvious advantage of this possibility is that NE will be used instead of true fluid replacement which may minimize fluid replacement during operation.

Recently, a method was described to estimate the changes in intravascular volume and vascular capacitance by calculating mean systemic filling pressure (MSFP) . MSFP is the driving pressure in venous return, and it allows calculation of the arterial and venous components of systemic vascular resistance .

Enrollment

31 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All Adults (age > 18 years) patients undergoing living donor liver transplant (LDLT) will be considered for inclusion in the study..

Exclusion criteria

  • Patients less than 18 years.
  • Patients undergoing liver transplantation for acute liver failure .
  • All Chronic Hypertensive patients on medication , whether controlled on not controlled
  • Those with high risk of post transplant renal dysfunction (serum creatinine >1.5 mg/dL at time of transplant)

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

31 participants in 1 patient group

Noradrenaline group
Experimental group
Treatment:
Drug: Noradrenaline

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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