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Biliary Atresia, Hepatic Buffer Response and Sevoflurane

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02471209
Enrollment
25
Registered
2015-06-15
Start date
2012-01-31
Completion date
2014-02-28
Last updated
2015-06-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Biliary Atresia

Brief summary

To evaluate the effects of sevoflurane on hepatic blood flow (HBF) and hepatic arterial buffer response (HABR) in infants with obstructive jaundice by Doppler ultrasound.Twenty-five infants with biliary atresia (1-3 months-of-age) scheduled for a Kasai procedure were enrolled. portal vein blood flow (PBF), hepatic arterial blood flow (HABF) and hepatic blood flow (HBF) were measured by Doppler ultrasound before induction, and after inhalation of 2 and 3% sevoflurane.

Detailed description

Children suffering from hepatobiliary disease also have an hepatic arterial buffer response (HABR) with reduced portal vein blood flow (PBF) and compensatory increases in hepatic arterial blood flow (HABF) which can help maintain hepatic blood flow (HBF). For infants with obstructive hepatobiliary disease, reduced HBF may affect drug metabolism and increase the risk of respiratory depression during analgesia, which can be life-threatening. To evaluate the effects of sevoflurane on HBF and HABR in infants with obstructive jaundice by Doppler ultrasound.Twenty-five infants with biliary atresia (1-3 months-of-age) scheduled for a Kasai procedure were enrolled. PBF, HABF and HBF were measured by Doppler ultrasound before induction, and after inhalation of 2 and 3% sevoflurane.

Interventions

DRUGSevoflurane

general anesthesia with 2% followed by 3% sevoflurane

Sponsors

Children's Hospital of Fudan University
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
1 Months to 3 Months
Healthy volunteers
No

Inclusion criteria

* persistent yellow skin or sclera, pale stool (in severe cases, clay-like), and hepatomegaly; * increased serum bilirubin (progressively or no decline after increase), increased total bilirubin (TBil) dominated by increased direct bilirubin (DBil) (\>60%); * elevated liver enzymes; * ultrasound confirmation of poor gallbladder filling and signs of liver fibrosis; * with radionuclide imaging confirmation of obstructed biliary excretion

Exclusion criteria

* concomitant cardiovascular or abdominal organ malformations

Design outcomes

Primary

MeasureTime frame
portal blood flow10 minutes
hepatic arterial blood flow10 minutes
hepatic blood flow10 minutes

Secondary

MeasureTime frameDescription
blood pressure5 minutesnoninvasive blood pressure
renal blood flow10 minutes
femoral vein blood flow10 minutes

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026