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Voriconazole therapeutic drug monitoring and hepatotoxicity in critically ill patients: a national multicenter retrospective study

Voriconazole therapeutic drug monitoring and hepatotoxicity in critically ill patients: a national multicenter retrospective study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000039332
Enrollment
Unknown
Registered
2020-10-23
Start date
2020-10-22
Completion date
Unknown
Last updated
2021-01-25

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

Conditions

critically ill patients

Interventions

TDM group:Nil

Sponsors

The First Affiliated Hospital of Xi'an Jiaotong University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Patients were admitted to the ICU, and aged >= 18 years; (2) Patients were diagnosed with a proven, probable, and possible invasive fungal disease, or with high risk factors for fungal infection; (3) Using voriconazole for >= 7 d; (4) Monitoring voriconazole blood concentration at least once at a steady state (3 days after administration); (5) During voriconazole treatment, liver function tests should be performed at least once weekly.

Exclusion criteria

Exclusion criteria: (1) Pregnant women and patients are allergic to voriconazole; (2) Voriconazole blood concentration is lower than the lower limit of detection; (3) The time of administration of Medication is uncertain and laboratory test results are unavailable; (4) According to CTCAE standards, patients with liver dysfunction is greater than grade 3 or above when admitted to ICU; (5) Patients with severe liver diseases such as viral hepatitis, cirrhosis, drug-induced liver damage, liver cancer when admitted to ICU.

Design outcomes

Primary

MeasureTime frame
voriconazole plasma concentration;hepatotoxicity;

Countries

China

Contacts

Public ContactDong Yalin

The First Affiliated Hospital of Xi'an Jiaotong University

dongyalin@mail.xjtu.edu.cn+86 29-85323241

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026