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Risk Factors and Clinical Prevention Strategies for Antimicrobial-Related Hematologic Toxicity

Risk Factors and Clinical Prevention Strategies for Antimicrobial-Related Hematologic Toxicity

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500101353
Enrollment
Unknown
Registered
2025-04-23
Start date
2022-08-08
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Infectious disease

Interventions

Group 1:None
Group 2:None

Sponsors

Beijing Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: Part 1: (1) Age> 18 years old; (2) The patients met the indications and dosage of cefoperazone/sulbactam instructions; (3) The course of treatment of cefoperazone/sulbactam >= 3 days; (4) Complete clinical data, blood and liver function biochemical examination indexes and coagulation function test data before and after cefoperazone/sulbactam treatment; (5) The coagulation function is normal and there is no bleeding symptom before medication. Part 2: (1) Age> 18 years old; (2) The course of treatment of target antimicrobial drugs (cefoperazone/sulbactam, tigecycline, vancomycin) >= 3 days; (3) The platelet count was normal and there were no bleeding symptoms before medication.

Exclusion criteria

Exclusion criteria: Part 1:(1) Patients with incomplete clinical and laboratory data; (2) Patients with comorbid hematological diseases; (3) Patients with pre - existing coagulation abnormalities before the use of cefoperazone/sulbactam; (4) Patients without coagulation function monitoring before and after treatment. Part 2:(1) Patients with comorbid hematological diseases; (2) Patients with pre - existing coagulation abnormalities before the use of target antibacterial drugs; (3) Patients without platelet count monitoring before and after treatment; (4) Patients with concomitant use of other drugs that can affect coagulation function, such as linezolid.

Design outcomes

Primary

MeasureTime frame
safety;

Countries

China

Contacts

Public ContactZHU YUANCHAO

Beijing Hospital

yczhu-2009@163.com+86 137 1810 6819

Outcome results

None listed

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