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The impact of platelet transfusion therapy on 28-day mortality in septic patients with thrombocytopenia during ICU stay: a multicenter retrospective observational study

The impact of platelet transfusion therapy on 28-day mortality in septic patients with thrombocytopenia during ICU stay: a multicenter retrospective observational study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500110422
Enrollment
Unknown
Registered
2025-10-14
Start date
2025-11-01
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Sepsis-Associated Thrombocytopenia

Interventions

No Platelet Transfusion Group:None
Platelet Transfusion Group:None

Sponsors

Southern Medical University Southern Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients admitted to the ICU between January 2021 and May 2024 and subsequently discharged; 2. Age >= 18 years; 3. Meeting the Sepsis-3.0 diagnostic criteria; 4. Platelet count = 48 hours;

Exclusion criteria

Exclusion criteria: 1. Active bleeding (e.g., major gastrointestinal bleeding, intracranial hemorrhage) or hematologic malignancies (e.g., leukemia, myelodysplastic syndrome, lymphoma); 2. Liver cirrhosis (Child-Pugh class B/C), chronic kidney disease (CKD stage 4-5), or autoimmune diseases (e.g., systemic lupus erythematosus); 3. Receipt of chemotherapy, immunosuppressants (e.g., cyclosporine, rituximab), or hematopoietic stem cell/solid organ transplantation within 2 weeks; 4. Pregnancy or lactation; 5. Pre-existing chronic thrombocytopenia (baseline platelet count 1 month) or long-term use of antiplatelet/anticoagulant drugs (>2 weeks); 6. Significant baseline coagulation dysfunction at ICU admission:Prothrombin time (PT) >1.5 times the upper limit of normal; Activated partial thromboplastin time (APTT) >1.5 times the upper limit of normal; Fibrinogen level 20% of key data (e.g., daily platelet counts, ICU survival status within 28 days).

Design outcomes

Primary

MeasureTime frame
ICU mortality;

Secondary

MeasureTime frame
Laboratory indicator-related endpoints;Bleeding events;Thrombotic events;ICU length of stay within 28 days;Platelet transfusion therapy-related endpoints;

Countries

China

Contacts

Public ContactZhenhua Zeng

Southern Medical University Southern Hospital

zhenhuazeng.2008@163.com+86 20 6164 1884

Outcome results

None listed

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