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Published on: January 31, 2018
Standardization of prophylactic platelet transfusion dosing in a pediatric oncology population: a quality improvement
Michael Leibowitz1,2, Heather Wolfe1,3, Andrea Flynn1,2
1Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Insights
Standardizing prophylactic platelet transfusion dosing in oncology patients to lower volumes was safe and effective. This initiative reduced transfusions without increasing bleeding events, improving care consistency.
Area of Science:
- Hematology
- Oncology
- Transfusion Medicine
Background:
- Oncology patients often receive prophylactic platelet transfusions.
- Recent evidence suggests lower prophylactic platelet doses are safe.
- Variability in platelet dosing was observed due to lack of standardized guidelines.
Purpose of the Study:
- To establish and implement standardized dosing guidelines for prophylactic platelet transfusions in nonbleeding oncology patients.
- To improve consistency and safety in platelet transfusion practices within an academic hospital setting.
Main Methods:
- A collaborative project developed dosing guidelines: ≤10 mL/kg for patients ≤20 kg, 1 unit for patients >20 kg.
- Implemented a data display tool for monitoring compliance and electronic medical record decision support.
- Conducted educational initiatives for oncology prescribers over multiple plan-do-study-act cycles.
Main Results:
- Achieved 85-90% compliance with standardized prophylactic platelet transfusion dosing guidelines.
- No increase in emergency department visits for bleeding or platelet transfusions was observed.
- The time between platelet transfusions remained unchanged post-implementation.
Conclusions:
- Reducing prophylactic platelet transfusion volumes to align with published studies is safe.
- Guideline consensus, decision support, and education effectively standardized transfusion practices.
- The project demonstrated successful practice change in a large academic hospital.
Background:
Oncology patients are frequent recipients of prophylactic platelet transfusions. Recent studies have demonstrated that lower prophylactic doses of platelets were not associated with a higher incidence of bleeding. At our institution, we found wide variation in platelet dosing due to lack of guidance and support for standardized dosing.
Study Design And Methods:
A collaborative process improvement project between oncology, hematology, intensivists, and the transfusion service established guidelines for dosing of prophylactic platelet transfusions in nonbleeding oncology patients: 10 mL/kg or less of apheresis platelets for patients weighing up to 20 kg and 1 unit of apheresis platelets patients weighing 20 kg or more, with our stated goal of standardizing transfusion practice. A graphic data display tool that draws on the electronic medical record to monitor platelet ordering was created, with a target goal of greater than 80% compliance with the dosing guidelines. We implemented decision support for dosing consistent with the guideline, and provided educational materials to prescribers at various levels of training within oncology over multiple plan-do-study-act cycles.
Results:
We were able to consistently achieve between 85 and 90% compliance of prophylactic platelet transfusion orders without an increase in the number of emergency department visits for bleeding or platelet transfusions or changing the time between platelet transfusions after guideline implementation.
Conclusion:
This project demonstrates that reducing the volume of prophylactic platelet transfusions to doses consistent with published studies was safe and that a process of guideline consensus based on published studies, well-designed decision support for computerized physician order entry, and targeted educational efforts, were effective in changing practice at a large academic hospital.
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