Korean J Blood Transfus.  2015 Aug;26(2):132-141. 10.17945/kjbt.2015.26.2.132.

Evaluation of Clinical Parameters and Symptoms in Healthy Donors for Granulocyte Collection

Affiliations
  • 1Department of Laboratory Medicine, Center for Diagnostic Oncology, National Cancer Center, Goyang, Korea. ksy@ncc.re.kr
  • 2Hematology-Oncology Clinic, Center for Specific Organs, National Cancer Center, Goyang, Korea.
  • 3Translational Epidemiology Branch, Hospital and Research Institute, National Cancer Center, Goyang, Korea.
  • 4Department of System Cancer Science, Graduate School of Cancer Science and Policy, National Cancer Center, Goyang, Korea.

Abstract

BACKGROUND
Donor granulocyte transfusion has been used as a salvage treatment for neutropenic patients with severe infection who did not respond to antibiotics. Here we investigated hematological parameters of granulocyte collection to evaluate its efficacy and safety.
METHODS
The clinical data for 92 procedures of granulocyte collection performed on 82 healthy donors from April 2007 to July 2014 at National Cancer Center were reviewed retrospectively. Healthy donors were pre-medicated 12 hours before apheresis with subcutaneous injection of 600 microg of granulocyte-colony stimulating factor (G-CSF) with or without 8 mg of oral dexamethasone. Blood cell counts of donors at the time of pre- and post- granulocyte collection state of donors were investigated and any clinical symptoms and signs were monitored during the procedure.
RESULTS
he median age was 29 years old (range, 18~52). The mean of collected granulocyte volume was 230 mL, and the granulocyte yield in apheresis products was 4.90x10(10) (1.46~7.86). Granulocyte yields showed significant correlation with volume of granulocyte collection, total processing volume, pre-WBC count, and pre-ANC. Granulocyte yields of dexamethasone and G-CSF administration were greater than with G-CSF administration alone. Pain (low back, hip, knee, and whole body), insomnia, fatigue, abdominal discomfort, and/or headache occurred in 21% of donors during mobilization.
CONCLUSION
Granulocyte mobilization was safe and effective, and is well-tolerable in healthy donors because collection was possible in all donors without complications of G-CSF and dexamethasone administration and apheresis.

Keyword

Granulocyte collection; Granulocyte-colony-stimulating factor; Parameter

MeSH Terms

Anti-Bacterial Agents
Blood Cell Count
Blood Component Removal
Dexamethasone
Fatigue
Granulocyte Colony-Stimulating Factor
Granulocytes*
Headache
Hip
Humans
Injections, Subcutaneous
Knee
Retrospective Studies
Sleep Initiation and Maintenance Disorders
Tissue Donors*
Anti-Bacterial Agents
Dexamethasone
Granulocyte Colony-Stimulating Factor
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