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Peripheral Blood Stem Cell Rescue. Multiple Myeloma.
Liz Higgins BMT Co-ordinator St James’s Hospital, Dublin
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(BMT/ PBSCT) BMT/ PBSCT involves eliminating an individual’s bone marrow stem cells. They are then replaced with bone marrow/ stem cells either from another individual or with a previously harvested portion of the individuals own bone marrow or peripheral blood stem cells.
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Reasons for PBSCT To facilitate high dose therapy in some malignant conditions e.G. Lymphoma, testicular cancer, Multiple Myeloma.
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Autologous rescue / PBSCT involves two processes.
PBSCH/ BMH PBSCT/ BMT
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Sources of Bone Marrow Stem Cells
Bone marrow (BM) - aspirated from the posterior iliac crests under GA, usually mls in volume Peripheral blood stem cells (PBSC) - following the administration of growth colony stimulating factor (G-CSF) + / - chemotherapy
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Pathway Referral / Review PBSCH PBSCT Follow up
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PBSC Mobilisation Initial Review
Bloods Consider venous access – peripheral/central Medical assessment Nursing Assessment Discussion
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PBSC Mobilisation Regimens for MM
G-CSF 10mcg/kg x 4 days Cyclophosphamide 2g/m2 + G-CSF 10mcg/kg
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Cyclophosphamide 2g/m2 Chemo on Monday Commence G-CSF Tuesday
Leucapheresis day 8-10
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GSCF ( Neupogen) 10Mcg / kg Round up. Commence on Saturday.
CD34 Count Tuesday +/- Gcsf PBSCH
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Apheresis 1-3 Days 5-6 Hours Inpatient or Transfer as day patient
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Stem Cell Red Cell or White Cell or Platelet
Once the ‘decision’ is made it is probably irreversible
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Autologous Stem Cell Rescue
Approximately 4-6 weeks post Harvest
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Pre Autograft work-up Pulmonary function tests
Echocardiogram or MUGA scan Dental Assessment BM Aspirate & Bx Skeletal survey (if applicable) Insertion of PICC or CVC 24 hour urine collection
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Conditioning Regimens
Melphalan
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Denis Burkitt
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Shared care National referral centre. Facilitation.
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