Exemplos de uso de PBPC mobilisation em Inglês e suas traduções para o Português
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PBPC mobilisation in normal donors.
Normal donors undergoing PBPC mobilisation.
PBPC mobilisation in normal donors.
Filgrastim for PBPC mobilisation when used alone.
Special precautions in patients undergoing PBPC mobilisation.
In PBPC mobilisation in normal donors the most commonly reported undesirable effect was musculoskeletal pain.
Special precautions in normal donors undergoing PBPC mobilisation.
Donors who receive G-CSFs for PBPC mobilisation should be monitored until haematological indices return to normal.
Patients undergoing myelosuppressive ormyeloablative therapy followed by autologous PBPC transplantation The recommended dose of filgrastim for PBPC mobilisation when used alone is 1.0 MU/ kg/ day(10 μ g/ kg/ day) for 5- 7 consecutive days.
Filgrastim for PBPC mobilisation after myelosuppressive chemotherapy: Filgrastim should be given by subcutaneous injection.
However, during the period of administration of filgrastim for PBPC mobilisation, filgrastim should be discontinued or its dosage should be reduced if the leukocyte counts rise to> 70 x 109/ l.
PBPC mobilisation should be considered only in donors who meet normal clinical and laboratory eligibility criteria for stem cell donation.
However, during the period of administration of filgrastim for PBPC mobilisation, filgrastim should be discontinued or its dosage should be reduced if the leukocyte counts rise to> 70 x 109/L.
PBPC mobilisation should be considered only in donors who meet normal clinical and laboratory eligibility criteria for stem cell donation with special attention to haematological values and infectious disease.
The recommended dose of filgrastim for PBPC mobilisation when used alone is 1.0 MU/kg/day(10 micrograms/kg/day) for 5-7 consecutive days.
For PBPC mobilisation in normal donors, filgrastim should be administered at 1.0 MU kg/day(10 micrograms/kg/day)for 4- 5 consecutive days.
Normal donors prior to allogeneic PBPC transplantation For PBPC mobilisation in normal donors prior to allogeneic PBPC transplantation, filgrastim should be administered at 1.0 MU/ kg/ day(10 μ g/ kg/ day) for 4- 5 consecutive days.
PBPC mobilisation should be considered only in donors who meet normal clinical and laboratory eligibility criteria for stem cell donation with special attention to haematological values and infectious diseases.
The recommended dose of filgrastim for PBPC mobilisation when used alone is 1.0 MIU(10 μ g)/ kg/ day as a 24 hour subcutaneous continuous infusion or a single daily subcutaneous injection for 5 to 7 consecutive days.
The recommended dose of filgrastim for PBPC mobilisation when used alone is 1.0 MIU(10 μ g)/ kg/ day as a 24 hour subcutaneous continuous infusion or a single daily subcutaneous injection for 5 to 7 consecutive days.
The recommended dose of filgrastim for PBPC mobilisation after myelosuppressive chemotherapy is 0.5 MU/ kg/ day(5 μ g/ kg/ day) given daily from the first day after completion of chemotherapy until the expected neutrophil nadir is passed and the neutrophil count has recovered to the normal range.
The recommended dose of filgrastim for PBPC mobilisation after myelosuppressive chemotherapy is 0.5 MIU(5 μ g)/ kg/ day given daily by subcutaneous injection from the first day after completion of chemotherapy until the expected neutrophil nadir is passed and the neutrophil count has recovered to the normal range.
Mobilisation of PBPC.
Mobilisation of PBPC Subcutaneous injection.
In patients with Mobilisation of PBPC.
For the mobilisation of PBPC in patients undergoing myelosuppressive or myeloablative therapy followed by autologous peripheral blood progenitor cell transplantation.
Mobilisation of PBPC does not provide a direct clinical benefit to normal donors and should only be considered for the purposes of allogeneic stem cell transplantation.
Normal donors prior to allogeneic PBPC transplantation Mobilisation of PBPC does not provide a direct clinical benefit to normal donors and should only be considered for the purposes of allogeneic stem cell transplantation.
Patients who have undergone very extensive prior myelosuppressive therapy may not show sufficient mobilisation of PBPC to achieve the recommended minimum yield(2.0 x 106 CD34+ cells/kg) or acceleration of platelet recovery to the same degree.
Patients who have undergone very extensive prior myelosuppressive therapy may not show sufficient mobilisation of PBPC to achieve the recommended minimum yield(2.0 x 106 CD34+ cells/kg) or acceleration of platelet recovery to the same degree.