Примери за използване на Platelet transfusion на Английски и техните преводи на Български
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The second study involving 215 adults found that 65% of patients who took Mulpleo did not require platelet transfusion before their procedure, compared with 29% of patients who received placebo.
Of the patients in the Vidaza group who were platelet transfusion dependent at baseline, 40.6%(95% CI= 30.9, 50.8) of these patients became platelet transfusion independent during the treatment period, compared with 29.3% of(95% CI= 19.7,
Of the patients in the azacitidine group who were platelet transfusion dependent at baseline, 40.6%(95% CI= 30.9, 50.8) of these patients became platelet transfusion independent during the treatment period, compared with 29.3% of(95% CI= 19.7,
The proportion of subjects who required no platelet transfusion prior to the primary invasive procedure
The primary endpoint in Study M0634 was the proportion of subjects who required no platelet transfusion(i.e. achieved platelet count>
Proportion of subjects who required no platelet transfusion during the study(Day 1 through Day 35) The proportion of subjects who required no platelet transfusion during the study was significantly
Platelet transfusions may be required, if clinically indicated(see section 4.4).
Platelet transfusions were given to 10% of patients in 4% of courses.
However, platelet transfusions may be required as clinically indicated.
In addition, there may also be significant platelet dysfunction despite regular platelet transfusions;
Platelet transfusions were given in 4% of courses.
Platelet transfusions may be required as clinically indicated(see sections 4.2 and 4.8).
During the randomised period, platelet transfusions were administered to 4.7% of patients receiving ruxolitinib
bortezomib+ dexamethasone arm and 10.3% patients in the placebo+ bortezomib+ dexamethasone arm received platelet transfusions during treatment.
In the BzmbR-CAP group, 22.5% of patients received platelet transfusions compared to 2.9% of patients in the R-CHOP group.
In the VcR-CAP group, 22.5% of patients received platelet transfusions compared to 2.9% of patients in the R-CHOP group.
Randomized clinical trials have shown similar outcomes for patients who received prophylactic platelet transfusions at a level of 10,000/mm3 rather than at a level of 20,000/mm3.
Randomized trials have shown similar outcomes for patients who received prophylactic platelet transfusions at a level of 10,000/mm3 rather than 20,000/mm3.
Rescue therapies allowed in the study were IVIG, platelet transfusions, anti-D immunoglobulin, and corticosteroids.
Rescue therapies allowed in the study were IVIG, platelet transfusions, anti-D immunoglobulin, and corticosteroids. e Stable dose