Примери за използване на Platelet transfusion на Английски и техните преводи на Български
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Platelet transfusion and red cell transfusion were used as appropriate.
Table 2 Proportion of subjects who required no platelet transfusion and no rescue therapy Study M0631.
Platelet transfusion should be considered when clinically appropriate(see section 4.2).
For patients with platelet count≤ 10,000/μL, platelet transfusion should be considered.
Platelet transfusion may be considered as supportive therapy should bleeding occur(see section 5.3).
In children, thrombocytopenia(<25x109/ l or requiring platelet transfusion) occurred in 100% of patients.
Platelet transfusion is unlikely to be of clinical benefit in patients with bleeding(see section 4.4).
Table 3 Proportion of Subjects who required no platelet transfusion during the study(Day 1 through Day 35).
A subject was considered a nonresponder if the subject met the responder criterion only after platelet transfusion.
Thrombocytopenia(< 25x109/ l or requiring platelet transfusion) occurred at a median of 5-6 days in 98% of patients.
Eighty-six percent of patients were RBC transfusion dependent, and91% were platelet transfusion dependent.
The proportion of subjects not requiring a platelet transfusion or any rescue procedure for bleeding was generally similar across the various subgroups.
For patients with active bleeding for whom reversal of the pharmacological effects of Efient is required, platelet transfusion may be appropriate.
P value[a] Proportion of subjects who required no platelet transfusion during the study(i.e., from Day 1 through Day 35).
Platelet transfusion did not reverse the antiplatelet effect of ticagrelor in healthy volunteers and is unlikely to be of clinical benefit in patients with bleeding.
If prompt correction of prolonged bleeding time is required, platelet transfusion may reverse the effects of clopidogrel.
In addition to subjects who received platelet transfusion, subjects who did not receive an invasive procedure regardless of the reason were considered as receiving platelet transfusion.
In the clinical programme, thrombocytopenia was managed with laboratory monitoring,dose modification and platelet transfusion where appropriate(see section 4.2).
Haematologic support such as platelet transfusion and haematopoietic growth factors can be used during treatment if clinically indicated.
However, thrombocytopenia is reversible(median time to recovery of 12 days) andcan usually be managed by dose adjustment and interruption with or without platelet transfusion(see section 4.4).
There are several reports, in both children and adults, of using recombinant activated factor VII(rFVIIa) for refractory bleeding during ECLS despite platelet transfusion and correction of all other coagulation factor deficiencies(27, 28).
Responders were defined as patients who did not require a platelet transfusion or any rescue procedure for bleeding after randomisation and up to 7 days following a scheduled procedure.
Figure 1 Time course profiles of platelet count in the Phase 3 studies in thrombocytopenic patients with chronic liver disease(lusutrombopag-treated subjects without platelet transfusion and placebo-treated subjects with platelet transfusion) Phase 3 Study M0631.
LUSU= lusutrombopag[a] Proportion of subjects who required no platelet transfusion prior to the primary invasive procedure and no rescue therapy(including platelet transfusion) for bleeding from randomisation through 7 days after the primary invasive procedure.
The primary endpoint in Study M0631 was the proportion of subjects who required no platelet transfusion(i.e. achieved platelet count> 50,000/µL) before the primary invasive procedure.
In patients who were platelet transfusion dependent at baseline and achieved transfusion independence on treatment, the median duration of platelet transfusion independence was 10.8 months in the Vidaza group and 19.2 months in the CCR group.
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.
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 greater in the lusutrombopag groups in the individual studies and the pooled(Studies M0631 and M0634) lusutrombopag group compared with placebo(Table 3).
The time course of platelet counts in lusutrombopag-treated subjects without platelet transfusion and placebo-treated subjects with platelet transfusion in Studies M0631 and M0634 is presented in Figure 1.