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Dose of prophylactic platelet transfusions and prevention of hemorrhage.

机译:预防性血小板输注的剂量和预防出血的剂量。

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BACKGROUND: We conducted a trial of prophylactic platelet transfusions to evaluate the effect of platelet dose on bleeding in patients with hypoproliferative thrombocytopenia. METHODS: We randomly assigned hospitalized patients undergoing hematopoietic stem-cell transplantation or chemotherapy for hematologic cancers or solid tumors to receive prophylactic platelet transfusions at a low dose, a medium dose, or a high dose (1.1x10(11), 2.2x10(11), or 4.4x10(11) platelets per square meter of body-surface area, respectively), when morning platelet counts were 10,000 per cubic millimeter or lower. Clinical signs of bleeding were assessed daily. The primary end point was bleeding of grade 2 or higher (as defined on the basis of World Health Organization criteria). RESULTS: In the 1272 patients who received at least one platelet transfusion, the primary end point was observed in 71%, 69%, and 70% of the patients in the low-dose group, the medium-dose group, and the high-dose group, respectively (differences were not significant). The incidences of higher grades of bleeding, and other adverse events, were similar among the three groups. The median number of platelets transfused was significantly lower in the low-dose group (9.25x10(11)) than in the medium-dose group (11.25x10(11)) or the high-dose group (19.63x10(11)) (P=0.002 for low vs. medium, P<0.001 for high vs. low and high vs. medium), but the median number of platelet transfusions given was significantly higher in the low-dose group (five, vs. three in the medium-dose and three in the high-dose group; P<0.001 for low vs. medium and low vs. high). Bleeding occurred on 25% of the study days on which morning platelet counts were 5000 per cubic millimeter or lower, as compared with 17% of study days on which platelet counts were 6000 to 80,000 per cubic millimeter (P<0.001). CONCLUSIONS: Low doses of platelets administered as a prophylactic transfusion led to a decreased number of platelets transfused per patient but an increased number of transfusions given. At doses between 1.1x10(11) and 4.4x10(11) platelets per square meter, the number of platelets in the prophylactic transfusion had no effect on the incidence of bleeding. (ClinicalTrials.gov number, NCT00128713.)
机译:背景:我们进行了一项预防性血小板输注试验,以评估血小板剂量对增生性血小板减少症患者出血的影响。方法:我们随机分配住院的接受造血干细胞移植或化学疗法治疗的血液系统癌症或实体瘤患者,分别接受低剂量,中剂量或高剂量的预防性血小板输注(1.1x10(11),2.2x10(11 ),或当早晨血小板计数为每立方毫米10,000或更低时,则分别为每平方米体表面积4.4x10(11)血小板)。每天评估出血的临床体征。主要终点是2级或更高级别的出血(根据世界卫生组织的标准定义)。结果:在1272例接受至少一次血小板输注的患者中,低剂量组,中剂量组和高剂量组的71%,69%和70%的患者观察到主要终点剂量组(差异不显着)。三组之间较高级别的出血和其他不良事件的发生率相似。低剂量组(9.25x10(11))输注的血小板中位数显着低于中剂量组(11.25x10(11))或高剂量组(19.63x10(11))(低剂量组与中等剂量组的P = 0.002,高剂量组与低剂量组的P <0.001,高剂量组与中等剂量组的P <0.001),但是低剂量组的平均输注血小板数要高得多(5个,中等组为3个) -高剂量组中,P <0.001;低与中,P <0.001;高与低组。 25%的研究日发生出血,早晨血小板计数为每立方毫米5000或更低,而17%的研究日血小板计数为每立方毫米6000至80,000(P <0.001)。结论:预防性输注低剂量的血小板导致每位患者输注的血小板数量减少,但输血次数增加。在每平方米1.1x10(11)和4.4x10(11)血小板之间的剂量下,预防性输血中的血小板数量对出血的发生率没有影响。 (ClinicalTrials.gov编号,NCT00128713。)

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