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Oral enoxacin for infection prevention in adults with acute nonlymphocytic leukemia. The Enoxacin Prophylaxis Study Group.

机译:口服依诺沙星预防成人急性非淋巴细胞白血病的感染。依诺沙星预防研究小组。

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摘要

A randomized, double-blind, placebo-controlled trial was conducted in eight hematologic units to determine the efficacy and safety of oral enoxacin for infection prevention in adult patients with acute nonlymphocytic leukemia. One hundred nineteen patients undergoing remission induction or consolidation chemotherapy were enrolled; 62 of them received enoxacin (400 mg orally every 12 h). Patients received antifungal prophylaxis with oral mycostatin (1,000,000 U four times daily) or clotrimazole (1 troche five times daily). Analysis was performed on an intent-to-treat basis. There was no significant difference between groups in race, age, or type and stage of leukemia, but there were more males in the placebo group (P = 0.073 [Fisher's exact test]). Fewer enoxacin patients had gram-negative bacteremia (1 versus 14 [P < 0.001]), gram-negative infection at any site (2 versus 19 [P < 0.001]), or bacterial and/or fungal infection (17 versus 26 [P = 0.056]). There was no significant difference in the number of patients with gram-positive infection at any site (12 versus 16), gram-positive bacteremia (9 versus 10), deep fungal infection (6 versus 2), death (2 versus 3), other antimicrobial therapy required (48 versus 48), therapy with amphotericin B (15 versus 7 [P = 0.105]), any adverse event (45 versus 36), or any study drug-associated adverse events (13 versus 6). Logistic regression confirmed (odds ratios and 95% confidence intervals are given in parentheses) that enoxacin reduced the risk of gram-negative infection (0.07; 0.01 to 0.30), especially gram-negative bacillary bacteremia (0.05; 0.01 to 0.37), without altering the risk of gram-positive bacterial (0.63; 0.26 to 1.5), deep fungal (2.57; 0.47 to 13.9), or Clostridium difficile (1.16; 0.3 to 4.56) infection. The median time to the onset of fever of more than or equal 102.8 F (39.3 degree C) was 32 days for the enoxacin group versus 15 days for patients receiving placebo (P=0.0007 [Wilcoxon test]). In patients with acute nonlymphocytic leukemia, oral enoxacin prevents gram-negative infections, delays the onset of fever, does not alter the incidence of gram-positive or proven deep fungal infections, and is well tolerated.
机译:在八个血液学部门进行了一项随机,双盲,安慰剂对照试验,以确定口服依诺沙星预防成人急性非淋巴细胞白血病患者的疗效和安全性。 119名接受缓解诱导或巩固化疗的患者;其中62人接受依诺沙星(每12小时口服400 mg)。患者接受口服霉菌抑素(每天四次,每次1,000,000 U)或克霉唑(每天五次,一次小剂量)的抗真菌药物预防。分析是按意向进行的。白血病的种族,年龄,类型和阶段在两组之间没有显着差异,但安慰剂组中的男性更多(P = 0.073 [Fisher精确检验])。较少的依诺沙星患者发生革兰氏阴性菌血症(1比14 [P <0.001]),在任何部位发生革兰氏阴性菌感染(2比19 [P <0.001])或细菌和/或真菌感染(17比26 [P]) = 0.056]。在任何部位发生革兰氏阳性感染(12对16),革兰氏阳性菌血症(9对10),深部真菌感染(6对2),死亡(2对3),需要其他抗微生物治疗(48对48),两性霉素B治疗(15对7 [P = 0.105]),任何不良事件(45对36)或任何与研究药物相关的不良事件(13对6)。逻辑回归确认(括号中给出了奇数比和95%置信区间),依诺沙星降低了革兰氏阴性菌感染的风险(0.07; 0.01至0.30),尤其是革兰氏阴性菌菌血症(0.05; 0.01至0.37),而没有改变革兰氏阳性细菌(0.63; 0.26至1.5),深部真菌(2.57; 0.47至13.9)或艰难梭菌(1.16; 0.3至4.56)感染的风险。依诺沙星组的发烧中位时间大于或等于102.8 F(39.3摄氏度)为32天,而接受安慰剂的患者为15天(P = 0.0007 [Wilcoxon测试])。在患有急性非淋巴细胞性白血病的患者中,口服依诺沙星可预防革兰氏阴性感染,延缓发烧发作,不改变革兰氏阳性或深部真菌感染的发生率,并且耐受性良好。

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