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在淋巴瘤患者严重短期中性粒细胞减少期间,使用氧氟沙星加利福平强化预防发热性中性粒细胞减少。

Intensified prophylaxis of febrile neutropenia with ofloxacin plus rifampin during severe short-duration neutropenia in patients with lymphoma.

作者信息

Muñoz L, Martino R, Subirà M, Brunet S, Sureda A, Sierra J

机构信息

Division of Clinical Hematology, Hospital De La Santa Creu i Sant Pau, Barcelona, Spain.

出版信息

Leuk Lymphoma. 1999 Aug;34(5-6):585-9. doi: 10.3109/10428199909058487.

Abstract

To analyse the impact of intensified prophylaxis with ofloxacin plus rifampin (O+R) in neutropenic patients we used this combination in 40 consecutive cycles of ifosfamide, cytarabine, prednisolone and etoposide (IAPVP-16). This salvage chemotherapy regimen for lymphoma usually produces four to six days of severe neutropenia without significant extrahematologic toxicities. We compared the infectious morbidity during neutropenia under O+R with 58 consecutives cycles using either norfloxacin or no prophylaxis (control group). Fifty-three percent of control group patients and 20% of the O+R group developed febrile neutropenia that required hospital admission (p<0.001, 95% CI for the difference between both proportions of 16% to 51%). Bacteremia was documented in two patients in the O+R group and six in the control group (p=0.08). Gram-positive cocci (GPC) accounted for all six bacteremias in the control group, while both cases in O+R group were due to a quinolone-resistant gram-negative bacteria (GNB) (p<0.01 for GPC). Five patients (13%) who received O+R and 23 (40%) in control group developed fever of unknown origin, p<0.001, while the total duration of hospitalization due to febril neutropenia was 42 days and 158 days, respectively (p<0.001). In conclusion, intensified prophylaxis with O+R appears to reduce the rate of febrile neutropenia and GPC bacteremia in patients with short and severe neutropenia, which translates into a reduction in the need for hospitalization.

摘要

为分析氧氟沙星联合利福平(O+R)强化预防对中性粒细胞减少患者的影响,我们在40个连续周期的异环磷酰胺、阿糖胞苷、泼尼松龙和依托泊苷(IAPVP-16)治疗中使用了该联合方案。这种淋巴瘤挽救化疗方案通常会导致四到六天的严重中性粒细胞减少,且无明显血液学外毒性。我们将O+R预防下中性粒细胞减少期间的感染发病率与使用诺氟沙星或不进行预防的58个连续周期(对照组)进行了比较。对照组53%的患者和O+R组20%的患者发生了需要住院治疗的发热性中性粒细胞减少(p<0.001,两组比例差异的95%置信区间为16%至51%)。O+R组有2例患者发生菌血症,对照组有6例(p=0.08)。对照组的6例菌血症均由革兰氏阳性球菌(GPC)引起,而O+R组的2例均由喹诺酮耐药革兰氏阴性菌(GNB)引起(GPC的p<0.01)。接受O+R的5例患者(13%)和对照组的23例患者(40%)出现不明原因发热,p<0.001,而因发热性中性粒细胞减少导致的住院总时长分别为42天和158天(p<0.001)。总之,O+R强化预防似乎可降低短期严重中性粒细胞减少患者的发热性中性粒细胞减少率和GPC菌血症发生率,这意味着住院需求的减少。

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