Espinouse D, Chomarat M
Service d'Hématologie Clinique, Centre Hospitalier Lyon-Sud, Pierre-Bénite.
Pathol Biol (Paris). 1990 Jun;38(5 ( Pt 2)):552-6.
The efficacy and the safety of teicoplanin were evaluated for the treatment of febrile episodes in neutropenic patients. A total of 18 patients received teicoplanin once daily as an intravenous injection of 200 mg in 6 patients (after a loading dose of 400 mg) or 400 mg in 12 patients (loading dose: 800 mg). The mean duration of therapy was 15.9 days (range 9 to 39 days). In all patients teicoplanin was combined with another antibiotic usually a beta-lactam. Thirteen of 18 patients were successfully treated. Three febrile episodes proved to be microbiologically documented infections and were cured by teicoplanin: one Streptococcus mitis and two methicillin-resistant (methi-R) Staphylococcus epidermidis bacteremias. Neither toxicity nor side effects were observed in the reported group. Six patients experiencing reactions to vancomycin (2 cases of cutaneous allergy) or to vancomycin and amphotericin B combination (4 cases of nephrotoxicity) were subsequently treated with teicoplanin without any evidence of cross-sensitivity. We observed emergence of teicoplanin-resistant coagulase-negative Staphylococcus in 3 patients receiving teicoplanin: 20, 18 and 8 days after a first febrile episode cured by teicoplanin and a beta-lactam, they developed fever while receiving the same antibiotic regimen. Methi-R Staphylococcus epidermidis was isolated from blood cultures in the first patient and methi-R Staphylococcus haemolyticus in the two other patients. In one patient, successfully treated by teicoplanin for a first febrile episode related to a methi-R Staphylococcus epidermidis, emergence of Staphylococcus haemolyticus occurred 8 days later while the patient was on teicoplanin therapy (6 mg/kg). MICs of teicoplanin were 16 mg/l for the two Staphylococcus strains isolated in this patient.(ABSTRACT TRUNCATED AT 250 WORDS)
评价替考拉宁治疗中性粒细胞减少患者发热性疾病的疗效和安全性。18例患者接受替考拉宁治疗,6例患者静脉注射200mg/日(首剂负荷量400mg),12例患者静脉注射400mg/日(首剂负荷量800mg)。平均治疗时间为15.9天(范围9至39天)。所有患者中,替考拉宁均与另一种抗生素联合使用,通常为β-内酰胺类。18例患者中有13例成功治愈。3例发热性疾病经微生物学证实为感染,且被替考拉宁治愈:1例缓症链球菌和2例耐甲氧西林表皮葡萄球菌败血症。报道的病例组中未观察到毒性或副作用。6例对万古霉素有反应(2例皮肤过敏)或对万古霉素和两性霉素B联合用药有反应(4例肾毒性)的患者随后接受替考拉宁治疗,未出现交叉敏感的证据。我们观察到3例接受替考拉宁治疗的患者出现了耐替考拉宁凝固酶阴性葡萄球菌:在首次发热性疾病被替考拉宁和β-内酰胺类治愈后20天、18天和8天,他们在接受相同抗生素方案治疗时出现发热。第1例患者血培养分离出耐甲氧西林表皮葡萄球菌,另外2例患者分离出耐甲氧西林溶血葡萄球菌。1例因耐甲氧西林表皮葡萄球菌引起的首次发热性疾病被替考拉宁成功治愈的患者,在接受替考拉宁治疗(6mg/kg)8天后出现溶血葡萄球菌。该患者分离出的2株葡萄球菌对替考拉宁的最低抑菌浓度均为16mg/l。(摘要截选至250词)