Hirose T, Kumamoto Y, Sakai S, Shimamura S, Shibuya A, Yamazaki K, Umehara T, Miyake M, Takatsuka K, Aoki M
Department of Urology, School of Medicine, Sapporo Medical University.
Kansenshogaku Zasshi. 1995 Jan;69(1):45-53. doi: 10.11150/kansenshogakuzasshi1970.69.45.
Female acute uncomplicated cystitis responds relatively well to antimicrobial chemotherapy, but this is also a disease which shows a high frequency of recurrence. However, there have been no published reports regarding long-term monitoring of the course of this disease after therapy has been administered. Accordingly, using primarily a questionnaire, the authors carried out long-term monitoring (for a mean of 242 days) of the natural course of cases of female acute uncomplicated cystitis after single-dose therapy with lomefloxacin (LFLX), a new quinolone antimicrobial agent. The subjects of this study were female patients diagnosed as having acute uncomplicated cystitis with pain upon urination, pyuria (> or = 10 WBCs/hpf) and bacteriuria (> or = 10(4) cfu/ml). LFLX was orally administered as a single dose of 100 mg or 300 mg, and the therapeutic efficacy was evaluated on the 3rd and 7th days thereafter. In principle, the evaluation of cure was performed on the 7th day after LFLX administration, and monitoring was conducted to detect early recurrence during the next 7 days (i.e., through the 14th day after treatment). Then the subjects were monitored for late recurrence during a mean follow-up period of 242 days by means of a questionnaire. Confirmation of recurrence was carried out to the greatest extent possible. It was possible to carry out long-term monitoring of the natural course of 101 cases of female acute uncomplicated cystitis in which the clinical efficacy on the 3rd day after LFLX treatment had been evaluated as good or excellent.(ABSTRACT TRUNCATED AT 250 WORDS)
女性急性单纯性膀胱炎对抗菌化疗反应相对良好,但这也是一种复发频率较高的疾病。然而,关于该病治疗后病程的长期监测尚无发表的报告。因此,作者主要通过问卷调查,对新型喹诺酮类抗菌药物洛美沙星(LFLX)单剂量治疗女性急性单纯性膀胱炎病例的自然病程进行了长期监测(平均242天)。本研究的对象为诊断为急性单纯性膀胱炎且有排尿疼痛、脓尿(≥10个白细胞/高倍视野)和菌尿(≥10⁴菌落形成单位/毫升)的女性患者。LFLX口服单剂量100毫克或300毫克,并于给药后第3天和第7天评估治疗效果。原则上,在LFLX给药后第7天进行治愈评估,并在接下来的7天内(即治疗后第14天前)进行监测以检测早期复发。然后通过问卷调查对受试者进行平均242天的随访以监测晚期复发。尽可能对复发进行确认。对101例女性急性单纯性膀胱炎病例的自然病程进行长期监测是可行的,这些病例在LFLX治疗后第3天的临床疗效被评估为良好或优秀。(摘要截断于250字)