Xu Hua, Shang Xue-jun, Cai Xia, Teng Wen-hui, Huang Yu-feng
Reproductive Medicine Research Center, the First Affiliated Hospital of Xinjiang Medical University, 830054, China.
Zhonghua Nan Ke Xue. 2007 Apr;13(4):338-41.
To study the therapeutic efficacy of Longqingpian combined with Levofloxacin on Type IIIA prostatitis.
Eighty patients with Type IIIA prostatitis were equally randomized into a Longqingpian group and a Puleanpian group, both treated for 12 weeks. The former were given Longqingpian (once 6 tablets, twice a day) combined with Levofloxacin (once 0.2 g, twice a day) during the first 4 weeks, followed by Longqingpian alone (once 6 tablets, twice a day) for 8 weeks. The latter received Puleanpian (once 4 tablets, 3 times a day) combined with Levofloxacin (once 0.2 g, twice a day) in the initial 4 weeks, followed by Puleanpian alone (once 4 tablets, 3 times a day) for 8 weeks. Before and 4, 8, and 12 weeks after the treatment, all the patients were evaluated by The National Institutes of Health Chronic Prostatitis Symptom Index (NIH-CPSI) and EPS examination.
After 4-week, 8-week and 12-week treatment, total score of NIH-CPSI, and the score of pain, voiding symptoms and the quality of life dropped significantly in both groups compared with pre-treatment (P < 0.05 or 0.01), so did the leukocyte count in EPS (P < 0.05). Compared with the 4-week treatment, total score of NIH-CPSI, and the score of pain, voiding symptoms and the quality of life were shown to be significantly different (P < 0.05) in the Longqingpian group from the 8-week and 12-week treatment, except the leukocyte count in EPS. However, there was no significant difference between the 8-week and 12-week treatment in any of the indexes (P > 0.05). Longqingpian effected significant differences in the above indexes (P < 0.05), while Puleanpian did not after the treatment (P > 0.05). And the lecithin Amato body analysis revealed no significant changes in EPS after the treatment in either group (P > 0.05).
Longqingpian combined with Levofloxacin is highly effective for Type IIIA prostatitis, by relieving pain and voiding symptoms, decreasing the leukocyte count in EPS and improving the life quality of the patients.
研究龙清片联合左氧氟沙星治疗ⅢA型前列腺炎的疗效。
将80例ⅢA型前列腺炎患者随机分为龙清片组和普乐安片组,每组40例,疗程均为12周。龙清片组前4周给予龙清片(一次6片,一日2次)联合左氧氟沙星(一次0.2g,一日2次),后8周单用龙清片(一次6片,一日2次);普乐安片组前4周给予普乐安片(一次4片,一日3次)联合左氧氟沙星(一次0.2g,一日2次),后8周单用普乐安片(一次4片,一日3次)。治疗前及治疗后4、8、12周,采用美国国立卫生研究院慢性前列腺炎症状指数(NIH-CPSI)及前列腺液(EPS)检查对所有患者进行评估。
治疗4周、8周、12周后,两组患者NIH-CPSI总分及疼痛、排尿症状、生活质量评分均较治疗前显著下降(P<0.05或0.01);EPS中白细胞计数亦显著下降(P<0.05)。龙清片组治疗8周、12周时NIH-CPSI总分及疼痛、排尿症状、生活质量评分与治疗4周时比较差异均有统计学意义(P<0.05);而治疗8周与12周时各指标比较差异均无统计学意义(P>0.05);治疗后龙清片组上述各指标改善差异均有统计学意义(P<0.05);普乐安片组治疗前后差异均无统计学意义(P>0.05)。两组治疗后EPS中卵磷脂小体分析差异均无统计学意义(P>0.05)。
龙清片联合左氧氟沙星治疗ⅢA型前列腺炎疗效显著,能有效缓解疼痛和排尿症状,降低EPS中白细胞计数,提高患者生活质量。