Johnson Theodore M, Burrows Pamela K, Kusek John W, Nyberg Leroy M, Tenover J Lisa, Lepor Herbert, Roehrborn Claus G
Birmingham/Atlanta Geriatric Research, Education, and Clinical Center, Atlanta Veterans Affairs Medical Center, Decatur, Georgia 30033, USA.
J Urol. 2007 Nov;178(5):2045-50; discussion 2050-1. doi: 10.1016/j.juro.2007.07.013. Epub 2007 Sep 17.
We evaluated the effectiveness of single or combination drug therapy on nocturia in men with lower urinary tract symptoms suggestive of benign prostatic hyperplasia.
A total of 3,047 men with lower urinary tract symptoms/benign prostatic hyperplasia enrolled in the Medical Therapy of Prostatic Symptoms trial were randomly assigned to receive doxazosin alone, finasteride alone, combination therapy or placebo. Treatment effectiveness was assessed according to intent to treat by mean reduction in self-reported nightly nocturia at 1 and 4 years. A subgroup analysis by age (younger than 70 vs 70 years old or older) was also performed.
Of the men 2,583 reported 1 or more episodes of nocturia and finished 12 or more months of the trial. Mean nocturia was similar in all groups at baseline. Mean nocturia was reduced at 1 year by 0.35, 0.40, 0.54 and 0.58 in the placebo, finasteride, doxazosin and combination groups, respectively. Reductions with doxazosin and combination therapy were statistically greater than with placebo (p <0.05). At 4 years nocturia was also significantly reduced in patients treated with doxazosin and combination therapy (p <0.05 vs placebo). In men older than 70 years (495) all drugs significantly reduced nocturia at 1 year (finasteride 0.29, doxazosin 0.46 and combination 0.42) compared to placebo (0.11, p <0.05).
Doxazosin and combination therapy reduced nocturia more than placebo, but the net benefit of active drug compared to placebo was often modest with a net difference of less than 0.20 fewer nightly nocturia episodes at 1 and 4 years. Findings in men 70 years old or older were similar, with an even smaller effect observed for finasteride.
我们评估了单一药物治疗或联合药物治疗对有提示良性前列腺增生的下尿路症状的男性夜尿症的疗效。
共有3047名有下尿路症状/良性前列腺增生的男性参加了前列腺症状医学治疗试验,他们被随机分配接受单独使用多沙唑嗪、单独使用非那雄胺、联合治疗或安慰剂。根据意向性分析,通过1年和4年时自我报告的夜间夜尿次数的平均减少量来评估治疗效果。还按年龄(70岁以下与70岁及以上)进行了亚组分析。
2583名男性报告有1次或更多次夜尿症发作并完成了12个月或更长时间的试验。所有组在基线时的平均夜尿次数相似。安慰剂组、非那雄胺组、多沙唑嗪组和联合治疗组在1年时的平均夜尿次数分别减少了0.35、0.40、0.54和0.58次。多沙唑嗪组和联合治疗组的减少量在统计学上大于安慰剂组(p<0.05)。在4年时,接受多沙唑嗪和联合治疗的患者夜尿症也显著减少(与安慰剂组相比,p<0.05)。在70岁以上的男性(495名)中,与安慰剂组(0.11次,p<0.05)相比,所有药物在1年时均显著减少了夜尿次数(非那雄胺组0.29次,多沙唑嗪组0.46次,联合治疗组0.42次)。
多沙唑嗪和联合治疗比安慰剂更能减少夜尿次数,但与安慰剂相比,活性药物的净益处通常不大,在1年和4年时每晚夜尿发作次数的净差异小于0.20次。70岁及以上男性的结果相似,非那雄胺的效果甚至更小。