Chrouser K L, Fick F, Goel A, Itano N B, Sweat S D, Lightner D J
Mayo Clinic, Rochester, Minnesota, USA.
J Urol. 2004 Mar;171(3):1152-5. doi: 10.1097/01.ju.0000103688.83606.06.
The durability of Durasphere (Carbon Medical Technologies, Saint Paul, Minnesota), used to treat stress urinary incontinence, has not been shown beyond 12 months of followup. Women treated with Durasphere and Contigen (Bard, Inc., Covington, Georgia) at 1 institution between 1996 and 2000 were compared to determine patient satisfaction and urinary continence after extended followup.
Between April 1996 and September 2000, 56 women were treated with Durasphere at this institution, of whom 43 were available for extended followup. Aged matched patients treated with Contigen were analyzed for comparison. Patient satisfaction and continence at last followup were subjectively assessed via telephone interview. Survival methods (Kaplan-Meier and Cox proportional hazards model) were used to analyze time to failure as a function of treatment group and other potential predictors.
Treatment groups (Contigen and Durasphere) were similar with respect to all baseline factors. Treatment was initially effective in 63% of Durasphere and Contigen cases (p = 1.0). At 24 and 36 months Durasphere remained effective in 33% and 21% of patients compared with 19% and 9% for Contigen, respectively. At last followup only 9 patients (21%) treated with Durasphere and 2 (5%) treated with Contigen (median followup 51 and 62 months, respectively) claimed that treatment was still effective. After controlling for differences in followup time there was no significant difference in time to failure between the treatment groups (p = 0.25). A third of patients in each group believed that treatment was a success.
Neither Contigen nor Durasphere provides durable improvement in continence. Despite this outcome a third of patients in the 2 groups were satisfied with the treatment outcome.
用于治疗压力性尿失禁的Durasphere(碳医疗技术公司,明尼苏达州圣保罗)的耐用性在随访超过12个月后尚未得到证实。对1996年至2000年期间在1家机构接受Durasphere和Contigen(巴德公司,佐治亚州科温顿)治疗的女性进行比较,以确定延长随访后的患者满意度和尿失禁情况。
1996年4月至2000年9月期间,该机构有56名女性接受了Durasphere治疗,其中43名可供延长随访。对接受Contigen治疗的年龄匹配患者进行分析以作比较。通过电话访谈对末次随访时的患者满意度和尿失禁情况进行主观评估。采用生存方法(Kaplan-Meier法和Cox比例风险模型)分析治疗失败时间与治疗组及其他潜在预测因素的关系。
治疗组(Contigen和Durasphere)在所有基线因素方面相似。治疗最初在63%的Durasphere和Contigen病例中有效(p = 1.0)。在24个月和36个月时,Durasphere分别在33%和21%的患者中仍有效,而Contigen分别为19%和9%。在末次随访时,只有9名接受Durasphere治疗的患者(21%)和2名接受Contigen治疗的患者(5%)(中位随访时间分别为51个月和62个月)称治疗仍有效。在控制随访时间差异后,治疗组之间的治疗失败时间无显著差异(p = 0.25)。每组中有三分之一的患者认为治疗是成功的。
Contigen和Durasphere均未持久改善尿失禁情况。尽管如此,两组中仍有三分之一的患者对治疗结果满意。