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确定接受NASHA(®)/Dx注射治疗大便失禁患者临床成功的相关因素。

Identifying factors associated with clinical success in patients treated with NASHA(®)/Dx injection for fecal incontinence.

作者信息

Franklin Howard, Barrett Andrew C, Wolf Ray

机构信息

Department of Medical Affairs, Salix, a Division of Valeant Pharmaceuticals North America LLC, Bridgewater, NJ, USA.

Department of Medical Affairs, Valeant Pharmaceuticals North America LLC, Wilton Manors, FL, USA.

出版信息

Clin Exp Gastroenterol. 2016 Mar 2;9:41-7. doi: 10.2147/CEG.S95238. eCollection 2016.

Abstract

PURPOSE

Injection with the bulking agent consisting of non-animal stabilized hyaluronic acid/dextranomer (NASHA(®)/Dx) is well tolerated and efficacious for the treatment of fecal incontinence (FI); however, the patient population that may derive maximum benefit has not been established. This post hoc responder analysis assessed demographic and baseline characteristics predictive of responsiveness to NASHA/Dx treatment.

METHODS

Adults with a Cleveland Clinic Florida fecal incontinence score (CCFIS) ≥10 were randomized to receive NASHA/Dx or sham treatment. The primary end point was response to treatment (ie, decrease from baseline of ≥50% in number of FI episodes) at 6 months; a prespecified secondary end point was change in fecal incontinence quality of life (FIQL) score at 6 months. Post hoc subgroup analyses were performed for baseline and demographic characteristics and prior FI treatments.

RESULTS

Overall, response to treatment was significantly greater with NASHA/Dx versus sham injection (52.7% vs 32.1%; P=0.0089). All subgroups analyzed demonstrated evidence of improvement, favoring NASHA/Dx versus sham treatment for both response to treatment and change in the FIQL coping/behavior subscale score. For the primary end point, a significantly greater percentage of patients with CCFIS ≤15, FI symptoms ≤5 years' duration, or obstetric causes of FI responded to NASHA/Dx treatment versus patients receiving sham treatment (51.1% vs 28.3%, P=0.0169; 55.4% vs 25.7%, P=0.0026; and 53.6% vs 23.1%, P=0.0191, respectively). The mean change in the FIQL coping/behavior score significantly favored NASHA/Dx versus sham treatment for patients with CCFIS ≤15 (P=0.0371), FI symptoms ≤5 years' duration (P=0.0289), or obstetric causes of FI (P=0.0384). Patients without a history of specific FI treatments (eg, antidiarrheal medications, biofeedback, surgery) were more likely to respond to NASHA/Dx versus sham treatment for both end points.

CONCLUSION

Although all subgroups analyzed showed evidence of quantitative and qualitative benefit from NASHA/Dx therapy, patients with characteristics indicative of mild-to-moderate FI may exhibit the greatest benefit.

摘要

目的

注射由非动物稳定化透明质酸/葡聚糖微球(NASHA(®)/Dx)组成的填充剂耐受性良好,对治疗大便失禁(FI)有效;然而,可能从治疗中获得最大益处的患者群体尚未确定。这项事后反应者分析评估了预测对NASHA/Dx治疗反应性的人口统计学和基线特征。

方法

佛罗里达克利夫兰诊所大便失禁评分(CCFIS)≥10的成年人被随机分配接受NASHA/Dx或假治疗。主要终点是6个月时对治疗的反应(即FI发作次数较基线减少≥50%);一个预先设定的次要终点是6个月时大便失禁生活质量(FIQL)评分的变化。对基线和人口统计学特征以及既往FI治疗进行事后亚组分析。

结果

总体而言,与假注射相比,NASHA/Dx治疗的反应明显更好(52.7%对32.1%;P = 0.0089)。所有分析的亚组均显示出改善的证据,在治疗反应和FIQL应对/行为子量表评分变化方面,NASHA/Dx优于假治疗。对于主要终点,CCFIS≤15、FI症状持续时间≤5年或因产科原因导致FI的患者中,对NASHA/Dx治疗有反应的患者比例明显高于接受假治疗的患者(分别为51.1%对28.3%,P = 0.0169;55.4%对25.7%,P = 0.0026;53.6%对23.1%,P = 0.0191)。对于CCFIS≤15(P = 0.0371)、FI症状持续时间≤5年(P = 0.0289)或因产科原因导致FI的患者(P = 0.0384),FIQL应对/行为评分的平均变化明显有利于NASHA/Dx而非假治疗。对于两个终点,既往无特定FI治疗史(如止泻药物、生物反馈、手术)的患者对NASHA/Dx治疗有反应的可能性高于假治疗。

结论

尽管所有分析的亚组均显示出NASHA/Dx治疗在数量和质量上有益的证据,但具有轻度至中度FI特征的患者可能获益最大。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1203/4780737/4af65065e3be/ceg-9-041Fig1.jpg

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