Dickersin Kay, Munro Malcolm, Langenberg Patricia, Scherer Roberta, Frick Kevin D, Weber Anne M, Johns Alan, Peipert Jeffrey F, Clark Melissa
Brown Medical School, Providence, Rhode Island 02912, USA.
Control Clin Trials. 2003 Oct;24(5):591-609. doi: 10.1016/s0197-2456(03)00023-0.
The Surgical Treatments Outcomes Project for Dysfunctional Uterine Bleeding (STOP-DUB) was a multicenter, randomized clinical trial that assessed the efficacy and effectiveness of hysterectomy versus endometrial ablation (EA) for dysfunctional uterine bleeding (DUB) in women for whom medical management has not provided relief. Resource centers included a coordinating center, a chair's office, the American College of Obstetricians and Gynecologists, the Agency for Healthcare Research and Quality Project Office and 33 clinical centers in the United States and Canada. STOP-DUB enrolled: (1) eligible patients for whom medical treatment had not been successful and who were randomized to either hysterectomy or EA and (2) an observational cohort of patients who were "provisionally ineligible" or who were eligible but did not wish to be randomized. Enrollment began in October 1997 and ended in June 2001. The primary outcome addressed by the randomized trial was the impact of surgery on bleeding, pain, fatigue, and the major problem (symptom) that led the woman to seek treatment for her condition, measured 1 year following surgery. Additional outcomes included the impact of surgery at time points after 1 year; changes in quality of life, activity limitation, sexual functioning, and urinary incontinence; surgical complications; additional surgery; and resource utilization. The costs and the relative cost-effectiveness of the two surgeries were calculated. The main scientific objective for the observational study was to examine changes over time in terms of treatment selected, DUB-related symptoms, and quality of life.
功能失调性子宫出血手术治疗结果项目(STOP-DUB)是一项多中心随机临床试验,旨在评估子宫切除术与子宫内膜消融术(EA)对药物治疗无效的功能失调性子宫出血(DUB)女性的疗效和有效性。资源中心包括一个协调中心、一位主席办公室、美国妇产科医师学会、医疗保健研究与质量局项目办公室以及美国和加拿大的33个临床中心。STOP-DUB纳入了:(1)药物治疗未成功且被随机分配接受子宫切除术或EA的符合条件患者,以及(2)一组“暂时不符合条件”或符合条件但不希望被随机分配的观察性队列患者。入组于1997年10月开始,2001年6月结束。随机试验关注的主要结局是手术对出血、疼痛、疲劳以及导致该女性因病情寻求治疗的主要问题(症状)的影响,在术后1年进行测量。其他结局包括术后1年之后各时间点手术的影响;生活质量、活动受限、性功能和尿失禁的变化;手术并发症;额外的手术;以及资源利用情况。计算了两种手术的成本及其相对成本效益。观察性研究的主要科学目标是考察所选治疗方法、与DUB相关的症状以及生活质量随时间的变化情况。