Ann Arbor, Mich. From the Section of Plastic Surgery, The University of Michigan Medical School; the Section of Plastic Surgery, Department of Surgery, University of Michigan Health System; and the Center for Statistical Consultation and Research, University of Michigan.
Plast Reconstr Surg. 2012 Jul;130(1):225-237. doi: 10.1097/PRS.0b013e318254b43b.
In 2006, the U.S. Food and Drug Administration recommended screening of all women with silicone gel breast implants with magnetic resonance imaging 3 years after implantation and every 2 years thereafter to assess their integrity. The cost for these serial examinations over the lifetime of the breast implants is an added burden to insurance payers and to women. The authors performed an economic analysis to determine optimal screening strategies by considering the diagnostic accuracy of the screening tests, costs of the tests, and subsequent implant removal.
The authors determined aggregate/pooled values for sensitivity and specificity of the screening tests of ultrasound and magnetic resonance imaging in detecting silicone breast implant ruptures from the data obtained from published literature. They compiled costs, based on Medicare reimbursements for 2011, for the following elements: imaging modalities, anesthesia, and three surgical treatment options for detected ruptures. A decision tree was used to compare three alternate screening strategies of ultrasound only, magnetic resonance imaging only, and ultrasound followed by magnetic resonance in asymptomatic and symptomatic women.
The cost per rupture of screening and management of rupture with ultrasound in asymptomatic women was $1090; in symptomatic women, it was $1622. A similar cost for magnetic resonance imaging in asymptomatic women was $2067; in symptomatic women it was $2143. A similar cost for ultrasound followed by imaging in asymptomatic women was $637; in symptomatic women, it was $2908.
Screening with ultrasound followed by magnetic resonance imaging was optimal for asymptomatic women, and screening with ultrasound was optimal for symptomatic women.
2006 年,美国食品和药物管理局建议对所有接受硅凝胶乳房植入物的女性进行磁共振成像筛查,植入后 3 年进行一次,并在此后每 2 年进行一次,以评估其完整性。这些连续检查在乳房植入物的使用寿命内给保险公司和女性带来了额外的负担。作者进行了一项经济分析,通过考虑筛查试验的诊断准确性、试验成本以及随后的植入物移除,来确定最佳的筛查策略。
作者从已发表的文献中获得的数据,确定了超声和磁共振成像筛查试验检测硅酮乳房植入物破裂的敏感性和特异性的综合/汇总值。他们根据 2011 年医疗保险的报销情况,编制了以下各项的成本:成像方式、麻醉和三种检测到的破裂的手术治疗选择。使用决策树比较了三种不同的筛查策略:仅超声、仅磁共振成像以及无症状和有症状女性的超声后磁共振成像。
无症状女性中,超声筛查和管理破裂的成本为 1090 美元/每破裂;有症状女性的成本为 1622 美元/每破裂。无症状女性中,磁共振成像的类似成本为 2067 美元/每破裂;有症状女性的成本为 2143 美元/每破裂。无症状女性中,超声后影像学检查的类似成本为 637 美元/每破裂;有症状女性的成本为 2908 美元/每破裂。
无症状女性最佳的筛查策略是超声后磁共振成像,有症状女性最佳的筛查策略是超声。