Fábregues Francisco, Tàssies Dolors, Reverter Juan C, Carmona Francisco, Ordinas Antonio, Balasch Juan
Hospital Clínic-Institut d'Investigacions Biomèdiques August Pi i Sunyer, Faculty of Medicine-University of Barcelona, Barcelona, Spain.
Fertil Steril. 2004 Apr;81(4):989-95. doi: 10.1016/j.fertnstert.2003.09.042.
To determine the prevalence of markers of thrombophilia in patients with severe ovarian hyperstimulation syndrome (OHSS) and to evaluate the cost-effectiveness of screening for factor V Leiden and prothrombin G20210A mutations in women entering an IVF program.
Case-control study and cost-effectiveness analysis.
University teaching hospital.
PATIENT(S): Women undergoing controlled ovarian hyperstimulation for IVF complicated by severe OHSS (group 1, n = 20), women undergoing controlled ovarian hyperstimulation for IVF without development of severe OHSS (group 2, n = 40), and healthy control subjects (group 3, n = 100).
INTERVENTION(S): Investigation of markers of thrombophilia. Estimate of number of IVF patients needed to detect a case of severe OHSS and thrombosis associated with thrombophilia genetic mutation was calculated from the available data.
MAIN OUTCOME MEASURE(S): Blood samples were analyzed for inherited (resistance to activated protein C due to the factor V Leiden mutation; prothrombin G20210A mutation; deficiencies in antithrombin, protein C, and protein S) and acquired (presence of circulating lupus anticoagulants and/or anticardiolipin antibodies; deficiencies of antithrombin and protein S; acquired protein C resistance) markers of thrombophilia. The cost of preventing one thrombotic event in a patient developing severe OHSS after IVF and having factor V Leiden or prothrombin G20210A mutations was calculated.
RESULT(S): None of the OHSS patients or controls had antithrombin, protein C, or free protein S deficiencies. All of them tested negative for antiphospholipid antibodies. No patient in group 1 had the factor V Leiden or prothrombin G20210A mutations. The prothrombin G20210A mutation was detected in 1 out of 40 patients (2.5%) in group 2. Both factor V Leiden and prothrombin G20210A mutations were detected in two of the control subjects (2%) (group 3). The estimated cost of preventing one thrombotic event arising as a consequence of screening for factor V Leiden and prothrombin G20210A mutation is a minimum of 418,970 dollars and 2,430,000 dollars, respectively.
CONCLUSION(S): The prevalence of thrombophilia is not increased in women with severe OHSS. Screening for V Leiden and prothrombin G20210A mutation in an IVF general population is not cost-effective.
确定重度卵巢过度刺激综合征(OHSS)患者中血栓形成倾向标志物的患病率,并评估对接受体外受精(IVF)治疗的女性进行凝血因子V莱顿突变和凝血酶原G20210A突变筛查的成本效益。
病例对照研究和成本效益分析。
大学教学医院。
接受IVF控制性卵巢过度刺激并并发重度OHSS的女性(第1组,n = 20);接受IVF控制性卵巢过度刺激但未发生重度OHSS的女性(第2组,n = 40);健康对照者(第3组,n = 100)。
调查血栓形成倾向标志物。根据现有数据计算检测1例与血栓形成倾向基因突变相关的重度OHSS和血栓形成所需的IVF患者数量。
分析血样中的遗传性(因凝血因子V莱顿突变导致的对活化蛋白C抵抗;凝血酶原G20210A突变;抗凝血酶、蛋白C和蛋白S缺乏)和获得性(循环狼疮抗凝物和/或抗心磷脂抗体的存在;抗凝血酶和蛋白S缺乏;获得性蛋白C抵抗)血栓形成倾向标志物。计算预防IVF后发生重度OHSS且有凝血因子V莱顿或凝血酶原G20210A突变的患者发生1次血栓事件的成本。
OHSS患者或对照组中均无抗凝血酶、蛋白C或游离蛋白S缺乏。所有患者抗磷脂抗体检测均为阴性。第1组中无患者有凝血因子V莱顿或凝血酶原G20210A突变。第2组40例患者中有1例(2.5%)检测到凝血酶原G20210A突变。第3组(对照组)的2名受试者(2%)检测到凝血因子V莱顿和凝血酶原G20210A突变。因筛查凝血因子V莱顿和凝血酶原G20210A突变预防1次血栓事件的估计成本分别至少为418,970美元和2,430,000美元。
重度OHSS女性中血栓形成倾向的患病率未增加。在IVF普通人群中筛查凝血因子V莱顿和凝血酶原G20210A突变不具有成本效益。