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Treatment of Bone Marrow Edema of the Foot and Ankle With the Prostacyclin Analog Iloprost

机译:用前列环素类似ILOPROST治疗脚和踝关节和踝关节的骨髓水肿

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Background: Bone marrow edema (BME) of the foot and ankle is challenging to treat. One approach is intravenous Iloprost treatment, which is a vasoactive prostacyclin analog. The aim of this study was to evaluate the early and intermediate outcome of intravenous Iloprost therapy on BME of the foot and ankle and to analyze the influence of its etiology and Association Research Circulation Osseous (ARCO) stage on the outcome. Methods: This was a retrospective study with prospective follow-up. All patients treated by intravenous Iloprost for BME of the foot and ankle (ARCO I-III) at a single orthopedic reference center were included. Demographics, medical history, and MRIs were assessed prior to treatment (t0). MRIs were used to assess the BMEs’ etiology (idiopathic/ischemic/metabolic, mechanical/degenerative, traumatic) and severity (ARCO). Complications as well as changes in pain, treatment, and MRI were evaluated after 3 months (t1). The following patient-rated outcome measures (PROMs) were assessed prospectively (t2): 12-Item Short Form Health Survey (SF-12), Visual Analog Scale Foot and Ankle (VAS FA), and the Foot Function Index (FFI) (also at t0). The descriptive outcomes and the influence of the etiology and ARCO on the outcome parameters were evaluated. Out of 70 eligible patients, 42 patients (60%; 47 ± 15 years; 30% female) with a mean follow-up of 28 ± 19 months were included. Results: Twelve patients reported minor complications during Iloprost therapy. At t1, pain decreased significantly in 56%, and the amount of BME decreased in 83% of patients. Both parameters correlated moderately (r = ?0.463, P = .015). The PROMs at t2 revealed moderate results. The overall FFI improved from 59 ± 21 to 30 ± 22 ( P < .001), the overall VAS FA was 68 ± 20, the SF-12 Physical Component Summary 42 ± 12 and Mental Component Summary 50 ± 9. Subgroup analysis revealed no significant influence of the etiology or ARCO stage on any outcome measure. Conclusion: Iloprost therapy for BME of the foot and ankle resulted in a 60% pain and 80% edema decrease after 3 months. After 2 years, patient-rated outcome measures showed residual impairment. Neither the etiology nor ARCO stage significantly influenced the outcome. Level of Evidence: Level III, comparative study.
机译:背景:脚和脚踝的骨髓水肿(BME)是挑战治疗。一种方法是静脉内伊洛普斯特治疗,即血管活性前列腺类别。本研究的目的是评估徒步和脚踝BME静脉内钛合体治疗的早期和中间结果,并分析其病因和关联研究循环骨质(ARCO)阶段对结果的影响。方法:这是一个具有前瞻性随访的回顾性研究。包括脚内伊洛替洛斯科(Arco I-III)在单个整形外科参考中心治疗的所有患者均受静脉和踝关节(ARCO I-III)治疗。在治疗之前评估人口统计,病史和MRIS(T0)。 MRIS用于评估BMES的病因(特发性/缺血性/代谢,机械/退行性,创伤)和严重程度(ARCO)。 3个月后评估并发症以及疼痛,治疗和MRI的变化进行评估(T1)。预期评估以下患者额定的结果措施(PROMS)(T2):12项短型健康调查(SF-12),视觉模拟尺寸脚和脚踝(VAS FA)和脚功能指数(FFI)(也在t0)。评估了描述性结果和病因和ARCO对结果参数的影响。除了70名符合条件的患者中,42名患者(60%; 47±15岁; 30%女性)包括28±19个月的平均随访。结果:12名患者报告了ILOPROST治疗过程中的次要并发症。在T1,疼痛在56%下显着下降,患者的83%的BME含量下降。两个参数适度相关(r = 0.463,p = .015)。 T2的PROM揭示了中等结果。总体FFI从59±21到30±22增加(p <.001),整体VAS FA为68±20,SF-12物理成分概要42±12和精神组件概要50±9.亚组分析显示没有病因或ARCO阶段对任何结果措施的重大影响。结论:脚压脚和踝关节的ILOPROST治疗导致60%的疼痛和80%的水肿减少3个月后。经过2年后,患者额定的结果措施显示剩余减值。病因既不明显影响结果。证据水平:第三级,比较研究。

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