Hörterer Hubert, Baumbach Sebastian Felix, Gregersen Johanne, Kriegelstein Stefanie, Gottschalk Oliver, Szeimies Ulrike, Walther Markus
1 Schön Klinik München Harlaching, Center for Foot and Ankle Surgery, Munich, Germany.
2 Paracelsus Medical Private University, Salzburg, Austria.
Foot Ankle Int. 2018 Oct;39(10):1183-1191. doi: 10.1177/1071100718778557. Epub 2018 Jun 4.
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.
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.
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.
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 III, comparative study.
足踝部骨髓水肿(BME)的治疗颇具挑战性。一种治疗方法是静脉注射伊洛前列素,它是一种血管活性前列环素类似物。本研究的目的是评估静脉注射伊洛前列素治疗足踝部骨髓水肿的早期和中期疗效,并分析其病因和骨循环研究协会(ARCO)分期对疗效的影响。
这是一项具有前瞻性随访的回顾性研究。纳入了在单一骨科参考中心接受静脉注射伊洛前列素治疗足踝部骨髓水肿(ARCO I - III期)的所有患者。在治疗前(t0)评估患者的人口统计学资料、病史和磁共振成像(MRI)。MRI用于评估骨髓水肿的病因(特发性/缺血性/代谢性、机械性/退行性、创伤性)和严重程度(ARCO分期)。在3个月后(t1)评估并发症以及疼痛、治疗和MRI的变化。前瞻性评估以下患者自评结局指标(PROMs)(t2):12项简短健康调查问卷(SF - 12)、足踝视觉模拟量表(VAS FA)和足功能指数(FFI)(也在t0时评估)。评估描述性结局以及病因和ARCO分期对结局参数的影响。在70例符合条件的患者中,纳入了42例患者(60%;年龄47±15岁;30%为女性),平均随访时间为28±19个月。
12例患者在伊洛前列素治疗期间报告有轻微并发症。在t1时,56%的患者疼痛显著减轻,83%的患者骨髓水肿量减少。这两个参数呈中度相关(r = -0.463,P = 0.015)。t2时的患者自评结局指标显示结果中等。总体FFI从59±21改善至30±22(P < 0.001),总体VAS FA为68±20,SF - 12身体成分总结评分为42±12,精神成分总结评分为50±9。亚组分析显示病因或ARCO分期对任何结局指标均无显著影响。
足踝部骨髓水肿的伊洛前列素治疗在3个月后使疼痛减轻60%,水肿减轻80%。2年后,患者自评结局指标显示仍有残余功能障碍。病因和ARCO分期均未对结局产生显著影响。
III级,比较性研究。