UOSD Spine Surgery, AOU Consorziale Policlinico di Bari, Piazza Giulio Cesare 11, 70124, Bari, Italy.
Department of Spine Surgery, IRCCS Istituto Ortopedico Rizzoli, Bologna, Italy.
J Orthop Traumatol. 2024 Apr 15;25(1):17. doi: 10.1186/s10195-024-00758-2.
Capacitively coupling electric fields (CCEF) is a method of non-invasive biophysical stimulation that enhances fracture repair and spinal fusion. This multicentre randomized controlled trial aimed to further examine the roles of CCEF in (1) the resolution of vertebral bone marrow oedema (VBME) using a follow-up MRI study and (2) pain relief, analgesic drug consumption and quality of life improvement in stimulated patients who were referred with acute vertebral fragility fractures (VFFs) compared to non-stimulated patients.
Between September 2016 and December 2019, patients who were referred to the spine centres that participated in this multicentre randomized clinical study with acute VFFs of type OF1 or OF2 were included in the present study. All the VFFs were conservatively managed according to Good Clinical Practice. Moreover, the patients were randomized into two groups: the CCEF group received, as an adjunct to the clinical study protocol, biophysical stimulation with a CCEF device (Osteospine, IGEA) for 8 h per day for 60 days, whereas the control group was treated according to the clinical study protocol. At baseline (T0), the 30-day follow-up (T1), the 60-day follow-up (T2), and the 6-month follow-up (T3), each patient underwent clinical evaluation using the Visual Analogue Scale (VAS) for Pain and the Oswestry Disability Index (ODI). Analgesic therapy with paracetamol 1000 mg tablets for 7 days-or longer, depending on the pain intensity-was performed; patients were required to report their paracetamol consumption on a specific sheet between study day 8 to 180 days of follow-up. MRI studies of the thoracolumbar spine were performed at 0 (T0), 30 (T1) and 60 days of follow-up (T2) using a 1.5-T MRI system in all of the centres that took part in the study. For each VBME area examined via MRI, the vertebral body geometry (i.e. anterior wall height/posterior wall height and vertebral kyphosis) were assessed.
A total of 66 patients (male: 9, 13.63%; mean age: 73.15 years old) with 69 VFFs were included in the present study and randomized as follows: 33 patients were included in the control group and the remaining 33 patients were randomized into the CCEF group. In the CCEF group, good compliance with CCEF therapy was observed (adherence = 94%), and no adverse effects were recorded. In the stimulated patients, faster VBME resolution and significantly less vertebral body collapse during follow-up were observed compared to the control patients. Moreover, in the active group, faster pain reduction and improvement in the ODI mean score were observed. Stimulated patients also reported a significantly lower paracetamol consumption rate from the third follow-up after treatment until the 6-month follow-up. In terms of sex-related differences, in the CCEF group, VBME showed a faster resolution in male patients compared with females.
Biophysical stimulation with CCEF, as an adjunct to traditional conservative treatment, is a useful tool to hasten the VBME resolution process and prevent vertebral body deformation. These MRI findings also correlate with faster back pain resolution and quality of life improvement. From the third follow-up after treatment until the 6-month follow-up, stimulated patients reported a significantly lower paracetamol consumption than control patients, even though back pain and quality of life showed no significant differences between the two groups.
II. Trial Registration Register: ClinicalTrials.gov, number: NCT05803681.
电容耦合电场 (CCEF) 是一种非侵入性生物物理刺激方法,可增强骨折修复和脊柱融合。这项多中心随机对照试验旨在进一步研究 CCEF 在以下方面的作用:(1) 使用后续 MRI 研究解决椎骨骨髓水肿 (VBME),以及 (2) 在接受急性椎体脆性骨折 (VFF) 的刺激患者中缓解疼痛、减少镇痛药消耗和改善生活质量,与未接受刺激的患者相比。
2016 年 9 月至 2019 年 12 月,参与这项多中心随机临床试验的脊柱中心收治了 OF1 或 OF2 型急性 VFF 的患者,将其纳入本研究。所有 VFF 均根据良好临床实践进行保守治疗。此外,患者被随机分为两组:CCEF 组接受 CCEF 设备(Osteospine,IGEA)进行 8 小时/天、60 天的生物物理刺激作为辅助治疗,而对照组则根据临床研究方案进行治疗。在基线(T0)、30 天随访(T1)、60 天随访(T2)和 6 个月随访(T3)时,每位患者均使用视觉模拟量表(VAS)进行疼痛评估和 Oswestry 残疾指数(ODI)评估。根据疼痛强度,使用扑热息痛 1000mg 片剂进行 7 天或更长时间的镇痛治疗;患者需要在研究第 8 天至 180 天的随访期间在特定表上报告扑热息痛的消耗量。所有参与研究的中心均使用 1.5-T MRI 系统在 0(T0)、30(T1)和 60 天随访(T2)时进行胸腰椎 MRI 研究。对于通过 MRI 检查的每个 VBME 区域,评估椎体几何形状(即前壁高度/后壁高度和椎体后凸)。
共有 66 名患者(男性 9 名,占 13.63%;平均年龄 73.15 岁)和 69 个 VFF 被纳入本研究并随机分组如下:33 名患者被纳入对照组,其余 33 名患者被随机分为 CCEF 组。在 CCEF 组中,观察到 CCEF 治疗的良好依从性(依从性=94%),没有记录到不良反应。在接受刺激的患者中,与对照组患者相比,VBME 更快得到解决,椎体塌陷在随访过程中明显减少。此外,在活跃组中,疼痛减轻和 ODI 平均评分的改善更快。接受刺激的患者还报告说,从治疗后的第三次随访开始,直到 6 个月的随访,扑热息痛的消耗量明显降低。就性别相关差异而言,在 CCEF 组中,男性患者的 VBME 比女性患者更快得到解决。
CCEF 作为传统保守治疗的辅助手段,进行生物物理刺激是一种有用的工具,可以加速 VBME 解决过程并防止椎体变形。这些 MRI 发现还与更快的背痛缓解和生活质量改善相关。从治疗后的第三次随访开始,直到 6 个月的随访,接受刺激的患者报告的扑热息痛消耗量明显低于对照组患者,尽管两组患者的背痛和生活质量没有显著差异。
II。试验注册:ClinicalTrials.gov,编号:NCT05803681。