Department of Rheumatology/Clinical Immunology, Asclepios-Clinic, 93077 Bad Abbach, Germany.
Rheumatology (Oxford). 2010 Aug;49(8):1479-82. doi: 10.1093/rheumatology/kep424. Epub 2009 Dec 17.
OBJECTIVE: IA injections of SIJs with corticosteroids are often performed in patients suffering from low back pain due to active sacroiliitis. However, SIJ injections are technically demanding, and therefore the clinical outcome of ultrasound-guided corticosteroid SIJ injections was analysed in relation to the accuracy of the injection. METHODS: Ultrasound-guided injections were performed with 40 mg triamcinolone and 0.78 mg gadolinium in 20 SIJ of 14 consecutive patients suffering from active sacroiliitis. Immediately following SIJ injection, MRI scanning was initiated to verify the correct placement of the drug. Clinical outcome of the intervention was determined using a numerical pain rating scale (NRS) at Days 1 and 28. RESULTS: Despite ultrasound guidance, only 8 injections (40%) were exactly positioned into the SIJ space, whereas the other 12 injections (60%) missed the SIJ. However, there were no significant differences observed in the clinical outcome between the IA-injected group and the peri-articular-injected group. There was similar pain relief observed in both groups 24 h and 28 days following the intervention [IA injection group: mean NRS-baseline: 6.8 (range 4-9), NRS-24 h: 4.3 (range 1-7) and NRS-day 28: 3.5 (range 1-5); peri-articular injection group: mean NRS-baseline: 7.0 (range 5-10), NRS-24 h: 4.1 (range 1-10) and NRS-day 28: 4.5 (range 1-8)]. CONCLUSION: These results demonstrate that IA SIJ injections remain technically challenging despite ultrasound guidance. However, peri-articular deposition of triamcinolone appears sufficient for pain and symptom control in patients suffering from active sacroiliitis.
目的:在患有活动性骶髂关节炎的腰痛患者中,常进行骶髂关节内注射皮质类固醇的 IA 注射。然而,骶髂关节注射技术要求较高,因此分析了超声引导下皮质类固醇骶髂关节注射的临床疗效与注射准确性的关系。
方法:对 14 例连续患有活动性骶髂关节炎的患者的 20 个骶髂关节进行了超声引导下注射,每个关节注射 40mg 曲安奈德和 0.78mg 钆。骶髂关节注射后立即开始 MRI 扫描,以验证药物的正确位置。干预后的临床结果采用数字疼痛评分量表(NRS)在第 1 天和第 28 天进行评估。
结果:尽管进行了超声引导,但只有 8 次注射(40%)准确地进入了骶髂关节间隙,而另外 12 次注射(60%)错过了骶髂关节。然而,IA 注射组和关节周围注射组的临床结果没有显著差异。两组在干预后 24 小时和 28 天均有相似的疼痛缓解[IA 注射组:平均 NRS-基线:6.8(范围 4-9),NRS-24 小时:4.3(范围 1-7)和 NRS-第 28 天:3.5(范围 1-5);关节周围注射组:平均 NRS-基线:7.0(范围 5-10),NRS-24 小时:4.1(范围 1-10)和 NRS-第 28 天:4.5(范围 1-8)]。
结论:尽管有超声引导,但 IA 骶髂关节注射仍然具有技术挑战性。然而,在患有活动性骶髂关节炎的患者中,曲安奈德的关节周围沉积似乎足以控制疼痛和症状。
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