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The posterolateral fluoroscopy-guided injection technique into the posterior subtalar joint: description of the procedure and pilot study on patient outcomes

机译:后侧透视引导下距下sub骨关节下注射技术:对过程的描述以及对患者预后的初步研究

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摘要

Objective To describe a posterolateral fluoroscopy-guided\udinjection technique into the posterior subtalar joint and to\udreport patient outcomes 1 month post-injection.\udMaterials and methods Twenty-three consecutive adult\udpatients who underwent fluoroscopy-guided injection into\udthe posterior subtalar joint using a direct posterolateral\udapproach and who returned an outcomes-based postal\udquestionnaire after receiving this injection were included.\udNumerical pain rating scale (NRS) data were collected prior\udto injection. NRS and Patient’s Global Impression of\udChange (PGIC) scales were completed 1 day, 1 week, and\ud1 month after injection. The proportion of patients who\udimproved was calculated for each time period. Baseline\udNRS data were compared to each time point using the\udWilcoxon test to assess differences. Spearman’s correlation\udcoefficient was used to compare the 20 min NRS score with\udall follow-up NRS scores. All available images were\udreviewed for the presence of subtalar osteoarthritis (OA).\udPatient charts were reviewed to identify characteristics of\udpatients referred for subtalar injections. Risk ratios were\udcalculated comparing presence of OA or other abnormalities\udwith improvement.\udResults A posterolateral approach for fluoroscopy-guided\udinjections into the subtalar joint is described. There was a\udsignificant reduction in the mean NRS score at all time\udperiods compared to baseline (p ≤ 0.004). One-third of\udpatients (7/21) reported clinically relevant improvement at\ud1 month.\udConclusions Fluoroscopy-guided puncture of the posterior\udsubtalar joint using a posterolateral approach is possible.\udClinically significant improvement is reported in 33% of\udpatients after 1 month.
机译:目的描述在后距骨下关节后路透视引导下的注胶技术,并在注射后1个月报告患者的预后。材料和方法二十三名连续的成人患者在透视后距骨下注药。包括使用直接后外侧\ udapproach的关节,并在接受此注射后返回基于结果的邮政\ udquestionnaire。\ ud在\ udud注射前收集了疼痛数字量表(NRS)。注射后1天,1周和\ ud1个月完成了NRS和患者的udChange全球印象(PGIC)量表。在每个时间段计算\ dimproved的患者比例。使用\ udWilcoxon检验将基线\ udNRS数据与每个时间点进行比较,以评估差异。 Spearman的相关性\ udcoefficient用于比较20分钟的NRS得分和\ udall随访的NRS得分。对所有可用的图像进行了\ udreview检查是否存在距下骨关节炎(OA)。\ ud患者的病历经过检查,以确定\ taltalal注射转诊患者的特征。通过比较OA的存在或其他异常的发生率来计算风险比率\改善情况。\ ud结果描述了一种后外侧方法,用于透视引导下\距下关节的注射。与基线相比,所有时间\结束时的NRS平均得分均显着降低(p≤0.004)。 \ ud1的患者中有三分之一(7/21)在ud1个月时报告了临床相关的改善。\ ud结论使用后外侧方法在透视下引导穿刺距后距/距下距的关节是可行的。\ ud临床上有显着改善的患者占33%\ 1个月后接受急诊。

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