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星状神经节阻滞治疗嗅觉障碍患者的长期疗效。

Long-term Results of Stellate Ganglion Block in Patients with Olfactory Dysfunction.

机构信息

Department of Anesthesiology and Pain Medicine, College of Medicine, The Catholic University of Korea, Seoul, Korea.

出版信息

Korean J Pain. 2013 Jan;26(1):57-61. doi: 10.3344/kjp.2013.26.1.57. Epub 2013 Jan 4.

Abstract

BACKGROUND

Olfactory dysfunction, including anosmia and hyposmia is difficult to treat. Although the mechanism is not well known, stellate ganglion block (SGB) is used to treat olfactory dysfunction. There are no prior studies on the long-term effects of SGB on olfactory dysfunction. The purpose of this study was to evaluate the continuity of therapeutic effects and patient satisfaction with SGB treatment.

METHODS

This was a follow-up study carried out via a telephonic survey. The olfactory function of the patient was evaluated using a visual analog scale (VAS). We checked VAS three times: VAS-I (pre-treatment VAS), VAS-A (post-treatment VAS), and VAS-C (VAS at follow up telephone survey). We divided the subjects into 2 groups according to their responsiveness to SGB: the responsive (R group) and the unresponsive groups (UR group). Patient satisfaction was evaluated using a Likert scale.

RESULTS

Out of the 40 subjects, 37 responded to the telephone survey. In the UR group, there was difference in the olfactory function. However, in the R group, there were significant VAS differences; VAS-I was 9.6 ± 0.7, VAS-A was 5.1 ± 4.2, and VAS-C was 2.7 ± 2.7 (P < 0.05). On the Likert scale, patient satisfaction was as follows: grade 1, 17 patients (45.9%); grade 2, 6 patients (16.2%); grade 3, 6 patients (16.2%); and grade 4, 8 patients (21.6%).

CONCLUSIONS

SGB is a safe, long-lasting, and effective therapeutic modality for olfactory dysfunction treatment.

摘要

背景

嗅觉功能障碍,包括嗅觉丧失和嗅觉减退,难以治疗。虽然其机制尚不清楚,但星状神经节阻滞(SGB)被用于治疗嗅觉功能障碍。目前尚无关于 SGB 对嗅觉功能障碍的长期疗效的研究。本研究旨在评估 SGB 治疗嗅觉功能障碍的疗效持续性和患者满意度。

方法

这是一项通过电话调查进行的随访研究。使用视觉模拟量表(VAS)评估患者的嗅觉功能。我们检查了 VAS 三次:VAS-I(治疗前 VAS)、VAS-A(治疗后 VAS)和 VAS-C(随访电话调查时的 VAS)。我们根据患者对 SGB 的反应将患者分为两组:有反应组(R 组)和无反应组(UR 组)。使用李克特量表评估患者满意度。

结果

在 40 名患者中,有 37 名患者回应了电话调查。在 UR 组中,嗅觉功能存在差异。然而,在 R 组中,VAS 存在显著差异;VAS-I 为 9.6 ± 0.7,VAS-A 为 5.1 ± 4.2,VAS-C 为 2.7 ± 2.7(P < 0.05)。在李克特量表上,患者满意度如下:1 级,17 名患者(45.9%);2 级,6 名患者(16.2%);3 级,6 名患者(16.2%);4 级,8 名患者(21.6%)。

结论

SGB 是一种安全、持久且有效的治疗嗅觉功能障碍的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61ec/3546212/ac253f218568/kjpain-26-57-g001.jpg

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