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随机临床试验“COVID-19 后的嗅觉功能障碍:棕榈酸乙醇酰胺和芦丁嗅觉康复治疗与干预治疗的比较”:初步结果。

Randomized clinical trial "olfactory dysfunction after COVID-19: olfactory rehabilitation therapy vs. intervention treatment with Palmitoylethanolamide and Luteolin": preliminary results.

机构信息

Department of Head and Neck Surgery, Institute of Otorhinolaryngology, Santa Croce Hospital AORMN, Fano, Italy.

出版信息

Eur Rev Med Pharmacol Sci. 2021 Jun;25(11):4156-4162. doi: 10.26355/eurrev_202106_26059.

Abstract

OBJECTIVE

Approximately 30% of patients with confirmed COVID-19 report persistent smell or taste disorders as long-term sequalae of infection. Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) infection is associated with inflammatory changes to the olfactory bulb, and treatments with anti-inflammatory properties are hypothesized to attenuate viral injury and promote recovery of olfaction after infection. Our study investigated the efficacy of a supplement with Palmitoylethanolamide (PEA) and Luteolin to support recovery of olfaction in COVID-19 patients.

PATIENTS AND METHODS

We conducted a randomized-controlled pilot study in outpatients with history of confirmed COVID-19 with post-infection olfactory impairment that persisted ≥ 90 days after SARS-CoV-2 negative testing. Patients were randomized to two times a day olfactory rehabilitation alone or weekly olfactory rehabilitation plus daily oral supplement with PEA and Luteolin. Subjects with preexisting olfactory disorders were excluded. Sniffin' Sticks assessments were performed at baseline and 30 days after treatment.  Data on gender, age, and time since infection were collected. Kruskal-Wallis (KW) test was used to compare variances of Sniff scores between groups over time, and Spearman's correlation coefficients were calculated to assess for correlations between Sniff Score and gender or duration of infection.

RESULTS

Among 12 patients enrolled (n=7, supplement; n=5, controls), patients receiving supplement had greater improvement in olfactory threshold, discrimination, and identification score versus controls (p=0.01). Time since infection was negatively correlated with Sniff Score, and there was no correlation between gender.

CONCLUSIONS

Treatment combining olfactory rehabilitation with oral supplementation with PEA and Luteolin was associated with improved recovery of olfactory function, most marked in those patients with longstanding olfactory dysfunction. Further studies are necessary to replicate these findings and to determine whether early intervention including olfactory rehabilitation and PEA+Luteolin oral supplement might prevent SARS-CoV-2 associated olfactory impairment.

摘要

目的

约 30%的确诊 COVID-19 患者报告称,感染后长期存在嗅觉或味觉障碍等后遗症。严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)感染与嗅球的炎症变化有关,具有抗炎特性的治疗方法被假设可以减轻病毒损伤并促进感染后嗅觉的恢复。我们的研究调查了含有棕榈酸乙醇酰胺(PEA)和木樨草素的补充剂治疗 COVID-19 患者嗅觉恢复的疗效。

患者和方法

我们对有确诊 COVID-19 病史且在 SARS-CoV-2 检测阴性后持续≥90 天出现感染后嗅觉障碍的门诊患者进行了一项随机对照的初步研究。患者被随机分为两组,每天两次进行嗅觉康复治疗或每周进行嗅觉康复治疗加每日口服 PEA 和木樨草素补充剂。排除有嗅觉障碍的患者。在基线和治疗 30 天后进行 Sniffin' Sticks 评估。收集了性别、年龄和感染时间的数据。Kruskal-Wallis(KW)检验用于比较不同组间随时间变化的嗅探评分方差,Spearman 相关系数用于评估嗅探评分与性别或感染持续时间之间的相关性。

结果

在纳入的 12 名患者中(补充组 n=7,对照组 n=5),与对照组相比,接受补充剂的患者在嗅觉阈值、辨别和识别评分方面的改善更大(p=0.01)。感染时间与嗅探评分呈负相关,性别之间无相关性。

结论

将嗅觉康复与口服 PEA 和木樨草素补充剂相结合的治疗方法与嗅觉功能的恢复有关,在长期存在嗅觉障碍的患者中更为明显。需要进一步的研究来复制这些发现,并确定是否包括嗅觉康复和 PEA+木樨草素口服补充在内的早期干预措施可能预防 SARS-CoV-2 相关的嗅觉障碍。

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