Department of Otorhinolaryngology, Head and Neck Surgery, Skane University Hospital, Lund, Sweden.
Division of ENT Diseases, Department of Clinical Sciences, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden.
Sci Rep. 2023 Nov 10;13(1):19649. doi: 10.1038/s41598-023-46869-4.
Intramuscular injections with methylprednisolone treating allergic rhinitis (AR) have a long history. Modern guidelines are designed to dissuade this treatment, but it´s frequently used, especially in primary care. This despite of concern for side effects and lack of modern placebo-controlled studies. This study was designed to evaluate if methylprednisolone, could significantly improve symptoms of birch pollen induced AR and reduce the concomitant use of standard of care medication. Forty-two patients with birch pollen induced AR were randomized to treatment with methylprednisolone (80 mg) or placebo (NaCl 0.9%). Daily symptom- and medication scores was registered for 3 weeks. Quality of life questionnaires Sino-nasal Outcome Test-22 (SNOT-22) and Juniper Rhinoconjunctivitis Quality of Life Questionaire (Juniper RQLQ) were registered at trial start and at the end of the 3 weeks period. The combined symptom- and medication scores indicate that the methylprednisolone treated group [mean Area Under the Curve (AUC) 37.1 (SD 16.2 (95% CI 29.9-44.6))] was significantly better off than the placebo group [mean AUC 49.1 (SD 10.1 (95% CI 44.5-53.7))], p = 0.008. No significant difference between the groups were found in the SNOT-22 and Juniper RQLQ analysis. Registered side effects were few and mild. The limited beneficial effects of systemic steroids when added to standard of care in combination of its potential risk for side effects, speaks against its use for treatment of severe seasonal allergic rhinitis. The lack of difference in quality-of-life further underscores this result.
肌肉内注射甲基强的松龙治疗过敏性鼻炎(AR)已有很长的历史。现代指南旨在劝阻这种治疗方法,但它经常被使用,尤其是在初级保健中。尽管人们担心副作用和缺乏现代安慰剂对照研究。本研究旨在评估甲基强的松龙是否能显著改善桦树花粉诱导的 AR 症状,并减少标准护理药物的同时使用。42 例桦树花粉诱导的 AR 患者随机分为甲基强的松龙(80mg)或安慰剂(0.9%NaCl)治疗组。登记了 3 周的每日症状和药物评分。在试验开始和 3 周结束时,登记了 Sino-nasal Outcome Test-22(SNOT-22)和 Juniper Rhinoconjunctivitis Quality of Life Questionnaire(Juniper RQLQ)的生活质量问卷。综合症状和药物评分表明,甲基强的松龙治疗组[平均 AUC 37.1(SD 16.2(95%CI 29.9-44.6))]明显优于安慰剂组[平均 AUC 49.1(SD 10.1(95%CI 44.5-53.7))],p=0.008。在 SNOT-22 和 Juniper RQLQ 分析中,两组之间没有发现显著差异。登记的副作用很少且轻微。当与标准护理联合使用时,全身类固醇的有限有益作用及其潜在的副作用风险,反对将其用于治疗严重的季节性过敏性鼻炎。生活质量的差异进一步强调了这一结果。