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首页> 外文期刊>Otology and neurotology: official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology >Longitudinal results of intratympanic injection of budesonide for Otitis media with effusion in children over 12 years and adults
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Longitudinal results of intratympanic injection of budesonide for Otitis media with effusion in children over 12 years and adults

机译:鼓膜内注射布地奈德治疗12岁以上儿童和成人中耳炎的纵向结果

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OBJECTIVE: To assess the longitudinal curative effect and improvement of subjective symptoms by using intratympanic injection of Budesonide(BUD) for otitis media with effusion (OME) patients older than 12 years and adults. STUDY DESIGN: A single-blind, randomized, parallel-controlled prospective study. SETTING: Hospital, outpatient. PATIENTS: Ninety patients (112 ears) who were diagnosed as having OME were recruited and then randomized to BUD, dexamethasone (DEX), and sodium chloride (NS) groups, the latter two served as controls. INTERVENTIONS: The randomly allocated patients received intratympanic injection of BUD (0.5 mg/1 ml), DEX (2 mg/1 ml), or 0.9% NS solution (1 ml) once a week. MAIN OUTCOME MEASURES: Survival analysis was applied to compare the longitudinal curative effects among the 3 groups. Meanwhile, the 6 main subjective symptoms were scored by 10-point visual scale, and physician's evaluations were preformed during treatment and follow-up. RESULTS: After adjustment for course of disease, volume, and characters of effusion, the relative risk (RR) of BUD is 0.139 (95% CI, 0.054-0.358) when compared with NS. Survival curve demonstrated that the rank of longitudinal therapeutic efficacy was BUD, DEX, and NS (p < 0.05). Both BUD and DEX showed improvements in subjective symptoms and quality of life compared with NS (p < 0.05). In the aspect of improving the symptom of stuffy ear, BUD showed advantage over both DEX and NS. During and after treatment, no serious complications or sequelae were observed. CONCLUSION: Intratympanic injection with BUD for OME patients showed advantages in improving long-term therapeutic efficacy, it was a safe and effective intervention for adolescents and adults with OME.
机译:目的:通过鼓膜内注射布地奈德(BUD)治疗12岁以上成人渗出性中耳炎(OME)患者,评估纵向治疗效果和主观症状的改善。研究设计:单盲,随机,平行对照的前瞻性研究。地点:医院,门诊。患者:招募了90名被诊断患有OME的患者(112耳),然后随机分为BUD,地塞米松(DEX)和氯化钠(NS)组,后两组作为对照组。干预措施:随机分配的患者每周一次接受鼓膜内注射BUD(0.5 mg / 1 ml),DEX(2 mg / 1 ml)或0.9%NS溶液(1 ml)。主要观察指标:采用生存分析比较3组患者的纵向疗效。同时,通过10点视觉量表对6个主要主观症状进行评分,并在治疗和随访期间进行医师评估。结果:在调整了病程,数量和积液特征后,与NS相比,BUD的相对风险(RR)为0.139(95%CI,0.054-0.358)。生存曲线表明,纵向治疗效果的等级为BUD,DEX和NS(p <0.05)。与NS相比,BUD和DEX均显示出主观症状和生活质量的改善(p <0.05)。在改善闷耳症状方面,BUD优于DEX和NS。在治疗期间和之后,未观察到严重的并发症或后遗症。结论:鼓膜腔内注射BUD对OME患者具有改善长期治疗效果的优势,对于青少年和成人OME是一种安全有效的干预措施。

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