在亚急性期基孔肯雅病毒感染患者中,高剂量皮质类固醇缺乏额外的益处

C. A. Muniz Caldas
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摘要

背景:关于治疗亚急性期基孔肯雅病毒(CHIKV)感染以缓解症状的最佳皮质类固醇剂量的科学证据缺乏。目的:本研究旨在评价皮质类固醇治疗亚急性基孔肯雅热的效果。方法:这项前瞻性队列研究涉及在巴西帕尔联邦大学热带医学中心接受治疗的亚急性CHIKV患者。数据收集于2019年1月至2020年1月,收集于患者初诊和复诊两个时间段。由风湿病学家进行体格检查,检查炎症体征的发生,评估疼痛和肿胀关节的数量。结果:共分析65例患者资料,以女性为主(80%),平均年龄53.5±13.5岁,病程50.0±20.8天。在本研究中,75.4%的患者使用皮质类固醇,其中73.8%的患者进展为慢性疾病,26.2%的患者治愈。虽然重新评估咨询显示初始症状有明显改善,但与小于或等于350mg泼尼松的剂量相比,使用超过350mg泼尼松的皮质类固醇累积剂量对结果没有影响。结论:总之,对于亚急性期感染CHIKV的患者,强的松剂量大于350mg不影响预后,应加强在最短时间内以最低剂量使用皮质类固醇的偏好。
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Lack of Additional Benefit with High Doses of Corticosteroids Among Patients with Chikungunya Viral Infection in the Subacute Phase
Background: Scientific evidence regarding the best dose of corticosteroids for the treatment for Chikungunya virus (CHIKV) infection in the subacute phase to relieve symptoms is lacking. Objectives: This study aimed to evaluate the effect of corticosteroid therapy on the treatment of subacute Chikungunya. Methods: This prospective cohort study involved patients with subacute CHIKV treated at the Tropical Medicine Center of Pará Federal University, Brazil. The data were collected between January 2019 and January 2020 during the following two periods: the initial consultation of patients and the return visit. A physical examination, in which the occurrence of inflammatory signs was checked and the number of painful and swollen joints was evaluated, was performed by a rheumatologist. Results: Data from 65 subjects were analysed with a predominance of females (80%), a mean age of 53.5±13.5 years and a disease duration of 50.0±20.8 days. In this study, 75.4% of the patients used corticosteroids, 73.8% of whom progressed to chronic disease and 26.2% of whom were cured. Although the re-evaluation consultation showed evident improvement in the initial symptoms, the use of a cumulative dose of corticosteroids above 350 mg of prednisone did not affect the outcomes compared to doses less than or equal to 350mg of prednisone. Conclusion: In conclusion, for patients infected with CHIKV in the subacute phase, doses of prednisone above 350 mg do not affect the outcome, and the preference for the use of corticosteroids at the lowest dose for the shortest possible time should be reinforced.
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