Clinical Course and Prognosis of Acute Rheumatic Fever with Carditis in Six Patients

Takumi Ishiodori, H. Horigome, Yusuke Yano, Y. Shima, Yoshihiro Nozaki, N. Ishikawa, Lisheng Lin, M. Takahashi, Takashi Murakami, J. Shiono, H. Takada
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Abstract

Background : In recent years, acute rheumatic fever (ARF) has been considered an extremely rare condition in Japan, with an incidence of 5 ‒ 10 cases annually. However, it should be recognized as a serious illness because some patients may develop heart failure (HF) if diagnosis and treatment are delayed. Methods : The clinical course and prognoses of ARF with carditis in six patients ( n = 3 women) diagnosed in our institutions from 1994 to 2018 were investigated by retrospectively reviewing medical records. Results : The age at diagnosis was 3 ‒ 13 (median: 8.5) years. The symptoms at onset were fever and arthralgia/ arthritis in four, arthralgia/arthritis alone in one, and shortness of breath and fatigability due to HF in one patient. The duration from the initial presentation to the diagnosis of ARF ranged from 3 days to 4 years and 10 months (median: 11.5 days). None of the patients presented with major symptoms other than carditis and polyarthritis based on the revised Jones Criteria. Similar to valvulitis, aortic valve regurgitation (AR), mitral regurgitation (MR), and both AR and MR were observed in 5, 3, and 2 cases, respectively. The patients were treated with prednisolone and/or aspirin and antibiotics (provided as prophylaxis drugs). During follow-up (range: 1 ‒ 15 [median: 9] years), MR almost disappeared; however, AR remained. Moreover, aortic valve replacement was required in two cases, and recurrence of ARF was not noted. Conclusion : In this study, arthritis-related symptoms were more likely to be observed during the initial presentation, and the diagnosis of carditis was delayed, resulting in a critical clinical course in some cases. Patients with streptococcal infection-related polyarthritis should be screened for carditis by a pediatric cardiologist.
急性风湿热合并心炎6例临床病程及预后分析
背景:近年来,急性风湿热(ARF)在日本被认为是一种极其罕见的疾病,每年的发病率为5 - 10例。然而,它应该被视为一种严重的疾病,因为如果诊断和治疗延迟,一些患者可能会发展为心力衰竭(HF)。方法:回顾性分析1994年至2018年我院诊断的6例ARF合并心炎患者(n = 3名女性)的临床病程和预后。结果:诊断年龄3 ~ 13岁,中位8.5岁。4例患者发病时出现发热和关节痛/关节炎,1例患者仅出现关节痛/关节炎,1例患者因心衰导致呼吸急促和疲劳。从最初出现到ARF诊断的时间从3天到4年零10个月不等(中位数:11.5天)。根据修订后的琼斯标准,除心炎和多发性关节炎外,所有患者均无其他主要症状。与瓣膜炎相似,主动脉瓣反流(AR) 5例,二尖瓣反流(MR) 3例,AR和MR均有2例。患者接受泼尼松龙和/或阿司匹林和抗生素治疗(作为预防药物提供)。随访期间(1 ~ 15年[中位9]年),MR几乎消失;然而,AR仍然存在。此外,有2例患者需要主动脉瓣置换术,未发现ARF复发。结论:在本研究中,关节炎相关症状在首发时更容易被观察到,导致心炎的诊断延迟,导致一些病例出现关键的临床病程。患有链球菌感染相关的多发性关节炎的患者应该接受儿科心脏病专家的心脏炎筛查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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