澳大利亚北部地区侵袭性A组链球菌病的社会环境和临床特征。

Q3 Medicine
Johanna M Birrell, Bart J Currie, Asanga Abeyaratne, Sandawana William Majoni, Rowena Boyd
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引用次数: 0

摘要

目的描述10年来澳大利亚北领地(NT)侵袭性A群链球菌(iGAS)感染的社会环境特征和临床特征。方法从NT法定疾病系统和电子健康记录中回顾性鉴定2011年5月1日至2021年4月30日期间诊断的iGAS疾病病例。记录居住的偏远程度、社会经济指数、季节性和临床特征。结果2011年5月1日至2021年4月30日期间,NT共发现692例iGAS疾病。iGAS疾病的年龄标准化发病率在生活在非常偏远地区(每100000人57.1例,95%置信区间[95%CI]:48.6-65.5)和偏远地区(每个100000人40.9例,95%CI:34.7-4.7.2)的人群中显著高于NT的外部地区(每10万人15.7例,95%CI:13.4-17.9)同样受到不成比例的影响,1-3分位数人群的发病率为52.6例/10万人(95%CI:46.2-5.89),而7-10分位数人群为8.9例/10万人口(95%CI:6.9-10.9)。对于有记录严重程度数据的病例,378例中有135例(36%)符合当地定义的严重iGAS疾病标准。在透析队列中经常观察到复发性iGAS疾病,在研究期间影响了106名患者中的17名(复发率为16%),并导致两人死亡。从研究期间鉴定出五个分子证实的iGAS疾病簇。结论iGAS疾病对NT人群的影响不均衡。生活在社会经济劣势地区的人群、偏远和非常偏远社区的人群以及接受透析的人群受到的影响最大。重要的是,初级、初级和二级预防措施应针对支持这些弱势群体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Socio-environmental and clinical features of invasive group A streptococcal disease in the Northern Territory of Australia.

Objective: To describe the socio-environmental profile and clinical features of invasive group A streptococcal (iGAS) infections in the Northern Territory (NT) of Australia over 10 years.

Methods: Cases of iGAS disease diagnosed between 1 May 2011 and 30 April 2021 were retrospectively identified from the NT Notifiable Diseases System and electronic health records accessed. Remoteness of residence, socio-economic index, seasonality and clinical characteristics were recorded.

Results: There were 692 cases of iGAS disease identified in the NT during the period 1 May 2011 - 30 April 2021. The age-standardised incidence of iGAS disease was significantly higher in people living in very remote (57.1 cases per 100,000 population, 95% confidence interval [95% CI]: 48.6-65.5) and remote areas (40.9 cases per 100,000 population, 95% CI: 34.7-47.2) than in outer regional areas of the NT (15.7 cases per 100,000 population, 95% CI: 13.4-17.9). People with socio-economic disadvantage were also disproportionately affected, with an incidence of 52.6 cases per 100,000 population (95% CI: 46.2-58.9) in decile 1-3 populations, compared to 8.9 cases per 100,000 population (95% CI: 6.9-10.9) for decile 7-10. For cases with recorded severity data, 135 of 378 (36%) met locally-defined criteria for severe iGAS disease. Recurrent iGAS disease was commonly observed in the dialysis cohort, affecting 17 of the 106 patients during the study period (16% recurrence rate) and causing two deaths. Five molecularly-confirmed clusters of iGAS disease were identified from the study period.

Conclusions: iGAS disease is unevenly affecting people in the NT. Those living in areas of socio-economic disadvantage, those in remote and very remote communities, and those receiving dialysis were most affected. It is important that primordial, primary and secondary prevention measures be directed towards supporting these disadvantaged population groups.

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