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根据感染性心内膜炎的微生物学病因的时间变化、患者特征和死亡率:一项全国性研究。

Temporal Changes, Patient Characteristics, and Mortality, According to Microbiological Cause of Infective Endocarditis: A Nationwide Study.

机构信息

The Heart Centre, Rigshospitalet University of Copenhagen Copenhagen Denmark.

Department of Cardiology Bispebjerg-Frederiksberg Hospital University of Copenhagen Copenhagen Denmark.

出版信息

J Am Heart Assoc. 2022 Aug 16;11(16):e025801. doi: 10.1161/JAHA.122.025801. Epub 2022 Aug 10.

DOI:10.1161/JAHA.122.025801
PMID:35946455
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9496298/
Abstract

Background Monitoring of microbiological cause of infective endocarditis (IE) remains key in the understanding of IE; however, data from large, unselected cohorts are sparse. We aimed to examine temporal changes, patient characteristics, and in-hospital and long-term mortality, according to microbiological cause in patients with IE from 2010 to 2017. Methods and Results Linking Danish nationwide registries, we identified all patients with first-time IE. In-hospital and long-term mortality rates were assessed according to microbiological cause and compared using multivariable adjusted logistic regression analysis and Cox proportional hazard analysis, respectively. A total of 4123 patients were included. was the most frequent cause (28.1%), followed by species (26.0%), species (15.5%), coagulase-negative staphylococci (6.2%), and "other microbiological causes" (5.3%). Blood culture-negative IE was registered in 18.9%. The proportion of blood culture-negative IE declined during the study period, whereas no significant changes were seen for any microbiological cause. Patients with species were older and more often had a prosthetic heart valve compared with other causes. For species IE, in-hospital and long-term mortality (median follow-up, 2.3 years) were 11.1% and 58.5%, respectively. Compared with species IE, the following causes were associated with a higher in-hospital mortality: IE (odds ratio [OR], 3.48 [95% CI, 2.74-4.42]), species IE (OR, 1.48 [95% CI, 1.11-1.97]), coagulase-negative staphylococci IE (OR, 1.79 [95% CI, 1.21-2.65]), "other microbiological cause" (OR, 1.47 [95% CI, 0.95-2.27]), and blood culture-negative IE (OR, 1.99 [95% CI, 1.52-2.61]); and the following causes were associated with higher mortality following discharge (median follow-up, 2.9 years): IE (hazard ratio [HR], 1.39 [95% CI, 1.19-1.62]), species IE (HR, 1.31 [95% CI, 1.11-1.54]), coagulase-negative staphylococci IE (HR, 1.07 [95% CI, 0.85-1.36]), "other microbiological cause" (HR, 1.45 [95% CI, 1.13-1.85]), and blood culture-negative IE (HR, 1.05 [95% CI, 0.89-1.25]). Conclusions This nationwide study showed that was the most frequent microbiological cause of IE, followed by species and species. Patients with IE had the highest in-hospital mortality

摘要

背景监测感染性心内膜炎(IE)的微生物病因仍然是了解 IE 的关键;然而,来自大型、未选择队列的数据仍然很少。我们旨在根据 2010 年至 2017 年 IE 患者的微生物病因,研究时间变化、患者特征以及住院和长期死亡率。

方法和结果通过链接丹麦全国性登记处,我们确定了所有首次 IE 的患者。根据微生物病因评估住院和长期死亡率,并分别使用多变量调整的逻辑回归分析和 Cox 比例风险分析进行比较。共纳入 4123 例患者。最常见的病因是 (28.1%),其次是 物种(26.0%)、 物种(15.5%)、凝固酶阴性葡萄球菌(6.2%)和“其他微生物病因”(5.3%)。血培养阴性 IE 占 18.9%。研究期间,血培养阴性 IE 的比例下降,而任何微生物病因均未见明显变化。与其他病因相比, 物种 IE 患者年龄较大,且更常患有人工心脏瓣膜。对于 物种 IE,住院和长期死亡率(中位随访 2.3 年)分别为 11.1%和 58.5%。与 物种 IE 相比,以下病因与更高的住院死亡率相关:IE(比值比 [OR],3.48 [95%CI,2.74-4.42])、 物种 IE(OR,1.48 [95%CI,1.11-1.97])、凝固酶阴性葡萄球菌 IE(OR,1.79 [95%CI,1.21-2.65])、“其他微生物病因”(OR,1.47 [95%CI,0.95-2.27])和血培养阴性 IE(OR,1.99 [95%CI,1.52-2.61]);与出院后死亡率更高相关的病因包括:IE(风险比 [HR],1.39 [95%CI,1.19-1.62])、 物种 IE(HR,1.31 [95%CI,1.11-1.54])、凝固酶阴性葡萄球菌 IE(HR,1.07 [95%CI,0.85-1.36])、“其他微生物病因”(HR,1.45 [95%CI,1.13-1.85])和血培养阴性 IE(HR,1.05 [95%CI,0.89-1.25])。

结论这项全国性研究表明, 是 IE 最常见的微生物病因,其次是 物种和 物种。IE 患者的住院死亡率最高。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9498/9496298/89549482a176/JAH3-11-e025801-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9498/9496298/fbc63a7faad9/JAH3-11-e025801-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9498/9496298/6044b3720157/JAH3-11-e025801-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9498/9496298/8b44a72a944b/JAH3-11-e025801-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9498/9496298/3e5706e00c1c/JAH3-11-e025801-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9498/9496298/89549482a176/JAH3-11-e025801-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9498/9496298/fbc63a7faad9/JAH3-11-e025801-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9498/9496298/6044b3720157/JAH3-11-e025801-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9498/9496298/8b44a72a944b/JAH3-11-e025801-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9498/9496298/3e5706e00c1c/JAH3-11-e025801-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9498/9496298/89549482a176/JAH3-11-e025801-g002.jpg

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