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Validation of a new risk stratification system-based management for methicillin-resistant Staphylococcus aureus bacteraemia: analysis of a multicentre prospective study

Authors
Kim, TaeeunLee, Sang-RokPark, Seong YeonMoon, Song MiJung, JiwonKim, Min JaeSung, HeungsupKim, Mi-NaKim, Sung-HanChoi, Sang-HoLee, Sang-OhKim, Yang SooSong, Eun HeeChong, Yong Pil
Issue Date
May-2024
Publisher
SPRINGER
Keywords
Staphylococcus aureus bacteraemia; Methicillin-resistance; Complicated bacteraemia; Metastatic infection; Risk stratification
Citation
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, v.43, no.5, pp 841 - 851
Pages
11
Journal Title
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES
Volume
43
Number
5
Start Page
841
End Page
851
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/91452
DOI
10.1007/s10096-024-04790-2
ISSN
0934-9723
1435-4373
Abstract
Purpose Distinguishing between complicated and uncomplicated Staphylococcus aureus bacteraemia (SAB) is therapeutically essential. However, this distinction has limitations in reflecting the heterogeneity of SAB and encouraging targeted diagnostics. Recently, a new risk stratification system for SAB metastatic infection, involving stepwise approaches to diagnosis and treatment, has been suggested. We assessed its applicability in methicillin-resistant SAB (MRSAB) patients. Methods We retrospectively analysed data of a 3-year multicentre, prospective cohort of hospitalised patients with MRSAB. We classified the patients into three risk groups: low, indeterminate, and high, based on the new system and compared between-group management and outcomes. Results Of 380 patients with MRSAB, 6.3% were classified as low-, 7.6% as indeterminate-, and 86.1% as high-risk for metastatic infection. No metastatic infection occurred in the low-, 6.9% in the indeterminate-, and 19.6% in the high-risk groups (P < 0.001). After an in-depth diagnostic work-up, patients were finally diagnosed as 'without metastatic infection (6.3%)', 'with metastatic infection (17.4%)', and 'uncertain for metastatic infection (76.3%)'. 30-day mortality increased as the severity of diagnosis shifted from 'without metastatic infection' to 'uncertain for metastatic infection' and 'with metastatic infection' (P = 0.09). In multivariable analysis, independent factors associated with metastatic complications were suspicion of endocarditis in transthoracic echocardiography, clinical signs of metastatic infection, Pitt bacteraemia score >= 4, and persistent bacteraemia. Conclusions The new risk stratification system shows promise in predicting metastatic complications and guiding work-up and management of MRSAB. However, reducing the number of cases labelled as 'high-risk' and 'uncertain for metastatic infection' remains an area for improvement.
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