TY - JOUR
T1 - Clinical aspects of invasive infections with Streptococcus dysgalactiae ssp. equisimilis in Japan
T2 - Differences with respect to Streptococcus pyogenes and Streptococcus agalactiae infections
AU - Takahashi, T.
AU - Sunaoshi, K.
AU - Sunakawa, K.
AU - Fujishima, S.
AU - Watanabe, H.
AU - Ubukata, K.
N1 - Funding Information:
This work was supported in part by a grant under the category, ‘Research Project for Emerging and Re-emerging Infectious Diseases’ (H-19-002), from the Ministry of Health, Labour and Welfare of Japan (to K. Ubukata). None of the authors is aware of any relationship or any degree of conflicting or dual interest, financial or of any other nature, that may affect professional judgement in relation to the article.
PY - 2010/8
Y1 - 2010/8
N2 - Streptococcus dysgalactiae ssp. equisimilis (SDSE) is increasingly being identified as a pathogen responsible for invasive and non-invasive infections. We compared the clinical features of invasive SDSE infections with those of invasive infections caused by Streptococcus pyogenes (group A streptococcus (GAS)) and Streptococcus agalactiae (group B streptococcus (GBS)). Active surveillance for invasive SDSE, GAS and GBS was maintained over 1 year at 142 medical institutions throughout Japan. Clinical information was collected together with isolates, which were characterized microbiologically. Two hundred and thirty-one invasive SDSE infections were identified, 97 other patients had infections with GAS, and 151 had infections with GBS. The median age of the SDSE patients was 75 years; 51% were male and 79% had underlying diseases. Forty-two SDSE patients (19%) presented to the emergency department. Among the 150 patients (65%) for whom follow-up was completed, 19 (13%) died and eight (5%) had post-infective sequelae (poor outcome). Insufficient white blood cell responses (<5000 cells/μL) and thrombocytopenia on admission each suggested significantly higher risk of poor outcome (ORs 3.6 and 4.5, respectively). Of 229 isolates, 55 (24%) showed an stG6792 emm type, which was significantly associated with poor outcome (OR 2.4). Clinical manifestations of invasive SDSE infections were distinct from those of invasive GBS infections. Primary-care doctors should consider invasive SDSE infections when treating elderly patients.
AB - Streptococcus dysgalactiae ssp. equisimilis (SDSE) is increasingly being identified as a pathogen responsible for invasive and non-invasive infections. We compared the clinical features of invasive SDSE infections with those of invasive infections caused by Streptococcus pyogenes (group A streptococcus (GAS)) and Streptococcus agalactiae (group B streptococcus (GBS)). Active surveillance for invasive SDSE, GAS and GBS was maintained over 1 year at 142 medical institutions throughout Japan. Clinical information was collected together with isolates, which were characterized microbiologically. Two hundred and thirty-one invasive SDSE infections were identified, 97 other patients had infections with GAS, and 151 had infections with GBS. The median age of the SDSE patients was 75 years; 51% were male and 79% had underlying diseases. Forty-two SDSE patients (19%) presented to the emergency department. Among the 150 patients (65%) for whom follow-up was completed, 19 (13%) died and eight (5%) had post-infective sequelae (poor outcome). Insufficient white blood cell responses (<5000 cells/μL) and thrombocytopenia on admission each suggested significantly higher risk of poor outcome (ORs 3.6 and 4.5, respectively). Of 229 isolates, 55 (24%) showed an stG6792 emm type, which was significantly associated with poor outcome (OR 2.4). Clinical manifestations of invasive SDSE infections were distinct from those of invasive GBS infections. Primary-care doctors should consider invasive SDSE infections when treating elderly patients.
KW - Invasive infections
KW - Non-invasive infections
KW - Streptococcus agalactiae
KW - Streptococcus dysgalactiae ssp. equisimilis
KW - Streptococcus pyogenes
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U2 - 10.1111/j.1469-0691.2009.03047.x
DO - 10.1111/j.1469-0691.2009.03047.x
M3 - Article
C2 - 19732082
AN - SCOPUS:77955169378
SN - 1198-743X
VL - 16
SP - 1097
EP - 1103
JO - Clinical Microbiology and Infection
JF - Clinical Microbiology and Infection
IS - 8
ER -