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Clostridioides (Clostridium) difficile infection burden in Japan: A multicenter prospective study.
Kato, Haru; Senoh, Mitsutoshi; Honda, Hitoshi; Fukuda, Tadashi; Tagashira, Yasuaki; Horiuchi, Hiroko; Chiba, Hiroshi; Suzuki, Daisuke; Hosokawa, Naoto; Kitazono, Hidetaka; Norisue, Yasuhiro; Kume, Hisashi; Mori, Nobuaki; Morikawa, Hideo; Kashiwagura, Saeko; Higuchi, Akiko; Kato, Hideaki; Nakamura, Makoto; Ishiguro, Saori; Morita, Sayuri; Ishikawa, Hideaki; Watanabe, Takuya; Kojima, Katsuyuki; Yokomaku, Izumi; Bando, Tatsuya; Toimoto, Kayoko; Moriya, Kei; Kasahara, Kei; Kitada, Seigo; Ogawa, Junko; Saito, Haruko; Tominaga, Harumi; Shimizu, Yousuke; Masumoto, Fumi; Tadera, Kayoko; Yoshida, Junichi; Kikuchi, Tetsuya; Yoshikawa, Ichiro; Watanabe, Tatsuyuki; Honda, Masahisa; Yokote, Kuniko; Toyokawa, Takao; Miyazato, Hiroko; Nakama, Mika; Mahe, Cedric; Reske, Kimberly; Olsen, Margaret A; Dubberke, Erik R.
Affiliation
  • Kato H; Department of Bacteriology II, National Institute of Infectious Diseases, Tokyo, Japan. Electronic address: cato@nih.go.jp.
  • Senoh M; Department of Bacteriology II, National Institute of Infectious Diseases, Tokyo, Japan.
  • Honda H; Division of Infectious Diseases, Tokyo Metropolitan Tama Medical Center, Tokyo, Japan.
  • Fukuda T; Department of Bacteriology II, National Institute of Infectious Diseases, Tokyo, Japan.
  • Tagashira Y; Division of Infectious Diseases, Tokyo Metropolitan Tama Medical Center, Tokyo, Japan.
  • Horiuchi H; Hachinohe City Hospital, Aomori, Japan.
  • Chiba H; Hachinohe City Hospital, Aomori, Japan.
  • Suzuki D; Kameda Medical Center, Chiba, Japan.
  • Hosokawa N; Kameda Medical Center, Chiba, Japan.
  • Kitazono H; Tokyo Bay Urayasu Ichikawa Medical Center, Chiba, Japan.
  • Norisue Y; Tokyo Bay Urayasu Ichikawa Medical Center, Chiba, Japan.
  • Kume H; Tokyo Bay Urayasu Ichikawa Medical Center, Chiba, Japan.
  • Mori N; National Hospital Organization Tokyo Medical Center, Tokyo, Japan.
  • Morikawa H; National Hospital Organization Tokyo Medical Center, Tokyo, Japan.
  • Kashiwagura S; National Hospital Organization Tokyo Medical Center, Tokyo, Japan.
  • Higuchi A; National Hospital Organization Tokyo Medical Center, Tokyo, Japan.
  • Kato H; Toyokawa City Hospital, Aichi, Japan.
  • Nakamura M; Toyokawa City Hospital, Aichi, Japan.
  • Ishiguro S; Toyokawa City Hospital, Aichi, Japan.
  • Morita S; Toyokawa City Hospital, Aichi, Japan.
  • Ishikawa H; Tokai Central Hospital, Gifu, Japan.
  • Watanabe T; Tokai Central Hospital, Gifu, Japan.
  • Kojima K; Tokai Central Hospital, Gifu, Japan.
  • Yokomaku I; Tokai Central Hospital, Gifu, Japan.
  • Bando T; Tokai Central Hospital, Gifu, Japan.
  • Toimoto K; Nara Medical University, Nara, Japan.
  • Moriya K; Nara Medical University, Nara, Japan.
  • Kasahara K; Nara Medical University, Nara, Japan.
  • Kitada S; National Hospital Organization Toneyama National Hospital, Osaka, Japan.
  • Ogawa J; National Hospital Organization Toneyama National Hospital, Osaka, Japan.
  • Saito H; National Hospital Organization Toneyama National Hospital, Osaka, Japan.
  • Tominaga H; National Hospital Organization Kure Medical Center and Chugoku Cancer Center, Hiroshima, Japan.
  • Shimizu Y; National Hospital Organization Kure Medical Center and Chugoku Cancer Center, Hiroshima, Japan.
  • Masumoto F; National Hospital Organization Kure Medical Center and Chugoku Cancer Center, Hiroshima, Japan.
  • Tadera K; National Hospital Organization Kure Medical Center and Chugoku Cancer Center, Hiroshima, Japan.
  • Yoshida J; Shimonoseki City Hospital, Yamaguchi, Japan.
  • Kikuchi T; Shimonoseki City Hospital, Yamaguchi, Japan.
  • Yoshikawa I; University Hospital, University of Occupational and Environmental Health, Fukuoka, Japan.
  • Watanabe T; University Hospital, University of Occupational and Environmental Health, Fukuoka, Japan.
  • Honda M; University Hospital, University of Occupational and Environmental Health, Fukuoka, Japan.
  • Yokote K; University Hospital, University of Occupational and Environmental Health, Fukuoka, Japan.
  • Toyokawa T; Okinawa Prefectural Nanbu Medical Center and Children's Medical Center, Okinawa, Japan.
  • Miyazato H; Okinawa Prefectural Nanbu Medical Center and Children's Medical Center, Okinawa, Japan.
  • Nakama M; Okinawa Prefectural Nanbu Medical Center and Children's Medical Center, Okinawa, Japan.
  • Mahe C; Sanofi Pasteur, Lyon, France.
  • Reske K; Section of Transplant Infectious Diseases, Washington University School of Medicine, St. Louis, Missouri, USA.
  • Olsen MA; Section of Transplant Infectious Diseases, Washington University School of Medicine, St. Louis, Missouri, USA.
  • Dubberke ER; Section of Transplant Infectious Diseases, Washington University School of Medicine, St. Louis, Missouri, USA.
Anaerobe ; 60: 102011, 2019 Dec.
Article in En | MEDLINE | ID: mdl-30872073
Clostridioides (Clostridium) difficile is the leading cause of healthcare-associated infectious diarrhea in the developed world. Retrospective studies have shown a lower incidence of C. difficile infection (CDI) in Japan than in Europe or North America. Prospective studies are needed to determine if this is due lack of testing for C. difficile or a true difference in CDI epidemiology. A prospective cohort study of CDI was conducted from May 2014 to May 2015 at 12 medical facilities (20 wards) in Japan. Patients with at least three diarrheal bowel movements (Bristol stool grade 6-7) in the preceding 24 h were enrolled. CDI was defined by positive result on enzyme immunoassay for toxins A/B, nucleic acid amplification test for the toxin B gene or toxigenic culture. C. difficile isolates were subjected to PCR-ribotyping (RT), slpA-sequence typing (slpA-ST), and antimicrobial susceptibility testing. The overall incidence of CDI was 7.4/10,000 patient-days (PD). The incidence was highest in the five ICU wards (22.2 CDI/10,000 PD; range: 13.9-75.5/10,000 PD). The testing frequency and CDI incidence rate were highly correlated (R2 = 0.91). Of the 146 isolates, RT018/018″ was dominant (29%), followed by types 014 (23%), 002 (12%), and 369 (11%). Among the 15 non-ICU wards, two had high CDI incidence rates (13.0 and 15.9 CDI/10,000 PD), with clusters of RT018/slpA-ST smz-02 and 018"/smz-01, respectively. Three non-RT027 or 078 binary toxin-positive isolates were found. All RT018/018" isolates were resistant to moxifloxacin, gatifloxacin, clindamycin, and erythromycin. This study identified a higher CDI incidence in Japanese hospitals than previously reported by actively identifying and testing patients with clinically significant diarrhea. This suggests numerous patients with CDI are being overlooked due to inadequate diagnostic testing in Japan.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Clostridioides difficile / Clostridium Infections Type of study: Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Country/Region as subject: Asia Language: En Journal: Anaerobe Year: 2019 Document type: Article Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Clostridioides difficile / Clostridium Infections Type of study: Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Country/Region as subject: Asia Language: En Journal: Anaerobe Year: 2019 Document type: Article Country of publication: