Population-based incidence of hospitalized Clostridioides difficile infection among older adults in Ota-ku, Japan: A prospective surveillance study.


Journal

Anaerobe
ISSN: 1095-8274
Titre abrégé: Anaerobe
Pays: England
ID NLM: 9505216

Informations de publication

Date de publication:
Aug 2022
Historique:
received: 06 04 2022
revised: 15 06 2022
accepted: 18 06 2022
pubmed: 6 7 2022
medline: 14 9 2022
entrez: 5 7 2022
Statut: ppublish

Résumé

Clostridioides difficile infection (CDI) burden is not well-characterized in Japan. Therefore, we conducted a population-based, hospitalized CDI incidence study, compared the results with standard-of-care (SOC) CDI testing, and generalized the results for nationwide incidence estimates. Surveillance identified inpatients ≥50 years-of-age with diarrhea in nine Tokyo hospitals from December 17, 2018-March 30, 2020. A CDI case was defined as a patient with a PCR-positive/cell cytotoxicity neutralization assay (CCNA)-positive stool or a PCR-positive stool and pseudomembranous colitis (PMC). Incidence estimates were adjusted for the hospitalization share of participating hospitals and, in the sensitivity analysis, for missing CDI test results. SOC specimen collection and CDI testing occurred independently. Surveillance during 318 840 patient-days identified 4633 inpatients with diarrhea. Sixty-three CDI cases were identified; 11 (17·5%) had PMC, eight (12·7%) recurrent CDI, and nine (14·3%) died. The hospitalized CDI incidence was 97/100 000 population per year (PPY) in persons ≥50 years-of-age and, in the sensitivity analysis, 324/100 000 PPY. The incidence was 170 and 481/100 000 PPY in persons ≥65 and ≥85 years-of-age, respectively; these estimates increased to 569 and 1609/100 000 PPY in the sensitivity analysis, respectively. There were 12 primary SOC CDI cases in persons ≥50 years-of-age (18/100 000 PPY). The CDI incidence was high in older adults, with severe clinical consequences. SOC specimen collection and testing under-estimated CDI burden. There are >57 000 hospitalized CDI cases per year in Japan in persons ≥50 years-of-age. Public health interventions are needed to reduce the CDI burden in Japan.

Identifiants

pubmed: 35787452
pii: S1075-9964(22)00098-1
doi: 10.1016/j.anaerobe.2022.102607
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

102607

Informations de copyright

Copyright © 2022 The Pfizer, The Author(s). Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest Shuhei Ito, Elisa Gonzalez, Pingping Zhang, Michael Pride, Sharon Gray, Nadia Minarovic, Frederick J. Angulo, Jennifer C. Moïsi, and Luis Jodar are employees of Pfizer Inc. Shuhei Ito, Elisa Gonzalez, Pingping Zhang, Michael Pride, Sharon Gray, Frederick J. Angulo, Jennifer C. Moïsi, and Luis Jodar hold stock and stock options in Pfizer Inc. Pfizer Inc. provided support for medical writing and article publication. Kazuhiro Tateda declares consulting fees from Pfizer for Advisory Board participation and payment from Pfizer for presentations. Junro Ishida and Satoshi Yoshizumi declare no competing interests.

Auteurs

Kazuhiro Tateda (K)

Toho University School of Medicine, Department of Microbiology and Infectious Diseases, 5-21-16, Omori-Nishi Ota-ku, Tokyo 143-8530, Japan. Electronic address: kazu@med.toho-u.ac.jp.

Junro Ishida (J)

Den-en-chofu Central Hospital, Department of General Medicine, 2-43-1, Den-en-chofu, Ota-ku, Tokyo 145-0071, Japan. Electronic address: j_ishida@tmg.or.jp.

Shuhei Ito (S)

Vaccine Medical Affairs, Pfizer Japan Inc., 3-22-7 Yoyogi, Shibuya-ku, Tokyo 151-8589, Japan. Electronic address: Shuhei.Ito@pfizer.com.

Elisa Gonzalez (E)

Medical Development and Scientific/Clinical Affairs, Pfizer Vaccines, Collegeville, PA 19301, USA. Electronic address: Elisa.N.Gonzalez2@pfizer.com.

Satoshi Yoshizumi (S)

Parexel International, 1-21-2 Shinkawa, Chuo-ku, Tokyo 104-0033, Japan. Electronic address: Satoshi.Yoshizumi@parexel.com.

Pingping Zhang (P)

Medical Development and Scientific/Clinical Affairs, Pfizer Vaccines, Collegeville, PA 19301, USA. Electronic address: Pingping.Zhang@pfizer.com.

Michael Pride (M)

Vaccine Research and Development, Pfizer, Pearl River, NY 10965, USA. Electronic address: Michael.Pride@pfizer.com.

Sharon Gray (S)

Medical Development and Scientific/Clinical Affairs, Pfizer Vaccines, Collegeville, PA 19301, USA. Electronic address: Sharon.Gray@pfizer.com.

Cátia Matos Ferreira (CM)

Medical Development and Scientific/Clinical Affairs, Pfizer Vaccines, Collegeville, PA 19301, USA. Electronic address: catia.s.ferreira@icloud.com.

Nadia Minarovic (N)

Medical Development and Scientific/Clinical Affairs, Pfizer Vaccines, Collegeville, PA 19301, USA. Electronic address: Nadia.Minarovic@pfizer.com.

Frederick J Angulo (FJ)

Medical Development and Scientific/Clinical Affairs, Pfizer Vaccines, Collegeville, PA 19301, USA. Electronic address: Frederick.J.Angulo@pfizer.com.

Jennifer C Moïsi (JC)

Medical Development and Scientific/Clinical Affairs, Pfizer Vaccines, Collegeville, PA 19301, USA. Electronic address: Jennifer.Moisi@pfizer.com.

Luis Jodar (L)

Medical Development and Scientific/Clinical Affairs, Pfizer Vaccines, Collegeville, PA 19301, USA. Electronic address: Luis.Jodar@pfizer.com.

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