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Streptococcus Pneumoniae septic arthritis in adults in Bristol and Bath, United Kingdom, 2006-2018: a 13-year retrospective observational cohort study.

Hyams, C; Amin-Chowdhury, Z; Fry, NK; North, P; Finn, A; Judge, A; Ladhani, SN; Williams, OM (2021) Streptococcus Pneumoniae septic arthritis in adults in Bristol and Bath, United Kingdom, 2006-2018: a 13-year retrospective observational cohort study. Emerg Microbes Infect, 10 (1). pp. 1369-1377. ISSN 2222-1751 https://doi.org/10.1080/22221751.2021.1945955
SGUL Authors: Ladhani, Shamez Nizarali

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Abstract

Few studies on adult pneumococcal septic arthritis are sufficiently large enough to assess both epidemiological trends following routine pneumococcal immunization and clinical disease. With major shifts in serotypes causing invasive pneumococcal disease (IPD), we wanted to determine the clinical phenotype of adult septic arthritis caused by Streptococcus pneumoniae. We conducted a retrospective cohort study of pneumococcal infections in Bristol and Bath, UK, 2006-2018. We defined pneumococcal septic arthritis as adults with clinically-confirmed septic arthritis, with pneumococcus isolated from sterile-site culture or urinary antigen test positivity. Clinical records were reviewed for each patient in the cohort. Septic arthritis accounted for 1.7% of all IPD cases. 45 cases of adult pneumococcal septic arthritis occurred, with disease typically affecting older adults and those with underlying comorbidity. 67% patients had another focus of infection during their illness. 66% patients required increased care on discharge and 43% had reduced range of movement. In-hospital case fatality rate was 6.7%. One-year patient mortality was 31%. Currently most cases of adult pneumococcal septic arthritis are due to non-PCV13 serotypes which are associated with more severe disease. Non-PCV-13 serotypes had higher prevalence of concomitant pneumococcal infection at another site (73.7% versus 36.6%), increased intensive care or high-dependency unit requirement (32.4% versus 0%), and increased inpatient and 1-year case fatality rate (8.8% versus 0%, and 32.4% versus 27.4% respectively) compared to PCV-13 serotypes. Pneumococcal septic arthritis remains a small proportion of IPD. However, there is significant associated morbidity and mortality, and pneumococcal septic arthritis requires monitoring in coming years.

Item Type: Article
Additional Information: © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Keywords: PCV-13, Pneumococcus, Streptococcus pneumoniae, invasive pneumococcal disease, pneumococcal vaccines, septic arthritis, Adult, Aged, Aged, 80 and over, Arthritis, Infectious, Comorbidity, Female, Humans, Male, Middle Aged, Pneumococcal Infections, Retrospective Studies, Risk Factors, Serogroup, Streptococcus pneumoniae, Treatment Outcome, United Kingdom, Young Adult, Humans, Streptococcus pneumoniae, Pneumococcal Infections, Arthritis, Infectious, Treatment Outcome, Risk Factors, Retrospective Studies, Comorbidity, Adult, Aged, Aged, 80 and over, Middle Aged, Female, Male, Young Adult, Serogroup, United Kingdom, Pneumococcus, Streptococcus pneumoniae, septic arthritis, PCV-13, pneumococcal vaccines, invasive pneumococcal disease, 0605 Microbiology
SGUL Research Institute / Research Centre: Academic Structure > Infection and Immunity Research Institute (INII)
Journal or Publication Title: Emerg Microbes Infect
ISSN: 2222-1751
Language: eng
Dates:
DateEvent
December 2021Published
5 July 2021Published Online
16 June 2021Accepted
Publisher License: Creative Commons: Attribution 4.0
Projects:
Project IDFunderFunder ID
ACF-2015-25-002National Institute for Health Researchhttp://dx.doi.org/10.13039/501100000272
PubMed ID: 34151740
Web of Science ID: WOS:000669697300001
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/114698
Publisher's version: https://doi.org/10.1080/22221751.2021.1945955

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