Infections and hospital bed-days among aging adults: A five-year retrospective study in a Belgian general hospital.
aging adults
geriatrics
hospitalization
infectious disease
pulmonology
Journal
Frontiers in medical technology
ISSN: 2673-3129
Titre abrégé: Front Med Technol
Pays: Switzerland
ID NLM: 101772626
Informations de publication
Date de publication:
2022
2022
Historique:
received:
04
04
2022
accepted:
25
08
2022
entrez:
7
11
2022
pubmed:
8
11
2022
medline:
8
11
2022
Statut:
epublish
Résumé
Infectious disease in aging adults (≥61 years) often occurs in combination with other health conditions leading to long hospital stays. Detailed studies on infection in aging adults investigating this problem are sparse. To quantify the effect of primary and secondary diagnosed infections on hospitalization bed-days among aging adult patients. Retrospective patient-file study. Ziekenhuis Netwerk Antwerpen (ZNA) Hospital, a 1,858-bed general hospital in Belgium, with 364 beds allocated to geriatric patients. Database of hospitalized adult patients aged ≥61 years. All adult patients aged ≥61 years hospitalized on two wards, Geriatrics and Pulmonology, from 2010 to 2014 were included. Primary diagnosed infections were defined as infections known at entry to be treated first. Secondary diagnosed infections included infections known at entry but treated in parallel to primary non-infectious causes of entry, infections unknown at entry, and hospital-acquired (nosocomial) infections. Data were analyzed by patient age, gender, year, ward type, bed-days of hospitalization, infection rates, and seasonality. There were 3,306 primary diagnosed infections (18%) and 14,758 secondary infections (82%) identified in the two wards combined (54.7% of all hospital stays at those 2 wards). Secondary diagnosed infections accounted for a significantly higher proportion of hospitalizations in both wards (+40% for Geriatric ward; +20% for Pulmonology ward; Real-world data showed that secondary diagnosed infections in aging adults imposed a high burden on hospital care along with longer hospital stays. This hampered bed availability during peak seasons.
Sections du résumé
Background
UNASSIGNED
Infectious disease in aging adults (≥61 years) often occurs in combination with other health conditions leading to long hospital stays. Detailed studies on infection in aging adults investigating this problem are sparse.
Aim
UNASSIGNED
To quantify the effect of primary and secondary diagnosed infections on hospitalization bed-days among aging adult patients.
Design
UNASSIGNED
Retrospective patient-file study.
Setting
UNASSIGNED
Ziekenhuis Netwerk Antwerpen (ZNA) Hospital, a 1,858-bed general hospital in Belgium, with 364 beds allocated to geriatric patients.
Data source
UNASSIGNED
Database of hospitalized adult patients aged ≥61 years.
Methods
UNASSIGNED
All adult patients aged ≥61 years hospitalized on two wards, Geriatrics and Pulmonology, from 2010 to 2014 were included. Primary diagnosed infections were defined as infections known at entry to be treated first. Secondary diagnosed infections included infections known at entry but treated in parallel to primary non-infectious causes of entry, infections unknown at entry, and hospital-acquired (nosocomial) infections. Data were analyzed by patient age, gender, year, ward type, bed-days of hospitalization, infection rates, and seasonality.
Results
UNASSIGNED
There were 3,306 primary diagnosed infections (18%) and 14,758 secondary infections (82%) identified in the two wards combined (54.7% of all hospital stays at those 2 wards). Secondary diagnosed infections accounted for a significantly higher proportion of hospitalizations in both wards (+40% for Geriatric ward; +20% for Pulmonology ward;
Conclusion
UNASSIGNED
Real-world data showed that secondary diagnosed infections in aging adults imposed a high burden on hospital care along with longer hospital stays. This hampered bed availability during peak seasons.
Identifiants
pubmed: 36340588
doi: 10.3389/fmedt.2022.912469
pmc: PMC9632861
doi:
Types de publication
Journal Article
Langues
eng
Pagination
912469Informations de copyright
© 2022 De Cock, Strens, Van Osta and Standaert.
Déclaration de conflit d'intérêts
BS is employed by HEBO. DS is employed by Realidad. BS has received consultancy fees, unrelated to the present work, from GSK Vaccines, Biondvax, and Evidera-PMM. DS received a consultancy fee from GSK Vaccines to initiate the study in 2019. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Références
Lancet Public Health. 2019 Mar;4(3):e123-e124
pubmed: 30851865
J Gerontol A Biol Sci Med Sci. 2019 Sep 15;74(10):1643-1649
pubmed: 30329033
Clin Infect Dis. 2000 Jun;30(6):931-3
pubmed: 10880303
Vaccine. 2020 Aug 18;38(37):5896-5904
pubmed: 32713682
J Gerontol A Biol Sci Med Sci. 2004 Mar;59(3):255-63
pubmed: 15031310
Lancet. 2015 Feb 14;385(9968):658-661
pubmed: 25468151
Sci Data. 2020 Oct 15;7(1):329
pubmed: 33057040
Am Fam Physician. 2001 Jan 15;63(2):257-68
pubmed: 11201692
Epidemiol Rev. 2000;22(1):95-106
pubmed: 10939013
Vaccine. 2016 Feb 10;34(7):942-9
pubmed: 26752065
JAMA. 1996 Jan 17;275(3):189-93
pubmed: 8604170
Antimicrob Resist Infect Control. 2020 Jan 13;9(1):13
pubmed: 31956402
Ann Intern Med. 1983 Mar;98(3):395-400
pubmed: 6830081
J Am Geriatr Soc. 2017 Mar;65(3):631-641
pubmed: 28140454
Euro Surveill. 2018 Nov;23(46):
pubmed: 30458912
Crit Care Med. 2006 Oct;34(10):2576-82
pubmed: 16915108
Lancet Infect Dis. 2019 Jan;19(1):56-66
pubmed: 30409683
J Infect Dis. 2021 Apr 8;223(7):1132-1138
pubmed: 33388780
Virulence. 2017 Jul 4;8(5):577-585
pubmed: 27540686
Med Sci (Basel). 2018 Apr 30;6(2):
pubmed: 29710871
Clin Geriatr Med. 2016 Aug;32(3):433-41
pubmed: 27394015
Hum Vaccin Immunother. 2015;11(9):2266-73
pubmed: 25902371
Euro Surveill. 2018 Apr;23(16):
pubmed: 29692315
Int J Environ Res Public Health. 2021 May 17;18(10):
pubmed: 34067797
Eur J Intern Med. 2016 Jun;31:11-4
pubmed: 26997416
Aging Clin Exp Res. 2021 Mar;33(3):689-701
pubmed: 31656032
Ochsner J. 2009 Spring;9(1):27-31
pubmed: 21603406
Clin Microbiol Rev. 2011 Jan;24(1):141-73
pubmed: 21233510