Abstract
Objective: We aimed to estimate the effectiveness of influenza and 23-valent pneumococcal polysaccharide vaccination on reducing the burden of community-acquired lower respiratory tract infection (LRTI) among older people with diabetes, and whether this varied by chronic kidney disease (CKD) status. Research design and methods: We used linked UK electronic health records for a retrospective cohort study of 190 492 patients ≥65 years with diabetes mellitus and no history of renal replacement therapy, 1997-2011. We included communityacquired LRTIs managed in primary or secondary care. Infection incidence rate ratios were estimated using the Poisson regression. Pneumococcal vaccine effectiveness (VE) was calculated as (1-effect measure). To estimate influenza VE, a ratio-of-ratios analysis (winter effectiveness/summer effectiveness) was used to address confounding by indication. Final VE estimates were stratified according to estimated glomerular filtration rate and proteinuria status. Results: Neither influenza nor pneumococcal vaccine uptake varied according to CKD status. Pneumococcal VE was 22% (95% CI 11% to 31%) against community-acquired pneumonia for the first year after vaccination, but was negligible after 5 years. In the ratio-of-ratios analysis, current influenza vaccination had 7% effectiveness for preventing community-acquired LRTI (95% CI 3 to 12). Pneumococcal VE was lower among patients with a history of proteinuria than among patients without proteinuria ( p=0.04), but otherwise this study did not identify variation in pneumococcal or influenza VE by markers of CKD. Conclusions: The public health benefits of influenza vaccine may be modest among older people with diabetes. Pneumococcal vaccination protection against community-acquired pneumonia declines swiftly: alternative vaccination schedules should be investigated.
| Original language | English |
|---|---|
| Article number | e000332 |
| Journal | BMJ Open Diabetes Research and Care |
| Volume | 5 |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - 3 Apr 2017 |
| Externally published | Yes |
Bibliographical note
Funding Information:Funding This work was supported by National Institute for Health Research (grant number CDF 2010-03-32 to SLT) and Kidney Research UK (grant number ST2/2011 to HIMD). JQ was funded on an MRC Population Health Scientist Fellowship (grant number G0902135).
Funding
Funding This work was supported by National Institute for Health Research (grant number CDF 2010-03-32 to SLT) and Kidney Research UK (grant number ST2/2011 to HIMD). JQ was funded on an MRC Population Health Scientist Fellowship (grant number G0902135).
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
ASJC Scopus subject areas
- Endocrinology, Diabetes and Metabolism
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