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Case Series: Efficacy of Polyclonal Intravenous Immunoglobulin for Refractory Clostridioides difficile Infection

Ragan, Sophie A.; Doyle, Caitlin; Datta, Neha; Abdic, Heather; Wilcox, Mark H.; Montgomery, Ros; Crusz, Shanika A.; Mahida, Yashwant R.; Monaghan, Tanya M.

Case Series: Efficacy of Polyclonal Intravenous Immunoglobulin for Refractory Clostridioides difficile Infection Thumbnail


Authors

Sophie A. Ragan

Caitlin Doyle

Neha Datta

Heather Abdic

Mark H. Wilcox

Ros Montgomery

Shanika A. Crusz

YASH MAHIDA yash.mahida@nottingham.ac.uk
Professor of Medicine

TANYA MONAGHAN Tanya.Monaghan@nottingham.ac.uk
Clinical Associate Professor in Luminal Gastroenterology



Abstract

Background: Intravenous immunoglobulin (IVIg) for Clostridioides difficile infection (CDI) no longer features in treatment guidelines. However, IVIg is still used by some clinicians for severe or recurrent CDI (rCDI) cases. The main objective of this study was to investigate the efficacy of IVIg and to identify possible predictors of disease resolution post IVIg administration for patients with CDI. Methods: This retrospective observational cohort study of patients ≥2 years old hospitalised with severe, relapsing, or rCDI treated with IVIg therapy was performed in a large UK tertiary hospital between April 2018 and March 2023. Scanned electronic notes from patient admissions and clinical reporting systems were used to collect relevant data. Results: In total, 20/978 patients diagnosed with CDI over the 5-year study were treated with IVIg. Twelve (60%) had hospital-onset CDI. Eleven of the twenty patients (55%) responded to treatment, with a mean of 8.6 (SD 10.7) days to disease resolution. Sixteen (80%) patients were treated for severe CDI and four (20%) for rCDI (n = 3) and relapsing CDI (n = 1). There were no statistically significant differences in possible independent predictors of disease resolution post IVIg administration between groups. There was an average of 6.2 (4.9) days to IVIg administration after diagnosis with no difference between responders and non-responders (p = 0.88) and no further significant difference in additional indicators. Four (36%) of the responders were immunosuppressed compared to just one (11%) of the non-responders (p = 0.15). Six of the responders (two with recurrent and four with severe CDI) improved rapidly within 2 days, and three of these were immunosuppressed. Conclusion: We observed disease resolution post IVIg therapy in over 50% of patients with refractory CDI. Our data also support a potential enhanced effect of IVIg in immunosuppressed individuals. Thus, the role of IVIg for CDI treatment, particularly in the immunosuppressed, warrants future case–control studies coupled to mechanistic investigations to improve care for this ongoing significant healthcare-associated infection.

Citation

Ragan, S. A., Doyle, C., Datta, N., Abdic, H., Wilcox, M. H., Montgomery, R., …Monaghan, T. M. (2024). Case Series: Efficacy of Polyclonal Intravenous Immunoglobulin for Refractory Clostridioides difficile Infection. Antibodies, 13(2), Article 26. https://doi.org/10.3390/antib13020026

Journal Article Type Article
Acceptance Date Mar 22, 2024
Online Publication Date Apr 1, 2024
Publication Date 2024-06
Deposit Date Mar 22, 2024
Publicly Available Date Apr 1, 2024
Journal Antibodies
Electronic ISSN 2073-4468
Publisher MDPI
Peer Reviewed Peer Reviewed
Volume 13
Issue 2
Article Number 26
DOI https://doi.org/10.3390/antib13020026
Keywords Drug Discovery; Immunology; Immunology and Allergy
Public URL https://nottingham-repository.worktribe.com/output/32752898
Publisher URL https://www.mdpi.com/2073-4468/13/2/26

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