JMIR Research Protocols (Jul 2023)

Duration of Protection From Pneumonia After Pneumococcal Vaccination in Hemodialysis Patients (DOPPIO): Protocol for a Prospective Multicenter Study

  • Sibylle Mellinghoff,
  • Gero von Gersdorff,
  • Caroline Bruns,
  • Kerstin Albus,
  • Vassiliki Dimitriou,
  • Angela Steinbach,
  • Mathias Schaller,
  • Jörg Janne Vehreschild,
  • Oliver A Cornely,
  • Blasius Janusch Liss

DOI
https://doi.org/10.2196/45712
Journal volume & issue
Vol. 12
p. e45712

Abstract

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BackgroundPneumonia is a leading cause of death in patients with end-stage chronic kidney disease treated with dialysis. Current vaccination schedules recommend pneumococcal vaccination. However, this schedule disregards findings of rapid titer decline in adult hemodialysis patients after 12 months. ObjectiveThe primary objective is to compare pneumonia rates between recently vaccinated patients and patients vaccinated more than 2 years ago. As an exploratory objective, antipneumococcal antibody titers in hemodialysis patients will be determined as a function. Factors influencing antibody kinetics will be identified. MethodsWithin this prospective multicenter study, we aim to compare 2 strata of vaccinated patients: those recently vaccinated and those vaccinated more than 2 years ago. A total of 792 patients will be enrolled. Twelve partner sites (within the German Centre for Infection Research [DZIF]) with allocated dialysis practices participate in this study. All dialysis patients who are vaccinated against pneumococcal infection in accordance with Robert Koch Institute guidelines prior to enrollment will be eligible. Data on baseline demographics, vaccination history, and underlying disease will be assessed. Pneumococcal antibody titers will be determined at baseline and every 3 months for 2 years. DZIF clinical trial units coordinate titer assessment schedules and actively follow-up on study patients for 2-5 years after enrollment, including validation of end points of hospitalization, pneumonia, and death. ResultsThe study has enrolled 792 patients and the last follow-up has been completed. Currently, the statistical and laboratory analyses are ongoing. ConclusionsResults will increase physician adherence to current recommendations. Establishing a framework for the efficient evaluation of guideline recommendations through a combination of routine and study data will inform the evidence base for future guidelines. Trial RegistrationClinicalTrials.gov NCT03350425; https://clinicaltrials.gov/ct2/show/NCT03350425 International Registered Report Identifier (IRRID)DERR1-10.2196/45712