Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Multicenter Study
. 2019 Mar 1;173(3):260-268.
doi: 10.1001/jamapediatrics.2018.4954.

Incidence of Hospitalization for Vaccine-Preventable Infections in Children Following Solid Organ Transplant and Associated Morbidity, Mortality, and Costs

Affiliations
Multicenter Study

Incidence of Hospitalization for Vaccine-Preventable Infections in Children Following Solid Organ Transplant and Associated Morbidity, Mortality, and Costs

Amy G Feldman et al. JAMA Pediatr. .

Erratum in

  • Coding Error in Cohort Study.
    [No authors listed] [No authors listed] JAMA Pediatr. 2019 Mar 1;173(3):296. doi: 10.1001/jamapediatrics.2019.0231. JAMA Pediatr. 2019. PMID: 30830160 Free PMC article. No abstract available.

Abstract

Importance: Pediatric transplant recipients are at risk for vaccine-preventable infections owing to immunosuppression, suboptimal response to vaccines before and after transplant, and potential underimmunization if transplant occurred early in life. However, the incidence and burden of illness from vaccine-preventable infections in this population is unknown.

Objectives: To evaluate in pediatric solid organ transplant recipients the number of hospitalizations for vaccine-preventable infections in the first 5 years after transplant and to determine the associated morbidity, mortality, and costs.

Design, setting, and participants: A retrospective cohort study from January 1, 2004, to December 31, 2011, with 5 years of follow-up per participant (unless they died during the study period). The participants of this multicenter study through the Pediatric Health Information System were solid organ transplant recipients who were younger than 18 years at the time of transplant. Analysis began in July 2017.

Exposures: Transplant.

Main outcomes and measures: Hospitalizations for a vaccine-preventable infection during the first 5 years after transplant were ascertained using International Classification of Diseases, Ninth Revision, and International Statistical Classification of Diseases and Related Health Problems, Tenth Revision, clinical modification diagnosis codes. Data were collected on clinical care, outcomes, and costs during these hospitalizations.

Results: Of 6980 transplant recipients identified, there were 3819 boys (54.7%), and the mean (SD) age at transplant was 8 (6.2) years. Overall, 1092 patients (15.6%) had a total of 1471 cases of vaccine-preventable infections. There were 187 of 1471 cases (12.7%) that occurred during transplant hospitalization. The case fatality rate was 1.7% for all infections. Excluding infections that occurred during transplant hospitalization (when all patients go to the intensive care unit), 213 of 1257 patients (17.0%) were hospitalized with a vaccine-preventable infection requiring intensive care. In multivariable analysis, age younger than 2 years at time of transplant and receipt of a lung, heart, intestine, or multivisceral organ were positively associated with increased risk of a hospitalization from a vaccine-preventable infection.Transplant hospitalizations complicated by vaccine-preventable infections were $120 498 more expensive (median cost) than transplant hospitalizations not complicated by vaccine-preventable infections.

Conclusions and relevance: Hospitalization for vaccine-preventable infections occurred in more than 15% of solid organ transplant recipients in the first 5 years after transplant at a rate of up to 87 times higher than in the general population. There was significant morbidity, mortality, and costs from these infections, demonstrating the importance of immunizing all transplant candidates and recipients. Further research on improving immunization delivery, preventing nosocomial infections, and monitoring response to vaccines in the transplant population is needed.

PubMed Disclaimer

Conflict of interest statement

Conflict of Interest Disclosures: Dr Feldman was funded by the Children’s Hospital Colorado Research Institute Research Scholar Award and the National Institutes of Health/National Center for Advancing Translational Sciences Colorado (CTSA KL2 TR002534). Dr Curtis received funding from Sanofi Pasteur for a separate high-dose influenza vaccine study.

Figures

Figure.
Figure.. Incidence of Respiratory Syncytial Virus (RSV)/Vaccine-Preventable Infection (VPI) by Organ Type
The mean cumulative function of RSV or a VPI by days alive per transplanted organ type. Each mark represents an infection. MCF indicates mean cumulative function.

Similar articles

Cited by

References

    1. Fishman JA. Infection in solid-organ transplant recipients. N Engl J Med. 2007;357(25):2601-2614. doi:10.1056/NEJMra064928 - DOI - PubMed
    1. Kumar D, Humar A, Plevneshi A, et al. ; Toronto Invasive Bacterial Diseases Network . Invasive pneumococcal disease in solid organ transplant recipients: 10-year prospective population surveillance. Am J Transplant. 2007;7(5):1209-1214. doi:10.1111/j.1600-6143.2006.01705.x - DOI - PubMed
    1. Apalsch AM, Green M, Ledesma-Medina J, Nour B, Wald ER. Parainfluenza and influenza virus infections in pediatric organ transplant recipients. Clin Infect Dis. 1995;20(2):394-399. doi:10.1093/clinids/20.2.394 - DOI - PubMed
    1. Madeleine MM, Finch JL, Lynch CF, Goodman MT, Engels EA. HPV-related cancers after solid organ transplantation in the United States. Am J Transplant. 2013;13(12):3202-3209. doi:10.1111/ajt.12472 - DOI - PMC - PubMed
    1. Olarte L, Lin PL, Barson WJ, et al. . Invasive pneumococcal infections in children following transplantation in the pneumococcal conjugate vaccine era. Transpl Infect Dis. 2017;19(1). doi:10.1111/tid.12630 - DOI - PubMed

Publication types