ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • ACR Convergence 2020
    • 2020 ACR/ARP PRSYM
    • 2019 ACR/ARP Annual Meeting
    • 2018-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings

Abstract Number: 001

Serious Infections Among Children with Systemic Lupus Erythematosus in the Pediatric Health Information System

Jordan Roberts, Anna Faino, Mersine Bryan, Jonathan Cogen and Esi Morgan, Seattle Children's Hospital, Seattle, WA

Meeting: 2023 Pediatric Rheumatology Symposium

Keywords: Administrative Data, Infection, juvenile SLE, Pediatric rheumatology, Systemic lupus erythematosus (SLE)

  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print
Session Information

Date: Thursday, March 30, 2023

Title: Plenary Abstracts Session I

Session Type: Plenary Session

Session Time: 2:30PM-3:30PM

Background/Purpose: High rates of serious infection have beenreported in pediatric systemic lupus erythematosus (pSLE), but modern care practices including pneumococcal vaccination, changing corticosteroid use, and B-cell-depletion may modify infectious risks. The current burden of infections in pSLE is unknown. We conducted a retrospective study using the Pediatric Health Information System (PHIS) to determine number and type of serious infections in hospitalized children with pSLE, and to identify risk factors for poor outcomes.

Methods: We included patients 2-21 years of age with ICD-9 or ICD-10 code for SLE (710.0, M32*) during admission to a hospital participating in PHIS, an administrative database of 50 freestanding childrens hospitals in the United States, from 2009-2021. Serious infections were identified using ICD-9 and ICD-10 codes and antimicrobial medication use. Summary statistics were used to describe demographic and disease features of the entire PHIS pSLE cohort, and the subset hospitalized with serious infection. We calculated the frequency of admission, intensive care admission, and mortality by type of infection. Logistic regression using generalized estimating equations was used to identify risk factors for ICU admission and in-hospital mortality among children hospitalized with infection.

Results: We identified 11,178 unique patients with pSLE and at least one hospitalization in PHIS. Among this cohort, there were 32,414 hospitalizations, of which 3,839 (11.8%) had codes for serious infections. Patients hospitalized with serious infections were similar in demographic and disease characteristics to the entire PHIS pSLE cohort (Table 1). Specific infections and outcomes of hospitalization are reported in Table 2. The most common infections were bacterial pneumonia (n=1159), cellulitis (n=810), sepsis (n=693) and urinary tract infections (n=498). In-hospital mortality occurred in 1% of children with pSLE hospitalized for all indications and in 3% of hospitalizations with a code for serious infection. The highest in-hospital mortality rates occurred in hospitalizations with codes for pneumocystis jirovecii pneumonia (22%), aspergillosis (15%), and other fungal infections (18%). Approximately half of children who died had ≥2 serious infections during the hospitalization in which death occurred. Lupus nephritis and end-stage renal disease (ESRD) were significantly associated with increased odds of ICU admission (OR [95% CI] of 1.6 [1.3, 1.8] and 2.1 [1.6, 2.7], respectively) and in-hospital mortality (OR [95% CI] 2.3 [1.3, 4.0] and 2.1 [1.0, 4.2]) among children admitted for a serious infection (Figure 1).

Conclusion: Hospitalizations including codes for serious infection comprised a small proportion of pSLE admissions but accounted for the majority resulting in in-hospital mortality among patients with pSLE in the PHIS cohort. While bacterial infections were more common, mortality rates of hospitalizations with codes for fungal infections were high. Patients with pSLE and renal disease were at increased risk for poor outcomes. Further research is needed to understand modifiable risk factors for infection and severe outcomes, including immunosuppressant medication use.

Supporting image 1Table 1: Characteristics of children with pSLE hospitalized for any indication and with serious infection from 2009_2021

Supporting image 2Table 2: Hospitalization Outcome by Type of Infection and Disease Characteristics

*Death during hospitalization was considered either with or without ICU admission.

Supporting image 3Figure 1: Odds of ICU admission and mortality among children with pSLE hospitalized with infection


Disclosures: J. Roberts: None; A. Faino: None; M. Bryan: None; J. Cogen: None; E. Morgan: None.

To cite this abstract in AMA style:

Roberts J, Faino A, Bryan M, Cogen J, Morgan E. Serious Infections Among Children with Systemic Lupus Erythematosus in the Pediatric Health Information System [abstract]. Arthritis Rheumatol. 2023; 75 (suppl 4). https://acrabstracts.org/abstract/serious-infections-among-children-with-systemic-lupus-erythematosus-in-the-pediatric-health-information-system/. Accessed .
  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print

« Back to 2023 Pediatric Rheumatology Symposium

ACR Meeting Abstracts - https://acrabstracts.org/abstract/serious-infections-among-children-with-systemic-lupus-erythematosus-in-the-pediatric-health-information-system/

Advanced Search

Your Favorites

You can save and print a list of your favorite abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract. View your favorites »

All abstracts accepted to ACR Convergence are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of our scientific journal, Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. In an exception to the media embargo, academic institutions, private organizations, and companies with products whose value may be influenced by information contained in an abstract may issue a press release to coincide with the availability of an ACR abstract on the ACR website. However, the ACR continues to require that information that goes beyond that contained in the abstract (e.g., discussion of the abstract done as part of editorial news coverage) is under media embargo until 10:00 AM ET on November 14, 2024. Journalists with access to embargoed information cannot release articles or editorial news coverage before this time. Editorial news coverage is considered original articles/videos developed by employed journalists to report facts, commentary, and subject matter expert quotes in a narrative form using a variety of sources (e.g., research, announcements, press releases, events, etc.).

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying colleagues, institutions, communications firms, and all other stakeholders related to the development or promotion of the abstract about this policy. If you have questions about the ACR abstract embargo policy, please contact ACR abstracts staff at [email protected].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2025 American College of Rheumatology