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Abstract Number: 462

Steroid Use in Pediatric Proliferative Lupus Nephritis

Nathalie Chalhoub1, Jianghong Deng2, Natasha M. Ruth3, Stacy P. Ardoin4, Mileka Gilbert5, Theresa Hennard6, Linda Hiraki7, Paul T. Jensen8, Andrea M. Knight9, Rebecca Kunder10, Laura Lewandowski11, Siok Hoon Lily Lim12, Angela Merritt13, Sonia Iqbal Savani14, Mary Beth Son15, Emily von Scheven16, Scott E. Wenderfer17 and Hermine I. Brunner6, 1Division of Immunology, Allergy, and Rheumatology, University of Cincinnati College of Medicine, Cincinnati, OH, 2Division of Rheumatology, Beijing Children’s Hospital and Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 3Rheumatology, Medical University of South Carolina, Charleston, SC, 4Division of Rheumatology, Nationwide Children’s Hospital, Columbus, OH, 5Pediatric Rheumatology, Medical University of South Carolina, Charleston, SC, 6Division of Rheumatology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 7Child Health Evaluative Sciences, The Hospital for Sick Children, Toronto, ON, Canada, 8Internal Medicine, The Ohio State University Wexner Medical Center, Columbus, OH, 9Division of Pediatric Rheumatology, Children's Hospital of Philadelphia, Philadelphia, PA, 10Gilead Sciences, Inc, Redwood City, CA, 11NIAMS/NIH, Bethesda, MD, 12Children's Hospital Research Institute of Manitoba, University of Manitoba, Winnipeg, MB, Canada, 13Pediatric Rheumatology, Division of Rheumatology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 14Medical University of South Carolina, Charleston, SC, 15Boston Children's Hospital, Harvard Medical School, Brookline, MA, 16Pediatric Rheumatology, University of California San Francisco, San Francisco, CA, 17Pediatrics-Renal, Baylor College of Medicine, Houston, TX

Meeting: 2018 ACR/ARHP Annual Meeting

Keywords: corticosteroids, lupus nephritis and systemic lupus erythematosus (SLE)

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Session Information

Date: Sunday, October 21, 2018

Title: Pediatric Rheumatology – Clinical Poster I: Lupus, Sjögren’s Disease, and Myositis

Session Type: ACR Poster Session A

Session Time: 9:00AM-11:00AM

Background/Purpose: Corticosteroids (CS) are the mainstay of childhood-onset lupus (cSLE) and proliferative lupus nephritis (LN) therapy. However, there are no widely accepted CS dosing regimens for LN. We aim to identify the CS treatment approaches employed by providers for newly diagnosed pediatric proliferative LN in response to common and challenging clinical scenarios.

Methods: Pediatric rheumatologists and nephrologists attending the 2018 Childhood Arthritis and Rheumatology Research Alliance (CARRA) meeting participated in a working group addressing CS use in newly diagnosed pediatric LN. Participants responded to 3 scenarios in live polling and 12 questions of CS management in small groups. A post meeting survey was sent to each participant.

Results: In total, 51 physicians participated in the working group and 25 answered the survey. Of the 51 participants, 42 (82%) reported prednisone to be the oral CS of choice to treat newly diagnosed pediatric LN and 64.7% favored liquid prednisolone if swallowing pills is problematic. Once daily dosing was the preferred regimen (15/25, 60%) to help patients with adherence. Some (8/25, 32%) use a twice daily regimen for prednisone doses >2mg/kg/day or 60mg. A 3-4 times daily regimen was considered for hospitalized patients with severe disease manifestations by 6/25, 24%. Factors leading to the use of intravenous (IV) pulse methylprednisolone during the initial 12 months of therapy for proliferative LN are shown in Figure 1. Laboratory results prompting a CS dose change are shown in Table 1 (Panels A/B). Side effects such as weight gain (20/25, 80%), difficult to control blood pressure (19/25, 76%) or hyperglycemia (21/25, 84%) were reported as reasons to taper CS. In patients with inactive LN on mycophenolate mofetil, the extra-renal features that prompt an increase in CS are new/worsening neuropsychiatric disease (24/25, 96%), cardiac (23/25, 92%), or pulmonary involvement (23/25, 92%). In cases of non-adherence, all physicians would discuss reasons for non-adherence with 72% choosing to start/increase the frequency of IV steroids.

Conclusion: Prescribed CS dosing regimens vary widely in the U.S. when used for the treatment of children with proliferative LN.  Decisions on initial CS dosing regimens and subsequent management strategies remain provider dependent.

 

Figure 1.

 

 

 

 

 

 

 

 

Table 1.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 


Disclosure: N. Chalhoub, None; J. Deng, None; N. M. Ruth, None; S. P. Ardoin, None; M. Gilbert, None; T. Hennard, None; L. Hiraki, None; P. T. Jensen, None; A. M. Knight, None; R. Kunder, Gilead Sciences, Inc, 3; L. Lewandowski, None; S. H. L. Lim, None; A. Merritt, None; S. I. Savani, None; M. B. Son, None; E. von Scheven, None; S. E. Wenderfer, None; H. I. Brunner, None.

To cite this abstract in AMA style:

Chalhoub N, Deng J, Ruth NM, Ardoin SP, Gilbert M, Hennard T, Hiraki L, Jensen PT, Knight AM, Kunder R, Lewandowski L, Lim SHL, Merritt A, Savani SI, Son MB, von Scheven E, Wenderfer SE, Brunner HI. Steroid Use in Pediatric Proliferative Lupus Nephritis [abstract]. Arthritis Rheumatol. 2018; 70 (suppl 9). https://acrabstracts.org/abstract/steroid-use-in-pediatric-proliferative-lupus-nephritis/. Accessed .
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