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The use of non-steroidal anti-inflammatory drugs in paediatric rheumatic diseases

P Hollingworth1

  • 1Rheumatology Department, Southmead Hospital, Bristol.

Insights

Nonsteroidal anti-inflammatory drugs (NSAIDs) are effective for juvenile idiopathic arthritis (JIA). While generally well-tolerated in children, specific NSAIDs are recommended for fever or joint symptoms, with careful monitoring for potential toxicities.

Area of Science:

  • Pediatric Rheumatology
  • Pharmacology
  • Clinical Therapeutics

Background:

  • Juvenile idiopathic arthritis (JIA) management differs significantly from adult arthritis due to pediatric-specific pharmacokinetics and assessment challenges.
  • Fewer nonsteroidal anti-inflammatory drugs (NSAIDs) are available or indicated for pediatric use compared to adults.
  • Children may underreport pain, influencing assessment and treatment strategies for arthritis.

Purpose of the Study:

  • To review the distinct indications, uses, pharmacokinetics, and available NSAIDs for managing arthritis in children.
  • To compare the efficacy and safety profiles of different NSAIDs for fever and joint symptom control in pediatric arthritis.
  • To highlight potential toxicities, drug interactions, and optimal therapeutic trial duration for NSAIDs in children.

Main Methods:

  • Literature review focusing on NSAID use in pediatric arthritis.
  • Comparison of efficacy and tolerance data for salicylates, indomethacin, ibuprofen, diclofenac, tolmetin, and naproxen.
  • Analysis of safety data, including gastrointestinal, renal, and hepatic toxicities, and drug interactions.

Main Results:

  • For systemic JIA fever, salicylates, indomethacin, and ibuprofen are used.
  • Diclofenac, ibuprofen, tolmetin, and naproxen show equal efficacy and tolerance for joint symptoms; salicylates and indomethacin are less effective and more toxic.
  • Children generally tolerate NSAIDs well, with fewer gastrointestinal issues reported than in adults, though evidence on endoscopic changes is conflicting. Renal toxicity is rare, but specific NSAIDs carry risks (tolmetin: pseudoproteinuria, naproxen: pseudoporphyria). Liver toxicity is a concern in systemic JIA.

Conclusions:

  • NSAIDs are a cornerstone in managing pediatric arthritis, with specific agents favored for different symptoms.
  • While generally safe, careful consideration of potential toxicities and drug interactions is crucial for optimal pediatric NSAID therapy.
  • An 8-week therapeutic trial is recommended for NSAIDs in children with arthritis, necessitating vigilant monitoring.

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