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Hypersensitivity pneumonitis: Lessons from a randomized controlled trial in children. | LitMetric

Hypersensitivity pneumonitis: Lessons from a randomized controlled trial in children.

Pediatr Pulmonol

Department of Pediatric Pneumology, Dr. von Haunersches Kinderspital, German Center for Lung Research, University of Munich, Munich, Germany.

Published: August 2021

AI Article Synopsis

  • Hypersensitivity pneumonitis (HP) in children is a serious lung disease that could turn chronic if not treated correctly, but there are no established treatment guidelines, particularly regarding the use of glucocorticoids.
  • A clinical trial was conducted to compare the effects of 3 months of oral prednisolone against a placebo over 6 months, but it was halted early after only four children participated due to limited responses and side effects from the medication.
  • The study highlights the urgent need for evidence-based treatment for pediatric HP and suggests that future research could include children in broader studies that also examine adult HP cases.

Article Abstract

Introduction: Hypersensitivity pneumonitis (HP) in children is a severe interstitial lung disease and potentially, a chronic condition, if not treated appropriately. No evidence-based guidelines are available; in particular, the role of systemic glucocorticoid therapy is unclear.

Methods: The aim of this randomized, double-blind, placebo-controlled, parallel-group, multi-center, phase II trial in pediatric HP was to assess the outcome of HP in children after 6 months of treatment and to compare 3 months of treatment with oral prednisolone or placebo.

Results: After 1.5 years and the inclusion of only four children, we terminated the study prematurely. Two of the children randomized to prednisolone did not achieve the predefined response of FVC to normal. One child treated with placebo recovered to normal, similar to another child treated with prednisolone. All children treated with steroids developed drug-related side effects.

Discussion: This uncompleted study illustrates the urgent medical need for evidence-based treatment protocols for this condition. We discuss the hurdles which were specific for completion of this trial in a rare condition. Among other options, we suggest the inclusion of children into an all-age study of HP, as in adults the same questions are unanswered.

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Source
http://dx.doi.org/10.1002/ppul.25513DOI Listing

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