[Clinical features and early diagnostic clues of chronic granulomatous disease]

H Liu1, H M Li1, J R Liu1

  • 1Department No.2 of Respiratory Medicine, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing 100045, China.

Insights

Early diagnosis of chronic granulomatous disease (CGD) in children is crucial. Key clinical clues like large BCG scars and recurrent infections can significantly shorten diagnosis time and reduce healthcare costs.

Area of Science:

  • Pediatrics
  • Immunology
  • Infectious Diseases

Background:

  • Chronic granulomatous disease (CGD) is a primary immunodeficiency characterized by impaired phagocyte function.
  • Delayed diagnosis of CGD leads to increased morbidity and mortality due to recurrent, severe infections.
  • Identifying early clinical indicators is essential for timely diagnosis and management of CGD.

Purpose of the Study:

  • To identify and evaluate early clinical clues for the diagnosis of chronic granulomatous disease (CGD) in children.
  • To assess the impact of utilizing these early diagnostic clues on the time to diagnosis and healthcare utilization.

Main Methods:

  • Retrospective analysis of clinical features of 139 children diagnosed with CGD between January 2007 and October 2020.
  • Evaluation of clinical manifestations, age of onset, reasons for hospitalization, and diagnostic delays.
  • Comparison of diagnostic time, length of stay, and hospital charges between patients diagnosed before and after 2015, following the identification of early diagnostic clues.

Main Results:

  • CGD onset was typically early (74.1% before 1 year), with a median diagnostic delay of 1 year.
  • Pulmonary infections were the most common presentation (97.1%), often with misdiagnosis rates as high as 96.3%.
  • Eight key early diagnostic clues were identified: large BCG scar, left axillary lymphadenopathy/calcification, skin/lymph node infections, skin scars, multiple lung nodules, perianal abscess, and pulmonary infections with Aspergillus or Burkholderia.

Conclusions:

  • CGD often presents in young children with significant diagnostic delays, primarily due to recurrent pulmonary infections.
  • The identified early clinical clues, including specific infection patterns and physical findings, can significantly aid in the early diagnosis of CGD.
  • Implementing these early diagnostic clues led to shorter diagnosis times, reduced hospital stays, and lower charges in the post-2015 cohort.

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