Affiliations 

  • 1 Department of Pediatrics, College of Medicine, Kuwait University, Kuwait City, Kuwait
  • 2 Department of Community Medicine and Behavioral Sciences, Faculty of Medicine, Kuwait University, Kuwait City, Kuwait
  • 3 Division of Immunology and Allergy, Sidra Medicine and Hamad Medical Corporation, Doha, Qatar
  • 4 Department of Pediatric Allergy and Clinical Immunology, The Royal Hospital, Muscat, Oman
  • 5 College of Medicine, Mohammed Bin Rashid University for Medicine and Health Sciences, Dubai, United Arab Emirates
  • 6 Department of Pediatrics, Tawam Hospital, Al-Ain, United Arab Emirates
  • 7 Division of Allergy and Immunology, Internal Medicine, Hamad Medical Corporation, Doha, Qatar
  • 8 Department of Child Health, Sultan Qaboos University Hospital, Muscat, Oman
Pediatr Allergy Immunol, 2022 Dec;33(12):e13901.
PMID: 36564872 DOI: 10.1111/pai.13901

Abstract

BACKGROUND: There is an increased demand for hematopoietic stem cell transplant (HSCT) to treat various diseases including combined immunodeficiencies (CID), with limited worldwide availability. Variables affecting the decision regarding CID patients' prioritization for HSCT are not known. We aimed to determine general, clinical, and immunologic factors associated with the higher risk of early death (≤6 months after diagnosis) in untransplanted CID patients.

METHODS: Data collection was done retrospectively from five centers and included general patients' information, and clinical and laboratory variables. Inclusion criteria were untransplanted patients who are either dead or alive with a follow-up period ≥6 months after diagnosis.

RESULTS: Two hundred and thirty-six CID patients were reported by participating centers, of whom 111 were included in the study with a cumulative follow-up period of 278.6 years. Seventy-two patients died with the median age of death of 10.5 months. 35.1% of the patients succumbed within 6 months after the diagnosis. Having a history of Candida infections, sepsis or hepatomegaly was associated with an increased risk of early death. None of the other general or clinical variables was associated with such risk. Bivariate analysis of lymphocyte subsets showed that patients with the following counts: CD3+  

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.