Thalassemia‐related complications in pediatric, adolescent, and young adult patients with transfusion‐dependent thalassemia: A multicenter study in Thailand

Abstract

AbstractIntroductionManagement of transfusion‐dependent thalassemia (TDT) can be challenging due to numerous potential disease‐related complications and comorbidities in particular age groups. The objective of this study was to report thalassemia‐related complications and risk factors in pediatric, adolescent, and young adult patients with TDT.MethodsA multicenter web‐based registry was conducted in patients with TDT aged 25 years and younger from eight university hospitals covering all parts of Thailand. Factors significantly associated with each complication were analyzed by logistic regression methods.ResultsOf 605 patients, 267 thalassemia‐related complications were reported from 231 pediatric, adolescent, and young adult patients with TDT patients (38.2%). The most common complications were infections, followed by cholelithiasis and growth failure. Splenectomy and elevated pre‐transfusion hemoglobin were statistically significant risk factors for infections (adjusted odds ratio [AOR] = 2.3, 95% confidence interval [CI]: 1.2–4.5, p‐value = .01 and AOR = 1.5, 95% CI: 1.2–1.7, p‐value < .005, respectively). There were two statistically significant risk factors conferred endocrinopathies, including older age (AOR = 1.06, 95% CI: 1.01–1.1, p‐value = .01) and being male (AOR = 2.4, 95% CI: 1.4–4.0, p‐value = .002).ConclusionNearly 40% of the patients in this cohort had thalassemia‐related complications. Periodic surveillance and optimal care for respective complications may minimize comorbidities in pediatric, adolescent, and young adult patients with TDT.