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Iron burden and endocrine complications in transfusion-dependent thalassemia patients In Sarawak, Malaysia: a retrospective study.
Chow, L C; Lee, B S; Tang, S O; Loh, E W; Ng, S C; Tan, X Y; Ahmad Noordin, M N; Ong, G B; Chew, L C.
Afiliação
  • Chow LC; Sarawak General Hospital, Department of Medicine, Haematology Unit, Jalan Hospital, Kuching, Sarawak, Malaysia. connie_chow2002@hotmail.com.
  • Lee BS; Sarawak General Hospital, Department of Paediatrics, Jalan Hospital, Kuching, Sarawak, Malaysia.
  • Tang SO; Miri Hospital, Department of Medicine, Jalan Cahaya, Miri, Sarawak, Malaysia.
  • Loh EW; Bintulu Hospital, Department of Medicine, Jalan Nyabau, Bintulu, Sarawak, Malaysia.
  • Ng SC; Limbang Hospital, Department of Medicine, Jalan Pandaruan, Limbang, Sarawak, Malaysia.
  • Tan XY; Sibu Hospital, Department of Medicine, Jalan Ulu Oya, Sibu, Sarawak, Malaysia.
  • Ahmad Noordin MN; Lawas Hospital, Department of Medicine, Jalan Hospital, Lawas, Sarawak, Malaysia.
  • Ong GB; Sarawak General Hospital, Department of Paediatrics, Paediatric Haemato-Oncology Unit, Kuching, Sarawak, Malaysia.
  • Chew LC; Sarawak General Hospital, Department of Medicine, Haematology Unit, Jalan Hospital, Kuching, Sarawak, Malaysia.
Med J Malaysia ; 79(3): 281-287, 2024 May.
Article em En | MEDLINE | ID: mdl-38817060
ABSTRACT

INTRODUCTION:

Thalassaemia is one of the major health problems in Malaysia. With safe blood transfusion regime, the lifespan of patients with transfusion-dependent thalassaemia (TDT) has improved but at the cost of a higher risk of developing endocrine disorders. It is crucial for us to monitor the iron overload to prevent end organ damage. This study aims to evaluate the iron burden and prevalence of endocrinopathies in patients with TDT in Sarawak. MATERIALS AND

METHODS:

This retrospective cohort study was conducted between January 2020 to June 2020 in six government hospitals in Sarawak. A total of 89 patients with TDT, aged 10 years and above, were recruited.

RESULTS:

Out of the 89 patients, there were 54 males (60.7%) and 35 females (39.3%) with a median age of 21 years (range 10.0-65.0). Sixty-seven (75.3%) patients had betathalassaemia major and 15 (16.9%) patients had haemoglobin E beta-thalassaemia (HbE beta-thalassaemia), remaining seven patients had other genotypes. Thirty-one (34.8%) patients had mean serum ferritin 2500ng/ml and above, and 44 (66.6%) had liver iron concentration (LIC) ≥7mg/g. The prevalence of endocrine disorders in our cohort was 69.7%. The most common endocrinopathies were short stature (n=46, 51.7%), followed by hypogonadism (n=24, 26.9%), delayed puberty (n=23, 25.8%), hypothyroidism (n=10, 11.2%), diabetes mellitus (n=9, 10.1%), impaired glucose tolerance (n=6, 6.7%) and hypoparathyroidism (n=3, 3.3%). Endocrinopathies were significantly associated with age (p=0.01), age at initiating regular blood transfusion (p<0.01) and duration of regular blood transfusion (p<0.01).

CONCLUSION:

Our data shows that the development of endocrinopathies in TDT can be time dependent. Early detection of endocrine-related complications and prompt treatment with iron chelation therapy are important to improve morbidity and mortality. A multidisciplinary approach with good patient-doctor collaboration is the key to improving patient care in our settings.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Talassemia / Transfusão de Sangue / Sobrecarga de Ferro / Doenças do Sistema Endócrino Limite: Adolescent / Adult / Aged / Child / Female / Humans / Male / Middle aged País/Região como assunto: Asia Idioma: En Revista: Med J Malaysia Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Malásia
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Talassemia / Transfusão de Sangue / Sobrecarga de Ferro / Doenças do Sistema Endócrino Limite: Adolescent / Adult / Aged / Child / Female / Humans / Male / Middle aged País/Região como assunto: Asia Idioma: En Revista: Med J Malaysia Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Malásia