Transfusion in haemoglobinopathies: Review and recommendations for local blood banks and transfusion services in Oman

Arwa Z. Al-Riyami, Shahina Daar

Research output: Contribution to journalReview article

2 Citations (Scopus)


Sickle cell disease and homozygous β-thalassaemia are common haemoglobinopathies in Oman, with many implications for local healthcare services. The transfusions of such patients take place in many hospitals throughout the country. Indications for blood transfusions require local recommendations and guidelines to ensure standardised levels of care. This article summarises existing transfusion guidelines for this group of patients and provides recommendations for blood banks and transfusion services in Oman. This information is especially pertinent to medical professionals and policy-makers developing required services for the standardised transfusion support of these patients.

Original languageEnglish
Pages (from-to)e3-e12
JournalSultan Qaboos University Medical Journal
Issue number1
Publication statusPublished - Feb 1 2018



  • Blood Banks
  • Blood Transfusion
  • Hemoglobinopathies
  • Oman
  • Sickle Cell Disease
  • Thalassemia Major

ASJC Scopus subject areas

  • Medicine(all)

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