Vaccination practices and knowledge among adults with hemoglobinopathies in Greece: a nationwide survey

Background: Hemoglobinopathies, such as sickle cell disease and thalassemia, are genetic disorders that affect hemoglobin structure or production, leading to various health complications, including an increased risk of infections. Vaccinations play a crucial role in managing these conditions by prov...

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Main Authors: Sophia Delicou (Author), Konstantinos Manganas (Author), Aikaterini Xydaki (Author), Loukia Evliati (Author), Ioanna Myrilla (Author), Leonidas Rubatis (Author), Stavroula Kostaridou (Author)
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Published: SAGE Publishing, 2024-09-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Sophia Delicou  |e author 
700 1 0 |a Konstantinos Manganas  |e author 
700 1 0 |a Aikaterini Xydaki  |e author 
700 1 0 |a Loukia Evliati  |e author 
700 1 0 |a Ioanna Myrilla  |e author 
700 1 0 |a Leonidas Rubatis  |e author 
700 1 0 |a Stavroula Kostaridou  |e author 
245 0 0 |a Vaccination practices and knowledge among adults with hemoglobinopathies in Greece: a nationwide survey 
260 |b SAGE Publishing,   |c 2024-09-01T00:00:00Z. 
500 |a 2515-1363 
500 |a 10.1177/25151355241278869 
520 |a Background: Hemoglobinopathies, such as sickle cell disease and thalassemia, are genetic disorders that affect hemoglobin structure or production, leading to various health complications, including an increased risk of infections. Vaccinations play a crucial role in managing these conditions by providing essential protection against preventable diseases. Ensuring timely and appropriate immunizations is vital for reducing infection-related morbidity and improving the overall health and quality of life for affected individuals. Objectives: Our objective was to assess vaccination coverage, as well as knowledge, attitudes, and practices toward vaccination in Greek patients with hemoglobinopathies. Design and methods: A nationwide survey of hemoglobinopathy patients in Greece using a 37-item questionnaire was conducted anonymously via Google Forms. It covered demographics, previous vaccinations, vaccine-preventable infections, beliefs about vaccines, and antibiotic prophylaxis post-splenectomy. The survey was distributed through Thalassemia and Sickle Cell Units and organizations. Results: Participants were predominantly university-educated married women aged 30-50 years with transfusion-depended thalassemia ( n  = 149, 60.5%) or sickle cell anemia ( n  = 52, 21.1%). Reported childhood vaccination rates aligned with Greece's national immunization program. However, adult coverage was suboptimal across all age groups for measles (10%), varicella (27%), zoster (2% for over 50 years old individuals), hepatitis A (13.9% of those with chronic liver disease) and hepatitis B (41%), pneumococcal (81.3%), meningococcal (37%), tetanus (20.3%), and influenza (67.1%) vaccines compared to guidelines. Participants relied predominantly on healthcare providers for vaccine information but perceived limited engagement. Those over age 50 demonstrated lower adult vaccination rates and higher misconceptions compared to younger cohorts. Conclusion: Addressing educational and access gaps could help protect this vulnerable population. Our findings highlight the need for coordinated efforts to optimize adult immunization for those with hemoglobinopathies. 
546 |a EN 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
690 |a Immunologic diseases. Allergy 
690 |a RC581-607 
655 7 |a article  |2 local 
786 0 |n Therapeutic Advances in Vaccines and Immunotherapy, Vol 12 (2024) 
787 0 |n https://doi.org/10.1177/25151355241278869 
787 0 |n https://doaj.org/toc/2515-1363 
856 4 1 |u https://doaj.org/article/6c35e8414a3146e0902f0b9e31a99d9c  |z Connect to this object online.