Evidence map›Paper›PMID 41939118›Full record

ArticleAnnals of medicine and surgery (2012)2026

Insights into the clinical features of thalassemia patients: a single-center study.

Suad M Jatal, Sawsan J Harfouch, Rim M Harfouch

Abstract read
In one paragraph

Article in Annals of medicine and surgery (2012), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

3 authors.

Suad M JatalFaculty of Pharmacy, Alsham Private University (ASPU), Latakia, Syria.
Sawsan J HarfouchFaculty of Pharmacy, Alsham Private University (ASPU), Latakia, Syria.
Rim M HarfouchFaculty of Pharmacy, Latakia (Tishreen) University, Latakia, Syria.ORCID https://orcid.org/0000-0001-7002-8728

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Thalassemia is a hereditary hemoglobinopathy that requires lifelong care, with β-thalassemia major being the most prevalent and severe form in the Mediterranean region, including Syria. Despite national programs for diagnosis and treatment, data on clinical patterns and healthcare challenges among Syrian patients remain scarce. Objective: This study aimed to characterize the demographic and clinical features of thalassemia patients in a city in Syria and identify gaps in management and preventive care. Methods: A cross-sectional study was conducted on 53 patients at the Thalassemia Center, between October 2024 and April 2025. Data were collected via patient interviews and a review of medical records. Variables included age, sex, thalassemia type, transfusion frequency, iron chelation therapy, splenectomy status, hemoglobin electrophoresis, ferritin levels, and vaccination status. Descriptive statistics and chi-square tests were used in the analysis. Results: The cohort comprised 28 males and 25 females, with β-thalassemia major accounting for 79.2% of cases and sickle cell thalassemia (15%). Elevated ferritin (>1000 ng/mL) was observed in 83% of patients, and 83% received iron chelation, mostly orally. Sickle hemoglobin was significantly associated with sickle cell thalassemia ( Conclusions: Thalassemia patients exhibit high rates of iron overload and undervaccination, reflecting the challenges in disease monitoring and preventive care. Despite the availability of treatment, significant gaps remain in patient education, genetic counseling, and healthcare infrastructure. Strengthening multidisciplinary care, improving vaccination strategies, and enforcing genetic screening are essential for enhancing outcomes in this vulnerable population.

Indexed as

cross-sectional studyiron overloadSyriaThalassemia

Identifiers

PMID41939118
PMCPMC13048676

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