Ocular manifestations in patients with transfusion-dependent β-thalassemia.

IF 0.3 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL
Hippokratia Pub Date : 2021-04-01
F Akritidou, A Praidou, T Papamitsou, V Kozobolis, G Labiris
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引用次数: 0

Abstract

Background: Ocular involvement in patients with transfusion-dependent β-thalassemia is quite common, and its frequency differs among studies. This case series aimed to describe the ocular abnormalities occurring in β-thalassemia patients who need regular blood transfusions and receive iron chelation therapy.

Case series: This is a case series prospectively studied 32 β-thalassemia patients from Northern Greece receiving regular blood transfusions and iron-chelating therapy. Patients' average age was 35.5 years. Eighteen patients with major phenotypes and fourteen patients with intermedia type underwent comprehensive ophthalmic examination at the time of enrolment, including visual acuity evaluation, refraction and color vision tests, Amsler grid test, slit-lamp, and dilated-pupil fundus examination. Additionally, we performed visual field testing and optical coherence tomography in all patients and fluorescein angiography only in selected cases. After six months, patients' complete ophthalmic examination was repeated for any new ocular findings due to the disease process and iron chelation therapy. Ocular involvement was detected in 46.87 % of the patients. Lesions were most frequently seen in elderly patients with thalassemia major. Lens opacities were present in 21.8 %, and degeneration of the retinal pigment epithelium was described in 15.6 % of the patients, representing the commonest fundus alteration observed, followed by fundus atrophy. The most severe and vision-threatening condition described in this study was the presence of angioid streaks with choroidal neovascularisation. Six months follow-up of patients did not reveal any new ocular findings.

Conclusion: Early detection of severe ocular abnormalities is important in patients with thalassemia; thus, an ophthalmologic examination should be included at regular check-ups. An annual examination is currently indicated for asymptomatic patients, while in symptomatic and complicated cases, patients should be closely followed-up. HIPPOKRATIA 2021, 25 (2):79-82.

输血依赖性β-地中海贫血患者的眼部表现。
背景:输血依赖性β-地中海贫血患者的眼部受累是相当常见的,其频率在不同的研究中有所不同。本病例系列旨在描述需要定期输血并接受铁螯合治疗的β-地中海贫血患者发生的眼部异常。病例系列:这是对来自希腊北部接受常规输血和铁螯合治疗的32例β-地中海贫血患者进行前瞻性研究的病例系列。患者平均年龄35.5岁。18例主要表现型患者和14例中间表现型患者在入组时进行了全面的眼科检查,包括视力评估、屈光和色视测试、Amsler网格测试、裂隙灯和扩大瞳孔眼底检查。此外,我们对所有患者进行了视野测试和光学相干断层扫描,仅在选定的病例中进行了荧光素血管造影。6个月后,再次对患者进行完整的眼科检查,以检查因疾病进程和铁螯合治疗而出现的任何新的眼部发现。46.87%的患者眼部受累。病变最常见于老年重度地中海贫血患者。21.8%的患者出现晶状体混浊,15.6%的患者出现视网膜色素上皮变性,这是观察到的最常见的眼底改变,其次是眼底萎缩。本研究中描述的最严重和视力威胁的情况是血管样条纹伴脉络膜新生血管的存在。6个月的随访未发现任何新的眼部发现。结论:早期发现严重眼部异常对地中海贫血患者有重要意义;因此,眼科检查应包括在定期检查。目前对无症状的患者应每年检查一次,对有症状和并发症的患者应密切随访。中华医学杂志,2015,25(2):79-82。
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来源期刊
Hippokratia
Hippokratia MEDICINE, GENERAL & INTERNAL-
CiteScore
1.10
自引率
0.00%
发文量
0
审稿时长
6-12 weeks
期刊介绍: Hippokratia journal is a quarterly issued, open access, peer reviewed, general medical journal, published in Thessaloniki, Greece. It is a forum for all medical specialties. The journal is published continuously since 1997, its official language is English and all submitted manuscripts undergo peer review by two independent reviewers, assigned by the Editor (double blinded review process). Hippokratia journal is managed by its Editorial Board and has an International Advisory Committee and over 500 expert Reviewers covering all medical specialties and additionally Technical Reviewers, Statisticians, Image processing Experts and a journal Secretary. The Society “Friends of Hippokratia Journal” has the financial management of both the printed and electronic edition of the journal.
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