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DOI 10.2147/opth.s128341

Медицинская библиотека · Clinical ophthalmology (Auckland, N.Z.) · 2017

Systemic abnormalities associated with retinal vein occlusion in young patients.

Sinawat Suthasinee, Bunyavee Chavisa, Ratanapakorn Tanapat, Sinawat Supat, Laovirojjanakul Wipada, Yospaiboon Yosanan

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Аннотация

OBJECTIVES

To study the systemic abnormalities associated with retinal vein occlusion in patients aged ≤50 years with a particular emphasis on atherosclerotic diseases and thrombophilic disorders.

METHODS

Medical charts of patients, aged ≤50 years whose diagnoses were retinal vein occlusions during the period 1995-2015 were retrospectively reviewed. The primary outcome was the number of systemic abnormalities associated with these patients. Secondary outcomes included types of retinal vein occlusion and sites of occlusion.

RESULTS

Atherosclerotic diseases were the most common systemic abnormalities associated with retinal vein occlusion and accounted for 55.1% of the patients in the study. Hypertension in 27.55%, diabetes mellitus in 16.33%, and 5.1% with dyslipidemia were noted. The number of thrombophilic disorders seemed to be less than expected and were noted in only 5.1%. Other systemic abnormalities included viral hepatitis infection, systemic lupus erythematosus, and acquired immunodeficiency syndrome. Oral contraceptives were used by some patients.

CONCLUSION

Atherosclerotic diseases remained the most commonly associated systemic diseases in the majority of these patients. Approach to these patients should include a screening for hypertension, diabetes mellitus, and lipid abnormalities. Thrombophilia should also be considered where no obvious atherosclerotic diseases are found or if the patient is <40 years old, a history of thrombosis or a family history of thrombosis is possible.

Для цитирования: Sinawat Suthasinee, Bunyavee Chavisa, Ratanapakorn Tanapat, Sinawat Supat, Laovirojjanakul Wipada, Yospaiboon Yosanan. Systemic abnormalities associated with retinal vein occlusion in young patients.. Clinical ophthalmology (Auckland, N.Z.). 2017. DOI: 10.2147/opth.s128341.
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