Ocular toxicity of psychotropic medications in a tertiary hospital in Lagos, Nigeria.

Modupe Medina Balogun, Olurotimi Ayodele Coker
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Abstract

Objective: This study aimed to determine the ocular toxicity of the psychotropic drugs used by patients and to proffer suggestions on how to prevent visual impairment or blindness in patients on antipsychotics. Methodology: This was a prospective, hospital-based cross-sectional study. Participants were adult patients between 18 and 70 years, diagnosed with psychosis, and who had been on antipsychotic medications for at least one year. All the recruited participants had an examination of the anterior and posterior segments of the eyes done. Schirmer's test, Tear film Break-up time (TBUT), Central Corneal thickness (CCT), Colour vision test, and Contrast sensitivity test were done. The collected data was analyzed using IBM SPSS 28.0. Results: The study enrolled patients who were mainly females (55.1%). The highest age group of the cases was 29-38 years (29.7%). The examination of the eyes and investigations revealed that 10.2% of the respondents on antipsychotics had color vision deficiency and 25.4% - loss of contrast sensitivity. Lid pigmentation was observed in 20.3% and cataract in 32.2%. Degeneration of the peripheral retina was observed in 4.2% of patients on antipsychotic medication. Schirmer's test showed mild, moderate, and severe dry eyes in 11%,17.8%, and 20.3% of the participants respectively. The test for Central Corneal Thickness (CCT) showed 50.0% of the respondents had a thin cornea and 24.6% had a thick cornea. 17.8% of the surveyed respondents manifested high eye pressure. Discussion: Psychotropics are the gold standard for the treatment of psychotic episodes and disorders. The choice of drug, dosing, and mode of administration depends on the severity of the psychotic disorder. Higher doses of psychotropics were reported to cause toxicity in different organs in the body including the eyes, especially on long-term use and high dosage and this can affect the quality of life of the individual negatively. Conclusion: The earliest and most prominent side effect seen in patients on psychotic medication was dry eyes. There were a few cases of blinding eye diseases like glaucoma, and cataract. For these reasons, ophthalmic assessments should be included as part of the management of psychiatric patients early at the start of antipsychotic treatment. Abbreviations: FGA = First Generation Antipsychotics, SGA = Second Generation Antipsychotics, TCAs = Tricyclic Antidepressants, CCT = Central Corneal Thickness, IOP = Intraocular Pressure, TBUT =Tear film Break-up Time, BIO = Binocular Indirect Ophthalmoscope.

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尼日利亚拉各斯一家三级医院精神药物的眼毒性。
研究目的本研究旨在确定患者使用的精神药物对眼部的毒性,并就如何预防服用抗精神病药物的患者视力受损或失明提出建议。研究方法这是一项以医院为基础的前瞻性横断面研究。研究对象为年龄在 18 岁至 70 岁之间、确诊为精神病、服用抗精神病药物至少一年的成年患者。所有受试者都接受了眼球前后节的检查。检查项目包括施尔默试验、泪膜破裂时间(TBUT)、中央角膜厚度(CCT)、色觉测试和对比敏感度测试。收集的数据使用 IBM SPSS 28.0 进行分析。结果研究中的患者主要为女性(55.1%)。最高年龄段为 29-38 岁(29.7%)。对眼睛的检查和调查显示,10.2%服用抗精神病药物的受访者有色觉障碍,25.4%的受访者对比敏感度下降。20.3%的受访者出现眼睑色素沉着,32.2%的受访者出现白内障。在服用抗精神病药物的患者中,有 4.2% 的人出现周边视网膜退化。施尔默氏测试显示,分别有 11%、17.8% 和 20.3%的参与者患有轻度、中度和重度干眼症。角膜中央厚度(CCT)测试显示,50.0% 的受访者角膜较薄,24.6% 的受访者角膜较厚。17.8%的受访者眼压偏高。讨论精神药物是治疗精神病发作和精神障碍的金标准。药物的选择、剂量和给药方式取决于精神病的严重程度。据报道,大剂量的精神药物会对包括眼睛在内的人体不同器官产生毒性,尤其是长期服用和大剂量时,这会对患者的生活质量产生负面影响。结论在服用精神药物的患者中,最早和最突出的副作用是眼睛干涩。青光眼和白内障等致盲性眼病的病例也不在少数。因此,在开始抗精神病药物治疗的早期,就应将眼科评估作为精神病患者管理的一部分。缩写:缩写:FGA = 第一代抗精神病药物,SGA = 第二代抗精神病药物,TCAs = 三环抗抑郁药,CCT = 中央角膜厚度,IOP = 眼内压,TBUT = 泪膜破裂时间,BIO = 双眼间接检眼镜。
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