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印度南部一家三级眼科护理中心史蒂文斯-约翰逊综合征的眼部并发症及治疗

Ophthalmic complications and management of Stevens-Johnson syndrome at a tertiary eye care centre in south India.

作者信息

Kompella Viswanadh B, Sangwan Virender S, Bansal Aashish K, Garg Prashant, Aasuri Murali K, Rao Gullapalli N

机构信息

Cornea Service, L V Prasad Eye Institute, L V Prasad Marg, Banjara Hills, Hyderabad-500 034, India.

出版信息

Indian J Ophthalmol. 2002 Dec;50(4):283-6.

Abstract

PURPOSE

To review the possible aetiological factors, ocular complications and their management in patients of Stevens-Johnson syndrome with ocular involvement, seen at a tertiary eye care centre.

METHODS

We retrospectively reviewed the medical records of patients with Stevens-Johnson syndrome seen between 1987-1998 at L V Prasad Eye Institute. The demographic and possible aetiological factors data causing Stevens-Johnson syndrome were collected. The details of the ocular examination and treatment were collected and examined to determine the pattern of presentation, complications, treatment response and outcome.

RESULTS

A total of 95 patients, 40 males (42.10%) and 55 females (57.89%), were identified during the 11-year period. A majority of the patients (n = 53; 55.78%) were between 20 and 40 years of age. All patients had bilateral involvement and most (n = 93; 97.89%) had bilateral symmetrical presentation. The duration from the onset of symptoms to the time of presentation at the institute varied from 6 days to 18 years with most patients presenting after one year (n = 39; 41.05%). The most commonly identified possible causative factor was drugs (n = 55; 51.89%). No definitive cause was identified in 37 (38.94%) patients, and 3 (3.15%) patients had a history of viral fever preceding the onset of Stevens-Johnson syndrome. The best corrected visual acuity at initial presentation was 6/12 or better in 32 (33.68%) patients. Lid abnormalities were observed in 87 (91.51%) patients, conjunctival abnormalities in 92 (96.84%) and corneal complications in 93 (97.89%). All patients were managed medically and 26 (27.36%) patients underwent surgery.

CONCLUSION

Stevens-Johnson syndrome remains an important cause of severe visual loss and ocular morbidity, both of which significantly affect the quality of life. Not many medical or surgical options are available even in tertiary eye-care centres. Future advances in immune modulation techniques may prevent many of the sequelae that continue to occur despite the best possible medical care.

摘要

目的

回顾在一家三级眼科护理中心就诊的史蒂文斯-约翰逊综合征眼部受累患者可能的病因、眼部并发症及其治疗方法。

方法

我们回顾性分析了1987年至1998年间在L V普拉萨德眼科研究所就诊的史蒂文斯-约翰逊综合征患者的病历。收集了导致史蒂文斯-约翰逊综合征的人口统计学和可能的病因学因素数据。收集并检查了眼部检查和治疗的详细信息,以确定其表现形式、并发症、治疗反应和结果。

结果

在这11年期间,共确定了95例患者,其中男性40例(42.10%),女性55例(57.89%)。大多数患者(n = 53;55.78%)年龄在20至40岁之间。所有患者均为双侧受累,且大多数(n = 93;97.89%)表现为双侧对称。从症状出现到在该研究所就诊的时间间隔从6天到18年不等,大多数患者在一年后就诊(n = 39;41.05%)。最常见的可能致病因素是药物(n = 55;51.89%)。37例(38.94%)患者未确定明确病因,3例(3.15%)患者在史蒂文斯-约翰逊综合征发病前有病毒热病史。初次就诊时最佳矫正视力为6/12或更好的患者有32例(33.68%)。87例(91.51%)患者出现眼睑异常,92例(96.84%)出现结膜异常,93例(97.89%)出现角膜并发症。所有患者均接受药物治疗,26例(27.36%)患者接受了手术。

结论

史蒂文斯-约翰逊综合征仍然是严重视力丧失和眼部疾病的重要原因,这两者均会显著影响生活质量。即使在三级眼科护理中心,可用的药物或手术选择也不多。免疫调节技术的未来进展可能会预防许多尽管接受了最佳医疗护理仍会出现的后遗症。

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