Horwath-Winter Jutta, Berghold Andrea, Schmut Otto, Floegel Ingrid, Solhdju Verena, Bodner Elizabeth, Schwantzer Gerold, Haller-Schober Eva-Maria
Department of Ophthalmology, University Hospital, Graz, Austria.
Arch Ophthalmol. 2003 Oct;121(10):1364-8. doi: 10.1001/archopht.121.10.1364.
To assess subjective symptoms, tear function factors, and ocular surface morphology in the clinical course of patients with dry eye syndrome under treatment within an observation period of up to 8 years.
In 97 patients (78 women and 19 men) with ocular discomfort, a clinical diagnosis of dry eye syndrome was made based on typical symptoms and a reduced tear film breakup time of less than 10 seconds. Subsequent evaluations revealed a diagnosis of aqueous tear deficiency in 9 patients, meibomian gland dysfunction in 32 patients, and aqueous tear deficiency combined with meibomian gland dysfunction in 30 patients, aqueous tear deficiency associated with Sjögren syndrome in 12 patients, and aqueous tear deficiency and meibomian gland dysfunction associated with Sjögren syndrome in 14 patients. Follow-up assessments were performed 12 to 94 months (mean follow-up, 40 months) after the initial diagnosis.
In different subgroups of dry eye tear film breakup time, Schirmer test without local anesthesia (Schirmer I), fluorescein and rose bengal staining, impression cytology, as well as subjective dry eye symptoms and frequency of tear substitute application were compared at baseline and after a follow-up of 1 to 8 years (mean, 3.3 years).
At baseline, tear film function and ocular surface test results found more pathologic abnormalities and more severe subjective symptoms in patients with aqueous tear deficiency associated with Sjögren syndrome and aqueous tear deficiency and meibomian gland dysfunction associated with Sjögren syndrome compared with the other groups who had dry eye syndrome. No differences in frequency of tear substitute application were observed. At follow-up, tear breakup time, Schirmer I test results, and corneal fluorescein staining improved compared with baseline values, whereas rose bengal staining and impression cytology of the conjunctival surface remained almost unchanged. Subjective symptoms and frequency of artificial tear application were reduced.
Within the observation period of up to 8 years, the dry eye syndrome improved or stabilized under appropriate treatment. Although no patient was completely cured, subjective reports as well as frequency of artificial tear application were reduced.
在长达8年的观察期内,评估干眼症综合征患者治疗过程中的主观症状、泪液功能因素及眼表形态。
对97例(78例女性和19例男性)有眼部不适的患者,根据典型症状及泪膜破裂时间缩短至10秒以内做出干眼症综合征的临床诊断。随后评估显示,9例患者诊断为水样泪液缺乏,32例患者诊断为睑板腺功能障碍,30例患者诊断为水样泪液缺乏合并睑板腺功能障碍,12例患者诊断为与干燥综合征相关的水样泪液缺乏,14例患者诊断为与干燥综合征相关的水样泪液缺乏和睑板腺功能障碍。在初次诊断后12至94个月(平均随访40个月)进行随访评估。
比较不同亚组干眼症患者在基线时以及随访1至8年(平均3.3年)后的泪膜破裂时间、无局部麻醉的Schirmer试验(Schirmer I)、荧光素和孟加拉红染色、印迹细胞学检查,以及主观干眼症状和泪液替代剂应用频率。
在基线时,与其他干眼症综合征患者组相比,与干燥综合征相关的水样泪液缺乏以及与干燥综合征相关的水样泪液缺乏和睑板腺功能障碍患者的泪膜功能和眼表检查结果显示出更多的病理异常和更严重的主观症状。泪液替代剂应用频率未见差异。随访时,与基线值相比,泪膜破裂时间、Schirmer I试验结果和角膜荧光素染色有所改善,而结膜表面的孟加拉红染色和印迹细胞学检查几乎保持不变。主观症状和人工泪液应用频率降低。
在长达8年的观察期内,干眼症综合征在适当治疗下有所改善或稳定。虽然没有患者完全治愈,但主观报告以及人工泪液应用频率降低。