Heiligenhaus Arnd, Dück Nadine, Michel Delia, Hudde Tobias, Koch Jörg, Steuhl Klaus Peter
Augenabteilung am St.-Franziskus-Hospital, Münster.
Klin Monbl Augenheilkd. 2003 Jul;220(7):471-80. doi: 10.1055/s-2003-40936.
The value of immunosuppressive drugs for the therapy of scleritis patients is unclear. The authors investigated the indications and effects of immunosuppression in a group of patients with scleral inflammation.
Retrospective study of patients treated for scleritis (n = 87) or episcleritis (n = 18). The demographic factors, clinical symptoms, visual outcome, course of inflammation, ocular complications resulting from inflammation, topical and systemic antiinflammatory medication, and associated systemic diseases were analysed.
Only one patient with episcleritis, but 37 with scleritis presented with ocular complications (P = 0.003). The vision was impaired in 15 patients with scleritis, but not in episcleritis patients (P = 0.022). In the group of patients with episcleritis, only those with frequent relapses required more than topical antiinflammatory drugs, especially systemic non-steroidals. In contrast, systemic therapy was indicated in all of the scleritis patients. Ocular complications were found more often in patients with necrotising (n = 7/10) or posterior scleritis (n = 10/11) than in those with diffuse (9/39) or nodular (11/27) scleritis. Compared with the other patients, associated systemic autoimmune diseases were more common in patients with necrotising scleritis (P = 0.03). The need for immunosuppression was associated with vision-threatening complications (glaucoma, uveitis, peripheral ulcerative keratitis) (P < 0.01), systemic autoimmune disease, and necrotising and posterior form of scleritis (P < 0.01). Quiescence of scleritis was obtained in 59 of the scleritis patients, and improvement of inflammation was achieved in further 21. In 26 patients, scleritis did not improve with systemic steroid or non-steroidal treatment, but with immunosuppression.
Scleritis is often associated with life-threatening systemic diseases and vision-threatening ocular complications. In patients with severe scleritis, especially with the posterior and necrotising form, improvement can often be achieved with immunosuppression.
免疫抑制药物治疗巩膜炎患者的价值尚不清楚。作者调查了一组巩膜炎症患者免疫抑制的指征及效果。
对87例巩膜炎患者和18例表层巩膜炎患者进行回顾性研究。分析了人口统计学因素、临床症状、视力预后、炎症病程、炎症导致的眼部并发症、局部和全身抗炎药物以及相关的全身性疾病。
仅1例表层巩膜炎患者出现眼部并发症,而巩膜炎患者有37例出现眼部并发症(P = 0.003)。15例巩膜炎患者视力受损,而表层巩膜炎患者视力未受损(P = 0.022)。在表层巩膜炎患者组中,只有那些频繁复发的患者需要使用除局部抗炎药物之外更多的药物,尤其是全身用非甾体类药物。相比之下,所有巩膜炎患者均需全身治疗。坏死性(7/10)或后巩膜炎(10/11)患者比弥漫性(9/39)或结节性(11/27)巩膜炎患者更常出现眼部并发症。与其他患者相比,坏死性巩膜炎患者合并全身性自身免疫性疾病更为常见(P = 0.03)。免疫抑制的需求与威胁视力的并发症(青光眼、葡萄膜炎、周边溃疡性角膜炎)(P < 0.01)、全身性自身免疫性疾病以及坏死性和后巩膜炎形式相关(P < 0.01)。59例巩膜炎患者巩膜炎病情静止,另有21例炎症得到改善。26例患者的巩膜炎经全身用类固醇或非甾体类治疗无改善,但免疫抑制治疗有效。
巩膜炎常与危及生命的全身性疾病和威胁视力的眼部并发症相关。在重度巩膜炎患者中,尤其是后巩膜炎和坏死性巩膜炎患者,免疫抑制治疗通常可使病情改善。