O'Gallagher Michael, Bunce Catey, Hingorani Melanie, Larkin Frank, Tuft Stephen, Dahlmann-Noor Annegret
Moorfields Eye Hospital NHS Foundation Trust, 162 City Road, London, UK, EC1V 2PD.
Department of Primary Care & Public Health Sciences, Kings College London, 4th Floor, Addison House, Guy's Campus, London, UK, SE1 1UL.
Cochrane Database Syst Rev. 2017 Feb 7;2(2):CD011965. doi: 10.1002/14651858.CD011965.pub2.
Blepharokeratoconjunctivitis (BKC) is a type of inflammation of the surface of the eye and eyelids that involves changes of the eyelids, dysfunction of the meibomian glands, and inflammation of the conjunctiva and cornea. Chronic inflammation of the cornea can lead to scarring, vascularisation and opacity. BKC in children can cause significant symptoms including irritation, watering, photophobia and loss of vision from corneal opacity, refractive error or amblyopia.Treatment of BKC is directed towards modification of meibomian gland disease and the bacterial flora of lid margin and conjunctiva, and control of ocular surface inflammation. Although both topical and systemic treatments are used to treat people with BKC, this Cochrane review focuses on topical treatments.
To assess and compare data on the efficacy and safety of topical treatments (including antibiotics, steroids, immunosuppressants and lubricants), alone or in combination, for BKC in children from birth to 16 years.
We searched CENTRAL (which contains the Cochrane Eyes and Vision Trials Register) (2016, Issue 6), Ovid MEDLINE, Ovid MEDLINE In-Process and Other Non-Indexed Citations, Ovid MEDLINE Daily, Ovid OLDMEDLINE ( January 1946 to 11 July 2016), Embase (January 1980 to 11 July 2016), the ISRCTN registry (www.isrctn.com/editAdvancedSearch), ClinicalTrials.gov (www.clinicaltrials.gov) and the World Health Organization (WHO) International Clinical Trials Registry Platform (ICTRP) (www.who.int/ictrp/search/en). We did not use any date or language restrictions in the electronic searches for trials. We last searched the electronic databases on 11 July 2016. We searched the reference lists of identified reports and the Science Citation Index to identify any additional reports of studies that met the inclusion criteria.
We searched for randomised controlled trials that involved topical treatments in children up to 16 years of age with a clinical diagnosis of BKC. We planned to include studies that evaluated a single topical medication versus placebo, a combination of treatments versus placebo, and those that compared two or multiple active treatments. We planned to include studies in which participants received additional treatments, such as oral antibiotics, oral anti-inflammatories, warm lid compresses and lid margin cleaning.
Two review authors independently screened the results of the literature search (titles and abstracts) to identify studies that met the inclusion criteria of the review and applied standards as expected for Cochrane reviews. We graded the certainty of the evidence using GRADE.
We included one study from the USA that met the inclusion criteria. In the study, 137 children aged zero to six years old with blepharoconjunctivitis were randomised to treatment in one of four trial arms (loteprednol etabonate/tobramycin combination, loteprednol etabonate alone, tobramycin alone or placebo) for 15 days, with assessments on days 1, 3, 7 and 15. We judged the study to be at high risk of attrition bias and bias due to selective outcome reporting. The study did not report the number of children with improvement in symptoms nor with total or partial success as measured by changes in clinical symptoms.All children showed a reduction in blepharoconjunctivitis grade score, but there was no evidence of important differences between groups. Visual acuity was not fully reported but the authors stated that there was no change in visual acuity in any of the treatment groups. The study reported ocular and non ocular adverse events but was underpowered to detect differences between the groups. Ocular adverse events were as follows: loteprednol/tobramycin 1/34 (eye pain); loteprednol 4/35 (eye pain, conjunctivitis, eye discharge, eye inflammation); tobramycin 0/34; placebo (vehicle) 0/34. The evidence was limited for all these outcomes and we judged it to be very low certainty.There was no information on clinical signs (aside from grade score), disease progression or quality of life.
AUTHORS' CONCLUSIONS: There is no high-quality evidence of the safety and efficacy of topical treatments for BKC, which resulted in uncertainty about the indications and effectiveness of topical treatment. Clinical trials are required to test efficacy and safety of current and any future treatments. Outcome measures need to be developed which can capture both objective clinical and patient-reported aspects of the condition and treatments.
睑缘角结膜炎(BKC)是一种眼表和眼睑的炎症,涉及眼睑变化、睑板腺功能障碍以及结膜和角膜炎症。角膜的慢性炎症可导致瘢痕形成、血管化和混浊。儿童BKC可引起明显症状,包括刺激感、流泪、畏光以及因角膜混浊、屈光不正或弱视导致的视力丧失。BKC的治疗旨在改善睑板腺疾病、调整睑缘和结膜的细菌菌群,并控制眼表炎症。虽然局部和全身治疗都用于治疗BKC患者,但本Cochrane综述聚焦于局部治疗。
评估和比较局部治疗(包括抗生素、类固醇、免疫抑制剂和润滑剂)单独或联合使用对16岁及以下儿童BKC的疗效和安全性数据。
我们检索了CENTRAL(其中包含Cochrane眼和视力试验注册库)(2016年第6期)、Ovid MEDLINE、Ovid MEDLINE在研及其他非索引引文、Ovid MEDLINE日报、Ovid OLDMEDLINE(1946年1月至2016年7月11日)、Embase(1980年1月至2016年7月11日)、ISRCTN注册库(www.isrctn.com/editAdvancedSearch)、ClinicalTrials.gov(www.clinicaltrials.gov)以及世界卫生组织(WHO)国际临床试验注册平台(ICTRP)(www.who.int/ictrp/search/en)。在电子检索试验时,我们未使用任何日期或语言限制。我们最后一次检索电子数据库是在2016年7月11日。我们检索了已识别报告的参考文献列表和科学引文索引,以识别符合纳入标准的任何其他研究报告。
我们检索了随机对照试验,这些试验涉及对临床诊断为BKC的16岁及以下儿童进行局部治疗。我们计划纳入评估单一局部药物与安慰剂、联合治疗与安慰剂,以及比较两种或多种活性治疗的研究。我们计划纳入参与者接受额外治疗(如口服抗生素、口服抗炎药、热敷眼睑和清洁睑缘)的研究。
两位综述作者独立筛选文献检索结果(标题和摘要),以识别符合综述纳入标准的研究,并应用Cochrane综述预期的标准。我们使用GRADE对证据的确定性进行分级。
我们纳入了一项来自美国的符合纳入标准的研究。在该研究中,137名0至6岁的睑结膜炎儿童被随机分配到四个试验组之一(氯替泼诺/妥布霉素联合用药、单独使用氯替泼诺、单独使用妥布霉素或安慰剂)进行15天的治疗,并在第1、3、7和15天进行评估。我们判断该研究存在较高的失访偏倚风险和因选择性报告结果导致的偏倚。该研究未报告症状改善的儿童数量,也未报告根据临床症状变化衡量的完全或部分成功情况。所有儿童的睑缘角结膜炎分级评分均有所降低,但没有证据表明各组之间存在重要差异。视力未得到充分报告,但作者表示任何治疗组的视力均无变化。该研究报告了眼部和非眼部不良事件,但检测组间差异的能力不足。眼部不良事件如下:氯替泼诺/妥布霉素组1/34(眼痛);氯替泼诺组4/35(眼痛、结膜炎、眼分泌物、眼部炎症);妥布霉素组0/34;安慰剂(赋形剂)组0/34。所有这些结果的证据都很有限,我们判断其确定性非常低。没有关于临床体征(除分级评分外)、疾病进展或生活质量的信息。
没有高质量证据证明局部治疗对BKC的安全性和有效性,这导致局部治疗的适应症和有效性存在不确定性。需要进行临床试验来测试当前及未来任何治疗的疗效和安全性。需要制定能够同时捕捉该疾病和治疗的客观临床及患者报告方面的结局指标。