Rahi Jugnoo S, Cable Noriko
Centre for Paediatric Epidemiology and Biostatistics and the Department of Ophthalmology/Visual Sciences Unit, Institute of Child Health, Great Ormond Street Hospital, UK.
Lancet. 2003 Oct 25;362(9393):1359-65. doi: 10.1016/S0140-6736(03)14631-4.
Prevention of visual impairment and blindness in childhood is an international priority. However, many countries do not have contemporary information about incidence and causes, from which the scope and priorities for prevention and treatment can be identified.
In the UK, children aged younger than 16 years newly diagnosed with severe visual impairment or blindness (SVI/BL, WHO criteria) during 2000 were identified through national active surveillance schemes in ophthalmology and paediatrics. From these data, we calculated yearly age-group specific incidence and cumulative incidence. Causes were classified by the anatomical site or sites affected and by timing of the insult or insults and causal factors, where known.
Of 439 newly diagnosed children, 336 (77%) had additional non-ophthalmic disorders or impairments (SVI/BL plus). Total yearly incidence was highest in the first year of life, being 4.0 (95% CI 3.6-4.5) per 10000, with a cumulative incidence by 16 years of age of 5.9 (5.3-6.5) per 10000. 10% (44) of all children died within 1 year of diagnosis of blindness. Prenatal causal factors affected 61% (268) of children, with perinatal or neonatal and childhood factors each affecting 18% (77). Incidence and causes varied with presence of non-ophthalmic impairments or disorders, birthweight, and ethnic origin. At least 75% (331) of children had disorders that were neither potentially preventable nor treatable, with current knowledge.
Severe visual impairment and blindness in childhood in the UK is more common, occurs more frequently in the context of complex non-ophthalmic impairments, and has greater associated mortality, than previously assumed. An increased rate in children of low birthweight and from ethnic minority groups, together with the observed diversity and complexity of the causes, reflect recent secular changes in the population at risk, specific risk factors, and strategies available for treatment.
预防儿童视力损害和失明是一项国际重点工作。然而,许多国家没有关于发病率和病因的最新信息,而据此才能确定预防和治疗的范围及重点。
在英国,通过眼科和儿科的全国主动监测计划,确定了2000年期间新诊断为严重视力损害或失明(根据世界卫生组织标准的SVI/BL)的16岁以下儿童。根据这些数据,我们计算了各年龄组的年发病率和累积发病率。病因按受影响的解剖部位或部位,以及已知的损伤时间或损伤及因果因素进行分类。
在439名新诊断的儿童中,336名(77%)有其他非眼科疾病或损伤(SVI/BL加)。年发病率在出生后第一年最高,每10000人中有4.0(95%可信区间3.6 - 4.5),到16岁时累积发病率为每10000人中有5.9(5.3 - 6.5)。所有儿童中有10%(44名)在失明诊断后1年内死亡。产前因果因素影响了61%(268名)的儿童,围产期或新生儿期以及儿童期因素各影响18%(77名)。发病率和病因因非眼科损伤或疾病的存在、出生体重和种族而有所不同。根据目前的知识,至少75%(331名)的儿童患有既无法潜在预防也无法治疗的疾病。
英国儿童严重视力损害和失明比以前认为的更常见,在复杂的非眼科损伤情况下更频繁发生,且相关死亡率更高。低出生体重儿童和少数族裔儿童的发病率增加,以及观察到的病因多样性和复杂性,反映了高危人群、特定风险因素和现有治疗策略的近期长期变化。