Kotaniemi K, Kautiainen H, Karma A, Aho K
Rheumatism Foundation Hospital, Heinola, Finland.
Ophthalmology. 2001 Nov;108(11):2071-5. doi: 10.1016/s0161-6420(01)00773-4.
To examine the occurrence and characteristics of uveitis in patients with recently diagnosed juvenile chronic arthritis (JCA).
A prospective observational case series.
PARTICIPANTS/METHODS: The study covered the new cases detected with JCA (426 children), all of whom were referred to an ophthalmologic consultation during 1989 to 1996 at the Pediatric Department of the Rheumatism Foundation Hospital, Heinola, Finland.
The children with JCA were followed by ophthalmologic and pediatric examinations two to four times a year. The type and course of arthritis and presentation and characteristics of uveitis were examined prospectively.
Uveitis was detected in 104 of 426 children (24%). Two thirds of all patients and the same proportion of those with uveitis were girls. Proportionally, uveitis was found to be as common among children with oligoarthritis (27%) as among those with seronegative polyarthritis (25%). Antinuclear antibodies (ANA) were detected significantly more frequently in patients with uveitis (66%) than among those without uveitis (37%) (P < 0.001). The uveitis was asymptomatic in 99 cases; only 5 children had episodes of acute anterior symptomatic uveitis. Uveitis was found before or within 3 months from the onset of recent arthritis in 51 of 104 children (49%) and later on in 53 of 104 children (51%). The mean age at diagnosis of uveitis was 5.9 years (range, 1.1-17.7; median, 4.9 years). The mean period from the diagnosis of JCA to the diagnosis of uveitis was 1.1 years (range, -2.4-6.5; median, 0.3 years). The mean age at diagnosis of JCA was 4.8 years (range, 0.6-15; median, 3.2 years) among those with uveitis and 7.3 years (range, 0.9-16; median, 6.7 years) among those who did not have it (P < 0.001). Uveitis was ongoing in 63 children at the end of the follow-up period. The mean follow-up time was 4.5 years (range, 0-9.7) for all children and 5.6 years (range, 1.3-9.6) for those with uveitis. In most instances, the visual prognosis was good. In 25 of 104 patients (24%) one or more complications of uveitis were found, but in only three children did the visual acuity decrease to 20/60 or less, and none became blind. All the other patients had visual acuity > or = 20/40.
In this patient group, uveitis in JCA frequently appeared very early after the onset of arthritis. The uveitis was significantly more common in patients with an early onset of arthritis combined with ANA positivity. The proportion of children with uveitis was as large in those with polyarthritis as in those with oligoarthritis, with no predilection to girls.
研究近期诊断的青少年慢性关节炎(JCA)患者葡萄膜炎的发生情况及特征。
前瞻性观察病例系列研究。
研究对象/方法:本研究涵盖新诊断的JCA患者(426名儿童),他们于1989年至1996年期间均被转诊至芬兰海诺拉风湿基金会医院儿科进行眼科会诊。
对JCA患儿每年进行2至4次眼科和儿科检查。前瞻性地检查关节炎的类型和病程以及葡萄膜炎的表现和特征。
426名儿童中有104名(24%)被检测出患有葡萄膜炎。所有患者中有三分之二以及葡萄膜炎患者中相同比例为女孩。按比例计算,寡关节炎患儿中葡萄膜炎的发生率(27%)与血清阴性多关节炎患儿中相同(25%)。葡萄膜炎患者中抗核抗体(ANA)的检测频率(66%)显著高于无葡萄膜炎患者(37%)(P<0.001)。99例葡萄膜炎患者无症状;只有5名儿童出现急性前葡萄膜炎症状发作。104名儿童中有51名(49%)在近期关节炎发作前或发作后3个月内发现葡萄膜炎,另外53名(51%)在之后发现。葡萄膜炎诊断时的平均年龄为5.9岁(范围1.1 - 17.7岁;中位数4.9岁)。从JCA诊断到葡萄膜炎诊断的平均时间为1.1年(范围 - 2.4 - 6.5年;中位数0.3年)。有葡萄膜炎患者JCA诊断时的平均年龄为4.8岁(范围0.6 -