Pennefather P M, Tin W, Clarke M P, Dutton J, Fritz S, Hey E N
Department of Ophthalmology, Royal Victoria Infirmary, Newcastle upon Tyne.
Br J Ophthalmol. 1999 Jun;83(6):643-5. doi: 10.1136/bjo.83.6.643.
To investigate the bias introduced by incomplete follow up in a cohort study of ocular outcome after premature birth.
A geographically defined cohort of children born before 32 weeks' gestation was prospectively recruited at birth to study the ocular outcome at 2 years. On the basis of attendance at 2 years, the children's families were allocated to one of three groups: group 1 attended for follow up, group 2 were difficult to trace, and group 3 were very reluctant for assessment. All children were examined by a single ophthalmologist, masked to these groupings.
558 children (98.8% of study group) were examined, of whom 505 were in group 1, 20 in group 2, and 33 in group 3. The groups which were more difficult to study (groups 2 and 3) showed a significantly higher prevalence of ocular abnormalities, including strabismus (p=0. 02) and cicatricial retinopathy of prematurity (p=0.002) compared with those attending for follow up. Further, not all of these cases could have been identified by review of the children's previous records. Ocular abnormalities would be underestimated by 16% (11.3% in group 1 compared with 13.4% in the total cohort, p=0.77).
This study suggests that the prevalence of abnormalities would be underestimated by incomplete follow up, as those subjects who were most difficult to obtain for study had a significantly higher prevalence of abnormalities.
在一项关于早产患儿眼部结局的队列研究中,调查不完全随访所引入的偏倚。
前瞻性招募了一个地理区域内孕周小于32周出生的儿童队列,以研究其2岁时的眼部结局。根据2岁时的随访情况,将儿童家庭分为三组:第1组接受随访,第2组难以追踪,第3组非常不愿意接受评估。所有儿童均由一名对分组情况不知情的眼科医生进行检查。
共检查了558名儿童(占研究组的98.8%),其中505名在第1组,20名在第2组,33名在第3组。较难研究的组(第2组和第3组)与接受随访的组相比,眼部异常的患病率显著更高,包括斜视(p=0.02)和早产儿瘢痕性视网膜病变(p=0.002)。此外,并非所有这些病例都能通过查阅儿童既往记录来识别。眼部异常的漏诊率为16%(第1组为11.3%,总队列中为13.4%,p=0.77)。
本研究表明,不完全随访会低估异常情况的患病率,因为最难纳入研究的受试者异常情况的患病率显著更高。