Department of Ophthalmology, Boston Children's Hospital, Boston, Massachusetts.
Harvard Medical School, Boston, Massachusetts; Division of Developmental Medicine, Boston Children's Hospital, Boston, Massachusetts.
J AAPOS. 2023 Oct;27(5):276.e1-276.e8. doi: 10.1016/j.jaapos.2023.07.014. Epub 2023 Sep 21.
To compare amblyopia treatment outcomes between patients with neurodevelopmental disorders and their typically developing peers.
Of 2,311 patients diagnosed with amblyopia between 2010 and 2014 at Boston Children's Hospital, 460 met inclusion criteria (age 2-12 with anisometropic, strabismic, or mixed amblyopia [interocular difference (IOD) ≥2 lines]). Treatment and visual outcomes were analyzed according to neurodevelopmental status: neurodevelopmental delay (DD) versus typical development (TD).
The DD group (n = 54) and TD group (n = 406) were similar in demographics, amblyogenic risk factors, baseline visual measures, prescribed therapy, and adherence (P ≥ 0.10). Between-visit follow-up time was longer for the DD group (0.65 [0.42- 0.97] years) than for the TD group (0.5 [0.36-0.82] years; P = 0.023). IOD improved similarly in each group by the last visit (DD, -0.15 logMAR [-0.31 to -0.02]; TD, -0.2 logMAR [-0.38 to -0.1]; P = 0.09). Each group reached amblyopia resolution by the last visit at similar frequencies (DD, 23/54 [43%]; TD, 211/406 [52%]; P > 0.2). DD diagnosis did not independently influence amblyopia resolution (HR, 0.77; 95% CI, 0.53-1.12; P = 0.17), but each additional month of interval time between follow-up visits reduced the likelihood of resolution by 2.7% (HR, 0.67; 95% CI, 0.51-0.87; P = 0.003).
Patients with DD and those with TD responded similarly to amblyopia therapy; however, follow-up intervals were longer in patients with DD and correlated with the likelihood of persistent amblyopia, suggesting that greater efforts at assuring follow-up may benefit patients with DD.
比较神经发育障碍患者与正常发育同龄人之间弱视治疗结果。
在波士顿儿童医院 2010 年至 2014 年间诊断为弱视的 2311 名患者中,有 460 名符合纳入标准(年龄 2-12 岁,患有屈光不正性、斜视性或混合性弱视[双眼间差异(IOD)≥2 行])。根据神经发育状况分析治疗和视觉结果:神经发育迟缓(DD)与典型发育(TD)。
DD 组(n=54)和 TD 组(n=406)在人口统计学、弱视发病危险因素、基线视力测量、处方治疗和依从性方面相似(P≥0.10)。DD 组的随访时间(0.65[0.42-0.97]年)长于 TD 组(0.5[0.36-0.82]年;P=0.023)。在最后一次随访时,两组的 IOD 均有相似程度的改善(DD,-0.15 对数 MAR[-0.31 至-0.02];TD,-0.2 对数 MAR[-0.38 至-0.1];P=0.09)。两组在最后一次随访时以相似的频率达到弱视缓解(DD,23/54[43%];TD,211/406[52%];P>0.2)。DD 诊断并不能独立影响弱视缓解(HR,0.77;95%CI,0.53-1.12;P=0.17),但随访间隔每增加一个月,缓解的可能性就会降低 2.7%(HR,0.67;95%CI,0.51-0.87;P=0.003)。
DD 患者和 TD 患者对弱视治疗的反应相似;然而,DD 患者的随访间隔时间较长,且与持续性弱视的可能性相关,这表明加强随访可能对 DD 患者有益。