Browning David J, Koonce Donnie R, Mentreddy Akshay, Punjabi Omar
From the Wake Forest University School of Medicine (D.J.B. and A.M.), Winston-Salem, North Carolina, USA.
W.G.Hefner Salisbury Department of Veterans Affairs Medical Center (D.R.K.), Salisbury, North Carolina, USA.
Am J Ophthalmol. 2025 Sep;277:335-348. doi: 10.1016/j.ajo.2025.05.030. Epub 2025 May 28.
To examine the progression of hydroxychloroquine retinopathy (HCR) from the time of drug cessation to the last follow-up.
Retrospective, consecutive case series SUBJECTS: 17 patients with HCR in whom drug was stopped and follow-up maintained.
Charts, visual fields, and retinal images were reviewed. Four ancillary studies were investigated: 10-2 visual fields (10-2 VF), multifocal electroretinography (mfERG), spectral domain optical coherence tomography (SD-OCT), and fundus autofluorescence (FAF) imaging. Retinopathy was graded as none, early, and advanced.
Progression of retinopathy by the four test methods.
Of the 17 patients, the numbers with at least two follow-up studies to allow comparison for progression were 17, 8, 16, and 9 for 10-2 VF, mfERG, SD-OCT, and FAF, respectively. Median follow-ups were 25, 22, 41, and 37 months for 10-2 VF, mfERG, SD-OCT, and FAF, respectively. The proportions of eyes with no retinopathy at drug cessation that progressed were 0/0, 3/5, 0/0, and 2/6 for 10-2 VF, mfERG, SD-OCT, and FAF, respectively. The proportions of eyes with early retinopathy that progressed were 4/6, 0/6, 2/15, and 3/7 for 10-2 VF, mfERG, SD-OCT, and FAF, respectively. The proportions of eyes with advanced retinopathy that progressed were 16/20, 0/5, 10/17, and 5/5 for 10-2 VF, mfERG, SD-OCT, and FAF, respectively. Progression of retinopathy was seen in cases without retinal pigment epithelium loss at the time of drug cessation. Not all ancillary studies show retinopathy at the time of diagnosis of HCR. Multifocal ERG shows a floor effect. Once response densities are low, detecting further progression of toxicity by this modality is not possible. A greater breadth of retinopathy progression is possible with 10-2 VF, SD-OCT, and FAF.
If HC is stopped when decreased reflectivity of the parafoveal ellipsoid zone is detected by SD-OCT, the probability of retinopathy progression is low. The cut point at which progression of retinopathy is acknowledged to be likely despite drug cessation needs to be moved earlier to discontinuity of the ellipsoid zone.
研究羟氯喹视网膜病变(HCR)从停药时到最后一次随访期间的进展情况。
回顾性、连续性病例系列
17例停用药物并持续随访的HCR患者。
查阅病历、视野检查结果和视网膜图像。研究了四项辅助检查:10-2视野检查(10-2 VF)、多焦视网膜电图(mfERG)、频域光学相干断层扫描(SD-OCT)和眼底自发荧光(FAF)成像。视网膜病变分为无、早期和晚期。
通过四种检查方法评估视网膜病变的进展情况。
17例患者中,有至少两项随访检查可用于比较进展情况的患者数量,10-2 VF为17例,mfERG为8例,SD-OCT为16例,FAF为9例。10-2 VF、mfERG、SD-OCT和FAF的中位随访时间分别为25个月、22个月、41个月和37个月。停药时无视网膜病变且发生进展的眼的比例,10-2 VF为0/0,mfERG为3/5,SD-OCT为0/0,FAF为2/6。早期视网膜病变且发生进展的眼的比例,10-2 VF为4/6,mfERG为0/6,SD-OCT为2/15,FAF为3/7。晚期视网膜病变且发生进展的眼的比例,10-2 VF为16/20,mfERG为0/5,SD-OCT为10/17,FAF为5/5。在停药时无视网膜色素上皮缺失的病例中可见视网膜病变进展。并非所有辅助检查在诊断HCR时都能显示视网膜病变。多焦视网膜电图显示有下限效应。一旦反应密度较低,就无法通过这种检查方式检测到毒性的进一步进展。10-2视野检查、SD-OCT和FAF可显示更广泛的视网膜病变进展情况。
如果在SD-OCT检测到黄斑旁椭圆体带反射率降低时停用羟氯喹,视网膜病变进展的可能性较低。尽管停药,但仍被认为可能发生视网膜病变进展的切点需要提前至椭圆体带的连续性中断。