Study design and participants
The study was a retrospective, consecutive, observational case series. The study followed the tenets of the Declaration of Helsinki and was approved by the Medical Ethics Committee of Tianjin Eye Hospital.
Patients who were diagnosed with IMH and had undergone 25G PPV and ILM flap surgery in Tianjin Eye Hospital between January 1, 2015 and May 31, 2017 were included. The exclusion criteria included prior vitreoretinal surgery, pathologic myopia [refractive error of more than − 6.00 diopters (D) or axial length (AL) more than 26.0 mm], neovascular age-related macular degeneration, proliferative diabetic retinopathy, solar retinopathy, and traumatic MH. Of the original 123 eyes, there were 65 eyes whose ILM could be found in the first time follow-up OCT images. A total of 5 eyes were excluded because of the presence of retinal diseases, including treated rhegmatogenous retinal detachment, diabetic retinopathy, and high myopia with an axial length of more than 26.0 mm or refractive error less than − 6.0 diopters. Eight other eyes were excluded because the patients were lost to follow-up within 6 months postoperatively. In total, 52 eyes of 52 patients (13 men, 39 women) met the study criteria for the data analysis. All the macular holes of 52 patients were closed after the first operation and ILM flap was attained surgically in these 52 eyes.
According to whether there was glial proliferation in the healing process of the macular hole one month post operation, the patients were divided into two groups. Patients with functional closure of the macular region were designated as group A, which is defined as the presence of normal layers in the macular region without blocking by hyper reflective substances. Patients with anatomical closure, which was characterized by discontinuous macular layers filled with hyper reflective material, were designated group B [11].
Ophthalmologic examinations
A detailed eye examination including a slit-lamp examination, fundus examination by indirect binocular ophthalmoscopy, and SD-OCT (RTVue XR 100–2, Optovue, USA) to scan the foveal microstructures were performed. The preoperative data included age, sex, symptom duration, right or left eye, BCVA, AL, refractive status, MLD, height (H) and the base linear diameter (BD) of the macular hole, and the central choroid thickness (CCT). This SD-OCT device used an 840-nm wavelength, and a scanning speed of 70,000 A-scans/second. A 6 mm × 6 mm scanning pattern was performed. The MLD, BD and H of the macular hole and CCT were manually measured with the calipers included in the software (Fig. 1). Two masked professional physicians evaluated all the images with excellent inter-and-intra-observer reliability for all measured macular structures.
Operation method
All the surgeries included in the study were performed by the same vitreoretinal specialist (H. QH.). A standard sutureless (25G) 3-port pars plana vitrectomy (PPV) was performed in all cases. An intravitreal injection of indocyanine green (5 mg/mL) was performed to make the ILM more visible. The ILM was peeled off in a circular fashion around the MH, and the remaining ILM around the macular hole was trimmed short then massaged gently over the MH until the ILM became inverted. Phacoemulsification with implantation of intraocular lens and circular dissection of the posterior capsule was performed simultaneously in patients with cataracts or those older than 50 years. Sterile air was used to tamponade the vitreous cavity in all patients, and patients were instructed to maintain a prone position while awake for at least 4 days postoperatively.
Follow-up data
Comprehensive ophthalmologic examinations and SD-OCT examinations were performed 1, 3, 6, 9, and 12 months after surgery for all patients. The follow-up model of the SD-OCT device we used, which could identify previous scan locations and automatically guide the instrument to scan the same location again for every visit. The same scanning location was determined by the eye-tracking system but not by the location of the fixation light. In the process of image acquisition, the position of the fovea was manually repositioned for patients with eccentric fixation to correct the scanning deviation from the fovea. The examinations included BCVA, IOP, slit-lamp examinations, and fundus examinations by indirect binocular ophthalmoscopy. BCVA was converted to the logarithm of the minimum angle of resolution (logMAR) to evaluate VA changes and for statistical analysis. The length of the ELM and EZ line defect was analyzed by the horizontal B scan in the fovea region. These images were analyzed by two masked observers who evaluated all the photographs with inter and intra-observer reliability for all OCT data measured.
Statistical analysis
Statistical analysis was carried out using SPSS, v 19.0 (IBM, Armonk, New York, USA). Continuous data were reported as the median ± standard deviation (SD). An independent sample t-test was used to compare data between groups. The chi-square test was used for categorical variables. A p < 0.05 was considered as statistically significant.