Front. Med. Frontiers in Medicine Front. Med. 2296-858X Frontiers Media S.A. 10.3389/fmed.2025.1537402 Medicine Original Research The short term impact of uncomplicated cataract surgery on retinal layers thickness Gioia Marco De Bernardo Maddalena * La Marca Aniello De Luca Martina Pagliarulo Sergio Avella Mariagrazia Mignone Alfredo Rosa Nicola Department of Medicine, Surgery and Dentistry “Scuola Medica Salernitana”, University of Salerno, Baronissi, Italy

Edited by: Gregor S. Reiter, Medical University of Vienna, Austria

Reviewed by: Mehmet Icoz, Yozgat City Hospital, Türkiye

Giovanni Neri, University of Turin, Italy

 *Correspondence: Maddalena De Bernardo, mdebernardo@unisa.it 21 07 2025 2025 12 1537402 30 11 2024 01 07 2025 Copyright © 2025 Gioia, De Bernardo, La Marca, De Luca, Pagliarulo, Avella, Mignone and Rosa. 2025 Gioia, De Bernardo, La Marca, De Luca, Pagliarulo, Avella, Mignone and Rosa

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 Objective or purpose

To detect the short-term impact of cataract surgery on retinal layers thickness, as the exact mechanism of fundus changes after phacoemulsification has not yet been fully clarified.

 Design

A retrospective observational study.

 Subjects, participants, and/or controls

Seventy eyes of 70 patients with age ranging from 49 to 92 years, scheduled for cataract surgery, were included.

 Methods, intervention, or testing

All subjects underwent a complete ophthalmological examination, including ART-OCT volume with Heidelberg Spectralis before and approximately one month later cataract surgery.

 Main outcome measures

The macula was divided into a central foveal region and four parafoveal regions (superior, inferior, nasal, temporal). The scans were then automatically segmented into the different retinal layers and the changes in each layer were assessed.

 Results

The results revealed that both the inner retinal layers and the entire retina exhibited a statistically significant thickening in foveal and parafoveal region: IRL (p < 0.001), ONL (p < 0.001), GCL (p = 0.010), RNFL (p = 0.020), and ALL (p < 0.001). Conversely, the outer retinal layers showed a statistically significant reduction in thickness only within the parafoveal regions: ORL (p < 0.001).

 Conclusion

This study may provide a pathophysiological explanation for post-phacoemulsification changes affecting the retina.

 cataract surgery cataract retina retinal thickness OCT SD-OCT retinal layers section-at-acceptance Ophthalmology Introduction

Cataract is the leading cause of treatable vision loss worldwide, affecting approximately 20 million individuals, (1) and cataract extraction is the most frequently performed surgical procedure (2). Any invasive eye surgery, including cataract surgery, initiates a biochemical cascade resulting in an immunological response. Advancements in surgical techniques and pharmacological treatments have effectively reduced this response in recent years, thereby lowering the risk of postoperative complications such as posterior capsule tear, vitreous presence in the anterior chamber, and the development of cystoid macular edema.

Phacoemulsification is the most widely utilized surgical technique, recognized as a well-standardized and safe procedure (3) generally yielding favorable visual outcomes. However, it is not entirely risk-free, as it can lead to side effects impacting various ocular structures, including the retina. Research indicates that cataract surgery can be a contributing factor in the development of posterior segment complications, including cystoid macular edema in pseudophakic patients, potential onset of age-related macular degeneration, and worsening of diabetic retinopathy (4–8). Even uncomplicated cataract surgery can induce retinal changes that are not detectable through ophthalmoscopic examination, often leading to unnoticed damage and subsequent decline in visual function (9–11).

The advent of optical coherence tomography (OCT) has enabled increasingly detailed imaging of retinal and choroidal structures (12, 13). This method is straightforward, safe, non-invasive, and highly precise, allowing for macular measurements with a resolution of 8–10 micrometers (14). Modern OCT equipment also permits precise and detailed segmentation of retinal layers. OCT has become a fundamental tool for identifying subclinical alterations affecting the macula after cataract surgery, leading to a growing number of studies in this area.

Previous research has largely focused on examining modifications across the entire retinal area, with somewhat conflicting results, (15–22) or on changes affecting specific retinal layers involved in common postoperative complications [e.g., outer plexiform/inner nuclear layers in Irvine Gass syndrome; (21–23) retinal nerve fiber layer (RNFL) in elevated IOP (24)].

In 2018, for the first time, Kurt and Kılıç (25) published a study that focused on the segmentation of all retinal layers and individually analyzed the alterations following phacoemulsification. Their findings revealed non-uniform thickening across different retinal layers (25). The present study aims to analyze retinal segmentation thickness before and one month after cataract surgery to detect any short-term surgically induced changes in each layer.

 Materials and methods

This research study was conducted in accordance with the ethical guidelines outlined in the Declaration of Helsinki, and the necessary approval from the Institutional Review Board (IRB) (CECS, South Campania Ethics Committee, protocol no. 16544) was secured. All individuals gave a written consent to take part in the study.

Subjects with lens opacities, eligible to cataract surgery at the Ophthalmology Unit of the University of Salerno, which underwent uneventful cataract surgery with in the bag IOL implantation, were recruited for this retrospective observational study.

Patients with corneal leukoma, epiretinal membrane, diabetic retinopathy, advanced hypertensive retinopathy (grade II to IV), age-related macular degeneration, central serous chorioretinopathy, glaucoma, macular hole, previous laser treatment or intravitreal injections, presence of vitreomacular disease, previous ocular surgery, optic neuropathy, uveitis, uncontrolled hypertension with medication, autoimmune diseases, glycated hemoglobin A1c (HbA1c) level > 6.5% and ocular or systemic conditions that could cause retinal alterations were excluded. Only patients with nuclear or cortical opacities that allowed the preoperative OCT examination were recruited.

Therefore, 70 eyes of a total of 70 subjects (42 female and 28 male patients), aged 49 to 92 years (mean age 73 ± 9 years), were selected.

Clinical and instrumental assessment

During the preoperative visit, the participants undertook a complete ophthalmological examination, which involved assessing their clinical history, measuring their uncorrected and corrected visual acuity using the Snellen chart, conducting slit-lamp biomicroscopy and anterior segment evaluation, determining their IOP with a Goldmann applanation tonometer, performing fundus examination, and measuring their axial length using an IOLMaster 500 device (Carl Zeiss Meditec AG, Jena, Germany, version 5.4.4.0006), and spectral domain OCT scanning (Spectralis; Heidelberg Engineering; Heidelberg, Germany, version 6.0) using the “automatic real-time” (ART) volume program. One month later (an interval between 28 and 31 days), the OCT evaluation was reperformed using the device’s follow-up mode.

 Surgical technique

Before surgery, a Mydriasert® tablet (Théa Pharma) (containing a combination of tropicamide and phenylephrine hydrochloride, 0.28 mg/5.4 mg) was located in the lower conjunctival fornix to promote mydriasis. Peribulbar anesthesia with 0.75% ropivacaine, followed by eyelids, eyelashes, and conjunctiva disinfection with 5% povidone iodine, and phacoemulsification with Constellation® Vision System (Alcon Laboratories, Inc.) were performed.

All surgeries followed the established protocol, including emulsification of cataractous lenticular nucleus passing through a clear corneal main tunnel of 3 mm on the vertical axis and the “Divide and Conquer” surgical technique, by different surgeons.

In all cases, the same preloaded hydrophobic intraocular lens Tecnis® Monofocal (PCB00) was implanted in the capsular bag. Injection of 0.1 mL/1 mg of cefuroxime (Ximaract®; Bausch & Lomb UK Ltd.) into the anterior chamber and closure of the main tunnel and two paracentesis were final steps of the surgery. In the postoperative period, the use of dexamethasone and levofloxacin 1 mg/ml + 5 mg/ml (Ducressa; Santen Italia S.r.l.) five times daily for one week, then diclofenac 1 mg/ml (Visunac; Visufarma S.p.A.) three times daily for the following three weeks were prescribed as post-surgical antibacterial and anti-inflammatory prophylaxis.

 OCT analysis: retinal parameters

The study involved the use of Spectral-Domain Optical Coherence Tomography (SD-OCT) with the Heidelberg Spectralis (Heidelberg Engineering, Heidelberg, Germany) to image participants’ retinas. The key details of the imaging process and analysis used are the following:

- Imaging Parameters: Scan Area: 20° × 15° (5.9 × 4.4 mm)

Frames: average of 100 frames using Automatic Real-Time (ART) mode

Sections: 19 horizontal scans spaced at 240 μm intervals

Resolution: 512 A-scans per B-scan

- Image Quality: images with a signal-to-noise ratio (SNR) less than 15 dB were excluded to ensure high-quality data.

- Retinal Layer Segmentation: the segmentation of retinal layers was performed automatically by the Heidelberg Spectralis software. The system identified 11 optical interfaces to study the 10 distinct retinal layers.

- Thickness Measurement: the standard Early Treatment Diabetic Retinopathy Study (ETDRS) grid was used. Measurements were taken at the following regions: fovea-centered Circle, 1 mm in diameter, and Parafoveal Regions, in superior, nasal, inferior, and temporal regions each with a 3 mm diameter. Finally, the average thickness of the retinal layers was calculated for the fovea (1 mm), parafoveal regions (3 mm each), and the combined average of these five regions (Figures 1–3).

Retinal layers before cataract surgery.

Optical coherence tomography (OCT) scan of the retina showing cross-sectional layers with labeled segments such as ILM, RNFL, GCL, and others. Each layer is highlighted with a distinct color line for differentiation. The left panel displays a cross-section selection on a retinal image.

Retinal layer after cataract surgery.

Optical coherence tomography (OCT) scan of a human retina showing cross-sectional layers with labeled boundaries. A sidebar lists retinal layers from ILM to CHO. The macular region is centrally indented.

Thickness map before and after cataract surgery and differential thickness map.

Optical coherence tomography scan of the retina showing various layers and structures. Color-coded maps illustrate retinal thickness and changes, with detailed measurements in micrometers. Visual data includes charts for average thickness, changes, and central measurements.

This detailed protocol ensures consistent and high-quality retinal imaging and analysis, crucial for accurate assessment and study of retinal health and diseases.

Therefore, values were collected for total thickness (ALL), outer retinal layers (ORL), inner retinal layers (IRL), retinal pigment epithelium (RPE), outer nuclear layer (ONL), outer plexiform layer (OPL), inner nuclear layer (INL), inner plexiform layer (IPL), ganglion cell layer (GCL), and nerve fiber layer (NFL). IRL included the sum of the layers between NFL and external limiting membrane (ELM), while ORL included layers from RPE to ELM.

Photoreceptor layer (PRL) measurement resulted from the subtraction of RPE measurements from the ORL.

Then, the same trained ophthalmologist (M.D.B.) checked the automatic retinal layers segmentation, misalignments, decentration or motion artifacts and reviewed data extrapolated from collected OCT scans to avoid measurement biases.

The ETDRS grid was manually aligned with the foveal pit, if not correctly positioned.

All examinations were performed between 12:00 and 2:00 PM. All measurements were made using the Heidelberg Spectralis software (Heidelberg Engineering; Heidelberg, Germany, version 6.0).

 Statistical analysis

SPSS software (IBM SPSS Statistics version 25) was used to conduct statistical assessment.

The normality of data distribution was computed with the Kolmogorov–Smirnov test. All parameters of patients and controls between the preoperative and the control visits were compared using a two-tailed t-test, for data distributing in accordance with the Gaussian curve, and the Wilcoxon signed-rank test, for data distributing according to a different trend. Statistical significance was considered for a p-value of less than 0.05. To perform the analysis G*Power software (version 3.1.9.4) was utilized. To maximize the statistical power utilizing a paired t-test, the sample size with α error = 0.05, 1-β error = 0.95 and effect size = 0.437 was set. Non-centrally parameter δ = 3.656, critical t = 1.995, Df = 69, total sample size = 70 and actual power = 0.95 were then calculated. In addition, to maximize the statistical power utilizing Wilcoxon test, the sample size with α error = 0.05, 1-β error = 0.95 and effect size = 0.450 was decided. Non-centrally parameter δ = 3.68, critical t = 1.997, Df = 65.84, total sample size = 70 and actual power = 0.95 were calculated.

 Results

Table 1 provides a summary of the retinal layers’ measurements, whereas Table 2, illustrates the differences between pre- and post-surgical measurements, which can be summarized as follows:

Thickness of retinal layers (μm).

PRE POST
Mt 3S 3I 3N 3T 3MT mt 3S 3I 3N 3T 3MT
ORL Mean 85 81 80 82 81 81 85 79 79 80 79 79
SD 5.9 3.2 3.6 3.6 3.3 3.2 4.8 4 3.3 3.6 3.7 3.5
Min 75 74 74 74 74 74 74 74 72 73 69 74
Max 109 89 98 97 90 92 99 91 87 91 90 90
Median 84 80 80 81 80 80 85 79 78 80 79 79
IRL Mean 176 245 243 245 234 242 187 258 257 260 247 255
SD 21.1 19 20 19.2 22 18.9 3.4 25 21.2 18 16.9 18.6
Min 111 146 149 154 132 145 134 146 160 210 208 200
Max 216 291 284 286 323 281 241 302 313 304 282 299
Median 177 246 245 245 233 244 183 260 256 261 247 256
EPR Mean 15 15 14 14 14 14 16 15 14 15 14 14
SD 3.1 1.4 1.3 1.3 1.1 1 2.8 1.9 1.7 1.8 1.6 1.6
Min 12 12 11 12 12 12 13 12 11 12 12 12
Max 30 18 17 18 16 17 24 20 18 19 18 18
Median 15 14 14 14 14 14 15 14 14 15 14 14
ONL Mean 81 68 69 69 74 70 91 74 73 79 80 77
SD 15.4 18.4 17.7 17.2 12.6 13 15.7 22.9 19.6 15.6 13 15.6
Min 42 33 37 31 46 45 51 31 34 34 48 48
Max 112 122 131 101 109 102 139 238 193 134 140 170
Median 84 69 69 70 73 69 91 73 74 79 80 77
OPL Mean 27 435 33 36 29 33 27 34 34 33 30 33
SD 7.8 8.4 7.4 10.7 5.5 5 8.5 7.6 6.1 7.2 5.4 3.7
Min 12 20 21 23 19 22 2 8 24 24 20 25
Max 52 62 56 64 48 46 61 59 54 60 56 44
Median 26 33 30 33 27 33 25 32 32 31 29 32
INL Mean 25 41 42 43 38 41 24 42 42 42 39 41
SD 8.8 4.51 5.9 5.7 3.8 3.4 7.3 3.9 5 4.1 4 3.1
Min 12 20 21 23 19 22 2 8 24 24 20 25
Max 56 55 71 67 47 49 46 50 65 54 48 48
Median 23 41 41 43 38 41 23 42 42 42 38 38
IPL Mean 19 36 35 37 36 36 20 3 38 39 38 38
SD 3.9 4.8 5.9 5.1 5.3 4.4 3.9 4.8 4.8 4.9 5.1 4.3
Min 13 17 19 21 23 23 11 17 17 24 23 25
Max 33 51 47 48 52 52 31 51 51 49 51 50
Median 18 39 37 38 36 36 20 39 39 39 39 39
GCL Mean 14 45 44 43 39 43 14 49 48 47 43 47
SD 4 8.2 9.6 7.2 7.6 7.2 4 8.1 8.2 7.8 7.8 7.2
Min 7 21 14 24 16 21 7 9 20 25 17 23
Max 25 68 68 60 60 64 25 70 70 67 68 68
Median 14 46 46 44 40 44 14 50 49 46 42 47
RNFL Mean 12 21 22 19 18 20 12 24 24 21 18 22
SD 2.8 3.4 3.9 2.1 2.5 1.9 2.8 4 3.9 2.7 1.8 2.4
Min 6 12 9 15 14 14 6 9 15 15 13 17
Max 22 31 30 24 27 24 22 35 37 27 22 28
Median 12 21 22 19 17 20 12 24 24 21 18 21
ALL Mean 258 327 325 328 315 324 270 339 336 340 326 336
SD 26.3 15.9 16.4 15.7 15.1 14.8 25.8 16.7 17.5 17.8 16.7 16.3
Min 136 260 267 271 278 277 170 284 284 288 291 292
Max 302 375 363 371 351 363 324 380 392 386 362 378
Median 261 327 325 329 314 324 268 337 337 341 326 334

mt: thickness of retinal layers at the foveal location (1 mm diameter). 3MT: mean thickness of retinal layers at the macular location (3 mm diameter). 0.3S: retinal layers thickness 3 mm superior to the fovea. 3I: thickness of retinal layers 3 mm inferior to the fovea. 3N: thickness of retinal layers 3 mm nasal to the fovea. 3T: thickness of retinal layers 3 mm temporal to the fovea. ORL, outer retinal layers. IRL, inner retinal layers; RPE, retinal pigment epithelium; ONL, outer nuclear layer; OPL, outer plexiform layer; INL, inner nuclear layer; IPL, inner plexiform layer; GCL, ganglion cell layer; RNFL, retinal nerve fiber layer; ALL, total retinal thickness.

Difference in thickness (μm) of retinal layers pre/post-operation.

Δ PRE/POST
Mt 3S 3I 3N 3T 3MT
ORL Mean 0 1 1 1 2 1
SD 0 −1 0 0 0 0
Min 1 0 2 1 5 1
Max 10 −2 11 6 0 2
Median −1 1 2 1 1 1
P 0.742 0.002 < 0.001 0.002 < 0.001 < 0.001
IRL Mean −11 −13 −13 −15 −13 −14
SD −2 −6 1 1 5 0
Min −23 0 −11 −56 −76 −55
Max −22 −11 −29 −18 41 −19
Median −7 −14 −11 −15 −14 −12
P < 0.001 < 0.001 < 0.001 < 0.001 < 0.001 < 0.001
EPR Mean 0 0 0 0 0 0
SD 1 −1 0 0 −1 −1
Min −1 0 0 0 0 1
Max 6 −2 −2 −1 −2 −1
Median 0 0 0 −1 0 0
P 0.232 0.721 0.284 0.394 0.861 0.563
ONL Mean −10 −6 −4 −10 −5 −6
SD 0 −5 −2 2 0 −3
Min −9 2 3 −3 −2 −3
Max −27 −116 −62 −33 −31 −68
Median −8 −5 −5 −10 −6 −7
P < 0.001 < 0.001 0.008 < 0.001 0.001 < 0.001
OPL Mean 0 1 −1 3 −1 1
SD −1 1 1 4 0 1
Min 10 12 −3 −1 −1 −3
Max −9 3 2 4 −8 2
Median 1 1 −2 2 −2 0
P 0.388 0.526 0.147 0.015 0.119 0.187
INL Mean 1 −1 0 1 −1 0
SD 2 1 1 2 0 0
Min 0 5 −1 −2 −1 −3
Max 10 5 6 13 −1 1
Median 1 −1 −1 1 −1 1
P 0.915 0.110 0.803 0.404 0.144 0.542
IPL Mean 0 −2 −2 −2 −2 −2
SD 0 0 1 0 0 0
Min 2 6 −4 −3 0 −2
Max 2 −1 −4 −1 1 −1
Median −2 −2 −1 −1 −3 −2
P 0.156 < 0.001 < 0.001 < 0.001 < 0.001 < 0.001
GCL Mean −1 −4 −4 −3 −4 −4
SD 0 1 1 −1 0 0
Min 0 12 −6 −1 −1 −2
Max −3 −2 −2 −7 −8 −5
Median −1 −4 −3 −2 −2 −4
P 0.010 < 0.001 < 0.001 < 0.001 < 0.001 < 0.001
RNFL Mean −1 −3 −3 −2 0 −2
SD 0 −1 0 −1 1 0
Min 0 3 −6 0 1 −3
Max 2 −4 −7 −3 5 −4
Median 0 −3 −2 −2 −1 −2
P 0.020 < 0.001 < 0.001 < 0.001 < 0.001 < 0.001
ALL Mean −12 −13 −12 −13 −11 −12
SD 1 −1 −1 −2 −2 −1
Min −34 −24 −17 −17 −13 −14
Max −22 −5 −29 −15 −11 −15
Median −8 −10 −12 −12 −13 −11
P < 0.001 < 0.001 < 0.001 < 0.001 < 0.001 < 0.001

mt: thickness of retinal layers at the foveal location (1 mm diameter). 0.3MT: mean thickness of retinal layers at the macular location (3 mm diameter). 0.3S: retinal layers thickness 3 mm superior to the fovea. 3I: thickness of retinal layers 3 mm inferior to the fovea. 3N: thickness of retinal layers 3 mm nasal to the fovea. 3T: thickness of retinal layers 3 mm temporal to the fovea. ORL, outer retinal layers; IRL, inner retinal layers; RPE, retinal pigment epithelium; ONL, outer nuclear layer; OPL, outer plexiform layer; INL, inner nuclear layer; IPL, inner plexiform layer; GCL, ganglion cell layer; RNFL, retinal nerve fiber layer; ALL, total retinal thickness.

The central foveal region (1 mm) exhibited a significant thickening in the IRL (p < 0.001), ONL (p < 0.001), GCL (p = 0.010), RNFL (p = 0.020), and ALL (p < 0.001). The other layers showed not statistically significant or negligible variations.

The superior parafoveal region (3 mm) presented a substantial increase in the IRL (p < 0.001), ONL (p < 0.001), IPL (p < 0.001), GCL (p < 0.001), RNFL (p < 0.001), and ALL (p < 0.001).

Additionally, a statistically significant thinning in the ORL (p = 0.002) was present in this region. The other layers showed not statistically significant or negligible variations.

The inferior parafoveal region (3 mm) displayed a statistically significant thickening in the IRL (p < 0.001), ONL (p = 0.008), IPL (p < 0.001), GCL (p < 0.001), RNFL (p < 0.001), and ALL (p < 0.001). A statistically significant reduction in the ORL thickness (p < 0.001) was also demonstrated. The other layers showed not statistically significant or negligible variations.

The nasal parafoveal region (3 mm) showed a statistically significant increase in the IRL (p < 0.001), ONL (p < 0.001), IPL (p < 0.001), GCL (p < 0.001), RNFL (p < 0.001), and ALL (p < 0.001). A meaningful decrease in the ORL (p = 0.002) and OPL (p = 0.015) was also shown.

The other layers showed not statistically significant or negligible variations.

The temporal parafoveal region (3 mm) displayed a statistically significant increase in the IRL (p < 0.001), ONL (p = 0.001), IPL (p < 0.001), GCL (p < 0.001), RNFL (p < 0.001), and ALL (p < 0.001). A statistically significant decrease in the ORL (p < 0.001) was also demonstrated.

The other layers showed not statistically significant or negligible variations.

The average of the five considered regions (foveal and parafoveal) demonstrated a statistically significant thickening of the IRL (p < 0.001), ONL (p < 0.001), IPL (p < 0.001), GCL (p < 0.001), RNFL (p < 0.001), and ALL (p < 0.001). A statistically significant thinning in the ORL layer (p < 0.001) was also displayed. The other layers showed not statistically significant or null variations.

In addition, PR layer showed a statistically significant reduction in the 4 parafoveal regions (p < 0.001), however not in the central foveal region (Tables 3, 4).

Thickness of photoreceptors layer (μm).

PRE POST
mt 3S 3I 3N 3T 3MT mt 3S 3I 3N 3T 3MT
PR Mean 70 66 66 67 67 66 69 65 64 65 65 65
SD 4.2 2.4 3.1 3.1 2.8 2.6 3.9 2.5 2.2 2.6 2.7 2.3
Min 61 62 62 62 61 62 61 61 61 61 56 61
Max 79 73 84 82 76 77 82 71 71 75 73 73
Median 69 66 66 66 66 66 69 65 64 65 65 65

mt: thickness of retinal layers at the foveal location (1 mm diameter). 3MT: mean thickness of retinal layers at the macular location (3 mm diameter). 0.3S: retinal layers thickness 3 mm superior to the fovea. 3I: thickness of retinal layers 3 mm inferior to the fovea. 3N: thickness of retinal layers 3 mm nasal to the fovea. 3T: thickness of retinal layers 3 mm temporal to the fovea.

Difference in thickness (μm) of photoreceptors layer pre/post-operation.

Δ PRE/POST
Mt 3S 3I 3N 3T 3MT
PR Mean 1 1 2 2 2 2
SD 0.3 0.1 0.9 0.5 0.1 0.3
Min 0 1 1 1 5 1
Max −3 2 13 7 3 5
Median −1 1 2 1 1 1
P 0.236 < 0.001 < 0.001 < 0.001 < 0.001 < 0.001

mt: thickness of retinal layers at the foveal location (1 mm diameter). 0.3MT: mean thickness of retinal layers at the macular location (3 mm diameter). 0.3S: retinal layers thickness 3 mm superior to the fovea. 3I: thickness of retinal layers 3 mm inferior to the fovea. 3N: thickness of retinal layers 3 mm nasal to the fovea. 3T: thickness of retinal layers 3 mm temporal to the fovea.

 Discussion

In recent years phacoemulsification for cataract treatment has been gradually improved, becoming a minimally invasive procedure that involves only the anterior segment of the eye.

However, post-operative retinal alterations can have serious consequences, such as cystoid macular edema, or they may present sub-clinically and seem to have no effect on visual outcome.

The precise cause and mechanism behind the fundus changes following emulsification of cataractous lenticular nucleus remain unclear. Several factors have been suggested, including vascular instability, vitreomacular traction, ocular hypotony, and increased light exposure (26).

Some studies indicate that post-operative inflammation may significantly contribute to the evelopment of retinal alterations (27–30).

Numerous factors related to phacoemulsification can affect ocular structures. Ultrasonic energy and fluid dynamics generate mechanical effects, albeit slight, that result in inflammation, compression, and oxygen drop in the surrounding tissues. Each step of this procedure can induce direct tissue changes and immediate pressure variations. Additionally, turbulent fluid flow exerts radiating pressure impacts similar to a shockwave and a small jet, directly affecting the anterior chamber structures and spreading in all directions (9).

Even if asymptomatic, these micro-alterations can be detected with optical coherence tomography (OCT).

Although several studies have been conducted in recent years to verify changes in macular thickness after cataract surgery, their conclusions were not in agreement (14–19, 25, 31, 32).

The present study focuses on changes one month after phacoemulsification, a significant increase in thickness is observed in many retinal layers (IRL, ONL, IPL, GCL, RNFL) both at the central foveal and parafoveal regions, leading to a statistically significant increase in ALL. This finding is consistent with the most recent studies that have examined retinal modifications in terms of thickness following cataract surgery (14–19, 25, 31, 32). However, among these studies, only one segmented the retina and examined the modifications individually.

Nevertheless, this research was limited by the modest number of examined eyes and segmenting the retina into the following layers: RPE, ONL, OPL, INL, IPL, GCL, RNFL (25).

This segmentation excluded the retinal structures between the RPE and ONL, which include photoreceptors and their connections with inner layers (33). Our study introduced further segmentation of the retina into IRL and ORL. The latter group includes all structures between RPE and the ELM, including PRL. Then we obtained the PRL from the ORL, and the results revealed that the ORL, in particular the PRL, is the only segment to show a statistically significant thinning in the 4 parafoveal regions, with no changes in the central foveal region.

This result, observed for the first time in this study, is in contrast with the findings of other studies and may indicate inflammation-induced suffering of the PRL, following phacoemulsification. This structural alteration was not evident during clinical examination, and the sparing of the central foveal region could explain the absence of clinical influence.

It is known that post-operative inflammatory effects can cause free radicals, growth factors and prostaglandins release, which could be leading factors for post-operative retinal alterations (5, 24, 34). By the literature, surgical wounds trigger releasing of prostaglandins into the aqueous humor and blood-aqueous barrier damage, with consequential start of an inflammatory cascade and production of other inflammatory mediators in the aqueous humor and their dispersion into the vitreous cavity. Posterior segment inflammation, consecutive to the anterior segment ones, disrupts both inner and outer blood-retinal barrier (35), inducing choroidal thickness and Vascularity Index increase at the first postoperative month (35–37). Nevertheless, lacking strong evidence, the exact mechanism of retinal structure changes and their impact on the ocular fundus–whether beneficial or harmful–remains unclear.

Menapace et al. (38) published a study involving 120 eyes from 60 patients, with complete follow-up data for 56 patients. The participants were divided into two groups: those undergoing femtosecond laser-assisted cataract surgery and those undergoing manual cataract surgery. The findings indicated similar patterns of macular thickness and volume increase, with no statistically significant differences between the two groups. Our results are consistent with those of the authors, despite our focus on individual retinal layers, to achieve a meticulous assessment of retinal changes (38).

Schwarzenbacher et al. (39) conducted a study involving 112 eyes from 56 patients, also divided into femtosecond laser-assisted and manual cataract surgery groups. They evaluated changes over postoperative periods of 1 week, 3 weeks, 6 weeks, and 18 months, focusing on the inner nuclear layer (INL), outer plexiform layer (OPL), outer nuclear layer (ONL), photoreceptor (PR) layer, and total retinal thickness. Notably, a significant decrease in PR thickness was observed 1 week post-surgery across all zones. Conversely, the other evaluated layers and the overall retina exhibited an increase in thickness during the initial weeks, remaining significantly elevated 18 months post-surgery in all zones. Our findings align with those of the authors in the early postoperative period; however, our study utilized a larger sample size of 70 eyes from a total of 70 subjects and assessed all individual retinal layers (39).

Großpötzl et al. (40) investigated a cohort of 41 patients who underwent uneventful cataract surgery, with evaluations conducted preoperatively and at 1 day, 1 month, and 3 months postoperatively. The authors focused on all layers of the inner retina, including the OPL, ONL, and total retinal thickness. They reported a decrease in retinal thickness on the first postoperative day, followed by a significant increase at 1 month and a subsequent reduction at 3 months. Our results are consistent with these findings at 1 month post-surgery; however, the strength of our research lies in its comprehensive assessment of all retinal layers. Unlike the authors, we observed a statistically significant decrease in the OPL and PR layer at 1 month post-surgery (40).

Recently, Balog et al. (41) published a study involving 102 eyes from 79 consecutive subjects without any other ocular or systemic diseases who underwent cataract surgery. The authors reported a statistically significant increase in nearly all retinal layers and a decrease in OPL at 7, 30 and 90 days post-phacoemulsification. This finding aligns with our results; we also observed thickening in nearly all retinal layers and thinning of the OPL. The authors suggested that the decrease might be attributed to PR loss. While we cannot confirm this hypothesis, our study specifically focused on the PR layer and found a statistically significant reduction. This decrease may indeed be explained by PR loss; however, our results indicate a reduction in thickness that could also be attributed to structural cellular changes within the PR layer (41).

In conclusion, our study, conducted on 70 eyes of 70 patients scheduled for cataract surgery supports the existing literature, highlighting an increase in retinal thickness following the procedure, and also reveals a previously unobserved reduction in the thickness of the ORL and PRL, observed through a more detailed segmentation of retinal layers than ever before. Due to the retrospective nature of this study, longer follow up visit were not available, because nor morphological signs of retinal changes by OCT neither best corrected visual acuity reduction were present. For the same reason, only the routine pharmacological treatment with NSAID drops was applied to these patients.

The lack of longer follow-up to strengthen our observation represents a limitation of this study. Nevertheless, our results provide a basis for further studies that may provide a pathophysiological explanation for this phenomenon, contributing to an understanding of post-phacoemulsification complications affecting the retina.

 Data availability statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

 Ethics statement

The studies involving humans were approved by the Comitato etico “Cometico Campania Sud.” The studies were conducted in accordance with the local legislation and institutional requirements. The participants provided their written informed consent to participate in this study.

 Author contributions

MG: Data curation, Writing – original draft. MDB: Validation, Writing – review and editing. AL: Writing – original draft. MDL: Data curation, Writing – original draft. SP: Investigation, Writing – original draft. MA: Methodology, Writing – original draft. AM: Writing – original draft. NR: Supervision, Validation, Writing – review and editing.

 Funding

The authors declare that no financial support was received for the research and/or publication of this article.

 Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

 Generative AI statement

The authors declare that no Generative AI was used in the creation of this manuscript.

 Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

 Abbreviations

AMD, age-related macular degeneration; OCT, optical coherence tomography; RNFL, retinal nerve fiber layer; IRB, Institutional Review Board; CECS, Cometico Campania Sud; HbA1c, glycated hemoglobin A1c; IOP, intraocular pressure; AL, axial length; ART, automatic real-time; ETDRS, early treatment diabetic retinopathy study; ALL, total thickness; ORL, outer retinal layers; IRL, inner retinal layers; RPE, retinal pigment epithelium; ONL, outer nuclear layer; OPL, outer plexiform layer; INL, inner nuclear layer; IPL, inner plexiform layer; GCL, ganglion cell layer; NFL, nerve fiber layer; ELM, external limiting membrane; PR, photoreceptor layer.

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