Open Access

Artificial intelligence and deep learning in ophthalmology - present and future (Review)

  • Authors:
    • Andreea Dana Moraru
    • Danut Costin
    • Radu Lucian Moraru
    • Daniel Constantin Branisteanu
  • View Affiliations

  • Published online on: August 12, 2020     https://doi.org/10.3892/etm.2020.9118
  • Pages: 3469-3473
  • Copyright: © Moraru et al. This is an open access article distributed under the terms of Creative Commons Attribution License.

Metrics: Total Views: 0 (Spandidos Publications: | PMC Statistics: )
Total PDF Downloads: 0 (Spandidos Publications: | PMC Statistics: )


Abstract

Since its introduction in 1959, artificial intelligence technology has evolved rapidly and helped benefit research, industries and medicine. Deep learning, as a process of artificial intelligence (AI) is used in ophthalmology for data analysis, segmentation, automated diagnosis and possible outcome predictions. The association of deep learning and optical coherence tomography (OCT) technologies has proven reliable for the detection of retinal diseases and improving the diagnostic performance of the eye's posterior segment diseases. This review explored the possibility of implementing and using AI in establishing the diagnosis of retinal disorders. The benefits and limitations of AI in the field of retinal disease medical management were investigated by analyzing the most recent literature data. Furthermore, the future trends of AI involvement in ophthalmology were analyzed, as AI will be part of the decision‑making regarding the scientific investigation, diagnosis and therapeutic management.

1. Introduction

In 1956 artificial intelligence (AI) was first described as a technology capable of thinking independently and reproducing human behavior after training (1). Machine learning (ML) was introduced in 1959 as an algorithm that, after exposure to multiple inputs can modify its behavior, automatically (2). Today, by developing computational power and neural networks, deep learning determines the perfection of automatic learning. Deep learning (DL), as a subset of machine learning, uses a programmable neural network that enables the machine to make its own decisions, without human aid. Convolutional neural networks (CNNs) play an important role in the development of these technologies (3). Convolutional layers, which are the basis of these networks, learn to extract the image features with the aid of convolutional filters (4).

Deep learning is used in ophthalmology for data analysis, segmentation, automated diagnosis and possible outcome predictions (5). The association of deep learning and optical coherence tomography (OCT) technologies has proven reliable for the detection of retinal diseases and improving the diagnostic performance of the eye's posterior segment diseases (6-8).

At present, some difficulties of translating these algorithms into the clinical practice may be encountered, such as inconsistency in the reporting metrics when analyzing data from multiple OCT devices, imaging protocols that are not standardized between devices, and limited capabilities in graphics processing.

The increase in the number of retinal disease cases has produced an ever-growing demand for retinal image readers. The development of artificial intelligence (AI) and deep learning analysis of retinal imaging can reduce the number of ophthalmologists needed for image interpretation and the time allocated for this procedure. At the same time, AI may increase the efficiency of healthcare providers by establishing the correct and rapid diagnosis of retinal diseases.

In this review, the possibility of implementing and using AI in establishing the diagnosis of retinal disorders was explored. Moreover, the benefits and limitations of AI in the field of retinal disease medical management were reviewed.

2. AI, ML, DL and computer programming

AI technologies entered the field of ophthalmology recently and have been in continue expansion ever since. In the near future AI will have an important impact on aiding research to achieve new discoveries and improving clinical practice.

Artificial intelligence

AI was defined by John McCarthy as the ‘science of creating intelligent machines which replicate human behavior’ (1).

Machine learning

ML is a subtype of AI. The computer software learns from large volumes, without explicit instructions, on how to derive the required output (through trial and error). It becomes better at making its own decisions but still needs human guidance.

Deep learning

DL is a subtype of ML. It uses multiple layers of CNNs. These are made of software-defined ‘neurons’ which together are processing data in order to get the required information. The neural networks are designed to be similar to the ones inside the human brain and reason in a similar manner. Thus the algorithm is able to determine on its own if the prediction made by the DL process is accurate or not.

Generative adversarial networks

GANs are paired neural networks used for unsupervised ML. This neural network generates images or other data and the discriminative neural network evaluates it and gives feedback to help in the learning process. GANs are used for fully supervised, semi-supervised and reinforcement learning.

Computer programming

The computer programming is very important. The software programmer has to know in advance how to process the data to produce the required information. When the ML software has finished learning, it will generate the required output (9).

3. OCT and AI/deep learning

OCT images are used for the diagnosis, monitoring and management of many retinal conditions such as diabetic macular edema (DME) and age-related macular degeneration (AMD). Investigative efforts have been directed at utilizing deep learning algorithms as tools for automated reading of OCT images, for diagnostic purposes. Numerous algorithms have been developed and various landmarks identified in order to recognize non-pathologic OCT images (10-12).

There are 10 relevant anatomic layers visible on spectral-domain OCT. Algorithms can identify anywhere from 4 to all 10 of these layers. Studies have shown wide variability in the identification of various landmarks. At the moment, the development of a consistently accurate algorithm is critically needed. The integration of these algorithms into a tele-retinal screening pathway will be one way of integrating automated OCT reading into clinical practice.

Automated OCT reading has shown promising results in DME and identifying exudative AMD (7,8,13). In a recent study, Kermany et al (8) found 97.8% sensitivity, 97.4% specificity, and 0.99 AUROC (area under the receiver operating characteristic) curve for detecting referable AMD. An AUROC curve score over 0.7 relates to good and outstanding results, while under 0.5 proves no discrimination was made. Thus, DL can accurately diagnose AMD in the early stages.

OCT demonstrates high accuracy in detecting small amounts of fluid and the need to commence treatment in neovascular AMD (14-17). Chakravarthy et al (16) recorded 91.0% accuracy for diagnosing exudative AMD and Prahs et al (15) showed 95.5% accuracy for predicting the need for intravitreal injections.

Automated OCT reading has also been proven useful in the diagnosis of diabetic retinopathy, central serous chorioretinopathy, polypoidal choroidal vasculopathy and macular holes (13,18,19). Obviously, physicians may benefit from OCT reading algorithms as a triaging mechanism and a guide in the therapy decision-making process.

4. AI and retinal diseases

Deep learning and the retinopathy of prematurity

ROP is a vasoproliferative disease that affects premature infants and it may lead to blindness (20). The initiation of ROP treatment is based on the International Classification Guide (ICROP), which is used to standardize the diagnosis and to determine treatment thresholds (21).

When examining a ROP eye, it is possible to visualize, at the level of the posterior pole, abnormal arterial tortuosity and venous dilatations, which define PLUS disease (22). The screening is performed by direct examination, by an ophthalmologist. For the same purpose, the images can be obtained with portable cameras examined afterward by a specialist.

Numerous clinical trials indicated that there are significant variability and inconsistency in the ROP diagnosis, which may lead to differences in treatment recommendations (23-25).

Some deep learning algorithms have been created to minimize the clinical reasoning variability and inconsistency in diagnosing ROP, many of them showing accuracy in detecting ‘plus’ or ‘pre-plus’ disease (lower degree of vascular tortuosity) (26-28). Brown et al (29) used deep learning for training a deep convolutional neural network on a set of 5,511 images. These images were previously rated by experts as ‘plus’, ‘pre-plus’ or ‘normal’. The validation of a set of 100 retinal images showed: 93% sensitivity and 94% specificity for the detection of ‘plus’ disease and 100% sensitivity and 94% species in detecting ‘pre-plus’ disease. Similar studies showed that deep learning may be able to minimize inter-observer variability.

In order to generate reliable image analysis algorithms, it is very important to have a clinically accepted reference standard for diagnosis. The effectiveness of deep learning image analysis as a screening tool for ROP needs to be evaluated in clinical daily practice.

Deep learning and diabetic retinopathy (DR)

The incidence of DR is on the rise as the prevalence of obesity increases and the population ages. Undiagnosed DR is one of the main causes of vision loss (30-32).

There are currently many studies aiming at the development of software programs that increase the efficiency of DR screening and management. Recent literature data showed that machine learning classes (MLC, support vector machine, multiple layer perceptron classes and radial basis function neural network) can recognize and classify DR from images (30-35). The results obtained (MLCs, AI programs) are comparable to those obtained when the retinal images were analyzed by ophthalmologists. In these studies, Ting et al (37), Gulshan et al (36), and Gargeya and Leng (38) used large data sets to create MLCs.

The researchers used as training images normal images and DR images (separated into categories of mild, moderate, severe, proliferative DR; referable DME and referable DR were additional categories from the same data set, but separate from the others classifications) (36). The results obtained were remarkable. The data validated DR (sensitivity, 0.87-0.98; specificity, 0.90-0.98 and AUROC, 0.936-0.991) (36-38). The software is able to recognize hemorrhages, exudation, microaneurysms, cotton-wool spots and neovascularization, build a model and based on it, is able to classify DR in stages.

Further research into how deep learning fits in the screening pathway is warranted.

Deep learning and age-related macular degeneration

AMD is a frequent disease in the aging population, with the potential to cause important and irreversible visual function loss. AI has contributed significantly to the progress that has been made in screening AMD and may help both patients and health-providers benefit from implementing AI as support in ophthalmological decision making (39).

Lee et al (40) created an AMD screening system capable of differentiating between normal and AMD, OCT images. They obtained a peak sensitivity of 0.926, a specificity of 0.937 and an AUROC of 0.9746. Their studies analyzed smaller size samples.

In a larger study, Treder et al (17) used 1112 OCT images. They created an MLC software which differentiates a healthy macula of one showing exudative AMD and obtained a sensitivity of 1.00 and a specificity of 0.92.

Besides diagnosis, formulating a visual prognosis is a challenge for many researchers.

Some studies are focused on AMD grading and predicting the final visual acuity by using OCT images. The presumptive prognosis may influence the clinician's decision in establishing the treatment of the disease.

Schmidt-Erfurth et al (39) predicted best-corrected visual acuity at 1 year immediately after establishing the diagnosis of the disease with the help of AI. The registered error was 12.9 letters. They trained their MLC on data sets from 614 eyes (2456 OCT scans). Aslam et al (41), in a similar study, reported a mean error of 8.21 letters. They analyzed only 847 OCT scans.

Burlina et al (42,43) made imaging assessment more efficient through grading systems, which have the potential to function as a decision support system for clinicians. The study group developed software for different MLCs using more than 130,000 OCT images from 4,613 patients. Their conclusion was that deep CNN is the most precise. They obtained an accuracy of the analysis comprised between 0.884 and 0.916.

Some studies look at the role of AI as support to therapy decision-making in AMD (if and when the anti-vascular endothelial growth factor, anti-VEGF, treatment is necessary). AI and predictive treatment technology have been proven as a useful addition to clinical practice. This is possible by training MLCs using OCT imaging. Prahs et al (44), Chakravarthy et al (16), Schlegl et al (45) found that their deep learning CNN was able to correctly predict the need for anti-VEGF therapy (intravitreal injection) in 95% of the cases, similar to an average specialist. The researchers analyzed different features of the scan, particularly retinal fluid presence (46). Central retinal thickness and fluid localization are important biomarkers in OCT images.

Schmidt-Erfurth and Waldstein (47) performed an analysis able to predict the functional prognosis (best-corrected visual acuity outcomes) in neovascular AMD patients about to receive ranibizumab treatment. Bogunovic et al (48), applied an algorithm on 61 eyes with AMD. This algorithm used OCT biomarkers to reasonably predict drusen regression over the next 2 years. They obtained an AUROC curve of 0.75. Drusen regression has been shown to precede the progression of non-exudative AMD (49-52).

The above studies demonstrate that deep learning can be utilized to extract data that ophthalmologists cannot read. Deep learning results in image analysis are comparable to that of human performance (43). Many studies have already validated the potential of neural networks in diagnosing AMD.

5. Limitations

AI usage in clinical practice might present some potential risks. Some software programs are based on algorithms that lead to high false-negative rates of detection of retinal diseases. Improper interpretation of the false-positive results may lead to diagnostic errors and could be clinically disastrous for patients' vision.

Sometimes the ophthalmologist can not evaluate the metrics values used by the AI computer software to analyze the clinical data. The method by which a computer algorithm came to its conclusion, the reasoning process, is not always obvious.

It is possible that remote screening (patient's home screening) by automated AI systems, may become a problem due to a lack of patient confidence. Some studies show that many patients do not trust computer-aided diagnosis and prefer in-person ophthalmology visits (53).

Also, there is a risk for doctors to become addicted to technology and lose diagnostic abilities.

For some particular situations, when a physician disagrees with the results obtained by deep learning assessment, or when a patient does not receive counseling related to the required treatment it is necessary to introduce and apply medicolegal and ethical regulations.

All these potential shortcomings highlight the need for continuous improvement in AI technology.

6. The future

In the near future, AI will become more involved in the decision-making regarding the scientific investigation, diagnosis and therapeutic management. Tele-ophthalmology applications can transmit information to less developed regions that face a shortage of specialists (54). Already, a hybrid algorithm, with high sensitivity and specificity, named IDx-DR, approved by FDA as a low to moderate risk device, is used for diabetic retinopathy screening, aiding the management of patients that need referral to an ophthalmologist.

AI can quickly analyze large databases. Based on these analyzes, AI can explore the associations between disease features that may not be easily obvious to humans.

The clinical analysis of the ophthalmologist supported by the DL analysis results will improve the individualization of the medical management, for the benefit of the patients (55).

AI also plays an important role in scientific research. With the help of AI, the features of newly discovered eye diseases can be identified (53). It is expected that AI algorithms will help in identifying new biomarkers, specific to each disease, as they are able to search for characteristics themselves and are not limited to only recognizing clinical features.

Ongoing research aims to develop autonomous software able to diagnose simultaneously AMD, diabetic retinopathy and glaucoma, predict progression and recommend personalized treatment.

7. Conclusions

AI/ DL (deep learning) algorithms using both OCT and fundus images will revolutionize techniques and methodologies of image analysis. Optimizing these (combined) technologies will accelerate the progress in this area. Currently, there are software programs that standardize OCT images from various devices and the results of these software packages are comparable when the appropriate metrics are used consistently. Nevertheless, large databases, using real patient data, are required to optimize the performance of this type of analysis. Thus, computer-assisted screening, diagnosis and prediction of the ophthalmic disease will reach new frontiers.

In ophthalmology AI has the potential to increase patient access to clinical screening/diagnosis and decrease health-care costs, especially when the risk of the disease occurrence is high or the communities confront with low financial resources. However, legal regulations and solving of the reproducibility issues are required before AI based screening is incorporated in clinical practice.

Acknowledgements

Not applicable.

Funding

No funding was received.

Availability of data and materials

Not applicable.

Authors' contributions

ADM and DC contributed to the design of the study, participated in the entire review process and prepared the manuscript. DCB, ADM and RLM performed the literature research and contributed to the analysis and critical interpretation of the data. ADM, DCB and RLM conceived the review and revised the manuscript. DC gave the final approval of the version to be published. All authors read and approved the final version of the manuscript.

Ethics approval and consent to participate

Not applicable.

Patient consent for publication

Not applicable.

Competing interests

All authors declare that they have no competing interests.

References

1 

McCarthy J, Minsky ML, Rochester N and Shannon CE: A proposal for the Dartmouth Summer Research Project on Artificial Intelligence. AI Mag. 27:12. 2006.

2 

Samuel AL: Some studies in machine learning using the game of checkers. IBM J Res Develop. 3:210–229. 1959.

3 

Lee A, Taylor P, Kalpathy-Cramer J and Tufail A: Machine learning has arrived! Ophthalmology. 124:1726–1728. 2017.PubMed/NCBI View Article : Google Scholar

4 

LeCun Y, Bengio Y and Hinton G: Deep learning. Nature. 521:436–444. 2015.PubMed/NCBI View Article : Google Scholar

5 

Schmidt-Erfurth U, Sadeghipour A, Gerendas BS, Waldstein SM and Bogunović H: Artificial intelligence in retina. Prog Retin Eye Res. 67:1–29. 2018.PubMed/NCBI View Article : Google Scholar

6 

De Fauw J, Ledsam JR, Romera-Paredes B, Nikolov S, Tomasev N, Blackwell S, Askham H, Glorot X, O'Donoghue B, Visentin D, et al: Clinically applicable deep learning for diagnosis and referral in retinal disease. Nat Med. 24:1342–1350. 2018.PubMed/NCBI View Article : Google Scholar

7 

Lee CS, Tyring AJ, Deruyter NP, Wu Y, Rokem A and Lee AY: Deep-learning based, automated segmentation of macular edema in optical coherence tomography. Biomed Opt Express. 8:3440–3448. 2017.PubMed/NCBI View Article : Google Scholar

8 

Kermany DS, Goldbaum M, Cai W, Valentim CCS, Liang H, Baxter SL, McKeown A, Yang G, Wu X, Yan F, et al: Identifying medical diagnoses and treatable diseases by image-based deep learning. Cell. 172:1122–1131.e9. 2018.PubMed/NCBI View Article : Google Scholar

9 

Sayres R, Taly A, Rahimy E, Blumer K, Coz D, Hammel N, Krause J, Narayanaswamy A, Rastegar Z, Wu D, et al: Using a deep learning algorithm and integrated gradients explanation to assist grading for diabetic retinopathy. Ophthalmology. 126:552–564. 2019.PubMed/NCBI View Article : Google Scholar

10 

Hussain MA, Bhuiyan A, Turpin A, Luu CD, Smith RT, Guymer RH and Kotagiri R: Automatic identification of pathology distorted retinal layer boundaries using SD-OCT imaging. IEEE Trans Biomed Eng. 64:1638–1649. 2017.PubMed/NCBI View Article : Google Scholar

11 

Fabritius T, Makita S, Miura M, Myllylä R and Yasuno Y: Automated segmentation of the macula by optical coherence tomography. Opt Express. 17:15659–15669. 2009.PubMed/NCBI View Article : Google Scholar

12 

Yazdanpanah A, Hamarneh G, Smith B and Sarunic M: Intra-retinal layer segmentation in optical coherence tomography using an active contour approach. Med Image Comput Comput Assist Interv. 12:649–656. 2009.PubMed/NCBI View Article : Google Scholar

13 

Liu YY, Ishikawa H, Chen M, Wollstein G, Duker JS, Fujimoto JG, Schuman JS and Rehg JM: Computerized macular pathology diagnosis in spectral domain optical coherence tomography scans based on multiscale texture and shape features. Invest Ophthalmol Vis Sci. 52:8316–8322. 2011.PubMed/NCBI View Article : Google Scholar

14 

Fang L, Cunefare D, Wang C, Guymer RH, Li S and Farsiu S: Automatic segmentation of nine retinal layer boundaries in OCT images of non-exudative AMD patients using deep learning and graph search. Biomed Opt Express. 8:2732–2744. 2017.PubMed/NCBI View Article : Google Scholar

15 

Prahs P, Radeck V, Mayer C, Cvetkov Y, Cvetkova N, Helbig H and Märker D: OCT-based deep learning algorithm for the evaluation of treatment indication with anti-vascular endothelial growth factor medications. Graefes Arch Clin Exp Ophthalmol. 256:91–98. 2018.PubMed/NCBI View Article : Google Scholar

16 

Chakravarthy U, Goldenberg D, Young G, Havilio M, Rafaeli O, Benyamini G and Loewenstein A: Automated identification of lesion activity in neovascular age-related macular degeneration. Ophthalmology. 123:1731–1736. 2016.PubMed/NCBI View Article : Google Scholar

17 

Treder M, Lauermann JL and Eter N: Automated detection of exudative age-related macular degeneration in spectral domain optical coherence tomography using deep learning. Graefes Arch Clin Exp Ophthalmol. 256:259–265. 2018.PubMed/NCBI View Article : Google Scholar

18 

Syed AM, Hassan T, Akram MU, Naz S and Khalid S: Automated diagnosis of macular edema and central serous retinopathy through robust reconstruction of 3D retinal surfaces. Comput Methods Programs Biomed. 137:1–10. 2016.PubMed/NCBI View Article : Google Scholar

19 

Xu Y, Yan K, Kim J, Wang X, Li C, Su L, Yu S, Xu X and Feng DD: Dual-stage deep learning framework for pigment epithelium detachment segmentation in polypoidal choroidal vasculopathy. Biomed Opt Express. 8:4061–4076. 2017.PubMed/NCBI View Article : Google Scholar

20 

Gilbert C and Foster A: Childhood blindness in the context of VISION 2020 - the right to sight. Bull World Health Organ. 79:227–232. 2001.PubMed/NCBI

21 

No authors listed. Cryotherapy for retinopathy of prematurity cooperative group: Multicenter trial of cryotherapy for retinopathy of prematurity. Preliminary results. Arch Ophthalmol. 106:471–479. 1988.PubMed/NCBI View Article : Google Scholar

22 

International Committee for the Classification of Retinopathy of Prematurity. The International Classification of Retinopathy of Prematurity Revisited. Arch Ophthalmol. 123:991–999. 2005.PubMed/NCBI View Article : Google Scholar

23 

Reynolds JD, Dobson V, Quinn GE, Fielder AR, Palmer EA, Saunders RA, Hardy RJ, Phelps DL, Baker JD, Trese MT, et al: CRYO-ROP and LIGHT-ROP Cooperative Study Groups: Evidence-based screening criteria for retinopathy of prematurity: Natural history data from the CRYO-ROP and LIGHT-ROP studies. Arch Ophthalmol. 120:1470–1476. 2002.PubMed/NCBI View Article : Google Scholar

24 

Chiang MF, Jiang L, Gelman R, Du YE and Flynn JT: Interexpert agreement of plus disease diagnosis in retinopathy of prematurity. Arch Ophthalmol. 125:875–880. 2007.PubMed/NCBI View Article : Google Scholar

25 

Chernyshov PV, Sampogna F, Pustišek N, Marinovic B, Manolache L, Suru A, Salavastru CM, Tiplica GS, Stoleriu G, Kakourou T, et al: Validation of the dermatology-specific proxy instrument the infants and toddlers dermatology quality of life. J Eur Acad Dermatol Venereol. 33:1405–1411. 2019.PubMed/NCBI View Article : Google Scholar

26 

Bajwa A, Aman R and Reddy AK: A comprehensive review of diagnostic imaging technologies to evaluate the retina and the optic disk. Int Ophthalmol. 35:733–755. 2015.PubMed/NCBI View Article : Google Scholar

27 

Gelman R, Jiang L, Du YE, Martinez-Perez ME, Flynn JT and Chiang MF: Plus disease in retinopathy of prematurity: Pilot study of computer-based and expert diagnosis. J AAPOS. 11:532–540. 2007.PubMed/NCBI View Article : Google Scholar

28 

Ataer-Cansizoglu E, Bolon-Canedo V, Campbell JP, Bozkurt A, Erdogmus D, Kalpathy-Cramer J, Patel S, Jonas K, Chan RV, Ostmo S, et al: i-ROP Research Consortium: i-ROP Research Consortium. Computer-based image analysis for plus disease diagnosis in retinopathy of prematurity: Performance of the ‘i-ROP’ system and image features associated with expert diagnosis. Transl Vis Sci Technol. 4(5)2015.PubMed/NCBI View Article : Google Scholar

29 

Brown JM, Campbell JP, Beers A, Chang K, Ostmo S, Chan RV, Dy J, Erdogmus D, Ioannidis S, Kalpathy-Cramer J, et al: Imaging and Informatics in Retinopathy of Prematurity (i-ROP) Research Consortium: Imaging and Informatics in Retinopathy of Prematurity (i-ROP) Research Consortium. Automated diagnosis of plus disease in retinopathy of prematurity using deep convolutional neural networks. JAMA Ophthalmol. 136:803–810. 2018.PubMed/NCBI View Article : Google Scholar

30 

Safi H, Safi S, Hafezi-Moghadam A and Ahmadieh H: Early detection of diabetic retinopathy. Surv Ophthalmol. 63:601–608. 2018.PubMed/NCBI View Article : Google Scholar

31 

Schaas BA, Ivan S, Titianu M, Condratovici CP, Maier A and Schaas CM: Biochemical markers predicting the risk of gestational diabetes mellitus. Mater Plast. 54:133–136. 2017.

32 

Alexe O, Gainaru C, Serafinceanu C, Pleseacondratovici A, Danciulescu-Miulescu R and Pleseacondratovici C: Patient- Reported Outcomes (PROs) in Romanian type 2 diabetic patients - Results from a Multicentre National Registry. In: Interdisciplinary Approaches In Diabetic Chronic Kidney Disease. Bucuresti, pp76-88, 2015.

33 

Abbas Q, Fondon I, Sarmiento A, Jiménez S and Alemany P: Automatic recognition of severity level for diagnosis of diabetic retinopathy using deep visual features. Med Biol Eng Comput. 55:1959–1974. 2017.PubMed/NCBI View Article : Google Scholar

34 

Raju M, Pagidimarri V, Barreto R, Kadam A, Kasivajjala V and Aswath A: Development of a deep learning algorithm for automatic diagnosis of diabetic retinopathy. Stud Health Technol Inform. 245:559–563. 2017.PubMed/NCBI

35 

Xu K, Feng D and Mi H: Deep convolutional neural network-based early automated detection of diabetic retinopathy using fundus image. Molecules. 22(2054)2017.PubMed/NCBI View Article : Google Scholar

36 

Gulshan V, Peng L, Coram M, Stumpe MC, Wu D, Narayanaswamy A, Venugopalan S, Widner K, Madams T, Cuadros J, et al: Development and validation of a deep learning algorithm for detection of diabetic retinopathy in retinal fundus photographs. JAMA. 316:2402–2410. 2016.PubMed/NCBI View Article : Google Scholar

37 

Ting DSW, Cheung CY-L, Lim G, Tan GSW, Quang ND, Gan A, Hamzah H, Garcia-Franco R, San Yeo IY, Lee SY, et al: Development and validation of a deep learning system for diabetic retinopathy and related eye diseases using retinal images from multiethnic populations with diabetes. JAMA. 318:2211–2223. 2017.PubMed/NCBI View Article : Google Scholar

38 

Gargeya R and Leng T: Automated identification of diabetic retinopathy using deep learning. Ophthalmology. 124:962–969. 2017.PubMed/NCBI View Article : Google Scholar

39 

Schmidt-Erfurth U, Bogunovic H, Sadeghipour A, Schlegl T, Langs G, Gerendas BS, Osborne A and Waldstein SM: Machine learning to analyze the prognostic value of current imaging biomarkers in neovascular age-related macular degeneration. Ophthalmol Retina. 2:24–30. 2018.PubMed/NCBI View Article : Google Scholar

40 

Lee CS, Baughman DM and Lee AY: Deep learning is effective for classifying normal versus age-related macular degeneration OCT images. Ophthalmol Retina. 1:322–327. 2017.PubMed/NCBI View Article : Google Scholar

41 

Aslam TM, Zaki HR, Mahmood S, Ali ZC, Ahmad NA, Thorell MR and Balaskas K: Use of a neural net to model the impact of optical coherence tomography abnormalities on vision in age-related macular degeneration. Am J Ophthalmol. 185:94–100. 2018.PubMed/NCBI View Article : Google Scholar

42 

Burlina P, Pacheco KD, Joshi N, Freund DE and Bressler NM: Comparing humans and deep learning performance for grading AMD: A study in using universal deep features and transfer learning for automated AMD analysis. Comput Biol Med. 82:80–86. 2017.PubMed/NCBI View Article : Google Scholar

43 

Burlina PM, Joshi N, Pekala M, Pacheco KD, Freund DE and Bressler NM: Automated grading of age related macular degeneration from color fundus images using deep convolutional neural networks. JAMA Ophthalmol. 135:1170–1176. 2017.PubMed/NCBI View Article : Google Scholar

44 

Prahs P, Märker D, Mayer C and Helbig H: Deep learning to support therapy decisions for intravitreal injections. Ophthalmologe. 115:722–727. 2018.PubMed/NCBI View Article : Google Scholar : (In German).

45 

Schlegl T, Waldstein SM, Bogunovic H, Endstrasser F, Sadeghipour A, Philip AM, Podkowinski D, Gerendas BS, Langs G and Schmidt-Erfurth U: Fully automated detection and quantification of macular fluid in OCT using deep learning. Ophthalmology. 125:549–558. 2018.PubMed/NCBI View Article : Google Scholar

46 

Bogunovic H, Waldstein SM, Schlegl T, Langs G, Sadeghipour A, Liu X, Gerendas BS, Osborne A and Schmidt-Erfurth U: Prediction of anti-VEGF treatment requirements in neovascular AMD using a machine learning approach. Invest Ophthalmol Vis Sci. 58:3240–3248. 2017.PubMed/NCBI View Article : Google Scholar

47 

Schmidt-Erfurth U and Waldstein SM: A paradigm shift in imaging biomarkers in neovascular age-related macular degeneration. Prog Retin Eye Res. 50:1–24. 2016.PubMed/NCBI View Article : Google Scholar

48 

Bogunovic H, Montuoro A, Baratsits M, Karantonis MG, Waldstein SM, Schlanitz F and Schmidt-Erfurth U: Machine learning of the progression of intermediate age-related macular degeneration based on OCT imaging. Invest Ophthalmol Vis Sci. 58:BIO141–BIO150. 2017.PubMed/NCBI View Article : Google Scholar

49 

Stanca HT, Petrović Z and Munteanu M: Transluminal Nd:YAG laser embolysis - A reasonable method to reperfuse occluded branch retinal arteries. Vojnosanit Pregl. 71:1072–1077. 2014.PubMed/NCBI View Article : Google Scholar

50 

Munteanu M, Rosca C and Stanca H: Sub-inner limiting membrane hemorrhage in a patient with Terson syndrome. Int Ophthalmol. 39:461–464. 2019.PubMed/NCBI View Article : Google Scholar

51 

Stanca HT, Stanca S, Tabacaru B, Boruga M and Balta F: Bevacizumab in Wet AMD treatment: A tribute to the thirteen years of experience from the beginning of the anti-VEGF era in Romania. Exp Ther Med. 18:4993–5000. 2019.PubMed/NCBI View Article : Google Scholar

52 

Danielescu C, Stanca HT and Balta F: The Management of lamellar macular holes: A review. J Ophthalmol. 2020(3526316)2020.PubMed/NCBI View Article : Google Scholar

53 

Keel S, Lee PY, Scheetz J, Li Z, Kotowicz MA, MacIsaac RJ and He M: Feasibility and patient acceptability of a novel artificial intelligence-based screening model for diabetic retinopathy at endocrinology outpatient services: A pilot study. Sci Rep. 8(4330)2018.PubMed/NCBI View Article : Google Scholar

54 

Armstrong GW and Lorch AC: A(eye): A review of current applications of artificial intelligence and machine learning in ophthalmology. Int Ophthalmol Clin. 60:57–71. 2020.PubMed/NCBI View Article : Google Scholar

55 

Consejo A, Melcer T and Rozema JJ: Introduction to machine learning for ophthalmologists. Semin Ophthalmol. 34:19–41. 2019.PubMed/NCBI View Article : Google Scholar

Related Articles

Journal Cover

October-2020
Volume 20 Issue 4

Print ISSN: 1792-0981
Online ISSN:1792-1015

Sign up for eToc alerts

Recommend to Library

Copy and paste a formatted citation
x
Spandidos Publications style
Moraru AD, Costin D, Moraru RL and Branisteanu DC: Artificial intelligence and deep learning in ophthalmology - present and future (Review). Exp Ther Med 20: 3469-3473, 2020
APA
Moraru, A.D., Costin, D., Moraru, R.L., & Branisteanu, D.C. (2020). Artificial intelligence and deep learning in ophthalmology - present and future (Review). Experimental and Therapeutic Medicine, 20, 3469-3473. https://doi.org/10.3892/etm.2020.9118
MLA
Moraru, A. D., Costin, D., Moraru, R. L., Branisteanu, D. C."Artificial intelligence and deep learning in ophthalmology - present and future (Review)". Experimental and Therapeutic Medicine 20.4 (2020): 3469-3473.
Chicago
Moraru, A. D., Costin, D., Moraru, R. L., Branisteanu, D. C."Artificial intelligence and deep learning in ophthalmology - present and future (Review)". Experimental and Therapeutic Medicine 20, no. 4 (2020): 3469-3473. https://doi.org/10.3892/etm.2020.9118