Literature DB >> 30767402

The utility of a new fundus camera using a portable slit lamp combined with a smartphone.

Mitsuru Arima1, Takuya Majima1, Shoko Tsukamoto1, Takuya Hara2, Iori Wada1, Shintaro Nakao1, Koh-Hei Sonoda1.   

Abstract

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Year:  2019        PMID: 30767402      PMCID: PMC6767703          DOI: 10.1111/aos.14049

Source DB:  PubMed          Journal:  Acta Ophthalmol        ISSN: 1755-375X            Impact factor:   3.761


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Editor, A contact‐type camera is commonly used for paediatric fundus photography. With its use, we can easily photograph the fundus while controlling the eye movement in arbitrary direction. However, it is difficult to use a contact‐type camera for infants in poor general condition because ocular compression with the camera lens risks a reduction of vital signs. Furthermore, its continuous use for different infants has a risk to spread infection. Therefore, we attempted to develop a new non‐contact‐type camera. Fundus imaging methods using an LED light from a smartphone were reported (Haddock et al. 2013; Russo et al. 2015). These methods are effective, but every time a smartphone is replaced with a new model, we must ensure that the LED light is not harmful to the retina. We therefore decided to use the light source of a portable slit lamp. Because this instrument does not use the LED light of a smartphone itself, it can be used with every existing smartphone model. Moreover, because portable slit lamps have already been introduced in almost all ophthalmic institutions, we can reduce the initial cost. Our instrument is shown in Fig. 1A. Instead of a forehead rest, we fixed the original attachment containing a front‐end lens (Super VitreoFundus or SuperPupil XL; Volk, Mentor, OH, USA), a polarizing plate (to reduce reflected light) and a barrier filter [to cut the blue excitation light in fluorescein angiography (FA)] to the portable slit lamp (SL‐17; Kowa Ltd., Tokyo, Japan). We also fixed an iPhone6s (Apple, Cupertino, CA, USA) to the eyepiece of the slit lamp. We tested the safety of our instrument and confirmed that it complies with ISO 15004‐2: 2007. This study was conducted in accord with the Declaration of Helsinki, and approval was obtained from the Institutional Review Board of Kyushu University Hospital. All images were captured from video data recorded in 4K resolution using FiLMiC Pro v6 (Cinegenix, Seattle, WA, USA).
Figure 1

(A) Our camera combined with a portable slit lamp and a smartphone. (B) Optical layouts of our camera and fundus images of a healthy adult. The diameter of the incident light is 12 mm. (C,D) The fundus of an infant with retinopathy of prematurity. A Super VitreoFundus was used. (E,F) The image of the posterior segment (E) and anterior segment (F) of an infant with persistent foetal vasculature. A Super VitreoFundus was used (E). (G) The fundus of an infant with optic nerve hypoplasia. The double ring signs (arrowheads) could be recognized. We used a Super VitreoFundus. (H,I) The fundus image (H) and fluorescein angiography image (I) of an 8‐week‐old wild‐type mouse. A SuperPupil XL was used. A = artery, V = vein. (J) The fundus image of an 8‐week‐old mouse with experimental autoimmune uveitis. We used a SuperPupil XL.

(A) Our camera combined with a portable slit lamp and a smartphone. (B) Optical layouts of our camera and fundus images of a healthy adult. The diameter of the incident light is 12 mm. (C,D) The fundus of an infant with retinopathy of prematurity. A Super VitreoFundus was used. (E,F) The image of the posterior segment (E) and anterior segment (F) of an infant with persistent foetal vasculature. A Super VitreoFundus was used (E). (G) The fundus of an infant with optic nerve hypoplasia. The double ring signs (arrowheads) could be recognized. We used a Super VitreoFundus. (H,I) The fundus image (H) and fluorescein angiography image (I) of an 8‐week‐old wild‐type mouse. A SuperPupil XL was used. A = artery, V = vein. (J) The fundus image of an 8‐week‐old mouse with experimental autoimmune uveitis. We used a SuperPupil XL. The field of view is 80° or 96° when using the Super VitreoFundus or SuperPupil XL, respectively (Fig. 1B). Fundus images of retinopathy of prematurity are shown in Fig. 1C,D. The image quality was sufficient to recognize abnormalities such as tortuous vessels and proliferative membranes. Figure 1E,F provides images in a case of persistent foetal vasculature. Our camera could capture the image of the proliferating tissue extending from the optic disc (Fig. 1E). Because our camera is also capable of capturing photographs of the anterior segment by removing the attachment to which the front lens is fixed, we could record images of the proliferating tissue in contact with the posterior surface of the crystalline lens (Fig. 1F). We could also record the double ring sign in an infant with optic nerve hypoplasia (Fig. 1G). All images were photographed during outpatient care. Unlike a contact‐type camera, our camera cannot control the eye movement. We therefore captured the fundus using an eyelid speculum and a retractor when peripheral retinal images were needed. It took about 5 seconds to capture one field of view, and <1 min even when photographing the entire fundus. Another advantage of our instrument is that we can capture fundus photographs and FA of animals, because the portable slit lamp has the function of emitting blue excitation light. The fundus and FA images captured from the same mouse are shown in Fig. 1H,I. Our camera is also useful for measuring the clinical score of experimental autoimmune uveitis (Fig. 1J) (Agarwal et al. 2012; Takeda et al. 2018). Anyone can create a non‐contact‐type camera easily by fixing a simple attachment to a portable slit lamp. This instrument has versatility, and it can be used for clinical examinations and basic experiments.
  4 in total

1.  Rodent models of experimental autoimmune uveitis.

Authors:  Rajeev K Agarwal; Phyllis B Silver; Rachel R Caspi
Journal:  Methods Mol Biol       Date:  2012

2.  Crucial role of P2X7 receptor for effector T cell activation in experimental autoimmune uveitis.

Authors:  Atsunobu Takeda; Hisakata Yamada; Eiichi Hasegawa; Mitsuru Arima; Shoji Notomi; Sayaka Myojin; Takeru Yoshimura; Toshio Hisatomi; Hiroshi Enaida; Ryoji Yanai; Kazuhiro Kimura; Tatsuro Ishibashi; Koh-Hei Sonoda
Journal:  Jpn J Ophthalmol       Date:  2018-03-23       Impact factor: 2.447

3.  A Novel Device to Exploit the Smartphone Camera for Fundus Photography.

Authors:  Andrea Russo; Francesco Morescalchi; Ciro Costagliola; Luisa Delcassi; Francesco Semeraro
Journal:  J Ophthalmol       Date:  2015-06-02       Impact factor: 1.909

4.  Simple, inexpensive technique for high-quality smartphone fundus photography in human and animal eyes.

Authors:  Luis J Haddock; David Y Kim; Shizuo Mukai
Journal:  J Ophthalmol       Date:  2013-09-19       Impact factor: 1.909

  4 in total
  2 in total

1.  Diffuser-based computational imaging funduscope.

Authors:  Yunzhe Li; Gregory N McKay; Nicholas J Durr; Lei Tian
Journal:  Opt Express       Date:  2020-06-22       Impact factor: 3.894

2.  Mucosal-associated invariant T cells have therapeutic potential against ocular autoimmunity.

Authors:  Satoshi Yamana; Kensuke Shibata; Eiichi Hasegawa; Mitsuru Arima; Shotaro Shimokawa; Nobuyo Yawata; Atsunobu Takeda; Sho Yamasaki; Koh-Hei Sonoda
Journal:  Mucosal Immunol       Date:  2021-11-13       Impact factor: 7.313

  2 in total

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