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AJR 2001; 177:1199-1203
© American Roentgen Ray Society


2001 ARRS President's Award

Radiologic Differentiation of Intraocular Glass

Evaluation of Imaging Techniques, Glass Types, Size, and Effect of Intraocular Hemorrhage

Devang M. Gor1, Claudia F. Kirsch1, Jeffrey Leen2, Roger Turbin2 and Stanley Von Hagen3

1 Department of Radiology, University Hospital, University of Medicine and Dentistry of New Jersey, Rm. C-320 150 Bergen St., Newark, NJ 07103.
2 Department of Ophthalmology, University Hospital, University of Medicine and Dentistry of New Jersey, Newark, NJ 07103.
3 Department of Preventive Medicine and Community Health, Biostatistics Division, University Hospital, University of Medicine and Dentistry of New Jersey, Newark, NJ 07103.

Received March 22, 2001; accepted after revision May 23, 2001.

 
Address correspondence to D. M. Gor (roentgen1895{at}yahoo.com )


Abstract
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
OBJECTIVE. The accurate detection of intraocular foreign bodies is critically important in treating ocular trauma. The purpose of this study was to evaluate the efficacy of CT, MR imaging, and sonography in detecting seven types of glass varying in size and placed in three locations in the globe, and to examine the effect of intraocular hemorrhage.

MATERIALS AND METHODS. Glass pieces were cut into 1.5-, 1.0-, and 0.5-mm pieces and implanted on the corneal surface and the anterior and posterior chambers of 42 fresh porcine eyes. Twenty-one eyes were scanned comparing axial CT, helical CT, and MR imaging. The remaining 21 eyes were scanned using helical CT and sonography after implantation in a simulated human skull before and after placement of blood in the anterior chamber (hyphema).

RESULTS. Detection rates were 57.1% for helical CT, 41.3% for axial CT, and 11.1% for T1-weighted MR imaging (n = 63 fragments). Results were significant (p < 0.0001). Sonography detected 43% of glass fragments in the posterior chamber and 24% in the anterior chamber. Detectability was greatest for green beer bottle glass (90.3%) and least for spectacle glass (43.1%) (p < 0.0001). Detection rates for size ranged from 96.2% at 1.5 mm to 48.3% at 0.5 mm, which was also significant (p < 0.0001). On helical CT, anterior chamber glass was easiest to detect (91.7%) and corneal surface glass the most difficult (64.9%). Hyphema made no statistical difference (p < 0.0001).

CONCLUSION. Helical CT was the most sensitive imaging modality for the detection of intraocular glass. The sensitivity of detection was unaffected by hyphema but was determined by the type of glass, size, and location.


Introduction
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
The accurate detection and localization of intraocular foreign bodies is a critical component in preoperative ophthalmologic treatment and surgical planning [1,2,3,4]. Frequently, traumatic tissue damage or ocular media opacities such as traumatic cataracts or intraocular hemorrhage prevent adequate direct ophthalmologic evaluation, and the ophthalmologic surgeon must rely on available imaging techniques for the detection of intraocular foreign bodies [1,2,3,4,5,6,7,8]. Helical CT scanning is considered the diagnostic method of choice for the detection of intraocular foreign bodies and is preferred over both MR imaging and sonography [1,2,3,4,5,6,7,8,9,10,11,12].

The radiologic evaluation of metallic and wooden intraocular foreign bodies is well reported, including minimum detection limits [1,2,3, 5, 6, 9]. However, only a few studies have evaluated the detection of glass intraocular foreign bodies, noting minimum detection limits of 1.82-5 mm [2, 6]. To our knowledge, no reports evaluate the efficacy of improved helical CT in detecting various types of glass that commonly present in the emergency department as intraocular foreign bodies. The aim of this study was to evaluate the efficacy of current imaging techniques, including axial and helical CT, MR imaging, and sonography, for detecting seven types of glass intraocular foreign bodies, with attention to factors such as size, location, and the presence or absence of intraocular hemorrhage.


Materials and Methods
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
Seven types of glass commonly seen in the emergency department setting were scanned using helical CT. We then determined the Hounsfield unit attenuation for each type. The types of glass were green beer bottle glass, brown beer bottle glass, windshield glass, spectacle glass, window plateglass, 100-W incandescent glass, and 40-W fluorescent bulb glass. The glass subtypes were cut precisely into 1.5-, 1.0-, and 0.5-mm lengths.

Forty-two fresh porcine eyes were prepared in a standardized fashion by a single ophthalmologist. Each eye was assigned a particular fragment size and glass type, and the appropriate-sized glass fragment was placed in each of three locations in each eye (corneal surface, anterior chamber, and posterior chamber). Surface glass was placed on the anterior cornea using fine jeweler's forceps. Glass foreign bodies were placed in the anterior chamber using a microsurgical technique through a 4-mm limbal incision fashioned with a standard 15° ophthalmologic blade. Glass foreign bodies were placed in the posterior chamber using a microsurgical technique through a 4-mm pars plana incision fashioned with a standard 15° ophthalmologic blade.

In the first study, 63 fragments were placed in 21 porcine eyes: three fragments per eye, in the three locations. This procedure was repeated for each of the three sizes and seven glass types. The eyes were placed on a foam tray and were scanned with a LightSpeed 4DCT scanner (General Electric Medical Systems, Milwaukee, WI) with an orbital algorithm in both the helical and axial modes. Helical CT parameters included 120 kVp, 250 mA, 1.25-mm slice thickness, and a pitch of 3.75. Sequential 1.25-mm images were obtained in the axial mode. CT images were processed and printed in both bone (window width, 2000 H; level, 250 H) and soft-tissue (window width, 250 H; level, 50 H) window settings. A water bath was placed under the foam tray and the eyes were scanned with MR imaging. A 1.5-T MR imager (General Electric Medical Systems) was used and the following sequences were obtained: T1-weighted sequences with a TR/TE of 450/28, 5-mm slice thickness with a 1.5-mm interslice gap, with and without fat suppression; and T2-weighed sequences with 4000/84 and a 4-mm slice thickness with a 1.0-mm interslice gap.

The CT and MR images were printed and reviewed by five physicians, who were asked to determine the number of glass fragments they could identify in each set. The identifications were double-blinded, in that the person inserting the glass fragments did not communicate with the inspectors identifying them. Two of the physicians were board-certified radiologists and certificate-of-added-qualification-certified neuroradiologists, one was a board-certified neuroophthalmologist, one was a radiology resident, and one, an ophthalmology resident. The data were compiled and evaluated using logistic regression.

In the second series, an identical second set of 21 fresh porcine eyes was prepared with the same seven types of glass in 1.5-, 1.0-, and 0.5-mm increments, with three fragments placed in each eye. The glass fragments were again placed by the same ophthalmologist onto the corneal surface, anterior chamber, and posterior chamber of each eye. However, to simulate in vivo conditions, a simulated human skull was used. The orbits were filled with lipid vegetable shortening to simulate the orbital fat, and the prepared globes were placed in the appropriate anatomic position (Fig. 1). The skull containing the prepared globes was imaged using helical CT with the same orbital algorithm used in the first series.



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Fig. 1. Photograph of porcine eyes placed in skull with vegetable fat in orbits to simulate orbital fat.

 

After the images were obtained, fresh human blood was obtained from a volunteer by using a 21-gauge butterfly needle. Two drops of blood were placed by an ophthalmologist into the anterior chamber of each eye, using surgical loops and a syringe to create a hyphema. All eyes were then rescanned with the same helical CT orbital algorithm using the skull model containing the globes.

After the helical CT, the 21 porcine eyes were examined using ocular high-resolution sonography. An I3 System ABD sonography scanner (Innovative Imaging, Sacramento, CA) was used with a 10-MHz probe applied directly on the surface of the globe to obtain contact B-mode scans. To obtain the sonographic evaluation, the corneal surface glass was removed, and only the presence or absence of anterior or posterior chamber glass was assessed. The ocular sonography was performed and interpreted by an ophthalmologist with specialty training in orbital sonography. These data were evaluated separately from the helical CT and MR imaging data.

Image analysis on the second series of helical CT data was performed independently by four physicians who were unaware of the content of the eyes (one board-certified neuroradiologist, one board-certified neuroophthalmologist, and two radiology residents). All helical CT data were compiled and evaluated using logistic regression.

Plots were generated using contingency table analysis or logistic regression, one factor at a time (location [surface, anterior chamber, posterior chamber]; size [0.5, 1.0, 1.5 mm]; type of glass [green beer bottle, brown beer bottle, spectacle eyeglass, windshield, plateglass, 100- or 40-W bulb]; observer [the various interpreters]; imaging modality [helical CT; axial CT; T1-, T2-, or T1-weighted with fat saturation MR imaging]; and hyphema [present or absent]). Sonographic data were evaluated in a separate table. In certain cases, contingency tables were supplemented with a Cochran-Mantel-Haenszel test stratified by size or location. However, all p values cited in this study refer (unless otherwise noted) to multiple logistic regression models in which several main effect factors, together with one or more interaction factors, were analyzed simultaneously. The level of significance was set at an {alpha} value of 0.05.


Results
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
In comparing imaging modalities in the first series, with 63 glass intraocular foreign bodies to be identified, helical CT was the most sensitive technique, with a total of 57.1% of glass foreign bodies identified, followed by axial CT, which identified 41.3%. In the second series, simulating in vivo conditions, helical CT identified 74% of all glass intraocular foreign bodies (n = 63, p < 0.0001) (Fig. 2A,2B). No statistical difference in detection was noted between helical CT and axial CT in the first series (p = 0.05, Fisher's exact test). MR imaging results were poor, with only 11.1% of intraocular foreign bodies identified on T1-weighted MR imaging, 4.8% using T1-weighted imaging with fat saturation, and 4.8% using T2-weighted MR imaging (p < 0.0001). Sonography of the 21 porcine eyes was less reliable than helical CT and was able to identify only nine (43%) of 21 glass fragments in the posterior chamber and only five (24%) of 21 glass fragments in the anterior chamber (Fig. 3A,3B,3C,3D,3E,3F). The corneal surface glass fragments were removed to perform the sonographic examination and were therefore not evaluated. A graphic comparison of these results is presented in Figure 4.



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Fig. 2A. Axial CT scans of intraocular foreign bodies in porcine eyes. 1.5-mm glass foreign bodies on corneal surface (open arrow) and in posterior chamber (straight solid arrow) in right eye. Also seen is 0.5-mm glass intraocular foreign body in posterior chamber (curved arrow) of left eye.

 


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Fig. 2B. Axial CT scans of intraocular foreign bodies in porcine eyes. 0.5-mm glass foreign body in anterior chamber (arrow).

 


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Fig. 3A. Helical CT, sonography, and T1-weighted MR imaging of glass intraocular foreign bodies. Helical CT scan (A), sonogram (B), and T1-weighted MR image (C) show 1.5-mm glass fragment in anterior chamber of eye. Arrowheads indicate glass fragments.

 


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Fig. 3B. Helical CT, sonography, and T1-weighted MR imaging of glass intraocular foreign bodies. Helical CT scan (A), sonogram (B), and T1-weighted MR image (C) show 1.5-mm glass fragment in anterior chamber of eye. Arrowheads indicate glass fragments.

 


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Fig. 3C. Helical CT, sonography, and T1-weighted MR imaging of glass intraocular foreign bodies. Helical CT scan (A), sonogram (B), and T1-weighted MR image (C) show 1.5-mm glass fragment in anterior chamber of eye. Arrowheads indicate glass fragments.

 


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Fig. 3D. Helical CT, sonography, and T1-weighted MR imaging of glass intraocular foreign bodies. Helical CT scan (D), sonogram (E), and T1-weighted MR image (F) show 1.5-mm glass fragment in posterior chamber of eye. Arrowheads indicate glass fragments.

 


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Fig. 3E. Helical CT, sonography, and T1-weighted MR imaging of glass intraocular foreign bodies. Helical CT scan (D), sonogram (E), and T1-weighted MR image (F) show 1.5-mm glass fragment in posterior chamber of eye. Arrowheads indicate glass fragments.

 


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Fig. 3F. Helical CT, sonography, and T1-weighted MR imaging of glass intraocular foreign bodies. Helical CT scan (D), sonogram (E), and T1-weighted MR image (F) show 1.5-mm glass fragment in posterior chamber of eye. Arrowheads indicate glass fragments.

 


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Fig. 4. Bar graph shows contingency analysis of outcome by imaging modality mosaic plot. Data were compiled using logistic regression, one factor at a time. Fat. Sat. = fatsaturated.

 

The Hounsfield unit attenuation and detection rates varied on helical CT according to the subtype of glass. The average radiologic attenuation of the different types of glass was as follows: green beer bottle, 550 H; brown beer bottle, 539 H; 40-W fluorescent bulb, 285 H; 100-W incandescent bulb, 260 H; windshield glass, 175 H; window plateglass, 140 H; and spectacle glass, 80 H. The greatest detection rates were noted for green beer bottle glass at 90.3%, followed by brown beer bottle glass at 86.1%, windshield glass at 70.8%, plateglass at 75.0%, 100-W incandescent bulb glass at 83.3%, 40-W fluorescent bulb glass at 76.4%, and spectacle glass (the least detectable) at 43.1% (n = 504, p < 0.0001) (Fig. 5A,5B,5C,5D,5E,5F).



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Fig. 5A. Helical CT of intraocular foreign bodies of various sizes and types of glass. CT scans show green beer bottle glass fragments of 1.5 (A), 1 (B), and 0.5 mm (C) in posterior chamber of the eye, compared with spectacle glass fragments of 1.5 (D), 1 (E), and 0.5 mm (F) in same chamber. Arrowheads indicate glass fragments.

 


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Fig. 5B. Helical CT of intraocular foreign bodies of various sizes and types of glass. CT scans show green beer bottle glass fragments of 1.5 (A), 1 (B), and 0.5 mm (C) in posterior chamber of the eye, compared with spectacle glass fragments of 1.5 (D), 1 (E), and 0.5 mm (F) in same chamber. Arrowheads indicate glass fragments.

 


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Fig. 5C. Helical CT of intraocular foreign bodies of various sizes and types of glass. CT scans show green beer bottle glass fragments of 1.5 (A), 1 (B), and 0.5 mm (C) in posterior chamber of the eye, compared with spectacle glass fragments of 1.5 (D), 1 (E), and 0.5 mm (F) in same chamber. Arrowheads indicate glass fragments.

 


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Fig. 5D. Helical CT of intraocular foreign bodies of various sizes and types of glass. CT scans show green beer bottle glass fragments of 1.5 (A), 1 (B), and 0.5 mm (C) in posterior chamber of the eye, compared with spectacle glass fragments of 1.5 (D), 1 (E), and 0.5 mm (F) in same chamber. Arrowheads indicate glass fragments.

 


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Fig. 5E. Helical CT of intraocular foreign bodies of various sizes and types of glass. CT scans show green beer bottle glass fragments of 1.5 (A), 1 (B), and 0.5 mm (C) in posterior chamber of the eye, compared with spectacle glass fragments of 1.5 (D), 1 (E), and 0.5 mm (F) in same chamber. Arrowheads indicate glass fragments.

 


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Fig. 5F. Helical CT of intraocular foreign bodies of various sizes and types of glass. CT scans show green beer bottle glass fragments of 1.5 (A), 1 (B), and 0.5 mm (C) in posterior chamber of the eye, compared with spectacle glass fragments of 1.5 (D), 1 (E), and 0.5 mm (F) in same chamber. Arrowheads indicate glass fragments.

 

Helical CT detection rates depended on the location of the glass foreign body. The glass fragment was easiest to detect in the anterior chamber at 91.7%, followed by the posterior chamber at 68.5%, and the corneal surface (most difficult to detect) at 64.9% (n = 63, p < 0.0001). The size of the glass intraocular foreign body also significantly affected detection rates, with 96.2% detection at 1.5 mm, 81.3% at 1 mm, and only 48.3% at 0.5 mm (n = 63, p < 0.0001) (Fig. 6A,6B,6C). Interobserver variation in interpreting the axial and helical CT scans and MR images was not statistically significant (p = 0.86). The presence of blood in the anterior chamber (hyphema) had no effect on the detection rates of helical CT scanning and was not statistically significant (p > 0.99).



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Fig. 6A. Line graphs show contingency analysis of outcome based on size of glass fragment. Graphs indicate percentage of glass fragments detected using helical CT (A), MR imaging (B), and sonography (C).

 


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Fig. 6B. Line graphs show contingency analysis of outcome based on size of glass fragment. Graphs indicate percentage of glass fragments detected using helical CT (A), MR imaging (B), and sonography (C).

 


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Fig. 6C. Line graphs show contingency analysis of outcome based on size of glass fragment. Graphs indicate percentage of glass fragments detected using helical CT (A), MR imaging (B), and sonography (C).

 


Discussion
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
Treatment of patients with ocular trauma and suspected intraocular foreign bodies requires an accurate and reliable determination of the number and location of foreign bodies before surgery. Failure to recognize a retained intraocular foreign body may lead to a fulminant infectious or inflammatory endophthalmitis, with ultimate loss of sight or the eye itself [12,13,14]. If the ocular media are clear, an ophthalmologist may examine the globe; however, media opacities are seen in many cases of ocular trauma, and radiologic imaging is required [7].

CT has been used in the detection and localization of intraocular foreign bodies since 1977 [8]. Over time, conventional CT technology has evolved from axial to helical CT. Helical CT offers the advantage of continuous imaging in one plane with no time gap in image acquisition, reduced motion artifacts, a decreased radiation dose to the lens, and the ability to obtain multiplanar reconstructions without additional scanning [1, 2]. Of the imaging modalities currently available, helical CT is considered the most sensitive method overall for the detection of intraocular foreign bodies [1,2,3,4,5,6,7,8,9,10,11,12]. In certain cases, MR imaging may be considered superior to CT if the intraocular foreign body is composed of wood; however, MR imaging is contraindicated if any possibility exists that the intraocular foreign body is composed of metal [2, 9, 10]. Sonography may also be superior for certain types of intraocular foreign bodies such as wood fragments; however, sonography has multiple limitations, including the variations of a nonstandardized technique and the resolving capacity of the sonographic probe with small intraocular foreign bodies. In addition, even if sonography is performed by a highly skilled examiner, further damage to the eye may be caused if the probe comes into direct contact with a severely traumatized ruptured globe [2, 11, 12, 15].

Although previous CT studies examined the detection limits of metallic intraocular foreign bodies [5], only a few reports exist in the literature that evaluate the minimum detectability limits of glass intraocular foreign bodies, noting limits of 1.8-5 mm [2, 6]. To our knowledge, no studies evaluate the efficacy of the improved helical CT technology in detecting various types of glass. In our study, helical CT was superior to axial CT, MR imaging, and sonography for detecting intraocular glass. This finding has been noted by previous authors for multiple types of intraocular foreign bodies [1, 2, 4]. Although helical CT was superior to axial CT in the detection of the glass intraocular foreign bodies, the difference was not statistically significant in this study. Slightly improved detection rates on helical CT (not statistically different from axial CT) are also reported for metallic intraocular foreign bodies [5].

The first helical CT series in our study had an overall detection rate of 57.1% compared with 74.0% in our second series. The improved detection rate in the second series may reflect a difference in the preparation of the porcine eyes. The contour and morphology of the porcine eye may have remained more formed and intact when supported and surrounded by lipid material simulating in vivo conditions, as opposed to being placed on a tray. This finding may imply that glass intraocular foreign bodies are more difficult to detect in the absence of ocular integrity. Limitations of helical CT that should be considered include the need to monitor scanning times and tube currents to avoid overheating of the X-ray tube; however, if only the orbit is being imaged, this is usually not a significant problem [2].

A qualified ophthalmologist with specialty training in sonography performed the sonographic examinations in this study. The overall detection rate of glass intraocular foreign bodies in the posterior chamber was lower for sonography than for helical CT, with only 43% detected on sonography. However, sonography was better at detecting glass in the posterior chamber than in the anterior chamber, with an anterior detection rate of only 24%. Because of the small sample size for sonography (n = 42), no meaningful statistical inference could be made among the glass subtypes. Interestingly (although not evaluated in this study), the sonographer noted many morphologic changes occurring in the globe. These changes, which included small areas of retinal detachment, were not always apparent on CT. This advantage of sonography has also been previously reported in the imaging literature [11].

Three major factors affected the detection of intraocular glass on helical CT in this study: glass type, size, and location. The radiologic density of the glass subtype was statistically significant in the rate of helical CT detection. Green beer bottle glass had the highest radiologic density and was the easiest to detect, whereas spectacle glass was the least dense and most difficult to identify. As expected, this study showed the larger the size of glass, the easier it was to detect. A limitation of this study is that glass fragments smaller than 0.5 mm were not used because of the difficulty in physically identifying and handling fragments smaller than this size with microsurgical instruments. However, in the emergency department setting, the presence of one identifiable glass intraocular foreign body should raise the suspicion that multiple fragments may be present and the possibility of fragments smaller than 0.5 mm.

Location of the glass also affected detection rates. Using helical CT, detection was easiest for glass intraocular foreign bodies located in the anterior chamber, followed by the posterior chamber, and, most difficult, the corneal surface. Previous reports have also noted the difficulty of preoperative CT localization of foreign bodies with respect to intra- or extraocular positions [5, 12]. Also in our experiment, the presence of blood in the anterior chamber of the eye (hyphema) had no statistical effect on the detection rates for observers interpreting helical CT scans. In comparison, the sonographer was able to identify a greater overall percentage of glass intraocular foreign bodies in the posterior chamber than in the anterior chamber. This finding may be a result of the fact that, if any flattening of the anterior chamber occurs, scanning in this region becomes technically difficult.

In conclusion, helical CT was the most sensitive imaging technique for the detection of glass intraocular foreign bodies when compared with axial CT, MR imaging, and sonography. Green beer bottle glass was easiest to detect, and spectacle glass was the most difficult. On helical CT, glass fragments were easier to detect in the anterior chamber, and most difficult to detect on the corneal surface. Sonography, in comparison with CT, localized glass better in the posterior chamber than in the anterior chamber. On helical CT, 1.5-mm glass fragments were detected at a rate of 96.2%, and 0.5-mm fragments were detected at a rate of 48.0%. Therefore, the glass fragment subtype, location, and size affect detection on imaging and are important considerations in the evaluation of intraocular glass foreign bodies presenting in the emergency department setting.


References
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
 

  1. Latkis A, Prokesch R, Scholda C, et al. Orbital computed tomography in the diagnosis and management of eye trauma. Ophthalmology 1999;106:2330 -2335[Medline]
  2. Latkis A, Steiner E, Scholda C, et al. Evaluation of intraocular foreign bodies by spiral computed tomography and multiplanar reconstruction. Ophthalmology 1998;105:307 -312[Medline]
  3. Gaster RN, Duda EE. Localization of intraocular foreign bodies by computed tomography. Ophthalmic Surg 1980;11:25 -29[Medline]
  4. Kollarits CR, Chiro DG, Christiansen J, et al. Detection of orbital and intraocular foreign bodies by computed tomography. Ophthalmic Surg 1977;8:45 -53
  5. Chacko JG, Figueroa RE, Johnson MH, et al. Detection and localization of steel intraocular foreign bodies using computed tomography. Ophthalmology 1997;104:319 -323[Medline]
  6. Tate E, Cupples H. Detection of orbital foreign bodies with computed tomography: current limits. AJNR 1981;2:363 -365
  7. Lindahl S. Computed tomography of intraorbital foreign bodies. Acta Radiol 1987;28:235 -240[Medline]
  8. Topilow HW, Ackerman AL, Zimmerman RD. Limitations of computed tomography in the localization of intraocular foreign bodies. Ophthalmology 1984;91:1086 -1091[Medline]
  9. McGukin JF, Akhtar N, Ho VT, et al. CT and MR evaluation of a wooden foreign body in an in vitro model of the orbit. AJNR 1996;17:129 -133[Abstract]
  10. Lagouras PA, Langer BG, Peyman GA, et al. Magnetic resonance imaging and intraocular foreign bodies. Arch Ophthalmol 1987;105:551 -553[Abstract/Free Full Text]
  11. McNicholas MM, Brophy DP, Power WJ, et al. Ocular trauma: evaluation with US. Radiology 1995;195:423 -427[Abstract/Free Full Text]
  12. Deramo VA, Shah GK, Baumal CR, et al. Ultrasound biomicroscopy as a tool for detecting and localizing occult foreign bodies after ocular trauma. Ophthalmology 1999;106:301 -305[Medline]
  13. Jonas JB, Knorr HL, Budde WM. Prognostic factors in ocular injuries caused by intraocular or retrobulbar foreign bodies. Ophthalmology 2000;107:823 -828[Medline]
  14. Thompson JT, Parver LM, Enger CL, et al. Infectious endophthalmitis after penetrating injuries with retained intraocular foreign bodies: National Eye Trauma System. Ophthalmology 1993;100:1468 -1474[Medline]
  15. Barash D, Goldenberg-Cohen N, Tzadok D, et al. Ultrasound biomicroscopic detection of anterior ocular segment foreign body after trauma. Am J Ophthalmol 1998;126:197 -202[Medline]

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