Orthokeratology (OK) is the reduction, modification or elimination of myopia through application of contact lenses. With the development of high Dk/t lens materials, overnight therapy has become the modality of choice for OK. Overnight OK lens wear has been previously investigated in terms of its efficacy to reduce myopia. However, the underlying effects of overnight OK lens wear on the human cornea have received less attention. As well as the clinical efficacy of overnight OK, this study investigated the effects of overnight OK on topographical corneal thickness and the overnight corneal edema response, and corneal tissue changes with overnight OK. Eighteen subjects participated as the OK lens-wearing group, wearing BE lenses (UltraVision, Brisbane, Queensland) in both eyes. A further ten subjects participated as control subjects, wearing conventional rigid lenses (J-Contour, UltraVision) in the right eye (RE) only. The left eye (LE) acted as a non-lens-wearing control. Both groups wore lenses overnight only, with no lens wear during the day. Measurements were conducted at baseline then on day 1, 4, 10, 30, 60, and 90 for the OK lens-wearing eyes; and up to day 30 for the control group, in the morning (after overnight lens wear) and in the evening (after 8-10 hours of lens removal). Variables measured included best vision sphere (BVS), unaided logMAR visual acuity (VA), refractive astigmatism, apical corneal power (ACP), simulated K readings (Medmont E300 corneal topographer), topographical corneal thickness (Holden-Payor optical pachometer), and keratocyte and endothelial cell densities (ConfoScan2 confocal microscope). Approximately 75% of myopia was corrected after the first night of OK lens wear and the changes in refractive error stabilised by day 10. By day 90, myopia reduction averaged 2.54 ?? 0.63 D. This was associated with significant improvement in unaided VA of about 82% after the first night of lens wear. There was no change in refractive astigmatism over the 3-month period. There was significant reduction in ACP in the OK lens-wearing eyes after the first night of lens wear, which accounted for more than 70% of the total ACP change over the 3-month period (RE: -2.16 ?? 0.53 D; LE: -2.11 ?? 0.86 D). There was significant central epithelial thinning (about 30%) and significant thickening (about 3%) in the mid-peripheral stroma in the OK lens-wearing eyes. Significant central epithelial thinning was found after the first night of lens wear while thickening in the mid-peripheral stroma reached statistical significance by day 4. Further analysis suggests that topographical corneal thickness changes account for the refractive error changes with overnight OK lens wear, rather than corneal bending. The central overnight stromal edema response was significantly reduced in the OK lens-wearing eyes (1.2 ?? 0.5%) to a level lower than in the conventional RGP (6.2 ?? 1.2%) and non-lens-wearing eyes (2.5 ?? 0.9%) in the control group. Mid-peripheral and peripheral stromal edema responses showed similar levels to those predicted based on lens Dk/t. A single overnight wear of BE and Paragon Corneal Refractive Therapy (CRT) lenses showed that the edema response to BE lens wear is significantly less than in the CRT lens-wearing eyes (BE: 2.5 ?? 0.7%; CRT 3.5 ?? 1.3%) immediately on eye opening. No significant changes were found in either central stromal keratocyte or endothelial cell densities in either OK or control groups over the study period. In conclusion, overnight OK lens wear induces significant reductions in myopia after the first night of lens wear associated with improvement in unaided VA. Overnight OK lens wear causes significant thinning in the central epithelium and significant mid-peripheral stromal thickening which results in flattening of the central cornea and steepening in the mid-periphery. Although there were no significant changes in central stromal keratocyte and endothelial cell densities, thinning of the central epithelial layer raises concerns regarding the safety of the procedure, especially with the alarming number of corneal infections reported recently in the literature.

Orthokeratology (OK) is the reduction, modification or elimination of myopia through application of contact lenses. With the development of high Dk/t lens materials, overnight therapy has become the modality of choice for OK. Overnight OK lens wear has been previously investigated in terms of its efficacy to reduce myopia. However, the underlying effects of overnight OK lens wear on the human cornea have received less attention. As well as the clinical efficacy of overnight OK, this study investigated the effects of overnight OK on topographical corneal thickness and the overnight corneal edema response, and corneal tissue changes with overnight OK. Eighteen subjects participated as the OK lens-wearing group, wearing BE lenses (UltraVision, Brisbane, Queensland) in both eyes. A further ten subjects participated as control subjects, wearing conventional rigid lenses (J-Contour, UltraVision) in the right eye (RE) only. The left eye (LE) acted as a non-lens-wearing control. Both groups wore lenses overnight only, with no lens wear during the day. Measurements were conducted at baseline then on day 1, 4, 10, 30, 60, and 90 for the OK lens-wearing eyes; and up to day 30 for the control group, in the morning (after overnight lens wear) and in the evening (after 8-10 hours of lens removal). Variables measured included best vision sphere (BVS), unaided logMAR visual acuity (VA), refractive astigmatism, apical corneal power (ACP), simulated K readings (Medmont E300 corneal topographer), topographical corneal thickness (Holden-Payor optical pachometer), and keratocyte and endothelial cell densities (ConfoScan2 confocal microscope). Approximately 75% of myopia was corrected after the first night of OK lens wear and the changes in refractive error stabilised by day 10. By day 90, myopia reduction averaged 2.54 ?? 0.63 D. This was associated with significant improvement in unaided VA of about 82% after the first night of lens wear. There was no change in refractive astigmatism over the 3-month period. There was significant reduction in ACP in the OK lens-wearing eyes after the first night of lens wear, which accounted for more than 70% of the total ACP change over the 3-month period (RE: -2.16 ?? 0.53 D; LE: -2.11 ?? 0.86 D). There was significant central epithelial thinning (about 30%) and significant thickening (about 3%) in the mid-peripheral stroma in the OK lens-wearing eyes. Significant central epithelial thinning was found after the first night of lens wear while thickening in the mid-peripheral stroma reached statistical significance by day 4. Further analysis suggests that topographical corneal thickness changes account for the refractive error changes with overnight OK lens wear, rather than corneal bending. The central overnight stromal edema response was significantly reduced in the OK lens-wearing eyes (1.2 ?? 0.5%) to a level lower than in the conventional RGP (6.2 ?? 1.2%) and non-lens-wearing eyes (2.5 ?? 0.9%) in the control group. Mid-peripheral and peripheral stromal edema responses showed similar levels to those predicted based on lens Dk/t. A single overnight wear of BE and Paragon Corneal Refractive Therapy (CRT) lenses showed that the edema response to BE lens wear is significantly less than in the CRT lens-wearing eyes (BE: 2.5 ?? 0.7%; CRT 3.5 ?? 1.3%) immediately on eye opening. No significant changes were found in either central stromal keratocyte or endothelial cell densities in either OK or control groups over the study period. In conclusion, overnight OK lens wear induces significant reductions in myopia after the first night of lens wear associated with improvement in unaided VA. Overnight OK lens wear causes significant thinning in the central epithelium and significant mid-peripheral stromal thickening which results in flattening of the central cornea and steepening in the mid-periphery. Although there were no significant changes in central stromal keratocyte and endothelial cell densities, thinning of the central epithelial layer raises concerns regarding the safety of the procedure, especially with the alarming number of corneal infections reported recently in the literature.

Orthokeratology (OK) is the reduction, modification or elimination of myopia through application of contact lenses. With the development of high Dk/t lens materials, overnight therapy has become the modality of choice for OK. Overnight OK lens wear has been previously investigated in terms of its efficacy to reduce myopia. However, the underlying effects of overnight OK lens wear on the human cornea have received less attention. As well as the clinical efficacy of overnight OK, this study investigated the effects of overnight OK on topographical corneal thickness and the overnight corneal edema response, and corneal tissue changes with overnight OK. Eighteen subjects participated as the OK lens-wearing group, wearing BE lenses (UltraVision, Brisbane, Queensland) in both eyes. A further ten subjects participated as control subjects, wearing conventional rigid lenses (J-Contour, UltraVision) in the right eye (RE) only. The left eye (LE) acted as a non-lens-wearing control. Both groups wore lenses overnight only, with no lens wear during the day. Measurements were conducted at baseline then on day 1, 4, 10, 30, 60, and 90 for the OK lens-wearing eyes; and up to day 30 for the control group, in the morning (after overnight lens wear) and in the evening (after 8-10 hours of lens removal). Variables measured included best vision sphere (BVS), unaided logMAR visual acuity (VA), refractive astigmatism, apical corneal power (ACP), simulated K readings (Medmont E300 corneal topographer), topographical corneal thickness (Holden-Payor optical pachometer), and keratocyte and endothelial cell densities (ConfoScan2 confocal microscope). Approximately 75% of myopia was corrected after the first night of OK lens wear and the changes in refractive error stabilised by day 10. By day 90, myopia reduction averaged 2.54 ?? 0.63 D. This was associated with significant improvement in unaided VA of about 82% after the first night of lens wear. There was no change in refractive astigmatism over the 3-month period. There was significant reduction in ACP in the OK lens-wearing eyes after the first night of lens wear, which accounted for more than 70% of the total ACP change over the 3-month period (RE: -2.16 ?? 0.53 D; LE: -2.11 ?? 0.86 D). There was significant central epithelial thinning (about 30%) and significant thickening (about 3%) in the mid-peripheral stroma in the OK lens-wearing eyes. Significant central epithelial thinning was found after the first night of lens wear while thickening in the mid-peripheral stroma reached statistical significance by day 4. Further analysis suggests that topographical corneal thickness changes account for the refractive error changes with overnight OK lens wear, rather than corneal bending. The central overnight stromal edema response was significantly reduced in the OK lens-wearing eyes (1.2 ?? 0.5%) to a level lower than in the conventional RGP (6.2 ?? 1.2%) and non-lens-wearing eyes (2.5 ?? 0.9%) in the control group. Mid-peripheral and peripheral stromal edema responses showed similar levels to those predicted based on lens Dk/t. A single overnight wear of BE and Paragon Corneal Refractive Therapy (CRT) lenses showed that the edema response to BE lens wear is significantly less than in the CRT lens-wearing eyes (BE: 2.5 ?? 0.7%; CRT 3.5 ?? 1.3%) immediately on eye opening. No significant changes were found in either central stromal keratocyte or endothelial cell densities in either OK or control groups over the study period. In conclusion, overnight OK lens wear induces significant reductions in myopia after the first night of lens wear associated with improvement in unaided VA. Overnight OK lens wear causes significant thinning in the central epithelium and significant mid-peripheral stromal thickening which results in flattening of the central cornea and steepening in the mid-periphery. Although there were no significant changes in central stromal keratocyte and endothelial cell densities, thinning of the central epithelial layer raises concerns regarding the safety of the procedure, especially with the alarming number of corneal infections reported recently in the literature.

Orthokeratology (OK) is the reduction, modification or elimination of myopia through application of contact lenses. With the development of high Dk/t lens materials, overnight therapy has become the modality of choice for OK. Overnight OK lens wear has been previously investigated in terms of its efficacy to reduce myopia. However, the underlying effects of overnight OK lens wear on the human cornea have received less attention. As well as the clinical efficacy of overnight OK, this study investigated the effects of overnight OK on topographical corneal thickness and the overnight corneal edema response, and corneal tissue changes with overnight OK. Eighteen subjects participated as the OK lens-wearing group, wearing BE lenses (UltraVision, Brisbane, Queensland) in both eyes. A further ten subjects participated as control subjects, wearing conventional rigid lenses (J-Contour, UltraVision) in the right eye (RE) only. The left eye (LE) acted as a non-lens-wearing control. Both groups wore lenses overnight only, with no lens wear during the day. Measurements were conducted at baseline then on day 1, 4, 10, 30, 60, and 90 for the OK lens-wearing eyes; and up to day 30 for the control group, in the morning (after overnight lens wear) and in the evening (after 8-10 hours of lens removal). Variables measured included best vision sphere (BVS), unaided logMAR visual acuity (VA), refractive astigmatism, apical corneal power (ACP), simulated K readings (Medmont E300 corneal topographer), topographical corneal thickness (Holden-Payor optical pachometer), and keratocyte and endothelial cell densities (ConfoScan2 confocal microscope). Approximately 75% of myopia was corrected after the first night of OK lens wear and the changes in refractive error stabilised by day 10. By day 90, myopia reduction averaged 2.54 ?? 0.63 D. This was associated with significant improvement in unaided VA of about 82% after the first night of lens wear. There was no change in refractive astigmatism over the 3-month period. There was significant reduction in ACP in the OK lens-wearing eyes after the first night of lens wear, which accounted for more than 70% of the total ACP change over the 3-month period (RE: -2.16 ?? 0.53 D; LE: -2.11 ?? 0.86 D). There was significant central epithelial thinning (about 30%) and significant thickening (about 3%) in the mid-peripheral stroma in the OK lens-wearing eyes. Significant central epithelial thinning was found after the first night of lens wear while thickening in the mid-peripheral stroma reached statistical significance by day 4. Further analysis suggests that topographical corneal thickness changes account for the refractive error changes with overnight OK lens wear, rather than corneal bending. The central overnight stromal edema response was significantly reduced in the OK lens-wearing eyes (1.2 ?? 0.5%) to a level lower than in the conventional RGP (6.2 ?? 1.2%) and non-lens-wearing eyes (2.5 ?? 0.9%) in the control group. Mid-peripheral and peripheral stromal edema responses showed similar levels to those predicted based on lens Dk/t. A single overnight wear of BE and Paragon Corneal Refractive Therapy (CRT) lenses showed that the edema response to BE lens wear is significantly less than in the CRT lens-wearing eyes (BE: 2.5 ?? 0.7%; CRT 3.5 ?? 1.3%) immediately on eye opening. No significant changes were found in either central stromal keratocyte or endothelial cell densities in either OK or control groups over the study period. In conclusion, overnight OK lens wear induces significant reductions in myopia after the first night of lens wear associated with improvement in unaided VA. Overnight OK lens wear causes significant thinning in the central epithelium and significant mid-peripheral stromal thickening which results in flattening of the central cornea and steepening in the mid-periphery. Although there were no significant changes in central stromal keratocyte and endothelial cell densities, thinning of the central epithelial layer raises concerns regarding the safety of the procedure, especially with the alarming number of corneal infections reported recently in the literature.

<strong>Purpose:</strong> Although orthokeratology (non-surgical corneal reshaping, Corneal Refractive Therapy, CRT®) has been used for almost a half century, contemporary CRT's outcomes and mechanisms still require investigation. A series of studies was designed to examine different aspects of non-surgical corneal reshaping for myopic and hyperopic corrections, including the efficacy and stability of this procedure, the effect of the lens material characteristics (Dk/t), and the corneal or superficial structural change (e. g. corneal/epithelial thickness) in corneal reshaping. <br /> <strong>Methods:</strong> In the CRT® for myopia (CRT1) study, 20 myopes wore CRT® lenses on one eye and control lenses on the contralateral eye (eye randomized) for one night while sleeping. Corneal topography and refractive error were measured the night prior to lens insertion, immediately after lens removal on the following morning and at 20 and 60 minutes and 3, 6 and 12 hours later. In the CRT® for hyperopia (CRTH) study, 20 ametropes wore CRT®H lenses on one eye for one night while sleeping, the contralateral eye (no lens wear) served as control (eye randomized). Corneal topography, aberrations and refractive error were measured the night prior to lens insertion, immediately after lens removal on the following morning and at 1 and 3, 6, 12 and 28 hours later. In the relatively long term (4 weeks) CRT® for myopia (CRT2) study, 23 myopes wore CRT® lenses overnight and removed their lenses on awakening. Visual Acuity (VA), subjective vision, refractive error, aberrations, and corneal topography were measured at baseline, immediately after lens removal on the first day and 14 hours later, and these measurements were repeated on days 4, 10, and 28. The treatment zone size was demarcated by the change in corneal curvature from negative to positive and vice versa, using tangential difference maps from the corneal topographer. In the study of effects of Dk/t on CRT® for myopia (CRTHDK), 20 myopic subjects were fit with Menicon Z (MZ) lenses (Dk/t=90. 6, Paragon CRT®) on one eye and an Equalens II (EII) CRT® lenses (Dk/t=47. 2) on the contralateral eye (eye randomized). Corneal topography, refractive error and aberrations were measured before lens insertion (baseline), and the following day after overnight lens wear, on lens removal and 1, 3, 6, 12 hours later. In the study of short term effects of CRT® for myopia and hyperopia (STOK), 20 ametropes wore CRT® and CRT®H lenses in a random order on one eye (randomly selected). The lenses were worn for 15, 30 and 60 minutes (randomly ordered, with each period taking place on a different day). Refractive error, aberrations, corneal topography, and corneal/epithelial thickness (using OCT) were measured before and after lens wear. The measurements were performed on the control eyes at 60 minutes only. <br /> <strong>Results:</strong> In the CRT1 study, after one night of CRT® for myopia, the central cornea flattened and the mid-periphery steepened, and myopia reduced. In the CRTH study, after one night of CRT® for hyperopia, the central cornea steepened and the para-central region flattened, myopia was induced or hyperopia was reduced, all aberrations except for the astigmatism increased and signed spherical aberration (SA) shifted from positive to negative. In the CRT2 study, after 4 weeks of CRT® lens wear, in general, the treatment zones stabilized by day 10, vision improved, myopia diminished, total aberration and defocus decreased and higher order aberrations (HOAs) including coma and SA increased. The visual, optical and subjective parameters became stable by day 10. In the CRTHDK study, after one night of CRT® (MZ vs. EII) lens wear, the central corneal curvature and aberration were similar with a slight exception: The mid-peripheral corneal steepening was greater in the EII (lower Dk/t) lens-wearing eyes compared to the MZ (higher Dk/t) eyes. In the STOK study, after brief CRT® and CRT®H lens wear, significant changes occurred from the 15 minutes time point: The corneal shape and optical performance changed in a predictable way; the central cornea swelled less than the mid-periphery after CRT® lens wear, whereas the central cornea swelled more than the para-central region after CRT®H lens wear; the central epithelium was thinner than the mid-periphery after CRT® lens wear and was thicker than the para-central region after CRT®H lens wear. <br /> <strong>Conclusion:</strong> After one night of lens wear, CRT® and CRTH® lenses were effective for myopia and hyperopia correction, respectively. In the 4 week CRT study, the treatment zone size changed during the first 10 days. Its size was associated with VA, refractive error, aberrations, and subjective vision. In the CRTHDK study, after one night of lens wear, changes in corneal shape were slightly different, with more mid-peripheral steepening in the lower Dk lens-wearing eyes compared to the higher Dk lens-wearing eyes. Changes in central corneal shape and optical performance were similar in both eyes. In the STOK study, CRT® lenses for myopia and hyperopia induced significant structural and optical changes in as little as 15 minutes. The cornea, particularly the epithelium, is remarkably moldable, with very rapid steepening and flattening possible in a small amount of time.

<strong>Purpose:</strong> Although orthokeratology (non-surgical corneal reshaping, Corneal Refractive Therapy, CRT®) has been used for almost a half century, contemporary CRT's outcomes and mechanisms still require investigation. A series of studies was designed to examine different aspects of non-surgical corneal reshaping for myopic and hyperopic corrections, including the efficacy and stability of this procedure, the effect of the lens material characteristics (Dk/t), and the corneal or superficial structural change (e. g. corneal/epithelial thickness) in corneal reshaping. <br /> <strong>Methods:</strong> In the CRT® for myopia (CRT1) study, 20 myopes wore CRT® lenses on one eye and control lenses on the contralateral eye (eye randomized) for one night while sleeping. Corneal topography and refractive error were measured the night prior to lens insertion, immediately after lens removal on the following morning and at 20 and 60 minutes and 3, 6 and 12 hours later. In the CRT® for hyperopia (CRTH) study, 20 ametropes wore CRT®H lenses on one eye for one night while sleeping, the contralateral eye (no lens wear) served as control (eye randomized). Corneal topography, aberrations and refractive error were measured the night prior to lens insertion, immediately after lens removal on the following morning and at 1 and 3, 6, 12 and 28 hours later. In the relatively long term (4 weeks) CRT® for myopia (CRT2) study, 23 myopes wore CRT® lenses overnight and removed their lenses on awakening. Visual Acuity (VA), subjective vision, refractive error, aberrations, and corneal topography were measured at baseline, immediately after lens removal on the first day and 14 hours later, and these measurements were repeated on days 4, 10, and 28. The treatment zone size was demarcated by the change in corneal curvature from negative to positive and vice versa, using tangential difference maps from the corneal topographer. In the study of effects of Dk/t on CRT® for myopia (CRTHDK), 20 myopic subjects were fit with Menicon Z (MZ) lenses (Dk/t=90. 6, Paragon CRT®) on one eye and an Equalens II (EII) CRT® lenses (Dk/t=47. 2) on the contralateral eye (eye randomized). Corneal topography, refractive error and aberrations were measured before lens insertion (baseline), and the following day after overnight lens wear, on lens removal and 1, 3, 6, 12 hours later. In the study of short term effects of CRT® for myopia and hyperopia (STOK), 20 ametropes wore CRT® and CRT®H lenses in a random order on one eye (randomly selected). The lenses were worn for 15, 30 and 60 minutes (randomly ordered, with each period taking place on a different day). Refractive error, aberrations, corneal topography, and corneal/epithelial thickness (using OCT) were measured before and after lens wear. The measurements were performed on the control eyes at 60 minutes only. <br /> <strong>Results:</strong> In the CRT1 study, after one night of CRT® for myopia, the central cornea flattened and the mid-periphery steepened, and myopia reduced. In the CRTH study, after one night of CRT® for hyperopia, the central cornea steepened and the para-central region flattened, myopia was induced or hyperopia was reduced, all aberrations except for the astigmatism increased and signed spherical aberration (SA) shifted from positive to negative. In the CRT2 study, after 4 weeks of CRT® lens wear, in general, the treatment zones stabilized by day 10, vision improved, myopia diminished, total aberration and defocus decreased and higher order aberrations (HOAs) including coma and SA increased. The visual, optical and subjective parameters became stable by day 10. In the CRTHDK study, after one night of CRT® (MZ vs. EII) lens wear, the central corneal curvature and aberration were similar with a slight exception: The mid-peripheral corneal steepening was greater in the EII (lower Dk/t) lens-wearing eyes compared to the MZ (higher Dk/t) eyes. In the STOK study, after brief CRT® and CRT®H lens wear, significant changes occurred from the 15 minutes time point: The corneal shape and optical performance changed in a predictable way; the central cornea swelled less than the mid-periphery after CRT® lens wear, whereas the central cornea swelled more than the para-central region after CRT®H lens wear; the central epithelium was thinner than the mid-periphery after CRT® lens wear and was thicker than the para-central region after CRT®H lens wear. <br /> <strong>Conclusion:</strong> After one night of lens wear, CRT® and CRTH® lenses were effective for myopia and hyperopia correction, respectively. In the 4 week CRT study, the treatment zone size changed during the first 10 days. Its size was associated with VA, refractive error, aberrations, and subjective vision. In the CRTHDK study, after one night of lens wear, changes in corneal shape were slightly different, with more mid-peripheral steepening in the lower Dk lens-wearing eyes compared to the higher Dk lens-wearing eyes. Changes in central corneal shape and optical performance were similar in both eyes. In the STOK study, CRT® lenses for myopia and hyperopia induced significant structural and optical changes in as little as 15 minutes. The cornea, particularly the epithelium, is remarkably moldable, with very rapid steepening and flattening possible in a small amount of time.

Cornea is a part of the optical system of the eye, the condition of which is directly related with the eyesight and its quality. Due to the increasing popularity of the correction of refraction defects with the help of excimer laser, central cornea thickness acquires higher prognostic significance for the determination of the success of the operation and probable post-surgical complications. The objective of the survey is to measure the central corneal thickness of adult residents in Lithuania and the relevant factors having impact on it. In total 1650 residents of Lithuania in the age from 18 to 89 years of age were tested. The survey was carried out in the urban and regional primary health care institutions of the 10 counties of Lithuania and at the Centre of Eye Diseases of the Vilnius University Hospital Santariškių klinikos. The average central corneal thickness of men and women in Lithuania was defined in the survey. It was observed that central corneal thickness is neither conditioned by the gender, height or weight of an individual, nor by the eye refraction or the number and the size of corneal endothelia cells. The thickest cornea was observed in persons under 40 years of age, whereas it becomes thinner each decade from 2 to 8 µm after forty. It was identified in the survey that the thicker the cornea is - the smaller is its curvature. On the basis of the survey a table of central corneal thickness was developed for doctors ophthalmologists to be used in their... [to full text] / Ragena – tai akies optinės sistemos dalis, nuo kurios būklės tiesiogiai priklauso regėjimas ir jo kokybė. Populiarėjant refrakcijos ydų korekcijai eksimeriniu lazeriu, ragenos centrinės dalies storis turi vis didesnę prognostinę reikšmę operacijos sėkmės bei pooperacinių komplikacijų galimybės nustatymui. Darbo tikslas – nustatyti Lietuvos suaugusių gyventojų ragenos centrinės dalies storį bei jį veikiančius veiksnius. Ištirta 1650 Lietuvos gyventojų nuo 18 iki 89 metų amžiaus.Tyrimas vykdytas 10 Lietuvos apskričių miestų ir rajonų pirminėse sveikatos priežiūros įstaigose, bei VUL Santariškių klinikos Akių ligų centre. Tyrimo metu nustatytas Lietuvoje gyvenančių vyrų ir moterų vidutinis ragenos centrinės dalies storis. Nustatyta, kad ragenos centrinės dalies storis nepriklauso nuo žmogaus lyties, ūgio, svorio, bei akių refrakcijos ir ragenos endotelio ląstelių skaičiaus ir dydžio. Storiausia ragena nustatoma iki 40 metų amžiaus, vyresniems nei 40 metų ji plonėja kas dešimtmetį nuo 2 iki 8 µm. Nustatyta, kad kuo storesnė ragena, tuo jos gaubtumas yra mažesnis. Tyrimo pagrindu sukurta skirtingo amžiaus žmonių ragenos centrinės dalies storio lentelė, kuria savo praktiniame darbe galės naudotis visi gydytojai oftalmologai.

Ragena – tai akies optinės sistemos dalis, nuo kurios būklės tiesiogiai priklauso regėjimas ir jo kokybė. Populiarėjant refrakcijos ydų korekcijai eksimeriniu lazeriu, ragenos centrinės dalies storis turi vis didesnę prognostinę reikšmę operacijos sėkmės bei pooperacinių komplikacijų galimybės nustatymui. Darbo tikslas – nustatyti Lietuvos suaugusių gyventojų ragenos centrinės dalies storį bei jį veikiančius veiksnius. Ištirta 1650 Lietuvos gyventojų nuo 18 iki 89 metų amžiaus.Tyrimas vykdytas 10 Lietuvos apskričių miestų ir rajonų pirminėse sveikatos priežiūros įstaigose, bei VUL Santariškių klinikos Akių ligų centre. Tyrimo metu nustatytas Lietuvoje gyvenančių vyrų ir moterų vidutinis ragenos centrinės dalies storis. Nustatyta, kad ragenos centrinės dalies storis nepriklauso nuo žmogaus lyties, ūgio, svorio, bei akių refrakcijos ir ragenos endotelio ląstelių skaičiaus ir dydžio. Storiausia ragena nustatoma iki 40 metų amžiaus, vyresniems nei 40 metų ji plonėja kas dešimtmetį nuo 2 iki 8 µm. Nustatyta, kad kuo storesnė ragena, tuo jos gaubtumas yra mažesnis. Tyrimo pagrindu sukurta skirtingo amžiaus žmonių ragenos centrinės dalies storio lentelė, kuria savo praktiniame darbe galės naudotis visi gydytojai oftalmologai. / Cornea is a part of the optical system of the eye, the condition of which is directly related with the eyesight and its quality. Due to the increasing popularity of the correction of refraction defects with the help of excimer laser, central cornea thickness acquires higher prognostic significance for the determination of the success of the operation and probable post-surgical complications. The objective of the survey is to measure the central corneal thickness of adult residents in Lithuania and the relevant factors having impact on it. In total 1650 residents of Lithuania in the age from 18 to 89 years of age were tested. The survey was carried out in the urban and regional primary health care institutions of the 10 counties of Lithuania and at the Centre of Eye Diseases of the Vilnius University Hospital Santariškių klinikos. The average central corneal thickness of men and women in Lithuania was defined in the survey. It was observed that central corneal thickness is neither conditioned by the gender, height or weight of an individual, nor by the eye refraction or the number and the size of corneal endothelia cells. The thickest cornea was observed in persons under 40 years of age, whereas it becomes thinner each decade from 2 to 8 µm after forty. It was identified in the survey that the thicker the cornea is - the smaller is its curvature. On the basis of the survey a table of central corneal thickness was developed for doctors ophthalmologists to be used in their... [to full text]

Syfte: Studiens syfte var att kontrollera repeterbarhet och jämförbarhet hos tre kliniska instrument som används för att mäta hornhinnans tjocklek i friska ögon. Instrumenten som användes har flera olika användningsområden men fokus i denna studie ligger specifikt på pakymetri: mätning av hornhinnetjocklek. Metod: Det var 64 personer som deltog i studien. Alla var över 18 år och befann sig på Linnéuniversitetet i Kalmar vid tidpunkterna för mättillfällena. De tre optiska pakymetri instrumenten som användes var Topcon TRK-2P, Bon Sirius samt Essilor Wavefront Analyzer Medica 700+. Tre mätningar utfördes vid varje instrument på deltagarnas båda ögon. All data sammanställdes i Google Kalkyl och analyserades vidare i Graphpad Prism (version 9). Resultat: Repeterbarheten testades med ICC vilket var över 0,98 på samtliga instrument, CR var mellan 5,28-8,80 μm och CV var mellan 6,29-6,74%. Jämförbarheten visade att det finns en signifikant skillnad mellan de tre instrumenten (One-way RM- ANOVA,  p&lt;0,0001). Slutsats: Samtliga instrument som användes inom studien visade på en utmärkt repeterbarhet vid mätning av friska ögon, däremot förekom signifikanta skillnader dem emellan. Detta innebär att man bör hålla sig till ett och samma instrument vid uppföljning av patienter. / Purpose: The purpose of this study was to examine the repeatability and comparability of three clinical instruments used to measure the corneal thickness in healthy eyes. The different instruments all have various fields of usage but the focus in this study is pachymetry: measurement of the corneal thickness. Method: In total, 64 people participated in this study. Everyone that participated were above the age of 18 and were located at Linneaus university in Kalmar, Sweden at the time the measurements took place. The three optical pachymetry instruments used were Topcon TRK-2P, Bon Sirius and Essilor Wavefront Analyzer Medica 700+. Three measurements were taken on each instrument on the participants’ both eyes. All collected data was collated in Google Sheets and analyzed in Graphpad Prism (version 9).  Results: The repeatability was tested with ICC that was above 0,98 on all the instruments. CR was between 5,28-8,80 μm and CV was between 6,29-6,74%. The comparability showed that there was a significant difference between the three instruments (One-way RM- ANOVA,  p&lt;0,0001). Conclusion: All three instruments that were used during this study showed an excellent repeatability when measuring healthy eyes. However, there were significant differences between the instruments themselves. This means that you should stick to the same instrument while following up patients.

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