Beatriz Machado Fontes1; Bruno Machado Fontes2; Elaine Castro3
DOI: 10.1590/S0004-27492011000300004
ABSTRACT
PURPOSE: To compare the achieved refractive outcomes of patients undergoing cataract surgery with intraocular lens (IOL) power calculation performed by conventional immersion ultrasound (US) or partial coherence interferometry (PCI). METHODS: Prospective, comparative case series. Patients undergoing cataract surgery were randomly divided in two groups with regard to the IOL power calculation method. Group 1 had calculations performed by PCI (IOL Master; Carl Zeiss Meditec), while US was used in Group 2 (Ultrascan; Alcon), using the Holladay 1 formula. Differences between target and achieved refractions were then compared. RESULTS: The study comprised 120 eyes from 79 patients. Biometry with PCI was used in 50 eyes of 33 patients, and US was used in 70 eyes of 46 patients. Mean age of patients in the PCI Group was 69.8 ± 13.1 years (range 11 - 85) and 70.0 ± 9.3 (45 - 86) in the US Group (P=0.7165). Mean axial length measured by PCI was 23.22 ± 1.00 mm (range 21.01 - 25.45) and that by US was 23.22 ± 1.06 mm (20.05 - 25.78) (P=0.9110). Mean absolute error in the PCI group was 0.15 ± 0.33 D (range -0.65 - 0.9) and that in the US group was 0.26 ± 0.48 D (-1.05 - 1.76). All eyes in the PCI group and 94.3% of those in the US group were within 1.00 D of the planned refraction. CONCLUSION: Although both PCI and US yielded good prediction in IOL power calculation, the PCI group tended to show better accuracy and improved refractive outcome.
Keywords: Diagnostic techniques, ophthalmological; Preoperative care; Cataract extraction; Lens implantation, intraocular; Refractive errors
RESUMO
OBJETIVO: Comparar os resultados refracionais obtidos em pacientes submetidos à cirurgia de catarata com cálculo da lente intraocular realizado por meio de biometria ultrassônica de imersão (US) ou por interferometria de coerência parcial (ICP). MÉTODOS: Série de casos comparativa, prospectiva. Os pacientes submetidos à cirurgia de catarata foram aleatoriamente divididos em dois grupos em relação ao método de cálculo do poder da lente intraocular (LIO) a ser implantada. O grupo 1 teve seu cálculo efetuado por ICP (IOL Master; Carl Zeiss Meditec), enquanto o grupo 2 usou-se US (Ultrascan; Alcon). A fórmula Holladay 1 foi utilizada nos dois grupos. As diferenças entre os resultados refracionais planejados e obtidos foram então comparadas. RESULTADOS: O estudo contou com 120 olhos de 79 pacientes. Biometria por meio de ICP foi utilizada em 50 olhos de 33 pacientes e com US em 70 olhos de 46 pacientes. A idade média dos pacientes no grupo 1 foi de 69,8 ± 13,1 anos e de 70,0 ± 9,3 anos no grupo 2 (P=0,7165). O comprimento axial médio aferido pela ICP foi de 23,22 ± 1,00 mm (variando de 21,01 a 25,45 mm) e no grupo US foi de 23,22 ± 1,06 mm (variando de 20,05 a 25,78 mm) (P=0,9110). O erro absoluto médio (diferença entre o planejado e o obtido) no grupo 1 foi de 0,15 ± 0,33 D (variando de -0,65 a 0,9 D) e no grupo 2 de 0,26 ± 0,48 D (variando de -1,05 a 1,76 D). Todos os olhos do grupo 1 e 94,3% dos olhos do grupo 2 obtiveram resultados refracionais de até 1,00 D de diferença do resultado refracional inicialmente planejado. CONCLUSÃO: Os dois métodos estudados mostraram boa previsibilidade refracional quando utilizados para o cálculo do poder da LIO. No entanto, o grupo que utilizou ICP mostrou uma tendência a melhor acurácia, com menos dispersão de resultados.
Descritores: Técnicas de diagnóstico oftalmológico; Cuidados pré-operatórios; Extração de catarata; Implante de lente intraocular; Erros de refração
ORIGINAL ARTICLE ARTIGO ORIGINAL
Intraocular lens power calculation by measuring axial length with partial optical coherence and ultrasonic biometry
Cálculo da dioptria da lente intraocular medindo o comprimento axial através de interferometria de coerência parcial ou biometria ultrassônica
Beatriz Machado FontesI; Bruno Machado FontesII, III; Elaine CastroIII
IPhysician, Centro de Microcirurgia e Diagnóstico, Rio de Janeiro (RJ), Brazil
IIPhysician, Ophthalmology Department, Federal University of São Paulo - UNIFESP - São Paulo (SP), Brazil
IIIPhysician, Oftalmoclínica Méier, Rio de Janeiro (RJ), Brazil
ABSTRACT
PURPOSE: To compare the achieved refractive outcomes of patients undergoing cataract surgery with intraocular lens (IOL) power calculation performed by conventional immersion ultrasound (US) or partial coherence interferometry (PCI).
METHODS: Prospective, comparative case series. Patients undergoing cataract surgery were randomly divided in two groups with regard to the IOL power calculation method. Group 1 had calculations performed by PCI (IOL Master; Carl Zeiss Meditec), while US was used in Group 2 (Ultrascan; Alcon), using the Holladay 1 formula. Differences between target and achieved refractions were then compared.
RESULTS: The study comprised 120 eyes from 79 patients. Biometry with PCI was used in 50 eyes of 33 patients, and US was used in 70 eyes of 46 patients. Mean age of patients in the PCI Group was 69.8 ± 13.1 years (range 11 - 85) and 70.0 ± 9.3 (45 - 86) in the US Group (P=0.7165). Mean axial length measured by PCI was 23.22 ± 1.00 mm (range 21.01 - 25.45) and that by US was 23.22 ± 1.06 mm (20.05 - 25.78) (P=0.9110). Mean absolute error in the PCI group was 0.15 ± 0.33 D (range -0.65 - 0.9) and that in the US group was 0.26 ± 0.48 D (-1.05 - 1.76). All eyes in the PCI group and 94.3% of those in the US group were within 1.00 D of the planned refraction.
CONCLUSION: Although both PCI and US yielded good prediction in IOL power calculation, the PCI group tended to show better accuracy and improved refractive outcome.
Keywords: Diagnostic techniques, ophthalmological; Preoperative care; Cataract extraction; Lens implantation, intraocular; Refractive errors
RESUMO
OBJETIVO: Comparar os resultados refracionais obtidos em pacientes submetidos à cirurgia de catarata com cálculo da lente intraocular realizado por meio de biometria ultrassônica de imersão (US) ou por interferometria de coerência parcial (ICP).
MÉTODOS: Série de casos comparativa, prospectiva. Os pacientes submetidos à cirurgia de catarata foram aleatoriamente divididos em dois grupos em relação ao método de cálculo do poder da lente intraocular (LIO) a ser implantada. O grupo 1 teve seu cálculo efetuado por ICP (IOL Master; Carl Zeiss Meditec), enquanto o grupo 2 usou-se US (Ultrascan; Alcon). A fórmula Holladay 1 foi utilizada nos dois grupos. As diferenças entre os resultados refracionais planejados e obtidos foram então comparadas.
RESULTADOS: O estudo contou com 120 olhos de 79 pacientes. Biometria por meio de ICP foi utilizada em 50 olhos de 33 pacientes e com US em 70 olhos de 46 pacientes. A idade média dos pacientes no grupo 1 foi de 69,8 ± 13,1 anos e de 70,0 ± 9,3 anos no grupo 2 (P=0,7165). O comprimento axial médio aferido pela ICP foi de 23,22 ± 1,00 mm (variando de 21,01 a 25,45 mm) e no grupo US foi de 23,22 ± 1,06 mm (variando de 20,05 a 25,78 mm) (P=0,9110). O erro absoluto médio (diferença entre o planejado e o obtido) no grupo 1 foi de 0,15 ± 0,33 D (variando de -0,65 a 0,9 D) e no grupo 2 de 0,26 ± 0,48 D (variando de -1,05 a 1,76 D). Todos os olhos do grupo 1 e 94,3% dos olhos do grupo 2 obtiveram resultados refracionais de até 1,00 D de diferença do resultado refracional inicialmente planejado.
CONCLUSÃO: Os dois métodos estudados mostraram boa previsibilidade refracional quando utilizados para o cálculo do poder da LIO. No entanto, o grupo que utilizou ICP mostrou uma tendência a melhor acurácia, com menos dispersão de resultados.
Descritores: Técnicas de diagnóstico oftalmológico; Cuidados pré-operatórios; Extração de catarata; Implante de lente intraocular; Erros de refração
INTRODUCTION
Innovative techniques and advanced technology have greatly improved cataract surgery over the past few years. Modern techniques utilize small-incision phacoemulsification and foldable lens implantation(1). Premium accommodative, toric, aspheric, and multifocal intraocular lenses (IOLs) are now widely available. There is an increased quest for accuracy, and patients are now seeking better results.
As a result, accurate biometry and power precision of IOLs have gained greater importance. Several factors influence the refractive outcome. Keratometry measurements, axial length, IOL power formulas, and anterior chamber depth are all related to better accuracy and refractive success(2,3). Axial length (AL) measurements are essential for determining the accuracy of the IOL calculation and are probably the element with the largest potential for error. Inaccurate measurements can limit the predictability of refractive outcomes. Methods are still evolving, but ultrasound (US) biometry and partial coherence interferometry (PCI) are the most commonly used methods for determining the IOL power.
Traditionally, ALs have been measured using ultrasound biometry, a time consuming exam that requires skilled biometrists. Contact A-scan ultrasonography is a well established method for measuring AL but immersion A-scan technique is potentially more accurate, since it does not require indentation of the cornea. More recently, PCI has emerged as a new modality for biometry with the advantages of being fast, noninvasive and less dependent on technician expertise.
In this study, we performed IOL power calculations by conventional immersion US biometry or PCI and compared the refractive outcomes in patients who presented for cataract surgery.
METHODS
We employed a prospective, randomized, comparative case series study design. Consecutive patients were randomly separated into two groups based on the method used to calculate the IOL power, creating comparable groups. In Group 1, 50 eyes from 33 patients underwent biometry with PCI (IOL Master Carl Zeiss Meditec, Dublin, CA, USA) to calculate the IOL power. In Group 2, 70 eyes from 46 patients underwent immersion US (Ultrascan, Alcon, Fort Worth, TX, USA) for IOL power calculation. An experienced ophthalmologist performed the immersion US and PCI measurements in all cases. The Holladay 1 formula was also used to calculate the IOL power in all patients.
The same surgeon performed small-incision phacoemulsification with the standard phaco-chop technique and in-the-bag implantation using an Acrysoft IQ model (Alcon) IOL in all cases. The final manifest refraction was assessed by the same examiner at least 4 weeks after the procedure.
Since certain calculation formulas for intraocular lens may be more precise depending on the axial length of the eye and the Holladay 1 formula was used in the study, eyes with axial length <20 mm or >25.8 mm were excluded. Other exclusion criteria were corneal astigmatism >2.5 diopters (D), complications during surgery, and patients with poor visual prognosis (eg, macular scar, amblyopia).
The desired final refraction was determined prior to surgery, and the final refractive outcome was compared between the two groups. The differences between the programmed final refraction and the achieved final refractive outcome for the two methodologies were compared. Spherical equivalent in diopters was used for programmed final refraction, final refractive outcome and mean absolute error.
The Wilcoxon rank-sum test was used to compare numerical variables between the two groups, and the chi-square test was performed to compare frequencies of categorical variables within the same group. The level of significance was set at 0.05, and the S-Plus 8.0 program was used for the statistical analysis.
RESULTS
We enrolled 120 eyes from 79 patients undergoing cataract surgery. The mean age of patients was 69.8 ± 13.1 years (range, 11 - 85 years) in the PCI Group and 70.0 ± 9.3 (range, 45 - 86 years) in the US Group (P=0.7165). The mean AL measured by the PCI was 23.22 ± 1.00 mm (range, 21.01 - 25.45 mm) and that measured by US was 23.22 ± 1.06 mm (range, 20.05 - 25.78 mm) (P=0.9110) (Table 1).
Table 2 shows the mean preoperative planned refractive outcome, the mean final achieved refraction, and the difference between the two values (mean absolute error, MAE). The MAE was 0.15 ± 0.33 D (upper and lower of -0.65 and 0.9, respectively) in the PCI group and 0.26 ± 0.48 D (upper and lower of -1.05 and 1.76, respectively) in the US group (P=0.0836). Although there was no statistical difference in the MAE between the two groups, figure 1 suggests that the variability of these differences was higher for the US group than for the PCI group.
In the PCI group, 68% of the eyes achieved a postoperative refraction that differed by <0.25 D from the predicted value, as compared with 45.7% of the eyes in the US group. All eyes in the PCI group were within 1.00 D of the planned refraction, and 94.3% of the eyes in the US group met this criterion. The accuracies of the predictions are given in table 3.
The values for the final and programmed refractions showed a weak (r=0.3), but significant (P=0.0127), correlation in the US group (Figure 2 A). This weak correlation is seen in the Bland-Altman graphic (Figure 2 B). The mean refraction is represented on the horizontal axis, and the difference between the final and programmed refractions is indicated on the vertical axis. The chart demonstrates that the final values were generally higher, more hyperopic, than the programmed values (P<0.0001; Figure 2 C).
In the PCI group, the final and programmed refractions were strongly (r=0.73) and significantly correlated (P<0.0001). Figure 3 A indicates a better match between the final and programmed refractions in the PCI group than that shown in the corresponding US figure. The differences had less variation in the PCI group (Figure 3 B), and the programmed and final refractions were significantly different (P=0.0041; Figure 4).
DISCUSSION
Younger patients with less visual disability are now undergoing surgery with higher expectations and demands for an optimal final result. As a consequence, cataract surgery is no longer just for visual rehabilitation but has also become a form of refractive surgery in which the final refractive result can define visual outcome. With the emergence of the so-called "premium IOLs," it became clear that an IOL power calculation was essential for determining the success of cataract surgery. Small biometric errors can limit IOL performance and cause patient dissatisfaction and frustration. An incorrect lens power calculation is the main cause for dissatisfaction and lens exchange in modern cataract surgery(1-3). This led to several studies with the objective of improving the accuracy and precision of the IOL power calculation(4-8).
Classical ultrasound biometry is still used for IOL assortment, but the emergence of new technology using optical biometry has caused a great change in IOL selection. The advantages of the new technology include high precision, noncontact and noninvasive measurements, speed, and superior patient comfort. Among the disadvantages are the high cost of the equipment and the inability to measure dense cataracts, some serious corneal pathologies, lid abnormalities, and eyes with poor fixation.
Recent studies have compared the two methods(8-21). In our study, we found high precision and reproducibility with both methods. The high accuracy level of both technologies was also demonstrated by Packer et al.(14), Kiss et al.(11), and Haigis et al.(15).
The design of our study offered a limitation since axial length measurements were obtained with only one of the two methods used. We suggest and encourage other researchers to do further studies measuring axial length preoperatively with both methods in our population.
In conclusion, we found that PCI is directly comparable to US with regard to the accuracy and reproducibility of the IOL power calculation. There was a trend toward a subtle improvement in the prediction for postoperative refraction with PCI, especially within close ranges. This finding has also been reported by Bhatt et al.(16) and, more recently, by Landers et al.(22). As surgical methods and materials continue to evolve and as patients' expectations become greater, we should consider the pursuit of excellence with methods that yield superior precision.
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Correspondence address:
Beatriz M. Fontes
Av. das Américas 2.300 B casa 27
Rio de Janeiro - RJ
22640-101 - Brazil
E-mail: [email protected]
Submitted for publication: November 18, 2010
Accepted for publication: April 17, 2011
Study carried out at the Centro de Microcirurgia e Diagnóstico - Rio de Janeiro (RJ), Brazil.
Funding: No specific financial support was available for this study.
Disclosure of potential conflicts of interest: B.M.Fontes, None; B.M.Fontes, None; E.Castro, None.