Surgical techniques for cataract extraction have been refined over time because of better instruments, better machines, and improved implants. There is also a trend of surgeons doing more procedures per year. Indications for cataract surgery have moved toward better preoperative visual acuity and younger and healthier eyes. All these changes over time have contributed to improved outcomes. In this study, we investigated changes regarding indications, technique, and outcomes as reflected in the European Registry of Quality Outcomes for Cataract and Refractive Surgery (EUREQUO).
METHODS
The EUREQUO was instituted in 2008 as a coproject between the European Union and the ESCRS and has been described extensively in the literature. Mandatory parameters included in the EUREQUO and to be reported are as follows—patient-related parameters: patient number, year of birth, sex, and eye; preoperative parameters: corrected distance visual acuity (CDVA), biometry target refraction, coexisting eye disease (none, glaucoma, macular degeneration, diabetic retinopathy, amblyopia, and other), complicating comorbidity (none, previous corneal refractive surgery, white cataract, pseudoexfoliation, previous vitrectomy, corneal opacities, small pupil/intraoperative floppy iris syndrome, and other); intraoperative parameters: date of surgery, surgeon experience, type of operation, laser-assisted cataract surgery details, type of intraocular lens (IOL) optic biomaterial, and complications during surgery; and postoperative parameters: date of examination, CDVA of operated eye, and postoperative complications. This study analyzed the preoperative, intraoperative, and postoperative parameters over time. Preoperative parameters were age, sex, visual acuity, target refraction, and risk factors including ocular comorbidity and surgical difficulties; intraoperative parameters were anesthesia, surgical technique, IOL optic biomaterial, and surgical complications; and postoperative parameters were visual acuity, refraction, and short-term complications. Some parameters had different denominators because they were not available in all reporting national registries affiliated to EUREQUO. All data reported to the EUREQUO are anonymized. This study was approved by the Swedish Ethical Board (ref. number2020-01872) and was performed according to the tenets of the Declaration of Helsinki.
Statistical Methods
Trends over time were analyzed with a χ2 test for categorical data and analysis of variance for numerical data. All analyses were performed using IBM SPSS Statistics for Windows software (version 25.0, IBM Corp.) at a 5% significance level.
RESULTS
During the study period (January 1, 2008, to December 31, 2017), a total of 2 714 108 cataract extractions were reported to the EUREQUO from 14 to 16 countries per year.
Preoperative Data
The mean age of the patients in this study decreased significantly over time from 74.5 years in 2008 to 73.0 years in 2017 (<.001). Trends in patient age, sex, preoperative visual acuity, and anticipated surgical difficulties over the study period are summarized in Table 1.
Table 1.
Number of reported surgeries, mean age, sex distribution, mean preoperative CDVA, ocular comorbidity, and anticipated surgical difficulties per year.
| Year | N = 2 714 108 | Mean Age y (SD) | % Female Sex | Preoperative CDVA logMAR (SD) [Decimal] | % Ocular Comorbidity | % Anticipated Surgical Difficulties |
| 2008 | 165 648 | 74.5 (10.0) | 60.6 | 0.46 (0.29) [0.33] | 30.0 | 12.6 |
| 2009 | 201 377 | 74.5 (10.0) | 60.3 | 0.44 (0.28) [0.33] | 29.7 | 11.7 |
| 2010 | 227 179 | 74.2 (10.0) | 60.0 | 0.44 (0.28) [0.33] | 30.1 | 12.4 |
| 2011 | 249 449 | 74.2 (9.8) | 59.7 | 0.43 (0.28) [0.40] | 29.7 | 12.0 |
| 2012 | 260 789 | 74.1 (9.7) | 59.3 | 0.41 (0.27) [0.40] | 28.7 | 11.1 |
| 2013 | 280 869 | 74.2 (9.6) | 59.2 | 0.40 (0.27) [0.40] | 29.5 | 12.0 |
| 2014 | 300 078 | 74.0 (9.6) | 58.5 | 0.39 (0.27) [0.40] | 29.4 | 12.3 |
| 2015 | 261 651 | 73.7 (9.3) | 57.9 | 0.36 (0.25) [0.45] | 28.2 | 10.4 |
| 2016 | 282 143 | 73.7 (9.3) | 57.7 | 0.36 (0.25) [0.45] | 27.3 | 10.9 |
| 2017 | 305 708 | 73.0 (9.7) | 57.2 | 0.37 (0.27) [0.45] | 27.0 | 10.6 |
| P value (trend) | <.001 | <.001 | <.001 | <.001 | <.001 |
Reported ocular comorbidities in the registry include age-related macular degeneration (AMD), glaucoma, diabetic retinopathy, amblyopia, and other sight-threatening ocular comorbidities. Over the study period, the reported occurrence of AMD decreased from 12.6% (20 893/165 650) to 10.6% (32 329/305 846) (P < .001), glaucoma decreased from 7.8% (12 939/165 650) to 6.6% (20 288/305 846) (P < .001), diabetic retinopathy decreased from 3.9% (6501/165 650) to 2.7% (8219/305 846) (P < .001), and amblyopia remained stable around 1.1% (2017: 3252/305 856) (P = .389). Anticipated surgical difficulties were divided into 8 categories: none, white cataract, small pupil, corneal opacities, pseudoexfoliation, previous corneal refractive surgery, previous vitrectomy, and other difficulties. The total proportion of anticipated surgical difficulties decreased slightly over the study period: from 12.6% (20 790/165 560) to 10.6% (32 403/305 846) (P < .001); but within the group, previous corneal refractive surgery increased, and white cataract decreased over time. Previous vitrectomy, small pupil, and corneal opacities were quite stable over the study period.
Surgical Data
Anesthesia
The trends regarding type of anesthesia over time are summarized in Table 2. This parameter is an optional one and, so, is not reported for all cases in the database. The number of valid cases is also tabulated in Table 2. Combinations of anesthesia methods are not included in the list of parameters in the registry. A χ2 test showed significant changes (P < .001) over time for all types of anesthesia, except general anesthesia. Topical anesthesia increased over time, whereas retrobulbar, sub-Tenon, peribulbar, and intracameral anesthesia decreased and general anesthesia remained stable.
Table 2.
Type of anesthesia (%) reported to the database, 2008 to 2017.
| 2008 | 2009 | 2010 | 2011 | 2012 | 2013 | 2014 | 2015 | 2016 | 2017 | |
| Available data on anesthesia (cases) | 93 320 | 120 036 | 140 057 | 150 747 | 163 089 | 172 645 | 188 652 | 148 781 | 163 166 | 182 083 |
| Retrobulbar | 24.7 | 21.2 | 17.5 | 13.4 | 11.3 | 9.1 | 7.5 | 6.8 | 5.4 | 8.6 |
| Sub-Tenon | 29.6 | 27.7 | 26.6 | 24.7 | 25.5 | 25.4 | 25.3 | 17.7 | 16.7 | 15.4 |
| Peribulbar | 8.1 | 5.7 | 5.0 | 4.3 | 4.5 | 3.4 | 2.3 | 1.0 | 1.1 | 1.3 |
| Topical | 28.1 | 35.8 | 38.5 | 43.9 | 46.7 | 49.5 | 51.5 | 70.7 | 73.1 | 71.7 |
| Intracameral | 6.0 | 6.2 | 8.7 | 10.2 | 8.9 | 9.4 | 10.2 | 0.9 | 0.8 | 0.5 |
| General | 2.6 | 2.4 | 2.7 | 2.9 | 2.6 | 2.6 | 2.7 | 2.8 | 2.8 | 2.5 |
| Other | 0.9 | 1.0 | 1.0 | 0.6 | 0.5 | 0.6 | 0.5 | 0.1 | 0.1 | 0 |
Type of Surgery
The preferred type of surgery over the study period was phacoemulsification with implantation of an IOL; this was used in 98.9% (2 622 443/2 653 551) of all surgeries, with a range of 98.1% to 99.4% per year. Phacoemulsification combined with a filtering procedure was reported in 0.2% (4735/2 653 551) of all cases, with a decreasing trend from 0.4% (1137/292 336) in 2014 to 0% from 2015 onward. This combination of procedures is not reported in all affiliated registries. Femtosecond laser–assisted cataract surgery was reported for the first time in 2012, being used in 0.1% (257/260 805) of cases; this increased to 0.8% (2333/292 336) in 2014 and then stabilized at 0.2%. Other types of surgery not listed among the preset registry variables were reported in 0.6% (16 726/2 653 551) of the cases on average.
Intraocular Lens
EUREQUO contains data on type of IOL optic biomaterial. This is tabulated per year in Table 3. All changes in type of IOL optic biomaterial were statistically significant (P < .001). Hydrophobic acrylic IOLs showed a significant increase, whereas all other types of biomaterial showed a significant decrease. There was also a significant decrease in leaving the eye aphakic postoperatively (no IOL). IOL type other than monofocal IOL has been reported to the database only sparsely (Table 4).
Table 3.
Type of IOL optic biomaterial (%).
| 2008 | 2009 | 2010 | 2011 | 2012 | 2013 | 2014 | 2015 | 2016 | 2017 | |
| Valid no. of cases | 165 642 | 201 376 | 227 179 | 249 458 | 260 804 | 280 906 | 300 142 | 261 739 | 280 439 | 291 748 |
| Hydrophobic acrylic | 78.7 | 81.0 | 80.7 | 81.6 | 82.8 | 85.2 | 85.5 | 89.4 | 91.1 | 90.6 |
| Hydrophilic acrylic | 13.8 | 13.2 | 14.1 | 13.3 | 12.7 | 11.1 | 11.7 | 9.3 | 8.3 | 8.8 |
| Silicon | 5.8 | 4.1 | 3.5 | 2.4 | 1.9 | 1.6 | 0.8 | 0 | 0 | 0 |
| PMMA | 0.4 | 0.3 | 0.2 | 0.1 | 0.1 | 0.1 | 0.1 | 0 | 0 | 0 |
| No IOL | 0.22 | 0.19 | 0.18 | 0.22 | 0.18 | 0.14 | 0.12 | 0.09 | 0.09 | 0.09 |
Table 4.
Reported use of nonmonofocal IOL.
| 2008 | 2009 | 2010 | 2011 | 2012 | 2013 | 2014 | 2015 | 2016 | 2017 | |
| Valid no. of cases | 72 436 | 82 093 | 85 765 | 95 048 | 96 118 | 109 124 | 112 776 | 113 560 | 119 943 | 124 631 |
| Multifocal IOL (%) | 0.21 | 0.37 | 0.66 | 0.83 | 1.03 | 1.14 | 1.98 | 1.28 | 1.36 | 1.67 |
| Toric IOL (%) | 0.06 | 0.12 | 0.27 | 0.46 | 0.46 | 0.51 | 0.59 | 0.28 | 0.27 | 0.30 |
| Multifocal toric IOL (%) | 0.11 | 0.09 | 0.09 | 0.04 | 0.08 | 0.16 |
Surgical Complications
Surgical complications are reported to the EUREQUO with the following options: posterior capsule rupture, vitreous loss, dropped nucleus, iris damage, complications related to laser-assisted surgery, other surgical complications, and no complication (Table 5). Capsule complications include a break of the posterior capsule with or without loss of vitreous and surgically induced zonular dehiscence of one quadrant or more. Dropped nucleus does not include cortex material. A χ2 test showed significant decrease over time for all surgical complications (P < .001).
Table 5.
Reported surgical complications during the study period.
| 2008 | 2009 | 2010 | 2011 | 2012 | 2013 | 2014 | 2015 | 2016 | 2017 | |
| Any surgical complication (%) | 2.5 | 2.3 | 2.2 | 2.5 | 1.9 | 1.7 | 1.6 | 1.3 | 1.2 | 1.2 |
| Capsule complication (n) | 2387 | 2725 | 2708 | 3976 | 2896 | 4181 | 4958 | 1969 | 2025 | 2007 |
| Capsule complication (%) | 1.44 | 1.34 | 1.19 | 1.59 | 1.11 | 1.49 | 1.65 | 0.75 | 0.72 | 0.66 |
| Valid cases for dropped nucleus and iris damage* | 93 344 | 120 186 | 142 594 | 155 717 | 166 189 | 173 118 | 189 682 | 149 143 | 163 482 | 182 560 |
| Dropped nucleus (n) | 87 | 124 | 126 | 145 | 130 | 129 | 162 | 96 | 72 | 85 |
| Dropped nucleus (%) | 0.09 | 0.10 | 0.09 | 0.09 | 0.08 | 0.08 | 0.08 | 0.06 | 0.04 | 0.05 |
| Iris damage (n) | 380 | 437 | 550 | 474 | 547 | 559 | 495 | 393 | 423 | 357 |
| Iris damage (%) | 0.41 | 0.36 | 0.39 | 0.30 | 0.33 | 0.32 | 0.26 | 0.25 | 0.26 | 0.20 |
Outcomes Data
Visual Outcome
Table 6 gives the visual outcome as mean values for all patients and for patients without any coexisting eye disease, along with the proportions achieving a certain visual acuity. Over the study period, the mean postoperative CDVA improved over the years from 0.08 logarithm of minimum angle of resolution (logMAR) to 0.05 logMAR, and the percentage achieving a postoperative CDVA of 0.0 logMAR (decimal 1.0) increased from 58.3% (44 221/75 915) to 75.0% (124 865/166 433).
Table 6.
Visual outcome in mean CDVA logMAR [decimal] and percentage of cases with CDVA logMAR 0.0 [1.0] or better and CDVA logMAR 0.3 [0.5] or better.
| 2008 | 2009 | 2010 | 2011 | 2012 | 2013 | 2014 | 2015 | 2016 | 2017 | P Value | |
| No. of all cases | 75 915 | 100 257 | 110 061 | 115 338 | 124 101 | 132 189 | 148 199 | 146 022 | 159 281 | 166 433 | |
| Postop CDVA logMAR, mean (SD), all cases | 0.08 (0.18) [0.8] | 0.08 (0.18) [0.8] | 0.07 (0.18) [0.8] | 0.07 (0.18) [0.8] | 0.06 (0.17) [0.8] | 0.06 (0.17) [0.8] | 0.06 (0.17) [0.8] | 0.05 (0.17) [0.8] | 0.05 (0.17) [0.8] | 0.05 (0.18) [0.8] | <.001 |
| Postop CDVA logMAR 0.0 [1.0] or better (%), all cases | 58.3 | 60.8 | 62.2 | 62.9 | 64.7 | 66.0 | 66.9 | 70.8 | 73.0 | 75.0 | <.001 |
| Postop CDVA logMAR 0.3 [0.5] or better (%), all cases | 94.4 | 94.5 | 94.5 | 94.9 | 95.3 | 95.4 | 95.6 | 95.8 | 95.9 | 95.3 | <.001 |
| No. of cases without ocular comorbidity | 56 384 | 74 741 | 81 364 | 87 658 | 95 243 | 99 633 | 109 11 | 110 605 | 121 626 | 127 662 | |
| Postop CDVA logMAR mean (SD), cases without ocular comorbidity | 0.04 (0.12) [1.0] | 0.04 (0.12) [1.0] | 0.03 (0.11) [1.0] | 0.04 (0.12) [1.0] | 0.03 (0.11) [1.0] | 0.03 (0.11) [1.0] | 0.02 (0.11) [1.0] | 0.01 (0.10) [1.0] | 0.01 (0.11) [1.0] | 0.02 (0.13) [1.0] | <.001 |
| Postop CDVA logMAR 0.0 [1.0] or better (%), cases without ocular comorbidity | 66.7 | 69.3 | 71.0 | 70.9 | 72.4 | 74.7 | 76.5 | 79.6 | 80.6 | 82.1 | <.001 |
| Postop CDVA logMAR 0.3 [0.5] or better (%), cases without ocular comorbidity | 98.2 | 98.2 | 98.3 | 98.2 | 98.4 | 98.4 | 98.7 | 98.9 | 98.8 | 97.8 | <.001 |
Absolute Prediction Error
The absolute prediction error is calculated as the absolute difference between the target refraction and the actual refraction achieved postoperatively. Target refraction is the predicted refraction for each surgeon using his/her preferred/available formula and biometry device. The postoperative refraction means refraction of the operated eye when testing subjective best distance visual acuity. The mean follow-up time was 31 days. The median values are tabulated in Table 7 along with the proportions that achieved a difference of 0.50 diopter [D] or less and 1.00 D or less, respectively.
Table 7.
Absolute prediction error in deviation from the intended refraction with the absolute value.
| 2008 | 2009 | 2010 | 2011 | 2012 | 2013 | 2014 | 2015 | 2016 | 2017 | P Value | |
| No. of cases | 75 915 | 100 257 | 110 061 | 115 338 | 124 101 | 132 189 | 148 199 | 146 022 | 159 281 | 166 433 | |
| Absolute median PE | 0.38 | 0.35 | 0.33 | 0.30 | 0.30 | 0.30 | 0.30 | 0.30 | 0.30 | 0.28 | <.001 |
| Absolute PE ≤0.50 D (%) | 66.9 | 69.0 | 70.1 | 71.1 | 72.3 | 71.7 | 72.4 | 73.1 | 73.1 | 73.4 | <.001 |
| Absolute PE ≤1.00 D (%) | 89.6 | 91.4 | 91.8 | 92.6 | 93.1 | 92.6 | 92.7 | 93.4 | 93.4 | 93.6 | <.001 |
The impact of monofocal or nonmonofocal IOLs on the refractive outcome was not calculated per year due to the low annual numbers of nonmonofocal IOLs. When the absolute median prediction error was calculated for the whole study period for monofocal IOLs, the result was 0.30 D. An absolute prediction error of 0.50 D or less for the same group was 72.0% (1 041 441/1 446 281).
Postoperative complications
Can be reported as no complication, persistent central corneal edema, reduced vision because of posterior capsule opacification (PCO), uveitis with need for medication, endophthalmitis, uncontrolled elevated intraocular pressure, or other postoperative complications. Numbers per year are summarized in Table 8.
Table 8.
Postoperative complications reported to the EUREQUO (absolute numbers).
| Year | 2008 | 2009 | 2010 | 2011 | 2012 | 2013 | 2014 | 2015 | 2016 | 2017 |
| Valid no. of cases | 76 234 | 100 718 | 111 291 | 115 942 | 124 594 | 132 669 | 148 888 | 146 668 | 159 955 | 167 366 |
| Central corneal edema/striae | 108 | 136 | 168 | 162 | 162 | 174 | 198 | 148 | 164 | 648 |
| Uveitis | 36 | 50 | 52 | 55 | 59 | 90 | 112 | 3 | 1 | 3 |
| Endophthalmitis | 43 | 51 | 42 | 52 | 36 | 40 | 24 | 43 | 16 | 24 |
| Uncontrolled IOP | 52 | 52 | 83 | 55 | 43 | 50 | 59 | 47 | 56 | 64 |
| Other | 1220 | 1383 | 1526 | 1506 | 1567 | 3364 | 4528 | 2050 | 2077 | 2023 |
| Total number | 1436 | 1646 | 1867 | 1822 | 1844 | 3714 | 4935 | 2283 | 2340 | 3153 |
| Total % | 1.88 | 1.63 | 1.68 | 1.57 | 1.48 | 2.80 | 3.31 | 1.56 | 1.46 | 1.88 |
DISCUSSION
This study showed a significant decrease in the mean age of cataract surgery patients, from 74.5 years in 2008 to 73.0 years in 2017. This is close to the mean age of 73.2 years reported from Poland in 2010 to 2015 based on more than 1 million cataract extractions, although that study demonstrated no clear trend over the period. In a previous publication from the European Cataract Outcome Study (ECOS), the mean age of patients was 73.7 years at time of surgery. In this study, the proportion of women undergoing cataract extraction decreased significantly during the study period from 60.6% to 57.2%, whereas the proportion in the Polish study was fairly stable around 65.1%, and the ECOS study showed a proportion of 65.7% for 1 study year. The relationship between age and sex distribution might be influenced by the difference in life expectancy between the sexes. Another factor might be different patterns in requesting second-eye surgery.
Risk factors for ocular comorbidity showed a decreasing trend in our study. The mean occurrence of glaucoma in the surgery eye (from 7.8% to 6.6%) was in line with that of reports from the Malaysian national cataract registry (6.4%), but lower than that of reports from Israel (14%). Our finding of diabetic retinopathy in approximately 3% of eyes operated on for cataract is much lower than that reported from the Malaysian cataract register (approximately 10%), which might be due to the well-known high incidence of diabetes in Malaysia. These differences reflect the fact that different countries in different parts of the world might have great differences in baseline factors for cataract surgery patients. Our results offer a snapshot of cataract surgery practice from many surgeons and clinics in European countries.
These data show a clear transition from anesthetic injections to topical anesthesia. The same trend has been documented in surveys of preferred cataract surgery practices. The drop in intracameral anesthesia from 2015 and onward reflects a change in contributing country data.
Most surgeries reported in this study were phacoemulsification with implanted IOL, and this was stable over time. According to the coding guidelines, combined surgeries (cataract extraction plus vitrectomy or corneal transplantation) should not be reported to the registry. The only exception is a cataract extraction combined with a filtering procedure; this kind of surgery declined in frequency over time in this study. A low percentage of laser-assisted femtosecond cataract extraction has been reported since 2012. For 3 years between 2013 and 2015, the EUREQUO received data from a femtosecond laser–assisted cataract surgery study, which explains the increase of this surgical type in the registry. The study protocol included meticulous reporting of complications, which also affected the reporting of surgical and postoperative complications in these years.
Regarding choice of IOL, the registry includes type of optic biomaterial and different kinds of nonmonofocal IOLs (multifocal and toric IOLs). Hydrophobic acrylic IOLs dominate the material and their use has increased over time, whereas use of silicon and PMMA IOLs has declined to nearly zero. Biomaterial in IOLs has usually been studied with a focus on complications such as PCO, anterior capsule opacification, and glistening formation. The increase in the use of hydrophobic acrylic IOLs in this study is not surprising because the literature shows that this biomaterial is less related to anterior capsule opacification or PCO. On the other hand, the material also seems related to glistening, even if this complication seldom affects visual acuity. The number of nonmonofocal IOLs implanted was surprisingly low in this study, given the huge focus on these IOLs in the literature. The EUREQUO database is dominated by Dutch and Swedish data, and our interpretation is that nonmonofocal IOLs are mostly used in refractive lens exchange surgeries in these countries and not within ordinary cataract surgery. However, the frequency of these IOLs did increase over time in this study.
Capsule complications during surgery showed a decreasing trend in our study. A similar trend has also been reported from other registries collecting data over time. Although findings regarding surgical complications might be flawed by underreporting, we think that this decreasing trend is a solid finding. Reasons for this positive development might include better surgical quality and surgery on younger and healthier eyes. Our finding of decreasing complications regarding dropped nucleus has been extensively discussed in a previous article.
The visual outcome in mean CDVA improved over time in our study. In a previous article, we discussed the visual outcome and the baseline parameters that influenced it. The refractive outcome also showed an improving trend during the study period. Reasons for a poor refractive outcome based on data from the EUREQUO have been reported previously.
The postoperative complications in our study must be seen in the light of a 30-day follow up, which prevents late complications such as PCO from being represented in a fair way. The reported frequency of postoperative endophthalmitis showed a decreasing trend from approximately 0.05% to 0.02%, which again must also be seen in the light of the mean follow-up time. A weakness in our registration is the lack of information about preventive measures such as asepsis and intracameral antibiotic injection. However, we know from other sources that most surgeons in the Netherlands and Sweden use intracameral antibiotics as a prophylactic regimen.
Another weakness of our study is the fact that the data were self-reported by surgeons and clinics. We believe, however, that the data are reliable because the reason for surgeons to participate is benchmarking and comparison, and each surgeon’s or clinic’s data are only visible to themselves. Finally, the registry protocol includes a limited number of parameters and a limited follow-up time, to reduce the clinical burden of reporting data. A strength of our study is the large number of reported cases from many countries for more than a decade.
Trends in European cataract surgery practice patterns from 2008 to 2017 as reflected in the EUREQUO have moved toward slightly younger patients with better preoperative visual acuity, fewer surgical complications, and better visual outcomes and less absolute prediction error.
WHAT WAS KNOWN
Mean age and sex distribution, surgical complications, and outcomes in cataract surgery have previously been reported in cohort studies and from some national registry data.
WHAT THIS PAPER ADDS
Data extracted from a large database was used to describe trends in patient demographics, anesthetic and surgical techniques, visual and refractive outcomes, and complications over a decade.
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