ARTICLE

Changing practice patterns in European cataract surgery as reflected in the European Registry of Quality Outcomes for Cataract and Refractive Surgery 2008 to 2017

  • Mats Lundström
  • Mor Dickman
  • Ype Henry
  • Sonia Manning
  • Paul Rosen
  • Marie-José Tassignon
  • David Young
  • Anders Behndig
  • Ulf Stenevi
Journal of Cataract & Refractive Surgery 47(3):p 373-378, March 2021. | DOI: 10.1097/j.jcrs.0000000000000457

Purpose:

To study practice patterns in European cataract surgery over a 10-year period.

Setting:

European clinics affiliated to the European Registry of Quality Outcomes for Cataract and Refractive Surgery (EUREQUO).

Design:

Registry cohort study.

Methods:

The EUREQUO contains preoperative, intraoperative, and postoperative parameters reported by surgeons in many European clinics. All data reported to the registry are anonymized. Preoperative parameters included age, sex, visual acuity, target refraction, ocular comorbidity, and surgical difficulties. Surgical data included anesthesia, surgical technique, intraocular lens optic biomaterial, and complications. Postoperative parameters included visual acuity, refraction, and short-term complications.

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. Preoperative data changed over time, with decreases in mean age (74.5–73.0 years), proportion of women from 60.6% (100 373/165 628) to 57.2% (174 908/305 845), and proportion of coexisting eye diseases from 30.0% (49 638/165 650) to 27.0% (82 704/305 846) and with improvements in preoperative visual acuity (mean logarithm of minimum angle of resolution [logMAR] 0.46 to 0.37). The use of topical anesthesia increased over time from 28.1% (26 238/93 320) to 71.7% (130 525/182 083). Surgical complications showed a significant decrease from 2.5% (4107/165 650) to 1.2% (3573/305 846). The visual outcome improved over time (mean logMAR 0.08 to 0.05), as did the absolute median prediction error (0.38 diopter [D] to 0.28 D).

Conclusions:

Trends in European cataract surgery practice patterns from 2008 to 2017 have moved toward younger patients with better preoperative visual acuity, fewer surgical complications, and better predicted refractions and visual outcomes.

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.

YearN = 2 714 108Mean Age y (SD)% Female SexPreoperative CDVA logMAR (SD) [Decimal]% Ocular Comorbidity% Anticipated Surgical Difficulties
2008165 64874.5 (10.0)60.60.46 (0.29) [0.33]30.012.6
2009201 37774.5 (10.0)60.30.44 (0.28) [0.33]29.711.7
2010227 17974.2 (10.0)60.00.44 (0.28) [0.33]30.112.4
2011249 44974.2 (9.8)59.70.43 (0.28) [0.40]29.712.0
2012260 78974.1 (9.7)59.30.41 (0.27) [0.40]28.711.1
2013280 86974.2 (9.6)59.20.40 (0.27) [0.40]29.512.0
2014300 07874.0 (9.6)58.50.39 (0.27) [0.40]29.412.3
2015261 65173.7 (9.3)57.90.36 (0.25) [0.45]28.210.4
2016282 14373.7 (9.3)57.70.36 (0.25) [0.45]27.310.9
2017305 70873.0 (9.7)57.20.37 (0.27) [0.45]27.010.6
P value (trend)<.001<.001<.001<.001<.001

*

One-way analysis of variance.

χ2 test.

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.

2008200920102011201220132014201520162017
Available data on anesthesia (cases)93 320120 036140 057150 747163 089172 645188 652148 781163 166182 083
Retrobulbar24.721.217.513.411.39.17.56.85.48.6
Sub-Tenon29.627.726.624.725.525.425.317.716.715.4
Peribulbar8.15.75.04.34.53.42.31.01.11.3
Topical28.135.838.543.946.749.551.570.773.171.7
Intracameral6.06.28.710.28.99.410.20.90.80.5
General2.62.42.72.92.62.62.72.82.82.5
Other0.91.01.00.60.50.60.50.10.10

 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 (%).

2008200920102011201220132014201520162017
Valid no. of cases165 642201 376227 179249 458260 804280 906300 142261 739280 439291 748
Hydrophobic acrylic78.781.080.781.682.885.285.589.491.190.6
Hydrophilic acrylic13.813.214.113.312.711.111.79.38.38.8
Silicon5.84.13.52.41.91.60.8000
PMMA0.40.30.20.10.10.10.1000
No IOL0.220.190.180.220.180.140.120.090.090.09

PMMA = poly(methyl methacrylate)

*

Cases with reported optic biomaterial parameter.

Table 4.

Reported use of nonmonofocal IOL.

2008200920102011201220132014201520162017
Valid no. of cases72 43682 09385 76595 04896 118109 124112 776113 560119 943124 631
Multifocal IOL (%)0.210.370.660.831.031.141.981.281.361.67
Toric IOL (%)0.060.120.270.460.460.510.590.280.270.30
Multifocal toric IOL (%)0.110.090.090.040.080.16

*

Cases with reported nonmonofocal parameter.

 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.

2008200920102011201220132014201520162017
Any surgical complication (%)2.52.32.22.51.91.71.61.31.21.2
Capsule complication (n)2387272527083976289641814958196920252007
Capsule complication (%)1.441.341.191.591.111.491.650.750.720.66
Valid cases for dropped nucleus and iris damage*93 344120 186142 594155 717166 189173 118189 682149 143163 482182 560
Dropped nucleus (n)87124126145130129162967285
Dropped nucleus (%)0.090.100.090.090.080.080.080.060.040.05
Iris damage (n)380437550474547559495393423357
Iris damage (%)0.410.360.390.300.330.320.260.250.260.20

*Not available in Swedish registry

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.

2008200920102011201220132014201520162017P Value
No. of all cases75 915100 257110 061115 338124 101132 189148 199146 022159 281166 433
Postop CDVA logMAR, mean (SD), all cases0.08 (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 cases58.360.862.262.964.766.066.970.873.075.0<.001
Postop CDVA logMAR 0.3 [0.5] or better (%), all cases94.494.594.594.995.395.495.695.895.995.3<.001
No. of cases without ocular comorbidity56 38474 74181 36487 65895 24399 633109 11110 605121 626127 662
Postop CDVA logMAR mean (SD), cases without ocular comorbidity0.04 (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 comorbidity66.769.371.070.972.474.776.579.680.682.1<.001
Postop CDVA logMAR 0.3 [0.5] or better (%), cases without ocular comorbidity98.298.298.398.298.498.498.798.998.897.8<.001

*One-way analysis of variance.

χ2 test.

χ2 test.

 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.

2008200920102011201220132014201520162017P Value
No. of cases75 915100 257110 061115 338124 101132 189148 199146 022159 281166 433
Absolute median PE0.380.350.330.300.300.300.300.300.300.28<.001
Absolute PE ≤0.50 D (%)66.969.070.171.172.371.772.473.173.173.4<.001
Absolute PE ≤1.00 D (%)89.691.491.892.693.192.692.793.493.493.6<.001

PE = prediction error

*

One-way analysis of variance.

χ2 test.

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).

Year2008200920102011201220132014201520162017
Valid no. of cases76 234100 718111 291115 942124 594132 669148 888146 668159 955167 366
Central corneal edema/striae108136168162162174198148164648
Uveitis365052555990112313
Endophthalmitis43514252364024431624
Uncontrolled IOP52528355435059475664
Other1220138315261506156733644528205020772023
Total number1436164618671822184437144935228323403153
Total %1.881.631.681.571.482.803.311.561.461.88

IOP = intraocular pressure

The mean follow-up period is 30 days. One or more complications can be registered. Posterior capsule opacification is not displayed in the table because of the short follow-up time.

*

Cases from the ESCRS femtosecond laser–assisted cataract surgery study are included.

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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Copyright © 2021 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of ASCRS and ESCRS
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