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Indian Journal of Ophthalmology logoLink to Indian Journal of Ophthalmology
. 2022 Feb 25;70(3):740–748. doi: 10.4103/ijo.IJO_934_21

Accuracy of intraocular lens power calculation formulae in short eyes: A systematic review and meta-analysis

Ankur K Shrivastava 1,, Swatishree Nayak 1, Ashish Mahobia 1, Mary Anto 1, Pranay Pandey 1
PMCID: PMC9114558  PMID: 35225507

Abstract

This review article attempts to evaluate the accuracy of intraocular lens power calculation formulae in short eyes. A thorough literature search of PubMed, Embase, Cochrane Library, Science Direct, Scopus, and Web of Science databases was conducted for articles published over the past 21 years, up to July 2021. The mean absolute error was compared by using weighted mean difference, whereas odds ratio was used for comparing the percentage of eyes with prediction error within ±0.50 diopter (D) and ±1.0 D of target refraction. Statistical heterogeneity among studies was analyzed by using Chi-square test and I2 test. Fifteen studies including 2,395 eyes and 11 formulae (Barrett Universal II, Full Monte method, Haigis, Hill-RBF, Hoffer Q, Holladay 1, Holladay 2, Olsen, Super formula, SRK/T, and T2) were included. Although the mean absolute error (MAE) of Barrett Universal II was found to be the lowest, there was no statistically significant difference in any of the comparisons. The median absolute error (MedAE) of Barrett Universal II was the lowest (0.260). Holladay 1 and Hill-RBF had the highest percentage of eyes within ±0.50 D and ±1.0 D of target refraction, respectively. Yet their comparison with the rest of the formulae did not yield statistically significant results. Thus, to conclude, in the present meta-analysis, although lowest MAE and MedAE were found for Barrett Universal II and the highest percentage of eyes within ±0.50 D and ±1.0 D of target refraction was found for Holladay 1 and Hill-RBF, respectively, none of the formulae was found to be statistically superior over the other in eyes with short axial length.

Keywords: Cataract, intraocular lens, mean absolute error, median absolute error, power calculation formulae, short eyes


Cataract surgery remains one of the most commonly performed ophthalmological procedures worldwide owing to the aging population and increasing life expectancy.[1,2] Even in a meticulously performed surgery, the actual visual outcome can match the expected visual outcome by accurate biometry.

The advent of optical biometry circumvented the operator-induced bias encountered in ultrasound biometry. Soon partial coherence interferometry (PCI) became the gold standard optical biometer owing to its precision in measurements along with ease of use in clinical settings.[3] Optical low coherence reflectometry (OLCR) and swept-source optical coherence tomography biometers were its successors, which although maintained the same precision of measurements, provided additive information on several parameters such as lens thickness, central corneal thickness, anterior chamber depth (ACD), horizontal white-to-white diameter, and corneal radii.[4] The incorporation of these parameters into the intraocular lens (IOL) power calculation formulae gave a better prediction of the effective lens position.

However, among the wide range of available formulae, none is completely accurate in all scenarios. Modern formulae show comparable refractive outcomes in eyes with normal axial length (AL).[5] But when we deal specifically with short eyes (AL <22 mm), they gave variable results. Hence, the deliberation for choosing the most accurate formula, so as to obtain an optimal postoperative visual outcome in the subgroup of short eyes continues. In 2018, a meta-analysis on short eyes had already been carried out by Wang et al.[6] With set down of protocols for conducting a study on IOL power accuracy, it was recommended to compare median absolute error (MedAE) rather than mean absolute error (MAE) and also includes the percentage of eyes with prediction error (PE) within ±0.25, ±0.50, and ±1.0 diopter (D) of target refraction.[7,8] Hence, the present meta-analysis was carried out taking into account these recommendations.

Methods

We carried out this meta-analysis according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses statement.[9] Ethics committee approval was not required as our review relied entirely on publicly available data that are already published. Nonetheless, the study methods adhered to the tenets of the Declaration of Helsinki.

Search methods

Two authors independently searched PubMed, Embase, Cochrane Library, Science Direct, Scopus, and Web of Science databases for research articles published over the past 21 years, up to July 2021. Search terms used for PubMed were short eyes* OR short axial length* AND Phacoemulsification AND Calculat* OR Formula* AND IOL. The title and abstract of the retrieved literature were then screened. The selected articles were further filtered by reading the full text and assessed for eligibility. Articles cited in the reference list of these eligible articles were also screened manually.

Inclusion and exclusion criteria

The studies included in the meta-analysis met the following inclusion criteria: (1) population: (a) patients older than 18 years of age, (b) eyes with AL less than 22 mm; (2) intervention: (a) biometry done by optical method, (b) eyes that underwent uneventful phacoemulsification surgery; (3) comparison: at least two of the following IOL power calculation formulae used – Barrett Universal II, Haigis, Hill-RBF, Hoffer Q, Holladay 1, Holladay 2, and SRK/T; (4) outcome: studies that reported at least one of the three outcome measures – MAE, MedAE, or percentage of eyes with PE within ±0.50 and ±1.0 D of target refraction; (5) study design: Prospective and retrospective.

The exclusion criteria were as follows: (1) history of corneal refractive surgery; (2) any ocular pathology affecting refraction; (3) toric, multifocal, piggyback IOL, or IOLs not implanted in the bag; (4) older generation formulae such as Binkhorst II, SRK I, or SRK II used; (5) review articles, studies under trial, editorials, conference abstracts, previous meta-analysis, discussion papers, full text not available in English, or animal studies.

Data extraction

Two authors extracted data regarding study design, methodology, participant demographics, and baseline characteristics from all included studies independently and matched their results. Any discrepancy found was resolved by discussion and confirmation with the third author. If standard deviation (SD) data could not be extracted from full-text articles or even after contacting the authors, we used the mean SD of the remaining studies.

Quality assessment

The study quality was assessed by using a modified checklist adapted from the Quality Assessment of Diagnostic Accuracy Studies–2 (QUADAS-2) tool.[10] The evaluation of bias was divided into four domains: patient selection, index test, reference standard, and last, flow and timing of patients. Applicability concerns were assessed using three domains: patient selection, index test, and reference standard. Each domain could have a high risk, low risk, or unclear risk of bias.

Statistical analysis

Data were analyzed for MAE, MedAE, and percentage of eyes with PE within ±0.50 and ±1.0 D of target refraction. We analyzed the relative effect size of continuous outcomes like MAE using weighted mean difference (WMD) with 95% confidence interval (CI). The relative effect size of the percentage of eyes with PE within ±0.50 and ±1.0 D of target refraction, which was a binary outcome, was calculated as odds ratio (OR) with a 95% CI. Statistical methods utilized were inverse variance for continuous data and Mantel–Haenszel for dichotomous data. A P value less than 0.05 was considered statistically significant in both. Statistical heterogeneity among studies was analyzed by using Chi-square test and I2 test. When the I2 value was more than 50% and P value was less than 0.1, random-effect model was used for analysis; otherwise a fixed-effect model was used. Sensitivity analysis was conducted to identify sources of significant heterogeneity. Te funnel plot was used to assess publication bias. Only descriptive analysis was performed for MedAE as it is not suitable for meta-analysis. Statistical analysis was carried out using Review Manager software (RevMan, Version 5.4).[11]

Results

Literature selection results

The detailed process of literature search and study selection is depicted in Fig. 1. Initially, 2,094 studies were identified through a database search. After the removal of 48 duplicate studies, 2,046 eligible titles were identified and screened by review of the abstract. Of these, 28 full-text articles were retrieved. After excluding 13 studies based on predefined inclusion criteria, 15 studies were included in this meta-analysis.

Figure 1.

Figure 1

Flow chart of article selection. Abbreviations: FLACS = Femtosecond laser-assisted cataract surgery; IOL=Intraocular lens

Study characteristics

The characteristics of eligible studies are summarized in Table 1. A total of 2,395 eyes with AL in the range of 18.77 to 21.99 mm were included in the analysis. The sample size ranged from 15 to 608 eyes. Formulae included were Barrett Universal II, Haigis, Hill-RBF, Hoffer Q, Holladay 1, Holladay 2, and SRK/T. A few studies also used newer generation formulae such as the Full Monte method, Kane, Ladas Super formula, Olsen, and T2.

Table 1.

Characteristics of study participants

Study Year Country Study design Number of eyes Age (years±SD) Axial length, mm±SD (Range) Method of calculating RPE Lens Constant Used
Aristodemou et al.[15] 2011 United Kingdom Retrospective 608 NA 21.57 (20.00-21.99) Postop SE-PR Optimized constants
Cooke and Cooke[23] 2016 USA Retrospective 41 NA 21.69 (20.84-22.00) Postop SE-PR Optimized constants
Darcy et al.[25] 2020 UK Retrospective 766 NA ≤ 22 Postop SE-PR Optimized constants For Haigis a0- optimized, a1, a2- ULIB
Day et al.[17] 2012 UK Retrospective 163 57±10 21.2±0.60 (19.23-21.98) Postop SE-PR Optimized constants
Eom et al.[18] 2014 South Korea Retrospective cross-sectional 75 70.1±6.8 21.69±0.29 (20.32-21.99) Postop SE-PR Optimized constants
Gavin and Hammond[16] 2008 UK Retrospectively Prospective 41 NA 21.51 (20.29-21.96) PR-Postop SE Manufacturer’s constants
Gökce et al.[19] 2017 USA Retrospective case series 86 72±8 21.53±0.56 (18.80-22.00) Postop SE-PR Optimized constants
Kane et al.[5] 2016 Australia Retrospective case series 156 NA ≤22 Postop SE-PR Optimized constants
Kane et al.[26] 2017 Australia Retrospective case series 137 NA ≤22 Postop SE-PR Optimized constants
Khatib et al.[21] 2021 India Retrospective observational 66 NA Postop SE-PR Optimized constants
Shrivastava et al.[20] 2018 India Retrospective observational 50 58.54±10.36 21.61±0.27 (20.76-21.96) Postop SE-PR Optimized constants
Srivannaboon et al.[22] 2013 Thailand Prospective comparative 15 NA 21.44 (18.77-21.94) Postop SE-PR ULIB constants
Terzi et al.[27] 2009 Germany Retrospective 19 53±7 21.24±0.55 (20.13-21.97) PR-Postop SE Optimized constants
Wang et al.[6] 2013 China Retrospective 33 NA 21.52±0.47 Postop SE-PR Optimized constants
Zhao et al.[13] 2018 China Retrospective 139 NA <21 PR-Postop SE ULIB constants

Study Version of biometer Method of K measurement Follow-up Refraction IOL implanted Formulae used

Aristodemou et al.[15] NA IOLMaster 1 month Subjective Sofport IOL and Akreos Fit IOL Hoffer Q, Holladay 1, SRK/T
Cooke and Cooke[23] Lenstar LS 900 (Version 3.02) and IOLMaster (Version 5.4) Optical biometer (both OLCR and PCI) 3 weeks to 3 months Subjective AcrysofSN60WF Barrett Universal II, Haigis, Hoffer Q, Holladay 1, Holladay 2No Ref, Holladay 2Pre surg Ref, Olsenstandalone, OlsenOLCR SRK-T, Super Formula, T2
Darcy et al. IOLMaster (Carl Zeiss, Meditec, AG) IOLMaster NA Subjective SA60AT, Superflex Aspheric920 H, C-Flex Aspheric970C, AkreosAdaptAO Barrett Universal II, Haigis, Hill-RBF, Hoffer Q, Holladay1, Holladay 2, Kane, Olsen, SRK/T
Day et al.[17] IOLMaster (Carl Zeiss, Meditec, Inc, Dublin, CA, USA) IOLMaster 2-17.7 weeks Autorefraction (Topcon KR8000 series autorefractor) Topcon, Rotterdam, The Netherlands Akreos AO, Akreos Adapt, Corneal ACR6D, OculentisLentis L302-1 Haigis, Hoffer Q, Holladay1, SRK/T
Eom et al.[18] IOLMaster (Version 5.02) IOLMaster 3-10 weeks Autorefractor/Keratometer (RK-F1; Canon, Tokyo, Japan) Alcon Acrysof IQ Haigis, Hoffer Q
Gavin and Hammond[16] IOLMaster (Zeiss-Humphrey systems) IOLMaster 2-3 weeks Autorefractometer (Canon AR-2, Canon, Tokyo) AllerganMA60 Hoffer Q, SRK/T
Gökce et al.[19] Lenstar LS900 (Version V 4.1.1, Haag Streit AG) Lenstar >3 weeks Subjective Alcon Acrysof SN60WF, SN6AT, SA60AT, Tecnis, ZCBOO, ZCT Barrett Universal II, Haigis, Hill-RBF, Hoffer Q, Holladay 1, Holladay 2, and Olsen
Kane et al.[5] IOLMaster (Version 5.4, Carl Zeiss, Meditec, AG) IOLMaster 2 weeks Subjective AcrysofIQSN60WF Barrett Universal II, Haigis, Hoffer Q, Holladay1, Holladay 2, SRK/T, T2
Kane et al. IOLMaster (Version 5.4, Carl Zeiss, Meditec, AG) IOLMaster 2 weeks Subjective Acrysof IQ SN60WF Barrett Universal II, Full Monte method, Hill- RBF, Holladay 1, Ladas Super formula
Khatib et al.[21] Lenstar LS 900 Lenstar 2 weeks Subjective Acrysof IQ SN60WF, Tecnis ZCB00 Barrett Universal II, EVO, Hill-RBF
Shrivastava et al.[20] IOLMaster 500 (Version 5.4, Carl Zeiss, Meditec, AG) IOLMaster 1 month Autorefractometer (Accuref K-900/R-800, Rexxam Co. Ltd.) Acrysof SN6CWS Barrett Universal II, Haigis, Hill- RBF, Hoffer Q, Holladay 2, SRK/T
Srivannaboon et al.[22] IOLMaster (Carl Zeiss, Meditec, Jena, Germany) IOLMaster 3 months Subjective Hoya PY60AD Haigis, Hoffer Q, Holladay 2 with LT, Holladay 2 without LT
Terzi et al. IOLMaster (Carl Zeiss, Meditec, AG) AL by PCI, Keratometry not clear 1 month Subjective Acrysof SA60AT, Sensar AR40e Haigis, Hoffer Q, Holladay 2, SRK/T
Wang et al.[6] IOLMaster (Carl Zeiss, Jena, Germany) IOLMaster 3 months Autorefractometer (Topcon AR, Tokyo, Japan) Acrysof SA60AT Haigis, Hoffer Q, Holladay 1, SRK/T
Zhao et al.[13] Zeiss IOLMaster (Version 4.02) AL- IOLMaster, Manual keratometry 1-3 months Subjective AA4203 Haigis, Hoffer Q, Holladay 1, Holladay 2, SRK/T

Postop SE=postoperative spherical equivalent; PR=predicted refraction; ULIB=User Group for Laser Interference Biometry; AL=axial length; OLCR=optical low-coherence reflectometry; PCI=partial coherence interferometry

Quality of included studies

A modified checklist adapted from QUADAS-2 tool was employed to assess the study quality [Fig. 2]. Detailed assessment questionnaire and its results are provided [Additional File 1]. Ten of the 15 studies did not report whether the patient selection was consecutive or random and hence had an unclear risk of bias. On analyzing the reference standard used, 10 studies had a high risk of bias due to the use of subjective refraction for calculating postoperative spherical equivalent (SE). Most of the studies were of high quality as far as index tests, the inclusion of patients, the flow of patients, and applicability were concerned.

Figure 2.

Figure 2

Quality assessment of the included studies based on modified QUADAS-2 tool. Abbreviations: QUADAS-2 = Quality Assessment of Diagnostic Accuracy Studies-2

Outcomes

The outcome variables included in our analysis were MAE, MedAE, and the percentage of eyes with PE within ±0.50 and ±1.0 D of target refraction. This meta-analysis included 2,395 eyes, of which 1,302 eyes were analyzed for Barrett Universal II, 1,543 eyes for Haigis, 1,105 eyes for Hill-RBF, 2,192 eyes for Hoffer Q, 2,129 eyes for Holladay 1, 1,272 eyes for Holladay 2, and 2,016 eyes for SRK/T formulae.

Mean absolute error

The MAE and standard error of all the formulae included in the analysis showed the lowest value for Barrett Universal II [Fig. 3 (I)]. It performed equally well as Haigis, Hoffer Q, and SRK/T with WMD and 95% CI of −0.00 (−0.04, 0.03) for the three pairs [Fig. 3IIA, B, and C]. The WMD and 95% CI of Barrett Universal II with Hill-RBF, Holladay 1, and Holladay 2 were 0.02 (−0.01, 0.06); 0.02 (−0.01, 0.06), and 0.03 (−0.01, 0.06), respectively [Fig. 3II D, E, and F]. Although the MAE of Barrett Universal II was found to be the lowest, there was no statistically significant difference in any of the comparisons.

Figure 3.

Figure 3

(I) The overall MAE and standard error of all formulae included in analysis. (II) Forest plots showing comparison of MAE between Barrett Universal II and Haigis (A), Hoffer Q (B), SRK/T (C), Hill-RBF (D), Holladay 1 (E), and Holladay 2 (F). Abbreviations: MAE = Mean absolute error; D = Diopter; PE = Prediction error

Median absolute error

Table 2 shows the descriptive analysis of MedAE of all the formulae included in the analysis. Nine of the 15 studies have reported this parameter. The MedAE of Barrett Universal II was the lowest (0.260) followed by Hill-RBF (0.300), Holladay 1 (0.302), Haigis (0.308), Holladay 2 (0.320), SRK/T (0.327), and Hoffer Q (0.340).

Table 2.

Descriptive analysis of median absolute error of all the formulae included in the analysis

Formula Number of studies Range
Barrett Universal II 7 0.260-0.540
Full Monte 1 0.462
Haigis 11 0.308-0.570
Hill-RBF 5 0.300-0.520
Hoffer Q 13 0.340-0.580
Holladay 1 9 0.302-0.630
Holladay 2 8 0.320-0.560
Olsen 3 0.325-0.350
Super formula 2 0.320-0.370
SRK/T 10 0.327-0.690
T2 2 0.341-0.415

Percentage of eyes with prediction error within ±0.50 D of target refraction

Fig. 4(I) shows the percentage of eyes with PE within ±0.50 D of target refraction of all the formulae included in the analysis. Holladay 1 had the highest percentage of eyes. On analyzing the forest plots, OR and 95% CI of Holladay 1 as compared with Barrett Universal II, Haigis, Hill-RBF, Hoffer Q, Holladay 2, and SRK/T formulae were 0.91 (0.68,1.21), P value = 0.51, 0.95 (0.73, 1.25), P value = 0.73, 0.94 (0.63, 1.40), P value = 0.76, 0.85 (0.72, 1.02), P value = 0.08, 1.10 (0.77, 1.57), P value = 0.59, and 1.19 (0.99, 1.43), P value = 0.07, respectively, as shown in Fig. 4(II). None of the comparisons showed statistically significant results [Additional file 3 (4.4MB, tif) ].

Figure 4.

Figure 4

(I) Percentage of eyes with prediction error within ±0.50 D of target refraction of all the formulae included in the analysis. (II) Forest plots showing comparison between Holladay 1 and Barrett Universal II (A), Haigis (B), Hill-RBF (C), Hoffer Q (D), Holladay 2 (E), and SRK/T (F). Abbreviations: D = Diopter; PE = Prediction error

Percentage of eyes with prediction error within ±1.0 D of target refraction

Hill-RBF had the highest value when the percentage of eyes with PE within ±1.0 D of target refraction was considered [Additional file 4 (6.8MB, tif) (I)]. On analyzing the forest plots none of the comparisons yielded statistically significant results [Additional file 4 (6.8MB, tif) (II)].

There was only one study that reported the percentage of eyes with PE within ±0.50 and ±1.0 D for comparison between Hill-RBF and SRK/T formulae, and hence forest plots were not made according to the Cochrane Collaboration guidelines.[12]

Heterogeneity and I2

Additional file 2 (4.7MB, tif) (B, C, D, and E) shows both substantial as well as statistical heterogeneity on comparison of MAE of Haigis with Hoffer Q, Holladay 1, Holladay 2, and SRK/T. A random-effect model was chosen in these cases. On doing a sensitivity analysis [Additional file 5 (1.7MB, tif) ], it was observed that I2 reduced to 0% in all the four comparisons by omitting the study by Zhao et al.[13] The result was more in favor of Holladay 2, although not statistically significant when the above-mentioned study was excluded from the comparison between Haigis and Holladay 2. However, the results were not altered in the rest of the comparisons.

Publication bias

The funnel plot drawn for comparison between Haigis and Hoffer Q, which included 11 studies, showed that the study by Zhao et al.[13] was outside the funnel [Additional file 6 (399.5KB, tif) ].

Discussion

MAE had long been reported as a parameter for comparing formula accuracy. As suggested by Hoffer et al.,[7] absolute error does not follow normal Gaussian distribution; so reporting and comparing MedAE gives a better idea about formula accuracy. MedAE, by negating the effect of outliers, had an added advantage. The reporting percentage of eyes within ±0.50 and ±1.0 D of target refraction is also recommended as this parameter is most closely related to patient satisfaction after surgery. With this background present, meta-analysis was carried out by comparing all the recommended parameters, that is, MAE, MedAE, and percentage of eyes with PE within ±0.50 and ±1.0 D of target refraction, to find the best-performing formula in short AL eyes.

Studies conducted in various parts of the world have advocated different formulae for eyes with short AL. Hoffer Q, a preferred formula for short eyes, has been reported as the most accurate in the study done by Hoffer[14]; although the study included only 10 short eyes and used ultrasound biometry. Also a study by Aristodemou et al.[15] considered it to give the best refractive outcome in eyes shorter than 21.00 mm; while between 21.00 and 21.49 mm, it was found to be equally good as Holladay 1. It is worthwhile to mention here that MAE was the only parameter compared in this study. Gavin and Hammond[16] considered Hoffer Q as an accurate formula in short eyes, but the comparison was done only against SRK/T. In a study by Day et al.,[17] although Hoffer Q had the lowest MAE on using manufacturer’s constants; all formulae performed equally well after lens constant optimization.

Contrary to this, Haigis has been described as the most accurate formula in short eyes by some authors. Zhao et al.[13] found optimized Haigis formula more accurate than other formulae in eyes with AL less than 21 mm. A study done by Eom et al.[18] found it to be more accurate as compared with Hoffer Q when ACD was less than 2.4 mm. The meta-analysis carried out by Wang et al.[6] has also recommended Haigis as the formula of choice for short eyes. But a general consensus regarding the formula of choice in short eyes is still missing.

In the present analysis, although Barrett Universal II had the lowest MAE and MedAE, the results were not statistically significant when compared with the rest of the formulae. Holladay 1 and Hill-RBF had the highest percentage of eyes within ±0.50 and ±1.0 D of target refraction, respectively. Yet their comparison with the rest of the formulae also did not yield statistically significant results. Our results were in concordance with that of Kane et al.[5] who found no statistical difference between the formulae analyzed, thus making it difficult to choose any one IOL power calculation formula over the other, in eyes with short AL. The study results of Gökce et al.,[19] Shrivastava et al.,[20] and Khatib et al.[21] were in agreement with this.

Over a period of years, there have been continuous developments in the field of IOL power calculation. It is an established fact now that optimization of lens constant has to be mandatorily done for conducting any study on IOL calculation accuracy. In this analysis, Gavin and Hammond[16] used the manufacturer’s constant and found Hoffer Q better, whereas Srivannaboon et al.[22] and Zhao et al.[13] used User Group for Laser Interference Biometry constants. The results of Srivannaboon et al.[22] showed no statistically significant difference between the formulae, whereas Zhao et al.[13] found Haigis formula to be more appropriate. It is interesting to note that in studies using optimized constants, none of the formulae was found to be statistically superior over the other. Second, the method of calculating refractive prediction error (RPE) also influences the results. Although most studies have calculated RPE as postoperative SE minus predicted refraction (PR), there are also a few, which have taken PR minus postoperative SE as RPE. Hence, this fact has to be considered before statistical analysis and comparing formula accuracy. Third, the difference in version and make of the optical biometers also affects the study results. This fact has been clearly established in the study by Cooke and Cooke[23] who showed that, in the subgroup of short eyes, Barrett Universal II achieved the best results when PCI measurements were used, whereas Olsen outperformed other formulae on using OLCR values. The strength of the current meta-analysis is that we have contemplated on all the above-mentioned facts and hence put forth a complete picture by analyzing the recommended parameters of formula accuracy, that is, MAE, MedAE, and percentage of eyes with prediction errors within ±0.50 and ±1.0 D of target refraction rather than only MAE as done by Wang et al.[6]

As an effort to minimize heterogeneity and reduce bias, our meta-analysis excluded studies where optical biometry was not used. The random-effect model was used in cases with substantial as well as statistical heterogeneity. Sensitivity analysis showed that I2 reduced to 0% in all the four pairs of comparison (Haigis with Hoffer Q, Holladay 1, Holladay 2, and SRK/T) by omitting the study of Zhao et al.[13] On analyzing, we found that in a study by Zhao et al.,[13] although AL measurement was done by IOLMaster; keratometry was done manually. The subgroup analysis of the keratometry method showed that the difference is statistically significant (P = 0.03), which was accounted for the source of heterogeneity. It is also a well-known fact that racial differences can affect the accuracy of IOL calculations.[24] The studies included in this meta-analysis are from various regions of the world, thus making our results more generalized rather than pertaining to a particular subcontinent.

Conclusion

Thus, to conclude, in the present meta-analysis, although lowest MAE and MedAE were found for Barrett Universal II and highest percentage of eyes within ±0.50 D and ±1.0 D of target refraction was found for Holladay 1 and Hill-RBF, respectively, none of the formulae was found to be statistically superior over the other in eyes with short AL.

Availability of data and materials

All data analyzed in this study are included in the article and its additional files.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

Additional file 2
IJO-70-740_Suppl1.tif (4.7MB, tif)
Additional file 3
IJO-70-740_Suppl2.tif (4.4MB, tif)
Additional file 4
IJO-70-740_Suppl3.tif (6.8MB, tif)
Additional file 5
IJO-70-740_Suppl4.tif (1.7MB, tif)
Additional file 6
IJO-70-740_Suppl5.tif (399.5KB, tif)

Additional file 1

Modified check-list adapted from the QUADAS-2 tool

Assessment of risk of bias

Domain 1: Patient selection

Question 1: Was a consecutive or random sample of patients enrolled?

  • • ‘yes’ low risk of bias

  • • ‘unclear’ unclear risk of bias

  • • ‘no’ high risk of bias.

Question 2: Did the study avoid inappropriate exclusions?

  • • ‘no’ for < 10% of patients or ‘yes’ low risk of bias

  • • ‘unclear’ unclear risk of bias

  • • ‘no’ for 10% of patients high risk of bias.

Domain 2: Index test

Were the index test result read without knowing the result of the reference standard?

  • • ‘yes’ low risk of bias

  • • ‘unclear’ unclear risk of bias

  • • ’no’ high risk of bias

Domain 3: Reference standard

Could the calculation of refractive prediction error have introduced bias?

  • • Objective Refraction low risk of bias

  • • ‘unclear’ unclear risk of bias

  • • Subjective refraction high risk of bias

Domain 4: Flow and timing

Question 1: Did all patients receive the same reference standard?

  • • ‘no’ but for < 10% of patients or ‘yes’ low risk of bias

  • • ‘unclear’ unclear risk of bias

  • • ‘no’ for 10% of patients high risk of bias.

Question 2: Was there an appropriate interval between the index test and reference standard?

  • • post-operative refraction done two weeks or later after surgery low risk of bias

  • • ‘unclear’ unclear risk of bias

  • • post-operative refraction done within two weeks of surgery high risk of bias.

Assessment of applicability concerns

Domain 1: Patient selection

Is there concern that included patients do not match review question?

  • • ‘no’ low risk of bias

  • • ‘unclear’ unclear risk of bias

  • • ‘yes’ high risk of bias

Domain 2: Index test

Is there concern that index test, its conduct or interpretation differ from review question?

  • • ‘no’ low risk of bias

  • • ‘unclear’ unclear risk of bias

  • • ‘yes’ high risk of bias.

Domain 3: Reference standard

Is there concern that target condition as defined by the reference standard does not match the review question?

  • • ‘no’ low risk of bias

  • • ‘unclear’ unclear risk of bias

  • • ‘yes’ high risk of bias.

Quality assessment of the included studies based on modified QUADAS- 2 tool

Quality assessment of the included studies based on modified QUADAS- 2 tool

Study Risk of bias Applicability concerns


Patient selection Index test Reference standard Flow and timing Patient selection Index test Reference standard
Aristodemou 2011
Cooke 2016
Darcy 2020 ? ?
Day 2012
Eom 2014 ?
Gokce2017 ?
Gavin 2008 ?
Kane 2016 ?
Kane 2017 ?
Khatib 2021 ?
Shrivastava 2018 ?
Srivannaboon 2013
Terzi 2009 ?
Wang 2013 ?
Zhao 2018 ?

☺ Low Risk, ☹ High Risk, ? Unclear Risk

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Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Additional file 2
IJO-70-740_Suppl1.tif (4.7MB, tif)
Additional file 3
IJO-70-740_Suppl2.tif (4.4MB, tif)
Additional file 4
IJO-70-740_Suppl3.tif (6.8MB, tif)
Additional file 5
IJO-70-740_Suppl4.tif (1.7MB, tif)
Additional file 6
IJO-70-740_Suppl5.tif (399.5KB, tif)

Data Availability Statement

All data analyzed in this study are included in the article and its additional files.


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