Corneal biomechanical properties after SMILE versus FLEX ...€¦ · Photorefractive keratectomy (PRK) was the first re-fractive surgery approved by the U.S. Food and Drug Administration
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RESEARCH ARTICLE Open Access
Corneal biomechanical properties afterSMILE versus FLEX, LASIK, LASEK, or PRK: asystematic review and meta-analysisHui Guo1, Seyed M. Hosseini-Moghaddam2 and William Hodge1,3*
Abstract
Background: The aim of this study was to compare the postoperative corneal biomechanical properties betweensmall incision lenticule extraction (SMILE) and other corneal refractive surgeries.
Methods: A systematic review and meta-analysis were conducted. Articles from January 2005, to April 2019, wereidentified searching PubMed, EMBASE, Web of Science, and International Clinical Trials Registry Platform. Studiesthat compared SMILE with other corneal refractive surgeries on adult myopia patients and evaluated cornealbiomechanics were included. Multiple effect sizes in each study were combined. Random-effects model wasconducted in the meta-analysis.
Results: Twenty-two studies were included: 5 randomized controlled trials (RCTs), 9 prospective and 6retrospective cohort studies, and 2 cross-sectional studies. Using the combined effect of corneal hysteresis (CH)and corneal resistance factor (CRF), which were obtained from ocular response analyzer (ORA), the pooledHedges’ g of SMILE versus femtosecond laser-assisted in situ keratomileusis (FS-LASIK) was 0.41 (95% CI, 0.00 to0.81; p = 0.049; I2 = 78%), versus LASIK was 1.31 (95% CI, 0.54 to 2.08; p < 0.001; I2 = 77%), versus femtosecondlenticule extraction (FLEX) was − 0.01 (95% CI, − 0.31 to 0.30; p = 0.972; I2 = 20%), and versus the group ofphotorefractive keratectomy (PRK) and laser-assisted sub-epithelial keratectomy (LASEK) was − 0.26 (95% CI, − 0.67to 0.16; p = 0.230; I2 = 54%). The summary score of Corvis ST (CST) after SMILE was comparable to FS-LASIK/LASIKwith the pooled Hedges’ g = − 0.05 (95% CI, − 0.24 to 0.14; p = 0.612, I2 = 55%).
Conclusions: In terms of preserving corneal biomechanical strength after surgeries, SMILE was superior to eitherFS-LASIK or LASIK, while comparable to FLEX or PRK/LASEK group based on the results from ORA. More studiesare needed to apply CST on evaluating corneal biomechanics after refractive surgeries.
BackgroundMyopia is the most common type of refractive error andhas a 15 to 49% prevalence worldwide [1]. Refractivesurgery is a way to correct refractive error and reducedependence on eyeglasses or contact lenses.Photorefractive keratectomy (PRK) was the first re-
fractive surgery approved by the U.S. Food and DrugAdministration (FDA) in 1996 [2]. After epithelial
removal, an excimer laser is used to remodel the cor-nea [3]. The most frequent complication of PRK ispostoperative pain [4]. Soon after the development ofPRK, laser-assisted in situ keratomileusis (LASIK),which was approved by FDA in 1998, [5] replaced PRKand has been the predominant refractive surgeryworldwide since the 1990s [6–8]. In the LASIKprocedure, a lamellar corneal flap is created with amechanical microkeratome, then the flap is lifted upand excimer laser is used to make an ablation on theunderlying stromal bed. After the ablation is done, thecorneal flap is repositioned on the surface of thecornea [6]. After the femtosecond laser (FS) was
* Correspondence: [email protected] of Epidemiology and Biostatistics, Schulich School of Medicineand Dentistry, Western University, London, ON, Canada3Department of Ophthalmology, Ivey Eye Institute, St. Joseph’s Health CareLondon, 268 Grosvenor St., London, ON, CanadaFull list of author information is available at the end of the article
Guo et al. BMC Ophthalmology (2019) 19:167 https://doi.org/10.1186/s12886-019-1165-3
introduced to the market in 2002, the corneal flap canbe produced by FS laser instead of a microkeratome(FS-LASIK) [9]. Laser-assisted sub-epithelial keratec-tomy (LASEK) is another common type of refractivesurgery firstly published by Massimo Camelin in 1998[10]. Initially, an epithelial flap is detached using a di-luted alcohol solution (usually 18 to 20%) on the cor-nea [8]. The latter surgical procedure is the same asLASIK. In 2008, the efficacy and safety after femtosec-ond lenticule extraction (FLEX) were reported bySekundo et al [11]. In the FLEX procedure, a cornealflap and a lenticule from the corneal stroma under theflap are created by the femtosecond laser. The lenti-cule is removed with forceps [11]. In 2011, a new pro-cedure developed from FLEX named small incisionlentiule extraction (SMILE) was reported by Shah etal., and it was approved by FDA in 2016 [12, 13]. Inthis technique, both the lenticule and side-cut incisionare made using femtosecond laser. Different fromFLEX, the lenticule is removed through a small inci-sion rather than lifting the flap.Corneal ectasia is one of the complications of
refractive surgery [14]. Although its prevalence has
been reported at between only 0.04 and 0.6%, cornealectasia is sight-threatening and may require cornealtransplantation in some severe cases [15, 16]. Cornealbiomechanical property changes can occur before thediagnosis of corneal ectasia, which is characterized bychanges in corneal geometric features [17]. To evalu-ate corneal biomechanics, the most widespread de-vices at the time of writing are ocular responseanalyzer (ORA) and Corvis ST system (CST) [18, 19].Both of them are non-contact tonometry and sharesome common principle: an air pulse is produced andprojects to the cornea, then a set of different variablesare generated related to the cornea deformation [20].ORA uses a Scheimflug image to measure corneal de-
formation and produces two main biomechanical parame-ters. One is corneal hysteresis (CH), which is defined as thepressures (P1 and P2) difference and represents the abilityto absorb the energy from the external force [21]. This abil-ity is primarily related to corneal viscoelastic properties[22]. The other one is corneal resistance factor (CRF),which may indicate the overall corneal resistant ability [23].Corvis ST system applies air pulse on the cornea then ob-
serves and records the movements using a high-speed
Fig. 1 Flow Diagram of Literature Search And Study Selection
Guo et al. BMC Ophthalmology (2019) 19:167 Page 2 of 20
Scheimpflug video camera in real time [7]. The first air puff(A1) causes the cornea to cave inward to the highest con-cavity (HC) and the second application (A2) is produced be-fore it returns outwards to the natural shape. Accordingly,deformation amplitude (vertical deformation length of cor-neal apex), time, and length (horizontal deformation lengthof corneal apex) of A1, A2, and HC are calculated alongwith the velocity of A1 and A2. In some version of CST, de-flection amplitude (deformation amplitude corrected bywhole eye movement) and deflection length (deflectionlength of the cornea compared with the undeformed cor-nea) are provided at A1, A2 and HC [24, 25].With a growing volume of refractive surgeries world-
wide, the aim of this study was to compare SMILE withother corneal refractive surgeries for myopia studying thepostoperative change in corneal biomechanical properties,which are often a precursor of clinically significant ectasia.
MethodsInclusion and exclusion criteriaWe selected the studies which performed cornealrefractive surgery on adult myopia patients. Theintervention was small incision lenticule extraction(SMILE). The comparator was other corneal refractivesurgeries. We focused on the corneal biomechanics mea-sured by ORA or Corvis ST as the outcome. Regardingstudy design, we included randomized controlled trials(RCTs), cohort, case-control or cross-sectional studies.Only studies in English were included.
Literature search and selection strategiesThe following databases were used: PubMed, Embase,and Web of Science. The search was limited to litera-ture published from January 01, 2005 to April 17,2019. Search term “((((((((ora) OR ocular responseanalyzer) OR covis st) OR cst) OR biomechanics) ORbiomechanical)) AND ((lenticule[Title/Abstract]) OR
lenticules[Title/Abstract])” was applied to all theabove databases. Studies that may not be published inthose databases were identified by searchingInternational Clinical Trials Registry Platform withlenticule as the search term. All the identified publica-tions were screened independently by two authors(Hui Guo and Seyed M Hosseini-Moghaddam).Disagreements were reviewed and solved by Hui Guo,who was also responsible for data extraction. The flowchart of study selection is shown in Fig. 1 based onPRISMA guideline [26].
Data extractionData extracted from the identified studies included thefollowing information: name of the first author, year ofpublication, study location, surgery method, parametersof each surgery, sample size, length of follow-up, publi-cation language, patient baseline characteristics [age,spherical equivalent (SE), central corneal thickness(CCT), and intraocular pressure (IOP) before surgery].Regarding corneal biomechanical properties, we ex-tracted the data including measure method, baselinevalue, the last follow-up value, and the change valuefrom the baseline. If the study used ORA to measurecorneal biomechanical properties, only the CH and CRFdata were extracted. All the parameters achieved fromCST were collected. Mean, standard deviation or stand-ard error, and sample size were extracted for the sum-mary measures.
Quality assessmentWe used Downs and Black checklist to assess literaturequality, which includes reporting bias, external validity, in-formation bias, selection bias, and power [27]. There are 27questions for the five sections of assessment and a 32 scoremaximum. We modified the last question as to whetherpower and sample size were calculated and scored it 1 for
Table 1 Example of how to combine effect size and variance of change score of CH and CRF within studies
Guo et al. BMC Ophthalmology (2019) 19:167 Page 4 of 20
“yes” answer and 0 for “no” answer [28]. Then our modifiedDowns and Black score ranges are given four quality levels:excellent (26–28); good (20–25); fair (15–19); and poor(≤14) [29].
Statistical analysisImputation of varianceIn the study of Li et al., [30] the mean of postoperativevalues of CH and CRF were reported with the absenceof standard deviation (SD), standard error (SE), corre-lated p-value, or 95% confidence interval (CI). We im-puted the SD using the average of SD from the otherfour studies in the same subgroup.
Within study calculationWhen standard error (SE) rather than standard deviation(SD) was provided from the included studies, we com-puted SD = SE ×
ffiffiffiffi
Np
[31]. The effect sizes of the bio-mechanical outcomes achieved from ORA and CSTwere calculated with standardized mean difference(Hedges’ g) [32]. Then, we pooled the effect sizes andthe variances of effect sizes within each study using theformula.
Y ¼ 1m
Xm
jY j
� �
ð1Þ
and
var1m
Xm
i¼1Y i
� �
¼ 1m
� �2Xm
i¼1V i þ
X
i≠ j
rijffiffiffiffiffiffi
V i
p
ffiffiffiffiffiffi
V j
p
� �
!
ð2Þ
with Y referring to the effect size, m to the number ofoutcomes, V to the variance of effect size, and r to thecorrelation between outcomes [33].The correlation between CH and CRF was calculated
using the weighted mean of Pearson correlation
results from three studies, and we obtained an r ≈ 0.71[24, 34, 35]. The correlation values among the out-comes from CST were obtained from the study ofBak-Nielsen et al [24]. Among each study reportingCST data, only the parameters which were reportedwith the correlated r were used in the meta-analysis.The composites combined from the effect sizes of CHand CRF were named CH/CRF, and those of parame-ters achieved from CST were named CST outcome inthe following text.Since CH and CRF have a positive correlation, we
combined the effect sizes of CH and CRF directly. Bycontrast, the parameters from CST decreased or in-creased after surgeries [25, 36] and included positive andnegative correlations [24]. We changed the sign ofHedges’ g by multiplying − 1 if the outcomes were nega-tively correlated with A1 time [37]. We also identifiedA1 time decreased after surgeries from previous studies[25, 36]. Examples of the combination of effect size andvariance is shown in Table 1. If the study provides bothpostoperative and change values (postoperative valuessubtract preoperative values), the change values wereused in the meta-analyses.
Meta-analysisBoth the CH/CRF and CST outcomes were pooledamong studies using Hedges’g. Random-effects modelwas selected because heterogeneity was expected due todifferent population and treatment regimens.Heterogeneity among studies was evaluated by χ 2 testand quantified using the I2 statistics [42, 43]. All re-ported p-values are 2-sided. A p-value equal to or lessthan 0.05 was considered statistically significant.Comprehensive Meta-analysis Software version 3.3.070was used for synthesizing the outcomes among studies.
Table 2 Baseline characters of studies (Continued)First author Publication
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Subgroup analysisThe meta-analysis for FS-LASIK as the comparatorwas divided with two subgroups based on whetherfollow-up time was longer than 12 months. LASEKand PRK was two separated subgroups in the com-parison with SMILE. FS-LASIK and LASIK was ana-lysed as two subgroups in the CST meta-analysiscomparing SMILE and FS-LASIK/LASIK. Subgroupanalyses for RCT or observational studies were con-ducted if applicable.
ResultsStudy identification and study characteristicsUsing our search strategy, 1488 articles were identifiedwith database searching and another 60 were identi-fied in International Clinical Trials Registry Platform.After duplications were removed, 900 articles werereviewed for eligibility (Fig. 1). We included 22 studiesin this review. Notably, we excluded one study com-paring micro incision lenticule extraction and SMILE,because they are basically the same type of surgeryusing different incision length [44].
Five studies were RCTs, 9 were prospective cohortstudies, 6 were retrospective cohort studies, and 2were cross-sectional studies. FS-LASIK/LASIK wasconducted in 15 studies, FLEX was in 3 studies,LASEK was in four studies, and PRK was included in1 study. The length of follow-up was between 3 to 6months in 17 studies. Four studies followed patientsequal to or longer than 12 months. One study ob-served patients until 1 month postoperatively. Detailsof characters of the studies are provided in Table 2.
Surgical parametersSMILESeventeen studies reported a cap thickness between 100 to120 μ m [25, 30, 39–41, 45, 47–53, 55, 56, 58, 59]. Onlyone study reported a 90 μ m thickness cap [36]. The capdiameter was between 7.2 to 8mm in 16 studies, [25, 30,36, 38, 41, 45–51, 53, 58–60] and the diameter of the op-tical zone was between 6 to 7mm in 19 studies [25, 30, 36,38–41, 45, 47–49, 51–56, 58, 59]. Twelve studies were
performed with an energy between 115 to 190 nJ [30, 36,38, 40, 41, 45, 47, 49–51, 53, 54, 58].
LASIKAll the 14 studies [25, 30, 38–41, 47, 48, 50, 52, 55–57, 59] performed FS-LASIK except for the study ofOsman et al. and Elmohamady et al., [36, 57] in whichmicrokeratome is used for the flap creation. The flapthickness was between 90 to 110 μm among the 14studies which performed LASIK [25, 30, 36, 39–41, 47,48, 50, 52, 55–57, 59]. Eleven studies reported a flapdiameter of 7.3 to 9 mm, [25, 30, 36, 38–40, 47, 48, 50,52, 56] and the optical zone was between 5.75 to 6.75mm in another 11 studies [25, 36, 38–41, 47, 48, 52,55, 56]. The energy was described in 6 studies with110 to 175 nJ [30, 38, 41, 47, 50, 52].
FLEXFour studies included FLEX as a comparison treatment[45, 46, 48, 49]. In those four studies, the flap thicknesswas between 100 to 120 μ m with 7.5 to 7.9 mm indiameter and the diameter of lenticule was between 6 to6.5 mm. Energy setting was reported in two studies with125 to 170 nJ [45, 49].
LASEKTwo of the four studies which involved LASEK as thecomparator reported an 8.5 mm flap diameter in 2 stud-ies [50, 53] and optical zone was 6.25 to 6.75 mm in 1study [58] with and the energy for ablation of 150 nJ inall 3 studies [50, 53, 58].
PRKOne study performed PRK as comparative surgery [54].The optical zone was 6.5 mm. Following the PRK sur-gery, 0.02% mitomycin C was applied on the eyes.
ORA and CST outcomeThe data from ORA and CST measurement preparedfor meta-analysis are shown in Table 3 and Table 4.
Table 3 Data from ocular response analyzer (ORA) measurement (Continued)
First author Procedure N(eye)at lastfollow-up
PreoperativeCH (mmHg)
PostoperativeCH (mmHg)
CH change(mmHg)
PreoperativeCRF (mmHg)
PostoperativeCRF (mmHg)
CRF change(mmHg)
Mean ± SD Mean ± SD Mean ± SD Mean ± SD Mean ± SD Mean ± SD
Abbreviations: CH corneal hysteresis, CRF corneal resistance factor, FLEX femtosecond lenticule extraction, FS femtosecond Laser, LASEK laser-assisted subepithelialkeratectomy, LASIK laser-Assisted in situ keratomileusis, N/A not available, PRK photorefractive keratectomy, SMILE small incision lenticule extraction. a the value ofSD was imputed from the other four studies in the same subgroup. b The number of patients at the last follow-up visit differed from the number at baseline
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Meta-analyses for ORA outcomesIn the studies with FS-LASIK as the comparator, 10studies which provided postoperative or change value(postoperative value – preoperative value) of CH andCRF were included in the meta-analysis (Fig. 2). In thesubgroup with follow-up less than 12 months, the dif-ference of Hedges’ g between two groups was 0.24(95% CI, − 0.06 to 0.53; p = 0.117; I2 = 25%). The differ-ence in over 12-month follow-up subgroup was 0.66(95% CI, 0.19 to 0.13; p = 0.006; I2 = 92%). The overalldifference was 0.41 (95% CI, 0.00 to 0.81; p = 0.049;
I2 = 78%). Since there is only one RCT in this meta-analysis, we conducted a subgroup analysis with obser-vational studies only, the over-all effect size signifi-cantly favored SMILE.(Additional file 1) Compared toLASIK, SMILE also had a higher postoperative CH/CRF value with Hedges’ g = 1.31 (95% CI, 0.54 to 2.08,p = 0.001; I2 = 77%) (Fig. 3).Three studies reported the CH and CRF outcomes com-
paring SMILE and FLEX. The effect size was almost com-parable to SMILE with Hedges’ g =− 0.01 (95% CI, − 0.31 to0.30; p= 0.972; I2 = 20%) (Fig. 4). In the subgroup analysis
Fig. 2 Forest Plot of Corneal Hysteresis/Corneal Resistance Factor (CH/CRF) for Studies Comparing Small Incision Lenticule Extraction (SMILE) withFemtosecond Laser-assisted in Situ Keratomileusis (FS-LASIK)
Table 4 Postoperative outcomes of Corvis ST (CST)
First author Iben Bach Pedersen [48] Yang Shen [50] Sherivin Mir Mohi Sefat[25]
Abbreviations: A application, FS femtosecond laser, HC highest concavity, LASEK laser-assisted subepithelial keratectomy, LASIK laser-assisted in situ keratomileusis,N/A not available, SD standard deviation, SMILE small incision lenticule extraction. Specifically, we chose the subgroup data created in the study of Seafat et al. asthis subgroup had a balance of spherical equivalent at baseline between the two intervention groups. Only one study provided the preoperative data of CSTmeasurement. Therefore, we presented only the postoperative outcomes in this table
Guo et al. BMC Ophthalmology (2019) 19:167 Page 8 of 20
which included only the RCT studies of Vetergaard et al.and Kamiya et al., the difference of Hedges’ g was − 0.04(95% CI, − 0.54 to 0.47; p= 0.882; I2 = 55%). In 2019,Vestergaard et al. used the data from the same cohort to ob-tain the new parameters of ORA [46]. No differences be-tween SMILE and FLEX were found in the majority of 37outcomes except that w11 slightly favoured FLEX.One study performed PRK, and 3 performed LASEK
with ORA as the postoperative measurement. Since bothPRK and LASEK remove corneal epithelium before appli-cation laser on the corneal stromal bed, and the numberof the studies was too small, we pooled the effect size ofthese two surgeries as to compare with SMILE. Althoughthe difference was not significant, the result showedLASEK/PRK group had a less decrease of CH/CRF aftersurgery than SMILE with Hedges’ g = − 0.26 (95% CI, −0.67 to 0.16; p = 0.230; I2 = 54%). Both subgroup outcomesand overall outcomes are also provided in Fig. 5.
Meta-analyses for CST outcomesFive studies reported corneal biomechanical outcomeswith CST after FS-LASIK or LASIK. The studies and pa-rameters that were used in the meta-analysis are shown inTable 4. The difference between SMILE and FS-LASIKwas not significant with Hedges’ g = − 0.05 (95% CI, − 0.24to 0.14; p = 0.612, I2 = 55%) (Fig. 6). Shetty et al. foundboth linear corneal stiffness and mean corneal stiffness ob-tained from CST were comparable between SMILE andFS-LASIK [56]. Since the parameters used in this studydiffered from the other four studies, we did not include itin the meta-analysis.The study of Pedersen et al. [48] reported the CST
outcome longer than 12 months after SMILE or FLEX.They found that eyes after both SMILE and FLEX had asignificantly lower A1 deflection length compared withhealthy eyes. The difference between SMILE and FLEXwas not significant in HC deformation amplitude, HC
Fig. 3 Forest Plot of Corneal Hysteresis/Corneal Resistance Factor (CH/CRF) for Studies Comparing Small Incision Lenticule Extraction (SMILE) withLaser-assisted in Situ Keratomileusis (LASIK)
Fig. 4 Forest Plot of Corneal Hysteresis/Corneal Resistance Factor (CH/CRF) for Studies Comparing Small Incision Lenticule Extraction (SMILE) withFemtosecond Lenticule Extraction (FLEX)
Guo et al. BMC Ophthalmology (2019) 19:167 Page 9 of 20
radius, HC deflection length, HC time, A1 time, A1 de-flection length, and A2 time.Shen et al. [50] included LASEK as the comparator. At
the 3-month postoperative follow-up, the difference be-tween SMILE and LASEK was not significant in A1time, HC time, A2 time, A1 length, A2 length, peak dis-tance, A1 velocity, A2 velocity, radius, or deformationamplitude.
Study quality assessmentIn the 22 articles, the quality score ranged from 15 to23. Eight were within good scale, and 14 were fair. Detailof quality assessment results is illustrated in Table 5.
Sensitivity analysisWe removed two studies from the meta-analysis for com-paring SMILE and FS-LASIK. One is the study of Li et al.because the SD in this study was imputed [30]. Anotherone is the study of Elmohamady et al. since the effect sizeof the study was much higher than the rest of the studies.In this meta-analysis, the outcome was significantly
favoured SMILE with Hedges’ g = 0.25 (95% CI, 0.007 to0.08; p = 0.003, I2 = 28%) (Additional file 2).
DiscussionTo our best knowledge, this is the first systematic reviewand meta-analysis comparing SMILE with all the othercorneal refractive surgeries in corneal biomechanicalproperties. We included 22 articles in this review with19 articles in the meta-analyses.According to the CH and CRF value measured with
ORA, corneal biomechanical strength was preservedsignificantly better after SMILE than either FS-LASIKor LASIK. After conducting a sensitivity analysis, theresult was robust after removing the possible biaseddata. Similarly, Yan et al. performed a meta-analysiswith five studies, which are included in our meta-ana-lysis, and reported a significant larger CH and CRFvalue after SMILE than FS-LASIK [62]. Furthermore,we found the difference was greater after postopera-tive 12 months. This might indicate wound healing isbetter after SMLE. By contrast, we did not find a sig-nificant difference between SMILE and FS-LASIK in
Fig. 5 Forest Plot of Corneal Hysteresis/Corneal Resistance Factor (CH/CRF) for Studies Comparing Small Incision Lenticule Extraction (SMILE) withLaser-assisted Subepithelial Keratectomy (LASEK) /Photorefractive Keratectomy (PRK) Group
Fig. 6 Forest Plot of Postoperative Corvis ST System (CST) Outcome for Studies Comparing Small Incision Lenticule Extraction (SMILE) withFemtosecond Laser-assisted in Situ Keratomileusis (FS-LASIK)/Laser-assisted in Situ Keratomileusis (LASIK) Group
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Table
5Qualitychecklist
No.
ofqu
estio
nQuestion
Answer
Score
And
ersH.
Vestergaard
[45,46]
Danyang
Wang
[47]
Iben
Bach
Pede
rsen
[48]
Kazutaka
Kamiya
[49]
Di
Wu
[39]
Alper
Agca
[38]
Yang
Shen
[50]
Rui
Dou
[51]
Shrvin
Mir
Moh
iSefat
[25]
Wen
jing
Wu[40]
Hua
Li [30]
Ihab
Moh
amed
Osm
an[36]
Bing
jieWang
[41]
Lei
Xia
[52]
Minjie
Che
n[53]
Yusuf
Yidirim
[54]
Jun
Zhang
[55]
Rohit
Shetty
[56]
Moh
amed
Nagy
Elmoh
amady
[57]
Manrong
Yu[61]
EsraaEl-
Mayah
[59]
1Isthehypo
thesis
/aim
/objective
ofthestud
yclearly
describ
ed?
YES
1X
XX
XX
XX
XX
XX
XX
XX
XX
XX
XX
NO
0
2Are
themain
outcom
esto
bemeasuredclearly
describ
edin
the
Introd
uctio
nor
Metho
dssection?
YES
1X
XX
XX
XX
XX
XX
XX
XX
XX
XX
XX
NO
0
3Are
the
characteristicsof
thepatients
includ
edin
the
stud
yclearly
describ
ed?
YES
1X
XX
XX
XX
XX
XX
XX
XX
XX
XX
X
NO
0X
4Are
the
interven
tions
ofinterestclearly
describ
ed?
YES
1X
XX
XX
XX
XX
XX
XX
XX
XX
XX
XX
NO
0
5Are
the
distrib
utions
ofprincipal
confou
ndersin
each
grou
pof
subjectsto
becompared
clearly
describ
ed?
YES
2X
XX
XX
XX
XX
XX
XX
XX
XX
PARTIALLY
1X
XX
X
NO
0
6Are
themain
finding
sof
the
stud
yclearly
describ
ed?
YES
1X
XX
XX
XX
XX
XX
XX
XX
XX
XX
X
NO
0X
7Doe
sthestud
yprovide
estim
ates
ofthe
rand
omvariabilityin
the
data
forthe
mainou
tcom
es?
YES
1X
XX
XX
XX
XX
XX
XX
XX
XX
XX
X
NO
0X
8Haveall
YES
1X
XX
XX
XX
XX
XX
XX
Guo et al. BMC Ophthalmology (2019) 19:167 Page 11 of 20
Table
5Qualitychecklist(Con
tinued)
No.
ofqu
estio
nQuestion
Answer
Score
And
ersH.
Vestergaard
[45,46]
Danyang
Wang
[47]
Iben
Bach
Pede
rsen
[48]
Kazutaka
Kamiya
[49]
Di
Wu
[39]
Alper
Agca
[38]
Yang
Shen
[50]
Rui
Dou
[51]
Shrvin
Mir
Moh
iSefat
[25]
Wen
jing
Wu[40]
Hua
Li [30]
Ihab
Moh
amed
Osm
an[36]
Bing
jieWang
[41]
Lei
Xia
[52]
Minjie
Che
n[53]
Yusuf
Yidirim
[54]
Jun
Zhang
[55]
Rohit
Shetty
[56]
Moh
amed
Nagy
Elmoh
amady
[57]
Manrong
Yu[61]
EsraaEl-
Mayah
[59]
impo
rtant
adverseeven
tsthat
may
bea
conseq
uenceof
theinterven
tion
been
repo
rted
?
NO
0X
XX
XX
XX
X
9Havethe
characteristicsof
patientslostto
follow-upbe
ende
scrib
ed?
YES
1X
XX
XX
XX
XX
XX
XX
XX
NO
0X
XX
XX
X
10Haveactual
prob
ability
values
been
repo
rted
forthe
mainou
tcom
esexcept
whe
retheprob
ability
valueisless
than
0.001?
YES
1X
XX
XX
XX
XX
XX
XX
XX
XX
X
NO
0X
XX
11Werethe
subjectsasked
toparticipatein
thestud
yrepresen
tativeof
theen
tire
popu
latio
nfro
mwhich
they
were
recruited?
YES
1X
XX
XX
X
NO
0
UNABLE
TO DETERMINE
0X
XX
XX
XX
XX
XX
XX
XX
12Werethose
subjectswho
wereprep
ared
toparticipate
represen
tativeof
theen
tire
popu
latio
nfro
mwhich
they
were
recruited?
YES
1X
NO
0X
XX
UNABLE
TO DETERMINE
0X
XX
XX
XX
XX
XX
XX
XX
XX
13Werethestaff,
places,and
facilitieswhe
rethepatients
YES
1X
XX
XX
XX
XX
XX
XX
X
Guo et al. BMC Ophthalmology (2019) 19:167 Page 12 of 20
Table
5Qualitychecklist(Con
tinued)
No.
ofqu
estio
nQuestion
Answer
Score
And
ersH.
Vestergaard
[45,46]
Danyang
Wang
[47]
Iben
Bach
Pede
rsen
[48]
Kazutaka
Kamiya
[49]
Di
Wu
[39]
Alper
Agca
[38]
Yang
Shen
[50]
Rui
Dou
[51]
Shrvin
Mir
Moh
iSefat
[25]
Wen
jing
Wu[40]
Hua
Li [30]
Ihab
Moh
amed
Osm
an[36]
Bing
jieWang
[41]
Lei
Xia
[52]
Minjie
Che
n[53]
Yusuf
Yidirim
[54]
Jun
Zhang
[55]
Rohit
Shetty
[56]
Moh
amed
Nagy
Elmoh
amady
[57]
Manrong
Yu[61]
EsraaEl-
Mayah
[59]
weretreated,
represen
tativeof
thetreatm
ent
themajority
ofpatientsreceive?
NO
0X
UNABLE
TO DETERMINE
0X
XX
XX
X
14Was
anattempt
madeto
blind
stud
ysubjectsto
theinterven
tion
they
have
received
?
YES
1
NO
0X
XX
XX
XX
UNABLE
TO DETERMINE
0X
XX
XX
XX
XX
XX
XX
X
15Was
anattempt
madeto
blind
thosemeasurin
gthemain
outcom
esof
the
interven
tion?
YES
1
NO
0X
XX
X
UNABLE
TO DETERMINE
0X
XX
XX
XX
XX
XX
XX
XX
XX
16Ifanyof
the
results
ofthe
stud
ywere
basedon
“data
dred
ging
”,was
thismadeclear?
YES
1X
XX
XX
XX
XX
XX
NO
0X
XX
XX
XX
XX
UNABLE
TO DETERMINE
0X
17In
trialsand
coho
rtstud
ies,
dotheanalyses
adjustfor
different
leng
ths
offollow-upof
patients,or
incase-con
trol
stud
ies,isthe
timepe
riod
betw
eenthe
interven
tionand
outcom
ethe
sameforcases
YES
1X
XX
XX
XX
XX
XX
XX
XX
Guo et al. BMC Ophthalmology (2019) 19:167 Page 13 of 20
Table
5Qualitychecklist(Con
tinued)
No.
ofqu
estio
nQuestion
Answer
Score
And
ersH.
Vestergaard
[45,46]
Danyang
Wang
[47]
Iben
Bach
Pede
rsen
[48]
Kazutaka
Kamiya
[49]
Di
Wu
[39]
Alper
Agca
[38]
Yang
Shen
[50]
Rui
Dou
[51]
Shrvin
Mir
Moh
iSefat
[25]
Wen
jing
Wu[40]
Hua
Li [30]
Ihab
Moh
amed
Osm
an[36]
Bing
jieWang
[41]
Lei
Xia
[52]
Minjie
Che
n[53]
Yusuf
Yidirim
[54]
Jun
Zhang
[55]
Rohit
Shetty
[56]
Moh
amed
Nagy
Elmoh
amady
[57]
Manrong
Yu[61]
EsraaEl-
Mayah
[59]
andcontrols?
NO
0
UNABLE
TO DETERMINE
0X
XX
XX
X
18Werethe
statisticaltests
used
toasses
themain
outcom
esapprop
riate?
YES
1X
XX
XX
XX
XX
XX
XX
XX
XX
NO
0X
XX
X
UNABLE
TO DETERMINE
0
19Was
compliance
with
the
inerventions
reliable?
YES
1X
XX
XX
XX
XX
XX
XX
XX
XX
XX
XX
NO
0
UNABLE
TO DETERMINE
0
20Werethemain
outcom
emeasuresused
accurate
(valid
andreliable)?
YES
1X
XX
XX
XX
XX
XX
XX
XX
XX
XX
XX
NO
0
UNABLE
TO DETERMINE
0
21Werethe
patientsin
different
interven
tion
grou
ps(trials
andcoho
rtstud
ies)or
were
thecasesand
controls(case-
controlstudies)
recruitedfro
mthesame
popu
latio
n?
YES
1X
XX
XX
XX
XX
XX
XX
XX
XX
XX
NO
0
UNABLE
TO DETERMINE
0X
X
22Werestud
ysubjectsin
YES
1X
XX
XX
XX
XX
XX
XX
XX
XX
XX
Guo et al. BMC Ophthalmology (2019) 19:167 Page 14 of 20
Table
5Qualitychecklist(Con
tinued)
No.
ofqu
estio
nQuestion
Answer
Score
And
ersH.
Vestergaard
[45,46]
Danyang
Wang
[47]
Iben
Bach
Pede
rsen
[48]
Kazutaka
Kamiya
[49]
Di
Wu
[39]
Alper
Agca
[38]
Yang
Shen
[50]
Rui
Dou
[51]
Shrvin
Mir
Moh
iSefat
[25]
Wen
jing
Wu[40]
Hua
Li [30]
Ihab
Moh
amed
Osm
an[36]
Bing
jieWang
[41]
Lei
Xia
[52]
Minjie
Che
n[53]
Yusuf
Yidirim
[54]
Jun
Zhang
[55]
Rohit
Shetty
[56]
Moh
amed
Nagy
Elmoh
amady
[57]
Manrong
Yu[61]
EsraaEl-
Mayah
[59]
different
interven
tion
grou
ps(trials
andcoho
rtstud
ies)or
were
thecasesand
controls(case-
controlstudies)
recruitedover
thesamepe
riod
oftim
e?
NO
0
UNABLE
TO DETERMINE
0X
X
23Werestud
ysubjects
rand
omised
tointerven
tion
grou
ps?
YES
1X
XX
NO
0X
XX
XX
XX
UNABLE
TO DETERMINE
0X
XX
XX
XX
XX
XX
24Was
the
rand
omised
interven
tion
assign
men
tconcealedfro
mbo
thpatients
andhe
alth
care
staffun
tilrecruitm
entwas
completeand
irrevocable?
YES
1X
NO
0X
XX
XX
XX
XX
XX
UNABLE
TO DETERMINE
0X
XX
XX
XX
XX
25Was
there
adeq
uate
adjustmen
tfor
confou
ndingin
theanalyses
from
which
the
mainfinding
sweredraw
n?
YES
1X
XX
XX
XX
XX
X
NO
0X
XX
XX
XX
XX
X
UNABLE
TO DETERMINE
0X
26Werelosses
ofpatientsto
YES
1X
XX
XX
XX
XX
XX
X
Guo et al. BMC Ophthalmology (2019) 19:167 Page 15 of 20
Table
5Qualitychecklist(Con
tinued)
No.
ofqu
estio
nQuestion
Answer
Score
And
ersH.
Vestergaard
[45,46]
Danyang
Wang
[47]
Iben
Bach
Pede
rsen
[48]
Kazutaka
Kamiya
[49]
Di
Wu
[39]
Alper
Agca
[38]
Yang
Shen
[50]
Rui
Dou
[51]
Shrvin
Mir
Moh
iSefat
[25]
Wen
jing
Wu[40]
Hua
Li [30]
Ihab
Moh
amed
Osm
an[36]
Bing
jieWang
[41]
Lei
Xia
[52]
Minjie
Che
n[53]
Yusuf
Yidirim
[54]
Jun
Zhang
[55]
Rohit
Shetty
[56]
Moh
amed
Nagy
Elmoh
amady
[57]
Manrong
Yu[61]
EsraaEl-
Mayah
[59]
follow-uptaken
into
accoun
t?
NO
0X
XX
UNABLE
TO DETERMINE
0X
XX
XX
X
27Did
thestud
yhave
sufficien
tpo
wer
tode
tect
aclinically
impo
rtanteffect
whe
rethe
prob
ability
value
foradifference
beingdu
eto
chance
isless
than
5%
YES
1X
XX
XX
NO
0X
XX
XX
XX
XX
XX
XX
XX
Totalscores
2820
1722
1718
2219
1815
2015
2019
1715
1618
2316
2117
excellent
(26–
28);go
od(20–
25);fair(15–19);
poor
(≤14)
Goo
dFair
Goo
dFair
Fair
Goo
dFair
Fair
Fair
Goo
dFair
Goo
dFair
Fair
Fair
Fair
Fair
Goo
dFair
Goo
dFair
Guo et al. BMC Ophthalmology (2019) 19:167 Page 16 of 20
the postoperative outcomes from CST. The conclusionbased on CST agreed with the majority of the studiesin this review [25, 48, 50, 56]. The study of Osman etal. found A1 time, A2 time, A2 length, HC time HCradius, HC peak distance, and deformation amplitudewere significantly different between SMILE and LASIKgroup [36]. It is the only divergent study which used amicrokeratome to create a corneal flap rather thanfemtosecond laser used in the other three studies. Itmight be the reason for the discrepancy of theconclusion.In our meta-analysis, the corneal biomechanics was
not statistically different between SMILE and FLEX. Thisconclusion agreed with the meta-analysis of Ma et al[63]. They used postoperative CH and CRF value in dif-ferent subgroup analysis and pooled the results of thetwo subgroups. The difference between SMILE andFLEX was 0.08mmHg (95% CI, − 0.17 to 0.33; p = 0.54).We found only one study comparing SMILE with FLEXin CST outcomes [48]. The study did not find a signifi-cant difference in the postoperative values between thetwo surgeries.The CH/CRF value was greater after PRK/LASEK
compared with SMILE although the difference did notreach a significance. In the study of Yildirim et al., theamount of stromal tissue removed by SMILE was signifi-cantly greater than PRK [54]. This may bias the resultbecause of the greater lenticule thickness or ablationdepth the more decrease of CH and CRF value after re-fractive surgeries [51, 54]. By contrast, Dou et al. did notfind a significant difference between SMILE and LASEKin CH or CRF decrease [51]. However, the decrease ofCH or CRF per unit of removed tissue was significantlysmaller after SMILE than LASEK. We identified onlyone study comparing SMILE with LASEK in CST. Nostatistically significant difference between the two treat-ments was found in this study [50].
Explanations for the outcomeIt has been hypothesized by many authors that SMILE issuperior to LASIK in preserving the biomechanicalproperties of corneas because of its flapless procedure[39, 47, 48, 52]. The difference between flap versus flap-less procedure was also found in the study of Kamiya etal. finding that CH and CRF had a significantly greaterdecrease after LASIK than after PRK [64].A vitro experimental study found that the vertical side
cuts of corneal lamellae contributed more of the loss ofstructural integrity than horizontal delamination inci-sions [65]. This can explain why flap procedure is morelikely to lower corneal biomechanics.However, we found that although SMILE was better
than LASIK in the outcome from ORA, SMILE wascomparable to FLEX, which also included a flap-creation
procedure. This may be explained by: first, the numberof studies was too small to identify the difference be-tween SMILE and FLEX; second, CH and CRF were cor-related to the flap thickness.It is possible that the thickness of the flap, which was
created in the anterior lamellae was responsible for thesignificant decrease of CH and CRF value. In the in-cluded studies, the flap thickness in the LASIK groupwas between 90 to 110 μm and it was between 100 to120 μ m in FLEX group. A laboratory study found thatthe anterior part of the corneal stroma (100 to 120 μ m)was rigid due to the tightly interwoven anterior lamellae[66]. This physiological property of cornea was approvedin the vivo study from Wang et al [47]. They found thatthe significantly lower CH and CRF value after LASIKthan SMILE was only identified in high myopia sub-group while not in low myopia subgroup. They alsopointed out that the corneal flap was thinner in highmyopia patients than low myopia patients treated withLASIK. It indicated that the more anterior part of stro-mal lamellae was affected, the more biomechanicalstrength was weakened.
LimitationsThere were some limitations in our study. (1) Thenumber of studies was small, especially of the studiesperforming FLEX, PRK, or LASEK as comparators. (2)Only five studies in this review were RCT design.Confounders were possible to be introduced in othertypes of studies and bias the outcomes. (3) All themeta-analysis included no more than 10 studies, whichmade the test of publication bias problematic [67]. (4)The way in which we used to synthesize effect size ofCH and CRF in the meta-analysis made it impossibleto compare the two parameters in the efficacy of de-tecting the corneal biomechanical change. However,ignoring the correlation between multiple outcomesand treating the outcomes as a unit separately in themeta-analysis will overestimate the precision of thesummary effects [33]. (5) High heterogeneity acrossstudies made the mean estimate less certain in this re-view. It may be caused by the diverse characteristics ofpatients and different study design across studies.Meta-regression analysis may be the best way to ad-dress this problem. However, this method might notbe applicable to such a small number of study [37].Alternatively, we did subgroup analyses to reduce thispossible bias.
PerspectiveTo evaluate the impact of SMILE on corneal biomech-anical properties compared with other corneal refractivesurgeries, studies could be done based on several consid-erations. Initially, RCT would be the best study design
Guo et al. BMC Ophthalmology (2019) 19:167 Page 17 of 20
for this scientific question, and blinding for measure-ment is necessary. Second, it is better to do subgroupanalysis by dividing patients into low myopia and highmyopia groups. Furthermore, if available, both ORA andCST measurements can be performed to evaluate thecorneal biomechanical change and compare the out-comes. Longer follow-up time (more than 6months) isnecessary for better evaluation of the efficacy and safetyof refractive surgery. Adverse events should be reportedwhen publishing the study.
ConclusionsOur results from ORA indicated that SMILE was superiorto FS-LASIK/LASIK in preserving corneal biomechanicalstrength after surgery. SMILE versus FLEX, PRK, or LASEKregarding corneal biomechanical properties were studied inonly a few trials. The biomechanical outcomes betweenSMILE and FLEX were comparable. Although no signifi-cant difference was found, PRK/LASEK group showed bet-ter outcomes than SMILE. CST was not sensitive indetecting the difference of postoperative corneal biomech-anical properties between surgeries in our meta-analysis.
Additional files
Additional file 1: Forest Plot of Corneal Hysteresis/Corneal ResistanceFactor (CH/CRF) for Observational Studies Comparing Small IncisionLenticule Extraction (SMILE) with Femtosecond Laser-assisted in SituKeratomileusis (FS-LASIK). (PDF 54 kb)
Additional file 2: Forest Plot of Corneal Hysteresis/Corneal ResistanceFactor (CH/CRF) for Studies Comparing Small Incision Lenticule Extraction(SMILE) with Femtosecond Laserassisted in Situ Keratomileusis (FS-LASIK)from a Sensitivity Analysis. (PDF 53 kb)
AcknowledgementsI would thank for the tutorial of systematic review and meta-analysis fromDr. Monali Madhukar Malvankar (PhD) (Departments of Ophthalmology,Physiology and Health Sciences, The University of Western Ontario, London,Canada) and Rohin Jayaram Krishnan (Department of Epidemiology andBiostatistics, Schulich School of Medicine and Dentistry, The University ofWestern Ontario, London, Canada).
Authors’ contributionsHG was responsible for study design, literature search and screening as wellas data analyses and interpretation. SMH was responsible for literaturescreening and data analyses. WH was a major contributor of study designand writing. All authors read and approved the final manuscript.
FundingThe authors have no funding to disclose.
Availability of data and materialsData used in the analyses can be found in the published article, which werelisted in the references of this manuscript.
Ethics approval and consent to participateNot applicable.
Consent for publicationNot applicable.
Competing interestsThe authors declare that they have no competing interests.
Author details1Department of Epidemiology and Biostatistics, Schulich School of Medicineand Dentistry, Western University, London, ON, Canada. 2Toronto GeneralHospital, University of Toronto, Toronto, ON, Canada. 3Department ofOphthalmology, Ivey Eye Institute, St. Joseph’s Health Care London, 268Grosvenor St., London, ON, Canada.
Received: 29 January 2019 Accepted: 12 July 2019
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