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ORIGINAL RESEARCH article

Front. Public Health, 17 March 2022
Sec. Children and Health

A Retrospective Study on the Eye-Related Quality of Life, Functional Vision, and Their Determinants Among Children Following Congenital and Developmental Cataracts Surgery and Its Impact on Their Families Using the PedEyeQ

\nSiyi Gu,,&#x;Siyi Gu1,2,3Yiwen Hu,,&#x;Yiwen Hu1,2,3Yinying Zhao,,Yinying Zhao1,2,3Lulu Chen,,Lulu Chen1,2,3Weijie Sun,,Weijie Sun1,2,3Pingjun Chang,,Pingjun Chang1,2,3Dandan Wang,,Dandan Wang1,2,3Yune Zhao,,
Yune Zhao1,2,3*
  • 1Eye Hospital and School of Ophthalmology and Optometry, Wenzhou Medical University, Wenzhou, China
  • 2National Clinical Research Center for Ocular Diseases, Wenzhou, China
  • 3Eye Hospital of Wenzhou Medical University Hangzhou Branch, Hangzhou, China

Objectives: To evaluate the eye-related quality of life (ER-QOL), functional vision, and their determinants in children following congenital and developmental cataract surgery, as the impact on their families, using the Pediatric Eye Questionnaire (PedEyeQ).

Materials and Methods: This was a retrospective cross-sectional study involving 107 children (aged 0–11 years) with congenital and developmental cataracts who had undergone surgery, as well as 59 visually healthy controls (aged 0–11 years). One parent for each child completed either the Proxy 0–4 PedEyeQ, the Proxy 5–11 PedEyeQ, or the Parent PedEyeQ, depending on their child's age. Mann-Whitney U and Kruskal-Wallis tests were then conducted to compare the differences between groups and to analyze their determinants.

Results: PedEyeQ scores were found to be lower in postoperative children with congenital and developmental cataracts compared with the control group across all study domains. The PedEyeQ Proxy 0 to 4 years' greatest mean difference was 27 points worse in the Functional Vision domain (95% CI −34 to −19; p < 0.001). We also found that the occurrence of nystagmus (p < 0.005) and strabismus (p < 0.005) were the major factors affecting participants' functional vision. The PedEyeQ Proxy 5 to 11 years' greatest mean difference was 23 points worse in this same domain (95% CI −30 to −15; p < 0.001), with nystagmus (p < 0.05) being the main determinant herein. Parent PedEyeQ 0 to 4 years' greatest difference was 46 points worse on the Worry about their Child's Eye Condition domain (95% CI −57 to −36; p < 0.001). Similarly, parents of children with ophthalmologic abnormalities, including nystagmus (p < 0.001) and strabismus (p < 0.05), were significantly more worried about their children's eye condition. Parent PedEyeQ 5 to 11 years' greatest difference was also found to be 30 points worse on the Worry about their Child's Eye Condition domain (95% CI −43 to −17; p < 0.005).

Conclusions: Children who have undergone congenital and developmental cataract surgery experience a lower quality of life and reduced functional vision. Their families are also significantly and adversely affected herein. Thus, more attention is needed on these groups, with more focused measures being administered to both children and their families.

Introduction

The incidence of congenital and developmental cataracts is 0.4–8.5 per 10,000 children, and may actually be higher according to some research (1). Furthermore, it is the leading cause of childhood blindness, with the percentage of pediatric cataracts causing childhood blindness being 12–39% (2). Additionally, there is a long-term risk of postoperative complications for this condition. Furthermore, long-term treatment, involving follow-ups and rehabilitation post-surgery, is also necessary. Thus, pediatric cataracts can cause significant psychological, financial, and social problems for both the affected children and their families.

Although congenital and developmental cataracts are associated with reduced eye-related quality of life (ER-QOL) (3), the daily impact of the surgery for these conditions on children and their families is poorly understood. Furthermore, the effects of congenital and developmental cataracts on patients' functional vision (4) have not been rigorously studied because of a lack of validated eye-related measurements. Therefore, we used the Pediatric Eye Questionnaire (PedEyeQ), which is a Rasch-scored, child-and-parent-derived, and an age-specific measure of ER-QOL, as well as including a functional vision questionnaire. It was designed in 2019 for use among children with eye-related conditions and their parents by a pediatric eye disease investigator group (5, 6). In our secondary analyses, we found some additional influencing factors that have not been previously reported in either patients' basic or their surgical information.

Methods

Institutional Review Board approval for this retrospective cross-sectional study was obtained. All data collection and procedures adhered to the tenets of the Declaration of Helsinki. Informed consent was obtained from the parents or legal guardians of each participant. Between July 2020 and February 2021, eligible children with congenital and developmental cataracts, who had undergone surgery in the past three months, were prospectively enrolled. Participants were identified from pediatric ophthalmology outpatient clinics. Finally, a total of 178 participants were approached, with 166 being included in this study. Only 12 families declined participation as they did not have enough time to complete the questionnaires.

Postoperative Children With Congenital and Developmental Cataracts

Among the participants, 69 were 0–4 years old and 38 were 5–11 years old. The following exclusion criteria were utilized: those with systemic abnormalities, secondary glaucoma, or other severe associated ocular complications, and those who had undergone ophthalmic surgery (incisional or laser) in the past one month. Additionally, parents who were unable to respond were excluded.

We gave each parent the age-appropriate questionnaire and answered their concerns. Additionally, we collected participants' demographic characteristics, including their age, gender, place of residence, and highest level of education from the parent who filled in the questionnaire. Additional clinical characteristics were obtained from their medical notes, including the eyes, staging operation, postoperative timing, glasses, amblyopia treatment, postoperative nystagmus, and postoperative strabismus.

Visually Healthy Control

Additionally, 28 (0–4 years old) and 31 children (5–11 years old), with normal visual acuity (best-corrected visual acuity was 0.17logMAR or better at 3 years of age, 0.08logMAR or better at 4 years of age, 0.02logMAR or better at 5 years of age, and 0.0logMAR or better at 6 years or older) (79), no refractive corrections, and no history of eye diseases or surgeries, were enrolled as a control.

Questionnaires

In each of the clinics, we asked one parent of each child to complete both the Proxy and Parent PedEyeQ's on paper. However, some postoperative and normal groups were located across China. Thus, these parents completed questionnaires electronically on either a mobile phone or their personal computer.

Pediatric Eye Questionnaire

The PedEyeQ (5) includes the following sections: Child, Proxy, and Parent 0–4 PedEyeQ, as well as the Child, Proxy, and Parent 5–11 PedEyeQ. They all have distinct and separately scored domains. For responses, they each use a 3-point frequency scale (“Never,” “Sometimes,” and “All of the time”).

The Proxy 0–4 PedEyeQ contains the Functional Vision, Bothered by Eyes/Vision, and Social domains. The Proxy 5–11 PedEyeQ is composed of five domains: Functional Vision, Frustration/Worry, Social, Bothered by Eyes/Vision, and Eye Care. Additionally, the Parent PedEyeQ is composed of four domains: Worry About Their Child's Visual Function, Impact on the Parent/Family, Worry About Their Child's Self-Perception and Interactions, and Worry About Their Child's Eye Condition.

Analysis

Statistical analyses were performed using SPSS 26.0. As mentioned, the Rasch-calibrated PedEyeQ domain scores were used to convert the data from 0 (worst) to 100 (best) for each participant. Thus, in the primary analysis, we used a Mann-Whitney U test to compare the differences between the children who had undergone congenital and developmental cataract surgery and the controls. Furthermore, proxy parent differences were also tested. In the secondary analyses, both Mann-Whitney U and Kruskal-Wallis tests were conducted to analyze the determinants contributing to these disparities. Values of p ≤ 0.05 were considered statistically significant. Furthermore, we calculated mean differences using a 95% Confidence Interval (CI) so that our estimates were more precise. PASS 15.0 (NCSs, USA) was used to calculate the sample size. The score of kids' PedEyeQ was taken as the main parameter. The calculated sample size is 13 eyes in each group. Considering the loss of follow-up rate is 20%, at least 17 eyes in each group.

Results

Postoperative Children With Congenital and Developmental Cataracts

Of the participants, 69 (64.5%) were aged 0 to 4 years (median: 3 years; interquartile range: 2 years) and 38 (35.5%) were aged 5 to 11 years (median: 6 years; interquartile range: 3 years). Fifty-nine children with no visual impairment (caused by refractive error, amblyopia, strabismus, and astigmatism) or eye diseases were then enrolled as the control. Twenty-eight of them (47.5%) were aged 0 to 4 years (median: 2.5 years; interquartile range: 2.5 years) and 31 (52.5%) were aged 5 to 11 years (median: 7; interquartile range: 3 years).

The demographics and clinical characteristics of the different age groups are shown in Table 1. Of the 69 0–4-year-old postoperative participants, 23 (33.33%) developed nystagmus, 39 (56.52%) developed strabismus, and 58 (84.06%) developed amblyopia. Of the 38 postoperative children aged 5–11 years, 9 (23.68%) developed nystagmus, 21 (55.26%) developed strabismus, and 28 (73.68%) developed amblyopia.

TABLE 1
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Table 1. Demographics and clinic characteristics of children in different ages completing the Pediatric Eye Questionnaire and their parents.

Comparing PedEyeQ Scores in Postoperative Children and the Control Group

Proxy PedEyeQ

The postoperative children aged 0- to 4-years-old had lower scores than the controls on each of the three Proxy 0–4 years PedEyeQ domains (p < 0.001; Table 2; Figure 1A). The PedEyeQ Proxy scores for participants aged 0 to 4 years' greatest mean difference was 27 points worse in the Functional Vision domain (median 75 vs. 100; mean difference −27; 95% CI −34 to −19; p < 0.001; Table 2; Figure 1A).

TABLE 2
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Table 2. PedEyeQ domain scores for kids' age among 0–4 with congenital cataracts (N = 69), age among 0–4 normal controls (N = 28), age among 5–11 with congenital cataracts (N = 38), age among 5–11 normal controls (N = 31).

FIGURE 1
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Figure 1. PedEyeQ domain scores in children following congenital and developmental cataracts surgery compared to healthy controls; (A) Proxy PedEyeQ scores for children aged 0–4 years; (B) Proxy PedEyeQ scores for children aged 5–11 years; (C) PedEyeQ scores for parents of children aged 0–4 years; (D) PedEyeQ scores for parents of children aged 5–11 years. (E) Comparison of PedEyeQ scores for parents of children after surgery. * means the results between two groups have significant difference statistically and ** means a greater significant difference.

In the Proxy 5–11 years PedEyeQ, the postoperative children aged 5–11 years had worse scores across each of the five domains compared to the controls (p < 0.001; Table 2; Figure 1B). The greatest difference was in the Functional Vision domain (median 78 vs. 100; mean difference −23; 95% CI −30 to −15; p < 0.001; Table 2; Figure 1B). Additionally, nystagmus was the main determinant herein (p < 0.05).

Associations

Demographics and clinical characteristics were analyzed using the Mann-Whitney U test. Nystagmus (p < 0.005; Table 3) and strabismus (p < 0.005; Table 3) were found to be the most significant clinical factors affecting participants' functional vision. In particular, male children (p < 0.001; Table 3) and female parents (p < 0.05; Table 3) had lower scores in the Functional Vision domain. Additionally, the more uncooperative that children were to undergo amblyopia treatment, the lower their scores (p < 0.05; Table 3).

TABLE 3
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Table 3. Dominating factors on functional vision of age 0–4 and 5–11 PedEyeQ domains.

Parent PedEyeQ

Parents of children aged 0–4 years' PedEyeQ scores were lower in each domain for those of postoperative children compared to parents of those in the control (p < 0.001; Table 2; Figure 1C). Parent PedEyeQ 0 to 4 years' greatest difference was 46 points worse on Worry About Their Child's Eye Condition domain (median 45 vs. 100; mean difference −46; 95% CI −57 to −36; p < 0.001; Table 2; Figure 1C). Parents of patients with nystagmus (p < 0.001) or strabismus (p < 0.05) were significantly more worried about their children's eye condition.

In the Parent PedEyeQ, parents of children aged 5–11 years also reported worse scores across each of the four domains compared to those of the controls (p < 0.001; Table 2; Figure 1D). Parents responding to the PedEyeQ 5 to 11 years' greatest difference was 30 points worse on the Worry About Their Child's Visual Function domain (median 53 vs. 100; mean difference −30; 95% CI −43 to −17; p < 0.001; Table 2; Figure 1D). Nevertheless, the demographic and clinical factors had only small effects on participants' functional vision.

Comparing PedEyeQ Scores in Parents of Children Aged 0–4 vs. Those of Children Aged 5–11 Years

Parental PedEyeQ scores of those with children aged 0 to 4 years showed the greatest difference in their 10 points lower scores on the Worry About Their Child's Eye Condition Domain (median 45 vs. 50; mean difference −10; 95% CI −21 to 0; p < 0.05; Table 4; Figure 1E) compared to those of children aged 5–11 years.

TABLE 4
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Table 4. PedEyeQ domain scores for kids' age among 0–4 with congenital cataracts (N = 69), age among 5–11 with congenital cataracts (N = 38).

Discussion

This study was the first to use the PedEyeQ to examine the quality of life (QOL) of both postoperative children with congenital and developmental cataracts and their parents. Furthermore, we found that appearance abnormalities, such as nystagmus and strabismus, significantly influenced their QOL.

The impact of reduced functional visual abilities of children with congenital and developmental cataracts has seldom been evaluated in previous studies. Tailor et al. (10) used the Cardiovascular Visual Ability Questionnaire for Children (CVAQC) to measure the functional visual abilities of children treated for cataracts. They recorded the putative risk factors herein, such as visual acuity and the number of previous surgical interventions. However, they did not explore the associations between participants' functional vision impairments and these factors. Furthermore, they measured these factors using three validated instruments, which complicates their findings. Paryani et al. (11) found low scores in children who had undergone an operation for cataracts, especially bilateral cataracts. They used the LV Prasad Functional Vision Questionnaire (LVP-FVQ). However, both the CVAQC and the LVP-FVQ were specifically designed for children with vision impairment and not for all eye conditions (1214).

Chak et al. (4) used the PedsQL 4.0 to assess the health-related QOL (HRQOL) in children with congenital cataracts. Their HRQOL scores were found to be significantly impacted, which were comparable with those of children with systemic chronic, severe, or life-threatening diseases. However, the current literature still lacks sufficient content on eye condition impairments.

There are several questionnaires that measure ER-QOL; however, they primarily target adolescents and young adults (13, 1517). Due to improvements in medical technologies, the youngest viable age for undergoing pediatric cataract surgery has increased. Furthermore, undergoing surgery at a younger age is more likely to result in better visual outcomes (18, 19). Some experts have even suggested that surgery should be performed within 6–8 weeks of birth (20). Thus, more research is needed on the impact of these surgeries on younger children.

PedEyeQ, with its distinct domains, provides a means with which to compensate for these research gaps. The PedEyeQ is an accurate instrument that has been developed to assess the impact of children's eye conditions on both them and their caregivers. The Child, Proxy, and Parent pediatric eye questionnaires of the PedEyeQ were designed separately and can be used across a wide age range of respondents. Additionally, the PedEyeQ's Rasch scoring system is convenient as its frequency scale and question format are easily understood (21). Finally, it has more items than most other measures and can simultaneously examine respondents' functional vision and ER-QOL.

The factor structure and validity, as well as the known-group, discriminant, and convergent validities, of the PedEyeQ have been established in studies of children with bilateral visual impairment (6), residual amblyopia (22), strabismus (23), unilateral visual acuity deficit (24), and correlational research between functional measures and the Child PedEyeQ (25).

The present study confirms previous publications (26). Using the PedEyeQ, Leske et al. (26) reported reduced functional vision and ER-QOL across various age groups and a wide range of pediatric eye conditions. A total of 1,037 patients with pediatric eye conditions (cataract, n = 99) and 254 visually healthy controls were included in their study. However, specific eye conditions, such as congenital cataracts, still need further study. Furthermore, only 16% of the 1,037 patients were in active treatment, meaning that changes in their response to treatments, like surgery, may impact both their functional vision and ER-QOL. Thus, the children we recruited were those who had undergone congenital and developmental cataract surgery. Additionally, we further explored the associations of the study factors with demographic and clinical factors.

The Proxy PedEyeQ domain scores were significantly worse for the participants compared to those of the controls. This shows that postoperative children have reduced functional vision and ER-QOL. Using the Parent PedEyeQ, we also discovered that, unlike parents of visually healthy children, those of postoperative children experience a lower QOL. Our findings are consistent with those of prior research (3, 4, 11, 2628).

In our research, the greatest mean differences were in the Functional Vision domain. This is indubitable given the impaired visual acuity and poor eye condition found in the cataract group. The Functional Vision domain of the Proxy PedEyeQ focuses on children's daily activities and school-related tasks. Postoperative children with congenital and developmental cataracts are more likely to showcase slower reading skills and a reduced physical.

We further analyzed the determinants contributing to this outcome using Mann-Whitney U and Kruskal-Wallis tests. Demographic and clinical characteristics were both considered herein. Finally, we found that having either nystagmus or strabismus was the major clinical factor affecting participants' Functional Vision domain. Additionally, more willing cooperation during amblyopia treatment (0–4 years, p < 0.05; 5–11 years, p = 0.099) and the staging operation (5–11 years, p = 0.090) are important factors influencing respondents' functional vision. However, likely because of our small sample size, these two variables were not statistically significant.

Our findings accurately outline the clinical reality of postoperative children with congenital and developmental cataracts. For example, we found that nystagmus, strabismus, and amblyopia are all likely to have an impact on peoples' daily activities (22, 28, 29) because reduced visual acuity and stereoacuity all influence their functional vision. Patients with amblyopia are more likely to have a slower reading speed (30), with those with strabismus being more likely to also exhibit motor skill deficits (30). Furthermore, having physically noticeable strabismus (31) or nystagmus (32) is often problematic for school children as others may treat them as “different.” Thus, children's well-being and developmental progress are affected by these conditions. Likewise, needing to wear specific glasses or an eye patch due to these conditions can also draw negative attention to children with amblyopia form their peers (33).

Our findings are in accordance with prior studies on children with various eye conditions. For example, a series of studies by the American Pediatric Eye Disease Investigator Group reported that the PedEyeQ greatest mean differences are worse in the Functional Vision domain for patients with these conditions. However, they directly explored the association of specific eye conditions, such as strabismus (23), amblyopia (22), and nystagmus (26), with functional vision and ER-QOL in their participants. This means that nystagmus, strabismus, and amblyopia are significant factors in this relationship.

Notably, we compared functional vision and ER-QOL changes in postoperative children with unilateral and bilateral cataracts; however, no statistically significant difference was found. In contrast, other studies have reported that bilateral pediatric cataracts provide better visual functioning than unilateral ones (11, 3437). However, this discrepancy is likely because both the unilateral and bilateral cataracts used in our study were of congenital or developmental etiology, while the unilateral cataracts used in the prior research were traumatic ones. Due to an uneven visual deprivation, the prevalence of amblyopia (100% vs. 77.6%) and strabismus (65.0% vs. 53.1%) was slightly higher after participants had undergone unilateral cataract surgery in our study. However, the incidence of complications following traumatic cataract surgery was higher (34). Additionally, this type of unilateral cataracts' vision and VQL are much lower.

In addition to the demographic and clinical characteristics included in our study, there are still other factors impacting patients' functional vision, meaning that more research is needed.

Parents of children aged 0–11 years had significantly negative PedEyeQ domain scores. The greatest mean differences were in the Worry About Their Child's Eye Condition and the Worry About Their Child's Visual Function domains. Specifically, the scores were significantly lower for parents of 0–4 year old children following congenital and developmental cataracts surgery in the Worry About Their Child's Eye Conditions domain (p < 0.05). Furthermore, in previous research (6, 22, 23) that also used the PedEyeQ to study various eye conditions, the greatest mean differences were observed in these same two domains. After an analysis of certain factors, we found that parents of children with nystagmus (0–4 years, p < 0.001) or strabismus (0–4 years, p < 0.05) were significantly more worried about their children's eye condition. Our findings indicate that parents tend to overestimate the influence of nystagmus and strabismus on their children following surgery. Additionally, it has been documented that patients with nystagmus or strabismus have worsened stereo functioning and control (38). Furthermore, it is likely that pediatric patients do not openly communicate with their parents about their school life, which then adds to the latter's psychological concerns (39). For example, they may worry about their children's learning and social abilities (40). Moreover, if the children are very young, their treatments will need to start as early on as possible, which may then add to their parents' financial pressure. Finally, long-term expectations and their understanding of their children's health may also affect parents' QOL.

We also found that parent PedEyeQ scores of those with children aged 0 to 4 years were generally lower than those of children aged 5 to 11 years. It is likely that their children's poor eye condition is the cause because, when compared with postoperative children aged 5–11 years, the 0–4 year old ones had a higher prevalence of nystagmus (33.3% vs. 23.7%), strabismus (56.5% vs. 55.3%), and amblyopia (84.1% vs. 73.7%). Our findings are similar to those reported by Birch et al. (41). They also found a high prevalence of nystagmus and strabismus in children aged 0–4 years after cataract surgery. Therefore, Parent PedEyeQ's greatest difference between these two age groups is most likely to be in the Worry About Their Child's Eye Condition domain. Perhaps our sample size was not large enough, which is why these two groups did not show any significant differences in the other three domains.

Thus, interventions to improve the QOL of postoperative children with congenital and developmental cataracts, and that of their parents, are necessary. Both patients and their parents should actively participate in therapy, especially in terms of the management of nystagmus, strabismus, and amblyopia. Applying the concept of win-win cooperation herein is also worth applying for both parties. Alternatively, engaging in outpatient follow-up is important because these children's eye conditions change with time. As such, an experienced clinician is needed to formulate the correct diagnosis and treatment plan. To ameliorate the adverse effects of the ER-QOL on the patient's family, educational interventions, such as clinical lectures, may be helpful. Psychosocial interventions and peer support groups should also be evaluated.

Because our sample size was small, future studies should use larger populations to evaluate more impact factors in this relationship. Additionally, because the child PedEyeQ we used was proxy-reported, parental perceptions may also have influenced their children's answers. Finally, this was a retrospective cross-sectional study. A prospective study is thus needed to identify any differences at various stages after surgery.

Conclusions

Although treatments for congenital and developmental cataracts are highly successful, their effects on the QOL and functional vision of postoperative children and their families are still significant. Families and their children would benefit from receiving clinical support, educational interventions, psychosocial interventions, and peer support.

Data Availability Statement

The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding author.

Ethics Statement

The studies involving human participants were reviewed and approved by Ethics Committee of the Affiliated Ophthalmology Hospital of Wenzhou Medical University. Written informed consent from the participants' legal guardian/next of kin was not required to participate in this study in accordance with the national legislation and the institutional requirements.

Author Contributions

The study was designed by YuZ and YiZ. Conducting of the study, data collection, and its analysis and interpretation were completed by SG, YH, LC, WS, PC, and DW. All authors contributed to the article and approved the submitted version.

Funding

This study was supported by research grants from Natural Science Foundation of Zhejiang Province (Grant No. LQ19H120001) and National Natural Science Foundation of China (Grant No. 81870680).

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher's Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

1. Mndeme FG, Mmbaga BT, Kim MJ, Sinke L, Allen L, Mgaya E, et al. Red reflex examination in reproductive and child health clinics for early detection of paediatric cataract and ocular media disorders: cross-sectional diagnostic accuracy and feasibility studies from Kilimanjaro, Tanzania. Eye. (2020) 35:1347–53. doi: 10.1038/s41433-020-1019-5

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Wilson ME. Paediatric cataract blindness in the developing world: surgical techniques and intraocular lenses in the new millennium. Br J Ophthalmol. (2003) 87:14–9. doi: 10.1136/bjo.87.1.14

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Fox A, O'Keefe M, Lanigan B. A follow-on study on vision-related quality of life assessment using the NEI-VFQ-25 in those with a history of unilateral and bilateral congenital cataracts. Acta Ophthalmol. (2018) 96:e596–9. doi: 10.1111/aos.13692

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Chak M Rahi JS on on behalf of the British Congenital Cataract Interest Group. The health-related quality of life of children with congenital cataract: findings of the British Congenital Cataract Study. Br J Ophthalmol. (2007) 91:922–6. doi: 10.1136/bjo.2006.109603

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Hatt SR, Leske DA, Castañeda YS, Wernimont SM, Liebermann L, Cheng-Patel CS, et al. Development of pediatric eye questionnaires for children with eye conditions. Am J Ophthalmol. (2019) 200:201–17. doi: 10.1016/j.ajo.2019.01.001

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Leske DA, Hatt SR, Castañeda YS, Wernimont SM, Liebermann L, Cheng-Patel CS, et al. Validation of the pediatric eye questionnaire in children with visual impairment. Am J Ophthalmol. (2019) 208:124–32. doi: 10.1016/j.ajo.2019.07.018

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Ohlsson J, Villarreal G. Normal visual acuity in 17-18 year olds: acta ophthalmologica scandinavica 2005. Acta Ophthalmol Scand. (2005) 83:487–91. doi: 10.1111/j.1600-0420.2005.00516.x

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Drover JR, Felius J, Cheng CS, Morale SE, Wyatt L, Birch EE. Normative pediatric visual acuity using single surrounded HOTV optotypes on the electronic visual acuity tester following the amblyopia treatment study protocol. J Am Assoc Pediatr Ophthalmol Strabismus. (2008) 12:145–9. doi: 10.1016/j.jaapos.2007.08.014

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Pan Y, Tarczy-Hornoch K, Cotter SA, Wen G, Borchert MS, Azen SP, et al. Visual acuity norms in pre-school children: the multi-ethnic pediatric eye disease study. Optometr Vis Sci. (2009) 86:607–12. doi: 10.1097/OPX.0b013e3181a76e55

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Tailor VK, Abou-Rayyah Y, Brookes J, Khaw PT, Papadopoulos M, Adams GGW, et al. Quality of life and functional vision in children treated for cataract—a cross-sectional study. Eye. (2017) 31:856–64. doi: 10.1038/eye.2016.323

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Paryani M, Khandekar R, Dole K, Rishikeshi N, Dharmadhikari S. Visual outcome and impact on quality of life after surgeries differ in children operated for unilateral and bilateral cataract (Pune study 2011). Oman J Ophthalmol. (2012) 5:150. doi: 10.4103/0974-620X.106094

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Khadka J, Ryan B, Margrain TH, Court H, Woodhouse JM. Development of the 25-item Cardiff Visual Ability Questionnaire for Children (CVAQC). Br J Ophthalmol. (2010) 94:730–5. doi: 10.1136/bjo.2009.171181

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Felius J, Stager DR, Berry PM, Fawcett SL, Stager DR, Salomão SR, et al. Development of an instrument to assess vision-related quality of life in young children. Am J Ophthalmol. (2004) 138:362–72. doi: 10.1016/j.ajo.2004.05.010

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Gothwal VK, Lovie-Kitchin JE, Nutheti R. The development of the LV Prasad-functional vision questionnaire: a measure of functional vision performance of visually impaired children. Invest Ophthalmol Vis Sci. (2003) 44:4131–9. doi: 10.1167/iovs.02-1238

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Cochrane G, Lamoureux E, Keeffe J. Defining the content for a new quality of life questionnaire for students with low vision (The impact of vision impairment on children: IVI_C). Ophthalmic Epidemiol. (2008) 15:114–20. doi: 10.1080/09286580701772029

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Weih LM, Hassell JB, Keeffe J. Assessment of the Impact of Vision Impairment. Invest Ophthalmol Vis Sci. (2002) 43:927–35.

PubMed Abstract | Google Scholar

17. Frost NA, Sparrow JM, Durant JS, Donovan JL, Peters TJ, Brookes ST. Development of a questionnaire for measurement of vision-related quality of life. Ophthalmic Epidemiol. (1998) 5:185–210. doi: 10.1076/opep.5.4.185.4191

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Hartmann EE Lynn MJ Lambert SR for the Infant Aphakia Treatment Study Group. Baseline characteristics of the infant Aphakia treatment study population: predicting recognition acuity at 45 years of age Invest Ophthalmol Vis Sci. (2015) 56:388–95. doi: 10.1167/iovs.14-15464

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Hartmann EE, Stout AU, Lynn MJ, Yen KG, Kruger SJ, Lambert SR, et al. Stereopsis results at 4.5 years of age in the infant Aphakia treatment study. Am J Ophthalmol. (2015) 159:64–70.e1–2. doi: 10.1016/j.ajo.2014.09.028

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Shrestha U. Cataract surgery in children: Controversies and practices. Nep J Oph. (2012) 4:138–49. doi: 10.3126/nepjoph.v4i1.5866

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Hatt SR, Leske DA, Wernimont SM, Birch EE, Holmes JM. Comparison of rating scales in the development of patient-reported outcome measures for children with eye disorders. Strabismus. (2017) 25:33–8. doi: 10.1080/09273972.2016.1276941

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Hatt SR, Leske DA, Castañeda YS, Wernimont SM, Liebermann L, Cheng-Patel CS, et al. Understanding the impact of residual amblyopia on functional vision and eye-related quality of life using the PedEyeQ. Am J Ophthalmol. (2020) 218:173–81. doi: 10.1016/j.ajo.2020.05.039

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Hatt SR, Leske DA, Castañeda YS, Wernimont SM, Liebermann L, Cheng-Patel CS, et al. Association of strabismus with functional vision and eye-related quality of life in children. JAMA Ophthalmol. (2020) 138:528. doi: 10.1001/jamaophthalmol.2020.0539

PubMed Abstract | CrossRef Full Text | Google Scholar

24. Leske DA, Hatt SR, Wernimont SM, Castañeda YS, Cheng-Patel CS, Liebermann L, et al. Association of visual acuity with eye-related quality of life and functional vision across childhood eye conditions. Am J Ophthalmol. (2021) 223:220–8. doi: 10.1016/j.ajo.2020.10.019

PubMed Abstract | CrossRef Full Text | Google Scholar

25. Birch EE, Castañeda YS, Cheng-Patel CS, Morale SE, Kelly R, Jost RM, et al. Associations of eye-related quality of life with vision, visuomotor function, and self-perception in children with strabismus and anisometropia. Invest Ophthalmol Vis Sci. (2020) 61:22. doi: 10.1167/iovs.61.11.22

PubMed Abstract | CrossRef Full Text | Google Scholar

26. Leske DA, Hatt SR, Wernimont SM, Castañeda YS, Cheng-Patel CS, Liebermann L, et al. Quality of life and functional vision across pediatric eye conditions assessed using the PedEyeQ. J AAPOS. (2021) 25:23.e1–e5. doi: 10.1016/j.jaapos.2020.10.010

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Kirwan C, Lanigan B, O'Keefe M. Vision-related quality of life assessment using the NEI-VFQ-25 in adolescents and young adults with a history of congenital cataract. J Pediatr Ophthalmol Strabismus. (2012) 49:26–31. doi: 10.3928/01913913-20110517-02

PubMed Abstract | CrossRef Full Text | Google Scholar

28. Uzun A, Atilla H. Health-related quality of life in children operated for pediatric cataracts. Eur J Ophthalmol. (2014) 24:707–11. doi: 10.5301/ejo.5000429

PubMed Abstract | CrossRef Full Text | Google Scholar

29. Chai Y, Shao Y, Lin S, Xiong K-Y, Chen W-S, Li Y-Y, et al. Vision-related quality of life and emotional impact in children with strabismus: a prospective study. J Int Med Res. (2009) 37:1108–14. doi: 10.1177/147323000903700415

PubMed Abstract | CrossRef Full Text | Google Scholar

30. Birch EE, Castañeda YS, Cheng-Patel CS, Morale SE, Kelly KR, Beauchamp CL, et al. Self-perception of school-aged children with amblyopia and its association with reading speed and motor skills. JAMA Ophthalmol. (2019) 137:167. doi: 10.1001/jamaophthalmol.2018.5527

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Archer SM, Musch DC, Wren PA, Guire KE. Social and emotional impact of strabismus surgery on quality of life in children. J AAPOS. (2005) 9:4. doi: 10.1016/j.jaapos.2004.12.006

PubMed Abstract | CrossRef Full Text | Google Scholar

32. Pilling RF. Social and visual function in nystagmus. Br J Ophthalmol. (2005) 89:1278–81. doi: 10.1136/bjo.2005.070045

PubMed Abstract | CrossRef Full Text | Google Scholar

33. Webber AL, Wood JM, Gole GA, Brown B. Effect of amblyopia on self-esteem in children. Optom Vis Sci. (2008) 85:1074–81. doi: 10.1097/OPX.0b013e31818b9911

PubMed Abstract | CrossRef Full Text | Google Scholar

34. Louison S, Blanc J, Pallot C, Alassane S, Praudel A, Bron A-M, et al. Visual outcomes and complications of congenital cataract surgery. J Français d'Ophtalmologie. (2019) 42:368–74. doi: 10.1016/j.jfo.2018.10.007

PubMed Abstract | CrossRef Full Text | Google Scholar

35. Lu Y, Ji Y-H, Luo Y, Jiang Y-X, Wang M, Chen X. Visual results and complications of primary intraocular lens implantation in infants aged 6 to 12 months. Graefes Arch Clin Exp Ophthalmol. (2010) 248:681–6. doi: 10.1007/s00417-010-1310-4

PubMed Abstract | CrossRef Full Text | Google Scholar

36. Borisovsky G, Silberberg G, Wygnanski-Jaffe T, Spierer A. Results of congenital cataract surgery with and without intraocular lens implantation in infants and children. Graefes Arch Clin Exp Ophthalmol. (2013) 251:2205–11. doi: 10.1007/s00417-013-2327-2

PubMed Abstract | CrossRef Full Text | Google Scholar

37. Vera L, Lambert N, Sommet J, Boulkedid R, Alberti C, Bui Quoc E. Visual outcomes and complications of cataract surgery with primary implantation in infants. Journal Français d'Ophtalmologie. (2017) 40:386–93. doi: 10.1016/j.jfo.2016.12.010

PubMed Abstract | CrossRef Full Text | Google Scholar

38. Wang Y. Health-related quality of life correlated with the clinical severity of intermittent exotropia in children. Eye (Lond). (2020) 34:400–7. doi: 10.1038/s41433-019-0557-1

PubMed Abstract | CrossRef Full Text | Google Scholar

39. Morita Y, Hiraoka T, Oshika T. Influence of intermittent exotropia surgery on general health-related quality of life: different perception by children and parents. Jpn J Ophthalmol. (2021) 65:326–30. doi: 10.1007/s10384-020-00811-7

PubMed Abstract | CrossRef Full Text | Google Scholar

40. Lim SB, Wong WL, Ho RC, Wong IB. Childhood intermittent exotropia from a different angle: does severity affect quality of life? Br J Ophthalmol. (2015) 99:1405–11. doi: 10.1136/bjophthalmol-2014-306545

PubMed Abstract | CrossRef Full Text | Google Scholar

41. Birch EE, Wang J, Felius J, Stager DR, Hertle RW. Fixation control and eye alignment in children treated for dense congenital or developmental cataracts. J Am Assoc Pediatr Ophthalmol Strabismus. (2012) 16:156–60. doi: 10.1016/j.jaapos.2011.11.007

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: congenital and developmental cataracts, quality of life, functional vision, PedEyeQ, determinants

Citation: Gu S, Hu Y, Zhao Y, Chen L, Sun W, Chang P, Wang D and Zhao Y (2022) A Retrospective Study on the Eye-Related Quality of Life, Functional Vision, and Their Determinants Among Children Following Congenital and Developmental Cataracts Surgery and Its Impact on Their Families Using the PedEyeQ. Front. Public Health 10:788384. doi: 10.3389/fpubh.2022.788384

Received: 07 November 2021; Accepted: 21 February 2022;
Published: 17 March 2022.

Edited by:

Dipika Bansal, National Institute of Pharmaceutical Education and Research S.A.S. Nagar, India

Reviewed by:

Danying Zheng, Sun Yat-sen University, China
Haiying Jin, Department of Ophthalmology Shanghai East Hospital, China
Annegret Dahlmann-Noor, Moorfields Eye Hospital NHS Foundation Trust, United Kingdom

Copyright © 2022 Gu, Hu, Zhao, Chen, Sun, Chang, Wang and Zhao. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Yune Zhao, zyehzeye@126.com

These authors have contributed equally to this work

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