Standardized Assessment of Health-Related Quality of Life in Patients with Congenital Aniridia

Congenital aniridia is a rare panocular disorder that is associated with varying degrees of impairment of visual acuity. The COST Action (CA18116) developed a survey (aniridia-net.eu) to assess patient-reported experiences with congenital aniridia and its impacts on vision and daily life. Here, we c...

Full description

Saved in:
Bibliographic Details
Published inKlinische Monatsblatter fur Augenheilkunde Vol. 242; no. 3; p. 228
Main Authors Hoxha, Zamira, Fries, Fabian Norbert, Hecker, Dietmar, Seitz, Berthold, Käsmann-Kellner, Barbara, Náray, Annamária, Lagali, Neil, Grupcheva, Christina, Szentmáry, Nóra, Stachon, Tanja
Format Journal Article
LanguageEnglish
Published Germany 01.03.2025
Subjects
Online AccessGet more information

Cover

Loading…
Abstract Congenital aniridia is a rare panocular disorder that is associated with varying degrees of impairment of visual acuity. The COST Action (CA18116) developed a survey (aniridia-net.eu) to assess patient-reported experiences with congenital aniridia and its impacts on vision and daily life. Here, we correlate the survey responses of German patients with congenital aniridia with clinical ophthalmology data acquired at the Homburger Aniridia Center. The patients completed the German-language version of a 20-point ANIRIDIA-NET survey. The survey included demographic information, the most common symptoms caused by the disease, difficulties caused by visual impairment in various life situations, and the frequency of using visual aids in daily life. As for clinical data, best-corrected visual acuity (BCVA) as well as corneal, lens, and glaucoma status were collected. A total of 71 participants, 27 (38.0%) children and 44 (61.7%) adults, completed the questionnaire, with an age range of 28.8 ± 20.2 years (6 - 78 years). Among them, 55 (77.4%) reported daily light sensitivity, 34 (47.8%) experienced dry eyes, 17 (23.9%) had fluctuating vision, 11 (15.4%) reported eye pain, and 5 (7.0%) experienced daily watering eyes. Older patients reported significantly more eye complaints than children (p < 0,001). Notably, patients with more advanced aniridia-associated keratopathy (AAK) exhibited a discernibly lower quality of life (ρ = 0.28, p = 0.027). Similarly, cataract surgery early in life was associated with a more pronounced decline in quality of life (ρ = - 0.36, p = 0.002). Thirty-five (49.2%) patients never needed assistance for their commute to school/work, 27 (38.0%) and 22 (30.9%) never needed assistance for their daily routines at home or various social activities, respectively. Regarding the use of visual aids, 39 (24.9%) reported that they always used visual aids at work or school, 24 (33.8%) during social activities, and 32 (45.1%) during free time activities. Although congenital aniridia is associated with reduced visual acuity, the majority of affected individuals, especially during childhood, report that they were able to manage personal communication and various life situations independently and without significant difficulties, despite their eye-related issues. Visual aids serve as crucial support for them during their transition into adulthood and as they age. Symptoms of congenital aniridia subjects, described by the ANIRIDIA-NET survey, correlated well with clinical findings. Therefore, the questionnaire may provide important information for the treating ophthalmologist for follow-up examination of these patients and improvement in their life quality.
AbstractList Congenital aniridia is a rare panocular disorder that is associated with varying degrees of impairment of visual acuity. The COST Action (CA18116) developed a survey (aniridia-net.eu) to assess patient-reported experiences with congenital aniridia and its impacts on vision and daily life. Here, we correlate the survey responses of German patients with congenital aniridia with clinical ophthalmology data acquired at the Homburger Aniridia Center. The patients completed the German-language version of a 20-point ANIRIDIA-NET survey. The survey included demographic information, the most common symptoms caused by the disease, difficulties caused by visual impairment in various life situations, and the frequency of using visual aids in daily life. As for clinical data, best-corrected visual acuity (BCVA) as well as corneal, lens, and glaucoma status were collected. A total of 71 participants, 27 (38.0%) children and 44 (61.7%) adults, completed the questionnaire, with an age range of 28.8 ± 20.2 years (6 - 78 years). Among them, 55 (77.4%) reported daily light sensitivity, 34 (47.8%) experienced dry eyes, 17 (23.9%) had fluctuating vision, 11 (15.4%) reported eye pain, and 5 (7.0%) experienced daily watering eyes. Older patients reported significantly more eye complaints than children (p < 0,001). Notably, patients with more advanced aniridia-associated keratopathy (AAK) exhibited a discernibly lower quality of life (ρ = 0.28, p = 0.027). Similarly, cataract surgery early in life was associated with a more pronounced decline in quality of life (ρ = - 0.36, p = 0.002). Thirty-five (49.2%) patients never needed assistance for their commute to school/work, 27 (38.0%) and 22 (30.9%) never needed assistance for their daily routines at home or various social activities, respectively. Regarding the use of visual aids, 39 (24.9%) reported that they always used visual aids at work or school, 24 (33.8%) during social activities, and 32 (45.1%) during free time activities. Although congenital aniridia is associated with reduced visual acuity, the majority of affected individuals, especially during childhood, report that they were able to manage personal communication and various life situations independently and without significant difficulties, despite their eye-related issues. Visual aids serve as crucial support for them during their transition into adulthood and as they age. Symptoms of congenital aniridia subjects, described by the ANIRIDIA-NET survey, correlated well with clinical findings. Therefore, the questionnaire may provide important information for the treating ophthalmologist for follow-up examination of these patients and improvement in their life quality.
Author Hoxha, Zamira
Lagali, Neil
Käsmann-Kellner, Barbara
Fries, Fabian Norbert
Stachon, Tanja
Hecker, Dietmar
Grupcheva, Christina
Szentmáry, Nóra
Seitz, Berthold
Náray, Annamária
Author_xml – sequence: 1
  givenname: Zamira
  surname: Hoxha
  fullname: Hoxha, Zamira
  organization: Department of Ophthalmology, Saarland University Medical Center and Faculty of Medicine, Homburg/Saar, Germany
– sequence: 2
  givenname: Fabian Norbert
  orcidid: 0000-0002-8526-4712
  surname: Fries
  fullname: Fries, Fabian Norbert
  organization: Department of Ophthalmology, Saarland University Medical Center and Faculty of Medicine, Homburg/Saar, Germany
– sequence: 3
  givenname: Dietmar
  surname: Hecker
  fullname: Hecker, Dietmar
  organization: Department of Experimental Audiology/Neurootology, Saarland University Medical Center and Faculty of Medicine, Homburg/Saar, Germany
– sequence: 4
  givenname: Berthold
  orcidid: 0000-0001-9701-8204
  surname: Seitz
  fullname: Seitz, Berthold
  organization: Department of Ophthalmology, Saarland University Medical Center and Faculty of Medicine, Homburg/Saar, Germany
– sequence: 5
  givenname: Barbara
  orcidid: 0000-0002-5137-8658
  surname: Käsmann-Kellner
  fullname: Käsmann-Kellner, Barbara
  organization: Department of Ophthalmology, Saarland University Medical Center, Kinderophthalmologie, Orthoptik, Low Vision und Neuroophthalmologie KiOLoN, Homburg/Saar, Germany
– sequence: 6
  givenname: Annamária
  surname: Náray
  fullname: Náray, Annamária
  organization: Department of Ophthalmology, Semmelweis University, Budapest, Hungary
– sequence: 7
  givenname: Neil
  surname: Lagali
  fullname: Lagali, Neil
  organization: Department of Biomedical and Clinical Sciences, Linköping University, Linköping, Sweden
– sequence: 8
  givenname: Christina
  surname: Grupcheva
  fullname: Grupcheva, Christina
  organization: Department of Ophthalmology and Visual Science, Varna Medical University, Varna, Bulgaria
– sequence: 9
  givenname: Nóra
  surname: Szentmáry
  fullname: Szentmáry, Nóra
  organization: Dr. Rolf M. Schwiete Center for Limbal Stem Cell and Congenital Aniridia Research, Saarland University, Saarbrücken, Germany
– sequence: 10
  givenname: Tanja
  surname: Stachon
  fullname: Stachon, Tanja
  organization: Dr. Rolf M. Schwiete Center for Limbal Stem Cell and Congenital Aniridia Research, Saarland University, Saarbrücken, Germany
BackLink https://www.ncbi.nlm.nih.gov/pubmed/39694046$$D View this record in MEDLINE/PubMed
BookMark eNo1j0tLAzEURoMottau3Ev-QDSPSTp3ORS1QsH31pLHHRuYScskReqvt6KuzuIcPvjOyHHaJCTkQvArwbW-tkxWRjFVz-CIjEWlgCkAGJFpztFxrRRIqMUpGSkwUPHKjMn7S7Ep2CHELwy0yRlz7jEVumnpAm1X1uwZO1sO8mlnu1j2P2YZW6Qx0Udb4iHO9DOWNZ1v0gemWGxHmxSHGKI9Jyet7TJO_zghb7c3r_MFWz7c3c-bJfNK8sLQCeQOjFJcaNmiDQJ9bWYGtOLopTPGOcHBYqikCb7mEkFLryFANfNeTsjl7-5253oMq-0QezvsV_9H5TfeR1XN
ContentType Journal Article
Copyright Thieme. All rights reserved.
Copyright_xml – notice: Thieme. All rights reserved.
DBID CGR
CUY
CVF
ECM
EIF
NPM
DOI 10.1055/a-2463-3879
DatabaseName Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
DatabaseTitle MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
DatabaseTitleList MEDLINE
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
DeliveryMethod no_fulltext_linktorsrc
DocumentTitleAlternate Standardisierte Erfassung der gesundheitsbezogenen Lebensqualität bei Patienten mit kongenitaler Aniridie
EISSN 1439-3999
ExternalDocumentID 39694046
Genre Journal Article
GeographicLocations Germany
GeographicLocations_xml – name: Germany
GroupedDBID ABJNI
ALMA_UNASSIGNED_HOLDINGS
CGR
CUY
CVF
ECM
EIF
NPM
ID FETCH-LOGICAL-c320t-eb1e0b96330152fead1ec86769530ec2b66bb109aed426dc802e952c59d947cc2
IngestDate Wed Apr 30 01:42:30 EDT 2025
IsPeerReviewed true
IsScholarly true
Issue 3
Language English
License Thieme. All rights reserved.
LinkModel OpenURL
MergedId FETCHMERGED-LOGICAL-c320t-eb1e0b96330152fead1ec86769530ec2b66bb109aed426dc802e952c59d947cc2
ORCID 0000-0002-8526-4712
0000-0002-5137-8658
0000-0001-9701-8204
PMID 39694046
ParticipantIDs pubmed_primary_39694046
PublicationCentury 2000
PublicationDate 2025-03-01
PublicationDateYYYYMMDD 2025-03-01
PublicationDate_xml – month: 03
  year: 2025
  text: 2025-03-01
  day: 01
PublicationDecade 2020
PublicationPlace Germany
PublicationPlace_xml – name: Germany
PublicationTitle Klinische Monatsblatter fur Augenheilkunde
PublicationTitleAlternate Klin Monbl Augenheilkd
PublicationYear 2025
SSID ssib053392981
Score 2.3530452
Snippet Congenital aniridia is a rare panocular disorder that is associated with varying degrees of impairment of visual acuity. The COST Action (CA18116) developed a...
SourceID pubmed
SourceType Index Database
StartPage 228
SubjectTerms Adolescent
Adult
Aged
Aniridia - diagnosis
Aniridia - epidemiology
Aniridia - psychology
Child
Female
Germany - epidemiology
Humans
Male
Middle Aged
Quality of Life - psychology
Reproducibility of Results
Surveys and Questionnaires
Vision Disorders - diagnosis
Vision Disorders - epidemiology
Vision Disorders - psychology
Young Adult
Title Standardized Assessment of Health-Related Quality of Life in Patients with Congenital Aniridia
URI https://www.ncbi.nlm.nih.gov/pubmed/39694046
Volume 242
hasFullText
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3fSxwxEA5nheJLabG_a8mDb0fsXpJdL49XrYhVKaggfagkuSwN9fbkugfF_8T_1plkf6TalrYvy7LJHsvOt3PfTGa-ELK5XVhlnDBMjqVgUgrJNHx0TEGsYiUy4hLzHUfHxf6ZPDjPzweDm6RqaVmbLXv9y76S_7EqXAO7YpfsP1i2-1G4AOdgXziCheH4VzY-afIA_hpo46TT2AzJ-VDXxUKtGwxGqYywmn7oyyAU8ikqqjbtbTtzbLLCHUSGk8ov_NTrlLd-xAZKCISDE9D1d3MZdDmH5XIxnCzhzq_OX37DhrQOJ_MfcS3ps575Ref89zA0D4xZo9o5rhthaXefkm3LPHa9q2e6Kx0-cT7sPDt8D7NxySxNV_C8r9factHFAgViQItU6oO55AnYROpRY-_4PU-f5SiKoRmXhUCBYJXOAjNdzYLRhSoAdjHL-efRO7Lb7dAKWYEABHdU7dNAQJGBVY5HTb8nPMq75EHWyMP25juxSuAsp4_JoybYoJOInCdk4Kp18iVFDe1RQ-cl_Rk1tEENjiBqqK9oixqKqKE9amiLmqfkbO_D6c4-a3bZYFbwrGbwZ-0yA34YXH3OS_AsI2fHWPmci8xZborCmFGmtJsCm5vaccadyrnN1VTJbWv5M_KgmlfuBaFajLguFEw0VhZSG6Et8F-jnNNKi_IleR5fx8VVlFK5aF_Uq9-OvCZrPYzekNUSvl23AUSwNm-DUW4B7MRhRg
linkProvider National Library of Medicine
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Standardized+Assessment+of+Health-Related+Quality+of+Life+in+Patients+with+Congenital+Aniridia&rft.jtitle=Klinische+Monatsblatter+fur+Augenheilkunde&rft.au=Hoxha%2C+Zamira&rft.au=Fries%2C+Fabian+Norbert&rft.au=Hecker%2C+Dietmar&rft.au=Seitz%2C+Berthold&rft.date=2025-03-01&rft.eissn=1439-3999&rft.volume=242&rft.issue=3&rft.spage=228&rft_id=info:doi/10.1055%2Fa-2463-3879&rft_id=info%3Apmid%2F39694046&rft_id=info%3Apmid%2F39694046&rft.externalDocID=39694046