Treatment outcomes of conventional or high-dose ranibizumab for vascularized pigment epithelial detachment based on lesion subtypes

A post hoc study was conducted to compare visual and anatomic outcomes of vascularized serous pigment epithelial detachment (Group 1) with fibrovascular pigment epithelial detachment (Group 2) due to age-related macular degeneration treated with either 0.5 or 2.0 mg ranibizumab injections. A prospec...

Full description

Saved in:
Bibliographic Details
Published in:European journal of ophthalmology Vol. 28; no. 6; p. 677
Main Authors: Chan, Clement K, Sarraf, David, Abraham, Prema
Format: Journal Article
Language:English
Published: United States 01.11.2018
Subjects:
ISSN:1724-6016, 1724-6016
Online Access:Get more information
Tags: Add Tag
No Tags, Be the first to tag this record!
Abstract A post hoc study was conducted to compare visual and anatomic outcomes of vascularized serous pigment epithelial detachment (Group 1) with fibrovascular pigment epithelial detachment (Group 2) due to age-related macular degeneration treated with either 0.5 or 2.0 mg ranibizumab injections. A prospective, randomized trial was performed with the following regimens for 12 months: (1) 0.5 mg monthly, (2) 0.5 mg monthly for 4 months followed by pro re nata injections, (3) 2.0 mg monthly, and (4) 2.0 mg monthly for 4 months followed by pro re nata injections. Primary measure was best-corrected standardized vision. Secondary measures included central subfield, thickness surface area A , greatest linear diameter, heights of pigment epithelial detachment and choroidal neovascularization (CNV), subretinal fluid, cystoid macular edema, and adverse events. For 36 eyes (8 in Group 1 and 28 in Group 2), follow-up time was 12 months. There were no differences in baseline features between groups except for pigment epithelial detachment A (Group 2 > Group 1). Two-way analysis of variance showed comparable improvements in anatomic and vision outcomes. Three-way analysis of variance also showed similar responses for both lesion subtypes with high-dose treatment. There was a trend toward greater pigment epithelial detachment resolution in Group 1 eyes. There were no differences in retinochoroidal angiomatous proliferation (Type-3 CNV) and cataracts between groups, although greater percentages of eyes in Group 1 developed retinal pigment epithelial tears (25% vs 10.7%). There were no differences in vision and anatomic outcomes between lesion subtypes, and similarly, more rapid responses to high-dose than conventional-dose ranibizumab occurred for eyes with both lesion subtypes. More retinal pigment epithelial tears may develop in eyes with vascularized serous pigment epithelial detachment.
AbstractList A post hoc study was conducted to compare visual and anatomic outcomes of vascularized serous pigment epithelial detachment (Group 1) with fibrovascular pigment epithelial detachment (Group 2) due to age-related macular degeneration treated with either 0.5 or 2.0 mg ranibizumab injections.INTRODUCTION:A post hoc study was conducted to compare visual and anatomic outcomes of vascularized serous pigment epithelial detachment (Group 1) with fibrovascular pigment epithelial detachment (Group 2) due to age-related macular degeneration treated with either 0.5 or 2.0 mg ranibizumab injections.A prospective, randomized trial was performed with the following regimens for 12 months: (1) 0.5 mg monthly, (2) 0.5 mg monthly for 4 months followed by pro re nata injections, (3) 2.0 mg monthly, and (4) 2.0 mg monthly for 4 months followed by pro re nata injections. Primary measure was best-corrected standardized vision. Secondary measures included central subfield, thickness surface area A2, greatest linear diameter, heights of pigment epithelial detachment and choroidal neovascularization (CNV), subretinal fluid, cystoid macular edema, and adverse events.METHODS:A prospective, randomized trial was performed with the following regimens for 12 months: (1) 0.5 mg monthly, (2) 0.5 mg monthly for 4 months followed by pro re nata injections, (3) 2.0 mg monthly, and (4) 2.0 mg monthly for 4 months followed by pro re nata injections. Primary measure was best-corrected standardized vision. Secondary measures included central subfield, thickness surface area A2, greatest linear diameter, heights of pigment epithelial detachment and choroidal neovascularization (CNV), subretinal fluid, cystoid macular edema, and adverse events.For 36 eyes (8 in Group 1 and 28 in Group 2), follow-up time was 12 months. There were no differences in baseline features between groups except for pigment epithelial detachment A2 (Group 2 > Group 1). Two-way analysis of variance showed comparable improvements in anatomic and vision outcomes. Three-way analysis of variance also showed similar responses for both lesion subtypes with high-dose treatment. There was a trend toward greater pigment epithelial detachment resolution in Group 1 eyes. There were no differences in retinochoroidal angiomatous proliferation (Type-3 CNV) and cataracts between groups, although greater percentages of eyes in Group 1 developed retinal pigment epithelial tears (25% vs 10.7%).RESULTS:For 36 eyes (8 in Group 1 and 28 in Group 2), follow-up time was 12 months. There were no differences in baseline features between groups except for pigment epithelial detachment A2 (Group 2 > Group 1). Two-way analysis of variance showed comparable improvements in anatomic and vision outcomes. Three-way analysis of variance also showed similar responses for both lesion subtypes with high-dose treatment. There was a trend toward greater pigment epithelial detachment resolution in Group 1 eyes. There were no differences in retinochoroidal angiomatous proliferation (Type-3 CNV) and cataracts between groups, although greater percentages of eyes in Group 1 developed retinal pigment epithelial tears (25% vs 10.7%).There were no differences in vision and anatomic outcomes between lesion subtypes, and similarly, more rapid responses to high-dose than conventional-dose ranibizumab occurred for eyes with both lesion subtypes. More retinal pigment epithelial tears may develop in eyes with vascularized serous pigment epithelial detachment.CONCLUSION:There were no differences in vision and anatomic outcomes between lesion subtypes, and similarly, more rapid responses to high-dose than conventional-dose ranibizumab occurred for eyes with both lesion subtypes. More retinal pigment epithelial tears may develop in eyes with vascularized serous pigment epithelial detachment.
A post hoc study was conducted to compare visual and anatomic outcomes of vascularized serous pigment epithelial detachment (Group 1) with fibrovascular pigment epithelial detachment (Group 2) due to age-related macular degeneration treated with either 0.5 or 2.0 mg ranibizumab injections. A prospective, randomized trial was performed with the following regimens for 12 months: (1) 0.5 mg monthly, (2) 0.5 mg monthly for 4 months followed by pro re nata injections, (3) 2.0 mg monthly, and (4) 2.0 mg monthly for 4 months followed by pro re nata injections. Primary measure was best-corrected standardized vision. Secondary measures included central subfield, thickness surface area A , greatest linear diameter, heights of pigment epithelial detachment and choroidal neovascularization (CNV), subretinal fluid, cystoid macular edema, and adverse events. For 36 eyes (8 in Group 1 and 28 in Group 2), follow-up time was 12 months. There were no differences in baseline features between groups except for pigment epithelial detachment A (Group 2 > Group 1). Two-way analysis of variance showed comparable improvements in anatomic and vision outcomes. Three-way analysis of variance also showed similar responses for both lesion subtypes with high-dose treatment. There was a trend toward greater pigment epithelial detachment resolution in Group 1 eyes. There were no differences in retinochoroidal angiomatous proliferation (Type-3 CNV) and cataracts between groups, although greater percentages of eyes in Group 1 developed retinal pigment epithelial tears (25% vs 10.7%). There were no differences in vision and anatomic outcomes between lesion subtypes, and similarly, more rapid responses to high-dose than conventional-dose ranibizumab occurred for eyes with both lesion subtypes. More retinal pigment epithelial tears may develop in eyes with vascularized serous pigment epithelial detachment.
Author Chan, Clement K
Abraham, Prema
Sarraf, David
Author_xml – sequence: 1
  givenname: Clement K
  surname: Chan
  fullname: Chan, Clement K
  organization: 3 Department of Ophthalmology, Loma Linda University, Loma Linda, CA, USA
– sequence: 2
  givenname: David
  surname: Sarraf
  fullname: Sarraf, David
  organization: 4 Jules Stein Eye Institute/UCLA, Los Angeles, CA, USA
– sequence: 3
  givenname: Prema
  surname: Abraham
  fullname: Abraham, Prema
  organization: 5 Black Hills Regional Eye Institute, Rapid City, SD, USA
BackLink https://www.ncbi.nlm.nih.gov/pubmed/29575941$$D View this record in MEDLINE/PubMed
BookMark eNpNkD1PwzAQhi1UBKWwMyGPLAF_xsmIKr6kSixljhzn0lhK7BA7ldqVP05aisR0r9577hnuCs2cd4DQLSUPlCr1SCkjqWKHLBTh4gzNqWIiSQlNZ__yBbpkuVQyF3SOvtcD6NiBi9iP0fgOAvY1Nt5tp856p1vsB9zYTZNUPgAetLOl3Y-dLnE9bbY6mLHVg91DhXu7Oaqgt7GB1k7HFURtmmNb6jAx3uEWwmTGYSzjrodwjc5r3Qa4Oc0F-nx5Xi_fktXH6_vyaZUYzlVMuNSMM5NJoiUVWnNTQwZcgoGcSZNXGRBaK5OVwoiqUoaVEyZoboShVGZsge5_vf3gv0YIsehsMNC22oEfQ8EIzdJUcHZA707oWHZQFf1gOz3sir_HsR_ko3Jc
CitedBy_id crossref_primary_10_3390_jpm14101041
crossref_primary_10_1177_11206721211006572
crossref_primary_10_1016_j_survophthal_2020_05_003
ContentType Journal Article
DBID CGR
CUY
CVF
ECM
EIF
NPM
7X8
DOI 10.1177/1120672117747034
DatabaseName Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
MEDLINE - Academic
DatabaseTitle MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
MEDLINE - Academic
DatabaseTitleList MEDLINE - Academic
MEDLINE
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: 7X8
  name: MEDLINE - Academic
  url: https://search.proquest.com/medline
  sourceTypes: Aggregation Database
DeliveryMethod no_fulltext_linktorsrc
EISSN 1724-6016
ExternalDocumentID 29575941
Genre Randomized Controlled Trial
Journal Article
GroupedDBID CGR
CUY
CVF
ECM
EIF
NPM
7X8
ID FETCH-LOGICAL-c337t-35a232c850a514aa3cfe8e35ece925c9d8e01f7c8b4c4dd7c2b14a419c4c11582
IEDL.DBID 7X8
ISICitedReferencesCount 2
ISICitedReferencesURI http://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestLinkType=CitingArticles&DestApp=WOS_CPL&KeyUT=000449834800010&url=https%3A%2F%2Fcvtisr.summon.serialssolutions.com%2F%23%21%2Fsearch%3Fho%3Df%26include.ft.matches%3Dt%26l%3Dnull%26q%3D
ISSN 1724-6016
IngestDate Fri Jul 11 10:30:05 EDT 2025
Thu Jan 02 23:04:05 EST 2025
IsPeerReviewed true
IsScholarly true
Issue 6
Keywords retinal pigment epithelial tears
vascularized pigment epithelial detachment
Fibrovascular pigment epithelial detachment
vascularized serous pigment epithelial detachment
Language English
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c337t-35a232c850a514aa3cfe8e35ece925c9d8e01f7c8b4c4dd7c2b14a419c4c11582
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ObjectType-Undefined-3
PMID 29575941
PQID 2018664328
PQPubID 23479
ParticipantIDs proquest_miscellaneous_2018664328
pubmed_primary_29575941
PublicationCentury 2000
PublicationDate 2018-Nov
20181101
PublicationDateYYYYMMDD 2018-11-01
PublicationDate_xml – month: 11
  year: 2018
  text: 2018-Nov
PublicationDecade 2010
PublicationPlace United States
PublicationPlace_xml – name: United States
PublicationTitle European journal of ophthalmology
PublicationTitleAlternate Eur J Ophthalmol
PublicationYear 2018
Score 2.1743102
Snippet A post hoc study was conducted to compare visual and anatomic outcomes of vascularized serous pigment epithelial detachment (Group 1) with fibrovascular...
SourceID proquest
pubmed
SourceType Aggregation Database
Index Database
StartPage 677
SubjectTerms Aged
Aged, 80 and over
Analysis of Variance
Angiogenesis Inhibitors - therapeutic use
Choroidal Neovascularization - drug therapy
Choroidal Neovascularization - pathology
Contrast Sensitivity - physiology
Female
Humans
Intravitreal Injections
Male
Middle Aged
Prospective Studies
Ranibizumab - therapeutic use
Retinal Detachment - drug therapy
Retinal Detachment - pathology
Retinal Detachment - physiopathology
Retinal Pigment Epithelium - pathology
Tomography, Optical Coherence
Vascular Endothelial Growth Factor A - antagonists & inhibitors
Visual Acuity - physiology
Title Treatment outcomes of conventional or high-dose ranibizumab for vascularized pigment epithelial detachment based on lesion subtypes
URI https://www.ncbi.nlm.nih.gov/pubmed/29575941
https://www.proquest.com/docview/2018664328
Volume 28
WOSCitedRecordID wos000449834800010&url=https%3A%2F%2Fcvtisr.summon.serialssolutions.com%2F%23%21%2Fsearch%3Fho%3Df%26include.ft.matches%3Dt%26l%3Dnull%26q%3D
hasFullText
inHoldings 1
isFullTextHit
isPrint
link http://cvtisr.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV2_a9wwFBZpL0OXtCFpe2kTVOgqcpZkW55CKA1ZetxwgduM_PTUGlL7Gt9lyJp_PO_5bNKlUMhiZGMJI33S-_x-CvG1wMr7mGcqAMyUjS5RDojIBchIePk0Md72xSby-dytVsViULh1g1vleCb2B3VogXXk9JPOqdms0e5i_Udx1Si2rg4lNF6JiSEqw6jOV330W66t4kwjz5bJc2IWbHfktiWc239zyl62XL196Ve9EwcDq5SXOxgcij1sjsTjcnQil-12Q-NhJ9so__Yzl-2d5ITFKrQdShJbdVU_bH_7ShKXlaOXav2AQa7rn_1QuOYojluCrWT3U_jVP2VhGGTbyFtk9ZvsthUrd7tjcXP1ffntWg01FxQYk2-UST1xLHDpjNbJem8gokOTImChUyiCw1kSc3CVBRtCDrqi12xSgAUil06_F6-btsGPQlpErT31A5tazJzLIkQNmdOxMK7Kp-LLOKclYZoNFb7BdtuVz7M6FR92C1Oud8k3Sl1wSVGbnPxH70_iDd_sQgc_i0mkHY2nYh_uN3V3d9aDha7zxY8n9lPO4Q
linkProvider ProQuest
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=Treatment+outcomes+of+conventional+or+high-dose+ranibizumab+for+vascularized+pigment+epithelial+detachment+based+on+lesion+subtypes&rft.jtitle=European+journal+of+ophthalmology&rft.au=Chan%2C+Clement+K&rft.au=Sarraf%2C+David&rft.au=Abraham%2C+Prema&rft.date=2018-11-01&rft.issn=1724-6016&rft.eissn=1724-6016&rft.volume=28&rft.issue=6&rft.spage=677&rft_id=info:doi/10.1177%2F1120672117747034&rft.externalDBID=NO_FULL_TEXT
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1724-6016&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1724-6016&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1724-6016&client=summon