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Central retinal artery occlusion – rethinking retinal survival time
BACKGROUND: The critical time from onset of complete occlusion of the central retinal artery (CRA) to functionally significant inner retinal infarction represents a window of opportunity for treatment and also has medical-legal implications, particularly when central retinal artery occlusion (CRAO)...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5907384/ https://www.ncbi.nlm.nih.gov/pubmed/29669523 http://dx.doi.org/10.1186/s12886-018-0768-4 |
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author | Tobalem, Stephan Schutz, James S. Chronopoulos, Argyrios |
author_facet | Tobalem, Stephan Schutz, James S. Chronopoulos, Argyrios |
author_sort | Tobalem, Stephan |
collection | PubMed |
description | BACKGROUND: The critical time from onset of complete occlusion of the central retinal artery (CRA) to functionally significant inner retinal infarction represents a window of opportunity for treatment and also has medical-legal implications, particularly when central retinal artery occlusion (CRAO) complicates therapeutic interventions. Here, we review the evidence for time to infarction from complete CRAO and discuss the implications of our findings. METHODS: A Medline search was performed using each of the terms “central retinal artery occlusion”, “retinal infarction”, “retinal ischemia”, and “cherry red spot” from 1970 to the present including articles in French and German. All retrieved references as well as their reference lists were screened for relevance. An Internet search using these terms was also performed to look for additional references. RESULTS: We find that the experimental evidence showing that inner retinal infarction occurs after 90–240 min of total CRAO, which is the interval generally accepted in the medical literature and practice guidelines, is flawed in important ways. Moreover, the retinal ganglion cells, supplied by the CRA, are part of the central nervous system which undergoes infarction after non-perfusion of 12–15 min or less. CONCLUSIONS: Retinal infarction is most likely to occur after only 12–15 min of complete CRAO. This helps to explain why therapeutic maneuvers for CRAO are often ineffective. Nevertheless, many CRAOs are incomplete and may benefit from therapy after longer intervals. To try to avoid retinal infarcton from inadvertent ocular compression by a headrest during prone anesthesia, the eyes should be checked at intervals of less than 15′. |
format | Online Article Text |
id | pubmed-5907384 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-59073842018-04-30 Central retinal artery occlusion – rethinking retinal survival time Tobalem, Stephan Schutz, James S. Chronopoulos, Argyrios BMC Ophthalmol Research Article BACKGROUND: The critical time from onset of complete occlusion of the central retinal artery (CRA) to functionally significant inner retinal infarction represents a window of opportunity for treatment and also has medical-legal implications, particularly when central retinal artery occlusion (CRAO) complicates therapeutic interventions. Here, we review the evidence for time to infarction from complete CRAO and discuss the implications of our findings. METHODS: A Medline search was performed using each of the terms “central retinal artery occlusion”, “retinal infarction”, “retinal ischemia”, and “cherry red spot” from 1970 to the present including articles in French and German. All retrieved references as well as their reference lists were screened for relevance. An Internet search using these terms was also performed to look for additional references. RESULTS: We find that the experimental evidence showing that inner retinal infarction occurs after 90–240 min of total CRAO, which is the interval generally accepted in the medical literature and practice guidelines, is flawed in important ways. Moreover, the retinal ganglion cells, supplied by the CRA, are part of the central nervous system which undergoes infarction after non-perfusion of 12–15 min or less. CONCLUSIONS: Retinal infarction is most likely to occur after only 12–15 min of complete CRAO. This helps to explain why therapeutic maneuvers for CRAO are often ineffective. Nevertheless, many CRAOs are incomplete and may benefit from therapy after longer intervals. To try to avoid retinal infarcton from inadvertent ocular compression by a headrest during prone anesthesia, the eyes should be checked at intervals of less than 15′. BioMed Central 2018-04-18 /pmc/articles/PMC5907384/ /pubmed/29669523 http://dx.doi.org/10.1186/s12886-018-0768-4 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Tobalem, Stephan Schutz, James S. Chronopoulos, Argyrios Central retinal artery occlusion – rethinking retinal survival time |
title | Central retinal artery occlusion – rethinking retinal survival time |
title_full | Central retinal artery occlusion – rethinking retinal survival time |
title_fullStr | Central retinal artery occlusion – rethinking retinal survival time |
title_full_unstemmed | Central retinal artery occlusion – rethinking retinal survival time |
title_short | Central retinal artery occlusion – rethinking retinal survival time |
title_sort | central retinal artery occlusion – rethinking retinal survival time |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5907384/ https://www.ncbi.nlm.nih.gov/pubmed/29669523 http://dx.doi.org/10.1186/s12886-018-0768-4 |
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