Utilização da microscopia confocal in vivo no diagnóstico de ceratites micóticas e por Acanthamoeba, na observação do dano e no processo de regeneração neuronal em ceratites infecciosas

Detalhes bibliográficos
Autor(a) principal: Muller, Rodrigo Thiesen [UNIFESP]
Data de Publicação: 2021
Tipo de documento: Tese
Idioma: por
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: https://sucupira.capes.gov.br/sucupira/public/consultas/coleta/trabalhoConclusao/viewTrabalhoConclusao.jsf?popup=true&id_trabalho=11180379
https://repositorio.unifesp.br/handle/11600/68292
Resumo: Purpose: (1) and (2) to determine the factors that influence the accuracy of in vivo confocal microscopy (IVCM) for diagnosing infectious keratitis (IK) caused by Acanthamoeba and fungi; (3) to evaluate long-term alterations of corneal innervation in patients with herpes simplex virus (HSV) keratitis using IVCM; (4) to investigate the alterations of corneal nerves in patients with IK using IVCM; and (5) to report long-term alterations of corneal nerves in patients with bacterial IK using IVCM. Methods: (1) the first study analyzed 27 patients with Acanthamoeba IK and 34 patients with bacterial IK. Sensitivity and specificity of IVCM for diagnosing Acanthamoeba IK were investigated; (2) the second study included 21 patients with fungal IK and 24 patients with bacterial IK. IVCM images were evaluated for the presence of fungal filamentous; (3) the third study included 16 patients with history of HSV keratitis and 15 agematched normal controls. IVCM images were performed at two time-points: baseline and then after a mean follow-up of 37.3 ± 1.7 months; (4) the fourth study recruited 56 patients with IK as well as 30 normal healthy controls. Corneal sensation and IVCM images were obtained prospectively; and (5) in the fifth study, 13 patients with unilateral bacterial keratitis and 12 controls were enrolled in the study. IVCM was performed in all patients at two-time points: acute phase of the infectious keratitis and after 28 ± 0.6 months from resolution of the infection. Results: In relation to (1) and (2), IVCM had average sensitivity and specificity for Acanthamoeba IK diagnosis of 69% ± 2% and 97% ± 4% for experienced observers, and 59% ± 7% and 92% ± 10% for inexperienced observers, respectively, and sensitivity and specificity for fungal filamentous detection of 71% ± 0% and 89% ± 3% for experienced observers, and 42% ± 6% and 87% ± 17% for inexperienced observers; (3) in the third study, corneal nerve density was significantly decreased in both affected and contralateral unaffected eyes with IK by HSV. There was an increase on nerve density in the affected eyes with HSV overtime; (4) in the fourth study, corneal nerves were significantly reduced during the acute phase in eyes with IK. Despite significant regeneration overtime, the nerve density was still significantly reduced compared to controls; (5) in the fifth study, corneal nerve density was significantly reduced in patients with bacterial keratitis compared to controls. There was partial regeneration of the corneal nerves over the 28-month follow-up. Conclusion: IVCM reveals high sensitivity and moderate specificity on identification of Acanthamoeba cysts and filamentous fungal. There is modest corneal nerve regeneration overtime in patients with HSV keratitis. Patients with IK show profound corneal nerve diminishment during the acute phase of the infection. Despite significantly regeneration of nerves overtime, the subbasal nerve density sustain altered even after more than 2 years after cornea infection resolution.
id UFSP_ec0d598c25d6e36915a32c7a60be4e5b
oai_identifier_str oai:repositorio.unifesp.br/:11600/68292
network_acronym_str UFSP
network_name_str Repositório Institucional da UNIFESP
repository_id_str 3465
spelling Utilização da microscopia confocal in vivo no diagnóstico de ceratites micóticas e por Acanthamoeba, na observação do dano e no processo de regeneração neuronal em ceratites infecciosasOphtahmologyCorneaInfectious KeratitisIn Vivo Confocal MicroscopyCorneal NervesOftalmologiaCorneaCeratite InfecciosaMicroscopia Confocal In VivoInervação CorneanaPurpose: (1) and (2) to determine the factors that influence the accuracy of in vivo confocal microscopy (IVCM) for diagnosing infectious keratitis (IK) caused by Acanthamoeba and fungi; (3) to evaluate long-term alterations of corneal innervation in patients with herpes simplex virus (HSV) keratitis using IVCM; (4) to investigate the alterations of corneal nerves in patients with IK using IVCM; and (5) to report long-term alterations of corneal nerves in patients with bacterial IK using IVCM. Methods: (1) the first study analyzed 27 patients with Acanthamoeba IK and 34 patients with bacterial IK. Sensitivity and specificity of IVCM for diagnosing Acanthamoeba IK were investigated; (2) the second study included 21 patients with fungal IK and 24 patients with bacterial IK. IVCM images were evaluated for the presence of fungal filamentous; (3) the third study included 16 patients with history of HSV keratitis and 15 agematched normal controls. IVCM images were performed at two time-points: baseline and then after a mean follow-up of 37.3 ± 1.7 months; (4) the fourth study recruited 56 patients with IK as well as 30 normal healthy controls. Corneal sensation and IVCM images were obtained prospectively; and (5) in the fifth study, 13 patients with unilateral bacterial keratitis and 12 controls were enrolled in the study. IVCM was performed in all patients at two-time points: acute phase of the infectious keratitis and after 28 ± 0.6 months from resolution of the infection. Results: In relation to (1) and (2), IVCM had average sensitivity and specificity for Acanthamoeba IK diagnosis of 69% ± 2% and 97% ± 4% for experienced observers, and 59% ± 7% and 92% ± 10% for inexperienced observers, respectively, and sensitivity and specificity for fungal filamentous detection of 71% ± 0% and 89% ± 3% for experienced observers, and 42% ± 6% and 87% ± 17% for inexperienced observers; (3) in the third study, corneal nerve density was significantly decreased in both affected and contralateral unaffected eyes with IK by HSV. There was an increase on nerve density in the affected eyes with HSV overtime; (4) in the fourth study, corneal nerves were significantly reduced during the acute phase in eyes with IK. Despite significant regeneration overtime, the nerve density was still significantly reduced compared to controls; (5) in the fifth study, corneal nerve density was significantly reduced in patients with bacterial keratitis compared to controls. There was partial regeneration of the corneal nerves over the 28-month follow-up. Conclusion: IVCM reveals high sensitivity and moderate specificity on identification of Acanthamoeba cysts and filamentous fungal. There is modest corneal nerve regeneration overtime in patients with HSV keratitis. Patients with IK show profound corneal nerve diminishment during the acute phase of the infection. Despite significantly regeneration of nerves overtime, the subbasal nerve density sustain altered even after more than 2 years after cornea infection resolution.Objetivos: (1) e (2) determinar os fatores que influenciam na acurácia da microscopia confocal in vivo (MCIV) em diagnosticar ceratite infecciosa (CI) por Acanthamoeba e fúngica; (3) avaliar alterações na inervação corneana em pacientes com CI pelo vírus do herpes simples (VHS) utilizando MCIV; (4) investigar o comprometimento nos nervos corneanos em pacientes com CI utilizando MCIV; e (5) reportar alterações no plexo nervoso corneano em pacientes com CI bacteriana. Métodos: (1) o primeiro estudo analisou 27 pacientes com CI por Acanthamoeba e 34 pacientes com ceratite bacteriana (grupo-controle). Foram investigados sensibilidade e especificidade da MCIV em diagnosticar ceratite por Acanthamoeba; (2) o segundo estudo incluiu 21 pacientes com diagnóstico de ceratite fúngica e 24 pacientes com ceratite bacteriana. As imagens da MCIV foram avaliadas considerando presença de filamentos fúngicos; (3) o terceiro estudo incluiu 16 pacientes com história de ceratite por VHS e 15 pacientes para grupo-controle. Imagens da MCIV foram obtidas em 2 momentos: exame inicial de base e após uma média de seguimento de 37,3 ± 1,7 meses; (4) o quarto estudo recrutou 56 pacientes com diagnóstico de CI, além de 30 voluntários saudáveis para grupo-controle. Foram obtidos prospectivamente sensibilidade corneana e imagens com MCIV; e (5) o quinto estudo incluiu 13 pacientes com ceratite bacteriana e 12 pacientes saudáveis para o grupo-controle. Realizou-se MCIV em dois momentos: durante a fase aguda da CI e após uma média de 28,3 ± 0,6 meses da resolução da infecção corneana. Resultados: Para (1) e (2), a MCIV apresentou sensibilidade e especificidade no diagnóstico de ceratite por Acanthamoeba de 69% ± 2% e 97% ± 4% para examinadores experientes e de 59% ± 7% e 92% ± 10% para examinadores inexperientes, respectivamente. Para a detecção de filamentos fúngicos, houve sensibilidade e especificidade de 71% ± 0% e 89% ± 3% para examinadores experientes e de 42% ± 6% e 87% ± 17% para examinadores inexperientes; (3) no terceiro, a densidade dos nervos corneanos foi significativamente menor tanto em olhos afetados com ceratite por VHS, quanto no olho contralateral não afetado, em comparação com grupo-controle. Houve aumento na densidade dos nervos corneanos em olhos afetados ao longo do tempo; (4) no quarto estudo, observou-se significativa redução dos nervos corneanos durante a fase aguda da CI. Houve aumento na densidade dos nervos corneanos ao longo do tempo, porém, ainda significativamente diminuída quando comparada à do grupo-controle; e (5) no quinto estudo, a densidade dos nervos corneanos em pacientes com ceratite bacteriana foi significativamente diminuída comparada à do grupo-controle. Houve regeneração parcial dos nervos corneanos ao longo dos 28 meses de seguimento. Conclusão: A MCIV apresenta alta especificidade e moderada sensibilidade na identificação de cistos de Acanthamoeba e filamentos fúngicos. Ocorre discreta regeneração dos nervos corneanos em pacientes com ceratite por VHS ao longo do tempo. Na fase aguda da doença, pacientes com CI apresentam profunda redução na densidade dos nervos corneanos do plexo sub-basal, a qual se mantém alterada mesmo após mais de 2 anos da resolução da infecção.Dados abertos - Sucupira - Teses e dissertações (2021)Universidade Federal de São Paulo (UNIFESP)Sousa, Luciene Barbosa De [UNIFESP]Universidade Federal de São PauloMuller, Rodrigo Thiesen [UNIFESP]2023-06-27T12:33:06Z2023-06-27T12:33:06Z2021info:eu-repo/semantics/doctoralThesisinfo:eu-repo/semantics/publishedVersion80 p.application/pdfhttps://sucupira.capes.gov.br/sucupira/public/consultas/coleta/trabalhoConclusao/viewTrabalhoConclusao.jsf?popup=true&id_trabalho=11180379RODRIGO THIESEN MULLER-A.pdfhttps://repositorio.unifesp.br/handle/11600/68292porinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-12T22:32:14Zoai:repositorio.unifesp.br/:11600/68292Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-12T22:32:14Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Utilização da microscopia confocal in vivo no diagnóstico de ceratites micóticas e por Acanthamoeba, na observação do dano e no processo de regeneração neuronal em ceratites infecciosas
title Utilização da microscopia confocal in vivo no diagnóstico de ceratites micóticas e por Acanthamoeba, na observação do dano e no processo de regeneração neuronal em ceratites infecciosas
spellingShingle Utilização da microscopia confocal in vivo no diagnóstico de ceratites micóticas e por Acanthamoeba, na observação do dano e no processo de regeneração neuronal em ceratites infecciosas
Muller, Rodrigo Thiesen [UNIFESP]
Ophtahmology
Cornea
Infectious Keratitis
In Vivo Confocal Microscopy
Corneal Nerves
Oftalmologia
Cornea
Ceratite Infecciosa
Microscopia Confocal In Vivo
Inervação Corneana
title_short Utilização da microscopia confocal in vivo no diagnóstico de ceratites micóticas e por Acanthamoeba, na observação do dano e no processo de regeneração neuronal em ceratites infecciosas
title_full Utilização da microscopia confocal in vivo no diagnóstico de ceratites micóticas e por Acanthamoeba, na observação do dano e no processo de regeneração neuronal em ceratites infecciosas
title_fullStr Utilização da microscopia confocal in vivo no diagnóstico de ceratites micóticas e por Acanthamoeba, na observação do dano e no processo de regeneração neuronal em ceratites infecciosas
title_full_unstemmed Utilização da microscopia confocal in vivo no diagnóstico de ceratites micóticas e por Acanthamoeba, na observação do dano e no processo de regeneração neuronal em ceratites infecciosas
title_sort Utilização da microscopia confocal in vivo no diagnóstico de ceratites micóticas e por Acanthamoeba, na observação do dano e no processo de regeneração neuronal em ceratites infecciosas
author Muller, Rodrigo Thiesen [UNIFESP]
author_facet Muller, Rodrigo Thiesen [UNIFESP]
author_role author
dc.contributor.none.fl_str_mv Sousa, Luciene Barbosa De [UNIFESP]
Universidade Federal de São Paulo
dc.contributor.author.fl_str_mv Muller, Rodrigo Thiesen [UNIFESP]
dc.subject.por.fl_str_mv Ophtahmology
Cornea
Infectious Keratitis
In Vivo Confocal Microscopy
Corneal Nerves
Oftalmologia
Cornea
Ceratite Infecciosa
Microscopia Confocal In Vivo
Inervação Corneana
topic Ophtahmology
Cornea
Infectious Keratitis
In Vivo Confocal Microscopy
Corneal Nerves
Oftalmologia
Cornea
Ceratite Infecciosa
Microscopia Confocal In Vivo
Inervação Corneana
description Purpose: (1) and (2) to determine the factors that influence the accuracy of in vivo confocal microscopy (IVCM) for diagnosing infectious keratitis (IK) caused by Acanthamoeba and fungi; (3) to evaluate long-term alterations of corneal innervation in patients with herpes simplex virus (HSV) keratitis using IVCM; (4) to investigate the alterations of corneal nerves in patients with IK using IVCM; and (5) to report long-term alterations of corneal nerves in patients with bacterial IK using IVCM. Methods: (1) the first study analyzed 27 patients with Acanthamoeba IK and 34 patients with bacterial IK. Sensitivity and specificity of IVCM for diagnosing Acanthamoeba IK were investigated; (2) the second study included 21 patients with fungal IK and 24 patients with bacterial IK. IVCM images were evaluated for the presence of fungal filamentous; (3) the third study included 16 patients with history of HSV keratitis and 15 agematched normal controls. IVCM images were performed at two time-points: baseline and then after a mean follow-up of 37.3 ± 1.7 months; (4) the fourth study recruited 56 patients with IK as well as 30 normal healthy controls. Corneal sensation and IVCM images were obtained prospectively; and (5) in the fifth study, 13 patients with unilateral bacterial keratitis and 12 controls were enrolled in the study. IVCM was performed in all patients at two-time points: acute phase of the infectious keratitis and after 28 ± 0.6 months from resolution of the infection. Results: In relation to (1) and (2), IVCM had average sensitivity and specificity for Acanthamoeba IK diagnosis of 69% ± 2% and 97% ± 4% for experienced observers, and 59% ± 7% and 92% ± 10% for inexperienced observers, respectively, and sensitivity and specificity for fungal filamentous detection of 71% ± 0% and 89% ± 3% for experienced observers, and 42% ± 6% and 87% ± 17% for inexperienced observers; (3) in the third study, corneal nerve density was significantly decreased in both affected and contralateral unaffected eyes with IK by HSV. There was an increase on nerve density in the affected eyes with HSV overtime; (4) in the fourth study, corneal nerves were significantly reduced during the acute phase in eyes with IK. Despite significant regeneration overtime, the nerve density was still significantly reduced compared to controls; (5) in the fifth study, corneal nerve density was significantly reduced in patients with bacterial keratitis compared to controls. There was partial regeneration of the corneal nerves over the 28-month follow-up. Conclusion: IVCM reveals high sensitivity and moderate specificity on identification of Acanthamoeba cysts and filamentous fungal. There is modest corneal nerve regeneration overtime in patients with HSV keratitis. Patients with IK show profound corneal nerve diminishment during the acute phase of the infection. Despite significantly regeneration of nerves overtime, the subbasal nerve density sustain altered even after more than 2 years after cornea infection resolution.
publishDate 2021
dc.date.none.fl_str_mv 2021
2023-06-27T12:33:06Z
2023-06-27T12:33:06Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/doctoralThesis
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format doctoralThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://sucupira.capes.gov.br/sucupira/public/consultas/coleta/trabalhoConclusao/viewTrabalhoConclusao.jsf?popup=true&id_trabalho=11180379
RODRIGO THIESEN MULLER-A.pdf
https://repositorio.unifesp.br/handle/11600/68292
url https://sucupira.capes.gov.br/sucupira/public/consultas/coleta/trabalhoConclusao/viewTrabalhoConclusao.jsf?popup=true&id_trabalho=11180379
https://repositorio.unifesp.br/handle/11600/68292
identifier_str_mv RODRIGO THIESEN MULLER-A.pdf
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 80 p.
application/pdf
dc.publisher.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
publisher.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
_version_ 1814268272993894400