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Pediatric posterior reversible encephalopathy syndrome: Age related clinico‐radiological profile and neurologic outcomes
Background The aim of this study was to analyze the characteristics of pediatric posterior reversible encephalopathy syndrome (PRES) to determine clinical and radiologic differences between younger and older age groups, and to identify risk factors for development of any neurologic sequelae. Methods...
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Published in: | Pediatrics international 2023-01, Vol.65 (1), p.e15562-n/a |
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creator | Ekinci, Faruk Yildizdas, Dincer Horoz, Ozden Ozgur Gul Mert, Gulen Kaya, Omer Bayram, Ibrahim Atmis, Bahriye Leblebisatan, Goksel Sezgin, Gulay Yavas, Damla Pinar |
description | Background
The aim of this study was to analyze the characteristics of pediatric posterior reversible encephalopathy syndrome (PRES) to determine clinical and radiologic differences between younger and older age groups, and to identify risk factors for development of any neurologic sequelae.
Methods
The study cohort consisted of confirmed pediatric PRES patients in a tertiary care university hospital from January, 2015, to December, 2020. Demographic and clinical properties, radiological manifestations, and neurologic outcomes were noted. Children aged ≤6 years were compared with those older than 6 years and factors affecting neurologic outcomes were evaluated.
Results
The most common underlying diseases were oncological (37%) and kidney diseases (29%). Epileptic seizures were the most frequent symptoms at initial clinical presentation. The regions in the brain that were most commonly involved were the occipital region (n = 65, 96%), the parietal region (n = 52, 77%), and the frontal lobe (n = 35, 54%). Magnetic resonance imaging (MRI) findings were consistent with atypical patterns in most of the study cohort (71%). Patients with unfavorable clinical outcomes (n = 13, 19.1%) had longer initial seizure times and longer encephalopathy times, lower leucocyte and absolute neutrophil counts, and lower neutrophil to lymphocyte ratios. No relationship was found between MRI findings, involvement patterns, and neurologic outcomes.
Conclusions
No clinically specific differences between two different age groups were found. Atypical imaging manifestations of pediatric PRES in our study had an incidence that was as high as those found in earlier adult studies. Multivariate logistic regression analysis showed that the initial neutrophil to lymphocyte ratio, absolute neutrophil counts, and white cell counts could not predict poor neurologic outcomes. |
doi_str_mv | 10.1111/ped.15562 |
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The aim of this study was to analyze the characteristics of pediatric posterior reversible encephalopathy syndrome (PRES) to determine clinical and radiologic differences between younger and older age groups, and to identify risk factors for development of any neurologic sequelae.
Methods
The study cohort consisted of confirmed pediatric PRES patients in a tertiary care university hospital from January, 2015, to December, 2020. Demographic and clinical properties, radiological manifestations, and neurologic outcomes were noted. Children aged ≤6 years were compared with those older than 6 years and factors affecting neurologic outcomes were evaluated.
Results
The most common underlying diseases were oncological (37%) and kidney diseases (29%). Epileptic seizures were the most frequent symptoms at initial clinical presentation. The regions in the brain that were most commonly involved were the occipital region (n = 65, 96%), the parietal region (n = 52, 77%), and the frontal lobe (n = 35, 54%). Magnetic resonance imaging (MRI) findings were consistent with atypical patterns in most of the study cohort (71%). Patients with unfavorable clinical outcomes (n = 13, 19.1%) had longer initial seizure times and longer encephalopathy times, lower leucocyte and absolute neutrophil counts, and lower neutrophil to lymphocyte ratios. No relationship was found between MRI findings, involvement patterns, and neurologic outcomes.
Conclusions
No clinically specific differences between two different age groups were found. Atypical imaging manifestations of pediatric PRES in our study had an incidence that was as high as those found in earlier adult studies. Multivariate logistic regression analysis showed that the initial neutrophil to lymphocyte ratio, absolute neutrophil counts, and white cell counts could not predict poor neurologic outcomes.</description><identifier>ISSN: 1328-8067</identifier><identifier>EISSN: 1442-200X</identifier><identifier>DOI: 10.1111/ped.15562</identifier><identifier>PMID: 37310120</identifier><language>eng</language><publisher>Australia: Blackwell Publishing Ltd</publisher><subject>Age groups ; Encephalopathy ; Epilepsy ; Frontal lobe ; Kidney diseases ; Leukocytes (neutrophilic) ; Lymphocytes ; Magnetic resonance imaging ; Neuroimaging ; Neurological complications ; Neutrophils ; outcome ; Patients ; pediatric ; Pediatrics ; posterior reversible encephalopathy syndrome ; risk factor ; Risk factors ; Seizures</subject><ispartof>Pediatrics international, 2023-01, Vol.65 (1), p.e15562-n/a</ispartof><rights>2023 Japan Pediatric Society.</rights><rights>2023 Japan Pediatric Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3772-5e0ce3f5913b79f17fc6c183fea6b8d45417cd8b1cc0a70425095f62f464d0ce3</citedby><cites>FETCH-LOGICAL-c3772-5e0ce3f5913b79f17fc6c183fea6b8d45417cd8b1cc0a70425095f62f464d0ce3</cites><orcidid>0000-0001-7590-650X ; 0000-0002-1160-5617 ; 0000-0003-0739-5108 ; 0000-0003-2396-5692 ; 0000-0001-7998-0686 ; 0000-0001-6675-3150 ; 0000-0003-3435-757X ; 0000-0003-0330-4766 ; 0000-0002-1133-4845 ; 0000-0002-0424-4155</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37310120$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ekinci, Faruk</creatorcontrib><creatorcontrib>Yildizdas, Dincer</creatorcontrib><creatorcontrib>Horoz, Ozden Ozgur</creatorcontrib><creatorcontrib>Gul Mert, Gulen</creatorcontrib><creatorcontrib>Kaya, Omer</creatorcontrib><creatorcontrib>Bayram, Ibrahim</creatorcontrib><creatorcontrib>Atmis, Bahriye</creatorcontrib><creatorcontrib>Leblebisatan, Goksel</creatorcontrib><creatorcontrib>Sezgin, Gulay</creatorcontrib><creatorcontrib>Yavas, Damla Pinar</creatorcontrib><title>Pediatric posterior reversible encephalopathy syndrome: Age related clinico‐radiological profile and neurologic outcomes</title><title>Pediatrics international</title><addtitle>Pediatr Int</addtitle><description>Background
The aim of this study was to analyze the characteristics of pediatric posterior reversible encephalopathy syndrome (PRES) to determine clinical and radiologic differences between younger and older age groups, and to identify risk factors for development of any neurologic sequelae.
Methods
The study cohort consisted of confirmed pediatric PRES patients in a tertiary care university hospital from January, 2015, to December, 2020. Demographic and clinical properties, radiological manifestations, and neurologic outcomes were noted. Children aged ≤6 years were compared with those older than 6 years and factors affecting neurologic outcomes were evaluated.
Results
The most common underlying diseases were oncological (37%) and kidney diseases (29%). Epileptic seizures were the most frequent symptoms at initial clinical presentation. The regions in the brain that were most commonly involved were the occipital region (n = 65, 96%), the parietal region (n = 52, 77%), and the frontal lobe (n = 35, 54%). Magnetic resonance imaging (MRI) findings were consistent with atypical patterns in most of the study cohort (71%). Patients with unfavorable clinical outcomes (n = 13, 19.1%) had longer initial seizure times and longer encephalopathy times, lower leucocyte and absolute neutrophil counts, and lower neutrophil to lymphocyte ratios. No relationship was found between MRI findings, involvement patterns, and neurologic outcomes.
Conclusions
No clinically specific differences between two different age groups were found. Atypical imaging manifestations of pediatric PRES in our study had an incidence that was as high as those found in earlier adult studies. Multivariate logistic regression analysis showed that the initial neutrophil to lymphocyte ratio, absolute neutrophil counts, and white cell counts could not predict poor neurologic outcomes.</description><subject>Age groups</subject><subject>Encephalopathy</subject><subject>Epilepsy</subject><subject>Frontal lobe</subject><subject>Kidney diseases</subject><subject>Leukocytes (neutrophilic)</subject><subject>Lymphocytes</subject><subject>Magnetic resonance imaging</subject><subject>Neuroimaging</subject><subject>Neurological complications</subject><subject>Neutrophils</subject><subject>outcome</subject><subject>Patients</subject><subject>pediatric</subject><subject>Pediatrics</subject><subject>posterior reversible encephalopathy syndrome</subject><subject>risk factor</subject><subject>Risk factors</subject><subject>Seizures</subject><issn>1328-8067</issn><issn>1442-200X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp1kc9qFTEUh4MotlYXvoAE3Ohi2vyd5LortVWhYBcK7kImOWlTcidjMlO5rnwEn7FPYuq0G8FsTjjny8chP4ReUnJI2zmawB9SKXv2CO1TIVjHCPn2uN05050mvdpDz2q9JoRopcVTtMcVp4Qyso9-XoCPdi7R4SnXGUrMBRe4gVLjkADD6GC6silPdr7a4bobfclbeIePL6Fxyc7gsUtxjC7f_vpdrI855cvobMJTySE2hx09HmEp6wDnZXZNUZ-jJ8GmCi_u6wH6enb65eRjd_75w6eT4_POcaVYJ4E44EFuKB_UJlAVXO-o5gFsP2gvpKDKeT1Q54hVRDBJNjL0LIhe-LunB-jN6m37fF-gzmYbq4OU7Ah5qYZpJiURnKiGvv4Hvc5LGdt2hm1Iz5RWvG_U25VyJddaIJipxK0tO0OJuQvEtEDM30Aa--reuAzb1n0gHxJowNEK_Ghftfu_yVycvl-VfwDXZZfh</recordid><startdate>202301</startdate><enddate>202301</enddate><creator>Ekinci, Faruk</creator><creator>Yildizdas, Dincer</creator><creator>Horoz, Ozden Ozgur</creator><creator>Gul Mert, Gulen</creator><creator>Kaya, Omer</creator><creator>Bayram, Ibrahim</creator><creator>Atmis, Bahriye</creator><creator>Leblebisatan, Goksel</creator><creator>Sezgin, Gulay</creator><creator>Yavas, Damla Pinar</creator><general>Blackwell Publishing Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-7590-650X</orcidid><orcidid>https://orcid.org/0000-0002-1160-5617</orcidid><orcidid>https://orcid.org/0000-0003-0739-5108</orcidid><orcidid>https://orcid.org/0000-0003-2396-5692</orcidid><orcidid>https://orcid.org/0000-0001-7998-0686</orcidid><orcidid>https://orcid.org/0000-0001-6675-3150</orcidid><orcidid>https://orcid.org/0000-0003-3435-757X</orcidid><orcidid>https://orcid.org/0000-0003-0330-4766</orcidid><orcidid>https://orcid.org/0000-0002-1133-4845</orcidid><orcidid>https://orcid.org/0000-0002-0424-4155</orcidid></search><sort><creationdate>202301</creationdate><title>Pediatric posterior reversible encephalopathy syndrome: Age related clinico‐radiological profile and neurologic outcomes</title><author>Ekinci, Faruk ; Yildizdas, Dincer ; Horoz, Ozden Ozgur ; Gul Mert, Gulen ; Kaya, Omer ; Bayram, Ibrahim ; Atmis, Bahriye ; Leblebisatan, Goksel ; Sezgin, Gulay ; Yavas, Damla Pinar</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3772-5e0ce3f5913b79f17fc6c183fea6b8d45417cd8b1cc0a70425095f62f464d0ce3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Age groups</topic><topic>Encephalopathy</topic><topic>Epilepsy</topic><topic>Frontal lobe</topic><topic>Kidney diseases</topic><topic>Leukocytes (neutrophilic)</topic><topic>Lymphocytes</topic><topic>Magnetic resonance imaging</topic><topic>Neuroimaging</topic><topic>Neurological complications</topic><topic>Neutrophils</topic><topic>outcome</topic><topic>Patients</topic><topic>pediatric</topic><topic>Pediatrics</topic><topic>posterior reversible encephalopathy syndrome</topic><topic>risk factor</topic><topic>Risk factors</topic><topic>Seizures</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ekinci, Faruk</creatorcontrib><creatorcontrib>Yildizdas, Dincer</creatorcontrib><creatorcontrib>Horoz, Ozden Ozgur</creatorcontrib><creatorcontrib>Gul Mert, Gulen</creatorcontrib><creatorcontrib>Kaya, Omer</creatorcontrib><creatorcontrib>Bayram, Ibrahim</creatorcontrib><creatorcontrib>Atmis, Bahriye</creatorcontrib><creatorcontrib>Leblebisatan, Goksel</creatorcontrib><creatorcontrib>Sezgin, Gulay</creatorcontrib><creatorcontrib>Yavas, Damla Pinar</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Pediatrics international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ekinci, Faruk</au><au>Yildizdas, Dincer</au><au>Horoz, Ozden Ozgur</au><au>Gul Mert, Gulen</au><au>Kaya, Omer</au><au>Bayram, Ibrahim</au><au>Atmis, Bahriye</au><au>Leblebisatan, Goksel</au><au>Sezgin, Gulay</au><au>Yavas, Damla Pinar</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pediatric posterior reversible encephalopathy syndrome: Age related clinico‐radiological profile and neurologic outcomes</atitle><jtitle>Pediatrics international</jtitle><addtitle>Pediatr Int</addtitle><date>2023-01</date><risdate>2023</risdate><volume>65</volume><issue>1</issue><spage>e15562</spage><epage>n/a</epage><pages>e15562-n/a</pages><issn>1328-8067</issn><eissn>1442-200X</eissn><abstract>Background
The aim of this study was to analyze the characteristics of pediatric posterior reversible encephalopathy syndrome (PRES) to determine clinical and radiologic differences between younger and older age groups, and to identify risk factors for development of any neurologic sequelae.
Methods
The study cohort consisted of confirmed pediatric PRES patients in a tertiary care university hospital from January, 2015, to December, 2020. Demographic and clinical properties, radiological manifestations, and neurologic outcomes were noted. Children aged ≤6 years were compared with those older than 6 years and factors affecting neurologic outcomes were evaluated.
Results
The most common underlying diseases were oncological (37%) and kidney diseases (29%). Epileptic seizures were the most frequent symptoms at initial clinical presentation. The regions in the brain that were most commonly involved were the occipital region (n = 65, 96%), the parietal region (n = 52, 77%), and the frontal lobe (n = 35, 54%). Magnetic resonance imaging (MRI) findings were consistent with atypical patterns in most of the study cohort (71%). Patients with unfavorable clinical outcomes (n = 13, 19.1%) had longer initial seizure times and longer encephalopathy times, lower leucocyte and absolute neutrophil counts, and lower neutrophil to lymphocyte ratios. No relationship was found between MRI findings, involvement patterns, and neurologic outcomes.
Conclusions
No clinically specific differences between two different age groups were found. Atypical imaging manifestations of pediatric PRES in our study had an incidence that was as high as those found in earlier adult studies. Multivariate logistic regression analysis showed that the initial neutrophil to lymphocyte ratio, absolute neutrophil counts, and white cell counts could not predict poor neurologic outcomes.</abstract><cop>Australia</cop><pub>Blackwell Publishing Ltd</pub><pmid>37310120</pmid><doi>10.1111/ped.15562</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0001-7590-650X</orcidid><orcidid>https://orcid.org/0000-0002-1160-5617</orcidid><orcidid>https://orcid.org/0000-0003-0739-5108</orcidid><orcidid>https://orcid.org/0000-0003-2396-5692</orcidid><orcidid>https://orcid.org/0000-0001-7998-0686</orcidid><orcidid>https://orcid.org/0000-0001-6675-3150</orcidid><orcidid>https://orcid.org/0000-0003-3435-757X</orcidid><orcidid>https://orcid.org/0000-0003-0330-4766</orcidid><orcidid>https://orcid.org/0000-0002-1133-4845</orcidid><orcidid>https://orcid.org/0000-0002-0424-4155</orcidid></addata></record> |
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subjects | Age groups Encephalopathy Epilepsy Frontal lobe Kidney diseases Leukocytes (neutrophilic) Lymphocytes Magnetic resonance imaging Neuroimaging Neurological complications Neutrophils outcome Patients pediatric Pediatrics posterior reversible encephalopathy syndrome risk factor Risk factors Seizures |
title | Pediatric posterior reversible encephalopathy syndrome: Age related clinico‐radiological profile and neurologic outcomes |
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