Death in Shunted Hydrocephalic Children in the 1990s
Using a combined search of the Children’s Hospital (Birmingham, Ala., USA) medical records and the Jefferson County Health Department death records, we reviewed all shunt-related deaths that occurred between January 1990 and July 1996. Of these, we excluded patients who died of nonhydrocephalus-rela...
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Veröffentlicht in: | Pediatric neurosurgery 1998-04, Vol.28 (4), p.173-176 |
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creator | Iskandar, Bermans J. Tubbs, Shane Mapstone, Timothy B. Grabb, Paul A. Bartolucci, Alfred A. Oakes, W. Jerry |
description | Using a combined search of the Children’s Hospital (Birmingham, Ala., USA) medical records and the Jefferson County Health Department death records, we reviewed all shunt-related deaths that occurred between January 1990 and July 1996. Of these, we excluded patients who died of nonhydrocephalus-related reasons, such as bronchopulmonary dysplasia, as well as patients who had other serious neurological illnesses such as brain tumor and hydranencephaly. Twenty-eight patients died of shunt-related causes in the 6.5-year period. A survival analysis showed that 96% survived 32 months after first shunting. Of 28 patients, 23 were beyond help prior to medical evaluation. However, at least 10 of these patients had symptoms suggestive of shunt failure at least 24 h and as long as 2 weeks prior to their demise. We conclude that hydrocephalic children still die of shunt failure despite the modern technology of the 1990s. Some of these causes may be avoidable through early detection of symptoms. Guidelines to patients, families, and primary caregivers should be emphasized. |
doi_str_mv | 10.1159/000028644 |
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We conclude that hydrocephalic children still die of shunt failure despite the modern technology of the 1990s. Some of these causes may be avoidable through early detection of symptoms. Guidelines to patients, families, and primary caregivers should be emphasized.</description><identifier>ISSN: 1016-2291</identifier><identifier>EISSN: 1423-0305</identifier><identifier>DOI: 10.1159/000028644</identifier><identifier>PMID: 9732242</identifier><identifier>CODEN: PDNEEV</identifier><language>eng</language><publisher>Basel, Switzerland: Karger</publisher><subject>Adolescent ; Biological and medical sciences ; Cerebrospinal Fluid Shunts - methods ; Cerebrospinal fluid. Meninges. 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Jerry</creatorcontrib><title>Death in Shunted Hydrocephalic Children in the 1990s</title><title>Pediatric neurosurgery</title><addtitle>Pediatr Neurosurg</addtitle><description>Using a combined search of the Children’s Hospital (Birmingham, Ala., USA) medical records and the Jefferson County Health Department death records, we reviewed all shunt-related deaths that occurred between January 1990 and July 1996. Of these, we excluded patients who died of nonhydrocephalus-related reasons, such as bronchopulmonary dysplasia, as well as patients who had other serious neurological illnesses such as brain tumor and hydranencephaly. Twenty-eight patients died of shunt-related causes in the 6.5-year period. A survival analysis showed that 96% survived 32 months after first shunting. Of 28 patients, 23 were beyond help prior to medical evaluation. However, at least 10 of these patients had symptoms suggestive of shunt failure at least 24 h and as long as 2 weeks prior to their demise. We conclude that hydrocephalic children still die of shunt failure despite the modern technology of the 1990s. Some of these causes may be avoidable through early detection of symptoms. Guidelines to patients, families, and primary caregivers should be emphasized.</description><subject>Adolescent</subject><subject>Biological and medical sciences</subject><subject>Cerebrospinal Fluid Shunts - methods</subject><subject>Cerebrospinal fluid. Meninges. Spinal cord</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Equipment Failure</subject><subject>Female</subject><subject>Humans</subject><subject>Hydrocephalus - mortality</subject><subject>Hydrocephalus - surgery</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Nervous system (semeiology, syndromes)</subject><subject>Neurology</subject><subject>Original Paper</subject><subject>Postoperative Complications</subject><subject>Retrospective Studies</subject><subject>Survival Rate</subject><subject>Time Factors</subject><issn>1016-2291</issn><issn>1423-0305</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqF0NFr1TAUBvAgk21OH3wegzJE8KF6TpKm9zzKdTphbILbc0nTE9vZ294l7cP-ezNvuYII5iWB78cJ5xPiNcJ7xII-QDpyZbR-Jo5RS5WDguIgvQFNLiXhkXgR4z1AwqQPxSGVSkotj4X-xHZqs27IvrfzMHGTXT42YXS8bW3fuWzddn0TeHgSU8sZEkF8KZ5720d-tdwn4u7zxe36Mr-6-fJ1_fEqdxr1lOsV0koiawWeG-lrKC0weyBjwRmUBTTk2Hpq0BoyhmSNzpaSjfd1TepEvN3N3YbxYeY4VZsuOu57O_A4x6pUhAUS_hdKIAXGFAme_wXvxzkMaYkq9YHKrEqZ0LsdcmGMMbCvtqHb2PBYIVRPfVf7vpM9WwbO9YabvVwKTvmbJbfR2d4HO7gu7plUmhJN7HTHftrwg8OffPnk_J_pt-uL36DaNl79An4CmBM</recordid><startdate>19980401</startdate><enddate>19980401</enddate><creator>Iskandar, Bermans J.</creator><creator>Tubbs, Shane</creator><creator>Mapstone, Timothy B.</creator><creator>Grabb, Paul A.</creator><creator>Bartolucci, Alfred A.</creator><creator>Oakes, W. 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Spinal cord</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Equipment Failure</topic><topic>Female</topic><topic>Humans</topic><topic>Hydrocephalus - mortality</topic><topic>Hydrocephalus - surgery</topic><topic>Infant</topic><topic>Infant, Newborn</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Nervous system (semeiology, syndromes)</topic><topic>Neurology</topic><topic>Original Paper</topic><topic>Postoperative Complications</topic><topic>Retrospective Studies</topic><topic>Survival Rate</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Iskandar, Bermans J.</creatorcontrib><creatorcontrib>Tubbs, Shane</creatorcontrib><creatorcontrib>Mapstone, Timothy B.</creatorcontrib><creatorcontrib>Grabb, Paul A.</creatorcontrib><creatorcontrib>Bartolucci, Alfred A.</creatorcontrib><creatorcontrib>Oakes, W. 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A survival analysis showed that 96% survived 32 months after first shunting. Of 28 patients, 23 were beyond help prior to medical evaluation. However, at least 10 of these patients had symptoms suggestive of shunt failure at least 24 h and as long as 2 weeks prior to their demise. We conclude that hydrocephalic children still die of shunt failure despite the modern technology of the 1990s. Some of these causes may be avoidable through early detection of symptoms. Guidelines to patients, families, and primary caregivers should be emphasized.</abstract><cop>Basel, Switzerland</cop><pub>Karger</pub><pmid>9732242</pmid><doi>10.1159/000028644</doi><tpages>4</tpages></addata></record> |
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subjects | Adolescent Biological and medical sciences Cerebrospinal Fluid Shunts - methods Cerebrospinal fluid. Meninges. Spinal cord Child Child, Preschool Equipment Failure Female Humans Hydrocephalus - mortality Hydrocephalus - surgery Infant Infant, Newborn Male Medical sciences Nervous system (semeiology, syndromes) Neurology Original Paper Postoperative Complications Retrospective Studies Survival Rate Time Factors |
title | Death in Shunted Hydrocephalic Children in the 1990s |
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