Developmental impairments following severe falciparum malaria in children

Summary Objective  Neurological deficits are reported in children after cerebral malaria (CM) but little is known about the prevalence and characteristics of persisting neurocognitive consequences. The prevalence of developmental impairments following other complications of falciparum malaria, such...

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Veröffentlicht in:Tropical medicine & international health 2005-01, Vol.10 (1), p.3-10
Hauptverfasser: Carter, Julie A., Ross, Amanda J., Neville, Brian G. R., Obiero, Elizabeth, Katana, Khamis, Mung'ala‐Odera, Victor, Lees, Janet A., Newton, Charles R. J. C.
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container_end_page 10
container_issue 1
container_start_page 3
container_title Tropical medicine & international health
container_volume 10
creator Carter, Julie A.
Ross, Amanda J.
Neville, Brian G. R.
Obiero, Elizabeth
Katana, Khamis
Mung'ala‐Odera, Victor
Lees, Janet A.
Newton, Charles R. J. C.
description Summary Objective  Neurological deficits are reported in children after cerebral malaria (CM) but little is known about the prevalence and characteristics of persisting neurocognitive consequences. The prevalence of developmental impairments following other complications of falciparum malaria, such as multiple, prolonged or focal seizures, is not known. Thus, our objective was to investigate the long‐term developmental outcome of CM and malaria with complicated seizures (M/S). Methods  We followed up a cohort of children previously exposed to CM or M/S and children unexposed to either condition. All children between 6 and 9 years of age, exposed to CM, and an equal number of children exposed to M/S were identified from databases of hospital admissions from 1991 to 1998. The unexposed group was randomly selected from a census database. The children's performance was measured using assessments of cognition, motor, speech and language, hearing and vision. A parental questionnaire was used to identify children with epilepsy. Results  CM group scores were significantly lower than unexposed group scores on the assessments of higher level language (adjusted mean difference −1.63, 95% CI: −2.99 to −0.27), vocabulary (−0.02, 95% CI: −0.04 to −0.01), pragmatics (OR 2.81, 95% CI: 1.04–7.6) and non‐verbal functioning (−0.33, 95% CI: −0.61 to −0.06). The areas of significantly reduced functioning for the M/S group were concentrated on phonology (OR 2.74, 95% CI: 1.26–5.95), pragmatics (OR 3.23, 95% CI: 1.2–8.71) and behaviour (OR 1.8, 95% CI: 1.0–3.23). The performance of the active epilepsy group was significantly poorer than that of the group without epilepsy on the tests of comprehension, syntax, pragmatics, word finding, memory, attention, behaviour and motor skills. Conclusions  CM and M/S are associated with developmental impairments. If these impairments persist, this may have implications for least 250 000 children in Sub‐Saharan Africa each year. Active epilepsy significantly increases the risk of cognitive and behavioural problems in children with a history of severe malaria.
doi_str_mv 10.1111/j.1365-3156.2004.01345.x
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R. ; Obiero, Elizabeth ; Katana, Khamis ; Mung'ala‐Odera, Victor ; Lees, Janet A. ; Newton, Charles R. J. C.</creator><creatorcontrib>Carter, Julie A. ; Ross, Amanda J. ; Neville, Brian G. R. ; Obiero, Elizabeth ; Katana, Khamis ; Mung'ala‐Odera, Victor ; Lees, Janet A. ; Newton, Charles R. J. C.</creatorcontrib><description>Summary Objective  Neurological deficits are reported in children after cerebral malaria (CM) but little is known about the prevalence and characteristics of persisting neurocognitive consequences. The prevalence of developmental impairments following other complications of falciparum malaria, such as multiple, prolonged or focal seizures, is not known. Thus, our objective was to investigate the long‐term developmental outcome of CM and malaria with complicated seizures (M/S). Methods  We followed up a cohort of children previously exposed to CM or M/S and children unexposed to either condition. All children between 6 and 9 years of age, exposed to CM, and an equal number of children exposed to M/S were identified from databases of hospital admissions from 1991 to 1998. The unexposed group was randomly selected from a census database. The children's performance was measured using assessments of cognition, motor, speech and language, hearing and vision. A parental questionnaire was used to identify children with epilepsy. Results  CM group scores were significantly lower than unexposed group scores on the assessments of higher level language (adjusted mean difference −1.63, 95% CI: −2.99 to −0.27), vocabulary (−0.02, 95% CI: −0.04 to −0.01), pragmatics (OR 2.81, 95% CI: 1.04–7.6) and non‐verbal functioning (−0.33, 95% CI: −0.61 to −0.06). The areas of significantly reduced functioning for the M/S group were concentrated on phonology (OR 2.74, 95% CI: 1.26–5.95), pragmatics (OR 3.23, 95% CI: 1.2–8.71) and behaviour (OR 1.8, 95% CI: 1.0–3.23). The performance of the active epilepsy group was significantly poorer than that of the group without epilepsy on the tests of comprehension, syntax, pragmatics, word finding, memory, attention, behaviour and motor skills. Conclusions  CM and M/S are associated with developmental impairments. If these impairments persist, this may have implications for least 250 000 children in Sub‐Saharan Africa each year. Active epilepsy significantly increases the risk of cognitive and behavioural problems in children with a history of severe malaria.</description><identifier>ISSN: 1360-2276</identifier><identifier>EISSN: 1365-3156</identifier><identifier>DOI: 10.1111/j.1365-3156.2004.01345.x</identifier><identifier>PMID: 15655008</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Science Ltd</publisher><subject>Africa ; Biological and medical sciences ; Child ; child development ; Children &amp; youth ; Cognition &amp; reasoning ; Cognition Disorders - epidemiology ; Cognition Disorders - etiology ; Convulsions &amp; seizures ; Developmental Disabilities - epidemiology ; Developmental Disabilities - etiology ; Epilepsy - psychology ; falciparum malaria ; Female ; Follow-Up Studies ; Human protozoal diseases ; Humans ; Infectious diseases ; Kenya - epidemiology ; Language Development Disorders - epidemiology ; Language Development Disorders - etiology ; Malaria ; Malaria, Cerebral - psychology ; Malaria, Falciparum - psychology ; Male ; Medical sciences ; Neurology ; Parasitic diseases ; Plasmodium falciparum ; Prevalence ; Protozoal diseases ; Seizures - parasitology ; Seizures - psychology ; Speech Disorders - epidemiology ; Speech Disorders - etiology</subject><ispartof>Tropical medicine &amp; international health, 2005-01, Vol.10 (1), p.3-10</ispartof><rights>2005 INIST-CNRS</rights><rights>2005 Blackwell Publishing Ltd</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5715-b925a26721ec065eb034998c2121578088cec9d8e8c25d1c04cfe4c47f166cd13</citedby><cites>FETCH-LOGICAL-c5715-b925a26721ec065eb034998c2121578088cec9d8e8c25d1c04cfe4c47f166cd13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1365-3156.2004.01345.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1365-3156.2004.01345.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,1433,4024,27923,27924,27925,45574,45575,46409,46833</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=16512155$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15655008$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Carter, Julie A.</creatorcontrib><creatorcontrib>Ross, Amanda J.</creatorcontrib><creatorcontrib>Neville, Brian G. R.</creatorcontrib><creatorcontrib>Obiero, Elizabeth</creatorcontrib><creatorcontrib>Katana, Khamis</creatorcontrib><creatorcontrib>Mung'ala‐Odera, Victor</creatorcontrib><creatorcontrib>Lees, Janet A.</creatorcontrib><creatorcontrib>Newton, Charles R. J. C.</creatorcontrib><title>Developmental impairments following severe falciparum malaria in children</title><title>Tropical medicine &amp; international health</title><addtitle>Trop Med Int Health</addtitle><description>Summary Objective  Neurological deficits are reported in children after cerebral malaria (CM) but little is known about the prevalence and characteristics of persisting neurocognitive consequences. The prevalence of developmental impairments following other complications of falciparum malaria, such as multiple, prolonged or focal seizures, is not known. Thus, our objective was to investigate the long‐term developmental outcome of CM and malaria with complicated seizures (M/S). Methods  We followed up a cohort of children previously exposed to CM or M/S and children unexposed to either condition. All children between 6 and 9 years of age, exposed to CM, and an equal number of children exposed to M/S were identified from databases of hospital admissions from 1991 to 1998. The unexposed group was randomly selected from a census database. The children's performance was measured using assessments of cognition, motor, speech and language, hearing and vision. A parental questionnaire was used to identify children with epilepsy. Results  CM group scores were significantly lower than unexposed group scores on the assessments of higher level language (adjusted mean difference −1.63, 95% CI: −2.99 to −0.27), vocabulary (−0.02, 95% CI: −0.04 to −0.01), pragmatics (OR 2.81, 95% CI: 1.04–7.6) and non‐verbal functioning (−0.33, 95% CI: −0.61 to −0.06). The areas of significantly reduced functioning for the M/S group were concentrated on phonology (OR 2.74, 95% CI: 1.26–5.95), pragmatics (OR 3.23, 95% CI: 1.2–8.71) and behaviour (OR 1.8, 95% CI: 1.0–3.23). The performance of the active epilepsy group was significantly poorer than that of the group without epilepsy on the tests of comprehension, syntax, pragmatics, word finding, memory, attention, behaviour and motor skills. Conclusions  CM and M/S are associated with developmental impairments. If these impairments persist, this may have implications for least 250 000 children in Sub‐Saharan Africa each year. 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R.</au><au>Obiero, Elizabeth</au><au>Katana, Khamis</au><au>Mung'ala‐Odera, Victor</au><au>Lees, Janet A.</au><au>Newton, Charles R. J. C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Developmental impairments following severe falciparum malaria in children</atitle><jtitle>Tropical medicine &amp; international health</jtitle><addtitle>Trop Med Int Health</addtitle><date>2005-01</date><risdate>2005</risdate><volume>10</volume><issue>1</issue><spage>3</spage><epage>10</epage><pages>3-10</pages><issn>1360-2276</issn><eissn>1365-3156</eissn><abstract>Summary Objective  Neurological deficits are reported in children after cerebral malaria (CM) but little is known about the prevalence and characteristics of persisting neurocognitive consequences. The prevalence of developmental impairments following other complications of falciparum malaria, such as multiple, prolonged or focal seizures, is not known. Thus, our objective was to investigate the long‐term developmental outcome of CM and malaria with complicated seizures (M/S). Methods  We followed up a cohort of children previously exposed to CM or M/S and children unexposed to either condition. All children between 6 and 9 years of age, exposed to CM, and an equal number of children exposed to M/S were identified from databases of hospital admissions from 1991 to 1998. The unexposed group was randomly selected from a census database. The children's performance was measured using assessments of cognition, motor, speech and language, hearing and vision. A parental questionnaire was used to identify children with epilepsy. Results  CM group scores were significantly lower than unexposed group scores on the assessments of higher level language (adjusted mean difference −1.63, 95% CI: −2.99 to −0.27), vocabulary (−0.02, 95% CI: −0.04 to −0.01), pragmatics (OR 2.81, 95% CI: 1.04–7.6) and non‐verbal functioning (−0.33, 95% CI: −0.61 to −0.06). The areas of significantly reduced functioning for the M/S group were concentrated on phonology (OR 2.74, 95% CI: 1.26–5.95), pragmatics (OR 3.23, 95% CI: 1.2–8.71) and behaviour (OR 1.8, 95% CI: 1.0–3.23). The performance of the active epilepsy group was significantly poorer than that of the group without epilepsy on the tests of comprehension, syntax, pragmatics, word finding, memory, attention, behaviour and motor skills. Conclusions  CM and M/S are associated with developmental impairments. If these impairments persist, this may have implications for least 250 000 children in Sub‐Saharan Africa each year. Active epilepsy significantly increases the risk of cognitive and behavioural problems in children with a history of severe malaria.</abstract><cop>Oxford, UK</cop><pub>Blackwell Science Ltd</pub><pmid>15655008</pmid><doi>10.1111/j.1365-3156.2004.01345.x</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects Africa
Biological and medical sciences
Child
child development
Children & youth
Cognition & reasoning
Cognition Disorders - epidemiology
Cognition Disorders - etiology
Convulsions & seizures
Developmental Disabilities - epidemiology
Developmental Disabilities - etiology
Epilepsy - psychology
falciparum malaria
Female
Follow-Up Studies
Human protozoal diseases
Humans
Infectious diseases
Kenya - epidemiology
Language Development Disorders - epidemiology
Language Development Disorders - etiology
Malaria
Malaria, Cerebral - psychology
Malaria, Falciparum - psychology
Male
Medical sciences
Neurology
Parasitic diseases
Plasmodium falciparum
Prevalence
Protozoal diseases
Seizures - parasitology
Seizures - psychology
Speech Disorders - epidemiology
Speech Disorders - etiology
title Developmental impairments following severe falciparum malaria in children
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