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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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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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 & 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</subject><ispartof>Tropical medicine & 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&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 & 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. Active epilepsy significantly increases the risk of cognitive and behavioural problems in children with a history of severe malaria.</description><subject>Africa</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>child development</subject><subject>Children & youth</subject><subject>Cognition & reasoning</subject><subject>Cognition Disorders - epidemiology</subject><subject>Cognition Disorders - etiology</subject><subject>Convulsions & seizures</subject><subject>Developmental Disabilities - epidemiology</subject><subject>Developmental Disabilities - etiology</subject><subject>Epilepsy - psychology</subject><subject>falciparum malaria</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Human protozoal diseases</subject><subject>Humans</subject><subject>Infectious diseases</subject><subject>Kenya - epidemiology</subject><subject>Language Development Disorders - epidemiology</subject><subject>Language Development Disorders - etiology</subject><subject>Malaria</subject><subject>Malaria, Cerebral - psychology</subject><subject>Malaria, Falciparum - psychology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Neurology</subject><subject>Parasitic diseases</subject><subject>Plasmodium falciparum</subject><subject>Prevalence</subject><subject>Protozoal diseases</subject><subject>Seizures - parasitology</subject><subject>Seizures - psychology</subject><subject>Speech Disorders - epidemiology</subject><subject>Speech Disorders - etiology</subject><issn>1360-2276</issn><issn>1365-3156</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkclOwzAQhi0EYn8FFCHBLcF24qUHDqhslYq4wNlynQm4chbshpa3x6EVSFzAF48934z-mR-hhOCMxHMxz0jOWZoTxjOKcZFhkhcsW22h_e_E9leMU0oF30MHIcxxJAvGd9FeTDOGsdxHk2t4B9d2NTQL7RJbd9r64RGSqnWuXdrmJQmR8ZBU2hnbad_XSa2d9lYntknMq3Wlh-YI7UQgwPHmPkTPtzdP4_t0-ng3GV9NU8MEYelsRJmmXFACBnMGM5wXo5E0lFDChMRSGjCjUkL8YiUxuDAVFKYQFeHclCQ_ROfrvp1v33oIC1XbYMA53UDbB8VFLkQc9U-QCJlTgoeOp7_Aedv7Jg6hoqZCRsU8QnINGd-G4KFSnbe19h-KYDWYouZq2L0adq8GU9SXKWoVS082_ftZDeVP4caFCJxtAB2MdpXXjbHhh-NsWA6L3OWaW1oHH_8WoJ4eJkOUfwLL7aaC</recordid><startdate>200501</startdate><enddate>200501</enddate><creator>Carter, Julie A.</creator><creator>Ross, Amanda J.</creator><creator>Neville, Brian G. R.</creator><creator>Obiero, Elizabeth</creator><creator>Katana, Khamis</creator><creator>Mung'ala‐Odera, Victor</creator><creator>Lees, Janet A.</creator><creator>Newton, Charles R. J. C.</creator><general>Blackwell Science Ltd</general><general>Blackwell Science</general><general>Blackwell Publishing Ltd</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T2</scope><scope>7U9</scope><scope>C1K</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>7X8</scope></search><sort><creationdate>200501</creationdate><title>Developmental impairments following severe falciparum malaria in children</title><author>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.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5715-b925a26721ec065eb034998c2121578088cec9d8e8c25d1c04cfe4c47f166cd13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Africa</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>child development</topic><topic>Children & youth</topic><topic>Cognition & reasoning</topic><topic>Cognition Disorders - epidemiology</topic><topic>Cognition Disorders - etiology</topic><topic>Convulsions & seizures</topic><topic>Developmental Disabilities - epidemiology</topic><topic>Developmental Disabilities - etiology</topic><topic>Epilepsy - psychology</topic><topic>falciparum malaria</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Human protozoal diseases</topic><topic>Humans</topic><topic>Infectious diseases</topic><topic>Kenya - epidemiology</topic><topic>Language Development Disorders - epidemiology</topic><topic>Language Development Disorders - etiology</topic><topic>Malaria</topic><topic>Malaria, Cerebral - psychology</topic><topic>Malaria, Falciparum - psychology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Neurology</topic><topic>Parasitic diseases</topic><topic>Plasmodium falciparum</topic><topic>Prevalence</topic><topic>Protozoal diseases</topic><topic>Seizures - parasitology</topic><topic>Seizures - psychology</topic><topic>Speech Disorders - epidemiology</topic><topic>Speech Disorders - etiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Virology and AIDS Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>MEDLINE - Academic</collection><jtitle>Tropical medicine & international health</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Carter, Julie A.</au><au>Ross, Amanda J.</au><au>Neville, Brian G. 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 & 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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