Severe neurological sequelae and behaviour problems after cerebral malaria in Ugandan children
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Published on: June 8, 2017
Richard Idro1, Angelina Kakooza-Mwesige, Stephen Balyejjussa
1Department of Paediatrics and Child Health, Mulago Hospital and Makerere University School of Medicine, PO Box 7072, Kampala, Uganda. ridro1@gmail.com.
Insights
Children surviving cerebral malaria often experience severe neurological deficits, including motor weakness, speech and vision loss, and epilepsy. Some behavioral issues, similar to ADHD, may also arise, highlighting the need for comprehensive care.
Area of Science:
- Neurology
- Pediatrics
- Infectious Diseases
Background:
- Cerebral malaria (CM) is a severe complication of falciparum malaria, causing significant death and neuro-disability in sub-Saharan Africa.
- Understanding the long-term functional deficits and behavioral problems in children surviving CM is crucial for effective management.
Purpose of the Study:
- To describe functional deficits and behavioral problems in children with severe neurological sequelae after CM.
- To identify patterns of brain injury associated with these sequelae.
Main Methods:
- Retrospective review of records from a child neurology clinic in Uganda (2007-2008).
- Analysis of deficits in gross motor function, speech, vision, hearing, behavior, and epilepsy.
- Classification of deficits by onset (immediate/late) and injury pattern (focal/generalized).
Main Results:
- 23 children with CM sequelae were analyzed.
- Common deficits included spastic motor weakness (14), speech loss (14), blindness (12), epilepsy (12), and behavioral problems (11).
- Behavioral issues resembled Attention Deficit Hyperactivity Disorder (ADHD) and conduct disorders; some deficits resolved, while others persisted.
Conclusions:
- Severe behavioral problems are significant sequelae of childhood cerebral malaria.
- Varied patterns of sequelae suggest different pathogenic mechanisms or injury types.
- CM offers a potential model for studying ADHD pathogenesis.
Background:
Cerebral malaria is the most severe neurological complication of falciparum malaria and a leading cause of death and neuro-disability in sub-Saharan Africa. This study aimed to describe functional deficits and behaviour problems in children who survived cerebral malaria with severe neurological sequelae and identify patterns of brain injury.
Findings:
Records of children attending a specialist child neurology clinic in Uganda with severe neurological sequelae following cerebral malaria between January 2007 and December 2008 were examined to describe deficits in gross motor function, speech, vision and hearing, behaviour problems or epilepsy. Deficits were classified according to the time of development and whether their distribution suggested a focal or generalized injury. Any resolution during the observation period was also documented.Thirty children with probable exposure to cerebral malaria attended the clinic. Referral information was inadequate to exclude other diagnoses in 7 children and these were excluded. In the remaining 23 patients, the commonest severe deficits were spastic motor weakness (14), loss of speech (14), hearing deficit (9), behaviour problems (11), epilepsy (12), blindness (12) and severe cognitive impairment (9). Behaviour problems included hyperactivity, impulsiveness and inattentiveness as in attention deficit hyperactivity disorder (ADHD) and conduct disorders with aggressive, self injurious or destructive behaviour. Two patterns were observed; a) immediate onset deficits present on discharge and b) late onset deficits. Some deficits e.g. blindness, resolved within 6 months while others e.g. speech, showed little improvement over the 6-months follow-up.
Conclusions:
In addition to previously described neurological and cognitive sequelae, severe behaviour problems may follow cerebral malaria in children. The observed differences in patterns of sequelae may be due to different pathogenic mechanisms, brain regions affected or extent of injury. Cerebral malaria may be used as a new model to study the pathogenesis of ADHD.
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