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Risk factors for persisting neurological and cognitive impairments following cerebral malaria
1Centre for Geographic Medicine Research-Coast, Kenya Medical Research Institute/Wellcome Trust Research Labs, Kilifi, Kenya. ridro@kilifi.mimcom.net
Insights
Persistent neurological and cognitive impairments after cerebral malaria are linked to factors like seizures and coma. Identifying these risk factors is crucial for developing future prevention strategies.
Area of Science:
- Neurology
- Pediatrics
- Infectious Diseases
Background:
- Cerebral malaria frequently leads to lasting neurological and cognitive deficits.
- While risk factors for severe outcomes are known, those for persistent impairments require further investigation.
Purpose of the Study:
- To identify risk factors associated with persistent neurological and cognitive impairments following cerebral malaria in children.
Main Methods:
- A retrospective study analyzed hospital records of 143 children (aged 6-9 years) with cerebral malaria.
- Assessments for motor, speech, language, and cognitive impairments were conducted at least 20 months post-discharge.
Main Results:
- 23.8% of children exhibited impairments, including motor (9.8%), speech/language (11.2%), and cognitive (14.0%).
- Independent risk factors for persistent impairments included previous seizures, deep coma, focal neurological signs, and discharge neurological deficits.
- Specific impairments were associated with factors like multiple seizures, young age, malnutrition, intracranial hypertension, and hypoglycemia.
Conclusions:
- Key risk factors for persistent impairments are multiple seizures, deep/prolonged coma, hypoglycemia, and intracranial hypertension.
- Distinct risk factors for specific functional impairments suggest varied mechanisms of neuronal damage.
- These findings can inform the development of preventive strategies for post-cerebral malaria impairments.
Background:
Persisting neurological and cognitive impairments are common after cerebral malaria. Although risk factors for gross deficits on discharge have been described, few studies have examined those associated with persistent impairments.
Methods:
The risk factors for impairments following cerebral malaria were determined by examining hospital records of 143 children aged 6-9 years, previously admitted with cerebral malaria, who were assessed at least 20 months after discharge to detect motor, speech and language, and other cognitive (memory, attention, and non-verbal functioning) impairments.
Results:
The median age on admission was 30 months (IQR 19-42) and the median time from discharge to assessment was 64 months (IQR 40-78). Thirty four children (23.8%) were defined as having impairments: 14 (9.8%) in motor, 16 (11.2%) in speech and language, and 20 (14.0%) in other cognitive functions. Previous seizures (OR 5.6, 95% CI 2.0 to 16.0), deep coma on admission (OR 28.8, 95% CI 3.0 to 280), focal neurological signs observed during admission (OR 4.6, 95% CI 1.1 to 19.6), and neurological deficits on discharge (OR 4.5, 95% CI 1.4 to 13.8) were independently associated with persisting impairments. In addition, multiple seizures were associated with motor impairment, age <3 years, severe malnutrition, features of intracranial hypertension, and hypoglycaemia with language impairments, while prolonged coma, severe malnutrition, and hypoglycaemia were associated with impairments in other cognitive functions.
Conclusions:
Risk factors for persisting neurological and cognitive impairments following cerebral malaria include multiple seizures, deep/prolonged coma, hypoglycaemia, and clinical features of intracranial hypertension. Although there are overlaps in impaired functions and risk factors, the differences in risk factors for specific functions may suggest separate mechanisms for neuronal damage. These factors could form the basis of future preventive strategies for persisting impairments.
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