Abstract |
Cerebral malaria is a rapidly progressive encephalopathy with up to 50% mortality. A cardinal feature is the massing of red cells containing mature Plasmodium falciparum within the cerebral capillaries. Adhesion of these parasitised red cells to endothelium, an event which may initiate cerebral malaria, is being studied at the molecular level. However, the relevance of these studies to the pathophysiology and treatment of human cerebral malaria is uncertain. Although chloroquine is still widely used to treat falciparum malaria, resistance has spread to most of the endemic zone. Quinine is emerging as the only effective treatment for cerebral malaria, though resistance to this drug threatens to become a problem. Alternative drugs are urgently needed.
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Authors | R E Phillips, T Solomon |
Journal | Lancet (London, England)
(Lancet)
Vol. 336
Issue 8727
Pg. 1355-60
(Dec 01 1990)
ISSN: 0140-6736 [Print] England |
PMID | 1978171
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Review)
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Chemical References |
- Antimalarials
- Tumor Necrosis Factor-alpha
- Quinine
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Topics |
- Adult
- Animals
- Antimalarials
(administration & dosage, therapeutic use)
- Blood-Brain Barrier
(physiology)
- Brain Diseases
(blood, drug therapy, etiology, parasitology)
- Child, Preschool
- Developing Countries
- Erythrocytes
(metabolism, parasitology)
- Humans
- Hypoglycemia
(blood, etiology)
- Malaria
(blood, complications, diagnosis, drug therapy, epidemiology)
- Plasmodium falciparum
- Prognosis
- Quinine
(administration & dosage, therapeutic use)
- Tumor Necrosis Factor-alpha
(analysis)
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