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1. e-mail: jkcmp@rh.dk
Internet: http://www.cmp.dk Severe and complicated malaria Jørgen Kurtzhals
Centre for Medical Parasitology
Rigshospitalet, Copenhagen, Denmark
2. e-mail: jkcmp@rh.dk
Internet: http://www.cmp.dk Cerebral malaria kills ½-1 million children every year
3. e-mail: jkcmp@rh.dk
Internet: http://www.cmp.dk Correct treatment: 85% survival – most without sequelae
4. e-mail: jkcmp@rh.dk
Internet: http://www.cmp.dk 15% of cerebral malaria patients die
5. e-mail: jkcmp@rh.dk
Internet: http://www.cmp.dk The asexual parasite multiplication cycle
6. e-mail: jkcmp@rh.dk
Internet: http://www.cmp.dk Sequestration interferes with splenic removal of schizont-infected erythrocytes
7. e-mail: jkcmp@rh.dk
Internet: http://www.cmp.dk Sequestration of erythrocytes in the brain
8. e-mail: jkcmp@rh.dk
Internet: http://www.cmp.dk Cerebral malaria – clinical features P. falciparum – often (not always) high parasitaemia
High temperature – (or hypothermia)
Impaired consciousness
From prostration and convulsions -> deep coma
Convulsions
Partial motor seizures
Convulsions is a bad sign
Classical definition of cerebral malaria
Unrousable coma
Mortality 5-15%
9. e-mail: jkcmp@rh.dk
Internet: http://www.cmp.dk Cerebral malaria - diagnosis Exclusion diagnosis
Other manifestations of malaria (may co-exist)
Hypoglycaemia
Hyponatriaemia
Multi-organ failure
Prolonged post-ictal state
Other infections (may co-exist!)
Meningitis
Sepsis
Metabolic diseases (e.g. DM)
Neurologic diseases
Head trauma
10. e-mail: jkcmp@rh.dk
Internet: http://www.cmp.dk Cerebral malaria – treatment Effective anti-malarial – i.v. quinine
Alternative: artemisinin, artesunate… i.v. or rectal
Anti-convulsive therapy
Only when clinically indicated (respiration depression)
Avoid hypoglycaemia
Ensure vital functions
Correct electrolyte derangement
11. e-mail: jkcmp@rh.dk
Internet: http://www.cmp.dk Severe anaemia - pathogenesis
12. e-mail: jkcmp@rh.dk
Internet: http://www.cmp.dk Severe anaemia P. falciparum – often, not always, high parasitaemia
Often prolonged duration
Hb < 5 g/dl (3 mmol/l)
Lactic acidosis – ’respiratory distress’
Hypovolaemia
Haemolysis
Hyperbilirubinaemia
Haemoglobinuria
13. e-mail: jkcmp@rh.dk
Internet: http://www.cmp.dk Severe anaemia – treatment Effective anti-malarial treatment
Parasite clearance restores bone marrow function
Blood transfusion
At >20% parasitaemia ~ exchange transfusion
Optimise circulation and oxygenation
Keep high urinary output
Caveat: do not precipitate pulmonary oedema
General supportive treatment
14. e-mail: jkcmp@rh.dk
Internet: http://www.cmp.dk Other severe complications Pulmonary oedema
ARDS
Renal insufficiency
Haemolysis
Thrombocytopaenia, DIC
Superinfections
Septicaemia
15. e-mail: jkcmp@rh.dk
Internet: http://www.cmp.dk Recommended laboratory investigations Blood film (x3)
Blood culture
Hb, thrombocytes, WBC and differential count
Na, K, creatinine
Bilirubin, ASAT, factor II-VII-X, LDH
Glucose
(Arterial blood gas, lactate)
16. e-mail: jkcmp@rh.dk
Internet: http://www.cmp.dk Case 1 53 year old male civil engineer, resident in Ghana for 6 years.
No malaria prophylaxis due to fear of side effects (and general opposition toward doctors)
During field work feeling feverish, treated with aspirin
Returned after 5 days. Wife finds the patient extremely ill looking and rushes him to hospital
17. e-mail: jkcmp@rh.dk
Internet: http://www.cmp.dk Case 1 (ctd.) On arrival pale, acutely ill, tp. 41.2oC, slow cerebrated
Blood film: 17% P. falciparum (ring stages)
Hb 8.2 g/dl, thrombocyte count 46, WBC normal range
Creatinine 320 mmol/l, Na 120 mmol/l, K 4.0 mmol/l
Glucose 3.8 mmol/l
Treatment suggestion?
18. e-mail: jkcmp@rh.dk
Internet: http://www.cmp.dk Case 1 (ctd.) Quinine 10 mg/kg infusion in 5% dextrose/saline over 4 h stat.
Quinine 10 mg/kg infusion tds
After parasite clearance (marked reduction) continue oral quinine at same dosage for 7 days
Alternatively doxycycline 100 mg/day for 7 days
CAVE! Never use mefloquine after quinine
Other necessary measures?
19. e-mail: jkcmp@rh.dk
Internet: http://www.cmp.dk Case 1 (ctd.) Hyponatraemia treated with isotonic saline and frusemide
Renal function did not deteriorate but was normalised after rehydration
Follow blood glucose carefully
Thrombocytes normalised after parasite clearance
20. e-mail: jkcmp@rh.dk
Internet: http://www.cmp.dk Theories about pathogenesis of cerebral malaria Impaired cerebral blood flow?
Sequestration of infected RBC in blood vessels
Histological picture
Ophthalmoscopy
21. e-mail: jkcmp@rh.dk
Internet: http://www.cmp.dk Near infrared spectrophotometry (NIRS)
22. e-mail: jkcmp@rh.dk
Internet: http://www.cmp.dk ScO2 on admission
23. e-mail: jkcmp@rh.dk
Internet: http://www.cmp.dk Theories about pathogenesis of cerebral malaria Impaired cerebral blood flow?
Regional blood flow changes
24. e-mail: jkcmp@rh.dk
Internet: http://www.cmp.dk Theories about pathogenesis of cerebral malaria Generalised excessive inflammation
High TNF levels
Association with TNF promoter polymorphism
Animal experiments
25. e-mail: jkcmp@rh.dk
Internet: http://www.cmp.dk Increased levels of inflammation markers in cerebral malaria
26. e-mail: jkcmp@rh.dk
Internet: http://www.cmp.dk Theories about pathogenesis of cerebral malaria Impaired cerebral blood flow?
Regional blood flow changes
Excessive inflammation
Regional inflammation
27. e-mail: jkcmp@rh.dk
Internet: http://www.cmp.dk Theories about pathogenesis of severe malarial anaemia Destruction of erythrocytes
Schizogony
Infected cells removed in spleen
Uninfected cells removed in spleen
28. e-mail: jkcmp@rh.dk
Internet: http://www.cmp.dk Complement binding to erythrocytes- direct Coombs’ test
29. e-mail: jkcmp@rh.dk
Internet: http://www.cmp.dk Pathogenesis of severe malaria Cerebral malaria – too much
Excessive inflammation
Localised in the brain
Local neuronal excitation
Possible focal impairment of micro-circulation
Redirection of circulation
Severe anaemia – too little
Insufficient inflammation
Long term infection
Low grade inflammation
Bone marrow suppression
Erythrocyte destruction