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Justifications
Sensitive for detecting malarial parasites than
thin films, as the blood is more concentrated
which allow for a greater volume of blood to be
Coagulation
profile
Renal function
test
Liver function
test
Arterial blood
gas
Urinalysis
Random blood
sugar
Blood culture
examined.
Identification and calculation of the parasitaemia
(percentage of parasitised red blood cells).
Necessary to determine appropriate treatment.
High parasitaemia (>2% of erythrocytes
parasitised) is a sign of more severe disease
Low platelet count secondary to consumptive
coagulopathy
Variable white blood cell count
Anemia
Elevated prothrombin time
Elevated urea and creatinine due to pre-renal AKI
Renal failure may develop due to microvascular
obstruction, filtration of free haemoglobin and
myoglobin, volume depletion, and hypotension,
with reduced urine output and proteinuria.
Elevated unconjugated bilirubin and
aminotransferase
Metabolic acidosis/lactic acidosis in severe
disease
Tissue hypoxia due to microvascular obstruction,
impaired red cell deformability, anaemia,
hypovolaemia, and hypotension can lead to lactic
acidosis, which may contribute to impaired level
of consciousness.
Massive haemolysis combined with acute tubular
necrosis produce acute renal failure with
haemoglobinuria and proteinuria.
May show trace to moderate protein;
urobilinogen and conjugated bilirubin may be
present
Hypoglycemia / hyperglycemia
Hypoglycemia secondary to quinine therapy
To rule out septicemia
(g)What are the laboratory findings associated with severe malaria. Name
three (3) such laboratory findings.
Hypoglycaemia (blood glucose < 3.0 mmol/l)
Metabolic acidosis (plasma bicarbonate < 18 mmol/l)
Severe normocytic anaemia (Hb < 8 g/dl, packed cell volume <
24%)
Haemoglobinuria
Hyperparasitaemia
(> 20,000/l for P. knowlesi or > 100,000/ l for other Plasmodium
species)
Hyperlactataemia
Renal impairment
Candidates are not expected to quantify the laboratory results
above.
(h)What are the clinical features associated with severe malaria. Name 3
such clinical features.
Impaired consciousness or unrousable coma
Prostration (generalized weakness so that the patient is unable to
walk or sit up without assistance)
Failure to feed/ not tolerating orally
Convulsion
Deep breathing, respiratory distress (acidotic breathing)
Circulatory collapse or shock, systolic blood pressure < 90 mm Hg
(**please refer to physician for local figure) in adults and < 50 mm
Hg in children
Clinical jaundice and evidence of other vital organ dysfunction
Haemoglobinuria
Abnormal spontaneous bleeding
Pulmonary oedema (radiological)
Chronic complications
Tropical splenomegaly
Quartan malarial nephropathy
(Distinction)
(j) For each of the complication stated above, describe the principle(s) of
management.
Shown
Plasmodi
Plasmodium
Plasmodi
um
Plasmodi Plasmodi
knowlesi
um
falciparu um vivax um ovale
malariae
m
Asexual
72
cycle
48 (tertian) 48 (tertian) 48 (tertian)
(QUARTAN)
(hours)
Relapse
No
YES
YES
No
Chloroquin
e
YES
Rare
No
No
resistance
Rings
predomina
Oval RBCs
te, multiply
Trophozoit
Enlarged
with
infected
e
RBCs,
fringed
RBCs, high
cytoplasm
Schffners edges,
parasitemi
compact
dots,
Schffners
a, rings
(band
Characteris
trophozoite
dots,
with
forms), 6tic on thin
cytoplasm trophozoite
thread-like
12
blood film
ameboid, cytoplasm
cytoplasm,
merozoites
12-24
compact,
double
in mature
merozoites
6-16
nuclei,
schizont,
in mature merozoites
bananaRBC
schizont in mature
shaped
unchanged
schizont
gametocyt
es
24 (tertian)
No
No
Similar to P.
malariae , 8-10
merozoites in
mature
schizont, often
in rosette
pattern with
central clump
of pigment