Malaria clinical features
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Transcript of Malaria clinical features
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MALARIA
Clinical features and diagnosis
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EPIDEMIOLOGY
Malaria is a major public health problem Malaria is the fifth most common infectious
cause of mortality 3.3 billion ( half of world’s population ) are at
risk of malaria in 109 countries In 2009 Cases-225 million deaths -7.81 million
www.searo.who.int
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DISEASE BURDEN IN SOUTH EAST ASIA REGION
Out of 11 countries of the Region 10 countries
are malaria endemic
15% of the global reported confirmed cases
and 2.7% of the global mortality.
In southeast Asia region India accounts for 80%
of cases
www.searo.who.int
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INDIA
80.5% of the population lives in malaria risk areas
In 2010 15.9 million cases were reported No of deaths- 1023
nvbdcp.gov.in
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KSCH DATA(2010-2011)
Total no of slides examined -7092
Total no of positives- 336
P vivax-291
P falciparum-45
Deaths- 10
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CLINICAL FEATURES
Children are asymptomatic during the initial phase– the incubation period
P falciparum ---- 9-14 days P vivax---- 12-17 days P ovale---- 16-18 days P malariae--- 18-40 days Prolonged in p vivax, partial immunity
and incomplete chemoprophylaxis.
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PRODROMAL SYMPTOMS
Headache Fatigue Anorexia Myalgia Pain in joints Chest and abdominal pain
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CLINICAL FEATURES (CONT..)
The classic presentation is paroxysms of fever alternating with periods of
fatigue but otherwise relative wellness
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CLINICAL FEATURES (CONT…)
Fever is the cardinal symptom of malaria Febrile paroxysms associated with rigors ,
headache, myalgia , back pain, abdominal pain, nausea and vomiting.
Paroxysms coincide with rupture of schizonts P vivax: every 48 hours( benign tertian
malaria) P falciparum and mixed infections: no
periodicity or less appparent.
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PRESENTATION
Fever 96% Chills 96% Headache 79% Muscle Pain 60% Palpable liver 33% Palpable Spleen 28% Nausea or vomiting 23% Abdominal pain/diarrhea 6%
(According to the working group of WHO,2001)
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On the basis of severity malaria can be classified as
uncomplicated complicated
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UNCOMPLICATED MALARIA
Uncomplicated malaria is defined as symptomatic malaria without signs of severity or evidence (clinical or laboratory) of vital organ dysfunction.
The signs and symptoms of uncomplicated malaria are nonspecific.
Malaria is usually suspected clinically on the basis of fever or a history of fever.
Guidelines for the treatment of malaria – 2nd edition World Health Organization, 2010
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COMPLICATED OR SEVERE MALARIA
In a patient with P. falciparum parasitaemia presence of certain clinical features or laboratory parameters classify the patient as severe or complicated malaria
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COMPLICATED MALARIA (CONT..)
Clinical features
Impaired consciousness or unrousable coma
prostration
Failure to feed
Multiple convulsions (more than 2 episodes in
24 h)
Deep breathing, respiratory distress
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COMPLICATED MALARIA (CONT..)
Clinical features (cont..) Circulatory collapse or shock, systolic blood
pressure < 70 mm Hg in adults and < 50 mm Hg in children
Clinical jaundice ( serum bil > 3 mg/dl) plus evidence of other vital organ dysfunction
Haemoglobinuria Abnormal spontaneous bleeding Pulmonary oedema (radiological)
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COMPLICATED MALARIA (CONT…)
Laboratory parameters
Hypoglycemia (blood glucose < 2.2 mmol/l or < 40 mg/dl)
Metabolic acidosis (plasma bicarbonate < 15 mmol/l)
Severe normocytic anaemia (Hb < 5 g/dl)
Haemoglobinuria
Hyperparasitaemia (> 2%in low intensity transmission areas or >
5% in ar eas of high stable malaria transmission intensity)
Hyperlactataemia (lactate > 5 mmol/l)
Renal impairment (serum creatinine 3 mg/dl)
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CLINICAL PROFILE OF SEVERE MALARIA IN INDIACharacteristics Frequency(46) Mortality
Cerebral malaria 76% 22%
Severe anemia 34% 56%
Hypoglycemia 21% 40%
Jaundice 15% 57%
Renal failure 8% 75%
Blackwater fever 6% 66%
Algid malaria 4% 50%
Indian Pediatrics 2003; 40:939-945
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CEREBRAL MALARIA
Cerebral malaria is the most severe
neurological complication of
Plasmodium falciparum
It is a major cause of acute non-
traumatic encephalopathy in tropical
countries
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CEREBRAL MALARIA (CONT..)
Clinical syndrome characterised by Coma (inability to localise a painful
stimulus) at least 1 h after termination of a seizure or correction of hypoglycaemia
Detection of asexual forms of P falciparum malaria parasites on peripheral blood smears, and exclusion of other causes
WHO. Severe falciparum malaria. Trans R Soc Trop Med Hyg 2000
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CEREBRAL MALARIA (CONT...)
Seizures Seizures are commonly reported and occur in
over 60% of children causes of seizures In children not associated with fever at the
time of the seizure or electrolyte disturbances. Sequestration of infected erythrocytes Parasite-derived toxins Immune mechanisms
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CEREBRAL MALARIA (CONT..)
Coma Cerebral malaria is a diffuse encephalopathy
characterised by coma and bilateral slowing on Electroencephalography
coma is potentially reversible. Brainstem signs Changes in pupillary size and reaction Disorders of conjugate gaze and eye movements. Abnormal respiratory patterns (such as
hyperventilatory, ataxic, and periodic breathing) posture (decerebrate, decorticate, or opisthotonic
posturing), and motor abnormalities of tone and reflexes
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CEREBRAL MALARIA (CONT..)
Cerebral malaria should be considered in the differential diagnosis of any patient who has a febrile illness with impaired consciousness who lives in or has recently travelled to malaria endemic areas
The mortality rate in children is about 20%, and most deaths happen within 24 h of admission.
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CEREBRAL MALARIA
Clinical feature Children (African) Adults
Onset Rapid Insidious
Seizures More common (in 80%)
In 20 %
Neurological signs
Brainstem signs, raised ICP,retinal changes
Symmetrical upper motor neuron signs
Mortality 18.6% 20%
Sequelae 11% <5%
Lancet Neurol 2005; 4: 827–40
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NEUROLOGICAL SEQUELAE
Hemiplegia
Cortical blindness
Aphasia
Ataxia
Cognitive impairment
Richard Idro ,Lancet Neurol 2005; 4: 827–40
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MALARIAL RETINOPATHY
Common in children with cerebral malaria(60%) and may be related to pathological changes
Malarial retinopathy consists of four main components: retinal whitening, vessel changes(whitening of retinal vessels), retinal hemorrhages, and papilledema
Bad prognostic indicator
Lancet Neurol 2005; 4: 827–40
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ANEMIA OF MALARIA
• Hemoglobin less than 8 g/dl, which is equivalent to a hematocrit of less than 24% in a parasitemic individual
Abdalla S, Weatherall D, Wickramasinghe SN and Hughes M (1980). The anaemia of P. falciparum malaria. Br. J. Haematol. 46: 171
• World Health Organization has defined severe malarial anemia (SMA) as a hemoglobin less than 5 g/dL or a hematocrit less than 15% seen in the context of malaria but without specifying parasitemia .
WHO (2000). Severe falciparum malaria. Trans. R. Soc. Trop. Med. Hyg. 94: Suppl. 1.
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PANCYTOPENIA
Pancytopenia can occur in both falciparum and vivax infections.
Can be due to microangiopathic hemolytic anemia, hypersplenism
Few cases due to bone marrow suppression have and hemophagocytosis have been reported
J Fam Community Med. 2009;16:71-73
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HEPATIC DYSFUNCTION
In patients with severe malarial infestation, the incidence of jaundice is reported to be around 2.5%
Transient abnormalities of liver enzymes are most commonly seen
If serum bil > 3 mg/dl---- severe malaria Hepatic encephalopathy is almost never
seen. Bhalla A J Postgrad Med 2006 Oct-
Dec;52(4):315-20.
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RENAL FAILURE
• In P. falciparum malaria, acute renal failure may develop in 0.1-0.6% of the patients
Defined as Urine output <400 ml/24 hours in adults (<12 ml/kg/24 hours in children) and a serum creatinine >265 µmol/l (> 3.0 mg/dl) despite adequate volume repletion
Renal failure is rare in children• High mortality (upto 45%)
Indian Academy of Clinical Medicine Vol. 3, No. 2 April-June 2002
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RENAL FAILURE CONTD..
The vulnerable group of patients are: with high parasitaemia with deep jaundice with prolonged dehydration patients receiving NSAIDs Manifests as ATN ,renal cortical
necrosis never develops
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METABOLIC ACIDOSIS
Venous lactate concentration at 4 hours after
admission to hospital is the BEST PROGNOSTIC
INDICATOR in severe malaria. (>5mmol/l has
bad prognosis)
This may result form renal failure, but more
commonly there is a primary lactic acidosis
Trans R Soc Trop Med Hyg. 1994 Jan-Feb;88(1):67-
73.
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HYPOGLYCEMIA
Hypoglycemia occurs in 30% of children
Hypoglycemia is a sign of poor prognosis
with a mortality rate as high as 40%.
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PULMONARY EDEMA/ADULT RESPIRATORYDISTRESS SYNDROME (ARDS)
May develop even after several days of
antimalarial therapy
Mortality >80%
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P VIVAX…. NEGLECTED AND NOT BENIGN
In recent years, complicated and even
fatal cases of malaria due to P. vivax
have been increasingly reported
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COMPLICATIONS OF P VIVAXCONTD..
Severe anemia Acute respiratory distress syndrome (ARDS) Incidence is less in children compared adults
Coma Malnutrition Splenic rupture Thrombocytopenia Acute renal failure and shock mortality rate - 1.6% among hospitalized patients
Trends in Parasitology Vol.25 No.5
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DIAGNOSIS
Symptom-based (clinical) diagnosis
Not possible to accurately diagnose malaria using
any one set of clinical criteria
Microscopy
Microscopy of stained thick and thin blood smears
remains the gold standard for confirmation of
diagnosis of malaria.
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DIAGNOSIS(CONT..)
In profound anemia ---parasite --often absent
malaria pigment in polymorphonuclear leukocytes and monocytes-- malaria
If more than 5% of PNM contains visible pigment it denotes poor prognosis.
Recommendations and IAP plan of action indian pediatrics volume 42 november 2005
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EXAMINATION OF BLOOD FILM
A minimum of 100 fields should be
examined before concluding the slide
to be negative.
Samples may be examined for at least
three consecutive days where clinical
suspicion of malaria persists.
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ADVANTAGE OF MICROSCOPY
Advantages of microscopy are: The sensitivity is high. It is possible to
detect malaria parasites at low densities.
It also helps to quantify the parasite load.
It is possible to distinguish the various species of malaria parasite and their different stages
WHO Expert Committee on Malaria. Twentieth report. Geneva, World Health Organization, 2000
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DIAGNOSIS (CONT..)
Rapid diagnostic tests are immunochromatographic tests that detect parasite-specific antigens in a finger-prick blood sample
WHO recommends that such tests should have a sensitivity of > 95% in detecting plasmodia at densities of more than 100 parasites per μl of blood
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DIAGNOSIS RDT..
Current tests are based on the detection of histidine-rich protein 2 (HRP2), (specific for P. Falciparum)
pan-specific or species-specific Plasmodium lactate dehydrogenase (pLDH)
pan-specific aldolase Commercially available kit can detect
falciparum, vivax and other malaria but cannot differentiate ovale and malarie malaria.
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DIAGNOSIS RDT..
HRP-II tests can remain positive for 7-14 days following malaria treatment even when blood doesn't show parasitemia by microscopy
p LDH is produced by only viable parasite so the tests detecting this antigen becomes negative within 3-5 days of treatment
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ADVANTAGES OF RDTS IN COMPARISON TOMICROSCOPY simple, straight forward ,less time
consuming, requiring no special equipment or skill/training
They can detect P. falciparum infection even when the parasite is sequestered
This test can exclude mixed falciparum and vivax malaria where the former may not be evident microscopically
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DISADVANTAGE OF RDTS IN COMPARISONTO MICROSCOPY
RDTs that target HRP-II of P. Falciparum is unsuitable for assessment of treatment failure and monitoring of drug resistance.
They do not quantify the parasite load so they do not have prognostic value
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DISADVANTAGES RDT CONT...
Under optimal conditions an expert microscopist can detect even 5-10 parasite per μl of blood, detection threshold of RDTs are 40- 60 parasite per μl of blood
Currently, available RDT kits are required
to be stored up to or under 30ºC