Malaria epidemiology, clinical features & treatment
Malaria is a protozoal disease caused by Plasmodium parasites, primarily transmitted by infected Anopheles mosquitoes. In 2018, approximately 228 million malaria cases were reported globally, with significant mortality, especially among children under five. The document details the epidemiology, symptoms, transmission, and recommended treatments for malaria, highlighting the importance of understanding risk factors and the effectiveness of different therapeutic approaches.
Malaria epidemiology, clinical features & treatment
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Dr Animesh Gupta
MBBS,MD, FDM, FAGE
Associate Professor
Dept. of Community Medicine, NMCH, Jamuhar (Bihar)
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▪Malaria is aprotozoal disease caused by infection with
parasites of the genus Plasmodium and transmitted by
certain species of infected female Anopheles mosquito.
▪Four species of Plasmodium can infect and be spread by
humans.
▪Humans occasionally become infected with Plasmodium
species that normally infect animals, such as P. knowlesi
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▪ Hippocrates wasthe first person who described feature of malaria
in man – 400 BC
▪ Charaka mentioned as fever is the main symptom of malaria – 300
BC
▪ Charles Louis Alphonse Laveran discovered P. malariae parasite
in the blood of soldier – 1880
▪ Ronald Ross discovered the disease transmission by mosquito
▪ Grassi and Feletti discovered P. vivax parasite 1890
▪ WilliamWelch discovered P. falcifarum parasite 1897
▪ Stephenes discovered P. ovale parasite
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▪In 2018 anestimated 228 million cases of malaria occurred
worldwide and 405 000 people died.
▪Children aged under 5 years are the most vulnerable group
affected by malaria.
Source :WHO Malaria Report 2019
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▪Globally, 53% ofthe P.
vivax burden is in the
WHO South-East Asia
Region, with the majority
being in India (47%).
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Reported cases ofMalaria (2018)
▪ Total cases- 429928
▪ P. falciparum cases- 204733
▪ P. vivax – 222730
▪ Mixed - 2465
▪ Deaths- 96
Source :WHO Malaria Report 2019
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▪ Tribal malaria– contributes about 50% of the cases in country
(AP, MP, Gujarat, Jharkhand, Bihar, Maharashtra, Odhisa).
▪ Infants, young children & pregnant women are considered as
high risk group.
▪ Rural malaria – irrigated areas of Haryana, Punjab, western
U.P., & parts of Rajasthan
▪ Urban malaria – 15 major cities like Delhi, Mumbai, Chennai,
Kolkata, Hyderabad, Bengaluru.
▪ Malaria in project areas
▪ Border malaria
▪ Forest malaria 5/7/2020 10Malaria - Epidemiology, Clinical Features & Treatment Dr. Animesh Gupta
▪Agent factor
▪ Malariais caused by 4 distinct species -
P.falciparum, P.vivax, P.ovale, and P.malariae.
▪ P.falciparum causes about 60% of the infections in India, 4-8%
is mixed infections, and rest due to P.vivax.
▪ P.malariae has a restricted distribution and contributes to 1%
of the infections.
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▪ Reservoir OfInfection
▪ With the possible exception of chimpanzees in tropical Africa,
which may carry P.Malariae.
▪ Human reservoir - one who harbours sexual forms of the parasite
▪ Conditions to serve as a reservoir :
▪ Must harbor both sexes of gametocyte in blood
▪ Gametocytes must be mature
▪ Gametocytes must be viable
▪ Gametocytes must be present in sufficient density to infect
mosquitoes.
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▪ Period OfCommunicability
▪ Malaria is communicable as long as mature, viable
gametocytes exist in the circulating blood in sufficient
densities to infect vector mosquitoes.
▪ Gametocytes appear in the blood 4-5 days after asexual
forms appear in P.vivax,and they do not appear until 10-12
days after asexual forms in P.falciparum.
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1. Age- Affectsall ages
2. Sex- Males are affected more frequently than females
3. Race- People with AS hemoglobin (sickle cell trait) have a
milder illness with falciparum infection. People whose RBC’s
are “Duffy negative” are resistant to P.vivax infection
4. Pregnancy- malaria during pregnancy have severe
manifestation
5. Housing- ill-ventilated, ill- lighted houses provide ideal
indoor resting place for mosquitoes.
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6. Occupation –predominantly a rural disease and is closely
related to agricultural practices.
7. Human habits – such as sleeping outdoors, not using
personal protection measures (example: bed nets)
8. Immunity – immunity is acquired only after repeated
exposure after several years.
In endemic areas a state of collective immunity becomes
established slowly and the people develop a considerable
degree of resistance.
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1. Season –maximum prevalence is from July to November (post
monsoon)
2. Temperature – 20 to 30 degree Celsius
3. Humidity – relative humidity of 60% ensures long life span. If
humidity is high they are more active and feed more.
4. Rainfall – provides opportunities for breeding of mosquitoes and may
give rise to epidemics.
5. Altitude – Anophelines are not found at altitudes above 2000 meters
6. Man-Made Malaria – burrow pits, garden pools, canals, irrigation
channels and engineering projects like construction of hydroelectric
dams, roads, bridges
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▪ An.culicifacies- Rural,periurban
▪ An.fluviatilis- Forest, Hilly areas
▪ An.stephensi- Urban, Industrial
▪ An.minimus,An.philippinensis,An.sundaicus – Foothills
▪ An. dirus : forest in NE states
▪ An. epiroticus – Andaman & Nicobar Island
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▪Life Span –10-12 days
▪Resting Habits – Endophily, Exophily, Endophagic,
Exophagic
▪Breeding Habits – moving water, wells, cisterns, fountains,
overhead tanks, garden pools
▪Time Of Biting – Nocturnal feeding between dusk to dawn
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▪ P.falciparum :12 days (9-14 days)
▪ P.vivax : 14 days (8-17 days)
▪ P.malariae : 28 days (18-40 days)
▪ P.ovale : 17 days (16-18 days)
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❑ Uncomplicated Malaria
▪The classical malaria attack lasts 6-10 hours. It consists of
▪ Cold stage (sensation of cold, shivering) – 1 hr
▪ Hot stage (fever, headaches, vomiting; seizures in young children &
Skin is hot and dry to touch) – 2 to 6 hrs
▪ Sweating stage (sweats, return to normal temperature, tiredness) – 2
to 4 hrs.
▪ Symptoms appear 7 days or more (usually 10–15 days) after the
infective mosquito bite.
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▪ Fever
▪ Chills
▪Sweats
▪ Headaches
▪ Nausea and vomiting
▪ Body aches
▪ General malaise
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The manifestations ofsevere malaria include
▪ Cerebral malaria
▪ Severe anemia due to hemolysis
▪ Hemoglobinuria due to hemolysis
▪ Acute respiratory distress syndrome (ARDS),
▪ Abnormalities in blood coagulation
▪ Low BP
▪ Hyperparasitemia, where > 5% of the RBCs are infected by malaria
parasites
▪ Metabolic acidosis often in association with hypoglycemia.
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▪ Microscopy- Thickfilm and Thin film.
Thick film – detection of parasite
Thin slide – identifying or confirmation of species
▪ Serological Tests- Malarial Fluorescent Antibody test usually
becomes positive two weeks or more after primary infection
▪ RDT- Rapid Diagnostic Tests- based on detection of circulating
parasite antigens by a simple dipstick.
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▪ P. vivaxcases
✓ Chloroquine 25 mg/kg bw – divided dosage – 3 days
✓Primaquine – 0.25 mg/kg bw daily – 14 days
✓ Primaquine is contraindicated in infants, pregnant women and
individuals with G6PD deficiency.
[When primaquine is administered to individuals with G6PD deficiency,
its metabolites lead to more severe hemolysis by inducing
oxyhemoglobin generation, GSH depletion and stimulation of the hexose
monophosphate pathway]
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Age in yearsChloroquine (10 mg/kg bw or
150 mg)
Primaquine
(2.5 mg)
Day 1 Day 2 Day 3 For 14 days
< 1 ½ ½ ¼ Nil
1-4 1 1 ½ 1
5-8 2 2 1 2
9-14 3 3 1½ 4
15 & above 4 4 2 6
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Chloroquine – 600 mg on day 1 & Day 2 ; 300 mg on day 3
Primaquine – 12.5 mg for 14 days
Malaria - Epidemiology, Clinical Features & Treatment Dr. Animesh Gupta
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▪ ACT isnot to be given
in 1st trimester of
pregnancy.
▪ Quinine can be given
in 1st trimester
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