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MALARIA
Dr.Benny PV
Professor & HOD
Department of Community Medicine
Malaria
Infection by parasite of the
genus Plasmodium, a protozoa
Transmitted to man by infected
female Anopheline mosquito
HISTORY
• Intermittent fever: High incidence during
rainy season, was first recognized by Romans
and Greeks
• They postulated that intermittent fevers
were due to ‘bad odour’ coming from
marshy areas and thus gave the name
‘malaria’ (‘mal’= bad + ‘air’)
Scientists
• In 1880, a French army surgeon, Charles
Louis Alphonse, first observed and
described the malarial parasite in red
blood cells
• In 1894, Sir Ronald Ross proved the
complete life cycle of plasmodium in
mosquitoes
History behind
anti-malarial
The indigenous people of Peru first used tincture
of Cinchona to control fever
In 1820, the active ingredient, Quinine, was first
extracted and named by 2 French chemists
It was the major drug till 1942.
In 1939, Paul Miller discovered the insecticidal
property of DDT
This opened a new avenue in control of malaria
worldwide
Artemisinins were discovered by Chinese
scientists in 1970s
BURDEN OF
DISEASE
• Globally in 2016:
• 216 million cases
• 4,45,000 deaths
• Population at risk - 3.5
billion (half of world’s
population)
• 91 countries had on-
going malaria
transmission
REGION CASES DEATHS
Sub-Saharan
Africa
90% 91%
SEAR 10% 7%
INDIA’S CONTRIBUTION TO
MALARIA IN SEAR
Epidemiology
Agent
Host &
Environment
Agent factors
Agent factors
• P. vivax
• P. falciparum
• P. malariae
• P. ovale
Agent
• Asexual cycle in humans & Sexual cycle in
mosquitoes
• Man – intermediate host, Mosquito –
definitive host
2 cycles of development
Hepatic phase
• In case of Pf, the intrahepatic
schizonts rupture almost
simultaneously & there is no
persistent tissue phase
• In Pv, Po, Pm they do not burst at
same time & some hepatic forms
persists and remain dormant in the
hepatocytes – “Relapses”
Reservoir of
infection
No animal reservoirs
A human reservoir is one who harbours the
sexual forms (gametocytes) of the parasite
Criteria for a man to serve as malaria carrier
• Person should have both the sexes of gametocytes in
the blood
• Gametocytes must be mature
• They must be viable
• Must be present in sufficient density to infect
mosquitoes (at least 12 per cubic mm of blood)
Period of
communicability
Relapses: vivax & ovale - upto 3 years, due to
liver schizonts
Recurrences in falciparum malaria: disappear
within 1-2 years
P.malariae: prolonged, low level, asymptomatic
parasitaemia
P.falciparum & P.malariae: chronic blood
infection (Erythrocytic schizogony persisting at
low level)
Host factors
Host factors
1. Age 6. Housing
2. Sex 7. Population mobility
3. Race 8. Occupation
4. Pregnancy 9. Human Habits
5. Socio- economic development 10. Immunity
Environmental
factors
Environmental
factors
Season: Maximum during July-November
Temperature: Affects life cycle of the parasite
inside vector; optimum range is 20-30 deg.C
Humidity: humidity of 60% is considered necessary
for mosquito to live its normal life span
Rainfall: Provides mosquito breeding places;
increases atmospheric humidity
Altitude: 2000-2500 metres, beyond which
anophelines are not found
Vector
45 species of Anopheles mosquitoes
in India
Six of them are vectors of important
• An. culicifacies-rural & peri-urban areas; highly
zoophilic
• An. stephensi- urban & industrial areas
• An. fluviatilis-hills & forest areas; highly
anthrophilic
• An. minimus-foothills of north eastern states
• An. dirus-forest vector in north east states
• An. epiroticus-Andaman and Nicobar islands
Vector factors
• Breeding habits-fresh water
collections
• Feeding habits-zoophilic / anthrophilic
• Resting habits- endophilic/exophilic
• Time of biting-nocturnal
• Density
• Life span
Mode of
transmission
Vector borne
Direct-blood transfusion; drug addicts
Congenital malaria
• It is the length of time between bite of infective
mosquito (inoculation of sporozoites) & the appearance
of clinical signs (fever)
• Pf - 10 days
• Pv - 12 days
• Po - 14 days
• Pm - 28 days
Incubation period
Types of
malaria
• Urban
• Rural
• Tribal
• Malaria in project areas
• Border
Epidemiological
• Uncomplicated
• Severe
Clinical
• Benign Tertian (Pv)
• Malignant Tertian (Pf)
• Quartan malaria
• Ovale tertian
Periodicity
Clinical
features
Stages of malaria
• Cold Stage
• Hot Stage
• Sweating Stage
Complications of malaria
• Cerebral malaria
• Anemia
• Dehydration
• Acute renal failure
• Liver damage
• GI symptoms
• Black water fever
Features of
severe
malaria
• Impaired consciousness /
coma
• Repeated generalized
convulsions
• Renal failure ( S.creatinine
>3mg/dl )
• Jaundice ( S.bilirubin
>3mg/dl)
• Severe anaemia ( Hb <
5g/dl)
• Pulmonary oedema /
ARDS
• Hypoglycemia ( Plasma
glucose < 40mg/dl)
• Metabolic acidosis
• Circulatory collapse or
shock - “Algid
malaria”
• Abnormal bleeding /
DIC
• Haemoglobinuria
• Hyperthermia (
Temperature >104 F)
• Hyper-parasitaemia
Diagnosis
Diagnosis of
malaria
Microscopy
• Stained thick and thin blood
smears
• Helps to quantify the parasite
load
• Thick smear shows whether the
slide is positive for MP or not
• Thin smear shows the species
of the MP & the stages of
development in red cells
Rapid diagnostic test (RDT)
• RDTs are based on the detection of
circulating parasite antigens
• Several types of RDTs are available
• Cassettes, cards or dip sticks
• Some of them can only detect P.falciparum,
while others can detect other parasite
species also
• Bivalent RDTs (for detecting P.falciparum
and P.vivax )
Serological test
• Malarial fluorescent antibody test
• Positive two weeks or more after primary
infection
• Useful in Epidemiological studies
Treatment
Treatment
• Early diagnosis & treatment of malaria aims
at
• Complete cure
• Prevention of progression of
uncomplicated malaria to severe disease
• Prevention of deaths
• Interruption of transmission
• Minimizing risk of selection and spread of
drug resistant malaria parasite
Treatment of
P.vivax cases
• 10 mg/kg on day 1
• 10 mg/kg on day 2
• 5 mg/kg on day 3
Chloroquine: 25 mg/kg body
wt divided over 3 days
• Primaquine is contraindicated in infants, pregnant
women and individuals with G6PD deficiency
• It can lead to haemolysis in G6PD deficiency
Primaquine: 0.25 mg/kg
body wt daily for 14 days
Treatment of
P.vivax cases
14 days regimen of Primaquine should be
given under supervision
Patient should be advised to stop
primaquine immediately if he/she develops
any of the following symptoms and should
report to the doctor immediately
• Dark coloured urine
• Yellow conjunctiva
• Bluish discolouration of lips
• Abdominal pain
• Nausea, vomiting etc
Paediatric
dose
Treatment of uncomplicated P.falciparum cases
• In states other than NE states
• Artemisinin based Combination Therapy
(ACT-SP)
• Artesunate: 4 mg/kg body wt daily for 3
days +
• Sulfadoxine (25 mg/kg body wt) &
Pyrimethamine (1.25 mg/kg body weight)
on day 1 +
• Primaquine: 0.75 mg/kg body wt on day 2
Treatment of
uncomplicated
P.falciparum
cases
ACT is not to be given in 1st trimester of
pregnancy & for children weighing < 5 kg
“Different coloured Blister Packs” have been
introduced for treatment of uncomplicated
falciparum malaria in different age groups
This has made administration of treatment
by field level staff easy
Monotherapy of Artemisinin derivatives is
BANNED in India
In Children
In North-
Eastern
states
Co-formulated ACT-AL tablets given
according to age group
Artemether 20mg &
Lumefantrine 120mg (
twice daily for 3 days )
Primaquine : 0.75 mg/kg
body wt on day 2
Due to resistance to currently used ACT-SP,
effective combination of Artemether-
Lumefantrine (ACT-AL) has been
recommended
In Children
Treatment of
uncomplicated
P.falciparum
cases in
pregnancy
• Quinine salt 10mg/kg 3 times daily for 7
days
• Quinine may induce hypoglycaemia
• Pregnant women should not start taking
quinine on an empty stomach
1st Trimester
• Area-specific ACT as per dosage schedule
• i.e. ACT-AL in North Eastern states
• ACT-SP in other states
2nd & 3rd Trimester
Treatment of mixed infections
(P.vivax + P.falciparum) cases
• All mixed infections should be treated with
full course of age-specific ACT and
Primaquine 0.25 mg/kg body wt daily for
14 days
• In NE states: ACT-AL for 3 days +
Primaquine 0.25 mg per kg body wt daily
for 14 days
• In other states: ACT-SP for 3 days +
Primaquine 0.25 mg per kg body wt daily
for 14 days.
Treatment of
severe malaria
cases
It’s an emergency and treatment
should be given as per severity
Should do RDT and take blood smear
first
Immediately give a parenteral dose of
artemisinin derivative (or) quinine in
suspected cerebral malaria cases
The parenteral treatment in severe malaria
cases should be given for minimum of 24
hours once started
Prevention and control
Malaria
Malaria
control
Strategic
action plan of
malaria
control in
India
• Case detection ( active & passive )
• Early diagnosis and complete treatment
• Sentinel surveillance
Surveillance and case management
• Indoor residual spray (IRS)
• Insecticidal treated nets (ITN)
• Long lasting insecticidal nets (LLIN)
Integrated vector management
Anti larval measures
Epidemic preparedness and early
response
Strategic action plan of
malaria control in India
• Supportive interventions
• Capacity building
• Behavioural change communication
• Intersectoral collaboration
• Monitoring & Evaluation
• Operational research & applied field
research
Malaria indices
• Annual Parasite Incidence (API)
• Annual Blood Examination Rate
(ABER)
• Annual falciparum incidence
• Slide positivity rate
• Slide falciparum rate
Vector
indices
• Human Blood Index
• Sporozoite Rate
• Mosquito Density
• Man biting Rate
• Inoculation Rate
Surveillance
• Malaria is under regular surveillance under IDSP
• Active case detection(ACD)
• Carried out by MPWs/ ASHAs through fortnightly house visits
• Under NVBDCP, Pf specific RDT kits have been deployed in Pf predominant
areas where microscopy results are not available in 24 hrs
• Since 2012, bivalent RDTs have been introduced
• Passive case detection
• All fever cases attending PHCs/hospitals should be screened for malaria
SHORT TERM
CHEMOPROPHYLAXIS
( UPTO 6 WEEKS )
CHEMOPROPHYLAXIS FOR
LONGER STAY
( MORE THAN 6 WEEKS )
Doxycycline Mefloquine
100 mg once daily & 1.5 mg/kg once daily for
children
250 mg weekly for adults
Should be started 2 days before travel &
continued for 4 weeks after leaving the area
Should be administered 2 weeks before & 4
weeks after exposure
Contraindicated in pregnant women &
children < 8 yrs
Contraindicated in individuals with history of
convulsions, neuropsychiatric problems &
cardiac conditions
Vector control
ANTI – ADULT
MEASURES
ANTI – LARVAL
MEASURES
PERSONAL
PROTECTION
Residual sprays Environmental
Control
Mosquito nets
Space Sprays Chemical control Repellents
Biological control
Anti-adult
measures
• DDT, Malathion,
Fenitrothion
Residual
spraying
• Pyrethrum, Residual
insecticides
Space
sprays
Genetic
control
Spraying
Anti-larval measures
• Environmental control
• Source reduction
• Chemical control
• Mineral oils, Paris green, Synthetic
insecticides
• Biological control
• Gambusia affinis, Lebister
reticulatus
Protection against mosquito
bite
• Mosquito net
• Insecticidal treated nets (ITN)
• Long lasting insecticidal nets (LLIN)
• Screening
• Repellents
• Diethyltoluamide
Chemoprophylaxis
Chemoprophylaxis
• Chemoprophylaxis should be administered
only in selective groups in high P.falciparum
endemic areas
• Use of personal protection measures
including Insecticide Treated bed Nets
(ITN) / Long Lasting Insecticidal Nets (LLIN)
should be encouraged for pregnant women
and other vulnerable population including
travellers for longer stay
Malaria vaccine
• Completed phase 3 trials
• RTS, S/ASO1- P.falciparum
circumsporozoite
• R+T segments of circumsporozoite protein
+ S (HbSAg)= RT (S+ S)
• Adjuvant- ASO1
• 1 vial= 1 mL (2 patients)
Malaria vaccine
• 0.5 mL IM
• WHO recommends 4 doses
• 1st dose at 5 months
• Repeat at 6th and 7th
months
• 4th dose at 18 months
after 3rd dose
THANK YOU

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Malaria (Community Medicine Class)

  • 1. MALARIA Dr.Benny PV Professor & HOD Department of Community Medicine
  • 2. Malaria Infection by parasite of the genus Plasmodium, a protozoa Transmitted to man by infected female Anopheline mosquito
  • 3. HISTORY • Intermittent fever: High incidence during rainy season, was first recognized by Romans and Greeks • They postulated that intermittent fevers were due to ‘bad odour’ coming from marshy areas and thus gave the name ‘malaria’ (‘mal’= bad + ‘air’)
  • 4. Scientists • In 1880, a French army surgeon, Charles Louis Alphonse, first observed and described the malarial parasite in red blood cells • In 1894, Sir Ronald Ross proved the complete life cycle of plasmodium in mosquitoes
  • 5. History behind anti-malarial The indigenous people of Peru first used tincture of Cinchona to control fever In 1820, the active ingredient, Quinine, was first extracted and named by 2 French chemists It was the major drug till 1942. In 1939, Paul Miller discovered the insecticidal property of DDT This opened a new avenue in control of malaria worldwide Artemisinins were discovered by Chinese scientists in 1970s
  • 6. BURDEN OF DISEASE • Globally in 2016: • 216 million cases • 4,45,000 deaths • Population at risk - 3.5 billion (half of world’s population) • 91 countries had on- going malaria transmission REGION CASES DEATHS Sub-Saharan Africa 90% 91% SEAR 10% 7%
  • 7.
  • 11. Agent factors • P. vivax • P. falciparum • P. malariae • P. ovale Agent • Asexual cycle in humans & Sexual cycle in mosquitoes • Man – intermediate host, Mosquito – definitive host 2 cycles of development
  • 12.
  • 13. Hepatic phase • In case of Pf, the intrahepatic schizonts rupture almost simultaneously & there is no persistent tissue phase • In Pv, Po, Pm they do not burst at same time & some hepatic forms persists and remain dormant in the hepatocytes – “Relapses”
  • 14. Reservoir of infection No animal reservoirs A human reservoir is one who harbours the sexual forms (gametocytes) of the parasite Criteria for a man to serve as malaria carrier • Person should have both the sexes of gametocytes in the blood • Gametocytes must be mature • They must be viable • Must be present in sufficient density to infect mosquitoes (at least 12 per cubic mm of blood)
  • 15. Period of communicability Relapses: vivax & ovale - upto 3 years, due to liver schizonts Recurrences in falciparum malaria: disappear within 1-2 years P.malariae: prolonged, low level, asymptomatic parasitaemia P.falciparum & P.malariae: chronic blood infection (Erythrocytic schizogony persisting at low level)
  • 17. Host factors 1. Age 6. Housing 2. Sex 7. Population mobility 3. Race 8. Occupation 4. Pregnancy 9. Human Habits 5. Socio- economic development 10. Immunity
  • 19. Environmental factors Season: Maximum during July-November Temperature: Affects life cycle of the parasite inside vector; optimum range is 20-30 deg.C Humidity: humidity of 60% is considered necessary for mosquito to live its normal life span Rainfall: Provides mosquito breeding places; increases atmospheric humidity Altitude: 2000-2500 metres, beyond which anophelines are not found
  • 20. Vector 45 species of Anopheles mosquitoes in India Six of them are vectors of important • An. culicifacies-rural & peri-urban areas; highly zoophilic • An. stephensi- urban & industrial areas • An. fluviatilis-hills & forest areas; highly anthrophilic • An. minimus-foothills of north eastern states • An. dirus-forest vector in north east states • An. epiroticus-Andaman and Nicobar islands
  • 21. Vector factors • Breeding habits-fresh water collections • Feeding habits-zoophilic / anthrophilic • Resting habits- endophilic/exophilic • Time of biting-nocturnal • Density • Life span
  • 22. Mode of transmission Vector borne Direct-blood transfusion; drug addicts Congenital malaria • It is the length of time between bite of infective mosquito (inoculation of sporozoites) & the appearance of clinical signs (fever) • Pf - 10 days • Pv - 12 days • Po - 14 days • Pm - 28 days Incubation period
  • 23. Types of malaria • Urban • Rural • Tribal • Malaria in project areas • Border Epidemiological • Uncomplicated • Severe Clinical • Benign Tertian (Pv) • Malignant Tertian (Pf) • Quartan malaria • Ovale tertian Periodicity
  • 25. Stages of malaria • Cold Stage • Hot Stage • Sweating Stage
  • 26. Complications of malaria • Cerebral malaria • Anemia • Dehydration • Acute renal failure • Liver damage • GI symptoms • Black water fever
  • 27. Features of severe malaria • Impaired consciousness / coma • Repeated generalized convulsions • Renal failure ( S.creatinine >3mg/dl ) • Jaundice ( S.bilirubin >3mg/dl) • Severe anaemia ( Hb < 5g/dl) • Pulmonary oedema / ARDS • Hypoglycemia ( Plasma glucose < 40mg/dl) • Metabolic acidosis • Circulatory collapse or shock - “Algid malaria” • Abnormal bleeding / DIC • Haemoglobinuria • Hyperthermia ( Temperature >104 F) • Hyper-parasitaemia
  • 30. Microscopy • Stained thick and thin blood smears • Helps to quantify the parasite load • Thick smear shows whether the slide is positive for MP or not • Thin smear shows the species of the MP & the stages of development in red cells
  • 31. Rapid diagnostic test (RDT) • RDTs are based on the detection of circulating parasite antigens • Several types of RDTs are available • Cassettes, cards or dip sticks • Some of them can only detect P.falciparum, while others can detect other parasite species also • Bivalent RDTs (for detecting P.falciparum and P.vivax )
  • 32. Serological test • Malarial fluorescent antibody test • Positive two weeks or more after primary infection • Useful in Epidemiological studies
  • 34. Treatment • Early diagnosis & treatment of malaria aims at • Complete cure • Prevention of progression of uncomplicated malaria to severe disease • Prevention of deaths • Interruption of transmission • Minimizing risk of selection and spread of drug resistant malaria parasite
  • 35. Treatment of P.vivax cases • 10 mg/kg on day 1 • 10 mg/kg on day 2 • 5 mg/kg on day 3 Chloroquine: 25 mg/kg body wt divided over 3 days • Primaquine is contraindicated in infants, pregnant women and individuals with G6PD deficiency • It can lead to haemolysis in G6PD deficiency Primaquine: 0.25 mg/kg body wt daily for 14 days
  • 36. Treatment of P.vivax cases 14 days regimen of Primaquine should be given under supervision Patient should be advised to stop primaquine immediately if he/she develops any of the following symptoms and should report to the doctor immediately • Dark coloured urine • Yellow conjunctiva • Bluish discolouration of lips • Abdominal pain • Nausea, vomiting etc
  • 38.
  • 39. Treatment of uncomplicated P.falciparum cases • In states other than NE states • Artemisinin based Combination Therapy (ACT-SP) • Artesunate: 4 mg/kg body wt daily for 3 days + • Sulfadoxine (25 mg/kg body wt) & Pyrimethamine (1.25 mg/kg body weight) on day 1 + • Primaquine: 0.75 mg/kg body wt on day 2
  • 40. Treatment of uncomplicated P.falciparum cases ACT is not to be given in 1st trimester of pregnancy & for children weighing < 5 kg “Different coloured Blister Packs” have been introduced for treatment of uncomplicated falciparum malaria in different age groups This has made administration of treatment by field level staff easy Monotherapy of Artemisinin derivatives is BANNED in India
  • 42. In North- Eastern states Co-formulated ACT-AL tablets given according to age group Artemether 20mg & Lumefantrine 120mg ( twice daily for 3 days ) Primaquine : 0.75 mg/kg body wt on day 2 Due to resistance to currently used ACT-SP, effective combination of Artemether- Lumefantrine (ACT-AL) has been recommended
  • 44. Treatment of uncomplicated P.falciparum cases in pregnancy • Quinine salt 10mg/kg 3 times daily for 7 days • Quinine may induce hypoglycaemia • Pregnant women should not start taking quinine on an empty stomach 1st Trimester • Area-specific ACT as per dosage schedule • i.e. ACT-AL in North Eastern states • ACT-SP in other states 2nd & 3rd Trimester
  • 45. Treatment of mixed infections (P.vivax + P.falciparum) cases • All mixed infections should be treated with full course of age-specific ACT and Primaquine 0.25 mg/kg body wt daily for 14 days • In NE states: ACT-AL for 3 days + Primaquine 0.25 mg per kg body wt daily for 14 days • In other states: ACT-SP for 3 days + Primaquine 0.25 mg per kg body wt daily for 14 days.
  • 46.
  • 47. Treatment of severe malaria cases It’s an emergency and treatment should be given as per severity Should do RDT and take blood smear first Immediately give a parenteral dose of artemisinin derivative (or) quinine in suspected cerebral malaria cases The parenteral treatment in severe malaria cases should be given for minimum of 24 hours once started
  • 48.
  • 49.
  • 52. Strategic action plan of malaria control in India • Case detection ( active & passive ) • Early diagnosis and complete treatment • Sentinel surveillance Surveillance and case management • Indoor residual spray (IRS) • Insecticidal treated nets (ITN) • Long lasting insecticidal nets (LLIN) Integrated vector management Anti larval measures Epidemic preparedness and early response
  • 53. Strategic action plan of malaria control in India • Supportive interventions • Capacity building • Behavioural change communication • Intersectoral collaboration • Monitoring & Evaluation • Operational research & applied field research
  • 54. Malaria indices • Annual Parasite Incidence (API) • Annual Blood Examination Rate (ABER) • Annual falciparum incidence • Slide positivity rate • Slide falciparum rate
  • 55. Vector indices • Human Blood Index • Sporozoite Rate • Mosquito Density • Man biting Rate • Inoculation Rate
  • 56. Surveillance • Malaria is under regular surveillance under IDSP • Active case detection(ACD) • Carried out by MPWs/ ASHAs through fortnightly house visits • Under NVBDCP, Pf specific RDT kits have been deployed in Pf predominant areas where microscopy results are not available in 24 hrs • Since 2012, bivalent RDTs have been introduced • Passive case detection • All fever cases attending PHCs/hospitals should be screened for malaria
  • 57. SHORT TERM CHEMOPROPHYLAXIS ( UPTO 6 WEEKS ) CHEMOPROPHYLAXIS FOR LONGER STAY ( MORE THAN 6 WEEKS ) Doxycycline Mefloquine 100 mg once daily & 1.5 mg/kg once daily for children 250 mg weekly for adults Should be started 2 days before travel & continued for 4 weeks after leaving the area Should be administered 2 weeks before & 4 weeks after exposure Contraindicated in pregnant women & children < 8 yrs Contraindicated in individuals with history of convulsions, neuropsychiatric problems & cardiac conditions
  • 58. Vector control ANTI – ADULT MEASURES ANTI – LARVAL MEASURES PERSONAL PROTECTION Residual sprays Environmental Control Mosquito nets Space Sprays Chemical control Repellents Biological control
  • 59. Anti-adult measures • DDT, Malathion, Fenitrothion Residual spraying • Pyrethrum, Residual insecticides Space sprays Genetic control
  • 61. Anti-larval measures • Environmental control • Source reduction • Chemical control • Mineral oils, Paris green, Synthetic insecticides • Biological control • Gambusia affinis, Lebister reticulatus
  • 62. Protection against mosquito bite • Mosquito net • Insecticidal treated nets (ITN) • Long lasting insecticidal nets (LLIN) • Screening • Repellents • Diethyltoluamide
  • 63.
  • 65. Chemoprophylaxis • Chemoprophylaxis should be administered only in selective groups in high P.falciparum endemic areas • Use of personal protection measures including Insecticide Treated bed Nets (ITN) / Long Lasting Insecticidal Nets (LLIN) should be encouraged for pregnant women and other vulnerable population including travellers for longer stay
  • 66. Malaria vaccine • Completed phase 3 trials • RTS, S/ASO1- P.falciparum circumsporozoite • R+T segments of circumsporozoite protein + S (HbSAg)= RT (S+ S) • Adjuvant- ASO1 • 1 vial= 1 mL (2 patients)
  • 67. Malaria vaccine • 0.5 mL IM • WHO recommends 4 doses • 1st dose at 5 months • Repeat at 6th and 7th months • 4th dose at 18 months after 3rd dose