7. MALARIA
• Malaria is a protozoal disease
caused by infection with
parasites of the genus
PLASMODIUM and transmitted
to man by certain species of
infected female ANOPHELINE
mosquito.
8. • A typical attack comprises three
distinct stages:
• 1. COLD STAGE.
• 2. HOT STAGE.
• 3. SWEATING STAGE.
9. • The clinical features of malaria
vary from mild to severe, and
complicated according o the
species of parasite present,
immunological status of the
patient, intensity of infection
and presence of concomitant
conditions (malnutrition & other
disease).
10. • The febrile paroxysms occur with
definite intermittent periodicity
repeating every third or fourth
day depending upon the species
of the parasite involved.
14. • Malaria in man is caused by four
distinct species of the malaria
parasite.
• Plasmodium vivax, Plasmodium
falciparum, Plasmodium
malariae & Plasmodium ovale.
23. HEPATIC PHASE
• The sporozoites dissappear within
60 minutes from peripheral
circulation.
• Many of them are destroyed by
phagocytes but a few reach the
liver.
24. • After 1-2 weeks the sporozoited
develop into HEPATIC
SCHIZONTS.
• The hepatic schizonts eventually
burst releasing a shower of
meroziotes.
25. • Sometimes the intrahepatic
schizonts (which are not burst –
they remain dormant inside the
liver) grow and become pre-
erythrocytic schizogony thus
liberating merozoites into the
blood stream (causing relapse).
26. • Once the parasites enter the
liver they do not reinvade the
liver.
• This is followed by erythrocytic
phase.
27. ERYTROCYTIC PHASE
• May meroziotes are quickly
destroyed.
• But a significant number of them
attach to a specific receptor sites
in RBC.
28. • The merozoites then penetrate
the RBC and pass through the
stages of trophozoites and
schizont.
• The erythrocytic phase ends with
the liberation of merozoites that
infect fresh RBC.
29. • The cycle is repeated over and
over again until it is slowed
down by the immune response.
• The duration of the erythrocytic
phase is constant for each
species.
30. • P falciaprum, P vivax & P. ovale -
48 hours.
• P malariae – 72 hours.
31. GAMETOGENY
• In all Plasmodium species some
erythrocytic forms do not divide
but become male and female
gametocytes.
32. • These are the sexual forms of the
parasites which are infective to
mosquito. (GAMETOCYTES)
33. SEXUAL CYCLE
• The sexual cycle ( sporogony)
begins when the gametocytes
are ingested by the vector
mosquito when feeding on an
infected person.
34. • The gametocytes continue
further development in the
mosquito.
• The first event to take place
inside the stomach of the
mosquito is the exflagellation of
the male gametocyte.
35. • 4-8 thread like filaments called
“macro-gametes” are developed.
• The female gametocyte
undergoes a process of
maturation and becomes a
female gamete of
“MACROGAMETE”.
36. • By a process called chemotaxis,
microgametes are attracted
towards the female gamete and
one of which (microgamete)
causes fertilization of the female
gamete.
37. • A zygote is formed. The zygote is
at first a motionless body, but
within 18-24 hours, it becomes
motile.
38. • This is known as OOKINETE,
which penetrates the stomach
wall of mosquito and develops
into a oocyst on the outer
surface of the stomach.
39. • The oocyst grows rapidly and
develops within its numerous
sporozoites. Into the body cavity
of the mosquito.
• Many of the sporozoites migrate
to the salivary glands of the
mosquito.
40. • Now the mosquito becomes
infective to man.
• The period of time required for
the development of the parasite
from the gametocyte to sporozoite
stage in the body of the mosquito
is about 10-20 days depending
upon favourable conditions.
41.
42.
43. • The conditions include
atmospheric temperature and
humidity.
• This period is also referred to as
EXTRINSIC INCUBATION PERIOD”
45. • A human reservoir is a person
who harbours the sexual forms (
gametocytes).
• A patient can be a carrier of
several plasmodial species at the
same time.
46. • Children are more likely to be
carriers than adults.
• There are certain conditions to
be fulfilled to be in the state of
reservoir.
47. • The person must harbour both
the sexes of the gametocyte in
the blood.
• The gametocytes must be
mature.
48. • The gametocytes must be viable.
• The gametocytes must be
present in sufficient density to
infect mosquitoes.
49. • There must be at least 12
gametocytes per cubic mm of
blood.
50. PERIOD OF
COMMUNICABILITY
• Malaria is communicable as long
as, mature, viable gametocytes
exist in the circulating blood in
sufficient density to infect vector
mosquitoes.
51. • Gametocytes are the most
numerous during the early
stages of the infection when
their density may exceed 1,000
per cubic mm of blood.
• They also tend to occur in waves
in the peripheral blood.
52. RELAPSES
• Vivax & Ovale malaria tend to
relapse more than 3 years after
the patient’s first attack.
• Recurrence of falciparum usually
disappear within 1-2 years.
53. • P. malariae has a tendency to
cause prolonged low-level,
asymptomatic parasitaemia.
55. AGE
• Malaria affects all ages.
• Newborn infants have
considerable resistance to
infection due to a high
concentration of foetal
haemoglobin during the first
months of life.
56. GENDER
• Males are more frequently
exposed more than females due
to their outdoor life.
• Females are better clothed than
males.
58. PREGNANCY
• Pregnancy increases the risk of
malaria in women.
• Malaria during pregnancy may
cause intra uterine death in
foetus.It may cause pre mature
labour or abortion
62. POPULATION MOBILITY
• Labourers connected with
engineering, irrigation
agricultural and other projects,
migrating nomads are more
disposed to develop malaria.
63. OCCUPATION
• Malaria is predominantly a rural
disease and has direct
connection with agriculture and
related occupation.
64. HUMAN HABITS
• Human habits such as sleeping
out of doors, nomadism,
absence of personal protection
measures increase the risk of
contracting malaria.
65. IMMUNITY
• Epidemic malaria is influenced
by the immune status of the
population.
• Immunity is acquired only after
repeated exposure over several
years.