Malaria in pregnancy.
 Definitions.
 Pathophysiology
 Complications
 Clinical features.
 Management.
Definition.
 Febrile condition caused by a protozoan in
plasmodium species ie plasmodium
falciparum, plasmodium vivax and plasmodium
ovale.
 Transmission occurs through bites of infected
anopheles mosquito
 Plasmodium falciparum is the commonest
species in kenya and it is associated with
significant morbidity and mortality.
Pathophysiology.
 The infected RBCs become rigid, irregular and
sticky.
 There is blockage of microcirculaton due to the
squestrated red cells
 The infected red blood cells are broken
down(haemolysis).
 The fetal effects are due to high fever or due to
placental parasitisation
 The intervillous spaces become blocked with
macrophages and parasites leading to diminished
placental blood flow.
Effects of malaria on the
mother.
 Anemia due to haemolysis and folic acid
deficiency.
 Hypoglycaemia due to increased glucose
consumption both by the host and the parasites.
Also quinine treatment.
 Metabolic acidosis.
 Jaundice due to hepatic dysfunction and
hemolysis.
 Renal failure due to blockage of renal
microcirculation
 Pulmonary edema and respiratory distress.
Effects of malaria on the fetus.
 Increased pregnancy complications such as:
 Abortion
 Preterm labor.
 Prematurity
 IUGR
 IUFD.
Effects of pregnancy on
malaria.
 Risk and severity of infection are high due to
immunocompromised state.
 Complications are high.
Clinical features.
 Joint pains
 Headaches
 Backaches
 General malaise
 Loss of appetite with
vomitting at times.
 Fever
 Chills rigors
 Abdominal pain accompanied by
diarrhoea or constipation.
 Fever
 Severe headache
 Confusion
 Convulsions
 Coma
 Haematuria
 Renal failure.
 Pulmonary edema.
 Hypoglycaemia.
 Dissemnated intravascular
coagulopathy.
Mild (uncomplicated) Severe(complicated)
Diagnosis.
 History of the above symptoms
 Physical examinations
 Investigations
 Blood slide for MPS
 Haemoglobin level-if <5g/dl take blood for
grouping and cross matching.
 Lumbar puncture when indicated to R/O
meningitis
 Blood sugar
 Widal test.
Differential diagnosis.
 Meningitis.
 Typhoid.
 HIV infection.
 Urinary tract infection.
 Pneumonia.
 Trypanosomiasis.
 Other viral infections.
Management.
 Treatment with oral medications
such as
 Artemisin/halofantrine
combinations.
 Other drugs that can be used
include
 Sulfadoxime/pyrimethamine
combination
 Amodiaquine.
 Quinine
 Take care of the fever.
 Tocolytics to prevent premature
labor.
 Intravenous quinine
 Loading dose 20mg/kg in
5%dextrose infused over 4 hours
 Repeat doses 10mg/kg every 8
hrs
 Discontinue infusion as soon as
patient is able to take orally.
 Take care of the fever
 Tocolytics to prevent premature
labor.
 Folic acid supplementation
 Fluid input and output
monitoring.
Mild. Severe.
Prevention.
 Use of treated mosquito nets.
 Routine antimalarial prophylaxis-SP 3 tablets
as a single oral dose in 2nd and 3rd trimesters.
 Use of mosquito repellenta
 Clear stagnant waters and bushes
 Routine folic acid and ferrous sulphate.
 Questions.

Malaria in pregnancy-1.ppt

  • 1.
    Malaria in pregnancy. Definitions.  Pathophysiology  Complications  Clinical features.  Management.
  • 2.
    Definition.  Febrile conditioncaused by a protozoan in plasmodium species ie plasmodium falciparum, plasmodium vivax and plasmodium ovale.  Transmission occurs through bites of infected anopheles mosquito  Plasmodium falciparum is the commonest species in kenya and it is associated with significant morbidity and mortality.
  • 3.
    Pathophysiology.  The infectedRBCs become rigid, irregular and sticky.  There is blockage of microcirculaton due to the squestrated red cells  The infected red blood cells are broken down(haemolysis).  The fetal effects are due to high fever or due to placental parasitisation  The intervillous spaces become blocked with macrophages and parasites leading to diminished placental blood flow.
  • 4.
    Effects of malariaon the mother.  Anemia due to haemolysis and folic acid deficiency.  Hypoglycaemia due to increased glucose consumption both by the host and the parasites. Also quinine treatment.  Metabolic acidosis.  Jaundice due to hepatic dysfunction and hemolysis.  Renal failure due to blockage of renal microcirculation  Pulmonary edema and respiratory distress.
  • 5.
    Effects of malariaon the fetus.  Increased pregnancy complications such as:  Abortion  Preterm labor.  Prematurity  IUGR  IUFD.
  • 6.
    Effects of pregnancyon malaria.  Risk and severity of infection are high due to immunocompromised state.  Complications are high.
  • 7.
    Clinical features.  Jointpains  Headaches  Backaches  General malaise  Loss of appetite with vomitting at times.  Fever  Chills rigors  Abdominal pain accompanied by diarrhoea or constipation.  Fever  Severe headache  Confusion  Convulsions  Coma  Haematuria  Renal failure.  Pulmonary edema.  Hypoglycaemia.  Dissemnated intravascular coagulopathy. Mild (uncomplicated) Severe(complicated)
  • 8.
    Diagnosis.  History ofthe above symptoms  Physical examinations  Investigations  Blood slide for MPS  Haemoglobin level-if <5g/dl take blood for grouping and cross matching.  Lumbar puncture when indicated to R/O meningitis  Blood sugar  Widal test.
  • 9.
    Differential diagnosis.  Meningitis. Typhoid.  HIV infection.  Urinary tract infection.  Pneumonia.  Trypanosomiasis.  Other viral infections.
  • 10.
    Management.  Treatment withoral medications such as  Artemisin/halofantrine combinations.  Other drugs that can be used include  Sulfadoxime/pyrimethamine combination  Amodiaquine.  Quinine  Take care of the fever.  Tocolytics to prevent premature labor.  Intravenous quinine  Loading dose 20mg/kg in 5%dextrose infused over 4 hours  Repeat doses 10mg/kg every 8 hrs  Discontinue infusion as soon as patient is able to take orally.  Take care of the fever  Tocolytics to prevent premature labor.  Folic acid supplementation  Fluid input and output monitoring. Mild. Severe.
  • 11.
    Prevention.  Use oftreated mosquito nets.  Routine antimalarial prophylaxis-SP 3 tablets as a single oral dose in 2nd and 3rd trimesters.  Use of mosquito repellenta  Clear stagnant waters and bushes  Routine folic acid and ferrous sulphate.
  • 12.