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Malaria
Dr. Irfan Ali Qambrani.
Introduction
• Malaria is the most important parasitic disease
of humans
• The disease is endemic in most of the tropics
• Malaria is transmitted by the bite of infected
female anopheline mosquitoes
Species
• P falciparum
• P vivax
• P ovale
• P malariae
P falciparum
• Most malignant form
• High levels of parasitemia (>5% RBCs infected)
• Sequestration is a specific property of P
falciparum
P vivax
• 50% experience a relapse within a few weeks
to 5 years after the initial illness
• Only immature RBCs ---limited parasitemia
P ovale
• Resolves without treatment
• Infects only immature RBCs, and parasitemia
is usually less
P malariae
• Remain asymptomatic for a much longer
period of time
• Associated with a nephrotic syndrome ---
deposition of antibody-antigen complex on
the glomeruli
Etiology
• Endemic area following a mosquito bite
• Secondary to transfusion of infected blood---
extremely rare
• Congenital
Symptoms
• Headache (noted in virtually all patients with malaria)
• Cough
• Fatigue
• Malaise
• Shaking chills
• Arthralgia
• Myalgia
• Paroxysm of fever, shaking chills, and sweats (every
48 or 72 hours, depending on species)
Physical examination
• Anemia
• Jaundice
• Splenomegaly and
• Mild hepatomegaly
Severe malaria
• Characterized by signs of severe illness
• Organ dysfunction, or
• A high parasite load (peripheral parasitemia
greater than 5% or greater than 200,000
parasites/mcL)
Organ damage
• Neurologic abnormalities progressing to
alterations in consciousness, repeated seizures,
and coma (cerebral malaria)
• Severe anemia
• Hypotension and shock
• Non cardiogenic pulmonary edema
• Acute respiratory distress syndrome
• Acute kidney injury
• Severe hemolysis
• Hypoglycemia
• Lactic acidosis
• Hepatic dysfunction
• Retinal hemorrhages
• Coagulopathy
• Disseminated intravascular coagulation
• Secondary bacterial infections, including
pneumonia and Salmonella bacteremia
Investigations
• Giemsa-stained thick and thin blood films
• Immunochromatographic tests for malaria
antigens
• DNA detection (PCR)
MP smear P Vivax
P falciparum P falciparum(high parasitemia)
Contd.
• CBC
• Liver function test
• Renal function, electrolytes (especially
sodium) test
• Hemolysis (haptoglobin, LDH, reticulocyte
count)
Contd.
• G-6-PD level
• RBS
• CXR – if respiratory symptoms are present
Poor prognosis
• High parasitemias (especially greater than 10-
20% of erythrocytes infected
or
• The presence of malarial pigment (a
breakdown product of hemoglobin) in more
than 5% of neutrophils
Species Management
Plasmodium vivax
and
Plasmodium ovale
Infections
Chloroquine
sensitive P
falciparum and P
malariae
Chloroquine phosphate,
1 g at 0, followed by 500 mg at
6, 24, and 48 hours
then (if G6PD normal)
Primaquine, 30 mg base daily for 14 days
Chloroquine phosphate,
1 g at 0, followed by 500 mg at
6, 24, and 48 hours
Uncomplicated
infections
P falciparum
(Coartem) Artemether 20 mg,
lumefantrine 120 mg,
four tablets twice daily for 3 days
Or Malarone 4 tablets (1g of atovaquone,
400mg of proguanil) daily for 3 days.
Species Management
Contn.
Severe or
complicated
infections with
P falciparum
Or Quinine sulfate 650mg three times
daily for 3-7 days plus one of the
following (when quinine given for
<7days):
Doxycycline 100mg twice daily for
7days OR Clindamycin 600mg twice
daily for 7days.
Artesunate
2.4 mg/kg intravenously every 12 hours
for
1 day, then daily
Prevention of malaria in travelers
Complications
Are same as discussed in organ damage
Prognosis
• Most patients with uncomplicated malaria –
prognosis good
• P falciparum infection ---poor prognosis ---
high mortality rate if untreated
thanks

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MALARIA.pptx

  • 2. Introduction • Malaria is the most important parasitic disease of humans • The disease is endemic in most of the tropics • Malaria is transmitted by the bite of infected female anopheline mosquitoes
  • 3.
  • 4. Species • P falciparum • P vivax • P ovale • P malariae
  • 5.
  • 6. P falciparum • Most malignant form • High levels of parasitemia (>5% RBCs infected) • Sequestration is a specific property of P falciparum
  • 7. P vivax • 50% experience a relapse within a few weeks to 5 years after the initial illness • Only immature RBCs ---limited parasitemia
  • 8. P ovale • Resolves without treatment • Infects only immature RBCs, and parasitemia is usually less
  • 9. P malariae • Remain asymptomatic for a much longer period of time • Associated with a nephrotic syndrome --- deposition of antibody-antigen complex on the glomeruli
  • 10. Etiology • Endemic area following a mosquito bite • Secondary to transfusion of infected blood--- extremely rare • Congenital
  • 11. Symptoms • Headache (noted in virtually all patients with malaria) • Cough • Fatigue • Malaise • Shaking chills • Arthralgia • Myalgia • Paroxysm of fever, shaking chills, and sweats (every 48 or 72 hours, depending on species)
  • 12. Physical examination • Anemia • Jaundice • Splenomegaly and • Mild hepatomegaly
  • 13. Severe malaria • Characterized by signs of severe illness • Organ dysfunction, or • A high parasite load (peripheral parasitemia greater than 5% or greater than 200,000 parasites/mcL)
  • 14. Organ damage • Neurologic abnormalities progressing to alterations in consciousness, repeated seizures, and coma (cerebral malaria) • Severe anemia • Hypotension and shock • Non cardiogenic pulmonary edema • Acute respiratory distress syndrome • Acute kidney injury
  • 15. • Severe hemolysis • Hypoglycemia • Lactic acidosis • Hepatic dysfunction • Retinal hemorrhages • Coagulopathy • Disseminated intravascular coagulation • Secondary bacterial infections, including pneumonia and Salmonella bacteremia
  • 16. Investigations • Giemsa-stained thick and thin blood films • Immunochromatographic tests for malaria antigens • DNA detection (PCR)
  • 17. MP smear P Vivax
  • 18. P falciparum P falciparum(high parasitemia)
  • 19. Contd. • CBC • Liver function test • Renal function, electrolytes (especially sodium) test • Hemolysis (haptoglobin, LDH, reticulocyte count)
  • 20. Contd. • G-6-PD level • RBS • CXR – if respiratory symptoms are present
  • 21. Poor prognosis • High parasitemias (especially greater than 10- 20% of erythrocytes infected or • The presence of malarial pigment (a breakdown product of hemoglobin) in more than 5% of neutrophils
  • 22. Species Management Plasmodium vivax and Plasmodium ovale Infections Chloroquine sensitive P falciparum and P malariae Chloroquine phosphate, 1 g at 0, followed by 500 mg at 6, 24, and 48 hours then (if G6PD normal) Primaquine, 30 mg base daily for 14 days Chloroquine phosphate, 1 g at 0, followed by 500 mg at 6, 24, and 48 hours Uncomplicated infections P falciparum (Coartem) Artemether 20 mg, lumefantrine 120 mg, four tablets twice daily for 3 days Or Malarone 4 tablets (1g of atovaquone, 400mg of proguanil) daily for 3 days.
  • 23. Species Management Contn. Severe or complicated infections with P falciparum Or Quinine sulfate 650mg three times daily for 3-7 days plus one of the following (when quinine given for <7days): Doxycycline 100mg twice daily for 7days OR Clindamycin 600mg twice daily for 7days. Artesunate 2.4 mg/kg intravenously every 12 hours for 1 day, then daily
  • 24. Prevention of malaria in travelers
  • 25. Complications Are same as discussed in organ damage
  • 26. Prognosis • Most patients with uncomplicated malaria – prognosis good • P falciparum infection ---poor prognosis --- high mortality rate if untreated