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Summary of Malaria & 
Antimalarial therapy 
Abdul Waris Khan 
Soepel: 12 
Internal medicine
Malaria 
• Human malaria is usually caused by one of 
four species of the genus Plasmodium: 
– P. falciparum 
– P. vivax 
– P. ovale 
– P. malariae
• Malaria probably originated from animal 
malarias in Central Africa, but was spread 
around the globe by human migration. 
• Public health measures and changes in land 
use have eradicated malaria in most 
developed countries.
Epidemiology 
• Some 400 million people are infected every year and 
over 1 million die annually. 
• 25 000 international travellers per year are infected. 
• Australia, the USA and most of the Mediterranean are 
malaria-free. 
• Mortality is still mainly seen in infants, but older 
children and adults may develop chronic ill health due 
to repeated infections.
• Malaria is transmitted by the bite of female 
anopheline mosquitoes. 
• The parasite undergoes a temperature-dependent 
cycle of development in the gut of 
the insect.
Pathogenesis 
• The pathology of malaria is related to anaemia, cytokine 
release and in the case of P. falciparum, widespread organ 
damage due to impaired microcirculation. 
• The anaemia seen in malaria is multifactorial. In P. 
falciparum malaria, red cells containing schizonts adhere to 
the lining of capillaries in the brain, kidneys, gut, liver and 
other organs. 
• As well as causing mechanical obstruction these schizonts 
rupture, releasing toxins and stimulating further cytokine 
release.
Clinical features 
• Typical malaria is seen in non-immune individuals. 
• The normal incubation period is 10–21 days, but can be 
• longer. 
• The most common symptom is fever, although 
• malaria may present initially with general malaise, 
headache, 
• vomiting, or diarrhoea. 
• The temperature often reaches 41°C and is accompanied by 
rigors and drenching sweats.
P. vivax or P. ovale infection 
• The illness is usually relatively mild (although P. vivax can 
occasionally cause severe disease). 
• Anaemia develops slowly and there may be tender 
hepatosplenomegaly. 
• Spontaneous recovery usually occurs within 2–6 weeks, but 
hypnozoites in the liver can cause relapses for many years 
after infection. 
• Repeated infections often cause chronic ill health due to 
anaemia and hyperreactive splenomegaly.
P. malariae infection 
• This also causes a relatively mild illness, but 
tends to run a more chronic course. 
• Parasitaemia may persist for years, with or 
without symptoms. 
• In children, P. malariae infection is associated 
with glomerulonephritis and nephrotic 
syndrome.
P. falciparum infection 
• This causes, in many cases, a self-limiting illness similar to the other types of 
malaria, although the paroxysms of fever are usually less marked. 
• However, it may also cause serious complications and the vast majority of malaria 
deaths are due to P. falciparum. 
• Patients can deteriorate rapidly and children in particular progress from 
reasonable health to coma and death within hours. 
• A high parasitaemia (>1% of red cells infected) is an indicator of severe disease. 
• Cerebral malaria is marked by diminished consciousness, confusion and 
convulsions, often progressing to coma and death. 
• Blackwater fever is due to widespread intravascular haemolysis, affecting both 
parasitized and unparasitized red cells, giving rise to dark urine.
Diagnosis 
• Malaria should be considered in the differential diagnosis of anyone 
who presents with a febrile illness or having recently left, a 
malarious area. 
• Falciparum malaria is unlikely to present more than 3 months after 
exposure, even if the patient has been taking prophylaxis, but vivax 
malaria may cause symptoms for the first time up to a year after 
leaving a malarious area. 
• Diagnosis is usually made by identifying parasites on a Giemsa-stained 
thick or thin blood film 
• At least three films should be examined before malaria is declared 
unlikely.
Treatment of uncomplicated malaria. 
• The drug of choice for susceptible parasites is chloroquine. 
• P. vivax, P. ovale and P. malariae are usually sensitive to this drug. 
• Following successful treatment of P. vivax or P. ovale malaria, it is necessary to give 
a 2- to 3-week course of primaquine (15 mg daily) to eradicate the hepatic 
hypnozoites and prevent relapse. 
• The artemisinin-based drugs are the most effective treatment for both 
uncomplicated and severe infections with P. falciparum, in adults and in children. 
• Artemisinin-based combination therapy (ACT) is the recommended oral treatment 
for uncomplicated falciparum malaria worldwide. 
• Artemisinin should not be given as monotherapy to limit resistance. 
• The WHO recommends that a single dose of primaquine should be given as a 
gametocide, to decrease transmission.
Treatment of severe falciparum malaria 
• Severe malaria, indicated by the presence of the complications, or a 
parasite count above 1% in a nonimmune patient, is a medical 
emergency. 
• Intravenous artesunate is more effective than intravenous quinine 
and should be used where available. 
• Absorption from intramuscular injection is less reliable than from 
intravenous injection. 
• Intensive care facilities may be needed, including mechanical 
ventilation and dialysis. 
• Severe anaemia may require transfusion.
Prevention and control 
• Mosquito eradication is usually achieved either by the 
use of insecticides, house spraying with DDT or by 
manipulation of the habitat (e.g. marsh drainage). 
• Non-immune travellers to malarious areas should take 
measures to avoid insect bites, such as using insect 
repellent (diethyltoluamide, DEET, 20–50% in lotions 
and sprays) and sleeping under mosquito nets. 
• Antimalarial prophylaxis should also be taken in most 
cases, although they are not 100% effective.
References 
• Kumar and Clark’s clinical medicine 8th edition

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malaria & anti malarial drugs

  • 1. Summary of Malaria & Antimalarial therapy Abdul Waris Khan Soepel: 12 Internal medicine
  • 2. Malaria • Human malaria is usually caused by one of four species of the genus Plasmodium: – P. falciparum – P. vivax – P. ovale – P. malariae
  • 3. • Malaria probably originated from animal malarias in Central Africa, but was spread around the globe by human migration. • Public health measures and changes in land use have eradicated malaria in most developed countries.
  • 4. Epidemiology • Some 400 million people are infected every year and over 1 million die annually. • 25 000 international travellers per year are infected. • Australia, the USA and most of the Mediterranean are malaria-free. • Mortality is still mainly seen in infants, but older children and adults may develop chronic ill health due to repeated infections.
  • 5.
  • 6. • Malaria is transmitted by the bite of female anopheline mosquitoes. • The parasite undergoes a temperature-dependent cycle of development in the gut of the insect.
  • 7.
  • 8.
  • 9.
  • 10. Pathogenesis • The pathology of malaria is related to anaemia, cytokine release and in the case of P. falciparum, widespread organ damage due to impaired microcirculation. • The anaemia seen in malaria is multifactorial. In P. falciparum malaria, red cells containing schizonts adhere to the lining of capillaries in the brain, kidneys, gut, liver and other organs. • As well as causing mechanical obstruction these schizonts rupture, releasing toxins and stimulating further cytokine release.
  • 11.
  • 12. Clinical features • Typical malaria is seen in non-immune individuals. • The normal incubation period is 10–21 days, but can be • longer. • The most common symptom is fever, although • malaria may present initially with general malaise, headache, • vomiting, or diarrhoea. • The temperature often reaches 41°C and is accompanied by rigors and drenching sweats.
  • 13. P. vivax or P. ovale infection • The illness is usually relatively mild (although P. vivax can occasionally cause severe disease). • Anaemia develops slowly and there may be tender hepatosplenomegaly. • Spontaneous recovery usually occurs within 2–6 weeks, but hypnozoites in the liver can cause relapses for many years after infection. • Repeated infections often cause chronic ill health due to anaemia and hyperreactive splenomegaly.
  • 14. P. malariae infection • This also causes a relatively mild illness, but tends to run a more chronic course. • Parasitaemia may persist for years, with or without symptoms. • In children, P. malariae infection is associated with glomerulonephritis and nephrotic syndrome.
  • 15. P. falciparum infection • This causes, in many cases, a self-limiting illness similar to the other types of malaria, although the paroxysms of fever are usually less marked. • However, it may also cause serious complications and the vast majority of malaria deaths are due to P. falciparum. • Patients can deteriorate rapidly and children in particular progress from reasonable health to coma and death within hours. • A high parasitaemia (>1% of red cells infected) is an indicator of severe disease. • Cerebral malaria is marked by diminished consciousness, confusion and convulsions, often progressing to coma and death. • Blackwater fever is due to widespread intravascular haemolysis, affecting both parasitized and unparasitized red cells, giving rise to dark urine.
  • 16.
  • 17. Diagnosis • Malaria should be considered in the differential diagnosis of anyone who presents with a febrile illness or having recently left, a malarious area. • Falciparum malaria is unlikely to present more than 3 months after exposure, even if the patient has been taking prophylaxis, but vivax malaria may cause symptoms for the first time up to a year after leaving a malarious area. • Diagnosis is usually made by identifying parasites on a Giemsa-stained thick or thin blood film • At least three films should be examined before malaria is declared unlikely.
  • 18. Treatment of uncomplicated malaria. • The drug of choice for susceptible parasites is chloroquine. • P. vivax, P. ovale and P. malariae are usually sensitive to this drug. • Following successful treatment of P. vivax or P. ovale malaria, it is necessary to give a 2- to 3-week course of primaquine (15 mg daily) to eradicate the hepatic hypnozoites and prevent relapse. • The artemisinin-based drugs are the most effective treatment for both uncomplicated and severe infections with P. falciparum, in adults and in children. • Artemisinin-based combination therapy (ACT) is the recommended oral treatment for uncomplicated falciparum malaria worldwide. • Artemisinin should not be given as monotherapy to limit resistance. • The WHO recommends that a single dose of primaquine should be given as a gametocide, to decrease transmission.
  • 19.
  • 20.
  • 21. Treatment of severe falciparum malaria • Severe malaria, indicated by the presence of the complications, or a parasite count above 1% in a nonimmune patient, is a medical emergency. • Intravenous artesunate is more effective than intravenous quinine and should be used where available. • Absorption from intramuscular injection is less reliable than from intravenous injection. • Intensive care facilities may be needed, including mechanical ventilation and dialysis. • Severe anaemia may require transfusion.
  • 22.
  • 23. Prevention and control • Mosquito eradication is usually achieved either by the use of insecticides, house spraying with DDT or by manipulation of the habitat (e.g. marsh drainage). • Non-immune travellers to malarious areas should take measures to avoid insect bites, such as using insect repellent (diethyltoluamide, DEET, 20–50% in lotions and sprays) and sleeping under mosquito nets. • Antimalarial prophylaxis should also be taken in most cases, although they are not 100% effective.
  • 24.
  • 25.
  • 26. References • Kumar and Clark’s clinical medicine 8th edition