Tx of malaria Flashcards

1
Q

First line tx of malaria

A
  • Intravenous artesunate for severe falciparum malaria
  • Use intravenous quinine if artesunate is not available
  • Use quinine and clindamycin to treat uncomplicated P. falciparum
  • Use chloroquine to treat P. vivax, P. ovale or P. malariae
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2
Q

Artenusate for tx of severe malaria

A
  • 2.4 mg/kg at 0, 12 and 24 hours, then daily thereafter.
  • When the patient is well enough to take oral medication artesunate 2 mg/kg (or IM artesunate 2.4 mg/kg) once daily, plus clindamycin.
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3
Q

Quinine for tx of severe malaria

A
  • Quinine IV 20 mg/kg loading dose (no loading dose if patient already taking quinine or mefloquine) in 5% dextrose over 4 hours and then 10 mg/kg IV over 4 hours every 8 hours plus clindamycin IV 450 mg
    every 8 hours (max. dose quinine 1.4 g).
  • When the patient is well enough to take oral medication she can be switched to oral quinine
    600 mg 3 times a day to complete 5–7 days and oral clindamycin 450 mg 3 times a day 7 days
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4
Q

Side effects of quinine

A

Cinchonism: tinnitus, headache, nausea, diarrhoea, altered auditory acuity and blurred vision

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5
Q

Recurrence of malaria

A
  • Usually day 28–42
  • 85 days with quinine
  • 98 days with artesunate
  • 63 days with artemether-lumefantrine
  • 121 days with mefloquine
  • Weekly screening by blood film until delivery allows these women to be detected positive before becoming symptomatic
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6
Q

Complications of severe malaria infection - Hypoglycemia

A
  • Commonly asymptomatic, although it may be associated with fetal bradycardia and other signs of fetal distress
  • In the most severely ill women, it is associated with lactic acidosis and high mortality
  • Abnormal behaviour, sweating and
    sudden loss of consciousness are the usual manifestations of quinine related hypoglycemia
  • The hypoglycaemia of quinine is caused
    by hyperinsulinaemia and remains the most common and important adverse effect of this drug
  • It may be profound, recurrent and intractable in pregnancy
  • It may present late in the disease when the patient appears to be recovering
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7
Q

Complications of severe malaria infection - Pulmonary oedema

A
  • It may be present on admission or may develop suddenly and unexpectedly
  • It may develop immediately after childbirth
  • High mortality of over 50%
  • Monitor the central venous pressure and urine output
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8
Q

Complications of severe malaria infection - Anaemia

A
  • Maternal morbidity
  • Increased risk of postpartum haemorrhage
  • Perinatal mortality
  • May develop acute pulmonary oedema after separation of the placenta
  • Transfuse slowly packed red cells
  • Consider exchange transfusion
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9
Q

Complications of severe malaria infection - Secondary infection

A
  • Principally Gram-negative septicaemia

- Broad-spectrum antibiotics (such as ceftriaxone) should be started immediately

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