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DƯỢC LÍ Goodman & Gilman's The Pharmacological Basis of Therapeutics 12th, 2010

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Clinical suspicion of malaria

or history of travel to endemic area

1413

Consider

alternate diagnosis

Acquired in region

with chloroquine resistance:

Artemether-lumefantrine

(COARTEM)

or

Oral quinine sulate plus either

tetracycline or

doxycycline or clindamycin

or

Atovaquone-proguanil

(MALARONE)

or Mefloquine (LARIAM) if

above not available

Negative

Repeat thick and

thin blood smears every

12–24 h for 48–72 h

P. falciparum

or parasite species not determined

Uncomplicated malaria

Determine malaria parasite species and

likely country of aquisition of infection

Acquired in

chloroquine-sensitive

region:

Chloroquine phosphate

(ARALEN and genetrics)

or

Hydroxychloroquine

(PLAQUENIL and

generics)

Positive

Negative

P. vivax, P. ovale

P. malariae, P. knowlesi

CHLOROQUINE

PHOSPHATE

(ARALEN, generics)

or

Hydroxychloroquine

(PLAQUENIL and

generics)

plus

Primaquine for P. vivax

and P. ovale if not

G6PD deficient

Thick and thin blood smears, timely

interpretation by qualified microscopist

Positive

Assess clinical status and disease severity

Determine parasite density

P. vivax acquired in

Papua New guinea,

Indonesia or other

area with

chloroquine resistance

Quinine sulfate plus

either tetracycline or

doxycycline

or

Atovaquone-proguanil

(MALARONE)

or

Mefloquine (lariam) if

above not available

plus

Primaquine if not

G6PDdeficient

Complicated/severe malaria

or

Unable to absorb oral medication

(regardless of infecting species or

geographic region where

infection was acquired)

Intravenous artesunate* followed by

either atovaquone-proguanil (MALARONE)

or doxycycline (clindamycin

in pregnant women)

or mefloquine (LARIAM)

or

Intravenous quinidine gluconate

plus either tetracycline

or doxycycline or clindamycin

Admit to intensive care unit

Monitor cardiac function,

bood pressure, parasitemia, glucose,

hemoglobin, electrolytes

Prevent and treat complications

Consideration of exchange transfusion

for hyperparasitemia

Change to oral therapy

when oral bioavailability reliable

*investigational new drug available

through CDC Drug Service

CHAPTER 49

CHEMOTHERAPY OF MALARIA

Admit to hospital

Monitor symptoms daily

Repeat blood smears daily until negative or if

discharged prior to a negative smear, at day 7

Repeat blood smears if symptoms recur

Figure 49–4. Approach to the treatment of malaria. Atovaquone-proguanil, mefloquine, artemether-lumefantrine, tetracycline, and

doxycycline are not indicated during pregnancy. Tetracycline and doxycycline are not indicated in children <8 years of age. G6PD,

glucose- 6-phosphate dehydrogenase. (Adapted from Griffith KS, Lewis LS, Mali S, Parise ME. Treatment of malaria in the United

States: A systematic review. JAMA, 297(20):2264–77, 2007, with permission of the American Medical Association © 2007. All rights

reserved.)

Guidelines for treatment of malaria in the U.S. are

provided by the CDC and are shown in Table 49–3.

Updates should be checked on the CDC website.

Figure 49–4 presents an overview of the general strategy

for treatment of malaria in the U.S.

Treatment of Uncomplicated Malaria. Chloroquine is

the drug of choice for P. ovale, P. malariae, P. knowlesi,

and chloroquine-sensitive strains of P. vivax and P. falciparum.

For P. vivax and P. ovale infections, a 2-week

course of primaquine should be added to eradicate hypnozoites

that may remain dormant in the liver, and thus

prevent relapse. Some patients with P. vivax infection

may require more than one course of primaquine to

obtain radical cure. Primaquine must not be given to

patients with G6PD deficiency or to pregnant women.

The oral route of administration should be used if feasible.

Within 48-72 hours of initiating therapy, patients

should show marked clinical improvement (especially

clearance of fever) and a substantial decrease in parasitemia

as monitored by daily thin and thick blood

smears. Under controlled administration of treatment,

lack of such a response or failure to clear asexual forms of

the parasite from the blood by 7 days suggests the presence

of drug resistance (except for atovaquone-proguanil).

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