Chapter 248 MALARIA Flashcards

1
Q

Responsible for nearly all deaths of malaria

A

Plasmodium falciparum

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2
Q

merozoites then invade the red blood cells (RBCs) and multiply

A

six- to twentyfold every 48 h

(P. knowlesi, 24 h; P. malariae, 72 h).

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3
Q

When the parasites reach densities of ~50/μL of blood or ____ the symptomatic stage of the infection begins.

A

(~100 million parasites in the blood of an adult),

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4
Q

In ____ infec- tions, a proportion of the intrahepatic forms do not divide immediately but remain inert for a period ranging from 3 weeks to ≥1 year before reproduction begins.

A

P. vivax and P. ovale

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5
Q

____, are the cause of the relapses that characterize infection with these two species.

A

hypnozoites

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6
Q

The swollen infected liver cells eventually burst, discharging motile _____ into the bloodstream.

A

merozoites

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7
Q

After entry into the bloodstream, merozoites rapidly invade erythrocytes and become ____.

A

trophozoites

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8
Q

By the end of the intraerythrocytic life cycle, the para- site has consumed two-thirds of the RBC’s hemoglobin and has grown to occupy most of the cell. It is now called a ______.

A

schizont

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9
Q

This zygote matures into an _____, which penetrates and encysts in the mosquito’s gut wall.

A

ookinete

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10
Q

to transmit malaria, the mosquito must survive for___

A

> 7 days.

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11
Q

potentially toxic heme is detoxified by lipid-mediated crystallization to biologically inert

A

hemozoin (malaria pigment)

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12
Q

The processes of cytoadherence, rosetting, and agglutination are central to the pathogenesis of

A

falciparum malaria.

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13
Q

Manifestation of severe falciparum malaria:

A
  1. Unarousable coma or severe malaria
  2. Acidemia or acidosis
  3. Anemia
  4. Renal failure
  5. ARDS
    6: hypoglycemia
  6. Hypotension
  7. Bleeding
  8. Convulsions
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14
Q

Coma is a characteristic and ominous feature of falciparum malaria and, despite treatment, is associated with death rates of ~20% among adults and 15% among children.

A

Cerebral Malaria

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15
Q

Most common funduscopic abnormalities include discrete spots of

A

retinal opacification (30–60%)

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16
Q

Approximately ____% of children surviving cerebral malaria—especially those with hypoglycemia, severe anemia, repeated seizures, and deep coma—have residual neu- rologic deficits when they regain consciousness;

A

10%

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17
Q

Chronic or repeated infections with P. malariae (and possibly with other malarial species) may cause soluble immune complex injury to the renal glomeruli, resulting in the nephrotic syndrome.

A

QuARTAN MALARIAL NEPHROPATHY

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18
Q

The diagnosis of malaria rests on the demonstration of asexual forms of the parasite in stained

A

peripheral-blood smears.

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19
Q

Repeat blood smears should be performed at least _____ for 2 days if the first smears are negative and malaria is strongly suspected.

A

every 12–24 h

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20
Q

Treatment Known chloroquine- sensitive strains of Plasmodium vivax,
P. malariae, P. ovale, P. knowlesi,
P. falciparumb

A

Chloroquine (10 mg of base/kg stat followed by 5 mg/ kg at 12, 24, and 36 h or by 10 mg/kg at 24 h and
5 mg/kg at 48 h)

or

Amodiaquine (10–12 mg of base/kg qd for 3 days)

21
Q

Radical treatment for P. vivax or P. ovale infection

A

In addition to chloroquine or amodiaquine as detailed above,

primaquine (0.5 mg of base/kg qd in tropical regions and 0.25 mg/kg for temperate-origin P. vivax) should be given for 14 days to prevent relapse.
or
Artesunated (4 mg/kg qd for 3 days) plus amodiaquine (10 mg of base/kg qd for 3 days)e

22
Q

Sensitive
P. falciparum malaria treatment

A

Artesunated (4 mg/kg qd for 3 days) plus sulfadoxine (25 mg/kg)/pyrimethamine (1.25 mg/kg) as a single dose
Or
Artesunated (4 mg/kg qd for 3 days) plus amodiaquine (10 mg of base/kg qd for 3 days)

23
Q

Treatment for Multidrug-resistant P. falciparum malaria

A

Either artemether-lumefantrined (1.5/9 mg/kg bid for 3 days with food)
or
Artesunated (4 mg/kg qd for 3 days) plus mefloquine (24–25 mg of base/kg—either 8 mg/kg qd for 3 days or 15 mg/kg on day 2 and then 10 mg/kg on day 3)e
or
Dihydroartemisinin-piperaquined (2.5/20 mg/kg qd for 3 days)

24
Q

Second-line treat- ment/treatment of imported malaria

A

Either artesunated (2 mg/kg qd for 7 days) or quinine (10 mg of salt/kg tid for 7 days) plus 1 of the following 3:
1. Tetracyclinef (4 mg/kg qid for 7 days)
2. Doxycyclinef (3 mg/kg qd for 7 days)
3. Clindamycin (10 mg/kg bid for 7 days)
or
Atovaquone-proguanil (20/8 mg/kg qd for 3 days with food)

25
Q

Severe falciparum malaria

A

Artesunated (2.4 mg/kg stat IV followed by 2.4 mg/kg at 12 and 24 h and then daily if necessary)h

26
Q

remains a first-line treatment for the non-falciparum malarias (P. vivax, P. ovale, P. malariae, P. knowlesi) except in Indonesia and Papua New Guinea, where high levels of resistance in P. vivax are prevalent.

A

chloroquine

27
Q

World Health Organization (WHO) now recommends _____ as first-line treatment for uncomplicated falciparum malaria

A

artemisinin-based combinations (ACTs)

28
Q

has therefore become the drug of choice for all patients with severe malaria everywhere.

A

Artesunate

29
Q

total plasma concentrations of ___ for quinine and ____ for quinidine are effective and do not cause serious toxicity.

A

Quinine 8–15 mg/L

Quijidine 3.5–8.0 mg/L

30
Q

Infections due to sensitive strains of P. vivax, P. knowlesi, P. malariae, and P. ovale should be treated with

A

oral chloroquine (total dose, 25 mg of base/kg) or with an ATC known to be efficacious for UNCOMPLICATED MALARIA

31
Q

In areas with multidrug-resistant falciparum malaria (parts of Asia and South America, including those with mefloquine-resistant parasites; these regimens provide cure rates of >90%.

A

artemether-lumefantrine, artesunate-mefloquine, or dihydroartemisinin-piperaquine should be used;

32
Q

is the only drug advised for pregnant women traveling to areas with drug-resistant malaria; this drug is generally considered safe in the sec- ond and third trimesters of pregnancy, and the data on first-trimester exposure, although limited, are reassuring.

A

MEFLOQUINE

33
Q

Used for presumptive antirelapse therapy (terminal prophylaxis) to decrease risk of relapses of P. vivax and P. ovale

A

PRIMAQUINE

34
Q

For prevention of malaria in areas with mainly
P. vivax

A

PRIMAQUINE

35
Q

Prophylaxis in areas with chloroquine-resistant
P. falciparum

A

MEFLOQUINE

36
Q

An alternative to chloroquine for primary prophylaxis only in areas with chloroquine-sensitive P. falciparumc or areas with P. vivax only

A

Hydroxychloroquine sulfate (PLAQUENIL)

37
Q

Prophylaxis in areas with chloroquine- or mefloquine-resistant
P. falciparum

A

DOXYCYCLINE

38
Q

Prophylaxis only in areas with chloroquine-sensitive P. falciparumc or areas with P. vivax only

A

Chloroquine phosphate (Aralen and generic)

39
Q

Prophylaxis in areas with chloroquine- or mefloquine-resistant Plasmodium falciparum

A

Atovaquone- proguanil (Malarone)

40
Q

is a fixed-combination, once-daily prophylactic agent that is very well tolerated by adults and children, with fewer adverse gastrointestinal effects than chloroquine-proguanil and fewer adverse central nervous system effects than mefloquine.

A

Atovaquone-proguanil (Malarone; 3.75/1.5 mg/kg or 250/100 mg, daily adult dose)

41
Q

has been widely used for malarial prophylaxis because it is usually effective against multi- drug-resistant falciparum malaria and is reasonably well tolerated

A

Mefloquine (250 mg of salt weekly, adult dose)

42
Q

Daily administration of ____ is an effective alternative to atovaquone-proguanil or mefloquine and is generally well tolerated but may cause vulvovaginal thrush, diarrhea, and photosensitivity and cannot be used by children <8 years old or by pregnant women.

A

doxycycline (100 mg daily, adult dose)

43
Q

_____ taken with food), an 8-aminoquinoline compound, has proved safe and effective in the prevention of drug-resistant falciparum and vivax

A

Primaquine (daily adult dose, 0.5 mg of base/kg or 30 mg

44
Q

True or false

Children born to nonimmune mothers in endemic areas (usually expatriates moving to malaria-endemic areas) should receive prophylaxis from birth.

A

TRUE

45
Q

Travelers should start taking antimalarial drugs ____ before departure so that any untoward reactions can be detected and so that therapeutic antimalarial blood concentrations will be present when needed

A

2 days to 2 weeks

46
Q

Antimalarial prophylaxis should continue for 4 weeks after the traveler has left the endemic area, except if ____ has been taken; these drugs have significant activities against the liver stage of the infection

A

atovaquone-proguanil or primaquine

47
Q

chloroquine (a 4-aminoquinoline) act on the ____ stage of parasitic develop- ment

A

erythrocyte

48
Q

inhibitors also inhibit preerythro- cytic growth in the liver (causal prophylaxis) and development in the mosquito (sporontocidal activity).

A

dihydrofolate reductase

DHR

49
Q

Lumbar tap mean opening pressure

A

Approximately 180mmhg