Malaria - Dr. Karwa Flashcards

1
Q

Chloroquine-resistant P.
___ is widespread

A

falciparum

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2
Q

Transmission, distribution, and incidence of vector-born infections are impacted by:
- Extreme weather events
- Increasing temperatures

A

Changing climate has the potential to increase the distribution of malaria

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3
Q

Plasmodium species that cause infections in humans:
(5)

A
  • P. falciparum
  • P. malariae
  • P. knowlesi
  • P. vivax
  • P. ovale
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4
Q

MALARIA VACCINE

Indication: ___ living in regions with moderate to high Plasmodium ___ transmission

Malaria vaccines available:
* RTS,S/AS01
* R21/Matrix-M

  • 4 doses starting at ~5 months of age
  • can consider 5th
A
  • Children
  • falciparum
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5
Q

Selection of chemoprophylaxis depends on region

traveling to:

All malaria-endemic regions (3)

A
  • Atovaquone/proguanil
  • Doxycycline
  • Tafenoquine
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6
Q

Selection of chemoprophylaxis depends on region

traveling to:

Regions primarily with P. vivax (1)

A

Primaquine

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7
Q

Selection of chemoprophylaxis depends on region

Regions with chloroquine-sensitive malaria (2)

A
  • chloroquine
  • hydroxychloroquine
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8
Q

Selection of chemoprophylaxis depends on region

Regions with mefloquine- sensitive malaria (1)

A
  • Mefloquine
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9
Q

CHEMOPROPHYLAXIS

Atovaquone/Proguanil (Malarone)

Duration
- Begin __ - __ days before departure and continue for __ days after leaving endemic area

take with food/milk

avoid if:
- CrCl < 30
- pregnant/breastfeeding

A
  • 1-2, 7
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10
Q

CHEMOPROPHYLAXIS

Chloroquine & Hydroxychloroquine

Duration
- begin __ - __ weeks before departure and continue for __ weeks after leaving

SE
- blurred vision
- dizziness
- GI disturbance
- headache
- insomnia
- pruritus

avoid if leaving in less than 1 weel

A
  • 1-2 weeks
  • 4 weeks
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11
Q

CHEMOPROPHYLAXIS

Doxycycline

Duration
- begin __ - __ days before departure and continue ___ weeks after leaving

Counseling
- wear sunscreen
- 2 hrs apart from antacids

Reasons to Avoid Use
- pregnant
- kid < 8 yo
- allergy
- prone to getting yeast infections

A
  • 1-2 days
  • 4 weeks
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12
Q

CHEMOPROPHYLAXIS

Mefloquine

Duration
- Begin ≥ __ weeks before departure and continue for __ weeks after leaving

Counseling Points
- Has been associated with rare but serious reactions (e.g. psychosis, seizures)*
- Side effects: abnormal dreams, anxiety, depression, dizziness, GI disturbance, headache, insomnia, visual disturbances

Reasons to Avoid Use
- Active/recent ___
- Recent history of psychiatric disorders or seizures
- Cardiac conduction abnormalities

A
  • 2 weeks
  • 4 weeks
  • depression
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13
Q

CHEMOPROPHYLAXIS

Primaquine

Duration
- Begin __ - __ days before departure and continue for __ days after leaving

Counseling Points
- take with food to minimize stomach upset
- only use for places with > 90% P. ___

Reasons to Avoid Use
- ___ deficiency or not tested yet
- pregnant/breastfeeding (unless bb tested)

A
  • 1-2 days
  • 7 days
  • vivax
  • G6PD
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14
Q

CHEMOPROPHYLAXIS

Tafenoquine

Duration
- Begin __ days before departure and continue for __ week after leaving

Counseling Points
- Take with food to minimize GI upset

Reasons to avoid use
- ___ deficiency or if not tested
- pregnant/ breastfeeding
- ___ disorders
- children

A
  • 3 days, 1 week
  • G6PD
  • psychotic
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15
Q
A
  • doxycycline
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16
Q

WHEN TO CONSIDER MALARIA

Onset of malaria symptoms:
* Typically, __ - __ weeks after mosquito bite
* Can occur up to 3 years after exposure to P. ___ or P. ___

A
  • Fever AND has traveled to a malaria endemic region before fever onset
  • 2-4 weeks
  • vivax, ovale
17
Q

SIGNS & SYMPTOMS OF MALARIA

Clinical Symptoms

A
  • Fever
  • Headache
  • Weakness
  • Rigors
  • Night sweats
  • Insomnia
  • Arthralgias/myalgias
  • GI distress (N/V/D)
  • Neurologic complications
    (dizziness, confusion, coma,
    disorientation)
    Laboratory
    Findings
  • Anemia
  • Thrombocytopenia
  • Hyponatremia
  • Acidemia
  • Increased creatinine
  • Hypoglycemia
18
Q

SIGNS & SYMPTOMS OF MALARIA

Laboratory Findings

A
  • Anemia
  • Thrombocytopenia
  • Hyponatremia
  • Acidemia
  • Increased creatinine
  • Hypoglycemia
19
Q

DIAGNOSIS

Giemsa-stained blood smear
- Standard for malaria diagnosis!

Thick & thin smear
- Thick smear: RBCs are lysed so visualize parasite outside of cells - Use to estimate ___ density
- Thin smear: used to determine the ___ species

Rapid diagnostic tests

A
  • parasite
  • Plasmodium
20
Q

DETERMINATION OF PLASMODIUM SPP.

Why consideration of Plasmodium spp. is important:

Infection severity:
- P. ___ and P. ___ are more likely to progress to severe disease/death

Treatment
- P. ___ and P. __ also require treatment of hypnozoites (dormant liver stage

Antimalarial resistance:
- P. ___ and P. ___ have different drug resistance patterns in various regions

A
  • falciparum, knowlesi
  • vivax, ovale
  • falciparum, vivax
21
Q

SEVERE MALARIA

Patients have severe malaria if they have ≥1 of the following:
- Impaired consciousness/coma
* Hemoglobin < __ g/dL
- ___
* Acute respiratory distress syndrome (ARDS)
* Circulatory collapse/shock
* Acidosis
* Disseminated intravascular coagulation
* Parasite density of ≥ __ %

Typically caused by P. ___

A
  • 7
  • AKI
  • 5%
  • falciparum
22
Q

TREATMENT OPTIONS FOR UNCOMPLICATED MALARIA

Presence of chloroquine resistance or unknown resistance
- ___ - ___ (Coartem)*
- Atovaquone-proguanil ( ___ )
- ___ sulfate PLUS doxycycline, tetracycline, or clindamycin

A
  • Artemether–lumefantrine
  • Malarone
  • Quinine
23
Q

TREATMENT OPTIONS FOR UNCOMPLICATED

MALARIA

Presence of chloroquine resistance, no mefloquine resistance, or unknown resistance (1)

A

Mefloquine

24
Q

TREATMENT OPTIONS FOR UNCOMPLICATED

MALARIA

Chloroquine sensitive (2)

A
  • Chloroquine
  • Hydroxychloroquine
    (Plaquenil)
25
# ANTI-RELAPSE TREATMENT For P. vivax and P. ovale infections - ___ phosphate - ___ (Krintafel)
- Primaquine - Tafenoquine | only use if G6PD is normal
26
# TREATMENT OF UNCOMPLICATED MALARIA: P. FALCIPARUM OR UNKNOWN SPECIES P. Falciparum or unknown species acquired in area with chloroquine resistance Preferred: * ___ - ___ Alternatives: * Atovaquone-proguanil * Quinine PLUS tetracycline, doxycycline, or clindamycin * Mefloquine (if no other options and no regional mefloquine resistance)
- Artemether-lumefantrine
27
# TREATMENT OF UNCOMPLICATED MALARIA: P. FALCIPARUM OR UNKNOWN SPECIES P. Falciparum or unknown species acquired in area with no chloroquine resistance
Preferred: * Chloroquine * Hydroxychloroquine Alternatives: any options used for treatment of chloroquine-resistant infections
28
# TREATMENT OF UNCOMPLICATED MALARIA: P. OVALE OR P.VIVAX P. ovale or P. vivax acquired in area with chloroquine resistance Preferred: * ___ - ___ Alternatives: * Atovaquone-proguanil * Quinine PLUS tetracycline, doxycycline, or clindamycin * Mefloquine (if no other options) PLUS anti-relapse treatment (must do ___ testing first) * ___
- Artemether-lumefantrine - G6PD - primaquine
29
# TREATMENT OF UNCOMPLICATED MALARIA: P. OVALE OR P.VIVAX P. ovale or P. vivax acquired in area with no chloroquine resistance Preferred: * Chloroquine * Hydroxychloroquine Alternatives: any options used for treatment of chloroquine-resistant infections PLUS anti-relapse treatment (must do ___ testing first) * ___ * ___ (can only be used if received chloroquine for treatment)
- G6PD - Primaquine - Tafenoquine
30
# TREATMENT OF UNCOMPLICATED MALARIA: P. KNOWLESI OR P. MALARIAE Preferred: * ___ or ___ Alternatives: * Artemether-lumefantrine * Atovaquone-proguanil * Quinine PLUS tetracycline, doxycycline, or clindamycin * Mefloquine (if no other options)
- Chloroquine, Hydroxychloroquine
31
# TREATMENT OF SEVERE MALARIA - Perform blood smears every 12-24 hrs until negative - Can be fatal so initiate treatment ___ Treatment - IV ___ - Continue treatment until parasite density ≤ 1% (up to 7 days) After finishing, transition to one of the following oral treatment:* - ___ - ___ (preferred) - Atovaquone-proguanil - Quinine PLUS doxycycline or clindamycin - Mefloquine
- negative - artesunate - Artemether-lumefantrine
32
Severe or uncomplicated?
severe - over 5% parasitemia - possible AKI
33
Artesunate 2.4 mg/kg IV at 0, 12, and 24 hrs then 2.4 mg/kg IV daily for up to 7 days
34
Artemether-lumefantrine 4 tablets PO once then 4 tablets PO 8 hrs later then 4 tablets PO BID for 2 days