CHAPTER 4: MALARIA IN PDW Flashcards

1
Q

Where are %% of malaria incidences observed.

A

90% In Africa.

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2
Q

How may deaths a year are attributed to malaria.

A

400,000 deaths each year.

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3
Q

How much does antimalarial drugs cost.

A

<$1

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4
Q

What are the four countries that account for almost half the malaria deaths worldwide.

A

Nigeria.
Democratic Republic of Congo.
Tanzania.
Niger.

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5
Q

What are the two patient populations we are most concerned about when thinking about Malaria.

A

Mother/Pregnant women.
Children under the age of 5.

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6
Q

What are the complications associated with pregnant woman contracting malaria infection.

A

Placental malaria, plasmodium falciparum infected erythrocytes sequester in the placenta, resulting in maternal anaemia and also puts the mother at risk of death before and after childbirth.

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7
Q

(a) Describe briefly malaria life cycle in the liver and erythrocyte; (b) What stage is responsible for the clinical presentation of malaria symptoms.

A

a. In the liver cells, sporozoites infect the cells and undergo maturation that leads to the release of merozoites.
In the blood, erythrocytes are infected by merozoites which later becomes trophozoite. Trophozoite reproduce asexually and later the hemolysis leads to release of merozoites.
b. Symptoms of anaemia and fever is due to hemolysis and release of parasite in the blood.

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8
Q

What is the %% of children that account for Malaria death in Africa.

A

80% deaths attributed to children under age of 5, according to WHO malaria report 202

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9
Q

How is malaria transmitted.

A

Migrant workers e.g. Gold mining North East Myanmar.
Seasonal workers (farming). For example, seasonal workers who are carrier that transport parasites to the highlands and other location in Ethiopia where there is lower malaria prevalence.
Troops.

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10
Q

Which method is a quantitive in diagnosis of malaria.

A

Molecular methods such as PCR: expensive but accurate.

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11
Q

Which method is qualitative in diagnosis of malaria.

A

Antigen test ‘dipsticks’

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12
Q

What intervention in the future could lead to better diagnosis.

A

In mobile devices there is an inserted chip that could detect disease.

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13
Q

What are the drawbacks (figure associated) with subjective diagnosis vs blood film.

A

Subjective diagnosis leads to misdiagnosis and poorer patient prognosis. For example Malawi, one study showed that when clinical predicators (rectal temperature, nailbed pallor, and splenomegaly) were used as treatment indications, rather than using only a history of subjective fevers, a correct diagnosis increased from 2% to 41% of cases.

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14
Q

Fill the table for Malaria treatment, prevention and eradication.

A
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15
Q

List the malaria drugs.

A

Quinine derivatives
• Aminoquinolones: Primaquine , Chloroquine
• DiHydroFolate (DHF) inhibitors
• Artemesinin Combination Products (ACT’s)

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16
Q

What are the limitations associated with antimalarial drugs.

A

Compliance
Cost
Safety
GMP Counterfeit
Resistance.

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17
Q

What are the limitations associated with antimalarial drugs concerning safety: THINK DEFICIENCY.

A

Primaquine derivatives: Not effective in patient with G6PD deficiency because it causes hemolysis.

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18
Q

What are the limitations associated with antimalarial drugs concerning cost: THINK EXPENSE/POTENTIAL.

A

Malarone (fixed-dose combination): Too expensive to distribute and patient population in Africa don’t have the financial means to afford treatment or healthcare system that pays for it. Also there is resistance potential.

19
Q

What is the limitation of antimalarial drugs concerning course of treatment, PK, cost.

A

Anti-malarial combination is it tends to be long course, which again for patient population can be costly/not viable in their impoverished circumstances, and short half-life, for example artemisinin (1.4-2.6 h), means there is now no anti-malarial coverage over days which would be ideal.

20
Q

What are the limitations associated with antimalarial drugs concerning drug resistance (6 factors).

A
21
Q

What is your ideal antimalarial drug.

A

Short course (<3 days), full day coverage, OD administration, easily accessible form e.g. dispersible tablets for 5 year olds. (<$1 manufacture).

22
Q

What are the potential damage of self medicating at Medicine Sellers e.g. Africa Village Stalls (DDCQ).

A

Incorrect Diagnosis, Incorrect Dosing, Poor Compliance, Poor Quality medicines.

23
Q

How could self-medication at Medicine sellers be addressed: solution.

A

Solution employed by Indian government involved the setting up of specialised medical centres with specialist volunteers that can DDCQ: Diagnose, Dose correctly, help with Compliance, and provide Quality medicines.

24
Q

a. How can Malaria be prevented (3 methods, memorise). b. What is covered in the classes.

A
  1. Vector Control.
  2. Preventative Chemotherapy.
  3. Vaccine.
25
Q

What does seasonal malaria chemoprevention contain.

A

Sulfadoxine-pyrimethamine (SP).

26
Q

What has been the age extension of seasonal malaria chemoprevention and what have been the benefit.

A

Extending the SMC age range up to 10 years of age effective in Senegal with high coverage and impact.

27
Q

What is seasonal chemoprevention

A

Community-based intervention to prevent malaria in those most vulnerable to the disease’s effects (e.g. <5 years). It involves administering monthly courses of antimalarial medicines during peak malaria transmission season.

28
Q

What is mass administration chemoprevention

A

Involves giving treatment to an entire population or every person in a geographical area regardless of ascertainment of disease or infection status.

29
Q

What is classed in IRS.

A

IRS: Indoor Residual Spraying.
Indoor: Room Surfaces.
Outdoor: Larvicides onto stagnant water (surfactant).

30
Q

What is classed in ITN.

A

Bed nets.
Long-lasting insecticide treated nets (LLTN).

31
Q

For vector control: what are the the drugs used to impregnante bed nets and used in IRS.

A
32
Q

What are the issues associated with insecticides.

A

Insecticide resistance.
Pyrethroid resistance is occurring major malaria vector Anopheles in Africa.

33
Q

What are the genes involved in pyrethroid resistance.

A

Mutations on the gene encoding for the sodium channel, knockdown resistance (kdr) cause resistance to DDT and/or pyrethroid insecticides.

34
Q

How can insecticide resistance be combated.

A

Rotating insecticides.
Using combination of ITN non-pyrethroid + pyrethroid.
Mosaic nets instead of plastic nets impregnted with pyrethroid.

35
Q

What is an example of ITN non-pyrethroid + pyrethroid.

A

Piperonyl butoxide + pyrethroid.

36
Q

What does education vector control involve.

A

Trained healthcare professionals such as pharmacist, nurses, doctors to volunteer in teaching population of how to use bed nets, indoor spraying insecticides and when to seek medical help when symptoms of malaria arise.

Encouraging and educating pregnant women to seek antenatal care where they educate why preventative chemotherapy is required to prevent malaria causing deleterious effects to them.

Teaching school children on what malaria is and what to avoid- puddles, leakages

37
Q

What is the requirement for an effective vaccine for preventing malaria.

A

Malaria vaccine with protective efficacy if more than 80% against clinical disease and last longer than four years.

38
Q

Why is there no widely effective vaccine yet for Malaria.
( Look at My Whole Family)

A
39
Q

What is the name of the vaccine in pilot trial in Ghana, Kenya and Malwai fo Malaria.

A

Mosquirix piloted by WHO for children aged 5 to 17 months.

40
Q

What is the potential downside Mosquirix.

A

Not pragmatic, as vaccine who need to be administered x 4 a year and that increases cost to African countries that may not be able to afford it.

41
Q

Whats the name of the vaccine with 450 participants that showed good efficacy for Malaria protection.

A

New Oxford Vaccine showed 77% efficacy in the high dose group in the trial report.

42
Q

Fill the table for the method used in eradication of malaria.

A
43
Q

What type of blood films are preferred: thin or thick films and why.

A

Thin films allow for species identifications whereas thick films pick up lower level of infection due to larger volume of blood. Also the parasite is distorted so it is difficult to distinguish species.