VIP Call Girls Mumbai Arpita 9910780858 Independent Escort Service Mumbai
Malaria 17_03_2021 JC edits.pptx
1. National Malaria Control Programme-Ghana
National Malaria Control Programme-Ghana
Uncomplicated Malaria
MALARIA CASE MANAGEMENT TRAINING 2021
2. National Malaria Control Programme-Ghana
• Objectives of the session
• Definition and Introduction
• Classification of Malaria
• Basic pathogenesis of malaria
• Clinical Management of Uncomplicated Malaria
Outline
1
3. National Malaria Control Programme-Ghana
At the end of this module, participants should be able to:
1. Describe the basic pathogenesis of malaria
2. Perform a thorough clinical assessment of a patient with
suspected malaria
3. Identify a case of suspected malaria
4. Conduct appropriate investigations of suspected malaria
5. Provide appropriate anti-malarials
6. Provide appropriate supportive care
7. Provide follow-up care
Objectives
2
4. National Malaria Control Programme-Ghana
• Malaria is a parasitic disease caused by a
protozoan of the genus Plasmodium
• It is transmitted through the bite of an infective
female Anopheles mosquito
• Malaria is a major cause of illness and death in
Ghana, particularly among children and pregnant
women
Definition and Introduction
3
5. National Malaria Control Programme-Ghana
• Malaria cases are classified as either
"uncomplicated" or "severe“ based on the clinical
severity
Uncomplicated malaria:
• Fever or a recent history of fever with positive
malaria diagnostic test and absence of any signs
of severe disease (evidence of vital organ
dysfunction)
Classification of Malaria
4
6. National Malaria Control Programme-Ghana
Severe Malaria
• It is presence or recent history of fever plus
• Any signs and symptoms of severe disease or
evidence of vital organ dysfunction, and
• Positive malaria diagnostic test
Classification of Malaria
5
7. National Malaria Control Programme-Ghana
• Definitions
• Suspected Uncomplicated Malaria is
• the presence of fever (axillary/infrared temp ≥ 37.5° C
) or recent history of fever ( within the last 2-3 days)
• in the absence of any signs of severe disease or vital
organ dysfunction
• Confirmed Uncomplicated Malaria is
• Suspected uncomplicated Malaria plus
• Detection of the malaria parasite in the blood using
malaria diagnostic test (e.g. RDT or microscopy)
Uncomplicated Malaria
6
8. National Malaria Control Programme-Ghana
• Chills (feeling unusually
cold)
• Rigors (shivering)
• Headache
• Nausea and/or vomiting
• Generalised body and
joint pain
• Loss of appetite
• Sweating
• Abdominal pain
(especially in children)
• Bitter taste in mouth
• Irritability and refusal
to drink or breastfeed
7
Other symptoms of Uncomplicated Malaria
11. National Malaria Control Programme-Ghana
• The systemic manifestations of malaria are
attributable to various cytokines released in
response to the parasite and red cell membrane
products
• FEVER and rigors,
• Headache
• GIT symptoms – nausea and vomiting, diarrhea,
anorexia,
• Tiredness, aching joints and muscles
• Thrombocytopenia, immunosuppression, coagulopathy
• CNS manifestations
Pathogenesis of Malaria
10
13. National Malaria Control Programme-Ghana
• Appropriately assess and classify fever
• Promptly and effectively treat to avoid
progression to severe disease
• Minimize the risk of developing drug-resistant
parasites
• Limit the duration of disease
• Exclude other common causes of febrile illness
Specific Objectives in the Management of
Uncomplicated Malaria
12
14. National Malaria Control Programme-Ghana
• Age
• Presenting symptoms
• Ask for common symptoms of illness (especially
in children cough or difficulty in breathing,
diarrhoea, ear pain, rash, dysuria, frequency of
urination)
• Past Medical History: Sickle cell disease, HIV
infection, Malnutrition, Diabetes mellitus,
Hypertension etc.
History Taking …1
13
15. National Malaria Control Programme-Ghana
• Medication and vaccination history: antimalarials
(treatment or prophylaxis – time frame), herbal,
malaria vaccine etc.
• Place of residence and recent travel history
• Obstetrics and gynaecological history ( for clients
in child bearing age group)
History Taking …2
14
16. National Malaria Control Programme-Ghana
• Assess the patient for signs of severe
disease in a systematic manner using the
ASK, LOOK and FEEL approach
• For children < 5years
ASK:
• Is the child able to drink or breastfeed
• Does the child vomit everything
• Has the child had convulsions
• How long patient has had the fever (≥ 7days)
Assessment of Severe Disease …1
15
17. National Malaria Control Programme-Ghana
• For all patients, ask for:
• Generalised weakness, such that the patient cannot walk or sit
without assistance
• Change of behaviour, confusion, unresponsiveness
• Convulsions (fits)
• Difficulty in breathing
• Recurrent or prolonged bleeding from the nose, gums, vomiting
blood, dark foul smelling stool or bloody stool
• Yellowish colouration of the eyes, palms etc.
• Inability to take fluids or anything orally
• Repeated vomiting
• Cola-coloured urine
Assessment of Severe Disease …2
16
18. National Malaria Control Programme-Ghana
• Look for:
• Restless, irritable
• Lethargic, Unconscious
• Convulsion
• Jaundice
• Pallor
• Generalized rash
• Sunken eyes
• Cola-coloured urine
• Abnormal bleeding
• Feel for:
• Fast breathing
• Stiff neck
• Temperature
• 2months – 2 years: <
35.5oC or >37.5oC
• > 2 years : ≥ 38.5oC
• Shock
• Weak rapid pulse
• Cold extremities
17
Assessment of Severe Disease …3
For children < 5 years
19. National Malaria Control Programme-Ghana
• For all patients look and feel for:
• Altered consciousness (change of behaviour,
confusion, delirium, coma)
• Deep breathing and respiratory distress
• Unexplained abnormal bleeding
• Recurrent or prolonged bleeding from the nose,
gums or venipuncture site, haematemisis or
melena
• Jaundice (yellowish colouration of the eyes)
• Prostration i.e. generalised weakness, such that the
patient cannot walk or sit without assistance
• Axillary temperature ≥ 41.0 °C
Assessment of Severe Disease …4
18
20. National Malaria Control Programme-Ghana
• Circulatory collapse or shock
• cold limbs, weak rapid pulse, systolic BP of less 80mmHg in adults
and less than 50mmHg in children
• Signs of hypoglycemia
• sweating, pupillary dilation, abnormal breathing
• Pallor – confirm anaemia with diagnostic test
• Renal Impairment - passing very little urine
• Urine Output <25 - 30mls/hour for over at least 6 hours for Adults
or
• < 0.5ml/kg/hr over at least 6 hours for children
• Dark or cola-colored urine
Assessment of Severe Disease …5
19
21. National Malaria Control Programme-Ghana
• Uncomplicated Malaria is confirmed by either;
• Microscopy (GOLD STANDARD)
• Quantitative test
• It is done by reporting on species, stage and parasite density
when positive
• And reported No Malaria Parasites(No MPs seen) seen when
Negative
• RDT
• Qualitative test
• Reported as either Positive or Negative
• EITHER ONE CAN BE USED TO CONFIRM THE DIAGNOSIS
Laboratory Investigation
20
22. National Malaria Control Programme-Ghana
•If test is positive
• Diagnosis of uncomplicated malaria is
confirmed
•If test is negative
• Malaria is unlikely
• Investigate for other causes of the fever or
illness
Diagnosis of Uncomplicated Malaria
21
23. National Malaria Control Programme-Ghana
1. Viral Infections
• COVID-19
• Acute respiratory infections- Cough/cold, pneumonia,
pharyngitis, ear infections
• Viral exanthems
• Measles (high fever, generalised skin rash with cough, red eyes or
mouth sores)
• Rubella /German measles (Rash tends to spread more quickly, over
24hrs)
• Chicken pox / Varicella-zoster virus (will have a vesicular rash)
• Erythema Infectiosum/Fifth disease (low grade fever, “slapped cheeks”
generalised skin rash)
• Mumps (usually have swelling at the angle of the jaw)
• Hepatitis (jaundice, loss of appetite/vomiting, pain in right
upper abdomen)
• Meningoencephalitis
Other Causes of Febrile Illnesses
22
24. National Malaria Control Programme-Ghana
2. Bacterial infections
• Acute respiratory infection: Tonsillitis, sinusitis Pneumonia
(Cough with fast breathing
• Scarlet fever (Fever, sore throat and rash)
• Acute ear infection in children (ear pain and/or discharge)
• Urinary tract infection (frequency or pain on passing urine,
loin pains)
• Typhoid (persistent fever for over 7 days, general
weakness/prostration)
• Meningitis (fever, neck stiffness)
Other Causes of Febrile Illnesses
23
25. National Malaria Control Programme-Ghana
• The clinical objectives of treating uncomplicated
malaria are to:
• cure the infection as rapidly as possible (Cure is
defined as elimination of all parasites from the
peripheral blood)
• prevent progression to severe disease
• The public health objectives of treatment are to:
• prevent onward transmission of the infection to others
• prevent the emergence and spread of resistance to
antimalarial drugs
Objectives of Treatment
24
26. National Malaria Control Programme-Ghana
• Specific antimalarial treatment
• Supportive treatment
• Counselling on treatment
• Follow-up
Principles of Treatment
25
27. National Malaria Control Programme-Ghana
• Treatment of choice is Artemisinin-based Combination Therapy
• The national recommended options include:
• First – Line
• Artesunate – Amodiaquine (AS-AQ)
• Artemether – Lumefantrine (AL)
• Second – Line
• Dihydroartemisinin - Piperaquine (DHAP)
• Fixed dose formulation is recommended
• Dosage should be weight-based
• Demonstrate how to measure and give the correct dose to the
patients/caregiver
• Give first oral dose under supervision (esp. children)
• PARENTERAL ANTIMALARIALS SHOULD NOT BE GIVEN IN
UNCOMPLICATED MALARIA
Specific Antimalarial Treatment
26
28. National Malaria Control Programme-Ghana
• The concept of ACT is based on the use of 2 drugs with
different modes of action:
• an Artemisinin-derivative that causes rapid and effective reduction
of parasite biomass and gametocyte carriage and
• a partner drug that has a longer duration of action
• Advantage of Artemisinin include:
• rapid action of clearing parasites, acting on all blood stages
• Short half-life reducing the selection of resistant clones from new
infection
• Generally well-tolerated
Rationale for Artemisinin-Based Combination
Therapy (ACT)
27
29. National Malaria Control Programme-Ghana
• Dose:
• Artesunate - 4 mg/kg/day (therapeutic range: 2–10 mg/kg/day)
• Amodiaquine – 10mg/kg/day (therapeutic range: 7.5–15
mg/kg/day)
• It is given orally once or twice a day for 3 days
• Fixed-dose formulations available
• AS – AQ : 25/67.5 mg
• AS – AQ : 50/135 mg
• AS – AQ : 100/270 mg
Artesunate-Amodiaquine
28
30. National Malaria Control Programme-Ghana
Artesunate-Amodiaquine 25mg/67.5mg tablet
Fixed Dose Combination 12 hourly dosing
29
Weight
(kg)
Age
(yr)
Day 1 Day 2 Day 3
<8 2-11 months ½ ½ ½ ½ ½ ½
9-17 1-6 years 1 1 1 1 1 1
18-35 7-13 years
2 2 2 2 2 2
>36 >13 years
4 4 4 4 4 4
31. National Malaria Control Programme-Ghana
Artesunate – Amodiaquine 25mg/67.5mg Fixed
Dose Combination 24-hourly Dosing
30
32. National Malaria Control Programme-Ghana
Artesunate + Amodiaquine 50/135mg Tablets,
given once daily for all ages
31
33. National Malaria Control Programme-Ghana
Artesunate + Amodiaquine 50/135mg Tablets,
given 12hourly for all ages
32
34. National Malaria Control Programme-Ghana
Artesunate – Amodiaquine fixed dosing
100/270mg tablet 12 – hourly dosing
33
35. National Malaria Control Programme-Ghana
Artesunate – Amodiaquine fixed dosing
100/270mg tablet 24 – hourly
34
36. National Malaria Control Programme-Ghana
• Dose:
• Artemether – 1.7mg/kg/dose (therapeutic range: 1.4–4 mg/kg/dose)
• Lumefantrine – 12mg/kg/dose (therapeutic range: 10 –16
mg/kg/dose)
• It is given orally twice a day for 3 days
• First 2 doses should be given 8 hours apart
• Total of 6 doses
• Fixed-dose formulations available
• AL : 20/120 mg (can now be given to children <5kg or 6mths)
• Al : 40/240 mg
• AL : 80/480 mg
• The 80/480 artemether-lumefantrine fixed-dose formulation is
recommended for use in patients with weight 35kg and above
for ease of administration
• Lumefantrine is enhanced when taken with a fat – containing
meal e.g. milk
Artemether-Lumefantrine
35
40. National Malaria Control Programme-Ghana
• Dose:
• Dihydroartemisinin – 4mg/kg/day (therapeutic range: 2 – 10
mg/kg/day)
• Children < 25kg : Dihydroartemisin minimum of 2.5mg/kg/day
• Piperaquine – 18 mg/kg/day (therapeutic range: 16 – 26
mg/kg/day)
• Children < 25kg : Piperaquine minimum of 20mg/kg/day
• It is given orally once daily for 3 days
• Fixed-dose formulations available
• DHAP : 20/160 mg
• DHAP : 40/320 mg
• DHAP : 80/640 mg
• Avoid fatty meals with intake of DHAP as the risk of
arrythmias is increased as a result of accelerated
absorption of piperaquine.
Dihydroartemisinin - Piperaquine
39
44. National Malaria Control Programme-Ghana
• Patient with fever(temperature > 37.5oC or feels warm to touch)
• Tepid – sponging
• Give an antipyretic, preferably paracetamol.
• Ibuprofen, aspirin and non steroidal antipyretics are not
recommended because of the risks of gastrointestinal bleeding, renal
impairment and Reye’s syndrome (children).
• Vomiting
• Repeat the dose if patient vomits within 30mins of administration
• Anti-emetics are potentially sedative and may have neuropsychiatric
adverse effects and should therefore be used with caution
• In case of itching
• Explain that itching is a possible adverse drug reaction
• Give an antihistamine
• If mild patients should continue taking the drug
• If severe: consider stopping the medication and change to other
suitable ACTs
Supportive Treatment
43
45. National Malaria Control Programme-Ghana
• Advise mothers/caregivers to give extra fluids, such as
breast milk, drinking water, fresh fruit juices, coconut
water, Oral Rehydration Salt solution (ORS), etc.
• Feed the child during illness
• Tell patient or child’s caregiver the diagnosis
• Tell patient or child’s caregiver the reason for giving the
medicine
• Advise to administer the antimalarials after meals
• Explain that anti-malarials must be taken till the course of
treatment is completed even if the patient feels well
Supportive Treatment and Counselling
44
46. National Malaria Control Programme-Ghana
• Advise the patient to return immediately ( even
within the same day) if symptoms get worse, or if
signs of severe disease develop (even if within
same day)
• Note : Ensure the patient or care-giver has
understood all the treatment advice before
leaving the clinic.
Counselling
45
47. National Malaria Control Programme-Ghana
• Ask patient to come for a review after completion of ACTs
• Assess for anaemia and treat or refer appropriately
• If symptoms are persistent, reassess, treat or refer appropriately
• If patient is not improving i.e. Getting worse after initiation
of treatment or Not getting better after 48 hours
• Reassess (Ask, Look and Feel approach) for:
• Signs of severe disease
• Compliance with therapy
• Co-existing illness
• Request for microscopy
Follow-up Activities
46
50. National Malaria Control Programme-Ghana
Malaria Life Cycle
49
*assuming uncomplicated infection
1 given in days, unless specified otherwise
2 except those strains with prolonged
incubation periods
3 from infection to the appearance of
detectable parasitaemia
4 from infection to the appearance of
symptoms
5 after the appearance of parasitaemia
6 maximal duration of infection ever recorded
Uncomplicated malaria:
presence of fever or a recent history (2-3 days) of fever,
positive malaria test
absence of any signs of severe disease or evidence of vital organ dysfunction
1.All 3 must be present to make a diagnosis of uncomplicated Malaria.
signs and symptoms of severe disease life threatening complications
Malaria diagnostic test, i.e. microscopy, a rapid diagnostic test or a molecular diagnostic test
Presumed Malaria: Case suspected of being malaria that is not confirmed by a diagnostic test
Note: The designation “presumed malaria” is reserved for uncommon situations in which a diagnostic test cannot be performed in a timely manner.
Suspected malaria: Illness suspected by a health worker to be due to malaria, generally on the basis of the presence of fever with or without other symptoms
Confirmed Malaria: Malaria case (or infection) in which the parasite has been detected in a malaria diagnostic test, i.e. microscopy, a rapid diagnostic test or a molecular diagnostic test
The Host factors, Parasite factors, Geographical factors and Social Factors interplay to exhibit these clinical features or presentations.
Sexual life cycle of parasite occurs in mosquito and asexual life cycle occurs in the human being.
Ian A Clark, Alison C Budd, Lisa M Alleva, William B Cowden. Human malarial disease: a consequence of inflammatory cytokine release. Malaria Journal. 2006;5:85. doi:10.1186/1475-2875-5-85.
Thrombocytopenia- low platelets count
Coagulopathy- disorders with blood clotting
Cytokines –are proteins produced by the cells of the immune system that mediate and regulate immunity, inflammation and hematopoiesis
Further information should be asked on each presenting complaint (duration, frequency, interventions)
Further information should be asked on each presenting complaint (duration, frequency, interventions)
Place of Residence and recent travel history: essence is for time of possible exposure and incubation period
The first 3 signs/symptoms stated constitute general danger signs in children under 5 years. The 5 General danger signs in children <5 years are: inability to drink or breastfeed, vomiting everything, history of convulsions during the current illness, lethargy or unconsciousness and convulsions now.
Note- Fever for more than 7 days is not a sign/symptom of severe disease. It only points to the likelihood of severe disease.
More work will be done during the Diagnostic session
Malaria diagnostic test, i.e. microscopy, a rapid diagnostic test or a molecular diagnostic test
Molecular test is not done routinely. Usually done under research purposes to distinguish recrudescence and reinfection.
Stage: Developmental stages of the parasite
Closely follow-up the patient and inform client to report immediately any danger sign(s) is/are identified
“Cure” is defined as elimination of all parasites from the peripheral blood. The public health objectives of treatment are to prevent onward transmission of the infection to others and to prevent the emergence and spread of resistance to antimalarial drugs
first-line treatment; Treatment recommended in national treatment guidelines as the medicine of choice for treating malaria
second-line: Treatment used after failure of first-line treatment or in patients who are allergic to or unable to tolerate the first-line treatment
Ding et al., 2011, Trends Parasit, 27, 73-81
Hypothesis is that these 2 drugs together will achieve effective clinical and parasitological cure, protect each other from the development of resistance by P. falciparum, and reduce the overall rate of malaria transmission
For ease of administration, avoid in patients <9kg (<1 year) and use appropriate lower strength formulations
For ease of administration, avoid in patients <18kg (6 years) and use appropriate lower strength formulations
For ease of administration, avoid in patients <9kg (<1 year) and use appropriate lower strength formulations
Range perday
Arthemeter -1.4-4mg/kBW per dose
Lumefantrin-10-16mg/kBW per dose
Recommended for weight 35kg and above for ease of administration
Range
Dihydroartemisinin- 2-10mg/KBW
Piperaquine-16-26mg /KBW
Reyes Syndrome – condition that causes confusion, swelling in the brain and liver damage
Treatment of fever is especially important for children.
Use lukewarm water from the feet toward the upper part of the body. Do not pour cold water on the child
Anti-emetics are potentially sedative and may have neuropsychiatric adverse effects, which could mask or confound the diagnosis of severe malaria. They should therefore be used with caution
Vomiting is common in acute malaria and may be severe. Parenteral antimalarial treatment may therefore be required until oral administration is tolerated. Then a full 3-day course of ACT should be given. Anti-emetics are potentially sedative and may have neuropsychiatric adverse effects, which could mask or confound the diagnosis of severe malaria. They should therefore be used with caution
Microscopy must be the preferred parasitological test for malaria
At the higher level total re-assessment of patient and appropriate lab investigations(Full blood count, X-ray, Urine, etc.) including microscopy will be needed
Prepatent Period: Interval between inoculation of sporozoites into the skin and first appearance of merozoites in the blood; corresponds to the length of hepatic or pre-erythrocytic schizogony, which is usually fixed for the different parasite species.
Incubation Period: Interval between inoculation of the sporozoites and first appearance of the symptoms