Presentation Transcript
Malaria prophylaxis: Malaria prophylaxis Jørgen Kurtzhals
Centre for Medical Parasitology
Rigshospitalet, Copenhagen, Denmark
Indication for chemoprophylaxis: Indication for chemoprophylaxis Risk groups in populations of endemic countries
Pregnant women
Infants
Travel to high risk areas
The headlines: The headlines Principles of malaria prophylaxis
Individual counselling
Geographical
Traveller
Available drugs
Standby treatment
Risk
The need of the traveller
The need of the doctor
Purpose of malaria prophylaxis: Purpose of malaria prophylaxis Give the traveller a tool to
Reduce risk of malaria
Minimise risk of severe malaria
Avoid fatal malaria
NOT a guarantee against malaria
Principles of malaria prophylaxis: Principles of malaria prophylaxis A – awareness about the risk of malaria
B – bites of mosquitoes should be avoided
C – chemoprophylaxis and compliance
D – diagnosis of febrile illness without delay
Awareness about the risk: Awareness about the risk The risk of contracting malaria
In spite of taking prophylaxis
Alert your doctor
The risk of dying from malaria (P. falciparum)
Particularly if treatment is delayed
Adjust level of information to the traveller
Mosquito bite prophylaxis: Mosquito bite prophylaxis Malaria transmitted by anopheline mosquitoes
Bite at night (dusk to dawn)
Stay indoor at night
Mosquito screen
Impregnated bed nets
Air conditioning
Long clothing and repellent outdoors at night
Also repellent in face – apart from proximity of eyes and mouth
Chemoprophylaxis: Chemoprophylaxis Take prescribed drug exactly as advised
Start one dose interval before (Lariam® 3-4 weeks)
Continue 4 weeks after (Malarone® 1 week)
Side effects
Serious: Discontinue. Seek immediate medical advise
Mild/moderate: Continue. Seek medical advise
Will chemoprophylaxis blurr symptoms?
Possibly, but no cause to discontinue
Diagnosis and treatment: Diagnosis and treatment Incubation period 1 week - months
Fever must be examined without delay
Fever fluctuates (not always clear periodicity)
Other symptoms can vary (nausea, headache, pains….)
Falciparum malaria may become severe in 24-48 hours
Standby treatment
Only when no other possibility
Always medical care (certify cure, differential diagnosis)
Drugs for prophylactic use: Drugs for prophylactic use Chloroquine
Benign malaria or sensitive P. falciparum
Acceptable in pregnancy and infants
One weekly dosage
Rare and acceptable side effects
GI
Vision
Itching
May worsen psoriasis (and epilepsy?)
Drugs for prophylactic use: Drugs for prophylactic use Proguanil (Paludrine®)
In combination with Chq for sensitive P. falciparum
Acceptable in pregnancy – folate 5 mg daily
Acceptable in infants – no syrup available
One daily dosage (evening meal)
Acceptable side effects
GI
Mouth ulceration, hair loss
Drugs for prophylactic use: Drugs for prophylactic use Mefloquine – I (Lariam®)
Documented effect against P. falciparum (not S-E Asia)
Useful from 5 kg body weight and > 3 months
Contra indicated in pregnancy and lactation
One weekly dose
Begin 3-4 weeks before (tolerance testing)
Quinine use relative contra indication
Drugs for prophylactic use: Drugs for prophylactic use Mefloquine – II
Side effects
Sleep disorders
Neuropsychiatric
Cardiac arrythmia
GI – vomiting
Public opinion!
Drugs for prophylactic use: Drugs for prophylactic use Doxycycline – I
Prevention of P. falciparum in S-E Asia (and alternative in other areas)
Absolutely contraindicated in
Pregnant and lactating women
Growing children (<12 years)
One daily dose (NOT with milk products or iron)
Broad spectrum antibiotic – ecological perspective
Drugs for prophylactic use: Drugs for prophylactic use Doxycycline – II
Side effects
GI – potentially severe (e.g. Cl. difficile)
Vaginal candidiasis
Photo sensitivity
Drugs for prophylactic use: Drugs for prophylactic use Atovaquone + proguanil (Malarone®)
Apparently effective against all P. falciparum
Not documented against other plasmodia
Used from 10 kg
Contra indicated in pregnancy and lactation
One daily dose (with food or milk product)
Expensive
Well tolerated (head ache, GI, mouth ulcers, hair loss rare)
Choice of prophylaxis: Choice of prophylaxis Destination
WHO International travel and health
www.who.int/ith
National guidelines
Duration and type of travel
Short term, business
Low risk, high economic performance
Long term, adventure
High risk, low economic performance
Choice of prophylaxis: Choice of prophylaxis Long term, residence
Mosquito free housing
Increased risk during journeys/field work
Awareness about malaria
Take responsibility
Knowledge about good local clinics
Long duration of drug intake
Side effects (real/perceived)
Economy
Choice of chemoprophylaxis: Choice of chemoprophylaxis
Standby treatment: Standby treatment Definition
Self administration of antimalarial
When malaria is suspected
And when medical care is unavailable within 24 hours
Rational for standby treatment: Rational for standby treatment Rapid progression from symptom start to possible complications
High risk area: Prophylaxis only 50-90% effective
Low risk area: Toxicity from prophylaxis may outweigh benefit of avoiding malaria
Indication for standby treatment: Indication for standby treatment Tp > 37.50C +/- malaise, head ache etc.
Medical aid unavailable within 24 hours
Minimum 7 days after entering malarious area
Take standby treatment
Seek medical care without delay
Choice of standby treatment: Choice of standby treatment Fansidar® (Sulfadoxin-pyrimethamine)
Easy administration, effective, well tolerated
S/P resistance in East Africa and South East Asia
Allergy
Malarone
Highly effective in all areas
Very expensive
Choice of standby treatment: Choice of standby treatment Mefloquine
Highly effective – except S-E Asia
Common side effects at therapeutic dosage
Not recommended for treatment if used as prophylaxis
Quinine
Highly effective in all areas
Common side effects
Compliance: Long treatment duration
Not if mefloquine used as prophylaxis
Choice of standby treatment: Choice of standby treatment Chloroquine
Effective against benign malaria and P. falciparum where there is no resistance (~WHO)
Well tolerated
Artemisinin derivatives
Not available in many countries – available in Africa
Effective in all areas
Well tolerated
Risk of recrudescence
Risk: Risk The traveller
The risk of malaria
Transmission intensity
Type
Benefit
Resistance
Adverse effects (and cost)
The level of awareness
The willingness to be responsible
Risk: Risk The doctor
Responsibility
Standard procedure
All deviations recorded
Signed contract for all sub-optimal choices?
E.g. long term travellers
Insurance!
Short cases 1: Short cases 1 18 year old girl, going on an international exchange programme to rural Kenya for 9 months
Suggest prophylaxis
Mefloquine
Father has epilepsy – alternative?
Ask about specific risk plus treatment facilities
Low risk, good facilities: Chloroquine and proguanil
High risk and/or doubtful facilities: Doxycycline
Short case 2: Short case 2 35 year old, pregnant woman (8 weeks) travelling to Solomon Islands on a 2 month trip
Advise: Stay at home
Insists on going – choose chemoprophylaxis
Chloroquine and proguanil
Suggest stand by treatment
Fansidar (or quinine)
Case 1: Case 1 17 students of West African architecture (Mali, Ghana)
Various prophylactic regimens
Two febrile cases treated as malaria by local clinic (Ghana)
Both were on doxycycline
Contact by e-mail: What do we do?
Case 1 – ctd.: Case 1 – ctd. Your advise: continue. Take care of mosquito bites
Confirmed diagnosis?
No better alternative
Two students on doxycykline have moderate-severe side effects
Suggest alternative
Case 1 – ctd.: Case 1 – ctd. Malarone if cost is not an issue
Chloroquine and proguanil plus warning!
Mefloquine not nice to start in the middle of journey
Case 1 – ctd.: Case 1 – ctd. One student on artemisia drops (herbal drug) x 2 weekly
Suggests this to fellow travellers, one takes the advise
After 3 months total of 11 suspected malaria, all treated with chloroquine
Who had malaria antibodies (merozoite IFAT)?
Case 1 – ctd.: Case 1 – ctd. The 2 on artemisia had confirmed malaria
Lessons learned:
Local diagnosis not always reliable
Do not change accepted principles due to single event
Artemisia not suitable for prophylaxis (short half life)
Herbal artemisia unreliable content
Case 2: Case 2 64-year old woman with fever and ’hot’ sensation when passing urine
Returned from the Gambia after beach journey 2 weeks ago
Good compliance with chloroquine and proguanil (ongoing)
Diagnosis?
Case 2 – ctd.: Case 2 – ctd. Could be malaria
Local doctor suspects cystitis – antibiotic treatment
Admitted after additional 3 days with 11% P. falciparum
Lessons:
Chq+proguanil not optimal in West Africa
No prophylaxis is safe – always suspect malaria
Symptoms of malaria can mimick many conditions
Case 3: Case 3 38-year old Danish woman, had been living in northern Ghana for 3 years
Developed fever with chills, malaise, womiting
Local clinic found <1% P. falciparum
Treated with halofantrine (Halfan®) 500 mg x 3 for one day
What next?
Case 3 (ctd.): Case 3 (ctd.) No serious side effects
No repeated dose after one week
Prolonged convalescence – not really well for 2 months
Anaemia, Hb 9.4 g/dl; normal MCV and MCHC
Repeated blood films: Malaria parasites not found
What next?
Case 3 (ctd.): Case 3 (ctd.) Returned to Denmark at end of contract period
Routine check including 3 blood films: Anaemia, no malaria parasites found
What next?
Case 3 (ctd.): Case 3 (ctd.) Stool examination x 3: No bacterial pathogens, Entamoeba coli cysts ++, Chilomastix mesnili cysts
Total WBC 8.7, <1% eosinophils, 102 thrombocytes
Normal renal function
Bilirubin 26 mmol/l, liver enzymes normal
No obvious clinical explanation for the tiredness and anaemia. Bone marrow investigation, cerebral CT, and other investigations considered
What next?
Case 3 (ctd.): Case 3 (ctd.) 4 weeks after return, discontinuation of malaria prophylaxis (chloroquine and proguanil)
Six days later rushed to hospital, reduced consciousness, tp. 39.70C
Lumbar puncture: CSF with 8 cells, glucose and protein normal
Blood film: 8% P. falciparum
Diagnosis: cerebral malaria
Case 3 – lessons learned: Case 3 – lessons learned Halfan® is never first choice
Halfan® should always be repeated after one week
Malaria prophylaxis is intended to suppress the infection
This may sometimes blurr the clinical and laboratory picture
HOWEVER: Prophylaxis should be given in any case
Thrombocytopaenia and anaemia are suggestive of malaria
Choose most effective prophylaxis?