Infectious diseases (Disease summaries) Flashcards
(96 cards)
types of malaria
Most common tropical disease in the UK
* 75% falciparum (90% of cases from Africa)
* 25% Ovale (90% of cases from India)
Initially ALWAYS TREAT AS FACIPARUM
5 species of malaria
Plasmodium:
- falciparum
- Vivax
- Ovale
- Malaria
Vector: female anopheles mosquito
course of illness: malaria
Incubation period: Minimum 7 days
- Most cases of falciparum malaria present within 2-3 months and nearly all within 6 months
- Non-falciparum malaria may present after months-years due to the reactivation of hypnozoites- Vivax/ ovale up to a year (lay dormant in the liver)
pathophysiology behind malaria
- Sporozoites are transmitted by Anopheles mosquito bites and travel through the blood to hepatocytes, where they mature into schizonts and release merozoites into the bloodstream.
- The merozoites invade red blood cells, mature into schizonts and rupture to release merozoites and the cycle repeats.
- Plasmodium vivax and Plasmodium ovale can remain dormant for months in the liver by producing hypnozoites which can lead to relapses after the initial infection.
- Plasmodium falciparum does not produce hypnozoites and is not associated with relapse.
- Plasmodium malariae also does not produce hypnozoites but can persist in the blood for years.
presentations of malaria
often non-speciifc symptoms with a history of travel to endemic area and fever
- high fever, sweats and rigors
- headache, myalgia, arthralgia
- lethargy
- reduced appetite, nausea, jaundice, abdominal pain
- hepatomegaly and splenomegaly
presentation of faliciparum malaria
Falciparum malaria is the most severe type of malaria. Features include suggesting severe malaria include:
- Cerebral involvement – reduced consciousness, seizures
- Renal impairment – oliguria
- Acidosis – may cause deep breathing
- Hypoglycaemia – more common in pregnant people
- Respiratory distress – pulmonary oedema or acute respiratory distress syndrome (ARDS) – more common in pregnant people
- Severe anaemia
- Haemorrhage – specifically disseminated intravascular coagulopathy
- Shock
- Sepsis – more common in pregnant people
- Haemoglobinuria – falciparum malaria can cause severe haemolysis and dark red urine (also known as ‘blackwater fever’)
- Parasitaemia (>10%.)
- Schizonts on a blood film
pesentation of Non-falciparum malaria
Plasmodium vivax is them most common cause of non-falciparum malaria. Features of non-falciparum malaria include:
- The general features of malaria discussed above
- Cyclical fever – paroxysms of fever based on the parasite’s lifecycle:
- Plasmodium vivax and Plasmodium ovale – every 48 hours
- Plasmodium malariae – every 72 hours
investigations for malaria
Blood film- gold standard
- x 3 blood films
Bloods (FBC, UE, LFT, glucose, coagulation)
- anaemia
- thrombocytopenia
- leukopenia
- abnormal liver test- unconjugated bilirubin
- blood glucose - hypoglycaemia
Imaging- cT
- if symptoms
management of: non-falciparum malaria
oral artemisinin combination therapy (ACT)
management of: uncomplicated Falciparum
admit all patients with falciparum
- artemisinin combination therapy (ACT)
- or quinine with doxycyline
management of: complicated Falciparum
admit
- IV artesunate
- or intravenous quinine (need to monitor for hypoglycaemia)
preventing malaria
General advice for preventing malaria when travelling to endemic areas:
- No method is 100% effective alone
- Use mosquito spray (e.g., 50% DEET spray)
- Use mosquito nets and barriers in sleeping areas
- Seek medical advice if symptoms develop
- Take antimalarial medication as recommended
Antimalarial medications are not 100% effective. The main options are:
- Proguanil with atovaquone (Malarone)
- Doxycycline
- Mefloquine (risk of psychiatric side effects)
Proguanil / atovaquone (Malarone)
is slightly more expensive than the other options but has the least side effects. It is taken from two days before until seven days after travel to an endemic area.
Doxycycline
is a broad-spectrum antibiotic that can cause side effects such as diarrhoea and thrush. It also causes skin sensitivity to sunlight, increasing the risk of sunburn and skin reactions. It is taken two days before until four weeks after travel to an endemic area.
Dengue fever
found in Africa, Asia, India and S and C America
- Arbovirus
- Vector : mosquito
Course of illness: Dengue fever
1) First infection ranges from asymptomatic to non-specific febrile illness (classic dengue)
- Lasts 1-5 days
- Improves 3-4 days after rash
- Supportive treatment only
2) Re-infection with different serotype is very dangerous
- Antibody dependent enhancement (immune system overdrive)
- Dengue haemorrhagic fever (children)
- Dengue shock syndrome
presentation of Dengue fever
- a high temperature, or feeling hot or shivery.
- a severe headache.
- thrombocytopenia and haemorrhage
- pain behind the eyes
- muscle and joint pain.
- feeling or being sick.
- a widespread red rash.
- tummy pain and loss of appetite.
investigations for dengue
- PCR
- Serology e.g. IgM and IgG
management of dengue fever
NO SPECIFIC TREATMENT
- paracetamol
prevention of dengue
Vaccine
severe dengue
Severe dengue is a more virulent form which can cause:
- Disseminated intravascular coagulopathy
- Shock – known as dengue shock syndrome
typhoid fever
- also known as ‘enteric fever’
- associated with poor sanitation- Asia, Africa and S America
Pathogen: Salmonella typhi and Salmonella parathyphi (Paratyphoid)
- gram negative bacilli
- faecal oral route
- fimbriae adhere to ileal lymphoid
Paratyphoid
is similar to typhoid fever, but less severe and is caused by Salmonella paratyphi. Both species are spread via the faecal-oral route through contaminated food and water.