"Oh Doc", says Brian, "I reckon I’ve got the flu. Either that or I never saw the truck that hit me."
He gives a brief history — "I’ve been working for Dave over at his new place, we’re putting up extra fences ‘cause he’s just started running sheep.
It’s all a bit of a panic ‘cause I don’t reckon he’s thought it out much, there’s pregnant ewes everywhere and some are giving birth and he’s running round like a blue arsed fly and I’m putting up fences and now I’ve got this flu and I can’t work and Centrelink say I’ve got to put in a certificate."
Brian does not complain of any respiratory symptoms.
Contact with animals permits the transfer of a variety of infective organisms.
Infections might involve viruses, bacteria, yeasts, protozoa and helminths.
The role of animals in disease transmission includes being reservoir, vector or both.
Zoonoses are common. 75% of newly discovered infectious diseases are zoonotic. 60% of existing infectious diseases are zoonoses.
Zoonoses should be considered in diseases affecting any body system.
History taking about exposure to animals including vertebrates, arthropods and insects may identify reservoirs and vectors of possible implicated organisms.
Zoonoses often have both an acute and a chronic form.
For patients presenting with any condition, accurate diagnosis and the possibility of treatment relies on a comprehensive history and examination.
A common, although by no means universal, presentation in zoonotic disease is acute febrile illness that may be ‘flu-like’ and may or may not have respiratory symptoms.
Some zoonoses have additional clinical signs that suggest the most likely causative organism.
Probability diagnosis is influenced by history of geography, exposure to species and the patient’s activities.
History for patients with chronic debilitating conditions may well disclose exposure to animals and thus suggest a zoonosis as the cause of their symptoms.
Proper establishment of pre-test probabilities before ordering investigations is essential for avoiding harms through false positives/negatives and unnecessary financial and other costs to both the patient and the health system.
Common conditions that might be considered in the differential diagnoses include:
Less likely conditions not to be missed include EBV, CMV, HIV, and atypical pneumonia.
Influenza during the influenza season is far more common1 than the most common zoonosis, Q fever2. [Influenza 20 to 34 per 100,000 compared with a Q fever incidence of about 2 per 100,000].
However, Brian has a significant risk factor for Q fever (exposure to livestock, and in this case, placental tissues from parturient ewes).
Between 1 and 10 coxiella burnetii bacteria are required to confer Q fever. Placental tissues from infected livestock may have as many as one billion such bacteria in every gram of tissue.
Scrub typhus, Queensland tick typhus and other tick related rickettsial diseases often have an eschar associated with a tick bite:
Other zoonoses that can produce symptoms similar to Brian’s include:
As to non-zoonotic chronic conditions marked by a persistent sense of fatigue, common complaints would include:
Murtagh’s General Practice provides a comprehensive list of conditions to consider.
Zoonoses to consider include:
Leptospirosis and rat bite fever could reasonably be considered in respect of an acute febrile illness following exposure to rats.
Rat bite fever
Rat bite fever is rare within the general population although rat fanciers, particularly those who kiss their rats, are more likely to have the illness.
Leptospirosis
Leptospirosis is more common and can be contracted by people who are exposed not only to infected rats and rat urine (exterminators, commercial cleaners, veterinarians and so on) but also from contact with infected sheep, cattle, domestic and working dogs and contaminated floodwaters, for example.
Common tick-borne diseases in Australia are:
All of these diseases are well treated with doxycycline in both adults and children over 6 months of age.
Common tick bite effects include:
Allergic reactions
Allergic reactions are related to proteins in the anaesthetic saliva of the tick. Reactions can range from itch, often mild but sometimes severe, to anaphylaxis.
Inoculation
Inoculation with bacteria can cause diseases such as Lyme (in appropriate circumstances), scrub typhus, and Queensland tick typhus and skin infections, including staphylococcal and streptococcal infections.
Intoxication
When large enough, ticks can deliver a potent neurotoxin that is capable of killing small animals such as dogs and cats. Cattle, if infested with a great many large ticks, may die as a result of the neurotoxin. Treatment of neurotoxin poisoning in humans is supportive only.
Ticks should be removed mechanically principally by firmly grasping close to the skin and extracting the head including mouthparts.
In some cases where ticks are really deeply embedded, an approach is to administer local anaesthetic to the skin and use a biopsy punch.
Ticks should not be doused in chemicals as this may trigger the discharge of neurotoxin.
What signs and symptoms would indicate that a person who had been bitten by a tick had contracted a Rickettsial disease?
The patient will typically complain of:
The patient is likely to be febrile, often with a temperature of about 39 to 41°C.
The site of the tick bite will usually be evident, displaying an eschar.
A few days after the onset of symptoms, a rash may appear — widely spaced erythematous macules.
Which invariably fatal zoonoses should be discussed during the travel medicine consult?
Rabies is common in Bali. There have been hundreds of deaths over the last decade. Rabies in conferred by bites or scratches from infected mammals including monkeys and bats as well as dogs and cats.
What preventative measures should Miriam and her husband take?
Immunisation against rabies (e.g. Rabipur®) is an option. The immunisations are not funded, they cost about $110 - $150 each, and three pre-exposure doses are required at 0, 7 and 21-28 days. Many travellers opt to not be immunised and simply avoid being bitten. It is important that irrespective of immunisation status, travellers have an appropriate post-exposure plan.
What action plan should Miriam follow if she is exposed to rabies – dependent upon her immunisation status?
A travelling patient who is exposed to rabies needs to make their way immediately to a US-style hospital (this may require repatriation) to be treated.
| Immunised | Un-immunised |
|---|---|
| Post exposure immunisation days 0 and 3 | Post exposure immunisation days 0, 3, 7 and 21-28 |
| Immunoglobulin — into wound, remainder as deep IM dose into tissues remote from bite |
If however a patient presents to your surgery following rabies exposure on a recent trip, you may need to discuss with your local public health unit in order to obtain appropriate treatment advice and the rabies vaccinations.
Brian could be suffering from Q fever.
Q fever was first discovered in Brisbane in 1935 and is named because of 'query fever'.
The disease appears to have an almost global distribution.
Caused by the bacterium Coxiella burnettii, it has a wide variety of clinical presentations ranging from no acute episode at all to a 'flu-like' illness, pneumonia or hepatitis (and others).
Even in a patient with very small exposure to sources of Coxiella burnettii, Q fever infection is possible.
Appropriate tests include FBE, E/LFTs, chest XRAY, rickettsial serology, and PCR respiratory viruses.
Mortality from untreated acute Q fever is about 1.5%.
Q fever does not always present as an acute illness.
Chronic Q fever may arise in patients who have been infected but have never manifested an acute episode.
The consequences of untreated chronic Q fever can be life-threatening.
Infectious disease specialist:
Before administering the Q Fever vaccination by SC injection it is imperative that a person is tested for pre-existing Q fever immunity.
People who are already immune to coxiella burnetti can suffer significant reactions including febrile reactions and granulomatous abscess formation at the site.
Pre-testing consists of serology and an intradermal skin test using a dilute formulation of the vaccine antigen.
This skin test is read after 7 days, and if either the skin test or serology is positive the person should not be vaccinated.
Further details can be found on the RRMEO module through ACRRM.