1. Introduction
Snakebite envenomation in Australia is not common, with 3000 cases, 500 hospital admissions, and an average of 2 deaths in Australia each year [
1,
2]. Since 2007, there have been 1054 calls to the Victorian Poison Information Centre (VPIC) relating to snake bite exposures, an average of 81 patients per year. In the 2020 calendar year, there were 128 calls regarding snake bite exposure, of which 63 patients were reported to be asymptomatic at initial call and 31 were reported to be symptomatic (all but four reporting minor symptoms), while symptoms were not reported or documented as unknown in 34 patients. Of this cohort, 72 were male, 54 female, and 2 unknown (Personal communication VPIC Medical Director). The VPIC serves a population of 6.681 million (as of September 2020); hence, the call rate is 0.0001% (Personal communication VPIC Medical Director).
A recent review of national data showed that brown snakes cause the majority of deaths in Australia, and the overall causes of death are due to cardiotoxic and coagulopathic effects [
1]. Data from animal experiments [
3,
4,
5,
6], case series [
7,
8,
9,
10,
11,
12,
13], analyses of fatal snakebites [
1,
14], and prospective observational studies [
15,
16,
17] have provided information about the epidemiology and clinical aspects of snakebite in Australia in order to inform clinical practice guidelines for patients with actual or suspected envenoming across all Australian jurisdictions. However, there are no data related to whether current clinical practice adheres to available clinical guidelines.
Australia has had a long and esteemed history of snakebite research, led over a 30-year period from 1960 by Stuhan Sutherland, who also pioneered the use of the pressure immobilisation bandage for the treatment of Australian elapids and the funnel web spider (Atrax Robustus) in the late 1970s. His contribution was acknowledged in a publication in Toxicon in 2006 [
18].
Our study was conducted following concerns raised during a coronial enquiry into two snakebite deaths in Victoria. In seeking expert opinion, the coroner noted a lack of consensus in treatment guidelines amongst three experts, all of whom are well respected and two of whom are well published in the area [
19]. We surmised that if experts could not agree, how were front line clinicians managing snake bite and what was guiding their care?
Some of the challenges in managing snake envenoming in Australia have included the controversy over the number of ampoules of antivenom required for treating envenoming cases [
13,
20,
21], the role of laboratory investigation in determining the use of antivenom, and the source of information commonly used by clinicians.
Our study was designed to gain an understanding of the “real world” experience of clinicians who have treated snake envenoming in Australia. The number of clinicians in this cohort is small, given the low volume of symptomatic calls received by our poison information services. Over a 10-year period in 1548 patients recruited from 171 hospitals in all Australian states and territories, 755 patients received antivenom, including 49 non-envenomed patients. This is less than eight patients a year [
22]. Our aim was to understand current attitudes and practice in the management of snake envenoming; identify sources of information; document the type and quantity of antivenom used; identify any barriers to management; and document compliance with clinical practice guidelines to inform, strengthen, and standardise recommendations in the future.
Our aim was to determine if there was a need for further work on information sources and we have shown that this is the case. More work needs to be done to align practice across the country. We have not set out to provide the medical expertise (and consensus) but to establish the need to do this. The study was not designed to provide clearer instructions on behaviour in emergency situations—it was to ascertain current treatment and sources of knowledge and referral
3. Discussion
Over the last two decades, there has been significant controversy over the number of ampoules of antivenom required for the initial dose in treating snake envenoming in Australia. The Australian Snakebite Project (ASP) study, an in vitro venom/antivenom neutralisation study, concluded that one ampoule of tiger snake antivenom appeared to be sufficient to bind all circulating tiger snake venom [
24]. On the basis of this work, product information for both tiger snake and brown snake antivenom was changed to recommend one ampoule of antivenom for the treatment for envenomation [
25,
26]. However, while this recommendation is based upon the average yield of venom, actual venom yields can be higher than anticipated [
2], and concern has been raised that the ASP methodology did not account for outliers [
27].
A recent coronial investigation into two fatal deaths in Victoria highlighted different opinions amongst experts about the optimal dose and type of antivenom and directed health department authorities to review and develop a consistent set of guidelines for suspected and established snake bite [
19,
28].
In this study, most respondents were fellows or trainees of the ACEM. This is not surprising, given most antivenom is administered in an ED setting. Clinicians reported that they felt confident in treating snakebite but not in choice of antivenom. There was very little difference in the frequency of use of the tiger snake antivenom and brown snake antivenom, and this result was similar to a previous report of 133 patients [
29], with the exception of a less frequent use of polyvalent antivenom—31% versus 19.3%.
Accurate diagnosis relies on the combination of a good history (e.g., a snake was seen, or the bite was felt), targeted examination for symptoms of envenoming (e.g., ptosis, dysarthria), and appropriate laboratory investigations (e.g., coagulation studies). In our study, clinical presentation was relied upon the most, and while laboratory investigations were identified as vital in determining the presence and/or severity of snake envenoming, access to pathology services was reported to be a major barrier to management.
While antivenom therapy can be associated with adverse reactions, our study did not identify adverse reactions as a barrier to prescribing, and our respondents demonstrated a high level of confidence (91.8%) in their ability to treat a reaction if it occurred.
A total of 39.6% of medical respondents stated that they were uncertain or disagreed that publications in peer-reviewed journals were useful in guiding the management of snake bite envenoming, possibly reflecting the conflicting recommendations.
Challenges in managing envenoming are not limited to antivenom dosing. There are concerns about the costs of stocking high quantity of antivenoms in the hospitals. Antivenom costs AUD 347 to AUD 2320 per ampoule and has a shelf-life of 1 to 3 years. Anecdotally, the high cost of antivenoms and the low incidence of envenoming cases have caused some hospitals to stop stocking antivenom. In our study, while over a third of physician respondents (35.5.%) identified that availability was or could be a barrier to managing snake envenoming, cost was identified as the least important factor (92.7%) Similarly, pharmacists also considered cost and shelf life as the least important factors to influence their decision to stock antivenom.
Limitations to Our Study
The results of this study are limited by the small sample size. We were unable to determine a response rate as the number of practitioners who have treated a snakebite is unknown. We piloted the survey to improve its usability and widely distributed it to our target group; however, despite this, most responses were from clinicians located in Victoria. The study was a questionnaire and respondents may have provided answers that were “expected” rather than actual, and responses were subject to recall bias. The high mortality rate (5%) may have been due to incomplete records or selection bias as clinicians who cared for a patient who died may have been more likely to contribute to the survey.
4. Conclusions
Our data confirm variation in management. Over one-third of respondents stated that they were uncertain or disagreed that publications in peer-reviewed journals were useful in guiding the management of snake bite envenoming. While two-thirds of respondents felt that the availability of guidelines was not a barrier, a third were uncertain or agreed they were a barrier to snake bite management. A different number and combination of antivenom was administered in the 67 patients who received antivenom, which highlights the concerns and the premise upon which the survey was conducted.
This study provides an insight into the management of snake bite as reported by those clinicians who have treated a snake bite patient over the last 36 months. The study highlights that for one in four patients, the number of ampoules administered differs from the current manufacturer guidelines. Nearly a quarter of our respondents reported that they were uncertain or did not agree that they would make the correct choice of antivenom. Multiple sources of information were accessed with least confidence provided by peer reviewed literature. Cost was not a factor in the decision to prescribe antivenom. Access to pathology was identified as a major barrier.