Tom* had been sexually assaulted by his partner and was referred to an after-hours sexual assault team as part of a hospital crisis care response. Tom had experienced significant injuries because of the sexual assault which required surgery. Police were involved and were investigating the assault.
Tom was unfamiliar with the service system and was overwhelmed by professionals which was compounded by his experiences of trauma while navigating a complex health system. Tom was on a lengthy waitlist for surgery which created increased stress. Tom had also been experiencing thoughts of suicide. The long-term outcomes for Tom are not clear.
Specialist sexual assault, family violence, police, General Practice, mental health, crisis housing and brokerage services, and both general and surgery hospital staff were involved. Coordination between numerous services was required within a short timeframe, thus creating the potential for miscommunication and the risk of replicating a loss of control central to trauma. Numerous services and professionals were involved with Tom in a condensed period which increased the potential for miscommunication and confusion between professionals. Responsive collaboration and advocacy resulted in Tom being offered a range of services through a more cohesive referral process. Clear processes and cooperative information sharing, with Tom’s consent, contributed to positive outcomes throughout Tom’s journey. Tom’s experience of trauma could occasionally present as agitation, so a key function of support from the sexual assault service was to elevate a trauma informed lens when conceptualising Tom’s responses. Furthermore, advocacy with professionals ensured consent and empowerment were central to Tom’s care. A key component of the support was to find out how Tom wanted to be supported including which conversations he was able to have with other services and which ones he felt comfortable to have himself
“You know, when sexual assault or family violence occurs, people’s rights are impacted, their choice is impacted, and their sense of control is impacted. It’s taken by away by the behaviour of the perpetrator. And so, any step that we could take where a person can feel like they could choose and can exercise their rights‘
Care team meetings were established with professionals, and input from those unable to attend were sought prior to meetings to ensure their input would be included. Communication that reduced the need for repeated communication from Tom, including re-telling traumatic detail, was key.
Advocacy occurred with the hospital which placed Tom on the priority waitlist for surgery. Police involvement in completing welfare checks were important to Tom’s care and due to the positive relationship, police were more actively involved. Strong communication made the process to escalate concerns easier, and police quickly attended when a concern for Tom’s welfare was raised. Family violence services and the Victim Support Agency coordinated material aid and housing support.
‘It was good to have that collaboration and to have…. specialist services (including) the police … to make sure… when at a time we were concerned about safety, we were able to kind of escalate that really quickly.’
Numerous professionals were involved with Tom in a brief period of time. Tom was supported by a cohesive referral process which prevented the requirement for Tom to repeat his story. Tom chose to take a step back from his engagement with services and was able to articulate that choice for themselves. Tom’s choice to disengage from services represented his decision to take control of his journey. The long-term outcomes for Tom are not known as service involvement was brief.
‘Even the choice to disengage is still a choice. So, we’re really focused on people’s rights options and control and if that’s what this person needs, and I suspected at that stage they did, they took that option for themselves‘
There were a range of key features that were critical to the multidisciplinary practice and outcomes achieved in this case example.
Enablers:
‘So, it was about bringing the information together so that everyone had a sense of what the support needs were a lot more clearly rather than this person having to tell the story and this being increasingly disturbing and distressing for them.’
Challenges:
‘I think for all practitioners, it’s nice to know that there’s someone there because the service user is getting more support but also that that you’re not left trying to kind of do things that you don’t have the time, the ability or the agency to do.‘