To respond appropriately is having the knowledge of how to ask patients about their experiences of DVA in the first place. Through training and on-going support, clinicians gain essential skills in how to ask direct questions about patients’ experiences of DVA. It also prepares them to be ready to hear the answer and to give supportive key messages to patients when they most need it. We know that clinicians want to support their patients affected and so we need to be providing tools and resources to enable this.
A best practice response clearly includes offering patients a referral to a specialist, independent, DVA service. The more knowledge the primary care teams have of this service the better. Following simple care pathways, which must account for children and risk, appropriate support can be accessed for survivors and perpetrators. Primary care is a busy place and the simpler the referral process the more accessible it becomes. A referral to a named advocate within a specialist service is better for everyone; the clinician, the advocate and most importantly the patient. The advocate can then walk alongside the patient and provide the specialist support they deserve.
An embedded relationship between the health sector and specialist DVA sector is essential for primary care to respond appropriately to DVA. Working together enables an on-going conversation, a consistent partnership approach that puts patients at the centre. This is integral to delivering a best practice approach, it allows for experts in the right places making services accessible and making a difference to the lives of people who really need it.