The inspection took place on 15, 16 and 17 June and was unannounced. Pilgrims Hospice Thanet is one of three hospice locations for the provider, Pilgrims Hospices in East Kent. The hospice offers specialist palliative care, advice and clinical support for adults with life limiting illness and their families. They deliver physical, emotional and holistic care through a multi-disciplinary team of nurses, doctors, counsellors, social workers, occupational therapists, physiotherapists, spiritual leaders and a range of volunteers. The location has a day centre and capacity for 18 in-patients. At the time of our inspection up to 12 people were using the service as in patients. The community team provide services for people in their own homes and at an outreach clinic in Deal. There is a Rapid Response Service that provides personal care to people in the community and is available on the same day it is needed. Support groups for carers are available and there is a 24 hour advice. The service was providing services to 349 people in the community and in the hospice at the time of the inspection.
A registered manager was in post. A registered manager is a person who has registered with the Care Quality Commission to manage the service. Like registered providers, they are ‘registered persons’. Registered persons have legal responsibility for meeting the requirements in the Health and Social Care Act 2008 and associated Regulations about how the service is run.
Safe systems were in place for the ordering and administration of medicines. However, medicines which had passed their expiry date were stored with current medicines. This was not safe practice. Guidance was not in place for the use of prescribed creams nor if people were able to self-administer their medicines.
The service had not followed its policy in providing staff with regular supervision which offers staff support and learning to help with their development. Opportunities for staff to reflect on their practice and to learn what they were doing well and what they could improve in supporting people, had not been formalised throughout the service.
There had been a lack of consistency in leadership at the service and not all staff had not been protected from bullying and harassment. The staff team had not felt valued, listened to or supported for a number of years. Even though some staff morale was low, all staff continued to give a high standard of care for people who used the service. The new management team was aware of staff’s feelings and that it took a long time to change the culture of a service. They had put in a range of initiatives to engage with staff.
Staff understood how to safeguard adults and children and this was central to the running of the service. Staff received training in safeguarding and demonstrated they knew how to recognise and report potential abuse.
Potential risks to people had been assessed and action and guidance was in place which identified how they could be minimised. Environmental and health and safety checks were carried out to ensure that the environment was safe and that equipment was in good working order. There were systems in place to review accidents and incidents and to identify any patterns or trends. The service was clean and infection control guidance was followed to help minimise the spread of any infection if it should occur.
Checks were carried out on all staff at the service, to ensure that they were fit and suitable for their role. Staffing levels were flexible so staff could support people in the part of the service where there was the greatest need.
New staff received a comprehensive induction and were provided with the training necessary to their roles. This included specialist training in bereavement and end of life care to make sure that they had the right knowledge and skills to meet people’s needs effectively.
People’s health, medical, nutritional and hydration needs were assessed and closely monitored. Their changing needs were effectively communicated within the multi-disciplinary team and with other professionals so that everyone involved in their care was knowledgeable about their needs.
The Mental Capacity Act 2005 (MCA) provides a legal framework for making particular decisions on behalf of people who may lack the mental capacity to do so for themselves. The Act requires that as far as possible people make their own decisions and are helped to do so when needed. When they lack mental capacity to take particular decisions, any made on their behalf must be in their best interests and as least restrictive as possible. People can only be deprived of their liberty to receive care and treatment when this is in their best interests and legally authorised under the MCA. The application procedures for this in care homes, hospitals and hospices are called the Deprivation of Liberty Safeguards (DoLS). The service understood their responsibilities under the Mental Capacity Act 2005 and Deprivation of Liberty Safeguards (DoLS).
The service provided a relaxed, comfortable and clean environment. There were a range of areas available for people and their visitors to sit and a large area for day patients to undertake activities.
Staff were kind, compassionate and caring and spent time listening and talking to people in a way that they understood. Supporting people’s family members was key to the service and they received support before and after the death of their loved one through counselling, bereavement counselling and carers groups. People also benefitted from spiritual support and complimentary therapies being available.
People’s individual wishes with regards to their care were recorded and the staff team advocated for people when necessary to ensure these were met. People and family members were involved in planning their care and treatment and care plans were personalised.
People’s needs were thoroughly assessed before and at the time of being admitted to the service. The service could immediately respond to people’s nursing and care needs to ensure they died in their preferred place.
People were supported to maintain their mobility and to manage their symptoms through exercise and breathlessness management. The day hospice offered a range of activities and information sessions and promoted conversation in a comfortable environment.
The service had built links with the local community through offering services and fundraising events. People were able to make their views known and knew how to make a complaint or raise a concern. When complaints had been received, these had been investigated so that lessons were learned to improve the service.
The service had a clear management structure and lines of accountability. There was a programme of clinical governance and audit to identify and take action to address any shortfalls. Research and education was undertaken to help improve the care offered for people at the end of their lives.
We found two breaches of the Health and Social Care Act 2008 (Regulated activities 2014). You can see what action we told the provider to take at the back of the full version of the report.