Children with non-oncological life-limiting conditions deserve the same high-quality palliative care as children with incurable cancer

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Children with non-oncological life-limiting conditions deserve the same high-quality palliative care as children with incurable cancer Results of a retrospective case-notes audit Archana Soman Consultant Paediatrician

Aims of the audit To determine if all children with LLCs have their palliative care needs assessed, planned and delivered - as per standards set out by Together for Short Lives (TfSL). To aid the development of a local guideline and framework (care pathway) to ensure the above happens.

TfSL Core Care pathway for Children with Lifelimiting and Life-threatening Conditions Stage 1 : Diagnosis and/ or recognition Sharing significant news diagnosis and prognosis Liaison with and/ or transferring to community services Stage 2 : Ongoing care Multidisciplinary assessment of needs Child and family care plan/s Stage 3 : End of life End of Life plan Bereavement support

Methods Inclusion Criteria Children who had died as a direct result of a condition/s that is clearly life-limiting, 2011-2015 Exclusion criteria Sudden/ unexpected deaths even in children with a LLC diagnosis Children whose care was mainly led by another hospital Deaths on the neonatal unit, or within a month of diagnosis of LLC Data collection Case notes, electronic databases, M&M minutes

Distribution of main diagnoses Total: 20 Oncology: 8 Severe neurodisability: 10 Complex congenital heart disease: 1 Cystic Fibrosis: 1 CHD Severe neurodisability CF Cancer oncology severe ND CCHD CF

Age at death Sex <1 11 to 1[VALUE] 1 to 4 Female Male 5 to 10 <1 1 to 4 5 to 10 11 to 16 Male Female

Time from confirmation of LLC to death >10 years < 1mo 2 mo 2 10 years 3 11mo 12 23 mo 1 mo 2 mo 3 to 11 mo 12-23 mo 2 to 10 years > 10 years

Audit Standards and results 1. There should be an honest discussion with the parent/s of all children with life-limiting conditions when such is identified, in an appropriate setting, and this should be documented in the hospital notes: 100% Documented in 19/20: 95% But discussions about the life-limiting nature hardly documented Oncology: no more curative options

Audit standards and results 2. An initial MDT meeting should be held to assess needs and plan delivery of care: 100% Result: 17/20: 85% (Onc: 100%, Non-onc: 75%) 3. The MDT should identify a key worker and a lead clinician: 100% Result: Both clearly identified in 9/ 20: 45% (Onc: 87.5%, non-onc: 20%, p = 0.01 ) One or the other in 9 Neither in 2

Audit standards and results 4. The child s palliative care needs including current and anticipated symptoms) should be assessed by the MDT and documented Result: 12/20 60% (Onc: 100%, non-onc: 33.3%, p = 0.015 ) 5. Symptom management plans (including roles of clinicians and lines of communication) made Result: 13/20 66.7% (onc: 100%, non-onc: 41.7%, p = 0.0225)

Audit Standards and results 6. Family structure and psychosocial and cultural needs should be assessed and documented Result: 15/20 75% (Onc: 100%, non-onc: 58.3%)

Audit Standards and results 7. End of life care plans should be discussed and documented: a) DNACPR: 13/20 66.7% (including 3 that did not engage) (Onc: 100%, non-onc: 41.7%) b) Place of EoL care/ death: 11/20 55% (Onc: 100%, non-onc: 25%) c) Other wishes and desires: 9/20 45% (Onc: 75%, non-onc: 25%) d) All 3: 8/20 40% (Onc: 75%, non-onc: 16.7%, p = 0.0325 )

Comparison cancer vs non-cancer 120% 100% all onc non-onc p = 0.01 p = 0.015 p = 0.0225 p = 0.0325 80% 60% 40% 20% 0% standard 3 standard 4 standard 5 standard 7

Other observations (1) 80% Place of death 60% 40% 20% 0% all patients cancer non-cancer home hospice hospital

Other observations (2) Intensive care: 4 (0 oncology) 1 for 3 weeks 1 for 32 days Resuscitation: 4 (0 oncology) 2 prolonged full CPR (one had SUDIC protocol) 2 partial (short of cardiac massage and drugs)

Summary of findings Poor documentation especially of communication of prognosis and lead professional/ key worker. MDT assessment and planning incl. end-of-life care planning grossly inadequate especially in nononcological LLC Clear disparities between oncological and nononcological LLC

Oncology versus non-oncology Often clear demarcation between potentially curable and non-curable Futility more acceptable a concept given the social and cultural connotations of the C word? Clear regional palliative care pathway for children with oncological diagnoses Limited research suggests that this is reflected in families perception of services (Price et al, 2012)

Recommendations/actions Care pathway and guideline for MDT management of children with LLCs - written Database of CYP with life-limiting conditions LLC forum and care coordinator Named paediatrician/s for palliative care Rolling (annual/biannual) MDTs for all children with LLCs Education programme : several completed already County-wide clinicians group Commissioners and acute Trust beginning to engage

References MCNAMARA, K. 2013. Standards Framework for Children s Palliative Care, 2/e. Bristol: Together for Short Lives. A framework for the development of Integrated Multi-Agency Care Pathways for children with life-threatening and life-limiting conditions, ACT, 2004 CRAIG, F., et al. 2007. IMPaCCT: Standards for paediatric palliative care in Europe. European Journal of Palliative Care, 14(3), 109-114. Rushton, C.H., 2005. A Framework for Integrated Pediatric Palliative Care Being with Dying. Journal of Pediatric Nursing, 20(5), 311-325 Better Care: Better Lives. 2008. Improving outcomes and experiences for children, young people and their families living with lifelimiting and life-threatening conditions. Department of Health. NHS STANDARD CONTRACT FOR PAEDIATRIC MEDICINE: PALLIATIVE CARE 2013/14. NHS Commissioning Board (now NHS England) Child & Young Person s Advance Care Plan Policy - April 2011 West Midlands Paediatric Palliative Care Network PRICE, J. et al., 2012. Comparing the needs of families of children dying from malignant and non-malignant disease: an in-depth qualitative study. BMJ Supportive & Palliative Care, 2, 127-132. HAIN, R., DEVINS, M., HASTINGS, R. & NOYES, J. 2013. Paediatric palliative care: development and pilot study of a 'Directory' of lifelimiting conditions. BMC Palliat Care, 12, 43. FRASER, L. K., et al., 2012. Rising national prevalence of life-limiting conditions in children in England. Pediatrics, 129, e923-9.