- Child with a new life-threatening or life-limiting illness diagnosis - Difficult pain management or other symptoms - Three or more urgent hospitalisations for serious clinical crises over a period of 6 months - Prolonged hospitalisation (over 3 weeks) without evidence of clinical improvement - Prolonged admission to intensive care (over 1 week) without evidence of clinical improvement - Fitting of invasive medical devices (e.g., tracheostomy) - Child and/or family with complex psychosocial needs, limited social support or both - Child assisted by more than three specialised services, with potential interdisciplinary communication difficulties - Child with difficult and complex management of care handover between the hospital setting and the home - Child and/or family obliged to make difficult and significant decisions - Difficulties in achieving consensus between child, family and medical team on treatment and illness management goals (e.g., resuscitation actions, use of parenteral nutrition/IV hydration or continuation of chemotherapy in the terminal stages) - Child and/or family experiencing difficulty making decisions concerning resuscitation actions - Ethical debates about palliative care expressed by the child, family or medical team - Needs for continuous medical support or medical devices or frequent laboratory services by home care services if these facilities are not readily available within the primary care territorial resources - The prospect of complex outcomes in case of survival, such as a serious toxicity condition from long-term therapy - The prospect of complex needs during the mourning period |