William E Rosa, Jacopo D’Andria Ursoleo, Stephen R. Connor, Oladayo Afolabi, Shrikant Atreya, Lindsay Farrant, Adrian E Go, Richard Harding, Matthew Maddocks, Scott Murray, David Musyoki, Roselyne A Omolo, Katherine Pettus, Kateřina Rusinová, Grant M Smith, Peter Tanuseputro, Frederic Ivan L Ting, William C W Wong, Matthew Allsop, Afsan Bhadelia, Rosa Buitrago, Juan Esteban Correa‐Morales, Edward Christopher Dee, Julia D. Downing, Libby Sallnow, Donald R. Sullivan, Eric L. Krakauer
Annually, more than 70 million people worldwide have health-related suffering amenable to palliative care. However, this need remains unmet for more than 85% of cases, predominantly in low-income and middle-income countries. Because most people with serious illness live in community settings and wish to remain there through the end of life, integration of palliative care into primary health care (PHC) is crucial. Primary care teams are well positioned to deliver generalist palliative care but often face insufficient training, weak PHC infrastructure, and poor policy support, among other barriers. In this Viewpoint, we provide an evidence-based rationale for improved integration of palliative care into PHC and share best practice exemplars that show feasible pathways to strengthen integration through training, mentorship, service development, international collaboration, and system adaptation. Informed by lessons learned and recommendations, our international and interprofessional team emphasises that successful integration of palliative care into PHC will require evidence-based advocacy, community partnerships, context-specific implementation, sustainable resourcing, and coordination between generalist and specialist teams to strengthen community-based, person-centred services across the life course.