What I find most astonishing is the lack of research going on at the Tavistock.
I was an HIV nurse specialist in the early 1990s and, as a new disease, research was fundamental to our care and treatment. Every week something new emerged from the whirlwind of trials. Then when I moved into cancer care in the late 90s, there was again so much research going on, every aspect of patients “cancer journeys” was analysed, findings implemented, practice adapted accordingly. National cancer care standards and practice are based on clinical research. Most oncology patients are eligible for - and informed about - current trials, be they new treatment trials or quality of life/end of life studies.
As the only GIDS in the UK, why was there so little research and audit?