British Association of Perinatal Medicine

[1] Combined with many others problems like paediatricians who were single handed, underfunded and distributed across large areas of the population, with the result that perinatal mortality in the UK was five times higher than it need have been and that as many newborn infants died in the first three days of life as in the whole of the remainder of childhood.

[1] When The Lancet article was published, it aroused the interest of the government, and the Department of Health contacted the British Paediatric Association to investigate the matter.

[1] In 1975 June Lloyd acting for the government,[6] wrote to Dunn to ask him for help in finding all the paediatricians who were specifically working, i.e. caring for newborn babies in the UK[6] After Dunn wrote to all the medical universities and maternity hospitals in the United Kingdom, to all paediatricians who were spending more than 60% of their time with newborn children and collected 20 people in total, he decided to try and advance an idea to provide help, where ever he could.

Dunn approached several colleagues who were specialists in obstetrics, who were initially enthused by the idea, but was subsequently dissuaded by the Royal College of Obstetricians and Gynaecologists.

In conversation with the BPA, they replied that neonatology was likely to remain in the domain of general paediatrician's and therefore perinatal or neonatal paediatrics would not be recognised as a sub-speciality.

[7] For much of the 1980s, neither the BPA nor the Royal College of Obstetricians and Gynaecologists felt that a country-wide, coordinated service for specialist neonatology and high risk obstetrics were of much use.

In 1982, the chairman of the Royal College of Obstetricians and Gynaecologists working party, Charlie Whitfield suggested that the group should be called the British Association of Perinatal Medicine.

The most important recommendations from BAPM's perspective from the report, was that in future all infants should be recognised at birth as a patient, as well as defining a data set for the baby as well as the mother, in part to move the NHS into the digital age.