Question to the Department of Health and Social Care:

To ask the Secretary of State for Health and Social Care, what steps her Department is taking to reduce waiting times for (a) diagnosis, (b) treatment and (c) care for people living with pulmonary fibrosis; and if she will make an assessment of the impact of waiting times on patient care.

The Department funds research through the National Institute for Health and Care Research (NIHR). The NIHR welcomes funding applications for research into any aspect of human health, including pulmonary fibrosis, although it is not usual practice to ring-fence funds for particular topics or conditions. Applications are subject to peer review and judged in open competition, with awards being made on the basis of the importance of the topic to patients and health and care services, value for money, and scientific quality.

In order to increase awareness of pulmonary fibrosis, NHS England has established 13 Respiratory Clinical Networks across the country. These have been vital in providing clinical leadership for respiratory services and supporting services in primary care, including restoring spirometry, which is one of the tests used to diagnose pulmonary fibrosis.

Furthermore, community diagnostic centres are also being established to deliver additional, digitally connected, diagnostic capacity in England, providing patients with co-ordinated diagnostic tests in the community, on a range of clinical pathways, including pulmonary fibrosis. With the aim of raising the standard of care that people with this idiopathic pulmonary fibrosis receive, the National Institute for Health and Care Excellence also publishes quality standards that define best practice, and areas in need of improvement.