AAT Deficiency: Health Services
The question
To ask the Secretary of State for Health and Social Care, what steps his Department is taking to support patients with Alpha-1 Antitrypsin Deficiency (A1AT).
Answered by Mrs Sharon Hodgson
Alpha-1 Antitrypsin Deficiency (A1AT) is a rare inherited condition which can affect the lungs and liver. The Government is committed to improving the lives of those living with rare diseases, including work to improve diagnosis and the use of genomics in rare disease care. NHS England’s National Genomic Test Directory includes testing for A1AT, where clinically appropriate.
The Government also supports patients with A1AT through wider action to improve care for people living with rare conditions and long-term respiratory disease.
NHS England’s respiratory disease programme is focused on earlier and more accurate diagnosis, reducing inequalities, and improving treatment and support. This includes support for diagnostic testing such as spirometry, expansion of pulmonary rehabilitation, and improvements in medicines optimisation and personalised care. NHS England has also published commissioning standards for spirometry, and community diagnostic centres are providing respiratory diagnostic tests to improve access closer to home.
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