Postural Tachycardia Syndrome: Training

(asked on 12th November 2025) - View Source

Question to the Department of Health and Social Care:

To ask the Secretary of State for Health and Social Care, what recent assessment he has made of the adequacy of the level of training provided to General Practitioners on (a) the treatment and (b) symptoms of Postural Tachycardia Syndrome .


Answered by
Ashley Dalton Portrait
Ashley Dalton
Parliamentary Under-Secretary (Department of Health and Social Care)
This question was answered on 21st November 2025

The Royal College of General Practitioners (RCGP) provides education on postural tachycardia syndrome (PoTS) through its Syncope Toolkit, which includes an e-learning module, a podcast and a webinar. These resources cover diagnosis and management and include patient perspectives to improve clinical understanding. The toolkit is available to GPs via the RCGP e-learning platform.

As part of its Clinical Knowledge Summary (CKS) resources, the National Institute for Health and Care Excellence (NICE) has also published detailed guidance on the assessment and management of syncope and blackouts, which includes advice on PoTS. The purpose of CKSs is to provide primary care practitioners with quick, accessible, and evidence-based guidance on best practice for commonly occurring conditions.

The guidance is available at the following link:

https://cks.nice.org.uk/topics/blackouts-syncope/diagnosis/assessment/

PoTS is diagnosed by a combination of GPs and specialist clinicians. GPs can diagnose PoTS in many cases but, if they are unsure of symptoms or if symptoms are complex, they will refer patients to specialists for diagnosis. The RCGP’s Syncope Toolkit provides diagnostic information to GPs, including the use of the active stand test, to rule out other conditions and potentially diagnose PoTS more quickly.

Where patients are referred to secondary care for diagnosis, we are investing in additional capacity to deliver appointments to help bring waiting lists and times down. The Elective Reform Plan, published in January 2025, sets out the specific productivity and reform efforts needed to return to the constitutional standard, that 92% of patients to wait no longer than 18 weeks from Referral to Treatment, by March 2029.

By expanding community-based services for routine monitoring and follow up, employing artificial intelligence for productivity and investing in digital tools and data, as outlined in the 10-Year Health Plan, we can ensure that consultants’ time is reserved for complex cases of PoTS, including specialist diagnostic assessments.

While the Department recognises the significant challenges of PoTS diagnosis, responsibility for specific clinical pathways and specialist training rests with local NHS bodies.

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