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NICE confirms first-line SGLT-2 prescribing in final type 2 diabetes guidance

NICE confirms first-line SGLT-2 prescribing in final type 2 diabetes guidance
OlenaMykhaylova via Getty Images

Most people with type 2 diabetes should be offered SGLT-2 inhibitors much earlier in their treatment, final NICE guidance has recommended.

In guidance published today, NICE recommended that most people with type 2 diabetes should now be offered metformin along with an SGLT-2 inhibitor from the start of treatment.

The guidance also expands access to GLP-1 receptor agonists – such as semaglutide, dulaglutide and liraglutide – and tirzepatide. Semaglutide will now be recommended for people with type 2 diabetes who also have cardiovascular disease caused by blocked arteries.

GLP-1 receptor agonists and tirzepatide will be recommended for people who were diagnosed before age 40, or who are living with obesity. Around 810,000 more people could benefit from these medicines, NICE said.  

But NICE also added that this is not a ‘one-size-fits-all approach’ as people will ‘work with their healthcare professional to decide the best treatment for them’, based on their own circumstances and preferences (see box for the key recommendations).

GP leaders have told Pulse that GP practices will need ‘appropriate support’ to implement the recommendations ‘consistently and safely’, following concerns that the new guidelines could cause a significant rise in prescribing and monitoring workload.

Analysis by NICE suggests using SGLT-2 medicines earlier in the treatment pathway, and the introduction of GLP-1 receptor agonists and tirzepatide for some people, could prevent around 17,000 deaths over a three-year period across the UK by reducing the risk of heart attacks, strokes and kidney problems.

The decision, which had been anticipated in draft guidance and represents a major ‘shake-up’ to current practice, was based on a ‘significant body of evidence’ that diabetes management should consider cardiovascular and renal protection not just HbA1c targets.

Publishing the final guidance, NICE said that the NHS is set to save millions of pounds because one of the most commonly prescribed SGLT-2 medicines, dapagliflozin, is now available as a clinically equivalent generic version. 

The estimated cumulative savings in total for 2025/26 and 2026/27 from generic dapagliflozin would be £560m and this money could be reinvested in other areas of diabetes care, such as education programmes and community support services or other parts of the NHS, according to NICE.

The guidance also asked healthcare professionals to work with each person to ‘find the right treatment for them’, based on their other health conditions, the medicines they already take, and what matters most to them.

Healthcare professionals will check each person’s heart and kidney health before starting treatment, and new medicines should be introduced one at a time to make sure they are well tolerated, NICE added.

A new prescribing guide published alongside this guidance will help healthcare professionals ‘have these conversations and prescribe safely’. 

NICE interim director of the centre for guidelines Eric Power said: ‘This is a landmark moment for diabetes care. Our independent committee conducted a rigorous review of the evidence and concluded that by offering certain medicines earlier, we can prevent thousands of heart attacks, strokes and cases of kidney failure — keeping people healthier for longer while reducing pressure on NHS services.

‘But we also found something troubling: these life-saving medicines are currently under-prescribed to women, older people and Black patients.

‘Tackling health inequalities is at the heart of what NICE does, and these recommendations will help ensure everyone with type 2 diabetes gets fair access to the best available treatments.

‘By recommending generic dapagliflozin where clinically appropriate, we’re also freeing up hundreds of millions of pounds that can be reinvested elsewhere in NHS care. This is evidence-based guidance that saves lives and delivers value for the taxpayer.’

NICE guideline committee chair Dr Waqaar Shah said: ‘As a GP, I see first-hand how type 2 diabetes affects my patients’ lives.

‘Right now, only around 1 in 5 people with type 2 diabetes and heart disease are receiving the medicines that could protect them from heart attacks, strokes and kidney failure.

‘By recommending these treatments earlier, we have a real opportunity to prevent thousands of serious complications. 

‘But every person is different, and the decision about which medicine is right should always be made together with the patient, taking into account their individual circumstances, preferences and what matters most to them.’

RCGP chair Professor Victoria Tzortziou Brown said that supporting ‘early, effective treatment’ in primary care has the potential to improve outcomes for patients, but will also require time, resources, and system support for general practice teams to be implemented safely.

She said: ‘With the right support, this approach can help prevent avoidable complications and contribute to a more sustainable NHS over the longer term.

‘These changes to the type 2 diabetes treatment pathway are based on the latest evidence and could prove to be a significant step forward in improving care for people living with this common condition. 

‘For eligible patients, earlier access to medicines shown to reduce the risk of heart and kidney complications, has the potential to save lives and reduce the risk of serious, long-term complications.  

‘GPs and our teams are central to delivering high-quality diabetes care. We support patients from diagnosis onwards, helping them manage their condition alongside other health needs and tailoring treatment to what works best for them.

‘Guidance that recognises individual circumstances and supports shared decision-making and appropriate prescribing fits closely with how care is delivered in general practice.’  

Professor Azeem Majeed, head of the department of primary care and public health at Imperial College London, told Pulse that for most GPs, this represents ‘an evolution rather than a revolution in care’, as many are already prescribing SGLT-2 inhibitors widely.

However, the guidance formalises their earlier use, strengthens the cardiovascular–renal focus, and embeds equity and personalised care ‘more firmly’ into routine diabetes management, he said.

He added: ‘Starting metformin alongside an SGLT-2 inhibitor for most people at diagnosis marks an important shift away from a purely glucose-centric model towards one that prioritises long-term cardiovascular and renal protection.

‘The emphasis on shared decision-making, use of slow-release metformin to improve tolerability, and tailored treatment for younger people, those living with obesity, or those with established cardiovascular or kidney disease are also very positive developments.

‘In primary care, this will mean earlier use of combination therapy, more proactive assessment of cardiovascular and renal risk, and careful discussions with patients about the benefits and potential side effects of newer medicines. General practices will need appropriate support to implement these changes consistently and safely.’

Researchers have recently argued that the recommendation could save many thousands of lives a year.

Key recommendations

1.13 People with type 2 diabetes and no relevant comorbidities

1.13.1 For adults with type 2 diabetes and no relevant comorbidity, offer:
• modified-release metformin, and
• an SGLT-2 inhibitor. 

1.13.2 If metformin is contraindicated or not tolerated, offer monotherapy with an SGLT-2 inhibitor. 

1.14 People with heart failure (with any ejection fraction, unless specified)

1.14.1 For adults with type 2 diabetes and heart failure offer:
• modified-release metformin, and
• an SGLT-2 inhibitor.

1.14.2 If metformin is contraindicated or not tolerated, offer monotherapy with an SGLT-2 inhibitor. 

1.15 People with atherosclerotic cardiovascular disease

1.15.1 For adults with type 2 diabetes and atherosclerotic cardiovascular
disease, offer:
• modified-release metformin, and
• an SGLT-2 inhibitor, and
• subcutaneous semaglutide (Ozempic), up to 1 mg once a week, for its cardiovascular, renal and glycaemic benefits. 

1.15.2 If metformin is contraindicated or not tolerated, offer:
• an SGLT-2 inhibitor, and subcutaneous semaglutide (Ozempic), up to 1 mg once a week,
for its cardiovascular, renal and glycaemic benefits.

1.16 People with early onset type 2 diabetes

1.16.1 For adults with early onset type 2 diabetes, offer modified-release metformin and an SGLT-2 inhibitor, and consider adding either:
• a GLP-1 receptor agonist for its cardiovascular, renal and glycaemic benefits or
• tirzepatide for its glycaemic benefits. 

1.16.2 If metformin is contraindicated or not tolerated, offer an SGLT-2 inhibitor and consider adding either:
• a GLP-1 receptor agonist for its cardiovascular, renal and glycaemic benefits or
• tirzepatide for its glycaemic benefits. 

1.17 People living with obesity

1.17.1 For adults with type 2 diabetes who are living with obesity, offer:
• modified-release metformin and
• an SGLT-2 inhibitor.

1.17.2 If metformin is contraindicated or not tolerated, offer monotherapy with an SGLT-2 inhibitor. 

1.18 People with chronic kidney disease

1.18.1 For adults with type 2 diabetes and an estimated glomerular filtration rate (eGFR) above 30 ml/min/1.73 m2:
• Offer modified-release metformin and an SGLT-2 inhibitor. If metformin is contraindicated or not tolerated, offer
monotherapy with an SGLT-2 inhibitor. 

1.18.2 For adults with type 2 diabetes and an eGFR of 20 ml/min/1.73 m2 and up to 30 ml/min/1.73 m2, offer:
• either dapagliflozin or empagliflozin and
• a DPP-4 inhibitor. 

1.18.3 For adults with type 2 diabetes and an eGFR below 20 ml/min/1.73 m2, consider a DPP-4 inhibitor. 

1.18.4 If a DPP-4 inhibitor is contraindicated, not tolerated or not effective,
consider:
• pioglitazone or
• an insulin-based treatment. 

1.19 People with frailty

1.19.1 For adults with type 2 diabetes and frailty:
• Offer modified-release metformin.
• Only offer an SGLT2 inhibitor if the person’s level of frailty does not place them at risk of adverse events from such a medicine (for example, volume depletion or hypotension). 

1.19.2 If metformin is contraindicated or not tolerated, assess whether their level of frailty places the person at risk of adverse events from SGLT-2 inhibitors:
• if it does not, consider monotherapy with a SGLT-2 inhibitor
• if it does, consider monotherapy with a DPP-4 inhibitor. 

Source: NICE

 


			

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READERS' COMMENTS [3]

Please note, only GPs are permitted to add comments to articles

Edoardo Cervoni 18 February, 2026 2:55 pm

The final NICE guidance on type 2 diabetes is a welcome, evidence-driven revolution. It abandons the outdated glucose-only focus and prioritises cardiorenal protection from diagnosis onward, recommending metformin + SGLT2 inhibitor for most patients, plus earlier access to GLP-1RAs and tirzepatide for those with early-onset disease or obesity.
Yet the onus is on ICBs. As I have repeatedly argued in prior comments, calling for broader, earlier use of potent agents like tirzepatide in obesity-linked type 2 diabetes, too many ICBs remain frustratingly inert, delaying high-impact changes despite overwhelming evidence. They persist in siloed thinking, treating diabetes, cardiovascular disease, chronic kidney disease, osteoarthritis, and obesity as disconnected rather than a unified systemic disorder (not such a surprise as we are a “corpus”), thereby squandering the cross-border, pleiotropic benefits these therapies deliver across metabolic, cardiac, renal, and musculoskeletal domains. GPs are prepared. ICBs must end the procrastination, deliver urgent training, resources, and support, and implement promptly. Anything less risks patient harm, inequity, and NHS waste.

Tj Motown 18 February, 2026 9:16 pm

Metformin 1£, Semaglutide £78, that is the only thing they see my friend

David Banner 20 February, 2026 11:09 am

There is now a perverse incentive for obese patients to be diagnosed with T2diabetes.

Diabetic? Congratulations, the smorgasbord of magic weight loss drugs is now all yours on FREE prescription for life!!

Non-diabetic? Tough luck, tubby, re-mortgage your house and pay through the nose, then put all the weight back on when the money runs out.

“Doctor, my HbA1c is 46. What fattening sugary weight-gaining foods would you recommend so I can drag it up to 48 and receive free Ozempic please?”