People have the right to be involved in discussions and make informed decisions about their care, as described in making decisions about your care.
Making decisions using NICE guidelines explains how we use words to show the strength (or certainty) of our recommendations, and has information about prescribing medicines (including off-label use), professional guidelines, standards and laws (including on consent and mental capacity), and safeguarding.
1.4 Diagnosing and managing hypertension
The recommendations on diagnosing and managing hypertension have been removed. For recommendations on hypertension in people with type 2 diabetes, see the NICE guideline on hypertension in adults. Diagnosis, treatment and monitoring of hypertension is broadly the same for people with type 2 diabetes as for other people. When a different approach is needed for people with type 2 diabetes, this is specified in the hypertension guideline.
1.7 Drug treatment
Recommendations in this section that cover dipeptidyl peptidase‑4 (DPP‑4) inhibitors, glucagon‑like peptide‑1 (GLP‑1) mimetics, sulfonylureas and sodium–glucose cotransporter‑2 (SGLT2) inhibitors refer to each of these groups of drugs at class level unless otherwise stated.
NICE technology appraisals for SGLT2 inhibitors recommend the use of these medicines only in specific populations and in certain circumstances. The 2022 update of this guideline looked at the clinical- and cost-effectiveness evidence for SGLT2 inhibitors in people with cardiovascular disease or at high risk of developing cardiovascular disease. The guideline recommends SGLT2 inhibitors in a wider population than the technology appraisals that were published before February 2022.
Rescue therapy at any phase of treatment
1.7.2
If an adult with type 2 diabetes is symptomatically hyperglycaemic, consider insulin (see the section on insulin-based treatments) or a sulfonylurea, and review treatment when blood glucose control has been achieved. [2015]
First-line drug treatment
Also see the visual summary on first-line drug treatment for an overview of the recommendations and additional information to support medicines choice.
For adults with type 2 diabetes and chronic kidney disease, follow recommendations on SGLT2 inhibitors in the section on chronic kidney disease in this guideline.
1.7.3
Offer standard-release metformin as first-line drug treatment to adults with type 2 diabetes. [2015]
1.7.4
1.7.5
Based on the cardiovascular risk assessment for the person with type 2 diabetes:
1.7.6
When starting an adult with type 2 diabetes on dual therapy with metformin and an SGLT2 inhibitor as first-line therapy, introduce the drugs sequentially, starting with metformin and checking tolerability. Start the SGLT2 inhibitor as soon as metformin tolerability is confirmed. [2022]
1.7.7
Gradually increase the dose of standard-release metformin over several weeks to minimise the risk of gastrointestinal side effects in adults with type 2 diabetes. [2015]
1.7.8
If an adult with type 2 diabetes experiences gastrointestinal side effects with standard‑release metformin, consider a trial of modified‑release metformin. [2015]
1.7.9
For first-line drug treatment in adults with type 2 diabetes, if metformin is contraindicated or not tolerated:
1.7.10
For first-line drug treatment in adults with type 2 diabetes, if metformin is contraindicated or not tolerated and if they are not in either of the groups in recommendation 1.7.9, consider:
1.7.11
Before starting an SGLT2 inhibitor, check whether the person may be at increased risk of diabetic ketoacidosis (DKA), for example if:
1.7.12
Address modifiable risks for DKA before starting an SGLT2 inhibitor. For example, for people who are following a very low carbohydrate or ketogenic diet, they may need to delay treatment until they have changed their diet. [2022]
1.7.13
Advise adults with type 2 diabetes who are taking an SGLT2 inhibitor about the need to minimise their risk of DKA by not starting a very low carbohydrate or ketogenic diet without discussing it with their healthcare professional, because they may need to suspend SGLT2 inhibitor treatment. [2022]
Reviewing drug treatments
1.7.14
When reviewing or considering changing treatments for adults with type 2 diabetes, think about and discuss the following with the person:
1.7.15
For adults with type 2 diabetes who start taking an SGLT2 inhibitor before they are 40 because they have an elevated lifetime risk of cardiovascular disease, do not stop the SGLT2 inhibitor when they turn 40 even if their QRISK2 score is below 10%. Only stop the SGLT2 inhibitor if the person's circumstances have changed and the SGLT2 inhibitor is no longer appropriate. [2022]
Adding an SGLT2 inhibitor at any stage after first-line treatment has been started
1.7.16
For adults with type 2 diabetes at any stage after they have started first-line treatment:
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If they have or develop chronic heart failure or established atherosclerotic cardiovascular disease, offer an SGLT2 inhibitor with proven cardiovascular benefit in addition to current treatment or replace an existing drug with the SGLT2 inhibitor.
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If they are or become at high risk of developing cardiovascular disease, consider adding an SGLT2 inhibitor with proven cardiovascular benefit to current treatment or replacing an existing drug with the SGLT2 inhibitor.
Take into account the person's current treatment regimen and preferences and make a shared decision about switching treatments or adding an SGLT2 inhibitor, as appropriate (also see recommendations 1.7.12 and 1.7.13 on starting an SGLT2 inhibitor). [2022]
In February 2022, using ertugliflozin to reduce cardiovascular risk when blood glucose is well controlled was off-label. See NICE's information on prescribing medicines.
Treatment options if further interventions are needed
Also see our visual summary on treatment options if further interventions are needed for an overview of the recommendations and additional information to support medicines choice.
1.7.17
Introduce drugs used in combination therapy in a stepwise manner, checking for tolerability and effectiveness of each drug. [2015]
1.7.18
For adults with type 2 diabetes, if monotherapy has not continued to control HbA1c to below the person's individually agreed threshold for further intervention, consider adding:
1.7.19
For adults with type 2 diabetes, if dual therapy with metformin and another oral drug has not continued to control HbA1c to below the person's individually agreed threshold for further intervention consider either:
1.7.20
In adults with type 2 diabetes, if metformin is contraindicated or not tolerated and dual therapy with 2 oral drugs has not continued to control HbA1c to below the person's individually agreed threshold for intervention, consider insulin-based treatment (see the section on insulin-based treatments). [2015, amended 2022]
1.7.21
If triple therapy with metformin and 2 other oral drugs is not effective, not tolerated or contraindicated, consider triple therapy by switching one drug for a GLP‑1 mimetic for adults with type 2 diabetes who:
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have a body mass index (BMI) of 35 kg/m2 or higher (adjust accordingly for people from Black, Asian and other minority ethnic groups) and specific psychological or other medical problems associated with obesity or
-
have a BMI lower than 35 kg/m2 and:
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for whom insulin therapy would have significant occupational implications or
-
weight loss would benefit other significant obesity-related comorbidities. [2015, amended 2022]
1.7.22
Only continue GLP‑1 mimetic therapy if the adult with type 2 diabetes has had a beneficial metabolic response (a reduction of at least 11 mmol/mol [1.0%] in HbA1c and weight loss of at least 3% of initial body weight in 6 months). [2015]
1.7.23
For adults with type 2 diabetes, only offer combination therapy with a GLP‑1 mimetic and insulin along with specialist care advice and ongoing support from a consultant-led multidisciplinary team. [2015]
Insulin-based treatments
1.7.24
For adults with type 2 diabetes starting insulin therapy, provide a structured programme using active insulin dose titration that encompasses:
-
injection technique, including rotating injection sites and avoiding repeated injections at the same point within sites
-
continuing telephone support
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self-monitoring
-
dose titration to target levels
-
dietary advice
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the DVLA's Assessing fitness to drive: a guide for medical professionals
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managing hypoglycaemia
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managing acute changes in plasma glucose control
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support from an appropriately trained and experienced healthcare professional. [2015]
1.7.25
For adults with type 2 diabetes starting insulin therapy, continue to offer metformin for people without contraindications or intolerance. Review the continued need for other blood glucose lowering therapies. [2015]
1.7.26
Start insulin therapy for adults with type 2 diabetes from a choice of the following insulin types and regimens:
-
Offer neutral protamine Hagedorn (NPH) insulin injected once or twice daily according to need.
-
Consider starting both NPH and short‑acting insulin (particularly if the person's HbA1c is 75 mmol/mol [9.0%] or higher), administered either:
-
Consider, as an alternative to NPH insulin, using insulin detemir or insulin glargine if:
-
the person needs help from a carer or healthcare professional to inject insulin, and use of insulin detemir or insulin glargine would reduce the frequency of injections from twice to once daily or
-
the person's lifestyle is restricted by recurrent symptomatic hypoglycaemic episodes or
-
the person would otherwise need twice‑daily NPH insulin injections in combination with oral glucose‑lowering drugs.
-
Consider pre-mixed (biphasic) preparations that include short‑acting insulin analogues, rather than pre‑mixed (biphasic) preparations that include short‑acting human insulin preparations, if:
-
the person prefers injecting insulin immediately before a meal or
-
hypoglycaemia is a problem or
-
blood glucose levels rise markedly after meals. [2015]
1.7.27
Consider switching to insulin detemir or insulin glargine from NPH insulin in adults with type 2 diabetes:
-
who do not reach their target HbA1c because of significant hypoglycaemia or
-
who experience significant hypoglycaemia on NPH insulin irrespective of the level of HbA1c reached or
-
who cannot use the device needed to inject NPH insulin but could administer their own insulin safely and accurately if a switch to one of the long‑acting insulin analogues was made or
-
who need help from a carer or healthcare professional to administer insulin injections and for whom switching to one of the long‑acting insulin analogues would reduce the number of daily injections. [2015]
1.7.28
Monitor adults with type 2 diabetes who are on a basal insulin regimen (NPH insulin, insulin detemir or insulin glargine) for the need for short‑acting insulin before meals (or a pre‑mixed [biphasic] insulin preparation). [2015]
1.7.29
Monitor adults with type 2 diabetes who are on pre‑mixed (biphasic) insulin for the need for a further injection of short‑acting insulin before meals or for a change to a basal-bolus regimen with NPH insulin or insulin detemir or insulin glargine, if blood glucose control remains inadequate. [2015]
1.7.30
When starting an insulin for which a biosimilar is available, use the product with the lowest acquisition cost. [2021]
1.7.31
Ensure the risk of medication errors with insulins is minimised by following the Medicines and Healthcare products Regulatory Agency (MHRA) guidance on minimising the risk of medication error with high strength, fixed combination and biosimilar insulin products, which includes advice for healthcare professionals when starting treatment with a biosimilar. [2021]
1.7.32
When people are already using an insulin for which a lower cost biosimilar is available, discuss the possibility of switching to the biosimilar. Make a shared decision with the person after discussing their preferences. [2021]
For guidance on using insulin in combination with SGLT2 inhibitors, see:
Terms used in this guideline
This section defines terms that have been used in a particular way for this guideline. For other definitions, see the NICE glossary and the Think Local, Act Personal Care and Support Jargon Buster.
Atherosclerotic cardiovascular disease
This includes coronary heart disease, acute coronary syndrome, previous myocardial infarction, stable angina, previous coronary or other revascularisation, cerebrovascular disease (ischaemic stroke and transient ischaemic attack) and peripheral arterial disease.
Consultant-led multidisciplinary team
A consultant-led multidisciplinary team may include a wide range of staff based in primary, secondary and community care.
Continuous glucose monitoring
This covers both real-time continuous glucose monitoring (rtCGM) and intermittently scanned continuous glucose monitoring (isCGM, commonly referred to as 'flash').
A continuous glucose monitor is a device that measures blood glucose levels and sends the readings to a display device or smartphone.
High risk of developing cardiovascular disease
Adults with type 2 diabetes who have:
Cardiovascular disease risk factors: hypertension, dyslipidaemia, smoking, obesity, and family history (in a first-degree relative) of premature cardiovascular disease.
Insulin glargine
The recommendations in this guideline also apply to any current or future biosimilar product of insulin glargine that has an appropriate marketing authorisation that allows the use of the biosimilar in the same indication.
Multiple daily injections
Two or more daily insulin injections, which could either be a basal-bolus regimen or more than one daily insulin injection.
Periodontitis
A chronic inflammatory gum disease that destroys the supporting tissues of the teeth (the periodontium).
Gingivitis is a milder form of periodontal disease than periodontitis. However, gingivitis still causes inflammation in the gum, and if not treated it can lead to periodontitis.
Severe hypoglycaemia
Episodes of hypoglycaemia that require assistance from another person to treat.
Recurrent hypoglycaemia
Frequent events of hypoglycaemia that occur each week or month and have an impact on quality of life.
Very low carbohydrate and ketogenic diets
A very low carbohydrate diet has 20 to 50 grams per day of carbohydrate or less than 10% of a 2000 kcal/day diet. A ketogenic diet is a very low carbohydrate, high fat diet that is designed to induce ketosis.