- Check CBG on everyone admitted, diabetic or not (hyperglycaemia is often not noted on a VBG if patient not known to be diabetic – look for it)
- Risk of DM can be calculated – need to know demographics, family history, waist circumference, BMI, history of HTN
- Typical symptoms include polydipsia, polyuria, blurred vision, weight loss, recurrent infections, fatigue. But can be absent.
- Ask about
-
- Family history of DM and autoimmune disorders
- Previous gestational DM
- Medications (in case causative)
- Any other symptoms (which may suggest an atypical cause, such as endocrine)
-
- Examine for
-
- Skin – Striae (cushings), acanthosis nigricans (insulin resistance), necrobiosis lipidoica (see other diabetic complications)
- Features of endocrine or pancreatic disease
- Complications of DM – feet, peripheral nerves, eyes
-
Criteria for diagnosis
- Any of
-
- Fasting blood glucose > 7
- Or HbA1c >48
- Or random glucose > 11 + symptoms
-
- If no symptoms – check blood sugar (not CBG) on two occasions, and/or HbA1c (but see below)
- If repeat CBG normal – monitor (transient hyperglycaemia can be caused by infection, trauma, other stresses)
- Oral glucose tolerance test – Generally only performed in pregnancy now (any degree of glucose intolerance in pregnancy is gestational DM)
HbA1C
- Not the whole story – hides glycaemic variability
- Do not use to diagnose DM if:
-
- Pregnant
- Symptoms of DM < 2 months
- Acutely unwell
- On drugs that cause hyperglycaemia
- Pancreatic disease
- End stage renal disease
- HIV
-
- Interpret with caution if haemoglobinopathy, severe anaemia, splenectomy, recent blood transfusion
- HbA1c in anaemia
-
- Normochromic anaemia secondary to CKD and haemolysis lead to falsely low HbA1c
- Iron Deficient Anaemia (IDA) and B12/folate deficiency falsely elevate HbA1c
-
- Cause of falsely elevated HbA1c
-
- Uraemia
- Acidosis
- IDA
- B12 or folate deficiency
- Splenectomy
- Untreated hypothyroidism
- Severe hypertriglyceridaemia
- Haemoglobin variants
-
- Causes of falsely low HbA1c
-
- Blood loss
- Blood transfusions
- Haemolysis
- Anaemia and haemoglobinopathies
- EPO treatment
- Drugs (sulphasalazine, dapsone, ARVs)
- G6PD deficiency
- Splenomegaly
- Advanced CKD
- Pregnancy
- Liver disease
-
- If HbA1C > 48, patient probably has DM – manage accordingly (but not valid for T1DM which starts acutely).
- 42-48 – probably pre-diabetes
- Target HbA1C depends upon the patient
- Suspect falsely low HbA1C if discordant with history or if consistently high CBGs. You can get a 7-day glucose sensor from a diabetes clinic in this instance
Diagnosing Type 1 DM
- Often (but not always): ketosis, rapid weight loss / BMI < 25, aged <50, personal/family of autoimmunity
- Antibodies and c-peptide are not routine to conform diagnosis
-
- Indicated if aged > 50, BMI >25, slowly evolving hyperglycaemia, suspected monogenic DM, DM type uncertain
- In practice almost always done in suspected new T1DM
-
- Antibodies
-
- GAD (antiglutamic decarboxylase autoantibodies) – 70% positive at diagnosis
- ICA (anti-islet cell autoantibodies) – present in 90% of T1DM
- ZnT8 (zinc transporter) – 55% present at diagnosis
- IA-2 – 55% positive at diagnosis, and higher in kids
- Absence of antibodies does not rule out T1DM
- False negative rate increases as time from diagnosis increases
-
- C-peptide levels tend to be low / reduced in new type 1 DM (normal or high in type 2)
- Screen for pancreatic cancer if there is new onset type 2 diabetes in older people with dramatic weight loss and features of exocrine insufficiency / risk factors
- Kit to consider on discharge after new diagnosis of T1DM
-
- Insulin pens and needles, sharps box
- CBG and ketone meters
- Test strips & lancets for both
- Glucose gel +/- glucagon 1mg IM injection
- Insulin passport, medic alert bracelet or diabetes card
-