Chronic disease management

Type 2 Diabetes Mellitus

Diagnosis, screening, complication surveillance and staged glucose/BP/lipid management for type 2 diabetes.

Source: Murtagh's General Practice, 9th ed. — Part 2, Ch 11 (pp. 91-106) · Reviewed 2026-10-05

Red flags — escalate / refer urgently
  • Unwell child/young person with a high finger-prick glucose — treat as diabetic ketoacidosis until proven otherwise; this is a medical emergency requiring hospital assessment.
  • Reduced conscious state or 'strange' behaviour in a known diabetic — consider hypoglycaemia first; also consider DKA (especially on SGLT2 inhibitors) and withhold the SGLT2 inhibitor.
  • Marked hyperglycaemia with dehydration and altered conscious state in (often elderly) type 2 diabetes without ketosis — hyperosmolar hyperglycaemic state (HHS); mortality higher than DKA.
  • Very unwell patient on metformin with hyperventilation ('air hunger') and confusion — consider lactic acidosis, especially if kidney function is impaired.
  • 'Never let the sun go down on pus in a diabetic foot' — admit to hospital.
  • Foot ulcer not healed in 6 weeks — exclude osteomyelitis (MRI) and investigate the vasculature.
1

Definition & classification

Relative or absolute insulin deficiency causing hyperglycaemia. Type 1 (~10%): usually young, rapid onset, thin, insulin-deficient, ketosis-prone. Type 2 (~85-90%): usually >40y, insidious/mild or asymptomatic, often obese, insulin-resistant, associated with metabolic syndrome/PCOS/fatty liver. This page focuses on type 2.

FeatureType 1Type 2
Relative frequency10%85-90%
Peak age of onset10-30 years>40 years
OnsetRapidInsidious/slow
PresentationPolyuria, polydipsia, weight lossMilder, often asymptomatic
Weight at onsetLow (thin)High (obese)
KetoacidosisYesRare
Insulin statusDeficientResistant
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Diagnostic approach

History
  • Specific symptoms: polyuria, polydipsia, weight loss, polyphagia, tiredness/malaise/fatigue, nocturia
  • Systems review: cardiovascular (chest pain, dyspnoea), urinary function, sexual function, neurological (tingling in feet/hands), vision (blurred), infection tendency (skin, urine, genital), genital itching
  • Family history, medications, smoking/alcohol, obstetric history, physical activity, nutrition/eating habits
  • DxT pattern: thirst + polyuria + weight loss → type 1 diabetes (typically an unwell child/young person with a high finger-prick glucose — this is a medical emergency)
Risk factors
  • Age >40 years
  • Family history
  • Overweight/obesity, sedentary lifestyle
  • History of gestational diabetes or pancreatitis
  • Polycystic ovarian syndrome
  • Hypertension/ischaemic heart disease
  • Medication causing hyperglycaemia (thiazides, high-dose oestrogen, corticosteroids)
  • High-prevalence ethnic groups: Aboriginal and Torres Strait Islander, Pacific Islander, Indian subcontinent, Chinese, Afro-Caribbean
Screening

AUSDRISK every 3 years from age 40; if score ≥12 do fasting glucose or HbA1c. Screen earlier/more often (annually in very high-risk groups) if: known prediabetes, age >40 (or >30 with risk factors: first-degree relative, BMI >30, high-prevalence ethnicity), age >18 in Aboriginal and Torres Strait Islander people, previous gestational diabetes, long-term steroids/antipsychotics, PCOS with overweight, previous CV event.

Examination
  • General inspection including skin; BMI (weight/height); waist circumference; visual acuity
  • Blood pressure — lying and standing
  • Peripheral neuropathy: tendon reflexes, sensation (e.g. cotton wool, 10g monofilament)
  • Urinalysis: glucose, albumin, ketones, nitrites
Diagnostic criteria
  • Symptomatic (≥2 of polydipsia, polyuria, frequent skin infections or genital thrush): fasting venous glucose ≥7.0 mmol/L, OR random venous glucose (≥2h after eating) ≥11.1 mmol/L, OR HbA1c >6.5% (>48 mmol/mol)
  • Asymptomatic: at least two separate elevated values (fasting, ≥2h postprandial, or the two OGTT values) on different occasions
  • Uncertain/borderline range (fasting or random venous glucose 5.5-11.0 mmol/L in a symptomatic patient or one with risk factors): perform an OGTT — 2-hour value ≥11.1 mmol/L confirms diabetes, <7.8 makes it unlikely, 7.8-11 = impaired glucose tolerance
  • Avoid glucose tolerance tests where diagnosis can be made on symptoms plus fasting/random glucose or HbA1c — an OGTT carries a small risk of precipitating hyperosmolar coma
  • Prediabetes = impaired fasting glucose (6.1-6.9 mmol/L) or impaired glucose tolerance — not itself a reason to start medication, but raises urgency of lifestyle change
  • Urinalysis for glucose is unreliable for diagnosis — renal glucose threshold varies between patients
3

Investigations

Recommended
  • Fasting or random venous blood glucose — Initial diagnostic test
  • HbA1c — Diagnosis and 3-6 monthly monitoring of control (reflects mean glucose over 2-3 months)
  • Oral glucose tolerance test (OGTT) — Only for true borderline cases, and for diagnosing gestational diabetes (75g OGTT at 24-28 weeks)
  • Lipids (total/HDL/LDL cholesterol, triglycerides) — CV risk stratification and management target
  • Kidney function (serum urea/creatinine, eGFR) — Baseline, monitor nephropathy and drug safety (e.g. metformin, SGLT2 inhibitors)
  • Urine albumin:creatinine ratio (ACR), first morning sample — Screens for diabetic nephropathy — microalbuminuria is an early, reversible marker; dipstick is unreliable and 24h collection impractical in general practice
  • ECG — Baseline cardiovascular assessment
Ongoing monitoring
  • HbA1c — Every 3-6 months
  • Blood glucose self-monitoring — Mainly useful if on insulin (fasting and postprandial); not routinely needed on oral agents alone — HbA1c preferred
  • Urine ACR — Annual nephropathy screen
  • Lipids — Every 12 months
  • Fundoscopy / retinal photography — Every 1-2 years via direct ophthalmoscopy (dilated pupils), retinal photography, or fluorescein angiography if needed
  • Foot examination (including footwear, injection sites) — Annually, and opportunistically — foot problems are among the commonest diabetes complications
4

Risk stratification

Cardiovascular disease causes most of the excess morbidity/mortality in type 2 diabetes. Diabetes often co-exists with obesity, hypertension and dyslipidaemia (the 'deadly quartet' / metabolic syndrome).

Risk factors
  • Obesity / abdominal obesity
  • Hypertension
  • Dyslipidaemia
  • Smoking
  • Sedentary lifestyle
  • Elevated triglycerides ≥1.7 mmol/L
  • Reduced HDL <1.03 mmol/L
Target organ damage
  • Microalbuminuria/proteinuria
  • Retinopathy
  • Peripheral/autonomic neuropathy
  • Macrovascular disease (coronary, cerebrovascular, peripheral vascular)
5

Management

Principles
  • GP's main objectives: prevent cardiovascular disease and other complications
  • Core targets: reduce lifestyle risks (weight, smoking, inactivity); glycaemic control (HbA1c usually ≤7%); blood pressure control (<140/90, lower if tolerated — has more mortality benefit than glucose control alone); blood lipid control
  • NEAT mnemonic for lifestyle review: Nutrition, Exercise, Avoidance of toxins (alcohol, tobacco, salt, sugar, illicit drugs), Tranquillity (rest, stress reduction)
  • Remission of established type 2 diabetes is a realistic aim in general practice using intensive dietary measures for 3 months followed by structured weight-loss support (DiRECT trial)
Who to treat

In prediabetes, medication is not indicated — focus on lifestyle. In confirmed type 2 diabetes, trial diet and exercise first (most symptoms improve within 1-4 weeks); if unsatisfactory control persists after 3-6 months, add an oral hypoglycaemic agent.

Lifestyle / non-drug measures
  • Diet: protein 10-20%, fat 20-40%, carbohydrate 35-60%; reduce saturated fat, added sugar and alcohol; follow glycaemic index; increase vegetables/fruit/wholegrain; special diabetic foods not necessary; low-carb diets are an option
  • Exercise: at least 150 minutes/week (e.g. 30 min, 3+ times/week, ideally daily) — brisk walking, jogging, swimming, aerobics; start gradually and increase pace
  • Weight loss support, ideally with a dietitian / diabetes education service
  • Smoking cessation, alcohol ≤2 standard drinks/day
  • Immunisation: influenza, pneumococcus, COVID-19, dTpa
Treatment targets
ParameterGoal
HbA1c≤7% (53 mmol/mol)
Fasting blood glucoseideal 4-6 mmol/L (NHMRC 6-8 mmol/L)
Postprandial blood glucose8-10 mmol/L
Blood pressure<140/90 mmHg, lower if tolerated; ≤125/80 if proteinuria ≥1g/day
Total cholesterol<4.0 mmol/L
LDL cholesterol<2.0 mmol/L
HDL cholesterol≥1.0 mmol/L
Triglycerides<2.0 mmol/L
BMI18-25 where practicable
Cigarette consumptionZero
Blood pressure & lipids

Preferred antihypertensives: ACE inhibitors/ARBs (first-line if albuminuria present) and calcium-channel blockers; target <140/90 (lower if tolerated, stricter with proteinuria). Try non-pharmacological measures first. For dyslipidaemia, preferred agents are HMG-CoA reductase inhibitors (statins) ± resins for hypercholesterolaemia, fibrates/resins for mixed hyperlipidaemia; non-pharmacological measures tried first. Aspirin is not routinely indicated unless there has been a prior cardiovascular event (then 75-150mg/day).

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Medications

Verify before prescribing: All drug names and doses below are Murtagh's printed reference figures — cross-check against current eTG/local formulary, renal function (eGFR) and the individual's cardiovascular/renal risk profile before prescribing. Diabetes pharmacotherapy is a fast-moving area (SGLT2/GLP-1 positioning in particular) — treat this list as a starting structure, not current best practice.
Staged approach
  1. 1. Lifestyle (diet + exercise) trial for 3-6 months first in type 2 diabetes
  2. 2. If HbA1c target not met: start metformin (first-line) — usual starting dose 500mg once or twice daily
  3. 3. If target not met after further 3-6 months: add a second agent — SGLT2 inhibitor or GLP-1 receptor agonist are now preferred second-line (particularly with cardiovascular disease, heart failure, multiple CV risk factors or kidney disease); DPP-4 inhibitors are an option where CV/renal risk is low or SGLT2/GLP-1 not tolerated; sulfonylureas and glitazones are valid but now largely superseded given they lack proven CV/renal benefit
  4. 4. Insulin may be required at any stage, particularly if symptomatic hyperglycaemia or HbA1c remains well above target — for less experienced GPs, shared care with an endocrinologist is recommended
  5. Review the need for continued oral therapy after 3 months of treatment; avoid prescribing an oral hypoglycaemic agent prematurely without a genuine lifestyle trial first
First-line agents

Biguanide — metformin

Verify dose
Examples: Metformin 500mg once or twice daily, titrated; duration of action ~12h (slow-release once-daily formulation available); usual range 0.5-3g/day
Favoured in: First-line for essentially all type 2 diabetes — good tolerance, low cost, no significant weight gain, no hypoglycaemia, improved lipid profile
Avoid / caution: Avoid in significant cardiac, hepatic or kidney disease (eGFR <30)
Key side effects: GI disturbance (diarrhoea, nausea/vomiting) — common; lactic acidosis — rare but serious, risk low if therapeutic dose not exceeded and renal function adequate
Second-line agents

SGLT2 inhibitor ('gliflozin')

Verify dose
Examples: Empagliflozin 10-25mg daily; Dapagliflozin 5-10mg daily; Ertugliflozin 5-15mg daily
Favoured in: Preferred second-line, particularly with CVD, heart failure, multiple CV risk factors or kidney disease — proven cardiovascular/renal protective benefits; also causes meaningful weight loss
Avoid / caution: Withhold during acute illness, fasting, or peri-surgery (risk of euglycaemic DKA)
Key side effects: Genitourinary infections, dehydration, dizziness, hypoglycaemia (when combined with insulin/sulfonylurea); diabetic ketoacidosis risk if withheld incorrectly during illness/fasting

GLP-1 receptor agonist

Verify dose
Examples: Dulaglutide 1.5mg weekly (SC); Exenatide 5mcg bd or 2mg weekly MR (SC); Liraglutide 0.6-1.8mg daily (SC)
Favoured in: Preferred second-line alongside SGLT2 inhibitors; greatest HbA1c reduction of any non-insulin agent when added to metformin (0.6-1.5%); proven CV benefit in high-risk patients; substantial sustained weight loss (2-6kg over 12 months)
Key side effects: Nausea (common), pancreatitis (rare)

DPP-4 inhibitor ('gliptin')

Verify dose
Examples: Sitagliptin 25-100mg daily; Linagliptin 5mg daily; Vildagliptin 50-100mg daily; Alogliptin 25mg daily
Favoured in: Where cardiovascular/renal risk is low, or an SGLT2 inhibitor/GLP-1 agonist is contraindicated or not tolerated
Key side effects: Slight pancreatitis risk; rhinorrhoea, headache, hypersensitivity (e.g. urticaria); dizziness/fatigue (vildagliptin)

Sulfonylurea

Verify dose
Examples: Gliclazide 40-320mg daily; Glipizide 2.5-40mg daily; Glibenclamide 2.5-20mg daily; Glimepiride 1-4mg daily
Favoured in: Valid option but increasingly superseded by SGLT2i/GLP-1 agonists, which have proven CV/renal benefit that sulfonylureas lack
Avoid / caution: Caution in elderly — prefer a shorter-acting agent (e.g. gliclazide); longer-acting potent agents cause troublesome hypoglycaemia in the elderly
Key side effects: Hypoglycaemia (most common), weight gain (common), rash and GI effects (rare)

Alpha-glucosidase inhibitor

Verify dose
Examples: Acarbose 150-600mg daily
Favoured in: Adjunct option
Key side effects: Flatulence, skin rashes, diarrhoea, liver effects

Thiazolidinedione ('glitazone')

Verify dose
Examples: Pioglitazone 15-45mg daily; Rosiglitazone 4-8mg daily
Favoured in: Dubious mortality benefit — largely superseded
Avoid / caution: Heart failure (caution)
Key side effects: Oedema, weight gain, heart failure; hepatic effects and fracture risk (rosiglitazone)

Insulin

Verify dose
Examples: Ultra-short (lispro/aspart/glulisine, e.g. Humalog/NovoRapid/Apidra); short-acting neutral (Actrapid/Humulin R); intermediate isophane/NPH (Protaphane/Humulin NPH); long-acting analogues (glargine/detemir, e.g. Lantus/Levemir); pre-mixed combinations (e.g. Humalog Mix 25/50, NovoMix 30)
Favoured in: Any stage if HbA1c remains above target on oral therapy, or symptomatic hyperglycaemia; shared care with endocrinology recommended for less experienced GPs; continuous subcutaneous insulin infusion (pump) uses rapid-acting insulin
Key side effects: Hypoglycaemia — teach recognition and treatment; injection site issues
7

Acute / severe presentations

Four metabolic emergencies to recognise promptly in a person with diabetes.

Hypoglycaemia (BGL <4.0 mmol/L, serious <3.0) Most common with insulin (any type) and sulfonylureas (metformin rarely causes it). Warning symptoms: sweating, tremor, palpitations, hunger, peri-oral paraesthesia — may progress rapidly to loss of consciousness without warning ('hypoglycaemic unawareness' after recurrent episodes). If alert and able to swallow: 15g refined carbohydrate orally (e.g. 7 jelly beans, 3 tsp sugar/honey, half glass juice/soft drink); recheck BGL every 15 min, repeat if still <4; once >4 give a complex carbohydrate snack. If reduced conscious state/unconscious: 30mL 50% glucose slow IV push (or rectally via syringe nozzle if no IV access, 10mL in children) OR 1mL (1 ampoule) glucagon IM/SC (0.5mL if child <25kg); call an ambulance if unconscious. Follow up with snack/meal once conscious; admit if concerned; identify the cause.
Diabetic ketoacidosis (DKA) Life-threatening; develops over days (hours in 'brittle' diabetes), usually when insulin is omitted during illness (opposite advice applies to SGLT2 inhibitors — withhold these when unwell or fasting, including peri-surgery or during deliberate low-calorie intake, to avoid precipitating DKA). Features: hyperglycaemia (often >20 mmol/L, can be lower/normal if on an SGLT2 inhibitor), polyuria/polydipsia/drowsiness, vomiting and abdominal pain, dehydration, hyperventilation (acidotic breathing) with low BP and high pulse/resp rate, ketosis. Management: urgent hospital admission; early IV fluids (normal saline fast first litre, then caution); IV insulin (e.g. 10U in first hour); sodium, potassium (KCl) and fluid replacement; ECG for arrhythmia from electrolyte disturbance.
Hyperosmolar hyperglycaemic state (HHS) Altered conscious state (stupor to coma) with marked dehydration, typically insidious onset over weeks with fatigue/polyuria/polydipsia, in uncontrolled type 2 diabetes (especially elderly) without significant ketosis. Often an underlying precipitant (e.g. pneumonia, UTI). Mortality is even higher than DKA. Treatment: IV fluids (normal to half-normal saline, given slowly) and insulin at relatively lower doses than for DKA.
Lactic acidosis Marked hyperventilation ('air hunger') and confusion, high mortality; consider in the very ill patient taking metformin, especially with impaired kidney function. Investigations show low pH, low bicarbonate, high lactate, absent serum ketones, large anion gap. Treatment: remove the cause, rehydration, IV sodium bicarbonate.
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Other considerations

  • Erectile dysfunction affects up to 50% of men with type 2 diabetes over 40 — may be macrovascular, autonomic-neuropathic or psychological; phosphodiesterase inhibitors appropriate if organic and not on nitrates
  • Female sexual dysfunction — reduced vaginal lubrication from autonomic dysfunction; lubricants, education, reassurance
  • Postural hypotension (autonomic neuropathy ± antihypertensive/anti-anginal medication) — may need relaxed BP targets, compression stockings, occasionally fludrocortisone if severe
  • Gastroparesis — fullness, dysphagia, reflux, recurrent nausea/vomiting after meals; dietary modification or domperidone/cisapride/erythromycin
  • Driving — hypoglycaemia and visual complications are the main risks; diet-controlled patients unrestricted, insulin-treated patients may need a conditional licence with periodic review (see Austroads 'Assessing Fitness to Drive')
  • Contraception — long-acting reversibles (Implanon, Mirena) or combined OCP are appropriate; consider coexisting PCOS
  • Diabetes-related stigma and discrimination are common (up to 4/5 report experiencing it) — empathetic care has a measurable positive effect on HbA1c/LDL target attainment
9

When to refer

  • Type 1 diabetes — specialist evaluation then 1-2 yearly review
  • Type 2 diabetes: consider referral for young people, those requiring insulin, or those with complications (level depends on GP's comfort/experience)
  • Treatable complications: retinopathy, nephropathy, neuropathy (test annually)
  • Foot ulcer not healing within 6 weeks, or any pus/infection in a diabetic foot
10

Safety netting

  • Teach recognition and self-treatment of hypoglycaemia to all patients on insulin or sulfonylureas; 'recurrent hypoglycaemia begets hypoglycaemic unawareness' — ask about symptoms often
  • Instruct patients on SGLT2 inhibitors to withhold the medication when acutely unwell, fasting, or around surgery (euglycaemic DKA risk)
  • Foot care education — check footwear, inspect feet, treat minor cuts/infections promptly
  • Sick-day guidance: do not stop insulin during illness (opposite advice to SGLT2 inhibitors); monitor more closely when unwell
  • Arrange structured follow-up: 3-monthly review (symptoms, weight/BMI, BP, urine, self-monitoring, exercise, HbA1c at least 6-monthly) and annual review (full history, examination incl. eyes/feet/pulses, biochemistry incl. lipids)
11

Practice tips

  • Many cases of type 2 diabetes remain undiagnosed — maintain vigilance, especially in at-risk groups
  • Hyperglycaemia is a common cause of tiredness in the elderly with type 2 diabetes — consider long-acting insulin to improve symptoms if very tired
  • If a person with diabetes (particularly type 1) is very drowsy and looks sick, consider ketoacidosis first and withhold SGLT2 inhibitors
  • Management is a team effort — family, nurse educator, podiatrist, dietitian, GP, and sometimes endocrinologist or domiciliary nursing
  • 'Never let the sun go down on pus in a diabetic foot' — admit to hospital
  • Prevention/detection of coronary heart disease should be integral to every consultation

This page summarises structure and content from Murtagh's General Practice for personal point-of-care use. Medication names and doses are the book's printed reference figures and are explicitly flagged to verify — check current eTG/local formulary guidance and the individual patient's renal function, comorbidities and interactions before prescribing.