Type 1 diabetes mellitus
Type 1 diabetes: shared care, CGM, and annual review in AU general practice
Type 1 diabetes mellitus (T1DM) is an autoimmune condition destroying the pancreatic beta cells, causing absolute insulin deficiency. Unlike type 2 diabetes, it is not related to lifestyle and requires lifelong insulin — by multiple daily injection or pump — regardless of diet or exercise.
Continuous glucose monitoring (CGM) is fully subsidised for all Australians with T1DM through the NDSS, improving glucose management and quality of life. Specialist endocrinology teams lead overall care; the GP's shared-care role covers annual complication screening, mental health, vaccinations, sick day planning, and chronic disease management.
Type 1 diabetes mellitus (T1DM) is an autoimmune condition requiring lifelong insulin. It affects approximately 120,000 Australians — about 0.5% of the population — and incidence is rising by around 3% each year. Peak onset is between 5 and 14 years, but adult-onset is increasingly recognised; many adults with slowly progressive autoimmune beta-cell failure are initially misdiagnosed with type 2 diabetes.
Care is led by an endocrinologist and diabetes team. The GP’s shared-care role is to be the consistent presence in a person’s care: coordinating the annual review checklist, managing comorbidities and mental health, supporting self-management, and ensuring sick day plans and driving requirements remain current.
A. Core clinical — the AU general-practice framework
What happens in type 1 diabetes
The immune system attacks and destroys the insulin-producing beta cells in the islets of Langerhans in the pancreas. Without insulin, cells cannot use glucose for energy. Blood glucose rises dangerously; simultaneously, without insulin signalling, the body breaks down fat, producing ketone bodies — in excess, this causes diabetic ketoacidosis (DKA).
A honeymoon phase — partial residual beta-cell function — may persist for months after diagnosis, temporarily reducing insulin requirements. This is transient; eventually beta-cell function is lost completely and lifelong insulin replacement is necessary.
Key autoantibodies — present in about 90% of people at diagnosis — include: GAD (anti-glutamic acid decarboxylase, most useful in adults), IA-2 (anti-tyrosine phosphatase), ZnT8 (zinc transporter 8), and insulin autoantibodies (particularly in children). Combined with a low or undetectable C-peptide level (confirming absent beta-cell function), these distinguish T1DM from type 2 diabetes and MODY (maturity-onset diabetes of the young, a monogenic form).
Insulin therapy — MDI and pump options
Multiple daily injections (MDI) — the most common regimen:
- Long-acting basal insulin once or twice daily: glargine (Lantus, Toujeo), detemir (Levemir), or degludec (Tresiba)
- Rapid-acting bolus insulin before each meal: aspart (NovoRapid, Fiasp), lispro (Humalog), or glulisine (Apidra)
- Insulin doses are adjusted using an insulin-to-carbohydrate ratio (ICR) and an insulin sensitivity factor (ISF/correction factor)
Insulin pump therapy (CSII) delivers continuous subcutaneous insulin via a pump worn on the body, with boluses programmed at mealtimes. Pump therapy suits motivated patients with recurrent hypoglycaemia, dawn phenomenon, active lifestyles, pregnancy, or children who struggle with injection schedules.
Hybrid closed-loop systems (“artificial pancreas”) integrate a CGM sensor with an insulin pump and an algorithm that automatically adjusts basal insulin delivery in response to real-time glucose readings. Systems include Tandem t:slim X2 with Control-IQ, Medtronic 780G, and Omnipod 5. Multiple RCTs — including the DCCT landmark trial and more recent closed-loop studies — confirm that tighter glucose control reduces both microvascular and cardiovascular complications over time.
Continuous glucose monitoring (CGM)
CGM measures glucose every one to five minutes via a subcutaneous sensor, alerting to rising or falling glucose before symptomatic hypoglycaemia develops. Dexcom G6 and G7 are factory-calibrated 10-day sensors; FreeStyle Libre 2 and 3 are 14-day sensors with integrated alarms in the newer models.
The NDSS has subsidised CGM for all Australians with type 1 diabetes since 1 July 2022 — previously limited to children and those with complex management. Registration with the NDSS (via Diabetes Australia or a state diabetes organisation) is the first step. Any person with type 1 diabetes not yet using CGM should be supported to register and access this subsidy.
Glycaemic targets
Per Australasian Diabetes Society (ADS) and eTG:
- HbA1c < 7.0% (53 mmol/mol) — typical adult target
- HbA1c < 6.5% — pre-pregnancy and during pregnancy
- HbA1c 8–8.5% — appropriate for older adults with frailty, hypoglycaemia unawareness, or limited life expectancy
CGM-based targets:
- Time in range (TIR) > 70% (glucose 3.9–10.0 mmol/L)
- Time below range (TBR) < 4% (below 3.9 mmol/L)
- Time very below range < 1% (below 3.0 mmol/L)
Acute complications
Hypoglycaemia — blood glucose below 3.9 mmol/L — is the most immediate danger.
Mild (person can self-treat): 15 g fast-acting carbohydrate (jelly beans, glucose tablets, fruit juice or soft drink 150–200 mL), wait 15 minutes, retest, repeat if needed. Follow with a complex carbohydrate snack when glucose is stable.
Severe (requires assistance from another person): buccal glucose gel or glucagon. Nasal glucagon spray (Baqsimi 3 mg) is easier for bystanders to administer than the traditional intramuscular injection (GlucaGen 1 mg), and should be accessible to family members and carers of anyone with type 1 diabetes.
Hypoglycaemia unawareness — loss of the warning symptoms of low blood glucose — is dangerous and requires specialist review. CGM with alarms and pump low-glucose suspend features significantly reduce severe hypoglycaemia events in those with impaired awareness.
Diabetic ketoacidosis (DKA) — hyperglycaemia, metabolic acidosis (pH below 7.3, bicarbonate below 15 mmol/L), and ketosis (blood beta-hydroxybutyrate above 3 mmol/L) — is a medical emergency. Common precipitants are insulin omission (the most frequent cause), intercurrent illness, and pump failure. Never stop insulin in type 1 diabetes, even when unwell and not eating. Every person with type 1 diabetes should have a written sick day plan.
B. Annual complication review — the GP checklist
Annual structured review of complications is the core contribution of general practice to shared diabetes care. The following should be completed at least once per year per ADS and RACGP:
Glycaemic control:
- HbA1c
- CGM download review (time in range, low events, pattern analysis)
Cardiovascular risk:
- Blood pressure (target < 130/80 mmHg)
- Fasting lipids (LDL target < 2.0 mmol/L, consider statin from age 30–40)
- Smoking status
Kidney function:
- Urine albumin-to-creatinine ratio (UACR) — first morning void; annual from diagnosis
- Serum creatinine and eGFR
- ACE inhibitor or ARB indicated if microalbuminuria is confirmed (UACR ≥ 3 mg/mmol) — even in normotensive patients, to slow nephropathy progression
Eye screening:
- Retinal photography or dilated fundoscopy — annual from five years after diagnosis in adults; before conception and during pregnancy
- KeepSight registry provides a recall system for retinal screening
Neuropathy:
- 10 g monofilament test on the soles of both feet
- 128 Hz tuning fork for vibration sense at the hallux
- History of numbness, burning, pins and needles, orthostatic symptoms, bowel or bladder change
Foot examination:
- Pulses (dorsalis pedis, posterior tibial)
- Skin integrity, callus, ulcer, nail health, deformities
Mental health:
- Depression screening (PHQ-9)
- Diabetes distress (Problem Areas in Diabetes scale, PAID) — a distinct concept from depression; very common and under-recognised
- Eating disorders — particularly insulin omission for weight loss (“diabulimia”) in adolescent and young adult women — requires specialist team involvement
- Anxiety, particularly hypoglycaemia-related fear
Autoimmune comorbidities:
- TSH — autoimmune thyroid disease (Hashimoto’s or Graves’) affects 15–25% of people with type 1 diabetes
- TTG-IgA coeliac serology — coeliac disease affects 5–10% of T1DM; relevant to glycaemic control and nutrition
Vaccinations:
- Annual influenza vaccination
- COVID-19 boosters as per current ATAGI schedule
- Pneumococcal vaccination (PCV20 or PCV13 + PPSV23)
- Herpes zoster vaccine (Shingrix — non-live; appropriate from age 18 if immunocompromised)
C. Evidence appraisal — key points for general practice
CGM is standard care. Multiple RCTs confirm CGM reduces HbA1c and severe hypoglycaemia rates. The NDSS subsidy makes it accessible. If a patient with type 1 diabetes is not using CGM, ask why, and help address the barrier.
SGLT2 inhibitors are not recommended for type 1 diabetes in Australia. Empagliflozin and dapagliflozin carry Authority-required PBS listing for type 2 diabetes and CKD/heart failure indications — these indications do not include type 1 diabetes. The risk of euglycaemic diabetic ketoacidosis (DKA occurring without markedly elevated blood glucose, and therefore easily missed) is significantly increased in type 1 diabetes. SGLT2 inhibitors should not be prescribed for type 1 diabetes outside specialist-supervised research or compassionate access contexts.
GLP-1 receptor agonists in type 1 diabetes — evidence exists in selected obese patients but the drugs are off-label and not PBS-approved for this indication in Australia. Specialist context only.
D. Australian operations
NDSS and PBS access
The National Diabetes Services Scheme (NDSS) (phone 1800 637 700) provides subsidised access to: blood glucose strips, lancets, syringes, pen needles, insulin pump consumables, and CGM sensors for all Australians with type 1 diabetes. Free registration is through Diabetes Australia or a state diabetes organisation.
Insulin (all forms) is PBS Authority Required (Streamlined) for diabetes mellitus. Glucagon (GlucaGen IM and Baqsimi nasal) are general PBS schedule. ACE inhibitors and ARBs are general PBS.
The Insulin Pump Program (IPP) provides subsidised insulin pump access for paediatric patients in most states; adult access is more variable, often requiring private health insurance, and is an area of ongoing advocacy by JDRF Australia.
GP care planning — MBS
Chronic complex type 1 diabetes qualifies for:
- GPCCMP (MBS items 965 / 967) — chronic condition management plan with review; enables allied health referrals
- Allied health visits under GPCCMP — diabetes educator (item 10951), accredited practising dietitian (item 10954), exercise physiologist (item 10968), podiatrist (item 10960) — up to five combined visits per calendar year
- Retinal photography (MBS item 12325) for diabetes eye check
- Mental Health Treatment Plan (MBS items 2715 / 2717) — for comorbid depression, anxiety, or eating disorders
Driving requirements
Per Austroads Assessing Fitness to Drive 2022, people with type 1 diabetes on insulin driving a private vehicle must:
- Check blood glucose (or CGM reading confirmed by blood glucose meter) and confirm ≥5 mmol/L before every drive
- Keep glucose in the vehicle at all times
- Recheck every two hours on journeys over two hours
- Stop driving immediately if glucose falls below 5 mmol/L; treat; wait 45 minutes before resuming
- Report severe hypoglycaemia while driving to the licensing authority
Commercial licence (truck, bus, taxi, heavy vehicles) requirements are significantly more restrictive and require specialist endocrinology assessment.
Australian patient resources
- NDSS — registration, education, subsidised supplies, helpline
- Diabetes Australia — peak body; advocacy, education, state organisations
- JDRF Australia — research, peer support, T1D Family Centre, closed-loop advocacy
- HealthDirect — Type 1 diabetes
E. Special populations
Pregnancy. Pre-conception care is essential: achieve HbA1c below 6.5% before conception; start folate 5 mg daily; obtain retinal review before and during pregnancy; optimise CGM and consider pump initiation with specialist team. Insulin requirements increase throughout pregnancy. Closed-loop systems are showing benefit in pregnancy outcomes in emerging trial data. Gestational endocrinology and shared maternity care are required.
Children and adolescents. Paediatric diabetes team-led care; pump and CGM access is well-supported. Transition to adult services is a high-risk period — young people commonly disengage and glycaemic control deteriorates. Eating disorders (including “diabulimia”) are most prevalent in this group. General practice plays a supportive role during transition.
Older adults. Relaxed glycaemic targets (HbA1c 8–8.5%) are appropriate in the context of frailty, cognitive impairment, or limited life expectancy, where the risks of hypoglycaemia outweigh the long-term microvascular benefits of tight control. Severe hypoglycaemia is associated with cognitive harm. Deprescribing of insulin may be relevant in end-of-life care.
Sport and exercise. Exercise lowers blood glucose and increases hypoglycaemia risk during and after activity — particularly after prolonged aerobic exercise. Strategies include reducing basal insulin, consuming carbohydrate before and during exercise, and checking CGM alerts. CGM is particularly useful during sport.
When to escalate
Send to emergency department immediately for:
- Suspected DKA — blood glucose above 14 mmol/L, blood ketones above 1.5 mmol/L, vomiting, drowsiness, or Kussmaul breathing (deep, sighing respirations)
- Severe hypoglycaemia with altered consciousness — administer glucagon while calling 000
- Any unexplained deterioration in a person with type 1 diabetes
Refer to endocrinologist urgently when:
- HbA1c is above 9% despite current management
- Recurrent severe hypoglycaemia or significant hypoglycaemia unawareness
- Preparing for pregnancy or newly pregnant
- Considering insulin pump or closed-loop system
- Suspected LADA in an adult initially diagnosed with type 2 diabetes — autoantibodies and C-peptide will guide the diagnosis
What this article is and is not
This article draws on current Australian guidelines — Australasian Diabetes Society, NDSS, Therapeutic Guidelines (eTG), RACGP, and Diabetes Australia resources — to provide general health information about type 1 diabetes and shared care with general practice. It is not personal medical advice and does not create a doctor–patient relationship.
All decisions about insulin dose adjustments, choice of technology, and specialist referral are made with your diabetes team and GP based on your individual management plan.
For consumer-friendly information: NDSS, Diabetes Australia, JDRF Australia, HealthDirect.
Sources cited
- Australasian Diabetes Society — Type 1 diabetes management
- NDSS — National Diabetes Services Scheme
- Therapeutic Guidelines (eTG) — Type 1 diabetes
- RACGP — Diabetes management resources
- Diabetes Australia
- JDRF Australia
- HealthDirect — Type 1 diabetes
- ADA Standards of Care in Diabetes
- DCCT Research Group — NEJM 1993
Frequently asked questions
-
What is the difference between type 1 and type 2 diabetes?
Type 1 diabetes is an autoimmune condition: the immune system destroys the insulin-producing cells in the pancreas, causing complete insulin deficiency. It is not caused by diet or weight and occurs at any age, though peak onset is between 5 and 14 years. Type 2 diabetes involves insulin resistance — the body cannot use insulin efficiently — and develops over years, strongly linked to weight, inactivity, and family history. Treatment is fundamentally different: type 1 always requires insulin; type 2 is usually managed first with lifestyle changes and oral medications, with insulin added if needed. Neither is anyone's fault.
-
Is CGM (continuous glucose monitoring) available on the NDSS?
Yes. Since 1 July 2022, CGM is fully subsidised for all Australians with type 1 diabetes through the National Diabetes Services Scheme (NDSS), regardless of age or management complexity. Previously subsidised only for children and those with complex management, the expansion means that CGM sensors — Dexcom G6/G7 and FreeStyle Libre 2/3 — are now available at subsidised cost to anyone with type 1 diabetes registered with the NDSS. CGM measures glucose continuously and can alert to impending hypoglycaemia, reducing the risk of severe low blood sugar events, and provides time-in-range data that guides insulin adjustments.
-
What are the annual review items in type 1 diabetes shared care?
Annual review in type 1 diabetes is a structured checklist covering: HbA1c (target typically <7.0% / 53 mmol/mol for adults); blood pressure and cholesterol; urine albumin-to-creatinine ratio (UACR) and kidney function (eGFR); retinal photograph or eye examination; peripheral neuropathy screening (monofilament test, vibration sense); foot examination; mental health screening for depression, diabetes distress, and eating disorders (including insulin omission for weight loss); thyroid function (TSH) and coeliac serology — both autoimmune conditions are more common in type 1 diabetes; vaccination status; and review of the sick day plan and driving requirements.
-
What should I do if I am sick and cannot eat — do I stop my insulin?
Never stop insulin in type 1 diabetes, even if you cannot eat. Without insulin, the body breaks down fat for energy, producing ketones — this can lead to diabetic ketoacidosis (DKA), a life-threatening emergency. The sick day rule for type 1 is: check your blood glucose or CGM hourly; check ketones with blood or urine strips; continue your basal insulin and adjust your correction doses as directed in your sick day plan; drink plenty of fluids; and seek help urgently if your blood glucose is above 15 mmol/L with ketones ≥1.5 mmol/L, or if you cannot keep fluids down. Your diabetes team should have given you a written sick day plan — keep it accessible.
-
What are the driving rules for people with type 1 diabetes on insulin?
Austroads 2022 sets specific requirements for people with type 1 diabetes driving on a private licence: check your blood glucose (or CGM reading) and confirm it is 5 mmol/L or above before every drive; carry glucose in the car at all times; recheck every two hours on long trips; stop and treat immediately if glucose falls below 5 mmol/L; wait at least 45 minutes after treating a low before resuming driving. For a commercial licence (truck, bus, taxi), requirements are considerably more restrictive and require specialist endocrinology assessment. These rules exist because hypoglycaemia impairs concentration and reaction time.
-
What is LADA and how does it differ from typical type 2 diabetes?
LADA — Latent Autoimmune Diabetes of Adults — is a slowly progressing form of type 1 diabetes that begins in adulthood, often after age 30, and is frequently misdiagnosed as type 2 diabetes. People with LADA are typically leaner than those with type 2, may have a personal or family history of autoimmune conditions, and tend to respond poorly to oral diabetes medications over months to years. The distinguishing tests are a positive autoantibody (particularly GAD antibody) and a low or falling C-peptide level, confirming declining beta-cell function. Early identification matters because appropriate insulin treatment from the outset avoids the progressive deterioration seen when LADA is treated as type 2.
Source quality
Sources grouped by evidence tier. AU primary tier first; international where AU is silent or lagging; named-author reconstruction where guidelines have not yet caught up. How tiers work.
-
T1 AU primary 7 sources -
T2 International primary 1 source -
T3 Named-author reconstruction 1 source