Hypoglycaemia occurs when a person’s blood glucose level (BGL) drops to a very low level (below 4 mmol/L) (Diabetes Australia 2024).
How Does the Body Respond to Hypoglycaemia?
The body’s most important glucose sensors are located in the brain (the brainstem and hypothalamus), with 30% of blood glucose being used to sustain normal brain activity (Amiel 2021).
When the brain is starved of energy, it will start to shut down certain areas that control memory and balance and stimulate hunger. The brain will also release stress hormones. Following treatment of a hypo, it can take 40 minutes to re-establish full brain function.
It’s crucial to treat hypoglycaemia quickly in order to prevent the person’s BGL from continuing to decrease, which can cause them to become seriously unwell (Diabetes Australia 2024).
It’s also important to be aware that not all people with diabetes can experience hypoglycaemia. Those treated with either insulin or sulfonylurea tablets (gliclazide, glimepiride, glipizide, glibenclamide) are at risk of hypoglycaemia. The remaining glucose-lowering medicines do not cause hypoglycaemia.
How Serious is Hypoglycaemia?
Hypoglycaemia is a significant contributor to morbidity and mortality. In US hospitals, admission trends between 1999 to 2011 showed a reduction in hyperglycaemia presentations but an increase in hypoglycaemia (Lipska et al. 2014).
English hospital admission data for hypoglycaemia between 2005 and 2014 shows that 72% (72,568 admissions) occurred in people aged 60 years or older, whilst nearly one in five people had more than one admission during this nine-year period (Zaccardi et al. 2016).
Hypoglycaemia can be classified into 3 levels:
Glycaemic criteria/description
Level 1
BGL < 3.9 mmol/L
Level 2
BGL < 3.0 mmol/L
Level 3
A severe event characterised by altered mental and/or physical status requiring assistance for treatment.
(ADA 2021)
The fear and anticipation of hypoglycaemia impacts the self-management of a person with diabetes and often prevents them from achieving optimal glycaemic control. Amiel (2021) explains that for people with diabetes, hypoglycaemia may be better defined by the degree of distress and disruption each episode causes, ranging from ingesting carbohydrate when not wishing to do so, to the acute stress response symptoms, and in some cases, confusion and coma.
What Causes Hypoglycaemia?
Hypoglycaemia risk can be divided into key areas for people with diabetes who are prescribed either insulin or a sulfonylurea agent:
Incorrect type of insulin or glucose-lowering medication prescribed and administered
Change of insulin administration site
Intravenous insulin with or without glucose infusion
Failure to monitor BGLs adequately whilst intravenous insulin infusion is in situ
Inadequate mixing of intermediate or pre-mixed insulins
Sudden discontinuation of long-term corticosteroids
Recovery from acute illness or stress
Mobilisation after illness
Major limb amputation.
Carbohydrate intake issues:
Missed or delayed meals
Less carbohydrate than normal
Change in the timing of the biggest meal of the day
Lack of access to usual between-meal or bedtime snacks
Prolonged starvation or fasting time
Vomiting
Reduced appetite.
Enteral/parenteral feeding issues:
Blocked/displaced tube
Change in feed regimen
Discontinuation of enteral feed
Discontinuation of TPN or IV glucose
Insulin or sulfonylurea medicines administered at an inappropriate time to feed regimen
Feed intolerance.
(JBDS-IP 2023)
When people who have diabetes use the same spot to inject insulin, they can develop fibrous and hardened areas. Therefore, the insulin does not get absorbed from that site, causing the patient to increase their dose. If the patient then administers that higher dose of insulin in a non-affected area, they are at risk of a severe hypo, because they are absorbing 100% of that insulin, as opposed to injecting it into the affected areas of lipohypertrophy.
Those with impaired renal function, including patients on haemodialysis, will have an increased hypo risk. This is because people need less insulin once they’re on dialysis. Furthermore, as the kidneys (or renal function) deteriorate, they are unable to remove the byproducts of these medicines.
Individuals with chronic kidney disease, heart failure and/or cardiovascular disease have a higher rate of severe hypos than those without comorbidity.
Hypoglycaemia in People with Type 1 Diabetes
People with type 1 diabetes experience around two episodes of mild hypoglycaemia every week. The annual prevalence of severe hypos in people with type 1 diabetes is close to 30%. Factors such as how long the person has had the condition may increase their risk.
People with type 1 diabetes are highly likely to have a hypo (83%). 40% of those people will experience hypos at night and 15% of these cases will be deemed severe (Frier 2014).
Hypoglycaemia in People with Type 2 Diabetes
Adults with insulin-treated type 2 diabetes experience a lower frequency of mild and severe hypoglycaemia episodes compared to those with type 1. However, the frequency of those hypos rises progressively the longer they are treated with insulin (Frier 2014).
In people with type 2 diabetes, less than half will experience a hypo over a month. Only 15% will experience them at night, and a much lower number (8%) will experience a severe hypo.
Patients with insulin-treated type 2 diabetes are more likely to require hospital admission for a severe hypoglycaemic episode compared to those with type 1 diabetes (Frier 2014).
Signs and Symptoms of Hypoglycaemia
Autonomic symptoms
Neuroglycopenic symptoms
Pallor
Sweating
Shaking
Impaired attention and cognition
Tingling of mouth/fingers
Anxiety
Palpitations
Dizziness
Hunger
Impaired/double vision
Slurred speech
Disorientation and confusion
Inappropriate behaviour
Coma
Seizures
(Tauchmann 2024)
In addition, headache (especially frontal) and nausea can also be experienced.
Management of Hypoglycaemia
Treatment of hypoglycaemia will depend on four factors:
Is the patient conscious and cooperative?
Is the patient on an insulin infusion?
Is the patient nil by mouth or nil by tube?
Is the patient receiving food orally or by tube?
It is vital to remember that you are treating low blood glucose, not low blood sugar. According to the American Diabetes Association Standards of Medical Care (2021), hypoglycaemic treatment with pure glucose is the preferred option as it correlates with a quicker response compared to carbohydrate foods.
One tube of oral glucose gel (now available in a variety of flavours)
Glucose tablets or glucose chews equivalent to 15 grams of carbohydrate (now available in a variety of flavours).
In the absence of available glucose, consume 15 grams of fast-acting carbohydrate. Examples include:
150 ml regular (non-diet) soft drink
Three teaspoons of sugar or honey
125 ml fruit juice
Note: Chocolate is no longer recommended due to its high fat content, which slows down the absorption of carbohydrates.
Wait 15 minutes and then check BGL.
Step 2: If BGL is still 4.0 mmol/L or less, repeat step 1 (or step 2 if glucose is not available) and recheck blood glucose in 15 minutes.
Step 3: If BGL has increased to above 4 mmol/L, consume a nutritious meal to maintain BGL.
If the next meal is more than an hour away, consume a snack containing 15 grams of longer-acting carbohydrate. Examples of snacks include:
One slice of bread
One glass of milk
One piece of fruit
Two to three pieces of dried apricots, figs or other dried fruit
One tablespoon of sultanas
One tub of natural low-fat yoghurt.
(NDSS 2022; JBDS-IP 2023; Better Health Channel 2021; CDC 2024)
For patients prescribed a thickened fluid/vitamised diet, initial hypoglycaemia treatment requires one tube of oral glucose gel that can be squeezed onto a spoon for ease of use. The use of thickened cordial or adding sugar to vitamised food will delay the initial reversal of hypoglycaemia. If BGL has risen above 4.0 mmol/L, the patient should consume a meal or a 15 g snack (if their next meal is more than an hour away) within 15-20 minutes. Ensure the meal or snack is appropriately prepared in line with the patient’s texture modification requirements (Better Health Channel 2021).
For patients on enteral tube feeding, initial treatment of 15 g glucose powder administered by the tube and flushed with 40 to 50 ml to prevent tube blockage should be administered. If BGL has risen above 4.0 mmol/L, commence the next feed within 15 to 20 minutes.
If BGL is under 4 mmol/L and the patient is nil by mouth or nil by tube:
Contact the doctor urgently and if IV access is in situ, administer 30 ml 50% glucose as a slow IV push. If no IV access, administer 1 mg glucagon IM.
Commence or revise IV glucose infusion.
Recheck BGLs in 15 minutes.
If BGL remains < 4.0 mmol/L, repeat initial treatment. If BGL is > 4.0 mmol/L, follow up with oral carbohydrate or IV glucose.
If BGL is under 4 mmol/L and the patient is on an insulin infusion:
Stop insulin infusion, continue glucose infusion and contact the doctor urgently.
If the patient is nil by mouth, administer 30 ml 50% glucose as a slow IV push. If the patient is not nil by mouth, implement usual oral hypo treatment.
Recheck BGL in 15 minutes.
If BGL < 4.0mmol/L, repeat initial treatment. If BGL > 4.0 mmol/L, revise insulin infusion rate and concurrent glucose infusion.
Recommence insulin infusion and glucose infusion at adjusted rate for 15 minutes after the hypoglycaemic event has resolved.
If BGL is under 4 mmol/L and the patient is not conscious or cooperative, is drowsy or is unable to swallow in a subacute setting:
Place the person on their side, ensuring their airway is clear.
Administer 1 mg glucagon IM if available and trained to do so.
Call the ambulance on triple zero (000) and state ‘diabetic emergency’.
Stay with the person and monitor airway and cardiac status.
Notify the treating doctor.
If the patient regains consciousness before the ambulance arrives, give 15 g of fast-acting carbohydrate.
Recheck BGL and if < 4.0 mmol/L and safe to do so, give another 15 g of fast-acting carbohydrate.
Repeat BGL checks every 15 minutes until the ambulance arrives.
The Impacts of Hypoglycaemia
A cumulative impact of hypoglycaemia exists that can include:
Societal impacts:
Loss of driving privileges
Restricted employment
Breakdown of family relationships and restricted access to children
Carer stress and burden
Additional home based resources/services or relocation to residential care.
Economic impacts:
Additional medical care costs
Time lost from work
Costs of accidents (road/workplace) occurring as a result of hypoglycaemia.
Impaired awareness of hypoglycaemia:
Occurring as a result of recurrent hypoglycaemia.
Future mortality:
Severe hypoglycaemia is estimated to be associated with an increased future mortality risk of 50 to 600%.
Cognitive function:
Recurrent hypoglycaemia in children may have a lasting impact on cognition as adults
There is a relationship between dementia and hypoglycaemia in older adults with diabetes.
(Amiel 2021)
It’s helpful and useful to acknowledge the fears and concerns people with diabetes have towards hypoglycaemia. Self-management behaviour can change as a result, for example, suboptimal dosing of insulin, overeating and avoiding social situations or sporting activities.
Wearable technology such as continuous glucose monitoring with alarm alerts for low blood glucose levels has significantly reduced the number of hypoglycaemic events by notifying when blood glucose levels reach a specified level.
Smart insulin pumps and hybrid closed-loop systems also reduce the time spent in a hypoglycaemic range. With the future development of full closed-loop systems, technology will adapt to the individual's changing insulin demands, taking into account meals, exercise, emotions and stress (Mathieu 2021).
The future may include ‘smart’ insulin that is activated/deactivated depending on ambient glucose levels, thus eliminating the risk of hypoglycaemia.
Lipska, KJ, Ross, JS & Wang, Y 2014, ‘National Trends in US Hospital Admissions for Hyperglycemia and Hypoglycemia Among Medicare Beneficiaries, 1999 to 2011’, JAMA Intern Med., vol. 174, no. 17, pp. 1116-1124, viewed 20 August 2024, https://jamanetwork.com/journals/jamainternalmedicine/article-abstract/1871566