Blood glucose <4.0 mmol/L (<72 mg/dL) in patients with diabetes. Some guidelines define the threshold as <3.9 mmol/L. In non-diabetic individuals, hypoglycaemia is defined by Whipple's Triad: low glucose + symptoms + resolution with glucose.
Earlier warning signs — triggered by catecholamine release
- Tremor / shakiness
- Diaphoresis (sweating)
- Palpitations / tachycardia
- Anxiety / feeling of dread
- Hunger / nausea
- Pallor
- Paraesthesia (tingling lips)
Later, more dangerous signs — inadequate CNS glucose
- Confusion / cognitive impairment
- Slurred speech
- Blurred / double vision
- Difficulty concentrating
- Focal neurological deficits (stroke mimic)
- Seizure
- Loss of consciousness / coma
| Hormone | Source | Effect |
|---|---|---|
| Glucagon | Pancreatic alpha cells | Stimulates hepatic glycogenolysis & gluconeogenesis |
| Adrenaline | Adrenal medulla | Glycogenolysis, lipolysis; triggers autonomic symptoms |
| Cortisol | Adrenal cortex | Gluconeogenesis, reduces peripheral glucose uptake |
| Growth Hormone | Anterior pituitary | Anti-insulin effects, promotes lipolysis |
Glucagon response is lost early in T1DM (within 5 years). Adrenaline response diminishes later — leading to hypoglycaemia unawareness, where patients lose autonomic warning symptoms.
- Loss of autonomic warning symptoms
- Patient does not recognise hypoglycaemia until neuroglycopenic
- Higher risk of Level 2 and Level 3 events
- Caused by recurrent hypoglycaemia lowering the glycaemic threshold for counterregulation
- Management: relax glucose targets, use CGM with alarms, consider DAFNE education programme
- Often undetected during sleep
- Somogyi Effect: rebound hyperglycaemia next morning due to counterregulatory response
- Suspect if: nightmares, morning headaches, high fasting glucose despite evening insulin
- CGM is gold standard for detection
| Cause | Mechanism / Notes |
|---|---|
| Excess insulin dose | Injection error, incorrect calculation |
| Wrong insulin type | High Risk Mix-up e.g. Humulin M3 (premix) vs Humulin S (short-acting). Always double-check |
| Timing mismatch | Rapid-acting insulin given without subsequent meal |
| Accidental double dose | Patient or carer administered second dose — common cause in hospital |
| IM injection | Faster absorption than SC — especially in thin patients or using long needles |
| Lipohypertrophy | Variable absorption from affected sites — erratic glucose control |
| Exercise without adjustment | Increased insulin sensitivity; delayed effect up to 24h post-exercise |
Sulphonylureas (e.g., glibenclamide, glipizide, gliclazide) stimulate insulin secretion regardless of glucose level. Hypoglycaemia may be prolonged (hours–days) requiring continuous dextrose infusion and hospital admission.
| Factor | Detail |
|---|---|
| Prolonged action | Glibenclamide (half-life up to 45h) — avoid in elderly |
| Renal impairment | Reduced clearance → accumulation → severe prolonged hypoglycaemia |
| Erratic eating | Missed meals with full sulphonylurea effect |
| Drug interactions | Fluconazole, fibrates, NSAIDs potentiate sulphonylurea effect |
| Alcohol | Inhibits hepatic gluconeogenesis — synergistic risk |
- Insulin not withheld or adjusted before procedure
- Patient taken to theatre late without interim glucose
- Ensure VRIII (variable rate insulin infusion) or basal-bolus adjustment protocol followed
- Check glucose pre-op and every 1–2h intra-op
- Feed interruption while insulin (bolus or infusion) continues running
- Nasogastric tube dislodged or blocked
- Feed rate reduced without adjusting insulin
- Check glucose at least every 4–6h in enterally-fed patients on insulin
- High-dose steroids cause hyperglycaemia → insulin prescribed
- Steroids tapered or stopped → hyperglycaemia resolves → insulin dose not reduced
- Review insulin at every steroid dose change
- If Dexamethasone given once daily (usually morning), glucose peaks in afternoon
- Patient admitted for poor oral intake — insulin increased
- Discharged on increased dose without review
- Always reconcile insulin dose at discharge against usual home dose
| Group | Risk Factor | Action |
|---|---|---|
| Elderly patients | Impaired counterregulation, renal impairment, polypharmacy, reduced hypoglycaemia awareness | Relaxed targets (HbA1c 7.5–8%), avoid glibenclamide, consider CGM |
| Longstanding T1DM | Hypoglycaemia unawareness, absent glucagon response | Relaxed targets, CGM with low alarms, hypoglycaemia awareness training |
| Tight glycaemic control | Narrowed margin; intensive insulin regimens | Structured education (DAFNE), CGM, frequent SMBG |
| Chronic Kidney Disease | Reduced insulin clearance, reduced gluconeogenesis, reduced renal glucose release | Reduce insulin doses (eGFR <30), avoid sulphonylureas (except gliquidone), monitor frequently |
| Liver disease (cirrhosis) | Reduced glycogen storage, impaired gluconeogenesis | Frequent monitoring, reduce insulin doses, nutritional support |
| Alcohol misuse | Suppresses hepatic gluconeogenesis; masked by symptoms | Never attribute confusion to intoxication without checking glucose first |
Ramadan fasting (typically 12–16 hours) significantly alters meal timing and carbohydrate distribution. Patients on insulin or sulphonylureas are at high risk of hypoglycaemia at pre-iftar (end of fast) and post-suhoor periods. Pre-Ramadan structured assessment and dose adjustment is essential. Break fast immediately if glucose <4.0 mmol/L. See Tab 4 for management protocols.
Community / Home
- ● 150–200 mL fruit juice (no added sugar variety)
- ● 150–200 mL regular (non-diet) cola
- ● 3–4 glucose tablets
- ● 5 jelly babies
- ● 1 tablespoon of sugar/honey dissolved in water
Hospital
- ● GlucoGel (40% dextrose oral gel) — 2 tubes = ~20g glucose; can be applied buccally if slightly impaired swallow but some protection reflex present
- ● Glucose tablets (Dextro Energy)
- ● 200 mL Lucozade Original
- ● 200 mL orange juice
After BG rises >4.0 mmol/L — give a long-acting carbohydrate snack: 2 biscuits, 1 slice bread/toast, a sandwich, or next meal if due within 30 minutes. This prevents recurrence as the fast-acting sugar effect wanes.
- 75–100 mL of 20% glucose IV (preferred concentration)
- Avoid 50% dextrose — highly hypertonic, severe vein irritant, risk of thrombophlebitis and extravasation injury
- Administer over 10–15 minutes via large vein
- Recheck glucose 15 minutes post-infusion
- Repeat if glucose <4.0 mmol/L
- If no IV access: glucagon IM
- Use when IV access unavailable
- Stimulates hepatic glycogenolysis — requires intact glycogen stores
- NOT reliable in sulphonylurea hypoglycaemia — limited glycogen stores, stimulates endogenous insulin
- NOT effective in malnourished patients, liver disease, or after prolonged fasting
- May cause nausea/vomiting on recovery
- Available as: GlucaGen HypoKit (1mg vial)
- Patient may take 10–15 min to respond
Risk of aspiration pneumonia. Establish IV access. Place in recovery position if airway at risk. Call for urgent medical assistance.
- Admit to hospital — observation for minimum 24h (longer for long-acting agents)
- Continuous IV glucose infusion (10% dextrose) — titrate to maintain BG 6–10 mmol/L
- Octreotide (somatostatin analogue) — suppresses ongoing sulphonylurea-driven insulin secretion; 50–100 mcg SC/IV TID
- Activated charcoal if within 1h of ingestion (overdose scenario)
- Notify endocrinology/diabetology team
- Review renal function (dose reduction/agent change on discharge)
Ensure patient eats regular meal within 30–60 min of recovery to stabilise glucose
Check every 30–60 min until glucose stable >5.0 mmol/L for 2 readings
All Level 2 and Level 3 episodes require senior review. Complete incident report for all in-hospital hypoglycaemia.
Insulin dose adjustment, sulphonylurea review, timing correction, patient education
Suspend pump during active hypoglycaemia. Do not resume until glucose >5.0 mmol/L and patient has eaten. Notify pump team for basal rate review.
Time of event, glucose value, symptoms, treatment given, response time, post-treatment glucose, actions taken, patient education provided
- Recognise early autonomic warning symptoms
- Always carry fast-acting glucose (glucose tablets, juice)
- Inform family/colleagues of hypoglycaemia recognition and glucagon use
- Medical ID bracelet / diabetes alert card
- DAFNE (Dose Adjustment For Normal Eating) programme
- SMBG (Self-monitoring blood glucose): before meals, 2h post-meal, bedtime, before driving
- CGM with low glucose alarms (<4.0 mmol/L threshold)
- Hybrid closed-loop systems reduce nocturnal hypoglycaemia significantly
- Check glucose before exercise and adjust carbohydrate/insulin
- Avoid glibenclamide in elderly and those with CKD
- Review insulin doses at every clinic visit
- Rotate injection sites — prevent lipohypertrophy
- Consistent injection technique and site
- SGLT2 inhibitors and GLP-1 agonists have low intrinsic hypoglycaemia risk
Even if not eating, T1DM patients MUST continue insulin to prevent diabetic ketoacidosis (DKA). Illness typically increases insulin requirements due to counterregulatory hormone release.
- Continue basal insulin — may need to increase
- Correct high glucose with additional rapid-acting insulin
- Check blood ketones every 2–4h if glucose >14 mmol/L
- Maintain fluid intake (water, sugar-free fluids)
- If eating reduced: replace meals with carbohydrate-containing drinks
- Contact diabetologist / diabetes specialist nurse if ketones >1.5 mmol/L
- Seek emergency care if vomiting, unable to keep fluids down
- Hold SGLT2 inhibitors during illness (DKA risk, dehydration)
- Hold metformin if vomiting/dehydration (lactic acidosis risk)
- Sulphonylureas: omit if not eating
- Continue basal insulin at reduced dose if eating less
- Monitor glucose more frequently
Islamic scholars unanimously permit (and many consider obligatory) breaking the fast if blood glucose falls below 4.0 mmol/L, rises above 16.7 mmol/L, or if the patient feels unwell. Illness negates the obligation to fast (Quran 2:185). Medical teams should reinforce this ruling.
- Classify risk: very high, high, moderate, low
- HbA1c, renal function, CGM/SMBG review
- Structured education on dose adjustments, glucose targets, when to break fast
- Discuss with patient their intention and ability to fast safely
- Review all diabetes medications
- Sulphonylureas: Reduce dose or avoid; shift main dose to iftar. Glibenclamide — avoid entirely
- Basal insulin: Reduce by 20–30% and shift timing to post-iftar or pre-suhoor
- Premix insulin: Reduce morning (suhoor) dose; adjust evening (iftar) dose
- SGLT2 inhibitors: Consider holding (dehydration risk, DKA)
- Metformin, DPP-4 inhibitors, GLP-1: Usually safe; adjust timing to iftar
- Break immediately if glucose <4.0 mmol/L — treat hypoglycaemia first
- Break if glucose <4.0–4.9 mmol/L and in first few hours of fast (likely to worsen)
- Break if glucose >16.7 mmol/L — check ketones, seek medical advice
- Break if feeling unwell, dizzy, or displaying any hypoglycaemia symptoms
- Document and reassess daily during Ramadan
- General ward: 6–10 mmol/L (NICE NG17)
- Acceptable range: 4–12 mmol/L (if targets not immediately achievable)
- Critically ill (ITU): 6–10 mmol/L (ADA/AACE joint guidelines)
- Avoid: <4.0 mmol/L or >12 mmol/L for prolonged periods
- Review insulin at every meal round
- Pre-op fasting glucose check — delay surgery if <4.0 or >12 mmol/L
- T1DM: always use VRIII (variable rate insulin infusion / sliding scale) during prolonged fasting
- T2DM on insulin: VRIII or modified basal-bolus approach depending on local protocol
- T2DM on oral agents: omit morning doses; restart when eating and drinking normally
- Hourly glucose monitoring intra-operatively when on VRIII
- First on operating list preferred to minimise fasting time
| Type | Examples | Key Feature |
|---|---|---|
| rtCGM Real-time CGM | Dexcom G6/G7, Medtronic Guardian 3/4 | Continuous automatic reading every 5 min; alarms for high/low; no scan required |
| isCGM Intermittent scan CGM | FreeStyle Libre 2 / Libre 3 | Requires scan (phone/reader) to get reading; Libre 2/3 also has optional alarms; Libre 3 continuous transmission |
Measures interstitial glucose (not blood glucose directly) via a small sensor wire inserted subcutaneously. There is a 5–10 minute physiological lag between blood glucose and interstitial glucose. Calibration: Dexcom G7 factory-calibrated; Medtronic Guardian requires fingerstick calibration.
| Arrow | Meaning | Nursing Action |
|---|---|---|
| → Horizontal | Stable — changing <1 mmol/L per 15 min | No immediate action unless at threshold |
| ↗ Slight rise | Rising 1–2 mmol/L per 15 min | Monitor; consider pre-meal rapid insulin if appropriate |
| ↑ Rising rapidly | Rising >2 mmol/L per 15 min | Check for missed dose; notify medical team if >12 mmol/L |
| ↘ Slight fall | Falling 1–2 mmol/L per 15 min | Give snack if borderline; increase monitoring frequency |
| ↓ Falling rapidly | Falling >2 mmol/L per 15 min | Act now — treat as hypoglycaemia even if not yet <4.0 mmol/L |
| ↓↓ Very rapid fall | Falling >3 mmol/L per 15 min | Urgent — treat immediately, notify team, prepare IV glucose |
A glucose of 5.2 mmol/L with rapid downward arrows (↓↓) requires immediate treatment. The patient will likely be <4.0 mmol/L within 10–15 minutes. Do not wait for the alarm to trigger.
TIR measures the percentage of time glucose is within target range (3.9–10.0 mmol/L / 70–180 mg/dL). Agreed by international consensus (Battelino et al. 2019).
| Patient Group | TIR Target | TBR Target | TIR Target (Elderly/High-Risk) |
|---|---|---|---|
| T1DM | >70% | <4% (<3.9), <1% (<3.0) | >50% (relaxed) |
| T2DM on insulin | >70% | <4% | >50% (relaxed) |
| Pregnancy (T1DM) | >70% (3.5–7.8 mmol/L) | <4% | N/A |
| Critically ill | N/A — use point-of-care BG | Avoid <4.0 mmol/L | N/A |
- Delivers rapid-acting insulin continuously as basal rate (unit/hour, customisable)
- Bolus delivered for meals (calculated by pump wizard using carb ratio, ISF, active insulin)
- Sick day rules: Never leave CSII interrupted for >2 hours without giving subcutaneous injection — risk of DKA rapid onset (no long-acting insulin reservoir)
- Infusion site change every 2–3 days
- Hospital: document pump settings; involve DSN; do not arbitrarily stop pump
- CGM + insulin pump + algorithm communicating automatically
- Algorithm adjusts basal rate in real-time to maintain glucose in range
- Examples: Medtronic MiniMed 780G, Tandem Control-IQ, CamAPS FX
- Significantly reduces nocturnal hypoglycaemia and TBR
- Still requires patient bolus for meals (hybrid, not fully closed)
- If CGM and capillary BG agree within 1.0 mmol/L — use CGM-guided trend arrows with confidence
- If discordant by >1.5 mmol/L — use capillary glucose for treatment decisions
- Always use capillary BG to confirm before treating severe hypoglycaemia (Level 2–3) if time allows
- Discordance common with: rapid glucose change, poor sensor placement, oedema, peripheral shutdown
Mean Absolute Relative Difference (MARD) <10% considered clinically adequate. Dexcom G7: MARD ~8.2%. FreeStyle Libre 3: MARD ~7.9%. Accuracy is lower at extremes of glucose range (hypoglycaemia and hyperglycaemia >20 mmol/L).
- Patients on dexamethasone (e.g., for multiple myeloma, post-transplant) during Ramadan
- Dexamethasone given post-iftar to minimise fasting hours of hyperglycaemia
- Insulin requirement peaks 6–12h after dexamethasone dose — anticipate and adjust
- Requires daily review and flexible insulin protocols during Ramadan
- Coordinate with haematology/oncology teams
- DHA (Dubai): Dubai Health Authority — exam and licensing authority for Dubai
- DOH (Abu Dhabi): Department of Health Abu Dhabi — licensing authority
- SCFHS (Saudi Arabia): Saudi Commission for Health Specialties — exam body for Saudi healthcare workers
- All follow international evidence-based guidelines (NICE, ADA, IDF)
- Localised diabetes guidelines for Ramadan: IDF-SACA Ramadan Guidelines
| Topic | Key Point to Remember |
|---|---|
| Hypoglycaemia definition | <4.0 mmol/L in diabetics; Level 1 <3.9, Level 2 <3.0, Level 3 = any with severe cognitive impairment |
| Rule of 15 | 15g carbohydrate → 15 min wait → recheck; repeat if still <4.0; always follow with long-acting carb |
| 50% dextrose | Avoid — use 20% dextrose 75–100 mL instead; 50% causes vein damage |
| Glucagon limitations | NOT reliable in sulphonylurea OD, liver disease, malnourishment — limited glycogen stores |
| Sulphonylurea hypoglycaemia | Most dangerous — prolonged; needs octreotide + continuous dextrose infusion + hospital admission |
| Hypoglycaemia unawareness | Loss of autonomic warnings in longstanding T1DM; treated by relaxing targets, CGM, education |
| Somogyi effect | Nocturnal hypoglycaemia → rebound morning hyperglycaemia; diagnose with CGM or 3am glucose check |
| Stroke vs hypoglycaemia | Always check BG before assuming stroke — focal neurology can be neuroglycopenic |
| Insulin in T1DM sick days | NEVER stop insulin in T1DM illness — risk DKA; increase monitoring; check ketones |
| Ramadan — break fast | BG <4.0 mmol/L or >16.7 mmol/L → must break fast; Islam permits this for medical necessity |
| CGM arrows | Rapid fall (↓↓) = treat now even if glucose borderline; do not wait for alarm |
| CSII pump failure | DKA within hours (no long-acting insulin depot); never interrupt CSII >2h without injection |
| Time In Range | Target >70% in 3.9–10 mmol/L; TBR <4% <3.9 mmol/L; <1% <3.0 mmol/L |
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