DKA — Diabetic Ketoacidosis
| Parameter | Threshold |
|---|---|
| Blood Glucose | >11 mmol/L |
| Blood Ketones | ≥3 mmol/L |
| Urinary Ketones | ≥++ (alternative if blood ketones unavailable) |
| pH | <7.3 |
| Bicarbonate | <15 mmol/L |
| Severity | pH | Bicarbonate | Ketones | Management |
|---|---|---|---|---|
| Mild | 7.25–7.30 | 15–18 mmol/L | 3–6 mmol/L | Ambulatory management possible |
| Moderate | 7.00–7.24 | 10–14 mmol/L | 3–6 mmol/L | Ward admission |
| Severe | <7.00 | <10 mmol/L | >6 mmol/L | HDU / ICU |
- Rate: 0.1 units/kg/hr Actrapid in 0.9% NaCl (1 unit/mL)
- Continue until: pH >7.3 AND bicarbonate >18 AND ketones <0.6 mmol/L
- Do NOT stop insulin simply because glucose normalises
- When glucose falls to <14 mmol/L: add 10% dextrose at 125 mL/hr alongside continued 0.9% NaCl
Recheck serum K+ every 1–2 hours
| Serum K+ | Action |
|---|---|
| < 3.5 mmol/L | 40 mmol/hr K+ replacement — senior review required before giving |
| 3.5–5.5 mmol/L | Add 40 mmol to each litre of IV fluid |
| > 5.5 mmol/L | No K+ replacement — recheck in 1 hour |
Resolution criteria (all must be met)
- pH >7.3
- Bicarbonate >18 mmol/L
- Blood ketones <0.6 mmol/L
- Glucose stabilising
Transition protocol
- Patient eating and drinking
- Give long-acting SC insulin (basal dose)
- Wait 30–60 minutes (overlap period — essential)
- Stop FRII
HHS — Hyperosmolar Hyperglycaemic State
| Parameter | Threshold |
|---|---|
| Blood Glucose | >30 mmol/L |
| Plasma Osmolarity | >320 mOsm/kg |
| Ketonaemia | Absent or minimal |
| Acidosis | Absent (pH >7.3) |
Formula: 2(Na + K) + Urea + Glucose
| Feature | HHS | DKA |
|---|---|---|
| Typical patient | Elderly T2DM | T1DM (any age) |
| Onset | Days to weeks | Hours |
| Glucose | >30 mmol/L | >11 mmol/L |
| Ketones | Absent/minimal | ≥3 mmol/L |
| Acidosis | No | Yes (pH <7.3) |
| Fluid deficit | 8–10 L | 3–6 L |
| Osmolarity | >320 mOsm/kg | Usually normal–mildly elevated |
| VTE/stroke risk | Very high | Moderate |
| Initial presentation | Often first diagnosis of DM | Known T1DM usually |
- Start: 0.9% NaCl 1 L over 1 hour, then reassess
- Correct osmolarity at <10 mOsm/kg/hr to avoid cerebral oedema
- Total correction over 48–72 hours
- As glucose falls, sodium rises — monitor closely
- Switch to 0.45% NaCl if plasma sodium is rising rapidly (>150 mmol/L)
- Do NOT start insulin until 1–2 L fluid replacement given
- Low-dose FRII: 0.05 units/kg/hr (half the DKA dose)
- Avoid rapid glucose fall — risk of cerebral oedema
- If glucose not falling with fluids alone, then consider insulin
Mandatory anticoagulation
- Enoxaparin 40 mg SC daily — all HHS patients
- High VTE risk: hyperosmolar state + elderly + immobile
- Elevated stroke risk — neuro observations required
Monitoring frequency
- Blood glucose: hourly
- Electrolytes (Na, K, urea): every 2 hours
- Calculated osmolarity: every 4 hours
- Neurological observations: every 2 hours
- Fluid balance: continuous
Hypoglycaemia
| Category | BGL | Symptoms |
|---|---|---|
| Autonomic (Early warning) |
3–4 mmol/L | Sweating, palpitations, tremor, anxiety, hunger, pallor |
| Neuroglycopenic (Brain glucose deprived) |
<3 mmol/L | Confusion, slurred speech, weakness, vision changes, seizure, coma |
| Hypoglycaemia Unawareness | Variable | No autonomic warning symptoms — common after many years of DM. Risk of sudden severe hypoglycaemia. |
Give 15 g fast-acting carbohydrates:
• 4 glucose tablets OR 150 mL fruit juice OR 3 jelly beans
Recheck BGL in 15 minutes. Repeat if still <4.0 mmol/L.
• Oral dextrose gel (buccal absorption) if safe to swallow
• Then 15 g carbohydrates once tolerating oral intake
• Do NOT give oral glucose if swallow is unsafe
• IV 50% dextrose: 50 mL IV push (adults)
• OR Glucagon 1 mg IM (if no IV access)
• Recovery snack once conscious: 20 g long-acting carbohydrate
• Investigate and document cause
- Position patient in recovery position (seizure or unconscious)
- Remove from case — do NOT shake
- Remove needle cap
- Inject into outer thigh or upper arm IM (through clothing if needed)
- Hold in place for 5 seconds
- Call emergency services simultaneously
- When patient responds: give 20 g carbohydrate snack
- Patients on insulin or sulphonylureas face elevated hypoglycaemia risk during Ramadan fasting
- Cultural and religious pressure to complete the fast — patients may not report symptoms
- Islamic fatwa supports breaking the fast for medical necessity — nurse education role is critical
- Timing of medications must be re-aligned to Iftar and Suhoor
- Pre-Ramadan structured education programme recommended for all insulin-dependent patients
Chronic Complications of Diabetes
- UAE, Kuwait, and Saudi Arabia rank among the top 10 countries globally for diabetes prevalence
- Diabetes accounts for approximately 17% of all deaths in the GCC
- GCC has the highest rates of diabetic ESRD (end-stage renal disease) requiring dialysis worldwide
- Diabetic retinopathy is the leading cause of blindness in GCC working-age adults
Leading cause of death in T2DM. Accelerated atherosclerosis driven by hyperglycaemia, dyslipidaemia, hypertension.
| Condition | Key Points | Nurse Actions |
|---|---|---|
| Coronary Artery Disease / MI | 2–4× higher risk than non-diabetic; may present silently (silent MI) | Monitor BP, lipids, ECG; aspirin adherence; statins |
| Stroke / TIA | 2–4× higher risk; lacunar infarcts common | FAST assessment; atrial fibrillation screening; anticoagulation review |
| Peripheral Arterial Disease | Claudication, absent pulses, critical ischaemia | ABI measurement; wound care; vascular surgery referral |
- Begins with microalbuminuria → macroalbuminuria → declining eGFR → ESRD
- Annual urine ACR (albumin:creatinine ratio) and eGFR monitoring
- ACEi / ARB are nephroprotective — prescribe even in normotensive patients with proteinuria
- GCC: highest rates of diabetic ESRD globally — early detection is critical
- Target BP <130/80 mmHg in diabetic nephropathy
- Leading cause of preventable blindness in working-age GCC adults
- Annual ophthalmology review — even without visual symptoms (early retinopathy is asymptomatic)
- Background → pre-proliferative → proliferative retinopathy progression
- Treatments: laser photocoagulation, intravitreal anti-VEGF injections (ranibizumab, bevacizumab)
- Tight glycaemic and BP control slows progression
Peripheral Neuropathy
- Symmetrical "stocking-glove" pattern — starts in feet
- Painful: burning, electric, worse at night
- Loss of protective sensation → undetected injury → ulceration
Autonomic Neuropathy
- Gastroparesis: delayed gastric emptying, nausea, vomiting, erratic glucose control
- Orthostatic hypotension: fall risk — measure lying/standing BP
- Bladder dysfunction: urinary retention, overflow incontinence
- Erectile dysfunction: early marker in men
Pharmacological Management
| Drug | Mechanism | Notes |
|---|---|---|
| Gabapentin | Calcium channel modulation | Start low, titrate; sedation, dizziness |
| Duloxetine (SNRI) | Noradrenaline/serotonin reuptake | First-line in many guidelines |
| Amitriptyline (TCA) | Pain modulation | Anticholinergic side-effects; use low dose |
| Pregabalin | Calcium channel modulation | Effective but higher abuse potential |
Annual Foot Examination
- Monofilament testing (10 g) — 10 sites per foot for protective sensation
- Vibration sense (128 Hz tuning fork) — great toe
- Ankle Brachial Index (ABI) — peripheral arterial disease screening
- Inspection: callus, deformity, nail changes, inter-digital maceration, ulceration
- Pulse assessment: dorsalis pedis + posterior tibial
High-Risk Foot
Patient Education
- Inspect feet daily (use a mirror for the sole)
- Wash with lukewarm water — test temperature with elbow, not feet
- Dry carefully between toes
- Never walk barefoot — even indoors
- Wear properly fitted footwear — no tight shoes, sandals with straps
- Trim nails straight across — refer podiatry if unsure
- Report any wound or new pain immediately — do not self-treat
Sick Day Rules
| Letter | Rule | Detail |
|---|---|---|
| S | Sugar | Test BGL every 1–4 hours. If BGL >14 mmol/L, test blood ketones. Keep a log. |
| I | Insulin | NEVER stop insulin when unwell — even if not eating. The liver continues to release glucose during illness. |
| C | Carbohydrates | Maintain carbohydrate intake. If vomiting, use liquids: fruit juice, regular (non-diet) cola, oral rehydration solution. |
| K | Ketones | If ketones ≥3 mmol/L AND vomiting AND unable to eat/drink = seek emergency medical help. |
Ramadan Management
Break-Fast Rules (patient must break fast if)
Insulin Adjustments for Ramadan
- Reduce evening long-acting insulin by 20–30% at Suhoor (pre-dawn meal)
- Adjust rapid-acting insulin timing: pre-Iftar and pre-Suhoor
- Omit or reduce lunchtime doses (no midday meal)
- Sulphonylureas: consider dose reduction or switch — high hypoglycaemia risk
- SGLT2 inhibitors: consider withholding during Ramadan (DKA risk in fasting state)
Knowledge Quiz — 10 Questions
1. What is the blood glucose threshold for diagnosing DKA?
2. A patient in DKA has a serum K+ of 3.2 mmol/L. What is the correct potassium action?
3. Which feature best distinguishes HHS from DKA?
4. DKA insulin infusion (FRII) should be stopped when:
5. A Level 3 hypoglycaemia patient is unresponsive. There is no IV access. What is the correct treatment?
6. According to sick day rules, when should an insulin-dependent diabetic patient seek emergency help?
7. The osmolarity formula used in HHS assessment is:
8. Why is the FRII rate lower in HHS than in DKA?
9. Which GCC-specific factor is a leading cause of end-stage renal disease?
10. A Ramadan fasting patient reports BGL of 3.6 mmol/L mid-afternoon. What should the nurse advise?