7 Tangdom of Sau Rrabia
Ministry of Defense
General stati Command
Medical Senice General Directorate
‘Armed Forces Hospital, Southern Region
Department: Hospital Wide Policy No: AFHSR-COP 033
Tile Protocol for Management of Patients with DKA (Diabetic
ketoacidosis) Inflation Date; 1-08-2017
Replaces New | Effective Date: 1-09-2017
| Revision Date. 1-09-2020
Edition. 1" Edition
Standard Reference JCI & CBAHI
1, PURPOSE:
1.1. To standardize and improve the patient care provided in accordance with evidence based
information
2, RESPONSIBILITIES:
2.1 Clinical Director. Head of ER, and all medical doctors.
3, SCOPE:
3.1 All Armed Forces Hospital, Southern Region Medical, nursing and allied healthcare staff
4, DEFINITION:
4.1 To identify and update proper management of DKA
5. PROCEDURE:
5.1. Diagnostic criteria: (All 3 of the following must be present)
5.1.1 BS>11 mmol,
51.2 Venous pH <7.3 andlor bicarbonate <15 mmol/L
51.3. Capillary ketones >3 mmol/L or urine ketones ++ or more
5.2 Assessment of Severity of DKA:
DKA
Z z Mild ~ Moderate Severe
‘Arterial pH (iaavas7 aime e700 724: <7.00
Serum bicarbonate (£E4/l) 15:18 Oto <15 10
>10 >
Alert Alert/drowsy | Stupor/coma |
5.3. Initial Clinical Assessment:
5.3.1 Respiratory rate. temperature: blood pressure; pulse: oxygen saturation
53.2 Glasgow Coma Scale
53.3 Full clinical examination
54 Initial Investigations:
5.4.1. Capillary blood glucose (BG)
5.4.2 Urine ketones
Protoceltor Management of Patents wih OKA (Diabet Ketoasisis) Page tot,5.43
544
5.45
5.46
SAT
5.48
5.49
Venous plasma glucose
Urea and electrolytes
Venous blood gases (VBG)
Full blood count (CBC)
ECG
Chest cardiograph, urinalysis and culture, blood cultures as needed
Identify and treat precipitating factors
5.5 Resolution of DKA is defined by:
551
552
563
Venous pH over 7.3 or anion gap <12 mEq/L
Venous bicarbonate 2 18 mmol/L
BS < 11 mmol
5.6 IV Fluids Management:
561 If systolic BP (SBP) <90 mmHg
5.6.2. Give 500 mi of 0.9% NaCl solution over 15 minutes
5.6.2.1 Repeat if SBP remains <90 mmHg
5.6.3 Once SBP above 90 mmHg follow fluid replacement as below
56.4 If systolic BP 2 90 mmHg
565 515 years: the recommended rate of fluid replacement (0.9% NaCl) is 15 mUkg/hr
fot the first hour then, 5 mi/kg/hr
566 >15 years: Give
5.6 6.10.9% NaCl 1L over 1% hour
5.6.6.20.9% NaC! 1L over next 2 hours.
5.6.6 30.9% NaCl 1L over next 4 hours
5.6.6.40.9% Na Gl 1L over 6 hours
56.7 If BS <14 mmol/L, change to 5% Dextrose with 0.45% Na Cl at 100-150 mifhr: If
extra fluid is needed, use NaCl 0.9%
568 if the BP remains <90 mmHg, reconsider other causes of hypotension and
consider involving the ICU/eritical care team. A plasma expander can be
considered in this situation
5.6.9. A slower infusion rate should be considered in: young people (<18 years (risk of
cerebral edema), elderly, pregnant heart or kidney failure, other serious co-
morbidities
5.6.10 Fluids should be replaced cautiously (monitor BP, cardiac and pulmonary
auscultation), check the inputs and the outputs (diuresis)
56.11 Re-assessment of cardiovascular status at 12 hours is mandatory, further fluid may
be required
Protocol ter Managers of Paberts with OKA (Oabet Ketoscxos Page 204557 Insulin Management:
5.7.1. Start continuous fixed rate of intravenous insulin infusion (IVI)
5.7.2 Put 50 units human soluble insulin made up to 50 mi with 0.9% NaCI solution
5.7.3. Infuse at a fixed rate of 0.1 unitikgikr (i.e. 7 mU/hr if weight is 70 kg)
57.4 Only give a stat dose f IV insulin bolus (0.1 unit/kg) if there is a delay in setting up a
fixed rate IVI
57.5 Check BS hourly
5.7.5.1 If BS is not faling by at least 3 mol/L/hr. check the insulin infusion pump
's working and connected and increase insulin infusion rate by 1 to 2
Unitfhr increments hourly until the glucose falls at this rate
5.76 If BS <14 mmol/L, the rate of insulin infusion should be decreased. If the rate of
IVIl required 2 required 2 7UWhr, decrease by 30%. If the rate of IVI <7Ul, see
algorithm,
Algorithm: rate of IVI if BS <14 mmol/l.
Units/hr
Off
05
1
15
B
3
4
577 Transfer to subcutaneous insulin if patient is able to eat, drink and passing urine
5.7.8 Ensure subcutaneous insulin is started at least 1 hour before IV insulin is
discontinued
579 Give subcutaneous fast acting insulin and a meal and discontinue IV insulin one
hour later (see conversion to subcutaneous insulin
5.7.10 Give intermediate or long acting insulin (NPH, Lantus, etc.) 8 to 10 UI with the
short acting insulin
Conversion to subcutaneous insulin
5.7.11 Restarting subcutaneous insulin for patients already established on insulin,
57.111 Previous regimen should generally be re-started. The insulin infusion
should not be stopped until some form of background basal insulin has
been given. Check glucose levels regularly (every 4 to 6 hours)
57.12 Calculating subcutaneous insulin dose in insulin-naive patients: The Total Dose
Daily (TOD) of insulin can be calculated by multiplying the patients weight (in kg)
Prtacoifor Managemen of Patents wih OKA (Diabetic Ketoaodos) Paget,
____|ee
by 0.5 units. Use 0.75 units/kg for those thought to be more insulin resistant ie
teens, obese. Give 50% of total dose in the form of long acting insulin and divide
remaining dose equally pre-breakfast, pre-lunch and pre-evening meal
NB: In patients new to insulin therapy dose requirements may decrease within a
few days as the insulin resistance associated with DKA resolves. Close supervision
from the specialist diabetes team and the diabetic educator is required
58 Potassium Management:
5.8.1 Add potassium as per protocol below hourly in 100 mi in a burette
5.82 Take this as a part of hourly fluid replacement
5.8.2.1 NB: maximum concentration of IV KCl is 20 mEq in 100 ml fof peripheral
vein administration and 40 mEq/L in 100 ml for central vein
administration
583. If serum K $3 mmol/L, hold insulin and give KC! 30-40 mEqihr until >3 mmol/L
58.4 IfserumK 3.1 to 3.9 mmol/L, give KC! 20 mEqinour
585 If K 25 mmol/L, do not give KCI but check K every 2 hours
Potassium replacement cautions:
5.8.6 If potassium is infused rapidly or in high dose intravenous, it may cause cardiac
arrest. Intravenous potassium must NEVER be administered undiluted
5.8.7 ECG monitoring is required when the infusion rate is greater than 20 mEqihr
58.88 tis preferable to replace potassium in a separate line
5.9. Bicarbonate Management:
59.1 IfpH>6.9, noHCO3
5.9.2 If pH $6.9: NaHCO3 (50 mmol) dilute in 200 mi H20 infuse at 200 mi/hr. Repeat
every 2 hours until pH > 6 9, monitor K+ level
59.3 Take this a part of fluid replacement
5.10.1 Consider urinary catheterization if incontinent or anuric (i.e not passed urine by 60
minutes)
5.10.2 Consider nasogastric tube if patient obtunded or if persistently vomiting
5.10.3 If oxygen saturation falling perform arterial blood gases and request repeat chest
5.10 Re-assess patient, monitor vital signs:
radiograph |
5.10.4 Accurate fluid balance chart, minimum urine output 0.5 mi/kg/hr
5.10.5 Continuous cardiac monitoring in those with severe DKA
Proacolr Managemen of Patents wih OKA (Diabet Ketoaedosi Page sot5. |
———5.10.6 Discuss low molecular weight heparin in patients with high risk of thrombosis.
5.10.7 Continue IV fluids if not eating and drinking
5.10.8 Re-assess for complications of treatment e.g. fluid overload, cerebral edema
5.11 Review metabolic parameters:
5.11.1 Measure BS hourly (note: if meter reads “HI”, venous blood should be sent to the
laboratory hourly)
5.11.2 Measure VBG for pH and bicarbonate and serum potassium at 60 minutes and 2
hourly thereafter til the resolution of DKA
5.11.3 Assess the appropriateness of potassium replacement and check it 2 hourly
5.114 Do not rely on urinary ketone clearance to indicate resolution of DKA, because
these will be present when DKA has resolved.
6, ATTACHMENTS:
None
7. REFERENCE: |
8. APPROVAL:
Prepared by: ———T Signaiyger ALF Date —
brow ar Bre ge —
Clinical Director. Medicine _ cant ada Ww
Reviewed by: —
Dr. Reda Refale
Chairman, Evidence Based Medicine
Reviewed by:
Col Dr Faisal Al Banah
Director of Diabetic Cente
Reviewed by:
| Dr Jawad Khaled
| Head of Ambulance & Emergency
Reviewed by:
| Dr. Abdullah Haram
| Director of Pharmacy
Reviewed by:
Ms. Samirah Asi
|_COIBPS Director
‘Approved by:
| Ms: Krshnavelie Chetty
Director of Nursin
‘Approved by:
Dr Yanya Al Qahtani
Medical Director
Approved by:
Brig. Gen, Abdullah Al Ghamdi
| Hospital Director
Protocol fr Management of Patents with OKA (Disbetic Ketosedors)
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