Diabetes Mellitus: new presentation


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    This guideline has been adapted for statewide use with the support of the Victorian Paediatric Clinical Network

  • See also

    Diabetes insipidus
    Diabetic ketoacidosis
    Diabetes mellitus: Management of unwell children with established diabetes at home
    Diabetes mellitus: Management of unwell children with established diabetes in hospital
    Diabetes mellitus and surgery
    Hyperosmolar hyperglycaemic state

    Key points

    1. This CPG is for children with a new diagnosis of diabetes mellitus who are not in diabetic ketoacidosis (DKA)
    2. A blood glucose level (BGL) should be checked in most acutely unwell children, as diabetes can present non-specifically
    3. Random BGL ≥11.1 mmol/L or fasting BGL ≥7.0 mmol/L, together with symptoms of hyperglycaemia, are diagnostic of diabetes in a child
    4. A child with a new diagnosis of diabetes mellitus who is not in DKA can be managed with subcutaneous insulin injections

    Background

    • Classic symptoms of hyperglycaemia that should prompt consideration of diabetes include:
      • polydipsia (excessive thirst)
      • polyuria (excessive urination)
      • new onset nocturnal enuresis (ie in a child who was previously dry overnight)
      • unexplained weight loss
      • unexplained fatigue
    • Other non-specific presentations (which may indicate ketosis/ketoacidosis) include vomiting, respiratory distress, dehydration, abdominal pain, altered consciousness
    • A diagnosis of diabetes should not be based on a single BGL reading in the absence of symptoms of hyperglycaemia. If the diagnosis is in doubt additional testing may be required (eg HbA1c, OGTT, continued monitoring of BGLs) in discussion with a paediatric specialist
    • Most cases of diabetes in children are due to Type 1 diabetes mellitus
    • The possibility of other types of diabetes should be considered in the following circumstances, when diabetes autoantibodies are negative:
      • Type 2 diabetes: obesity, acanthosis nigricans, strong family history
      • Monogenic diabetes: <6 months of age at presentation (neonatal diabetes mellitus), autosomal dominant family history of diabetes (MODY)
    • Diabetes can also be secondary to certain medications (eg glucocorticoids, tacrolimus) and other disease processes that can affect the pancreas eg cystic fibrosis, hereditary haemochromatosis

    Assessment

    History

    • Presence and duration of symptoms:
      • excessive thirst
      • excessive urination
      • weight loss
      • vomiting
      • abdominal pain
      • fatigue
    • Concurrent illness
    • Medications
    • Past medical history
    • Family history of diabetes and other autoimmune conditions

    Examination

    • Conscious state (AVPU/GCS)
    • Respiratory signs: respiratory rate, increased work of breathing
    • Assess hydration status
    • Weight

    Management

    Investigations

    • Formal serum blood glucose level
    • Point of care blood ketones if random BGL ≥11.1 mmol/L
      • urine ketones may be used for initial assessment if blood ketones are unavailable
    • Venous blood gas

    If pH <7.3 or bicarbonate <18 mmol/L, manage as per Diabetic ketoacidosis

    Other investigations

    • UEC
    • Diabetes autoantibodies: anti-GAD, insulin autoantibodies (IAA), insulinoma-associated-2 autoantibodies (anti-IA2), zinc transporter 8 (ZnT8)
    • Coeliac serology (transglutaminase IgA and total IgA)
    • TSH, FT4
    • Additional investigations may be required as part of diagnostic workup, or for associated conditions
      • C-peptide
      • Insulin level
      • Thyroid autoantibodies: thyroid peroxidase, thyroglobulin
      • Coeliac screen
      • Lipid profile
      • Liver function tests

    Treatment

    Intravenous fluids if required for dehydration. See Intravenous fluids

    Choice of insulin therapy

    Chioce of insulin theraphy

    Note that some centres use different management guidelines, see local protocols

    Subcutaneous insulin (for children not in DKA)

    If ketones are elevated (≥0.6) insulin should be started as soon as possible to prevent DKA

    The two most common regimens for insulin dosing are fixed multiple daily injection (MDI) and flexible insulin dosing

    • MDI insulin dosing (also called basal-bolus insulin):
      • Calculate total daily insulin (TDD), see guide below. Give 40% as long-acting basal insulin (daily) and 60% as rapid-acting insulin divided into 3 x boluses with meals ie 20% TDD rapid-acting insulin with each meal
    • Flexible insulin dosing:
      • The dose of rapid-acting insulin is calculated before each meal (or snack) based on pre-meal BGL and the amount of carbohydrates being consumed
      • In addition, rapid acting insulin is given to correct hyperglycaemia before and between meals
      • The insulin carbohydrate ratio (ICR) is the number of grams of carbohydrate that require 1 unit of insulin to be administered, and is used to determine the rapid-acting insulin dose for a quantity of carbohydrates
      • The insulin correction factor (CF) is the expected BGL decrease (in mmol/L) with 1 unit of insulin administered, and is used to determine the rapid-acting insulin dose to correct hyperglycaemia
        Note: the CF is also called the insulin sensitivity factor (ISF)
      • Long-acting insulin is given daily, typically in the evening
      Note: twice daily (BD dosing) injections are rarely used as a standard regimen and are limited to extremely rare circumstances where more precise dosing cannot be achieved in extraneous circumstances

    A guide to initial insulin doses is given below. Insulin regimens will need to be individualised to the child's needs as indicated by BGL levels

    • Where possible, discuss ongoing insulin dosing with a paediatric endocrinologist or paediatrician with experience in paediatric diabetes and always consult local guidelines where available
    • Pre-meal BGL target is 4-8 mmol/L. If BGL >8 mmol/L use CF to determine dose of rapid-acting insulin to return BGL to 6 mmol/L (unless insulin has already been given in preceding 2 hours)
    • Pre-meal rapid-acting insulin should be given 15 minutes prior to the meal (except Fiasp®, which can be given at the time of the meal due to faster onset)

    Suggested dosing for initiation of subcutaneous insulin therapy

    Multiple daily injections (MDI)
    Insulin type
    and frequency
    Long-acting (basal) insulin once daily (typically at night)
    and
    Pre-meal injections of rapid-acting insulin
    Finger prick blood glucose monitoring* Pre-meals (breakfast, lunch, dinner)
    2 am (during initial stabilisation/admission)
    Whenever hypoglycaemia is suspected

    Note: more frequent BGL monitoring may be required on initial administration eg 2 hours following first insulin dose and 4-hourly overnight, especially if child is ketotic
    Initial total daily dose
    (TDD)
    For children <1 year consult paediatric endocrinologist

    1-5 years: 0.5 units/kg/day

    5-10 years: 0.7 units/kg/day

    >10 years: 0.7-1.0 units/kg/day

    Dosing
    1. Calculate total daily dose as above

    2. Give 40% of TDD as long-acting insulin in the evening

    3. Divide remaining 60% into 3 doses of rapid-acting insulin and give pre-meal at breakfast, lunch and dinner ie ~0.1 - 0.2 units/kg before each main meal
    Comments

    If commencing first dose rapid-acting insulin >2 hours before mealtime, consider giving stat 0.2 units/kg of insulin; then begin regular rapid-acting insulin with meals as above

    Children presenting during the day may need slightly higher pre-meal doses (eg 0.25 units/kg) until basal insulin is given that evening

    Round insulin dose down to nearest 0.5 unit

    Flexible insulin dosing
    Insulin type
    and frequency

    Long-acting (basal) insulin once daily (typically evening)


    Rapid-acting insulin is given:

    • pre-meals (breakfast, lunch dinner)
    • with snacks containing >15 grams of carbohydrat
    • if BGL >8 mmol/L and taken >2 hours after last insulin during the day dose, or BGL >15 mmol/L overnight
    Finger prick blood glucose monitoring*

    Pre-breakfast

    Pre-lunch

    Pre-afternoon tea (>2 hours following lunchtime insulin)

    Pre-dinner

    Pre-bed (>2 hours following dinner)

    2 am (during initial stabilisation/admission)

    Whenever hypoglycaemia is suspected

    Note: some centres also check BGL at morning tea and 4-hourly overnight on initiating insulin

    Long-acting insulin dosing Daily long-acting insulin given in the evening (see table below for dosing guide)
    Rapid-acting insulin dosing Insulin dose =

    1) Insulin needed to correct BGL (child's BGL minus target BGL 6 mmol/L, then divide by correction factor)

    plus

    2) Insulin needed to cover carbohydrate being eaten (grams of carbohydrate divided by insulin:carbohydrate ratio)

    eg pre-lunch BGL 16, eating 20 g carb, child has CF 2 and ICR 5

    1) Insulin required to correct BGL =

    16 (child's BGL) - 6 (target BGL) = 10 mmol/L

    10 mmol/L ÷ 2 (CF) = 5 units

    2) Insulin to cover carbohydrates being eaten (ICR) =

    20 grams ÷ 5 (ICR) = 4 units

    3) Give insulin 5 + 4 = 9 units

    If giving insulin to correct BGL but child is not eating or eating <15 grams carbohydrate, calculate insulin dose using CF only
    ie step 1 only

    If giving insulin with food and BGL 4-8 mmol/L, use step 2 only

    Initial ICR and CF Please see Appendix 1 and 2 for suggest initial ICR and CF ratios.
    ICR and CF ratios will change based on BGLs following initiation of insulin. This document provides a guide for initiation only
    Comments Round insulin dose down to nearest 0.5 unit

    *Note: many children will be started on a continuous glucose monitor (CGM) early in their admission. Finger prick BGL may vary in this instance. Please see CGM

    Ketone monitoring

    • If ketones are present at diagnosis, continue to measure with each BGL every 2 hours until ketones <0.6
    • As part of ongoing management, ketones should be checked whenever
      BGL ≥15 or child is unwell

    Consider consultation with local paediatric team

    • For all new presentations of diabetes in children. In most centres these children need to be admitted for initiation of insulin therapy and diabetes education
    • In some tertiary centres, hospital in the home (HITH)/ambulatory care programs may be considered in appropriate cases; discuss with paediatric endocrinology team first

    Consider transfer when

    Child requiring care beyond the level of comfort of the treating hospital

    For emergency advice and paediatric or neonatal ICU transfers, see Retrieval Services

    Consider discharge when

    • Child tolerating oral intake
    • Child linked in with local diabetes care team and contact information provided
    • Initial diabetes education completed, usually involves input from diabetes nurse educator, dietician, social work
    • Family competent in monitoring BGLs and administering insulin and treating hypoglycaemia

    Parent information

    Kids Health Information: Diabetes

    Diabetes Australia

    RCH-specific info:

    Sick day and ketone management for injections

    Sick day and ketone management for pumps

    Diabetes at the RCH

    Diabetes at the RCH : Type 1 diabetes toolkit

    Appendix 1: Initial recommended insulin:carbohydrate ratio (ICR), correction factor (CF) and long-acting insulin

    Initial ICR and CF and long-acting insulin dose
    Weight ICR CF Long-acting insulin
    10 kg 30 10 mmol/L 2 units
    15 kg 20 6.5 mmol/L 3 units
    20 kg 20 5 mmol/L 4-6 units
    25 kg 20 4 mmol/L 5-7 units
    30 kg 17 3.5 mmol/L 6-10 units
    35 kg 14 3 mmol/L 8-14 units
    40 kg 12.5 2.5 mmol/L 10-16 units
    45 kg 11 2 mmol/L 12-18 units
    50 kg 10 2 mmol/L 14-20 units
    55 kg 9 2 mmol/L 16-22 units
    60 kg 8 1.5 mmol/L 18-24 units
    >60 kg 8 1.5 mmol/L 20-25 units

    Appendix 2: Flexible dosing insulin with variable ICR throughout the day

    Takes into account insulin sensitivity variation throughout the day

    Child's weight ICR at breakfast
    (grams of carbohydrate per 1 unit short-acting insulin)
    ICR at lunch
    (grams of carbohydrate per 1 unit short-acting insulin)
    ICR at afternoon tea
    (grams of carbohydrate per 1 unit short-acting insulin)
    ICR at dinner
    (grams of carbohydrate per 1 unit short-acting insulin)
    Correction factor for BGL >6
    (mmol/L BGL drops with 1 unit insulin)
    Long acting insulin
    eg Detemir or glargine
    (units)
    10 kg 15 20 30 30 10 2.5
    11-13 kg 10 12 30 30 8 3
    14-16 kg 10 12 20 20 6.5 3.5
    17-20 kg 8 10 20 20 5.5 4
    21-25 kg 7 10 20 20 4 5.5
    26-30 kg 6 8 15 15 3.5 6.5
    31-35 kg 6 7 15 15 3 8
    36-40 kg 6 7 15 15 2.5 9
    41-45 kg 5 6 12 12 2 10
    46-50 kg 5 6 12 12 2 11
    51-55 kg 4 5 10 10 2 12
    56-60 kg 4 5 10 10 1.5 14
    >60 kg 3 4 8 8 1.5 18

    Last updated March 2025

    Reference List

    1. Anderson, K., Scott, F., Kenneady, A., O'Brien, J., Van Roon, S., Sharp, A., Pearce, H., Virgona, M. Paediatric management of a newly diagnosed child with T1DM without DKA -- Guide for hospital staff. Retrieved from PROMPT, Barwon Health (viewed 2022)
    2. Beckles, Z. L., Edge, J. A., Mugglestone, M. A., Murphy, M. S., & Wales, J. K. Diagnosis and management of diabetes in children and young people: summary of updated NICE guidance. Bmj. 2016. 352.
    3. Cengiz, E., Danne, T., Ahmad, T., Ayyavoo, A., Beran, D., Ehtisham, S., Fairchild, J., Jarosz-Chobot, P., Ng, S. M., Paterson, M., Codner, E. ISPAD Clinical Practice Consensus Guidelines 2022: Insulin treatment in children and adolescents with diabetes. Pediatr Diabetes. 2022. 23(8), 1277-1296.
    4. Craig, M. E., Twigg, S. M., Donaghue, K. A., Cheung, N., Cameron, F., Conn, J., & Silink, M. National evidence-based clinical care guidelines for type 1 diabetes in children, adolescents and adults. 2011. Australian Government Department of Health and Ageing. Canberra.
    5. Mayer-Davis, E. J., Kahkoska, A. R., Jefferies, C., Dabelea, D., Balde, N., Gong, C. X., & Craig, M. E. ISPAD Clinical Practice Consensus Guidelines 2018: Definition, epidemiology, and classification of diabetes in children and adolescents. Pediatric diabetes. 2018. 19(Suppl 27), 7-19.