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28 Julai 2026, 17:31:54
Insulin therapy in diabetes mellitus
Insulin therapy is an essential component of diabetes management and remains the only effective treatment for individuals with type 1 diabetes mellitus. It is also indicated in many patients with type 2 diabetes mellitus when glycaemic targets cannot be achieved with lifestyle modification and oral hypoglycaemic agents alone or when insulin deficiency becomes clinically significant.
The aims of insulin therapy are to replace deficient endogenous insulin, achieve optimal glycaemic control, relieve symptoms of hyperglycaemia, prevent acute metabolic emergencies, reduce the risk of chronic complications, and improve quality of life.
Successful insulin therapy requires individualized dose adjustment, patient education, regular blood glucose monitoring, and careful attention to diet, physical activity, and injection technique.
Physiology of insulin
Insulin is a peptide hormone produced by the β-cells of the pancreatic islets of Langerhans. It promotes glucose uptake into skeletal muscle and adipose tissue, suppresses hepatic glucose production, stimulates glycogen synthesis, promotes protein synthesis, and inhibits lipolysis and ketogenesis.
Normal insulin secretion consists of:
Basal insulin secretion, which maintains glucose homeostasis during fasting.
Prandial (bolus) insulin secretion, which controls postprandial blood glucose following meals.
Insulin therapy aims to mimic these physiological patterns.
Indications for insulin therapy
Type 1 diabetes mellitus
All patients with type 1 diabetes mellitus require lifelong insulin therapy because of absolute insulin deficiency.
Type 2 diabetes mellitus
Insulin should be initiated in patients with:
Fasting blood glucose greater than 15 mmol/L at presentation
Hyperglycaemic emergencies
Severe symptomatic hyperglycaemia
Major surgery or the perioperative period
Serious medical illnesses requiring tight glycaemic control
Renal failure
Liver failure
Heart failure
Poor glycaemic control despite lifestyle modification and oral hypoglycaemic agents
Latent autoimmune diabetes in adults (LADA)
Contraindications to oral hypoglycaemic agents
Clinical note
The maximum glucose-lowering effect of oral hypoglycaemic agents is usually evident within six months. Patients who remain uncontrolled despite appropriate dose titration should have their treatment intensified rather than continuing ineffective therapy.
Types of insulin
Insulin preparations differ according to their onset, peak, and duration of action.
Type of insulin | Example | Clinical role |
Short-acting | Soluble (regular human) insulin | Prandial insulin |
Intermediate-acting | Isophane (NPH) insulin | Basal insulin |
Premixed insulin | Human insulin 70/30 | Basal and prandial coverage |
Short-acting insulin
Short-acting insulin controls postprandial blood glucose excursions and is commonly used before meals or intravenously during diabetic emergencies and perioperative care.
Examples include:
Soluble human insulin
Intermediate-acting insulin
Intermediate-acting insulin provides basal insulin coverage throughout the day and overnight.
Example:
Neutral protamine Hagedorn (NPH) insulin
Premixed insulin
Premixed insulin combines intermediate-acting and short-acting insulin in a fixed ratio, providing both basal and mealtime insulin coverage.
Common preparation:
Human insulin 70/30
Initiation of insulin therapy
Insulin should be initiated by a clinician experienced in diabetes management who is able to educate the patient regarding:
Injection technique
Dose adjustment
Storage of insulin
Blood glucose monitoring
Recognition of hypoglycaemia
Sick-day management
Once stabilized, patients may continue follow-up and prescription refills at lower-level health facilities.
Insulin as substitution therapy
Substitution therapy replaces endogenous insulin when oral hypoglycaemic agents are no longer adequate.
Oral medications
Discontinue oral hypoglycaemic agents.
Metformin may be continued in obese patients if appropriate.
Starting dose
Premixed insulin:
0.2 IU/kg/day
Divide the total daily dose into:
Two-thirds before breakfast
One-third before the evening meal
Administration
Human insulin:
Inject approximately 30 minutes before meals
Insulin analogues:
Inject 0–15 minutes before meals
Dose adjustments should be based on fasting and postprandial blood glucose measurements.
Insulin as supplemental therapy
Supplemental insulin is added to existing oral therapy when oral agents alone fail to achieve adequate glycaemic control.
Regimen
Continue:
Metformin (up to 2 g/day)
Sulphonylurea (usually half of the maximum dose)
Add:
NPH insulin
Dose:
0.1–0.2 IU/kg once daily at bedtime (before 22:00 hours)
Regular blood glucose monitoring should guide subsequent dose adjustments.
Insulin therapy in type 1 diabetes mellitus
Because endogenous insulin production is absent, lifelong insulin replacement is mandatory.
Recommended total daily insulin dose:
Before puberty
0.5 IU/kg/day
During puberty
1–2 IU/kg/day
After puberty
Usually less than 2 IU/kg/day
Individual requirements vary according to weight, pubertal stage, illness, diet, and physical activity.
Basal-bolus insulin regimen
The total daily insulin dose is divided into basal and prandial components.
Time | Insulin | Percentage of total daily dose |
Breakfast | Short-acting insulin | 30% |
Lunch | Short-acting insulin | 20% |
Evening meal | Short-acting insulin | 10% |
Bedtime | Intermediate-acting (NPH) insulin | 40% |
This regimen closely mimics normal physiological insulin secretion and provides the best glycaemic control for most patients with type 1 diabetes.
Premixed insulin is generally not recommended in children because it offers less flexibility for meal timing and insulin adjustment.
Administration of insulin
Insulin is administered by subcutaneous injection into:
Abdomen
Anterior thigh
Upper arm
Buttocks
Injection sites should be rotated regularly to reduce the risk of lipohypertrophy and ensure consistent insulin absorption.
Patients should receive practical instruction on:
Injection technique
Needle disposal
Storage of insulin
Rotation of injection sites
Monitoring during insulin therapy
Regular monitoring is essential to achieve glycaemic control while minimizing hypoglycaemia.
Monitoring includes:
Self-monitoring of blood glucose
HbA1c every three months until stable
Weight
Blood pressure
Renal function
Injection site inspection
Review of hypoglycaemic episodes
Review of adherence and injection technique
Dose adjustment
Insulin doses should be adjusted according to:
Fasting blood glucose
Postprandial blood glucose
HbA1c
Physical activity
Dietary intake
Intercurrent illness
Pregnancy
Weight changes
Dose adjustments should generally be gradual to reduce the risk of hypoglycaemia.
Adverse effects
Potential adverse effects include:
Hypoglycaemia
Weight gain
Lipohypertrophy
Lipoatrophy
Injection site pain
Local allergic reactions
Peripheral oedema during initiation
Hypoglycaemia
Hypoglycaemia is the most common complication of insulin therapy.
Symptoms
Sweating
Tremor
Hunger
Palpitations
Anxiety
Confusion
Blurred vision
Dizziness
Behavioural changes
Seizures
Loss of consciousness
Common causes
Excess insulin
Delayed or missed meals
Excessive physical activity
Alcohol consumption
Incorrect insulin administration
Management
Mild hypoglycaemia:
Administer 15–20 g of rapidly absorbed carbohydrate.
Recheck blood glucose after 15 minutes.
Repeat if necessary.
Severe hypoglycaemia:
Intravenous dextrose or intramuscular glucagon (where available).
Identify and correct the precipitating cause.
Patient education
Patients should receive education regarding:
Nature and purpose of insulin therapy
Injection technique
Blood glucose monitoring
Recognition of hypo- and hyperglycaemia
Sick-day rules
Storage of insulin
Needle disposal
Diet and meal planning
Physical activity
Foot care
Importance of adherence and regular clinic attendance
Clinical pearls
Insulin is mandatory for all patients with type 1 diabetes mellitus.
In type 2 diabetes mellitus, insulin should be initiated promptly when oral therapy fails or when severe hyperglycaemia is present.
Basal insulin is commonly introduced before progressing to more intensive insulin regimens.
Premixed insulin provides both basal and prandial insulin coverage but offers less flexibility than basal-bolus therapy.
Regular self-monitoring of blood glucose and periodic HbA1c assessment are essential for safe insulin dose adjustment.
Proper injection technique, site rotation, and patient education reduce complications and improve treatment outcomes.
Imeandikwa:
28 Julai 2026, 10:38:29
Rejea za mada hii:
Ministry of Health, United Republic of Tanzania. Standard Treatment Guidelines and National Essential Medicines List for Tanzania Mainland. 2023 ed. Dodoma: Ministry of Health; 2021.
World Health Organization. Definition and diagnosis of diabetes mellitus and intermediate hyperglycaemia: report of a WHO/IDF consultation. Geneva: World Health Organization; 2006.
World Health Organization. Diagnostic criteria and classification of hyperglycaemia first detected in pregnancy. Geneva: World Health Organization; 2013.
American Diabetes Association. 2. Classification and Diagnosis of Diabetes: Standards of Care in Diabetes—2023. Diabetes Care. 2023;46(Suppl 1):S19–S40. doi:10.2337/dc23-S002.
American Diabetes Association. 3. Prevention or Delay of Type 2 Diabetes and Associated Comorbidities: Standards of Care in Diabetes—2023. Diabetes Care. 2023;46(Suppl 1):S41–S48.
American Diabetes Association. 9. Pharmacologic Approaches to Glycemic Treatment: Standards of Care in Diabetes—2023. Diabetes Care. 2023;46(Suppl 1):S140–S157.
Davies MJ, Aroda VR, Collins BS, et al. Management of hyperglycaemia in type 2 diabetes, 2022. A consensus report by the American Diabetes Association (ADA) and the European Association for the Study of Diabetes (EASD). Diabetes Care. 2022;45(11):2753–2786.
International Diabetes Federation. IDF Diabetes Atlas. 10th ed. Brussels: International Diabetes Federation; 2021.
World Health Organization. Global report on diabetes. Geneva: World Health Organization; 2016.
Disclaimer: The information provided on this platform is for educational and informational purposes only and does not replace professional medical advice, diagnosis, or treatment. Clinical recommendations are primarily based on the Tanzania Standard Treatment Guidelines and National Essential Medicines List (STG & NEMLIT), Seventh Edition, 2021, unless otherwise stated.
