Matthew (Diagnosis and treatment of T1DM) Flashcards

1
Q

What is type 1 diabetes?

A

When the pancreas no longer produces insulin.

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2
Q

Which cells in the pancreas are responsible for producing insulin?

A

Beta cells

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3
Q

What are the 3 functions of insulin?

A

1- Reduces blood glucose levels
2- Promotes body growth and development
3- Ensures we have adequate energy stores

Facilitates glucose uptake and utilisation in cells and tissues.
Stimulates breakdown of glucose and storage in the liver as glycogen serving as ‘energy’ storage

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4
Q

Signs and symptoms of T1DM

A
  • Excessive thirst
  • Excessive urination
  • Recurrent UTI
  • Sweet smelling urine
  • Superficial infections (ringworm or thrush)
  • Weight loss
  • Blurred vision
  • Confusion
  • Vomiting
  • Drowsiness
  • Slow healing wounds
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5
Q

Renal glucose reabsorption

A

Body wants to keep as much glucose as possible as it is our main energy source so it will be reabsorbed in the PCT.
There is a threshold to how much can be reabsorbed so one this is reached glucose will go out in the urine.
Because glucose has a high osmolarity it pulls water out with it which leads to dehydration (why T1DM have symptoms of excessive urination and thirst). This creates a state of hyper filtration- kidney is in overdrive.
When you start to treat the diabetes it can cause issues with kidney function- change creatinine clearance which can cause problems in the elderly

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6
Q

What is diagnosis based on?

A
  • Clinical presentation and symptoms
  • Family history - history of autoimmune diseases (Addisons, rheumatoid arthritis, hyperthyroidism, coeliac). In patients that have a strong family history of T1DM you can consider that there might be a genetic influence and that it is actually monogenic diabetes instead of type 1.
  • Capillary blood glucose - expect to be high, can’t diagnose without. Important to know if it is fed or fasted- ideally want fasted glucose levels. Above 11 is classed as hyperglycaemia
  • HbA!c- important for target setting
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7
Q

HbA1c

A

Measure blood glucose control over the past 3 months (because the lifespan of RBC is 90-120 days).
Not essential for diagnosis of T1DM as wouldn’t be raised in patients with classic acute onset as glucose won’t have had time to bind to Hb.
Still used in practice as is clinically useful to guide differential and monitoring.
Usually do test twice when diagnosing.

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8
Q

When diagnosis isn’t clear

A
  • High BMI
  • More advanced age (>50)
  • Insidious onset of symptoms

Further investigations:
- Urinary C peptide
- diabetes specific antibodies
- Genetic testing (MODY - monogenic diabetes- mutations in only a single gene)

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9
Q

What are the main parts of a beta cell?

A
  • Glutamate decarboxylase (GAD)
  • Insulin
  • Islet Antigen-2 (IA-2)
  • Zinc transporter 8 (ZnT8)
  • Insulin Granule

If you suspect type 1 then you should start treatment before waiting for autoantibody test results to come back as this can take a while.
Most commonly there will be a rise in GAD. The more positive antibodies they have the more likely they are to have type 1 diabetes.

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10
Q

Diabetes autoantibodies

A

Helpful if clinical picture is unclear or if needed for coding and access to health technologies which is a huge part of proper patient care.

  • Evidence T1DM is an autoimmune condition is based on the presence of DAAs most specific to islet cell destruction (ICAs, GAD65/67Abs, IA-2Abs, or IAAs)
  • Lack of these in a completely insulinopenic patient would suggest type 3c/type 1B (idiopathic)
  • ICAs (Islet Cell Autoantibodies) were previously the main method to confirm T1DM but GAD, IAA, and IA-2 have been shown to be more precise and definitive predictive/diagnostic measures

Presentation/presence of autoantibodies doesn’t;t always follow specific pattern so not definitive at time of diagnosis. In the majority of patients GAD will be the first indicator.

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11
Q

C-peptide

A
  • C-peptide is a by product of the breakdown of endogenous pro-insulin.
  • The bodies natural precursor to insulin
  • Made in equal amounts to insulin protein so marker for level of insulin productions

Not used routinely to monitor or test for type 1
- Requires endogenous insulin production
- Doesn’t account for ‘honeymoon’ period (when started on insulin some patients seem to ‘get better’ as the insulin that was given can kick the pancreas back into action. Usually stops after 12 months)

Most clinically useful to distinguish between forms of diabetes in those on insulin or to identify misdiagnosis 3-5 years into diagnosis or if unclear
- Benefit of which increase the further you are from point of diagnosis

Not useful early on in diagnosis.
Low C-peptide, high glucose = insulin deficient (type 1).
High C-peptide, high glucose = insulin resistance (type 2/MODY).

Often cheaper.
Faster to result as can e done at local labs rather than regional centres.

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12
Q

Goals of therapy

A

Glycaemic management- optimal insulin replacement with minimal episodes of hypoglycaemia

Prevention of microvascular and macrovascular complications
- Micro- retinopathy, neuropathy
- Macro- cardiovascular, peripheral vascular

Effectively managing cardiovascular risk factors
- Blood pressure, cholesterol, obesity

Providing approaches, treatments, and devices that minimise the psychosocial burden of living with type 1 diabetes and diabetes related distress while promoting psychological well-being.
- Can need a good understanding of maths and technology which can be hard for some people which leads to diabetes stress

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13
Q

Insulin formulation- Quick acting

A

Short acting (onset = 30-60 mins, duration = 6-8 hours)
- Actrapid
- Humulin S
- Hypurin Neutral

Rapid acting (onset = 10-20 mins, duration = 4 hours)
- Novorapid
- Humalog
- Apidra
- TruRapid
- Admelog

Very rapid acting (onset = 5-10 mins, duration = 3 hours)
- Fiasp
- Lyumjev

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14
Q

Insulin formulation- intermediate

A

Onset of action = 60-90 mins
Duration = 12-20 hours

  • Humulin I
  • Insulatard
  • Hypurin isophane
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15
Q

Insulin formulation- biphasic

A

Analogue mix (onset = 10-20 mins, duration = 12-24 hours)
- Novomix
- Humalog Mix 25
- Humalog Mix 50

Isophane (onset = 30-60 mins, duration = 12-24 hours)
- Humulin M3
- Hypurin Mix 30/70

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16
Q

Insulin formulation- long acting

A

Long acting (onset = 2-4 hours, duration = 20-24 hours)
- Lantus
- Levemir
- Abasaglar

Ultra long acting (onset = 30-90 minutes, duration = 24-42 hours)
- Tresiba
- Toujeo

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17
Q

Insulin safety

A

Standards for safe insulin prescribing;
- Correct brand name
- Beware of sound alike
- Never prescribe by salt always by brand
- Correct device
- Never abbreviate ‘units’ to ‘u’ or ‘iu’ due to risk of 10x overdose
- Correct time
- Correct strength
- Write in full

Insulin is in the top 5 most dangerous drugs used worldwide and errors are very common. Some errors are minor e.g. dose is given 30 mins late. Some errors are almost fatal e.g. insulin pump removed, go into ketoacidosis, then suffer a cardiovascular event

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18
Q

What are the 6 Rs in insulin safety?

A

Right patient
Right insulin
Right dose
Right time
Right device
Right way

19
Q

Insulin regimens

A
  1. Basal Bolus (multiple daily injections (MDI))- most common
  2. Twice or three times daily biphasic
  3. 5 minutes for insulin
20
Q

Basal bolus

A

3 Rapid acting + 2 intermediate acting Or 3 rapid acting + 1 long acting.

Best regimen at mimicking endogenous insulin production other than an insulin pump.
Doesn’t matter what kind of foods you eat, don’t have to avoid carbs as there is always a baseline of insulin.
It reduces the risk of hypoglycaemia overnight as they are not having any quick acting insulin which is what actively lowers the blood sugar.

21
Q

Basal bolus advantages and disadvantages

A

Advantages:
- More flexibility with meal times
- Tighter glycaemic control
- Rapid acting analogues- greater flexibility and control
- Longer acting analogues- decreases chance of nocturnal hypoglycaemia

Disadvantages
- Multiple injections required
- Can lead to more weight gain
- Increased risk of hypoglycaemia
- Required patient compliance and responsibility

22
Q

DAFNE (Dose Adjustment For Normal Eating)

A

It is a program to educate adults with type 1 diabetes and helps them lead aa normal a life as possible whilst maintaining blood glucose within healthy targets.
Teaches people how to count carbohydrates in complex situations (e.g. buffets, takeaways) where there are a lot of hidden carbohydrates and how to find the right dose of insulin.
Usually advise that patients underestimate and top up later as we don’t want them to become hypoglycaemic.

23
Q

Carbohydrate counting

A

10g of carbohydrate requires 1 unit of insulin (in an individual with correct background and no resistance)

24
Q

Twice or three times daily injections

A

2 or 3 analogue or isophane biphasic injections.

Mix of quick and long acting.
The number in the name tell you how much is quick acting e.g. Humalog 25 is 25% quick acting.

25
Q

Twice or three times daily injections advantages and disadvantages

A

Advantages
- Simple
- Convenient
- firs well into regular work routing
- Can be provided by health care professionals e.g. by community nurses for those unable to do their own insulin

Disadvantages
- Limited flexibility with timing of mealtimes (e.g. late lunch may cause hypo)
- May require inter-meal snacks
- Overnight blood sugar control issues (risk of hypos)
- Difficult to treat ‘highs’
- Less tight glycaemic control

26
Q

5 minutes for insulin

A

1 true long acting and 1 analogue biphasic.

Give 2 injections once a day
Keeps them out of diabetic ketoacidosis but very limited control so will probably end up with complications.

27
Q

5 minutes for insulin advantages and disadvantages

A

Advantages
- Patients actually do it
- Virtually no time spent thinking about diabetes if overwhelmed or stressed
- Keeps them out of DKA/HHS (very high BG)

Disadvantages
- Facilitates disengaged behaviour
- Virtually no ‘control’ for glucose other then keeping patients out of the danger zone
- Will certainly progress toward diabetes related complications such as heart attacks, heart failure, diabetic foot disease, kidney disease, and retinopathy
- Reduced life expectancy

28
Q

Insulin pumps and continuous glucose monitors

A

Filled with quick acting- slowly drops tiny amounts in to create basal insulin. You can change it hour by hour to design an individualised regimen specific to that person (when they eat, exercise, etc).

Closed loops- the monitors speak to the pumps and they act as an artificial pancreas. The monitor checks what the glucose is and it tells the pump whether to give more or less insulin. All the patient has to fo is put in how much food they are eating and the pump works out how much insulin to give.

29
Q

What is the disadvantage of using HbA1c as a marker?

A

It is an average of the blood glucose measurements. This means the patient could go above and below target multiple times in the day and the HbA1c will still say they are in range.

30
Q

Time in range

A

70% time in range is the aim but it takes a lot of patient engagement to get there.

For the elderly the target for time spent in hypos is much lower as they are more at risk of falls compared to a young person. A fall for an elderly person will have greater consequences as they may end up in bed for long periods of time leading to loss of muscle mass and functionality. To make sure they do not have hypos the time allowed above target range is increased.

Pregnant women should spend as little time above target range as possible. Glucose does cross the placenta and high glucose is poor for the vascular system and when there are tiny vessels being created in the womb it can be harmful to the baby.

31
Q

Inequality in insulin pump distribution

A

Massive inequality in pump distribution and care.
Patients from more affluent areas have more access to pumps.
NICE says everyone should have access to Hybrid Closed Loop Systems.

32
Q

Why use a closed loop?

A
  • Better glycaemic control- researchers found that HbA1c reduced by an average of 1.7% and time in range increased by an average of 28.3%
  • Better overnight control
  • Reduced risk of complications/admissions
  • Reduces diabetes burnout/mental burden- more than 70% of people reported that using a hybrid closed loop improved not just their food sugar levels but also their quality of life
  • Lower insulin requirements
33
Q

Drawbacks of closed loop systems

A
  • Complex to understand- not suitable for all (elderly, those with learning difficulties)
  • Complex to manage- extremely specialist skill set to review and adjust further complicating patient care in hospitals
  • Reluctant to trust (you can’t actually see the insulin going in you anymore)
  • Retinopathy risk
  • Using diabetes technology is like switching from driving a car with manual gears to driving an automatic car. It can take a while to get used to
  • Risk of failures
  • Exercise adjustments
  • Cost
34
Q

Treatment

A
  1. HbA1c test to measure overall blood glucose levels over the past 8-12 weeks
  2. Blood pressure measurement
  3. Cholesterol test to check for levels of harmful fats in the blood
  4. Eye screening using a digital camera to look for any changes to the back of the eye
  5. Foot examination to check the skin, circulation and nerve supply of legs and feet
  6. Kidney function to measure how well the kidneys are working- creatinine clearance
  7. Urinary albumin to check fr protein which may be a sign of kidney problems
  8. BMI measurement to check if you are a healthy weight
  9. Smoking review including advice and support for smokers
35
Q

Blood glucose targets

A

Adults with type 1 should aim for
- a fasting plasma glucose level of 5-7 mmol/litre on waking, and
- a plasma glucose level of 4-7 mmol/litre before meals at other times of the day

Those who chose to test after meals should aim for a plasma glucose level of 5-9 mmol/litre at leas 90 minutes after eating.

An agreed bedtime target plasma glucose level should be set that takes into account timing of last meal and its related insulin dose.

36
Q

Long term monitoring

A
  • HbA1c should be checked every 3-6 months until stable
  • NICE guidelines states patient should aim for a target A1c of 53mmol/mol
  • Targets should be individualised to the specific patient as diabetes is different is everyone
    (- Targets can be relaxed if patient is having lots of hypos or is very frail)
37
Q

Hypoglycaemia

A
  • Defined as blood glucose of less than 4mmol/mol (4 is the floor!!)
  • Early symptoms (adrenergic) include hunger, sweating, tingling lips, tremor, dizziness, tiredness, palpitations, irritation, pallor
    When blood glucose is low the body produces adrenaline which causes the symptoms of hypo. Adrenaline as a hormone resolves the hypo by increasing glucose output from the liver.
    -Later symptoms (neurological) include weakness, blurred vision, poor concentration, confusion slurred speech, seizures, collapse

Detect and treat
- 15-20g fast absorbing glucose

38
Q

What can be used to treat hypoglycaemia?

A
  • Full fat soda
  • 5 glucose tablets
  • 5 jelly babies
  • Fresh fruit
  • Tube of glucose gel
39
Q

Hospital treatment of hypoglycaemia

A

Severe hypos require either IM glucagon or IV glucose
- IM if they are fluid restricted
- Glucagon- opposing hormone to glucose. Makes the liver evacuate all glucose stored in one go. Cannot do repeated doses as all the glucose has been removed from the liver in the first dose

A RCT of patient in ED with hypo showed these two were equal effective overall in treating hypos with similar averse effect profiles but recovery levels were swifter with IV glucose in comparison to IM glucagon.

Glucagon will be less effective in those with depleted glycogen reserves such as those with impaired hepatic function.

Glucagon is effective and useful as a treatment option in an outpatient setting when IV access is unavailable. However, it can only be used once and provides slower recovery so IV glucose is the preferred option.

40
Q

Driving and diabetes

A
  • Must inform DVLA if using insulin
    • Complete a self declaration including contact details of specialist care provider and report on hypo awareness
    • Restricted license (no HGVs) and 3 year expiry
  • Always test glucose before any journey if driving
  • Need to be 5 to drive! If less than 5mmol/L treat as hypo and must wit at leats 45 minutes after glucose has returned to >5.
  • Test blood glucose every 2 hours as a minimum on long journeys
41
Q

Alcohol and diabetes

A
  • alcohol lowers blood glucose
  • Risk of hypoglycaemia
  • Harder to manage- thought processes impaired
  • More likely to forget and omit insulin
  • Some drinks like cocktails have lots of sugar in them so even though it has alcohol in it will still push blood glucose up.
  • Beers and larger can have carbohydrates in them.
  • Wines and Prosecco will also increase blood glucose but it will drop again
42
Q

Needle safety

A

Reusing needles can cause lipohypertrophy which is hard nodules under the skin and the insulin is not vascularised.

43
Q

Sick day rules

A

If vomiting and unable to keep fluids down go to A&E.
If someone has had an infection or trauma their need for glucose will increase. If they don’t have sufficient insulin no matter how much more glucose the liver produces they won’t absorb any more. Therefore, in illness they may need higher doses of insulin.
Glucose will normalise before ketones because they have to come out through the kidneys so patients need to stay hydrated.