Carbohydrates Flashcards

1
Q

Normal blood glucose?

A

3,5-5,5 mmol/l

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2
Q

Name 4 hormones that increase blood glucose

A

• Glucagon
• catecholamines (adrenaline)
• growth hormone
• cortisol

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3
Q

Name 3 factors that stimulate insulin release

A

•increased blood glucose
• incretin gut hormones during food intake:
-Glucagon like peptide 1 GLP 1
- glucose dependent insulinotropic peptide GIP

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4
Q

Name 2 electrolyte changes in insulin deficiency

A

Hyperkalaemia
Hyper P

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5
Q

Name 3 electrolyte changes in insulin therapy

A

(Increased cellular uptake)
• hypo K
• hypo p
• hypo mg

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6
Q

Name 4 causes diabetes mellitis

A

• Chronic pancreatitis
•Haemochromatosis ( excess iron)
• endocrine conditions with increased cortisol eg Cushing
• endocrine conditions with increased gh eg acromegaly

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7
Q

Define normal fasting glucose

A

<6,1

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8
Q

Define dm glucose

A

Fasting ≥7
2h post glucose ≥11,1

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9
Q

Diabetic hba1c?

A

> 6,5% (48 mmol/mol)
Repeat within 2. weeks to confirm
(If <6,5%, reassess in 6 months because high diabetes and cv risk)

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10
Q

Define intermediate HbA1C values and appropriate action

A

6-6.4% (42-47 mmol/mol)
Increased risk diabetes and cv risk, reassess in 1 year

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11
Q

Name 6 contraindications to using hba1c

A

• Rapidly changing glucose levels eg acute illness, new onset dm, drugs
• abnormal RBC lifespan: liver and kidney disease, hemolytic anemia, fe deficiency, b12/folate deficiency, hypersplenism, splenectomy
• pregnancy
• severe anaemia hb <6,5
• no HbA ( homozygous variant: S,C,D, E)
. Method specific interferences from certain hb variants

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12
Q

First line diagnosis for gestational diabetes?

A

2h ogtt > 7,8 mmol/ L

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13
Q

When should gestational diabetes be tested for

A

24-28 Weeks

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14
Q

Best method of measuring ketones in diabetes?

A

Plasma 3-oh-buturate (3-0h-b) with ketone meter
(Urine detect acetoacetate and acetone, which can underestimate DkA severity)

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15
Q

Which tests should be used to monitor nephropathy in diabetes (4)

A

• Creatinine
• eGFR
• screen for microalbuminaria (3-30 mg / mmol) with urine albumin: creatinine ratio
• once clinical proteinuria (acr>30), monitor with urine protein: creatinine ratio

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16
Q

Electrolyte derangements in DkA? (3)

A

• Hypo Na
• hyper K
• hyper p

17
Q

Treatment DKA? (5)

A

• Insulin for hyperglycaemia
• iv saline for hyponatraemia
• k, p, Mg supplements (insulin cause hypo)
• check uce, blood glucose every 6 hours
• monitor water balance with CvP and input output chart

18
Q

Define hyperosmolar hyperglycaemic state (3)

A

• DM 2 severe hyperglycaemia > 50 mmol /l without DkA
• extreme dehydration, very high serum osmolality >320 mosm/kg
• no or minimal metabolic acidosis, no/mild ketones (unlike dka)

19
Q

Treatment hyperosmolar hyperglycaemic state

A

• Rehydration
• low dose iv insulin
• thrombosis prophylaxis

20
Q

Define Whipple’s triad of hypoglycaemia

A

• Hypoglycaemic symptoms: neuroglycopaenia
• low glucose <3
• symptoms resolve after glucose load

21
Q

How determine cause of fasting hypoglycaemia? (3)

A

Measure insulin and C peptide while hypoglycaemic
• both increase: endogenous hyperinsulinism eg islet cell tumours, drug induced, anti-insulin antibodies
• both decrease: suppressed endogenous insulin secretion: liver diseases , CkD, non-islet cell tumours, endocrine deficiencies, drug, alcohol, severe starvation
•. increase insulin, decrease C peptide: exogenous insulin, anti-insulin receptor antibodies

22
Q

How calculate expected pCO2 for metabolic acidosis?

A

1.5 x HCO3 + 8
(Range +/- 2. Max compensation may take 12-24h to reach)

23
Q

Name 9 causes neonatal hypoglycaemia

A

• Fasting
• decreased liver glycogen ; muscle protein; fat in premature and iugr
• increased consumption in birth stress, RDS, infections, hypothermia
•Persistent hyperinsulinaemic hypoglycaemia of infancy
• decreased growth hormone, cortisol
• inborn errors of intermediary metabolism
-Galactosaemia
- organic acidemias
- Fatty acid oxidation disorders
- Glycogen storage diseases, hereditary fructose intolerance

24
Q

Which test can be done on newborns to confirm presence of mono or disaccharide that can’t be metabolised

A

Screen for urine reducing sugars with copper reduction test (urine change colour)