Endo Flashcards

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1
Q

What is the difference between hypocalcemic and hypophosphatemic rickets?

A

In Vitamin D deficiency (hypocalcemic) you have decreased calcium, normal (or mildly low) phosphate, increased ALP, PTH and decreased Vitamin D.

Hypophosphatemic: decreased phosph, normal caclium, normal vitamin D, increased ALP

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2
Q

What are 5 risk factors for cerebral edema in DKA?

A
Too much Bolus 
Insulin Bolus
First time presentation 
Young Age <5 years 
High BUN and Low CO2
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3
Q

What are the components of the critical sample? (11)

A

Serum:
Glucose, IGF-1, Cortisol, insulin
Fatty Acids: Free Fatty acids, Carnitine, beta hydroxy buturate
Gluconeogenesis: Pyruvate, Lactate

Urine: Ketones, Urine Amino Acids and Organic acids

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4
Q

5 Causes of Primary Amenorrhea

A
Turner Syndrome
Premature Ovarian Failure
Hypothalmic-Pituitary dysfunction 
Pan hypopit
Malnutrition
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5
Q

6 Causes of Secondary amenorrhea

A
Pregnancy
Premature Ovarian Failure 
Eating Disorder 
CNS Tumor 
Chronic Disease 
Thyroid
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6
Q

Rickets Monitoring

A

Monitoring is via ALP

You can test 25 Vitamin D initially

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7
Q

Signs of Rickets?

A
Ricketic Rosary 
Craniotabes 
Cupping, fraying and splaying
Widened growth plates 
Thickened risks
Bowed Legs
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8
Q

Canadian Guidelines for Screening for Type 2 Diabetes

A

Pre Pubertal = 3 or more
Post Pubertal = 2 or more

Obese
Signs of insulin resistance - Acanthosis nigricans
Family history
High risk ethnicity

Being on atypical antipsychotics will put you at increased risk.

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9
Q

Missing Insulin - what is the counselling

A
Check for Ketones - DKA?
Still need to give long acting Insulin
Will need to bolus for elevated glucose with rapid insulin 
ISF = 100/TDD
Aim for 6-10 - maybe around 8 
Check sugar again in 3 hours
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10
Q

What are the screening recommendations for Type 1 dm - Comorbidities and associated risks

A

Comorbidities:
Retinopathy - 15 years of age and diabetes for more than 5 years
Nephropathy - 12 years of age and diabetes for more than 5 years
Neuropathy - Only if symptomatic and poor control; diabetes for >5 years
Dyslipidemia - 12 and 17 years of age; if less than 12 if they have other risk factors
HTN: twice a year

thyroid - every 2 years; Celiac and Addisons - if symptomatic.

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11
Q

Sick day guidelines for Type 1 DM

A

Children may need extra insulin if they are sick. Use the 5-10-15-20 Rule.
Use this rule if their bg is greater than 15 or if there is ketones in urine or blood.
If the child is vomiting - may need a mini glucagon dose.

Urine Ketones/BG 15-20/BG>20
Negative - none or 5%
Small-5% or 10%
Medium-10% or 15%
Large-15% or 20%

The percentage of insulin is always a percentage of the total daily dose.

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12
Q

What are the cut offs for lipds?

A

No risk factors: 4.9 mmol
Risk factors: 4.1
Diabetes: 3.4

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13
Q

What is growth hormone approved for?

A

Turners, Prader Willi, Have not caught up after 2 years with IUGR/SGA, GH Deficiency, noonan, renal insufficiency, idiopathic short stature.

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14
Q

What are the antibodies in:
Graves
Hashimotos

A

Graves: Anti thyroid receptor, Thyroid stimulating hormone
Thyroglobulin

Hashimotos: Anti TPO (microsomal) - the thyroid is infiltrated by T lymphocytes.

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15
Q

What are the treatment for Graves and what are the side effects

A

Medications: PTU and Methimazole (1st line)
White, Yellow, Red, teratogen and hypothyroid
Agranulocytosis, liver toxx and rash/serum sickness
Radio iodine

Thyroidectomy

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16
Q

Explain premature thelarche and adrenarche

A

Thelarche: is common at 6 months and 24 months. The patient has a normal height velocity and bone age. Not common after 4 years of age.

Adrenarche: normal or mildly increased bone age
Increased DHEA and androsteine; normal testosterone

17
Q

How do you treat adrenal insufficiency/

A

Normal is 6-8 mg/m2 of Hydrocortisone
Mild Illness 20-30
Moderate 50
Severe 100

All children need to wear a medic alert bracelet.

18
Q

What are 5 side effects of steroid use?

A
Adrenal insufficiency
Weight Gain
Hyperglycaemia/hypertension 
Infection 
Cataracts
19
Q

What are the clinical signs of osteogenesis imperfecta and how many types are there?

A

It is an AUTOSOMAL DOMINANT condition with a genetic mutation in collagen.
Clinically: blue sclera, wormian bones, dentogenesis imperfecta, joint laxity, changes in face
4 types: type 2 is the worst. Type 1 multiple fractures but usually in adolescent. Type 3 and 4 are inbetween.

20
Q

Mcune Albright

A

Poly osteotic disease; cutaneaus manifestations that do not cross midline and precocious puberty

21
Q

Albright Hereditary Osteodystrophy

A

Like nephrogenic DI but for Vitamin D

Vitamin D dependent rickts - does not respond to parathyroid hormone (increased phosphate and decreased calcium)

Round faces, short stature, short 4th metacarpal and developmental delay, subcutaneous calcifications.

22
Q

What are the clinically significant fractures

A

2 or more long bone fractures by 10 years
3 or more long bone fractures by 19 years
1 or more vertebral compression fracture (loss of 20%)