Growth Flashcards

1
Q

How is prematurity adjusted for in a growth chart?

A

Prematurity= <37 weeks gestation
Actual age is plotted on the graph and then arrow is drawn to adjust to gestational age: go back the number of weeks they were born premature.

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2
Q

What is defined as a failure to thrive?

A

Growth that crosses two centiles on a growth chart - needs prompt assessment and investigation.

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3
Q

What is the definition of growth failure?

A

Where height is below the 25th centile for a period of at least 18 months.

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4
Q

How do you calculate the mid -parental height

A

(Father’s height (cm) - Mother’s height (cm) ) / 2 +7cm for boys, or - 7cm for girls

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5
Q

How is BMI calculated?

A

Weight (kg)/ Height (m)^2

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6
Q

What is are the upper and lower limits of normal birth weight?

A

Low birth weight = <2500g

High birth weight = >4000g

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7
Q

Why is some allowance for low weight allowed in the first 2 weeks?

A

Babies may lose up to 10% of the body weight within the first two weeks

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8
Q

What are the four phases of normal growth?

A
  1. Foetal growth:
    Fastest period of growth - determined by mother size and placental nutritional supply
    Hormones involved = IGF-2, insulin, HPL

2.Infancy phase:
Rapid deceleration of growth in the first 2-3 years of life.
Fastest period of growth apart from foetal - peak of 18cm per year .

3.Childhood phase:
Slowest phase - from 2/3 years to puberty.
Initially determined by nutrition, then later by hormones e.g. GH

4.Pubertal phase:
Growth spurt occurs from puberty to 14/15 in girls, and 16/17 in boys.
Determined by GH and sex hormones - peak is at around Tanner stage 3.

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9
Q

What marks the end of the pubertal growth spurt?

A

Fusion of the epiphyses due to action of oestrogen.

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10
Q

What are the Tanner Stages of development?

A

Male - testicular volume:
Tanner 1 = <1.5ml - small penis
Tanner 2 = 1.6-6ml - scrotum skin thins, penis length unchanged
Tanner 3 = 6-12ml - penis begins to lengthen
Tanner 4 = 12-20ml - scrotum enlarges and penis continues to lengthen
Tanner 5 = >20ml - adult scrotum and penis by 14/15 y/o

Female - breasts:
Mnemonic = No-Body Elevates 2 mountains in Adulthood
Tanner 1 = NO glandular tissue
Tanner 2 = Breast bud forms, with some glandular tissue and areola widening
Tanner 3 = Breast elevated and extends beyond borders of areola
Tanner 4 = Areola and papilla form secondary mound - increasing in size and elevation
Tanner 5 = Adult size breasts -

Both - pubic hair:
Mnemonic = she/he’s Not a Small CAT
Tanner 1 = No hair
Tanner 2 = Small amount of downy hair, with slight pigmentation
Tanner 3 = Coarse and wiry hair - extending laterally
Tanner 4 = Adult-like but thigh sparing
Tanner 5 = Thighs not spared

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11
Q

Explain the growth hormone axis…

A
  1. GH- releasing hormone (GHRH) and Somatotropin release inhibiting factor (SRIF / somatostatin) are released by hypothalamus.
  2. GHRH stimulates GH release from somatotrophs, and somatostatin inhibits release.
  3. GH has direct effecton promotion of bone growth AND stimulates production of IGF-1 in the liver - which is released as free IGF-1.
  4. IGF-1 is transported to bone where it stimulates proliferation of epiphyseal growth plate.
  5. IGF-1 has negative feedback on pituitary and hypothalamus.
    GH has negative feedback on hypothalamus.
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12
Q

What is the definition of short stature?

A

Height that is >2 SDs from the mean (below second centile)

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13
Q

What are some causes of short stature?

A

Commonest: familial short stature or constitutional delay

Primary growth disorders:

  • Genetic syndromes= Down’s, Turner’s
  • IUGR
  • Congenital bone disorders = osteogenesis imperfeta

Secondary growth disorders:

  • Psychosocial deprivation
  • Malnutrition
  • Chronic disease
  • Endocrine disorders e.g. GH deficiency
  • Medication e.g. steroids
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14
Q

If the child is small, but following the centile lines - what should be considered?

A
  • Familial short stature
  • Low birthweight
  • Constitutional delay
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15
Q

Important features of history in short stature…

A
  • Obstetric history - any prenatal complications, prematurity
  • Feeding history
  • Family history of growth disorders
  • Developmental milestones
  • Systems review to identify any underlying chronic disease
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16
Q

If no signs of disease in child with short stature, what should be done?

A

Review growth in 12 months - then calculate growth velocity.

17
Q

What investigations can be carried out for short stature?

A

Bloods:

  • FBC: anaemia in chronic disease e.g. IBD
  • U&Es: renal disorders
  • Bone profile: bone disorders
  • TSH: hypothyrodism
  • CRP/ ESR: IBD
  • EMA/ TTG: coeliac disease
  • IGF-1 measurement
  • Dexamethasone suppression test: Cushing’s (steroid excess)
  • Genetic karyotype: chromosomal disorders

Imaging:

  • X-ray of hand and wrist: identify bone age - delay in GH deficiency but no delay in familial short stature
  • MRI head: rule out intracranial tumours if neuro signs
  • Skeletal survey: Scoliosis present
18
Q

How do familial short stature and constitutional delay differ on growth charts?

A
  • Familial short stature will have consistent low level throughout growth chart
  • Constitutional delay will have low growth initially, followed by crossing centiles at puberty to a final normal adult height
19
Q

What are the causes of GH deficiency?

A
  • Isolated defect

- Secondary to panhypopituitarism - craniopharyngioma, head trauma , meningitis

20
Q

How is GH deficiency treated?

A

Subcutaenous GH injections at night- improves muscular strength, body composition and vertical height.

21
Q

What are the causes of failure to thrive?

A

Non-organic: environmental and social deprivation e.g. lack of food available

Organic:

  • Inadequate intake due to impaired suck/swallow reflex
  • Inadequate retention due to vomiting/ GORD
  • Increased nutritional requirements due to chronic illness
  • Failure to utilise nutrients
  • Impaired nutrient absorption e.g. coeliac