Thursday, October 20, 2022

cmecde 21546

 





Key stages for developmental assessment

Newborn

Supine infant (1.5–2 months)

Sitting infant (6–9 months)

Toddler (18–24 months)

Communicating child (3–4 years)

The four areas in which development is assessed

Gross motor skills

Vision and fine movement

Hearing and language

Social behaviour

Before starting

Introduce yourself to the parent and child, and confirm the child’s name and date of birth.

Explain that you would like to ask a few questions about how the child is doing, and obtain

consent.

Ensure that the child is comfortable. Younger children may need toys to keep them distracted.

Ask to look at the child health record or ‘red book’.

The assessment

Confirm the sex and preferred name of the child.

Do not ask whether the child is ‘developing normally’. Ask instead, “Do you have any concerns

with his development?”

Be sure to verify whether any delay is in just one area or all four (gross developmental delay).


Clinical Skills for OSCEs

160 Station 59 Developmental assessment

Table 23. Average age for the acquisition of milestones

Key stages Age Gross motor

skills

Vision & fine

movement

Hearing and

language

Social

behaviour

Newborn Birth –

1/12

Symmetrical

movements,

limbs flexed,

head lag on

pulling up

Looks at light/

faces in direct

line of vision

Startles to

noises and

voices, cries

Responds

to parents,

endogenous

smile

Supine infant 2/12 Raises head in

prone position

Eyes ‘fix and

follow’ to

midline

Coos and grunts Exogenous

smile, i.e. at

faces or objects

3–4/12 Rolls over

from supine to

prone, sits with

support

Eyes follow past

midline

Laughs

Sitting infant 6/12 Rolls over

from prone

to supine, sits

unsupported

Transfers

objects from

hand to hand

Babbles, single

syllable words

(yes, no)

Separation

anxiety

9/12 Crawls and,

from 10/12,

‘cruises’ (walks

holding on to

furniture)

Pincer grasp Double syllable

words (mama,

bye-bye)

Stranger

anxiety, plays

pat-a-cake and

peek-a-boo

Toddler 1 year Takes first steps Starts to feed

himself

Uses 10 words Onlooker and

parallel play

18/12 Runs, walks

carrying a toy

Stacks 3 cubes Uses 10–20

words

Temper

tantrums

2 years Ascends stairs

in child-like

manner, arm

throws a ball

Copies a line,

stacks 6 cubes

Uses 200 words,

pronouns,

2-word

sentences

Alone play

continued


Paediatrics and geriatrics

Station 59 Developmental assessment 161

Table 23. Average age for the acquisition of milestones – continued

Key stages Age Gross motor

skills

Vision & fine

movement

Hearing and

language

Social

behaviour

Communicating

child

3 years Climbs stairs

like an adult,

descends stairs

in child-like

manner, jumps

in one place,

rides tricycle,

catches ball

with arms

Copies a circle,

stacks 9 cubes,

builds bridge

with cubes

Uses 900

words and

understands

many more,

uses compound

sentences

Knows own

name and

gender,

understands

‘taking turns’,

i.e. co-operates

4 years Climbs down

stairs like

an adult,

hops on one

foot, throws

overhand

Copies a cross

and, from 4.5

years, a square

Tells stories Imitates

parents, has

imaginary

friends

5 years Stands on one

leg, catches ball

with hands

Copies a

triangle

Asks the

meaning of

words

Conforms with

peers

Red flags

‘Red flags’ that call for further investigation include the absence of:

– smiling at 2/12

– good eye contact at 3/12

– sitting at 9/12

– walking at 18/12

– 2–3 word sentence construction at 2.5 years

After the assessment

Ask the parent if there is anything they might add that you have forgotten to ask about.

Ask the parent if they have any specific questions or concerns.

Thank the parent and child.

Summarise your findings and offer a differential diagnosis.

Conditions most likely to come up in a developmental assessment station

Late walker (>18 months).

Visual or hearing impairment.

Developmental disorder, e.g. autism.

Emotional disorder, e.g. enuresis (>5 years), elective mutism, sleep disorder.

Behavioural disorder, e.g. conduct disorder, ADHD.

Gross developmental delay from e.g. mental retardation, genetic abnormality, brain injury,

congenital infection, endocrine disorder.


Clinical Skills for OSCEs

162 Station 60

Neonatal examination

Specifications: A mannequin in lieu of a baby. The baby’s ‘mother’ is also in the room.

Before starting

Introduce yourself to the mother, and confirm the baby’s name and date of birth.

Explain the examination, and ask for consent.

Wash your hands.

Ask the mother about:

– complications of the pregnancy, if any

– type of delivery and any complications

– the baby’s gestational age at the time of birth

– the baby’s birth weight

– the baby’s feeding, urination, and defecation

– any concerns that she might have about the baby

– how she herself is coping with the new arrival

The examination

General inspection

Although it is important to be systematic, an opportunistic approach to the examination may

be necessary.

Note size, colour (e.g. cyanosis, jaundice), posture, tone, movements, skin abnormalities (e.g.

birth marks, petechiae, rash, haemangioma, Mongolian blue spot), and any other obvious

abnormalities (e.g. dysmorphic features or birth trauma such as forceps marks or chignon). Are

there any signs of pain or respiratory distress?

Head

Gently palpate the anterior and posterior fontanelles for bulging (raised intracranial pressure)

or depression (dehydration).

Measure the head circumference with the tape measure passing above the ears. Head circumference in the neonate should be 33–38 cm.

Figure 39. Neonatal examination, general order of the

examination.


Paediatrics and geriatrics

Station 60 Neonatal examination 163

Face

Inspect the face for dysmorphological features, e.g. dysplastic or folded ears, upward slanting

palpebral fissures, and a flat nasal bridge (all may be seen in Down syndrome).

Inspect the sclerae for redness (subconjunctival haemorrhage related to birth trauma) and the

irises for Brushfield spots (Down syndrome).

Using an ophthalmoscope, test the red reflex (congenital cataracts if the red reflex is absent,

retinoblastoma if instead there is a white reflex) and pupillary reflexes.

Test eye movements (squint).

Check the patency of the ears and nostrils.

Elicit the rooting reflex by lightly touching a corner of the baby’s mouth.

Introduce a finger into the baby’s mouth and palpate the roof of the mouth with the finger pulp

to assess the sucking reflex and soft palate (cleft palate).

Also examine the soft palate using a torch and spatula.

Chest

Inspect the chest for signs of laboured breathing and for deformities, e.g. pectus carinatum,

pectus excavatum, shield-shaped chest with widely-spaced nipples (Turner syndrome).

Take the brachial and femoral pulses, one after the other and then both at the same time

(brachio-femoral delay). Pulse rate in the neonate should be 100–160.

Palpate the precordium and locate the apex beat.

Auscultate the heart using the bell of your stethoscope (congenital heart defects).

Auscultate the lungs using the diaphragm of your stethoscope. Turn the infant over and listen

over the back. The respiratory rate should be less than 60 breaths per minute.

Back

Examine the spine, focusing on the sacral pit (neural tube defects).

Check the position and patency of the anus (anal atresia).

Enquire as to when the baby first passed stool. Ideally, this should have been within 24 hours

of birth.

Abdomen

Inspect the abdomen and the umbilical stump.

Palpate the abdomen.

Palpate specifically for the spleen, liver, and kidneys (thumb in front, finger in the loin), and for

any masses.

Auscultate for bowel sounds.

Feel in the inguinoscrotal region for inguinal hernias.

Examine the genitalia, in male infants note the position of the urethral meatus (hypospadias)

and feel for the testicles (undescended testes).

Feel for the femoral pulses (coarctation of the aorta).

Hips

Ortolani test. With your thumbs on the inner aspects of the thighs and your index and middle

fingers over the greater trochanters, flex the hips and knees to 90 degrees and then abduct the

hips (an audible and palpable clunk indicates relocation of a dislocated hip).

Barlow test. Next, adduct them whilst applying downward pressure with your thumbs (an audible and palpable clunk indicates an unstable hip that can be dislocated).


Clinical Skills for OSCEs

164 Station 60 Neonatal examination

Arms and hands

Inspect the arms and hands, paying particular attention to the palmar creases (Simian crease –

Down syndrome).

Count the number of digits on each hand (polydactyly).

Feet

Inspect the feet for deformities such as club foot and ‘sandal gap’ and test their range of movement.

Count the number of digits on each foot (polydactyly).

Posture and reflexes

Head lag. Lay the baby supine and pull up the upper body by the arms – the head should first

‘lag’ back, then straighten and fall forward.

Ventral suspension. Hold the baby prone – the head should lie above the midline.

Moro or startle reflex. Lift the head and shoulders and then suddenly drop them back – the

arms and legs should abduct and extend symmetrically, and then adduct and flex (NB. This test

should be conducted as safely and sensitively as possible. For instance, it could be carried out

with the baby only slightly raised from the cot mattress.).

Grasp reflex. Place a finger in the baby’s hand – the hand should close around your finger.

Ortolani test

Barlow test Figure 40. The Ortolani and Barlow tests.


Paediatrics and geriatrics

Station 60 Neonatal examination 165

After the neonatal examination

State that you would also measure and weigh the baby and record your findings on a growth

centile chart.

Summarise your findings.

Reassure the mother, and tell her that you are going to have the baby examined by a senior

colleague.

Figure 41. Eliciting the Moro reflex.


Clinical Skills for OSCEs

166 Station 61

The six-week surveillance review

Specifications: A mannequin in lieu of a baby. The six-week ‘baby check’ is part of the Newborn and

Infant Physical Examination programme. It involves a physical examination and review of development.

However, it is also an opportunity to give health promotion advice and for the parent or parents to

express concerns.

Before starting

Introduce yourself to the parent, and confirm the baby’s name and date of birth.

Explain the nature of the examination and obtain consent.

Ask for the child health record or ‘red book’.

The history

Ask for the exact age, sex, and preferred name of the child.

Main concerns

Ask if the parent has any specific concerns.

Past medical history

Birth history:

– pregnancy

– gestation

– delivery

– birth weight

– neonatal history

Present health:

– current health status, including feeding regimen and weight gain

– medication

– social history

The examination

PART 1 – DEVELOPMENTAL ASSESSMENT

Motor skills

Symmetrical limb movements.

Head lag.

Vision and fine movement

Looks at light/faces.

Follows an object.

Hearing and language

Responds to noises/voices.

Normal cry.

Ask parent if they are concerned about the baby’s hearing.


Paediatrics and geriatrics

Station 61 The six-week surveillance review 167

Social behaviour

Smiles responsively.

PART 2 – PHYSICAL EXAMINATION

Wash your hands

General inspection

Overall size and colour, i.e. is the baby cyanosed or jaundiced?

Skin abnormalities such as birth marks, petechiae, or rash.

Other obvious abnormalities such as dysmorphic features.

Posture, tone, and movements.

Signs of respiratory distress

Growth

Weight.

Length.

Head circumference.

Plot findings on a centile chart.

Head

Palpate the fontanelles.

Face

Eyes: red reflex, pupillary reflexes, and eye movements (squints).

Ears.

Mouth – use a pen torch (high arched or cleft palate).

Chest

Feel for the radial and femoral pulses.

Auscultate the heart.

Auscultate the lungs.

Back

Examine the spine, particularly the sacral pit.

Abdomen

Inspect and palpate the abdomen.

Examine the external genitalia.

Hips

Abduct the hips (Ortolani test, see Figure 40).

Next, adduct them whilst applying downward pressure with your thumbs (Barlow test, see

Figure 40).


Clinical Skills for OSCEs

168 Station 61 The six-week surveillance review

After the surveillance review

Discuss your findings with the parent.

Use the opportunity for health promotion, e.g. immunisations, breastfeeding, car safety, accident prevention, risks of passive smoking, reducing the risk of sudden infant death syndrome,

services available for the parents of young children.

Consider maternal mental health. How is mum coping? Is there any suggestion of postnatal

depression?

Elicit any remaining concerns that the parent may have.

Thank the parent.


169Paediatrics and geriatrics

Station 62

Paediatric examination: cardiovascular system

Read in conjunction with Station 13.

If you are asked to examine the cardiovascular system of a younger child (an unlikely event), be

prepared to change the order of your examination and to modify your technique as appropriate. For

example, you may need to examine the child on his parent’s knees or auscultate his heart as soon

as he stops crying. As in all paediatric stations, the quality of your rapport with the child will be of

considerable importance.

Before starting

Introduce yourself to the child and the parent, and confirm the child’s name and date of birth.

Explain the examination and ask for consent to carry it out.

Position the child at 45 degrees, and ask him to remove his top(s).

Ensure that he is comfortable.

The examination

General inspection

From the end of the couch, inspect the child carefully, looking for any obvious abnormalities

in his general appearance and in particular for any dysmorphic features suggestive of Down

syndrome (e.g. oblique eye fissures, epicanthic folds, Brushfield spots, flat nasal bridge, Simian

crease), Turner syndrome (e.g. short stature, low-set ears, webbed neck, shield chest), or Marfan

syndrome (e.g. tall stature, elongated limbs, pectus carinatum or pectus excavatum).

Does the child look his age? Ask to look at the growth chart.

Is he breathless or cyanosed?

Look around the child for clues such as a oxygen, PEFR meter, inhalers, etc.

Inspect the precordium and the chest for any scars and pulsations. A median sternotomy or

thoracotomy scar under the axillae may indicate the repair of a congenital heart defect such as

a patent ductus arteriosus or a ventricular septal defect.

Inspection and examination of the hands

Take both hands and assess them for:

– colour and temperature

– clubbing (cyanotic congenital heart disease)

– nail signs

Determine the rate, rhythm, and character of both radial pulses (in younger infants, the brachial

pulses). Take both femoral pulses at the same time to exclude a radiofemoral delay (coarctation

of the aorta).

Indicate that you would record the blood pressure in both arms. If you are asked to record the

blood pressure, remember to use a cuff of appropriate size.


Clinical Skills for OSCEs

170 Station 62 Paediatric examination: cardiovascular system

Table 24. Normal pulse rates in children

Age in years Pulse (beats per minute)

< 1 100–160

2–4 90–140

4–10 80–140

> 10 65–100

Inspection and examination of the head and neck

Inspect the conjunctivae for signs of anaemia or jaundice.

Inspect the mouth and tongue for signs of central cyanosis and a high arched palate (Marfan

syndrome).

Assess the jugular venous pressure (difficult in very young infants).

Locate the carotid pulse and assess its character.

Palpation of the heart

Ask the child if he has any pain in the chest.

Determine the location and character of the apex beat. In children (up to 8 years), this is found

in the fourth intercostal space in the mid-clavicular line.

Palpate the precordium for thrills and heaves.

Auscultation of the heart

Warm up the diaphragm of your stethoscope.

Listen for heart sounds, additional sounds, and murmurs. Using the stethoscope’s diaphragm,

listen in:

– the aortic area

– the pulmonary area

– the tricuspid area

– the mitral area

(See Station 13, Figure 7.)

Any murmur heard must be classified according to:

– timing (systolic or diastolic)

– grading (I–VI)

– site (aortic, pulmonary, tricuspid, or mitral)

– radiation (carotids or axilla, or no radiation)

Innocent murmurs are common in childhood

Innocent murmurs are:

Systolic.

Low-grade.

Heard over only a relatively small area.

Asymptomatic.


No comments:

Post a Comment

cmecde 544458

  Paediatrics and geriatrics Station 67 Child immunisation programme 185 That having been said, they are still very common in some other cou...