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Book cover for Oxford Handbook of ENT and Head and Neck Surgery (2 edn) Oxford Handbook of ENT and Head and Neck Surgery (2 edn)

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Oxford University Press makes no representation, express or implied, that the drug dosages in this book are correct. Readers must therefore always … More Oxford University Press makes no representation, express or implied, that the drug dosages in this book are correct. Readers must therefore always check the product information and clinical procedures with the most up to date published product information and data sheets provided by the manufacturers and the most recent codes of conduct and safety regulations. The authors and the publishers do not accept responsibility or legal liability for any errors in the text or for the misuse or misapplication of material in this work. Except where otherwise stated, drug dosages and recommendations are for the non-pregnant adult who is not breastfeeding.

They are small and so is their anatomy

They are usually unable to give an accurate history

They have parents who may be very anxious

Their condition can deteriorate very quickly

Important learning points

Be able to assess a child in its entirety.

Gain knowledge of how a child feeds and its daily requirements, especially the total time it takes to feed.

Become familiar with height and weight charts and the centile ranges which chart a child’s physical development.

Become familiar with the developmental milestones showing a child’s speech development (graphic see Table 17.1).

Table 17.1
Language development
AgeNormal language developmentNormal speech developmentIntelligibility

Infant

Cooing

Babbling

Non-cry vocalic sounds

Consonant—vowel syllables with intonation patterns

1 year

Appearance of first 2–3 words

Imitates sounds of animals

Omits most final and some initial consonants

Substitutes consonants m, w, p, b, k, g, n, t, d, and h for more difficult sounds

Usually no more than 25% intelligible to familiar listener

2 years

Uses 2–3-word phrases

Uses above consonants with vowels but inconsistently and with substitution

50–65% of spoken language can be understood

Has a vocabulary of 250–300 words

Can put together simple 2–3-word phrases

Word usage and comprehension develops but comprehension lags behind expressive ability

Uses I, me, and you

Can understand much adult communication directed to them

3 years

Says 4–5-word sentences, with a vocabulary of about 900 words. Uses who, what, and where. Uses plurals, pronouns, and prepositions

Says b, t, d, k, and g, but r and l may be unclear. W is either omitted or substituted. Often repeats self.

75% of communications are intelligible

4–5 years

Vocabulary has increased to about 1500–2100 words. Sentences are complete and most grammar correct

Says f and v. May still have some distortion of r, l, s, z, sh, ch, y, and th

All speech can be understood, although some words may not be perfectly enunciated

5–6 years

Vocabulary of 3000 words

May still distort s, z, ch, sh, and j

AgeNormal language developmentNormal speech developmentIntelligibility

Infant

Cooing

Babbling

Non-cry vocalic sounds

Consonant—vowel syllables with intonation patterns

1 year

Appearance of first 2–3 words

Imitates sounds of animals

Omits most final and some initial consonants

Substitutes consonants m, w, p, b, k, g, n, t, d, and h for more difficult sounds

Usually no more than 25% intelligible to familiar listener

2 years

Uses 2–3-word phrases

Uses above consonants with vowels but inconsistently and with substitution

50–65% of spoken language can be understood

Has a vocabulary of 250–300 words

Can put together simple 2–3-word phrases

Word usage and comprehension develops but comprehension lags behind expressive ability

Uses I, me, and you

Can understand much adult communication directed to them

3 years

Says 4–5-word sentences, with a vocabulary of about 900 words. Uses who, what, and where. Uses plurals, pronouns, and prepositions

Says b, t, d, k, and g, but r and l may be unclear. W is either omitted or substituted. Often repeats self.

75% of communications are intelligible

4–5 years

Vocabulary has increased to about 1500–2100 words. Sentences are complete and most grammar correct

Says f and v. May still have some distortion of r, l, s, z, sh, ch, y, and th

All speech can be understood, although some words may not be perfectly enunciated

5–6 years

Vocabulary of 3000 words

May still distort s, z, ch, sh, and j

Reproduced with permission from Glasper, McEwing, and Richardson, Oxford Handbook of Children’s and Young Person’s Nursing, page 13, 2007 © Oxford University Press.

No group of patients demonstrates the principles of shared care better than the paediatric population

Help from paediatricians, midwives, neonatal intensivists, and anaesthetists with special paediatric training is invaluable.

Occasionally pre-delivery ultrasound scanning can detect congenital problems leading to a planned Caesarean section and possible ENT intervention, for example, cystic hygroma (graphic see ‘Congenital neck remnants’, p. 266).

The ENT team should be in the theatre, scrubbed and on standby for intubation or tracheostomy if the baby’s airway is compromised. Secondary treatment of cystic hygroma is given after further investigation.

Newborn infants are obligate nasal breathers.

Failure to breathe and the development of hypoxia may be related to choanal atresia. The attending paediatrician/anaesthetist may be able to restore breathing with an oral airway.

Bilateral choanal atresia is the likely diagnosis. Failure to pass the nasal suction tube is not always a good sign of atresia.

Placing a metal tongue depressor and watching whether it mists is a good method of measuring nasal airway patency.

Microtia

Branchial cysts or fistulas

Smaller cystic hygromas

Haemangiomas

These lesions may all be noticed at birth or during the neonatal examination.

Soon all newborn children will be tested for hearing problems in universal newborn hearing programmes. It is important that children who are too sick to be screened are not missed.

Many children have periods of noisy breathing. It is not normal.

Stertor and stridor are caused by turbulent airflow in the partially compressed airway:

—is the noise associated with snoring and is due to a supraglottic narrowing of the airway, e.g. enlarged tonsils.

—is due to narrowing of the airway in and around the glottis and upper airway.

Assessment and examination aim to establish a likely diagnosis and to set parameters for further intervention.

When did it start?

Related to feeding?

Position-dependent? Worse on back or front?

Growth and development

Neonatal history

General examination for birthmarks

Oral cavity

Tongue size

Palate—any clefts?

Tonsil size

Intercostal recession

Tracheal tug

Stridor—time stridor relative to breathing cycle. Is it inspiratory or expiratory?

is the commonest cause of stridor in children. It is usually benign and self-limiting. This is often the presumed diagnosis in children with stridor. (graphic See ‘Congenital laryngeal lesions’, p. 218.)

Examination under anaesthetic in children less than 12 months of age is associated with an increased mortality.

Failure to thrive

Cyanosis

Prolonged apnoeic episodes

Table 17.2
Different sites of airway obstruction lead to different clinical presentations
StridorVoiceCough

Nasal/oropharyngeal region

Stertor

Muffled

Supraglottis, glottis

Inspiratory

Hoarse

Barking

Subglottis, extrathoracic tracheal

Biphasic

Normal

Brassy

Intrathoracic tracheal, bronchi

Expiratory

Normal

+

StridorVoiceCough

Nasal/oropharyngeal region

Stertor

Muffled

Supraglottis, glottis

Inspiratory

Hoarse

Barking

Subglottis, extrathoracic tracheal

Biphasic

Normal

Brassy

Intrathoracic tracheal, bronchi

Expiratory

Normal

+

Reproduced with permission from Warner et al., Otolaryngology and Head and Neck Surgery, 2009, copyright, Oxford University Press.

Is this a primary feeding problem or secondary to an airway problem?

Investigations are usually conducted with the help of a paediatrician and paediatric SALT.

When did it start?

Regurgitation present?

Choking?

Aspiration?

Weight/height gain?

Stridor present or absent?

Nasal airway—clear or obstructed?

Mouth and tongue—any enlargement or tongue tie?

Palate—any clefts present?

Tonsils—are they enlarged?

Watch bottle or breastfeeding

Nasal endoscopy to examine larynx and vocal cord movement

Barium swallow with paediatric SALT in attendance

Consider examination under GA if no obvious cause and child is failing to thrive

Nutrition and fluid intake may necessitate NG feeding

Depends on underlying condition

This is a common problem in children. Commonest age is from 3–8 years when adenoidal hypertrophy is greatest. The aetiology is different to that in adults.

Mobile phone video often documents episodes

Apnoeic episodes

Daytime sleepiness is often not a feature

Irritability is probably the manifestation of inadequate sleep

Nasal obstruction not relieved by vasoconstrictor

Large tonsils

Developmental or syndromic children may have central apnoea as the cause of their snoring and sleep apnoea. Sleep study will show apnoea is not associated with respiratory efforts.

History of cardiac disease can be associated with central apnoea.

Useful for children with obvious rhinitis and hypertrophied turbinates. May also decrease the size of the adenoidal pad.

Use intranasal steroids, e.g. fluticasone 1 spray into each nostril od for at least 6 weeks.

Adenotonsillectomy is usually curative. However, it carries the risk of postoperative haemorrhage and is uncomfortable.

Cognitive ability interacts with the physical method of speech production:

—generates constant airflow to the larynx

—production of sound occurs via opposition of the vocal cords and mucosal wave of the vocal fold

—modification of the laryngeal sound by the tongue, oral cavity, and sinuses

ENT assessment is mandatory in children who are failing to develop speech properly.

The role of the team investigating the child is to identify the barrier to speech development. Often more than one factor can be responsible and may need to be addressed.

Neonatal history

Developmental landmarks

Any family history of developmental problems?

Neonatal history

Any risk factors?

Familial hearing problems?

Syndromic child

Physical examination

Microtia

EAC development

Tympanometry

Audiology

Dual pathology

Oral cavity

Tongue tie

Cleft palate

Bifid uvula

Massive tonsils

Examination of larynx

Examination under anaesthesia

It is important to treat any hearing problem with hearing aids or surgery, e.g. grommets for glue ear. This is particularly important for children with global developmental delay. Any language development is going to be improved by normal hearing.

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