Paeds I Flashcards

1
Q

If you have upper or lower airwway problem then what is resp symptom most likely to be? [2]

A

Upper: stridor

Lower: wheeze

If both - then both!

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2
Q

A neonate is born at term and under observation in the delivery room. At 5 minutes of life, the oxygen saturation (SpO2) reading is 85%, and the baby appears pink and is breathing normally. There are no other signs of distress, and other observations are unremarkable.

What is the most appropriate next step? [1]

A

In first 10 minutes of life, suboptimal SpO2 readings can be expected from a healthy neonate.

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3
Q

Describe what is meant by laryngomalacia [1]
Describe the structural changes that causes this condition [+]

A

Laryngomalacia:
- part of the larynx above the vocal cords (the supraglottic larynx) is structured in a way that allows it to cause partial airway obstruction.
- This leads to a chronic stridor on inhalation, when the larynx flops across the airway as the infant breathes in. Stridor is a harsh whistling sound caused by air being forced through an obstruction of the upper airway.

Structural changes:
- There are two aryepiglottic folds at the entrance of the larynx. They run between the epiglottis and the arytenoid cartilages.
- They are either side of the airway and their role is to constrict the opening of the airway to prevent food or fluids entering the larynx and trachea.
- In laryngomalacia the aryepiglottic folds are shortened, which pulls on the epiglottis and changes it shape to a characteristic “omega” shape.
- The tissue surrounding the supraglottic larynx is softer and has less tone in laryngomalacia, meaning it can flop across the airway.
- This happens particularly during inspiration, as the air moving through the larynx to the lungs pulls the floppy tissue across the airway to partially occlude it. This partial obstruction of the airway generates the whistling sound.

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4
Q

Describe the presentation of laryngomalacia [2]

A

Laryngomalacia occurs in infants, peaking at 6 months. It presents with:
inspiratory stridor, a harsh whistling sound when breathing in.
Usually this is intermittent and become more prominent when feeding, upset, lying on their back or during upper respiratory tract infections.
- Infants with laryngomalacia do not usually have associated respiratory distress.

Symptomatic relief may be provided by hyperextending the neck during episodes of stridor

It can cause difficulties with feeding, but rarely causes complete airway obstruction or other complication

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5
Q

Describe the disease course of Laryngomalacia [3]

A

The problem resolves as the larynx matures and grows and is better able to support itself, preventing it from flopping over the airway. Usually, no interventions are required and the child is left to grow out of the condition.

Rarely tracheostomy may be necessary. This involves inserting a tube through the front of the neck into the trachea, bypassing the larynx
Surgery is also an option to alter the tissue in the larynx and improve the symptoms.

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6
Q

Describe the three types of laryngomalacia [3]

A

Type I Laryngomalacia (Curling Type):
* Characterised by inward curling of the mucosa overlying the arytenoid cartilages during inspiration. This creates an omega-shaped laryngeal inlet instead of the normal V-shape.
* It’s the most common type, accounting for approximately 75% of cases.

Type II Laryngomalacia (Prolapsing Type):
* Involves prolapse of the mucosa overlying the cuneiform and corniculate cartilages into the glottis during inspiration.
* This type accounts for around 15% of laryngomalacia cases.

Type III Laryngomalacia (Posterior Displacement Type):
* Less common, only observed in about 10% of cases. It involves posterior displacement or malpositioning of the epiglottis and aryepiglottic folds.
* This type is often associated with more severe symptoms and may require early surgical intervention.

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7
Q

What is this ddx of LM? [1]
What previously has likely occured to this patient? [1]

How would it present differently? [2]
What is likely caused by? [1]

A

Subglottic stenosis
- likely previous intubations
- presents with biphasic stridor and is not limited to inspiration like laryngomalacia.
- It may also present with respiratory distress that is disproportionate to the degree of stridor.

Causes:
- The underlying causes are diverse including congenital malformations, prolonged intubation trauma or systemic diseases like Wegener’s granulomatosis.
- This differentiates it from laryngomalacia which is believed to be due to neuromuscular immaturity.

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8
Q

What is this ddx of LM? [1]

A

Laryngeal cleft

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9
Q

What is this ddx of LM? [1]

A

Laryngeal web

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10
Q

What is this ddx of LM? [1]

A

Laryngeal cyst

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11
Q

Describe the presentation of croup [4]

What is the classic cause of croup? [1] Which tx does it respond well to? [1] What are other common causes? [3]

A

Presentation:
* Increased work of breathing
* “Barking” cough, occurring in clusters of coughing episodes
* Hoarse voice
* Stridor
* Low grade fever

The classic cause of croup that you need to spot in your exams, is parainfluenza virus. It usually improves in less than 48 hours and responds well to treatment is steroids, particularly dexamethasone. Also by:
* Influenza
* Adenovirus
* Respiratory Syncytial Virus (RSV)

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12
Q

Which factors would make you admit a patient with croup? [3]

A

CKS suggest admitting any child with:
moderate or severe croup
* < 3 months of age
* known upper airway abnormalities (e.g. Laryngomalacia, Down’s syndrome)
* uncertainty about diagnosis (important differentials include acute epiglottitis, bacterial tracheitis, peritonsillar abscess and foreign body inhalation)

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13
Q

How would you differentiate croup from epiglottis and foreign body aspiration [+]

A

Epiglottitis
Similarities
* Stridor

Differences
* Usually seen in children 3-5 years of age
* Absence of barking cough
* Muffled hot potato voice
* Tripod or sniffing position
* An incomplete vaccination history more likely to be present

Foreign body aspiration
Similarities
* Often < 3 years of age
* Stridor
* Dysphonia depending on location of foreign body

Differences
* History suggestive of possible foreign body
* Abrupt onset during daytime (croup usually night-time)
* Minimal response to adrenaline nebuliser

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14
Q

How would you differentiate croup from Bacterial tracheitis [3]

A

Bacterial tracheitis
Similarities
* Stridor

Differences
* Usually school-age
* Soft stridor 2-7 days after onset of URTI symptoms
* Significant tracheal tenderness on palpation
* Reluctant to cough because of pain

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15
Q

NICE guidelines, last updated in 2019, suggest the following algorithm for the management of croup:
- Primary Care [3]
- Secondary care [4]

A

Primary care (mild illness):
* Supportive care
* Oral dexamethasone

Parents should be advised regarding:
* The expected course of croup, including that symptoms usually resolve within 48 hours.
* The need to take the child to hospital if stridor can be heard continually, the skin between the ribs is pulling in with every breath, and/or the child is restless or agitated.
* The use of antipyretics in children distressed due to fever.
* The need to check on the child regularly, including through the night.
* Arrange follow-up, using clinical judgment to determine the appropriate interval.

Secondary care (moderate - severe illness)
* All children with moderate-severe illness should be admitted
* Supportive care
* Oral dexamethasone
* Nebulised epinephrine
* Supplemental oxygen
* The above advice should also be given

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16
Q

Bacterial tracheitis is most likely cause by which organism? [1]

A

Haemophilus influenza

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17
Q

Lecture

Name three further ddx for croup and how you would differentiate between them [+]

A

Retropharyngeal/peritonsillar abscess
* dysphagia, drooling, stridor (occasionally), dyspnoea, tachypnoea, neck stiffness, and unilateral cervical adenopathy.
* Onset is typically more gradual than with croup and is often accompanied by fever.

Angioneurotic oedema
* acute swelling of the upper airway that may cause dyspnoea and stridor.
* Fever is uncommon. Swelling of face, tongue, or pharynx may be present. Can occur at any age.

Allergic reaction
* rapid onset of dysphagia, stridor, and possible cutaneous manifestations (urticarial rash).
* Can occur at any age
* Known allergies

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18
Q

Describe what is meant by bronchiolitis [1]
What is the most common cause? [1]

A

Bronchiolitis describes inflammation and infection in the bronchioles, the small airways of the lungs.

This is usually caused by a virus. Respiratory syncytial virus (RSV) is the most common cause.

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19
Q

Describe the presentation of bronchiolitis [+]

A

Symptoms noramlly usually get worse for 3-5 days, then improves

Coryzal symptoms - These are the typical symptoms of a viral upper respiratory tract infection:
* running or snotty nose, sneezing, mucus in throat and watery eyes.
* Signs of respiratory distress
* Dyspnoea (heavy laboured breathing)
* Tachypnoea (fast breathing)
* Poor feeding
* Mild fever (under 39ºC)
* Apnoeas are episodes where the child stops breathing
* Wheeze and crackles on auscultation

Signs of Resp. Distress:
* Raised respiratory rate
* Use of accessory muscles of breathing, such as the sternocleidomastoid, abdominal and intercostal muscles
* Intercostal and subcostal recessions
* Nasal flaring
* Head bobbing
* Tracheal tugging
* Cyanosis (due to low oxygen saturation)
* Abnormal airway noises

TOM TIP: You should become very confident in listing and spotting the signs of respiratory distress. This is very important when treating children, to distinguish between a well child and an unwell child. Your examiners will expect you to know the signs like the back of your hand.

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20
Q

TOM TIP: You should become very confident in listing and spotting the signs of respiratory distress. This is very important when treating children, to distinguish between a well child and an unwell child. Your examiners will expect you to know the signs like the back of your hand.

What are they? [+]

A

Signs of Resp. Distress:
* Raised respiratory rate
* Use of accessory muscles of breathing, such as the sternocleidomastoid, abdominal and intercostal muscles
* Intercostal and subcostal recessions
* Nasal flaring
* Head bobbing
* Tracheal tugging
* Cyanosis (due to low oxygen saturation)
* Abnormal airway noises

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21
Q

Describe the course of bronchiolitis [3]

A

Bronchiolitis usually starts as an upper respiratory tract infection (URTI) with coryzal symptoms.

From this point around half get better spontaneously.

The other half develop chest symptoms over the first 1-2 days following the onset of coryzal symptoms.

Symptoms are generally at their worst on day 3 or 4. Symptoms usually last 7 to 10 days total and most patients fully recover within 2 – 3 weeks.

Children who have had bronchiolitis as infants are more likely to have viral induced wheeze during childhood.

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22
Q

Which patients should you admit w/ bronchiolitis? [+]

A
  • Aged under 3 months or any pre-existing condition such as prematurity, Downs syndrome or cystic fibrosis
  • 50 – 75% or less of their normal intake of milk
  • Clinical dehydration
  • Respiratory rate above 70
  • Oxygen saturations below 92%
  • Moderate to severe respiratory distress, such as deep recessions or head bobbing
  • Apnoeas
  • Parents not confident in their ability to manage at home or difficulty accessing medical help from home
23
Q

Describe the managment plan for bronchiolitis [+]

A

Typically patients only require supportive management. This involves:
* Ensuring adequate intake. This could be orally, via NG tube or IV fluids depending on the severity. It is important to avoid overfeeding as a full stomach will restrict breathing. Start with small frequent feeds and gradually increase them as tolerated.
* Saline nasal drops and nasal suctioning can help clear nasal secretions, particularly prior to feeding
* Supplementary oxygen if the oxygen saturations remain below 92%
* Ventilatory support if required
* There is little evidence for treatments such as nebulised saline, bronchodilators, steroids and antibiotics.

24
Q

What are the best indicators of resp. failure? [2]

A

Rising pCO2, showing that the airways have collapsed and can’t clear waste carbon dioxide.

Falling pH, showing that CO2 is building up and they are not able to buffer the acidosis this creates. This is a respiratory acidosis. If they are also hypoxic, this is classed as type 2 respiratory failure.

25
Which babies might be given monthly injections to protect agaisnt bronchiolitis? [2] What injection would recieve? [1]
**Palivizumab** is a monoclonal antibody that targets the respiratory syncytial virus. A monthly injection is given as prevention against bronchiolitis caused by RSV. It is given to **high risk babies, such as ex-premature and those with congenital heart disease.** It is not a true vaccine as it does not stimulate the infant’s immune system. It provides passive protection by circulating the body until the virus is encountered, as which point it works as an antibody against the virus, activating the immune system to fight the virus. The levels of circulating antibodies decrease over time, which is why a monthly injection is required.
26
Describe the clinical dx of asthma [+]
**Spirometry** - The NICE guidelines suggest offering spirometry to children aged **over 5-years-old if a diagnosis of asthma is being considered**: - **(FEV1:FVC) ratio of less than 70%** is suggestive of obstructive airway disease **Bronchodilator reversibility**: * For **children aged 5 to 16-years-old,** an improvement in **FEV1 of >12% is suggestive of asthma** * For **children aged 17 years-old and older, an improvement in FEV1 of >12%**, plus an **increase in volume of >200mL, is suggestive of asthma** **FeNO**: - A fraction exhaled nitric oxide level of **greater than 35 parts per billion (ppb)** is suggestive of asthma **Peak Flow:** * The NICE guidelines suggest monitoring peak flow variability for **2-4 weeks if there is any diagnostic uncertainty** * **Greater than 20% variability** is considered a positive test, suggestive of asthma * After diagnosis and treatment, peak expiratory flow can also be used as an indicator of treatment effect and a marker of clinical improvement/deterioration
27
Describe the features of moderate, severe and life threatening asthma in children [+]
**Moderate**: - Peak flow > 50 % predicted - Normal speech - No features listed across **Severe**: * Peak flow < 50% predicted * Saturations < 92% * Unable to complete sentences in one breath * Signs of respiratory distress * Respiratory rate: > 40 in 1-5 years; > 30 in > 5 years * HR: > 140 in 1-5 years; > 125 in > 5 years **Life Threatening**: * Peak flow < 33% predicted * Saturations < 92% * Exhaustion and poor respiratory effort * Hypotension * Respiratory rate: * Silent chest * Cyanosis * Confusion
28
Describe the management plan for chronic asthma in children aged 5-16 [+]
**Mild cases** can be managed as an outpatient with **regular salbutamol inhalers via a spacer (e.g. 4-6 puffs every 4 hours)**. **Moderate-severe:** 1. **SABA** 2. **SABA + paediatric low-dose inhaled corticosteroid (ICS)** 3. **SABA + paediatric low-dose ICS + leukotriene receptor antagonist (LTRA)** 4. **SABA + paediatric low-dose ICS + long-acting beta agonist (LABA)** (Don't stop the LRTA like in adults) 5. **SABA + switch ICS/LABA for a maintenance** and **reliever therapy (MART), that includes a paediatric low-dose ICS** 6. **SABA + paediatric moderate-dose ICS MART** OR consider changing back to a **fixed-dose of a moderate-dose ICS and a separate LABA** 7. **SABA + one of the following options**: **increase ICS to paediatric high-dose, either as part of a fixed-dose regime or as a MART** OR **a trial of an additional drug (for example theophylline)** OR **seeking advice from a healthcare professional with expertise in asthma** ## Footnote double check - as asthma guidelines may have changed
29
Describe the management plan for chronic asthma in children aged < 5 [+]
**One. SABA** **Two:. SABA + an 8-week trial of paediatric MODERATE-dose inhaled corticosteroid (ICS)** * After **8-weeks stop the ICS** and monitor the **child's symptoms:** * if symptoms **did not resolve** during the trial period, **review whether an alternative diagnosis is likely** * if symptoms resolved then reoccurred within 4 weeks of stopping ICS treatment, **restart the ICS at a paediatric low dose as first-line maintenance therapy** * if symptoms resolved but reoccurred beyond 4 weeks after stopping ICS treatment, **repeat the 8-week trial of a paediatric moderate dose of ICS** **Three. SABA + paediatric low-dose ICS + leukotriene receptor antagonist (LTRA)** **Four. Stop the LTRA and refer to an paediatric asthma specialist**
30
What are the different definitions for low, moderate and high doses for ICS in asthma? [3]
<= **200 micrograms** budesonide or equivalent = paediatric low dose **200 micrograms - 400 micrograms** budesonide or equivalent = paediatric moderate dose **> 400 micrograms budesonide** or equivalent= paediatric high dose.
31
How do you treat acute moderate asthma in children > 5? [2]
**Supplementary oxygen** if required (i.e. oxygen saturations less than 94% or working hard) **Bronchodilator therapy** * give a beta-2 agonist via a spacer (for a child < 3 years use a close-fitting mask) * give 1 puff every 30-60 seconds up to a maximum of 10 puffs * if symptoms are not controlled repeat beta-2 agonist and refer to hospital **Steroid therapy** * should be given to all children with an asthma exacerbation * treatment should be given for 3-5 days * 20 mg oral prednisolone for children aged 2-5 years * 40 mg oral prednisolone for children over 5 years **Moderate asthma may be managed using oral prednisolone and beta 2 bronchodilator therapy as an outpatient.**
32
How do you treat acute severe asthma in children > 5? [+]
* **Administer inhaled salbutamol** with a pressurised metered dose inhaler and spacer * Proceed to **nebulised salbutamol** (2.5-5 mg) if necessary * All children should recieve **steroids** * Add **nebulised ipratropium bromide** * If the patient is not responding to salbutamol or ipratropium, **consult with a senior clinician** * For consideration of **IV magnesium, IV salbutamol or aminophylline** ## Footnote * **Salbutamol inhalers** via a spacer device: starting with **10 puffs every 2 hours**
33
How would you treat life threatening acute asthma in a child > 5?
34
**Acute asthma:** - Generally, discharge can be considered when the child well on **[]** **puffs** **[] hourly of salbutamol.** - They can be prescribed a reducing regime of salbutamol to continue at home, for example [] then [] then [] as required.
Generally, discharge can be considered when the child well on **6 puffs 4 hourly of salbutamol**. They can be prescribed a reducing regime of salbutamol to continue at home, **for example 6 puffs 4 hourly for 48 hours then 4 puffs 6 hourly for 48 hours then 2-4 puffs as required.**
35
# Lecture Describe the management of acute wheeze [+]
**ABCDE approach**, get help early **Assess severity** **Apply high-flow oxygen** (initially 15 litres via non-rebreathe mask,) titrate as needed aiming for target saturations 94-98% **Start bronchodilators:** * **Burst therapy of Salbutamol** (via spacer if Sats > 94% or **via nebulizer** if needing oxygen) and **Ipratropium Bromide** if severe exacerbation/poor response to Salbutamol **Give steroids** **Consider IV Magnesium Sulphate** if poor response to initial therapy **Also, can consider IV Salbutamol and IV Aminophylline**
36
A potential exam scenario is discussing inhaled steroids with a parent that is worried about potential side effects. A common question is whether they slow growth. Describe how you would discuss this answer
There is evidence that **inhaled steroids** can **slightly reduce growth velocity** and can cause a small **reduction in final adult height of up to 1cm when used long term (for more than 12 months)**. - This effect was **dose-dependent, meaning it was less of a problem with smaller doses.** It is worth putting this in **context** for the **parent** by **explaining that these are effective medications that work to prevent poorly controlled asthma and asthma attacks** that could lead to **higher doses of oral steroids being given.** - **Poorly controlled asthma** can lead to a **more significant impact on growth and development**. - The **child** will also have **regular asthma reviews** to ensure they are **growing** **well** and on the **minimal dose required** to effectively control symptoms.
37
Describe how you would tell a patient how to use an inhaler: **MDI technique without a spacer:** [+] **MDI technique with a spacer:** [+]
**MDI technique without a spacer:** * Remove the cap * Shake the inhaler (depending on the type) * Sit or stand up straight * Lift the chin slightly * Fully exhale * Make a tight seal around the inhaler between the lips * Take a steady breath in whilst pressing the canister * Continue breathing for 3 – 4 seconds after pressing the canister * Hold the breath for 10 seconds or as long as comfortably possible * Wait 30 seconds before giving a further dose * Rinse the mouth after using a steroid inhaler **MDI technique with a spacer:** * Assemble the spacer * Shake the inhaler (depending on the type) * Attach the inhaler to the correct end * Sit or stand up straight * Lift the chin slightly * Make a seal around the spacer mouthpiece or place the mask over the face * Spray the dose into the spacer * Take steady breaths in and out 5 times until the mist is fully inhaled ## Footnote **NB**: Spacers should be cleaned once a month. Avoid scrubbing the inside and allow them to air dry to avoid creating static. Static can interact with the mist and prevent the medication being inhaled.
38
A parent thinks their child might be suffering from acute asthma attack. What would initial at home advise be for parents? [1]
Parents/carers of children with acute asthma at home, should seek **urgent medical attention** if initial symptoms are not controlled with **up to 10 puffs of salbutamol via a spacer;**
39
what doses of pred. should be used for acute asthma for 2-5 yr olds [1] and 5+ ? [1]
* **20 mg oral prednisolone** for children aged **2-5 years** * **40 mg oral prednisolone** for children over **5 years**
40
When does CLDP usually occur? [1] How is a dx made [1] and at what age? [1]
It occurs in **premature babies**, typically those born **before 28 weeks gestation**. These babies suffer with **respiratory distress syndrome** and **require oxygen therapy or intubation and ventilation at birth**. **Diagnosis** is made based on **chest xray changes** and when the **infant requires** **oxygen** **therapy** after they **reach 36 weeks gestational age**.
41
How can you prevent CLDP: - pre-birth [1] - post-birth [3]
There are several measure that can be taken to minimise the risk of CLDP. **Giving corticosteroids (e.g. betamethasone)** to mothers that show **signs of premature labour at less than 36 weeks gestation** can help speed up the development of the fetal lungs before birth and reduce the risk of CLDP. Once the neonate is born the risk of CLDP can be reduced by: * **Using CPAP** rather than intubation and ventilation when possible * Using **caffeine** to stimulate the respiratory effort * **Not over-oxygenating** with supplementary oxygen
42
Describe the long term management of CLDP [2]
Babies with CLDP require **protection against respiratory syncytial virus (RSV)** to reduce the risk and severity of **bronchiolitis**. - This involves **monthly injections of a monoclonal antibody against the virus called palivizumab**. This is very expensive (around £500 per injection) so is reserved for babies meeting certain criteria. - **Babies may be discharged from the neonatal unit on a low dose of oxygen** to continue at home, for example **0.01 litres per minute via nasal cannula**. They are followed up to wean the oxygen level over the first year of life.
43
You perform a chest x-ray and find a patient to have dextrocardia and bronchiectasis. What is the most likely pathology? [1] Name two further signs of this pathology [2]
**Kartagener syndrome** (aka primary ciliary dyskinesia): - dextrocardia - bronchiectasis - recurrent sinisitis - subfertility
44
**Kartagner’s triad** describes the three key features of PCD. Not all patients will have all three features. These are:
* Paranasal sinusitis * Bronchiectasis * Situs Inversus
45
Describe the clinical significance of sinitus invertus [1]
Situs inversus on its own **does not cause any problems, and patients can expect to live a normal life**. A small number have associated congenital heart disease, such as **transposition of the great arteries.** ## Footnote **NB**: **Dextrocardia** is when **only** the **heart** is reversed.
46
Describe how you manage NAS - Monitoring [2] - Medical management [2]
**Monitoring**: - Babies are **kept in hospital with monitoring** on a **NAS** **chart** for at least **3 days (48 hours for SSRI antidepressants**) to monitor for withdrawal symptoms. - A **urine sample** can be collected from the **neonate to test for substances** **Medical treatmen**t options for **moderate to severe** symptoms are: * **Oral** **morphine** **sulphate** for **opiate** **withdrawal** * **Oral phenobarbitone** for **non-opiate withdrawal**
47
**Fetal alcohol syndrome** refers to certain effects and characteristics that are found in children of mothers that consumed significant alcohol during pregnancy What are they? [+]
* **Microcephaly** (small head) * **Thin upper lip** * **Smooth flat philtrum** (the groove between the nose and upper lip) * **Short palpebral fissure** (short horizontal distance from one side of the eye and the other) * **Cardiac malformations** * Learning disability * Behavioural difficulties * Hearing and vision problems * Cerebral palsy
48
How soon after birth should a baby pass their first meconium poo? Before birth Within 24 hrs Within 48 hrs Within 72 hrs
How soon after birth should a baby pass their first meconium poo? Before birth Within 24 hrs **Within 48 hrs** Within 72 hrs
49
What is Jitteriness? [1] How do you differentiate between a seizure in a newborn and Jitteriness? [1]
**Jitteriness**: immaturity of muscle spindle fibres - trying to find resting state **Seizure**: if you hold a limb, seizure will continue; **Jitteriness**: will not
50
A baby is born with polcythemia. What other abnormality might they have and why? [1]
**Hypoglycaemia** - due to energy demands to of +rbc
51
**Ceftriaxone** is CI in newborns - binds to albumin and bilirubin - so increase risk of jaundice
52
Which newborn screening tests are given to neonates? [3] What do they test for [+]
**NIPE**: * **Within 72 hrs**, then repeated by **GP in 6 weeks** **Hearing screening:** - Automated oto-acoustic emissions (basic screening for congenital deafness) - High risk babies: automated auditory brainstem response **Heelprick test (day) 5:** - SCD - CF - Hypothyroidism - 6 Metabolic diseases (including PKU)
53
Describe the examination steps of NIPE
**Ask** about FHx of eyes, heart and hips **Ask** about feeding, pooing and weeing **General assessment:** - Colour - Tone **Scalp**: - Feel for sutures and fontanelles for raised / decrease ICP - Measure head circumference - Any swellings or lacerations **Eyes**: - Assess for red reflex **Ears**: - Position? - Skin tags? **Mouth**: - Assess for teeth, soft and hard palate (for clefts) - Assess rooting and sucking reflex **Body**: - Feel for clavicles - Palpate for masses or organomegaly - Ascultate lung fields **Limbs**: - Resp. distress, tone **Heart** - Listen for murmurs **Pulses** - Feel femoral and brachial pulses **Genitals** - Look for urethral meatus - Assess two testes - Anus - clean meconium as can miss malformations **Hips**: - Form Ortalani and Bartoli tests **Reflexes**: - Assess for Moro reflex - Assess for Babinksi reflex **Toes**: - Assess for talipes **Spine** - Assess shape - Look for sacral pits / dimples **Assess pre and post ductal saturations** - difference should be within 3%
54
Describe Ortalini and Barlows tests
Barlow - can you dislocate hip? Ortolani - can you relocate an already dislocated hip