Respiratory Flashcards

1
Q

What is bronchiolitis?

How does it present?

A

Inflammation of the bronchioles with increased mucus secretions, due to a viral infection; most commonly RSV (respiratory syncytial virus). Adult bronchioles are a lot larger so would be unaffected by his level of inflammation and hypersecretion.
Commonly affects under 1yr old, typically under 6 months.
Baby’s who had bronchiolitis are more likely to get viral induced wheeze.

Starts off as an URTI for a few days, where some baby’s will recover, others will go on to develop a chest infection.

Children present with;
Coryzal symptoms (since starts off as URTI)- runny nose, sneezing, mucus throat and watery eyes.
Symptoms of respiratory distress
Mild fever
Poor feeding
Poor wt gain
Wheeze and crackles
Apnoea
Dyspnoea
Increased RR
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2
Q

What are the features of respiratory distress?

A
Cyanosis
Accessory muscles for breathing i.e. abdominal, SCM, intercostal
Subcostal recess
Intercostal recess
Head bobbing
Tracheal tug (pulled downward)
Nasal flaring
Abnormal Airway noise.
Increased RR

NB- Wheeze - small airway narrowing, high pitched heard on expiration.
Stridor- high pitch heard on expiration; large airway obstruction.
Grunt- Exhaling with partially closed glottis.

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3
Q

How is bronchiolitis managed?

A
Can manage at home with symptomatic relief.
Only admit when:
Under 3 months old
Has prematurity, Down's, CF etc
Parents can't manage at home
Clinically dehydrated
Reduced feeds by 50-75%
O2 sat <92%
RR>70
Apnoea
Moderate-severe respiratory distress
Hospital management is also supportive;
Ensure adequate intake; IV, NG
Nasal saline drips/nasal suctioning to clear nasal airways
Supplementary O2 if remains <92%
Ventilation if required

Ventilation is escalated to the next step if the previous is not sufficient:

1) High flow humidified O2- tight nasal cannula used to allow O2 intake and also pressure prevents airways collapsing.
2) CPAP- Similar to 1 but more pressure
3) Intubation and ventilation

To assess the effectiveness of ventilation take capillary blood gas. Increasing CO2 suggesting collapsing airways, as does a low pH where there has not been any compensation- leading to respiratory acidosis.

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4
Q

What is a viral induced wheeze?
How does it present?
How is it managed?

A

Essentially is an asthma caused by a virus.
Get inflammation and oedema of small airways, where inflammation leads to SM constriction (as with asthma).
Has a strong FHx and patients are more likely to develop asthma.

Children present with a viral prodrome (fever, cough coryzal symptoms) followed by SOB, expiratory wheeze throughout the chest and signs of respiratory distress.

Manage the same as acute asthma.

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5
Q

How does acute asthma present? RECAP

A

SOB
Cyanosis
Respiratory distress
Expiratory wheeze throughout the chest.

NB- Silent chest- suggests not enough air to create a wheeze- could be as a result of exhaustion leading to reduced respiratory effort.

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6
Q

How is acute asthma managed? RECAP

Also same for viral induced wheeze

A

Give O2 if sats <94%
If mild can discharge home with 2-6 puffs of salbutamol 4 hourly via a spacer.

If moderate to severe then requires stepping up the management ladder until control is gained:
1) Salbutamol inhaler with spacer 10 puffs 4hrly
2) Nebulised salbutamol/ipratropium bromide
3) Oral prednisolone (typically a 3 day course)
4) IV hydrocortisone
5) IV Magnesium Sulphate
6) IV Salbutamol
7) IV theophylline
If not gained control whilst approaching the end need to call anaesthetist to intubate and ventilate.

Once control is gained can wean pt down the ladder. Monitor K+ levels with salbutamol. Also salbutamol can cause tremors and tachycardia.

Discharge the child when they are well on 6 puffs 4hrly (prescribe a reducing regime alongside this for when they are at home i.e. after 48hrs 4 puffs 6hrly, after 48hrs 2-4 puffs PRN)
Ensure to finish course of oral prednisolone, safety net the family and discharge with an asthma action plan.

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7
Q

How is chronic asthma diagnosed in children?

A

Most children are not diagnosed until 5 yrs old.

Tests to use are:
Spirometry with bronchodilator reversibility.
FeNO test.
Peak flow variability- Keep a diary of peak flow test results for 2 weeks.

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8
Q

How is chronic asthma managed in children?

A

FInd out which guidelines we follow!!!

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9
Q

What is pneumonia?

How does it present?

A

Inflammation of the airway and alveoli, with sputum filling them. LRTI- common bacterial cause is strep.pneumonia, common viral cause is RSV, followed by influenza.

Presentation:
SOB
Increased RR
Increased HR
Fever
Cough (wet)
Lethargy
Increased worked breathing

Think sepsis if hypoxia, tachypnoea, tachycardia, hypotension, fever, confusion etc.

Characteristic signs of pneumonia:
Bronchial breathing (on inspiration and expiration)
Dull percussion
Focal coarse crackles

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10
Q

How is pneumonia diagnosed?

How is pneumonia managed?

A

CXR will indicate pneumonia (consolidation), although is not always needed for a diagnosis.
Sputum culture to find the organism and then guide treatment.

Management:
O2 if saturation below 92%
Mild- Amoxicillin +/- clarithromycin
Severe- Co-amoxiclav +/- clarithromycin

Penicillin allergy- use macrolide alone.

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11
Q

How is a patient with recurrent admissions of RTI requiring Abx treatment managed?

A
Need to test for underlying pathology.
Take thorough family history
Sweat test for CF
FBC- WBC anomalies
HIV
CXR- Any structural abnormality
Test immunoglobulins
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12
Q

What is croup?
How does it present?
How is it managed?

A

URTI- Oedema of the larynx, common in 6 months-2yrs old. Will resolve within 48hrs.

Presentation:
Barking cough
Increased work of breathing
Stridor
Low grade fever
Hoarse voice

Management:
Can manage at home with symptomatic relief.
If more severe then single dose of dexamethasone (can be repeated after 12hrs).
If not responding can escalate further.

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13
Q

What is epiglottitis?

How does it present?

A

Inflammation and swelling of the epiglottis which can obscure the airway, within hrs of symptoms- therefore life threatening.
Due to H.influenza, now seen mainly in unvaccinated children.

Presents:
Fever
Sore throat
Drooling
Tripod position (hands on both knees and head leaned forward)
Difficulty/painful swallowing
Upset/quiet child
Unwell/septic looking
Muffed voice
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14
Q

How is epiglottitis investigated?

How is it managed?

A

Don’t investigate- can aggravate the child and encourage airway closing. On lateral X-Ray of the neck, will see thumb print sign- epiglottis swollen pressing on the trachea.

Management is focused on securing the airway. Call a senior paediatrician and anaesthetist. Ensure also ENT surgeons present if airway closes and need to tracheostomy. If intubated need ICU admission.
Don’t bother the child, keep them comfortable.
Once airway secure- give IV ceftriaxone and dexamethasone.

Most children recover w/o intubation, those who are extubated recover well also. Few may die.
Complication includes epiglottis abscess; puss filled which can potentially compromise the airway- manage same as epiglottitis.

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15
Q

What is Laryngomalacia?

How is it managed?

A

Poorly developed supraglottic larynx; aryepiglottic folds (important for constricting the airway ot prevent food and fluid enering the larynx/trachea) are shortened and softer. So when the child breathes in the folds are pulled downwards, creating an upper respiratory tract obstruction.

Usually presents at 6 months old
Chronic inspiratory stridor- can be intermittent- worse on crying, lying on back, feeding etc.
Can cause poor feeding

Will self resolve as the larynx matures. However options for corrective surgery or tracheostomy are available.

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16
Q

What is whooping cough?

How does it present?

A

Caused by Bordetella.pertussis.
Pregnant women and children should be vaccinated against it.

Initially have mild coryzal symptoms- mild fever, dry cough.
Then develop more severe coughing fits, pt is unable to breathe in between the fits of coughing, once this has stopped they take a loud inspiratory whoop to force air in (hence whooping cough), equally some infants can become apnoeic.
Coughs can be so forceful they cause the pt to faint, vomit or develop a pneumothroax.

17
Q

How is whooping cough diagnosed?

How is it managed?

A

Diagnosis with nasopharyngeal/nasal swab for PCR/bacterial culture- results within 2-3 wks OR after having the cough for 2 wks, can test for anti-pertussis toxin immunoglobulin G in oral fluid of 5-16yrs old or blood of >16yrs old.

Management involves supportive care mainly but hospital admission if vulnerable i.e. < 6months or pregnant, also admit if cyanotic, severe coughs, apnoeic.
Give macrolides within the first 21 days or after if vulnerable- effective.
Notifiable disease
ensure prophylactic Abx given t vulnerable close contacts
Will resolve usually within 8 wks but can last several months. Pts can go on to develop bronchiectasis.

18
Q

What is chronic lung disease of prematurity?

How does it present?

A

Baby born before 28 wks gestation suffer from respiratory distress at birth so require O2 therapy or intubation + ventilation.

Features;
Low O2 saturations
Poor feeding
Increase susceptibility to infections
Increased work of breathing
Crackles and wheeze on auscultation
19
Q

How is chronic lung disease of prematurity investigated?

How is it managed?

A

Diagnosis on +ve CXR and requiring O2 after reaching 36wks gestational age.

Management:
Prevention of CLDP by:
Giving mothers betamethasone (steroid) injection if delivery <36wks.
Giving CPAP to neonates requiring O2, rather than intubation and ventilation
Giving caffeine to increase respiratory effort
Don’t over oxygenate when giving O2

Discharge from neonatal ward with lose dose O2, which is then slowly weaned off.
At increase risk of bronchiolitis therefore give monthly injection of palivizumab if criteria met.

20
Q

What is Cystic fibrosis?

How does it present?

A

Autosomal recessive condition, caused by a mutation in the CFTR gene. This affects the mucus gland, leading to thick mucus production.

Thick mucus secretions from the bile and pancreatic ducts can lead to blockage of the ducts- therefore don’t get pancreatic lipase- get steatorrhea.
Congenital bilateral absence of the vas deferens in males- infertility.
Thick mucus production of the respiratory tract- medium for bacterial growth- recurrent infections.

Presents usually with neonates not passing meconium within the first 24-48hrs of birth. this is due to sticky stool obstructing the bowels- meconium ileus. Can lead to abdominal pain, distension and vomiting. If do not present with this, CF is picked up later in childhood wit recurrent respiratory tract infections, failure to thrive or pancreatitis.

21
Q

What are the signs and symptoms of CF?

A
Symptoms-
Recurrent respiratory infections
Salty skin (kissing baby- tastes salty)
Poor feeding
Failure to thrive
Chronic cough
Thick sputum production
Steatorrhea
Abdominal pain/bloating
Signs-
Low weight
Finger clubbing
Nasal polyps
Abdominal distension
22
Q

How is CF diagnosed?

What are the common colonisers of the respiratory airways?

A

Gold standard- sweat test. Pilocarpine is place on pt skin, then the skin is stimulated by electrodes to make the skin sweat. The sweat is collected and tested for chloride concertation. Cl>60mM is diagnostic of CF.
New born blood spot test- Every child undergoes one- picks up most cases.
Genetic testing of CFTR gene either by amniocentesis, chorionic villous sampling or blood test after birth.

Main colonisers or respiratory airway are staph.aureus and pseudomonas. Staph.aureus is reduced by giving long term flucloxacillin prophylaxis. Pseudomonas is a very difficult infection to treat as it is Abx resistant. Therefore CF pt should stay away from other CF pt. Can give nebulised tobramycin or oral ciprofloxacin.

23
Q

How is CF managed?

What is the prognosis?

A

Chest physiotherapy- several times a day to clear secretions and reduce colonisation.
Exercise
Prophylactic flucloxacillin to prevent staph.aureus
Treat respiratory infections as they occur
CREON tablets to aid digestion (in place of pancreatic lipase)
Bronchodilators to help with bronchoconstriction
Nebulised DNase- to breakdown DNA material is respiratory mucus and allow better clearance
Nebulised hypertonic saline
Vaccinations- pneumococcal, influenza and varicella
High calorie diet since increased energy needed for respiratory effort, coughing, physiotherapy etc.

Can consider lung transplant in end stage disease, liver transplant in liver disease, fertility treatment and also genetic counselling.
Need to be monitored every 6 months- looking at colonisation, any pseudomonas? Also check risk of diabetes, osteoporosis, liver failure and Vitamin D deficiency.

Life expectancy is 47 yrs old.

24
Q

What is primary ciliary dyskinesia?

How does it present?

A

Autosomal recessive disease where the cilia of the body are affected.
Respiratory cilia- Build up of sputum, site for infection, poor growth- similar to CF.
Fallopian tube and flagella of serm cilia affected- infertility.

Can also have situs inversus and paranasal sinusitis alongside- Kartagner’s triad.

NB situs inversus can exist stand alone. If everything besides the heart is mirrored- dextrocardia.

25
Q

How is primary ciliary dyskinesia investigated?

How is it managed?

A

Can diagnose with semen sample, CXR (situs inversus in 50%), Hx from the parents to look for consanguinity (related parents)
Ultimate diagnosis is with biopsy of the respiratory ciliated epithelia to examine the cilia, obtained by nasal brushing or bronchoscopy. Several samples will be required.

Management is similar to CF with Abx, chest physiotherapy and high calorie diet.