Respiratory Flashcards

1
Q

Aetiology of asthma

A

Affects 15-20% of children
Genetic predisposition may be a factor
40% of children who suffer with asthma are atopic
Presence of one allergic disease increases the risk of another
The majority of asthma exacerbations are triggered by rhinovirus infection
Other triggers: URTIs, allergens, smoking, cold air, exercise, emotional upset/anxiety, chemical irritants

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2
Q

Asthma pathophysiology

A

Genetic predisposition/atopy/triggers leads to:
Bronchial inflammation: oedema, excessive mucus production, infiltration with eosinophils, mast cells, neutrophils, lymphocytes, oedema
Bronchial hyper-responsiveness: to inhaled stimuli
Airway narrowing: reversible airway obstruction
Symptoms: wheeze, cough, breathlessness, tight chest

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3
Q

Asthma presentation and history

A

Recurrent polyphonic wheeze
Symptoms worse at night and early AM
Symptoms with triggers (e.g. cold air, pets, dust)
Interval symptoms: symptoms between acute exacerbations
Personal/FH of atopy
Reversibility of symptoms with beta-2-agonist
Chest exam usually normal between attacks
Harrison’s sulci if onset in early childhood (depression at base of thorax)
Barrel chest & hyperinflation

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4
Q

Asthma differential diagnosis

A

Look for: evidence of eczema, allergic rhinitis
Wet cough/sputum production/clubbing/poor growth = indicates chronic infection such as cystic fibrosis/bronchiectasis
Bronchiolitis
Foreign body in the airway
Croup: inspiratory stridor and wheeze
Vocal chord dysfunction: mimics steroid refractory asthma
Ciliary dyskinesia
Post-nasal drip
Sinonasal manifestations of CF

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5
Q

Asthma investigations

A

Skin-prick testing for allergens/atopy
CXR: usually normal - rule out other conditions. Hyperinflation, flattened hemi-diaphragm, peribronchial cuffing, atelectasis
Peak flow: if uncertainty
Spirometry: check reversibility with beta-agonist, PEFR<80% predicted
FEV1/FVC <80% predicted

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6
Q

Chronic asthma initial management plan

A

Step-up/step-down approach:

1) short acting beta-2 agonist, consider very low-dose ICS
2) SABA + regular very low-dose ICS
3) SABA + low-dose ICS + LTRA(<5y)/LABA(>5y)
4) increase doses, theophylline?

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7
Q

Acute asthma initial management

A

Up to 10 puffs of a SABA (through nebuliser if )2 sats <92%)
Oral prednisolone (3d)/ i.v. hydrocortisone
Nebulised ipratropium bromide if poor response (anti muscarinic)
Repeat bronchodilators every 20-30m
Severe attack not responding: IV aminophylline

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8
Q

Coryza classical features + treatment

A

Clear/mucopurulent nasal discharge
Nasal blockage
Fever/pain: treat with paracetamol + ibuprofen
Unlikely to be bacterial in origin so antibiotics not indicated

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9
Q

Coryza pathogens

A

Viruses = commonest
Rhinovirus
Coronaviruses
Respiratory syncytial virus

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10
Q

Common causative organisms of pharyngitis

A

Adenoviruses
Entenoviruses
Rhinoviruses
Older children: group A beta-haemolytic streptococcus

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11
Q

Pharyngitis clinical presentation and common pathogens

A

Sore throat
Inflamed pharynx and soft palate
Enlarged/tender local lymph nodes

Adenovirus, enterovirus, rhinovirus. group A beta-haemolytic strep

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12
Q

Tonsillitis common causative organisms

A

Group A beta-haemolytic strep

Epstein-Barr virus –> infectious mononucleosis (glandular fever)

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13
Q

Tonsillitis presentation

A

Form of pharyngitis with intense inflammation of the tonsils, often with a purulent exudate

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14
Q

Markers of bacterial tonsillitis, and treatment

A

Headache, apathy, abdominal pain, white tonsillar exudate, cervical lymphadenopathy

Treatment: penicillin/erythromycin (if penicillin allergy)
Amoxicillin avoided: causes widespread maculopapular rash if tonsillitis is due to infectious mononucleosis
Recurrent severe tonsillitis –> tonsillectomy? Reduces tonsillitis episodes by 1/3

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15
Q

URTI clinical presentation + complications

A
Nasal discharge + blockage/sinusitis
Fever
Pharygitis/tonsillitis/sore throat
Acute otitis media/ear ache
Cough

Complications:
Infants may find feeding difficult if noses are blocked
Febrile convulsions
Acute exacerbation of asthma

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16
Q

Acute otitis media clinical presentation + complications

A

Most common at 6-12m of age
Ear pain + fever (check tympanic membranes of every child with a fever)
Tympanic membrane is bright red and bulging with loss of normal light reflection
Occasionally acute tympanic membrane perforation with pus visible in external canal

Complications: mastoiditis, meningitis
Recurrent infections: otitis media with effusion - most common cause of conductive hearing loss in children

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17
Q

Acute otitis media initial management plan

A

Pain: paracetamol/ibuprofen
Most cases resolve spontaneously
Amoxicillin may be prescribed, only to be used if no improvement within 2-3d

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18
Q

Types of wheezing patterns

A

Transient early wheezing: begins in infants with respiratory infection, result of small airways being
more likely to narrow and obstruct due to inflammation/aberrant immune response to viral infection

Recurrent persistent wheezing: triggered by a stimuli and presence of IgE in response to inhaled allergens, persistent symptoms, decreased lung function, association to other atopic diseases

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19
Q

Beta2-agonist examples and mechanism of action

A

Salbutamol/Terbutaline (SABA)
Salmeterol/Formoterol (LABA)
Act on beta receptors to directly –> bronchodilation
Less effective in very young children as they have fewer active beta receptors

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20
Q

Anti-muscarinic examples and mechanism of action

A

Ipratropium bromide

Similar effect to beta-agonists, but act via a different receptor to achieve their affect: sympathetic system

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21
Q

Methylxanthines examples and mechanism of action

A

Aminothylline or Theophylline
Pathway that leads to the relaxation of bronchiole smooth muscle
ADRs: vomiting, sleep disturbance, headaches, poor concentration, arrhythmias

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22
Q

Corticosteroids examples and mechanism of action

A

Budesonide/Beclometasone/Fluticasone (inhaled) Prednisolone (oral)
Prevent the creation of inflammatory proteins –> reduce IgE response
ADRs: impaired growth, adrenal suppression, oral candidiasis, altered bone metabolism

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23
Q

Leukotriene inhibitor examples and mechanism of action

A

Montelukast or Zafirlukast
Taken orally in children <5yrs instead of LABA
Antagonist that blocks the action of leukotriene –> reduces bronchoconstriction

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24
Q

Anti-IgE injections example and mechanism of action

A

Omalizumab

Monoclonal antibody designed to target IgE and prevent atopic reaction

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25
Bronchiolitis aetiology
90% occur in 1-9month olds Most common in winter months and urban areas RSV: 80% of cases. Remainder = Human metapneumovirus, Parainfluenza virus, Rhinovirus, Adenovirus, Influenza virus, Mycoplasma pneumoniae Severe bronchiolitis: associated with combined RSV & human metapneumovirus
26
Bronchiolitis risk factors
``` Older siblings Nursery attendance Passive smoking (particularly maternal) Prematurity/low birth weight Chronic lung disease: CF, bronchopulmonary dysplasia Immunocompromised ``` Breast-feeding = protective
27
Bronchiolitis presentation
Mild rhinorrhea, cough and fever, dry cough, increasing breathlessness Feeding difficulties associated with dyspnoea Apnoeas: especially young children Sharp, dry cough Tachypnoea Subcostal and intercostal recession Hyperinflation of the chest: prominent sternum or liver displaced downwards Fine end-inspiratory crackles or prolonged expiration High-pitched wheezes: expiratory > inspiratory Tachycardia Cyanosis or pallor
28
Bronchiolitis on CXR
``` Only performed if there is a diagnostic uncertainty or an atypical course Non-specific and patchy infiltrates Focal atelectasis Air trapping Flattened diaphragm Increased anteroposterior diameter Peribronchial cuffing ```
29
Acute bronchiolitis management
Supportive: primary care & at home --> fluid input, nutrition, temp control Secondary care if: Poor feeding, lethargy, apnoeas, >70 breaths/min, nasal flaring or grunting, severe chest wall recession, cyanosis, saturations <94% Humidified oxygen via nasal cannulae Monitored for apnoea Fluids: NG tube or IV If assisted ventilation is required: nasal/facemask CPAP/full ventilation
30
Common bacterial causes of pneumonia
Neonates: organisms from mother’s genital tract: group B streptococcus, E.coli, Klebsiella, Staph. Aureus (Gram –ve enterococci) Infants: Strep. pneumoniae, Chlamydia trachomatics, Haemophilus influenzae (more commonly RSV) School age: Strep pneumoniae, Staph aureus, group A streptococcus, Bordetella pertussis, Mycoplasma pneumoniae
31
Pneumonia presentation
Recent URTI, fevers, SOB, increased WOB, cough, lethargy, poor feeding Localised chest pain: indicative of pleuritic irritation from bacterial infection Temp>38.5 Signs of respiratory distress: tachypnoea, grunting, intercostal recession, nasal flaring Desaturation: <92 in air Dullness to percussion, tactile vocal fremitus Auscultation: coarse crackles, decreased breath sounds, bronchial breathing
32
Pneumonia investigations
CXR: confirm diagnosis, cannot differentiate between bacterial/viral Nasopharyngeal aspirate: identify viral causes Bloods & acute phase response markers may not differentiate between bacterial/viral
33
Abx therapy for a child with pneumonia <5yo
Supportive: O2 & analgesia, IV fluids, correct electrolytes Newborns: broad spectrum IV Abx <5yrs: Strep. Pneumoniae is most common 1st line = oral amoxicillin 2nd line = Co-amoxiclav or Cefaclor for typical cases Erythromycin, clarithromycin or azithromycin for atypical cases
34
Abx therapy for a child with pneumonia >5yo
Supportive: O2 & analgesia, IV fluids, correct electrolytes >5 yrs: Mycoplasma pneumoniae is most common 1st line = oral Amoxicillin or macrolide (Erythromycin) if mycoplasma/chlamydia suspected 2nd line = if Staph. Aureus is suspected consider using macrolide or combination of Flucloxacillin with Amoxicillin Severe pneumonia = Co-amoxiclav, Cefotaxime or Cefuroxime IV
35
Pertussis causative organisms, phases and according symptoms
Caused by Bordetella parapertussis Other causes = Mycoplasma pneumoniae, Chlamydia or adenovirus Catarrhal phase (1-2 weeks): mild symptoms with fever, cough and coryza Paroxysmal phase (2-6 weeks): develops characteristic paroxysmal or spasmodic cough followed by a inspiratory whoop Convalescent phase (2-4 weeks): symptoms gradually decrease, but may persist for many months
36
Pertussis investigations
Eyes: subconjunctival haemorrhage CXR: pneumonia sometimes develops Blood count: leucocytosis and lymphocytosis Diagnosis: culture nasal swab, marked lymphocytosis on blood film
37
Pertussis management
Erythromycin for 14 days (or Clarithromycin for 7 days): reduce infectivity Severe spasms of cough or cyanotic attack should be admitted to hospital and isolated from other children Erythromycin started in the catarrhal phase: can reduce symptoms and eradicate pertussis organisms Immunisation: reduces the risk of developing pertussis & severity
38
TB pathological sequence
4-8 weeks: Febrile illness Erythema nodosum: red swellings in fat tissue Phlyctenular conjunctivitis: allergic conjunctivitis 6-9 months: Progressive healing of primary complex Effusion: ghon focus may rupture into pleural space Cavitation: focus may rupture into bronchus Coin lesion on CXR: focus may enlarge Regional lymph nodes may obstruct bronchi or erode into bronchus/pericardial sac Miliary spread
39
Asymptomatic TB prevalence and explanation
50% of infants and 90% of older children show minimal signs & symptoms Local inflammatory reaction limits the progression of infection --> disease remains latent and therefore may develop into active disease at a later time Mantoux test may be positive = sufficient evidence to initiate treatment
40
TB presentation
``` Host response fails to contain the inhaled bacilli --> spread to regional lymph nodes Fever Anorexia and weight loss Cough CXR changes: ghon focus, miliary TB ``` Local enlargement of peribronchial lymph nodes: bronchial obstruction, lung consolidation & collapse Organs that may be involved: gut, skin, superficial lymph nodes (caseate forming cold abscess_ Post-primary TB: local disease or widely disseminated miliary TB to bones, joints, kidneys, pericardium and CNS: tuberculous meningitis
41
What is a ghon focus?
Lung lesions + infected lymph node = ‘Ghon or primary complex’
42
TB treatment
Triple/quadruple therapy: decreased to 1st 2 drugs after 2m Rifampicin, Isoniazid, Pyrazinamide, Ethambutol Pulmonary/lymph node TB: 6m treatment Disseminated TB/TB meningitis: >6m treatment TB meningitis: 1m course of dexamethasone Latent TB treatment: 3m rifampicin & isoniazid
43
CF aetiology
Autosomal recessive, annually 1/2500 live births and 1/25 carriers Projected life expectancy for current newborns: 40s Defective membrane protein = cystic fibrosis transmembrane conductance regulator (CFTR): cyclic AMP-dependent chloride channel CFTR gene = chromosome 7: most common defect is delta-F508 Additional factors important in determining the severity of lung disease: microbial pathogens, passive smoking, social deprivation and other ‘modifier’ genes
44
CF pathophysiology
Airways: reduction in airway surface mucus layer, impaired ciliary function, retention of mucopurulent secretions Chronic endobronchial infections: Pseudomonas aeruginosa Dysregulation of inflammation and defence against infection Intestine: meconium ileus in 10-20% of infants Pancreatic ducts: blocked by thick secretions --> pancreatic enzyme deficiency and malabsorption Sweat glands: excessive concentrations of sodium & chloride in sweat (salty)
45
CF clinical features in infancy
Meconium ileus: inspissated meconium causes intestinal obstruction, vomiting, abdominal distension, failure to pass meconium for the 1st few days Prolonged neonatal jaundice Failure to thrive Recurrent chest infections: Staphylococcus aereus, Haemophilus influenzae, Pseudomonas aeruginosa, Burkholderia Malabsorption: steatorrhoea Hypoproteinaemia and oedema
46
CF clinical features in young children
``` Bronchiectasis Rectal prolapse Nasal polyps Sinusitis Anorexia ```
47
CF clinical features in older children/adolescents
``` Allergic bronchopulmonary aspergillosis (ABPA) Diabetes mellitus Cirrhosis and portal hypertension Distal intestinal obstruction (DIOS): meconium ileus equivalent Pneumothorax/recurrent haemoptysis Sterility in males Arthropathy Psychological problems ```
48
CF chronic chest infection consequences
Results in viscous mucus in the smaller airways leading to damage of the bronchial wall, bronchiectasis and abscess formation --> may have persistent, loose cough and productive purulent sputum O/E: chest hyperinflation due to air trapping, coarse inspiratory crepitations and/or expiratory wheeze, finger clubbing
49
CF pancreatic exocrine insufficiency consequences
Insufficient lipase, amylase and proteases -->m maldigestion and malabsorption --> failure to thrive and passing frequent steatorrhoea Diagnosis: low elastase in faeces Meconium ileus: treated with gastrografin enemas
50
CF investigations
``` Newborn screening (heel-prick) Sweat test: increased chloride levels (>60mmol/L) CXR: hyperinflation, increased AP diameter, bronchial dilation, cysts, linear shadow and infiltrates Lung function: obstructive pattern with decreased FVC and increased lung volume ```
51
CF pulmonary management
b.d. physiotherapy: chest percussion, postural drainage, self-percussion, deep breathing exercises, flutter/acapello device Antibiotic therapy When well: oral Abx (flucloxacillin) against Staphylococcus aureus & Haemophilus influenzae Acute exacerbations: 14 day course of IV Abx through an indwelling long-line Chronic Pseudomonas aeruginosa infection: nebuliser Other therapies: annual flu vaccine, bronchodilators, mucolytics (before physio) and oral azithromycin
52
CF GI management
Distal intestinal obstruction: Lactulose (1mL/kg/day) Oral acetylcysteine solution (prophylaxis 15mL of 10%/day in <7yrs or 30mL in >7yrs, treatment doses 2-3x larger) Gastrografin: single oral dose treatment + fluid intake encouraged Pancreatic insufficiency: oral enteric-coated pancreatic supplements (Creon) taken will all meals and snacks, Ranitidine/omeprazole may be useful High calorie diet: 120-150% of normal energy intake Salt supplements: salt depletion is risk in 1st year and summer months Fat-soluble vitamin supplements: multivitamins, vitamin E and vitamin K (liver disease)
53
Epiglottitis aetiology
Life-threatening swelling of the epiglottis and septicaemia Haemophilus influenzae type B infection Most commonly in children 1-6yrs Rare due to routine HiB immunisation
54
Epiglottitis presentation
Pyrexic: ill, toxic-looking child Intensely painful throat that prevent swallowing or speech: saliva drools down chin Soft inspiratory stridor and rapidly increasing respiratory difficulty over hours Child sits immobile, upright and with an open mouth to optimise the airway
55
Epiglottitis management
ICU after endotracheal intubation Blood cultures and IV antibiotics 2nd or 3rd generation Cephalosporin IV for 7-10: Cefuroxime, Ceftriaxome or Cefotaxime Rifampicin prophylaxis to close contacts
56
Otitis media causative organisms
RSV and rhinovirus Pneumococcus Group A beta-haemolytic streptococcus Haemophilus influenza
57
Secretory otitis media features
Middle ear effusion without symptoms and signs of acute otitis media Course: months Effusions: serious, mucoid or purulent O/E: the drum may be retracted, does not move easily, with fluid effusions visible behind the tympanic membrane (opaque)
58
Childhood fever red flags
Fever: >38oC if <3 months or >39oC if 3-6 months Pale, mottled, blue Level of conscious: neck stiffness, bulging fontanelle, status epilepticus, focal neurological signs or seziures Significant respiratory distress: recession, stridor Bile-stained vomiting: obstruction Severe dehydration or shock Non-blanching rash
59
Septic screen components
``` Blood culture FBC: including differential WCC Acute phase proteins: CRP Urine sample CXR LP Rapid antigen screening (blood/urine/CSF), meningococcal/pneumococcal PCR (blood/CSF) or virus PCR for HSV or enterovirus (CSF) ```
60
Pyrexia treatment
Parenteral abx stat. if seriously unwell: 3rd-generation cephalosporin (cefotaxime or ceftriaxone) and ampicillin Aciclovir is given if HSV encephalitis is suspected Antipyretics: paracetamol or ibuprofen Not thought to prevent febrile seizures, but are in NICE guidelines
61
Croup causative organisms
``` Croup = laryngotracheobronchitis Viral croup (>95%): parainfluenza viruses, human metapneumovirus, RSV, influenza ```
62
Croup presentation
6m to 6 years: peak incidence 2yrs old in the autumn Barking cough, harsh stridor and hoarseness Usually preceded by fever and coryza Start and are worse at night
63
Croup management
Close observation at home, rest Oral dexamethasone, oral prednisolone and nebulised steroids (budesonide): reduce severity and duration of croup, and the need for hospitalization Severe cases with severe upper airway obstruction: nebulised adrenaline & oxygen provides transient improvement Beware rebound symptoms after 2hrs Only a few children require tracheal intubation Link between recurrent croup and atopy
64
Bacterial tracheitis clinical features & management
Similar to severe croup + high fever, appears toxic and has rapidly progressive airway obstruction due to thick airway secretions Staphylococcus aureus Management: IV antibiotics and intubuation/ventilation if required
65
Smoke inhalation symptoms
Cough: becomes useless to remove particulate matter SOB Sore throat Headache Confusions Mucosal oedema: hot smoke burning the mouth and throat Cyanosed: asphyxia due to deposition of smoke in the lower alveoli Increased RR accordingly
66
Smoke inhalation management
high flow and humidified oxygen: 100% oxygen helps to remove CO from blood quickly and reduces any poisoning affect CO is the leading cause of cardiac arrest and death before patients reach hospital 50% of patients will need intubation and PEEP to maintain the airway