Module 2.1 (Paediatrics, Childhood Infections, Febrile Seizures) Flashcards

1
Q

What questions to ask to get all information regarding paediatrics?

A

Age (or corrected age in pre-term infants)

Weight (actual vs ideal)

Route or acceptable administration methods

Allergies or ADR’s

Family and medical histories and co-morbidities

Medications

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2
Q

Age classification?

A
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3
Q

Define the following terms:

A) gestational age

B) chronological age

C) postmenstrual age

D) corrected age

A

A)

  • In completed weeks: time between the first day of the last menstraul period and day of delivery

B)

  • In days, weeks, months, or years: time since birth

C)

  • In weeks: gestational age plus chronological age (CGA)

D)

  • In weeks or months: chronological age minus the number of weeks born before 40 weeks’ gestation (only used for children born preterm upto 3 years of age)
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4
Q

What is absorption from the GI tract affected by?

A
  • Gastric acid secretion
  • Bile salt formation
  • Gastric emptying time
  • Intestinal motility
  • Bowel length and effective absorptive surface
  • Microbial flora

> all these factors are reduced in neonates (full-term and premature) and all may be reduced or increased in an ill child of any age.

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5
Q

How is absorption affected in neonates?

A

Rate of oral absorption is correlated with age

  • ↓ gastric acid secretion (higher gastric pH)
  • ↑ gastric emptying time

Immature production of pancreatic fluid and bile salts

Differences in intestinal microbial colonisation

IM absorption

  • Decreased muscle mass, erratic blood flow and painful
  • Generally should NOT be used – too painful in children (reserved for emergencies or if slower absorption is desired eg Vit K at birth)

Rectal: variation in blood flow to the rectum

Percutaneous absorption

  • Enhanced: thinner stratum corneum, better skin hydration, larger SA.
  • Potential for systemic toxicity
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6
Q

True or false preterm neonates have

> increased body water content

> less body fat

> lower albumin concentration

> increased blood brain barrier permeability

A

True

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7
Q

Higher doses (per kg of body weight) of water-soluble drugs are required in younger children because a higher percentage of their body weight is water

true or false

A

true

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8
Q

Albumin and total protein concentrations are lower in neonates but approach adult levels by 10-12 months = increased pharmacological effects and adverse effects at lower concentrations

True or False

A

True

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9
Q

Phase 1 and Phase 2 metabolism in neonates ?

A

Phase 1 metabolism

  • Activity is reduced in neonates and increases progressively during the first 6 months of life
  • Adult rates of metabolism may be achieved for some medications by 2-4 weeks of age

Phase 2 metabolism

> varies significantly by substrate

  • delay in maturation of enzymes required for bilirubin and paracetamol conjugation
  • enzymes required for morphine conjugation are fully developed even in pre-term neonates
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10
Q

Summary of drug absorption in neonates

A
  • Drug absorption may be erratic
  • Larger volume of distribution may result in the need for relatively larger doses (by weight) than might be expected
  • Reduced metabolism and clearance may result in longer half-lives and the need for extended dosing intervals
  • TDM may be helpful (in conjunction with clinical review)

> but not effective for valprotate –> doesn’t predict hepatotoxicity in children

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11
Q

What are some drugs that can manifest unusual toxicity in children?

A
  • Ceftriaxone
  • Codeine
  • Lindane
  • Prochloperazine
  • Tetracycline
  • SSRIs –> suicidal ideation
  • Fluoroquinolones
  • Diphenoxylate
  • Anesthetics, topical (eg benzocaine, mixture of lidocaine and prilocaine)
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12
Q

Should mix medications with breast milk/formula?

A

No –> may change the taste of it and child may refuse it.

  • small amount of apple puree on spoon may be ok
  • give favourite food after medicine if necessary to disguise taste
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13
Q

Excipients? What are they linked with?

A
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14
Q

What measurement should dose be prescribed in?

A

mg not mL

> Avoid trailing decimals and clearly indicated leading 0’s

> Eg 0.2mg NOT .2mg, 12mg NOT 12.0mg

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15
Q

What should HR, SBP and RR be in children aging from <1 year to 5-12 years?

A
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16
Q

What formul to use for creatinine clearance in children?

A

Schwartz clearance, NOT cockroft-gault (>18yo only)

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17
Q

What factors to consider when giving medication to children?

A
  1. Age/weight
  2. Appropriate dose

> when the calculated dose using mg/kg exceeds the adult dose, use the recommended adult dose instead, unless otherwise specified

> Prescribe sensible and practical doses for easy measurement and administration

  1. Appropriate interval

> don’t confuse total daily dose with dose/interval ‘prn’: include frequency and maximum daily dose

  1. Appropriate route of administration
  2. Formulation
  3. Monitoring parameters
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18
Q

Summary of introduction to paediatrics

A

Age classification

  • Including pre-term infants

Pharmacokinetic changes

Absorption

  • Higher gastric pH, increased gastric emptying time, increased percutaneous absorption

Distribution

  • Increased body water, lower albumin (less protein binding), increased BBB permeability

Metabolism

  • Reduced hepatic enzyme activity in neonates. Most drugs have longer t½ in neonates

Elimination

  • Renal plasma flow and GFR gradually improve over the first year or so

Specific medications

  • Gentamicin, codeine, theophylline, phenytoin, levetiracetam

Role of TDM?

Adverse effects and toxicity

  • Increased risk with paracetamol, valproate, topical anaesthetics, ceftriaxone, codeine, diphenoxylate, fluoroquinolones*, prochlorperazine, SSRI’s, tetracyclines*

Dosing in children

  • Mg/kg vs mg/dose vs mg/kg/day vs BSA (mg/m2)
  • IBW vs actual body weight

Administration

  • How to measure dose
  • How to give dose:

> Change medication, change route, tablet, disperse tablet, liquid, extemporaneous, SAS, half/quarter tab, injection via oral route

  • Timing of dose
  • Excipients

> Can cause issues (eg benzyl alcohol, gluten, ethanol, peanut oil, propylene glycol, colouring agents, carbohydrates)

Medication errors in children

  • Inconsistent presentation of dosing information
  • Calculations required
  • Lack of familiarity
  • Unlicensed/off-label use of products
  • Different strength products

> Eg paracetamol 24mg/mL, 48mg/mL, 50mg/mL, 100mg/mL

  • Parents giving doses in the middle of the night (tired/poor light)
  • Child getting into others medication (or other products)
  • Poisons information 13 11 26

Paediatric references

  • AMH CDC, KEMH, PCH and RCH information etc

Monitoring parameters in children

  • Different to adults and vary with age
  • do NOT use Cockroft-Gault
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19
Q

What is otitis media? When does it peak? What are the 3 different types?

A

Inflammation of the middle ear

Peaks between 6 months and 3 years

>Eustachian drainage tube dysfunction

1. Acute Otitis Media (OM)

  • Infected effusion and inflammation

2. Otitis Media with effusion

  • Effusion but not infected

3. Chronic Suppurative Otitis Media (CSOM)

  • infection of the middle ear with a perforated eardrum and discharge for >6 weeks
  • Can cause hearing impairment and disability
  • Occasionally serious complications can occur
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20
Q

What type of infection if AOM? Is it self-limiting?

A

Commonly viral infection

> antibiotics often (inappropriately) prescribed

> can also be bacterial or mixed infection

regardless of cause is usually self limiting

> Spontaneous resolution in 80% cases in 2-3 days

> Symptoms may persist up to 8 days in some children

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21
Q

True or false

for AOM: pull on ear and will feel better

for otitis externa: pull on ear and will hurt more

A

yessir true

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22
Q

How to diagnose acute otitis media?

A

Middle ear inflammation AND middle ear effusion

> Bulging tympanic membrane

> Otorrhoea (tympanic membrane perforation and effusion) –> discharge from the ear

PAIN ALONE IS NOT SUFFICIENT FOR DIAGNOSIS OF ACUTE OTITIS MEDIA

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23
Q

Acute otitis media where effusion is infected, what other symptoms will there be?

A
  • Acute onset ear pain (tugging, holding, rubbing ear)
  • Fever, irritability, poor feeding
  • Bulging tympanic membrane
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24
Q

How to manage otitis media? What medications are not used? Why antibiotics not helpful?

A

Adequate and regular analgesia with paracetamol +/- NSAID

> Antihistamines, decongestants and steroids are NOT beneficial for AOM

> Pain is a poor indicator of response to antibiotic

  • For every 100 children treated with antibiotics, only five children will be better at 2 to 3 days due to the antibiotics
  • Antibiotic therapy does not improve pain at 24 hours
  • Antibiotic therapy can cause harm through allergy, adverse effects and reistance
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25
Q

For most children antibiotics are not required for AOM, who are the exceptions?

A

Infants <6months

<2 years with bilateral infection

Systemically unwell (lethargic, pale, irritable +fever)

Children with otorrhoea (perforated eardrum)

Aboriginal and Torres Strait islander (ATSI) children

Children at high risk of complications (eg immunocompromised)

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26
Q

For normal patients, what does shared decision making with parent or carer mean for AOM?

A

Return to Dr if symptoms worsen, or don’t improve in 48-72 hours - antibiotics may be required

A delayed prescription for antibiotic therapy can be provided

Rare complications of AOM (without without antibiotics)

> mastoiditis and facial palsy –> urgent referral

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27
Q

Harms of antibiotic therapy?

A
  1. Adverse effects of antibiotics

Diarrhoea, rash or more serious hypersensitivity reactions

  1. Effect on microbiome

Full consequences not fully understood Yeast infections (eg thrush) to more serious infections (eg Clostridium difficile infection)

  1. Antibiotic Resistance

Multidrug-resistant bacteria (known as ‘superbugs’) can be spread between people, affecting your family and the community

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28
Q

If antibiotics are indicated for AOM:

A) what to use?

B) if no response to 48-72 hours, what to change to

C) for children with chronic otorrhea, add what?

D) if child very unwell or not responding to therapy?

A

A)

Amoxicillin

> do not use lower doses

B)

Amoxicillin/clavulanate

> B-lactamase producing H influenzae of M cattarhalis

C)

Ciporofloxacin ear drops until middle ear has been free of discharge for at least 3 days

D)

Urgent clinical review/hospital referral (may require IVABs)

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29
Q

If allergic to pencillins, what to use in place of amoxicillin or amoxicillin + clavulanate?

A) delayed non-severe hypersensitivity to penicillins

B) immediate (non severe or severe) or delayed severe hypersensitivity to pencillins

A

A)

  • cefuroxime for 5 days
  • trimethoprim + sulfamethoxazole for 5 days

B)

  • trimethoprim + sulfamethoxazole as above
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30
Q

What are risk factors for recurrent bacterial OM?

A

group child care

allergic rhinitis

adenoid disease

various structural anomalies, such as cleft palate and those associated with Down syndrome

exposure to smoke (eg cigarettes, wood fires)

socioeconomic disadvantage (eg crowded housing)

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31
Q

What vaccination should child have to prevent bacterial OM?

A

Streptococcus pneumoniae vaccination

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32
Q

What to do if recurrent infection of OM occurs?

A

Manage as for acute otitis media and consider referral to an otolaryngologist

> frequent recurrences may require myringotomy and insertion of tympanostomy tubes (grommets)

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33
Q

How long does effusion last after resolution of AOM? Does it go away? When would it not be appropriate to wait?

A

Middle ear effusion can persist for weeks after resolution of AOM

  • By 3 months 90% will have resolved spontaneously = wathcful waiting
  • May be appropriate to watch and wait 1st 3 months

> Watchful waiting would be appropriate in a child that is not experiencing persistent otitis media with effusion

> A child that is of a non-risk factor category would be indicated for observation (watchful waiting) and would be expected to completely resolve of their symptoms after 3 months (90% of cases)

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34
Q

What are the clinical signs of middle ear effusion?

A

Grey-white fluid behind an immobile tympanic membrane without signs of inflammation

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35
Q

What is persistent OM with effusion (glue ear) –> how long does it last for? What is the solution?

A

Middle effusion for > 3 months

  • Usually asymptomatic
  • May have hearing loss or balance/behavioural problems
  • Problem if affecting hearing and speech development
  • May need ENT referral and ?grommets
  • Some children (eg ATSI children (see guidelines – link in eTG) or children with risk factors for recurrent OM) are at high risk of developing chronic suppurative OM
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36
Q

What are the aims of management of OM with effusion?

A

Restore hearing (if affected)

Resolve and prevent recurrent infections

Address risk factors for recurrent OM

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37
Q

What is chronic suppurative otitis media (CSOM)? Symptoms?

A

Is an infection of the middle ear with a perforated eardrum and discharge for >6 weeks

  • Non-painful, copious discharge from ear
  • Can cause hearing impairment and disability
  • Occasionally serious complications can occur

> Intracranial infection and acute mastoiditis

> Increased risk in Aboriginal children

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38
Q

What is the treatment for CSOM?

A

Dry aural toilet

Topical antibiotic drops

  • Ciprofloxacin 0.3% ear drops – 5 drops 12hourly until the middle ear has been free of discharge for >3 days

Persistent discharge may require prolonged treatment –> ENT referral

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39
Q

Summary for AOM

A

Common presentation in primary care

  • Middle ear inflammation AND middle ear effusion

Often viral infection but antibiotics often prescribed

REGARDLESS OF CAUSE IS USUALLY SELF LIMITING

Management

Adequate and regular analgesia

> For most children antibiotics are NOT required

  • Shared decision making
  • Review or delayed prescription at 24-48 hours
  • Risk of adverse effects and increased resistance from antibiotic use

> If antibiotics required:

  • Amoxicillin (or if no response or concerns re resistance  amoxicillin/clavulanate)
  • Penicillin allergy (cefuroxime or sulfamethoxazole/trimethoprim)
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40
Q

Summary for preventing and managing recurrent bacterial OM

A

Reduce risk factors (smoke exposure, day care)

Pneumococcal vaccination

Consideration of ENT referral and grommets

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41
Q

Summary for otitis media with effusion

A

Not infected

Persistent OM with effusion if >3mths (Glue ear)

> May present with hearing or behavioural/balance problems

> Restore hearing, resolve and prevent infections, address risk factors

> Consider ENT referral +/- grommets

Risk of chronic suppurative OM (especially in Aboriginal and Torres Strait Islander children

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42
Q

Summary for chronic suppurative otitis media

A

Infection of the middle ear with perforated eardrum and discharge for >6wks

> Can cause hearing impairment and disability

> Occasionally serious complications can occur

Treatment

> aural toilet and ciprofloxacin ear drops

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43
Q

What is croup?

A

Acute laryngotracheobronchitis

  • Inflammation of upper airway, larynx and trachea
44
Q

How does croup present itself?

A

Coryzal (URTI) prodrome

> corzyal: acute inflammatory contagious disease involving the upper respiratory tract; especially.

> prodrome: an early symptom indicating the onset of a disease or illness.

Hoarseness/husky voice

Inspiratory stridor

Barking (brassy) cough (barking seal cough!)

Variable airway obstruction due to inflammatory oedema within the subglottis

45
Q

What age does croup occur in, how long does it last for?

A

Most common 1-3 years (6mths-6 years)

Duration 2-5 days (post-viral cough may last weeks)

46
Q

What is the cause for croup?

A

Most commonly parainfluenza viruses

Antibiotics are not indicated

47
Q

What is spasmodic croup? When and who does it occur in?

A

Typical croup symptoms that occur without acute viral infection

  • Usually in the early hours of the morning
  • Shorter course than acute laryngotracheobronchitis
  • Often recurrent
  • Occurs in older children

> have co-existing asthma

  • Treatment is the same as for acute croup
48
Q

Outline the severity of coup through the following

A) Mild airway obstruction

B) Moderate airway obstruction

C) Severe airway obstruction

D) Life-threatening airway obstruction

A

stridor = harsh vibrating noise when breathing

A)

Mild chest wall retractions and tachycardia, but no stridor at rest

B)

Stridor at rest, chest wall retractions, use of accessory respiratory muscles, and tachycardia

C)

Persisting stridor at rest, increasing fatigue, markedly decreased air entry and marked tachycardia

D)

Restlessness, LOC↓, hypotonia, cyanosis and pallor

> LOC: level of consciousness

> hypotonia: medical term for decreased muscle tone

> cyanosis: bluish-purple hue to the skin

> pallor: unhealthy pale appearance

Minimise distress to the child as this can worsen symptoms

49
Q

Differential diagnosis for croup?

A

Inhaled foreign body, anaphylaxis, bacterial tracheitis, epiglottitis

50
Q

What to use in croup? Why use these medications?

A

Good evidence to support the routine use of a single dose of corticosteroids in all children with croup

> Regardless whether mild, moderate or severe

> Reduces hospital admission and prevents re-presentation

> No evidence for use of humidifier or cough suppressants

51
Q

What corticosteroid to use in mild-moderate croup?

A

Budesonide inhalation single dose

Dexamethasone single dose

Prednisolone single dose

52
Q

What corticosteroid to use in severe croup?

A

Adrenaline by inhalation via nebuliser, repeated after 30 minutes if no improvement

PLUS EITHER

  • budesonide by inhalation via nebuliser as a single dose

OR

  • dexamethasone orally or IM/IV if vomiting as a single dose

OR

  • prednisolone as a single dose
53
Q

Croup summary

A

Acute laryngotracheobronchitis

Triggered by virus

  • Antibiotics are NOT indicated

URTI sx, inspiratory stridor, barking cough

Most common 1-3 years

Treatment

  • Single dose of corticosteroids in ALL children with croup
  • Plus nebulised adrenaline in severe croup

Spasmodic croup – sx without viral trigger (often in asthmatics)

54
Q

Influenza caused by?

A

Caused by influenza A and B viruses

Novel strains have potential to cause pandemics due to

> lack of immunity

> increased virulence

eg swine flu influenza A H1NI 2009

55
Q

Incubation period for influenza?

A

1-4 days

56
Q

Infection control for influenza?

A

Spread by droplets and contact with fomites

  • Hand hygiene, patient isolation, PPE

Notify HDWA

Prevent with vaccination

57
Q

How is the diagnosis of influenza done?

A
  • Rapid PCR from throat swab

Clinical features

  • Temperature >38.5 OR significant history of fever (rigors, chills, sweating) PLUS 2 or more of:

> Cough, sore throat, body aches, tiredness, SOB

Do not rule out influenza in vaccinated individual

58
Q

What are the complications of influenza?

A

Acute bronchitis, croup, AOM, pneumonia, myocarditis, pericarditis, post-infectious encephalitis, Reyes syndrome, haematological issues

59
Q

Treatment of influenza?

A

In healthy adults with a low risk of complications

  • Tx with a neuraminidase inhibitor –> decreased duration of influenza sx by <1 day on average, when tx started within 48 hrs of sx

> Limited benefit vs the potential AE’s of antiviral tx = N &V, headaches and neuropsychiatric events

60
Q

How to treat children with influenza? Which patients to treat?

A

Most children require NO antiviral treatment

Regardless of duration of symptoms -treat patients with

  • Established complications
  • Being admitted to hospital for mx influenza
  • With concurrent CAP
61
Q

Consider treatment for individuals at higher risk of poor outcomes from influenza, who are these individuals?

A

Children aged <5 years

ATSI people of any age People with heart disease, Down syndrome, obesity, chronic respiratory, neurological or other chronic conditions, immune compromise

People with heart disease, Down syndrome, obesity, chronic respiratory, neurological or other chronic conditions, immune compromise

62
Q

Which drugs used in treatment of influenza? What dose to use in different age groups?

A

Oseltamivir or zanamivir

63
Q

Oseltamivir in renal impairment?

A
64
Q

Treatment of influenza to prevent disease transmission, any backing to this?

A

May reduce risk of viral shedding and disease transmission

  • Hospitalised or aged-care facility residents
  • Have household contacts at risk of poor outcomes
65
Q

Rare side AE of oseltamivir?

A
  • Rare reports of self-injury, delirium and abnormal behaviour (some fatal) in children taking oseltamivir
66
Q

True or false

Data for use in children <1 year for the prevention of influenza are limited; consider using oseltamivir only in a pandemic.

A

true

67
Q

The earlier treatment starts, the shorter and less severe the illness, for oseltamivir. When to start?

A

Start within 48 hours (ideally within 24 hours) after onset of symptoms

However, in severe illness, later treatment, eg within 4 days of onset, is of benefit.

68
Q

A 15 mg/mL oseltamivir liquid can be made before each dose by asking the carer to?

A

Mix the contents of one 75 mg capsule in 5 mL water by stirring for about 2 minutes

Draw the correct dose volume into a syringe (discard unwanted liquid)

Mix the dose in soft food to disguise the taste before giving

Tamiflu oral liquid also available

69
Q

What is common in first couple of days with oseltamivir?

A

Nausea and vomiting in the first couple of days is common with this medicine

  • Take it with food to help reduce this
  • If swallowing capsules is difficult, you can take the contents of the capsule mixed in soft food, eg yoghurt, honey
70
Q

Zanamivir precuations?

A

Airways disease (eg asthma) – bronchospasm may occur

DPI – children may not be able to inhale sufficiently –> inadequate tissue levels

Neuropsychiatric AE’s – unclear if due to influenza or zanamivir

71
Q

Counselling from neuraminidase inhibitors

A

Neuraminidase inhibitors decrease, but do not suppress, viral excretion

treatment

  • Shortens the time you have symptoms, such as fever, headache, sore muscles, cough and sore throat.

prevention

  • May get flu even if you are taking this medicine

Otherwise healthy people should treat uncomplicated influenza by resting, drinking plenty of fluids and using paracetamol for symptom relief

Neuraminidase inhibitors have no effect in treating or preventing influenza-like illness (eg Coronavirus!)

72
Q

Annual influenza vaccination recommended for everyone > 6months of age. Especially who? How many doses to give?

A

Children 6mths -5years

ATSI

People with medical conditions that increase their risk (eg asplenia, immunosuppressed, Down syndrome, long

  • 1 dose per year
  • 2 doses if 6mths-9 years getting vaccine for the first time CHECK THE BRAND of vaccine is ok for use in children
73
Q

How is influenza vaccination given? How long does protection last for?

A

Preferably IM but can be given SC

Protection is expected to last for the whole season

> Optimal protection is within the first 3–4 months after vaccination

> Deferring vaccination to the beginning of winter may result in greater immunity later in the season, but may also lead to lack of protection if the influenza season starts early

> It’s never too late to vaccinate!

> Vaccinate children who need 2 doses (1st time vaccination) early in season to ensure the 2nd dose in time for winter

74
Q

CI to influenza vaccination?

A

Anaphylaxis after a previous dose of influenza vaccination

Anaphylaxis to any component of influenza vaccination

75
Q

Precuations to influenza vaccination?

A

Anaphylaxis to egg

  • Vaccinate in medical facility with trained staff
  • Remain for 30 minutes post-dose

Guillain-Barre syndrome within 6 weeks of influenza vaccination – vaccination generally not recommended

Immunotherapy – may be at increased risk of immune AE’s

Children who need both influenza and 13vPCV

> Can have both. Possible increased risk of febrile rxns

76
Q

Adverse events to influenza vaccination?

A

Can NOT cause influenza (not a live vaccine)

Symptoms may mimic influenza

  • Injection site reactions
  • Fever, malaise, myalgia
  • Immediate reactions rare (anaphylaxis, hives)
77
Q

Influenza summary

A

Caused by influenza A and B viruses

  • Infection control and vaccination important

Diagnosis

  • Rapid PCR and clinical features (fever, cough, sore throat, body aches, tiredness, SOB)

Complications

  • Acute bronchitis, croup, AOM, pneumonia, myocarditis, pericarditis, post-infectious encephalitis, Reyes syndrome, haematological issues

Treatment

  • Most children require NO antiviral treatment
  • Treat children with complications, CAP or being admitted to hospital
  • Consider treating those with ↑ risk of complications (<5yrs, ATSI, comorbidities)

Neuraminidase inhibitors

  • Oseltamivir (disperse capsule or liquid cc) or zanamivir (DPI – precaution asthma)
  • Treat for individual benefit or to prevent transmission
  • Rare reports of self-injury, delirium and abnormal behaviour (some fatal) in children taking oseltamivir and possibly zanamivir (?due to influenza)
  • The earlier treatment starts, the shorter and less severe the illness

Influenza vaccination

> Annual influenza vaccination recommended for everyone > 6months of age

  • Especially for high-risk (eg <5yrs, ATSI, immunocompromised etc)
  • 2 doses if 1st year vaccinated for 6mths -9 years
  • CHECK THE BRAND is ok for use in children
  • Optimal protection within 3-4 months of vaccination

CI

  • Previous anaphylaxis to flu vaccine or a component of flu vaccine
  • Caution - egg allergy, Guillain-Barre Syndrome, immunotherapy, 13v-PCV

AE

  • Mimics flu sx but it is NOT the flu, injection site reactions, anaphylaxis is rare
78
Q

What is hand,foot and mouth disease (HFMD)? Who does it affect?

A

Group of enteroviruses

  • Most commonly caused by the Coxsackie virus

Mainly children < 10yrs

Rarely causes further complications

HFMD is not linked to the foot and mouth disease which affects animals.

79
Q

What are the signs and symptoms of HFMD?

A

Fever, sore throat, poor appetite, lethargy, small blisters on the inside of the mouth and tongue, palms of the hands, fingers, soles of feet and nappy area (blisters should not be itchy)

  • Sx last ¬7-10 days
80
Q

How is HFMD spread?

A

Spread via droplets (cough/sneeze), blister fluid and in faeces

> Good hand hygiene

> Keep away from school etc until blisters dried

81
Q

Treatment for HFMD?

A

None – symptom management (painful mouth)

Complications extremely rare

82
Q

Definition for UTI?

A

Urinary tract infection (UTI) refers to a bacterial infection in the bladder (cystitis), or kidneys and ureters (pyelonephritis).

83
Q

Background for UTI?

A

Urinary tract infections in childhood are common and can be potentially serious in the first few years of life

The diagnosis of UTI should be considered in all febrile infants and young children, and in all infants with fever without focus.

84
Q

Key points for UTI?

A

Signs and symptoms of UTI can be non-specific in young children

Urinary dipstick is a useful screening test, but a positive urine culture with pyuria (white blood cells in urine) confirms the diagnosis

Oral antibiotics are appropriate for most children with UTI

> Children who are seriously unwell and most infants under 3 months usually require IV antibiotics

85
Q

Symptoms of UTI?

A

Infants and pre-verbal children often have non-specific symptoms (including jaundice in neonates)

> Fever, vomiting, poor feeding, lethargy and irritability

Older children may present with more typical symptoms

> Dysuria, urinary frequency, lower abdominal and loin pain

Ask about previous UTI

86
Q

Assessment of severity of UTI, lower and upper UTI differences? Cystitis and Pyelonephritis?

A

Clinical distinction between lower and upper UTI difficult, especially in younger children

  • Cystitis is suggested by features such as dysuria, frequency, urgency and lower abdominal discomfort
  • Pyelonephritis is suggested by systemic features such as fever, malaise, vomiting and loin tenderness
87
Q

How to investigate and manage UTI?

A

Collect urine sample

  • Dipstick and microscopy screening can guide initial management
  • Check culture results after 24hrs to confirm or adjust management

Urine samples should be collected prior to starting antibiotics (unless the child is seriously unwell and requires immediate IV therapy)

Older children able to void on request can provide a midstream urine sample

For younger pre-continent children, a clean catch is often suitable. Catheter or SPA may be required for seriously unwell infants

88
Q

What does urine dipstick test show for UTI?

A

useful screening test to guide initial management

  • The presence of leucocytes and nitrites is suggestive of a UTI Results ↓reliable in neonates/young infants, esp false negatives
89
Q

What does urine microscopy and culture test show for UTI?

A

laboratory microscopy can complement dipstick results to guide initial management

  • Bacteria and leucocytes on microscopy are suggestive of UTI
  • Epithelial cells suggest skin contamination and a poor sample
  • A positive culture with sufficient growth and pyuria confirms UTI
  • Growth of a single organism at >108 CFU/litre suggests infection
90
Q

What are other investigations used for UTI?

A

Check renal function and consider renal ultrasound if the child is seriously unwell, or not responding to appropriate therapy after 48hrs

Consider blood culture and lumbar puncture for unwell infants less than 4 weeks old, or if sepsis or meningitis is suspected at any age

  • FBC, (LFTs), UEC, CRP (all < 3mths and all systemically unwell)
91
Q

Treament for UTI in children? How does length change with cystitis and pyelonephritis?

A

Oral antibiotics are usually appropriate

Any child who is seriously unwell, and most infants under 3 months, should be admitted for initial IV antibiotics

3-7 day course for children with cystitis

7-10 day course for children with pyelonephritis

> E.coli causes 75% of UTI’s in otherwise healthy children

> Staph saprophyticus occasionally in adolescent females

> Wider range of organisms in patients with anatomical or functional abnormalities of urinary tract

92
Q

Treatment of UTI in infants?

A

Gentamicin > 1mth – 7.5mg/kg/dose once daily

IV aminoglycosides inactivated by IV penicillins and IV cephalosporins

> Aminoglycosides rapidly bactericidal so give 1st/flush well

Ceftriaxone

  • Avoid in <1 mth
  • May displace bilirubin from serum albumin
  • Caution in neonates with hyperbilirubinaemia
  • If < 1mth and penicillin allergic –> cefotaxime
  • Do NOT give IV Ca containing products to a neonate on ceftriaxone –> potentially fatal systemic calcinosis (Not within 48 hours (even if via different lines)
  • IM very painful – dilute with lidocaine
93
Q

What to do if multi-drug resistant organisms for UTI ab treatment?

A

Assess the response to therapy within 24 to 48 hours; if the child has not improved and results of culture and susceptibility testing are unavailable:

  • reconsider the diagnosis
  • consider if risk of multidrug-resistant bacterium
  • consider switching to intravenous therapy
94
Q

If resistance to all of the above drugs is confirmed, provided the pathogen is susceptible, use?

A

ciprofloxacin 12.5 mg/kg up to 500 mg orally, 12-hourly for 10 days

  • Liquid form not available and very bitter
  • Children with Pseudomonas aeruginosa UTI’s often have urological abnormalities and may require longer tx

If child is septic and MDR G-ve suspected (eg ESBL)

  • Use Meropenem 20mg/kg IV (up to 1g) q8h
95
Q

Summary of UTIs

A

Bacterial infection in the bladder (cystitis) OR kidneys/ureters (pyelonephritis)

Common and can be potentially serious if first years of life

  • Symptoms can be non-specific in young kids (fever, vomiting, poor feeding, irritable)
  • Older children more specific sx (dysuria, urinary frequency, lower abdo and loin pain)

Investigations

  • Urine dipstick can be a useful screening test
  • Can get false negatives in in neonates/young infants
  • Positive urine culture with pyuria confirms diagnosis Contamination rates of MSU, clean catch, SPA, in/out catheter
  • Other investigations FBC, UEC, CRP, BC, renal ultrasound

Treatment

  • Oral antibiotics are appropriate for most children
  • Children <3mths and very unwell children require IVAB’s
  • 3-7 day course for children with cystitis
  • 7-10 day course for children with pyelonephritis
96
Q

Summary of UTI treatment in infants

A

Birth – 3months: IV amoxicillin and gentamicin

  • Separate IV administration – give gentamicin first to avoid inactivation and flush well
  • Caution ceftriaxone <1 mth (Avoid with calcium containing IV fluids and displaces bilirubin from serum albumin)

Birth > 3 months

  • Toxic sx: IV amoxicillin and gentamicin OR ceftriaxone (note increased dose of gentamicin used)
  • Unwell but not toxic sx:

> Consider IM gentamicin or IM ceftriaxone (painful –give with lidocaine)

  • Discharge home with poAB’s (also for children that appear well but apparent UTI)
  • Cephalexin, cotrimoxazole, Augmentin Duo Cotrimoxazole

> Avoid in <1mth infants displace bilirubin from serum albumin (risk of kernicterus)

> Avoid in G6PDH deficiency (haemolytic anaemia)

If not responding to treatment consider

  • Multi-drug resistant organisms, alternative diagnosis, step-up to IVAB’s
97
Q

What are simple febrile seizures?

A

Infants and children have a predisposition to convulse in the presence of a fever.

Etiology and pathogenesis: unknown

Provoked seizures – they are NOT epilepsy

98
Q

What type of seizures are simple febrile seizures? How long do they last for?

A

Brief, generalised seizures (tonic-clonic)

Occurring only once in 24 hours

Last up to 15 minutes

Associated with a fever from a source outside the CNS

99
Q

How long does complicated febrile seizures last for? How often do they occur?

A

Seizure starts focally

Last >15 minutes

Occur more than once in 24 hours

Increased risk of developing epilepsy

100
Q

Prevalence of simple febrile seizures?

A
  • Increased risk if family hx febrile seizures
  • Occur in about 3% of children 6 months – 5 years of age
  • 30–50% risk of recurrent febrile seizures
  • Increased risk the younger the child when first febrile seizure

> 50% risk if 1yo, 30% risk if 2yo

  • Low risk of chronic epilepsy

> 1-2% if no other risk factors

  • No documented risk of other adverse outcomes

> Do not cause neurological damage (BENIGN condition)

101
Q

Cause of simple febrile seizure?

A

Temperature >38 degrees – triggers seizure

Infection

  • Usually viral (esp influenza, roseola virus) Can be bacterial

Post-immunisation temperature –> febrile seizure (MMR)

102
Q

Differential diagnosis of simple febrile seziures?

A

CNS infection (meningitis)

  • Esp if <12 months old or not up to date with immunisations (esp Hib, pneumococcus)

Epilepsy, metabolic disturbance

103
Q

Acute treatment for simple febrile seizures?

A

Standard 1st aid

Call 000 if lasts >5 minutes

Prolonged seizures

  • Diazepam (IV or rectal) or
  • Midazolam (IV, IM, intranasal, buccal)
104
Q

How to prevent simple febrile seizures?

A

Rarely necessary

Diazepam (oral or rectal) at the onset of fever for children at high risk of severe or complicated seizures

Rarely phenobarbitone or valproate

105
Q

Paediatric references?

A