Disease Profiles Flashcards

1
Q

Premature Infants: Altered Approach to Management (4 stages)

A

Delay cord clamping
Keep the baby warm
Gentle Lung Inflation
Saturation monitoring for careful oxygen control

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2
Q

The Sick Term Infant: APGAR scoring meaning

A

Appearance - skin colour
Pulse
Grimace - Reflex irritability
Activity - Muscle tone
Respiration

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3
Q

The Sick Term Infant: APGAR Appearance - Score of 0

A

Blue or Pale

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4
Q

The Sick Term Infant: APGAR Appearance - Score of 1

A

Blue in extremities but pink in the body

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5
Q

The Sick Term Infant: APGAR Appearance - Score of 2

A

No cyanosis

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6
Q

The Sick Term Infant: APGAR Pulse - Score of 0

A

Absent

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7
Q

The Sick Term Infant: APGAR Pulse - Score of 1

A

<100 BPM

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8
Q

The Sick Term Infant: APGAR Pulse - Score of 2

A

> 100 BPM

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9
Q

The Sick Term Infant: APGAR Grimace - Score of 0

A

No response

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10
Q

The Sick Term Infant: APGAR Grimace - Score of 1

A

Grimace or feeble cry when stimulated

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11
Q

The Sick Term Infant: APGAR Grimace - Score of 2

A

Cries or pulls away when stimulated

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12
Q

The Sick Term Infant: APGAR Activity - Score of 0

A

None

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13
Q

The Sick Term Infant: APGAR Activity - Score of 1

A

Some flexion

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14
Q

The Sick Term Infant: APGAR Activity - Score of 2

A

Flexed arms and legs that resist extension

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15
Q

The Sick Term Infant: APGAR Respiration - Score of 0

A

Absent

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16
Q

The Sick Term Infant: APGAR Respiration - Score of 1

A

Weak and irregular gasping

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17
Q

The Sick Term Infant: APGAR Respiration - Score of 2

A

Strong cry

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18
Q

The Sick Term Infant: Examples of respiratory problems (3)

A

TTN - Transient Tachypnoea of the Newborn
Pneumothorax
Congenital Respiratory Disease - Tracheo-oesophageal fistula or Diaphragmatic hernia

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19
Q

The Sick Term Infant: Examples of cardiac problems (3)

A

Hydrops foetalis - due to rhesus disease or chromosomal abnormalities
PPHN - Persistent pulmonary hypertension of the newborn
Congenital heart disease

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20
Q

The Sick Term Infant: Examples of Congenital Heart Disease (5)

A

Tetralogy of Fallot
Transposition of the Great Arteries
Coarctation of the Aorta
TAPVD - Total Anomalous Pulmonary Venous Drainage
Hypoplastic heart

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21
Q

The Sick Term Infant: Examples of Neurological Disease (3)

A

Hypoxic ischaemic encephalopathy
Microcephaly
Spina bifida

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22
Q

The Sick Term Infant: Example of a Renal Disease

A

Potters Syndrome

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23
Q

The Sick Term Infant: Main two causes of bacterial infection in neonates (2)

A

Group B Streptococcus
E. coli

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24
Q

The Sick Term Infant: Syphilis - Causative organism

A

Treponema Pallidum

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25
Q

The Sick Term Infant: Syphilis - Highest risk

A

Mothers infected within the last two years - early stage

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26
Q

The Sick Term Infant: Syphilis - Clinical Presentation (4)

A

Bone abnormalities
Anaemia
Hepatosplenomegaly
Jaundice

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27
Q

The Sick Term Infant: Syphilis - How to reduce risk to neonate?

A

Treat 30 days prior to delivery

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28
Q

The Sick Term Infant: Respiratory Distress Syndrome - Presentation (4)

A

Tachypnoea
Recession
Grunting
Blue - Cyanosed

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29
Q

The Sick Term Infant: Respiratory Distress Syndrome - Investigation and result

A

CXR - ground glass with air bronchograms

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30
Q

The Sick Term Infant: Transient Tachypnoea of the Newborn - Most at risk

A

Infants delivered by C-section

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31
Q

The Sick Term Infant: Transient Tachypnoea of the Newborn - How is lung fluid cleared in the normal neonate?

A

Active epithelial Sodium Channels pump it into the interstitium and then into the lymphatic system

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32
Q

The Sick Term Infant: Transient Tachypnoea of the Newborn - Investigations and result

A

CXR - fluid in the lungs within the horizontal fissure

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33
Q

The Sick Term Infant: Transient Tachypnoea of the Newborn - Management

A

Resolves within 24 hours

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34
Q

The Sick Term Infant: Pneumothorax - Aetiologies (4)

A

Meconium
Infection
Resuscitation
Surfactant deficiency

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35
Q

The Sick Term Infant: Pneumothorax - Management

A

Pig tail chest drains

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36
Q

The Sick Term Infant: Meconium Aspiration Syndrome - Pathophysiology

A

Foetus inhales liquor with meconium in it, leading to airway obstruction, inflammation and surfactant dysfunction

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37
Q

The Sick Term Infant: Meconium Aspiration Syndrome - Complications (2)

A

Asphyxia
Persistent pulmonary hypertension

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38
Q

The Sick Term Infant: Hypoxic Ischaemic Encephalopathy - Pathophysiology

A

Multi-organ damage due to tissue hypoxia - in the brains, kidneys, liver and gut

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39
Q

The Sick Term Infant: Hypoxic Ischaemic Encephalopathy - Primary aetiologies (3)

A

Placental failure
Cord prolapse
Uterine rupture

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40
Q

Cyanosed babies with congenital heart disease are often not responsive to what?

A

Oxygen

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41
Q

Bilious Vomiting

A

Green vomit

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42
Q

The Sick Term Infant: Hypoglycaemia - Aetiologies (3)

A

Low birth weight or small for gestational age
Maternal Disease - Diabetes
Mother on Labetalol

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43
Q

The Sick Term Infant: Inborn Errors of Metabolism - Presentation (3)

A

Acidosis
Hypoglycaemia
Jaundice

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44
Q

The Sick Term Infant: Pathophysiology of Potters Syndrome

A

Lack of amniotic fluid leads to kidney disease

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45
Q

Vital Signs: Heart rate normal

A

120-140 BPM

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46
Q

Vital Signs: Perfusion normal

A

Capillary refill of 2-3 seconds with >95% oxygen saturation

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47
Q

Vital Signs: Respiratory Rate Normal

A

40-60 per minute

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48
Q

Infection: Main three antibiotics used

A

Benzylpenicillin
Gentamicin
Cefotaxime

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49
Q

Infection: Main three antibiotics used

A

Benzylpenicillin
Gentamicine
Cefotaxime

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50
Q

Cover of Benzylpenicillin

A

Gram positive and negative

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51
Q

Cover of Gentamicin

A

Gram negative

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52
Q

Cover of Cefotaxime

A

Gram positive and negative

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53
Q

Neonatal Sepsis: Early Onset is mainly due to what? (2)

A

Bacteria acquired before or during delivery - Group B Streptococcus or Gram Negative Bacteria

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54
Q

Neonatal Sepsis: Late Onset is mainly due to what? (3)

A

Noscomial or Community Sources - Coagulase Negative Staphylococci, Gram Negative Bacteria or Staphylococcus aureus

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55
Q

Neonatal Sepsis: Symptoms (4)

A

Fever
Reduced tone and activity
Poor feeding
Vomiting

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56
Q

Neonatal Sepsis: Signs - Respiratory (2)

A

Respiratory distress or apnoea
Hypoxia

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57
Q

Neonatal Sepsis: Signs - Cardiovascular

A

Tachycardia or Bradycardia

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58
Q

Neonatal Sepsis: Signs - Gastrointestinal (2)

A

Jaundice - within 24 hours
Hypoglycaemia

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59
Q

Neonatal Sepsis: Signs - Neurological

A

Seizures

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60
Q

Neonatal Sepsis: Five Stages to Management (5)

A

Give high flow oxygen
Obtain IV access to take blood tests - cultures, glucose and lactate analysis
Give IV or IO antibiotics - broad spectrum
Fluid resuscitation
Consider Inotropic Support with Adenaline

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61
Q

Neonatal Sepsis: Management - Fluid Resuscitation

A

20ml/kg isotonic fluid over 5-10 minutes
Assess for fluid overload after 40ml/kg fluids and titrate further if no signs of overload

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62
Q

Neonatal Sepsis: Management - Adrenaline Dose

A

Administer with 3rd fluid bolus - 0.3mg/kg in 50ml 5% dextrose 1ml/hour

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63
Q

Anatomical Differences: Head (2)

A

Large head
Prominent occiput

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64
Q

Anatomical Differences: Ratios

A

Large Surface Area:Volume Ratio

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65
Q

Anatomical Differences: URTI (2)

A

High anterior larynx
Floppy epiglottis

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66
Q

Anatomical Differences: Ribs

A

More flexible

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67
Q

Anatomical Differences: Blood volume

A

80ml

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68
Q

Anatomical Differences: Haemoglobin

A

HbF at birth

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69
Q

Anatomical Differences: Over time what trend is seen with HR?

A

Reduces

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70
Q

Anatomical Differences: Over time what trend is seen with RR?

A

Reduces

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71
Q

Anatomical Differences: Over time what trend is seen with Systolic Blood pressure?

A

Increases

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72
Q

Bronchiolitis

A

Acute inflammatory injury to the bronchioles

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73
Q

Bronchiolitis: Causative organism

A

RSV

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74
Q

Medical word for Croup

A

Laryngotracheobronchitis

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75
Q

Croup: Most common causative organism

A

Parainfluenza Virus

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76
Q

Croup: Clinical presentation

A

Stridor - due to ~70% of airway impacted

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77
Q

Meningicoccaemia: Causative Organism

A

Neisseria meningitidis

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78
Q

Meningicoccaemia: Clinical Presentation

A

Purpura the spreads on the skin

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79
Q

Respiratory Distress in the Newborn: Most common in what patient group?

A

Infants born before 29 weeks - before the lungs begin producing surfactant

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80
Q

Respiratory Distress in the Newborn: Pathophysiology

A

Inadequate surfactant leads to high surface tension within the alveoli to cause lung collapse and thus inadequate gaseous exchange

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81
Q

Respiratory Distress in the Newborn: Clinical Presentation (5)

A

Tachypnoea
Grunting
Intercostal recession
Nasal flaring
Cyanosis

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82
Q

Respiratory Distress in the Newborn: Management (3)

A

Maternal steroid
Surfactant replacement
Ventilation

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83
Q

Respiratory Distress in the Newborn: Aetiologies - Metabolic (3)

A

Acidosis
Inborn errors of metabolism
Hypoglycaemia

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84
Q

Respiratory Distress in the Newborn: Aetiologies - Haematological (3)

A

Polycythaemia
Blood loss
Anaemia

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85
Q

Respiratory Distress in the Newborn: Aetiologies - Neurological (3)

A

Seizures
Intra-cranial bleed
Withdrawal

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86
Q

Hypochondroplasia: Clinical Presentation - Neurological (2)

A

Severe neonatal seizures
Temporal lobe epilepsy

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87
Q

Hypochondroplasia: Clinical Presentation - General (4)

A

Short stature
Bossed prominent forehead
Short triangular fingers
Rhizomelic limb shortening of the femurs and humeri

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88
Q

Hypochondroplasia: Genetic Mutation

A

FGFR3 - c.1620C>A or p.Asn540Lys

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89
Q

Hypochondroplasia: Example of Management

A

Vosoritide

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90
Q

Russell Silver Syndrome: Genetic mutation mechanisms (3)

A

Methylation on C bases just before G bases
Imprinting
UPD 7 mutations

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91
Q

Russell Silver Syndrome: Management

A

Growth Hormone

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92
Q

Russell Silver Syndrome: Clinical Presentation - Gastrointestinal (3)

A

Vomiting - due to Reflux
Poor weight gain
Poor Appetite

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93
Q

Russell Silver Syndrome: Clinical Presentation - General features (2)

A

Short stature
Elfin features - triangular face with ears that stick out

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94
Q

Turners Syndrome: General features (7)

A

Short and wide neck - due to cystic hygroma
Low hairline
Teeth probelms
Broad chest with wide spaced nipples
Short fourth finger or toe
Low weight
Short stature

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95
Q

Reactive Attachment Disorder

A

Markedly disturbed and developmentally inappropriate social relatedness that begins before the age of 5 years old

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96
Q

Reactive Attachment Disorder: Main Aetiologies (3)

A

Persistent disregard for the child’s emotional needs for comfort, stimulation and affection
Persistent disregard for child’s physical needs
Repeated changes for primary caregivers

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97
Q

Reactive Attachment Disorder: Risk Factors

A

Adverse childhood experiences - Abuse, Neglect or Household dysfunction

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98
Q

Reactive Attachment Disorder: More common in what children?

A

Children orphaned at a young age

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99
Q

Reactive Attachment Disorder: What are the subtypes? (2)

A

Inhibited
Disinhibited

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100
Q

Reactive Attachment Disorder: Inhibited Subtype

A

Children who continually fail to initiate and respond to social interactions in a developmentally appropriate way

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101
Q

Reactive Attachment Disorder: Inhibited Subtype - Interactions characterised by what? (4)

A

Avoidance
Resistance to comfort
Hyper-vigilance
Ambivalence

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102
Q

Reactive Attachment Disorder: Disinhibited Subtype

A

A child with an inability to display appropriate selective attachments

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103
Q

Reactive Attachment Disorder: Disinhibited Subtype - How is this displayed?

A

Displays excessive familiarity with strangers or lack of selectivity in their choices of an attachment figure

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104
Q

Reactive Attachment Disorder: Clinical Presentation - Signs in Relationships (4)

A

Neglectful behaviour by the primary caregiver
Lack of smiling or responsiveness from the baby or child
Lack of distress in situations that should cause distress
Excessive friendliness to healthcare workers

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105
Q

Reactive Attachment Disorder: Clinical Presentation - Common Co-morbidities (3)

A

Emotional Disorders
ADHD
Behavioural Disorders

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106
Q

Reactive Attachment Disorder: Diagnosis - 1-2 Years

A

Strange Situation Procedure

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107
Q

Reactive Attachment Disorder: Diagnosis - 2-4 Years

A

Modified Strange Situation Procedure

108
Q

Reactive Attachment Disorder: Diagnosis - 1-4 Years

A

Attachment Q-sort - children observed in a number of set environments

109
Q

Reactive Attachment Disorder: Diagnosis - 4-7 Years

A

Story Stem Attachment Profile - use toys or verbally communicate stories

110
Q

Reactive Attachment Disorder: Diagnosis - 7-15 Years

A

Child Attachment Interview

111
Q

Reactive Attachment Disorder: Diagnosis - 15+ Years

A

Adult Attachment Interview

112
Q

Reactive Attachment Disorder: Management - Pre-school (3)

A

Parental sensitivity and behaviour therapy
Home visiting programmes
Parent-child Psychotherapy

113
Q

Reactive Attachment Disorder: Management - School Age (4)

A

Parental sensitivity and behavioural training
Group play sessions
Group-based educational sessions for caregivers and children
Trauma-Based Behavioural Therapy

114
Q

Reactive Attachment Disorder: Complications if not Managed (3)

A

Developmental delay
Reduction in academic achievement
Increased risk of contact with youth justice

115
Q

Conduct Disorder

A

Repetitive and persistent pattern of behaviour in which the rights of others or major age-appropriate norms or rules are violated

116
Q

Conduct Disorder: Name in younger children

A

Oppositional Defiant Disorder

117
Q

Conduct Disorder: Aetiologies - Examples of Brain Injury (2)

A

Intrauterine trauma
Post-natal CNS trauma

118
Q

Conduct Disorder: Aetiologies - Family Circumstances (4)

A

Families with parents with mental illness
Drug and alcohol concerns
Domestic violence
Single parent families

119
Q

Conduct Disorder: Aetiologies - Parenting Style (4)

A

Lack of house rules
Lack of clarity on how a child should behave
Lack of supervision
Lack of techniques to deal with crises

120
Q

Conduct Disorder: Subtypes - Mild to Moderate

A

Restricted to the Family Environment

121
Q

Conduct Disorder: Subtypes - Severe two types

A

Unsocialised - predominantly violent behaviour

Socialised - anti-social acts or better ability to avoid getting involved with criminal justice system

122
Q

Conduct Disorder: Diagnosis

A

Presence of a3+ of the following criteria within 12 months and 1 in the last 6 months:
- Aggression towards people or animals
- Destruction of property
- Deceitfulness or theft
- Serious violations of rules

123
Q

Conduct Disorder: Clinical Presentation - Triad

A

Inattention
Hyperactivity
Impulsivity

124
Q

Conduct Disorder: Management - Under 11 years old

A

Parent or Foster parent training

125
Q

Conduct Disorder: Management - Aged between 9 and 14 years

A

Child-focused programmes

126
Q

Conduct Disorder: Management - Aged between 11 and 17 years

A

Multi-modal interventions

127
Q

Conduct Disorder: Management - Pharmacological main drug of choice

A

Risperidone - atypical anti-psychotic

128
Q

Conduct Disorder: Management - If co-existing ADHD

A

Stimulant medication

129
Q

Conduct Disorder: Management - If co-existing depression

A

SSRIs

130
Q

Prader-Willi Syndrome: Genetic Involvement

A

Deletion on the paternal chromosome 15 or complete loss of parental chromosome 15 causes uniparental maternal disomy

131
Q

Prader-Willi Syndrome: Presentation at Birth (3)

A

Hypotonia - floppy
Unable to suck or reduced ability - tube feeding is common
Hyperphagia - food seeking and lack of satiety

132
Q

Prader-Willi Syndrome: Facial Features

A

Small hands and feet with almond shaped eyes with a narrow face and high-arched palate

133
Q

Prader-Willi Syndrome: Stature

A

Short

134
Q

Prader-Willi Syndrome: Later stage features (2)

A

Developmental delay
Failure to thrive in infancy

135
Q

Prader-Willi Syndrome: Dysregulation in what region is present?

A

Hypothalamus

136
Q

Prader-Willi Syndrome: Endocrine features (3)

A

Hypogonadotropic hypogonadism
Cortisol deficiency
GH deficiency

137
Q

Prader-Willi Syndrome: Indications for Paediatric Review (3)

A

Obesity-related morbidity that requires weight loss - Intra-cranial hypertension, Sleep Apnoea or Orthopaedic problems
Suspected underlying cause of obesity
Children under 24 months that are >99.6th centile

138
Q

Prader-Willi Syndrome: Pharmaceutical Options for Obesity (2)

A

Orlistat
Saxenda

139
Q

Prader-Willi Syndrome: Surgical Options (3)

A

Laparoscopic Adjustable Gastric Banding
Roux-en-Y Gastric Bypass
Laparoscopic Sleeve Gastrectomy

140
Q

Prader-Willi Syndrome: Indications for surgery

A

Post-pubertal adolescents with severe to extreme obesity with severe co-morbidities

141
Q

Bardet-Biedl Syndrome: Genetic Pathophysiology

A

Autosomal recessive disease affecting the proteins of the cilia basal body to prevent intercellular sensing

142
Q

Bardet-Biedl Syndrome: Clinical Presentation (6)

A

Obesity
Neurocognitive Delay
Syn- or Polydactyly
Retinal dystrophy or pigmentary retinopathy
Hypogonadism
Renal dysfunction

143
Q

Neonatal Abstinence Syndrome

A

Withdrawal symptoms that happens in neonates of mothers that used substances in pregnancy

144
Q

Neonatal Abstinence Syndrome: Related Substances (6)

A

Opiates
Methadone
Benzodiazepines
Cocaine
Alcohol
Amphetamines

145
Q

Neonatal Abstinence Syndrome: Neurological Symptoms (3)

A

Irritability
Tremors
Seizures

146
Q

Neonatal Abstinence Syndrome: Vasomotor and Respiratory Symptoms (3)

A

Sweating
Unstable temperature
Tachypnoea

147
Q

Neonatal Abstinence Syndrome: Metabolic and GI Symptoms (3)

A

Poor feeding
Regurgitation
Hypoglycaemia

148
Q

Neonatal Abstinence Syndrome: Monitoring time

A

3 days of NAS chart

149
Q

Neonatal Abstinence Syndrome: Monitoring time for SSRI anti-depressants

A

48 hours of NAS chart

150
Q

Birth Asphyxia

A

Baby does not receive enough oxygen before, during or after birth

151
Q

Birth Asphyxia: Aetiologies (4)

A

Maternal shock
Intrapartum haemorrhage
Prolapsed cord
Nuchal cord - wrapped around the neck of the baby

152
Q

Birth Asphyxia: Main complication

A

Hypoxic Ischaemic Encephalopathy

153
Q

Hydrocephalus

A

Abnormal CSF build up within the brain and spinal cord

154
Q

Hydrocephalus: Clinical Presentation (5)

A

Enlarged and rapidly increasing head circumference
Bulging anterior fontanelle
Poor feeding with vomiting
Poor tone
Sleepiness

155
Q

Hydrocephalus: Management

A

Ventriculoperitoneal shunt

156
Q

Necrotising Enterocolitis

A

Disorder affecting premature neonates in which part of the bowel becomes necrotic

157
Q

Necrotising Enterocolitis: Aetiology

A

Intestinal injury to the immature gut causing perforation e.g. fed too early

158
Q

Necrotising Enterocolitis: Clinical Presentation (5)

A

Intolerance to feeds
Vomiting - green bilous vomit
Distended tender abdomen
Absent bowel signs
Blood in stools

159
Q

Necrotising Enterocolitis: Diagnosis - What test is used?

A

Abdominal X-ray

160
Q

Necrotising Enterocolitis: Diagnosis - Presentation on AXR (4)

A

Dilated loops of bowel
Bowel wall oedema
Gas within the bowel wall
Gas in the pertioneal cavity - indicates perforation

161
Q

Pneumoperitoneum

A

Gas within the peritoneal cavity

162
Q

Necrotising Enterocolitis: Management (3)

A

NBM
Clindamycin and Cefotaxime
Urgent referral to surgery

163
Q

Intraventricular Haemorrhage

A

Bleeding into the ventricles within the brain

164
Q

Intraventricular Haemorrhage: Most common type

A

Germinal Matrix Subtype

165
Q

Intraventricular Haemorrhage: When does risk reduce and why?

A

35-36 weeks gestation - as the germinal matrix has disappeared by then

166
Q

Jejunal Atresia

A

Congenital Anomaly characterised by obliteration of the lumen of the jejunum in that it is not connected to the large intestine

167
Q

Jejunal Atresia: Clinical Presentation

A

Abdominal distension and bilious vomiting within the first 24 hours of birth

168
Q

Jejunal Atresia: Diagnostic approach

A

Abdominal X-ray

169
Q

Jejunal Atresia: Management

A

Surgical correction

170
Q

Malrotation

A

Congenital anatomical anomaly that results from an abnormal rotation of the gut as it returns to the abdominal cavity during embryogenesis

171
Q

Malrotation: Clinical Presentation

A

Mid gut volvulus - presenting with bilious green vomiting mainly within the first month of life

172
Q

Malrotation: Diagnostic Test

A

Upper GI contrast test

173
Q

Malrotation: Management

A

Surgical correction

174
Q

Meconium Ileus

A

Bowel obstruction of the neonate due to thick and impacted meconium

175
Q

Meconium Ileus: Main aetiology

A

Cystic Fibrosis

176
Q

Meconium Ileus: Main diagnostic test

A

X-ray

177
Q

Inguinal Hernia

A

Weakness in the muscle around the groin resulting in a loop of bowel bulging through

178
Q

Cerebral Palsy

A

Permanent neurological problems resulting from damage to the brain near birth

179
Q

Cerebral Palsy: Aetiologies - Antenatal (2)

A

Maternal infections
Trauma during pregnancy

180
Q

Cerebral Palsy: Aetiologies - Peri-natal (2)

A

Birth Asphyxia
Pre-term Birth

181
Q

Cerebral Palsy: Aetiologies - Post-natal (3)

A

Meningitis
Severe neonatal jaundice
Head injury

182
Q

Duchenne’s Muscular Dystrophy

A

Genetic disease causing muscular weakness and wasting

183
Q

Duchenne’s Muscular Dystrophy: Genetic Pathophysiology

A

X-linked recessive mutation of dystrophin gene on the X-chromosome

184
Q

Duchenne’s Muscular Dystrophy: Clinical presentation

A

Progressive weakness in the muscles around the pelvis of boys at around 3-5 years old

185
Q

Duchenne’s Muscular Dystrophy: What sign is significant?

A

Gower’s Sign - Children with proximal muscle weakness use knees to stand up

186
Q

Bronchiolitis

A

Acute inflammatory injury of the bronchioles

187
Q

Bronchiolitis: Most common cause

A

RSV

188
Q

Bronchiolitis: Most common age

A

<6 months old

189
Q

Bronchiolitis: Clinical Presentation - Signs on auscultation

A

Wheeze and crackles

190
Q

Bronchiolitis: Clinical Presentation - Viral URTI symptoms (4)

A

Running or snotty nose
Sneezing
Mucous within the throat
Watery eyes

191
Q

Croup: Clinical Presentation (4)

A

Barking cough
Increased work of breathing
Hoarse voice
Stridor

192
Q

Croup: Management - First stage

A

Oral Dexamethasone

193
Q

Croup: Management - Second stage

A

IM Dexamethasone or Nebulised Budesonide

194
Q

Croup: Management - Third Stage

A

Oxygen

195
Q

Croup: Management - Fourth Stage

A

Nebulised adrenaline

196
Q

Croup: Management - Fifth Stage

A

Intubation and ventilation

197
Q

Most common heart rhythm disturbance in children

A

Supraventricular Tachycardia

198
Q

SVT

A

Supraventricular Tachycardia

199
Q

SVT: Pathophysiology

A

Abnormally fast heart rhythm arising from inappropriate electrical activity in the upper part of the heart

200
Q

SVT: 4 types

A

Atrial fibrillation
Paroxysmal SVT
Atrial flutter
Wolff-Parkinson-White Syndrome

201
Q

Infective Endocarditis: Most common causative organism in paediatrics (2)

A

Gram positive bacteria
Viridans group

202
Q

Main causes of Gastroenteritis in children? (2)

A

Rotavirus
Norovirus

203
Q

Congenital Pyloric Stenosis

A

Narrowing of the opening from the stomach to the first part of the small intestine

204
Q

Congenital Pyloric Stenosis: Clinical Presentation - Symptoms (2)

A

Projectile vomiting without the presence of bile (milk in vomit) after feeding
Keen to feed

205
Q

Congenital Pyloric Stenosis: Clinical Presentation - Typical age of symptoms

A

2-12 weeks old

206
Q

Congenital Pyloric Stenosis: Clinical Presentation - Signs (3)

A

Signs of dehydration
Peristalsis across the abdomen
Abdominal mass may be present - olive-like structure at the top right of the abdomen

207
Q

Congenital Pyloric Stenosis: Main Diagnostic Test

A

US scan of the upper abdomen

208
Q

Congenital Pyloric Stenosis: Management

A

Pyloromyotomy

209
Q

Congenital Pyloric Stenosis: Complications

A

Metabolic imbalance leading to metabolic acidosis

210
Q

Volvulus

A

Loop of intestine twists around itself and the mesentery supporting it, resulting in bowel obstruction

211
Q

Volvulus: Congenital intestinal malrotation increases the risk of what?

A

Midgut volvulus

212
Q

Volvulus: What increases the risk of segmental volvulus?

A

Meconium ileus

213
Q

Volvulus: Clinical Presentation (4)

A

Abdominal pain and bloating
Vomiting bile
Constipation
Bloody stool

214
Q

Volvulus: Diagnostic test

A

Abdominal X-Ray

215
Q

Intussusception

A

Bowel invaginates into itself, narrowing the lumen which results in a palpable mass in the abdomen and obstruction to the passage of faeces through the bowel

216
Q

Intussusception: Symptoms (3)

A

Severe colicky abdominal pain
Lethargy
Vomiting

217
Q

Intussusception: Signs (3)

A

Signs of dehydration
Redcurrant Jelly stool
Right upper quadrant mass

218
Q

Intussusception: Diagnostic test and result

A

USS - Shows a target sign

219
Q

Intussusception: Management - First line

A

Air reduction

220
Q

Intussusception: Management - Second line

A

Surgical reduction

221
Q

Intussusception: Characteristic symptom

A

Cycle of pain and then goes limp

222
Q

Appendicitis

A

Inflammation of the appendix

223
Q

Appendicitis: Classic Clinical Presentation

A

Abdominal pain that starts as central abdominal pain and migrates to the right iliac fossa over time

224
Q

Appendicitis: Signs - Tenderness is located where?

A

McBurney’s Point

225
Q

Appendicitis: Signs - What result is shown on Rosving’s Test?

A

Palpation of the left iliac fossa causes pain in the right iliac fossa

226
Q

Appendicitis: Management

A

Appendicectomy

227
Q

Urinary Tract Infection: More common in what sex?

A

Females

228
Q

Urinary Tract Infection: Diagnostic Test

A

Urine sample with microbiology

229
Q

Urinary Tract Infection: Management - Children <3 months with a fever

A

Immediate IV antibiotics

230
Q

Urinary Tract Infection: Management - Children with features of sepsis or pyelonephritis

A

IV antibiotics

231
Q

3 Causes of Acute Scrotal Pain (3)

A

Torsion of testicle
Epididymoorchitis
Hydatid of Morgagni - Torsion of the appendix testes

232
Q

Torsion of Testicles

A

Testicle rotates to twist the spermatic cord that is responsible for bringing blood to the scrotum

233
Q

Torsion of Testicles: Management

A

Surgical correction

234
Q

Epididymoorchitis

A

Acute bacterial infection of the epididymis involving the testis that occurs as a result of retrograde bacterial colonisation via the ejaculatory ducts and vas deferens

235
Q

Hydatid of Morgagni

A

Appendix testis is located at the upper pole of the testes between the testis and head of the epididymis

236
Q

Hydrocele

A

Collection of fluid within the tunica vaginalis that surrounds the testes

237
Q

Hydrocele: Clinical presentation

A

Soft, smooth non-tender swelling around one of the testes

238
Q

Hydrocele: Presentation on exmaination with pen torch

A

Transilluminate

239
Q

Hydrocele: Management - Simple Hydrocele

A

Resolves within 2 years

240
Q

Hydrocele: Simple Hydrocele definition

A

Has no connection with the peritoneal cavity

241
Q

Hydrocele: Management - Communicating Hydrocele

A

Surgical correction

242
Q

Hydrocele: Communicating Hydrocele definition

A

Connects with the peritoneal cavity

243
Q

Undescended Testes

A

Testes have not descended through the abdomen by birth

244
Q

Undescended Testes: Clinical presentation

A

Empty scrotum

245
Q

Undescended Testes: Management

A

Watch and wait for first 6 months - surgically correct between 6-12 months if not descended

246
Q

Normal Physiological Non-Retractability

A

The prepuce (foreskin) is attached to the glans with a tight opening (preputial ring) - this is not retractable in most newborns

247
Q

Bxo Balantis Xerotica Obliterans

A

Chronic inflammatory process that affects the foreskin - and can extend to the glans and external urethral meatus

248
Q

Bxo Balantis Xerotica Obliterans: Presentation

A

Keratinisation of the tip of the foreskin causes scarring and non-retractile foreskin

249
Q

Bxo Balantis Xerotica Obliterans: Management

A

Circumcision

250
Q

Paraphimosis

A

Foreskin cannot be returned to its original position after being retracted

251
Q

Paraphimosis: Conservative Management

A

Manual reduction following application of a local anaesthetic

252
Q

Hypospadias

A

Congenital defect causing the urethral meatus to be located at an abnormal site - normally on the under side of the penis

253
Q

Encephalitis

A

Inflammation of the brain

254
Q

Encephalitis: Most common cause

A

Herpes Simplex Virus

255
Q

Encephalitis: Diagnostic tests (2)

A

Lumbar puncture
Imaging

256
Q

Meningitis

A

Inflammation of the meninges of the brain and spinal cord

257
Q

Meningitis: Bacterial causes in children (2)

A

Neisseria meningitidis
Streptococcus pneumoniae

258
Q

Meningitis: Bacterial causes in neonates

A

Group B Streptococcus

259
Q

Meningitis: Viral Causes (3)

A

Herpes Simplex Virus
Enterovirus
Varicella Zoster Virus

260
Q

Meningitis: Diagnostic test

A

Lumbar puncture

261
Q

Meningitis: Management - <3 months

A

Cefotaxime + Amoxicillin

262
Q

Meningitis: Management - >3 months

A

Cefotaxime followed 6 hours later with Ceftriaxone

263
Q

Meningitis: Management - Can combine with what?

A

Dexamethasone

264
Q

Down Syndrome: Genetic Pathophysiology

A

Trisomy 21 - three copies of chromosome 21

265
Q

Down Syndrome: Distinctive Facial Features (4)

A

Prominent tongue
Flattened face and nose
Prominent epicanthic folds
Brushfield spots - speckled iris

266
Q

Down Syndrome: General features (4)

A

Hypotonia
Short neck
Short stature
Brachycephaly - small head with a flat back