Breathless Baby Flashcards

1
Q

History of poor feeding

A

Volumes of milk (before and now) (mls/kg/day)
Timescale of decline
Why/What happens when baby stops feeding?
Sleepiness?
Parents thoughts on precipitating factor

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2
Q

Minumum milk requirement for a baby up to a month of age

A

150mls/kg/day

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3
Q

Young child PMH

A

Scans and screening
Maternal health - congenital infections, vascular episodes following antenatal bleeds, trauma, medication, teratogenic agents including high sugar
Gestation
Mode of Delivery
Weight
Post delivery complications - neonatal unit

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4
Q

Intial inspection of a child

A
  • General dysmorphism
  • Neuro - alert, happy, interacting, responding to voice
  • colour? jaundiced, mottled
  • noises - grunting, stridor, wheeze, crying
  • Signs of pain?
  • marks or rashes present on his face?

secretions - eyes, nasal

Increased work of breathing

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5
Q

What is a tracheal tug (and AKA)?

A

Oliver’s sign

Abnormal downward movement of the trachea during systole that can indicate a dilation or aneurysm of the aortic arch

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6
Q
V
I
N
D
I
C
A
T
E
A
Vascular
Infective, Inflammation, Immune,
Neoplastic
Degenerative, Developmental
Iatrogenic, Idiopathic
Coneginital
Autoimmune
Trauma
Endocrine, Environmental
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7
Q

Signs of increased work of breathing?

A
Nasal flaring
Head bobbing, hed thrust back, leant forward
Tracheal tug
> RR
>HR
Noise - grunting, wheezing, stridor
Visible chest/abdominal movement
Colour changes
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8
Q

What is posseting?

A

The regurgitation of small quantities of undigested milk following each feed

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9
Q

What is tetralogy of fallot?

A

Four congenital abnormalities:

  • Ventricular septal defect (VSD)
  • Pulmonary Valve Stenosis
  • Misplaced Aorta
  • Right ventricular hypertrophy
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10
Q

What is paradoxical breathing?

A

Instead of moving out when taking a breath, the chest wall or the abdominal wall moves in. Often, the chest wall and the abdominal wall move in opposite directions with each breath.

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11
Q

What is recession? (sternal, intercostal, subcostal)

A

Recession is a clinical sign of respiratory distress which occurs as increasingly negative intrathoracic pressures cause indrawing

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12
Q

What is dextrocardia?

A

Dextrocardia is a congenital heart condition in which your heart points toward the right side of your chest instead of the left side

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13
Q

Where to auscultate for a PDA?

A

Medium pitched, high-grade continuous murmur heard best at the pulmonic position, with a harsh machinelike quality that often radiates to the left clavicle

Over left scapula posteriorly

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14
Q

What is respiratory splinting?

A

Respiratory splinting is defined as reduced inspiratory effort as a result of sharp pain upon inspiration (severe pleuritic chest pain).

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15
Q

Causes of abnormal respiratory examination in a child

A

Primary respiratory disease (bronchiolitis)
Cardiac cause - compensation for poor perfusion, hypoxia and possible acidosis
Congenital abnormality (diaphragmatic hernia)
Acute blood loss
Metabolic acidosis/alkalosis
Endocrine (DKA - Kussmauls breathing)

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16
Q

What is 3rd space loss?

A

Too much fluid moves from the intravascular space (blood vessels) into the interstitial or “third” space-the nonfunctional area between cells. This can cause potentially serious problems such as oedema, reduced cardiac output, and hypotension

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17
Q

Investigations for children with respiratory distress

A
FBC
U and Es
LFT
CRP
Glucose
Blood Cultures
Lactate
Ammonia
ECG
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18
Q

Causes of a large heart on X-ray

A
Large L to R shunts - VSD, PDA
Transposition of great arteries (can also be nirmal size)
Tricuspid Atresia
Truncus Arteriosus
Ebstein's Anomaly
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19
Q

Causes of a small heart on X-ray

A

Fallot’s tetralogy

TAPVD - Infradiaphragmatic(under diaphragm into IVC)

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20
Q

What is TAPVD?

A

Total Anomalous Pulmonary Venous Drainage

TAPVD is a rare form of congenital heart disease where all four pulmonary veins drain to the systemic venous circulation

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21
Q

Ebstein’s Anomaly

A

Ebstein’s anomaly is a rare heart defect in which the tricuspid valve fails to form properly

22
Q

What is truncus arteriosus?

A

Congenital heart disease in which a single blood vessel (truncus arteriosus) comes out of the right and left ventricles

23
Q

Define Plethoric and Oligaemic

A

Plethoric: lung full of fluid (blood)
- L to R shunts - VSD, PDA or cardiac failure

Oligaemic: Reduced volume of fluid (blood)
- Fallot’s tetralogy, pulmonary atresia/stenosis

24
Q

Areas of VSD

A
Membranous septum (most common)
Muscular septum
25
Q

Treatment of VSD

A

If asymptomatic (small and o2 levels adequate) no action taken

Large - surgery is required

26
Q

Systolic murmurs in children

A
Fallot's Tetralogy
VSD
Pul/Aortic stenosis
Truncus Arteriosus
DORV
TAPVD (can be no murmur)
Single Ventricle
27
Q

What is a DORV?

A

Double Outlet Right Ventricle

28
Q

Diastolic murmurs in children?

A

Truncus Arteriosus
Mitral Stenosis
Pul/ Aortic Regurg

29
Q

Acute management of VSD

A

Inform senior colleague
O2 (consider CPAP) - caution as can close duct dependent cardiac lesions
Stop oral feeds (consider NGT when stable)
IV maintenance with glucose
IV antibiotics (sepsis)

30
Q

Symptoms of cardiac failure in children

A
SOB - tachypnoea, dyspnoea
Poor feeding (Weight)
Inc. HR
Hepatomegaly 
Poor pulses
Acidosis
Sweating

Oedema not always seen in children younger than 2/3 years

31
Q

Management of Cardiac Failure

A
Diuretics: Furosemide, Amiloride etc.
ACE inhibitors: Captopril, Enlapril (shorter acting)
O2 (never for duct dependent lesions)
Prostin (Prostaglandin E1)
Diet/Fluid Intake
Inotropes: Dopamine, Dobutamine
Angioplasty
Surgery
32
Q

Effects of Prostin

A

Used in duct dependent lesions

Keeps duct open
Given intravenously
SE: Apnoea, pyrexia, hypotension

33
Q

Characteristics of PDA

A

Connects branch pulmonary arteries to the aorta

Bounding pulses
Continuous murmur

34
Q

Characteristics of Coarctation of the aorta

A

Constriction of aorta

Femoral weak/absent
Systemic HTN of upper limbs
Commonly associated with other left sided lesions - VSD, bicuspid aortic valve
Risk of necrotising enterocolitis

35
Q

Most common cyanotic Congenital Heart Disease

A

Fallot’s Tetalogy
TGA
Complete Atrio-Ventricular Septal Defects

36
Q

What is TGA?

A

Transposition of Great Arteries

Deoxygenated blood in aorta, oxygenated blood in pulmonary artery
No murmurs

37
Q

Clinical presentation of Fallot’s Tetralogy

A

Central cyanosis
Pulm. oligaemia on CXR
Hypercyanotic episodes
Loud ES murmur (from pulm. stenosis)

38
Q

Features of AVSD

A

Atrio-Ventricular Septal defects

Higher incidence in trisomy 21
Left axis deviation on ECG

39
Q

Conditions associated with congenital heart conditions

A
Trisomy 13
Trisomy 18
Trisomy 21
Turner's
Kartagener's Syndrome
DiGeorge
40
Q

What is Kartagener’s Syndrome?

A

Autosomal recessive genetic ciliary disorder

Triad of situs inversus (transposition of viscera), chronic sinusitis, and bronchiectasis.

Defective movement of cilia, leads to recurrent chest infections, ear/nose/throat symptoms, and infertility

41
Q

What is DiGeorge syndrome?

A

22q11 deletion
Autosomal Dominant

Symptoms include:
Heart defects
Learning difficulties
Cleft Palate

42
Q

Clinical features of Edward’s Syndrome (13)

1 / 8,000

A
Low birthweight
Prominent occiput
Small mouth and chin
Short sternum
Fixed, overlapping fingers
'Rocker-bottom' feet
Cardiac and renal malformations
43
Q

Clinical features of Patau syndrome (18)

1 / 14,000

A

Structural defect of brain
Scalp defects
Small eyes (microphthalmia) and other eye defects
Cleft lip and palate
Polydactyly
Cardiac and renal malformations (80% have CHD

44
Q

Clinical features of Turner’s syndrome? (45 X)

A
Lymphoedema of hands and feet in neonate (may persist)
Spooned-shaped nails
Short stature - cardinal features
Cubitus Valgus
Widely spaced nipples 
CHD (Coarctation of aorta)
Delayed puberty
Ovarian dysgenesis - Infertilty
Hypothyroidism 
Renal anomalies
Pigmented moles
Recurrent otitis media
45
Q

Treatment of Turner’s

A

Growth hormone therapy

Oestrogen replacement

46
Q

Which are tested for the neonatal heel prick test?

A

MCADD
HCU (Homocystinuria)
Isovalaric Acidaemia
Other metabolic conditions

Sickle Cell
Cystic Fibrosis
Hypothyroidism
Phenylketonuria

47
Q

Autosomal dominant conditions

A

Neurofibromatosis
Marfan’s
Familial Adenomatous Polyposis

48
Q

Features of autosomal dominant inheritance

A
Males and Females equally affected
Transmitted by both sexes
Incomplete penetrance
Variable expression
New mutations
Risk to offspring is 50%
49
Q

Parts of a chromosome?

A

Telomere
P arm
Centromere
Q arm

50
Q

What 3 things should you always check in a baby?

A

Ammonia
Glucose
Gas

51
Q

Sound and Site of VSD

A

Pansystolic murmur

Left lower sternal border