Child Health Flashcards
Haemorrhagic disease of the newborn
Bleeding problem that occurs in a baby during the first few days of life.
Babies are normally born with low levels of vitamin K, an essential factor in blood clotting.
A deficiency in vitamin K is the main cause of hemorrhagic disease in newborn babies.
Haemorrhagic disease of the newborn Mx
Vitamin K: IM or oral
hypoxic ischaemic encephalopathy
Brain injury caused by oxygen deprivation to the brain, also commonly known as intrapartum asphyxia.
Hypoxia (lack of oxygen), ischaemia (restriction of blood flow to brain) and encephalopathy (malfunctioning of the brain)
The newborn’s body can compensate for brief periods of depleted oxygen, but if the asphyxia lasts too long, brain tissue is destroyed. Leads to cerebral palsy and multisystem organ damage
hypoxic ischaemic encephalopathy signs/symptoms
events that could lead to hypoxia during the perinatal or intrapartum period
acidosis (pH < 7) on the umbilical artery blood gas
features of mild, moderate or severe HIE (see below) or evidence of multi organ failure.
Poor Apgar scores – active resuscitation required
Neurodevelopmental sequalae
hypoxic ischaemic encephalopathy causes
- Maternal shock
- Intrapartum haemorrhage
- Prolapsed cord, causing compression of the cord during birth
- Nuchal cord, where the cord is wrapped around the neck of the baby
hypoxic ischaemic encephalopathy Mx
active resuscitation required: ongoing optimal ventilation, circulatory support, nutrition, acid base balance
• monitoring and treatment of seizures
• therapeutic hypothermia: protect brain from hypoxic injury (reduce inflammation and neurone loss)
Neonatal Jaundice: physiological jaundice
exaggerated with prematurity and immature liver – increased risk of kernicterus
- Fetal red blood cells break down more rapidly than normal red blood cells, releasing lots of bilirubin.
- Normally this bilirubin is excreted via the placenta, however at birth the foetus no longer has access to a placenta to excrete bilirubin. Additionally liver systems have not fully matured
- This leads to a normal rise in bilirubin shortly after birth, causing a mild yellowing of skin and sclera from 2 – 7 days of age.
- This usually resolves completely by 10 days.
Neonatal Jaundice: Increased production of bilirubin
- Haemolytic disease of the newborn
- ABO incompatibility
- Haemorrhage including Intraventricular haemorrhage
- Cephalo-haematoma (scalp and the skull)
- Polycythaemia
- Sepsis and (DIC)
- G6PD deficiency
Neonatal Jaundice: Decreased clearance of bilirubin:
- Prematurity
- Breast milk jaundice
- Neonatal cholestasis
- Extrahepatic biliary atresia
- Endocrine disorders (hypothyroid and hypopituitary)
- Gilbert syndrome
Jaundice in first 24 hours?
first 24 hours of life is pathological. This needs urgent investigations and management. Neonatal sepsis is a common cause. Babies with jaundice within 24 hours of birth need treatment for sepsis if they have any other clinical features or risk factors.
Breast milk Jaundice why?
Components of breast milk inhibit the ability of the liver to process the bilirubin. Breastfed babies are more likely to become dehydrated if not feeding adequately.
Inadequate breastfeeding may lead to slow passage of stools, increasing absorption of bilirubin in the intestines.
Keep on breastfeeding – just extra support
Prolonged Jaundice
- More than 14 days in full term babies
- More than 21 days in premature babies
- biliary atresia, hypothyrodisim and G6PD deficiency common causes
Neonatal Jaundice Ix
FBC & blood film for polycythaemia or anaemia
- Conjugated bilirubin: elevated levels indicate a hepatobiliary cause
- mother and baby for ABO or rhesus incompatibility
• Direct Coombs Test (direct antiglobulin test) for haemolysis
• Thyroid function, particularly for hypothyroid
• Blood and urine cultures if infection is suspected.
• Glucose-6-phosphate-dehydrogenase (G6PD) levels for G6PD deficiency
Neonatal Jaundice Mx
Phototherapy
Exchange transfusion
Hypothermia - which babies at risk?
Small for dates / Preterm
o Low stores of brown fat
o Little subcutaneous fat
o Larger surface area: vol
Hypothermia Mx
Dry Hat Skin to skin blanket Heated mattress incubator
Intraventricular Hemorrhage
bleeding into the brain’s ventricular system, where the cerebrospinal fluid is produced and circulates through towards the subarachnoid space.
Intraventricular Hemorrhage classification grades
Grade 1 and 2 : Neurodevelopmental delay up to 20% and Mortality 10%
Grade 3 and 4: Neurodevelopmental delay up to 80% and Mortality 50%
Necrotizing enterocolitis (NEC)
Disorder affecting premature neonates, where part of the bowel becomes necrotic. Usually affects babies in the first week of life. It is a life-threatening emergency.
• Death of the bowel tissue can lead to bowel perforation.
• Bowel perforation leads to peritonitis and shock.
Risk factors for NEC
- Very low birth weight or very premature
- Formula feeds (it is less common in babies fed by breast milk feeds)
- Respiratory distress and assisted ventilation
- Sepsis
- Patient ductus arteriosus and other congenital heart disease
NEC signs/symptoms
Intolerance to feeds/poor feeding
Vomiting, particularly with green bile • Generally unwell – decreased activity • Distended, tender abdomen • Absent bowel sounds • Blood in stools • Perforation leading to peritonitis and shock
NEC Ix
FBC - thrombocytopenia, neutropenia, CRP and blood cultures - Cap blood gas: metabolic acidosis - stool cultures - AXR: Pneumatosis intestinalis & Pneumoperitoneum
NEC Mx
- stop feeding orally
- PN with IV fluids and broad spectrum antibiotics
NG tube - drain fluid and gas
Surgery - remove dead tissue and temp stoma
Tetralogy of Fallot
Four defects include a ventricular septal defect (VSD), pulmonary valve stenosis, a misplaced aorta and a thickened right ventricular wall (right ventricular hypertrophy)
Tetralogy of Fallot
- VSD: blood flow between ventricles.
- “overriding aorta” refers to the fact that the entrance to the aorta (the aortic valve) is placed further to the right than normal
- right ventricle contracts and sends blood upwards, the aorta is in the direction of travel of that blood, therefore a greater proportion of deoxygenated blood enters the aorta from the right side of the heart.
- Pulmonary stenosis promotes blood through VSD and into aorta - cyanosis
Tetralogy of Fallot signs/symptoms
- Cyanosis (blue discolouration of the skin due to low oxygen saturations)
- Clubbing
- Poor feeding & weight gain
- Ejection systolic murmur heard loudest in the pulmonary area (second intercostal space, left sternal boarder) – pulmonary stenosis
- “Tet spells”: intermittent symptomatic periods where the right to left shunt becomes temporarily worsened, precipitating a cyanotic episode (SVR decreases or PVR increases): irritable, cyanotic and short of breath
- Severe cases will present with heart failure before one year of age.
- In milder cases, they can present as older children once they start to develop signs and symptoms of heart failure.
Tetralogy of Fallot Mx
Tet spell: squat when a tet spell occurs (increases SVR) - supplementary oxygen - beta blockers (relax RV) - IV fluids - increase preload - morphine -sodium bicarbonate - phenylephrine infusion - increase SVR • Neonates: Prostaglandin infusion – ductus arteriosus is opened (blood flow from aorta back to pulmonary arteries)
Corrective surgery by 6 months
Transposition of great arteries
aorta and pulmonary artery swap
life threatening - no connection - cyanosed
Transposition of great arteries signs/symptoms
A patent ductus arteriosus or ventricular septal defect can initially compensate by allowing blood to mix between the systemic circulation and the lungs
However: within few weeks of life:
o Respiratory distress, tachycardia, poor feeding, poor weight gain and sweating.
Transposition of great arteries Mx
Prostaglandin infusion: maintain ductus arteriosus (blood from aorta to pulmonary arteries)
surgery
- balloon septostomy: create atrial septal defect
- open heart surgery is definitive management
Coarctation of the aorta
aortic narrowing, is a congenital condition whereby the aorta is narrow, usually in the area where the ductus arteriosus (ligamentum arteriosum after regression) inserts.
- Narrowing of the aorta reduces the pressure of blood flowing to the arteries that are distal to the narrowing.
- It increases the pressure in areas proximal to the narrowing, such as the heart and the first three branches of the aorta.
Coarctation of the aorta signs/symptoms
- weak femoral pulse
- radiofemoral pulse
- hypertension and ejection systolic murmur
- CXR: Rib notching 3-5
- ECG: LVH
Coarctation of the aorta Mx
- In mild cases patients can live symptom free until adulthood without requiring surgical input, and in severe cases patients will require emergency surgery shortly after birth.
- In cases of critical coarctation where there is a risk of heart failure and death: Prostaglandin E is used keep the ductus arteriosus open while waiting for surgery
- Surgery or stent by the age of 5 to avoid pulmonary hypertension or end organ damage
Hypoplastic heart
left side of the heart is severely underdeveloped. It may affect the left ventricle, aorta, aortic valve, or mitral valve
TAPVD
Pulmonary veins connect straight into systemic circulation
Patent Ductus Arteriosus
The ductus arteriosus (shunt: trunk of the pulmonary artery to the proximal descending aorta) normally stops functioning within 1-3 days of birth and closes completely within the first 2-3 weeks of life.
PDA pathology
aorta is higher than that in the pulmonary vessels, so blood flows from the aorta to the pulmonary artery.
• This creates a left to right shunt where blood from the left side of the heart crosses to the circulation to the right side.
• increases the pressure in the pulmonary vessels causing pulmonary hypertension, leading to right sided heart strain as the right ventricle struggles to contract against the increased resistance.
•lead to right ventricular hypertrophy.
increased blood flowing through the pulmonary vessels and returning to the left side of the heart leads to left ventricular hypertrophy.
PDA signs/symptoms
- Shortness of breath
- Difficulty feeding
- Poor weight gain
- Lower respiratory tract infections
- Continuous machine murmur below left clavicle
- Thrill, collapsing pulse, failure to thrive and loud S2
PDA management
oral or IV ibuprofen
• After 1 year of age it is highly unlikely that the PDA will close spontaneously and trans-catheter or surgical closure can be performed.
• Symptomatic patient or those with evidence of heart failure as a result of PDA are treated earlier.
Persistent Pulmonary Hypertension of the Newborn (PPHN)
defined as the failure of the normal circulatory transition that occurs after birth
marked pulmonary hypertension that causes hypoxemia secondary to right-to-left shunting of blood at the foramen ovale and ductus arteriosus..
BP in lungs does not drop, blood does not go to lungs, blood does not get oxygenated. Persistent pulmonary hypertension
Persistent Pulmonary Hypertension of the Newborn (PPHN) Ix
• Pre and post O2 sats (more than 3% difference)
o Pre: right hand
o Post: left foot
• Echo: right to left shunt
• Persisting desaturation despite intensive oxygen use
PPHN Mx
Ventilation O2 NO Sedation Inotropes ECMO
Transient tachypnoea of the newborn (TTN)
benign, self-limited condition that can present in infants of any gestational age, shortly after birth.
It is caused due to delay in clearance of fetal excess lung fluid after birth
Transient tachypnoea of the newborn (TTN) Signs/symptoms
ineffective gas exchange, respiratory distress, and tachypnea
Respiratory distress syndrome
occurs <32 weeks gestation
Surfactant deficiency
o Inadequate surfactant leads to high surface tension within alveoli.
o This leads to atelectasis (lung collapse), as it is more difficult for the alveoli and the lungs to expand.
o This leads to inadequate gaseous exchange, resulting in hypoxia, hypercapnia (high CO2) and respiratory distress.
• Structural immaturity
secondary causes of respiratory distress syndrome
intubation and ventilating
respiratory distress syndrome signs/symptoms
Respiratory distress •Tachypnoea o Grunting o Intercostal recessions o Nasal flaring o Cyanosis • Worsen over minutes to hours
respiratory distress syndrome Ix
CXR: Ground glass appearance
respiratory distress syndrome Mx
antenatal Dexamethasone -increase surfactant
Intubation and ventialtion
endotracheal intubation
CPAP
Microcephaly
condition where the head (circumference) is smaller than normal. Microcephaly may be caused by genetic abnormalities or by drugs, alcohol, certain viruses, and toxins that are exposed to the fetus during pregnancy and damage the developing brain tissue.
Neonatal sepsis risk factors
- Vaginal GBS colonisation
- GBS sepsis in a previous baby
- Maternal sepsis, chorioamnionitis or fever > 38ºC
- Prematurity (less than 37 weeks)
- Early (premature) rupture of membrane
- Prolonged rupture of membranes (PROM)
Neonatal sepsis organisms
Early Onset
o Gp B Streptococcus
o Gram negatives
Late Onset
o Coagulase negative staphylococci
o Gram negatives
o Staph Aureus
Neonatal sepsis signs/symptoms
- Fever
- Reduced tone and activity
- Poor feeding
- Respiratory distress or apnoea
- Vomiting
- Tachycardia or bradycardia
- Hypoxia
- Jaundice within 24 hours
- Seizures
- Hypoglycaemia
Red flags
o Confirmed or suspected sepsis in the mother
o Signs of shock
o Seizures
o Term baby needing mechanical ventilation
o Respiratory distress starting more than 4 hours after birth
o Presumed sepsis in another baby in a multiple pregnancy
Autism features
1) Communication
2) social interaction
3) Imagination
4) repetitive
5) sensory issues