Neonatology Flashcards

1
Q

describe the changes in pulmonary vascular resistance after birth

A

this decreases as baby takes its first breath

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2
Q

describe circulatory changes after birth

A
pulmonary vascular resistance drops 
systemic vascular resistance rises 
oxygen tension rises 
circulating prostaglandins drop 
duct constricts 
foramen ovale closes
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3
Q

what is persistent pulmonary hypertension

A

resistance in the lungs remains high and so blood bypasses the lungs and you get lower oxygen levels-ducts remain open and get shunting
significantly differnet pre and post right arm and right head and neck vessels

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4
Q

how is PPH managed

A

ventilation, O2, nitric oxide, sedation, ionotropes, ECLS (extracorporeal life support)

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5
Q

how is heat produced

A

breakdown of stored brown adipose tissue in response to catecholamines, not efficient in the first 12 hours
peripheral vasoconstriction

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6
Q

describe glucose homeostasis in newborns

A

very little oral intake of milk
drop in insulin increase in glucagon
mobilisation of hepatic glycogen stores for gluconeogenesis
ability to use ketones as brain fuel

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7
Q

describe haematological changes

A

fetal haemoglobin becomes disadvantageous
increase in 2,3 DPG shifts curve to the right
haematopoiesis moves to bone marrow
adult Hb synthesised more slowly than fetal hb is broken down
can get physiological anaemia

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8
Q

if baby is jaundice day 10 this is likely to be what type of bilirubin

A

unconjugated bilirubin

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9
Q

how does blue light help with increased unconjugated bilirubin

A

it makes it water soluble

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10
Q

what is HbH disease

A

excess B chains form tetramers, there is only one working alpha gene (–, -a)

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11
Q

what is raised HbA2 diagnostic of

A

B thal trait

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12
Q

what are the three stages of CML

A

chronic phase, accelerated phase, blast crisis

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13
Q

what are the mutation in polycythaemia

A

JAK2 mutation

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14
Q

what does the JAK2 muscle do

A

loss of auto-inhibition

activation of erythropoeis in absence of ligand

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15
Q

treatment of PRV

A

venesect to <0.45, aspirin, cytotoxic chemo-hydroxycarbamide

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16
Q

what is essential thrombocythamia

A

uncontrolled proliferation of abnormal platelets

17
Q

what genetic problems are associated with essential thrombocythaemia

A

JAK2, CALR and MPL mutation

18
Q

what are the treatments for essential thrombocythameia

A

aspirin, cytotoxic chemo eg hydroxycarbamide

19
Q

what are the types of myelofibrosis

A

idiopathic or post polycythaemia/ET

20
Q

what does the blood film look like in myelofibrosis

A

leukoerythroblastic film]tear shaped RBCs in peripheral blood