Path 3 Flashcards

1
Q

describe Pericardial disease

A
  • Fluid accumulation, inflammation, fibrous constriction, or some combination of these processes, usually in association with disease elsewhere in the heart or a systemic disease
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2
Q

define Tamponade

A
  • Acute sydrome (stabbed in the heart)
  • Heart can’t beat with the volume of blood in the pericardium
  • COnstrictive problems

–> develops Becks triad = Low arterial blood pressure, JVD, muffled heart sounds

–> paradoxus pulse = drop of >10mmHg in arterial blood pressure on inspiration

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3
Q

describe congenitial Heart disease (CHD)

A
  • abnormalities of the heart or great vessels that are present from birth

–> most disorders arise from faulty embryogenesis during weeks 3-8.

  • Most common is VSD > ASD > pulmonary stenosis > patent ductus arteriosus
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4
Q

Define shunt

A
  • abnormal cummunication or opening between cardiac chambers and/or blood vessels thru which abnormal blood flow will occur
  • L to R OR R to L depending on pressure gradient
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5
Q

define stenosis

A
  • abnormal narrowing causing partial obstruction to normal blood flow
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6
Q

define atresia

A
  • failure of a normal anatomic feature, usually a cardiac valve, to form or develop to a functionally adequate state
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7
Q

Left-to-right shunts

A
  • Initially raise BOTH flow volumes and pressures in the normally low-pressure, low resistance pulmonary circulation

–> leads to right ventricular hypertrophy and atherosclerosis of pulmonary vasculature

  • INITIAL INCREASE PULMONARY BLOOD FLOW and is not associated with cyanosis (NONCYANOTIC)
  • Eventually pulmonary vascular resistance = systemic levels, thereby producing a RIGHT TO LEFT SHUNT that introduces unoxygenated blood into systemic circulation (LATE CYANOTIC) –> called Eisenmenger syndrome
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8
Q

Ventricular septal defect

A
  • most common (2/3 of cases associated with anomalies)
  • mixed blood goes to heart
  • functional consequences of VSD depend on the size of the defect and whether there are associated with right-sided malforamtions
  • LARGE VSDs cause difficulties virtually from birth
  • type of Left-to-right shunt
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9
Q

Atrial septal defect

A
  • Fixed opening in the atrial septum
  • classified based on location

–> secundum (90% of all ASD) = result from deficient or fenestrated oval fossa near the center of atrial septum

–> Primum = results from defect in lower portion

–> sinus venosus = results from defect in upper portion

  • Right-sided volume overload - pulmonary blood flow may be two or four times normal
  • ASD are well tolerated and do not become symptomatic before age 30
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10
Q

Patent ductus arteriosus

A
  • results when the ductus arteriosus, an essential fetal structure that normally spontaneously closes, remains open after birth
  • may be essential to preserve life (pulmonary circulation) in hypoplastic heart syndromes
  • sounds like a harsh murmur (machinery like)
  • Usually asymptomatic at birth, and a narrow PDA may have no effect on child’s growth and development
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11
Q

Atrioventricular septal defect (AVSD)

A
  • Result from embryologic failure of the superior and inferior endocardial cusions of the AV canal to fuse adequately with malformation of tricuspid and mitral valves
  • Can be partial or complete

–> partial consists of primum ASD and a cleft anterior mitral leaflet, causing MITRAL INSUFFICIENCY

–> complete AVSD consisting of a large combined AV septal defect and a large common AV valve (essentially a hole in the center of heart)

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12
Q

Right to left shunts

A
  • Cause CYANOSIS EARLY in postnatal life
  • Most common is teralogy of fallot (others are transposition of the great arteries)
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13
Q

Tetralogy of Fallot (TOF)

A
  • 4 pathologies in one

–> obstruction of the right ventricular outlow tract (subpulmonary stenosis)

–> right ventricular hypertrophy

–> aorta that overrides the VSD

–> large VSD

  • Blood flow comes from right ventricle to the left ventricle –> cyanosis
  • Pulmonic stenosis protects pulmonary arteries from HTN PVD
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14
Q

what are the clinical complications + the types of Tetralogy of fallot

A
  • TYPES:

–> subpulmonary stenosis is mild = resembles isolated VSD, and the shunt may be left-to-right without cyanosis (so-called pink tetralogy)

–> Severe subpulmonary stenosis = results in greater resistance to right ventricular outflow (Right to Left shunting and cyanosis)

  • CLINICAL COMPLICATIONS:

–> systemic cyanosis, polycythemia/thromboses, endocarditis, cerebral abscess

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15
Q

Transposisiton of the Great arteries

A
  • Aorta arises from the right ventricle, and lies anterior and to the right of the pulmonary artery, which emanates from the left ventricle
  • embryologic defect in complete TGA stems from abnormal foramtion of the truncal and aortopulmonary septa
  • patients with TGA and a VSD may have a stable shunt
  • patients with patent foramen ovale or ductus arteriosus have unstable shunts that tend to close and require immediate interention to creat a new shunt
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16
Q

describe Obstructive congenital anomalies

A
  • obstruction of blood flow may occur at the level of heart valves or within a great vessel

–>includes stenosis or atresa of the aortic or pulmonary valves and COARCTATION OF THE AORTA

  • circulation must be shunted thru an ASD or PDA to sustain life
17
Q

coarctation of the aorta

A
  • Narrowing, constriction of the aorta, high in frequency
  • TWo forms:
  • proximal to the patent ductus arteriosus (infant/child)

–> severe, do not survive the neonatal period without surgical or catheter-based intervention (CYANOSIS LOWER HALF OF BODY)

  • distal to closed ductus arteriosus (ligamentum arteriosum) and distal to the arch vessels (adult)

–> Asymptomatic unless severe narrowing (may be weak pulses and hypotension in lower extremities, claudication, and coldness)

  • Coarctation of aorta results in high blood pressure before point of coarctation and low blood pressure byond that point