PEDS Flashcards

1
Q

Name the acynotic defeacts

A
  1. VSD
  2. ASD
  3. PDA
  4. Pulmonary stenosis
  5. Aortic stenosis
  6. coartcation of aorta
  7. Atriovetricular septal defect
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

cyanotic defects are:

A

TOF
Transposition of great vesssel
Truncus

“all start with T”

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

what type of shunt are “blue babies”

A

right to left

all the 3 T’s

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

what type of shunts are “blue kids”?

A

left to right shunts

Late developing shunting -
VSD
ASD
PDA

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

frequency of Left to right shunt in order:

A

VSD > ASD > PDA

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

most common congenital cardiac anomaly is?

A

VSD

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

describe Eisenmenger’s Syndrome:

A

Uncorrected VSD, ASD, or PDA leads to progressive pulmonary hypertension (too much blood is going to lungs, ultimately lungs clamp down). As pulmonary resistance increases, the shunt reverses from L –> R to R –>L, which causes late cyanosis (clubbing and polycythemia)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

quick way to describe eisenmenger’s syndrome -

A

Shunt reversal

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

ASD is a congenital “hole” in the

A

septum b/w atria

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

what are complications of uncorrected ASD?

A

Pulm HTN

Eisenmenger’s Disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

with ASD, what part of the heart is working harder?

A

RV - receiving more blood

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

AVOID the during repair of VSD:

A

-arrhythmia
RV dysfunction
Pulmonary vascular obstructive disease
paradoxical embolus

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

with Coarctation of aorta, which BP is accurate?

A

radial

femoral would be absent
normal flow to UE; lower flow to LE

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

PDA
Persistence of connection between pulmonary artery and aorta
L–> R shunt
Blood flow from aorta to pulmonary artery.
Additional blood is re-oxygenated in lungs and return to LA and LV –> increase work load –> LVH
Continuous murmur “machinery”
Small defect– No symptoms
Large defects
CHF
Delayed growth
Infections
Treatment
Surgical ligation
COX-1,COX-2 inhibtors and indomethacin “medical ligation”

A

PDA

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

describe a PDA murmur

A

Continuous (both systolic and diastolic)

“Machinery”

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

in a child with PDA; how is the SPO2 monitored?

%?

A

Preductal (right hand) and Postductal (foot) O2 saturation difference = 3%

High >10% in
Increase right to left shunt (Pulmonary hypertension)

17
Q

MC congenital heart disease causing cyanosis
Four features
Pulmonary stenosis – RV outflow obstruction
Overriding aorta (aorta comes out both from left ventricle and right ventricle ( BIG AORTA)
Large VSD
Right ventricular hypertrophy
Right ventricular outflow obstruction + VSD result ejection of mixed blood into the aorta

A

TOF

18
Q
Clinical presentation
Cyanosis
Squatting
A position that increases systemic vascular resistance and aortic pressure, which  right-to-left ventricular shunting and thus   arterial O2saturation.
Dyspnea
Hypercyanotic  and hypoxic spells ( TET spells) PO2 < 50 mmHg during feeding or crying
Unresponsive to supplemental O2
PE
RV heave
Harsh systolic ejection murmur
A

tof

19
Q

in TOF, squatting pt. tries to decrease the shunt so

A

lungs can get more blood

20
Q

Anesthetic management of TOF

A

Maintain intravascular volume and SVR
Avoid INCREASE in pulmonary vascular resistance (e.g. by N2O)

Ketamine is used because it maintains or INCREASES SVR and therefore does not aggravates R–> L shunt
VA and histamine-releasing drugs DECREASES SVR and INCREASES shunt

Phenylephrine INCREASES SVR and Reducing shunt

21
Q

what is the name of the procedure required to repair tricuspid atresia?

A

fontan procedure

22
Q

Conotruncal separation does not occur, one trunk

A

Truncus Arteriosus

23
Q
Pulmonary veins-->RA via; instead of going to left atrium
Coronary sinus --> RA
Innominate--> SVC
Portal vein--> IVC
Combination of routes
R->L shunt across ASD

Clinical presentation:
Cynosis
Tachypnea
Dyspnea

X-ray- Snowman shaped heart
Surgery- redirection of veins

A

Total anomalous pulmonary venous return TAPVR

24
Q

Gut herniate into thorax through ‘hole’ in diaphragm in CDH is known as:

A

Foramen of Bochdalek or Morgagni

25
Q
CDH Anesthetic consideration 
NG tube
Avoid high pressure PPV
Pre-oxygenation
Decrease conc. of VA, muscle relaxant
Nitrous oxide (N2O) is contraindicated 
High risk of pneumothorax --> avoid barotrauma 
Chest tube
A

know what to do and what NOT to do

***Positive pressure ventilation (PPV)

26
Q

Types of Tracheoesophageal fistula. What is the most common

A

Type IIIB

27
Q

Anesthesia consideration for Tracheoesphageal Fistula

A
  • Need frequent suction due to INCREASE secretion
  • Avoid PPV
  • Awake intubation
28
Q

cause of polyhydraminos?

A

excessive amount of amniotic fluid

-eeophageal atresia – baby no swallowing it so an increased level

29
Q

cause of oligohydraminos?

A

lack of amniotic fluid

- kidney issue or development delay

30
Q

Tell me about paradoxic aciduria

A

high alkalosis

  • low ph of urine
  • opposite effect
  • extreme alk and extreme shock

… finish