Volume 2 Flashcards

1
Q

Which of the following is not a side effect of intubation/laryngoscopy of the newborn infant?

a) systemic and pulmonary hypertension
b) tachycardia
c) hypoxia
d) intracranial hypertension

A

b) false - bradycardia is the side effect
bradycardia and hypoxia does not appear to be related
some of the side effects from laryngoscopy itself, it is thought to be vagal, pre oxygenation does not help with it.

the others are effects of laryngoscopy/intubation
systemic HTN - increased SVR from catecholamines
IC hypertension - coughing and struggling

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2
Q

Which of the following is not an effect of using premedication for intubation?

a) increased hypoxia when paralytics are used
b) reduce hypertension with analgesia
c) reduce intracranial hypertension with muscle relaxants
d) quicker intubation with paralytics

A

a) fase - quicker intubation with paralytics which leads to less hypoxia
2 recent studies - used muscle relaxants, additional benefits more than analgesia alone

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3
Q

Which of the following statements is false ?

a) a recent study showed that propofal leads to faster intubation with better maintaining of O2 sats and quicker recovery in neonates
b) thiopental is very slowly cleared by the neonate
c) midazolam has potent analgesic properties and is a good choice for neonatal intubation
d) fentanyl is faster acting than morphine

A

c)false - does not have analgesic properties, associated with serious adverse effects, doesn’t reduce physiological changes of intubation, should NOT be used for intubation in the newborn

the rest are true
a) true - a recent study shows this, concern that it doesn’t have analgesic properties (is a hypnotic agent ) and would need to be combined with an opiod
need more investigation, limited PK data
can cause hypotension in older people
b) one study does show it reduces pain, but big concern is very slow clearance (half life 14.9 hours)

d) is true, fentanyl is faster acting, morphine does not seem to reduce hypoxia because it is too slow

remifentanyl even quicker, onset within seconds and lasts minutes, limited PK and PD data
meperidine in one study - reduced endocrine responses to intubation, very limited data

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4
Q

Which of the following is not an adverse effect of midazolam?

a) hypotension
b) infusion results in adverse neurological outcomes
c) decreased cerebral flow velocity
d) increased cardiac output
e) long half life (22 hours)

A

d) in fact decreased cardiac output

the rest are adverse effects/reasons not to use midazolam

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5
Q

After giving fentanyl for intubation to give surfactant, how soon after can a baby be extubated?

a) <1 hour
b) 4 hoursh
c) 6 hours
d) 10 hours

A

a)half life of fentanyl is 10 hours in newborn) but can be safely extubated t want to give meds that will prolong resp depression when intubating for this reason
remifentanyl super short acting, even better from this perspective (only few minutes)

complications are a reason given to not give pre -meds
RCTs have not shown that pre-meds increase the complication rate
chest freeze - infrequent complication, can avoid by giving slowly and treating with muscle relaxant or opioid antagonist
after giving fentanyl

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6
Q

Which of the following patients is not an acceptable patient to intubate without pre medication?

a) severely abnormal airway
b) crashing patient
c) baby resuscitated by face mask who needs ongoing resp support
d) resuscitation

A

c) all other newborn babies should be offered pre med
the others are cases where you don’t need pre med
should NOT use pre med if severe abnormal airway and will take time to intubate, and want the patient to be able to breathe on their own; may need special techniques, if not trained, consider transfer with bagging to tertiary care centre
if can’t get IV, consider inhaled (i.e. sevoflurane) or intranasal (i.e. fentanyl) ; or consider awake intubation (clarify what they mean here)

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7
Q

Which of the following statements is true?

a) atropine is the most effective vagolytic
b) fentanyl has been compared to other analgesics and shown to be more effective as a pre med for intubation
c) succinylcholine can cause hypokalemia
d) chest freeze can be treated and potentially prevented with co-administration of muscle relaxing

A

d) true - muscle relaxants (i.e. succ) can be co administered, also, should administer the fentanyl slowly to prevent this effect, could also give naloxone for this; also remember that fentanyl can reduce the respiratory drive so need to be prepared to support respiratory whenever you give this drug

a) false - both atropine and glycopyrrolate are effective, have not been directly compared
atropine 10-20 ug/kg - no adverse effect at correct dosage, there is potential for CNS complications with overdose
b) false - has not been directly compared to others, morphine NOT ideal, takes too long, remifentanyl is appealing (quicker action) needs more study, thiopental and methohexital only studied in larger preterm and term infants
c) opposite - can cause hyperkalemia and malignant hyperthermia, can also cause rhabdomyolysis

**see table for details on all the studies

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8
Q

Which of the following statements is false?

a) succinylcholine should not be used in babies with hyperkalemia
b) succinylcholine should not be used in babies with family history of malignant hyperthermia
c) succinylcholine causes significant increase in blood pressure
d) succinylcholine is a non depolarizing agent

A

d) false - it is a depolarizing agent

the rest are true
rare series side effects
hyperkalemia - major elevations are uncommon, usually associated with significant tissue injury
malignant hyperthermia is autosomal dominant - symptoms include increased temperature, muscle rigidity, rhabdomyolysis etc, high HR etc, treatment is dantrolene

rocuronium - not a good choice of relaxant because lasts 1 hour
if intubating with opioid but no muscle relaxant, should have it available in case of chest freeze

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9
Q

Which of the following is not true?

a) fentanyl is the best choice of analgesic at a dose of 3-5 ug/kg (slow infusion over at least 1 minute)
b) full cardiorespiratory monitoring is required for intubation
c) succinylcholine is the best choice of muscle relaxant, at a dose of 2mg/kg
d) atropine is a suggested choice of vagolytic, at a dose of 20 ug/kg (may work at 10 ug/kg)

A

b) false - O2 sat monitoring is the minimum
Preoxygenation to reduce hypoxia, limiting the duration of attempts to a reasonable maximum duration (such as 30 s), careful observation and monitoring during the procedure (in particular with pulse oximetry), and confirmation of appropriate tube placement with exhaled carbon dioxide detection are required.

should always have muscle relaxant (i.e. succ) when giving fentanyl to non intubated infant

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10
Q

Which of the following is not a radiographic feature of respiratory distress syndrome?

a) increased lung volumes
b) air bronchograms
c) ground glass appearance

A

a) the opposite, reduced air volume

RDS - surfactant deficiency and poorly functioning surfactant in preterm infants

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11
Q

Which of the following is false about surfactant treatment ?

a) reduces mortality from RDS and increases survival
b) reduces morbidity from RDS
c) reduces the incidence of BPD
d) reduces duration of respiratory support and hospitalization
e) reduces pneumothorax in babies with RDS

A

c) false- increases the likelihood of survival without BPD (by increasing survival rather than incidence of BPD)

surfactant normally lines the surface of alveoli, reducing surface tension, and prevents atelectasis
treatment either as rescue or propylaxis
no cost of neurodevelopment outcome
the rest are benefits
also shorter and cheaper hospital stays
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12
Q

Which of the following infants does not meet criteria for surfactant therapy?

a) baby with meconium aspiration syndrome on 40% FiO2
b) intubated babies with RDS
c) sick newborns with pneumonia and OI>15
d) intubated infants with pulmonary hemorrhage leading to clinical deterioration

A

a) does not meet - criteria is : babies with MAS on >50% FiO2 should receive surfactant (grade A recommendation)

the other babies do meet criteria
albumin, meconium and blood inhibit surfactant function
for pneumonia, not adequately studied so is a grade C recommendation (one study showed in sepsis helped reduce ECMO, another said might be beneficial in pneumonia)
pulmonary hemorrhage - surfactant has been shown to INCREASE the risk of pulmonary hemorrhage, however because blood adversely affects surfactant function, has been tried, some studies showing that it helps (grade C recommendation)
lung hypoplasia and CDH - only small studies, no conclusions can be made

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13
Q

Which of the following is not a significant risk of surfactant treatment?

a) tube blockage
b) increased mortality from pulmonary haemorrhage
c) bradycardia
d) hypoxemia

A

b) there is an increased risk of pulmonary hemorrhage but not increased mortality from pulmonary hemorrhage or overall mortality (in fact overall mortality is decreased after surfactant treatment)

tube blockage, bradycardia and hypoxemia are short term risks during instillation
OVERALL, physiology of what all surfactant does
improvement in static compliance only, dynamic stays unchanged
large improvement in FRC (due to improvement in lung volume with recruitment)
get normalizing pressure volume loops, need to decrease administered pressures to avoid over distension
can also get accidental hyperventilation with low pCO2 (bad for brain)
immunological - babies treated with surfactant may have antibodies to surfactant proteins, but no evidence that this is increased compared to other babies with RDS

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14
Q

Which of the following statements is false?

a) natural surfactants lead to lower mortality than synthetic
b) natural surfactants decrease the O2 needs and ventilatory support more than synthetic surfactants
c) pulmonary air leak syndromes are lower with natural surfactant compared to synthetic surfactant
d) incidence of BPD is reduced with natural surfactant (vs synthetic)

A

d) false - not a difference in the incidence of BPD, but because there is less death, combined outcome of Bpd AND death is reduced (mortality is reduced with natural, but the amount of BPD is the same)

Therefore, natural surfactants improve survival without BPD and with a lower incidence of airleak, and they are to be preferred over synthetic surfactants (evidence level 1a). However, it must be noted that all studies comparing natural with synthetic surfactants have been done using synthetic preparations that did not contain surfactant protein analogues. New synthetic surfactants have been developed which may have enhanced efficacy and they are presently being investigated in clinical trials.

better survival with less pneumos says michelley

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15
Q

Which groups should one consider prophylactic surfactant therapy for in a peripheral hospital ?

A

all babies who are considered high risk of RDS should get prophylactic surfactant therapy as soon as they are stable (one study found there wasn’t a huge difference between giving ASAP vs giving as soon as stable) :

<29 weeks in a peripheral hospital, then should intubate immediately then give prophylactic surfactant

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16
Q

Which is true of surfactant treatment for babies with RDS?

a) > 3 doses can be of benefit
b) should be considered for babies with persistent O2 and ventilatory needs at 72 hours
c) increase in complications with repeated doses
d) retreatment should not be considered until 8 hours after initial dose

A

b) true
the rest are false
a) no benefit to more than 3 doses
c) no increased complications from repeated doses
d) can consider retreatment when there is persistent or recurrent FiO2 need of 30% or more as early as 2 hours after, more commonly 4-6 hours after

can consider early extubation to CPAP within 1 hour of surfactant
surfactant for babies on CPAP - should be considered if FiO2 >50% (greater risk of pneumothorax at this point if not)
if babies are initially managed with CPAP then need to make sure that we give them surfactant as soon as they show signs of worsening

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17
Q

Which of the following is false of steroid treatment for mothers with threatened pre term labour?

a) has been shown to reduce severe IVH
b) better outcomes when combined with surfactant that surfactant alone
c) should be considered for all moms GA

A

c)should be considered for women

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18
Q

Which of the following is false?

a) intrapartum antibiotic prophylaxis reduces the chance of sepsis by other organisms
b) currently in Canada, most babies with invasive GBS infection are born to women who tested GBS -ve
c) invasive GBS disease is possible, although rare, in women who received prophylaxis
d) any infant with signs of sepsis only needs to have cultures done before starting therapy

A

a) false - doesn’t reduce the chance of sepsis by other organisms

the rest

b) true - can still get GBS if cultures at 35-37 weeks are negative, because of IAP, most babies now who present with invasive GBS infection are born to mom’s who tested negative and got colonized between the test and birth
d) true - the predictive value of no other tests will allow you to prevent therapy, i.e.) normal CBC or diff should not prevent therapy, negative likelihood ratio is 0.7

most common organisms in early sepsis: GBS (strep agalactiae), other strep, E. coli, other gram negative, Listeria

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19
Q

Which of the following is not well covered by the empiric treatment of a neonate by ampicillin and gentamycin?

a) GBS meningitis
b) Listeria meningitis
c) E. coli meningitis
d) Staphylococcus meningitis

A

c) should treat with cefotax and gent

amp and gent is the usual empiric choice
if +ve CSF, then should target the organism and ensure that the antibiotic can cross the BBB (although I think that neonates have a pretty chill BBB from what I remember)

Gram positive cocci (GBS, staph, enterococci)- amp and gent
Gram positive rod (Listeria )- amp and gent
Gram negative rods (E. coli, less common Klebsiella, Pseudomonas, Citrobacter) - cefotaxime and gentamycin
gram negative cocci - uncommon -
if signs of meningitis but no organisms, or too unstable for LP- amp and gent

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20
Q

which of the following is a gram positive rod?

a) E. coli
b) Klebsiella
c) Citrobacter
d) Listeria

A

d) listeria is a gram positive rod

gram positive - dark purple
gram negative - red or pink

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21
Q

A healthy and well-looking baby baby is born at 36 weeks to a GBS +ve mom who received penicillin 6 hours prior to delivery, what is the appropriate management?

a) CBC and vitals x 24 hours
b) full septic work up but no antibiotics
c) full septic work up and antibiotics
d) routine care and can discharge as early as 24 hours after

A

d) if antibiotics >4 hours before, newborn healthy and >35 weeks gestational age, no therapy needed
if baby looks well at 24 hours and parents know how to get to hospital, can d/c home at this time
if did not get penicillin but got different antibiotic, treat as inadequate prophylaxis
if adequately treated 1% chance of GBS in kids

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22
Q

A baby is born at 38 weeks to a mom with GBS +ve who did not receive appropriate antibiotics, which is the appropriate management?

a) CBC and vitals x 24 hours
b) full septic work up but no antibiotics
c) full septic work up and antibiotics
d) routine care and can discharge as early as 24 hours after

A

a) is the answer

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23
Q

Which is the most predictive finding on a CBC for risk of sepsis (highest positive predictive value)?

a) WBC 30 x 109
b) WBC count <5.0 x 109
c) left shift
d) low platelets

A

b) <5.0, should move onto full septic work up and empiric antibiotics (flowchart in statement says up to 36 hours, i think it should be 48)
risk of kid with GBS in this case is 10-20%

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24
Q

Which of the following is an appropriate management for a well appearing baby born to a GBS -ve mother who had prolonged rupture of membranes of 20 hours?

a) routine neonatal care
b) CBC at birth and vitals q4 hours (limited diagnostic investigation)
c) full septic work up but no antibiotics
d) full septic work up and antibiotics

A

b)
GBS-ve ->still have risk of GBS but risk is low, even with prolonged ROM or intrapartum pyrexia
should do a limited diagnostic investigation - CBC and observation with vitals q4 hours
before, they used to say that even GBS -ve mom’s with any one of these risk factors should get IAP prophylaxis

**although in the recommendations they say that if a mother with GBS -ve and risk factors delivers a baby who remains well, don’t need further evaluation for GBS, clarify this

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25
Q

Which of the following is not one of the risk factors for GBS sepsis?

a) intrapartum pyrexia
b) ROM > 18 hours
c) prematurity

A

d) is not, GBS bacteria at any point in the pregnancy

the risk factors are present in 50% of babies with invasive GBS disease, and happen in about 20% of babies born at term

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26
Q

Which of the following is the appropriate management of a mom who is GBS unknown with intrapartum pyrexia?

a) routine care
b) should have a C/section
c) should receive antibiotic prophylaxis
d) none of the above

A

c) if GBS unknown with any of the risk factors, should get intrapartum antibiotics (vs if GBS unknown with no risk factors then no special care needed)

GBS unknown should then be treated same as GBS +ve ->if receive prophylaxis routine care and d/c in 24 hours, if no prophylaxis then do CBC at birth and vitals x 24 hours q4hour

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27
Q

Which of the following is the appropriate management for a 35 week baby who looks well and GBS has not yet been done?

a) routine neonatal care
b) CBC at birth and vitals q4 hours (limited diagnostic investigation) with discharge as early as 24 hours
c) CBC at birth and vitals q4 hours (limited diagnostic investigation) with discharge as early as 48 hours
d) full septic work up and antibiotics

A

c) is the answer, **same as above, has a risk factor (prematurity) so should have CBC and limited diagnostic evaluation (vitals q4 hour)
should NOT discharge prior to 48 hours
for babies

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28
Q

Which of the following is not one of the diagnostic criteria for chorioamnionitis?

a) fever
b) foul smelling discharge
c) lower uterine tenderness
d) left shift

A

b) is not
the other 3 are the criteria to diagnose definite chorioamnionitis
a lot of the time, it is classified as possible when the main sign is fever

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29
Q

Which of the following is the risk of sepsis in a baby born to a mother with definite chorioamnionitis?

a) 4%
b) 8%
c) 25%
d) 60%

A

b) 8% is the risk of sepsis (from all organisms) in a mother with definite chorio; when possible and definite are considered together it is 3-4 %
among all mothers with fever, 2-6% (depending on “height” of the fever)
babies who don’t have signs of sepsis at birth are unlikely to develop sepsis (odds ratio for those who are well at birth is 0.26)

therefore, should do a limited diagnostic evaluation (CBC and q4 hour vitals) for these babies, only do more if CBC is suggestive of infection

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30
Q

Which of the following statements is false?

a) babies born at <88% while sitting in car seat for 90 minutes

A

c) false - should repeat the test in recumbent car seat (i.e. reduced angle, from 45-30 degrees in many cases) and if they pass this can go home with that. this type of car seat might not provide as much protection in a crash
if they still desat in recumbent position may need to do further testing

the rest are true
O2 sat monitoring along should detect 99% of episodes
monitors don’t prevent SIDS
should test all prems (including late perms) and babies with abnormalities
use caution with slings etc until 1 month corrected age, and for neuro abnormalities kids, until they can sit independently

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31
Q

Which of the following statements is false?

a) Last menstrual period is the most accurate way to measure gestational age
b) early ultrasounds are more accurate with dating than later ultrasounds
c) estimated fetal weight cannot be used to date pregnancy at 22-25 weeks
d) most babies at 25 weeks onward should have active care unless there are any special risk factors for a worse outcome

A

a)false - early U/S is the most accurate, between 8-14 weeks with crown rump length
should figure out dates most accurate way (ultrasound) to help with decisions

the rest are true
early ultrasound +/-5 days, 16-22 week U/S is +/- 10 days
increasing imprecision with advancing gestational age
fetal weight estimates have accuracy of +/- 10% and tend to be underestimates
need to determine the estimated birth date as early as possible and tell the pregnant woman
25 weeks have decent neurodevelopment outcomes so should do active care (weak recommendation)
extremely preterm - 22 weeks-25 weeks and 6 days
154-181 days inclusive

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32
Q

Which of the following is not a recommended management option?

a) consider active care for babies of gestational age 22 weeks and over depending on wishes of the family
b) women with threatened birth at 22-25+6 weeks should be transferred to a tertiary care centre with a level 3 NICU
c) all women where active care is being considered should get antenatal corticosteroids
d) C section should not be done at

A

a) false - for 22 weekers (22+0 to 22+6) a non interventional approach should be considered with a focus on comfort care, any mothers in threatened preterm labour at 22-25+6 weeks should talk to neonatology and MFM

the rest are true
c) there is some debate about whether babies

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33
Q

Which country has the highest reported survival of 22 week baby?

a) Canada
b) U.K.
c) Sweden
d) Japan

A

d) Japan - 34%
these data are sometimes skewed cause some countries just won’t resuscitate super perms
Sweden is second at 10%

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34
Q

What is the survival of 24 weeker in Canada?

a) 8%
b) 36%
c) 62%
d) 78%

A

c) survival in Canada 62% of 24 weaker
<5% survival, also that overall 25 week onwards have good survival

more variability between studies with lower GA
also differences in different countries

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35
Q

Which of the following statements is false?

a) extremely preterm babies (23-25 weeks gestation) have worse neurodevelopment outcomes than more mature preterm babies
b) survival free of neurodevelopment consequences for extreme perms has range of estimates from roughly 18-60% in different studies
c) male sex leads to better outcomes for extreme perms
d) when plan of care is uncertain, should ensure that the birth is attended by people who are capable of caring for an extremely preterm infant

A

c) false female does better, other things which influence include steroids, tertiary care centre, twins (discuss if they generally do better or worse), so these factors can also affect decision making

when decision not made, have people around that can resuscitate the baby if needed
should do ongoing counselling and document as well as possible

some report that even within this group worse outcomes with decreasing GA, whereas others don’t find this
A large UK-wide study (EPICURE) showed that of the 283 survivors born at ≤ 25 completed weeks’ GA, 23% had a severe disability at 30 months corrected age [51] and 22% had a severe disability at age six years [56]. At 11 years of age [57], this cohort had serious cognitive impairment (score

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36
Q

What is the first step of grief and mourning?

a) avoidance
b) confrontation
c) disorganization
d) accommodation

A

a)avoidance or protestation is the first step
covers the period of time where the news is delivered and the period immediately after
usually lasts a few hours to days
often anger in this stage

2nd stage: grief is experienced most intensely, reactions to loss are most acute, awareness of finality , involves preoccupation with thoughts of the deceased, most intense phase

accommodation and reorganization - gradual decline in the feelings of acute grief, beginning of social and emotional reinvestment in the world
person learns to live with the death - typically lasts 1-2 years

grief - reaction to loss
absence of grief may be abnormal
perinatal death - multiple losses

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37
Q

Which of the following statements is false?

a) parents have difficulty recognizing loss, particularly of neonates
b) many secondary losses related to the self also occur when faced with the loss of a child
c) complicated grief is more likely to occur with the loss of an older child than a newborn
d) incongruence between spouses coping with the death of a child increases significantly between 2-4 years after the loss

A

c) false- the age of the child is irrelevant, similar process regardless of whether the child is new or older
loss of a child high risk for complicated grieving

the rest are true
incongruity increases 2-4 years after, decreases after year 5
each person copes with grief differently, and the ups and downs mean that couples may be at different stages of their grief
when a child dies, one must also struggle with the loss of their identify as a parent, harder to hold on to than other roles since parenting is a very active role
hard to readjust and reinvest in relationships, especially with another child

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38
Q

Which of the following does not help parents with critically ill children in the NICU?

a) parents should be encouraged to bring mementos to their infants in the NICU
b) heath care providers should use the child’s first name and sex when talking about a baby
c) limiting visiting hours for parents to avoid crowding and overwhelming parents with information and compromising confidentiality
d) bad news should be given in a timely manner by the attending staff physician

A

c) false - should not limit visiting hours for parents, including when there are rounds, 80%parents enjoyed attending bedside rounds, helped them learn about their baby and feel more confident in the heath care team
using name, mementos help parents form attachment during the time in the NICU and may help them mourn later on

should give news to the parents and an additional support person (i.e. social worker ) who will stick around afterwards
should give repeated offers to hold the baby, warn about gasping and muscle contractions
reassure parents, support them, allow family to see if the parents want, explain the process/need for autopsy if relevant, explain options for memorials

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39
Q

Which of the following is not part of the management of a perinatal loss ?

a) spiritual support, including baptism if it is wanted, should be offered
b) organ donation should only be mentioned when it is an option for the particular baby/family
c) health care providers should create a partnership with parents early in critical care setting, and withdrawal decisions should be taken with the parents and the team, to help relieve the parents of guilt regarding this
d) an attending should state that the team recommends withdrawal to the parents, rather than asking the parents what they want

A

b)patients who don’t get the discussion of organ donation are often upset it didn’t happen, should do it even when it is not an option

try to keep the burden of decision to withdraw away from the parents, emphasize the role to he team
attending should state that the team recommends withdrawal

may help for attending to talk to a second attending to say that the team recommends withdrawal

stillbirth - may lead to lower self esteem

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40
Q

Which of the following is false

a) grieving for the loss of a twin can be harder than a singleton
b) separation occurred in 12% of couples after a prenatal loss in one study
c) bereavement counselling should be part of training for health care providers
d) babies who are malformed/macerated should not be held by their mothers because it will disturb them

A

d) the opposite, mothers who were given the option to hold their babies say it helped, also parents will focus on the good features rather than the malformed ones, should get to hold the baby

pregnancy termination - also results in grieving, even when it is terminated for medical reasons

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41
Q

True or false - circumcision lowers the risk of UTI in boys <1 year old

A

true - it does lower the risk of UTI in first year of life
it also lowers the risk of penile cancer
AAP says that overall the benefits outweigh the risks but that ultimately the decision should be left up to parents since there are other cultural/religius factors that matter
Canadian ancient statement (1996) say that risks and benefits are equal - so no recommendation

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42
Q

True or false - some research suggests that circumcision lowers the risk of cervical cancer in partners of circumsized men

A

true -

also some evidence that it lowers the risk of heterosexual acquisition of STI and HIV rates

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43
Q

Name 3 risks of circumcision:

A

bleeding
infection
swelling
amputation of the glans
renal failure (???) in the old CPS statement
rarely death
very low risk of these complications (0.2-0.6% in the old statement)

should be done under sterile conditions with appropriate pain management
**this is not from the statement, this is from my brain)

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44
Q

Please name 3 conditions where you wouldn’t circumsize a boy immediately

A
  1. hypospadias
  2. prematurity
  3. bleeding disorders
  4. congenital abnormalities

circumcision should only be performed on stable, heathy babies

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45
Q

True or false - complication rates of circumcision done in the newborn period are similar to those done later in life

A

false - much lower complications when done in the newborn period

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46
Q

True or false - male circumcision adversely affects sexual function

A

false - does not appear to negatively affect sexual function

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47
Q

True or false - sucrose alone is appropriate analgesia for circumcision

A

false - non pharmacological interventions (i.e. sucrose, positioning, pacifiers) are not enough for pain control, therefore need to use analgesia , these (i.e. non pharm methods) should be adjuncts only

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48
Q

What is the best method of analgesia to use for the circumcision of low birth weight infants?

A

penile nerve blocks are the best; topical creams in this group may cause more skin irritation

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49
Q

What percentage of term newborns develop jaundice?

A

60%

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50
Q

What percentage of term newborns have a bilirubin level >340 umol/L

A

2%
jaundice very common, kernicterus very rare
kernicterus in term infants doesn’t occur until 340, and very rare until over 425 umol/L
most with kernicterus in the US registry had bili>500
also, milder bill levels (but not in the kernicterus range) may cause some impact on neuro outcome, although we aren’t sure of the details - therefore we should treat all hyperbili

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51
Q

Please name 9 factors that can increase the risk of acute encephalopathy in the presence of hyperbilirubinemia

A
  1. dehydration
  2. prematurity
  3. acidosis
  4. hypoxia
  5. seizures
  6. hyperosmolarity
  7. hydrops
  8. resp distress
  9. hypoalbuminemia
    * *however not great evidence for this

on the nomogram, the risk factors for kernicterus are

low risk is :>38 weeks and well
medium risk is: >38 weeks and risk factors or 35-376/7 weeks and well
high risk: 35-376/7 weeks and risk factors

risk factors: 1. isoimmune hemolytic disease 2. G6PD deficiency 3. asphyxia 4. respiratory distress 5. significant lethargy 6. temperature instability 7. sepsis 8. acidosis

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52
Q

True or false - sepsis is common in the well appearing infant with severe hyperbilirubinemia

A

false - some infants with severe hyperbili are found to have sepsis, however, sepsis is uncommon in the well appearing infant with severe hyperbili

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53
Q

What is the estimated incidence of acute bilirubin encepalopathy in Canada? of chronic bilirubin encephalopathy

A

based on study - 1/10 000
2002-2004 258 Canadian babies with severe bill (excluding those with Rh disease)
5% hearing loss or severe neuro outcome at discharge, 20% at least one sign
chronic bili encephalopathy 1/100000 (similar as danish study)

acute bili encephalopathy 1st in Rh disase - now this is rare
occurs in children with other risk factors

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54
Q

Please name 7 risk factors for the development of severe hyperbilirubinemia

A
  1. male sex - Odds Ratio (OR): 1.3-1.7
  2. previous sibling with hyperbili: OR 4.8
  3. gestation shorter < 38 weeks (for 36 weeks OR is 1.9 to 7.7)
  4. asian or european background (more for asian)
  5. visible bruising
  6. cephalohematoma
  7. maternal age older than 25 years old: 2.6
    * *effect of dehydration and breastfeeding are very variable in the literature
55
Q

True or false - breastfeeding increases the chance of jaundice

A

varied evidence, some studies show that it increases it, but one other study showed that it decreased it - may depend on cultural approaches/supports to breastfeeding
overal the evidence is variable
evidence is unclear for the association with visible jaundice<24 hours, before discharge at any age,

56
Q

true or false - severe dehydration increases the chance of jaundice

A

true - the chance of jaundice increases with increasing severity of dehydration

57
Q

True or false - cord Hg is a useful way to detect hyperbili

A

false - Although bilirubin is derived from the breakdown of hemoglobin, routine umbilical cord blood hemoglobin or hematocrit measurement does not aid in the prediction of severe hyperbilirubinemia

58
Q

True or false - babies of mothers with type O blood have an increased risk of severe hyperbilirubinemia

A

true by an OR of 2.9(because most infants with jaundice due to ABO isoimmunization are blood group A or B infants born to a mother with group O blood)
need for photo - increased in babies with DAT +ve

59
Q

True or false - all babies should have a blood group and DAT done

A

false - only for babies of mother with type O blood who have jaundice or are in the high intermediate risk group ->
also, may need to do for the babies of mothers who have positive antibodies in the prenatal panel which is done

Universal testing for incompatibility with blood grouping, and for isoimmunization using the DAT, on cord blood does not improve clinical outcomes compared with testing only infants whose mothers are group O [33][34] (evidence level 2b). Testing all babies whose mothers are group O does not improve outcomes compared with testing only those with clinical jaundice [35][36] (evidence level 2b). Therefore, it is reasonable to perform a DAT in clinically jaundiced infants of mothers who are group O and in infants with an elevated risk of needing therapy (ie, in the high-intermediate zone [Figure 1]).

this will also help determine at which level the baby will need photo

60
Q

True all false - a timed bilirubin concentration can accurate detect the babies at highest risk of having severe hyperbili

A

true - 2 studies, for late preterm and term

61
Q

In a study of North American babies, how many babies with bilirubin at discharge (18hour-3 days) between 40th=75th percentile had bilirubin level>95th percentile

A

2.2% had bili in this range
for bili 95%
for >75th percentile initially, 12% had >95th percentile bill
bili at 6 hours can also be used to predict (another study)

when you combine the bill measurement, with other risk factors (primarily gestational age) even better prediction tool ->between 40-75th percentile, increase in 12% risk of >95th percentile bill for 36 weaker, vs. only 3% for term infant

62
Q

What is the percentage risk of a term infant (39-40 weeker) with a initial timed bill >95th percentile of developing severe hyperbili?

A

> 10%
also for infant 10% (12%) of severe hyperbili
**discuss where the cut off of GA is (i.e. what do we do with a 38 weaker)

63
Q

What is the positive predictive value of an umbilical cord bilirubin level in a term infant?

A

only 4.8%, 10% in late preterm infant, specificity is very poor

64
Q

True or false - Because G6PD is X linked, only boys with severe hyperbilirubinemia need to be tested for G6PD

A

false - female heterozygotes can have up to 50% of their cells affected by inactivation of the X chromosome, so need to test both girls and boys with severe hyperbili

should consider for all with severe hyperbili
should also consider for those at risk (i.e. ethnic background)

65
Q

Which of the following statements is false?

a) G6PD increases the risk of severe hyperbili
b) in the presence of hemolysis G6PD levels can be over-exagerrated
c) G6PD increases the risk of exchange transfusion from hyperbili
d) only meditarreanan boys are at high risk of G6PD

A

d) false - other ethnicities at risk include
Mediterranean , Middle Eastern, African [37] or Southeast Asian origin
female heterozygotes can also be affected
so should consider testing in everyone (both sexes) from at risk backgrounds
test takes a while to come back
G6PD deficient individuals may need intervention at lower levels - since they can progress more quickly

66
Q

True or false - end tidal carbon monoxide in combination with time bill reading helps predict severe hyperbili

A

false - although end tidal CO is increased with hemolysis, prediction is not improved by measuring this in combo with timed measurements

67
Q

A baby is born to a mom with O+ve blood, the baby has jaundice needing phototherapy. What bloodwork should you do on baby?

a) blood group only
b) DAT only
c) blood group and DAT
d) none of the above

A

c) Blood group and DAT for babies of mothers with O blood and with early jaundice (in high intermediate zone)

all mothers should be tested for ABO and Rh blood types in pregnancy
if mother is not tested in pregnancy, then cord blood should be sent for evaluation of blood type and DAT

68
Q

When does the peak bill concentration usually occur?

A

day 3-5 of life, when most babies have already been discharged

69
Q

True or false - all infants should have their bilirubin checked between 24 hours and 72 hours of life

A

true - with using visual detection, risk factors etc, we were still missing cases
the best idea is to check everyone, decide what the risk of progressing to severe hyperbilirubinemia is, and give a copy to the parents, as well as arrange follow up testing as needed

70
Q

A 36 week baby who is DAT negative plots their bill in the high intermediate risk zone. What is your next step?

a) phototherapy
b) discharge with no follow up
c) discharge with follow up in 24-48 hours
d) none of the above

A

c) follow up in 24-48 hours

**look at the whole chart
for the some of the high risk babies, need phototherapy treatment anyways

71
Q

An infant is discharged from hospital at 24 hours of life. When should they next see a medical professional?

A

Should be reviewed within 24 hours by someone who can detect clinical jaundice/arrange lab test for bill and further treatment if needed. can be from any medical or nursing discipline.

72
Q

True or false - capillary sample of bilirubin are 10 higher than venous samples

A

false - there is no systemic difference between venous and capillary (used most often and in most samples) samples for bill, can use either

73
Q

Name 3 factors that affect the accuracy of transcutaneous bilirubin measurement

A
  1. become inaccurate after phototherapy started
  2. affected by skin colour
  3. affected by skin thickness

more accurate at lower bilirubin levels, so can use it as a screening tool is reasonable
confidence is interval is 37 - therefore as long as it is 37 or more lower than the treatment line, should be safe

74
Q

Name two cases where you would check a bill earlier than at discharge with the metabolic screen (i.e. within 24-72 hours)

A
  1. visible jaundice
  2. excessive weight loss
  3. ABO incompatibility (other risk factors for significant bill)
75
Q

What are 3 causes of conjugated neonatal hyperbilirubinemia?

A
  1. rhesus disease
  2. liver disease
  3. cholestasis
    should consider measuring the conjugated fraction for babies on phototherapy
76
Q

What conjugated bilirubin amount warrants further investigation?

A

> 18 umol/L or >20% warrants further investigation

should measure the conjugated fraction for persistent jaundice >2 weeks or HSM

77
Q

True or false - transcutaneous bilirubin is an acceptable screening method

A

true- Transcutaneous bilirubinometry is an acceptable method, either as a routine procedure or in infants with visible jaundice. The result should be summed with the 95% CI of the device to estimate the maximum probable TSB concentration (recommendation grade C). (i.e. within 37 umol/L)

78
Q

True or false - breastfeeding support should be offered to mother’s of jaundiced babies

A

true - while breastfed babies are at higher risk of jaundice than formula fed babies, but overall still so so many benefits of breastfeeding that we should offer it to these moms.
support of the breastfeeding mother increases the frequency and duration of breastfeeding
It is difficult to find reliable evidence that the risk of severe jaundice can be minimized by a program of breastfeeding support, but other aspects of breastfeeding difficulty can be reduced by such programs, and providing such support is reasonable

79
Q

When do exclusively breastfed infants lose their maximum weight by?

A

by day 3, usually lose 6-8%, if they lose >10% should be seen by a breastfeeding specialist

80
Q

True or false - routine supplementation of breastfed babies by dextrose water or water prevents hyperbiliribinemia

A

false - does not prevent hyperbili
other interventions that don’t help: Routine use of glycerine suppositories [64][67], routine glycerine enemas [65], L-aspartic acid, enzymatically hydrolyzed casein, whey/casein and clofibrate

81
Q

Which of the following has a clinically important benefit in reducing severe hyperbilirubinemia from hemolysis?

a) phenobarbitone
b) Tin-mesoporphyrin
c) prophylactic phototherapy
d) none of the above

A

d) none of the above

phenobarbitone-studied for G6PD kiddies, does not help clinical outcomes
tin-mesoporphyrin - one study of G6PD with historical controls in infants with G6PD deficiency, SnMP eliminated the need for phototherapy and appeared to prevent severe hyperbilirubinemia. However, prospective RCTs have as yet failed to demonstrate a clinically important benefit (evidence level 1b), and the compounds are not commercially available [71][72].
prophylactic phototherapy - no benefit

82
Q

What are two roles of phototherapy?

A
  1. treat severe hyperbili

2. prevent severe hyperbili in those with moderate hyperbili

83
Q

How does phototherapy work?

A

changes the conformation of the bilirubin molecule, making it water soluble
blue-green light works the best
effectiveness related to the area exposed and the intensity of the lights in the needed wavelengths
can get more intense by using more units or moving it closer

84
Q

Please list 5 side effects of phototherapy

A
  1. temperature instability
  2. intestinal hypermotility, diarrhea
  3. interference with maternal-infant interaction
  4. rarely, bronze discolouration of the skin
  5. increased anxiety and health care use by parents who perceive it as a serious illness
  • water loss from skin - NOT a clinically significant effect in heathy term infants who are drinking well
  • Reassurance of the parents importent
  • use eye patches - animal studies suggest a risk to the developing retina
85
Q

Should enteral feeding by continued in dehydrated infants with jaundice?

A

yes - it should
fluid supplementation will quickly bring down the bill level
enteral feeding should be continued - will replace missing fluid, supply energy, reduce hepatoenteric uptake of the bilirubin

86
Q

What are advantages of the fibre optic phototherapy?

disadvantages?

A
  1. don’t need eye patches
  2. can breastfeed the baby without interrupting phototherapy
    disadvantage: the peak intensity of phototherapy is less
87
Q

What type of light is most commonly used for phototherapy?

A

fluorescent light

88
Q

What type of phototherapy should be used for infants with severe hyperbilirubinemia?

A

intensive phototherapy mplies that a high intensity of light (greater than 30 µW/cm2/nm) is applied to the greatest surface area of the infant possible. In usual clinical situations, this will require two phototherapy units, or special high-intensity fluorescent tubes, placed approximately 10 cm from the infant, who can be nursed in a bassinet. Usually the diaper can be left in place

89
Q

Who can you consider conventional phototherapy for?

A

for babies with moderate hyperbili(i.e. if 35-50 below the thresholds for phototherapy)
conventional phototherapy – a single bank of fluorescent lights placed above the incubator of an infant nursed with a diaper in place – is, of course, less effective because both surface area and intensity are reduced; nevertheless, it will have an effect on TSB concentration.

90
Q

For a child who is approaching the exchange transfusion level, what do you add onto the phototherapy in question 88.

A

fibre optic blanket and remove the diaper

91
Q

True or false - continuing breastfeeding during phototherapy is associated with adverse clinical outcomes

A

false - is not associated with adverse clinical outcomes
however, stopping breastfeeding for phototherapy is associated with more discontinuation of breastfeeding at 1 month, however 1 observational study did show a slower response to phototherapy when breastfeeding was continued during phototherapy. no clinically significant difference observed

92
Q

True or false - we should encourage continued breastfeeding during phototherapy for hyperbili

A

true, see above

93
Q

Which newborns should get IVIG?

A
  1. Infants with a positive DAT who have predicted severe disease based on antenatal investigation
  2. infants with an elevated risk of progressing to exchange transfusion based on the postnatal progression of TSB concentration

should receive IVIG at a dose of 1 g/kg (recommendation grade A)

94
Q

True or false - SnMP (tin-porphyrin), synthetic analogues of Heme oxygenate, show no evidence for the reduction of improvement of outcomes in moderate hyperbili

A

true - it doesn’t show any evidence

95
Q

True or false - supplemental fluids should be indicated only for babies who are at high risk of exchange transfusion from severe hyperbilirubinemia

A

true -
oral and IV are equal
the study had a high rate of exchange transfusion, so shouldn’t give fluids to those who are at lower risk of exchange transfusion

96
Q

When should you check the bilirubin in a child with severe hyperbilirubinemia or who has progressed to severe hyperbilirubinemia despite treatment?

A

within 2-6 hours to ensure that they are responding

an infant who presents with severe hyperbilirubinemia or who progresses to severe hyperbilirubinemia despite treatment

97
Q

At which concentration (despite phototherapy) should one consider exchange transfusion?

A

375-425 umol/L

98
Q

In a child that is getting prepared for exchange transfusion, what bloodwork should you draw?

A

blood after exchange transfusion can’t be used for study of many rarer causes of hyperbili. therefore should draw the following:

  1. red cell fragility
  2. enzyme deficiency -G6PD and Pyruvate kinase deficency
  3. metabolic disorders
  4. hemoglobin electrophoresis
  5. chromosome analysis
99
Q

While getting set up for exchange transfusion, what interventions should you do?

A

phototherapy
fluids
IVIG (for isoimmunization)

**if already above exchange transfusion level at presentation, appropriate to check level right before the treatment as long as it doesn’t delay care (since it can help avoid some of the risks of exchange transfusion)

should do under supervision of experienced neonatologist

100
Q

A child presents with a bilirubin of 400 and a high pitched cry. What do you do?

A

immediate exchange transfusion for child with sign of acute bilirubin encephalopathy

101
Q

When should children with isoimmunization have a repeat hemoglobin performed after discharge if it was normal at discharge ?

A

at risk of severe anemia after several weeks, so should do a repeat Hg at 2 weeks if low at discharge and at 4 weeks if normal at discharge

102
Q

What type of hearing loss are children with severe hyperbilirubinemia at risk for?

A

neurosensory hearing loss

therefore they should all have brainstem auditory evoked potentials

103
Q

A child has severe hyperbili, what other bloodwork should you do?

A

conjugated and unconjugated bilirubin levels; direct Coombs test; hemoglobin and hematocrit levels; and complete blood cell count, including differential count, blood smear and red cell morphology); investigation for sepsis if warranted by clinical condition
always do complete hx and physical

104
Q

What are the 3 main questions one should ask when entering a resuscitation room?

A
  1. gestational age - term or not term
  2. is the baby crying or breathing?
  3. muscle tone

no longer about mec- BUT should be able to assess it in order to decide about need for suctioning

105
Q

Which is the most important indicator of PPV effectiveness?

A

increase in HR
best determined by auscultating the precordial pulse
need to do the initial evaluation and start PPV within the 1st minute (golden minute)

106
Q

What O2 concentration should be used for the resuscitation of term babies?

A

21% O2 (Room air)
for preterm, may be better to use slightly higher (30-90%) may be preferable until studies provide better direction
should always monitor pre ductal sat by oximetry when doing PPV
targets based on the chart of sats in first 10 minutes
self-inflating bags (even without a reservoir) can provide more O2 than previously thought

107
Q

What ratio of compressions to ventilation is indicated for neonatal resuscitation?

A

3:1
100% O2 for ventilation
in rare occasion where thought to be cardiac, may consider a higher ratio of compressions to ventilation

108
Q

Name 4 aspects of post-resucsitation care in NICU:

A
  1. monitor vital signs
  2. temperature control
  3. awareness of complications
  4. provisions of support
109
Q

Who should be present at every delivery according to NRP?

A

one person who is responsible for the care of the newborn, capable of initiating resuscitation who can start PPV and chest compressions; a second more skilled person who knows advance resuscitation should be readily available

110
Q

What is MR SOPA?

A
used to make sure you have effective ventilation - need to make sure of this before moving further down in the resus algorithm
Mask readjustment
Reposition airway
Suction mouth and nose
Open mouth
Pressure increase
Alternative airway
111
Q

What is the minimum gestational age and weight that LMA can be effective?

A

34 weeks

2000g

112
Q

What is the optimal training method for NRP?

A

simulation training

cognitive, technical and behavioural skills

113
Q

Within how many hours should cooling be considered for HIE?

A

within 6 hours

114
Q

After how long of no detectable heart rate should resuscitation efforts be discontinued?

A

10 minutes

115
Q

How long should cord clamping be delayed for in healthy term newborns?

A

1 minute after, don’t know what the appropriate time is for babies who need resuscitation

116
Q

What is the IV dose of epinephrine for neonatal resuscitation?

A

IV route is preferred
1:10000 epi
dose is 0.1 ml/kg

117
Q

What is the ETT dose of epinephrine for neonatal resuscitation?

A

1:10000 epi
dose is 1 ml/kg
max 3ml dose

118
Q

True or false - naloxone is a resuscitation drug

A

NO-it is not a rescucitation drug, NOT the first corrective therapy for a baby who is not breathing effectively, PPV is

119
Q

rocuronium for intubation in neonates ?

A

has rapid onset BUT the muscle relation lasts way too long

other non depolarizing - mivacurium is short acting and closest to ideal profile, however, it isn’t available in N/A

120
Q

In a tertiary level hospital, what gestational age should get prophylactic surfactant (this is a somewhat lousy goody recommendation)

A

t gotten adequate antenatal steroids

121
Q

should intubated infants with RDS get surfactant before transport?

A

yes

122
Q

what are the risk factors for sepsis (from GBS statement)?

A
  1. maternal fever/signs of chorio
  2. ROM >18 hours
  3. previous GBS sepsis
  4. preterm labour <36 hours
123
Q

mom has antibodies on the antenatal screen, what should you do for the baby

A

should do blood type and DAT

should consult neonatology or heme

124
Q

bili at 48 hours in a 39 week baby who is DAT negative is in the low intermediate range, when to follow?

A

routine care

125
Q

bili at 48 hours in a 35 week baby who is DAT positive in the low intermediate range, when to follow?

A

needs further testing and evaluation (i.e. within 24 hours +/- photo depending on the value)

126
Q

bili at 48 hours in a 35 week baby who is DAT -ve in the low intermediate range, when to follow

A

routine care

127
Q

bili at 48 hours in a 39 week baby who is DAT +ve in the high intermediate range

A

follow up within 24-48 hours

128
Q

bili at 48 hours in the high range

A

if term baby , still need very close follow up +/- treatment
if DAT +ve and perm then needs treatment for sure

129
Q

bili in 35 week baby DAT +ve in the low range

A

routine care

for all gestation age and DAT

130
Q

car seat testing who to do for

A

prem
neuro
cardio resp conditions

131
Q

evidence for car seat testing before discharge

A

not that great

132
Q

definition of failing car seat test

A

drop in sats to <88%

2 or more episodes lasting 10 seconds or more during a 90 minute monitoring period

133
Q

if baby fails car seat testing

A

try in recumbent car seat testing