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Flashcards in The Crashing Neonate Deck (61)
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1
Q

What should always come to mind with a crashing neonate?

A

Sepsis

2
Q

What does grunting signify?

A

Need for PEEP

3
Q

What is the first step in assessing a crashing neonate?

A

The pediatric assessment triangle:
Appearance: tone, interaction, vocalizations
Work of breathing: RR, retractions, nasal flaring, grunting, breath sounds
Circulation: pallor, cyanosis, mottling, warmth, cap refill
Also include the vitals, and probably a POC glucose

4
Q

What two signs are ominous in this age group?

A

Hypothermia

Bradycardia

5
Q

How is irritability defined?

A

It is paradoxical irritability where the kid gets more irritable when they are touched or handled and are not soothed by the means that usually work

6
Q

What are the first actions basically every patient gets?

A
IV, O2, Monitor
POC glucose, Hgb, check lytes, VBG
All cultures
Bolus 10–20 cc.kg of NS
First dose of Abx
7
Q

How rapidly should abnormalities be addressed?

A

Remember to fix abnormalities as fast as they developed. Slow onset issues should be corrected slowly.

8
Q

Name 6 rapid lab abnormalities that should be corrected?

A
Dehydration/shock
Low Ca
High K
Anemia
Low Na
Low glucose
9
Q

How is dehydration/hypovolemia treated?

A

NS bolus of 10–20 cc/kg

10
Q

How is Hypocalcemia treated? What level is treated?

A

<7 mg/dL is treated

Ca gluconate 100–200 mg/Kg

11
Q

How is Hyperkalemia treated?

A

Treat symptomatic or above 7 mEq/L
Regular insulin 0.1 u/Kg with D10W 2–3mL/Kg
Consider albuterol
Check EKG for peaked T’s, loss of P waves, wide QRS, Sine waves, dysrhythmias, asystole
Give Ca as this acts the fastest
Insulin takes 10–20 minutes to start working and peaks at 30–60 min
Check POC glucose 1 hour later
Bicarb and albuterol tend to be more transient

12
Q

How is anemia treated?

A

PRBC 10 mL/Kg

13
Q

How is hyponatremia treated?

A

If less than 125, give 3% Saline 5mL/Kg with goal of 125–130

Correct remaining over the next 1–2 days

14
Q

How is hypoglycemia treated?

A

if less than 60, give D10W 5mL/Kg

15
Q

What does an open fontanelle mean for head trauma and intracranial pressure?

A

Symptoms are less likely to develop and therefore less reliable to indicate an intracranial issue

16
Q

Where can neonates have bleeding to the point of hypovolemic shock where other patients cannot?

A

In their heads!

17
Q

What brain bleed pattern = abuse?

A

Subdural hematoma

18
Q

Neonates don’t break bones in trauma and are therefore more likely to have what injuries?

A

Pulmonary contusion

Liver and spleen injuries

19
Q

What labs are needed in neonatal trauma?

A

Type/screen/cross

Coags, LFT’s, Lipase, UA

20
Q

What imaging is indicated in neonatal trauma assessment?

A

CXR, Skeletal survey, CT’s (faster than MRI), and FAST exam

21
Q

What are broad categories to consider when evaluating a crashing neonate?

A
Trauma
Heart/Hypovolemia/Hypoxia
Endocrine
Metabolic
Inborn errors of metabolism
Seizures
Formula Issues
Intestinal catastrophes
Toxins/ingestions
Sepsis

Also remember: Botulism, Meningitis, Hydrocephalus

22
Q

What are the CSF findings suggestive of bacterial vs Viral meningitis?

A

Bacterial: low glucose, high protein, high WBC’s PMN predominant
Viral: normal glucose and protein, smaller increase in WBC’s with lymph predominance

23
Q

What should be the empiric antibiotic regimen when meningitis is possible?

A

Ampicillin + Gentamicin + 3rd/4th gen Cephalosporin
Cephalosporin is needed to improve CSF activity against pneumococcus, and to cover for GBS resistant to ampicillin and enteric G (-) resistant to ampicillin and to cover listeria (Cetotaxime, Ceftazidime, Cefepime)
Vanco is substituted for ampicillin if a hospitalized patient unless concern for GBS, Listeria, or Enteric bacteria are suspected based on gram stain, in which case ampicillin and vanco are both given because vanco is not bactericidal in the CSF for these organisms
Acyclovir included if any suspicion for viral infection
Meropenem sub for cephalosporin if concern for MDR G(-) organisms

24
Q

What are the two ways that cardiac disease can present?

A

Cyanosis and Shock

Both require prostaglandin

25
Q

When should empiric prostaglandin be given to a suspected cardiac issue?

A

When cyanosis/hypoxia doesn’t respond to 100% O2 or

Shock does not respond to fluid bolus

26
Q

What is a side effect of prostaglandin that should be remembered?

A

Causes apnea and the child should probably be intubated

27
Q

What are the two potential causes of central cyanosis that you should consider and how to differentiate the two?

A

Think primary respiratory vs cardiac
Give 100% O2 and if not >85% saturations after ten minutes then it is likely a shunt and cardiac in origin and PGE1 should be given

28
Q

In broad terms, what are the two types of congenital cardiac issues and how do they present?

A

Left and right sided obstructive lesions
Left: Present in shock
Right: Present with hypoxia and cyanosis

29
Q

What are the left sided obstructive CHD’s?

A

Coarctation, hypoplastic LV, aortic stenosis

PDA is needed for systemic flow

30
Q

What are the right sided obstructive CHD’s?

A

These are the cyanotic lesions, the five T’s
Truncus arteriosis, Transposition of the great vessels, Tricuspid atresia, Tetrology of fallot, Total anomalous venous return
PDA is needed for pulmonary flow

31
Q

What is the dosing of PGE1?

A

0.05–0.1 mcg/kg/min

32
Q

What presenting symptom equals heart disease until proven otherwise?

A

Diaphoresis with feeding

33
Q

An infant presents with hypotension. It is unclear if it is sepsis or heart disease. How should fluids be managed?

A

Give 10cc/Kg and reassess. Sepsis should get better but heart disease will not. Give the sepsis patients more fluid and the heart disease patient start with pressors (Epinephrine)

34
Q

What is the dosing for epinephrine as a pressor for infants?

A

0.01–0.1 mcg/kg/min

35
Q

A crashing neonate has hypotension and is not responding to fluids or pressors. What exam finding will be helpful and what intervention is needed?

A

Consider congenital adrenal hyperplasia
Check the genitalia for ambiguity or hyperpigmentation
Give hydrocortisone 25mg IV
Check labs: low glucose, high K, low Na

36
Q

Explain 21-alpha hydroxylase deficiency

A

Most common cause of congenital adrenal hyperplasia
Inhibits progression to aldosterone and cortisol pushing everything to sex hormones leading to excessive androgens
Lack of aldosterone leads to Na wasting and hyper K
Lack of cortisol leads to hypoglycemia and steroid deficient shock

37
Q

Explain 17-beta hydroxylase deficiency

A

Stops formation of sex steroids and cortisol

Causes lack of androgens and cortisol but high mineralcorticoid activity

38
Q

Explain 11-alpha hydroxylase deficiency

A

One step down from 21-alpha hydr. deficiency preventing cortisol production and increasing androgen production but paradoxically increasing mineralcorticoid function

39
Q

What endocrine issues should be considered?

A

Congenital adrenal hyperplasia
Thyroid
Glucose
Calcium

40
Q

What should always come to mind when a baby is found to be hypoglycemic?

A

Sepsis

And probably other things

41
Q

Patient comes in with jerks, seizures, tetany.

What lab abnormality should be suspected?

A

Low calcium

42
Q

What are the symptoms of low calcium? What disease causes this and what can be seen on imaging?

A

Seizures, jitteriness, tetany, apnea, dysrhythmias
DiGeorge syndrome
No thymus

43
Q

When hypocalcemia is found what other studies should be ordered?

A

ECG to check QTc

PTH levels, Vit D, Mg, Phos

44
Q

What is the treatment for hypocalcemia?

A

Ca gluconate 100mg/kg (1mL/Kg of 10%) IV over 5–10 minutes

Also find and correct other electrolyte abnormalities such as Mg (25–50mg/Kg IV)

45
Q

What are the labs that are helpful for inborn errors of metabolism? What can all these kids get empirically?

A

Ammonia, Lactate, Ketones, Glucose
Also include LFT’s
These all affect some form of the 3 energy sources: fat, protein, sugar
Give empiric glucose D10W in 0.5NS @ 1.5X maintenance

46
Q

What infectious bug should be suspected if a patient is septic and with seizures?

A

Remember to consider Herpes among others

47
Q

What history do you need from mom when working up sepsis?

A

PROM?, vaginal vs c-section, maternal infections?

48
Q

What do all kids less than 30 days old get when they present with a fever?

A

Septic workup, admission, +/- Abx
Labs: CBC, UA, all cultures, Lactate, CRP, Procal
CSF gram stain, cultures, protein, glucose, cell count and CSF for herpes
RPP, LFT’s, Coags
Fluid bolus
Epi if hypotensive despite fluids
Abx: ampicillin 50–100mg/kg
Gentamicin 4mg/Kg
Consider Vancomycin 15mg/kg
Consider Acyclovir 20mg/kg if CSF suggestive or other reasons to suspect herpes
Include 3rd gen cephalosporin if meningitis

49
Q

Describe omphalitis

A

Erythema, purulent drainage from stump with fever
Progresses rapidly! High mortality
Necrotizing infection
Needs surgical consultation, Abx, and septic workup
A clinical diagnosis

50
Q

What should you remember about localized infections in neonates?

A

There is no such thing as a “localized infection” in neonates

51
Q

When considering formula mishaps, what is a serious presenting symptom and the underlying cause?

A

Can present with seizures from hyponatremia from over dilution or too much free water
Kids under 3 months should not be given free water
Treat with hypertonic saline

52
Q

What is the treatment for seizure from low Na?

A

3% NaCl 3–5mL/Kg IV over 30–60 minutes
Goal Na 125–130
Correct remaining levels gradually over 24–48 hours

53
Q

Patient presents with seizures that are not responding to usual therapy. What causes should be considered?

A

Hyponatremia and Pyridoxime requiring seizures

54
Q

What are the symptoms of hypo and hyper natremia?

A

Hypo: seizures, lethargy, hypothermia, resp. insufficiency
Hyper: dehydration, lethargy, not fed enough, from concentrated formula

55
Q

What is the MI of pediatric surgery?

A

Malrotation with midgut volvulus

56
Q

Describe features of malrotation and midgut volvulus

A
50% present <1 month of age
Time is bowel
ANY TIME there is bilious vomiting
Belly can be benign or peritoneal
Workup with abd X-Ray flat and upright
Ultimately need an upper GI study looking for a corkscrew shape in the duodenum
57
Q

Describe features of necrotizing enterocolitis

A

Usually only in premies but can happen in shock states
Can mimic sepsis +/- hematochezia
Can perf bowel
Exam: distended abdomen, red abdomen, palpable bowel loops
Abd X-Ray: pneumatosis intestinalis, portal venous gas

58
Q

What is the workup and treatment for Hirschsprungs?

A

X-Ray, call GI for definitive Dx
Watch out for perforation
NPO, NGT, Abx, need surgery

59
Q

What are the features of infantile spasms?

A

Epileptic spasms in infancy or early childhood
Hypsarrhythmia on EEG
Developmental regression
Often develop seizures later in childhood
Poor neurodevelopmental prognosis
Often subtle findings and hard to recognize
Consider brain imaging and LP

60
Q

How are seizures managed?

A

Secure airway and give O2
Benzos first: Midazolam 0.2mg/kg IN
Phenobarb or keppra second line
Febrile seizures most common cause in kids
Low Na is the second most common cause and need to ask about formula and feeding
Give pyridoxine 100mg IV push to any kid not responding to benzos

61
Q

What are the doses and routes of administration for banzos in a seizing patient?

A

Lorazepam: 0.1mg/kg IV
Midazolam: 0.1mg/kg IV or 0.2mg/kg IN or IM
Diazepam: 0.2mg/kg IV

Repeat doses after 4 minutes