|
Medications used in the
NICU
Post Menstrual Age (PMA) = gestational age
at birth + postnatal age
Sedatives/Analgesics
|
Drug |
Doses |
Comments |
|
Acetaminophen |
Oral
Loading: 20 mg/kg/dose PO x 1 then 10-15 mg/kg/dose
<32 wks=q8hr
≥32
wks=q6hr
Rectal
Loading: 30 mg/kg x 1 then 20 mg/kg/dose
<32 wks=q12hr
≥32-40
wks=q8hr
≥40
wks =q6hr |
Administer 30 minutes prior to immunizations and continue for 24 hours.
Scheduled use should
not exceed 72 hours |
|
Chloral
Hydrate |
25-75 mg/kg/dose PO x1
|
Use repeat doses with caution. Contraindicated in patients with
significant hepatic or renal dysfunction.
|
|
EMLA |
1. Apply 0.5gm of topical
mixture of lidocaine/prilocaine (generic EMLA) in a 1 X 1 cm square
(dime sized) surface over the anticipated puncture sites (maximum of 3
sites)
2. Cover with an occlusive
dressing for 45 minutes (maximum 60 minutes)
3. Remove dressing
4. Wipe/wash away topical
medication |
Local anesthestic used for
procedural pain management such as central line placement and lumbar
punctures. |
|
Fentanyl
|
Intermittent: 1-2 mcg/kg/dose IV q2-4h prn
ELBW: 0.5 mcg/kg/dose IV q2-4h prn
Infusion:
Usual starting dose: 1-3 mcg/kg/hr
*ELBW: 0.5 mcg/kg/hr
Range: 1-12 mcg/kg/hr |
Intermittent doses may cause chest wall rigidity. Administer doses over
at least five minutes. Tachyphylaxis and opioid dependence will
often occur.
Tacyphylaxis to fentanyl may develop with
chronic use which may improve with a conversion to morphine.
Equipotent doses published
in standard tables are not applicable for chronic dosing and may result
in overdose. Please use the following conversion
(1:10) 10 mcg/kg/hr fentanyl = 0.1 mg/kg/hr morphine
|
|
Hydromorphone |
Infusion:
Usual starting dose: 4 mcg/kg/hr
Range: 2-20 mcg/kg/hr
|
Not first-line analgesic in
NICU. |
|
Lorazepam |
Intermittent:
0.05-0.1 mg/kg/dose IV q2-4h prn
Infusion:
Usual initial dose: 0.1-0.15 mg/kg/hr.
See:
Benzodiazepine Taper |
Do not administer through UAC. Used for sedation. Does not provide pain
relief. Seizure-like myoclonus has occurred in some premature
infants. Adverse effects: respiratory depression, hypotension. May
need to be tapered in neonates receiving > 7 days of therapy due to
physiologic dependence. |
|
Methadone
|
Please see
Methadone taper for opioid-dependent
neonates
for detailed dosing information. |
Used for iatrogenic opioid dependence and
neonatal withdrawal. |
|
Midazolam
|
Intermittent:
0.05-0.1 mg/kg/dose IV q2-4h prn
Infusion: Usual
initial dose: 0.1 mg/kg/hr.
Range 0.05-0.15
mg/kg/hr. |
Do not administer through UAC. Used for sedation. Does not provide pain
relief. Seizure-like myoclonus has occurred in some premature
infants. Adverse effects: respiratory depression, hypotension. May
need to be tapered in neonates receiving > 7 days of therapy due to
physiologic dependence. |
|
Morphine
|
Intermittent:
0.05-0.1 mg/kg/dose IV q2-4h prn
Infusion:
Initial
0.01 mg/kg/hr.
Range: 0.01 - 0.2 mg/kg/hr
|
Should be reserved for term and older infants without hemodynamic
compromise.
Tacyphylaxis to fentanyl may develop with
chronic use which may improve with a conversion to morphine.
Equipotent doses published
in standard tables are not applicable for chronic dosing and may result
in overdose. Please use the following conversion
(1:10) 10 mcg/kg/hr fentanyl = 0.1 mg/kg/hr morphine
|
|
Naloxone
|
0.01 -0.1 mg/kg/dose IV or ET. Repeat doses may be needed in some patients.
|
Reversal agent for opioids. May be used for maternal opioid use 4 hours
PTD. Avoid use in patients born to narcotic-addicted mothers as sudden
reversal may cause life-threatening withdrawal symptoms. |
Antimicrobials
|
Acyclovir |
< 1200 gm: 20 mg/kg/dose IV q12h
> 1200 gm: 20 mg/kg/dose IV q8h |
For
HSV encephalitis. May cause nephrotoxicity. Maintain good hydration to
prevent crystallization in kidneys. Monitor liver and renal function. |
|
Amikacin |
0-4weeks (<1200g): 7.5 mg/kg/dose IV q24h
< 7d (>
1200 g): 7.5 mg/kg/dose IV q12h
>7d
(1200-2000 g): 7.5 mg/kg/dose IV q8-12h
>7d
(>2000 g): 7.5 mg/kg/dose IV q8h
|
Aminoglycoside used only for organisms resistant to gentamicin and
tobramycin. Monitor serum levels and SCr. Desired trough: < 10 mcg/mL |
|
Amoxicillin |
UTI
Prophylaxis: 10 mg/kg/dose PO QD
|
|
|
Amphotericin B
Conventional |
1
mg/kg/dose IV q24h
Follow instructions in WIZ for ordering in patient’s current dextrose
concentration. Electrolyte and nutrition requirements should be
calculated to run over 20 hours as TPN or IVF will be turned off during
Amphotericin infusion. |
Should be infused over 4 hours. Administration through central line
preferred. Adverse effects: nephrotoxicity, infusion-reactions (fever,
rigors), hypokalemia, hypomagnesemia. |
|
Amphotericin B
Lipid Complex
Abelcet® |
5
mg/kg/dose IV q24h
Follow instructions in WIZ for ordering in patient’s current dextrose
concentration. Electrolyte and nutrition requirements should be
calculated to run over 20 hours as TPN or IVF will be turned off during
Amphotericin infusion.
|
Used if nephrotoxicity occurs with conventional Amphotericin B.
|
|
Ampicillin |
< 1
m.o.:100 mg/kg/dose IV q12h
> 1 m.o.: 50
mg/kg/dose IV q6h
Group B Strep Meningitis
< 7 d.o. 100
mg/kg/dose IV q8h
> 7
d.o.: 100 mg/kg/dose IV q6h
UTI
prophylaxis: 10 mg/kg/dose IV QD
|
Used empirically to cover for Group B streptococcus and Listeria sp.
Also covers Enterococcus. |
|
Azithromycin |
Pertussis
< 6 months: 10 mg/kg/day PO x 5 days |
Caution: No data available for appropriate dosing using IV.
|
|
Cefazolin |
<7d: 20
mg/kg/dose IV q12h
>7d
(<2000g): 20 mg/kg/dose IV q12h
>7d
(>2000g): 20 mg/kg/dose IV q8h |
1st
generation cephalosporin principally used for Staph aureus. |
|
Cefepime |
< 14 days: 30 mg/kg/dose IV q12h
14 -30 days: 50 mg/kg/dose IV q12h
> 30 days: 50 mg/kg/dose IV q8-12h
|
4th generation cephalosporin.
Limited information available regarding appropriate dosing in neonates.
Provides coverage against susceptible S. aureus and many
gram-negatives including Pseudomonas aeruginosa. |
|
Cefotaxime |
0-4
wks (<1200 g): 50 mg/kg/dose IV q12h
<7d (>1200
g): 50 mg/kg/dose IV q12h
>7d
(>1200 g): 50 mg/kg/dose IV q8h
Meningitis: 67 mg/kg/dose IV q8h (if pneumococcus not suspected) |
3rd generation cephalosporin.
Provides coverage against gram-negative organisms and susceptible
Streptococcus pneumoniae. . Not first line for rule-out sepsis
in neonates (associated with worse outcomes in neonates in combination
with ampicillin vs gentamicin + ampicillin). Can consider in rule-out
sepsis patients with renal issues in place of gentamicin. |
|
Ceftazidime |
0-4
weeks (<1200 g): 50 mg/kg/dose IV q12h
<
7d (>1200 g): 50 mg/kg/dose IV q12h
>7d
(>1200 g): 50 mg/kg/dose IV q8h |
3rd
generation cephalosporin used to treat susceptible strains of
Pseudomonas aeruginosa. |
|
Ceftriaxone |
Please see comments section.
|
3rd
generation cephalosporin with spectrum of activity similar to cefotaxime.
Use in the NICU is Prohibited risk of kernicterus and
life-threatening interactions when given with calcium containing
intravenous fluids. Refer to
Rocephin use in the NICU. |
|
Clindamycin |
< 7d (<
2000g): 5 mg/kg/dose IV q12h
< 7d (>
2000g): 5 mg/kg/dose IV q8h
>
7d (<1200g): 5 mg/kg/dose IV q12h
>
7d (1200-2000g): 5 mg/kg/dose IV q8h
>
7d (> 2000g): 7.5 mg/kg/dose IV q6-8h |
Provides coverage against anaerobes and Group A streptococcus.
|
|
Erythromycin
(see GI section for motility doses) |
<7d:
10 mg/kg/dose IV/PO q12h
>7d (<1200g): 10 mg/kg/dose IV/PO q12h
>7d (1200-2000g): 10 mg/kg/dose IV/PO q8h
>7d (>2000g): 10 mg/kg/dose IV/PO q6h
Pertussis and chlamydial pneumonia and conjunctivitis: 12.5
mg/kg/dose PO q6h |
Macrolide antibiotic used in neonates for Chlamydia trachomatis
pneumonia, Ureaplasma urealyticum infections and pertussis.
Cardiac arrhythmias have been reported with IV use (infuse slowly). Other
adverse effects: abdominal pain, vomiting, nausea,
pyloric stenosis,
thrombophlebitis. Fluconazole increases erythromycin
levels (monitor for cardiac arrhythmias). |
|
Fluconazole |
<29
wks and < 14 days:
5-6 mg/kg/dose IV/PO q72h
<29
wks and > 14 days:
5-6mg/kg/dose IV/PO q48h
30-36 wks and < 14 days:
3-6mg/kg/dose IV/PO q48h
30-36 wks and > 14 days:
3-6 mg/kg/dose IV/PO q24h
37-44 wks and < 7 days:
Loading dose 6-10 mg/kg IV/PO x1 followed by maintenance of 3-6
mg/kg/dose IV/PO Q48H
37-44 wks and > 7 days:
Loading dose 6-10 mg/kg IV/PO x1 followed by maintenance of 3-6
mg/kg/dose IV/PO Q24H
Neonates and infants > 45 weeks:
3-6 mg/kg/dose IV/PO q24h
Prophylaxis Dosing: <26wk (<750g) on vent with PICC/CVC line = 3
mg/kg/dose IV twice weekly x 6wk as long as line is in. Not if in liver
failure.
|
Treatment of systemic fungal infections including meningitis caused by
Candida albicans and other susceptible fungi.
.
Twice weekly prophylaxis may be used in high risk infants. Refer
to Fluconazole Prophylaxis
Protocol for Criteria.
Monitor hepatic
function with long courses of therapy. Monitor phenobarbital and
phenytoin levels as fluconazole can increase levels. Rifampin decreases
fluconazole and hydrochlorothiazide increases fluconazole levels. |
|
Gentamicin |
<
30 weeks and <= 7 days postnatal age: 5 mg/kg/dose
IV Q48H
<
30 weeks and >7 days postnatal age: 4 mg/kg/dose IV Q24H
>
30 weeks, < 30 days postnatal age: 4 mg/kg/dose IV Q24H
>
30 weeks, > 30 days postnatal age, < 2 kg: 4 mg/kg/dose
IV Q24H
>
30 weeks, > 30 days, > 2 kg: 5 mg/kg/dose IV Q24H
Impaired renal function: Give dose X 1 and base interval on drug levels. |
Aminoglycoside used for gram-negative organisms including E. coli
and Pseudomonas aeruginosa. Desired trough: < 2 mcg/mL prior to
the 4th dose. Patients being treated for meningitis should
have both peaks and troughs drawn. May cause nephro- and ototoxicity. |
|
Meropenem |
< 7d: 20 mg/kg/dose IV q12h
>
7d (1200-2000 g): 20 mg/kg/dose IV q12h
>
7d (> 2000 g): 20 mg/kg/dose IV q8h |
Carbapenem with a broad spectrum of activity to be used in cases of
documented resistance to other antibiotics. Should not be used as
monotherapy due to rapid development of resistance. |
|
Metronidazole |
0-4
weeks (< 1200 g): 7.5 mg/kg/dose IV q48h
< 7 d
(1200-2000 g): 7.5 mg/kg/dose IV q24h
< 7 d (>2000
g): 7.5 mg/kg/dose IV q12h
> 7
d (1200-2000 g): 7.5 mg/kg/dose IV q12h
> 7
d (>2000 g): 15 mg/kg/dose IV q12h
> 1
m.o.: 7.5 mg/kg/dose IV q6h |
Provides anaerobic coverage. |
|
Nystatin
(Oral) |
Preterm: 1 mL (100,000 units). Give 0.5 mL (50,000 units) to each side
of mouth QID
Term: 2 mL (200,000 units). Give 1 mL (100,000 units) to each side of
mouth QID |
Topical antifungal used for oral candidiasis. |
|
Oxacillin |
0-7d (<2000 g): 25 mg/kg/dose IV q12h
0-7d (>2000 g): 25 mg/kg/dose IV q8h
>7d
(<1200 g): 25 mg/kg/dose IV q12h
>7d
(1200-2000 g): 25 mg/kg/dose IV q8h
>7d
(>2000g): 25 mg/kg/dose IV q6h |
Penicillinase-resistant penicillin used in the treatment of confirmed
methicillin-susceptible Staph aureus. May cause significant
phlebitis. |
|
Penicillin G |
GBS Meningitis:
<7d=150,000 units/kg/dose IV q8h (450,000 units/kg/day)
>7d=125,000 units/kg/dose IV q6h (400,000 units/kg/day)
GBS Bacteremia:
<7d = 50,000 units/kg/dose IV q8h (150,000 units/kg/day)
>7d = 50,000 units/kg/dose IV q6h (200,000 units/kg/day)
Congenital Syphilis:
<7d(all
wts)=50,000 units/kg/dose IV q12h
>7d(all wts)=50,000 units/kg/dose IV q8h |
Used in treatment of confirmed susceptible Group B Streptococcus. May
also be used for congenital syphilis. |
|
Piperacillin/
Tazobactam (Zosyn®)
|
50-100 mg/kg/dose IV
<29wk, <28d = q 12hr
<29wk, > 28d = q 8hr
30-36 wk, <14d = q 12hr
30-36wk, >14d = q 8hr
>37wk, 0-7d = q 12hr
>37wk, >7d = q 8hr |
For empiric therapy for non-CNS infections that involve non-CoNS/MRSA
gram-positives, gram-negatives (including pseudomonas) and anaerobes
(e.g. gram-neg pneumonia, VAP with GNR in ETT aspirate, aspiration
pneumonia, abdominal infections, etc). It can be combined with
Gentamicin for double coverage of GNR, which would eliminate the use of
Metronidazole as a third drug. |
|
Rifampin |
5-20 mg/kg/day IV divided q12h |
Used for synergy for Staphylococcus aureus infections. |
|
Tobramycin |
<30 weeks (< 7 d): 5 mg/kg/dose IV q48h
<30 weeks (> 7 d): 4 mg/kg/dose IV q24h
>
30 weeks (< 30 d): 4 mg/kg/dose IV q24h
> 30 weeks (> 30 d, < 2 kg): 4 mg/kg/dose IV q24h
> 30 weeks (> 30 d, > 2 kg): 5 mg/kg/dose IV q24h
Impaired renal
function:
Give dose x 1 and base interval on
|
Aminoglycoside used for gram-negative organisms including E. coli
and Pseudomonas aeruginosa. Desired trough: < 2 mcg/mL prior to
the 4th dose. Patients being treated for meningitis should
have both peaks and troughs drawn. May cause nephro- and ototoxicity. |
|
Vancomycin |
Infants
< 1 month: 10 mg/kg/dose IV Q8H
Patients with impaired renal function:
15
mg/kg/dose X 1
Infants ≥ 1 month, > 2 kg: 15 mg/kg/dose IV Q8H
Infants ≥ 1 month, > 2 kg with documented/suspected meningitis:
15 mg/kg/dose IV q6h |
Initial gram positive
antibiotic coverage for clinically septic infants and infants with
indwelling hardware (central line, VP shunt, etc) pending culture and
sensitivity results.
Antibiotic of
choice for MRSA, Staph epidermidis, and where indicated by sensitivity
patterns of culture proven isolates.
Desired troughs: 5-12 mcg/mL
prior to the fourth dose. Patients being treated for meningitis should
have both peaks and troughs drawn. Monitor renal function.
|
|
Zidovudine |
Preterm:
< 30 weeks: 2
mg/kg/dose PO q12h or 1.5 mg/kg/dose IV q12h for first four weeks then
increase the interval to q8h thereafter.
30-34 weeks:
2 mg/kg/dose PO q12h or 1.5 mg/kg/dose IV q12h for first two weeks then
increase interval to q8h thereafter.
> 35
weeks: 2
mg/kg/dose PO q6h or 1.5 mg/kg/dose IV q6h
|
Post-exposure prophylaxis for patients born to HIV-infected mothers.
Should be started within 6-12 hours of birth. Adverse effects: anemia,
thrombocytopenia, neutropenia. Monitor CBC. |
Respiratory
Medications
|
Albuterol
0.083.%
|
2.5 mg in 3 mL via nebulizer q4-6h |
Do not give if HR over 180. Observe for hypoxia. May be used
to treat hyperkalemia |
|
Budesonide
|
0.25 mg via nebulization per ETT or mask q12h
|
A
trial may be used in some patients to reduce the risk of CLD.
|
|
Caffeine
citrate
|
Loading dose: 20 mg/kg IV/PO x1
Initial maintenance dose: 5 mg/kg/dose IV/PO q24h (starting 24 hours
after load)
Range: 5-10 mg/kg/dose IV/PO q24h
|
Used for apnea of prematurity. Monitor for feeding intolerance,
irritability, HR. Levels not routinely performed. Obtain levels if
toxicity suspected (usual range: 4-20 mcg/mL) |
|
Dexamethasone |
Extubation: 0.25 mg/kg/dose IV q8h x 3 doses, started 4-6 hours prior to
extubation
For chronic lung disease:
Day
1
0.1 mg/kg/dose IV q12h
2 0.1 mg/kg/dose IV q12h
3 0.075 mg/kg/dose IV q12h
4 0.075 mg/kg/dose IV q12h
5 0.05 mg/kg/dose IV q12h
6 0.05 mg/kg/dose IV q12h
7 0.025 mg/kg/dose IV q12h
8 0.025 mg/kg/dose IV q12h |
Please see Dexamethasone protocol
for criteria for use in the
patients with CLD.
Discuss
the use and potential risks with family.
Supplemental interventions for patients receiving 8
day taper: discontinue Vitamin A, initiate famotidine, avoid
indomethacin if possible, increase protein intake and monitor
triglycerides. |
|
Racemic
Epinephrine |
0.3 - 0.5 ml of racemic epinephrine (2.25%) diluted in NS to a final
volume of 3 ml |
Used for post-extubation stridor. |
|
Beractant
(Survanta)
|
4
ml/kg/dose via ETT
May give up to 4 doses in the first 48 hrs of life, no more frequently
than q6h.
|
Warm to room temperature by allowing to sit for 20 minutes or warm in
hand for 8 minutes. Do not shake dose. Avoid suctioning for 2 hours
post-dose unless clinically indicated. Observe for hypoxia and
bradycardia. |
|
Vitamin A
|
Initial: 2000 IU/kg/dose IM every other day starting DOL#1. Continue
until patient receiving full feeds then give 4000 IU/kg/dose PO/PT Q24H
until discharge
|
Used to decrease the incidence of BPD. See Vitamin A protocol for
criteria for use. Should be discontinued during dexamethasone
treatment. |
Cardiac
Medications
|
Adenosine |
0.1 mg/kg/dose IV. If no effect, give 0.2 mg/kg IV. If effective but
tachycardia reinitiates, repeat same dose rather than double the dose.
|
Acute treatment of sustained paroxysmal supraventricular tachycardia. |
|
Albumin
|
0.5-1 g/kg/dose IV x1
|
Can
also be added to TPN |
|
Amiodarone |
Consult
cardiology for dosing recommendations.
IV
bolus: Five separate 1 mg/kg aliquots
Infusion: 5-15 mg/kg/day |
For the
treatment of life-threatening refractory arrhythmias |
|
Alprostadil
|
0.05-0.1 mcg/kg/min |
Not to be given through UAC. Promotes dilation of the ductus arteriosus.
Used in neonates with CHD dependent upon ductal shunting for
oxygenation/perfusion. Adverse effects: apnea, fever, flushing,
hypotension, bradycardia, and seizures. |
|
Captopril
|
< 44 weeks and < 2
months:
Initial dosing: 0.01-0.05 mg/kg/dose PO Q8-12H Range: 0.01-0.1
mg/kg/dose
< 44 weeks
and > 2 months:
Initial dosing: 0.01-0.05 mg/kg/dose PO Q8-12H, Range: 0.01-0.1
mg/kg/dose
Maintenance dosing: Some infants may require 0.15-0.3 mg/kg/dose PO Q8H
Max: 6 mg/kg/day
|
ACE-inhibitor. Note: Use higher doses with caution in patients < 44
weeks and < 2 months as significant decreases in cerebral blood flow
have occurred in preterm infants with chronic hypertension who have
received doses higher than 0.15 mg/kg/dose.
|
|
Digoxin
|
Neonates > 40 weeks:
5
mcg/kg/dose PO q12h
4
mcg/kg/dose IV q12h
Preterm neonates < 40 weeks PMA:
3
mcg/kg/dose PO q12h
2.5 mcg/kg/dose IV q12h
|
Monitor HR, ECG, and potassium. Low potassium increases risk of
toxicity. Adverse effects: feeding intolerance, lethargy, bradycardia,
arrhythmias. |
|
Dobutamine
|
2-20 mcg/kg/min |
Do not give through a UAC. Increases myocardial contractility with less
of an impact on heart rate than other catecholamines. May cause
vasodilation at high doses. Adverse effects: tachycardia, arrhythmias,
hypotension. Use phentolamine if extravasation occurs. |
|
Dopamine
|
2-20 mcg/kg/min |
Do not give through a UAC. Low doses increase renal blood flow and urine
output. Intermediate doses increase renal blood flow, cardiac output,
contractility, and blood pressure. High doses cause alpha-adrenergic
effects with vasoconstriction and increased blood pressure. Adverse
effects: tachycardia, arrhythmias, tissue sloughing with extravasation.
Use phentolamine if extravasation occurs. |
|
Enalapril
|
Initial dosing:
0.05 mg/kg/dose PO q12-24h. Titrate upward based upon response.
Max daily dose: 0.5 mg/kg/day |
ACE-inhibitor used for hypertension and afterload reduction. Adverse
effects: hypotension, oliguria. Monitor potassium and renal function.
|
|
Enalaprilat |
0.005-0.01 mg/kg/dose IV Q8-24H |
ACE-inhibitor used for hypertension. Adverse effects: hypotension,
oliguria. Monitor potassium and renal function. |
|
Epinephrine
|
Resuscitation: 0.01-0.03 mg/kg/dose IV (0.1-0.3 mL/kg) of 1:10,000
dilution
Infusion: 0.05-2 mcg/kg/min. Usual max in neonates is 1 mcg/kg/min
|
Do not give through UAC. Stimulates alpha and beta adrenergic
receptors. Adverse effects: arrhythmias, renal vascular ischemia.
Use phentolamine if extravasation occurs. Extravasation may cause
ischemia and necrosis.
IV preferred but may be given ETT. Dosing ETT: 0.1 mg/kg/dose (1 mL/kg)
of a 1:10,000 dilution |
|
Heparin
|
Bolus: 75 units/kg IV x1
Infusion: 28 units/kg/hr |
Monitor aPTT. Monitor platelets for heparin-induced thrombocytopenia
(rare). |
|
Hydralazine
|
0.25-1 mg/kg/dose PO q6-8h
Hypertensive crisis: 0.1-0.4 mg/kg/dose IV q6h prn. Max daily dose: 3.5
mg/kg/day in 4-6 divided doses |
Direct acting arterial vasodilator. Reduces systemic vascular
resistance. Adverse effects: tachycardia, diarrhea, emesis, and
transient agranulocytosis. |
|
Indomethacin
|
0.2 mg/kg IV x1
|
Do not give via UAC. Please see indomethacin protocol for indications
and qualifying labs. Contraindicated if mother received indomethacin
within 72 hours of delivery. Maintain good oxygenation, fluid restrict
(decrease maintenance IVF by 30%), NPO for 12-24 hours after dose,
monitor UOP, and repeat labs q24h. |
|
Isoproterenol
|
0.05-2 mcg/kg/min |
Stimluates ß1 and ß2 receptors with no action on alpha receptors.
Positive inotropic and chronotropic effects. Adverse effects:
tachycardia, arrhythmias |
|
Milrinone |
0.25-1 mcg/kg/min |
Phosphodiesterase-inhibitor. Positive inotropic effect with decreases
in preload and afterload, increased cardiac output, and decreased
systemic and arterial pressures. Adverse effects: arrhythmias,
thromobocytopenia, hypokalemia, hepatotoxicity |
|
Nicardipine |
Infusion:
Initial: 0.5-5 mcg/kg/min
Usual: 1-4 mcg/kg/min
Max: 5 mcg/kg/min
|
Calcium channel
blocker. Inhibits the influx of Ca into myocardium and selectively into
coronary vascular smooth muscle without altering serum calcium
concentrations. Affects contractile functions of cardiac and vascular
smooth muscle. |
|
Nitroprusside
|
Initial: 0.3-0.5 mcg/kg/min. Doses above 4 mcg/kg/min are rarely
required. Max: 10 mcg/kg/min. |
Reduces preload and afterload through venous and arteriolar vasodilation.
Use cautiously in patients with renal, hepatic or thyroid dysfunction.
Adverse effects: excessive hypotension, ECG changes. Monitor
thiocyanate levels if > 3 days of therapy, > 4 mcg/kg/min or renal
impairment. Monitor cyanide in patients with hepatic dysfunction. |
|
Sotalol
|
Consult cardiology for dosing information
|
Anti-arrhythmic agent used to treat ventricular and supraventricular
tachycardias. Adverse effects: arrhythmias, hypotension, dyspnea.
Monitor ECG. |
Hematologic
Medications
|
Aquamephyton (Vitamin K)
|
<1500 g: 0.5 mg IM x1
>1500
g:1 mg IM x1 |
Administer within 1 hour of birth for prevention of hemorrhagic disease
of the newborn. |
|
Enoxaparin
|
Infants < 2 months old:
Treatment dose: 1.5 mg/kg/dose SC q12h
Prophylaxis: 0.75 mg/kg/dose SC q12h
Infants ≥ 2 mths old:
Treatment dose: 1 mg/kg/dose SC q12h
Prophylaxis: 0.5 mg/kg/dose SC q12h
|
Low-molecular weight heparin. Antifactor-Xa levels should be
monitored. Neonates often require higher doses. Please see
Thrombolytic Therapy protocol. |
|
Ferrous
sulfate drops
|
2-4 mg elemental iron/kg/day PO in 1-2 divided doses (maximum: 15 mg
elemental Fe/day) |
Refer to iron supplementation guidelines on website for more detailed
dosing information. May cause GI distress. Avoid use until patient
tolerating full feeds of an adequate caloric density for growth. |
Anticonvulsants
|
Fosphenytoin
|
Loading dose: 10 PE/kg IV x1, may repeat 10 PE/kg IV up to 20 PE/kg IV
total.
Initial maintenance: 2 PE/kg/dose IV q12h
|
Used for seizures refractory to phenobarbital. Monitor free phenytoin
levels (usual range: 1-2 mcg/mL). Infuse no faster than
1.5 PE/kg/min. |
|
Levetiracetam (Keppra®) |
20-60 mg/kg/day IV/PO q12h |
Limited information available on its use in neonates. Used for neonatal
seizures refractory to phenobarbital. Infuse over 15 minutes. PO and IV
doses are equivalent.
Blood serum levels do not need to be monitored. Caution in patients
with renal dysfunction. Adverse effects: drowsiness, agitation and
irritability
|
|
Lorazepam
|
0.05 mg/kg/dose IV, may repeat in 10-15 min. |
Used for status epilepticus. |
|
Phenobarbital
(see GI
section for cholestatis dosing) |
Loading dose: 20 mg/kg IV x1, may repeat 10 mg/kg IV x 2 up to 40 mg/kg
IV total
Initial maintenance dose: 2mg/kg/dose IV or PO q12h |
Drug of choice for most types of seizures in neonates. Desired serum
level: 15-40 mcg/mL. PO and IV doses are equivalent. |
|
Phenytoin
|
Initial maintenance: 2 mg/kg/dose IV/PO q12h
Note: IV formuation is
non-formulary. Use fosphenytoin instead.
|
Used for seizures refractory to phenobarbital. Monitor free phenytoin
levels (usual range: 1-2 mcg/mL). |
GI
Medications
|
Erythromycin
|
1
mg/kg/dose PO/IV q6h
|
Used for GI motility at low doses.
Adverse effects:
abdominal pain, vomiting, nausea, pyloric stenosis. |
|
Famotidine
|
0.5-1 mg/kg/dose IV/PO q12h
|
H2-antagonist used for GERD. Routine use is not recommended. May be added to TPN. |
|
Glycerin
suppository
|
Sliver as needed. |
|
|
Lansoprazole |
Infants < 3 months: 7.5 mg or 0.5 – 1.5 mg/kg/day PO
Infants > 3 months: 15 mg or 0.5 – 1.5 mg/kg/day PO
|
Limited data in neonates. Proton-pump inhibitor. Used in cases of GERD
unresponsive to H2-antagonists and metoclopramide. Solutabs may be
diluted in 1-5 mLs of water and given PO or PT.
|
|
Metoclopramide
|
0.1 mg/kg/dose q6h IV or PO
|
Treatment of GERD. Adverse effects: dystonic and extrapyramidal effects
at higher doses. |
|
Omeprazole
|
0.5-1.5 mg/kg/dose PO q24h
|
Proton-pump inhibitor. Used in cases of GERD unresponsive to
H2-antagonists and metoclopramide. |
|
Phenobarbital (for cholestasis)
|
2-2.5 mg/kg/dose IV/PO q12h
|
|
|
Ranitidine |
1-5
mg/kg/dose PO q12h |
H2-antagonist used for GERD. |
|
Simethicone
|
20 mg PO q6h prn
|
|
|
Ursodiol
|
TPN-cholestasis:
30 mg/kg/DAY
PO
divided q8-12h
Biliary atresia: 10-15 mg/kg/dose PO q24h |
Cholerectic agent. |
Diuretics
|
Furosemide
|
Intermittent:
1
mg/kg/dose IV q12-24h
2
mg/kg/dose PO q12-24h
Infants > 1 month: Administer doses above Q6-24H
Infusion:
Initial 0.1 mg/kg/hr
Range 0.05-0.4 mg/kg/hr |
Loop diuretic also used in patients with BPD. Monitor Na, K,
PO4, and Cl. Extra potassium supplementation should be considered when
initiating therapy. Can cause nephrocalcinosis. |
|
Hydrochlorothiazide |
1
mg/kg/dose PO q12h
|
Thiazide diuretic. Diuretic effect is potentiated when used with
furosemide or spironolactone. Calcium-sparing. May cause hyperglycemia,
hypokalemia, or hyperuricemia. |
|
Spironolactone
|
0.5-1.5 mg/kg/dose PO q12h
|
Potassium-sparing diuretic. Use cautiously in patients with renal
impairment. |
|
Spironolactone/Hydrochlorothiazide (Aldactazide®) |
Dosed based on spironolactone component: 0.5 – 1.5 mg/kg/dose PO q12h |
Combination thiazide and potassium-sparing diuretic.
|
Endocrine
|
Hydrocortisone
|
Physiologic replacement: 6-8 mg/m2/day IV/PO in 2-3 divided
doses
Pressor- or volume-resistant hypotension (stress dose): 1 mg/kg/dose
q8h x 3-5 days (usually equivalent to 20-40 mg/m2/day)
Please refer to
Hydrocortisone for Vasopressor-Resistant
Hypotension |
Adverse effects: hyperglycemia, hypertension, sodium and water
retention. |
|
Insulin
|
0.05-0.2 units/kg/hr. Usual initial dose is 0.1 units/kg/hr. |
Should be used in conjunction with dextrose infusion when used for the
treatment of hyperkalemia. (see hyperkalemia protocol in Wiz
for dosing information) |
|
Levothyroxine |
10-12 mcg/kg/dose PO q24h or
5-8 mcg/kg/dose IV q24h |
|
Neuromuscular
blockers
|
Pancuronium
|
Intermittent:
0.05–0.1 mg/kg/dose IV q1-2h prn
|
Neuromuscular blocking agent. Patient must be on ventilator. Must be
given with sedation. |
|
Vecuronium
|
Intermittent:
0.05-0.1 mg/kg/dose IV q1-2h prn
Infusion:
Usual starting dose: 0.1 mg/kg/hr
Range: 0.05-0.1 mg/kg/hr |
Neuromuscular blocking agent. Patient must be on ventilator. Must be
given with sedation.
Less
effect on BP and HR (hypotension and tachycardia) than pancruronium |
Electrolytes
|
Calcium
gluconate
(Ordered as salt not as elemental calcium)
|
Symptomatic hypocalcemia: 100-200 mg/kg/dose of calcium gluconate salt
IV x 1
Resuscitation: 60-100 mg/kg/dose IV |
Do not administer through UAC. Observe IV site closely for extravasation.
Use hyaluronidase (Amphadase®) if extravasation occurs. |
|
Magnesium
sulfate (ordered as salt not elemental Mg)
|
Hypomagnesemia: 25-50 mg/kg/dose IV x 1
|
Monitor blood pressure, HR and respiratory rate during infusion. |
|
Sodium
bicarbonate 4.2%
|
Resuscitation: 2 mEq/kg IV over 3-5 minutes.
*Full correction of metabolic acidosis=Wt (kg) x Base deficit (mEq/L) x
0.3 = mEq of HCO3. Give ½ of this dose.
|
Treats metabolic acidosis. Give slowly over several hours for VLBW.
Must have adequate ventilation. Do not give in presence of hypercarbia. |
|
THAM (Tromethamine
sulfate)
|
3.3 to 6.6 ml/kg/dose IV
Equation for
full correction:
Dose(mL)=weight(kg) x Base deficit(mEq/L) x 1.1
Max dose: 15-23 mL/kg/day
|
Do not give through umbilical line. Treats metabolic acidosis without
elevation of serum sodium. Do not give in patients that are anuric or
uremic. |
|
Potassium
(PO)
|
Prevention of hypokalemia associated with diuretics:
Initial: 1-2 mEq/kg/day PO in 1-2 divided doses
|
May cause GI distress. |
Immunizations:
|
DTaP (diphtheria and tetanus toxoids with acellular pertussis)
|
0.5 mL IM |
|
Hib (haemophilus influenzae type B) |
0.5 mL IM |
|
IPV (inactivated poliovirus) |
0.5 mL SC |
|
Hepatitis B (Recombivax HB®) |
0.5 mL IM |
|
PCV (pneumococcal 7-Valent Conjugate Vaccine; Prevnar®) |
0.5 mLIM |
Combinations:
Hib
and Hep B (Comvax®)
0.5 mL IM
Hep
B, IPV, DTaP (Pediarix®)
0.5 mL IM
Hepatitis B Immune Globulin for babies born to HBsAg+ mothers:
0.5
mL IM x1
Ophthalmic
Agents
|
Cyclopentolate/phenylephrine (Cyclomydril) |
Instill 1-2 drop in each eye X3 doses, 5 minutes between doses. |
|
Miscellaneous
|
Octreotide |
Chylothorax
dosing:
Infusion:
0.5-4 mcg/kg/hr,
titrate to effect – doses up to 40 mcg/kg/hr have been used |
Somatostatin
analog. Monitor for hyper/hypoglycemia. Pulmonary hypertension has
been reported in treated former premature infants with CLD. |
|