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In This Topic
Pediatrics
Infections in Neonates
Overview of Neonatal Infections
Risk factors
Symptoms and Signs
Diagnosis
Treatment
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Chapters in Pediatrics
  • Introduction
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  • Perinatal Physiology
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Topics in Infections in Neonates
  • Overview of Neonatal Infections
  • Congenital and Perinatal Cytomegalovirus Infection (CMV)
  • Congenital Rubella
  • Congenital Syphilis
  • Congenital Toxoplasmosis
  • Neonatal Conjunctivitis
  • Neonatal Hepatitis B Virus Infection
  • Neonatal Herpes Simplex Virus (HSV) Infection
  • Neonatal Hospital-Acquired Infection
  • Neonatal Listeriosis
  • Neonatal Bacterial Meningitis
  • Neonatal Pneumonia
  • Neonatal Sepsis
  • Perinatal Tuberculosis (TB)
 
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Overview of Neonatal Infections

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Neonatal infection can be acquired in utero transplacentally, through the birth canal during delivery (intrapartum), and from external sources after birth (postpartum).

In utero infection, which can occur any time before birth, results from overt or subclinical maternal infection. Consequences depend on the agent and timing of infection in gestation and include spontaneous abortion, intrauterine growth restriction, premature birth, stillbirth, congenital malformation (eg, rubella), and symptomatic neonatal infection (eg, cytomegalovirus [CMV], toxoplasmosis, syphilis).

Common viral agents include herpes simplex, HIV, CMV, and hepatitis B. Intrapartum infection with HIV or hepatitis B occurs from passage through an infected birth canal or by ascending infection if delivery is delayed after rupture of membranes; these viruses can less commonly be transmitted transplacentally. CMV is commonly transmitted transplacentally. Bacterial agents include group B streptococci, enteric gram-negative organisms (primarily Escherichia coli), gonococci, and chlamydiae.

Postpartum infections are acquired from contact with an infected mother either directly (eg, TB, which also is sometimes transmitted in utero) or through breastfeeding (eg, HIV, CMV) or from contact with health care practitioners and the hospital environment (numerous organisms—see Infections in Neonates: Neonatal Hospital-Acquired Infection).

Risk factors: Risk of contracting intrapartum and postpartum infection is inversely proportional to gestational age. Neonates are immunologically immature, with decreased polymorphonuclear leukocyte and monocyte function; premature infants are particularly so (see also Perinatal Physiology: Immunologic function). Maternal IgG antibodies are actively transported across the placenta, but effective levels for all organisms are not achieved until near term. IgM antibodies do not cross the placenta. Premature infants have decreased intrinsic antibody production and reduced complement activity. Premature infants are also more likely to require invasive procedures (eg, endotracheal intubation, prolonged IV access) that predispose to infection.

Symptoms and Signs

Symptoms and signs in neonates tend to be nonspecific (eg, vomiting, fever, petechiae, rashes, diarrhea, fever, hypothermia). Many congenital infections acquired before birth can cause or be accompanied by various symptoms or abnormalities (eg, growth restriction, deafness, microcephaly, anomalies, failure to thrive, hepatosplenomegaly, neurologic abnormalities).

Diagnosis

A wide variety of infections should be considered in neonates who are ill, febrile, or hypothermic. Infections such as congenital rubella, syphilis, toxoplasmosis, and CMV should be considered, particularly in neonates with abnormalities such as growth restriction, deafness, microcephaly, anomalies, failure to thrive, hepatosplenomegaly, or neurologic abnormalities.

Treatment

  • Antimicrobial therapy

The primary treatment is usually antimicrobial therapy. Drug selection is similar to that in adults, because infecting organisms and their sensitivities are not specific to neonates. However, numerous factors, including age and weight, affect dose and frequency (see Table 1: Infections in Neonates: Recommended Dosages of Selected Parenteral Antibiotics for NeonatesTables and Table 2: Infections in Neonates: Recommended Dosages of Selected Oral Antibiotics for Neonates*Tables).

Table 1

PrintOpen table in new window Open table in new window
Recommended Dosages of Selected Parenteral Antibiotics for Neonates

Interval of Administration

Antibiotic

Route of Administration

Individual Dose

Body Weight < 1200 g

Body Weight 1200 – 1999 g

Body Weight ≥ 2000 g

Age

Age

Age

≤ 7 days

8–28 days

0–7 days

≥ 8 days

0–7 days

≥ 8 days

Comments

AmikacinSome Trade Names
AMIKIN
Click for Drug Monograph
*

IV, IM

7.5–10 mg/kg

q 18–24 h

q 18–24 h

q 12 h

q 8 h

q 12 h

q 8 h

Monitoring of serum drug levels required (peak = 20–30 μg/mL; trough = < 10 μg/mL)

Dose reduction required for impaired renal function

For term neonates, may be given as a single dose of 15–20 mg/kg/day

Amphotericin BSome Trade Names
ABELCET
AMBISOME
AMPHOCIN
AMPHOTEC
Click for Drug Monograph

IV

0.25–1 mg/kg

After dilution in 5% or 10% D/W (saline solution should not be used), infusion of a test dose of 0.1 mg/kg (maximum 1 mg) over 1 h to assess patient's febrile and hemodynamic response;† if no serious adverse effects are observed, infusion of a therapeutic dose (usually 0.25–1.25 mg/kg over 2–4 h), which may be given the same day as the test dose

After the patient improves, may give the dose every other day until therapy is complete

Monitoring of K levels and hematologic and renal functions required

AmpicillinSome Trade Names
OMNIPEN
PRINCIPEN
Click for Drug Monograph

For meningitis

IV

50 mg/kg

q 12 h

q 12 h

q 12 h

q 8 h

q 8 h

q 6 h

IV as 15– to 30-min infusion (≤ 10 mg/kg/min)

For other diseases

IV, IM

25 mg/kg

q 12 h

q 12 h

q 12 h

q 8 h

q 8 h

q 6 h

AztreonamSome Trade Names
AZACTAM
Click for Drug Monograph

IV, IM

30 mg/kg

q 12 h

q 12 h

q 12 h

q 8 h

q 8 h

q 6 h

Limited data

For gram-negative bacilli only

CefazolinSome Trade Names
ANCEF
KEFZOL
Click for Drug Monograph
‡

IV, IM

20 mg/kg

q 12 h

q 12 h

q 12 h

q 12 h

q 12 h

q 8 h

Limited data

No primary indication; not used as initial therapy for sepsis or meningitis

CefepimeSome Trade Names
MAXIPIME
Click for Drug Monograph

IV, IM

30 mg/kg

q 12 h

q 12 h until age 14 days

q 12 h

q 12 h until age 14 days

q 12 h

q 12 h until age 14 days

May be used for Pseudomonas aeruginosa infections

Sometimes used for meningitis, although usually as a 2nd-line drug and not always recommended

50 mg/kg

—

q 8–12 h if age > 14 days

—

q 8–12 h if age > 14 days

—

q 8–12 h if age > 14 days

CefotaximeSome Trade Names
CLAFORAN
Click for Drug Monograph

IV, IM

50 mg/kg

q 12 h

q 8–12 h

q 12 h

q 8 h

q 8–12 h

q 6–8 h

Often a first-line therapy for neonatal meningitis

CeftazidimeSome Trade Names
FORTAZ
TAZICEF
Click for Drug Monograph

IV, IM

50 mg/kg

q 12 h

q 8 h

q 12 h

q 8 h

q 8 h

q 8 h

Penetrates well into inflamed meninges

70–90% of drug excreted unchanged in urine

CeftriaxoneSome Trade Names
ROCEPHIN
Click for Drug Monograph

IV, IM

25–50 mg/kg

q 24–36 h

q 24–36 h

q 24 h

q 24 h

q 24 h

q 24 h

Limited data

May cause biliary pseudolithiasis and, in jaundiced premature infants, may increase risk of bilirubin encephalopathy via displacement of bilirubin from albumin

Contraindicated for 48 h after the infusion of Ca-containing solutions in infants ≤ 28 days

For meningitis, 40–50 mg/kg q 12 h or 80–100 mg/kg q 24 h

ChloramphenicolSome Trade Names
CHLOROMYCETIN
Click for Drug Monograph

IV

25 mg/kg

q 24 h

q 24 h

q 24 h

q 24 h

q 24 h

q 12 h

Doses adjusted by monitoring serum drug levels and hematologic parameters

For meningitis, desired peak serum levels = 15–25 μg/mL and trough levels = 5–15 μg/mL

For other infections, dose adjusted to attain a peak level of 10–20 μg/mL and a trough level of 5–10 μg/mL

Large variability in serum levels and serum half life, especially in preterm neonates

ClindamycinSome Trade Names
CLEOCIN
Click for Drug Monograph

IV, IM

5 mg/kg

q 12 h

q 12 h

q 12 h

q 8 h

q 8 h

q 6 h

For anaerobes and gram-positive cocci (not enterococci)

GentamicinSome Trade Names
GARAMYCIN
Click for Drug Monograph
*

IV, IM

2.5 mg/kg

q 18–24 h

q 18–24 h

q 12 h

q 8–12 h

q 12 h

q 8 h

Monitoring of serum drug levels required (peak = 4–12 μg/mL; trough = 0.5–2 μg/mL)

Dose reduction required for impaired renal function

Reduction in frequency (to q 18–24 h) for very small, premature infants

For term infants, possibly gentamicinSome Trade Names
GARAMYCIN
Click for Drug Monograph
4 mg/kg q 24 h (peak serum levels are 2–3 times higher)

Imipenem

IV

20–25 mg/kg

q 18–24 h

q 18–24 h

q 12 h

q 12 h

q 12 h

q 8 h

Limited data

KanamycinSome Trade Names
KANTREX
Click for Drug Monograph
*

IV, IM

7.5–10 mg/kg

q 18–24 h

q 18–24 h

q 12–18 h

q 8–12 h

q 12 h

q 8 h

Monitoring of serum drug levels required (peak = 20–30 μg/mL; trough serum level should be < 10 μg/mL)

Dose reduction required for impaired renal function

Reduction in frequency (to q 18–24 h) required for very small, premature infants

MetronidazoleSome Trade Names
FLAGYL
Click for Drug Monograph

IV

7.5 mg/kg

q 24–48 h

q 24–48 h

q 24 h

q 12 h

q 12 h

15 mg q 12 h

Limited data

Loading dose of 15 mg/kg, then a subsequent dose 48 h later in preterm infants and 24 h later in term infants and then q 12 h

NafcillinSome Trade Names
UNIPEN
Click for Drug Monograph

For meningitis or endocarditis

IV

50 mg/kg

q 12 h

q 12 h

q 12 h

q 8 h

q 8 h

q 6 h

Monitoring of CBC and liver function required

Primarily excreted via the biliary tract

In jaundiced neonates, possible accumulation in serum, which may have adverse effects

For other diseases

IV, IM

25 mg/kg

q 12 h

q 12 h

q 12 h

q 8 h

q 8 h

—

37.5 mg/kg

—

—

—

—

—

q 6 h

OxacillinSome Trade Names
BACTOCILL
PROSTAPHLIN
Click for Drug Monograph

For meningitis or endocarditis

IV

50 mg/kg

q 12 h

q 12 h

q 12 h

q 8 h

q 8 h

q 6 h

For other diseases

IV, IM

25 mg/kg

q 12 h

q 12 h

q 12 h

q 8 h

q 8 h

—

37.5 mg/kg

—

—

—

—

—

q 6 h

Penicillin GSome Trade Names
BICILLIN
WYCILLIN
Click for Drug Monograph
, aqueous

For meningitis

IV

50,000–75,000 units/kg

q 12 h

q 12 h

q 12 h

q 8 h

q 8 h

q 6 h

Maximum for group B streptococcal meningitis = 500,000 units/kg/day

For most other diseases

IV, IM

25,000 units/kg

q 12 h

q 12 h

q 12 h

q 8 h

q 8 h

q 6 h

Penicillin GSome Trade Names
BICILLIN
WYCILLIN
Click for Drug Monograph
, procaine

IM

50,000 units/kg

Not recommended

Not recommended

q 24 h

q 24 h

q 24 h

q 24 h

Caution: Sterile abscess and procaine toxicity

Piperacillin/TazobactamSome Trade Names
ZOSYN

IV (dose based on piperacillinSome Trade Names
PIPRACIL
Click for Drug Monograph
component)

50 mg/kg

q 12 h

—

q 12 h

—

—

—

May be increased to 100 mg/kg q 6 h in infants > 28 days

100 mg/kg

—

q 8 h

—

q 8 h

q 12 h

q 8 h

TobramycinSome Trade Names
NEBCIN
TOBI
TOBREX
Click for Drug Monograph
*

IV, IM

2.5 mg/kg

q 18–24 h

q 18–24 h

q 12 h

q 8–12 h

q 12 h

q 8 h

Monitoring of serum drug levels (peak = 4–12 μg/mL; trough serum level should be < 2 μg/mL)

Dose reduction required for impaired renal function

Reduction in frequency (to q 18–24 h) required for very small, premature infants

For term neonates, may be given as 4 mg/kg once/day (peak serum levels are 2–4 times higher with once/day dosing)

VancomycinSome Trade Names
VANCOCIN
Click for Drug Monograph

IV

10–15 mg/kg

q 24 h

q 24 h

q 12–18 h

q 8–12 h

q 8–12 h

q 6–8 h

Loading dose of 15–20 mg/kg recommended by some clinicians

Given by slow IV infusion, over at least 60 min

Monitoring of serum trough level recommended (trough = 10–15 μg/mL)

Doses adjusted in patients with renal failure

For premature infants < 1000 g, 15 mg/kg q 24–36 h

*Sample should be obtained 30 min after a 30-min IV infusion.

†The need to administer a test dose of amphotericin BSome Trade Names
ABELCET
AMBISOME
AMPHOCIN
AMPHOTEC
Click for Drug Monograph
is controversial.

‡ CefazolinSome Trade Names
ANCEF
KEFZOL
Click for Drug Monograph
does not cross the blood-brain barrier.

Recommended Dosages of Selected Parenteral Antibiotics for Neonates

Interval of Administration

Antibiotic

Route of Administration

Individual Dose

Body Weight < 1200 g

Body Weight 1200 – 1999 g

Body Weight ≥ 2000 g

Age

Age

Age

≤ 7 days

8–28 days

0–7 days

≥ 8 days

0–7 days

≥ 8 days

Comments

AmikacinSome Trade Names
AMIKIN
Click for Drug Monograph
*

IV, IM

7.5–10 mg/kg

q 18–24 h

q 18–24 h

q 12 h

q 8 h

q 12 h

q 8 h

Monitoring of serum drug levels required (peak = 20–30 μg/mL; trough = < 10 μg/mL)

Dose reduction required for impaired renal function

For term neonates, may be given as a single dose of 15–20 mg/kg/day

Amphotericin BSome Trade Names
ABELCET
AMBISOME
AMPHOCIN
AMPHOTEC
Click for Drug Monograph

IV

0.25–1 mg/kg

After dilution in 5% or 10% D/W (saline solution should not be used), infusion of a test dose of 0.1 mg/kg (maximum 1 mg) over 1 h to assess patient's febrile and hemodynamic response;† if no serious adverse effects are observed, infusion of a therapeutic dose (usually 0.25–1.25 mg/kg over 2–4 h), which may be given the same day as the test dose

After the patient improves, may give the dose every other day until therapy is complete

Monitoring of K levels and hematologic and renal functions required

AmpicillinSome Trade Names
OMNIPEN
PRINCIPEN
Click for Drug Monograph

For meningitis

IV

50 mg/kg

q 12 h

q 12 h

q 12 h

q 8 h

q 8 h

q 6 h

IV as 15– to 30-min infusion (≤ 10 mg/kg/min)

For other diseases

IV, IM

25 mg/kg

q 12 h

q 12 h

q 12 h

q 8 h

q 8 h

q 6 h

AztreonamSome Trade Names
AZACTAM
Click for Drug Monograph

IV, IM

30 mg/kg

q 12 h

q 12 h

q 12 h

q 8 h

q 8 h

q 6 h

Limited data

For gram-negative bacilli only

CefazolinSome Trade Names
ANCEF
KEFZOL
Click for Drug Monograph
‡

IV, IM

20 mg/kg

q 12 h

q 12 h

q 12 h

q 12 h

q 12 h

q 8 h

Limited data

No primary indication; not used as initial therapy for sepsis or meningitis

CefepimeSome Trade Names
MAXIPIME
Click for Drug Monograph

IV, IM

30 mg/kg

q 12 h

q 12 h until age 14 days

q 12 h

q 12 h until age 14 days

q 12 h

q 12 h until age 14 days

May be used for Pseudomonas aeruginosa infections

Sometimes used for meningitis, although usually as a 2nd-line drug and not always recommended

50 mg/kg

—

q 8–12 h if age > 14 days

—

q 8–12 h if age > 14 days

—

q 8–12 h if age > 14 days

CefotaximeSome Trade Names
CLAFORAN
Click for Drug Monograph

IV, IM

50 mg/kg

q 12 h

q 8–12 h

q 12 h

q 8 h

q 8–12 h

q 6–8 h

Often a first-line therapy for neonatal meningitis

CeftazidimeSome Trade Names
FORTAZ
TAZICEF
Click for Drug Monograph

IV, IM

50 mg/kg

q 12 h

q 8 h

q 12 h

q 8 h

q 8 h

q 8 h

Penetrates well into inflamed meninges

70–90% of drug excreted unchanged in urine

CeftriaxoneSome Trade Names
ROCEPHIN
Click for Drug Monograph

IV, IM

25–50 mg/kg

q 24–36 h

q 24–36 h

q 24 h

q 24 h

q 24 h

q 24 h

Limited data

May cause biliary pseudolithiasis and, in jaundiced premature infants, may increase risk of bilirubin encephalopathy via displacement of bilirubin from albumin

Contraindicated for 48 h after the infusion of Ca-containing solutions in infants ≤ 28 days

For meningitis, 40–50 mg/kg q 12 h or 80–100 mg/kg q 24 h

ChloramphenicolSome Trade Names
CHLOROMYCETIN
Click for Drug Monograph

IV

25 mg/kg

q 24 h

q 24 h

q 24 h

q 24 h

q 24 h

q 12 h

Doses adjusted by monitoring serum drug levels and hematologic parameters

For meningitis, desired peak serum levels = 15–25 μg/mL and trough levels = 5–15 μg/mL

For other infections, dose adjusted to attain a peak level of 10–20 μg/mL and a trough level of 5–10 μg/mL

Large variability in serum levels and serum half life, especially in preterm neonates

ClindamycinSome Trade Names
CLEOCIN
Click for Drug Monograph

IV, IM

5 mg/kg

q 12 h

q 12 h

q 12 h

q 8 h

q 8 h

q 6 h

For anaerobes and gram-positive cocci (not enterococci)

GentamicinSome Trade Names
GARAMYCIN
Click for Drug Monograph
*

IV, IM

2.5 mg/kg

q 18–24 h

q 18–24 h

q 12 h

q 8–12 h

q 12 h

q 8 h

Monitoring of serum drug levels required (peak = 4–12 μg/mL; trough = 0.5–2 μg/mL)

Dose reduction required for impaired renal function

Reduction in frequency (to q 18–24 h) for very small, premature infants

For term infants, possibly gentamicinSome Trade Names
GARAMYCIN
Click for Drug Monograph
4 mg/kg q 24 h (peak serum levels are 2–3 times higher)

Imipenem

IV

20–25 mg/kg

q 18–24 h

q 18–24 h

q 12 h

q 12 h

q 12 h

q 8 h

Limited data

KanamycinSome Trade Names
KANTREX
Click for Drug Monograph
*

IV, IM

7.5–10 mg/kg

q 18–24 h

q 18–24 h

q 12–18 h

q 8–12 h

q 12 h

q 8 h

Monitoring of serum drug levels required (peak = 20–30 μg/mL; trough serum level should be < 10 μg/mL)

Dose reduction required for impaired renal function

Reduction in frequency (to q 18–24 h) required for very small, premature infants

MetronidazoleSome Trade Names
FLAGYL
Click for Drug Monograph

IV

7.5 mg/kg

q 24–48 h

q 24–48 h

q 24 h

q 12 h

q 12 h

15 mg q 12 h

Limited data

Loading dose of 15 mg/kg, then a subsequent dose 48 h later in preterm infants and 24 h later in term infants and then q 12 h

NafcillinSome Trade Names
UNIPEN
Click for Drug Monograph

For meningitis or endocarditis

IV

50 mg/kg

q 12 h

q 12 h

q 12 h

q 8 h

q 8 h

q 6 h

Monitoring of CBC and liver function required

Primarily excreted via the biliary tract

In jaundiced neonates, possible accumulation in serum, which may have adverse effects

For other diseases

IV, IM

25 mg/kg

q 12 h

q 12 h

q 12 h

q 8 h

q 8 h

—

37.5 mg/kg

—

—

—

—

—

q 6 h

OxacillinSome Trade Names
BACTOCILL
PROSTAPHLIN
Click for Drug Monograph

For meningitis or endocarditis

IV

50 mg/kg

q 12 h

q 12 h

q 12 h

q 8 h

q 8 h

q 6 h

For other diseases

IV, IM

25 mg/kg

q 12 h

q 12 h

q 12 h

q 8 h

q 8 h

—

37.5 mg/kg

—

—

—

—

—

q 6 h

Penicillin GSome Trade Names
BICILLIN
WYCILLIN
Click for Drug Monograph
, aqueous

For meningitis

IV

50,000–75,000 units/kg

q 12 h

q 12 h

q 12 h

q 8 h

q 8 h

q 6 h

Maximum for group B streptococcal meningitis = 500,000 units/kg/day

For most other diseases

IV, IM

25,000 units/kg

q 12 h

q 12 h

q 12 h

q 8 h

q 8 h

q 6 h

Penicillin GSome Trade Names
BICILLIN
WYCILLIN
Click for Drug Monograph
, procaine

IM

50,000 units/kg

Not recommended

Not recommended

q 24 h

q 24 h

q 24 h

q 24 h

Caution: Sterile abscess and procaine toxicity

Piperacillin/TazobactamSome Trade Names
ZOSYN

IV (dose based on piperacillinSome Trade Names
PIPRACIL
Click for Drug Monograph
component)

50 mg/kg

q 12 h

—

q 12 h

—

—

—

May be increased to 100 mg/kg q 6 h in infants > 28 days

100 mg/kg

—

q 8 h

—

q 8 h

q 12 h

q 8 h

TobramycinSome Trade Names
NEBCIN
TOBI
TOBREX
Click for Drug Monograph
*

IV, IM

2.5 mg/kg

q 18–24 h

q 18–24 h

q 12 h

q 8–12 h

q 12 h

q 8 h

Monitoring of serum drug levels (peak = 4–12 μg/mL; trough serum level should be < 2 μg/mL)

Dose reduction required for impaired renal function

Reduction in frequency (to q 18–24 h) required for very small, premature infants

For term neonates, may be given as 4 mg/kg once/day (peak serum levels are 2–4 times higher with once/day dosing)

VancomycinSome Trade Names
VANCOCIN
Click for Drug Monograph

IV

10–15 mg/kg

q 24 h

q 24 h

q 12–18 h

q 8–12 h

q 8–12 h

q 6–8 h

Loading dose of 15–20 mg/kg recommended by some clinicians

Given by slow IV infusion, over at least 60 min

Monitoring of serum trough level recommended (trough = 10–15 μg/mL)

Doses adjusted in patients with renal failure

For premature infants < 1000 g, 15 mg/kg q 24–36 h

*Sample should be obtained 30 min after a 30-min IV infusion.

†The need to administer a test dose of amphotericin BSome Trade Names
ABELCET
AMBISOME
AMPHOCIN
AMPHOTEC
Click for Drug Monograph
is controversial.

‡ CefazolinSome Trade Names
ANCEF
KEFZOL
Click for Drug Monograph
does not cross the blood-brain barrier.

Table 2

PrintOpen table in new window Open table in new window
Recommended Dosages of Selected Oral Antibiotics for Neonates*

Antibiotic

Dosage

Interval

Comments

AmoxicillinSome Trade Names
AMOXIL
TRIMOX
Click for Drug Monograph

15 mg/kg

q 8 h

Limited data

AzithromycinSome Trade Names
ZITHROMAX
Click for Drug Monograph

5–10 mg/kg

q 24 h

Preferred drug for treatment or prevention of pertussis in neonates < 1 mo

For treatment or prevention of pertussis, 10 mg/kg given once/day for 5 days

For most other infections, 10 mg/kg given on day 1 and then 5 mg/kg given on days 2–5

ClindamycinSome Trade Names
CLEOCIN
Click for Drug Monograph
†

5 mg/kg

q 6–8 h

Limited data

ErythromycinSome Trade Names
ERY-TAB
ERYTHROCIN
Click for Drug Monograph
ethylsuccinate

10 mg/kg

q 6–12 h

For chlamydial infections or pertussis in neonates > 1 mo

Associated with idiopathic hypertrophic pyloric stenosis

FluconazoleSome Trade Names
DIFLUCAN
Click for Drug Monograph

3–6 mg/kg

q 24–72 h

For minor candidal infections, 6 mg/kg on day 1, then 3 mg/kg/dose q 24–72 h

For serious infections, 12 mg/kg once/day recommend for all gestational and postnatal ages

A first (loading) dose of 25 mg/kg also possibly considered

During the 1st 2 wk of life, adjustment of dosing interval possibly necessary if renal function is abnormal

FlucytosineSome Trade Names
ANCOBON
Click for Drug Monograph

12.5–37.5 mg/kg

q 6 h

Limited data

Used only with amphotericin BSome Trade Names
ABELCET
AMBISOME
AMPHOCIN
AMPHOTEC
Click for Drug Monograph
to slow emergence of resistance

Monitoring of levels recommended

NeomycinSome Trade Names
NEO-FRADIN
NEO-RX
Click for Drug Monograph
sulfate

33 mg/kg

q 8 h

For gastroenteritis caused by enteropathogenic strains of Escherichia coli

May be systemically absorbed in neonates with severe diarrhea

RifampinSome Trade Names
RIFADIN
RIMACTANE
Click for Drug Monograph

10 mg/kg

q 24 h

For TB

5 mg/kg

q 12 h

For meningococcus prophylaxis, given for 2 days

10 mg/kg

q 24 h

For Haemophilus influenzae prophylaxis, given for 4 days

*Unless otherwise stated, doses are for neonates who are > 7 days and > 2000 g.

†The dose for neonates who are < 7 days old < 2000 g is 5 mg/kg q 12 h.

In neonates, the ECF constitutes up to 45% of total body weight, requiring relatively larger doses of certain antibiotics (eg, aminoglycosides) compared with adults. Lower serum albumin concentrations in premature infants may reduce antibiotic protein binding. Drugs that displace bilirubin from albumin (eg, sulfonamides, ceftriaxoneSome Trade Names
ROCEPHIN
Click for Drug Monograph
) increase the risk of kernicterus.

Absence or deficiency of certain enzymes in neonates may prolong the half-life of certain antibiotics (eg, chloramphenicolSome Trade Names
CHLOROMYCETIN
Click for Drug Monograph
) and increase the risk of toxicity. Changes in GFR and renal tubular secretion during the first month of life necessitate dosing changes for other drugs (eg, penicillins, aminoglycosides, vancomycinSome Trade Names
VANCOCIN
Click for Drug Monograph
).

Last full review/revision October 2009 by Mary T. Caserta, MD

Content last modified February 2012

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