nicu case presentation jon palma, md neonatology fellow march 2010

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NICU Case Presentation Jon Palma, MD Neonatology Fellow March 2010

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Page 1: NICU Case Presentation Jon Palma, MD Neonatology Fellow March 2010

NICU Case Presentation

Jon Palma, MDNeonatology Fellow

March 2010

Page 2: NICU Case Presentation Jon Palma, MD Neonatology Fellow March 2010

Clinical scenario

You are called to attend a delivery in L&D for a diagnosis of maternal chorioamnionitis.

Upon entering the delivery room, what minimal information must you obtain (according to NRP guidelines)?

Page 3: NICU Case Presentation Jon Palma, MD Neonatology Fellow March 2010

Question 1

Upon entering the delivery room, what minimal information must you obtain (according to NRP guidelines)?

•Singleton or multiple gestation•Estimated gestational age•Presence of meconium

Page 4: NICU Case Presentation Jon Palma, MD Neonatology Fellow March 2010

Case (cont’d): in the delivery room

The OB team tells you: Mom is a G1 P0 at 38 weeks, and meconium is not present. You were called because chorioamnionitis was diagnosed

for a fever of 38.3 celsius

Next questions: What are the diagnostic criteria for chorioamnionitis? In regards to sepsis risk factors, what items must you

determine from mom’s history? At LPCH, for what indications do we perform full sepsis

evaluations on newborn infants?

Page 5: NICU Case Presentation Jon Palma, MD Neonatology Fellow March 2010

Question 2What are the diagnostic criteria for

chorioamnionitis?

The essential clinical criteria is maternal fever > 38 degrees C (100.4 F); other criteria are insensitive.

For clinical research, diagnosis is typically based upon the presence of maternal fever and at least two of the following: Maternal leukocytosis (>15,000 cells/cubic millimeter) Maternal tachycardia (>100 beats/minute) Fetal tachycardia (>160 beats/minute) Uterine tenderness Foul smelling amniotic fluid

Bottom line: chorioamnionitis is a clinical diagnosis made by the obstetrician. If they say it’s chorio, then it is.

Page 6: NICU Case Presentation Jon Palma, MD Neonatology Fellow March 2010

Question 3:In regards to sepsis risk factors, what items must you determine from mom’s history?

Estimated gestation Preterm labor

Rupture of membranes (ROM) Prolonged ROM (PROM): >18 hrs Premature preterm ROM (PPROM):

ROM prior to the onset of labor at a gestation of <37 weeks

GBS status Including history of a prior infant with GBS infection

Page 7: NICU Case Presentation Jon Palma, MD Neonatology Fellow March 2010

Odds Ratios for Neonatal Sepsis Associated with Maternal Risk

Factors

Page 8: NICU Case Presentation Jon Palma, MD Neonatology Fellow March 2010

Question 4:At LPCH, for what indications do we perform full sepsis evaluations on newborn infants?

Certain babies are at such high risk for infection that they should be admitted to the NICU, regardless of clinical appearance. They should undergo a complete evaluation for possible sepsis and be started on empiric antibiotic therapy until infection is ruled out. These babies include those whose mothers have: premature pre-term ROM chorioamnionitis a history of having a prior infant with GBS infection*

Source: NICU Manual

*If mother received adequate IP prophylaxis, the CDC guidelines support observation, but clinicians and parents may opt for a complete diagnostic evaluation

Page 9: NICU Case Presentation Jon Palma, MD Neonatology Fellow March 2010

CDC GuidelinesApproach for empiric management of newborns born to women who

receive intrapartum antibiotics to prevent early-onset GBS disease or to treat suspected chorioamnionitis

Note: in the setting of adequate intrapartum antibiotic prophylaxis for GBS and no concern for chorio, labs are not required but a 48 hour observation period is recommended (no early discharge)

Page 10: NICU Case Presentation Jon Palma, MD Neonatology Fellow March 2010

Adequate IAP Penicillin, ampicillin, or cefazolin > 4 hrs before delivery

Penicillin is the agent of choice (narrower spectrum) Clindamycin or erythromycin > 4 hrs before delivery in:

Penicillin-allergic women at high risk for anaphylaxis With GBS isolates sensitive to clinda or erythro

Vancomycin > 4 hrs before delivery in: Penicillin-allergic women at high risk for anaphylaxis When clinda or erythro are not options because of in vitro

resistance or unknown susceptibility

Without susceptibility testing of GBS isolates clindamycin is not considered adequate IAP Usually would not send screening labs, but use clinical

judgment

CDC GuidelinesIntrapartum Antibiotic Prophylaxis (IAP)

Page 11: NICU Case Presentation Jon Palma, MD Neonatology Fellow March 2010

Case (cont’d): over to the NICU

The baby required only routine resuscitation (warmth, drying, suctioning, and stimulation) and had APGAR scores of 8 at one minute and 9 at five minutes of life.

You proceed to the NICU to perform a full sepsis evaluation.

What constitutes a full sepsis evaluation of a newborn in the LPCH NICU, including laboratory studies and empiric antibiotics?

Page 12: NICU Case Presentation Jon Palma, MD Neonatology Fellow March 2010

Question 5:What constitutes a full sepsis evaluation of a newborn

in the LPCH NICU, including laboratory studies and empiric antibiotics? CBC with differential, blood culture, glucose

2 CRPs at least 24h apart The first CRP should be drawn at > 8h after birth or after the blood culture is drawn,

whichever is later

Lumbar puncture Tube 1: CSF glucose, protein Tube 2: CSF culture/gram stain (changed to tube 2 to decrease false +’s) Tube 3: CSF cell count/diff Tube 4: if needed for other studies (e.g. HSV PCR)

Empiric antibiotics (while awaiting culture(s), CRPs) Ampicillin 50mg/kg IV q6h (meningitic dose100 mg/kg IV q6h for sicker babies) Gentamicin 4mg/kg IV loading dose, followed by 3 mg/kg IV q24h

For infants with respiratory symptoms CXR ETT aspirate (if intubated)

Page 13: NICU Case Presentation Jon Palma, MD Neonatology Fellow March 2010

from Pediatrics 1998; 102 (4): e41

“Serial CRP levels are useful in the diagnostic evaluation of neonates with suspected infection. Two CRP levels <1 mg/dL obtained 24 hours apart, 8 to 48 hours after presentation, indicate that bacterial infection is unlikely.”

“Serial CRP levels are useful in the diagnostic evaluation of neonates with suspected infection. Two CRP levels <1 mg/dL obtained 24 hours apart, 8 to 48 hours after presentation, indicate that bacterial infection is unlikely.”

Page 14: NICU Case Presentation Jon Palma, MD Neonatology Fellow March 2010

CRP has excellent negative predictive value

In the study, CRP #2 was the lab sent at least 8 hours after the initial evaluation, and CRP #3 was sent 24 hours later. CRP #1 was done at the time of the initial evaluation.

Page 15: NICU Case Presentation Jon Palma, MD Neonatology Fellow March 2010

What About ET Aspirates and Urine Specimens?

For babies who have just been intubated for respiratory distress and have an infiltrate on chest x-ray, culture of an endotracheal aspirate will be positive in approximately 8%. Fewer than half of these positive cultures are associated with positive blood cultures, so don’t forget to order an endotracheal aspirate Gram stain and culture.

Urine cultures are rarely positive in the first 48 hours of life. After that, they may be quite helpful. Because they are almost always contaminated, often with a single organism, bag urine specimens are useless. Specimens obtained by catheterization of the bladder are better, but also have a surprisingly high contamination rate. Learn to do suprapubic aspirates for urine cultures in neonates.

Source: NICU Manual

Page 16: NICU Case Presentation Jon Palma, MD Neonatology Fellow March 2010

Question 6:How do the LPCH NICU practices vary from CDC

guidelines?

*

*The CDC will be revising its guidelines in 2010 to clarify that for infants who are admitted because of risk factors (chorio) but are well appearing, the lumbar puncture may be deferred

Page 17: NICU Case Presentation Jon Palma, MD Neonatology Fellow March 2010

Question 6:How do the LPCH NICU practices vary from CDC

guidelines? CRP not part of CDC guidelines Lumbar puncture is always performed when an infant

demonstrates clinical symptoms of possible sepsis Rationale: there is no surrogate blood test for meningitis; only

CSF analysis provide diagnostic clues, and a diagnosis of meningitis impacts length of antibiotic therapy. Blood cultures are negative in about 1/3 of meningitis cases and thus should not be used in lieu of

Limited evaluation at LPCH does not include a blood culture Rationale: if the index of suspicion is high enough to perform a

blood culture, treatment with antibiotics is warranted What is the approach to sepsis screening in the LPCH Well Baby

Nursery? LPCH Well Baby Nursey Website - Sepsis Screen

Page 18: NICU Case Presentation Jon Palma, MD Neonatology Fellow March 2010

Practical Aspects of the Sepsis Evaluation

Draw the blood culture as soon as possible - preferably before antibiotics are given, but start treatment without delay. The initial dose of ampicillin can be given as an IV bolus, and the first dose of gentamicin can be given IM if the infant is not in shock.

As many as 50% of neonates with meningitis may have negative blood cultures, so the CSF culture may be the only source of a bacteriologic diagnosis. Do the LP as soon as possible; it is not appropriate to defer it for a few hours, either for the convenience of the caretakers or until the baby is more stable.

Source: NICU Manual

Page 19: NICU Case Presentation Jon Palma, MD Neonatology Fellow March 2010

Question 7:How are CRP results generally interpreted and

managed in the LPCH NICU?

In an asymptomatic infant with negative cultures:

In a symptomatic infant with negative cultures: Discuss with your attending

CRP < 1 negative d/c abx if CRP negative x 2 (24h apart)*

CRP 1 – 2

indeterminate

Follow up CRP in 24 hours

CRP > 2 positive Discuss with your attending regarding duration of abx

*Note: the NPV of serial CRPs means that antibiotics may be discontinued prior to the blood culture reaching 48 hours

Page 20: NICU Case Presentation Jon Palma, MD Neonatology Fellow March 2010

Question 8:What is the duration of treatment for neonates

with confirmed serious bacterial infections? Positive blood culture*, UTI, or pneumonia

Coag-negative Staph: 7d Other gram-positives: 10d Gram-negatives: 14d Candida: 21d

Meningitis#

Gram-positive: 14d Gram-negative: 21d

* Count should begin from first negative culture# Repeat lumbar puncture recommended to document negative culture prior to discontinuing antibiotics

Page 21: NICU Case Presentation Jon Palma, MD Neonatology Fellow March 2010

Additional references

Uptodate.com (Intraamniotic infections) Benitz. Suspected sepsis in newborn infants. NICU

Manual. http://www.cdc.gov/groupbstrep/guidelines/

summary.htm http://newborns.stanford.edu/ClinicalGuidelines.html