Sepsis

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Neonatal Sepsis

Author: Sherrill Roskam RNC MN NNP CNS

Updated presentation: Susan Greenleaf RNC, BSN

Objectives

Identify major causative organisms and routes of transmission of sepsis.

Discuss clinical manifestations and modalities used in diagnosis of sepsis.

Describe antibiotic therapy used in the treatment of neonatal sepsis.

Sepsis

Definition: A systemic response to an invasive organism. Frequently signified by a positive blood culture.

A systemic illness due to the presence of bacteria and or bacterial toxins in the blood

Neonatal Immune System

Sepsis occurs in 1-8:1000 term infants and 1:250 premature infants

Neonates are immunocompromised even at term gestation

The neonatal immune system is functional at birth, but not mature

Sepsis

Two types of sepsis

Early-onset sepsis, with in the first

72 hours of life

Late-onset sepsis, those infections acquired later by horizontal transmission. Highest risk for the first month of life

Predisposing Factors: Pregnancy

Prematurity

PROM < 36 weeks

Prolonged ROM

Prolonged labor

Excessive manipulation

Predisposing Factors: Maternal

History of infection

Bacterial

Viral

History of GBS bacteriuria

History of previously affected infant

Temperature in labor

Predisposing Factors: Neonatal

Invasive procedures

Resuscitation

Intubation

IV starts / PICC lines

Umbilical Catheterization

Skin colonization

Predisposing Factors: Nursery

Humidifiers

Respiratory therapy equipment

Staff members

Unsterile equipment

Scales

Stethoscopes

Thermometers

Transmission

Transplacental

Ascending

Birth

Nosocomial

Antibodies

IgG

IgM

IgA

Human Immunoglobulins

Antibodies are the immunoglobulins produced in response to specific antigens

IgG is the only antibody that crosses the placenta and provides immuological protection over the first few months

Transfer peaks at 32 weeks gestation

Immunoglobulins cont.

IgM and IgA are directly responsible for antibodies against bacteria

Neonatal IgM production starts at 30 weeks gestation and increases over the first year of life

IgA passes through breast milk to provide early defense against infection. Found in the intestinal tract.

Causative Organisms:

Bacterial

Group B strep

E Coli

Haemophilus Influenzae

Coagulase Negative Staph

Staph Aureus

Neisseria Meningitis

Listeria

Causative Organisms: Viral

Maternal in origin

Toxoplasmosis

Rubella

Cytomegalovirus

Herpes

Hepatitis B

HIV

Recognition: Clinical Signs

Temperature instability

Lethargy

Pallor, mottling, poor cap refill

Respiratory distress

Poor feeding

Apnea

Neurologic

Jaundice

Hypoglycemia

Recognition

Recognition is of utmost importance, because newborns with sepsis can get very sick very fast

Be aware of risk factors – review maternal history

Diagnostic tests for sepsis

CBC

Cultures

Blood ~ Most common Gold Standard

Urine

Surface - only indicates colonization

CSF Lumbar puncture

CRP

C-Reactive Protein

What is CRP?

Laboratory test that identifies an inflammatory response in the body.

Binds to Calcium and phosphocholine sites; forming CRP-ligand complexes.

CRP

CRP’s unique binding characteristics have led to the identification of elevated CRP levels in over 70 different infectious and

noninfectious disorders.

It is associated with acute and chronic inflammatory disorders.

CRP Continued. . .

Paired mother and infant sampling shows that CRP does not cross the placenta.

4 types of inflammatory response to tissue injury

Infectious, noninfectious, chemical, physical or immunologic toxins.

Use of CRP

2 schools of thought

Early diagnostic tool for confirming sepsis

Screening tool to r/o the presence of sepsis

CRP Levels: What is normal?

In the neonatal period: Level of 10mg/L is considered normal

Healthy full-term and preterm infants may range from 2 to 5mg/L during the first few days of life.

More than 1 Level?

Conflicting information about obtaining more than one level

Serial CRP levels drawn 12 to 24 hours after onset of S/S of sepsis may be superior to a single level.

More About the CBC: WBC

White cell count

Differential

Neutrophils - bacteria fighting cells

Polys, Segs - most mature

Bands - immature

Metas – really immature

Absolute Neutrophil Count

I:T Ratio

White Blood Cells

The main defense against invading microorganisms

Neutrophils (pack man cells) and macrophages(monocytes)

Circulating cells that migrate to sites of inflamation, ingesting and killing foreign material or bacteria (phagocytosis)

Small stores in neonates, not as effective in killing bacteria, quickly depleted

Differential of the WBC

Mature Neutrophils – Segmented

Immature Neutrophils – Bands

Monocytes

Basophils

Eosinophils

Lymphocytes

Neutrophils

As mature neutrophols (polys, segs, neuts, or PMNs) are mobilized and consumed in the presence of a pathogen, their numbers decrease and immature cells are released from the bone marrow.

Immature neutrophils (bands, metas or stabs)

Absolute Neutrophil Count

(ANC)

Helps determine how many neutrophils are available to fight bacterial infections

Premature infants have lower ANC than term infants

Must plot on the Manroe chart

How to calculate an ANC

Identify the immature and the mature neutrophils on the CBC.

Add the segs, bands and metas ( total number of neutrophils) together and turn it into a percentage

Multiply this number by the total

WBC

This resulting number is the ANC

Manroe Chart

WBC: 20,000

Differential is expressed as a percent of total white cells

Poly’s (Segs, Neuts): 48%

Bands

Lymphs:

Monos:

Eso:

12%

20%

17%

3%

ANC: Absolute number of neutrophils

WBC X % Neutrophils

ANC WBC X % Neutrophils

20,000 X .6 (60%) = 12,000

Manroe Chart

Immature to Total Ratio (I:T)

An Increased IT ratio is called a left shift.

It show an increase in the number of immature sells

An IT ratio of >.25 may indicate sepsis

I/T ratio: Ratio of immature to total neutrophils

___Bands + Meta___

Polys + Bands + Meta

WBC: 20,000

Differential is expressed as a percent of total white cells

Poly’s (Segs, Neuts): 48%

Bands

Lymphs:

Monos:

Eso:

12%

20%

17%

3%

I/T ratio: Bands + Metas

Polys + Bands + Metas

12/60=0.2 (not indicative of sepsis)

If WBC 3000 Polys 30 and Bands 15:

15/45=0.33 (indicative of sepsis)

3,000 X .45 (45%) = 1,350

Platelet Count

Normal Values

VLBW – 275,000 +/- 60,000

Preterm – 290,000 +/- 60,000

Term – 310,000 +/- 60,000

Infants with infection may have a low platelet count

Management

Support Systems

Neutral Thermal Environment

Monitor

Cardiac/Respiratory

Pulse Oximetry

Vital signs

Feedings

IV

Management (con’t)

Antibiotics

Ampicillin 50-100 mg/kg/dose IV q8-12 hours

Varies with gestation and age

Gentamicin 4 mg/kg/dose IV q24-48 hours

Varies with gestation

Give over 30 minutes

Monitor Gent levels

Antiviral

Acyclovir 20 mg/kg/dose IV q8

Give over 1 hour

Do not refrigerate

Prognosis

Prognosis depends on organism involved and when treatment started

A bit more practice

CBC results

WBC 10.4

Metamyelocytes 0

Band Neutrophils 14

Segmented neutrophils 5

Platelets 141,000

What is the ANC and the IT ratio?

CBC Practice

CBC results

WBC 1.3

Metamyelocytes 2

Band Neutrohils 17

Segmented Neutrophils 42

Platelets 262,000

Calculate the ANC and IT ratio

CBC Practice

CBC results

WBC 6.3

Metamyelocytes 6

Band Neutrophils 44

Segmented Neutrophils 23

Platelets 95,000

What is the ANC and the IT ratio?

Same patient, 6 hours later

CBC results

WBC 0.8

Metamyelocytes 2

Band Neutrophils 4

Segmented Neutrophils 2

Platelets 24,000

What is the ANC and IT ratio?

References

Behrman, R. E., Kliegman, R.M.,Editors (1998) Nelson

Essentials of Pediatrics, 3 rd Ed. Philadelphia: W.B.

Saunders Co.

Cloherty, J.P., Eichenwald, E.C., Stark, A.R. (2004) Manual

of Neonatal Care, 5 th Ed. Philadelphia: Lippincott, Williams

& Wilkins.

Hengst, J.M., The Role of C-Reactive Protein in the

Evaluation and Management of Infants with Suspected

Sepsis. Advances in Neonatal Care. 2003;3(1):3-13.

References

Karlsen, K.A. (2001) The S.TA.B.L.E. Program:

Transporting Newborns the S.T.A.B.L.E.Way, Learner

Manual, 8 th Ed.

Merenstein, G.B., Gardner, S.L. (2002) Handbook of

Neonatal Intensive Care, 5 th Ed. St. Louis:Mosby Inc.

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