Peds - Fever (3)

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    Fever in Neonates and Young

    Infants

    (0-3 months)

    K R Mahmood MDFAAP

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    Definition:

    Fever = 1-2C increase overnormal body temperature

    Axillary and Tympanictemperatures are unreliable in

    young children Bundling has minimal effect on

    rectal temperature

    Comparative Fever Definitions:

    Children 3-36 months c fevermanagement changes if well or illappearing and immunization status

    TRECTAL > 39C in children 3-36months require evaluation

    Caregiver Report of Fever

    92% pts with reported fever athome (rectal temp) had fever atpresentation-48hrs hospitalization

    46% pts with reported fever athome (tactile) had fever atpresentation-48hrs hospitalization

    5 of 19 infants with SBI wereafebrile at presentation

    TRECTAL > 38.0 C

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    Immunology:Cell-Mediated Immunity

    No maternal transfer of T-Cells cytotoxic CD8+ T cell response to CMV is

    similar in neonates and adults, although theCD4+ T cell response is reduced

    Humoral Immunity

    Transfer of maternal IgG across theplacenta during the 3rd trimester;

    (most of newborns serum Ig) Maternal Ig then gradually cleared

    while antibodies produced by infant o

    Only maternal IgG is transferred

    Innate-Immunity

    q neutrophil & monocyte fxn:

    Limited ability to accelerate neutrophilproduction response to infection/sepsis.

    Variability in classic & alternativepathway activity & components

    Complement levels o after birth;reach adult levels at 6 - 18 months

    Clinical Effects

    osusceptibility toHIV, CMV, and VSV; Normal responseto other viruses & graft rejection

    Strong antibody responses to proteinantigens/vaccinesSeverely blunted response topolysaccharide antigens until ~ 18 to

    24 months of age

    Breast Feeding

    Transfer of immunoglobulins (IgG, IgA),promotion of normal GI flora, transfer ofWBC, anti-microbials

    q incidence of gastroenteritis, Respinfections, Otitis media, UTIs, andSepsis

    Save ~$1000 per year

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    Etiology:Viral Illness

    Herpes simplex

    Varicella

    Enteroviruses

    Influenza virus

    Some adenoviruses

    Respiratory syncytial virus

    Serious Bacterial Infection GBS

    Bacterial meningitis

    Bacterial pneumonia

    Cellulitis

    Osteomyelitis

    Bacterial gastroenteritis Urinary tract infection

    Herpes Simplex

    Gen: -among etiologies of TORCH

    Eti: -generally transmitted from maternal genitaltrack at birth

    Sx: -temperature instability, respiratory distress,poor feeding, and lethargy

    -hypotension, jaundice, DIC, apnea, shock

    -Vesicular skin lesions may or may not bepresent and develop late in some patients

    Dx: -cultures of skin lesions, mouth/nasopharynx,eyes, urine, blood, stool or rectum, and CSF.-Serologic tests generally are not helpful.

    Tx: -parenteral high-dose Acyclovir(60/mg/kg per day) for 21 days

    -supportive care

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    Etiology:Viral Illness

    Herpes simplex

    Varicella

    Enteroviruses

    Influenza virus

    Some adenoviruses

    Respiratory syncytial virus

    Serious Bacterial Infection GBS

    Bacterial meningitis

    Bacterial pneumonia

    Cellulitis

    Osteomyelitis

    Bacterial gastroenteritis Urinary tract infection

    Congenital Varicella

    Gen: -among etiologies of TORCH

    Neonatal Varicella

    Pres: -Fever followed by a vesicular eruption.-Mild cases: lesions heal within 7-10 days-Disseminated disease: varicella pneumonia,hepatitis, and meningoencephalitis

    Dx: -clinically, upon characteristic appearance of

    skin lesions.-VZV may be cultured from vesicular fluid,but the virus takes several weeks to grow

    Post-exposure Prophylaxis:

    -Varicella-zoster immuneglobulin

    prepared from donors with high levels of

    VZV antibody- VariZIG

    purified human immune globulinpreparation; alternative to VZ-Ig

    Tx: -Acyclovir (30 mg/kg per day, 3 divided dosesIV) for 10 days

    -Breast Feeding

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    Etiology:Viral Illness

    Herpes simplex

    Varicella

    Enteroviruses

    Influenza virus

    Some adenoviruses

    Respiratory syncytial virus

    Serious Bacterial Infection GBS

    Bacterial meningitis

    Bacterial pneumonia

    Cellulitis

    Osteomyelitis

    Bacterial gastroenteritis Urinary tract infection

    Enteroviruses

    Micr:-Poliovirus, echovirus,coxsackievirus, enterovirus

    Early sx

    -may be mild and nonspecific:listlessness, anorexia, and transientrespiratory distress. -Approximately 1/3 of

    cases have a biphasic illness

    Generalized non-polio enterovirus disease inthe newborn most often occurs in one of twocharacteristic clinical syndromes:1. Neonatal myocarditis,

    2. Fulminant hepatitis-hypotension, profuse bleeding,jaundice, and multiple organ failure.

    Tx: -supportive-judicious fluid management inmyocarditis

    -IVIG in severe cases

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    Etiology:Viral Illness

    Herpes simplex

    Varicella

    Enteroviruses

    Influenza virus

    Some adenoviruses

    Respiratory syncytial virus

    Serious Bacterial Infection GBS

    Bacterial meningitis

    Bacterial pneumonia

    Cellulitis

    Osteomyelitis

    Bacterial gastroenteritis Urinary tract infection

    Influenza

    Complications:

    -Otitis Media (most common)

    -Laryngotracheitis

    -Pneumonia

    (2 bacterial)-Neuro: aseptic meningitis, transverse

    myelitis, Guillain-Barr syndrome, acutenecrotizing and postinfectiousencephalitis, encephalopathy, febrileseizures, acute mental status changes,and Reye syndrome with use of aspirin

    -Myositis & Rhabdomyositis

    Dx: -Rapid test, culture, serology

    Tx: -Supportive-Oseltamivir/Zanamivir (A&B)-Amantidine/Rimantidine (A)

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    Etiology:Viral Illness

    Herpes simplex

    Varicella

    Enteroviruses

    Influenza virus

    Some adenoviruses

    Respiratory syncytial virus

    Serious Bacterial Infection GBS

    Bacterial meningitis

    Bacterial pneumonia

    Cellulitis

    Osteomyelitis

    Bacterial gastroenteritis Urinary tract infection

    Adenovirus: clinical manifestations Rsp: -Pharyngitis

    -Coryza-Otitis Media-Pneumonia (causes 10% in children)

    Eye -Pharyngoconjuctival fever

    GI: -Diarrhea-Gastroenteritis

    GU -acute hemorrhagic cystitis CNS -occasional encephalitis, menningitis

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    Etiology:Viral Illness

    Herpes simplex

    Varicella

    Enteroviruses

    Influenza virus

    Some adenoviruses

    Respiratory syncytial virus

    Serious Bacterial Infection GBS

    Bacterial meningitis

    Bacterial pneumonia

    Cellulitis

    Osteomyelitis

    Bacterial gastroenteritis Urinary tract infection

    Respiratory Syncytial Virus

    Gen: -November-April (peak Jan, Feb)

    -strains shift yearly p reinfection possible Epi: -MCC LRTI in children < 1yoa

    -viral shedding = ~3-8 days-transmission: direct contact, aerosol droplets contact and aerosol precautions

    Prs: -Apnea (20% in hospitalized pts)

    -Bronchiolitis, bronchospasm,pneumonia, wheezing and acuterespiratory failure

    Cmp: -associaed with later development of reactiveairway disease

    Dx: -clinical-rapid assay of nasal secretions

    DDX:Influenza, parainfluenza, adenovirus

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    Etiology:Viral Illness

    Herpes simplex

    Varicella

    Enteroviruses

    Influenza virus

    Some adenoviruses

    Respiratory syncytial virus

    Serious Bacterial Infection GBS

    Bacterial meningitis

    Bacterial pneumonia

    Cellulitis

    Osteomyelitis

    Bacterial gastroenteritis Urinary tract infection

    Group-B Streptococcus

    Gen: -acquired in utero during vaginal passage

    Risk: -maternal GU GBS colonization

    Sepsis-irritability, lethargy, tachypnea, grunting,temperature instability, poor perfusion, andhypotension.-Most infants < 24hrs old will not have fever

    Pneumonia-tachhypnea, grunting, cyanosis, pulmonaryeffusion, and increased work of breathing

    Menningitis-Specific CNS Si

    Septic-arthritis & Osteomyelitis

    Eval: -CBC c diff, blood culture, CXR, and lumbar

    puncture (cell count, protein &glucose concentration, Gram stain & culture)-Urine culture if over 6 days of age

    Tx: -Initial emperic tx (cover streptococci, gram-neg enterics, staph, and Listeria)-PCN G (once GBS isolated)

    Prevention: Screen pregnant women for GBScolonization, tx with antibiotics

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    Etiology:Viral Illness

    Herpes simplex

    Varicella

    Enteroviruses

    Influenza virus

    Some adenoviruses

    Respiratory syncytial virus

    Serious Bacterial Infection GBS

    Bacterial meningitis

    Bacterial pneumonia

    Cellulitis

    Osteomyelitis

    Bacterial gastroenteritis Urinary tract infection

    Bacterial Meningitis

    Eti: Group B Streptococcus 50 %

    E. coli 25 %Other gram-negative rods 8 %Listeria monocytogenes 6 %Streptococcus pneumoniae 5 %Group A Streptococcus 4 %Haemophilus influenzae 3 %N. Mennigitidis, S. Aureus, enterococcus

    Si: -Temp. Instability (>38, 1000 WBC/microL)

    -oCSF protein concentration(>150 mg/dL preterm, >100 mg/dL term)

    -qCSF glucose concentration

    (

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    Etiology:Viral Illness

    Herpes simplex

    Varicella

    Enteroviruses

    Influenza virus

    Some adenoviruses

    Respiratory syncytial virus

    Serious Bacterial Infection GBS

    Bacterial meningitis

    Bacterial pneumonia

    Cellulitis

    Osteomyelitis

    Bacterial gastroenteritis Urinary tract infection

    Bacterial Meningitis

    Tx: -Supportive

    -1-7d: Ampicillin+Gentamycin+Cefoxaxime-7+d: -Non-hospitalized

    Ampicillin+Gentamycin+Cefoxaxime-7+d: -Hospitalized

    Vancomycin+Gentamycin+Cefoxaxime+Ampicillin

    -Selective tx once bacteria isolated

    F/U: -Repeat lumbar puncture in 24-48hrs

    -Ultrasound

    -Perform CT or MRI c contrast

    -F/u of hearing, visual acuity, developmentalstatus

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    Etiology:Viral Illness

    Herpes simplex

    Varicella

    Enteroviruses

    Influenza virus

    Some adenoviruses

    Respiratory syncytial virus

    Serious Bacterial Infection GBS

    Bacterial meningitis

    Bacterial pneumonia

    Cellulitis

    Osteomyelitis

    Bacterial gastroenteritis Urinary tract infection

    Bacterial Pneumonia-any infant with respiratory distress

    or illness should be evaluated forpneumonia/sepsis

    EARLY ONSET

    Respiratory distress soon after birth

    LATE ONSET

    Changes in condition: respiratory distress,tachypnea, apnea, poor feeding, juandice, emesis

    Labs: -Blood, CSF, pleural fluid-CXR

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    Etiology:Viral Illness

    Herpes simplex

    Varicella

    Enteroviruses

    Influenza virus

    Some adenoviruses

    Respiratory syncytial virus

    Serious Bacterial Infection GBS

    Bacterial meningitis

    Bacterial pneumonia

    Cellulitis

    Osteomyelitis

    Bacterial gastroenteritis Urinary tract infection

    Cellulitis

    Dx: -Clinical, Cx usually unhelpful

    Eti: -beta-hemolytic strep, S. Aureus

    Osteomyelitis

    Sx often non-specific in infants

    Warmth, inflammation, tenderness

    Plain films, MRI Staph Aureus, Gram(-) Bacilli, GBS

    3rd-gen Cephalosporin (Cefotaxime)+ anti-staph (nafcillin or vacomycin ifICUexposure)

    Bacterial Gastroenteritis MCC = Salmonella

    (esp. bloody diarrhea)

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    Etiology:Viral Illness

    Herpes simplex

    Varicella

    Enteroviruses

    Influenza virus

    Some adenoviruses

    Respiratory syncytial virus

    SeriousB

    acterialInfection

    GBS

    Bacterial meningitis

    Bacterial pneumonia

    Cellulitis

    Osteomyelitis

    Bacterial gastroenteritis Urinary tract infection

    Urinary Tract Infection

    Sx:Often fever only manifestation-Fever (20 to 40 %)-Failure to thrive (15 to 43 %)-Jaundice (3 to 41 %)-Vomiting (9 to 41 %)-Loose stools (3 to 5 %)-Poor feeding (3 to 5 %)

    Epi:16% of pt 39C had UT

    I

    -1/3 of infants with UTI have bacteremia

    -MCC = E-Coli

    -Higher incidence in girls and uncircumcised males

    Dx: Urine collection by catheter, suprapubic aspiration

    -UA and Urine Cx

    -renal US & voiding cystourethrogram(evaluate presence of GU abnormalities)

    Tx: -Ampicillin + Gentamycin

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    Evaluation/Management:Neonates (0 to 28 days)

    blood, urine, and CSF cultures performed regardless of clinical appearance. chest radiograph be obtained in those with any sign or symptom of pulmonary disease.

    admision to the hospital (Grade 1B).

    presumptive treatment with antibiotics (Ampicillin and gentamicin or ampicillin andcefotaxime provide adequate empiric therapy for the pathogens that are common in thisage group.)

    Infants 0 to 28 days who are ill-appearing and lethargic and have mucocutaneous vesicles,have had seizures, a CSF pleocytosis with a negative CSF Gram stain, or elevated livertransaminases may have a CNS or disseminated herpes simplex virus (HSV) infection. Inthis select population of infants, we suggest initiating presumptive treatment with acyclovir(60 mg/kg per day divided three times daily), particularly if the bacterial cultures remainnegative at 48 to 72 hours and the patient has not improved clinically (Grade 2B).Laboratory studies to confirm the diagnosis ofHSV should be sent prior to the initiation of

    acyclovir.

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    Evaluation/Management:Young infants (29 to 60 days)

    I

    ll-appearing infants all infants who are ill-appearing, have abnormal cry, or temperatures 38.5C undergo a completehx and physical exam, and full laboratory evaluation including CBC, blood culture, UA and culture,and CSF for cell count and culture.

    Stool culture is suggested if diarrhea is present.

    CXR if at least one clinical sign of pulmonary disease (respiratory rate >50 breaths/minute, rales,rhonchi, retractions, wheezing, coryza, grunting, stridor, nasal flaring, or cough).

    Admission regardless of the initial laboratory results and treated empirically with cefotaxime or

    ceftriaxone

    Well-appearing Infants complete history and physical examination with appropriate laboratory evaluation including CBC,

    blood culture, urinalysis and culture, and CSF for cell count and culture.

    Although lumbar puncture may not be necessary in some well-appearing infants, lumbar puncturebe should performed if empiric antibiotics are prescribed, including in infants who have anabnormal UA.

    Stool culture is suggested if diarrhea is present.

    CXR be obtained only in infants with at least one clinical sign of pulmonary disease (respiratoryrate >50 breaths/minute, rales, rhonchi, retractions, wheezing, coryza, grunting, stridor, nasalflaring, or cough).

    Infants who have a CSF pleocytosis or an abnormal chest radiograph be admitted to the hospitaland treated with presumptive antibiotic therapy

    Infants with an abnormal urinalysis also be admitted and treated with antibiotics

    well-appearing infants c normal laboratory evaluation and CXR, can be sent home as long asreliable follow-up within 24 hours can be arranged ; tx with ceftriaxone (50 mg/kg in a single dose) ;CSF be obtained if antibiotics are given empirically.

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    Evaluation/Management:Young infants (61 to 90 days)

    Ill-appearing full laboratory evaluation including blood, urine, and CSF.

    Signs of pulmonary disease should also receive CXR

    Admission for empiric antibiotic therapy (with cefotaxime or ceftriaxone), regardless ofthe initial laboratory results

    Infants with CSF pleocytosis should be treated with doses of antibiotics adequate to

    treat meningitis. Well-appearing

    CBC, urinalysis, and cultures of blood and urine

    Si of pulmonary disease should receive a chest radiograph

    CSF be obtained when empiric antibiotics are prescribed. (See "Lumbar puncture"above).

    Infants with an abnormal urinalysis consistent with a urinary tract infection may beadmitted to the hospital and treated with empiric antibiotics. However, outpatienttherapy possible for the well-appearing infant for whom follow-up can be assured.

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    Summary: Fever in neonates and infants less than three months of age is defined as a rectal

    temperature 38C (100.4F)

    A reliable caretaker report of fever should be carefully evaluated, even if the infant isafebrile at presentation.

    Presence of fever should be evaluated with complete H&P, laboratory evaluation--generally including CBC, blood culture, UA and culture, and CSF evaluation forculture for cell count, UA and culture; CXR and stool Cx if indicated--and, in most

    cases, admission.

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    References:Up To Date:

    Definition and etiology of fever in neonates and infants (less than 3 months of age)

    Strategies for the evaluation of fever in neonates and infants (less than 3 months of ag

    Overview of TORCH infections

    Varicella-zoster infection in the newborn

    Clinical manifestations and diagnosis of enterovirus infections

    Clinical features and diagnosis of influenza in children Epidemiology and clinical manifestations of adenovirus infection

    Clinical features and diagnosis of respiratory syncytial virus infection

    Groub B streptococcal infection in neonates and young infants

    Clinical features and diagnosis of bacterial meningitis in the neonate

    Treatment and outcome of bacterial meningitis in the neonate

    Clinical features and diagnosis of urinary tract infections in children

    Acute management, imaging, and prognosis of urinary tract infections in children