Pediatric fever of uncertain source: Difference between revisions

(Added algorithm for evaluation of pediatric fever.)
(Text replacement - "[[Ceftriaxone]]" to "Ceftriaxone")
(28 intermediate revisions by 6 users not shown)
Line 17: Line 17:
===Facts and Figures===
===Facts and Figures===
''From  ACEP's Clinical Policy on Pediatric Fevers<ref>Clinical Policy for Children Younger Than Three Years Presenting to the Emergency Department With Fever. Annuals of Emergency Medicine 2003 42. 530-545</ref>
''From  ACEP's Clinical Policy on Pediatric Fevers<ref>Clinical Policy for Children Younger Than Three Years Presenting to the Emergency Department With Fever. Annuals of Emergency Medicine 2003 42. 530-545</ref>
*7% of patients < 2 years old with fever have PNA, however the etiology (viral/bacterial) or even the presence of pneumonia has low inter-observer reliability even among pediatric radiologists
*7% of patients < 2 years old with fever have pneumonia, however the etiology (viral/bacterial) or even the presence of pneumonia has low inter-observer reliability even among pediatric radiologists
*4% Prevalence of UTI with common other sources of fever (OM, viral URI, et cetera)
*4% Prevalence of UTI with common other sources of fever (OM, viral URI, et cetera)
*1.5-2% background prevalence of asymptomatic bacteruria in healthy afebrile controls
*1.5-2% background prevalence of asymptomatic bacteruria in healthy afebrile controls
Line 23: Line 23:
*0.3% of previously well children aged 3-36 months who have a fever without a source will develop significant sequelae, 0.03% will develop sepsis or meningitis
*0.3% of previously well children aged 3-36 months who have a fever without a source will develop significant sequelae, 0.03% will develop sepsis or meningitis


=== Concomitant RSV or Infulenza Infection ===
===Concomitant RSV or Infulenza Infection===
*In RSV+ (by PCR) neonates aged 0-28 days, 6.1% had UTIs and 3.7% were bactremic; there was no difference in rates of SBI between RSV+ and RSV- neonates in a large prospective multicenter study entailing 1,248 children<ref>Greenes, D.S.M., & Harper, M. B.M. (1999). Low risk of bacteremia in febrile children with recognizable viral syndromes. Pediatric Infectious Disease Journal, 18(3), 258-261.</ref>
*In RSV+ (by PCR) neonates aged 0-28 days, 6.1% had UTIs and 3.7% were bactremic; there was no difference in rates of SBI between RSV+ and RSV- neonates in a large prospective multicenter study entailing 1,248 children<ref>Greenes, D.S.M., & Harper, M. B.M. (1999). Low risk of bacteremia in febrile children with recognizable viral syndromes. Pediatric Infectious Disease Journal, 18(3), 258-261.</ref>
*RSV+ infants aged 29-60 days, the SBI rate was 5.5%, all of which were UTIs
*RSV+ infants aged 29-60 days, the SBI rate was 5.5%, all of which were UTIs
Line 31: Line 31:
{{Pediatric fever DDX}}
{{Pediatric fever DDX}}


==Diagnosis & Management==
==Evaluation & Management==
[[File:Pediatric Fever.pngthumb|Algorithm for the evaluation of pediatric fever]]
[[File:Pediatric Fever2.png|thumb|Algorithm for the evaluation of pediatric fever]]
=== 0-28dy ===
===0-28dy===
{| class="wikitable"
{| class="wikitable"
|-
|-
Line 42: Line 42:
| '''Comments'''
| '''Comments'''
|-
|-
| '''Temp ≥38°'''  
| '''Temperature ≥38°'''  
'''Toxic or Well'''
'''Toxic or Well'''
|  
|  
*CBC  
*CBC  
*Blood Cx
*Blood cultures
*UA, Ucx
*[[Urinalysis]], Urine culture
*LP-CSF  
*LP-CSF  
*CXR
*[[CXR]]
*+/- Stool studies (if diarrhea)
*+/- Stool studies (if diarrhea)
|  
|  
Line 61: Line 61:
{{Pediatric fever acyclovir indications}}
{{Pediatric fever acyclovir indications}}


=== 28dy-90dy<ref> Jaskiewicz, J.A., McCarthy, C.A., Richardson, A.C., White, K.C., Fisher, D.J., Powell, K. R., et al. (1994). Febrile infants at low risk for serious bacterial infection-an appraisal of the Rochester criteria and implications for management. Pediatrics 94(3), 390-396.</ref> ===
===28dy-90dy<ref> Jaskiewicz, J.A., McCarthy, C.A., Richardson, A.C., White, K.C., Fisher, D.J., Powell, K. R., et al. (1994). Febrile infants at low risk for serious bacterial infection-an appraisal of the Rochester criteria and implications for management. Pediatrics 94(3), 390-396.</ref>===
{| class="wikitable"
{| class="wikitable"
|-
|-
Line 72: Line 72:
|  
|  
*CBC  
*CBC  
*Blood Cx
*Blood cultures
*UA, Ucx
*[[Urinalysis]], Urine culture
*[[LP]]-CSF  
*[[LP]]-CSF  
*+/- CXR
*+/- CXR
Line 86: Line 86:
|  
|  
*CBC  
*CBC  
*Blood Cx
*Blood cultures
*UA, UCx
*[[Urinalysis]], urine culture
*+/- [[LP]]-CSF (must do before giving antibiotics)  
*+/- [[LP]]-CSF (must do before giving antibiotics)  
*+/- CXR
*+/- CXR
|
|
*+/-[[Ceftriaxone]] (50-100 mg/kg IM/IV)  
*+/-[[Ceftriaxone]] (50-100mg/kg IM/IV)  
| Workup(+): Antibiotics and admit
| Workup(+): Antibiotics and admit
Workup(-): ?antibiotics; home with 24 follow-up  
Workup(-): ?antibiotics; home with 24 follow-up  
|-
|-
|}
|}
^^Can use [[ceftriaxone]] 50-100 mg/kg, but concern for bilirubin displacement  
^^Can use [[ceftriaxone]] 50-100mg/kg, but concern for bilirubin displacement  


{{Pediatric fever CXR indications}}
{{Pediatric fever CXR indications}}
Line 102: Line 102:
{{Pediatric fever acyclovir indications}}
{{Pediatric fever acyclovir indications}}


=== 90dy-36mo<ref>Jaskiewicz, J.A., McCarthy, C.A., Richardson, A.C., White, K.C., Fisher, D.J., Powell, K. R., et al. (1994). Febrile infants at low risk for serious bacterial infection-an appraisal of the Rochester criteria and implications for management. Pediatrics 94(3), 390-396.</ref> ===
===90dy-36mo<ref>Jaskiewicz, J.A., McCarthy, C.A., Richardson, A.C., White, K.C., Fisher, D.J., Powell, K. R., et al. (1994). Febrile infants at low risk for serious bacterial infection-an appraisal of the Rochester criteria and implications for management. Pediatrics 94(3), 390-396.</ref>===
{| class="wikitable"
{| class="wikitable"
|-
|-
Line 113: Line 113:
|  
|  
*CBC  
*CBC  
*Blood Cx
*Blood cultures
*UA, UCx
*[[Urinalysis]], urine culture
*[[LP]]-CSF  
*[[LP]]-CSF  
*CXR^
*[[CXR]]^
|  
|  
{{Pediatric fever antibiotics 90dy-36mo}}
{{Pediatric fever antibiotics 90dy-36mo}}
Line 124: Line 124:
(No [[Prevnar]] or <4 wks post 1st [[Prevnar]] dose)
(No [[Prevnar]] or <4 wks post 1st [[Prevnar]] dose)
|  
|  
*UA, Urine culture
*[[Urinalysis]], Urine culture
*CBC  
*CBC  
*+/- CXR
*+/- CXR
| If WBC(+):
| If WBC(+):
*[[Ceftriaxone]] 50mg-100 mg/kg (also then consider [[BCx]] and [[LP]], esp in <6mo old)
*[[Ceftriaxone]] 50mg-100mg/kg (also then consider [[blood culture]] and [[LP]], especially in <6mo old)
| Outpatient (24 hour follow-up)
| Outpatient (24 hour follow-up)
|-
|-
Line 134: Line 134:
(2 [[Prevnar]] or ≥4 wks post 1st [[Prevnar]] dose)
(2 [[Prevnar]] or ≥4 wks post 1st [[Prevnar]] dose)
|  
|  
*Urine workup (UA, UCx) for:
*Urine workup (UA, urine culture) for:
**Circumcised males <6 months
**Circumcised males <6 months
**Uncircumcised males <12 months
**Uncircumcised males <12 months
**All females
**All females
*+/- CXR
*+/- CXR
| Treat [[cystitis]] or [[PNA]] if postitive
| Treat [[cystitis]] or [[pneumonia]] if postitive
| Outpatient (48hour f/u)
| Outpatient (48hour follow up)
|-
|-
| '''T≥38-38.9°C + Well'''
| '''T≥38-38.9°C + Well'''
| Consider UA, CXR based on symptoms, etc
| Consider UA, CXR based on symptoms, etc
| Treat [[cystitis]] or [[PNA]] if positive
| Treat [[cystitis]] or [[pneumonia]] if positive
| Outpatient (48-72 hour follow-up)<ref>Baker, M.D., Bello, L.M., & Avner, J.R. (1993). Outpatient management without antibiotics of fever in selected infants. New England Jouranl of Medicine, 329(20), 1437-1441.</ref>
| Outpatient (48-72 hour follow-up)<ref>Baker, M.D., Bello, L.M., & Avner, J.R. (1993). Outpatient management without antibiotics of fever in selected infants. New England Jouranl of Medicine, 329(20), 1437-1441.</ref>
|-
|-
Line 159: Line 159:
*Neg Nitrate and Leukocyte esterase
*Neg Nitrate and Leukocyte esterase
*WBC <10/high powered field
*WBC <10/high powered field
===CSF===
===CSF===
====0-28 days====
====0-28 days====
Line 166: Line 165:
====>29 days====
====>29 days====
*WBC 0-7/mm<sup>3</sup>
*WBC 0-7/mm<sup>3</sup>
*Protein: 15-25 mg/dL
*Protein: 15-25mg/dL
 
===Low Risk by Step-By-Step Approach<ref>Gomez B, Mintegi S, Bressan S, et al. Validation of the “Step-by-Step” Approach in the Management of Young Febrile Infants. Pediatrics. 2016;138(2):e20154381</ref>===
''Study validated against Rocheter criteria and Lab-score for identifying low risk for invasive bacterial infections (IBI), with '''''NPV ~98%'''''
*Well appearing
*Age > 21 days
*No leukocyturia
*Procalcitonin < 0.5 ng/mL
*ANC < 10,000/mm3
*CRP < 20 mg/L
====Low Risk Management<ref>Mintegi S, Gomez B, Martinez-Virumbrales L, et al. Outpatient management of selected young febrile infants without antibiotics. Arch Dis Child. 2016 Jul 28. pii: archdischild-2016-310600. doi: 10.1136/archdischild-2016-310600.</ref>====
*Offer no LP, no antibiotics, 24 hrs observation
*Plan for prompt follow-up


==Symptomatic Managment==
==Symptomatic Managment==
Line 181: Line 192:
==External Links==
==External Links==
*[http://www.pemed.org/blog/2011/10/9/fever-of-unknown-source-part-1.html PEM ED Algorithm for Pediatric Fever]
*[http://www.pemed.org/blog/2011/10/9/fever-of-unknown-source-part-1.html PEM ED Algorithm for Pediatric Fever]
*[http://ddxof.com/pediatric-fever/ DDxOf: Pediatric Fever]


==References==
==References==
<references/>
<references/>


[[Category:Peds]]
[[Category:Pediatrics]]

Revision as of 04:51, 12 March 2017

Background

  • Medicine is an art as well as science, practice clinical judgment when using guidelines
  • Preemies: Count age by estimated postconception date (not by actual delivery date) for 1st-90d
Age 0-14 days 14-28 days 28-60 days (pre vaccine) 28-60 days (post vaccine) 60-90 days > 90 days
Meningitis/SBI Prevalence 1/10 1/20 1/100 1/1000 1/1000-10,000 > 1/10,000

Facts and Figures

From ACEP's Clinical Policy on Pediatric Fevers[1]

  • 7% of patients < 2 years old with fever have pneumonia, however the etiology (viral/bacterial) or even the presence of pneumonia has low inter-observer reliability even among pediatric radiologists
  • 4% Prevalence of UTI with common other sources of fever (OM, viral URI, et cetera)
  • 1.5-2% background prevalence of asymptomatic bacteruria in healthy afebrile controls
  • 0.3% Rate of occult bactremia with healthy, well-appearing child who has a fever 2-24 months
  • 0.3% of previously well children aged 3-36 months who have a fever without a source will develop significant sequelae, 0.03% will develop sepsis or meningitis

Concomitant RSV or Infulenza Infection

  • In RSV+ (by PCR) neonates aged 0-28 days, 6.1% had UTIs and 3.7% were bactremic; there was no difference in rates of SBI between RSV+ and RSV- neonates in a large prospective multicenter study entailing 1,248 children[2]
  • RSV+ infants aged 29-60 days, the SBI rate was 5.5%, all of which were UTIs
  • Influenza+, low risk of bacterial illness

Differential Diagnosis

Pediatric fever

Evaluation & Management

Algorithm for the evaluation of pediatric fever

0-28dy

Child Appearance Work Up Treatment Disposition & Follow-up Comments
Temperature ≥38°

Toxic or Well

  • CBC
  • Blood cultures
  • Urinalysis, Urine culture
  • LP-CSF
  • CXR
  • +/- Stool studies (if diarrhea)
Admit SBI incidence
  • Ill appearing: 13%–21%
  • Not ill appearing: <5%

^Acyclovir if:

  • HSV infection in baby or mother
  • CSF pleocytoisis
  • Concerning skin lesions
  • Seizures
  • Abnormal LFTs

28dy-90dy[3]

Appearance Work Up Treatment Disposition & Follow-Up
Temp≥38° + Toxic
  • CBC
  • Blood cultures
  • Urinalysis, Urine culture
  • LP-CSF
  • +/- CXR
  • +/- Stool studies (if diarrhea)
Admit

Temp≥°38 + Well

  • CBC
  • Blood cultures
  • Urinalysis, urine culture
  • +/- LP-CSF (must do before giving antibiotics)
  • +/- CXR
Workup(+): Antibiotics and admit

Workup(-): ?antibiotics; home with 24 follow-up

^^Can use ceftriaxone 50-100mg/kg, but concern for bilirubin displacement

  • Consider CXR for:
    • Respiratory symptoms
    • Fever >48 hrs
    • Tachypnea
    • Hypoxia

^Acyclovir if:

  • HSV infection in baby or mother
  • CSF pleocytoisis
  • Concerning skin lesions
  • Seizures
  • Abnormal LFTs

90dy-36mo[4]

Appearance Work Up Treatment Disposition & Follow-Up
T≥38° + Toxic Admit
T≥39°C + Well + Non-complete Prevnar

(No Prevnar or <4 wks post 1st Prevnar dose)

If WBC(+): Outpatient (24 hour follow-up)
T≥39°C + Well + Prevnar

(2 Prevnar or ≥4 wks post 1st Prevnar dose)

  • Urine workup (UA, urine culture) for:
    • Circumcised males <6 months
    • Uncircumcised males <12 months
    • All females
  • +/- CXR
Treat cystitis or pneumonia if postitive Outpatient (48hour follow up)
T≥38-38.9°C + Well Consider UA, CXR based on symptoms, etc Treat cystitis or pneumonia if positive Outpatient (48-72 hour follow-up)[5]
  • Consider CXR for:
    • Respiratory symptoms
    • Fever >48 hrs
    • Tachypnea
    • Hypoxia

Low Risk Lab Criteria

If low-risk criteria below not met, then perform the LP (if not done) and admit for inpatient antibiotics[6][7]

CBC

  • WBC 5-15 /mm3
  • Absolute Band count <1500 /mm3

Urinalysis

  • Clear
  • Neg Nitrate and Leukocyte esterase
  • WBC <10/high powered field

CSF

0-28 days

  • WBC: 0-22/mm3
  • Protein: <100mg/dL

>29 days

  • WBC 0-7/mm3
  • Protein: 15-25mg/dL

Low Risk by Step-By-Step Approach[8]

Study validated against Rocheter criteria and Lab-score for identifying low risk for invasive bacterial infections (IBI), with NPV ~98%

  • Well appearing
  • Age > 21 days
  • No leukocyturia
  • Procalcitonin < 0.5 ng/mL
  • ANC < 10,000/mm3
  • CRP < 20 mg/L

Low Risk Management[9]

  • Offer no LP, no antibiotics, 24 hrs observation
  • Plan for prompt follow-up

Symptomatic Managment

Acetaminophen Pediatric Dosing Chart

Weight (kg) Weight (lbs) Age Dosage (mg)
3-4 6-11 0-3 mo 40
5-7 12-17 4-11 mo 80
8-10 18-23 1-2 y 120
11-15 24-35 2-3 y 160
16-21 36-47 4-5 y 240
22-26 48-59 6-8 y 320
27-32 60-71 9-10 y 400
33-43 72-95 11 y 480
Dosage can be given q6 hours

See Also

External Links

References

  1. Clinical Policy for Children Younger Than Three Years Presenting to the Emergency Department With Fever. Annuals of Emergency Medicine 2003 42. 530-545
  2. Greenes, D.S.M., & Harper, M. B.M. (1999). Low risk of bacteremia in febrile children with recognizable viral syndromes. Pediatric Infectious Disease Journal, 18(3), 258-261.
  3. Jaskiewicz, J.A., McCarthy, C.A., Richardson, A.C., White, K.C., Fisher, D.J., Powell, K. R., et al. (1994). Febrile infants at low risk for serious bacterial infection-an appraisal of the Rochester criteria and implications for management. Pediatrics 94(3), 390-396.
  4. Jaskiewicz, J.A., McCarthy, C.A., Richardson, A.C., White, K.C., Fisher, D.J., Powell, K. R., et al. (1994). Febrile infants at low risk for serious bacterial infection-an appraisal of the Rochester criteria and implications for management. Pediatrics 94(3), 390-396.
  5. Baker, M.D., Bello, L.M., & Avner, J.R. (1993). Outpatient management without antibiotics of fever in selected infants. New England Jouranl of Medicine, 329(20), 1437-1441.
  6. Smitherman, H.F. & Macias, C.G. (2014). Evaluation and management of fever in the neonate and young infant (less than three months of age) [Electronic Version]. UpToDate,Teach, S.J., Kaplan, SL, Wiley, JF.
  7. Dagan, R. Sofer, S., Phillip, M., & Shachak, E. (1988). Ambulatory care of febrile infants younger than 2 months of age classified as being at low risk for having serous bacterial infections. Journal of Pediatrics, 112(3), 355-360.
  8. Gomez B, Mintegi S, Bressan S, et al. Validation of the “Step-by-Step” Approach in the Management of Young Febrile Infants. Pediatrics. 2016;138(2):e20154381
  9. Mintegi S, Gomez B, Martinez-Virumbrales L, et al. Outpatient management of selected young febrile infants without antibiotics. Arch Dis Child. 2016 Jul 28. pii: archdischild-2016-310600. doi: 10.1136/archdischild-2016-310600.