Kawasaki disease laboratory findings: Difference between revisions

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{{Kawasaki disease}}
{{Kawasaki disease}}


{{CMG}}; {{AE}}  
{{CMG}}; {{AE}} {{SH}}


==Overview==
==Overview==
An elevated/reduced concentration of serum/blood/urinary/CSF/other [lab test] is diagnostic of [disease name].
Kawasaki disease is diagnosed by clinical presentation, although the laboratory findings are non-specific for the diagnosis of Kawasaki disease - normocytic [[anemia]], [[thrombocytosis]], with [[Platelet|platelets]] ≥ 450×10<sup>3</sup>/μL (after first week of acute disease), [[Leukocytosis|leucocytosis]] with [[white blood cell count]] ≥ 15,000/μL, elevated [[erythrocyte sedimentation rate]], elevated [[liver enzyme]] levels, [[hypoalbuminemia]] with ≥ 3.0g/dL, elevated [[c-reactive protein]], [[hyponatremia]] and sterile [[pyuria]] can be noted on laboratory investigations.


OR
== Laboratory Findings ==
 
Although non-specific for diagnosis, the following laboratory findings are helpful in the diagnosis of Kawasaki disease:<ref name="McCrindleRowley2017">{{cite journal|last1=McCrindle|first1=Brian W.|last2=Rowley|first2=Anne H.|last3=Newburger|first3=Jane W.|last4=Burns|first4=Jane C.|last5=Bolger|first5=Anne F.|last6=Gewitz|first6=Michael|last7=Baker|first7=Annette L.|last8=Jackson|first8=Mary Anne|last9=Takahashi|first9=Masato|last10=Shah|first10=Pinak B.|last11=Kobayashi|first11=Tohru|last12=Wu|first12=Mei-Hwan|last13=Saji|first13=Tsutomu T.|last14=Pahl|first14=Elfriede|title=Diagnosis, Treatment, and Long-Term Management of Kawasaki Disease: A Scientific Statement for Health Professionals From the American Heart Association|journal=Circulation|volume=135|issue=17|year=2017|pages=e927–e999|issn=0009-7322|doi=10.1161/CIR.0000000000000484}}</ref><ref name="pmid15574639">{{cite journal |vauthors=Newburger JW, Takahashi M, Gerber MA, Gewitz MH, Tani LY, Burns JC, Shulman ST, Bolger AF, Ferrieri P, Baltimore RS, Wilson WR, Baddour LM, Levison ME, Pallasch TJ, Falace DA, Taubert KA |title=Diagnosis, treatment, and long-term management of Kawasaki disease: a statement for health professionals from the Committee on Rheumatic Fever, Endocarditis, and Kawasaki Disease, Council on Cardiovascular Disease in the Young, American Heart Association |journal=Pediatrics |volume=114 |issue=6 |pages=1708–33 |date=December 2004 |pmid=15574639 |doi=10.1542/peds.2004-2182 |url=}}</ref><ref name="pmid15505111">{{cite journal |vauthors=Newburger JW, Takahashi M, Gerber MA, Gewitz MH, Tani LY, Burns JC, Shulman ST, Bolger AF, Ferrieri P, Baltimore RS, Wilson WR, Baddour LM, Levison ME, Pallasch TJ, Falace DA, Taubert KA |title=Diagnosis, treatment, and long-term management of Kawasaki disease: a statement for health professionals from the Committee on Rheumatic Fever, Endocarditis and Kawasaki Disease, Council on Cardiovascular Disease in the Young, American Heart Association |journal=Circulation |volume=110 |issue=17 |pages=2747–71 |date=October 2004 |pmid=15505111 |doi=10.1161/01.CIR.0000145143.19711.78 |url=}}</ref><ref name="pmid26714775">{{cite journal |vauthors=Chen X, Zhao ZW, Li L, Chen XJ, Xu H, Lou JT, Li LJ, Du LZ, Xie CH |title=Hypercoagulation and elevation of blood triglycerides are characteristics of Kawasaki disease |journal=Lipids Health Dis |volume=14 |issue= |pages=166 |date=December 2015 |pmid=26714775 |pmc=4696131 |doi=10.1186/s12944-015-0167-2 |url=}}</ref>
Laboratory findings consistent with the diagnosis of [disease name] include [abnormal test 1], [abnormal test 2], and [abnormal test 3].
*[[Complete blood count]] (CBC) may reveal:
 
**[[Normocytic normochromic anemia]]
OR
**[[Thrombocytosis]]
 
***[[Platelet|Platelets]] ≥ 450×10<sup>3</sup>/μL (450 × 10<sup>9</sup>/L) after the first week and peaking to a mean of ≈700,000 per mm<sup>3</sup> and normalizing after 4-6 weeks of onset of acute episode of Kawasaki disease
[Test] is usually normal for patients with [disease name].
**[[Leukocytosis|Leucocytosis]]
 
***[[White blood cell count]] ≥ 15,000/μL (15.0 × 10<sup>9</sup>/L)
OR
*[[Lipid profile]]
 
**May demonstrate [[hypertriglyceridemia]]
Some patients with [disease name] may have elevated/reduced concentration of [test], which is usually suggestive of [progression/complication].
*Elevated [[erythrocyte sedimentation rate]]
 
*Elevated [[c-reactive protein]]
OR
*Hypercoagulation profile
 
**May or may not demonstrate evidence of hypercoagulability
There are no diagnostic laboratory findings associated with [disease name].
**Panel should include [[thrombomodulin]], [[tissue factor]], [[tissue factor pathway inhibitor]], [[Von Willebrand factor]], coagulation [[factor VII]], activated [[factor VII]], [[prothrombin]] fragment 1 + 2, and [[D-dimer]].
=== Laboratory Findings ===
*[[Liver function tests]] may reveal:
'''Blood tests'''
**Elevated [[liver enzyme]] levels
* [[Complete blood count]] (CBC) may reveal normocytic [[anemia]] and eventually [[thrombocytosis]]
**[[Hypoalbuminemia]] ≥ 3.0g/dL (30g/L)
* [[Erythrocyte sedimentation rate]] (ESR) will be elevated
*Electrolyte study may reveal [[hyponatremia]]
* [[C-reactive protein]] (CRP) will be elevated
*Urine analysis may demonstrate sterile [[pyuria]]
* [[Liver function tests]] may show evidence of hepatic inflammation and low [[serum albumin]]


==References==
==References==
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[[Category: (name of the system)]]
[[Category:Pediatrics]]
[[Category:Cardiovascular diseases]]
[[Category:Angiology]]
[[Category:Cardiology]]
[[Category:Rheumatology]]
[[Category:Dermatology]]
[[Category:Emergency medicine]]
[[Category:Up-To-Date]]

Latest revision as of 21:48, 16 April 2018

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Dildar Hussain, MBBS [2]

Overview

Kawasaki disease is diagnosed by clinical presentation, although the laboratory findings are non-specific for the diagnosis of Kawasaki disease - normocytic anemiathrombocytosis, with platelets ≥ 450×103/μL (after first week of acute disease), leucocytosis with white blood cell count ≥ 15,000/μL, elevated erythrocyte sedimentation rate, elevated liver enzyme levels, hypoalbuminemia with ≥ 3.0g/dL, elevated c-reactive proteinhyponatremia and sterile pyuria can be noted on laboratory investigations.

Laboratory Findings

Although non-specific for diagnosis, the following laboratory findings are helpful in the diagnosis of Kawasaki disease:[1][2][3][4]

References

  1. McCrindle, Brian W.; Rowley, Anne H.; Newburger, Jane W.; Burns, Jane C.; Bolger, Anne F.; Gewitz, Michael; Baker, Annette L.; Jackson, Mary Anne; Takahashi, Masato; Shah, Pinak B.; Kobayashi, Tohru; Wu, Mei-Hwan; Saji, Tsutomu T.; Pahl, Elfriede (2017). "Diagnosis, Treatment, and Long-Term Management of Kawasaki Disease: A Scientific Statement for Health Professionals From the American Heart Association". Circulation. 135 (17): e927–e999. doi:10.1161/CIR.0000000000000484. ISSN 0009-7322.
  2. Newburger JW, Takahashi M, Gerber MA, Gewitz MH, Tani LY, Burns JC, Shulman ST, Bolger AF, Ferrieri P, Baltimore RS, Wilson WR, Baddour LM, Levison ME, Pallasch TJ, Falace DA, Taubert KA (December 2004). "Diagnosis, treatment, and long-term management of Kawasaki disease: a statement for health professionals from the Committee on Rheumatic Fever, Endocarditis, and Kawasaki Disease, Council on Cardiovascular Disease in the Young, American Heart Association". Pediatrics. 114 (6): 1708–33. doi:10.1542/peds.2004-2182. PMID 15574639.
  3. Newburger JW, Takahashi M, Gerber MA, Gewitz MH, Tani LY, Burns JC, Shulman ST, Bolger AF, Ferrieri P, Baltimore RS, Wilson WR, Baddour LM, Levison ME, Pallasch TJ, Falace DA, Taubert KA (October 2004). "Diagnosis, treatment, and long-term management of Kawasaki disease: a statement for health professionals from the Committee on Rheumatic Fever, Endocarditis and Kawasaki Disease, Council on Cardiovascular Disease in the Young, American Heart Association". Circulation. 110 (17): 2747–71. doi:10.1161/01.CIR.0000145143.19711.78. PMID 15505111.
  4. Chen X, Zhao ZW, Li L, Chen XJ, Xu H, Lou JT, Li LJ, Du LZ, Xie CH (December 2015). "Hypercoagulation and elevation of blood triglycerides are characteristics of Kawasaki disease". Lipids Health Dis. 14: 166. doi:10.1186/s12944-015-0167-2. PMC 4696131. PMID 26714775.

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