Cyanosis laboratory findings: Difference between revisions

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{{Cyanosis}}
{{Cyanosis}}


{{CMG}}; {{AE}}  
{{CMG}}; {{AE}} {{Sara.Zand}} {{ADS}}


==Overview==
==Overview==
An elevated/reduced concentration of serum/blood/urinary/CSF/other [lab test] is diagnostic of [disease name].
Laboratory findings consistent with the diagnosis of [[central cyanosis]] include [[Polycythemia]] due to secondary [[erythrocytosis]], Elevated [[prothrombin time]] and [[partial thromboplastin time]] , decreased levels of factors 5,7,8,9 (qualitative and quantitative),[[Platelet disorder]], increased [[fibrinolysis]] and paradoxical [[thrombotic]] tendency, [[Proteinuria]], [[Hyperuricemia]], [[Renal failure]] and [[nephrolithiasis]].
 
OR
 
Laboratory findings consistent with the diagnosis of [disease name] include [abnormal test 1], [abnormal test 2], and [abnormal test 3].
 
OR
 
[Test] is usually normal for patients with [disease name].
 
OR
 
Some patients with [disease name] may have elevated/reduced concentration of [test], which is usually suggestive of [progression/complication].
 
OR
 
There are no diagnostic laboratory findings associated with [disease name].


==Laboratory Findings==
==Laboratory Findings==
*Laboratory findings consistent with the diagnosis of [[cyanosis]]  in older children include:<ref name="pmid28393783">{{cite journal |vauthors=Bhardwaj V, Malhotra P, Hasija S, Chowdury UK, Pangasa N |title=Coagulopathies in cyanotic cardiac patients: An analysis with three point - of - care testing devices (Thromboelastography, rotational thromboelastometry, and sonoclot analyzer) |journal=Ann Card Anaesth |volume=20 |issue=2 |pages=212–218 |date=2017 |pmid=28393783 |pmc=5408528 |doi=10.4103/aca.ACA_4_17 |url=}}</ref>


*There are no diagnostic laboratory findings associated with [disease name].
* [[Polycythemia]] due to secondary [[erythrocytosis]]
OR
* Elevated [[prothrombin time]] and [[partial thromboplastin time]]
*An elevated/reduced concentration of serum/blood/urinary/CSF/other [lab test] is diagnostic of [disease name].
* Decreased levels of factors 5,7,8,9: qualitative and quantitative
*[Test] is usually normal among patients with [disease name].
* [[Platelet disorder]]
*Laboratory findings consistent with the diagnosis of [disease name] include:
* Increased [[fibrinolysis]] and paradoxical [[thrombotic]] tendency
**[Abnormal test 1]
* [[Proteinuria]]
**[Abnormal test 2]
* [[Hyperuricemia]]
**[Abnormal test 3]
* [[Renal failure]]
 
* [[Uric acid]] [[nephrolithiasis]]
*Some patients with [disease name] may have elevated/reduced concentration of [test], which is usually suggestive of [progression/complication].


==References==
==References==
{{Reflist|2}}
{{Reflist|2}}
 
[[Category:Primary care]]
{{WH}}
{{WS}}
[[Category: (name of the system)]]

Latest revision as of 04:17, 26 December 2020

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Sara Zand, M.D.[2] Amandeep Singh M.D.[3]

Overview

Laboratory findings consistent with the diagnosis of central cyanosis include Polycythemia due to secondary erythrocytosis, Elevated prothrombin time and partial thromboplastin time , decreased levels of factors 5,7,8,9 (qualitative and quantitative),Platelet disorder, increased fibrinolysis and paradoxical thrombotic tendency, Proteinuria, Hyperuricemia, Renal failure and nephrolithiasis.

Laboratory Findings

  • Laboratory findings consistent with the diagnosis of cyanosis in older children include:[1]

References

  1. Bhardwaj V, Malhotra P, Hasija S, Chowdury UK, Pangasa N (2017). "Coagulopathies in cyanotic cardiac patients: An analysis with three point - of - care testing devices (Thromboelastography, rotational thromboelastometry, and sonoclot analyzer)". Ann Card Anaesth. 20 (2): 212–218. doi:10.4103/aca.ACA_4_17. PMC 5408528. PMID 28393783.