Cyanosis laboratory findings: Difference between revisions
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==Overview== | ==Overview== | ||
Laboratory findings consistent with the diagnosis of [[central cyanosis]] include | 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== | ||
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==References== | ==References== | ||
{{Reflist|2}} | {{Reflist|2}} | ||
[[Category:Primary care]] | |||
[[Category: |
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
- 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
- Uric acid nephrolithiasis
References
- ↑ 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.