Sickle-cell disease laboratory findings: Difference between revisions
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===Blood tests=== | ===Blood tests=== | ||
Laboratory findings consistent with the diagnosis of sickle cell disease include:<ref name="pmid1624972">{{cite journal |vauthors=West MS, Wethers D, Smith J, Steinberg M |title=Laboratory profile of sickle cell disease: a cross-sectional analysis. The Cooperative Study of Sickle Cell Disease |journal=J Clin Epidemiol |volume=45 |issue=8 |pages=893–909 |date=August 1992 |pmid=1624972 |doi= |url=}}</ref><ref name="pmid16549581">{{cite journal |vauthors=Bernard AW, Venkat A, Lyons MS |title=Best evidence topic report. Full blood count and reticulocyte count in painful sickle crisis |journal=Emerg Med J |volume=23 |issue=4 |pages=302–3 |date=April 2006 |pmid=16549581 |pmc=2579511 |doi=10.1136/emj.2006.035154 |url=}}</ref> | Laboratory findings consistent with the diagnosis of sickle cell disease include:<ref name="pmid1624972">{{cite journal |vauthors=West MS, Wethers D, Smith J, Steinberg M |title=Laboratory profile of sickle cell disease: a cross-sectional analysis. The Cooperative Study of Sickle Cell Disease |journal=J Clin Epidemiol |volume=45 |issue=8 |pages=893–909 |date=August 1992 |pmid=1624972 |doi= |url=}}</ref><ref name="pmid16549581">{{cite journal |vauthors=Bernard AW, Venkat A, Lyons MS |title=Best evidence topic report. Full blood count and reticulocyte count in painful sickle crisis |journal=Emerg Med J |volume=23 |issue=4 |pages=302–3 |date=April 2006 |pmid=16549581 |pmc=2579511 |doi=10.1136/emj.2006.035154 |url=}}</ref> | ||
*Anemia | |||
*High [[reticulocyte count]] (greater than 1.5%) | |||
*Target cells and Howell-Jolly bodies on pripheral blood smear | |||
*Abnormal [[hemoglobin]] forms on [[hemoglobin electrophoresis]] (Sickle-cell hemoglobin (HgbS) and [[hemoglobin C]] with sickling (HgbSC) are the two most common forms) | |||
==References== | ==References== | ||
Latest revision as of 16:25, 1 August 2018
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Aarti Narayan, M.B.B.S [2], Shyam Patel [3]
Overview
The most important laboratory test for sickle cell anemia is a complete blood count (CBC), specifically hemoglobin and hematocrit.
Laboratory findings
Blood tests
Laboratory findings consistent with the diagnosis of sickle cell disease include:[1][2]
- Anemia
- High reticulocyte count (greater than 1.5%)
- Target cells and Howell-Jolly bodies on pripheral blood smear
- Abnormal hemoglobin forms on hemoglobin electrophoresis (Sickle-cell hemoglobin (HgbS) and hemoglobin C with sickling (HgbSC) are the two most common forms)
References
- ↑ West MS, Wethers D, Smith J, Steinberg M (August 1992). "Laboratory profile of sickle cell disease: a cross-sectional analysis. The Cooperative Study of Sickle Cell Disease". J Clin Epidemiol. 45 (8): 893–909. PMID 1624972.
- ↑ Bernard AW, Venkat A, Lyons MS (April 2006). "Best evidence topic report. Full blood count and reticulocyte count in painful sickle crisis". Emerg Med J. 23 (4): 302–3. doi:10.1136/emj.2006.035154. PMC 2579511. PMID 16549581.