Sickle-cell disease laboratory findings

Revision as of 16:25, 1 August 2018 by Farima Kahe (talk | contribs) (→‎Laboratory findings)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Jump to navigation Jump to search

Sickle-cell disease Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Sickle-cell disease from other Diseases

Epidemiology & Demographics

Risk Factors

Screening

Natural History, Complications & Prognosis

Diagnosis

History & Symptoms

Physical Examination

Laboratory Findings

X Ray

CT

MRI

Echocardiography or Ultrasound

Other Imaging Findings

Other Diagnostic Studies

Treatment

Medical Therapy

Surgery

Primary Prevention

Secondary Prevention

Future or Investigational Therapies

Case Studies

Case #1

Sickle-cell disease laboratory findings On the Web

Most recent articles

Most cited articles

Review articles

CME Programs

Powerpoint slides

Images

American Roentgen Ray Society Images of Sickle-cell disease laboratory findings

All Images
X-rays
Echo & Ultrasound
CT Images
MRI

Ongoing Trials at Clinical Trials.gov

National Guidelines Clearinghouse

NICE Guidance

FDA on Sickle-cell disease laboratory findings

CDC on Sickle-cell disease laboratory findings

Sickle-cell disease laboratory findings in the news

Blogs onSickle-cell disease laboratory findings

Directions to Hospitals Treating Sickle-cell disease

Risk calculators and risk factors for Sickle-cell disease laboratory findings

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]

References

  1. 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.
  2. 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.

Template:WH Template:WS