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Analyzing Samples
Available Test Interpretations
C1 Esterase Inhibitor
C Reactive Protein
C Reactive Protein High Sensitivity
CA 125
CA 153
CA 19.9
CA 27.29
Caffeine
Calcitonin
Calcium
Calcium Ionized
Carbamazepine
Carbon Dioxide
Carbon Monoxide
Carcinoembryonic Antigen
Cardiac Marker Panel
Cardiovascular Risk Panel
Carotene
CCP Antibody
CD4 Enumeration
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Cerebrospinal Fluid
Ceruloplasmin
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Chlamydia Detection
Chloride
Cholesterol
Cholinesterase
Clindamycin Resistance
Clostridium Difficile
Coagulation Factor Assays
Coagulation Factor Inhibitor
Coagulation Screen
Cold Agglutinin Titer
Colloid Osmotic Pressure
Complement Profile
Complete Blood Count
Congenital Adrenal Hyperplasia
Cord Blood Gases
Cord Blood Studies
Corticotropin Releasing Hormone Stimulation Test
Cortisol
Cortisol in Critical Illness
Cortisol Salivary
Cortisol Urine Free
Cortrosyn Stimulation Test
Cotinine
Creatine Kinase
Creatine Kinase MB
Creatinine
Creatinine Clearance
Creatinine Kinase Isoenzymes
Crossmatch
CRP
Cryoglobulin
Cryptococcal Antigen
Cryptosporidium Antigen
Crystal Identification
Cushing Syndrome
Cyclosporine
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Cytomegalovirus PCR Quantitative
Test Interpretations
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

Coagulation Screen

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The best screening tests for disorders of coagulation are a history and physical examination. Coagulation screening, a useful combination of laboratory tests, consists of a prothrombin time (PT), activated partial thromboplastin time (APTT), fibrinogen and platelet count. The screening coagulation tests are designed to provide rapid, useful, non-specific information, which allows an initial broad categorization of the hemostatic problem. The results of these screening tests, in conjunction with the clinical history, will then direct the selection of further, more detailed and specific coagulation tests, such as specific factor assays, fibrin degradation products, D-dimer, thrombin time, platelet aggregation, or specific factor inhibitor assays.



Based on the results of the PT and APTT, a disorder of hemostasis can be broadly categorized as shown in Table I.

Protime

APTT

Possible Abnormality

Normal

Normal

Qualitative or Quantitative Platelet Defect

Vascular Defect

Factor XIII Deficiency

Alpha-2 Antiplasmin Deficiency

Increased

Normal

Hereditary Factor VII Deficiency

Warfarin therapy

Early Vitamin K deficiency

Early liver dysfunction

Normal

Increased

Hemophilia A

Hemophilia B

von Willebrand's Disease

Factor XI deficiency

Factor XII deficiency (no bleeding history)

HMWK deficiency (no bleeding history)

Prekallikrein deficiency (no bleeding history)

Coagulation inhibitor

Heparin

Increased

Increased

Factor X deficiency

Factor V deficiency

Factor II deficiency

Hypofibrinogenemia/Dysfibrinogenemia

Liver disease

Vitamin K deficiency

DIC

Warfarin therapy

Heparin



Reference ranges are:

Test

Reference Range

Critical Value

Prothrombin Time

11.4 - 14.2 sec

>17 sec

>25 sec if anticoagulated

APTT

22 - 32 sec

>45 sec

>130 sec if heparinized

Platelet count

140,000 - 400,000/uL

<30,000/uL

>1 million/uL

Fibrinogen

146 - 390 mg/dL

<100 mg/dL



Specimen requirement is one light blue top (sodium citrate) tube and one lavender top (EDTA) tube of blood.