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Consolidated Clinical Document Architecture (C-CDA) Abbreviation: C-CDA: Status: Published: First published: December 2011 () Latest version: 2.1 2015: Organization: Health Level Seven International: Committee: Structured Documents Group: Base standards
Congenital dyserythropoietic anemia (CDA) is a rare blood disorder, similar to the thalassemias. CDA is one of many types of anemia , characterized by ineffective erythropoiesis , and resulting from a decrease in the number of red blood cells (RBCs) in the body and a less than normal quantity of hemoglobin in the blood. [ 2 ]
In the opinion of HL7 and its members, the CDA CCD combines the benefits of ASTMs Continuity of Care Record (CCR) and the HL7 Clinical Document Architecture (CDA) specifications. It is intended as an alternate implementation to the one specified in ASTM ADJE2369 for those institutions or organizations committed to implementation of the HL7 ...
The anemia associated with CDA type II can range from mild to severe, and most affected individuals have jaundice, hepatosplenomegaly, and the formation of hard deposits in the gallbladder called bilirubin gallstones. This form of the disorder is usually diagnosed in adolescence or early adulthood.
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The CDA encompasses both working with children in the ECE setting and interaction with parents or guardians. The first CDA credential was awarded in 1975. [2] The CDA became the sole nationally recognized ECE credential, accepted in all 50 states and U.S. Territories. An initial CDA credential was valid for a period of five years, with a ...
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CDA type IV is characterized by mild to moderate splenomegaly. Hemoglobin is very low and patients are transfusion dependent. MCV is normal or mildly elevated. Erythropoiesis is normoblastic or mildly to moderately megaloblastic. Nonspecific erythroblast dysplasia is present. [2]