Sickle cell disease in North Carolina : facts for providers

[PDF-474.19 KB]

Details:

Corporate Authors:

National Center on Birth Defects and Developmental Disabilities (Centers for Disease Control and Prevention)‏. Division of Blood Disorders.

Description:

There were approximately

5,578 people with SCD

living in North Carolina in

2004-2008:

•• 39% younger than

18 years

•• 29% 18-35 years

•• 32% 35 years

and older

There were 92 babies born

with SCD in North Carolina

in 2008:

•• 95% Black or African-

American

•• 1% White

•• 0% Asian-American

•• 1% American Indian

•• 3% Other/Unknown race

•• 2% Hispanic-American

Note: There is overlap between the

race and ethnicity categories.

SCD affects all races and

ethnic groups. In North

Carolina, SCD occurs

among approximately

1 out of every

•• 1,435 births

•• 360 Black or African

American births

•• 10,800 Hispanic-

American births

CS238867_G

Publication date retrieved from document properties

Subject:

[+]

Document Type:

Pamphlet (or booklet)

Place as Subject:

North Carolina

Collection(s):

Stephen B. Thacker CDC Library collection

Main Document Checksum:

[+]

Supporting Files:

No Additional Files

You May Also Like:

Sickle cell disease in Georgia : facts for providers

Corporate Authors:

National Center on Birth Defects and Developmental Disabilities (Centers for Disease Control and Prevention)‏. Division of Blood Disorders.

Published Date:

6/3/2013

Series:

National Tobacco Control Program (NTCP) State Fact Sheets

Description:

What is RuSH?•• Registry and Surveillance System for Hemoglobinopathies(RuSH) was a pilot project of the Centers for DiseaseControl and Prevention (CDC), with the National Institutesof Health’s National Heart, Lung, and Blood Institute.•• T...

File Type:

[PDF - 1.16 MB]
Sickle cell disease national resource directory

Corporate Authors:

National Center on Birth Defects and Developmental Disabilities (Centers for Disease Control and Prevention), Division of Blood Disorders.. Centers for Disease Control and Prevention (U.S.).

Published Date:

June 2011

Description:

"The Sickle Cell Disease National Resource Directory is a compilation of national agencies, state-based health providers, and community-based organizations that provide services and resources for individuals and families affected by SCD. This directo...

File Type:

[PDF - 3.11 MB]
Sickle cell disease in North Carolina : facts for the public

Corporate Authors:

National Center on Birth Defects and Developmental Disabilities (Centers for Disease Control and Prevention)‏. Division of Blood Disorders.

Published Date:

4/23/2013

Series:

National Tobacco Control Program (NTCP) State Fact Sheets

Description:

There were approximately5,578 people with SCDliving in North Carolinain 2004-2008:•• 39% younger than18 years•• 29% 18-35 years•• 32% 35 yearsand olderThere were 92 babiesborn with SCD in NorthCarolina in 2008:•• 95% Black or African-...

File Type:

[PDF - 467.97 KB]
Sickle cell disease in Georgia : facts for the public

Corporate Authors:

National Center on Birth Defects and Developmental Disabilities (Centers for Disease Control and Prevention)‏. Division of Blood Disorders.

Published Date:

6/3/2013

Series:

National Tobacco Control Program (NTCP) State Fact Sheets

Description:

What is RuSH?•• Registry and Surveillance System forHemoglobinopathies (RuSH) was a pilot projectof the Centers for Disease Control and Prevention(CDC), with the National Institutes of Health’sNational Heart, Lung, and Blood Institute.•• Th...

File Type:

[PDF - 1.10 MB]
Registry and Surveillance System for Hemoglobinopathies -- RuSH : strategies from the field : Health promotion

Corporate Authors:

National Center on Birth Defects and Developmental Disabilities (Centers for Disease Control and Prevention). Division of Blood Disorders.. National Heart, Lung, and Blood Institute..

Published Date:

4/18/12

Description:

In 2010, the Registry and Surveillance System for Hemoglobinopathies (RuSH) pilot project was implemented by the Centers for Disease Control and Prevention (CDC) to collect state-specific, population-based data on people with sickle cell disease (SCD...

File Type:

[PDF - 6.06 MB]