Isbn: 9780197630839 - Management of Sickle Cell Pain (what Do I Do Now Pain Medicine) (20 results)

paperback. Condition: Very Good.

paperback. Condition: Fine.

Condition: New.

PAP. Condition: New. New Book. Shipped from UK. Established seller since 2000.

Condition: new.

PAP. Condition: New. New Book. Shipped from UK. Established seller since 2000.

Condition: As New. Unread book in perfect condition.

Paperback. Condition: New. Sickle cell disease is a group of inherited red blood cell disorders, named for the C-shaped "sickle" appearance of a patient's red blood cells. SCD affects millions of people throughout the world and is particularly common among those whose ancestors came from Sub-Saharan Africa, Spanish-speaking regions in the Western Hemisphere, Saudi Arabia, India, and Mediterranean countries such as Turkey, Greece, and Italy. Approximately 100,000 people in the US suffer from SCD, where SCD appears in one of 365 African-American births. When the sickle-shaped cells travel through small blood vessels, they get stuck and clog the blood flow, causing pain which can be a first indicator of other serious problems such as infection, acute chest syndrome, and stroke. Managing acute and chronic pain and understanding how pain relates to the disease and its related health problems is consequently an important but thorny concern for pain physicians, hematologists, pediatricians, and primary care clinicians. The sixth volume in the "What Do I Do Now? Pain Medicine" series, Sickle Cell Pain Management provides 26 case-based, clinically useful chapters with guidance for managing acute and chronic pain in pediatric and adult sickle cell patients.…

Paperback. Condition: Brand New. 288 pages. 6.23x0.66x9.14 inches. In Stock.

Condition: New.

Condition: New. In.

paperback. Condition: New.

Condition: New. 2025. paperback. . . . . .

Paperback / softback. Condition: New. New copy - Usually dispatched within 4 working days.

Condition: As New. Unread book in perfect condition.

Paperback. Condition: new. Paperback. Sickle cell disease is a group of inherited red blood cell disorders, named for the C-shaped " appearance of a patient> 's red blood cells. SCD affects millions of people throughout the world and is particularly common among those whose ancestors came from Sub-Saharan Africa, Spanish-speaking regions in the Western Hemisphere, Saudi Arabia, India, and Mediterranean countries such as Turkey, Greece, and Italy. Approximately 100,000 peoplein the US suffer from SCD, where SCD appears in one of 365 African-American births. When the sickle-shaped cells travel through small blood vessels, they get stuck and clog the blood flow, causing pain which can be a firstindicator of other serious problems such as infection, acute chest syndrome, and stroke.Managing acute and chronic pain and understanding how pain relates to the disease and its related health problems is consequently an important but thorny concern for pain physicians, hematologists, pediatricians, and primary care clinicians. The sixth volume in the "What Do I Do Now? Pain Medicine" series, Sickle Cell Pain Management provides 26 case-based, clinically usefulchapters with guidance for managing acute and chronic pain in pediatric and adult sickle cell patients. The sixth volume in the What Do I Do Now? Pain Medicine series Sickle Cell Pain Management provides readers useful guidance for managing a variety of scenarios in sickle cell patients. Shipping may be from multiple locations in the US or from the UK, depending on stock availability.…

Condition: New. 2025. paperback. . . . . . Books ship from the US and Ireland.

Condition: NEW.

Paperback. Condition: Brand New. 288 pages. 6.23x0.66x9.14 inches. In Stock.

Paperback. Condition: New. Sickle cell disease is a group of inherited red blood cell disorders, named for the C-shaped "sickle" appearance of a patient's red blood cells. SCD affects millions of people throughout the world and is particularly common among those whose ancestors came from Sub-Saharan Africa, Spanish-speaking regions in the Western Hemisphere, Saudi Arabia, India, and Mediterranean countries such as Turkey, Greece, and Italy. Approximately 100,000 people in the US suffer from SCD, where SCD appears in one of 365 African-American births. When the sickle-shaped cells travel through small blood vessels, they get stuck and clog the blood flow, causing pain which can be a first indicator of other serious problems such as infection, acute chest syndrome, and stroke. Managing acute and chronic pain and understanding how pain relates to the disease and its related health problems is consequently an important but thorny concern for pain physicians, hematologists, pediatricians, and primary care clinicians. The sixth volume in the "What Do I Do Now? Pain Medicine" series, Sickle Cell Pain Management provides 26 case-based, clinically useful chapters with guidance for managing acute and chronic pain in pediatric and adult sickle cell patients.…