Management of sickle cell pain:
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-...
Gespeichert in:
| Hauptverfasser: | , |
|---|---|
| Format: | Buch |
| Sprache: | English |
| Veröffentlicht: |
New York, NY, United States of America
Oxford University Press
[2025]
|
| Schriftenreihe: | What do I do now? - pain medicine
|
| Schlagworte: | |
| Zusammenfassung: | 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 |
| Beschreibung: | xvi, 310 Seiten Illustrationen 156 x 235 mm |
| ISBN: | 9780197630839 0197630839 |
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| 245 | 1 | 0 | |a Management of sickle cell pain |c edited by Wally R. Smith, MD, Thokozeni Lipato, MD |
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| 520 | |a 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 | ||
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| 650 | 4 | |a Clinical psychology / BIC2 | |
| 700 | 1 | |a Smith, Wally R. |4 edt |4 aut |4 aui | |
| 700 | 1 | |a Lipato, Thokozeni |4 edt |4 aut |4 aui | |
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Datensatz im Suchindex
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| author | Smith, Wally R. Lipato, Thokozeni |
| author2 | Smith, Wally R. Smith, Wally R. Lipato, Thokozeni Lipato, Thokozeni |
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| author2_variant | w r s wr wrs w r s wr wrs t l tl t l tl |
| author_facet | Smith, Wally R. Lipato, Thokozeni Smith, Wally R. Smith, Wally R. Lipato, Thokozeni Lipato, Thokozeni |
| author_role | aut aut |
| author_sort | Smith, Wally R. |
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| illustrated | Illustrated |
| indexdate | 2025-05-15T12:01:44Z |
| institution | BVB |
| isbn | 9780197630839 0197630839 |
| language | English |
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| physical | xvi, 310 Seiten Illustrationen 156 x 235 mm |
| publishDate | 2025 |
| publishDateSearch | 2025 |
| publishDateSort | 2025 |
| publisher | Oxford University Press |
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| series2 | What do I do now? - pain medicine |
| spelling | Management of sickle cell pain edited by Wally R. Smith, MD, Thokozeni Lipato, MD New York, NY, United States of America Oxford University Press [2025] xvi, 310 Seiten Illustrationen 156 x 235 mm txt rdacontent n rdamedia nc rdacarrier What do I do now? - pain medicine 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 Pain & pain management / BIC2 Clinical psychology / BIC2 Smith, Wally R. edt aut aui Lipato, Thokozeni edt aut aui Erscheint auch als Online-Ausgabe, PDF 978-0-19-763084-6 Erscheint auch als Online-Ausgabe, EPUB 978-0-19-763085-3 Erscheint auch als Online-Ausgabe 978-0-19-763122-5 |
| spellingShingle | Management of sickle cell pain Pain & pain management / BIC2 Clinical psychology / BIC2 Smith, Wally R. Lipato, Thokozeni |
| title | Management of sickle cell pain |
| title_auth | Management of sickle cell pain |
| title_exact_search | Management of sickle cell pain |
| title_full | Management of sickle cell pain edited by Wally R. Smith, MD, Thokozeni Lipato, MD |
| title_fullStr | Management of sickle cell pain edited by Wally R. Smith, MD, Thokozeni Lipato, MD |
| title_full_unstemmed | Management of sickle cell pain edited by Wally R. Smith, MD, Thokozeni Lipato, MD |
| title_short | Management of sickle cell pain |
| title_sort | management of sickle cell pain |
| topic | Pain & pain management / BIC2 Clinical psychology / BIC2 |
| topic_facet | Pain & pain management / BIC2 Clinical psychology / BIC2 |
| url | https://www.lehmanns.de/media/119643604 |
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