How I treat acute and persistent sickle cell pain
Sickle pain is the hallmark of sickle cell disease (SCD). It could be acute, persistent/relapsing, chronic or neuropathic. Although there is a general consensus that pain is a major manifestation of SCD there is a controversy as to the types of pain and their interrelationship between acute, chronic...
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| Format: | Article | 
| Language: | English | 
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            PAGEPress Publications
    
        2020-08-01
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| Series: | Mediterranean Journal of Hematology and Infectious Diseases | 
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| Online Access: | https://www.mjhid.org/index.php/mjhid/article/view/4297 | 
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| _version_ | 1846098517852946432 | 
    
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| author | Samir Ballas | 
    
| author_facet | Samir Ballas | 
    
| author_sort | Samir Ballas | 
    
| collection | DOAJ | 
    
| description | Sickle pain is the hallmark of sickle cell disease (SCD). It could be acute, persistent/relapsing, chronic or neuropathic. Although there is a general consensus that pain is a major manifestation of SCD there is a controversy as to the types of pain and their interrelationship between acute, chronic, relapsing, persistent, etc. This report first reviews the general approach to the management of acute vaso-occlusive crisis (VOC) pain including education, counseling, pharmacotherapy, non-pharmacotherapy, and fluid therapy. This is followed by the presentation of five patients that represent typical issues that are commonly encountered in the management of patients with SCD. These issues are: individualized treatment of pain, bilaterality of pain, use of illicit drugs, tolerance to opioids, opioid induced hyperalgesia and withdrawal syndrome. The clinical aspects and management of each of these issues are described. Moreover, such complications as tolerance and withdrawal may persist after discharge and may be mistaken as chronic pain rather than resolving, persistent or relapsing pain. | 
    
| format | Article | 
    
| id | doaj-art-cfeaaf9f40ce4d6b90db524c9dfbd470 | 
    
| institution | Kabale University | 
    
| issn | 2035-3006 | 
    
| language | English | 
    
| publishDate | 2020-08-01 | 
    
| publisher | PAGEPress Publications | 
    
| record_format | Article | 
    
| series | Mediterranean Journal of Hematology and Infectious Diseases | 
    
| spelling | doaj-art-cfeaaf9f40ce4d6b90db524c9dfbd4702025-01-02T00:22:50ZengPAGEPress PublicationsMediterranean Journal of Hematology and Infectious Diseases2035-30062020-08-0112110.4084/mjhid.2020.064How I treat acute and persistent sickle cell painSamir Ballas0Cardeza Foundation for Hematologic Research, Philadelphia.Sickle pain is the hallmark of sickle cell disease (SCD). It could be acute, persistent/relapsing, chronic or neuropathic. Although there is a general consensus that pain is a major manifestation of SCD there is a controversy as to the types of pain and their interrelationship between acute, chronic, relapsing, persistent, etc. This report first reviews the general approach to the management of acute vaso-occlusive crisis (VOC) pain including education, counseling, pharmacotherapy, non-pharmacotherapy, and fluid therapy. This is followed by the presentation of five patients that represent typical issues that are commonly encountered in the management of patients with SCD. These issues are: individualized treatment of pain, bilaterality of pain, use of illicit drugs, tolerance to opioids, opioid induced hyperalgesia and withdrawal syndrome. The clinical aspects and management of each of these issues are described. Moreover, such complications as tolerance and withdrawal may persist after discharge and may be mistaken as chronic pain rather than resolving, persistent or relapsing pain.https://www.mjhid.org/index.php/mjhid/article/view/4297Sickle cell diseaseSickle cell anemiaPainVaso-occlusive crisis | 
    
| spellingShingle | Samir Ballas How I treat acute and persistent sickle cell pain Mediterranean Journal of Hematology and Infectious Diseases Sickle cell disease Sickle cell anemia Pain Vaso-occlusive crisis  | 
    
| title | How I treat acute and persistent sickle cell pain | 
    
| title_full | How I treat acute and persistent sickle cell pain | 
    
| title_fullStr | How I treat acute and persistent sickle cell pain | 
    
| title_full_unstemmed | How I treat acute and persistent sickle cell pain | 
    
| title_short | How I treat acute and persistent sickle cell pain | 
    
| title_sort | how i treat acute and persistent sickle cell pain | 
    
| topic | Sickle cell disease Sickle cell anemia Pain Vaso-occlusive crisis  | 
    
| url | https://www.mjhid.org/index.php/mjhid/article/view/4297 | 
    
| work_keys_str_mv | AT samirballas howitreatacuteandpersistentsicklecellpain |