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Key Components of Pain Management for Children and Adults with Sickle Cell Disease
Sickle cell disease (SCD) pain manifests as severe acute pain episodes and also as a debilitating chronic pain syndrome. Acute pain episodes are the most common reason for health care utilization; however, acute pain episodes are also frequently managed at home. Chronic pain syndrome develops in 30–...
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| Udgivet i: | Hematol Oncol Clin North Am |
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| Main Authors: | , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
2018
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6800257/ https://ncbi.nlm.nih.gov/pubmed/29729787 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.hoc.2018.01.014 |
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