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- W99577887 abstract "Vaso-occlusive pain from sickle cell disease is one of the most challenging pain syndromes in pediatrics. Pain symptoms can occur in patients of all ages, from young infants to young adults. Pain can represent a very rare event for some individuals, but can be a daily occurrence for others. Pain symptoms in younger children are usually relatively mild and of short duration, and management strategies need to focus on the use of rapidly acting, short-duration analgesics, and comforting nonpharmacologic strategies. Symptoms become more frequent and of longer duration in older children and adolescents, requiring a more complex management strategy. Long-acting analgesics may provide more optimal relief for those with persistent pain, and short-acting analgesics may be needed for breakthrough pain. Selected patients may benefi t from adjuvant analgesics such as antidepressants or anxiolytics. If available, training in the use of cognitive-behavioral techniques may improve self-esteem and perceived control over pain symptoms. As pain symptoms are just one of many symptoms of this complex disorder, the family and the health care provider must work as a team, together with sickle cell disease specialists, so that optimal disease management can go hand-in-hand with optimal pain management. Ongoing clinical research is likely to lead to more effective disease management in the future, which may lessen the burden of pain for patients and families affected by this disorder." @default.
- W99577887 created "2016-06-24" @default.
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- W99577887 date "2008-01-01" @default.
- W99577887 modified "2023-09-24" @default.
- W99577887 title "Pain in Sickle Cell Disease" @default.
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- W99577887 doi "https://doi.org/10.1007/978-1-59745-476-6_20" @default.
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