COVID-19 infection and pain in adolescents with sickle cell disease: A case series

被引：2

作者：

Heyman, Heidi M. ^{[1
]}

Alberts, Nicole M. ^{[2
]}

Rees, Matthew ^{[3
]}

Puri, Latika ^{[4
]}

Frett, Michael J. ^{[1
]}

Anghelescu, Doralina L. ^{[1
]}

机构：

[1] St Jude Childrens Res Hosp, Dept Pediat Med, Div Anesthesiol, MS 130,Room IA 5302,262 Danny Thomas Pl, Memphis, TN 38105 USA

[2] Concordia Univ, Dept Psychol, Montreal, PQ, Canada

[3] St Jude Childrens Res Hosp, Dept Oncol, Memphis, TN USA

[4] Loma Linda Univ, Dept Hematol, Loma Linda, CA USA

来源：

EJHAEM | 2022年 / 3卷 / 04期

关键词：

anemia; chronic pain; COVID-19; neuropathic pain; sickle cell disease; vaso-occlusive crisis; CHILDREN; SURVIVAL; ADULTS;

D O I：

10.1002/jha2.587

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Adolescents with sickle cell disease (SCD) have been shown to have pain-related sequelae following COVID-19 infection. In this case series, we discuss five adolescents with SCD and SARS-CoV-2 infection who subsequently developed complex pain circumstances manifested as: (1) increased frequency of acute care visits or admissions for pain; (2) new onset chronic pain; (3) new onset neuropathic pain; (4) escalation in the complexity of pharmacologic therapies; (5) increased use of nonpharmacologic interventions. While more research is needed to fully understand the implications of COVID-19 infection on pain in adolescents with SCD, these cases suggest the presence of a complex relationship.

引用

页码：1310 / 1315

页数：6

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