脊髓裂患者乳胶过敏指南。
Latex allergy guidelines for people with spina bifida.
机构信息
Division of Developmental-Behavioral Pediatrics, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Pediatric Developmental Disabilities Department, Scottish Rite Hospital for Children, Dallas, TX, USA.
出版信息
J Pediatr Rehabil Med. 2020;13(4):601-609. doi: 10.3233/PRM-200741.
An estimated 85% of individuals with spina bifida (SB) survive into adulthood, warranting SB-specific transition to adult healthcare guidelines to address the diverse and complex medical, adaptive, and social needs particular to this condition. Latex allergy constitutes one important health concern for this population that requires ongoing and life-long evidence-based management. This article discusses management of latex allergy according to the SB Latex Allergy Healthcare Guidelines from the 2018 Spina Bifida Association's Fourth Edition of the Guidelines for the Care of People with Spina Bifida, reviews current care models in which such latex allergy guidelines can be implemented, and explores further relevant research topics in SB care relative to latex allergy.
估计有 85%的脊柱裂（SB）患者能存活到成年期，因此需要 SB 特定的过渡到成人保健指南，以满足该疾病特有的多样化和复杂的医疗、适应和社会需求。乳胶过敏是该人群的一个重要健康关注点，需要持续和终身的基于证据的管理。本文根据 2018 年脊柱裂协会第四版《脊柱裂患者护理指南》中的 SB 乳胶过敏保健指南讨论了乳胶过敏的管理，回顾了可以实施此类乳胶过敏指南的当前护理模式，并探讨了与 SB 护理相关的乳胶过敏的其他相关研究课题。
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