Pre-trial implementation study for ketamine in sickle cell disease

具体目标1：评估医疗保健利益相关者对以下方面的障碍和促进因素的看法： 亚麻醉氯胺酮输注早期给药作为VOE疼痛辅助治疗的RCT 使用实施研究综合框架（CFRIR）和普罗克特的 实施结果的分类。为了实现这一目标，我们将：1A：进行一次横向调查， EPPIC网络内为患有以下疾病的人提供护理的医疗保健专业人员的调查研究 SCD和/或在其医院系统内提供氯胺酮给药指南（即， 专业包括血液学、急诊医学、麻醉学和住院医学） 评估拟议RCT 1B的障碍和促进因素：进行半结构化 采访15-20名医疗保健专业人员，以评估建议的障碍和促进因素 RCT。

Specific Aim 1: Assess healthcare stakeholders' perceptions of barriers to and facilitators for a RCT of early administration of sub-anesthetic ketamine infusion as a pain adjunct for VOEs using the Consolidated Framework for Implementation Research (CFRIR) and Proctor's taxonomy for implementation outcomes. To achieve this, we will: 1A: Conduct a cross-sectional survey study of healthcare professionals within EPPIC-Net who provide care for people with SCD and/or provide guidance for administration of ketamine within their hospital system (i.e., specialties including hematology, emergency medicine, anesthesiology, and hospitalist medicine) to assess barriers to and facilitators for the proposed RCT 1B: Conduct semi-structured interviews of 15-20 healthcare professionals to assess barriers to and facilitators for the proposed RCT.