Rolston Aimee M, Gardner Melissa, van Leeuwen Kathleen, Mohnach Lauren, Keegan Catherine, Délot Emmanuèle, Vilain Eric, Sandberg David E
Department of Pediatrics and Communicable Diseases and the Child Health Evaluation and Research Center, University of Michigan Medical School, Ann Arbor, Michigan.
Department of Obstetrics and Gynecology, University of Michigan Medical School, Ann Arbor, Michigan.
Am J Med Genet C Semin Med Genet. 2017 Jun;175(2):268-278. doi: 10.1002/ajmg.c.31558. Epub 2017 May 30.
Following the principles of care recommended in the 2006 Consensus Statement on Disorders of Sex Development (DSD), along with input from representatives of peer support and advocacy groups, this study surveyed DSD clinical management practices at healthcare facilities in the United States. DSD are congenital conditions in which development of chromosomal, gonadal, or anatomic sex is atypical. Facilities providing care for patients with DSD were targeted for participation. Specialty providers completed a survey with questions in six broad categories: Institution Information, Nomenclature and Care Guidelines, Interdisciplinary Services, Staff and Community Education, DSD Management, and Research. Twenty-two of 36 targeted sites (61%) participated. Differences were observed between sites with regard to what conditions were considered to be DSD. All sites reported some degree of involvement of pediatric urology and/or surgery and pediatric endocrinology in the care of DSD patients. Gynecology and neonatology were most frequently not represented. Wide variation was observed across sites in continuing education standards, obtaining informed consent for clinical procedures, and in specific clinical management practices. This survey is the first to assess DSD clinical management practices in the United States. The findings establish a baseline of current practices against which providers delivering care to these patients and their families can benchmark their efforts. Such surveys also provide a practical framework for collaboration in identifying opportunities for change that enhance health and quality of life outcomes for patients and families affected by DSD.
遵循2006年性发育障碍(DSD)共识声明中推荐的护理原则,并结合同伴支持和倡导团体代表的意见,本研究对美国医疗机构的DSD临床管理实践进行了调查。DSD是指染色体、性腺或解剖学性别发育异常的先天性疾病。为DSD患者提供护理的机构被选为参与对象。专科提供者完成了一项涵盖六大类问题的调查:机构信息、命名法和护理指南、跨学科服务、工作人员和社区教育、DSD管理以及研究。36个目标地点中有22个(61%)参与了调查。不同地点在哪些疾病被视为DSD方面存在差异。所有地点都报告说,小儿泌尿外科和/或外科以及小儿内分泌科在DSD患者护理中都有一定程度的参与。妇科和新生儿科最常未被纳入。各地点在继续教育标准、临床程序获得知情同意以及具体临床管理实践方面存在很大差异。这项调查是首次对美国DSD临床管理实践进行评估。研究结果确立了当前实践的基线,为这些患者及其家庭提供护理的提供者可以以此为基准来衡量自己的工作。此类调查还为合作提供了一个实用框架,以确定变革机会,从而改善受DSD影响的患者及其家庭的健康和生活质量结果。