Disorders of sex development (DSD): Clinical service delivery in the United States

被引:34
作者
Rolston, Aimee M. [1 ,2 ,3 ]
Gardner, Melissa [1 ,2 ]
van Leeuwen, Kathleen [4 ]
Mohnach, Lauren [3 ,5 ]
Keegan, Catherine [6 ,7 ]
Delot, Emmanuele [8 ]
Vilain, Eric [8 ]
Sandberg, David E. [1 ,2 ]
机构
[1] Univ Michigan, Sch Med, Dept Pediat & Communicable Dis, Ann Arbor, MI USA
[2] Univ Michigan, Sch Med, Child Hlth Evaluat & Res Ctr, Ann Arbor, MI USA
[3] Univ Michigan, Dept Obstet & Gynecol, Sch Med, Ann Arbor, MI 48109 USA
[4] Phoenix Childrens Hosp, Dept Surg, Phoenix, AZ USA
[5] Univ Michigan, Sch Med, Dept Urol, Ann Arbor, MI USA
[6] Univ Michigan, Dept Pediat, Div Genet, Ann Arbor, MI 48109 USA
[7] Univ Michigan, Sch Med, Dept Human Genet, Ann Arbor, MI USA
[8] Univ Calif Los Angeles, David Geffen Sch Med, Dept Human Genet, Los Angeles, CA 90095 USA
关键词
disorders of sex development; intersex; quality improvement; survey; MANAGEMENT; CONSENSUS; CARE;
D O I
10.1002/ajmg.c.31558
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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.
引用
收藏
页码:268 / 278
页数:11
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