Heller Kathleen, Madura Grace, Nawara Nourhan, Salevitz Daniel, Coronado Janett, Chawla Reeti, Hansen Erik, Grimsby Gwen, van Leeuwen Kathleen, Weidler Erica M
Division of Surgery, Phoenix Children's, Phoenix, Arizona.
Mayo Clinic Alix School of Medicine, Phoenix, Arizona.
J Surg Res. 2025 Sep;313:291-296. doi: 10.1016/j.jss.2025.06.029. Epub 2025 Jul 17.
Improved patient/family education and shared decision-making (SDM) for congenital adrenal hyperplasia (CAH) is needed. We aimed to evaluate patient/family characteristics and management choices since implementation of an SDM tool for CAH.
CAH patients at a single institution from 2014 to 2024 were provided an SDM tool for management options. Families chose elective reconstruction of the clitoris and/or urogenital sinus (UGS) or only medically necessary procedures. Patients deferring surgery are followed for voiding difficulty, undergoing cystoscopy/vaginoscopy and imaging when indicated. UGS repair with introitoplasty is offered when obstruction is noted. Variables examined included race/ethnicity, procedures performed, clitoris and UGS anatomy, difficulty voiding, and imaging.
Sixteen patients fell into four categories: (1) full elective reconstruction (n = 4); (2) partial elective reconstruction (n = 2); (3) partial medically necessary reconstruction (n = 4) and; (4) deferral of reconstruction (n = 6). Common channel length of patients deferring surgery trended shorter without reaching statistical significance. When collapsed into non-Hispanic White versus persons of color, non-Hispanic White families were more likely to choose elective reconstruction versus delayed surgery (100% vs 0%, P = 0.001). Age in months at procedure was lower for elective reconstruction versus delayed reconstruction (8 versus 38, P = 0.05). Insurance type did not differ between groups.
Families of children with CAH who use an SDM process, combined with monitoring for voiding dysfunction, can choose to defer all or some reconstruction. Long-term follow-up and cultural and psychosocial factors influencing decision-making need to be investigated to ensure delivery of equitable care.
先天性肾上腺皮质增生症(CAH)需要改善患者/家庭教育及共同决策(SDM)。我们旨在评估自实施CAH的SDM工具以来患者/家庭的特征及管理选择。
2014年至2024年在单一机构的CAH患者被提供了用于管理选择的SDM工具。家庭选择阴蒂和/或泌尿生殖窦(UGS)的择期重建或仅选择必要的医疗程序。推迟手术的患者会接受排尿困难的随访,必要时进行膀胱镜检查/阴道镜检查及影像学检查。发现梗阻时提供UGS修复及阴道口成形术。所检查的变量包括种族/民族、实施的程序、阴蒂和UGS解剖结构、排尿困难及影像学检查。
16例患者分为四类:(1)完全择期重建(n = 4);(2)部分择期重建(n = 2);(3)部分必要医疗重建(n = 4);(4)重建推迟(n = 6)。推迟手术患者的共同通道长度有缩短趋势,但未达到统计学意义。分为非西班牙裔白人及有色人种后,非西班牙裔白人家庭比推迟手术更倾向于选择择期重建(分别为100%对0%,P = 0.001)。择期重建与推迟重建相比,手术时的月龄更低(分别为8个月对38个月,P = 0.05)。各组之间保险类型无差异。
使用SDM流程并结合排尿功能障碍监测的CAH患儿家庭,可以选择推迟全部或部分重建。需要调查长期随访以及影响决策的文化和社会心理因素,以确保提供公平的医疗服务。