Mapping of the current transition of care practice for patients with pituitary disease at Endo-ERN reference centers

Abstract

Rare endocrine conditions present specific diagnostic and management challenges to healthcare providers, one of which is the understudied transition of care. Despite the need for guidance regarding transition, consensus on structured and protocolled approaches are lacking. Therefore, we aimed to map the current clinical practice, and identify unmet needs regarding transition of care for patients with pituitary disease in the reference centers (RCs) of the European Reference Network on Rare Endocrine Conditions (Endo-ERN). A survey-based, cross-sectional study using the EU Survey tool was performed, and completed by 46 physicians (n) from 30 RCs (N). Transition is a common practice among RCs (n=44/46), usually accomplished by a multidisciplinary team meeting (N=20/30). Criteria for start and end of transition were defined in half of the RCs, with 16.7% of centers providing dissimilar answers. Transition readiness was assessed by >75% of the RCs, mostly by unvalidated means (e.g. subjective opinions, informal consultations). Pituitary-specific transition assessment tool was applied in one RC only. Transition protocols were present in only 9% of RCs, while in many RCs transition decisions were taken in combined adult-pediatric meetings, or based on clinicians’ personal judgment. A minority of physicians evaluated the effectiveness of transition-related interventions (n=11/46), or medical outcomes (n=8/46). Patient-reported outcome measures were infrequently used (n=4/46). Identified unmet needs included development of guidelines (n=5/46), and EU-wide approach (n=2/46). This study exemplifies the unmet needs for a structure the definition of the transition period and transition management for patients with rare hypothalamic and pituitary conditions from healthcare providers perspective.