Resource utilization during pediatric to adult transfer of care in IBD

Abstract

BackgroundThe transition from pediatric to adult care for inflammatory bowel disease (IBD) is poorly understood. AimsTo characterize this transfer of care, health resource utilization was assessed. MethodsPatients transferred between 1999 and 2008 were studied. Utilization of health resources one year before transfer and one year after transfer was compared. Resource units assessed included: i) emergency department (ED) visits; ii) hospitalizations; iii) clinic visits; iv) surgical procedures; and v) endoscopies. Secondary outcomes included: i) documentation of patient non-compliance; ii) reason(s) for ED visit; iii) diagnoses most responsible for hospital admission; iv) medications; v) indications for surgery; vi) endoscopic findings; vii) and disease activity. Results95 subjects were identified (48 female), of whom 69 had Crohn's disease (CD) and 26 had ulcerative colitis (UC). The average age of diagnosis was 12.9years. Over their adult care interval, subjects had fewer clinic visits (2.56 versus 3.05 (p=0.01)) and more documented non-compliance (43% versus 29% (p=0.01)). No differences in ED visits (0.15 versus 0.18 (p=0.71)), hospitalizations (0.13 versus 0.13 (p=0.23)), surgical intervention (0.03 versus 0.05 (p=0.53)) or endoscopies (0.37 versus 0.25 (p=0.11)) were observed. IBD was active 66.7% of endoscopies under pediatric care versus only 23.8% under adult care (p=0.003). The average activity of CD was also higher during the last year of pediatric care. ConclusionsUnderstanding the transition process can help to develop strategies needed to support patients and their families.