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Primary care use and depression screening among young adults with sickle cell disease during their final year of pediatric hematology care
被引:1
|作者:
Bangudi, Suzy
[1
]
Stanek, Charis
[2
]
Shankar, Divya
[1
]
Hart, Laura
[1
,2
]
Nahata, Leena
[1
,2
]
Cronin, Robert M.
[2
]
Creary, Susan E.
[1
,2
]
机构:
[1] Ohio State Univ, Coll Med, Columbus, OH 43201 USA
[2] Nationwide Childrens Hosp, Abigail Wexner Res Inst, Columbus, OH USA
关键词:
HEALTH-CARE;
ADOLESCENTS;
TRANSITION;
CHILDREN;
COMFORT;
D O I:
10.1002/pbc.30784
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Depression may contribute to transition risk among young adults with sickle cell disease (SCD). It is unclear if they receive depression screening because primary care providers (PCPs) routinely perform this screening, but PCP use declines with age. This retrospective study of young adults with SCD during their final year of pediatric hematology care identified 51 (91%) had PCPs. Among those with hospital system PCPs, 20% saw their PCP and 50% of those were screened for depression by the PCP. This suggests young adults with SCD may not receive depression screening or see PCPs, leading to potential missed opportunities for intervention.
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