Rybczynski Suzanne, Ryan Taylor C, Wilcox Holly C, Van Eck Kathryn, Cwik Mary, Vasa Roma A, Findling Robert L, Slifer Keith, Kleiner Daniel, Lipkin Paul H
Kennedy Krieger Institute, Baltimore, MD.
Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD.
J Dev Behav Pediatr. 2022 May 1;43(4):181-187. doi: 10.1097/DBP.0000000000001026. Epub 2021 Oct 15.
The purpose of this study was to describe the implementation of universal suicide risk screening in pediatric neurodevelopmental disabilities (NDD) medical clinics, analyze demographic and clinical characteristics of eligible patients, describe outcomes of positive screenings, and describe factors that influenced participation in screenings.
A suicide risk screening protocol was developed and implemented for medical clinic patients aged 8 to 18 years. Registered nurses screened patients using the "Ask Suicide-Screening Questions" tool during triage. Positive screenings were referred for further assessment and mental health management. Demographics and clinical data were extracted from medical records using retrospective chart reviews.
During the 6-month study period, 2961 individual patients presented for 5260 screening eligible patient visits. In total, 3854 (73.3%) screenings were completed with 261 (6.8%) positive screenings noted. Screenings were declined in 1406 (26.7%) visits. Parents of children with cognitive impairments were more likely to decline screening. Clinics serving children with autism spectrum disorder had higher rates of positive screenings compared with all other clinic attendees. Seventy-two of 187 children (38.5%) with positive screenings were identified and referred to outpatient mental health referrals. Seven (2.5%) of these children required acute psychiatric treatment.
Routine screening, identification of increased suicide risk, and referral to mental health care among children with NDD are feasible. It remains unclear whether variation in rates among youth with and without NDD may indicate true differences in suicide risk or cognitive impairments or reflect psychiatric comorbidities. High rates of declined participation may have influenced identification of children with NDD and suicide risk. Preliminary findings identified groups of children with NDD at heightened risk for suicidal ideation and behavior. Further research is needed to assess the validity of suicide risk screening tools in children with neurodevelopmental disorders.
本研究旨在描述儿科神经发育障碍(NDD)诊所中通用自杀风险筛查的实施情况,分析符合条件患者的人口统计学和临床特征,描述筛查呈阳性的结果,并描述影响参与筛查的因素。
为8至18岁的诊所患者制定并实施了自杀风险筛查方案。注册护士在分诊期间使用“询问自杀筛查问题”工具对患者进行筛查。筛查呈阳性者被转介进行进一步评估和心理健康管理。通过回顾性病历审查从医疗记录中提取人口统计学和临床数据。
在6个月的研究期间,2961名个体患者进行了5260次符合筛查条件的就诊。总共完成了3854次(73.3%)筛查,其中261次(6.8%)筛查呈阳性。1406次(26.7%)就诊的筛查被拒绝。认知障碍儿童的父母更有可能拒绝筛查。与所有其他诊所就诊者相比,为自闭症谱系障碍儿童服务的诊所筛查呈阳性的比例更高。187名筛查呈阳性的儿童中有72名(38.5%)被识别并转介至门诊心理健康机构。其中7名(2.5%)儿童需要急性精神病治疗。
在患有NDD的儿童中进行常规筛查、识别自杀风险增加情况并转介至心理健康护理是可行的。尚不清楚患有和未患有NDD的青少年在筛查率上的差异是否表明自杀风险或认知障碍的真正差异或反映精神疾病共病情况。高拒绝参与率可能影响了对患有NDD和自杀风险儿童的识别。初步研究结果确定了患有NDD且有自杀意念和行为高风险的儿童群体。需要进一步研究以评估自杀风险筛查工具在神经发育障碍儿童中的有效性。