Increasing and maintaining rates of standardized depression screening in youth with childhood-onset systemic lupus erythematosus in a pediatric rheumatology clinic.

IF 2.8 3区 医学 Q1 PEDIATRICS Pediatric Rheumatology Pub Date : 2025-01-04 DOI:10.1186/s12969-024-01038-3
Emily Datyner, Jodi Dingle, Victoria Newsome, Lisa H Buckley, Natasha Belsky, Seungweon Park, Manda Mitchell, Brooke Fine, Barron Patterson, T Brent Graham, Alaina Davis
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Abstract

Background: Depression adversely affects health outcomes in patients with childhood-onset systemic lupus erythematous (cSLE). By identifying patients with depressive symptoms, we can intervene early with referrals to mental health resources and improve outcomes. The aim of our quality improvement project was to increase and maintain rates of standardized depression screening for youth with cSLE seen within our pediatric rheumatology clinic.

Methods: Patients with cSLE 12 years of age or older seen for routine follow-up at our pediatric rheumatology clinic from September 16, 2019, through December 30, 2022, were offered the Patient Health Questionnaire-9 modified for adolescents (PHQ-A) to screen for depressive symptoms. A multidisciplinary team developed a key driver diagram to plan potential interventions to improve rates of screening. Plan‒Do‒Study‒Act (PDSA) cycles were used to prepare, implement, and evaluate interventions. Notable interventions focused on accurately identifying eligible patients, facilitating bidirectional communication between staff, and integrating and automating screening within the electronic health record (EHR). Statistical process control (SPC) methods were used for data analysis.

Results: The percentage of eligible patient encounters where depression screening was completed increased from 0 to 81% and was maintained for more than 6 months. This represents special cause variation, as evidenced by data shifts on our statistical process control chart. Among the 592 patients who completed depression screens, 114 (17%) were positive for moderate to severe symptoms, and 59 (9%) were positive for suicidal ideation (SI).

Conclusions: A high rate of standardized depression screening for youth with cSLE was achieved and maintained via integration and automation within our EHR. Establishing a highly reliable screening system is a critical first step in improving mental health care for this vulnerable population of youth.

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在儿童风湿病临床增加和维持儿童期全身性红斑狼疮青少年的标准化抑郁筛查率
背景:抑郁症对儿童期全身性红斑狼疮(cSLE)患者的健康结果有不利影响。通过识别抑郁症状的患者,我们可以通过转介到心理健康资源进行早期干预,并改善结果。我们的质量改进项目的目的是提高和维持在我们的儿科风湿病诊所看到的青少年cSLE的标准化抑郁筛查率。方法:从2019年9月16日至2022年12月30日,在我们的儿科风湿病诊所进行常规随访的12岁或以上的cSLE患者接受了青少年患者健康问卷-9 (PHQ-A)的筛查,以筛查抑郁症状。一个多学科团队制定了一个关键的驱动图,以计划潜在的干预措施,以提高筛查率。计划-执行-研究-行动(PDSA)循环用于准备、实施和评估干预措施。值得注意的干预措施侧重于准确识别符合条件的患者,促进工作人员之间的双向沟通,以及在电子健康记录(EHR)中集成和自动化筛查。采用统计过程控制(SPC)方法进行数据分析。结果:完成抑郁症筛查的合格患者的百分比从0增加到81%,并维持了6个多月。这代表了特殊原因的变化,正如我们统计过程控制图上的数据变化所证明的那样。在592名完成抑郁筛查的患者中,114名(17%)中度至重度症状呈阳性,59名(9%)自杀意念(SI)呈阳性。结论:通过电子病历的整合和自动化,实现并维持了青少年cSLE的高标准化抑郁筛查率。建立一个高度可靠的筛查系统是改善这一弱势青年群体心理卫生保健的关键的第一步。
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来源期刊
Pediatric Rheumatology
Pediatric Rheumatology PEDIATRICS-RHEUMATOLOGY
CiteScore
4.10
自引率
8.00%
发文量
95
审稿时长
>12 weeks
期刊介绍: Pediatric Rheumatology is an open access, peer-reviewed, online journal encompassing all aspects of clinical and basic research related to pediatric rheumatology and allied subjects. The journal’s scope of diseases and syndromes include musculoskeletal pain syndromes, rheumatic fever and post-streptococcal syndromes, juvenile idiopathic arthritis, systemic lupus erythematosus, juvenile dermatomyositis, local and systemic scleroderma, Kawasaki disease, Henoch-Schonlein purpura and other vasculitides, sarcoidosis, inherited musculoskeletal syndromes, autoinflammatory syndromes, and others.
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