Alkhatib Einas H, Patel Tejal, Harlam Julie, Pavuluri Padmaja, Naveed Maria, Dauber Andrew, Vaidyanathan Priya
From the Division of Endocrinology/Diabetes, Department of Pediatrics, Children's National Hospital, Washington, D.C.
Division of Endocrinology/Diabetes, Department of Pediatrics, Boston Children's Hospital, Boston, Mass.
Pediatr Qual Saf. 2025 Jun 25;10(4):e824. doi: 10.1097/pq9.0000000000000824. eCollection 2025 Jul-Aug.
Graves disease (GD) is the most common cause of pediatric hyperthyroidism, and if untreated, may result in multisystem complications and decreased quality of life. Through a multifaceted quality improvement (QI) approach, we aimed to address treatment barriers after a new diagnosis of GD and increase the percentage of patients attaining an euthyroid state within 3 months from diagnosis and sustain for 12 months.
Using standard QI methodologies from January to November 2023, our plan, do, study, act cycles focused on an educational handout and checklist at diagnosis, a standardized methimazole dose based on initial free thyroxine (T4) and age, and frequent provider check-ins with phone call at 2 weeks, telehealth visit at 4 weeks with laboratories, and continued QI follow-up for 3 months as process measures. Outcome measure was the percentage of patients achieving normalization of free T4 level by 3 months. We used an electronic dashboard to track patients.
Of the 46 patients, 76% (34) received written education; 67% (30) were initiated on standardized methimazole dosing; 80% (37) and 70% (32), respectively, attended the 2-week telephone and 1-month telehealth visits, and 83% (38) obtained 1-month laboratories. By 3 months, the outcome measure increased to 78% (36/46) from 47% (15/32) ( < 0.01), sustained at 6 months (58% versus 22%) but decreased by 12 months (45% versus 40%). Barriers included missed appointments/laboratories, language, medication adherence, and/or lack of insurance.
Through a multifaceted QI approach, we increased the percentage of newly diagnosed GD patients with normal free T4 levels and sustained for 6 months. Extension of follow-up is planned.
格雷夫斯病(GD)是儿童甲状腺功能亢进最常见的病因,若不治疗,可能导致多系统并发症并降低生活质量。通过多方面的质量改进(QI)方法,我们旨在解决GD新诊断后的治疗障碍,并提高患者在诊断后3个月内达到甲状腺功能正常状态并维持12个月的比例。
使用2023年1月至11月的标准QI方法,我们的计划、执行、研究、行动循环聚焦于诊断时的教育手册和检查表、基于初始游离甲状腺素(T4)和年龄的标准化甲巯咪唑剂量,以及在2周时通过电话、4周时通过远程医疗就诊并进行实验室检查的频繁医护人员检查,以及作为过程指标持续3个月的QI随访。结果指标是3个月内游离T4水平恢复正常的患者比例。我们使用电子仪表盘跟踪患者。
46例患者中,76%(34例)接受了书面教育;67%(30例)开始采用标准化甲巯咪唑剂量治疗;分别有80%(37例)和70%(32例)参加了2周的电话随访和1个月的远程医疗就诊,83%(38例)进行了1个月的实验室检查。到3个月时,结果指标从47%(15/32)提高到78%(36/46)(P<0.01),6个月时维持在该水平(58%对22%),但12个月时下降(45%对40%)。障碍包括错过预约/实验室检查、语言问题、药物依从性和/或缺乏保险。
通过多方面的QI方法,我们提高了新诊断的GD患者游离T4水平正常并维持6个月的比例。计划延长随访时间。