Brinkman William B, Hartl Jessica, Rawe Lauren M, Sucharew Heidi, Britto Maria T, Epstein Jeffery N
Department of Pediatrics, Center for Innovation in Chronic Disease Care, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA.
Arch Pediatr Adolesc Med. 2011 Nov;165(11):1013-9. doi: 10.1001/archpediatrics.2011.154.
To describe the amount of shared decision-making (SDM) behavior exhibited during treatment-planning encounters for children newly diagnosed as having attention-deficit/hyperactivity disorder and to explore relationships between participant characteristics and the amount of SDM.
Prospective cohort study.
Seven community-based primary care pediatric practices in the Cincinnati, Ohio; northern Kentucky; and southeast Indiana regions from October 5, 2009, through August 9, 2010.
Ten pediatricians and 26 families with a 6- to 10-year-old child newly diagnosed as having attention-deficit/hyperactivity disorder.
The amount of SDM behavior exhibited during videorecorded encounters, as coded by 2 independent raters using the validated Observing Patient Involvement (OPTION) scale, which was adapted for use in pediatric settings and produces a score ranging from 0 (no parental involvement) to 100 (maximal parental involvement).
Treatment decisions focused on initiation of medication treatment. The mean (SD) total OPTION score was 28.5 (11.7). More SDM was observed during encounters involving families with white vs nonwhite children (adjusted mean difference score, 14.9; 95% confidence interval [CI], 10.2-19.6; P < .001), private vs public health insurance coverage (adjusted mean difference score, 15.1; 11.2-19.0; P < .001), mothers with at least some college education vs high school graduate or less (adjusted mean difference score, 12.3; 7.2-17.4; P < .001), and parents who did not screen positive for serious mental illness vs those who did (adjusted mean difference score, 15.0; 11.9-18.1; P < .001).
Low levels of SDM were observed. Exploratory analyses identified potential disparities and barriers. Interventions may be needed to foster SDM with all parents, especially those of nonwhite race, of lower socioeconomic status, of lower educational level, and with serious mental illness.
描述新诊断为注意力缺陷/多动障碍儿童的治疗计划会诊中表现出的共同决策(SDM)行为量,并探讨参与者特征与SDM量之间的关系。
前瞻性队列研究。
2009年10月5日至2010年8月9日期间,俄亥俄州辛辛那提、肯塔基州北部和印第安纳州东南部地区的7家社区基层医疗儿科诊所。
10名儿科医生和26个家庭,每个家庭有一名新诊断为注意力缺陷/多动障碍的6至10岁儿童。
录像会诊期间表现出的SDM行为量,由2名独立评分者使用经过验证的《观察患者参与度》(OPTION)量表进行编码,该量表适用于儿科环境,得分范围为0(无父母参与)至100(父母最大参与度)。
治疗决策集中在药物治疗的启动上。OPTION量表总平均分(标准差)为28.5(11.7)。在涉及白人儿童家庭与非白人儿童家庭的会诊中观察到更多的SDM(调整后平均差异得分,14.9;95%置信区间[CI],10.2 - 19.6;P <.001),私人医疗保险与公共医疗保险覆盖的家庭(调整后平均差异得分,15.1;11.2 - 19.0;P <.001),母亲至少有一些大学教育与高中或以下学历的家庭(调整后平均差异得分,12.3;7.2 - 17.4;P <.001),以及未筛查出严重精神疾病阳性的父母与筛查出阳性的父母(调整后平均差异得分,15.0;11.9 - 18.1;P <.001)。
观察到SDM水平较低。探索性分析确定了潜在的差异和障碍。可能需要采取干预措施,促进与所有父母的SDM,特别是非白人种族、社会经济地位较低、教育水平较低以及患有严重精神疾病的父母。