Shiffman R N, Freudigman M d, Brandt C A, Liaw Y, Navedo D D
Department of Pediatrics, Yale School of Medicine, New Haven, CT 06520-8009, USA.
Pediatrics. 2000 Apr;105(4 Pt 1):767-73. doi: 10.1542/peds.105.4.767.
To evaluate effects on the process and outcomes of care brought about by use of a handheld, computer-based system that implements the American Academy of Pediatrics guideline on office management of asthma exacerbations.
A before-after trial with randomly selected, office-based Connecticut pediatricians. In both the control and intervention phases, physicians collected data from 10 patient encounters for acute asthma exacerbations. During the intervention phase, the computer provided for structured encounter documentation and offered recommendations based on the guideline of the American Academy of Pediatrics. Patients were contacted by telephone 7 to 14 days after the visit to assess outcomes.
Nine study-physicians enrolled 91 patients in the control phase and 74 in the intervention phase. Follow-up information was available for 93% of encounters. Use of the intervention was associated with increased mean frequency/visit of: 1) measurements of peak expiratory flow rate (2.18 vs 1.57) and oxygen saturation (1.12 vs.42), and 2) administration of nebulized beta2-agonists (1.25 vs.71). Visits in the intervention phase lasted longer and fees were higher ($145.61 vs $103.11). There were no significant differences in immediate disposition or subsequent emergency department visits, hospitalizations, missed school, or caretaker's missed work during the 7 days post visit.
Use of handheld computers that provide guideline-based decision support was associated with increased physician adherence to guideline recommendations; however, visits were prolonged, fees were higher, and no improvement could be demonstrated with regard to the observed intermediate-term patient outcomes. Guideline implementers (and users) should be cautious about putting unvalidated recommendations into practice.
评估使用一种基于计算机的手持式系统对哮喘急性发作门诊管理过程及护理结果的影响,该系统实施了美国儿科学会的哮喘急性发作门诊管理指南。
对随机选取的康涅狄格州门诊儿科医生进行前后对照试验。在对照阶段和干预阶段,医生均从10例急性哮喘发作患者的诊疗过程中收集数据。在干预阶段,计算机提供结构化的诊疗记录,并根据美国儿科学会的指南给出建议。就诊后7至14天通过电话联系患者以评估结果。
9名参与研究的医生在对照阶段纳入了91例患者,在干预阶段纳入了74例患者。93%的诊疗过程有随访信息。使用该干预措施与以下方面平均就诊频率增加相关:1)呼气峰值流速测量(2.18比1.57)和血氧饱和度测量(1.12比0.42),以及2)雾化吸入β2激动剂的使用(1.25比0.71)。干预阶段的就诊时间更长,费用更高(145.61美元比103.11美元)。就诊后7天内,在即刻处置、后续急诊就诊、住院、缺课或家长误工方面无显著差异。
使用提供基于指南决策支持的手持式计算机与医生对指南建议的依从性增加相关;然而,就诊时间延长,费用更高,且未观察到中期患者结局有改善。指南实施者(及使用者)在将未经验证的建议付诸实践时应谨慎。