Okeke Constance O, Quigley Harry A, Jampel Henry D, Ying Gui-shuang, Plyler Ryan J, Jiang Yuzhen, Friedman David S
Scheie Eye Institute, Department of Ophthalmology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104, USA.
Ophthalmology. 2009 Feb;116(2):191-9. doi: 10.1016/j.ophtha.2008.09.004. Epub 2008 Dec 12.
To assess patient adherence and behaviors with topical once-daily therapy for glaucoma.
Prospective, observational cohort study.
One hundred ninety-six patients with glaucoma who were being treated with a prostaglandin analog in 1 or both eyes at the Scheie or Wilmer Eye Institutes between August 2006 and June 2007.
Detailed medical history was obtained from each patient. All subjects used the Travatan Dosing Aid (DA; Alcon, Fort Worth, TX) to administer travoprost as prescribed. Devices were collected at 3 months and the data of drop usage was downloaded using software provided with the dosing aid. Data were analyzed for the 8-week period starting 2 weeks after the enrollment visit and ending 2 weeks before the 3-month visit.
Assessment of adherence and patterns of drop usage as indicated by the DA.
A total of 282 subjects consented to be in the study and 86 (30%) withdrew before study completion or had device errors, leaving 196 subjects (70%) with evaluable data at 3 months. The overall mean (+/-standard deviation) adherence rate was 0.71 (+/-0.24), ranging from 0.02 to 0.97. One hundred nine of these patients (55.6%) took greater than 75% of the expected doses. Those with adherence of less than 50% of expected doses showed substantially increased dose taking immediately after the office visit and just before the return visit at 3 months (P = 0.03). The mean adherence rate estimates of the physician and patient self-report were 0.77 and 0.95, respectively. The agreement between the physician assessment and DA-recorded adherence rate showed poor correlation for individual cases (intraclass correlation coefficient, 0.09; 95% confidence interval, 0.00-0.19).
Nearly 45% of patients using an electronic monitoring device who knew they were being monitored and were provided free medication used their drops less than 75% of the time. Patients reported far higher medication use than their actual behavior. The ability of the physician to identify which persons are poorly adherent from their self-report or from other subjective clues is poor.
FINANCIAL DISCLOSURE(S): Proprietary or commercial disclosure may be found after the references.
评估青光眼患者对每日一次局部治疗的依从性和行为。
前瞻性观察队列研究。
2006年8月至2007年6月期间在Scheie或Wilmer眼科研究所接受前列腺素类似物单眼或双眼治疗的196例青光眼患者。
获取每位患者的详细病史。所有受试者按照处方使用Travatan给药辅助装置(DA;爱尔康公司,沃思堡,德克萨斯州)来施用曲伏前列素。在3个月时收集装置,并使用给药辅助装置附带的软件下载滴眼剂使用数据。对从入组访视后2周开始至3个月访视前2周结束的8周期间的数据进行分析。
根据DA评估依从性和滴眼剂使用模式。
共有282名受试者同意参加研究,其中86名(30%)在研究完成前退出或出现装置错误,196名受试者(70%)在3个月时有可评估数据。总体平均(±标准差)依从率为0.71(±0.24),范围为0.02至0.97。其中109名患者(55.6%)服用的剂量超过预期剂量的75%。那些依从性低于预期剂量50%的患者在门诊就诊后和3个月复诊前立即出现服药量大幅增加(P = 0.03)。医生和患者自我报告的平均依从率估计值分别为0.77和