Weinberger Morris, Murray Michael D, Marrero David G, Brewer Nancy, Lykens Michael, Harris Lisa E, Seshadri Roopa, Caffrey Helena, Roesner J Franklin, Smith Faye, Newell A Jeffrey, Collins Joyce C, McDonald Clement J, Tierney William M
Regenstrief Institute for Health Care, Roudebush Veterans Affairs Medical Center, and Department of Medicine, Indiana University School of Medicine, Indianapolis, USA.
JAMA. 2002 Oct 2;288(13):1594-602. doi: 10.1001/jama.288.13.1594.
It is not known whether patient outcomes are enhanced by effective pharmacist-patient interactions.
To assess the effectiveness of a pharmaceutical care program for patients with asthma or chronic obstructive pulmonary disease (COPD).
DESIGN, SETTING, AND PARTICIPANTS: Randomized controlled trial conducted at 36 community drugstores in Indianapolis, Ind. We enrolled 1113 participants with active COPD or asthma from July 1998 to December 1999. Outcomes were assessed in 947 (85.1%) participants at 6 months and 898 (80.7%) at 12 months.
The pharmaceutical care program (n = 447) provided pharmacists with recent patient-specific clinical data (peak expiratory flow rates [PEFRs], emergency department [ED] visits, hospitalizations, and medication compliance), training, customized patient educational materials, and resources to facilitate program implementation. The PEFR monitoring control group (n = 363) received a peak flow meter, instructions about its use, and monthly calls to elicit PEFRs. However, PEFR data were not provided to the pharmacist. Patients in the usual care group (n = 303) received neither peak flow meters nor instructions in their use; during monthly telephone interviews, PEFR rates were not elicited. Pharmacists in both control groups had a training session but received no components of the pharmaceutical care intervention.
Peak expiratory flow rates, breathing-related ED or hospital visits, health-related quality of life (HRQOL), medication compliance, and patient satisfaction.
At 12 months, patients receiving pharmaceutical care had significantly higher peak flow rates than the usual care group (P =.02) but not than PEFR monitoring controls (P =.28). There were no significant between-group differences in medication compliance or HRQOL. Asthma patients receiving pharmaceutical care had significantly more breathing-related ED or hospital visits than the usual care group (odds ratio, 2.16; 95% confidence interval, 1.76-2.63; P<.001). Patients receiving pharmaceutical care were more satisfied with their pharmacist than the usual care group (P =.03) and the PEFR monitoring group (P =.001) and were more satisfied with their health care than the usual care group at 6 months only (P =.01). Despite ample opportunities to implement the program, pharmacists accessed patient-specific data only about half of the time and documented actions about half of the time that records were accessed.
This pharmaceutical care program increased patients' PEFRs compared with usual care but provided little benefit compared with peak flow monitoring alone. Pharmaceutical care increased patient satisfaction but also increased the amount of breathing-related medical care sought.
尚不清楚有效的药剂师 - 患者互动是否能改善患者预后。
评估一项针对哮喘或慢性阻塞性肺疾病(COPD)患者的药学服务项目的有效性。
设计、地点和参与者:在印第安纳州印第安纳波利斯的36家社区药店进行的随机对照试验。1998年7月至1999年12月,我们招募了1113名患有活动性COPD或哮喘的参与者。6个月时对947名(85.1%)参与者进行了结局评估,12个月时对898名(80.7%)参与者进行了评估。
药学服务项目组(n = 447)为药剂师提供了最新的患者特定临床数据(呼气峰值流速[PEFR]、急诊科就诊、住院和用药依从性)、培训、定制的患者教育材料以及促进项目实施的资源。PEFR监测对照组(n = 363)收到了一个峰值流量计、关于其使用的说明以及每月的电话以获取PEFR。然而,PEFR数据未提供给药剂师。常规护理组(n = 303)既未收到峰值流量计也未收到其使用说明;在每月的电话访谈中,未获取PEFR值。两个对照组的药剂师都参加了一次培训课程,但未接受药学服务干预的任何组成部分。
呼气峰值流速、与呼吸相关的急诊科或医院就诊、健康相关生活质量(HRQOL)、用药依从性和患者满意度。
在12个月时,接受药学服务的患者的峰值流速显著高于常规护理组(P = 0.02),但与PEFR监测对照组相比无显著差异(P = 0.28)。在用药依从性或HRQOL方面,组间无显著差异。接受药学服务的哮喘患者与呼吸相关的急诊科或医院就诊次数显著多于常规护理组(优势比,2.16;95%置信区间,1.76 - 2.63;P < 0.001)。接受药学服务的患者对其药剂师的满意度高于常规护理组(P = 0.03)和PEFR监测组(P = 0.001),并且仅在6个月时对其医疗保健的满意度高于常规护理组(P = 0.01)。尽管有充分的机会实施该项目,但药剂师仅约一半的时间获取了患者特定数据,并且在获取记录时约一半的时间记录了行动。
与常规护理相比,该药学服务项目提高了患者的PEFR,但与单独的峰值流速监测相比益处不大。药学服务提高了患者满意度,但也增加了与呼吸相关的医疗护理需求。