Simko R J, Stanek E J
College of Pharmacy, Midwestern University, Downers Grove, IL, USA.
Am J Manag Care. 1997 Nov;3(11):1669-76.
Little published information regarding current pharmacotherapeutic treatment patterns for congestive heart failure (CHF) in nonacademic, ambulatory care settings is available. We sought to assess, in a nonacademic primary care environment, pharmacotherapeutic treatment patterns for CHF with respect to consistency with clinical trial evidence and published treatment guideline recommendations. Over an 18-month period, we examined CHF pharmacotherapy using a computerized, integrated clinical diagnoses and prescription database from an outpatient community healthcare center without academic affiliations. We identified adult patients meeting contact criteria and with diagnosis of CHF by International Classification of Diseases (ICD-9-CM) coding and assessed prescribed therapy as well as select comorbid conditions. Drugs of interest included those with known or suspected benefit or detriment and those with unproven benefit. An eligible group of 14,983 patients was identified, from which a cohort of 148 patients with CHF was selected. Forty-one percent of these 148 patients were prescribed an angiotensin converting enzyme (ACE) inhibitor, 34% digoxin, 12% diuretic, 12% hydralazine + nitrate, 20% inhaled beta-agonists, and 66% warfarin. Only 5% of patients were prescribed the combination of an ACE inhibitor, digoxin, and diuretic. Thirty-one percent had a comorbid diagnosis of atrial fibrillation, of whom 44% were prescribed digoxin, 22% diltiazem, 15% beta-blockers, 15% digoxin and diltiazem, 7% digoxin and a beta-blocker, and 33% warfarin. In general, recommended therapies for CHF appeared underutilized in this cohort, whereas those of unclear benefit and potential detriment appeared overutilized. Although these results may not be readily generalized to the entire healthcare system, they do suggest a need for additional analysis and potential intervention.
关于非学术性门诊护理环境中充血性心力衰竭(CHF)当前药物治疗模式的公开信息很少。我们试图在非学术性初级护理环境中,评估CHF的药物治疗模式与临床试验证据和已发表的治疗指南建议的一致性。在18个月的时间里,我们使用一个来自无学术附属关系的门诊社区医疗中心的计算机化综合临床诊断和处方数据库,对CHF药物治疗进行了研究。我们通过国际疾病分类(ICD-9-CM)编码确定了符合接触标准并诊断为CHF的成年患者,并评估了所开的治疗药物以及选定的合并症。感兴趣的药物包括那些已知或疑似有益或有害的药物以及那些益处未经证实的药物。确定了一组符合条件的14983名患者,从中选出了148名CHF患者队列。这148名患者中,41%的患者开具了血管紧张素转换酶(ACE)抑制剂,34%开具了地高辛,12%开具了利尿剂,12%开具了肼屈嗪+硝酸盐,20%开具了吸入性β-激动剂,66%开具了华法林。只有5%的患者同时开具了ACE抑制剂、地高辛和利尿剂。31%的患者合并诊断为心房颤动,其中44%的患者开具了地高辛,22%开具了地尔硫䓬,15%开具了β受体阻滞剂,15%开具了地高辛和地尔硫䓬,7%开具了地高辛和β受体阻滞剂,33%开具了华法林。总体而言,该队列中CHF的推荐疗法似乎未得到充分利用,而那些益处不明确和有潜在危害的疗法似乎被过度使用。尽管这些结果可能无法轻易推广到整个医疗系统,但它们确实表明需要进行更多分析和可能的干预。