Gislason Gunnar H, Rasmussen Jeppe N, Abildstrom Steen Z, Schramm Tina Ken, Hansen Morten Lock, Buch Pernille, Sørensen Rikke, Folke Fredrik, Gadsbøll Niels, Rasmussen Søren, Køber Lars, Madsen Mette, Torp-Pedersen Christian
Department of Cardiology, Gentofte University Hospital, Hellerup, Denmark.
Circulation. 2007 Aug 14;116(7):737-44. doi: 10.1161/CIRCULATIONAHA.106.669101. Epub 2007 Jul 23.
Undertreatment with recommended pharmacotherapy is a common problem in heart failure and may influence prognosis. We studied initiation and persistence of evidence-based pharmacotherapy in 107,092 patients discharged after first hospitalization for heart failure in Denmark from 1995 to 2004.
Prescriptions of dispensed medication and mortality were identified by an individual-level linkage of nationwide registers. Inclusion was irrespective of left ventricular function. Treatment with renin-angiotensin inhibitors (eg, angiotensin-converting enzyme inhibitors and angiotensin-2 receptor blockers), beta-blockers, spironolactone, and statins was initiated in 43%, 27%, 19%, and 19% of patients, respectively. Patients who did not initiate treatment within 90 days of discharge had a low probability of later treatment initiation. Treatment dosages were in general only 50% of target dosages and were not increased during long-term treatment. Short breaks in therapy were common, but most patients reinitiated treatment. Five years after initiation of treatment, 79% patients were still on renin-angiotensin inhibitors, 65% on beta-blockers, 56% on spironolactone, and 83% on statins. Notably, multiple drug treatment and increased severity of heart failure was associated with persistence of treatment. Nonpersistence with renin-angiotensin inhibitors, beta-blockers, and statins was associated with increased mortality with hazard ratios for death of 1.37 (95% CI, 1.31 to 1.42), 1.25 (95% CI, 1.19 to 1.32), 1.88 (95% CI, 1.67 to 2.12), respectively.
Persistence of treatment was high once medication was started, but treatment dosages were below recommended dosages. Increased severity of heart failure or increased number of concomitant medications did not worsen persistence, but nonpersistence identified a high-risk population of patients who required special attention. A focused effort on early treatment initiation, appropriate dosages, and persistence with the regimen is likely to provide long-term benefit.
推荐的药物治疗未充分实施是心力衰竭领域的常见问题,且可能影响预后。我们研究了1995年至2004年在丹麦因心力衰竭首次住院后出院的107,092例患者中循证药物治疗的起始和持续情况。
通过全国登记册的个体层面关联确定所配发药物的处方和死亡率。纳入标准与左心室功能无关。分别有43%、27%、19%和19%的患者开始使用肾素 - 血管紧张素抑制剂(如血管紧张素转换酶抑制剂和血管紧张素2受体阻滞剂)、β受体阻滞剂、螺内酯和他汀类药物进行治疗。出院后90天内未开始治疗的患者后续开始治疗的可能性较低。治疗剂量通常仅为目标剂量的50%,且在长期治疗过程中未增加。治疗过程中的短期中断很常见,但大多数患者会重新开始治疗。开始治疗五年后,79%的患者仍在使用肾素 - 血管紧张素抑制剂,65%使用β受体阻滞剂,56%使用螺内酯,83%使用他汀类药物。值得注意的是,联合药物治疗和心力衰竭严重程度增加与治疗持续相关。肾素 - 血管紧张素抑制剂、β受体阻滞剂和他汀类药物治疗的中断与死亡率增加相关,死亡风险比分别为1.37(95%CI,1.31至1.42)、1.25(95%CI,1.19至1.32)、1.88(95%CI,1.67至2.12)。
一旦开始用药,治疗的持续性较高,但治疗剂量低于推荐剂量。心力衰竭严重程度增加或联合用药数量增加并未使治疗持续性恶化,但治疗中断识别出了需要特别关注的高危患者群体。集中精力于早期治疗起始、合适剂量以及治疗方案的持续性可能会带来长期益处。