Michael K A, Parnell K J
Department of Pharmacy Services, University of Virginia Health System, Charlottesville 22906-0002, USA.
AACN Clin Issues. 1998 May;9(2):172-91; quiz 327-8. doi: 10.1097/00044067-199805000-00003.
Improved understanding of the pathophysiologic course of heart failure has led to many advances in pharmacologic therapy. Angiotensin-converting enzyme inhibitors represent the first effort at targeting neurohormonal activation in chronic heart failure. More recently, beta-adrenergic receptor antagonists have been shown effective in blocking chronic sympathetic nervous system activation. The roles of digoxin and the newer, vasoselective calcium channel blockers in heart failure have been better defined. Other agents targeting the neurohormonal system are under investigation. These include angiotensin-receptor antagonists, aldosterone inhibitors, and endothelin antagonists. Experience with phosphodiesterase inhibitors and adrenergic agents has confirmed the importance of neurohormonal activation in progression of heart failure. Despite angiotensin-converting enzyme inhibitor, diuretic, and digoxin therapy, mortality in heart failure remains high. Careful manipulation of the neurohormonal response to heart failure holds promise for altering the course of the disease.
对心力衰竭病理生理过程的深入了解推动了药物治疗的诸多进展。血管紧张素转换酶抑制剂是针对慢性心力衰竭神经激素激活的首次尝试。最近,β-肾上腺素能受体拮抗剂已被证明可有效阻断慢性交感神经系统激活。地高辛和新型血管选择性钙通道阻滞剂在心力衰竭中的作用已得到更明确的界定。其他针对神经激素系统的药物正在研究中。这些药物包括血管紧张素受体拮抗剂、醛固酮抑制剂和内皮素拮抗剂。磷酸二酯酶抑制剂和肾上腺素能药物的使用经验证实了神经激素激活在心力衰竭进展中的重要性。尽管使用了血管紧张素转换酶抑制剂、利尿剂和地高辛进行治疗,但心力衰竭的死亡率仍然很高。谨慎调控对心力衰竭的神经激素反应有望改变疾病的进程。