Anderton J L, Gill M, Notghi A
Department of Medicine, Western General Hospital, Edinburgh, UK.
Nephrol Dial Transplant. 1994;9(6):607-12. doi: 10.1093/ndt/9.6.607.
Effective renal plasma flow (ERPF) and glomerular filtration rate (GFR) were measured in 53 hypertensive patients (26 renally impaired, 27 with normal renal function) before and after treatment with sufficient bunazosin retard or prazosin to control their high blood pressure. After a 3-week placebo run-in period, patients were classified as normal (creatinine clearance > 80 ml/min) or renally impaired (20-55 ml/min), and randomly assigned to bunazosin retard or prazosin. There followed a dose titration (T) phase of 6-7 weeks, and a maintenance (M) phase of 4 weeks. Blood pressure was satisfactorily controlled (sitting diastolic pressure < or = 90 mmHg or decreased by > or = 10 mmHg) by both drugs in both groups. Bunazosin Retard was associated with increases in GFR and ERPF in both normal and renally impaired groups; the increases were statistically significant in the renally impaired group (n = 14). Prazosin was associated with small decreases in both measures in both groups. One patient died of myocardial infarction during the placebo run-in. There were no other serious adverse events. Four patients reported dizziness (2 with each drug). We conclude that with appropriate dose titration, bunazosin retard is well tolerated and preserves renal blood flow when used to treat hypertension in patients with renal insufficiency.
在53例高血压患者(26例肾功能受损,27例肾功能正常)中,在使用足量缓释布那唑嗪或哌唑嗪治疗以控制其高血压之前和之后,测量了有效肾血浆流量(ERPF)和肾小球滤过率(GFR)。经过3周的安慰剂导入期后,患者被分为肾功能正常(肌酐清除率>80 ml/分钟)或肾功能受损(20 - 55 ml/分钟),并随机分配至缓释布那唑嗪组或哌唑嗪组。随后是一个为期6 - 7周的剂量滴定(T)阶段和一个为期4周的维持(M)阶段。两组患者使用两种药物后血压均得到满意控制(坐位舒张压≤90 mmHg或下降≥10 mmHg)。缓释布那唑嗪在正常和肾功能受损组中均与GFR和ERPF的增加相关;在肾功能受损组(n = 14)中,这些增加具有统计学意义。哌唑嗪在两组中均与这两项指标的小幅下降相关。在安慰剂导入期有1例患者死于心肌梗死。没有其他严重不良事件。4例患者报告头晕(每种药物各2例)。我们得出结论,通过适当的剂量滴定,缓释布那唑嗪耐受性良好,在用于治疗肾功能不全患者的高血压时可保留肾血流量。