Department of Cardiology, University of Basel Hospital, Basel, Switzerland.
Minerva Med. 2012 Oct;103(5):361-7.
"Optimal" medical therapy is mandatory before implantation of a cardiac resynchronization therapy (CRT) device, but "optimal" is not further specified. We determined the number of patients on a specific drug, the percentages of recommended target doses of the drugs the patients were on and their evolution over time.
Drug therapy (ACE-inhibitors (ACE-I), AT-receptor antagonists (ARBs), betablockers) of 140 patients with a follow-up of at least one year was studied. Response to CRT was defined as reduction in NYHA class ≥1.
Age was 66±9 years, follow-up 43±25 months during which 28 patients (20%) had died. At baseline, 81 % of patients were on a betablocker compared to 95% after 3 years (P-value 0.02). Percentages of target doses were 55±34% and increased to 68±41% after 3 years (P-value <0.02). Percentages were increased in responders (58±40% to 72±32%, P-value 0.01 after 3 years), but not in non-responders (57±31% to 56±38%). At baseline, 97% of patients were on ACE-Is/ARBs and 100% after 3 years. Mean percentages of target doses were 78±43% at implant and between 73±40% and 79±49% during follow-up. Percentages were stable both in responders (83% at implant, 78% after 3 years) and in non-responders (80%/87%, both P-value n.s.).
Even though quantity and quality of drug therapy at baseline was on an acceptable (betablockers) or high (ACE-Is/ARBs) level, physicians must be very observant on therapy during long-term follow-up, especially on target doses of betablockers in non-responders.
在植入心脏再同步治疗(CRT)装置之前,必须进行“最佳”药物治疗,但并未进一步具体说明“最佳”的含义。我们确定了接受特定药物治疗的患者数量、患者接受推荐药物靶剂量的百分比及其随时间的变化。
研究了至少随访 1 年的 140 例患者的药物治疗(ACE 抑制剂(ACE-I)、AT 受体拮抗剂(ARB)、β受体阻滞剂)。CRT 反应定义为 NYHA 心功能分级至少改善 1 级。
年龄为 66±9 岁,随访时间为 43±25 个月,在此期间有 28 例患者(20%)死亡。基线时,81%的患者使用β受体阻滞剂,3 年后增至 95%(P 值为 0.02)。靶剂量百分比为 55±34%,3 年后增至 68±41%(P 值<0.02)。在有反应者中,百分比增加(58±40%至 72±32%,3 年后 P 值为 0.01),但在无反应者中未增加(57±31%至 56±38%)。基线时,97%的患者使用 ACE-I/ARB,3 年后为 100%。植入时平均靶剂量百分比为 78±43%,随访期间为 73±40%至 79±49%。有反应者和无反应者的百分比均稳定(植入时为 83%,3 年后为 78%)(两者 P 值均为 n.s.)。
尽管基线时药物治疗的数量和质量处于可接受水平(β受体阻滞剂)或较高水平(ACE-I/ARB),但医生在长期随访期间必须密切关注治疗情况,特别是非反应者β受体阻滞剂的靶剂量。