N J Summerfield, A Boswood, M R O'Grady, S G Gordon, J Dukes-McEwan, M A Oyama, S Smith, M Patteson, A T French, G J Culshaw, L Braz-Ruivo, A Estrada, M L O'Sullivan, J Loureiro, R Willis, P Watson
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Dogs were allocated in a 1:1 ratio to receive pimobendan (Vetmedin capsules) or visually identical placebo. The composite primary endpoint was prospectively defined as either onset of CHF or sudden death. Time to death from all causes was a secondary endpoint.</p><p><strong>Results: </strong>The proportion of dogs reaching the primary endpoint was not significantly different between groups (P = .1). The median time to the primary endpoint (onset of CHF or sudden death) was significantly longer in the pimobendan (718 days, IQR 441-1152 days) versus the placebo group (441 days, IQR 151-641 days) (log-rank P = 0.0088). The median survival time was significantly longer in the pimobendan (623 days, IQR 491-1531 days) versus the placebo group (466 days, IQR 236-710 days) (log-rank P = .034).</p><p><strong>Conclusion and clinical importance: </strong>The administration of pimobendan to Dobermans with preclinical DCM prolongs the time to the onset of clinical signs and extends survival. 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引用次数: 128
摘要
背景:哌莫苯丹在延缓杜宾犬临床前扩张型心肌病(DCM)进展方面的益处尚未报道。假设:临床前DCM的杜宾犬长期口服匹莫苯丹可以延缓CHF或猝死的发生,提高生存率。动物:在英国和北美的10个中心招募了76只客户拥有的杜宾犬。方法:采用随机、盲法、安慰剂对照、平行组多中心研究。狗按1:1的比例被分配接受匹莫苯丹(维美丁胶囊)或视觉上相同的安慰剂。综合主要终点被前瞻性地定义为CHF发作或猝死。各种原因导致的死亡时间是次要终点。结果:两组间达到主要终点的犬只比例差异无统计学意义(P = 0.1)。与安慰剂组(441天,IQR 151-641天)相比,匹摩苯丹组(718天,IQR 441-1152天)到主要终点(CHF发作或猝死)的中位时间明显更长(log-rank P = 0.0088)。匹摩苯丹组的中位生存时间(623天,IQR 491-1531天)明显长于安慰剂组(466天,IQR 236-710天)(log-rank P = 0.034)。结论及临床意义:临床前DCM杜宾犬给予匹莫苯丹可延长临床症状出现时间,延长生存期。用哌摩苯丹治疗这种常见心血管疾病的临床前阶段的狗可以改善结果。
Efficacy of pimobendan in the prevention of congestive heart failure or sudden death in Doberman Pinschers with preclinical dilated cardiomyopathy (the PROTECT Study).
Background: The benefit of pimobendan in delaying the progression of preclinical dilated cardiomyopathy (DCM) in Dobermans is not reported.
Hypothesis: That chronic oral administration of pimobendan to Dobermans with preclinical DCM will delay the onset of CHF or sudden death and improve survival.
Animals: Seventy-six client-owned Dobermans recruited at 10 centers in the UK and North America.
Methods: The trial was a randomized, blinded, placebo-controlled, parallel group multicenter study. Dogs were allocated in a 1:1 ratio to receive pimobendan (Vetmedin capsules) or visually identical placebo. The composite primary endpoint was prospectively defined as either onset of CHF or sudden death. Time to death from all causes was a secondary endpoint.
Results: The proportion of dogs reaching the primary endpoint was not significantly different between groups (P = .1). The median time to the primary endpoint (onset of CHF or sudden death) was significantly longer in the pimobendan (718 days, IQR 441-1152 days) versus the placebo group (441 days, IQR 151-641 days) (log-rank P = 0.0088). The median survival time was significantly longer in the pimobendan (623 days, IQR 491-1531 days) versus the placebo group (466 days, IQR 236-710 days) (log-rank P = .034).
Conclusion and clinical importance: The administration of pimobendan to Dobermans with preclinical DCM prolongs the time to the onset of clinical signs and extends survival. Treatment of dogs in the preclinical phase of this common cardiovascular disorder with pimobendan can lead to improved outcome.
期刊介绍:
The mission of the Journal of Veterinary Internal Medicine is to advance veterinary medical knowledge and improve the lives of animals by publication of authoritative scientific articles of animal diseases.