Ang S Y, Peterson G M, Friesen W T, Vial J H
Tasmanian School of Pharmacy, Faculty of Health Science, University of Tasmania, Hobart Tas, Australia.
J Clin Pharm Ther. 1998 Apr;23(2):97-106. doi: 10.1046/j.1365-2710.1998.00148.x.
The important prophylactic role of antithrombotic therapy against stroke in nonrheumatic atrial fibrillation (AF) has been clearly established in recent clinical trials. There have been suggestions, however, that practice has been slow to change in light of the findings of these trials.
To review cases of AF at the major teaching hospital in Tasmania, Australia, to determine whether the recommendations from the results of the trials had been translated into local clinical practice.
A retrospective review of the medical records for consecutive patients who had AF documented on ECG between 1 January and 30 June 1997 was performed. An extensive range of demographic and clinical variables were recorded for patients with chronic or paroxysmal nonrheumatic AF. These included antithrombotic and other drug therapy at admission and discharge from hospital care, risk factors for stroke, contraindications to antithrombotic use, and incidents of ischaemic stroke and bleeding complications that occurred during the period from January 1996 up to 3 months after the hospital admission that was studied.
The 228 patients included in the study had a mean (+/-SD) age of 75.3+/-10.9 years. Sixty-eight per cent had chronic AF and 32% had paroxysmal AF. According to two risk stratification criteria, 91% and 86% of the patients with previously diagnosed chronic or paroxysmal nonrheumatic AF (n=186) had a high risk of developing stroke at the time of admission to hospital care. However, less than one-third of these patients were receiving warfarin (or warfarin plus aspirin), with almost another one-third receiving no antithrombotic agent. Of those who were not taking warfarin, about 60% had no apparent contraindication to warfarin. For those high risk patients who had a possible contraindication to warfarin, only approximately one-third had been prescribed aspirin. Only a slight increase in the use of antithrombotic agents had occurred by the time of discharge from hospital care. The majority of international normalized ratio (INR) values on admission for patients who had been taking warfarin were subtherapeutic. The estimated annual incidence of bleeding complications in patients taking warfarin was 15.0% overall, 5.0% for major bleeds and 3.8% for intracranial haemorrhages.
While a number of published trials have demonstrated that antithrombotic agents confer substantial protection against stroke in patients with nonrheumatic AF, the drugs were underused in our setting. There is a need to improve antithrombotic use and to develop a better monitoring system for the provision of safer and more effective antithrombotic therapy.
近期临床试验已明确抗血栓治疗在非风湿性心房颤动(AF)预防中风方面的重要作用。然而,有观点认为,鉴于这些试验结果,临床实践的改变较为缓慢。
回顾澳大利亚塔斯马尼亚主要教学医院的房颤病例,以确定试验结果的建议是否已转化为当地临床实践。
对1997年1月1日至6月30日期间心电图记录有房颤的连续患者的病历进行回顾性研究。记录了慢性或阵发性非风湿性房颤患者的一系列广泛的人口统计学和临床变量。这些变量包括入院和出院时的抗血栓及其他药物治疗、中风危险因素、抗血栓药物使用的禁忌症,以及1996年1月至所研究患者入院后3个月期间发生的缺血性中风和出血并发症事件。
纳入研究的228例患者的平均(±标准差)年龄为75.3±10.9岁。68%为慢性房颤,32%为阵发性房颤。根据两种风险分层标准,在入院接受医院治疗时,先前诊断为慢性或阵发性非风湿性房颤的患者(n = 186)中,91%和86%有发生中风的高风险。然而,这些患者中接受华法林(或华法林加阿司匹林)治疗的不到三分之一,近三分之一未接受抗血栓药物治疗。在未服用华法林的患者中,约60%没有明显的华法林使用禁忌症。对于那些对华法林可能有禁忌症的高风险患者,只有约三分之一被开了阿司匹林。到出院时,抗血栓药物的使用仅略有增加。服用华法林的患者入院时的国际标准化比值(INR)大多低于治疗水平。服用华法林的患者出血并发症的估计年发生率总体为15.0%,严重出血为5.0%,颅内出血为3.8%。
虽然多项已发表的试验表明抗血栓药物可显著预防非风湿性房颤患者中风,但在我们的研究环境中这些药物未得到充分利用。有必要改善抗血栓药物的使用,并建立更好的监测系统,以提供更安全、更有效的抗血栓治疗。