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Impact of internal audit on pacemaker prescription and the immediate costs of pacing in the northern region: towards implementation of the recommendations of the British Pacing and Electrophysiology Group.

机译:内部审计对北部地区起搏器处方和起搏直接成本的影响:实施英国起搏和电生理学小组的建议。

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摘要

BACKGROUND--In September 1990 a working party of the British Pacing and Electrophysiology Group recommended the routine use of physiological pacing systems in patients with bradycardia. An audit of the impact of these recommendations on pacemaker prescription in the Freeman Hospital between March 1990 and August 1991 has previously been reported. This paper considers the effect of that internal audit on subsequent pacemaker prescription from September 1991 to February 1993. PATIENTS AND METHODS--The records of 1228 patients who underwent first pacemaker implantation at the Freeman Hospital between March 1990 and February 1993 were audited retrospectively. The patient's age, indication for pacing, pacing mode, and cost of the generator and leads were recorded. The indications for pacing were sinus node dysfunction (24.9%) (including patients with coexistent sinus node dysfunction and atrioventricular block), atrioventricular block (57.2%), atrioventricular block and atrial fibrillation (12.2%), and carotid sinus syndrome (5.7%). There was an increase in carotid sinus syndrome (2.7% to 8.1%) between the two study periods but no other differences in the distribution of case mix or characteristics of patients. The cost of the working party's recommended optimal pacing mode was calculated from multiplication of the mean cost of the recommended unit over the second half of the study period by the number of patients who would have received that unit. RESULTS--Between March 1990 and August 1991 atrial pacing for sinus node dysfunction (AAI, AAIR, DDD, or DDDR) increased by 138% (from 25.0% to 59.6%), mainly because of increased use of AAI mode. Physiological pacing for atrioventricular block (DDD or VVIR) increased by 41% (from 17.0% to 24.0%), and VVIR pacing for atrioventricular block with atrial fibrillation increased by 111% (from 10.5% to 22.2%). After the internal audit (that is, between September 1991 and February 1993), physiological pacing for atrioventricular block increased by a further 126% (from 24.0% to 54.2%). Sixty three per cent of this increase was in the first six months after the internal audit. Pacemaker prescriptions in sinus node dysfunction and atrioventricular block with atrial fibrillation were unchanged (59.6% physiological pacing for sinus node dysfunction and 22.2% v 27.3% VVIR pacing for atrioventricular block with atrial fibrillation). These changes in practice were accompanied by an increase in the age of patients receiving physiological units. Costs of pacemaker hardware for the final six months of the audit (excluding carotid sinus syndrome) increased by 38% over the costs that would have accrued had pacing policy remained the same as for the initial six month period before the circulation of the recommendations of the working party. Adoption of the guidelines of the working party in full would lead to a further 66% increase in the costs of hardware. CONCLUSIONS--The principal effect of the recommendations of the working party alone was increased use of AAI pacing for sinus node dysfunction, with little change in the costs of hardware. The internal audit was followed by an increase in physiological pacing for atrioventricular block, and this has had important financial consequences. Internal audit was followed by closer adherence to the recommendations of the working party.
机译:背景技术-1990年9月,英国起搏和电生理学小组的一个工作组建议在心动过缓患者中常规使用生理起搏系统。先前曾有报道称,这些建议对Freeman医院1990年3月至1991年8月间起搏器处方的影响进行了审计。本文考虑了1991年9月至1993年2月内部审计对随后的起搏器处方的影响。病人和方法-回顾性分析了1990年3月至1993年2月在Freeman医院接受首次起搏器植入的1228例患者的记录。记录患者的年龄,起搏指示,起搏模式以及发生器和导线的成本。起搏的指征是窦房结功能障碍(24.9%)(包括合并存在的窦房结功能障碍和房室传导阻滞的患者),房室传导阻滞(57.2%),房室传导阻滞和房颤(12.2%)以及颈动脉窦综合征(5.7%) 。在两个研究期之间,颈动脉​​窦综合征增加(2.7%至8.1%),但病例组合的分布或患者特征没有其他差异。工作组推荐的最佳起搏模式的费用是根据研究期间下半年推荐单元的平均费用乘以该患者的患者人数得出的。结果-在1990年3月至1991年8月之间,窦房结功能障碍(AAI,AAIR,DDD或DDDR)的心房起搏增加了138%(从25.0%增至59.6%),这主要是因为增加了对AAI模式的使用。房室传导阻滞(DDD或VVIR)的生理起搏增加了41%(从17.0%增至24.0%),而房颤传导阻滞的VVIR起搏增加了111%(从10.5%增至22.2%)。在内部审核之后(即1991年9月至1993年2月),房室传导阻滞的生理起搏进一步增加了126%(从24.0%增加到54.2%)。其中增加的百分之六十三是在内部审计后的头六个月。对于窦房结功能不全和房室传导阻滞的起搏器处方没有改变(窦房结功能不全的生理起搏率为59.6%,对于房室传导阻滞的房室传导阻滞为22.2%v 27.3%VVIR起搏)。在实践中,这些变化伴随着接受生理学治疗的患者年龄的增加。在起搏政策的建议发布之前的最初六个月中,起搏器硬件的最后六个月的成本(不包括颈动脉窦综合征)比起搏政策保持最初六个月的成本增长了38%。工作组。完全采用工作组的准则将导致硬件成本进一步增加66%。结论-仅工作组建议的主要效果就是增加了对窦房结功能障碍使用AAI起搏的使用,而硬件成本几乎没有变化。内部审计之后,增加了房室传导阻滞的生理起搏,这对财务产生了重要影响。内部审计之后,工作组的建议更加严格。

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