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大型医疗群体中永久性心脏起搏器不必要植入的发生率。

Incidence of unwarranted implantation of permanent cardiac pacemakers in a large medical population.

作者信息

Greenspan A M, Kay H R, Berger B C, Greenberg R M, Greenspon A J, Gaughan M J

机构信息

Albert Einstein Medical Center, Philadelphia, PA 19141.

出版信息

N Engl J Med. 1988 Jan 21;318(3):158-63. doi: 10.1056/NEJM198801213180306.

Abstract

Because of allegations that the implantation of many permanent cardiac pacemakers has been unjustified, we reviewed the indications for all new pacemakers implanted at 30 hospitals in Philadelphia County between January 1 and June 30, 1983, and paid for by Medicare. Complete chart data were evaluated for 382 implants. We determined whether the indications for implantation were appropriate and adequately documented on the basis of standard clinical practice. Implants were classified as possibly indicated primarily because of inadequate diagnostic evaluation (63 percent) or inadequate documentation of an accepted indication (36 percent). Implants were classified as not indicated primarily because a rhythm abnormality was incorrectly identified as a justifiable indication (84 percent). We found that 168 implants (44 percent) were definitely indicated, 137 (36 percent) possibly indicated, and 77 (20 percent) not indicated. Unwarranted implantation was both prevalent (73 percent of hospitals had an incidence of 10 percent or more) and independent of the type of hospital (university teaching, university-affiliated, and community hospitals). The additional tests most often required to clarify the need for a pacemaker in inadequately evaluated cases included electrophysiologic studies (37 percent) and ambulatory monitoring (31 percent). We conclude that in a large medical population in 1983, the indications for a considerable number of permanent pacemakers were inadequate or incompletely documented.

摘要

由于有人指控许多永久性心脏起搏器的植入是不合理的,我们回顾了1983年1月1日至6月30日期间在费城县30家医院植入并由医疗保险支付费用的所有新起搏器的适应证。对382例植入病例的完整病历数据进行了评估。我们根据标准临床实践确定植入适应证是否恰当且记录充分。植入病例被分类为可能有适应证主要是因为诊断评估不充分(63%)或对公认适应证的记录不充分(36%)。植入病例被分类为无适应证主要是因为节律异常被错误地认定为合理适应证(84%)。我们发现168例植入(44%)明确有适应证,137例(36%)可能有适应证,77例(20%)无适应证。不必要的植入既很普遍(73%的医院发生率为10%或更高),且与医院类型(大学教学医院、大学附属医院和社区医院)无关。在评估不充分的病例中,最常需要的用于明确是否需要起搏器的额外检查包括电生理研究(37%)和动态监测(31%)。我们得出结论,在1983年的一大群患者中,相当数量的永久性起搏器的适应证不充分或记录不完整。

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