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1
Pacemaker assessment in the ambulant patient.门诊患者的起搏器评估
Br Heart J. 1981 Nov;46(5):531-8. doi: 10.1136/hrt.46.5.531.
2
Heart rate monitoring in implanted pacemakers.植入式起搏器中的心率监测
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Inhibition of a demand pacemaker and interference with monitoring equipment by radio-frequency transmissions.射频传输对按需起搏器的抑制及对监测设备的干扰。
Br Med J. 1969 May 24;2(5655):504-6. doi: 10.1136/bmj.2.5655.504.
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Detection of atrial fibrillation by permanent pacemakers: observations from the STOP AF trial.植入式心脏起搏器对心房颤动的检测:来自STOP AF试验的观察结果
Card Electrophysiol Rev. 2003 Dec;7(4):333-40. doi: 10.1023/B:CEPR.0000023133.43829.9a.
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[Management of patients after pacemaker implanation (author's transl)].起搏器植入术后患者的管理(作者译)
Herz. 1978 Dec;63(36):347-56.
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J Clin Eng. 1994 Jan-Feb;19(1):39-47. doi: 10.1097/00004669-199401000-00015.
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Am J Dis Child. 1989 Jan;143(1):105-7. doi: 10.1001/archpedi.1989.02150130115028.

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本文引用的文献

1
Diagnosis of occult arrhythmias by Holter electrocardiography.通过动态心电图诊断隐匿性心律失常。
Prog Cardiovasc Dis. 1974 May-Jun;16(6):569-99. doi: 10.1016/0033-0620(74)90019-x.
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Artifacts in portable electrocardiographic monitoring.便携式心电图监测中的伪迹
Am Heart J. 1976 Mar;91(3):349-57. doi: 10.1016/s0002-8703(76)80220-7.
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Ambulatory electrocardiographic records in patients with transient cerebral attacks or palpitation.短暂性脑缺血发作或心悸患者的动态心电图记录。
Br Med J. 1975 Dec 6;4(5996):569-71. doi: 10.1136/bmj.4.5996.569.
4
Pacemaker implantation based on ambulatory ECG monitoring in patients with cerebral symptoms.基于动态心电图监测的脑症状患者起搏器植入术
Chest. 1975 Mar;67(3):274-8. doi: 10.1378/chest.67.3.274.
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Ability of Holter electrocardiographic recording and atrial stimulation to detect sinus nodal dysfunction in symptomatic and asymptomatic patients with sinus bradycardia.
Am J Cardiol. 1977 Aug;40(2):189-94. doi: 10.1016/0002-9149(77)90007-8.
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World survey on cardiac pacing.心脏起搏全球调查。
Pacing Clin Electrophysiol. 1979 Sep;2(5):W1-17. doi: 10.1111/j.1540-8159.1979.tb04271.x.

门诊患者的起搏器评估

Pacemaker assessment in the ambulant patient.

作者信息

Murray A, Jordan R S, Gold R G

出版信息

Br Heart J. 1981 Nov;46(5):531-8. doi: 10.1136/hrt.46.5.531.

DOI:10.1136/hrt.46.5.531
PMID:7317218
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC482692/
Abstract

A new technique for assessing implanted cardiac pacemaker function in the ambulant patient has been introduced and assessed. A modified portable electrocardiograph recorder is used to store 24 hours of electrocardiograms along with marker pulses indicating the timing of pacemaker impulses. The recorder detects this narrow impulse and records a wider marker pulse on a second channel. The false positive detection rate was estimated from recordings, each of 24 hours, taken from 10 patients. All of these patients were ambulant and none had a cardiac pacemaker. There was on average less than one false positive per 24 hours. When similar recordings were taken from a group of 15 patients with pacemakers, the average false positive rate in 13 of these patients was also less than on per 24 hours. In the two other recordings artefacts resulted in false positive rates of 28 and 960 per 24 hours. Failure to detect pacemaker pulses was confirmed in only one patient. In addition to determining the accuracy of pacemaker pulse detection, the clinical usefulness of this technique was assessed. Two patients had fixed-rate pacemakers and 13 had demand pacemakers. Of the latter, two patients had a total of three episodes of failure to sense, one patient frequently failed to capture, and six patients had episodes of inappropriate inhibition of the pacemaker, the number of episodes ranging from one to 21 in 24 hours. Paced complexes were easily identified even when they occurred as fusion complexes. The frequency of paced complexes was quantified in each patient and varied from 21 to over 100 000 impulses in the 24 hour period.

摘要

一种用于评估门诊患者植入式心脏起搏器功能的新技术已被引入并进行了评估。使用一种改良的便携式心电图记录仪来存储24小时的心电图以及指示起搏器脉冲时间的标记脉冲。该记录仪检测到这个窄脉冲,并在第二个通道上记录一个更宽的标记脉冲。从10名患者身上采集的24小时记录中估计假阳性检测率。所有这些患者都是门诊患者,且都没有心脏起搏器。平均每24小时假阳性少于1次。当从一组15名有起搏器的患者身上进行类似记录时,其中13名患者的平均假阳性率也低于每24小时1次。在另外两份记录中,伪迹导致每24小时的假阳性率分别为28次和960次。仅在一名患者中证实未能检测到起搏器脉冲。除了确定起搏器脉冲检测的准确性外,还评估了该技术的临床实用性。两名患者有固定频率起搏器,13名患者有按需起搏器。在后者中,两名患者共有三次感知失败发作,一名患者经常未能夺获,六名患者有起搏器不适当抑制发作,发作次数在24小时内从1次到21次不等。即使起搏复合波以融合复合波的形式出现,也很容易识别。对每名患者的起搏复合波频率进行了量化,在24小时内从21次到超过100000次脉冲不等。