Bainbridge A D, Cave M, Newell S, Delaney M, Parameshwar J, Large S R, Wallwork J, Grace A A, Carey N R, Schofield P M
Transplant Unit, Papworth Hospital, Cambridge, United Kingdom.
Pacing Clin Electrophysiol. 1999 Jun;22(6 Pt 1):942-6. doi: 10.1111/j.1540-8159.1999.tb06819.x.
Previous work suggested that pacemaker evoked T wave amplitude (ETWA) may be a sensitive noninvasive marker of cardiac allograft rejection. A Topaz QT sensing rate responsive pacemaker (Vitatron Medical) was implanted at transplantation using epicardial ventricular leads in 45 recipients (35 males; median age 51 years, range 20-63). The median duration of follow-up was 129 days (range 4-327). The ETWA at a paced rate of 100 beats/min was measured daily during hospitalization and at each outpatient attendance (900 readings). Endomyocardial biopsies were at routine intervals or when otherwise clinically indicated (257 biopsies with concurrent ETWA data). There were 58 episodes of rejection > or = grade 3a in 28 patients. The biopsies were classed as either no rejection (grade < 3a) or rejection requiring treatment (grade > or = 3a). The median normalized ETWA was 100.8% (range 24.6-239.7) without rejection and 89.9% (17.0-189.7) with rejection (Mann-Whitney U Test: P = 0.028). The performance of ETWA monitoring as a diagnostic test for the individual recipient was evaluated with exponentially weighted moving average quality control charts. For the diagnosis of all rejection episodes, ETWA monitoring had a sensitivity of 55%, a specificity of 62%, a positive predictive value of 30%, and negative predictive value of 83%. It is concluded that although analysis of pooled data showed a significant reduction in normalized ETWA with biopsy proven rejection, ETWA monitoring requires further refinement to improve sensitivity before it can be considered a clinically useful technique for the non-invasive diagnosis of cardiac allograft rejection in individual recipients.
先前的研究表明,起搏器诱发的T波振幅(ETWA)可能是心脏移植排斥反应敏感的非侵入性标志物。45例接受者(35例男性;年龄中位数51岁,范围20 - 63岁)在移植时使用心外膜心室导联植入了Topaz QT感知频率应答式起搏器(Vitatron Medical公司)。随访时间中位数为129天(范围4 - 327天)。住院期间每日及每次门诊就诊时均测量起搏频率为100次/分钟时的ETWA(共900次读数)。心内膜活检按常规时间间隔进行,或在临床有其他指征时进行(257次活检并同时记录ETWA数据)。28例患者发生了58次≥3a级的排斥反应。活检结果分为无排斥反应(<3a级)或需要治疗的排斥反应(≥3a级)。无排斥反应时ETWA的标准化中位数为100.8%(范围24.6 - 239.7),有排斥反应时为89.9%(17.0 - 189.7)(Mann - Whitney U检验:P = 0.028)。使用指数加权移动平均质量控制图评估ETWA监测作为个体接受者诊断试验的性能。对于所有排斥反应发作的诊断,ETWA监测的敏感性为55%,特异性为62%,阳性预测值为30%,阴性预测值为83%。结论是,虽然汇总数据分析显示活检证实有排斥反应时标准化ETWA显著降低,但ETWA监测在被认为是个体接受者心脏移植排斥反应非侵入性诊断的临床有用技术之前,还需要进一步完善以提高敏感性。