Ritter S, Tani L Y, Etheridge S P, Williams R V, Craig J E, Minich L L
Department of Pediatrics, University of Utah, Salt Lake City, Utah, USA.
Pediatrics. 2000 May;105(5):E58. doi: 10.1542/peds.105.5.e58.
To determine the yield of screening echocardiography in the evaluation of pediatric syncope.
All patients diagnosed with syncope from January 1993 to January 1999 were identified and their records were reviewed for age, weight, sex, year of presentation, personal and family history, physical examination, and cardiac diagnostic testing. Cardiac defects were identified by reviewing echocardiograms and reports.
The 480 patients (268 females) ranged in age from 1.5 to 18.0 years old and ranged in weight from 10.3 to 113.6 kg. Final diagnoses included noncardiac causes in 458, long QT syndrome in 14, arrhythmias in 6, and cardiomyopathy in 2. An abnormal history, physical examination, or electrocardiogram identified 21 of the 22 patients with a cardiac cause of syncope. Of the 322 (67%) echocardiograms performed, abnormalities were detected in 37. These abnormalities included 26 minor valve anomalies, 7 hemodynamically insignificant shunt lesions, 2 mildly decreased left ventricular shortening fractions, and 2 cardiomyopathies. Only the 2 cardiomyopathies were considered to be potential causes of syncope, and in both cases, the electrocardiogram was markedly abnormal. A similar percentage of echocardiograms were ordered during the first and last 3 years of the study (61% vs 71%).
History, physical examination, and electrocardiography provide a screening protocol that allows the identification of a cardiac cause of syncope in the overwhelming majority of pediatric patients. In the absence of a positive screen result, the echocardiogram does not contribute to the evaluation of syncope in children. We speculate that primary care providers and pediatric cardiologists continue to use echocardiography because of the paucity of data regarding its value in pediatric syncope. However, this study shows little benefit of screening echocardiography and should discourage its routine use.
确定筛查超声心动图在评估小儿晕厥中的检出率。
确定1993年1月至1999年1月期间所有诊断为晕厥的患者,并查阅其记录,包括年龄、体重、性别、就诊年份、个人及家族史、体格检查和心脏诊断检查。通过查阅超声心动图和报告来确定心脏缺陷。
480例患者(268例女性)年龄在1.5至18.0岁之间,体重在10.3至113.6千克之间。最终诊断包括458例非心脏原因、14例长QT综合征、6例心律失常和2例心肌病。22例由心脏原因导致晕厥的患者中,21例通过异常病史、体格检查或心电图得以确诊。在进行的322例(67%)超声心动图检查中,发现37例异常。这些异常包括26例轻度瓣膜异常、7例血流动力学无显著意义的分流病变、2例左心室缩短分数轻度降低和2例心肌病。仅2例心肌病被认为可能是晕厥的原因,且在这两例中,心电图均明显异常。在研究的最初3年和最后3年,超声心动图检查的开具比例相似(61%对71%)。
病史、体格检查和心电图提供了一种筛查方案,能够在绝大多数小儿患者中识别出晕厥的心脏原因。在筛查结果为阴性的情况下,超声心动图无助于儿童晕厥的评估。我们推测,由于关于其在小儿晕厥中价值的数据匮乏,初级保健提供者和儿科心脏病专家仍继续使用超声心动图。然而,本研究显示筛查超声心动图益处不大,应不鼓励常规使用。