Gonvers J J, Burnand B, Froehlich F, Pache I, Thorens J, Fried M, Kosecoff J, Vader J P, Brook R H
Division of Gastroenterology, University Medical Outpatient Dept., Lausanne, Switzerland.
Endoscopy. 1996 Oct;28(8):661-6. doi: 10.1055/s-2007-1005573.
This prospective study tested the appropriateness of referrals for upper gastrointestinal endoscopy in an open-access endoscopy unit, using the criteria of the American Society for Gastrointestinal Endoscopy. It also examined whether there was any relationship between appropriateness of use and the presence of significant lesions detected by endoscopy.
Four hundred fifty consecutive upper gastrointestinal endoscopies were studied prospectively. The referral indication was recorded by the endoscopist before the procedure was performed, and was compared with the current criteria of the American Society for Gastrointestinal Endoscopy and with endoscopic findings.
The appropriateness of referral was assessed in 442 consecutive endoscopies. Of these, 252 (57%) were judged to be appropriate. In 168 (88%) of the 190 endoscopies rated as inappropriate, the reason was that the patient had not undergone empirical anti-ulcer therapy before endoscopy. The probability of finding a significant lesion did not differ between the endoscopies judged to be appropriate (50%) and those judged to be inappropriate (46%)
Upper gastrointestinal endoscopy was frequently used for inappropriate indications. The main reason for inappropriate use was insufficient treatment, or no treatment, of dyspeptic symptoms prior to endoscopy. In this study, the criteria for appropriateness did not predict the probability of finding a significant endoscopic lesion.
本前瞻性研究采用美国胃肠内镜学会的标准,对一家开放获取式内镜检查科室中上消化道内镜检查转诊的适宜性进行了测试。该研究还探讨了使用适宜性与内镜检查发现的显著病变之间是否存在关联。
前瞻性地研究了连续450例上消化道内镜检查。内镜医师在检查前记录转诊指征,并将其与美国胃肠内镜学会的现行标准以及内镜检查结果进行比较。
对连续442例内镜检查的转诊适宜性进行了评估。其中,252例(57%)被判定为适宜。在190例被评为不适宜的内镜检查中,有168例(88%)的原因是患者在内镜检查前未接受经验性抗溃疡治疗。在被判定为适宜的内镜检查(50%)和被判定为不适宜的内镜检查(46%)中,发现显著病变的概率没有差异。
上消化道内镜检查经常用于不适宜的指征。使用不当的主要原因是在内镜检查前对消化不良症状的治疗不足或未进行治疗。在本研究中,适宜性标准无法预测发现显著内镜病变的概率。