ERCP前后实验室值的临床相关性

Johny Salem, W. Arja, Jennifer Aoun, Nourhane Obeid, Anna-maria Abi-nehme, N. Gharib, Tala Ghorayeb, Said Farhat
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However, several complications were described post-procedure such as pancreatitis, perforation, cholangitis, post-sphincterotomy bleeding, etc. Data concerning variation in laboratory values before and after ERCP and its clinical significance with respect to endoscopic findings and possible complications is lacking in the literature.\nAim: To analyze the clinical significance of laboratory values in patients before and after ERCP.\nMethods: From a total of 723 patients, 363 with different sets of findings on ERCP were eligible to be included in the study and were divided into 8 different groups. 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引用次数: 0

摘要

背景:内窥镜逆行胆管造影(ERCP)已经从一种诊断方式发展成为胰腺和胆道疾病的主要治疗方法。然而,术后出现胰腺炎、穿孔、胆管炎、括约肌切开术后出血等并发症。文献中缺乏关于ERCP前后实验室值变化的数据及其与内镜检查结果和可能并发症的临床意义。目的:分析ERCP术前、术后实验室检查的临床意义。方法:从723例患者中选取363例具有不同ERCP检查结果的患者纳入研究,并将其分为8组。术前及术后测定血清丙氨酸转氨酶(ALT)、天冬氨酸转氨酶(AST)、γ -谷氨酰转移酶(GGT)、碱性磷酸酶(ALKP)、胆红素、淀粉酶、脂肪酶、c反应蛋白(CRP)、白细胞计数(WBC)、中性粒细胞、淋巴细胞、单核细胞、嗜酸性粒细胞、嗜碱性粒细胞、血小板计数和肌酐。结果:所有患者ercp前后AST和直接胆红素水平差异均有统计学意义(p值分别<0.01和p值<0.05)。恶性梗阻组肝功能指标明显高于胆管结石组(P <0.05),术后肝功能指标下降更为显著(P <0.05)。各组间脂肪酶显著升高(p值<0.05),淋巴细胞计数显著降低(p值<0.01)。结论:结论:(1)ERCP可显著降低梗阻性病因分层组术后AST、直接胆红素、淋巴细胞和单核细胞计数,证明ERCP对胆道梗阻性疾病的治疗价值。(2) T0时实验室值基线紊乱较高,尤其是肝功能检查如ALT、AST、GGT、ALKP,以及T1时淋巴细胞计数下降较大,与恶性梗阻(肿瘤组)有关,而与良性梗阻(结石、污泥、结石+污泥、狭窄)无关。(3)最后,结石组和狭窄组发生ERCP后胰腺炎的风险最高,因为这些组在ERCP后胰酶水平最高,因此应该是ERCP前药物预防(如双氯芬酸等)和ERCP后密切监测的最佳人选。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical Correlation Between Pre and Post ERCP Laboratory Values
Abstract  Background: Endoscopic retrograde cholangiopancreatography (ERCP) has evolved from a diagnostic modality to a primarily therapeutic procedure for pancreatic as well as biliary disorders. However, several complications were described post-procedure such as pancreatitis, perforation, cholangitis, post-sphincterotomy bleeding, etc. Data concerning variation in laboratory values before and after ERCP and its clinical significance with respect to endoscopic findings and possible complications is lacking in the literature. Aim: To analyze the clinical significance of laboratory values in patients before and after ERCP. Methods: From a total of 723 patients, 363 with different sets of findings on ERCP were eligible to be included in the study and were divided into 8 different groups. Serum levels of alanine aminotransferase (ALT), aspartate aminotransferase (AST), Gamma-glutamyl transferase (GGT), Alkaline phosphatase (ALKP), bilirubin, amylase, lipase, c-reactive protein (CRP), white blood count (WBC), neutrophil, lymphocyte, monocyte, eosinophils, basophils, platelets counts and creatinine were determined preoperatively as well as postoperatively in these patients. Results: AST and direct bilirubin showed a significant difference in all patients between pre and post-ERCP (p-value<0.01 and p-value<0.05, respectively). Liver tests were significantly higher in the malignant obstruction group than in the bile duct stones group (P <0.05) and decrease more significantly (P <0.05) after the procedure. A significant increase in lipase (p-value<0.05) among all groups was found, and interestingly, the lymphocytic count showed a significant decrease (p-value<0.01). Conclusion: In conclusion, (1) ERCP significantly decreases AST, direct bilirubin, lymphocytes, and monocytes count post procedure among all stratified groups of obstructive etiology thus proving its therapeutic value for biliary system obstructions. (2) Higher baseline disturbances in laboratory values at T0, especially in liver function tests such as ALT, AST, GGT, and ALKP as well as a bigger decrease in lymphocyte count at T1 are noted to be linked with malignant obstructions (tumor group), rather than benign obstructions (stone, sludge, stone+ sludge, and stricture).  (3) Finally, stone and stricture groups are at the highest risk of post-ERCP pancreatitis owing to those groups having the highest pancreatic enzyme levels post ERCP, and thus should be the best candidates for a pre-ERCP pharmacologic prophylaxis (such as diclofenac, etc) and post ERCP close monitoring.
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