CC BY-NC-ND 4.0 · Endosc Int Open 2017; 05(12): E1268-E1277
DOI: 10.1055/s-0043-119791
Original article
Eigentümer und Copyright ©Georg Thieme Verlag KG 2017

Low yield for non-targeted biopsies of the stomach and esophagus during elective esophagogastroduodenoscopy

Michael K. Dougherty
1   Division of Gastroenterology, Department of Medicine, University of North Carolina, Chapel Hill, North Carolina, United States
,
Phillip P. Santoiemma
2   Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois, United States
,
Andrew T. Weber
3   Department of Medicine, University of California Los Angeles, Los Angeles, California, United States
,
David C. Metz
4   Division of Gastroenterology, Department of Medicine, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania, United States
,
Yu-Xiao Yang
5   Division of Gastroenterology, Department of Medicine, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania, United States
› Author Affiliations
Further Information

Publication History

submitted 21 November 2016

accepted after revision 31 July 2017

Publication Date:
06 December 2017 (online)

Abstract

Background and study aims Biopsies of non-specific mucosal findings are often performed during esophagogastroduodenoscopy (EGD). We sought to determine the prevalence and clinical utility of non-targeted biopsies of the stomach and esophagus.

Patients and methods We conducted a retrospective review of 949 outpatient EGDs performed at a US tertiary referral center. Non-targeted biopsies of the stomach were defined as either “normal” or “mild” to “moderate” “erythema” or “inflammation” without other endoscopic features. Non-targeted biopsies of the esophagus and gastroesophageal junction (GEJ) were defined as endoscopically “normal” mucosa. The primary outcome was the proportion of non-targeted biopsies resulting in “definite management change.” Secondary outcomes included histopathologic diagnoses of Helicobacter pylori, intestinal metaplasia and esophageal eosinophilia.

Results Of 949 EGDs, 332 (35.0 %, 95 % CI 31.9 – 38.1 %) had a non-targeted biopsy taken at any site. Erythema in the gastric body and antrum was biopsied at a rate of 83 – 86 %, while biopsies of “normal”-appearing mucosa occurred at rates from 3 % (GEJ) to 15 % (body and antrum). The percentage of non-targeted biopsies that led to definite management change ranged from 5 % in the GEJ and esophagus to 9 % in the antrum, but did not significantly differ by mucosal appearance. Multivariable regression analyses suggested associations of language and age > 50 with management change from non-targeted gastric biopsy.

Conclusions Non-targeted biopsies of the stomach and esophagus led to definite management change in a small proportion of patients. Further studies are needed to identify patient and/or endoscopic characteristics and techniques to improve the yield of this practice.

 
  • References

  • 1 Cosgrove JC, Walke JD, Anderson TD. et al. Action needed to address higher use of anatomic pathology services by providers who self-refer. GAO; 2013 http://www.gao.gov/products/GAO-13-445 [Accessed July 16, 2017]
  • 2 Allen JI, Katzka D, Robert M. et al. American Gastroenterological Association Institute Technical Review on the Role of Upper Gastrointestinal Biopsy to Evaluate Dyspepsia in the Adult Patient in the Absence of Visible Mucosal Lesions. Gastroenterology 2015; 149: 1088-1118
  • 3 Carabotti M, Lahner E, Porowska B. et al. Are clinical features able to predict Helicobacter pylori gastritis patterns? Evidence from tertiary centers. Intern Emerg Med 2014; 9: 841-845
  • 4 Johnsen R, Bernersen B, Straume B. et al. Prevalences of endoscopic and histological findings in subjects with and without dyspepsia. BMJ 1991; 302: 749-752
  • 5 Moayyedi P. Helicobacter pylori eradication for functional dyspepsia: what are we treating? Comment on “Helicobacter pylori eradication in functional dyspepsia”. Arch Intern Med 2011; 171: 1936-1937
  • 6 Makris N, Crott R, Fallone CA. et al. Cost-effectiveness of routine endoscopic biopsies for Helicobacter pylori detection in patients with non-ulcer dyspepsia. Gastrointest Endosc 2003; 58: 14-22
  • 7 de Vries AC, Haringsma J, de Vries RA. et al. Biopsy strategies for endoscopic surveillance of pre-malignant gastric lesions. Helicobacter 2010; 15: 259-264
  • 8 El-Zimaity HM, Graham DY. Evaluation of gastric mucosal biopsy site and number for identification of Helicobacter pylori or intestinal metaplasia: role of the Sydney System. Hum Pathol 1999; 30: 72-77
  • 9 Breslin NP, Thomson AB, Bailey RJ. et al. Gastric cancer and other endoscopic diagnoses in patients with benign dyspepsia. Gut 2000; 46: 93-97
  • 10 Cadman B, Dixon MF, Wyatt JI. Value of routine, non-targeted biopsies in the diagnosis of gastric neoplasia. J Clin Pathol 1997; 50: 832-834
  • 11 Fiorenza JP, Tinianow AM, Chan WW. The Initial Management and Endoscopic Outcomes of Dyspepsia in a Low-Risk Patient Population. Digestive Diseases and Sciences 2016; 61: 2942-2948
  • 12 Areia M, Carvalho R, Cadime AT. et al. Screening for gastric cancer and surveillance of premalignant lesions: a systematic review of cost-effectiveness studies. Helicobacter 2013; 18: 325-337
  • 13 O'Connor A, McNamara D, OʼMorain CA. Surveillance of gastric intestinal metaplasia for the prevention of gastric cancer. Cochrane Database Syst Rev 2013; 9: CD009322
  • 14 Zullo A, Hassan C, Repici A. et al. Intestinal metaplasia surveillance: searching for the road-map. World J Gastroenterol 2013; 19: 1523-1526
  • 15 Evans JA, Chandrasekhara V, Chathadi KV. et al. The role of endoscopy in the management of premalignant and malignant conditions of the stomach. Gastrointest endosc 2015; 82: 1-8
  • 16 Chey WD, Wong BC. Practice Parameters Committee of the American College of Gastroenterology. American College of Gastroenterology guideline on the management of Helicobacter pylori infection. Am J Gastroenterol 2007; 102: 1808-1825
  • 17 Talley NJ, Vakil N. Practice Parameters Committee of the American College of Gastroenterology. Guidelines for the management of dyspepsia. Am J Gastroenterol 2005; 100: 2324-2337
  • 18 Ikenberry SO, Harrison ME, Lichtenstein D. et al. The role of endoscopy in dyspepsia. Gastrointest Endosc 2007; 66: 1071-1075
  • 19 Yang Y-X, Brill J, Krishnan P. et al. American Gastroenterological Association Institute Guideline on the Role of Upper Gastrointestinal Biopsy to Evaluate Dyspepsia in the Adult Patient in the Absence of Visible Mucosal Lesions. Gastroenterology 149: 1082-1087
  • 20 Dinis-Ribeiro M, Areia M, de Vries AC. et al. Management of precancerous conditions and lesions in the stomach (MAPS): guideline from the European Society of Gastrointestinal Endoscopy (ESGE), European Helicobacter Study Group (EHSG), European Society of Pathology (ESP), and the Sociedade Portuguesa de Endoscopia Digestiva (SPED). Endoscopy 2012; 44: 74-94
  • 21 Katz PO, Gerson LB, Vela MF. Guidelines for the diagnosis and management of gastroesophageal reflux disease. Am J Gastroenterol 2013; 108: 308-328; quiz 329
  • 22 Kahrilas PJ, Shaheen NJ, Vaezi MF. et al. American Gastroenterological Association Medical Position Statement on the management of gastroesophageal reflux disease. Gastroenterology 2008; 135: 1383-1391, 1391 e1381-1385
  • 23 Dellon ES, Gonsalves N, Hirano I. et al. ACG clinical guideline: Evidenced based approach to the diagnosis and management of esophageal eosinophilia and eosinophilic esophagitis (EoE). Am J Gastroenterol 2013; 108: 679-692; quiz 693
  • 24 Kim HP, Vance RB, Shaheen NJ. et al. The prevalence and diagnostic utility of endoscopic features of eosinophilic esophagitis: a meta-analysis. Clin Gastroenterol Hepatol 2012; 10: 988-996 e985
  • 25 Foroutan M, Norouzi A, Molaei M. et al. Eosinophilic esophagitis in patients with refractory gastroesophageal reflux disease. Dig Dis Sci 2010; 55: 28-31
  • 26 Dubin SM, Kwong WT, Kalmaz D. et al. Low yield of routine duodenal biopsies for evaluation of abdominal pain. World J Gastroenterol 2015; 21: 7495-7499
  • 27 Eriksson NK, Karkkainen PA, Farkkila MA. et al. Prevalence and distribution of gastric intestinal metaplasia and its subtypes. Dig Liver Dis 2008; 40: 355-360
  • 28 Lash JG, Genta RM. Adherence to the Sydney System guidelines increases the detection of Helicobacter gastritis and intestinal metaplasia in 400738 sets of gastric biopsies. Aliment Pharmacol Ther 2013; 38: 424-431
  • 29 Lahner E, Zullo A, Hassan C. et al. Detection of gastric precancerous conditions in daily clinical practice: a nationwide survey. Helicobacter 2014; 19: 417-424
  • 30 Simko V, Anand N, Ginter E. Gastric intestinal metaplasia – age, ethnicity and surveillance for gastric cancer. Bratisl Lek Listy 2015; 116: 3-8
  • 31 den Hoed CM, van Eijck BC, Capelle LG. et al. The prevalence of premalignant gastric lesions in asymptomatic patients: Predicting the future incidence of gastric cancer. European Journal of Cancer 2011; 47: 1211-1218
  • 32 Marques-Silva L, Areia M, Elvas L. et al. Prevalence of gastric precancerous conditions: a systematic review and meta-analysis. European Journal of Gastroenterology & Hepatology 2014; 26: 378-387
  • 33 Jensen ET, Eluri S, Lebwohl B. et al. Increased risk of esophageal eosinophilia and eosinophilic esophagitis in patients with active celiac disease on biopsy. Clin Gastroenterol Hepatol 2015; 13 (08) 1426-1431
  • 34 Dellon ES, Speck O, Woodward K. et al. Distribution and variability of esophageal eosinophilia in patients undergoing upper endoscopy. Mod Pathol 2015; 28: 383-390
  • 35 Muto M, Yao K, Kaise M. et al. Magnifying endoscopy simple diagnostic algorithm for early gastric cancer (MESDA-G). Digestive Endoscopy 2016; 28: 379-393
  • 36 Yao K. The endoscopic diagnosis of early gastric cancer. Annals of Gastroenterology: Quarterly Publication of the Hellenic Society of Gastroenterology 2013; 26: 11-22