How to measure quality in endoscopic ultrasound
Review Article on Quality in Gastrointestinal Endoscopy

How to measure quality in endoscopic ultrasound

Antonio Facciorusso, Rosario Vincenzo Buccino, Nicola Muscatiello

Department of Medical Sciences, Gastroenterology Unit, University of Foggia, Foggia, Italy

Contributions: (I) Conception and design: A Facciorusso; (II) Administrative support: N Muscatiello; (III) Provision of study materials or patients: RV Buccino; (IV) Collection and assembly of data: A Facciorusso; (V) Data analysis and interpretation: A Facciorusso; (VI) Manuscript writing: All authors; (VII) Final approval of manuscript: All authors.

Correspondence to: Antonio Facciorusso. Department of Medical Sciences, Gastroenterology Unit, University of Foggia, Viale L.Pinto, 1, 71100 Foggia, Italy. Email: antonio.facciorusso@virgilio.it.

Abstract: Quality is a key focus for gastrointestinal endoscopy and main international gastroenterology societies instituted specific task forces focused on this issue. Endoscopic ultrasound (EUS) represents one of the most fascinating fields to explore in gastrointestinal endoscopy due to its relatively limited availability out of high-volume centers. This leads to a particular need to define widely accepted quality indicators (QIs) and the ways to measure them. The current manuscript reviews these indicators in light of their impact on common clinical practice.

Keywords: Endoscopic ultrasound (EUS); fine-needle aspiration (FNA); outcome; performance


Submitted Nov 26, 2017. Accepted for publication Mar 19, 2018.

doi: 10.21037/atm.2018.03.36


Introduction

Quality is a key focus for gastrointestinal endoscopy aiming to promote best practices among endoscopists on the basis of available evidence-based care. The pressing need to properly define quality assessment in endoscopy, like in many other medical fields, was pushed by increasing alarming reports about medical errors (1). Since several areas of underperformance were perceived to impair main outcomes (1,2), great efforts to develop widely recognized performance measures have been initiated since early 2000s. This was the base for important health programs such as “pay for performance” and “value-based medicine” (3,4).

Quality improvement implies not only definition and achievement of standard outcomes, but also the impact on patient experience including other aims such as professionalism, and equitable care (5).

As a consequence, main international gastroenterology societies instituted specific task forces focused on quality in gastroenterology and endoscopy. Aim of this effort was to define all the elements of high-quality endoscopy, starting from definition of evidence-based indicators to standardization of their measurements. First manuscripts by American Society for Gastrointestinal Endoscopy (ASGE) quality task force were released in 2006 (6-11).

As our ability to measure real outcomes has considerably evolved, and since surrogate process is no longer accepted by the stakeholders, definition of what constitutes quality indicators (QIs) for endoscopy has necessarily been revised in last few years.

Moreover, the aforementioned papers published in 2006 were based mainly on expert opinion, while novel robust evidence is now available and capable to address satisfactorily the standard level of performance in daily endoscopy practice.

For example, great advances have been obtained concerning information from days after the examination, although capturing data on delayed events still remains a challenge (12).

Among the other aspects of gastrointestinal endoscopy, endoscopic ultrasound (EUS) represents one of the most fascinating to explore due to several specific features of this technique and its relatively limited availability out of high-volume centers. This leads to a particular need to define widely accepted QIs and the ways to measure them.


Importance of quality assessment in EUS practice

EUS represents the cornerstone in the diagnostic and staging algorithm of several GI and mediastinal conditions. Moreover, EUS allows direct tissue sampling through fine-needle aspiration (FNA) or biopsy (FNB). As for other endoscopic procedures, QIs may be classified into three categories depending on timing of assessment: pre-procedure, intra-procedure, and post-procedure (13).

In 2015 the ASGE task force updated the previous document published in 2006 and recommended a list of high-priority QIs based on their clinical relevance and feasibility of measurement (13). As a general rule, lower is the number of procedures needed to obtain a reliable estimate with narrow confidence interval (CI) easier is the measurement of the indicator. All endoscopists may compare their personal performance with commonly accepted standard measures for each QI, thus falling into a high- or low-performing group based on pre-defined thresholds.

Of course, most of these indicators are common to all endoscopy procedures.

EUS has largely benefited from quality control (QC) and QI analysis, as demonstrated by Bluen et al. who showed that accurate QC, including systemic monitoring and evaluation, is critical to rendering EUS-FNA more effective (14). Likewise, Coe et al. found endoscopist adherence to EUS QIs over an eight-year span to be strictly related to significant improvement in all EUS aspects (15). Lachter et al. explored adherence to EUS QIs at ten different Israeli medical centers keeping as standard the University of Chicago and observed that an overall improvement in documented quality of EUS exams was found in centers ensuring comprehensive documentation and stronger guideline adherence (16). Further confirm of these findings was provided in the study by Schwab et al., where significant improvements were demonstrated in QI adherence and thus EUS reporting and delivery quality in 2013–2014 reports as compared to 2009 results (17). Therefore, authors concluded that QI implementation facilitates effective high-quality EUS exams by ensuring comprehensive documentation while limiting error (17). However, adherence to quality guidelines remains still jeopardized across several centers, with some items such as description of FNA, or listing of adverse events largely lacking from procedural documentation (16).


Pre-procedure QIs

All contacts between the endoscopy team and the patient before the exam (conventionally before the administration of the sedation) fall into the “pre-procedure” category (18).

First fundamental point is the proper definition of the indications to the examination. This QI corresponds to a specific item: “Frequency with which EUS is performed for an indication that is included in a published standard list of appropriate indications, and the indication is documented”. The performance threshold required for this item is >80% (13). This means that the correct indication should be documented according to the current guidelines (19,20), and when it is “off-guidelines” its use should be justified in the documentation.

The correct use of the procedure should be always weighted in light of its impact on the diagnostic and therapeutic management of that single patient, specifically in comparison to other competitive procedures. For example, EUS is generally deemed not indicated in staging tumors already shown to be metastatic by non-invasive imaging methods (unless in the case of tissue sampling). However, the choice among different concurrent diagnostic procedures cannot be universally pre-defined since it should be “tailored” to the local availability and expertise of the center.

The endoscopist should be “up-to-date” on the changing scenario of the indications to EUS based on novel evidence and recent advances.

The correct and documented definition of the indication to the exam is a paramount quality measure for either the justification of this invasive procedure and to focus the attention of the endoscopist to a specific diagnostic question (for example, if the indication for EUS is the staging of an esophageal cancer, lengthening the duration of the procedure for a detailed study of pancreatic parenchyma is unnecessary).

Other important quality measure responds to the following question: “Frequency with which consent is obtained, including specific discussions of risks associated with EUS, and fully documented” with an accepted cut-off point >98% (13). The patient should be always fully aware of relevant potential adverse events of the procedure and he/she should be offered an appropriate alternative. Useless to say, every step of this process should be correctly documented and registered. Although the risks of diagnostic EUS with no tissue sampling are very low, anecdotal cases of perforation have been reported (21-23). Risks of adverse events are obviously higher when tissue sampling by means of FNA or FNB is performed (24,25). Among commonly reported adverse events, an increased risk of bleeding (0.5%), infection (<1%), and pancreatitis (2%) has been reported (25-30). Tumor seeding has been rarely observed (31-33). More serious complications are expected with interventional procedures such as celiac plexus neurolysis or tumor ablation (34-36).

Therefore the consent form should be comprehensive enough to include all these adverse events.

Related to the previous point is the use of antibiotics for FNA of cystic lesions. Given the lack of randomized-controlled trials (RCTs) and the low incidence of infectious events after EUS-FNA of pancreatic cysts/lesions, antibiotic prophylaxis is currently deemed unnecessary except for mediastinal EUS-FNA (37,38).

The patient has the right to know what is the level of experience of the endoscopist. Specific training requirements for EUS have been published (39,40). As a consequence, a specific question concerning the rate of examinations performed by a fully trained endoscopist is reported in the quality checklist with an accepted cut-off of 98% (13).

In summary, main questions to address properly before performing the procedure are whether EUS may really impact on the clinical management of the patient and if there are reasonable alternatives and finally whether the training of the endoscopist responsible of the procedure fulfils the standards required by current guidelines.


Intra-procedure QIs

The intra-procedure period corresponds to the time span between the administration of the sedation and the removal of the endoscope. Therefore, all the technical aspects of the procedure are included in this period.

The first question is about the frequency with which the appearance of relevant structures (those representing the target of that specific examination) is documented (threshold 98%) (13). For example, in the setting of pancreatobiliary disease, visualization of the whole pancreas and precise description of the biliary tree whereas in lower GI EUS definition of main perirectal structures comprehensive of lymph nodes. All relevant findings should be documented with clear photographs.

Likewise, when describing subepithelial masses, involvement of wall layers should be consistently reported and documented.

One of the main strengths of EUS is the capability to provide an accurate staging of GI malignancies. Hence T and N parameters of TNM staging system should be properly described by measuring the tumor mass and evaluating the vascular/lymph nodes involvement. On the other hand, EUS is reportedly less accurate in defining the presence of distant metastases (M parameter) (41,42).

Noteworthy, given the operator-dependent nature of the procedure, ASGE task force does not account accuracy of vascular or lymphatic invasion (widely ranging from 73% to 90% the former and from 40% to 85% the latter in the case of pancreatic cancer) (43-49) but only the presence of vascular/lymphatic invasion as a QI (13).

A crucial point is the diagnostic rate related to adequacy of sample when performing EUS-FNA (cut-off 85%). EUS-FNA is commonly performed in order to increase the diagnostic rate of EUS but its major drawback is the relatively low negative predictive value mainly due to inadequate sample or sampling errors (30). As for other diagnostic procedures, EUS-FNA recognizes specific indications and should be avoided when unnecessary (for example in the case of diagnosed pancreatic cancer already deemed surgically resectable). Accuracy of EUS-FNA is obviously dependent on the organ to study, with reported diagnostic rate for malignancy of 71% in the case of pancreatic adenocarcinoma (50,51) and 87% for nodal involvement due to esophageal cancer (52-55). Therefore, endoscopist’s personal score should be as close as possible to the aforementioned values reported in the literature.

Although comprehensive description of all technical aspects is beyond the scope of this review, the reader should be aware of the number of features described (even if not univocally) to be able to alter diagnostic accuracy of EUS-FNA, among them presence of on-site pathologist, use of the stylet, and number of needle passes (56-62).

However, availability of all these aspects (particularly the presence of on-site pathologist) is not universal even in high-volume centers. In this case, the endosonographer should obviate to this lacking by increasing the number of needle passes up to 5–7 for pancreatic masses and 2–4 for lymph nodes or metastases (63-65). No definitive recommendation on the needle calibre may be provided since a recent meta-analysis of RCTs failed to demonstrate superiority of EUS-FNA with 25-gauge needle as compared to 22 G (30). Initial reports with trucut biopsy reported higher complication rate with even decreased diagnostic accuracy in comparison to standard EUS-FNA (66), although interesting results have been recently published with novel flexible small-gauge core biopsy needles (67,68).

In conclusion, relevant intra-procedure “hot points” are defining the thresholds for accurate T and N staging, and increasing diagnostic accuracy of EUS-FNA (when tissue sampling is necessary).


Post-procedure QIs

The post-procedure period concerns the follow-up of the patient after the procedure and includes providing information/instructions to the patient, recognition and management of adverse events, pathology follow-up and assessing patient satisfaction (13).

As previously reported, complications after diagnostic EUS with no tissue sampling are extremely rare, whereas in the case of EUS-FNA acceptable rates of adverse events are reported (pancreatitis <2%, perforation <0.5%, bleeding <1%). Of note, most of these events are usually mild and easily to manage.

As for pathology follow-up, we previously described the false negative rate as a consequence of sampling errors or inadequate tissue. On the other hand, false positive results after EUS-FNA are reported in 1.1–5.3% of cases and are mainly due to pathologist misinterpretation (often in the setting of chronic pancreatitis) (69-71). Hence, although not due to direct responsibility of the endoscopic team, the endoscopist should cooperate with the pathologist in order to reach an accurate diagnosis.

Patient satisfaction, like in many other fields of endoscopy, is mainly related to the personal experience during the procedure, therefore sedation plays a pivotal role in this regard. Although satisfaction scores are usually optimal with propofol for complex upper endoscopic procedures, some concern were raised on the cardiopulmonary safety of this agent (72-74) thus pushing the research and testing of other drugs such as etomidate (75). It should be noted that patient satisfaction and preferences concern also aspects other than sedation, in particular the way to deliver “bad” diagnoses as reported in an interesting US study (76).

Therefore, main issues of the post-procedure period are interpretation of the clinical significance of the complications and management of eventual delayed adverse events, cooperation with the pathologist to increase the diagnostic yield of EUS-FNA, and patient satisfaction.


Conclusions

Great efforts of main gastroenterology and endoscopy societies led to the description of key QIs characterized by their ease of implementation, monitoring, and reporting. The current list of QIs is accurate and comprehensive although not every indicator is applicable to every practice setting. Therefore, facilities should select the subset most appropriate to their individual needs. Since EUS is one of the most dynamic fields in gastrointestinal endoscopy, new indications as well as new adverse events are very likely to appear in the next future, thus determining the need to continuously update the current documents. This is of particular importance since due to the increasing demand for EUS, the number of physicians performing this complex procedure will continue to grow. Therefore, quality assessment should be part of routine endoscopic training for all those residents/trainees willing to learn and practice this procedure.


Acknowledgements

None.


Footnote

Conflicts of Interest: The authors have no conflicts of interest to declare.


References

  1. Kohn LT, Corrigan JM, Donaldson MS. To err is human: building a safer health system. Washington (DC): National Academy Press, 2000.
  2. Institute of Medicine, Committee on Health Care in America. Crossing the quality chasm: a new health system for the 21st Century. Washington (DC): National Academy Press, 2001.
  3. Eijkenaar F. Pay for performance in health care: an international overview of initiatives. Med Care Res Rev 2012;69:251-76. [Crossref] [PubMed]
  4. Gross WL, Cooper L, Boggs S, et al. Value-Based Care and Strategic Priorities. Anesthesiol Clin 2017;35:725-31. [Crossref] [PubMed]
  5. Department of Health & Human Services. National Quality Strategy. National Strategy for Quality Improvement in Health Care. March 2011. Available online: http://www.ahrq.gov/workingforquality/nqs/nqs2011annlrpt.htm, accessed in November 2017.
  6. Bjorkman DJ, Popp JW. Measuring the quality of endoscopy. Gastrointest Endosc 2006;63:S1-2. [Crossref] [PubMed]
  7. Faigel DO, Pike IM, Baron TH, et al. Quality indicators for gastrointestinal endoscopic procedures: an introduction. Gastrointest Endosc 2006;63:S3-9. [Crossref] [PubMed]
  8. Cohen J, Safdi MA, Deal SE, et al. Quality indicators for esophagogastroduodenoscopy. Gastrointest Endosc 2006;63:S10-5. [Crossref] [PubMed]
  9. Rex DK, Petrini JL, Baron TH, et al. Quality indicators for colonoscopy. Gastrointest Endosc 2006;63:S16-28. [Crossref] [PubMed]
  10. Baron TH, Petersen BT, Mergener K, et al. Quality indicators for endoscopic retrograde cholangiopancreatography. Gastrointest Endosc 2006;63:S29-34. [Crossref] [PubMed]
  11. Jacobson BC, Chak A, Hoffman B, et al. Quality indicators for endoscopic ultrasonography. Gastrointest Endosc 2006;63:S35-8. [Crossref] [PubMed]
  12. Cohen J, Pike IM. Defining and measuring quality in endoscopy. Gastrointest Endosc 2015;81:1-2. [Crossref] [PubMed]
  13. Wani S, Wallace MB, Cohen J, et al. Quality indicators for EUS. Gastrointest Endosc 2015;81:67-80. [Crossref] [PubMed]
  14. Bluen BE, Lachter J, Khamaysi I, et al. Accuracy and Quality Assessment of EUS-FNA: A Single-Center Large Cohort of Biopsies. Diagn Ther Endosc 2012;2012. [Crossref] [PubMed]
  15. Coe SG, Raimondo M, Woodward TA, et al. Quality in EUS: an assessment of baseline compliance and performance improvement by using the American Society for Gastrointestinal Endoscopy-American College of Gastroenterology quality indicators. Gastrointest Endosc 2009;69:195-201. [Crossref] [PubMed]
  16. Lachter J, Bluen B. Establishing a quality indicator format for endoscopic ultrasound. World J Gastrointest Endosc 2013;5:574-80. [Crossref] [PubMed]
  17. Schwab R, Pahk E, Lachter J. Impact of endoscopic ultrasound quality assessment on improving endoscopic ultrasound reports and procedures. World J Gastrointest Endosc 2016;8:362-7. [Crossref] [PubMed]
  18. Gorospe EC, Oxentenko AS. Preprocedural considerations in gastrointestinal endoscopy. Mayo Clin Proc 2013;88:1010-6. [Crossref] [PubMed]
  19. Gan SI, Rajan E, Adler DG, et al. Role of EUS. Gastrointest Endosc 2007;66:425-34. [Crossref] [PubMed]
  20. Polkowski M, Jenssen C, Kaye P, et al. Technical aspects of endoscopic ultrasound (EUS)-guided sampling in gastroenterology: European Society of Gastrointestinal Endoscopy (ESGE) Technical Guideline - March 2017. Endoscopy 2017;49:989-1006. [Crossref] [PubMed]
  21. Adler DG, Jacobson BC, Davila RE, et al. ASGE guideline: complications of EUS. Gastrointest Endosc 2005;61:8-12. [Crossref] [PubMed]
  22. Das A, Sivak MV Jr, Chak A. Cervical esophageal perforation during EUS: a national survey. Gastrointest Endosc 2001;53:599-602. [Crossref] [PubMed]
  23. Eloubeidi MA, Tamhane A, Lopes TL, et al. Cervical esophageal perforations at the time of endoscopic ultrasound: a prospective evaluation of frequency, outcomes, and patient management. Am J Gastroenterol 2009;104:53-6. [Crossref] [PubMed]
  24. Dumonceau JM, Deprez PH, Jenssen C, et al. Indications, results, and clinical impact of endoscopic ultrasound (EUS)-guided sampling in gastroenterology: European Society of Gastrointestinal Endoscopy (ESGE) Clinical Guideline - Updated January 2017. Endoscopy 2017;49:695-714. [Crossref] [PubMed]
  25. Wang KX, Ben QW, Jin ZD, et al. Assessment of morbidity and mortality associated with EUS-guided FNA: a systematic review. Gastrointest Endosc 2011;73:283-90. [Crossref] [PubMed]
  26. Williams DB, Sahai AV, Aabakken L, et al. Endoscopic ultrasound guided fine needle aspiration biopsy: a large single centre experience. Gut 1999;44:720-6. [Crossref] [PubMed]
  27. Al-Haddad M, Wallace MB, Woodward TA, et al. The safety of fineneedle aspiration guided by endoscopic ultrasound: a prospective study. Endoscopy 2008;40:204-8. [Crossref] [PubMed]
  28. Eloubeidi MA, Tamhane A, Varadarajulu S, et al. Frequency of major complications after EUS-guided FNA of solid pancreatic masses: a prospective evaluation. Gastrointest Endosc 2006;63:622-9. [Crossref] [PubMed]
  29. Madhoun MF, Wani SB, Rastogi A, et al. The diagnostic accuracy of 22-gauge and 25-gauge needles in endoscopic ultrasound-guided fine needle aspiration of solid pancreatic lesions: a meta-analysis. Endoscopy 2013;45:86-92. [Crossref] [PubMed]
  30. Facciorusso A, Stasi E, Di Maso M, et al. Endoscopic ultrasound-guided fine needle aspiration of pancreatic lesions with 22 versus 25 Gauge needles: A meta-analysis. United European Gastroenterol J 2017;5:846-53. [Crossref] [PubMed]
  31. Chong A, Venugopal K, Segarajasingam D, et al. Tumor seeding after EUS-guided FNA of pancreatic tail neoplasia. Gastrointest Endosc 2011;74:933-5. [Crossref] [PubMed]
  32. Ahmed K, Sussman JJ, Wang J, et al. A case of EUS-guided FNArelated pancreatic cancer metastasis to the stomach. Gastrointest Endosc 2011;74:231-3. [Crossref] [PubMed]
  33. Doi S, Yasuda I, Iwashita T, et al. Needle tract implantation on the esophageal wall after EUS-guided FNA of metastatic mediastinal lymphadenopathy. Gastrointest Endosc 2008;67:988-90. [Crossref] [PubMed]
  34. Facciorusso A, Di Maso M, Serviddio G, et al. Echoendoscopic ethanol ablation of tumor combined with celiac plexus neurolysis in patients with pancreatic adenocarcinoma. J Gastroenterol Hepatol 2017;32:439-45. [Crossref] [PubMed]
  35. Facciorusso A, Maso MD, Barone M, et al. Echoendoscopic ethanol ablation of tumor combined to celiac plexus neurolysis improved pain control in a patient with pancreatic adenocarcinoma. Endosc Ultrasound 2015;4:342-4. [Crossref] [PubMed]
  36. Arcidiacono PG, Carrara S, Reni M, et al. Feasibility and safety of EUS-guided cryothermal ablation in patients with locally advanced pancreatic cancer. Gastrointest Endosc 2012;76:1142-51. [Crossref] [PubMed]
  37. Khashab MA, Acosta RD, Bruining DH, et al. Antibiotic prophylaxis for GI endoscopy. Gastrointest Endosc 2015;81:81-9. [Crossref] [PubMed]
  38. Banerjee S, Shen B, Baron TH, et al. Antibiotic prophylaxis for GI endoscopy. Gastrointest Endosc 2008;67:791-8. [Crossref] [PubMed]
  39. Wani S, Keswani R, Hall M, et al. A Prospective Multicenter Study Evaluating Learning Curves and Competence in Endoscopic Ultrasound and Endoscopic Retrograde Cholangiopancreatography Among Advanced Endoscopy Trainees: The Rapid Assessment of Trainee Endoscopy Skills Study. Clin Gastroenterol Hepatol 2017;15:1758-1767.e11. [Crossref] [PubMed]
  40. DiMaio CJ, Mishra G, McHenry L, et al. EUS core curriculum. Gastrointest Endosc 2012;76:476-81. [Crossref] [PubMed]
  41. Edge S, Byrd DR, Compton CC, et al. AJCC Cancer Staging Manual. New York: Springer, 2010.
  42. Sobin L, Gospodarowicz M, Wittekind C, et al. TNM classification of malignant tumours. Wiley-Blackwell, 2010.
  43. Soriano A, Castells A, Ayuso C, et al. Preoperative staging and tumor resectability assessment of pancreatic cancer: prospective study comparing endoscopic ultrasonography, helical computed tomography, magnetic resonance imaging, and angiography. Am J Gastroenterol 2004;99:492-501. [Crossref] [PubMed]
  44. Tio TL, Tytgat GN, Cikot RJ, et al. Ampullopancreatic carcinoma: preoperative TNM classification with endosonography. Radiology 1990;175:455-61. [Crossref] [PubMed]
  45. Legmann P, Vignaux O, Dousset B, et al. Pancreatic tumors: comparison of dual-phase helical CT and endoscopic sonography. AJR Am J Roentgenol 1998;170:1315-22. [Crossref] [PubMed]
  46. Gress FG, Hawes RH, Savides TJ, et al. Role of EUS in the preoperative staging of pancreatic cancer: a large single-center experience. Gastrointest Endosc 1999;50:786-91. [Crossref] [PubMed]
  47. Puli SR, Singh S, Hagedorn CH, et al. Diagnostic accuracy of EUS for vascular invasion in pancreatic and periampullary cancers: a meta-analysis and systematic review. Gastrointest Endosc 2007;65:788-97. [Crossref] [PubMed]
  48. Rösch T, Braig C, Gain T, et al. Staging of pancreatic and ampullary carcinoma by endoscopic ultrasonography. Comparison with conventional sonography, computed tomography, and angiography. Gastroenterology 1992;102:188-99. [Crossref] [PubMed]
  49. Ahmad NA, Lewis JD, Ginsberg GG, et al. EUS in preoperative staging of pancreatic cancer. Gastrointest Endosc 2000;52:463-8. [Crossref] [PubMed]
  50. Savides TJ, Donohue M, Hunt G, et al. EUS-guided FNA diagnostic yield of malignancy in solid pancreatic masses: a benchmark for quality performance measurement. Gastrointest Endosc 2007;66:277-82. [Crossref] [PubMed]
  51. Hewitt MJ, McPhail MJ, Possamai L, et al. EUS-guided FNA for diagnosis of solid pancreatic neoplasms: a meta-analysis. Gastrointest Endosc 2012;75:319-31. [Crossref] [PubMed]
  52. Vazquez-Sequeiros E, Wiersema MJ, Clain JE, et al. Impact of lymph node staging on therapy of esophageal carcinoma. Gastroenterology 2003;125:1626-35. [Crossref] [PubMed]
  53. Vazquez-Sequeiros E, Norton ID, Clain JE, et al. Impact of EUS-guided fine-needle aspiration on lymph node staging in patients with esophageal carcinoma. Gastrointest Endosc 2001;53:751-7. [Crossref] [PubMed]
  54. Eloubeidi MA, Wallace MB, Reed CE, et al. The utility of EUS and EUSguided fine needle aspiration in detecting celiac lymph node metastasis in patients with esophageal cancer: a single-center experience. Gastrointest Endosc 2001;54:714-9. [Crossref] [PubMed]
  55. Parmar KS, Zwischenberger JB, Reeves AL, et al. Clinical impact of endoscopic ultrasound-guided fine needle aspiration of celiac axis lymph nodes (M1a disease) in esophageal cancer. Ann Thorac Surg 2002;73:916-20; discussion 920-1. [Crossref] [PubMed]
  56. Jani BS, Rzouq F, Saligram S, et al. Endoscopic Ultrasound-Guided Fine-Needle Aspiration of Pancreatic Lesions: A Systematic Review of Technical and Procedural Variables. N Am J Med Sci 2016;8:1-11. [Crossref] [PubMed]
  57. Matsubayashi H, Matsui T, Yabuuchi Y, et al. Endoscopic ultrasonography guided-fine needle aspiration for the diagnosis of solid pancreaticobiliary lesions: Clinical aspects to improve the diagnosis. World J Gastroenterol 2016;22:628-40. [Crossref] [PubMed]
  58. Nelsen EM, Buehler D, Soni AV, et al. Endoscopic ultrasound in the evaluation of pancreatic neoplasms-solid and cystic: A review. World J Gastrointest Endosc 2015;7:318-27. [Crossref] [PubMed]
  59. Iglesias-Garcia J, Lariño-Noia J, Abdulkader I, et al. Rapid on-site evaluation of endoscopic-ultrasound-guided fine-needle aspiration diagnosis of pancreatic masses. World J Gastroenterol 2014;20:9451-7. [Crossref] [PubMed]
  60. Kim JH, Park SW, Kim MK, et al. Meta-Analysis for Cyto-Pathological Outcomes in Endoscopic Ultrasonography-Guided Fine-Needle Aspiration With and Without the Stylet. Dig Dis Sci 2016;61:2175-84. [Crossref] [PubMed]
  61. Varadarajulu S, Bang JY, Holt BA, et al. The 25-gauge EUS-FNA needle: Good for on-site but poor for off-site evaluation? Results of a randomized trial. Gastrointest Endosc 2014;80:1056-63. [Crossref] [PubMed]
  62. Wee E, Lakhtakia S, Gupta R, et al. Endoscopic ultrasound guided fine-needle aspiration of lymph nodes and solid masses: factors influencing the cellularity and adequacy of the aspirate. J Clin Gastroenterol 2012;46:487-93. [Crossref] [PubMed]
  63. Erickson RA, Sayage-Rabie L, Beissner RS. Factors predicting the number of EUS-guided fine-needle passes for diagnosis of pancreatic malignancies. Gastrointest Endosc 2000;51:184-90. [Crossref] [PubMed]
  64. LeBlanc JK, Ciaccia D, Al-Assi MT, et al. Optimal number of EUSguided fine needle passes needed to obtain a correct diagnosis. Gastrointest Endosc 2004;59:475-81. [Crossref] [PubMed]
  65. Wallace MB, Kennedy T, Durkalski V, et al. Randomized controlled trial of EUS-guided fine needle aspiration techniques for the detection of malignant lymphadenopathy. Gastrointest Endosc 2001;54:441-7. [Crossref] [PubMed]
  66. Jenssen C, Dietrich CF. Endoscopic ultrasound-guided fine-needle aspiration biopsy and trucut biopsy in gastroenterology - An overview. Best Pract Res Clin Gastroenterol 2009;23:743-59. [Crossref] [PubMed]
  67. Petrone MC, Poley JW, Bonzini M, et al. Comparison of pancreatic histology specimens obtained by EUS 19G versus 22G core biopsy needles: A prospective multicentre study among experienced pathologists. United European Gastroenterol J 2017;5:854-8. [Crossref] [PubMed]
  68. Bang JY, Hebert-Magee S, Navaneethan U, et al. EUS-guided fine needle biopsy of pancreatic masses can yield true histology: results of a randomised trial. Gut 2017. [Epub ahead of print]. [Crossref] [PubMed]
  69. Gleeson FC, Kipp BR, Caudill JL, et al. False positive endoscopic ultrasound fine needle aspiration cytology: incidence and risk factors. Gut 2010;59:586-93. [Crossref] [PubMed]
  70. Siddiqui AA, Kowalski TE, Shahid H, et al. False-positive EUS-guided FNA cytology for solid pancreatic lesions. Gastrointest Endosc 2011;74:535-40. [Crossref] [PubMed]
  71. Schwartz DA, Unni KK, Levy MJ, et al. The rate of false-positive results with EUS-guided fine-needle aspiration. Gastrointest Endosc 2002;56:868-72. [Crossref] [PubMed]
  72. Campbell JA, Irvine AJ, Hopper AD. Endoscopic ultrasound sedation in the United Kingdom: Is life without propofol tolerable? World J Gastroenterol 2017;23:560-2. [Crossref] [PubMed]
  73. van Riet PA, Cahen DL, Poley JW, et al. Mapping international practice patterns in EUS-guided tissue sampling: outcome of a global survey. Endosc Int Open 2016;4:E360-70. [Crossref] [PubMed]
  74. Jensen JT, Hornslet P, Konge L, et al. High efficacy with deep nurse-administered propofol sedation for advanced gastroenterologic endoscopic procedures. Endosc Int Open 2016;4:E107-11. [PubMed]
  75. Kim MG, Park SW, Kim JH, et al. Etomidate versus propofol sedation for complex upper endoscopic procedures: a prospective double-blinded randomized controlled trial. Gastrointest Endosc 2017;86:452-61. [Crossref] [PubMed]
  76. Siddiqui UD, Rossi F, Padda MS, et al. Patient preferences after endoscopic ultrasound with fine needle aspiration (EUS-FNA) diagnosis of pancreas cancer: rapid communication valued over long-term relationships. Pancreas 2011;40:680-1. [Crossref] [PubMed]
Cite this article as: Facciorusso A, Buccino RV, Muscatiello N. How to measure quality in endoscopic ultrasound. Ann Transl Med 2018;6(13):266. doi: 10.21037/atm.2018.03.36

Download Citation