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The field of endoscopy has revolutionized the diagnosis and treatment of gastrointestinal (GI) diseases in recent years. Besides the ‘traditional’ endoscopic procedures (esophagogastroduodenoscopy, colonoscopy, flexible sigmoidoscopy, and endoscopic retrograde cholangiopancreatography), advances in imaging technology (endoscopic ultrasonography, wireless capsule endoscopy, and double balloon enteroscopy) have allowed GI specialists to detect and manage disorders throughout the digestive system. This article reviews various endoscopic procedures and provides up-to-date endoscopic indications based on the recommendations of American Society for Gastrointestinal Endoscopy and American Cancer Society for primary care providers in order to achieve high-quality and cost-effective care.
Open access endoscopy (OAE) is becoming more common due to the cost-driven health care system. It allows general practitioners to schedule elective common endoscopic procedures without prior specialty consultation. Endoscopies ‘generally not indicated’ are accounted for 49% when the examination is prescribed by general practitioners compared to 14% by endoscopists.1 Because of this disparity, it is critical for primary care physicians to have a thorough understanding of endoscopic indications. The purpose of this article is twofold: 1) to provide up-to-date endoscopic indications for primary care physicians so that only ‘indicated’ procedures are performed in order to avoid unnecessary complications and cost and 2) to familiarize primary practitioners with new endoscopic procedures in order to promote closed communication with gastrointestinal (GI) specialists (Table 1). The following information is based on the American Society for Gastrointestinal Endoscopy (ASGE) and American Cancer Society (ACS) recommendations.
Esophagogastroduodenoscopy (EGD) is a procedure that visualizes the mucosal surfaces of the esophagus, stomach, and proximal duodenum. It allows both diagnostic and therapeutic functions. The gastroscope is used for EGD. It is a forward-viewing instrument and consists of a control head with valves for air insufflations and suction, an instrument channel for biopsy, an insertion length, and a bending length at the end of the scope. Patients should be kept nil per os (NPO) 6 h before the procedure. In preparation for EGD, the patient lies on the left side with the head resting on a pillow. A mouthguard is placed between the teeth to prevent biting on the endoscope. Then the gastroscope is inserted into the mouth, down to the esophagus, stomach, and ultimately ending in the second part of the duodenum. After this maneuver, the endoscope is withdrawn for further inspection of the GI lining. The fundus is examined by retroflexing the gastroscope’s tip to resemble the J-shape. Any abnormal lesions should be biopsied. Most GI endoscopic procedures (EGD and colonoscopy) are performed under conscious sedation. The patient is able to respond to verbal or tactile stimulation. Combinations of benzodiazepines (midazolam and diazepam) and opioids (meperidine and fentanyl) are used for sedation.2
Endoscopic retrograde cholangiopancreatography (ERCP) is a technique that combines endoscopy and fluoroscopy to diagnose and to treat biliary or pancreatic ductal diseases. Similar to EGD, an endoscope is inserted through the mouth down into the duodenum. Instead of using a forward-viewing gastroscope as in EGD, a side-viewing duodenoscope is used for accurate identification of the ampulla of Vater, the opening of the common bile duct (CBD) and pancreatic duct (PD). When the ampulla is identified, a catheter is inserted through the ampulla into the CBD and/or PD. Radiocontrast dye is then injected into these ducts for real-time visualization by fluoroscopy. Fluoroscopy uses X-ray to look for strictures, blockages, or ductal leakages, and it guides therapeutic procedures. The bowel preparation is similar to EGD. However, because of longer duration, more sedatives than the standard benzodiazepines/opioid agents are needed for patient comfort. General anesthesia with propofol has demonstrated to be more effective than the above combinations in complex ERCP.2
Endoscopic ultrasonography (EUS) uses a high-frequency ultrasound transducer that is incorporated into the tip of the endoscope to provide high-resolution images of the GI wall and adjacent structures. EUS-guided fine needle aspiration (EUS-FNA) is a technique using a thin needle under the ultrasonographic guidance to obtain an aspirate of the tissue. In addition, other therapeutic procedures, such as EUS-guided drainage and EUS-guided celiac plexus blockage, can be performed under the guidance of real-time ultrasound. For upper EUS, bowel preparation is similar to EGD; for lower EUS, it is similar to colonoscopy (will be discussed under ‘Colonoscopy’). More sedatives and analgesics may be required because these procedures are longer than EGD and colonoscopy.3
Colonoscopy allows for examination of the entire large bowel. The colonoscope is a forward-viewing instrument and has similar features to the gastroscope. As the patient lies on the left side, the endoscope is inserted through the anus, up the rectum, colon, and ultimately the terminal ileum. A thorough inspection is often done upon withdrawal of the colonoscope. Suspicious lesions are cauterized or removed for histopathology studies. Three accepted bowel preparations are polyethylene glycol (PEG), aqueous sodium phosphate (NaP), and tablet NaP. With the glycol-based product, patients either drink 4 L of PEG (Colyte®, GoLytely®) in one dose the day before the procedure or in divided doses (3 L the evening before and 1 L the morning of the procedure). The latter regimen is better tolerated. With the aqueous form, patients may take two doses of 30–45 mL of NaP (Fleet®) (at least 10–12 h apart) along with plenty of fluids to prevent dehydration because NaP osmotically draws plasma water into the bowel lumen to promote cleansing. The tablet NaP (Visicol®) is in a pill form that has the same salt doses as found in the solution without the unpleasant taste. It is also formulated to limit the volume of liquid required. The total dose is 32–40 tablets (20 on the evening before the procedure and 12–20 tablets 3–5 h before the colonoscopy). There are a few caveats with NaP laxative. It should be avoided in patients with congestive heart failure, renal impairment, and gut dysmotility due to significant fluid and electrolyte shifts. In addition, nonspecific aphthoid-like mucosal lesions have been associated with NaP. If a diagnosis of inflammatory bowel disease (IBD) is being considered, NaP should be avoided. Similar to EGD, conscious sedation is used for patient comfort.4
Until the introduction of wireless capsule endoscopy (WCE) in 1990s, diagnosing small bowel diseases was a challenge. Former techniques (Sonde enteroscopy and intraoperative enteroscopy) had many limitations and complications and were also associated with high mortality rate. WCE is purely a diagnostic tool. The system consists of a disposable ‘video-recorder’ capsule, a 7-h battery that allows images transmission to a data recorder that is carried around the patient’s waist, and a computer workstation with proprietary software that reviews and interprets the results. WCE can be performed in an ambulatory outpatient setting. Without sedation, the capsule is ingested after a 10–12-h fasting period and moves through the small intestine by peristalsis. Although bowel preparation is not required, some centers advocate bowel catharsis for improved visualization of the small bowel. At present, studies yield conflicting results and no consensus has been reached.5
While CE provides only a diagnostic workup, double balloon enteroscopy (DBE) allows for both diagnostic and therapeutic capabilities. DBE enables direct visualization of the small bowel by the push-and-pull technique with two balloons under fluoroscopic guidance. The system consists of a video endoscope, a flexible overtube, which covers the endoscope and enables it to slide freely, and two latex balloons that are inflated and deflated by a pressure-controlled pump system. The balloons are attached to the tip of the enteroscope and the overtube. The procedure is as follows:
The whole process (steps 1–4) is repeated.
DBE can be performed from the oral route, the anal route, or both. For the oral approach, the patient is kept NPO for at least 6 h. For the anal approach, bowel cleansing is similar to colonoscopy. Total enteroscopy is not possible in a single procedure, and it is usually terminated when abnormalities are found and treated. Due to the lengthy procedure (70–80 min), general anesthesia is preferred.6 Serious complications of DBE are pancreatitis (0.3%)7 and bowel perforation (3.4%).8
Instead of examining the entire colon, flexible sigmoidoscopy (FS) only inspects the rectum, sigmoid, and descending colon. Although the sigmoidoscope is shorter, it shares many similar designs with the colonoscope. Since no sedation is required, the procedure can be performed in office-based settings by nurses or physician assistants. For bowel preparation, two Fleet enemas are adequate. Patients with active colitis or diarrhea do not need bowel preparation. After placing the patient in left lateral decubitus position, the scope is inserted into the rectum through the anus and is ascended until 40 cm is reached for a high-quality exam in colorectal cancer (CRC) screening. Polyps are biopsied and sent to pathology lab.
Achalasia is an esophageal motility disorder. In this condition, the smooth muscle of the esophagus has impaired peristalsis, and the lower esophageal sphincter (LES) fails to relax properly in response to swallowing. Some achalasia cases result from esophageal cancer or Chagas disease, a lower esophageal condition that is infected by a parasite, Trypanosoma cruzi. However, the cause for most achalasia is unknown. Symptoms include dysphagia, regurgitation of undigested food, coughing, and weight loss. Esophageal manometry is the ‘gold standard’ for diagnosing achalasia. 9 EGD is required to exclude esophageal cancer at the gastroesophageal junction before therapeutic interventions. The treatment goal is to reduce the LES pressure. This can be accomplished with pneumatic balloon dilators, botulinum toxin injection, or surgery as the last-line intervention strategy.
Barrett’s esophagus is an acquired premalignant condition resulting from gastroesophageal reflux disease (GERD). It is marked by the presence of columnar epithelia in the lower esophagus, replacing the normal squamous epithelium. Compared to the normal population, patients with Barrett’s esophagus have 30–125 times the risk of developing esophageal adenocarcinoma.10 However, screening and surveillance are currently still controversial. Currently, the ASGE makes the following recommendations:11
Caustic injury is resulted from accidental or intentional ingestion of alkaline or acidic substances that include drain cleaners and other household cleaning products. Self- poisoning with these chemicals is common in Asia. The result is intense damage to the esophagus and stomach, often producing perforation. Late sequelae are stricture and squamous cell carcinoma. The incidence of carcinoma has been estimated to be 1%–4%. After 12–20 years of injury, EGD is recommended. Subsequently, surveillance should not be more than every 1–3 years.11
Approximately 13,000 cases of esophageal cancer are diagnosed annually in the United States. Adenocarcinoma of the esophagus has one of the fastest rising incidence rates of any malignancy. EGD is the primary method for direct visualization and allows the endoscopist to obtain multiple biopsies. The classic endoscopic appearance is an ulcerated mass projecting from a rigid, aperistaltic segment of the esophagus.12 EGD also plays an important role in detecting recurrence and in treating esophageal cancer.13
Sixty to seventy percent of all esophageal strictures are caused by GERD, and the remaining strictures are secondary to Schatzki’s ring (a ring found in lower esophagus causing dysphagia), esophageal cancer, radiation therapy, esophageal surgery, eosinophilic esophagitis (a disorder characterized by infiltration of a large number of eosinophils in the esophagus), sclerotherapy, caustic injury, or photodynamic therapy.14 Dysphagia to solid foods is a common symptom. EGD with biopsies should be performed in all patients with dysphagia to exclude neoplastic processes. After ruling out malignancy, benign strictures are managed by either balloon or bougie dilations.9 Balloon dilators are often used to treat achalasia for forceful disruption of the LES. Bougies consist of two types: 1) mercury or tungsten- filled dilator and 2) wire-guided polyvinyl dilator. The former type has a tapered tip and can pass either blindly or under fluoroscopy. The latter type is passed over a guidewire and used for complex strictures.15
Variceal bleeding is a serious complication of portal hypertension with the mortality rate as high as 50%.16 Because of high mortality, nonselective beta-blockers (propranolol or nadolol) have been shown to prevent or to delay the first episode of variceal bleeding.16 EGD is the only reliable method to confirm the presence of varices. Patients with cirrhosis and signs of portal hypertension (platelet count <140,000/mm3) should have screening endoscopy. Endoscopic variceal ligation (EVL) is indicated for primary prophylaxis in patients who cannot tolerate beta-blockers (asthma). EVL has also become the treatment of choice for variceal hemorrhage.
Once foreign bodies are diagnosed, the timing of endoscopy is dependent on the risks of aspiration or perforation. Urgent endoscopic intervention is required to remove sharp objects or disk batteries that are lodged in the esophagus. Urgent EGD is also required to prevent aspiration when an object creates a high-grade obstruction. Conservative management is indicated when a foreign body has entered the stomach. If an object fails to pass the stomach within 3–4 weeks, it should be removed endoscopically.17
The majority of gastric epithelial polyps found during EGD are benign. However, adenomatous polyps have malignant potential. They should be completely resected. One-year surveillance endoscopy is reasonable to assess recurrence. If the result is negative, endoscopy should be repeated at 3–5-year intervals.11
Dyspepsia is a condition characterized by a variety of symptoms (epigastric discomfort, bloating, anorexia, early satiety, belching, nausea, and heartburn). It can be caused by peptic ulcer disease (PUD), GERD, and malignancy. GERD and gastric cancer will be discussed in next two sections. Approximately, 15% of patients with dyspepsia have PUD, and the majority of them are tested positive for Helicobacter pylori antibody.18 In patients with PUD, H. pylori infection should be eradicated to improve healing and to reduce the risk of recurrence and rebleeding. At the experienced hands, 90% of gastroduodenal lesions can be detected by EGD.19 For patients with previous gastrectomy as a result of PUD, routine endoscopic surveillance is not indicated.18
GERD is defined as symptoms or mucosal damage produced by the abnormal reflux of gastric contents into the esophagus. Patients with mild GERD symptoms (typical heartburn or mild intermittent dyspepsia) may be given an initial trial of therapy without endoscopic evaluation. EGD is the preferred procedure when patients with GERD have one of the following alarming symptoms: dysphagia, odynophagia, persistent or progressive heartburn symptoms while on antacid therapy, or weight loss.20 Sole hiatal hernia on the upper GI series is not an indication for EGD.
Gastric cancer is the fourth most common cancer in the world, only behind lung, breast, and colon cancers. However, it still remains the second most common cause of death from cancer worldwide.21 Multiple biopsies (at least seven specimens) of the gastric ulcers are necessary to rule out malignancy. It remains to be determined whether it is cost-effective to repeat endoscopy to verify post-treatment healing of gastric ulcers. At the present time, a follow-up endoscopy should be performed in 8–12 weeks after the initial EGD and treatment to document healing and repeat biopsies of any nonhealing ulcers.22
Adenoma arising at the major duodenal papilla is called ampullary adenoma. It can occur sporadically or in association with familial adenomatous polyposis (FAP) (will be discussed later). In order to determine the ampullary involvement, a side-viewing endoscope is used in addition to a routine forward-viewing duodenoscope. ERCP and EUS are important tools in selecting patients for endoscopic or surgical resection (will be discussed later).23 For patients undergoing endoscopic resection, postprocedure endoscopic surveillance should be done to ensure complete tissue removal and lack of disease recurrence.23 Endoscopic resection techniques are not standardized and should only be performed by experienced endoscopists.
Nonampullary duodenal adenoma (NDA) occurs outside of the ampulla sporadically or in association with FAP (will be discussed in next section). Its endoscopic appearance is similar to Brunner’s gland tumor, inflammatory polyp, carcinoid tumor, and hamartoma, thus a suspicious lesion should be biopsied before attempted resection.23 Before endoscopic resection, it is important to determine that the lesion does not involve the ampulla because the approach for evaluating an ampullary lesion is different (as noted above). Similar to ampullary adenomas, postprocedure endoscopic surveillance is indicated to verify complete resection and lack of occurrence.23
The second leading cause of death in patients with FAP who have had colectomy is duodenal cancer.11 The risk of these patients developing duodenal adenocarcinoma is more than 100-fold when compared to the general population.11 Both forward-viewing and side-viewing endoscopes should be used to detect adenomas in the duodenum, particularly in the periampullary region. Patients with hereditary nonpolyposis colorectal cancer (HNPCC) have a higher risk of developing cancers of the stomach and small bowel. Small bowel cancer in patients with HNPCC occurs at a young age (median age of 39), and the duodenum involves 50% of the cases.11 As a result, regular upper endoscopy surveillance of patients with FAP/HNPCC should be started around the time of colectomy or after the age of 30.11
Approximately 13% of patients with Crohn’s disease (CD) have upper GI tract involvement.24 Duodenal biopsy often yields more granulomas (organized collections of macrophages are usually seen with CD) (40%–68%) than colonic biopsy.24 Hence, EGD is helpful in differentiating CD from ulcerative colitis (UC) in indeterminate colitis.
Percutaneous endoscopic gastrostomy (PEG) is an endoscopic procedure for placing a tube through the abdominal wall. Indications for PEG placement include impaired swallowing conditions (stroke), cancer of the oropharynx, larynx, and esophagus. PEG is also useful in patients with malignant bowel obstruction. PEG is not appropriate if peroral feeding is expected to resume within 30 days. Sometimes, the indication for PEG is debatable. In advanced dementia, PEG placement does not prolong life. Ethical considerations should be considered given the quality of life and prognosis.25
Patients with upper GI bleeding (UGIB) should be stabilized before the initiation of endoscopy. Prompt endoscopy in patients with UGIB is effective in diagnosing and treating most causes of UGIB. It is also associated with reduction in both blood transfusion and length of hospital stay.26 Starting intravenous erythromycin 30–90 min before EGD promotes gastric motility and emptying and significantly improves the mucosal visibility.26
Obscure GI bleeding is defined as persistence of bleeding from unknown origin, despite negative initial EGD and colonoscopy. A study demonstrated that push endoscopy diagnosed 64% of the bleeding lesions in patients with obscure GI bleeding within the reach of the standard endoscope. 27 As a result, a ‘second-opinion’ EGD may be indicated in these patients before proceeding to WCE.
Pernicious anemia is a form of megaloblastic anemia due to B12 deficiency in the setting of atrophic gastritis. Patients with this disorder have a 2–3-fold increase in the incidence of gastric cancer. Single endoscopy should be performed to identify prevalent lesions but routine subsequent endoscopic surveillance is not recommended.11
Obesity is a major health problem that contributes to increased morbidity and mortality as well as to other disorders worldwide. In the United States, annual cost of managing obesity is approximately $100 billion.28 Weight loss surgery is recommended for patients with the body mass index (BMI) ≥ 40 kg/m2 or those with BMI ≥ 35 kg/m2 and serious comorbid conditions.29 Patients with upper GI symptoms should be evaluated by EGD prior to undergoing bariatric surgery. A preoperative upper endoscopy is indicated for patients who are having gastric banding because a large hiatal hernia may be a contraindication. The European guidelines recommend preoperative upper endoscopy in all patients before surgery, regardless of whether or not symptoms are present.29 The rationale is that some bariatric surgical procedures render the stomach and duodenum inaccessible for upper endoscopic techniques. Nausea, vomiting, and abdominal pain are common symptoms commonly seen after bariatric surgery. However, patients with these persistent problems should have an upper endoscopy because the symptoms may indicate the presence of marginal ulcers, gastrogastric fistulas, postsurgical reflux disease, or anastomotic obstruction.
Choledocholithiasis is a disorder of gallstones in the CBD. Stone extraction ERCP is the treatment of choice for this condition with the success rate of more than 90%.30 The overall complication rate and mortality rate are approximately 5% and less than 1%, respectively.31
These benign conditions result from primary sclerosing cholangitis (PSC), congenital bile-duct abnormalities, chronic pancreatitis, or postoperative complications (liver transplantation).30 Endoscopic dilation is achieved by a graduated catheter, balloon, stent placement, or combination of interventions. Dominant strictures of patients with PSC should also undergo endoscopic brushing and biopsy for assessment of malignancy.
Pancreatic ductal leaks occur as a result of acute pancreatitis, chronic pancreatitis, trauma, or surgical injury. Pancreatic leaks can lead to pancreatic ascites and pseudocyst formation. The leaks can be ‘bridged’ with transpapillary stents.30
Sphincter of Oddi dysfunction (SOD) is a condition of biliary colic resulting from the obstruction of bile and pancreatic juice flow. Patients with this disorder can have abnormal liver chemistries, dilated bile duct, or both. The gold standard to diagnose SOD is biliary manometry, which is performed during ERCP.30 Biliary sphincterotomy alleviate pain in the majority of patients. SOD manometry has an increased rate of pancreatitis and should be performed by experienced endoscopists.
If other imaging modalities of patients with recurrent acute pancreatitis are equivocal, ERCP should be done to evaluate the ductal anatomy along with bile analysis for microlithiasis. Endoscopic sphincterotomy without cholecystectomy is a viable option for patients with microlithiasis.30
Both ERCP and EUS are useful for diagnosing CP, but ERCP should be reserved for patients in whom the diagnosis has not been established by less-invasive studies.32
ERCP can drain pancreatic fluid collections, such as acute pseudocyst, chronic pseudocysts, and pancreatic necrosis. Fluid collections communicating with the PD are drained via the transpapillary approach, while noncommunicating collections are amenable to the transmural (transgastric or transduodenal) therapy. The success rates for transpapillary and transmural routes are >90% and >80%, respectively.30 Acute and chronic pseudocysts will be further discussed in the EUS section.
Bariatric weight loss surgery has been discussed above in the EGD section. Postoperative rates for gallstones are high (22%–71%), and cholecystectomy was performed in 7%–41% of patients who underwent bariatric surgery.29 The rates of choledocholithiasis in these patients are unknown. ERCP is challenging due to altered anatomy. According to a small study, ERCP with successful papilla cannulation was only achieved in 66% of patients.29
Intraductal papillary mucinous neoplasm (IPMN) is defined as papillary proliferations of pancreatic mucin-producing epithelial cells with/without excessive mucin hypersecretion and/or cystic ductal dilation. (Please refer to the EUS section for further discussion.) On ERCP, the pathognomonic for IPMN is the finding of mucus extruding from a patulous ampulla.33 Pancreatographic findings during ERCP suggesting IPMN are segmental or diffuse dilatation of the main PD or focal side-branch dilatation. Sometimes filling defects in the main PD (caused by mucus) can be differentiated from stones by their transient nature when passed with a guidewire.
Before endoscopic resection of an ampullary adenoma, the extent of biliary and pancreatic involvement is evaluated by ERCP. Some authors recommend surgical resection if there is evidence of intraductal extension; other authors still favor endoscopic resection as long as the extension is <1 cm because, at this level, the invading tissue can be endoscopically ablated.23
Cholangiocarcinoma is a cancer of the bile ducts. It is rare and highly lethal due to local metastases at presentation. The common risk factor is PSC, which is closely associated with UC. Patients with unresectable cholangiocarcinoma and jaundice should undergo ERCP for stent placement.34
Pancreatic cancer is the fourth leading cause of death in the United States.35 The pathognomonic finding of pancreatic head cancer on ERCP is the ‘double-duct’ sign, biliary and pancreatic ductal strictures with proximal dilation. With recent advances in other noninvasive pancreatic imaging modalities, preoperative ERCP does not add further staging information and may result in complications (pancreatitis and perforation) that make surgery more difficult. However, for patients with cholangitis, severe pruritus, or patients who are not fit for surgery, ERCP with biliary stenting should be performed to relieve obstruction.34
These cancers are staged according to the ‘Tumor, Node, and Metastasis’ system. Accurate staging is important for therapeutic decision-making and prognostication. Staging with EUS is more accurate than computed tomography (CT) in these types of cancers.13
Similar to esophageal cancer, EUS is superior to both CT and intraoperative surgical assessment for staging gastric carcinoma and lymphoma. It is also useful in monitoring response to therapy in patients with lymphoma.36
Mediastinal adenopathy may be detected by CT, by chest X-ray, or by the presence of extrinsic compression of the esophagus detected during EGD. Mediastinal adenopathy is caused by both benign processes (sarcoidosis, tuberculosis, and histoplasmosis) and malignant processes (metastatic cancer and lymphoma). EUS-FNA avoids mediastinoscopy or thoracotomy and increases the yield of malignancy. Therefore, EUS-FNA is the preferred procedure for tissue sampling of posterior mediastinal lymph nodes or lesions seen on cross-sectional imaging.37
EUS and EUS-FNA are useful adjunctive techniques for the diagnosis and staging of pancreatic malignancies. In patients with unresectable carcinoma, EUS allows patient selection for stent placement and EUS-guided celiac plexus neurolysis.34
Pancreatic cystic lesions are a frequent incidental finding due to the increased use of high resolution abdominal radiographic imaging. These lesions are classified into either benign or malignant cysts, depending on whether they have the malignant potential. The benign cyst is pseudocyst, whereas the malignant cystic lesions consist of serous cystadenoma, mucinous cystadenoma, IPMN, and solid pseudopapillary neoplasm.33 EUS and EUS-guided procedures (EUS-FNA, EUS-guided drainage, and EUSguided celiac plexus blockage) play an important role in diagnosing and managing pancreatic cystic lesions. Some EUS features can differentiate a certain type of cystic lesion from others. EUS-FNA of the cystic lesions provides further information on the etiology of the cysts. The different types of pancreatic cystic lesions include the following:
Submucosal tumors are divided into two groups. The more common group is referred to as gastrointestinal stromal tumors, and the less common group includes lipomas, schwannomas, hemangiomas, leiomyomas, and their malignant counterparts (leiomyosarcoma). The diagnosis of these tumors is difficult by standard imaging. EUS can suggest the nature of a submucosal tumor by determining the layer of origin and echotexture of the lesion. Tumor size, an irregular border, echogenic foci, and cystic spaces are independently associated with malignancy.36
For ampullary adenoma, EUS and intraductal EUS (a small EUS probe passing inside the pancreatobiliary systems) allow us to evaluate periampullary lymph nodes, to select patients for endoscopic versus surgical resection, and to guide surgical therapy.23 For NDA, EUS allows us to determine the relationship of the polyp to the pancreaticobiliary tree when side-viewing examination is uncertain. In addition, EUS can also determine whether endoscopic removal is feasible when biopsy shows HGD.23
Ampullary carcinoma is a relatively rare cancer that accounts for approximately 0.2% of GI malignancies.41 It is suspected when a patient presents with obstructive jaundice, and abdominal imaging studies show pancreatic and biliary ductal dilatation. EUS allows not only more accurate diagnosis and staging of these lesions than CT, but it also permits tissue biopsies and FNA sampling.34 In addition, EUS selects appropriate patients for undergoing local resection instead of pancreaticoduodenectomy (Whipple procedure).
For patients with CD, EUS can accurately assess perianal fistula and abscess. EUS is also useful in monitoring medical and surgical therapy for CD perianal fistulae.24
Two modalities have complementary roles and are not mutually exclusive. The most common indication of WCE is for the evaluation of obscure GI bleeding (unknown bleeding origin after initial EGD and colonoscopy). A cost-analysis study showed that the initial DBE approach is more cost-effective. 42 However, because DBE is potentially associated with serious complications, such as pancreatitis and bowel perforation, the authors advocate using CE-directed DBE approach because this would reduce complications and decreased utilization of endoscopic resources.42
Other indications for WCE include CD, ulcers, polyps, foreign bodies, infiltrative diseases, and imaging abnormalities.6 It should be emphasized that in patients with CD and suspected strictures, WCE is contraindicated.
Acute colonic pseudo-obstruction (ACPO) is characterized by massive colonic dilation in the absence of mechanical obstruction. The symptoms include nausea, vomiting, abdominal pain, constipation, and paradoxically diarrhea. Spontaneous perforation occurs in 3%–15% of patients with a mortality rate of 50% or higher. Endoscopic decompression should be performed if conservative therapy fails or if neostigmine is contraindicated.43
Lower endoscopy can play a pivotal role in the evaluation of patients with chronic diarrhea. Endoscopy with colonic biopsy is helpful in ruling out IBD, ischemic colitis, collagenous and microscopic colitis, and neoplastic disease. When patients with human immunodeficiency virus and chronic diarrhea have negative basic stool test, lower endoscopy with biopsy is indicated to rule out infectious causes. Mucosal biopsies are the ‘gold standard’ to establish graft-versus-host-disease after bone marrow transplantation and to rule out other infections and pathologies. Upper GI evaluation may ensue when lower GI workup for chronic diarrhea is negative.44
Studies indicate that patients with sporadic ampullary adenomas or duodenal adenomas are at greater risk for CRC.23 Screening colonoscopy should be offered to patients with these polyps.
Mucosal biopsy during colonoscopy with ileoscopy is invaluable in the evaluation of IBD and the differentiation of UC from CD. Endoscopy along with other diagnostic modalities can distinguish CD from UC in ≥85% of patients.24 Surveillance colonoscopy every 1–2 years starting 8–10 years after disease onset is recommended for patients with CD and UC. Biopsy specimens are obtained in all four quadrants every 10 cm from the cecum to the rectum. Colectomy should be performed when there is the presence of HGD or multifocal LGD in a flat mucosa. Colonic strictures in patients with UC are considered malignant until proven otherwise. If a stricture is unable to be assessed thoroughly, colectomy is indicated.24 Chronic obstruction due to fibrotic strictures can be managed by endoscopic balloon dilation. For patients with CD undergoing partial colectomy or partial ileocolectomy, recurrence rates range from 70% to 90% after 1 year of surgery.24 Therefore, colonoscopy is recommended at 6–12 months after surgery to identify patients who may benefit from medical therapy.
CRC is the second leading cause of cancer-related deaths in the United States. Therefore, it is important for primary care physicians to understand the role of CRC screening and surveillance. The following recommendations for early detection of CRC and adenomatous polyps in average-risk adults (aged 50 years and older) are based on the most recent published guideline by the ACS.45 For CRC screening and surveillance in high-risk patients (family or personal history of CRC, IBD, or FAP/HNPCC), please refer to the actual guidelines.45 Screening tests are divided into two categories: fecal tests (guaiac fecal occult blood test (gFOBT), fecal immunochemical test (FIT), and stool-based DNA (sDNA)) and structural exams (FS, colonoscopy, double contrast barium enema (DCBE), and computerized topography colonography (CTC)). The appropriate test to be used depends on the individual’s preference and local resources. Patients should understand that positive findings with less invasive tests require follow-up colonoscopy.
Chronic constipation is associated with an increased risk of colon cancer.47 For this reason, patients with constipation who are above 50 years and have not had a colon cancer screening should have a colonoscopy.47 Patients and physicians should be aware that Medicare (health insurance program for the elderly administered by the US government) might not reimburse for colonoscopy if the sole indication is constipation.
Lower GI bleeding (LGIB) may present as occult fecal blood, iron deficiency anemia, melena, intermittent hematochezia, or acute bleeding. Colonoscopy is effective in the diagnosis and treatment of LGIB. If a bleeding source is not identified by colonoscopy, EGD should be performed to rule out upper GI bleeding.48
Patients with distal adenomas have an increased risk of advanced proximal neoplasia. If adenomas are found at FS, colonoscopy should be performed for complete examination of the colon. For surveillance of average-risk patients, either FS alone or FS with annual gFOBT or FIT is recommended every 5 years.45
Because of low malignant risk in younger patients (<50 years) with suspected distal colonic disease, FS should be considered instead of colonoscopy. In patients with IBD, FS is preferred when colonoscopy is considered high risk (fulminant colitis). In addition, when there is an exacerbation in patients with UC, FS is useful in evaluating superimposed infections (cytomegalovirus, Clostridium difficile) or condition (ischemic colitis).24
In the rapidly changing field of endoscopy as well as increasing referrals to OAE centers by nongastroenterologists, primary care practitioners should have an updated understanding of new endoscopic technologies and its indications in order to save resources, to provide optimal care with the least risk, and to facilitate effective communication between different specialties.
The authors report no conflicts of interest in this work.