Sphincter of Oddi Dysfunction

Etiology

The exact etiology of sphincter of Oddi dysfunction is unclear. Conceptualizing this disease process is easier when it is understood that Sphincter of Oddi Dysfunction is a broad term, describing a spectrum of hepatobiliary disorders. These clinical entities result from many types of sphincter dysfunction, including spasms, strictures, or inappropriate relaxation. Moreover, this disease process can involve either biliary or pancreatic sphincters or both.[1] Clinical sequelae are reflective of the comingled nature of these organ systems.

Epidemiology

Sphincter of Oddi dysfunction occurs most frequently in females, generally aged 20 to 50. The prevalence is approximately 1.5%, but this is likely an underestimate due to under testing and a lack of concrete biochemical markers for identification.[1] In persons with recurrent idiopathic pancreatitis and chronic pancreatitis, the prevalence of SOD may be as high as 72% and 59%, respectively.[2] Therefore, SOD should be much higher in the astute provider's differential.

Risks factors for the development of SOD multiple, and include prior cholecystectomy, gallbladder agenesis, cholelithiasis, previous gallstone lithotripsy, liver transplantation, alcohol use disorder, hypothyroidism, and irritable bowel syndrome (IBS).[1][3] And while this list is quite varied, in each setting, an insult to the pancreaticobiliary system that could impact sphincter function or flow of bile is conceivable.

Pathophysiology

The Sphincter of Oddi has three main functions: regulation of bile flow into the duodenum, prevention of reflux into the bile or pancreatic duct, and promotion of gallbladder filling in between digestive cycles (see Image. Sphincter of Oddi, Anatomy). The basal pressure of the sphincter is 10 mmHg with an intermittent phasic increase in tone 2 to 6 times per min of 50 to 140 mmHg. Cholecystokinin (CCK) has been demonstrated to relax basal tone and inhibit phasic contractions. Cholecystokinin is released from enteroendocrine cells in response to a meal, exerting direct hormonal effects on the sphincter. Other gastrointestinal peptides have varying influence on the sphincter; these include gastrin, secretin, motilin, and octreotide. Additionally, there is extrinsic control of the sphincter via parasympathetic innervation. This vagal innervation is mostly excitatory.

As referenced above, sphincter of Oddi dysfunction commonly presents with recurrent biliary colic type abdominal complaints. Both stenosis and/or dyskinesia of the sphincter can result in the hallmark constellation of symptoms seen in this disease. It is theorized that trauma from stone passage can result in sphincter stenosis. While congenital syndromes and motility disorders may serve as the nidus for dyskinetic sphincter function, all of these can result in a pathologic process that falls under the umbrella of SOD.

History and Physical

Most patients presenting with SOD will complain of biliary type pain. Their discomfort is mostly located in the epigastrium and right upper quadrant, with radiation to the back and shoulder. It usually lasts around 30 minutes to several hours before resolving spontaneously.[1] This pain can be accompanied by nausea and vomiting. In contrast to biliary colic, symptoms are generally not post-prandial in nature, unless the primary source of their sphincter dysfunction relates to the pancreatic ductal component of the sphincter. Recurrent or chronic pancreatitis may also signify underlying sphincter dysfunction.

Evaluation

Given the overlap of sphincter of Oddi dysfunction symptoms with other biliary pathology, most patients will undergo abdominal imaging (US, CT, HIDA scan, etc.). However, in the algorithm for SOD, these studies are generally low-yield. But they can be beneficial in ruling out other more sinister pathology prior to focusing on SOD as the cause of the patient's complaints. Endoscopic retrograde cholangiopancreatography (ERCP) with manometry is considered the gold standard test for sphincter of Oddi dysfunction.[4] Basal sphincter pressures of more than 35 to 40 mmHg on manometry are consistent with the diagnosis of SOD.[1] Importantly, however, even this modality may overlook patients with clinically apparent SOD. For types, I, II, and III, the frequency of abnormal sphincter of Oddi manometry were (shown to be) 85.7%, 55.1%, and 28.1%, respectively.[5] Thus, for even the most clinically sound patient presentations (type I), some 15% of people failed to demonstrate the expected manometry, suggesting that isolated sphincter pressure measurements may not fully assess a disease process whose symptoms are more intermittent in nature. Thus, although ERCP with manometry is the gold standard, it is only a single component of the diagnostic workup, which should be considered alongside other measures.

Laboratory evaluation should also be performed, specifically, a comprehensive metabolic panel (CMP), amylase, and lipase, to evaluate for hepato-pancreatic dysfunction. Functional examinations, such as the Nardi test, can also help confirm the diagnosis. The Nardi test involves the simultaneous administration of morphine and neostigmine. The former causes biliary contraction, and the latter contracts the Sphincter of Oddi. The forward pulsion of bile into a contracted sphincter should reproduce the patient's symptoms if sphincter of Oddi dysfunction is the source of their symptoms.[1]

The patient's presentation, in combination with the results of their examination, should be used to stratify them to into three classes of sphincter of Oddi dysfunction. Specific diagnostic criteria for SOD include:

• Transaminitis (greater 2 times the upper limit of normal on 2 or more occasions
• Common bile duct dilation (greater than 10 mm on US; greater than 12 mm on ERCP)
• Biliary pain

Utilizing these criteria, patients are classified as follows:

• Type I SOD: all three
• Type II SOD: biliary pain and one of the other two criteria.
• Type II SOD: biliary pain only[3]

The results of this classification will impact the subsequent treatment plan.

Treatment / Management

The treatment of sphincter of Oddi dysfunction is aimed at reducing the basal pressure and resistance of the valve.[1] Noninvasive options include calcium channel blockers, tricyclic antidepressants, glyceryl trinitrate, and somatostatin, each with varying levels of success. For example, in a randomized controlled trial, nifedipine was shown to decrease cumulative pain scores and the number of symptom episodes, number of emergency department visits, and pain medication consumption compared to placebo.[6] However, combinations of the aforementioned therapies show even greater levels of symptom reduction. One study utilizing a combination of nifedipine, tricyclic antidepressants, and glyceryl trinitrate, showed that 15.3% and 59.3% of patients reported complete symptom resolution or improvement in symptoms, respectively.[7](A1)

Invasive interventions for the treatment of SOD include ERCP with sphincterotomy. This modality has been shown to be highly effective and generally safe for patients with SOD, with reports of 90% and 70% resolution of symptoms in types I and II SOD, respectively.[1] Intrasphincteric botulinum toxin injections have been shown to reduce sphincter tone by approximately 50%, but unfortunately, did not resolve patient symptoms in a small case series.[8] However, botulinum toxin and stent placement both have been suggested as possible interim steps to clarify whether or not sphincter relaxation/stenting resolves symptoms, thereby providing a means to predict patient response to a more definitive sphincterotomy. (B3)

Patients with type I and type II sphincter of Oddi dysfunction should be referred for management with ERCP and sphincterotomy. Type III SOD has been shown in a trial not to respond to procedural intervention.[9] These patients should instead be referred for medical management, including pain control, as discussed above.(A1)

Differential Diagnosis

As stated previously, sphincter of Oddi dysfunction is generally regarded as a diagnosis of exclusion. The differential for epigastric and/or right upper quadrant pain is wide. It is, therefore, important that appropriate testing is performed to rule out other disease processes prior to formally diagnosing and treating sphincter of Oddi dysfunction. The spectrum of obstructive biliary pathologies, including choledocholithiasis and malignant conditions such as cholangiocarcinoma, should receive specific attention. These must especially be considered if bile duct dilation and elevated transaminases are present. 

Prognosis

While this disease process is not inherently dangerous, effective treatment may improve the patient's quality of life. While all-comers with suspected sphincter of Oddi dysfunction may undergo ERCP and possible sphincterotomy, this is not necessarily warranted. Those that see the greatest improvement in symptoms are types I and II, particularly with abnormal sphincter manometry. However, even in these patients, symptoms generally do not resolve entirely, suggesting a multifactorial cause for pain.[10] Predictions regarding responsiveness to intervention can be derived from the Milwaukee classification of SOD. Here, patient presentation, laboratory data, and imaging findings stratify patients to SOD types 1, 2, and 3, with clinically predictable responses to sphincterotomy available in this framework.[1]

Complications

Complications to the management of sphincter of Oddi dysfunction generally related to those seen with ERCP and other endoscopy evaluations. Perforation, anesthetic morbidities, and post-ERCP pancreatitis are inherent risks.