Elsevier

Disease-a-Month

Volume 65, Issue 12, December 2019, 100851
Disease-a-Month

A comprehensive review and update on ulcerative colitis,,✰✰

https://doi.org/10.1016/j.disamonth.2019.02.004Get rights and content

Abstract

Ulcerative colitis (UC) is a chronic idiopathic inflammatory bowel disorder of the colon that causes continuous mucosal inflammation extending from the rectum to the more proximal colon, with variable extents. UC is characterized by a relapsing and remitting course. UC was first described by Samuel Wilks in 1859 and it is more common than Crohn's disease worldwide. The overall incidence and prevalence of UC is reported to be 1.2–20.3 and 7.6–245 cases per 100,000 persons/year respectively. UC has a bimodal age distribution with an incidence peak in the 2nd or 3rd decades and followed by second peak between 50 and 80 years of age. The key risk factors for UC include genetics, environmental factors, autoimmunity and gut microbiota. The classic presentation of UC include bloody diarrhea with or without mucus, rectal urgency, tenesmus, and variable degrees of abdominal pain that is often relieved by defecation. UC is diagnosed based on the combination of clinical presentation, endoscopic findings, histology, and the absence of alternative diagnoses. In addition to confirming the diagnosis of UC, it is also important to define the extent and severity of inflammation, which aids in the selection of appropriate treatment and for predicting the patient's prognosis. Ileocolonoscopy with biopsy is the only way to make a definitive diagnosis of UC. A pathognomonic finding of UC is the presence of continuous colonic inflammation characterized by erythema, loss of normal vascular pattern, granularity, erosions, friability, bleeding, and ulcerations, with distinct demarcation between inflamed and non-inflamed bowel. Histopathology is the definitive tool in diagnosing UC, assessing the disease severity and identifying intraepithelial neoplasia (dysplasia) or cancer. The classical histological changes in UC include decreased crypt density, crypt architectural distortion, irregular mucosal surface and heavy diffuse transmucosal inflammation, in the absence of genuine granulomas. Abdominal computed tomographic (CT) scanning is the preferred initial radiographic imaging study in UC patients with acute abdominal symptoms. The hallmark CT finding of UC is mural thickening with a mean wall thickness of 8 mm, as opposed to a 2–3 mm mean wall thickness of the normal colon. The Mayo scoring system is a commonly used index to assess disease severity and monitor patients during therapy. The goals of treatment in UC are three fold—improve quality of life, achieve steroid free remission and minimize the risk of cancer. The choice of treatment depends on disease extent, severity and the course of the disease. For proctitis, topical 5-aminosalicylic acid (5-ASA) drugs are used as the first line agents. UC patients with more extensive or severe disease should be treated with a combination of oral and topical 5-ASA drugs +/− corticosteroids to induce remission. Patients with severe UC need to be hospitalized for treatment. The options in these patients include intravenous steroids and if refractory, calcineurin inhibitors (cyclosporine, tacrolimus) or tumor necrosis factor-α antibodies (infliximab) are utilized. Once remission is induced, patients are then continued on appropriate medications to maintain remission. Indications for emergency surgery include refractory toxic megacolon, colonic perforation, or severe colorectal bleeding.

Introduction

Ulcerative colitis (UC) is a chronic idiopathic inflammatory bowel disease (IBD) of the colon that causes a superficial mucosal inflammation in a continuous fashion extending from the rectum to the more proximal colon, in varying extents.1 UC is characterized by a relapsing and remitting course.1 The hallmark symptoms of UC include bloody diarrhea with rectal urgency and tenesmus. Although the etiology of UC remains a subject of debate, increasing evidence suggests the presence of an underlying autoimmune component.2, 3 Many UC patients experience extraintestinal manifestations (EIM) that involve multiple organs sharing features with other autoimmune disorders. The annual direct and indirect cost related to UC is estimated to be as high as $8.1–14.9 billion in the United States of America (USA).4 Here, we review the current literature on the pathophysiology, diagnosis, and treatment of UC.

Section snippets

Epidemiology and risk factors

UC was first described by Samuel Wilks in 1859. Worldwide, UC is more common than Crohn's disease (CD).5 UC is most common in industrialized countries and the incidence has been rising in Asia.6, 7 A prospective study from the United Kingdom (UK) showed that second generation South Asian immigrants to the UK had a higher incidence of UC when compared with the European population (17.2 vs. 7 per 100,000 population/year).8,9 The overall incidence and prevalence of UC is reported to be 1.2 - 20.3

Clinical features and extra intestinal manifestations (EIM)

The classic presentation of UC includes symptoms of bloody diarrhea with or without mucus, rectal urgency, tenesmus, and variable degrees of abdominal pain that is often relieved by defecation.10 Perhaps underappreciated, a minority of patients may present with constipation.10, 41 Ford et al. reported that a combination of anemia, weight loss of more than 5 kg in the past year, and having more than 4 bowel movements daily, had a positive likelihood ratio (LR) of 14.6 for diagnosis of UC; while

Natural course

UC is a chronic disease with variable rates of relapse and remission. Multiple factors that play a role in its etiology could be responsible for a unique profile of the disease. The disease manifests by waxing and waning symptoms, with random episodes of varying severity. At the time of presentation, approximately 40% of patients present with proctitis, 30% present with left-sided colitis, and 30% with pancolitis. Disease progression most often follows a gradual course with only 14%–16% of

Diagnosis of ulcerative colitis

UC is diagnosed based on a combination of clinical presentation, endoscopic findings, histology, and the exclusion of alternative diagnoses (Table 2). In addition to confirming and accurately diagnosing UC, it is also important to define the extent and severity of inflammation, which guides the selection of appropriate treatments and for predicting the patient's prognosis.

Medical management

The goals of treatment in UC focus on improving quality of life, achieving steroid free remission and minimizing the risk of cancer. During the initial endoscopic assessment, it is important to delineate the proximal margin of inflammation. If the inflammation is limited to below the splenic flexure, it is considered to be "distal" and hence within the reach of topical therapy. If the inflammation extends proximal to the splenic flexure, then systemic therapy is warranted. The histologic

Surgery

Advances in medical therapy have allowed UC to be treated more effectively and thereby decreased the surgical rates. However, 10% of UC patients will require surgery within the first year of diagnosis and up to 30% will require surgical intervention in their lifetime.221 The most commonly performed surgery for UC is restorative proctocolectomy with ileal pouch-anal anastomosis (IPAA).221 Most studies have reported improvement in health-related quality of life (QOL) in patients with severe UC

Post-operative management of UC

Surgical management of UC through TPC with IPAA is curative but is associated with short-term (≤30 days) and long-term (>30 days) complications that require monitoring and management.263 Short-term complications include bleeding, pouch leakage, pelvic abscess, anastomotic stricture, and small bowel obstruction.236 Common long-term complications include pouchitis, cuffitis, anastomotic ulcer, pouch fistula, fecal incontinence, irritable pouch syndrome, sexual dysfunction, and CD of the pouch.236

Conclusion

In summary, it is difficult to predict the prognosis of patients with UC. It is necessary to individualize each patients’ assessment and treatment plan in order to produce the best health outcomes. Not one approach is a perfect fit for every patient and one patient may require multiple treatment modalities to achieve remission. It is also essential to be able to identify higher risk patients, as their treatment approach may require more frequent and aggressive interventions.

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    Author Contributions: Mahesh Gajendran is the article guarantor.

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    Financial disclosure: None to report.

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