Share Facebook
Crohn's Disease Forum » Books, Multimedia, Research & News » Review Article: The Optimal Medical Management of Acute Severe UC


11-16-2010, 06:45 PM   #1
David in Seattle
Senior Member
 
David in Seattle's Avatar
 
Join Date: Feb 2010
Review Article: The Optimal Medical Management of Acute Severe UC

A. L. Hart; S. C. Ng

Alimentary Pharmacology & Therapeutics. 2010;32(5):615-627. © 2010 Blackwell Publishing

Abstract and Introduction
Abstract

Background Management of acute severe ulcerative colitis (UC) is a clinical challenge, with a mortality rate of approximately 1–2%. The traditional management with intravenous corticosteroids has been modified by introduction of ciclosporin and more recently, infliximab.
Aim To provide a detailed and comprehensive review of the medical management of acute severe UC.
Methods PubMed and recent conference abstracts were searched for articles relating to treatment of acute severe UC.
Results Two-thirds of patients respond to intravenous steroids in the short term. In those who fail steroids, low-dose intravenous ciclosporin at 2 mg/kg/day is effective. Approximately 75% and 50% of patients treated with ciclosporin avoid colectomy in the short and long-terms, respectively. Long-term outcome of ciclosporin therapy is improved by introduction of azathioprine on discharge from hospital, together with oral ciclosporin as a bridging therapy. Controlled data show that infliximab is effective as rescue therapy for acute severe UC and the effect appears to be durable, although longer-term follow-up data are needed.
Conclusions Both ciclosporin and infliximab have demonstrated efficacy as rescue medical therapies in patients with acute severe UC, but surgery needs to be considered if there is failure to improve or clinical deterioration.
Introduction

Acute severe ulcerative colitis (UC) will affect 15% of UC patients at some point in their disease course.1 Twenty per cent of first attacks of UC are 'acute severe' in nature.[1] Acute severe UC has been defined by the Truelove and Witt's[2] criteria: the patient passing more than 6 bloody stools/day plus one or more of the following: temperature >37.8 °C; pulse >90 bpm; Hb <10.5 g/dL or erythrocyte sedimentation ratio (ESR) >30 mm/h. In this review, we will focus on the management of patients classified as having acute severe UC by the Truelove and Witt's criteria and who are hospitalized.

The goal of medical therapy is to avoid colectomy while preventing complications of disease, side effects of medications and mortality. Corticosteroids, ciclosporin and infliximab have been used in the setting of acute UC. In addition to these medical therapies, optimization of the overall supportive care of patients with acute severe UC is essential. This includes intravenous fluid replacement with potassium supplementation, careful exclusion of enteric infection by stool cultures and Clostridium difficile toxin testing, and an unprepared flexible sigmoidoscopy (and biopsy) with minimal air insufflation in patients not responding or those slow to respond to medical therapy to assess mucosal severity of inflammation and to exclude cytomegalovirus infection. Patients presenting with acute UC with co-existing C. difficile infection have an increased colectomy rate and worse long-term clinical outcome[3] and should be treated with metronidazole or vancomycin.[4] The presence of cytomegalovirus inclusion bodies on colonic biopsies should prompt treatment with ganciclovir, particularly in patients slow to respond to conventional therapy. Malnourished patients should be considered for calorie supplementation and should be weighed and reviewed by a dietician. In addition, prophylactic subcutaneous heparin to reduce the risk of thromboembolism, and blood transfusions to maintain the Hb >10 g/dL are crucial.[5, 6] Any medication which may precipitate toxic dilatation in the colon including opioids, nonsteroidal anti-inflammatory drugs and anti-cholinergics should be stopped. Topical therapy (mesalazine or corticosteroids) is effective if tolerated, although there are no systematic studies in acute severe UC.[7] Careful daily monitoring of the patient with clinical assessment (bowel frequency and presence of blood, abdominal pain, temperature, pulse, abdominal tenderness), biochemical assessment (blood count, inflammatory markers, biochemistry) and radiological monitoring (abdominal radiography with the frequency determined by the clinical status and response of the patient) with integration of input from the physician and surgeon is imperative for optimal outcome.

Corticosteroids

The mainstay of therapy for acute severe UC is corticosteroids. In 1955, Truelove and Witt published a 'final report on a therapeutic trial' of cortisone in UC. A total of 213 patients were randomized to receive cortisone 100 mg each day or placebo for 6 weeks. The cortisone-treated patients did better than the corresponding control patients with cortisone being particularly beneficial in those with a first attack of disease. Furthermore, in 120 patients who had a sigmoidosopic examination at the end of treatment in addition to pre-treatment, normal or improved sigmoidoscopic appearances were more frequent in the cortisone group than in the control group.[8] Subsequently, in 1974, Truelove and Jewell published the results of a trial using an intensive intravenous regimen for severe attacks of UC. Forty-nine patients were treated with intensive intravenous corticosteroids and 36 of 49 (73%) were in complete remission at day 5.[7] A recent systematic review of 32 trials consisting of over 2000 patients treated with steroids for acute severe UC between 1974 and 2006 showed that the overall response rate to steroids was 67%. Approximately one-third of patients came to a colectomy in the short term.[9] The introduction of steroids for the management of acute severe UC has dramatically reduced mortality figures from more than 50% to 1–2%.[8] Mortality from acute severe UC in the first year from a study in Birmingham in 1933 and a study from Oxford in 1950 was 75% and 22% respectively. However, after the introduction of steroids in 1955, the mortality rate from acute severe UC had fallen to 7%. The current overall mortality in specialist centres is <1%.[10]

Acute severe UC is associated with both early postcolectomy inpatient mortality and long-term mortality postcolectomy. The UK inflammatory bowel disease (IBD) audit of more than 6000 adult patients admitted to UK hospitals between 2007 and 2008 with IBD (863 patients had acute severe UC), and a national study from Canada reported early postcolectomy mortalities of 2.9% and 2.3% respectively.[11, 12] In the UK IBD audit, the reported inpatient mortality of 1.2% was strongly associated with increased age, male gender and the presence of C. difficile infection.[13] Kaplan et al. [14] showed that short-term mortality after surgery for UC was higher in those who had emergency than in those who underwent elective surgery. Both advanced age and low volume of surgery at a given centre contributed towards increased mortality.[15, 16]

In a record linkage study from England, which included more than 20 000 patients admitted to hospital for more than 3 days for IBD, mortality rates for patients admitted with UC 3 years after elective colectomy (3.7%) appeared to be significantly lower than for those who had an emergency colectomy (13.2%) or no colectomy (13.6%).[17] Mortality was highest in the first 12 months after admission. It was suggested that the threshold for elective colectomy for UC in England may be too high. Using a national record linkage database from 1998 to 2000, Nicholls et al. [18] recently demonstrated that in patients with UC requiring hospital admission, the overall 3-year mortality rate is lowest in patients who had an elective colectomy (5.6%) and highest in those who did not have surgery (9.8%). Age >50 years at admission, male gender, co-morbidity, hospital stay beyond 2 weeks and prior hospital admission for IBD were independently associated with mortality.[18]

The timing of surgery is critical and should not be delayed for more than 5 days if the patient is not responding to medical therapy. Kaplan et al. [14] showed that in patients admitted urgently for a UC flare, those whose surgery is performed more than 6 days after admission, had an odds ratio (OR) of in-hospital mortality of two compared with those who had earlier surgery. A multidisciplinary approach involving the gastroenterologist, surgeon, dietician, stomatherapist to educate patients on the options of rescue therapy and surgery is of paramount importance.

Last edited by David in Seattle; 11-16-2010 at 06:57 PM.
11-16-2010, 06:46 PM   #2
David in Seattle
Senior Member
 
David in Seattle's Avatar
 
Join Date: Feb 2010
Predictors of Response to Steroids

In clinical practice, clinical response is assessed by improvement in symptoms (reduced bowel frequency, reduced urgency, improved stool constituency, reduced abdominal pain, reduced rectal bleeding, improved general well being, increased energy, reduced lethargy) and improvement in blood test parameters [reduced C- reactive protein (CRP), ESR and platelet count, improved albumin and haemoglobin].

Clinical response to steroids can be assessed on day 3. In a prospective study by Travis et al. [19] on 51 episodes of severe UC, more than 8 stools/day or 3–8 stools/day plus a CRP >45 mg/L predicted a colectomy rate of 85%. In 1998, Lindgren et al. [20] performed a prospective study on 97 episodes of severe UC and devised the following mathematical model to predict colectomy: number of stools/day + 0.14 Χ CRP (mg/L) ≥ 8 predicted a colectomy rate of 72%. In a retrospective study by Ho et al. in 2004 on 167 episodes of severe UC, the number of stools/day (score 1–4); hypoalbuminaemia <30 g/L (score 1) and colonic dilatation >5.5 cm (score 4) were useful in predicting a colectomy or the need for second line intervention. Eight-five per cent of patients with a score greater than or equal to four required a colectomy or second line intervention.[21]

These studies highlight the importance of a time-bound approach in the management of patients with acute severe UC. Indeed, in a group of 80 patients undergoing emergency colectomy for severe UC treated between 1994 and 2000 in Oxford, patients who had a significantly longer duration of preoperative medical therapy were more likely to have major post-operative complications. If medical therapy was continued for 8 days or more, a higher complication rate was noted if surgery ensued.[22]

We suggest that at day 3, careful assessment is made of the response of the patient in terms of stool frequency, inflammatory markers and radiological assessment (Figure 1). In cases of clear nonresponse, the decision should be made to consider other medical or surgical options. If there is a degree of response in the parameters mentioned, a balanced judgement needs to be taken regarding continuing with current therapy for a further time-bound period. We suggest that if a patient's clinical condition does not improve after 5–7 days of IV steroid treatment, consideration should be made for other medical options or surgery. Recently, Ananthakrishnan et al. [23] showed that anaemia, the requirement for blood transfusion, malnutrition and total parenteral nutrition were independent predictors of colectomy and a simple risk score has been proposed to stratify the severity of UC hospitalizations which helped to predict colectomy. Preliminary data suggested that faecal calprotectin may be a potential non-invasive biomarker to predict response to corticosteroids and colectomy. In 90 patients with acute severe UC treated with corticosteroids, faecal calprotectin was significantly higher in patients requiring colectomy with a trend towards significance when comparing corticosteroid responders and nonresponders.[24] In daily clinical practice, we propose using simple clinical and biochemical parameters including stool frequency, CRP, serum albumin levels and abdominal radiograph as predictive factors in assessing response to medical therapy. The use of a simple index in clinical practice may help quantify the risk of colectomy and aid decision making.

Figure 1.

Proposed algorithm for the treatment of patients with acute severe ulcerative colitis. No response: defined as > 8 stools daily or 3–8 stools with a CRP> 45mg/L.

fig 1.jpg

Last edited by David in Seattle; 11-16-2010 at 06:52 PM.
11-16-2010, 06:48 PM   #3
David in Seattle
Senior Member
 
David in Seattle's Avatar
 
Join Date: Feb 2010
Ciclosporin
Short-term Efficacy

Approximately one-third of patients with acute severe UC will fail to respond to corticosteroids. Several medical options exist for these patients. One option is ciclosporin, the fungal metabolite originally derived from a Norwegian soil sample. Two controlled trials have assessed the efficacy of ciclosporin in the setting of severe UC. In 1994, Lichtiger et al. performed a randomized placebo-controlled trial of intravenous ciclosporin at a dose of 4 mg/kg/day administered over a mean of 7 days. The study was stopped early for ethical reasons because of the marked favourable response to ciclosporin. Nine of 11 and zero of nine patients treated with ciclosporin and placebo respectively had a response. When five patients who had placebo were crossed over to ciclosporin, all five patients responded.[25] A subsequent European controlled trial compared intravenous ciclosporin (4 mg/kg) with intravenous steroids. Nine of 14 (64%) ciclosporin-treated patients and eight of 15 (53%) corticosteroid-treated patients responded.[85] Ciclosporin was used as monotherapy and not as an adjunct to corticosteroid therapy. This trial highlights the efficacy of ciclosporin monotherapy in severe attacks of UC and it can be considered as an option for patients who wish/need to avoid steroids or who have failed oral steroid therapy. The largest ciclosporin trial to date of 73 patients by Van Assche et al. [26] in 2003 was a head-to-head comparison study of ciclosporin 4 vs. 2 mg/kg. Response rate at day 8 was not different in the 'high-dose' group (84%) vs. the 'low-dose' group (86%). Several other uncontrolled trials have also assessed the initial response of UC to intravenous ciclosporin[27–33, 43, 44, 86] and these are detailed in Table 1. Overall, the short-term response to ciclosporin is in the range of 64–86%.

tbl 1.jpg

Side-effect Profile

One of the major issues pertaining to the use of ciclosporin relates to its side effect profile. As ciclosporin is generally used as a bridge to azathioprine in the setting of acute severe UC, the short-term side effects represent the main issue and include hypertension, tremor, nausea/vomiting, renal insufficiency, headaches, anaphylaxis, infection, paraesthesia and seizures.[34] There is a mortality rate associated with ciclosporin in IBD (approximately 1.8%),[34] although some centres have reported higher mortality rates of up to 3.5%. Side effects of ciclosporin can be limited in a number of ways. One such way is by using a reduced dose. Actis et al. [35] in 1993 treated eight patients with severe steroid resistant UC with 2 mg/kg a day of intravenous ciclosporin. Seven patients responded and two patients had reversible renal insufficiency. In a separate cohort of patients treated at St Mark's Hospital, 31 patients with acute severe steroid resistant UC were given 2 mg/kg a day of intravenous ciclosporin followed by the early introduction of azathioprine. Of these patients, 77% responded and no deaths, major infective episodes or seizures were reported.[28] In the trial by Van Assche et al. comparing 2 mg/kg with 4 mg/kg ciclosporin, although no seizures, infections or deaths were reported, there was a trend towards increased hypertension in the 4 mg/kg dose group.

The neurotoxicity and seizure risk associated with ciclosporin can be limited by monitoring and ensuring normal levels of magnesium and cholesterol or alternatively, the use of oral ciclosporin. Data from the transplant literature have shown an increased seizure risk with low total cholesterol. In liver transplant patients treated with ciclosporin, toxicity occurred with a cholesterol concentration below 3.1 mmol per litre.[36, 37] It has been suggested that lower cholesterol levels increased ciclosporin bound to low-density lipoprotein particles and that this may result in increased delivery of ciclosporin to astrocytes, which have low-density lipoprotein receptors.[38] Hypomagnesaemia increases the risk of seizures in patients treated with ciclosporin; therefore, correcting deficiencies can limit neurotoxicity. Oral ciclosporin is also effective in the treatment of acute severe colitis[33] and there is also some evidence that oral formulations of ciclosporin may limit neurotoxicity.[39] In a retrospective study of patients with severe UC, 54 patients were treated with intravenous ciclosporin and 22 patients with oral ciclosporin. Oral ciclosporin (used as rescue therapy) was superior to intravenous ciclosporin with regard to the time to first relapse and time to surgery at a median follow-up of 2.9 years (range: 0.2–7 years).[33] Once ciclosporin has been started, drug levels should be monitored on days 2–3 and dosage should be adjusted to the levels of 150–300 ng/mL.[28, 33] Random levels can be measured during intravenous infusion, and trough levels for oral formulations.

Limiting infective complications associated with intravenous ciclosporin can be achieved by minimizing concomitant immunosuppressant use and using prophylactic antibiotics. The risk of infection is greater with triple and double immunosuppressive therapy than with single therapy. In a case–control study, the relative risk of opportunistic infections is the highest in those who are on two or three immunosuppressive agents (OR 14.5) compared with those on any one of steroids, azathioprine or infliximab (OR 2.9).[40] In clinical practice, rapid weaning of steroids as appropriate is one means of limiting the risk of infections. Prophylaxis with Cotrimoxazole for patients on triple immunomodulators is advised. In patients on two immunomodulators, one of which is a calcineurin inhibitor or an anti-tumour necrosis factor (TNF) agent, the European Crohn's and Colitis Organisation consensus could not reach a verdict on the use of prophylactic Cotrimoxazole.[41]
Long-term Efficacy

The long-term benefit of ciclosporin is an important issue. In a cohort of 42 patients with severe UC treated with intravenous ciclosporin and followed up long term, the probability of avoiding colectomy was 67% within 1 year and 58% at 5.5 years. If only the patients who initially responded to ciclosporin were included in the analysis, the probability of avoiding colectomy was 80% at 1 year and 70% at 5.5 years.[31] In a separate cohort of 31 patients with acute UC treated with intravenous ciclosporin, 45% of patients did not require a colectomy over a median of 17.5 months.[28] In a retrospective long-term follow-up study from Oxford of 76 patients with acute UC treated with ciclosporin, 42% of patients had avoided colectomy after 7 years.[33] A recent study from the same unit in Oxford showed that incomplete responders to ciclosporin within 1 week after admission with acute severe UC had a 50% chance of colectomy within a year and 70% within 5 years.[42]

Investigators from Leuven showed that of all treated patients, 55% would avoid colectomy during a period of 3 years using prediction from life table analysis.[43] When this cohort of patients was followed up long term, the probability of avoiding colectomy after successful intravenous ciclosporin therapy was 63% at 1 year, 41% at 4 years, 16% at 6 years and 12% at 7 years.[44] Overall, there is a long-term benefit in preventing colectomy when ciclosporin is used in a subgroup of patients. The likelihood of avoiding colectomy over 2–3 years is approximately 50%.
11-16-2010, 06:49 PM   #4
David in Seattle
Senior Member
 
David in Seattle's Avatar
 
Join Date: Feb 2010
Influence of Immunomodulators on Long-term Efficacy

What is the influence of concurrent immunomodulator therapy on the long-term outcome of patients with acute severe colitis treated with intravenous ciclosporin? Data from the trial by Cohen et al. [31] in 1999 showed that the probability of avoiding colectomy was 66% at long-term follow-up (5.5 years) in patients receiving ciclosporin and azathioprine/mercaptopurine (MP) compared with 40% in those who received ciclosporin alone, suggesting that azathioprine improves the long-term efficacy of ciclosporin. In patients who had an initial response to ciclosporin, this rate increased to 71% in those who were treated with azathioprine/MP, vs. 55% in those who received ciclosporin alone. The timing of azathioprine/MP in the ciclosporin responders was such that 28% had started azathioprine/MP a mean of 15 months before starting ciclosporin; 32% started azathioprine/MP 'during' ciclosporin therapy; 8% started azathioprine/MP simultaneously with stopping ciclosporin and the remaining started azathioprine/MP a mean of 8 months after stopping ciclosporin.

Further studies have suggested that in patients who were already on immunomodulators at the time of admission with acute severe UC, the likelihood of needing a colectomy following treatment with ciclosporin is high. Moskowitz et al. showed that 77% of patients who were taking azathioprine at the time of admission with acute severe colitis required a colectomy compared with 35% of patients who were started on azathioprine during the same admission as their intravenous ciclosporin; 88% of patients already on azathioprine and requiring colectomy underwent surgery within the first year of receiving ciclosporin.[44]

Overall, it is beneficial in patients with acute severe UC naive to thiopurine to be started on thiopurine during the acute admission when treated with intravenous ciclosporin to optimize long-term outcome and avoid colectomy. If a patient presenting with acute severe UC is already taking a thiopurine at the time of admission, the outcome with ciclosporin is less favourable and other medical options or early surgery needs to be considered.[45]
Predictive Factors of Response to Ciclosporin

In addition to determining predictive factors for response or nonresponse to corticosteroids, several studies have assessed predictive factors for response to ciclosporin. In one study, two clinical parameters (body temperature >37.5 and pulse rate >90 bpm) and one biochemical marker (CRP level >45) predicted colectomy. Rates of colectomy at 6 months were 0.22, 0.47, 0.55 and 0.90 when 0, 1, 2 and 3 of these factors were present respectively.[46] Cautious sigmoidoscopy within a few days of starting ciclosporin can be helpful. Severe endoscopic lesions (deep ulcers or large mucosal abrasion or weld-like ulcers or mucosal detachment) were independent predictors of colectomy. The rate of colectomy at 6 months in patients with severe endoscopic lesions was 73% vs. 42% in patients without them. Colonoscopy was particularly helpful in patients with intermediate clinical and biological severity of their disease such that colonoscopy changed the therapeutic decision in patients with one or two of the criteria mentioned above: 71% of the patients with severe endoscopic lesions had a colectomy vs. 17% of the patients without severe endoscopic lesions.[46] Rowe et al. [47] showed that low serum albumin, tachycardia and neutrophils were predictors of poor response to ciclosporin. Taken together, the monitoring of ciclosporin using clinical, biological and endoscopic criteria is crucial to help predict response to the drug. This is necessary to help a timely move to the next therapy and minimize procrastination.

In summary, ciclosporin is effective in the treatment of acute severe UC in the short term. In the longer term, ciclosporin can prevent colectomy in a subgroup of patients. Careful patient selection is critical to identify those most likely to benefit in the short term and long term; patients who are naοve to thiopurines and those who show good early response with clinical, biological and endoscopic parameters are most likely to do well. The side effect profile of ciclosporin needs to be taken into consideration in each individual patient and its safety optimized by careful monitoring.

Infliximab

Infliximab is a chimeric monoclonal antibody to human TNF-α which is known to play an important role in the inflammation process of UC. Increased levels of TNF-α have been found in faeces from patients with active UC.[48]

In an open label study, six patients with severe steroid refractory UC were treated with a single infusion of infliximab 5 mg/kg. All patients experienced marked clinical improvement at the end of 7 days and colonoscopy confirmed significant healing of endoscopic lesions. Four of the six patients experienced long-term remission at median follow-up of 5.5 months.[49] Sands et al. reported the results of a placebo-controlled trial of infliximab in patients with severe steroid refractory UC, which was terminated early due to slow enrolment. Of the patients treated with infliximab, four of eight (50%) were treatment successes at 2 weeks compared with zero of three patients treated with placebo.[50] A further randomized controlled trial was performed in 13 hospitalized patients with acute UC randomized to three infusions of 5 mg/kg of infliximab or high dose corticosteroids. Five of six patients on infliximab and six of seven patients on high dose corticosteroids were better.[51]

The largest randomized placebo-controlled trial to date of infliximab in acute severe UC was reported in 2004 by Jarnerot et al. Forty-five patients with moderately severe UC were given a single infusion of 5 mg/kg infliximab 4 days after initiation of steroids. Significantly more patients who had placebo (67%) required surgery than those who had infliximab (29%) within 90 days of randomization.[52] The greatest benefit of infliximab was seen in patients who had severe or moderately severe, but not fulminant UC. Lees et al. [53] reported experience of 39 patients hospitalized for acute severe UC treated with infliximab. They found that 66% responded and avoided colectomy during the acute admission and higher early responses were reported by Kohn et al. [54]with 85% of hospitalized patients with acute severe UC avoiding colectomy initially. Table 2 summarized clinical studies of infliximab in acute UC.

tbl 2.jpg

Last edited by David in Seattle; 11-16-2010 at 06:51 PM.
11-16-2010, 06:50 PM   #5
David in Seattle
Senior Member
 
David in Seattle's Avatar
 
Join Date: Feb 2010
Influence of Immunosuppression

Does treatment with Azathioprine influence the outcome of patients with acute severe UC treated with infliximab? Some studies suggest that whether the patient was on existing azathioprine or not at the time of admission with acute severe UC did not affect the outcome.[52] If patients were on azathioprine at the initiation of infliximab, 80% avoided a colectomy at 90 days. This is in contrast with the data using ciclosporin, where the chance of a colectomy in patients who were already on azathioprine and needed ciclosporin was high. However, other studies suggest that infliximab is less efficacious as rescue therapy if patients are on immunosuppression at the time of admission. In a Scottish cohort of 39 patients with acute severe colitis treated with infliximab, although previous treatment with azathioprine/MP did not affect urgent colectomy rates, two additional colectomies were performed at longer follow-up in patients who had had prior exposure to azathioprine.[53]
Screening for Opportunistic Infections

A complete history of risk factors for infection and an immunization history need to be obtained prior to infliximab (and immunomodulators). Recommended screening tests include a full blood count, hepatitis B virus serology, varizella zoster virus serology (in the absence of a history of chickenpox), HIV serology, a chest radiograph and tuberculin skin test or interferon γ release assay according to local or national practice guidelines.[41, 55, 56]
Side Effect Profile

The periodic safety update report (2008) showed that the benefit–risk profile of infliximab is well defined and positive. There are over 15 years of clinical trial experience and over 10 years of postmarketing experience in which 1 700 682 infliximab-treated patients have been assessed. There are two registries in Crohn's Disease, The Crohn's Disease Therapy, Resource, Evaluation and Assessment Tool (TREAT) and European National Crohn's Observational Registry (ENCORE) with a total of approximately 10 000 patients monitored for 5 years. Although data in such registries may be incomplete and/or biased, they do serve to provide information on drug safety. Data from the US TREAT registry that consists of more than 6000 patients treated with infliximab with a mean follow-up of 3.4 year have not shown a significant increase in malignancy, mortality, incidence of lymphoma in IBD patients treated with infliximab compared with other therapies.[57] A recent meta-analysis assessing the safety of anti-TNF therapy showed that there was no increased risk of death, serious infection, or malignancy in overall, subgroup and sensitivity analyses.[58] The TREAT registry and the European ENCORE CD registry have identified steroid use as an independent risk factor for serious infections. In a recent longer-term study of the TREAT registry with a follow-up of 4.8 years, infliximab-treated patients showed similar rates of mortality and malignancy (including lymphoma), but an increased risk of serious infections compared with non-infliximab-treated patients.[59] A very rare form of non-Hodgkin's lymphoma, hepatosplenic T-cell lymphoma, has been reported in patients with IBD, predominantly Crohn's disease, usually treated with combination anti-TNF-α agents and azathioprine. This malignancy was first described in 1990 as distinct subtype of lymphoma. There are only about 150 cases documented in the literature. It predominantly affects paediatric and young adult patients (predominantly male) and tends to have a very aggressive disease course with a usually fatal outcome. This form of lymphoma has been described in 14 Crohn's disease patients, one patient with indeterminate colitis and one with UC (age 12–40 years).[60]
Long-term Efficacy

As with ciclosporin, it is important to determine the duration of response with infliximab. There have been data up to 1 year in 110 patients with severe steroid refractory UC from ten Italian centres treated with infliximab 5 mg/kg at 0, 2 and 6 weeks and subsequently maintained on infliximab, azathioprine or both. The colectomy rate at 1 year was 24.5%.[61] These data are consistent with a separate study of 20 patients hospitalized for acute severe UC demonstrating that colectomy was prevented in 75% of patients 1 year following initiation of infliximab.[62] In addition, data up to 3 years from a Swedish/Danish trial showed a 50% colectomy rate in infliximab-treated patients compared with a 76% colectomy rate in placebo-treated patients. However, in this study, the use of subsequent immunomodulators in the two groups was not equal, and this may influence the long-term outcome.[63, 64]

Several other uncontrolled studies have also examined the long-term effects of infliximab treatment for acute severe UC. A study from Edinburgh reported that approximately two-thirds of patients treated with infliximab avoided colectomy during the acute admission and when patients were followed up to a median of 203 days, there were two additional colectomies.[53] A study from Oxford showed that about half of their patients with refractory UC treated with infliximab came to a colectomy at a median of 140 days after the first infusion.[65] In a large Italian study of 83 patients with severe steroid-refractory UC treated with infliximab, 15% of patients underwent colectomy within 2 months, and more than 50% of the patients avoided colectomy up to a median of 23 months. Two or more infliximab infusions appeared to be more effective than a single infusion in the short term.[54]

Overall, infliximab is effective in preventing colectomy in acute severe UC in the short term and the response may be durable. A recent systematic review of 34 studies including 896 patients with moderate-to-severe UC showed that infliximab was more effective than placebo for inpatients and outpatients with severe UC. At approximately 9 months follow-up, 40% of patients were in remission.[66]
11-16-2010, 06:54 PM   #6
David in Seattle
Senior Member
 
David in Seattle's Avatar
 
Join Date: Feb 2010
Predictors of Response to Infliximab

Investigators from Leuven identified predictors of early clinical response to infliximab in their first 100 patients with severe UC treated with infliximab. A majority of patients received a single dose 5 mg/kg infliximab, whereas one-third of patients received a three-dose infliximab induction at weeks 0, 2 and 6. More than half of the patients were on concomitant immunomodulators. Younger patients and those without a pANCA+/ASCA− serotype tended to have an early clinical response.[67]

Independent predictors of failure to infliximab as rescue therapy for severe intravenous steroid-refractory UC have been assessed in another retrospective study and these factors include a disease duration of ≤3 years, bowel frequency of greater than six times per day on admission and prior hospitalization in the past 3 months for UC.[68]

Lees et al. showed that serum albumin at admission and day 3 of intravenous steroids predicted response to infliximab. A serum albumin of <34 g/L at day 3 showed a sensitivity of 57% and specificity of 90% for colectomy.[53]

Infliximab vs. Ciclosporin

No head-to-head trials comparing ciclosporin and infliximab in acute severe UC have been published, but controlled trials comparing these two drugs for this indication are in progress. In a retrospective study presented in abstract form of an Austrian cohort of UC patients treated with ciclosporin (n = 49) and a Swedish cohort of UC patients treated with infliximab (n = 46), a lower colectomy rate was observed at 3 and 12 months after rescue therapy with ciclosporin (12%, 33%) than with a single infusion of infliximab 5 mg/kg (33%, 45%) in patients presenting with acute severe steroid-refractory UC. Both groups received subsequent maintenance therapy with azathioprine. However, severity and extent of disease were not comparable in the two cohorts.[69] In a separate Italian study of severe steroid-resistant UC, 19 infliximab-treated patients were compared with a historical cohort of ciclosporin-treated patients (33 patients). Re-hospitalization rates in the two groups up to 20 months were similar.[70] Both ciclosporin and infliximab are effective in the treatment of acute severe UC and the therapeutic decision should be individualized. In patients naοve to thiopurine therapy presenting with their first episode of acute severe UC, intravenous ciclosporin followed by the introduction of azathioprine while still in hospital after having demonstrated a response, together with 3 months of bridging oral ciclosporin, is an effective strategy. In these patients, ciclosporin is being used as a bridge to azathioprine, which is used as a maintenance therapy. In contrast, in patients who have been maintained on optimal dose azathioprine and present with a severe episode of UC, ciclosporin and probably infliximab are less likely to be successful[44] and there is the issue of what further maintenance therapy can be used. In this setting, the use of infliximab can be considered, as this can be used as a maintenance therapy. However, consideration for early surgery may be more appropriate.

Switching between Ciclosporin and Infliximab

Some patients with acute severe UC will fail ciclosporin or infliximab. There have been reports of switching from ciclosporin to infliximab and vice versa. However, the strategy of switching between ciclosporin and infliximab or vice versa has significant risks, which are outlined below and needs to be considered very carefully weighing up the risks and benefits of surgery with the risks and benefits of continuing medical therapy. We would not advocate switching as a 'standard' treatment strategy. It is theoretically safer to use infliximab after ciclosporin than to use these drugs in the reverse order in view of the shorter half life of ciclosporin. In a Spanish study, 16 patients with acute UC were treated with infliximab after failing ciclosporin; 37.5% of patients required a colectomy at a median follow-up of 195 days from the first infliximab infusion.[71] In a study from Mount Sinai, 19 patients with fulminant UC failed to respond to either ciclosporin or infliximab and crossed over to the other medication. Ten patients received infliximab after failing ciclosporin and nine patients received ciclosporin after failing infliximab. Four (40%) and three (33%) patients in the infliximab- and ciclosporin-salvage groups achieved remission respectively. Remission lasted a mean of 10.4 and 28.5 months respectively. One patient treated with infliximab salvage died of sepsis. Two patients who had Ciclosporin salvage developed herpetic oesophagitis and pancreatitis.[72] In the largest study to date by the GETAID group of 86 patients, 65 patients had ciclosporin first followed by infliximab after a median time of 2 days after ciclosporin withdrawal, and 21 patients had infliximab first followed by ciclosporin after a median of 17 days since last infliximab infusion. Corticosteroids or immunosuppressants were continued in about three-quarter of patients. Thirty-three patients had a colectomy within 3 months. About one-third of patients had adverse effects consisting mostly of infections. One patient died after surgery from pulmonary embolism.[73]
11-16-2010, 06:55 PM   #7
David in Seattle
Senior Member
 
David in Seattle's Avatar
 
Join Date: Feb 2010
Drug-related Mortality

A single centre study from Leuven showed that ciclosporin was associated with deaths (3.5%) from opportunistic infections (two aspergillus and one pneumocystis carinii) in three of 86 patients with UC.[40] Other trials have reported a mortality rate associated with ciclosporin in IBD of approximately 1.8%.[34] The Scottish study showed that the major complication and mortality rate was 5.2% and 2.6% respectively in patients with acute UC treated with infliximab. An older man died of pseudomonas pneumonia following successful response to infliximab for severe UC, and a young patient had severe fungaemia postcolectomy after failing infliximab.[53] Switching between infliximab and ciclosporin is associated with serious adverse effects and death as discussed above, and is not recommended as 'standard' approach.[72, 73] Infliximab and ciclosporin appear to be efficacious as rescue therapy for patients with acute severe UC, but serious adverse events do occur. A risk–benefit analysis of medical therapy needs to be compared with 'curative' surgery, which carries a mortality of about 2–3% in the early post-operative period. Both short- and long-term postcolectomy mortality rates are substantially reduced when an elective colectomy, but not an emergency colectomy, is performed.

Other Experimental Therapies

There are no published studies reporting the efficacy of the humanized anti-TNF agent, adalimumab, in the setting of acute severe UC defined by the Truelove and Witt's criteria, although two small studies have investigated the use of Adalimumab in patients with moderately severe UC who had failed infliximab.[74, 75] A recent larger study of 186 patients assessing the use of Adalimumab in moderately to severely active UC showed disappointing results at 8 weeks with 19.2% of patients in the adalimumab group (160 mg/80 mg) in clinical remission compared with 9.2% in the placebo group.[76] Other agents such as tacrolimus and leukocytapheresis have been studied and recently biological agents such as basiliximab and visiluzumab have been assessed. Intravenous and oral tacrolimus showed results similar to those of ciclosporin.[77] A dose-ranging study of Visiluzimab, an anti-CD3 monoclonal antibody, in acute severe UC based on the Modified Truelove and Witt's score, showed a 30-day remission and response rates of 30% and 60% respectively.[78]

Surgery

Surgery may be unavoidable in some patients with acute severe UC; therefore, optimal management requires close collaboration between the gastroenterologist and the surgeon, and the surgeon and stoma nurse should be involved early in the management. Indications for surgery include toxic megacolon, perforation, severe haemorrhage or clinical deterioration during medical therapy. Delayed surgery for patients who do not respond to medical therapy is associated with an increased risk of post-operative complications. In a group of 80 patients undergoing emergency colectomy for severe UC treated between 1994 and 2000 in Oxford, patients who had a significantly longer duration of preoperative medical therapy were more likely to have major post-operative complications. If medical therapy was continued for 8 days or more, a higher complication rate was noted if surgery ensued.[22] This emphasizes the importance of having a time-bound approach with both medical and surgical teams monitoring patients closely and making the decision to operate at the appropriate time. It has to be a part of the medical management plan to optimize the condition of the patient for potential surgery with regard to maximizing nutrition and tapering steroids, where possible.

Ferrante et al. compared post-operative infectious complications between patients who had infliximab 3 months prior to surgery and those who did not have. Corticosteroids and a restorative proctocolectomy without defunctioning ileostomy, but not infliximab, were associated with an increased risk of short-term post-operative infectious complications in UC.[79] However, a recent meta-analysis showed that pre-operative infliximab use increased the risk of total short-term post-operative complications (OR 1.8), which included wound infection, sepsis and abscess.[80]

The recommended operation in the acute setting is total colectomy and ileostomy, with the rectum left in situ. Reconstructive surgery is best performed approximately 6 months after primary surgery.[81] Although ileal pouch anal anastomosis offers the prospect of a life without a permanent stoma, surgery does not always restore all aspects of quality of life to normal and a substantial number of patients still have problems with leakage, urgency, nocturnal soiling, sexual dysfunction, and pouchitis, and some patients may require conversion to a permanent ileostomy after ileal J-pouch-anal anastomosis failure.[82]

Conclusions

Approximately 15% of patients with UC will have a severe acute attack that requires admission to hospital. Standard intensive treatment with intravenous steroids is still the first line approach. Patients who do not respond within 3 days to first line medical therapy should be considered for second line rescue medical therapy or surgery. This decision should take into account the patient's previous immunosuppressant history, age and co-morbidity. Delaying surgery, especially in older patients, those who had prior IBD admissions and prolonged hospital stays, carries risk and is associated with increased mortality up to 3 years. Surgeons and stoma nurses should be involved early in the management of patients with acute severe UC. A time-limited approach with assessment of predictors of response to therapies and close collaboration between physicians and surgeons are needed to ensure optimized management of patients with acute severe UC.

As we gain more information regarding the genetics of IBD, there may well be genotypic predictors of disease course, likelihood of colectomy and response to drugs, including, but not limited to, infliximab and ciclosporin, for the treatment of acute severe UC.[83] Ultimately, additional data are required to define better the efficacy and safety of current treatment in the short term and long term, and the optimal timing of colectomy if unavoidable, in an individual patient.
11-16-2010, 06:55 PM   #8
David in Seattle
Senior Member
 
David in Seattle's Avatar
 
Join Date: Feb 2010
References

1. Edwards FC, Truelove SC. The course and prognosis of ulcerative colitis. Gut 1963; 4: 299–315.
2. Truelove SC, Witts LJ. Cortisone in ulcerative colitis; preliminary report on a therapeutic trial. Br Med J 1954; 2: 375–8.
3. Jodorkovsky D, Young Y, Abreu MT. Clinical outcomes of patients with ulcerative colitis and co-existing Clostridiumdifficile infection. Dig Dis Sci 2010; 55: 415–20.
4. Ananthakrishnan AN, Issa M, Binion DG. Clostridium difficile and inflammatory bowel disease. Med Clin North Am 2010; 94: 135–53.
5. Garcia-Erce JA, Gomollon F, Munoz M. Blood transfusion for the treatment of acute anaemia in inflammatory bowel disease and other digestive diseases. World J Gastroenterol 2009; 15: 4686–94.
6. Gasche C, Berstad A, Befrits R, et al. Guidelines on the diagnosis and management of iron deficiency and anemia in inflammatory bowel diseases. Inflamm Bowel Dis 2007; 13: 1545–53.
7. Truelove SC, Jewell DP. Intensive intravenous regimen for severe attacks of ulcerative colitis. Lancet 1974; 1: 1067–70.
8. Truelove SC, Witts LJ. Cortisone in ulcerative colitis; final report on a therapeutic trial. Br Med J 1955; 2: 1041–8.
9. Turner D, Walsh CM, Steinhart AH, et al. Response to corticosteroids in severe ulcerative colitis: a systematic review of the literature and a metaregression. Clin Gastroenterol Hepatol 2007; 5: 103–10.
10. Jakobovits SL, Travis SP. Management of acute severe colitis. Br Med Bull 2005; 75–76: 131–44.
11. UK IBD Audit second round. Available at: http://www.rcplondon.ac.uk/clinicals.../Overview.aspx. Accessed March 2009.
12. Arnott IDR, Leiper K, Down C, et al. Outcome of acute severe ulcerative colitis: data from the national UK IBD audit. Gut 2009; 58: A33.
13. Arnott ID, Leiper K, Down C, et al. Outcome of acute severe ulcerative colitis: data from the UK National IBD audit. Gastroenterology 2010; 138(Suppl 1): S106.
14. Kaplan GG, McCarthy EP, Ayanian JZ, et al. Impact of hospital volume on postoperative morbidity and mortality following a colectomy for ulcerative colitis. Gastroenterology 2008; 134: 680–7.
15. Ananthakrishnan AN, McGinley EL, Binion DG. Inflammatory bowel disease in the elderly is associated with worse outcomes: a national study of hospitalizations. Inflamm Bowel Dis 2009; 15: 182–9.
16. Nguyen GC, Steinhart AH. Nationwide patterns of hospitalizations to centers with high volume of admissions for inflammatory bowel disease and their impact on mortality. Inflamm Bowel Dis 2008; 14: 1688–94.
17. Roberts SE, Williams JG, Yeates D, et al. Mortality in patients with and without colectomy admitted to hospital for ulcerative colitis and Crohn's disease: record linkage studies. BMJ 2007; 335: 1033.
18. Nicholls RJ, Clark DN, Kelso L, et al. Nationwide linkage analysis in Scotland implicates age as the critical overall determinant of mortality in ulcerative colitis. Aliment Pharmacol Ther 2010; 31: 1310–21.
19. Travis SP, Farrant JM, Ricketts C, et al. Predicting outcome in severe ulcerative colitis. Gut 1996; 38: 905–10.
20. Lindgren SC, Flood LM, Kilander AF, et al. Early predictors of glucocorticosteroid treatment failure in severe and moderately severe attacks of ulcerative colitis. Eur J Gastroenterol Hepatol 1998; 10: 831–5.
21. Ho GT, Mowat C, Goddard CJ, et al. Predicting the outcome of severe ulcerative colitis: development of a novel risk score to aid early selection of patients for second-line medical therapy or surgery. Aliment Pharmacol Ther 2004; 19: 1079–87.
22. Randall J, Singh B, Warren BF, et al. Delayed surgery for acute severe colitis is associated with increased risk of postoperative complications. Br J Surg 2010; 97: 404–9.
23. Ananthakrishnan AN, McGinley EL, Binion DG, et al. Simple score to identify colectomy risk in ulcerative colitis hospitalizations. Inflamm Bowel Dis 2010 [Epub ahead of print].
24. Ho GT, Lee HM, Brydon G, et al. Fecal calprotectin predicts the clinical course of acute severe ulcerative colitis. Am JGastroenterol 2009; 104: 673–8.
25. Lichtiger S, Present DH, Kornbluth A, et al. Cyclosporine in severe ulcerative colitis refractory to steroid therapy. NEngl J Med 1994; 330: 1841–5.
26. Van Assche G, D'Haens G, Noman M, et al. Randomized, double-blind comparison of 4 mg/kg versus 2 mg/kg intravenous cyclosporine in severe ulcerative colitis. Gastroenterology 2003; 125: 1025–31.
27. Santos J, Baudet S, Casellas F, et al. Efficacy of intravenous cyclosporine for steroid refractory attacks of ulcerative colitis. J Clin Gastroenterol 1995; 20: 285–9.
28. Rayner CK, McCormack G, Emmanuel AV, et al. Long-term results of low-dose intravenous ciclosporin for acute severe ulcerative colitis. Aliment PharmacolTher 2003; 18: 303–8.
29. Stack WA, Long RG, Hawkey CJ. Shortand long-term outcome of patients treated with cyclosporin for severe acute ulcerative colitis. Aliment PharmacolTher 1998; 12: 973–8.
30. Hyde GM, Thillainayagam AV, Jewell DP. Intravenous cyclosporin as rescue therapy in severe ulcerative colitis: time for a reappraisal? Eur J Gastroenterol Hepatol 1998; 10: 411–3.
31. Cohen RD, Stein R, Hanauer SB. Intravenous cyclosporin in ulcerative colitis: a five-year experience. Am J Gastroenterol 1999; 94: 1587–92.
32. Message L, Bourreille A, Laharie D, et al. Efficacy of intravenous cyclosporin in moderately severe ulcerative colitis refractory to steroids. Gastroenterol Clin Biol 2005; 29: 231–5.
33. Campbell S, Travis S, Jewell D. Ciclosporin use in acute ulcerative colitis: a longterm experience. Eur J GastroenterolHepatol 2005; 17: 79–84.
34. Sternthal MB, Murphy SJ, George J, et al. Adverse events associated with the use of cyclosporine in patients with inflammatory bowel disease. Am J Gastroenterol 2008; 103: 937–43.
35. Actis GC, Ottobrelli A, Pera A, et al. Continuously infused cyclosporine at low dose is sufficient to avoid emergency colectomy in acute attacks of ulcerative colitis without the need for high-dose steroids. J Clin Gastroenterol 1993; 17: 10–3.
36. de Groen PC, Aksamit AJ, Rakela J, et al. Central nervous system toxicity after liver transplantation. The role of cyclosporine and cholesterol. N Engl JMed 1987; 317: 861–6.
37. de Groen PC, Wiesner RH, Krom RA. Cyclosporine A-induced side effects related to a low total serum cholesterol level: an indication for a free cyclosporine A assay? Transplant Proc 1988; 20: 374–6.
38. de Groen PC. Cyclosporine, low-density lipoprotein, and cholesterol. Mayo Clin Proc 1988; 63: 1012–21.
39. Wijdicks EF, Dahlke LJ, Wiesner RH. Oral cyclosporine decreases severity of neurotoxicity in liver transplant recipients. Neurology 1999; 52: 1708–10.
40. Toruner M, Loftus EV Jr, Harmsen WS, et al. Risk factors for opportunistic infections in patients with inflammatory bowel disease. Gastroenterology 2008; 134: 929–36.
41. Rahier JF, Ben-horin S, Chowers Y, et al. European evidence-based consensus on the prevention, diagnosis and management of opportunistic infection in inflammatory bowel disease. Journal of Crohn's Colitis 2009; 3: 47–91.
42. Bojic D, Radojicic Z, Nedeljkovic-Protic M, et al. Long-term outcome after admission for acute severe ulcerative colitis in Oxford: the 1992–1993 cohort. Inflamm Bowel Dis 2009; 15: 823–8.
4.
11-16-2010, 06:56 PM   #9
David in Seattle
Senior Member
 
David in Seattle's Avatar
 
Join Date: Feb 2010
43. Arts J, D'Haens G, Zeegers M, et al. Long-term outcome of treatment with intravenous cyclosporin in patients with severe ulcerative colitis. Inflamm Bowel Dis 2004; 10: 73–8.
44. Moskovitz DN, Van AG, Maenhout B, et al. Incidence of colectomy during long-term follow-up after cyclosporineinduced remission of severe ulcerative colitis. Clin Gastroenterol Hepatol 2006; 4: 760–5.
45. Stange EF, Travis SPL, Vermeire S, et al. European evidence-based Consensus on the diagnosis and management of ulcerative colitis: definitions and diagnosis. Journal of Crohn's Colitis 2008; 2:1: 1–23.
46. Cacheux W, Seksik P, Lemann M, et al. Predictive factors of response to cyclosporine in steroid-refractory ulcerative colitis. Am J Gastroenterol 2008; 103: 637–42.
47. Rowe FA, Walker JH, Karp LC, et al. Factors predictive of response to cyclosporin treatment for severe, steroidresistant ulcerative colitis. Am JGastroenterol 2000; 95: 2000–8.
48. Nicholls S, Stephens S, Braegger CP, et al. Cytokines in stools of children with inflammatory bowel disease or infective diarrhoea. J Clin Pathol 1993; 46: 757–60.
49. Kaser A, Mairinger T, Vogel W, et al. Infliximab in severe steroid-refractory ulcerative colitis: a pilot study. Wien KlinWochenschr 2001; 113: 930–3.
50. Sands BE, Tremaine WJ, Sandborn WJ, et al. Infliximab in the treatment of severe, steroid-refractory ulcerative colitis: a pilot study. Inflamm Bowel Dis 2001; 7: 83–8.
51. Ochsenkuhn T, Sackmann M, Goke B. Infliximab for acute, not steroidrefractory ulcerative colitis: a randomized pilot study. Eur J Gastroenterol Hepatol 2004; 16: 1167–71.
52. Jarnerot G, Hertervig E, Friis-Liby I, et al. Infliximab as rescue therapy in severe to moderately severe ulcerative colitis: a randomized, placebo-controlled study. Gastroenterology 2005; 128: 1805–11.
53. Lees CW, Heys D, Ho GT, et al. A retrospective analysis of the efficacy and safety of infliximab as rescue therapy in acute severe ulcerative colitis. Aliment Pharmacol Ther 2007; 26: 411–9.
54. Kohn A, Daperno M, Armuzzi A, et al. Infliximab in severe ulcerative colitis: short-term results of different infusion regimens and long-term follow-up. Aliment Pharmacol Ther 2007; 26: 747–56.
55. Rahier JF, Yazdanpanah Y, Colombel JF, et al. The European (ECCO) Consensus on infection in IBD: what does it change for the clinician? Gut 2009; 58: 1313–5.
56. Rahier JF, Yazdanpanah Y, Viget N, et al. Review article: influenza A (H1N1) virus in patients with inflammatory bowel disease. Aliment Pharmacol Ther 2010; 31: 5–10.
57. Lichtenstein GR, Feagan BG, Cohen RD, et al. Serious infections and mortality in association with therapies for Crohn's disease: TREAT registry. Clin Gastroenterol Hepatol 2006; 4: 621–30.
58. Peyrin-Biroulet L, Deltenre P, de SN, et al. Efficacy and safety of tumor necrosis factor antagonists in Crohn's disease: meta-analysis of placebo-controlled trials. Clin Gastroenterol Hepatol 2008; 6: 644–53.
59. Lichtenstein GR, Cohen RD, Feagan BG, et al. Safety of Infliximab and other Crohn's disease therapies: Treat Registry data with 27762 patient-year follow-up. Gastroenterology 2010; 138(Suppl 1): S475.
60. Mackey AC, Green L, Leptak C, et al. Hepatosplenic T cell lymphoma associated with infliximab use in young patients treated for inflammatory bowel disease: update. J Pediatr Gastroenterol Nutr 2009; 48: 386–8.
61. Monterubbianesi R, Armuzzi A, Papi C, et al. Infliximab for severe ulcerative colitis: short-term and one year outcome of three dose regimen. An Italian multicentre open-label study. Gastroenterology 2009; 138(Suppl 1): S685.
62. Venu M, Naik AS, Ananthakrishnan AN. Early infliximab infusion in hospitalised severe UC patients: one year outcome. Gastroenterology 2009; 136(Suppl 1): A201.
63. Gustavsson A, Jarnerot G, Hertevig E, et al. Colectomy after rescue therapy in intravenous steroid-resistant acute ulcerative colitis: a 3-year follow-up study of the Swedish/Danish Infliximab/Placebo Trial. Gut 2008; 57: A79.
64. Gustavsson A, Jarnerot G, Hertevig E. A 2-year follow up study of the Swedish–Danish infliximab trial in steroid resistant acute ulcerative colitis. Gastroenterology 2007; 132: 983–4.
65. Jakobovits SL, Jewell DP, Travis SP. Infliximab for the treatment of ulcerative colitis: outcomes in Oxford from 2000 to 2006. Aliment Pharmacol Ther 2007; 25: 1055–60.
66. Gisbert JP, Gonzalez-Lama Y, Mate J. Systematic review: infliximab therapy in ulcerative colitis. Aliment Pharmacol Ther 2007; 25: 19–37.
67. Ferrante M, Vermeire S, Katsanos KH, et al. Predictors of early response to infliximab in patients with ulcerative colitis. Inflamm Bowel Dis 2007; 13: 123–8.
68. Zisman TL, Lewis JR, Stein AC, et al. Predictors of avoidance of colectomy with infliximab initiation in severe, IV steroid refractory ulcerative colitis. Gastroenterology 2009; 136(Suppl 1): A660.
69. Walch A, Sjoberg M, Meshkat M, et al. Outcome of rescue therapy in steroidresistant ulcerative colitis: a retrospective study comparing cyclosporine and infliximab. Gut 2008; 57: P0801.
70. Moccario F, Oliva L, Orlando A, et al. Infliximab or cyclosporine in severe steroid- refractory ulcerative colitis: short and long term results in two groups of treated patients (a historical comparison). Gut 2009; 58: A324.
71. Manosa M, Lopez San RA, Garcia- Planella E, et al. Infliximab rescue therapy after cyclosporin failure in steroid-refractory ulcerative colitis. Digestion 2009; 80: 30–5.
72. Maser EA, Deconda D, Lichtiger S, et al. Cyclosporine and infliximab as acute salvage therapies for each other, in severe steroid-refractory ulcerative colitis. Gut 2007; 132: S1132.
73. Leblanc S, Allez M, Seksik P, et al. Successive treatment with cyclosporine and infliximab in severe ulcerative colitis. Gastroenterology 2009; 136(Suppl 1): A88.
74. Estelles J, Fernandez-Blanco I, Mendoza JL, et al. Initial response and long-term outcome of adalimunab for ulcerative colitis previously treated with infliximab. Gut 2009; 58: A69.
75. Peyrin-Biroulet L, Laclotte C, Roblin X, et al. Adalimumab induction therapy for ulcerative colitis with intolerance or lost response to infliximab: an open-label study. World J Gastroenterol 2007; 13: 2328–32.
76. Reinisch W, Sandborn WJ, Hommes DW, et al. Adalimumab for induction of clinical remission in moderately to severely active ulcerative colitis. Journalof Crohn's Colitis 2010; 4(Suppl 1): 7.
77. Baumgart DC, Wiedenmann B, Dignass AU. Rescue therapy with tacrolimus is effective in patients with severe and refractory inflammatory bowel disease. Aliment Pharmacol Ther 2003; 17: 1273–81.
78. Targan SR, Salzberg BA, Mayer L. A phase I–II study: multiple doe levels of visilizumab are well tolerated and produce rapid and sustained improvement in ulcerative colitis patients refractory to treatment with intravenous steroids. Gastroenterology 2005; 128: A75.
79. Ferrante M, D'Hoore A, Vermeire S, et al. Corticosteroids but not infliximab increase short-term postoperative infectious complications in patients with ulcerative colitis. Inflamm Bowel Dis 2009; 15: 1062–70.
80. Yang Z, Wu Q, Wu K, et al. Metaanalysis: pre-operative infliximab treatment and short-term post-operative complications in patients with ulcerative colitis. Aliment Pharmacol Ther 2010; 31: 486–92.
81. Andersson P, Soderholm JD. Surgery in ulcerative colitis: indication and timing. Dig Dis 2009; 27: 335–40.
82. Lichtenstein GR, Cohen R, Yamashita B, et al. Quality of life after proctocolectomy with ileoanal anastomosis for patients with ulcerative colitis. J ClinGastroenterol 2006; 40: 669–77.
83. Haritunians T, Taylor K, Rotter JI, et al. Genetic predictors of medically refractive ulcerative colitis requiring colectomy. Gastroenterology 2009; 136(Suppl 1): A131.
84. Bressler B, Law JK, Al Nahdi SN, et al. The use of infliximab for treatment of hospitalized patients with acute severe ulcerative colitis. Can J Gastroenterol 2008; 22: 937–40.
85. D'Haens G, Lemmens L, Geboes K, et al. Intravenous cyclosporine versus intravenous corticosteroids as single therapy for severe attacks of ulcerative colitis. Gastroenterology 2001; 120: 1323–9.
86. Holme Φ, Thiis-Evensen E, Vatn MH. Treatment of fulminant ulcerative colitis with cyclosporine A. Scand Journal ofGastro 2009; 44: 1310–
Reply

Crohn's Disease Forum » Books, Multimedia, Research & News » Review Article: The Optimal Medical Management of Acute Severe UC
Thread Tools


All times are GMT -5. The time now is 02:42 PM.
Copyright 2006-2017 Crohnsforum.com