All Boards >> Irritable Bowel Syndrome Research Library

Posts     Flat       Threaded

Pages: 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | (show all)
Doctors group launches war on drug ads new
      #274351 - 07/17/06 11:17 AM
HeatherAdministrator

Reged: 12/09/02
Posts: 7799
Loc: Seattle, WA

Doctors group launches war on drug ads

American Medical Association seeks waiting period for FDA approval before marketing new prescriptions, devices to public.

By BLYTHE BERNHARD
The Orange County Register


Dr. Melvyn Sterling, internist practicing in Orange
"The reason those ads are there is to sell the drug, not to educate the public."


If there's an ailment, there's an ad for a prescription drug aimed at fighting it – from toe fungus to impotence.

Prescription drug advertising has swelled to a $4.8 billion industry since the U.S. Food and Drug Administration relaxed its restrictions on the ads in 1997, allowing for descriptions of the drugs' purpose. Many doctors say the ads are coming so fast that they don't have time to learn about the benefits and risks of a new drug before patients start requesting prescriptions.

Last month, the American Medical Association asked the FDA to impose a waiting period before new drugs and devices can be marketed to consumers.

"Doctors just want to make sure they have a chance to get up to speed on new drugs before the patients are being urged to seek these medications because of heavy advertising," said Dr. Ron Davis, the association's president-elect.

The ads can disrupt the patient-doctor relationship and contribute to risinghealth-care costs when patients insist on receiving new, more expensive drugs, said Davis, who works in the Henry Ford Health System in Detroit.

The drug industry's lobby, Pharmaceutical Research and Manufacturers of America, is opposed to a mandatory waiting period for drug ads. The lobby has voluntary guidelines encouraging drug companies to educate doctors and submit ads to the FDA for approval.

In response to the medical association's ruling, the lobby released a statement that reads, in part:

"Direct-to-consumer advertising provides doctors and patients with accurate, educational information about disease and treatment options."

Davis acknowledged that drug advertising can raise awareness and encourage communication between doctors and patients, but added that tighter regulations are necessary.

"We hope that the FDA will step forward and show leadership in this area," Davis said. "If that doesn't happen then legislation may be needed to make it a requirement."

Dr. Melvyn Sterling, an internist who practices in Orange, attended the medical association meetings that led to the policy changes. He said people should consider the source when reading or watching drug ads.

"The reason those ads are there is to sell the drug, not to educate the public," Sterling said.

And the ads aren't just coming in magazines and television.

A local pharmaceutical company, Valeant, flies a yellow banner off its Costa Mesa building: "New Zelapar orally disintegrating tablets. Now FDA approved!" The banner doesn't mention what the drug is used for (Parkinson's disease).

Officials for Valeant did not respond to requests for comment for this story. Irvine pharmaceutical company Allergan, which markets wrinkle smoothers and dry eye treatments in magazines, also did not respond.

Drug safety is another reason doctors are hoping for an advertising moratorium. Clinical drug trials sometimes are conducted with too few subjects for serious side effects to show up.

One famous example – the heavily promoted arthritis pill Vioxx – was later recalled because of a serious risk of heart attacks and strokes.

Patients should be aware of safer, cheaper alternatives, doctors said.

"A patient with arthritis should typically be given a trial on regular aspirin," Davis said. "The ads sometimes are for very expensive drugs when there are much less expensive drugs available that the patient should try first … A lot of patients are looking for that magic pill. "

It's not just new drugs for old ailments that concern doctors. Drugs are marketed for conditions that a few years ago didn't have a name: irritable bowel syndrome, restless leg syndrome and female sexual dysfunction, among others. Depending on the marketing, "SAD" can mean seasonal affective disorder or social anxiety disorder.

"To market a drug, it's best to market a disease," said Dr. John Abramson, author of "Overdo$ed America" and a clinical instructor at Harvard Medical School. "Much of the advertising is convincing people that they need drugs when often they don't need drugs, or what's being treated is ordinary, regular life."

Abramson said a moratorium on new drug advertising is a good first step, but that it's getting harder for doctors to find objective information on drugs.

Drug companies sponsor most of the clinical trials that appear in the doctors' medical journals, often next to ads for the drugs.

"There's now much, so much commercial influence that doctors aren't able to get the unbiased, non-commercial scientific truth," he said.

http://www.ocregister.com/ocregister/money/homepage/article_1203782.php

--------------------
Heather is the Administrator of the IBS Message Boards. She is the author of Eating for IBS and The First Year: IBS, and the CEO of Heather's Tummy Care. Join her IBS Newsletter. Meet Heather on Facebook!

Print     Remind Me     Notify Moderator    

Marijuana eases chronic pain new
      #274356 - 07/17/06 11:49 AM
HeatherAdministrator

Reged: 12/09/02
Posts: 7799
Loc: Seattle, WA

Marijuana eases chronic pain, study finds

Cannabis extract from marijuana gives powerful relief for chronic pain, and should be studied for future clinical use, a medical researcher has told a conference in Glasgow.

Dr William Notcutt of the James Paget Hospital in Great Yarmouth, England, said the cannabis extract used in his study - applied as a spray under the tongue - was remarkably effective in easing chronic pain. He announced the findings at the annual meeting of the British Association for the Advancement of Science.

"The cannabis extracts can produce high-quality pain relief, symptom control, and improvement in the quality of life, without significant side effects," said Dr Notcutt.

He tested cannabis extracts collected from cloned plants, in 23 sufferers of chronic pain.

Subjects were mostly patients with multiple sclerosis or spinal injury. Nine had used marijuana regularly in the past, while the remainder were 'naïve': they had either not used it at all, or had tried it infrequently.

The cannabinoid extract was given over eight weeks, and participants' pain levels monitored. Asked to rate their improvement in pain relief on a scale from one to 10, the majority rated it at "between 9 and 10".

Without their knowledge, a placebo was introduced during the trial, and later replaced with cannabinoid. When the extract was removed, pain levels shot up 20 to 30 per cent, and subsequently dropped off once the extract was again provided.

Dr Notcutt said subjects reported improvements ranging from 'life-changing' to allowing them to get a good night's sleep. One subject had returned to work; others had started driving, gardening and caring for children again.

In all, 17 of the 23 subjects found the extract useful in reducing pain. Of the remainder, three said it had little or no effect, two disliked the euphoria produced, and one was withdrawn from the program due to 'protocol violations'.

Previous anecdotal reports from multiple sclerosis patients have suggested that smoking cannabis has a beneficial effect. Dr Notcutt said he was interested in establishing if this was true, whether there were any side effects and what appropriate dosages might be.

Although cannabis use is illegal in most countries, some multiple sclerosis and cancer patients have been lobbying to legalise its medicinal use, particularly in Britain and the United States.

Despite his positive results, however, Dr Notcutt said more research was needed before scientists could recommend cannabis as a treatment.

"I think it's too early - we need a lot more basic information on just on how to use the drug," he told reporters. He decried the fact that, because of its status as a prohibited substance, very little is known about its pain-relieving properties.

"What we're trying to do is study it in depth, get a lot of information. What is going on, what are the effects on individual patients?"

Notcutt did the study in his own time, with cannabis extract supplied by GW Pharmaceuticals, a company licensed by the British government to grow and supply cannabis for medical research.

He said the use of cannabis extracts for pain alleviation could pave the way for the drug to be used for other conditions, including rheumatoid arthritis, epilepsy and cancer.

Studies in Europe suggest that 18 per cent of people suffer chronic pain, defined as pain that lasts six months or more.

Wilson da Silva - ABC Science Online

http://www.abc.net.au/science/news/health/HealthRepublish_358716.htm

--------------------
Heather is the Administrator of the IBS Message Boards. She is the author of Eating for IBS and The First Year: IBS, and the CEO of Heather's Tummy Care. Join her IBS Newsletter. Meet Heather on Facebook!

Print     Remind Me     Notify Moderator    

Citalopram (Celexa) Improves Symptoms of Irritable Bowel Syndrome new
      #286472 - 10/14/06 12:57 PM
HeatherAdministrator

Reged: 12/09/02
Posts: 7799
Loc: Seattle, WA

Citalopram Improves Symptoms of Irritable Bowel Syndrome

News Author: Laurie Barclay, MD
CME Author: Charles Vega, MD, FAAFP


Citalopram improves the symptoms of irritable bowel syndrome (IBS), according to the results of a placebo-controlled crossover trial reported in the August issue of Gut.

"Selective serotonin reuptake inhibitors (SSRIs) are frequently used in the treatment of IBS, although evidence of their efficacy is scarce," write J. Tack, MD, from the University of Leuven in Belgium, and colleagues. "Recently, we demonstrated that administration of the SSRI citalopram in healthy subjects decreases the sensitivity of the colon to distension and inhibits the colonic response to feeding. These observations may provide a rationale for use of citalopram in the treatment of IBS."

At a tertiary care center, 23 patients without depression and with IBS were recruited from and included in this crossover trial comparing 6 weeks of treatment with the SSRI citalopram (20 mg daily for 3 weeks and 40 mg daily for 3 weeks) with placebo. The primary outcome measure was IBS symptom severity, and depression and anxiety scores were also recorded. As a hypothesized predictor of symptomatic response to the drug, the effect of acute administration of citalopram on colonic sensitivity and on colonic response to feeding was evaluated.

Compared with placebo, citalopram significantly improved abdominal pain, bloating, impact of symptoms on daily life, and overall well-being after 3 and 6 weeks of treatment. However, there was only a modest effect on stool pattern, and changes in depression or anxiety scores were not related to symptom improvement. The effect of acute administration of citalopram during a colonic barostat study did not predict clinical response to the drug. Analysis of the first treatment period as a double-blind, parallel-group study confirmed that citalopram was significantly more beneficial than placebo.

"The SSRI citalopram significantly improves IBS symptoms, including abdominal pain, compared with placebo," the authors write. "The therapeutic effect is independent of effects on anxiety, depression, and colonic sensorimotor function."

Study limitations include criticisms of the crossover design, selection of patients from a tertiary care center only, and inability to determine the mechanism underlying the beneficial effect of citalopram.

"Based on the present study, the SSRI citalopram is a potentially valuable addition to our therapeutic options in IBS," the authors conclude. "Citalopram provided symptomatic benefit of rapid onset, was well tolerated, and was not associated with the side effects of tricyclic antidepressants, such as drowsiness or constipation.... Larger scale studies will be required to study the efficacy of citalopram or other SSRIs in the IBS patient population seen in primary practice and in secondary care."


Gut. 2006;55:1095-1103.


http://www.medscape.com/viewarticle/541393

--------------------
Heather is the Administrator of the IBS Message Boards. She is the author of Eating for IBS and The First Year: IBS, and the CEO of Heather's Tummy Care. Join her IBS Newsletter. Meet Heather on Facebook!

Print     Remind Me     Notify Moderator    

Antibiotic Rifaximin Appears Safe and Effective for Irritable Bowel Syndrome new
      #288017 - 10/26/06 10:29 AM
HeatherAdministrator

Reged: 12/09/02
Posts: 7799
Loc: Seattle, WA

Rifaximin Appears Safe and Effective for Irritable Bowel Syndrome

NEW YORK (Reuters Health) Oct 16 - Treatment with the nonabsorbed oral antibiotic rifaximin for 10 days can improve the symptoms of irritable bowel syndrome (IBS) for up to 10 weeks, findings from a small study suggest.

Previous reports have suggested that alterations in gut flora, primarily bacterial overgrowth, may influence the pathogenesis of irritable bowel syndrome. Therefore, treatment with agents that modify this flora might have an effect on disease outcomes, Dr. Mark Pimentel, from the Cedars-Sinai Medical Center in Los Angeles, and colleagues note in the Annals of Internal Medicine for October 17.

Neomycin therapy has proven useful in reducing IBS symptoms, but the bacterial overgrowth elimination rate is just 25%. By contrast, rifaximin, which has broad-spectrum activity, has been shown to achieve rates as high as 70%.

The present study involved 87 patients with IBS who were randomized to receive rifaximin 400 mg or placebo three times daily for 10 days. In addition to completing IBS-related questionnaires before and 7 days after treatment, the subjects kept weekly symptom diaries for 10 weeks.

Patients treated with rifaximin experienced significantly greater improvements in IBS symptoms than did controls (p = 0.02). This primarily related to a drop in bloating as no major differences were noted between the groups in abdominal pain, diarrhea, or constipation.

Rifaximin was generally well tolerated and was associated with only rare, minor side effects that occurred with similar frequency in the control group.

"The clinical challenge is to identify the subset of patients with IBS who are most likely to have bacterial overgrowth that produces symptoms relative to the many other factors contributing to patients' clinical state," Dr. Douglas A. Drossman, from the University of North Carolina at Chapel Hill, comments in a related editorial.

"Pimentel and colleagues should be congratulated for their efforts to increase awareness of this important subgroup of patients with IBS symptoms who need to be identified and treated. However, until better evidence is available, decisions relating to diagnosis and treatment remain within the art of medicine," he adds.

Ann Intern Med 2006;145:557-563,626-628.


http://www.medscape.com/viewarticle/546127

--------------------
Heather is the Administrator of the IBS Message Boards. She is the author of Eating for IBS and The First Year: IBS, and the CEO of Heather's Tummy Care. Join her IBS Newsletter. Meet Heather on Facebook!

Print     Remind Me     Notify Moderator    

Rifaximin vs Placebo in Reducing Symptoms in Adults With IBS new
      #291305 - 11/26/06 02:39 PM
HeatherAdministrator

Reged: 12/09/02
Posts: 7799
Loc: Seattle, WA

Efficacy of Rifaximin vs Placebo in Reducing Symptoms in Adults With IBS


David A. Johnson, MD, FACG, FACP

The Effect of a Nonabsorbed Oral Antibiotic (Rifaximin) on the Symptoms of the Irritable Bowel Syndrome: A Randomized Trial
Pimentel M, Park S, Mirocha J, Kane SV, Kong Y

Ann Intern Med. 2006;145:557-563

Summary
Irritable bowel syndrome (IBS) is a prevalent condition that has been labeled as a "functional bowel disorder." By this delineation, its cause has been thought to be indefinable. The primary symptoms of this disorder include constipation, diarrhea, abdominal bloating, and cramping. Recent attention has focused on a potential infectious component of IBS.

In this study, Pimental and colleagues investigated the use of rifaximin in patients diagnosed with IBS as defined by the Rome I criteria. Rifaximin is a nonabsorbable, gut-selective antibiotic derived from the rifamycin family that may reduce bacterial overgrowth due to its broad-spectrum activity in vitro against gram-positive, gram-negative, aerobic, anaerobic, and microaerophilic bacteria.

This was a prospective, double-blind randomized controlled trial that involved 43 patients who received 400 mg of rifaximin 3-times daily and 44 who received placebo for 10 days. Patient symptom and stool diaries were completed prior to entry, during the study, and the week following treatment.

Global improvement was found to vary widely across weeks for most patients, and the data were reported as an averaging of the symptoms over all 10 weeks of the study. This percentage was significant as a function of group (P = .020), but not as a function of week (P = .78) or group-by-week (P = .96). The patients in the rifaximin group had a 36.4% improvement in global symptoms compared with 21.0% for the placebo group.

The rifaximin group also reported significantly less bloating on a visual analog scale compared with the placebo group (P = .010), a difference that persisted after controlling for differences between groups in baseline pain scores (P = .001). Besides bloating, none of the secondary endpoints improved with treatment compared with placebo on the visual analog scale: abdominal pain (P = .32), diarrhea (P = .67), and constipation (P = .069).

Viewpoint
Rifaximin is currently US Food and Drug Administration-approved for the treatment of traveler's diarrhea, although these study findings suggest a more expanded potential role for this antibiotic. However, before recommending widespread globalized use of this medication for all patients with IBS, healthcare providers should be aware of several limitations of this study. First, although this was a "multicenter study," there was a considerable imbalance between enrollment from the 2 study sites (83 participants vs 3 participants). Second, because the global measure includes pain, it is important to note that there was an imbalance in baseline pain scores between the 2 patient groups at entry. The imbalance (higher baseline pain scores in the rifaximin group) potentially favors the reduction in the global scores. Additionally, this primary outcome measure is unique in the spectrum of the recent treatment intervention evaluations for IBS trials, and therefore makes comparisons with other trials somewhat difficult. Third, the study authors relied solely on the use of the lactose breath test to define small bowel bacterial overgrowth. Future tests in this area should evaluate the use of other breath tests to define bacterial overgrowth in the small intestine. Fourth, the data suggest that rifaximin may be of more help in the subset of patients with bloating. In IBS, abdominal bloating is reported in more than 50% of patients, and a recent study suggests that changes in abdominal girth can reach 12 cm in more than 50% of patients.[1]

Clearly, this study highlights a new concept in the potential pathogenesis of IBS. An infectious cause may offer a tremendous opportunity to manage an otherwise somewhat frustrating disease -- both for patients and their treating physicians.

Abstract

References
Houghton LA, Lea R, Agrawal A, Reilly B, Whorwell PJ. Relationship of abdominal bloating to distention in irritable bowel syndrome and effect of bowel habit. Gastroenterology. 2006;131:1003-1010.


David A. Johnson, MD, FACG, FACP, Professor of Medicine, Chief of Gastroenterology, Eastern Virginia School of Medicine, Norfolk, Virginia


David A. Johnson, MD, FACG, FACP, has disclosed that he has received grants for clinical research from AstraZeneca, TAP, Wyeth, Novartis, and Abbott, and grants for educational activities from AstraZeneca and Novartis. Dr. Johnson has also disclosed that he has served as an advisor or consultant to AstraZeneca, TAP, and Novartis.


Medscape Gastroenterology. 2006;8(2) ©2006 Medscape

http://www.medscape.com/viewarticle/547055?src=mp

--------------------
Heather is the Administrator of the IBS Message Boards. She is the author of Eating for IBS and The First Year: IBS, and the CEO of Heather's Tummy Care. Join her IBS Newsletter. Meet Heather on Facebook!

Print     Remind Me     Notify Moderator    

Enteric Bacteria and IBS new
      #291306 - 11/26/06 02:51 PM
HeatherAdministrator

Reged: 12/09/02
Posts: 7799
Loc: Seattle, WA

Advances in Functional Gastrointestinal Disorders -- Enteric Bacteria and IBS


Brooks D. Cash, MD, FACP, FACG
Las Vegas, Nevada; Monday, October 23, 2006 --

The functional gastrointestinal disorders (FGIDs), chief among them the irritable bowel syndrome (IBS), are extremely common reasons for seeking healthcare and can be extremely frustrating to patients and clinicians because of the lack of a reliably identifiable pathophysiologic etiology and an even less reliable response to therapy. Considered by many as heterogeneous disorders with a variety of organic and psychological causes, the FGIDs have been the topic of a great deal of groundbreaking research and clinical developments over the last several years. In IBS, organic abnormalities such as abnormal serotonin signaling and homeostasis, altered densities of inflammatory cells and humoral inflammatory mediators, and disturbed visceral proprioception and central processing of pain have all been demonstrated in select groups of patients. More recently, significant attention has been directed toward clarifying the role of intestinal bacteria in the evolution of IBS symptoms. The recognition of postinfectious IBS as a common sequel of acute infectious gastroenteritis,[1] in addition to data demonstrating prevalence values of small intestinal bacterial overgrowth (SIBO) between 30% and 70% in patients with IBS, is driving forward research into the fields of probiotic therapy as well as antibiotic therapy to ease IBS symptoms.[2,3] This report highlights the research in this area, as presented on Monday, October 23, 2006, at the annual scientific meeting of the American College of Gastroenterology (ACG).

Diagnosing SIBO in IBS

The typical methods involved in diagnosing SIBO are breath-test measurements of expired gases after a sugar load (most commonly glucose or lactulose) or small bowel fluid aspiration and culture. The prevalence of SIBO diagnosed via breath testing rages from 10% to as high as 84% in the literature.[4,5] Breath testing can be difficult to perform because of the strict requirements for patient compliance and, in the case of glucose breath testing, variability in the absorption of glucose. Similarly, the gold standard, jejunal aspirate and culture, is limited by the invasiveness of the procedure and the anatomic extent of aspirating tube advancement, usually to the proximal 40-60 cm of the small intestine. Several investigators reported their experience with each of these diagnostic techniques during this year's ACG meeting. Bratten and colleagues[6] from Northwestern University in Chicago, Illinois, performed lactulose breath testing (for hydrogen [H+] and methane [CH4+]) in 175 patients with IBS and 23 non-IBS controls. They found that 21% (37/175) of the IBS patients produced CH4+ compared with 9% (2/23) of controls (P = .16). They also found that patients who had CH4+-positive breath tests were more than twice as likely as CH4+-negative IBS patients to have constipation as their predominant stool pattern (odds ratio [OR] = 2.61; 95% confidence interval [CI]: 1.24-5.54; P = .01) and were significantly less likely to have diarrhea (OR = 0.28; 95% CI: 0.13-0.63; P = .001). The observation that CH4+-positive breath tests correlate with constipation has been made by other investigators, but the mechanisms underlying the association between CH4+ and constipation remain poorly understood.[7]

Ruff and colleagues[8] from the Mayo Clinic College of Medicine in Rochester, Minnesota, reported the results of a retrospective analysis of clinical parameters and results of duodenal aspirate culture in 690 patients. Using the criteria of > 100,000 colony-forming units (cfu)/mL of aspirate for the diagnosis of SIBO, these investigators failed to detect an increased prevalence of SIBO in patients with diagnosed IBS or the symptom of bloating. These results contrast with previous reports using less restrictive cfu/mL criteria for the diagnosis of SIBO, and should be viewed cautiously. Potential pitfalls in this analysis include that many of the patients were taking narcotics, a systematic program of aspiration in patients with IBS was not undertaken, and the duodenal aspirates may not be adequate to rule out distal SIBO.

Bacterial Overgrowth -- Is it Hype or Hope?

During a clinical symposium convened during this year's ACG meeting, leading experts in the field addressed issues surrounding the diagnosis of SIBO and the use of antibiotics and probiotics.[9-11] Dr. Jack DiPalma[9] opened the symposium with a discussion of bacterial overgrowth. He highlighted some of the clinical conditions that predispose patients to bacterial overgrowth, such as postsurgical states, age extremes, and motility abnormalities, as well as the symptoms of overgrowth such as chronic diarrhea, malabsorption, and nutrient deficiencies. He touched on the various diagnostic tests for bacterial overgrowth and identified the best predictive factors among these tests: fasting elevations in H+ or CH4+, a positive 14C D-xylose test, or jejunal culture with > 105 cfu/mL. Dr. DiPalma also discussed the well-known limits of the so-called "gold standard" of small bowel fluid aspiration and culture, which include the invasive nature of the test, oral floral contamination, culture transport difficulties, limited access to the distal small bowel, and the unclear relevance of colonization in the elderly. He concluded by reviewing the ideal testing measures that should be present when testing for bacterial overgrowth. These include measuring both H+ and CH4+, using a standard dose of breath-test substrate, confirming the fasting state of patients undergoing testing when fasting elevations are found during fructose or glucose testing, and the need to test before a colon cleansing (or waiting for at least 30 days after a colon cleansing to test).

Dr. Lawrence Schiller[10] followed with a discussion of prebiotics and probiotics. It is interesting to note that there are more than 1015 bacteria in the human gut, of which 500 different species have been identified and one third have been cultured. In comparison, the average human body contains approximately 1014 cells. The bacteria have been selected, through the innate immune system (that part of the immune system that responds to immunogenic patterns rather than specific antigens), to coexist in the gut and provide for enterocyte nutrients, vitamin production, defense against pathogenic bacteria, and to modulate mucosal inflammation and permeability. Prebiotics are substances that can be ingested and which foster bacterial growth, and include fructo-oligosaccharides, inulin, and lactulose. Very few data exist regarding the role of prebiotics as therapies for IBS. The probiotics are live organisms that can be ingested for health benefits, but there is little theoretical basis for the selection of particular strains of probiotics, and the exact contributions of probiotics to intestinal health are unknown. Examples of probiotics include Lactobacillus and Bifidobacterium species and Escherichia coli Nissle 1917. Yeasts such as Saccharomyces species can also be used as probiotic therapy. Potential mechanisms of action for probiotics include displacement of pathogens, enhancement of bacterial function, and modification of signaling. Although complications of probiotic therapy are rare and some mixtures have been reported to improve IBS symptoms, many unanswered questions remain. These include whether live organisms need to be ingested, whether enteric colonization occurs, the ideal duration of therapy, and what biochemical signatures are most predictive of treatment success.

Dr. Mark Pimentel[11] concluded the symposium with a discussion of the rationale for the use of antibiotics in IBS. He eloquently presented the evidence for the role of enteric bacteria in the etiology of IBS symptoms and how intrinsic or extrinsic factors can produce alterations in the normal motility pattern of the gut, leading to abnormal levels of enteric bacteria which then induce inflammation and/or further alterations in gut function through the elaboration of H+ and/or CH4+. Dr. Pimentel then reviewed the evidence supporting the use of antibiotics, often in combination with promotility agents such as tegaserod, for the effective treatment of IBS. The promotility agents are used to promote more effective peristalsis and intestinal stripping waves and may have a role in preventing recurrence, although this concept has not been studied rigorously. When used for this purpose, tegaserod is usually administered at a lower dose (2 mg) and in a fasting state (every night at bedtime) rather than the standard regimen used in the settings of IBS with constipation and chronic constipation (6 mg twice daily) in order to minimize potential motility-related side effects such as diarrhea. Although it is clear that there is much that we do not know regarding the role and effects of modulation of the enteric flora in patients with IBS, this is a very exciting corner of the IBS world and additional data are eagerly awaited.

One of the overarching concerns surrounding the use of probiotics is their safety. In another abstract presented during this meeting, Adler and colleagues[12] reported results of a safety study evaluating the effects of the probiotic E coli strain M-17 in 138 healthy individuals. Subjects ingested 120 mL/day of E coli strain M-17 every day for 8 weeks, a dose that represents a 10-fold increase over standard dosing regimens. The M-17 was generally well tolerated, with associated adverse events seen in 6.5% of patients, most of which were mild. Multiple laboratory parameters were followed, and although there were some changes from baseline, all laboratory values remained within normal limits. Additional clinical data reflecting effects on symptoms in patients with IBS are eagerly awaited.

Concluding Remarks
The field of FGIDs continues to generate meaningful and important research. Emerging data surrounding the role of enteric bacteria in the origin of IBS symptoms are among the hottest topics in this field. During this year's ACG meeting, excellent overviews and original research were presented regarding the yield of diagnostic maneuvers for the detection of SIBO and the various treatment approaches to IBS involving the manipulation of the intestinal flora; such data will no doubt add to this controversial growing body of literature.

References
Halvorson H, Schlett CD, Riddle MS. Postinfectious irritable bowel syndrome--a meta-analysis Am J Gastroenterol. 2006;101:1-6.
Whorwell PJ, Altringer L, Morel J, et al. Efficacy of an encapsulated probiotic Bifidobacterium infantis 35624 in women with irritable bowel syndrome. Am J Gastroenterol. 2006;101:1581-1590. Abstract
Pimentel M, Park S, Mirocha J, et al. The effect of a nonabsorbed oral antibiotic (rifaximin) on the symptoms of the irritable bowel syndrome: a randomized trial. Ann Intern Med. 2006;145:557-563. Abstract
Harris LA, Crowell MD, DiBaise JK, et al. Is small intestinal bacterial overgrowth (SIBO) really prevalent in irritable bowel syndrome (IBS)? Am J Gastroenterol. 2005;100:S336.
Pimentel M, Chow EJ, Lin HC. Normalization of lactulose breath testing correlates with symptom improvement in irritable bowel syndrome. a double-blind, randomized, placebo-controlled study. Am J Gastroenterol. 2003;98:412-419. Abstract
Bratten J, Spanier J, Jones MP Lactulose hydrogen breath testing (LHBT) in patients with IBS and controls: differences in methane (CH4) but not hydrogen (H2). Am J Gastroenterol. 2006;101;S479. [Abstract 1236]
Pimental M, Lin H, Enayati P, et al. Methane, a gas produced by enteric bacteria, slows intestinal transit and augments small intestinal contractile activity. Am J Physiol Gastrointest Liver Physiol. 2006;290:G1089-G1095. Abstract
Ruff KC, Saio-Loftus YA, Locke GR, et al. Failure to detect association with irritable bowel syndrome (IBS) and small intestinal bacterial overgrowth (SIBO). Am J Gastroenterol. 2006;101;S486. [Abstract 1261]
DiPalma JA. Diagnosis and treatment of bacterial overgrowth. In: ACG Clinical Symposium: Bacterial Overgrowth: Hype or Hope. Program and abstracts of the American College of Gastroenterology 2006 Annual Scientific Meeting and Postgraduate Course; October 20-25, 2006; Las Vegas, Nevada.
Schiller LR. Prebiotics and probiotics. In: ACG Clinical Symposium: Bacterial Overgrowth: Hype or Hope. Program and abstracts of the American College of Gastroenterology 2006 Annual Scientific Meeting and Postgraduate Course; October 20-25, 2006; Las Vegas, Nevada.
Pimentel M. IBS: Is SBO really a factor? In: ACG Clinical Symposium: Bacterial Overgrowth: Hype or Hope. Program and abstracts of the American College of Gastroenterology 2006 Annual Scientific Meeting and Postgraduate Course; October 20-25, 2006; Las Vegas, Nevada.
Adler SN, Jacob H, Levine L. An open label, high dose prospective trial of the safety of the probiotic E. coli strain M-17 in healthy volunteers. Am J Gastroenterol. 2006;101:S134. [Abstract 273]




Copyright © 2006 Medscape.

http://www.medscape.com/viewarticle/546502

--------------------
Heather is the Administrator of the IBS Message Boards. She is the author of Eating for IBS and The First Year: IBS, and the CEO of Heather's Tummy Care. Join her IBS Newsletter. Meet Heather on Facebook!

Print     Remind Me     Notify Moderator    

Neuromuscular Dysfunction and IBS: Clinical Implications for Drug Use new
      #298897 - 02/04/07 04:30 PM
HeatherAdministrator

Reged: 12/09/02
Posts: 7799
Loc: Seattle, WA

Neuromuscular Dysfunction and IBS: Clinical Implications
Brooks D. Cash, MD, FACP, FACG

Conclusion
The heterogeneity in the pathogenesis of IBS creates unique challenges when designing and assessing the efficacy of novel therapies. As our knowledge continues to evolve regarding the various factors that may play a role in causing symptoms of IBS, so too will our approach to designing effective therapies. For the foreseeable future, it is unlikely that there will be a "magic bullet" for IBS sufferers. Given our current level of understanding, the practice of subgrouping IBS patients on the basis of predominant bowel pattern is a good first step, but clearly it is not the final answer to defining which drugs will be most effective for which patients. As the process of new drug discovery proceeds, emphasis should be placed not only on how often or how much a drug improves global and individual symptoms in IBS sufferers, but also on ways in which the clinician can identify the subset of patients most likely to benefit from a specific drug. This strategy will not only allow the clinician to more effectively treat his/her patients, but should allow scientists to add further pieces to the ever evolving puzzle of IBS.

http://www.medscape.com/viewarticle/548600_4

Medscape Gastroenterology. 2006;8(2) ©2006 Medscape

--------------------
Heather is the Administrator of the IBS Message Boards. She is the author of Eating for IBS and The First Year: IBS, and the CEO of Heather's Tummy Care. Join her IBS Newsletter. Meet Heather on Facebook!

Print     Remind Me     Notify Moderator    

Antidepressant Therapy (Imipramine and Citalopram) for Irritable Bowel Syndrome new
      #309446 - 06/20/07 01:56 PM
HeatherAdministrator

Reged: 12/09/02
Posts: 7799
Loc: Seattle, WA

Dig Dis Sci. 2007 May 15;

Antidepressant Therapy (Imipramine and Citalopram) for Irritable Bowel Syndrome: A Double-Blind, Randomized, Placebo-Controlled Trial.

Talley NJ, Kellow JE, Boyce P, Tennant C, Huskic S, Jones M.
Department of Medicine, Nepean Hospital, University of Sydney, Sydney, NSW, Australia.

BACKGROUND: The efficacy of antidepressants in irritable bowel syndrome (IBS) is controversial. No trials have directly compared a tricyclic with a selective serotonin reuptake inhibitor. Our aim was to determine whether imipramine and citalopram are efficacious in IBS.

METHODS: This was a randomized, double-blind, placebo-controlled, parallel group pilot trial with imipramine (50 mg) and citalopram (40 mg).

RESULTS: Of 51 IBS patients randomized, baseline characteristics were comparable among the treatment arms; the majority was diarrhea-predominant. Adequate relief of IBS symptoms (primary endpoint) was similar for each treatment arm. Improvements in bowel symptom severity rating for interference (P = 0.05) and distress (P = 0.02) were greater with imipramine versus placebo, but improvements in abdominal pain were not. There was a greater improvement in depression score (P = 0.08) and in the SF-36 Mental Component Score (P = 0.07), with imipramine. Citalopram was not superior to placebo. Approximately 20% of the variance in scores was explained by treatment differences for abdominal pain, bowel symptom severity disability, depression and the mental component of the SF-36.

CONCLUSION: Neither imipramine nor citalopram significantly improved global IBS endpoints over placebo.

PMID: 17503182 [PubMed - as supplied by publisher]

http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&Cmd=ShowDetailView&TermToSearch=17503182&ordinalpos=40&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum

--------------------
Heather is the Administrator of the IBS Message Boards. She is the author of Eating for IBS and The First Year: IBS, and the CEO of Heather's Tummy Care. Join her IBS Newsletter. Meet Heather on Facebook!

Print     Remind Me     Notify Moderator    

FDA permits the restricted use of Zelnorm new
      #312922 - 08/09/07 11:41 AM
HeatherAdministrator

Reged: 12/09/02
Posts: 7799
Loc: Seattle, WA

Under an investigational new drug protocol program, restricted use of tegaserod maleate has been approved to benefit certain patients who have no other treatment options. Under the protocol, tegaserod may only be used to treat irritable bowel syndrome with constipation and chronic idiopathic constipation in women younger than 55 years who have had no satisfactory response to other available treatments or had satisfactory improvement of symptoms during prior tegaserod therapy.

Key exclusion criteria for tegaserod use include a history or current diagnosis of cardiovascular ischemic disease, symptoms suggestive of cardiovascular ischemic disease, the presence of any cardiovascular risk factors according to National Institutes for Health guidelines, and uncompensated depression or anxiety or suicidal ideation or behavior. Tegaserod will remain off the market for general use.

http://www.fda.gov/cder/drug/infopage/zelnorm/default.htm



--------------------
Heather is the Administrator of the IBS Message Boards. She is the author of Eating for IBS and The First Year: IBS, and the CEO of Heather's Tummy Care. Join her IBS Newsletter. Meet Heather on Facebook!

Print     Remind Me     Notify Moderator    

Role of Antibiotics vs Conventional Pharmacotherapy in Treating Symptoms of Irritable Bowel Syndrome
      #321612 - 01/03/08 04:45 PM
HeatherAdministrator

Reged: 12/09/02
Posts: 7799
Loc: Seattle, WA

Review Article: The Role of Antibiotics vs Conventional Pharmacotherapy in Treating Symptoms of Irritable Bowel Syndrome

C. L. Frissora; B. D. Cash

Conclusion: Antibiotics are an emerging therapeutic option for IBS, and many questions surrounding the exact role of enteric bacteria in the diagnosis and management of IBS remain unanswered. Results to date suggest that appropriately targeted antibiotic therapy may offer important benefits as an alternative to, or in addition to, symptom-directed pharmacotherapies in the treatment of IBS. Clear demonstration of superiority of one treatment approach over another will require a suitably designed, randomized, placebo-controlled trial. Given the breadth of the IBS symptom spectrum and current limitations in symptom-directed therapies related to adverse effects and blinding, it is unlikely that such a trial will be conducted. More likely, continued reports of efficacy with directed antibiotic therapy in patients with symptoms consistent with IBS or other functional GI disorders will lead to the complementary use of these medications in a stepwise or combined fashion. The potential benefit of antibiotics in diminishing the need for chronic daily pharmacotherapy or reducing the frequency of repeated courses of therapy in IBS warrants additional exploration.

Aliment Pharmacol Ther. 2007;25(11):1271-1281. ©2007 Blackwell Publishing


http://www.medscape.com/viewarticle/557851_4

--------------------
Heather is the Administrator of the IBS Message Boards. She is the author of Eating for IBS and The First Year: IBS, and the CEO of Heather's Tummy Care. Join her IBS Newsletter. Meet Heather on Facebook!

Print     Remind Me     Notify Moderator    

Pages: 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | (show all)

Extra information
0 registered and 24 anonymous users are browsing this forum.

Moderator:  Heather 

Print Thread

Permissions
      You cannot post until you login
      You cannot reply until you login
      HTML is enabled
      UBBCode is enabled

Thread views: 500233

Jump to

| Privacy statement Help for IBS Home

*
UBB.threads™ 6.2


HelpForIBS.com BBB Business Review