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Dive into the research topics where Lani Prideaux is active.

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Featured researches published by Lani Prideaux.


The Lancet | 2015

Crohn's disease management after intestinal resection: a randomised trial.

Peter De Cruz; Michael A. Kamm; Amy L. Hamilton; Kathryn J. Ritchie; Efrosinia O. Krejany; Alexandra Gorelik; Danny Liew; Lani Prideaux; Ian C. Lawrance; Jane M. Andrews; Peter A. Bampton; Peter R. Gibson; Miles Sparrow; Rupert W. Leong; Timothy H. Florin; Richard B. Gearry; Graham L. Radford-Smith; Finlay Macrae; Henry Debinski; Warwick Selby; Ian Kronborg; Michael J. Johnston; Rodney Woods; P. Ross Elliott; Sally Bell; Steven J. Brown; William Connell; Paul V. Desmond

BACKGROUND Most patients with Crohns disease need an intestinal resection, but a majority will subsequently experience disease recurrence and require further surgery. This study aimed to identify the optimal strategy to prevent postoperative disease recurrence. METHODS In this randomised trial, consecutive patients from 17 centres in Australia and New Zealand undergoing intestinal resection of all macroscopic Crohns disease, with an endoscopically accessible anastomosis, received 3 months of metronidazole therapy. Patients at high risk of recurrence also received a thiopurine, or adalimumab if they were intolerant to thiopurines. Patients were randomly assigned to parallel groups: colonoscopy at 6 months (active care) or no colonoscopy (standard care). We used computer-generated block randomisation to allocate patients in each centre to active or standard care in a 2:1 ratio. For endoscopic recurrence (Rutgeerts score ≥i2) at 6 months, patients stepped-up to thiopurine, fortnightly adalimumab with thiopurine, or weekly adalimumab. The primary endpoint was endoscopic recurrence at 18 months. Patients and treating physicians were aware of the patients study group and treatment, but central reading of the endoscopic findings was undertaken blind to the study group and treatment. Analysis included all patients who received at least one dose of study drug. This trial is registered with ClinicalTrials.gov, number NCT00989560. FINDINGS Between Oct 13, 2009, and Sept 28, 2011, 174 (83% high risk across both active and standard care groups) patients were enrolled and received at least one dose of study drug. Of 122 patients in the active care group, 47 (39%) stepped-up treatment. At 18 months, endoscopic recurrence occurred in 60 (49%) patients in the active care group and 35 (67%) patients in the standard care group (p=0.03). Complete mucosal normality was maintained in 27 (22%) of 122 patients in the active care group versus four (8%) in the standard care group (p=0.03). In the active care arm, of those with 6 months recurrence who stepped up treatment, 18 (38%) of 47 patients were in remission 12 months later; conversely, of those in remission at 6 months who did not change therapy recurrence occurred in 31 (41%) of 75 patients 12 months later. Smoking (odds ratio [OR] 2.4, 95% CI 1.2-4.8, p=0.02) and the presence of two or more clinical risk factors including smoking (OR 2.8, 95% CI 1.01-7.7, p=0.05) increased the risk of endoscopic recurrence. The incidence and type of adverse and severe adverse events did not differ significantly between patients in the active care and standard care groups (100 [82%] of 122 vs 45 [87%] of 52; p=0.51) and (33 [27%] of 122 vs 18 [35%] of 52; p=0.36), respectively. INTERPRETATION Treatment according to clinical risk of recurrence, with early colonoscopy and treatment step-up for recurrence, is better than conventional drug therapy alone for prevention of postoperative Crohns disease recurrence. Selective immune suppression, adjusted for early recurrence, rather than routine use, leads to disease control in most patients. Clinical risk factors predict recurrence, but patients at low risk also need monitoring. Early remission does not preclude the need for ongoing monitoring. FUNDING AbbVie, Gutsy Group, Gandel Philanthropy, Angior Foundation, Crohns Colitis Australia, and the National Health and Medical Research Council.


Journal of Gastroenterology and Hepatology | 2012

Inflammatory bowel disease in Asia: a systematic review.

Lani Prideaux; Michael A. Kamm; Peter De Cruz; Francis K.L. Chan; Siew C. Ng

The incidence and prevalence of inflammatory bowel diseases (IBD), Crohns disease (CD) and ulcerative colitis (UC), are lower in Asia than in the West. However, across Asia the incidence and prevalence of IBD has increased rapidly over the last two to four decades. These changes may relate to increased contact with the West, westernization of diet, increasing antibiotics use, improved hygiene, vaccinations, or changes in the gut microbiota. Genetic factors also differ between Asians and the Caucasians. In Asia, UC is more prevalent than CD, although CD incidence is rapidly increasing in certain areas. There is a male predominance of CD in Asia, but a trend towards equal sex distribution for UC. IBD is diagnosed at a slightly older age than in the West, and there is rarely a second incidence peak as in the West. A positive family history is much less common than in the West, as are extra‐intestinal disease manifestations. There are clear ethnic differences in incidence within countries in Asia, and an increased incidence in IBD in migrants from Asia to the West. Research in Asia, an area of rapidly changing IBD epidemiology, may lead to the discovery of critical etiologic factors that lead to the development of IBD.


Inflammatory Bowel Diseases | 2012

Serological antibodies in inflammatory bowel disease: a systematic review.

Lani Prideaux; Peter De Cruz; Siew C. Ng; Michael A. Kamm

&NA; The diagnosis of inflammatory bowel disease (IBD) is traditionally based on a combination of clinical, endoscopic, histological, and radiological criteria. However, further testing is needed in cases of diagnostic uncertainty and in predicting disease course. This systematic review focuses on the potential for 10 serological antibodies to fill these roles: pANCA, ASCA, anti‐OmpC, anti‐CBir1, anti‐I2, ALCA, ACCA, AMCA, anti‐L, and anti‐C. We discuss their prevalence in IBD and health; their role in disease diagnosis and risk stratification; their stability over time; their presence in unaffected relatives; their association with genetic variants; and differences across ethnic groups. Serological antibodies have some role in primary diagnosis and in differentiating between Crohns disease and ulcerative colitis. In indeterminate colitis, preoperative measurement of serological antibodies can help to predict the likelihood of complications among patients undergoing pouch surgery. The combined presence and magnitude of a large panel of antibodies appear to be of value in predicting disease progression. There is currently insufficient evidence to recommend the use of antibody testing to predict responses to treatment or surgery in patients with IBD. (Inflamm Bowel Dis 2011;)


Inflammatory Bowel Diseases | 2012

Postoperative recurrent luminal Crohn's Disease: A systematic review

Peter De Cruz; Michael A. Kamm; Lani Prideaux; Patrick B. Allen; Paul V. Desmond

Despite improved immunosuppressive therapy, surgical resection is still often required for uncontrolled inflammatory disease and the stenosing and perforating complications of Crohns disease. However, surgery is not curative. A majority of patients develop disease recurrence at or above the anastomosis. Subclinical endoscopically identifiable recurrence precedes the development of clinical symptoms; identification and treatment of early mucosal recurrence may therefore prevent clinical recurrence. Therapy to achieve mucosal healing should now be the focus of postoperative therapy. A number of clinical risk factors for the development of earlier postoperative recurrence have been identified, and reasonable evidence is now available regarding the efficacy of drug therapies in preventing recurrence. This evidence now needs to be incorporated into prospective treatment strategies.


Inflammatory Bowel Diseases | 2013

Mucosal healing in Crohn's disease: a systematic review.

Peter De Cruz; Michael A. Kamm; Lani Prideaux; Patrick B. Allen; Gregory Thomas Charles Moore

Abstract:The traditional goals of Crohns disease therapy, to induce and maintain clinical remission, have not clearly changed its natural history. In contrast, emerging evidence suggests that achieving and maintaining mucosal healing may alter the natural history of Crohns disease, as it has been associated with more sustained clinical remission and reduced rates of hospitalization and surgical resection. Induction and maintenance of mucosal healing should therefore be a goal toward which therapy is now directed. Unresolved issues pertain to the benefit of achieving mucosal healing at different stages of the disease, the relationship between mucosal healing and transmural inflammation, the intensity of treatment needed to achieve mucosal healing when it has not been obtained using standard therapy, and the means by which mucosal healing is defined using current endoscopic disease activity indices. The main clinical challenge relates to defining the means of achieving high rates of mucosal healing in clinical practice.


Inflammatory Bowel Diseases | 2012

Characterization of the gastrointestinal microbiota in health and inflammatory bowel disease

Peter De Cruz; Lani Prideaux; Josef Wagner; Siew C. Ng; Chris McSweeney; Carl D. Kirkwood; Mark Morrison; Michael A. Kamm

&NA; The enteric bacterial flora play a key role in maintaining health. Inflammatory bowel disease is associated with quantitative and qualitative alterations in the microbiota. Early characterization of the microbiota involved culture‐dependent techniques. The advent of metagenomic techniques, however, allows for structural and functional characterization using culture‐independent methods. Changes in diversity, together with quantitative alterations in specific bacterial species, have been identified. The functional significance of these changes, and their pathogenic role, remain to be elucidated. (Inflamm Bowel Dis 2011;)


Journal of Gastroenterology and Hepatology | 2015

Association between specific mucosa‐associated microbiota in Crohn's disease at the time of resection and subsequent disease recurrence: A pilot study

Peter De Cruz; Seungha Kang; Josef Wagner; Michael Buckley; Winnie H. Sim; Lani Prideaux; Trevor Lockett; Chris McSweeney; Mark Morrison; Carl D. Kirkwood; Michael A. Kamm

Crohns disease pathogenesis involves alterations in the gut microbiota. We characterized the mucosa‐associated microbiota at the time of surgical resection and 6 months later to identify bacterial profiles associated with recurrence and remission.


Inflammatory Bowel Diseases | 2013

Impact of ethnicity, geography, and disease on the microbiota in health and inflammatory bowel disease.

Lani Prideaux; Seungha Kang; Josef Wagner; Michael Buckley; Jackie E. Mahar; De Cruz P; Zezhang Wen; Liping Chen; Bing Xia; van Langenberg Dr; Trevor Lockett; Siew C. Ng; Joseph J.Y. Sung; Paul V. Desmond; Christopher S. McSweeney; Mark Morrison; Carl D. Kirkwood; Michael A. Kamm

Background:The gut microbiota is central to health and disorders such as inflammatory bowel disease. Differences in microbiota related to geography and ethnicity may hold the key to recent changes in the incidence of microbiota-related disorders. Methods:Gut mucosal microbiota was analyzed in 190 samples from 87 Caucasian and Chinese subjects, from Australia and Hong Kong, comprising 22 patients with Crohns disease, 30 patients with ulcerative colitis, 29 healthy controls, and 6 healthy relatives of patients with Crohns disease. Bacterial 16S rRNA microarray and 454 pyrosequencing were performed. Results:The microbiota was diverse in health, regardless of ethnicity or geography (operational taxonomic unit number and Shannon diversity index). Ethnicity and geography, however, did affect microbial composition. Crohns disease resulted in reduced bacterial diversity, regardless of ethnicity or geography, and was the strongest determinant of composition. In ulcerative colitis, diversity was reduced in Chinese subjects only, suggesting that ethnicity is a determinant of bacterial diversity, whereas composition was determined by disease and ethnicity. Specific phylotypes were different between health and disease. Chinese patients with inflammatory bowel disease more often than healthy Chinese tended to have had a Western diet in childhood, in the East and West. Conclusion:The healthy microbiota is diverse but compositionally affected by geographical and ethnic factors. The microbiota is substantially altered in inflammatory bowel disease, but ethnicity may also play an important role. This may be key to the changing epidemiology in developing countries, and emigrants to the West.


Alimentary Pharmacology & Therapeutics | 2015

Efficacy of thiopurines and adalimumab in preventing Crohn's disease recurrence in high‐risk patients – a POCER study analysis

P. De Cruz; Michael A. Kamm; Amy L. Hamilton; Kathryn J. Ritchie; Efrosinia O. Krejany; Alexandra Gorelik; Danny Liew; Lani Prideaux; Ian C. Lawrance; Jane M. Andrews; Peter A. Bampton; Simon Jakobovits; Timothy H. Florin; Peter R. Gibson; Henry Debinski; Richard B. Gearry; Finlay Macrae; Rupert W. Leong; Ian Kronborg; Graham L. Radford-Smith; Warwick Selby; Michael J. Johnston; R. Woods; Peter R. Elliott; Sally Bell; Steven J. Brown; William Connell; Paul V. Desmond

Crohns disease recurs in the majority of patients after intestinal resection.


Colorectal Disease | 2013

Postoperative recurrence of Crohn's disease: impact of endoscopic monitoring and treatment step-up.

P. De Cruz; M.‐P. Bernardi; Michael A. Kamm; Patrick B. Allen; Lani Prideaux; J. Williams; Michael J. Johnston; J. Keck; Richard Brouwer; Alexander G. Heriot; R. Woods; Steven J. Brown; Sally Bell; Ross Elliott; William Connell; Paul V. Desmond

Aim  Eighty per cent of patients with Crohn’s disease require surgery, of whom 70% will require a further operation. Recurrence occurs at the anastomosis. Although often recommended, the impact of postoperative colonoscopy and treatment adjustment is unknown.

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Michael A. Kamm

St. Vincent's Health System

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William Connell

St. Vincent's Health System

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Steven J. Brown

St. Vincent's Health System

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Sally Bell

St. Vincent's Health System

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Amy L. Hamilton

St. Vincent's Health System

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Ian C. Lawrance

University of Western Australia

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Henry Debinski

St. Vincent's Health System

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Kathryn J. Ritchie

St. Vincent's Health System

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