M. G. Bramble
James Cook University Hospital
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Featured researches published by M. G. Bramble.
British Journal of Cancer | 2012
Gill; M. G. Bramble; Colin Rees; T. J. W. Lee; Dm Bradburn; S. J. Mills
Background:The NHS Bowel Cancer Screening Programme (BCSP) offers biennial faecal occult blood testing (FOBt) followed by colonoscopy after positive results. Colorectal cancers (CRCs) registered with the Northern Colorectal Cancer Audit Group database were cross-referenced with the BCSP database to analyse their screening history.Methods:The CRCs in the screening population between April 2007 and March 2010 were identified and classified into four groups: control (diagnosed before first screening invite), screen-detected, interval (diagnosed between screening rounds after a negative FOBt), and non-uptake (declined screening). Patient demographics, tumour characteristics and survival were compared between groups.Results:In all, 511 out of 1336 (38.2%) CRCs were controls; 825 (61.8%) were in individuals invited for screening of which 322 (39.0%) were screen detected, 311 (37.7%) were in the non-uptake group, and 192 (23.3%) were interval cancers. Compared with the control and interval cancer group, the screen-detected group had a higher proportion of men (P=0.002, P=0.003 respectively), left colon tumours (P=0.007, P=0.003), and superior survival (both P<0.001). There was no difference in demographics, tumour location/stage, or survival between control and interval groups.Conclusion:The FOBt is better at detecting cancers in the left colon and in men. The significant numbers of interval cancers weren’t found to have an improved outcome compared with the non-screened population.
Alimentary Pharmacology & Therapeutics | 2003
Martin Prince; H. C. Mitchison; D. Ashley; D. A. Burke; N. Edwards; M. G. Bramble; Oliver F. W. James; David Jones
Background : We have previously reported, in an uncontrolled trial, an improvement in fatigue scores in patients with primary biliary cirrhosis given oral antioxidant supplementation. We now present data from a controlled trial.
Journal of Gastroenterology and Hepatology | 1999
Jonathan P Watson; David Jones; Oliver F. W. James; Paul A Cann; M. G. Bramble
Background : The symptoms of the chronic cholestatic liver disease primary biliary cirrhosis (PBC), in particular fatigue and chronic pruritus, adversely affect quality of life and respond only poorly to treatment. Recent studies have suggested that oxidative stress may play a role in tissue damage in cholestatic liver disease and may contribute to symptoms, such as fatigue. We have, therefore, examined, in an open‐label pilot study, the therapeutic effects of antioxidant medication on the biochemistry and symptomatology of PBC.
British Journal of Cancer | 2014
Gill; M. G. Bramble; Mark A. Hull; S. J. Mills; Eva Morris; Dm Bradburn; Y Bury; Parker Ce; T J W Lee; Colin Rees
Background:Colorectal cancers (CRCs) detected through the NHS Bowel Cancer Screening Programme (BCSP) have been shown to have a more favourable outcome compared to non-screen-detected cancers. The aim was to identify whether this was solely due to the earlier stage shift of these cancers, or whether other factors were involved.Methods:A combination of a regional CRC registry (Northern Colorectal Cancer Audit Group) and the BCSP database were used to identify screen-detected and interval cancers (diagnosed after a negative faecal occult blood test, before the next screening round), diagnosed between April 2007 and March 2010, within the North East of England. For each Dukes’ stage, patient demographics, tumour characteristics, and survival rates were compared between these two groups.Results:Overall, 322 screen-detected cancers were compared against 192 interval cancers. Screen-detected Dukes’ C and D CRCs had a superior survival rate compared with interval cancers (P=0.014 and P=0.04, respectively). Cox proportional hazards regression showed that Dukes’ stage, tumour location, and diagnostic group (HR 0.45, 95% CI 0.29–0.69, P<0.001 for screen-detected CRCs) were all found to have a significant impact on the survival of patients.Conclusions:The improved survival of screen-detected over interval cancers for stages C and D suggest that there may be a biological difference in the cancers in each group. Although lead-time bias may have a role, this may be related to a tumour’s propensity to bleed and therefore may reflect detection through current screening tests.
Alimentary Pharmacology & Therapeutics | 2005
Alastair Forbes; A. Al-Damluji; S. Ashworth; M. G. Bramble; K. Herbert; J. Ho; J. Y. Kang; R. Przemioslo; A. Shetty
Background : 5‐Aminosalicylates remain important in the treatment of ulcerative colitis, but it is uncertain if the various preparations currently available are equivalent given the different delivery systems that exist. Generic prescription of mesalazine (mesalamine) is therefore inappropriate. Ipocol has recently become available as an alternative to Asacol‐MR.
Alimentary Pharmacology & Therapeutics | 2004
S. J. Panter; H. O'Flanagan; M. G. Bramble; A. P. S. Hungin
Background : Upper gastrointestinal cancer carries a poor prognosis. Although the incidence of gastric adenocarcinoma is falling, oesophageal adenocarcinoma is increasing. This has been attributed to an increasing prevalence of gastro‐oesophageal reflux disease, commonly treated empirically in primary care with antisecretory drugs. Treatment has been associated with delayed diagnosis but it is unclear if this influences prognosis.
Colorectal Disease | 2012
P. T. Rajasekhar; Matt Rutter; M. G. Bramble; Douglas Wilson; James E. East; J. R. Greenaway; Brian P. Saunders; T. J. W. Lee; R. Barton; A. P. S. Hungin; Colin Rees
Aim Completeness and thoroughness of colonoscopy are measured by the caecal intubation rate (CIR) and the adenoma detection rate (ADR). National standards are ≥ 90% and ≥ 10% respectively. Variability in CIR and ADR have been demonstrated but comparison between individuals and units is difficult. We aimed to assess the performance of colonoscopy in endoscopy units in the northeast of England.
Gastrointestinal Endoscopy | 2012
Praveen T. Rajasekhar; Colin Rees; Matthew D. Rutter; Brian P. Saunders; M. G. Bramble; Pali Hungin; James E. East
1. Blomberg J, Lagergren P, Martin L, et al. Albumin and C-reactive protein levels predict short-term mortality after percutaneous endoscopic gastrostomy in a prospective cohort study. Gastrointest Endosc 2011;73: 29-36. 2. McMillan DC, Crozier JE, Canna K, et al. Evaluation of an inflammationbased prognostic score (GPS) in patients undergoing resection for colon and rectal cancer. Int J Colorectal Dis 2007;22:881-6. 3. Forrest LM, McMillan DC, McArdle CS, et al. Evaluation of cumulative prognostic scores based on the systemic inflammatory response in patients with inoperable non-small-cell lung cancer. Br J Cancer 2003;89: 1028-30. 4. McMillan DC. An inflammation-based prognostic score and its role in the nutrition-based management of patients with cancer. Proc Nutr Soc 2008;67:257-62. 5. Moyes LH, Leitch EF, McKee RF, et al. Preoperative systemic inflammation predicts postoperative infectious complications in patients undergoing curative resection for colorectal cancer. Br J Cancer 2009;100:1236-9. 6. Ishizuka M, Nagata H, Takagi K, et al. Influence of inflammation-based prognostic score on mortality of patients undergoing chemotherapy for far advanced or recurrent unresectable colorectal cancer. Ann Surg 2009; 250:268-72. 7. Pfitzner T, Krocker D, Perka C, et al. C-reactive protein. an independent risk factor for the development of infection after primary arthroplasty [German]. Orthopade 2008;37:1116-20. doi:10.1016/j.gie.2011.09.035
British Journal of Cancer | 2016
E Walsh; Colin Rees; M Gill; Parker Ce; R Bevan; Sarah L. Perry; Y Bury; S. J. Mills; Dm Bradburn; M. G. Bramble; Mark A. Hull
Background:We measured biomarkers of tumour growth and vascularity in interval and screen-detected colorectal cancers (CRCs) in the English Bowel Cancer Screening Programme in order to determine whether rapid tumour growth might contribute to interval CRC (a CRC diagnosed between a negative guaiac stool test and the next scheduled screening episode).Methods:Formalin-fixed, paraffin-embedded sections from 71 CRCs (screen-detected 43, interval 28) underwent immunohistochemistry for CD31 and Ki-67, in order to measure the microvessel density (MVD) and proliferation index (PI), respectively, as well as microsatellite instability (MSI) testing.Results:Interval CRCs were larger (P=0.02) and were more likely to exhibit venous invasion (P=0.005) than screen-detected tumours. There was no significant difference in MVD or PI between interval and screen-detected CRCs. More interval CRCs displayed MSI-high (14%) compared with screen-detected tumours (5%). A significantly (P=0.005) higher proportion (51%) of screen-detected CRC resection specimens contained at least one polyp compared with interval CRC (18%) resections.Conclusions:We found no evidence of biological differences between interval and screen-detected CRCs, consistent with the low sensitivity of guaiac stool testing as the main driver of interval CRC. The contribution of synchronous adenomas to occult blood loss for screening requires further investigation.
Endoscopy | 2015
Praveen T. Rajasekhar; Colin Rees; M. G. Bramble; Douglas Wilson; Rutter; Brian P. Saunders; Ap Hungin; James E. East