Andrea Sheel
University of Liverpool
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Featured researches published by Andrea Sheel.
Pancreatology | 2017
Asbjørn Mohr Drewes; Stefan A.W. Bouwense; C. Campbell; Güralp O. Ceyhan; Myriam Delhaye; Ihsan Ekin Demir; Pramod Kumar Garg; Harry van Goor; Christopher Halloran; Shuiji Isaji; John P. Neoptolemos; Søren Schou Olesen; Tonya Palermo; Pankaj J. Pasricha; Andrea Sheel; Tooru Shimosegawa; Eva Szigethy; David C. Whitcomb; Dhiraj Yadav
Abdominal pain is the foremost complication of chronic pancreatitis (CP). Pain can be related to recurrent or chronic inflammation, local complications or neurogenic mechanisms with corresponding changes in the nervous systems. Both pain intensity and the frequency of pain attacks have been shown to reduce quality of life in patients with CP. Assessment of pain follows the guidelines for other types of chronic pain, where the multidimensional nature of symptom presentation is taken into consideration. Quantitative sensory testing may be used to characterize pain, but is currently used in a research setting in advanced laboratories. For pain relief, current guidelines recommend a simple stepwise escalation of analgesic drugs with increasing potency until pain relief is obtained. Abstinence from alcohol and smoking should be strongly advised. Pancreatic enzyme therapy and antioxidants may be helpful as initial treatment. Endoscopic treatment can be used in patients with evidence of ductal obstruction and may be combined with extracorporeal shock wave lithothripsy. The best candidates are those with distal obstruction of the main pancreatic duct and in early stage of disease. Behavioral interventions should be part of the multidisciplinary approach to chronic pain management particularly when psychological impact is experienced. Surgery should be considered early and after a maximum of five endoscopic interventions. The type of surgery depends on morphological changes of the pancreas. Long-term effects are variable, but high success rates have been reported in open studies and when compared with endoscopic treatment. Finally, neurolytical interventions and neuromodulation can be considered in difficult patients.
The American Journal of Gastroenterology | 2018
Andrea Sheel; Sara Harrison; I Sarantitis; J. A. Nicholson; Thomas Hanna; C. Grocock; Michael Raraty; Jayapal Ramesh; A. Farooq; Eithne Costello; Richard J. Jackson; Michael H. Chapman; A. Smith; Ross Carter; Colin J. McKay; Z. Hamady; Guruprasad P. Aithal; R. Mountford; Paula Ghaneh; Pascal Hammel; Markus M. Lerch; Christopher Halloran; Stephen P. Pereira; William Greenhalf
OBJECTIVES: Intraductal papillary mucinous neoplasms (IPMNs) are associated with risk of pancreatic ductal adenocarcinoma (PDAC). It is unclear if an IPMN in individuals at high risk of PDAC should be considered as a positive screening result or as an incidental finding. Stratified familial pancreatic cancer (FPC) populations were used to determine if IPMN risk is linked to familial risk of PDAC. METHODS: This is a cohort study of 321 individuals from 258 kindreds suspected of being FPC and undergoing secondary screening for PDAC through the European Registry of Hereditary Pancreatitis and Familial Pancreatic Cancer (EUROPAC). Computerised tomography, endoscopic ultrasound of the pancreas and magnetic resonance imaging were used. The risk of being a carrier of a dominant mutation predisposing to pancreatic cancer was stratified into three even categories (low, medium and high) based on: Mendelian probability, the number of PDAC cases and the number of people at risk in a kindred. RESULTS: There was a median (interquartile range (IQR)) follow-up of 2 (0–5) years and a median (IQR) number of investigations per participant of 4 (2–6). One PDAC, two low-grade neuroendocrine tumours and 41 cystic lesions were identified, including 23 IPMN (22 branch-duct (BD)). The PDAC case occurred in the top 10% of risk, and the BD-IPMN cases were evenly distributed amongst risk categories: low (6/107), medium (10/107) and high (6/107) (P = 0.63). CONCLUSIONS: The risk of finding BD-IPMN was independent of genetic predisposition and so they should be managed according to guidelines for incidental finding of IPMN.
Pancreatology | 2018
Jens Brøndum Frøkjær; Fatih Akisik; Ammad Farooq; Burcu Akpinar; Anil K. Dasyam; Asbjørn Mohr Drewes; Ingfrid S. Haldorsen; Giovanni Morana; John P. Neoptolemos; Søren Schou Olesen; Maria Chiara Petrone; Andrea Sheel; Tooru Shimosoegawa; David C. Whitcomb
The paper presents the international guidelines for imaging evaluation of chronic pancreatitis. The following consensus was obtained: Computed tomography (CT) is often the most appropriate initial imaging modality for evaluation of patients with suspected chronic pancreatitis (CP) depicting most changes in pancreatic morphology. CT is also indicated to exclude other potential intraabdominal pathologies presenting with symptoms similar to CP. However, CT cannot exclude a diagnosis of CP nor can it be used to exclusively diagnose early or mild disease. Here magnetic resonance imaging (MRI) and MR cholangiopancreatography (MRCP) is superior and is indicated especially in patients where no specific pathological changes are seen on CT. Secretin-stimulated MRCP is more accurate than standard MRCP in the depiction of subtle ductal changes. It should be performed after a negative MRCP, when there is still clinical suspicion of CP. Endoscopic ultrasound (EUS) can also be used to diagnose parenchymal and ductal changes mainly during the early stage of the disease. No validated radiological severity scoring systems for CP are available, although a modified Cambridge Classification has been used for MRCP. There is an unmet need for development of a new and validated radiological CP severity scoring system based on imaging criteria including glandular volume loss, ductal changes, parenchymal calcifications and parenchymal fibrosis based on CT and/or MRI. Secretin-stimulated MRCP in addition, can provide assessment of exocrine function and ductal compliance. An algorithm is presented, where these imaging parameters can be incorporated together with clinical findings in the classification and severity grading of CP.
Pancreatology | 2018
David C. Whitcomb; Tooru Shimosegawa; Suresh T. Chari; Chris E. Forsmark; Luca Frulloni; Pramod Kumar Garg; Péter Hegyi; Yoshiki Hirooka; Atsushi Irisawa; Takuya Ishikawa; Shuiji Isaji; Markus M. Lerch; Philippe Lévy; Atsushi Masamune; Charles M. Wilcox; John A. Windsor; Dhiraj Yadav; Andrea Sheel; John P. Neoptolemos
Pancreatology | 2018
Andrea Sheel; Ryan Baron; Ioannis Sarantitis; Jayapal Ramesh; Paula Ghaneh; Michael Raraty; Vincent Yip; Robert Sutton; Michael R. Goulden; Fiona Campbell; Ammad Farooq; Priya Healey; Richard J. Jackson; Christopher Halloran; John P. Neoptolemos
Pancreatology | 2018
Andrea Sheel; Ryan Baron; Jayapal Ramesh; Paula Ghaneh; Michael Raraty; Vincent Yip; Robert Sutton; Fiona Campbell; Ammad Farooq; Christopher Halloran; John P. Neoptolemos
Pancreatology | 2018
Ioannis Sarantitis; Andrea Sheel; James Nicholson; Emma McCarthy; Emma Howard; Ryan Baron; Jennifer Law; Paula Ghaneh; Roger Mountford; Eithne Costello-Goldring; Vinciane Rebours; John P. Neoptolemos; Christopher Halloran; William Greenhalf
Pancreatology | 2018
Jennifer Law; Ioannis Sarantitis; Andrea Sheel; Eithne Costello; Zaed Hamady; Aithal Guru; Andrew Paul Smith; Richard Charnley; Stephen P. Pereira; John P. Neoptolemos; Christopher Halloran; William Greenhalf
Pancreatology | 2018
Andrea Sheel; Klaire Exarchou; Ryan Baron; Val Akintunde; Jo Garry; Phil Whelan; Robert Sutton; Christopher Halloran; Paula Ghaneh; John P. Neoptolemos; Michael Raraty; Vincent Yip
Archive | 2018
Michael Raraty; Andrea Sheel; John P. Neoptolemos