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1.
BMJ Open Gastroenterol ; 10(1)2023 06.
Article in English | MEDLINE | ID: mdl-37399433

ABSTRACT

OBJECTIVE: Endoscopic ultrasound-guided through-the-needle microbiopsy (EUS-TTNB) forceps is a recent development that facilitates sampling of the walls of pancreatic cystic lesions (PCL) for histological analysis. We aimed to assess the impact of EUS-TTNB and its influence on patient management in a tertiary pancreas centre. DESIGN: A prospective database of consecutive patients who underwent EUS-TTNB from March 2020 to August 2022 at a tertiary referral centre was retrospectively analysed. RESULTS: Thirty-four patients (22 women) were identified. Technical success was achieved in all cases. Adequate specimens for histological diagnosis were obtained in 25 (74%) cases. Overall, EUS-TTNB led to a change in management in 24 (71%) cases. Sixteen (47%) patients were downstaged, with 5 (15%) discharged from surveillance. Eight (24%) were upstaged, with 5 (15%) referred for surgical resection. In the 10 (29%) cases without change in management, 7 (21%) had confirmation of diagnosis with no change in surveillance, and 3 (9%) had insufficient biopsies on EUS-TTNB. Two (6%) patients developed post-procedural pancreatitis, and 1 (3%) developed peri-procedural intracystic bleeding with no subsequent clinical sequelae. CONCLUSION: EUS-TTNB permits histological confirmation of the nature of PCL, which can alter management outcomes. Care should be taken in patient selection and appropriately consented due to the adverse event rate.


Subject(s)
Endoscopic Ultrasound-Guided Fine Needle Aspiration , Pancreatic Cyst , Humans , Female , Retrospective Studies , Endoscopic Ultrasound-Guided Fine Needle Aspiration/adverse effects , Pancreas/pathology , Endosonography , Pancreatic Cyst/diagnosis
2.
Catheter Cardiovasc Interv ; 86(6): 1078-84, 2015 Nov 15.
Article in English | MEDLINE | ID: mdl-26105198

ABSTRACT

Patent foramen ovale has been identified as a conduit for paradoxical embolism resulting in cryptogenic stroke or transient ischemic attack (TIA). We aimed to establish rates of death, recurrent stroke or TIA among patients undergoing PFO closure for stroke or TIA at our unit. A retrospective analysis of all PFO closure patients was performed between May 2004 and January 2013. Follow up was performed by mortality tracing using the Medical Research Information Service of the Office of National Statistics. With regard to stroke or TIA recurrence, written consent forms and questionnaires were mailed with follow up telephone calls. Medical notes and imaging records were consulted where adverse events were noted. 301 patients aged 48.6 ± 11.0 years, 54.4% male, with ≥1 thromboembolic neurovascular event had percutaneous PFO closure with one of eight devices, with successful implantation in 99% of cases. Follow-up duration was 40.2 ± 26.2 months (range 1.3-105.3); complete in 301 patients for mortality (100%) and 283 patients (94.0%) for neurovascular events. Two patients died during follow-up (respiratory failure n = 1; road traffic accident n = 1). Recurrent stroke (MRI or CT confirmed) was observed in five patients (0.5%; 0.55 per 100 person-years) and TIA in 9 (1.1%; 0.98 per 100 person-years). Atrial fibrillation requiring treatment was documented in 14 patients (1.7%). Percutaneous PFO closure in patients with cryptogenic stroke or TIA is a safe treatment with a low incidence of procedural complications and recurrent neurovascular events. Registry data like these may help to demonstrate the utility of PFO closure in stroke.


Subject(s)
Cardiac Catheterization/methods , Foramen Ovale, Patent/complications , Foramen Ovale, Patent/therapy , Ischemic Attack, Transient/etiology , Septal Occluder Device , Stroke/etiology , Adult , Cohort Studies , Female , Follow-Up Studies , Foramen Ovale, Patent/mortality , Humans , Ischemic Attack, Transient/mortality , Ischemic Attack, Transient/therapy , Kaplan-Meier Estimate , Male , Middle Aged , Retrospective Studies , Risk Assessment , Stroke/mortality , Stroke/therapy , Survival Rate , Time Factors , Treatment Outcome
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