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Viscosity Cup (Ford Cup) Analytical Instruments
Viscosity Cup (Ford Cup) Analytical Instruments
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Manufacture of Viscosity Cup (Ford Cup) Analytical Instruments
Method of Use Ford Cup Viscometer: Viscosity Flow Cups are very easy to use instruments made of anodized aluminium with a stainless steel orifice, for measuring the consistency of paints, varnishes and similar products. The measured kinematic viscosity is generally expressed in seconds(s) flow time. If the Standards stipulate conversion methods the flow time can be converted into Centistokes (cSt) using the Elcometer ElcoCalc Mobile App. Calibration certificates which offer traceability and assurance that each viscosity cup has been individually tested and comply to Standards are also available. The cups can be supplied separately or with an adjustable stand which includes aprecision level and an overflow glass draw plate.
Gut is a leading international journal in gastroenterology and hepatology and has an established reputation for publishing first class clinical research of the alimentary tract, the liver, biliary tree and pancreas. Gut delivers up-to-date, authoritative, clinically oriented coverage in all areas of gastroenterology and hepatology. Regular features include articles by leading authorities describing novel mechanisms of disease and new management strategies, both diagnostic and therapeutic, likely to impact on clinical practice within the foreseeable future.
Our new online collection highlights all research relating to the COVID-19 pandemic published by Gut, Frontline Gastroenterology and BMJ Open Gastroenterology. It is updated regularly as new articles are published.
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Barrett’s oesophagus may be the precursor of all oesophageal adenocarcinomas
To cite: Curtius K, Rubenstein JH, Chak A, et al. Gut 2021;70:1435-1440.
Read the full article here: link
Objective: Barrett’s oesophagus (BE) is a known precursor to oesophageal adenocarcinoma (OAC) but current clinical data have not been consolidated to address whether BE is the origin of all incident OAC, which would reinforce evidence for BE screening efforts. We aimed to answer whether all expected prevalent BE, diagnosed and undiagnosed, could account for all incident OACs in the US cancer registry data.
Conclusion: There are likely few additional OAC cases arising in the US population outside those expected from individuals with BE. Effective screening of high-risk patients could capture the majority of population destined for OAC progression and potentially decrease mortality through early detection and curative removal of small (pre)cancers during surveillance.