1.Towards a Standard Protocol for Fecal Microbiota Transplantation in IrritableBowel Syndrome
Magdy EL-SALHY ; Maura CORSETTI ; Odd Helge GILJA ; Sutep GONLACHANVIT ; Jan Gunnar HATLEBAKK ; Dag Arne Lihaug HOFF ; Perttu LAHTINEN ; Johan Axel LUNDING ; Tarek MAZZAWI ; Tanya M MONAGHAN ; Bodil OHLSSON ; Tanisa PATCHARATRAKUL ; Yong Sung KIM ; Cheol Min SHIN
Journal of Neurogastroenterology and Motility 2026;32(2):185-197
Randomized controlled trials (RCTs) of fecal microbiota transplantation (FMT) in patients with irritable bowel syndrome (IBS) have produced outcomes varying from no effect at all to high efficacy and durable effects over time. This review analyzed differences in the protocols used in FMT RCTs for IBS in the recently published literature with the aim of identifying the factors responsible for the success or failure of these RCTs. The results of this analysis might be useful in formulating an effective standard protocol for FMT in IBS. A systematic search was conducted in the PubMed database of the literature published in English from January 2015 to December 2023 using several search phrases comprising MeSH expressions. Those RCTs that carefully selected donors based on environmental factors that are known to affect the gut microbiota positively and ensured bacterial diversity before and during FMT produced successful outcomes. Furthermore, direct freezing of the donor’s fecal transplant, storing it at −80°C until the FMT is performed, and then thawing it at 4°C and mixing it manually appear to be factors associated with the success of FMT in IBS. Administering the donor’s fecal transplant into the small intestine results in durable effects of FMT and long-term colonization of beneficial bacteria. A standard protocol for FMT with large and durable effects should include (1) careful donor selection, (2) handling the donor’s fecal transplant in a way that preserves its microbiota contents, and (3) administering the transplant into the small intestine.
2.The AFSUMB Consensus Statements and Recommendations for the Clinical Practice of Contrast-Enhanced Ultrasound using Sonazoid
Jae Young LEE ; Yasunori MINAMI ; Byung Ihn CHOI ; Won Jae LEE ; Yi-Hong CHOU ; Woo Kyoung JEONG ; Mi-Suk PARK ; Nobuki KUDO ; Min Woo LEE ; Ken KAMATA ; Hiroko IIJIMA ; So Yeon KIM ; Kazushi NUMATA ; Katsutoshi SUGIMOTO ; Hitoshi MARUYAMA ; Yasukiyo SUMINO ; Chikara OGAWA ; Masayuki KITANO ; Ijin JOO ; Junichi ARITA ; Ja-Der LIANG ; Hsi-Ming LIN ; Christian NOLSOE ; Odd Helge GILJA ; Masatoshi KUDO
Ultrasonography 2020;39(3):191-220
The first edition of the guidelines for the use of ultrasound contrast agents was published in 2004, dealing with liver applications. The second edition of the guidelines in 2008 reflected changes in the available contrast agents and updated the guidelines for the liver, as well as implementing some nonliver applications. The third edition of the contrast-enhanced ultrasound (CEUS) guidelines was the joint World Federation for Ultrasound in Medicine and Biology-European Federation of Societies for Ultrasound in Medicine and Biology (WFUMB-EFSUMB) venture in conjunction with other regional US societies such as Asian Federation of Societies for Ultrasound in Medicine and Biology, resulting in a simultaneous duplicate on liver CEUS in the official journals of both WFUMB and EFSUMB in 2013. However, no guidelines were described mainly for Sonazoid due to limited clinical experience only in Japan and Korea. The new proposed consensus statements and recommendations provide general advice on the use of Sonazoid and are intended to create standard protocols for the use and administration of Sonazoid in hepatic and pancreatobiliary applications in Asian patients and to improve patient management.

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