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1.
Curr Opin Pharmacol ; 73: 102414, 2023 Dec.
Article in English | MEDLINE | ID: mdl-38029641

ABSTRACT

With technical progress of gastrointestinal functional testing, there has been a demand for more comprehensive examination of esophageal physiology and pathophysiology beyond high-resolution manometry. A new interventional technology based on impedance planimetry, the functional lumen imaging probe (FLIP), enables intraluminal measurement of distensibility and compliance of hollow organs. EndoFLIP uses balloon catheters to measure diameter and distension pressure to calculate cross-sectional area and distensibility in different organs (mostly esophagus, stomach, anorectal region) and can be used in wide variety of indications (diagnostics, pre- and post-treatment evaluation) and currently serves as a helpful adjunctive tool in ambiguous clinical cases. EsoFLIP is a therapeutic variation that uses a stiffer balloon catheter allowing for dilation. The trend to simplify the clinical process from diagnosis to treatment tends to a one-session procedure combining diagnostics and therapeutic interventions. In specified conditions like e.g. achalasia or gastroparesis, a combination of EndoFLIP and EsoFLIP procedures may therefore be useful. The aim of this narrative review is to introduce the clinical use of FLIP and its potential benefit in combined diagnostic-therapeutic procedures.


Subject(s)
Esophageal Achalasia , Humans , Esophageal Achalasia/diagnosis , Endoscopy, Gastrointestinal , Manometry/methods , Stomach
2.
Diagnostics (Basel) ; 12(3)2022 Feb 27.
Article in English | MEDLINE | ID: mdl-35328157

ABSTRACT

Since the beginning of the COVID-19 pandemic, SARS-CoV-2 has caused a global burden for health care systems due to high morbidity and mortality rates, leading to caseloads that episodically surpass hospital resources. Due to different disease manifestations, the triage of patients at high risk for a poor outcome continues to be a major challenge for clinicians. The AIFELL score was developed as a simple decision instrument for emergency rooms to distinguish COVID-19 patients in severe disease stages from less severe COVID-19 and non-COVID-19 cases. In the present study, we aimed to evaluate the AIFELL score as a prediction tool for clinical deterioration and disease severity in hospitalized COVID-19 patients. During the second wave of the COVID-19 pandemic in Switzerland, we analyzed consecutively hospitalized patients at the Triemli Hospital Zurich from the end of November 2020 until mid-February 2021. Statistical analyses were performed for group comparisons and to evaluate significance. AIFELL scores of patients developing severe COVID-19 stages IIb and III during hospitalization were significantly higher upon admission compared to those patients not surpassing stages I and IIa. Group comparisons indicated significantly different AIFELL scores between each stage. In conclusion, the AIFELL score at admission was useful to predict the disease severity and progression in hospitalized COVID-19 patients.

3.
Braz. j. infect. dis ; 24(5): 458-461, Sept.-Oct. 2020. tab
Article in English | LILACS, Coleciona SUS | ID: biblio-1142556

ABSTRACT

Abstract Clinical prediction scores support the assessment of patients in the emergency setting to determine the need for further diagnostic and therapeutic steps. During the current COVID-19 pandemic, physicians in emergency rooms (ER) of many hospitals have a considerably higher patient load and need to decide within a short time frame whom to hospitalize. Based on our clinical experiences in dealing with COVID-19 patients at the University Hospital in Zurich, we created a triage score with the acronym "AIFELL" consisting of clinical, radiological and laboratory findings.The score was then evaluated in a retrospective analysis of 122 consecutive patients with suspected COVID-19 from March until mid-April 2020. Descriptive statistics, Student's t-test, ANOVA and Scheffe's post-hoc analysis confirmed the diagnostic power of the score. The results suggest that the AIFELL score has potential as a triage tool in the ER setting intended to select probable COVID-19 cases for hospitalization in spontaneously presenting or referred patients with acute respiratory symptoms.


Subject(s)
Humans , Pneumonia, Viral , Coronavirus Infections , Pandemics , Pneumonia, Viral/epidemiology , Retrospective Studies , Triage , Coronavirus Infections/epidemiology , Emergency Service, Hospital , Betacoronavirus , SARS-CoV-2 , COVID-19
4.
Braz J Infect Dis ; 24(5): 458-461, 2020.
Article in English | MEDLINE | ID: mdl-32828735

ABSTRACT

Clinical prediction scores support the assessment of patients in the emergency setting to determine the need for further diagnostic and therapeutic steps. During the current COVID-19 pandemic, physicians in emergency rooms (ER) of many hospitals have a considerably higher patient load and need to decide within a short time frame whom to hospitalize. Based on our clinical experiences in dealing with COVID-19 patients at the University Hospital in Zurich, we created a triage score with the acronym "AIFELL" consisting of clinical, radiological and laboratory findings. The score was then evaluated in a retrospective analysis of 122 consecutive patients with suspected COVID-19 from March until mid-April 2020. Descriptive statistics, Student's t-test, ANOVA and Scheffe's post-hoc analysis confirmed the diagnostic power of the score. The results suggest that the AIFELL score has potential as a triage tool in the ER setting intended to select probable COVID-19 cases for hospitalization in spontaneously presenting or referred patients with acute respiratory symptoms.


Subject(s)
Coronavirus Infections , Pandemics , Pneumonia, Viral , Betacoronavirus , COVID-19 , Coronavirus Infections/epidemiology , Emergency Service, Hospital , Humans , Pneumonia, Viral/epidemiology , Retrospective Studies , SARS-CoV-2 , Triage
5.
Stem Cells Transl Med ; 3(7): 801-8, 2014 Jul.
Article in English | MEDLINE | ID: mdl-24855275

ABSTRACT

We present a method to efficiently culture primary chromaffin progenitors from the adult bovine adrenal medulla in a defined, serum-free monolayer system. Tissue is dissociated and plated for expansion under support by the mitogen basic fibroblast growth factor (bFGF). The cultures, although not homogenous, contain a subpopulation of cells expressing the neural stem cell marker Hes3 that also propagate. In addition, Hes3 is also expressed in the adult adrenal medulla from where the tissue is taken. Differentiation is induced by bFGF withdrawal and switching to Neurobasal medium containing B27. Following differentiation, Hes3 expression is lost, and cells acquire morphologies and biomarker expression patterns of chromaffin cells and dopaminergic neurons. We tested the effect of different treatments that we previously showed regulate Hes3 expression and cell number in cultures of fetal and adult rodent neural stem cells. Treatment of the cultures with a combination of Delta4, Angiopoietin2, and a Janus kinase inhibitor increases cell number during the expansion phase without significantly affecting catecholamine content levels. Treatment with cholera toxin does not significantly affect cell number but reduces the ratio of epinephrine to norepinephrine content and increases the dopamine content relative to total catecholamines. These data suggest that this defined culture system can be used for target identification in drug discovery programs and that the transcription factor Hes3 may serve as a new biomarker of putative adrenomedullary chromaffin progenitor cells.


Subject(s)
Adrenal Medulla/metabolism , Cell Culture Techniques , Chromaffin Cells/metabolism , Neural Stem Cells/metabolism , Transcription Factors/metabolism , Adrenal Medulla/cytology , Adrenal Medulla/drug effects , Angiopoietin-2/pharmacology , Animals , Biomarkers/metabolism , Catecholamines/metabolism , Cattle , Cell Differentiation , Cell Proliferation , Cells, Cultured , Cholera Toxin/pharmacology , Chromaffin Cells/drug effects , Fibroblast Growth Factor 2/metabolism , Gene Expression Regulation, Developmental , Intracellular Signaling Peptides and Proteins/pharmacology , Janus Kinases/antagonists & inhibitors , Janus Kinases/metabolism , Membrane Proteins/pharmacology , Neural Stem Cells/drug effects , Protein Kinase Inhibitors/pharmacology , Signal Transduction , Time Factors , Transcription Factors/genetics
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