Search results for "diagnostic techniques"

showing 10 items of 122 documents

A nanomaterial-based breath test for distinguishing gastric cancer from benign gastric conditions

2013

Background: Upper digestive endoscopy with biopsy and histopathological evaluation of the biopsy material is the standard method for diagnosing gastric cancer (GC). However, this procedure may not be widely available for screening in the developing world, whereas in developed countries endoscopy is frequently used without major clinical gain. There is a high demand for a simple and non-invasive test for selecting the individuals at increased risk that should undergo the endoscopic examination. Here, we studied the feasibility of a nanomaterial-based breath test for identifying GC among patients with gastric complaints. Methods: Alveolar exhaled breath samples from 130 patients with gastric …

Malevolatile organic compoundCancer Researchmedicine.medical_specialtyPathologydiagnosisPilot Projects02 engineering and technologyGastroenterology03 medical and health sciences0302 clinical medicineStomach NeoplasmssensorInternal medicineBiopsymedicineHumansStomach Ulcerbreath analysisStage (cooking)Molecular DiagnosticsBreath testVolatile Organic Compoundsmedicine.diagnostic_testbiologybusiness.industrygastric cancerConfoundingCancerMiddle AgedHelicobacter pylori021001 nanoscience & nanotechnologybiology.organism_classificationmedicine.diseaseNanostructures3. Good healthEndoscopyClinical trialBreath TestsMolecular Diagnostic TechniquesOncology030220 oncology & carcinogenesisFemale0210 nano-technologybusinessBiomarkersBritish Journal of Cancer
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The Dual/Global Value of SARS-CoV-2 Genome Surveillance on Migrants Arriving to Europe via the Mediterranean Routes.

2021

Despite the pandemic, 34,154 migrants, refugees or asylum-seekers landed in Sicily (Italy) in 2020, representing the main point of entry by sea into Europe. The SARS-CoV-2 surveillance program among migrants arriving to Sicily via the Mediterranean Sea, made by the combination of clinical examination and molecular testing, has been integrated by full-genome sequencing strains using the NGS technology from the last week of February. To date, more than one hundred full-genome strains have been sequenced and 8 different lineages have been identified mostly belonging to the lineages B.1.1.7 and B.1.525. As global access to COVID-19 vaccines should be ensured, the need to provide more detailed i…

Mediterranean climatePoint of entryCOVID-19 VaccinesCoronavirus disease 2019 (COVID-19)Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)RefugeeInfectious and parasitic diseasesRC109-216Genome ViralSettore MED/42 - Igiene Generale E ApplicataGenomeMediterranean seaPandemicHumansSocioeconomicsLetters to the EditorSicilyTransients and MigrantsSARS-CoV-2COVID-19General MedicineGeographyCOVID-19 COVID-19 Vaccines Genome Viral Humans Molecular Diagnostic Techniques SARS-CoV-2Sicily Transients and MigrantsMolecular Diagnostic TechniquesPublic aspects of medicineRA1-1270Annals of global health
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Cytomegalovirus Infection Management in Allogeneic Stem Cell Transplant Recipients: a National Survey in Spain.

2015

ABSTRACT This study gathered information about current practices of cytomegalovirus (CMV) infection management in allogeneic stem cell transplant recipients at Spanish centers. A wide variety of preemptive antiviral therapy strategies for CMV infection guided by real-time PCR assays was found, yet the incidence of CMV disease was low (<3%).

Microbiology (medical)AdultPcr assayCongenital cytomegalovirus infectionReal-Time Polymerase Chain ReactionAntiviral AgentsChemopreventionVirologyMedicineHumansTransplantation Homologousbusiness.industryIncidence (epidemiology)Antiviral therapyvirus diseasesCase managementmedicine.diseaseCytomegalovirus infectionTransplantationMolecular Diagnostic TechniquesSpainImmunologyCytomegalovirus InfectionsStem cellbusinessCase ManagementStem Cell Transplantation
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Epidemiological cutoff values for fluconazole, itraconazole, posaconazole, and voriconazole for six Candida species as determined by the colorimetric…

2013

ABSTRACT In the absence of clinical breakpoints (CBP), epidemiological cutoff values (ECVs) are useful to separate wild-type (WT) isolates (without mechanisms of resistance) from non-WT isolates (those that can harbor some resistance mechanisms), which is the goal of susceptibility tests. Sensititre YeastOne (SYO) is a widely used method to determine susceptibility of Candida spp. to antifungal agents. The CLSI CBP have been established, but not for the SYO method. The ECVs for four azoles, obtained using MIC distributions determined by the SYO method, were calculated via five methods (three statistical methods and based on the MIC 50 and modal MIC). Respectively, the median ECVs (in mg/lit…

Microbiology (medical)AzolesPosaconazolemedicine.medical_specialtyAntifungal AgentsItraconazoleMycologyMicrobial Sensitivity TestsBiologyMicrobiology:Organisms::Eukaryota::Animals::Chordata::Vertebrates::Mammals::Primates::Haplorhini::Catarrhini::Hominidae::Humans [Medical Subject Headings]EpidemiologymedicineHumansCutoffCandida albicansPruebas de sensibilidad microbianaCandidaVoriconazoleCandidiasisLiter:Chemicals and Drugs::Heterocyclic Compounds::Heterocyclic Compounds 1-Ring::Azoles [Medical Subject Headings]:Diseases::Bacterial Infections and Mycoses::Mycoses::Candidiasis [Medical Subject Headings]biology.organism_classification:Chemicals and Drugs::Chemical Actions and Uses::Pharmacologic Actions::Therapeutic Uses::Anti-Infective Agents::Antifungal Agents [Medical Subject Headings]:Analytical Diagnostic and Therapeutic Techniques and Equipment::Diagnosis::Diagnostic Techniques and Procedures::Clinical Laboratory Techniques::Microbiological Techniques::Microbial Sensitivity Tests [Medical Subject Headings]:Organisms::Eukaryota::Fungi::Mitosporic Fungi::Candida [Medical Subject Headings]AntifúngicosFluconazolemedicine.drug
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Characterization and multicentric validation of a common standard for Toxoplasma gondii detection using nucleic acid amplification assays.

2014

ABSTRACT The molecular diagnosis of toxoplasmosis essentially relies upon laboratory-developed methods and suffers from lack of standardization, hence the large diversity of performances between laboratories. Moreover, quantifications of parasitic loads differ among centers, a fact which prevents the possible prediction of the severity of this disease as a function of parasitic loads. The objectives of this multicentric study performed in eight proficient laboratories of the Molecular Biology Pole of the French National Reference Center for Toxoplasmosis (NRC-T) were (i) to assess the suitability of a lyophilized preparation of Toxoplasma gondii as a common standard for use in this PCR-base…

Microbiology (medical)MESH: Reference Standards*MESH: Molecular Diagnostic Techniques/methods*MESH: Parasite Load/standards[SDV]Life Sciences [q-bio]Toxoplasma gondiidiagnosticParasitic loadsParasite LoadMESH: Nucleic Acid Amplification Techniques/standards*MESH: Toxoplasma/isolation & purification*medicineMolecular diagnostic techniquesHumansNational levelReference standardsMESH: Parasite Load/methodsstandardizationMESH: HumansbiologyMESH: Nucleic Acid Amplification Techniques/methods*Toxoplasma gondiiNucleic acid amplification techniqueMESH: Toxoplasmosis/diagnosis*MESH: Molecular Diagnostic Techniques/standards*Reference Standardsbiology.organism_classificationmedicine.diseaseVirologyToxoplasmosisquantification3. Good healthMESH: FranceMolecular Diagnostic TechniquesImmunologyNucleic acidMESH: Toxoplasma/geneticsParasitologyFranceNucleic Acid Amplification TechniquesToxoplasmaToxoplasmosisJournal of clinical microbiology
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Molecular Diagnosis of Toxoplasmosis in Immunocompromised Patients: a 3-Year Multicenter Retrospective Study

2015

ABSTRACT Toxoplasmosis is a life-threatening infection in immunocompromised patients (ICPs). The definitive diagnosis relies on parasite DNA detection, but little is known about the incidence and burden of disease in HIV-negative patients. A 3-year retrospective study was conducted in 15 reference laboratories from the network of the French National Reference Center for Toxoplasmosis, in order to record the frequency of Toxoplasma gondii DNA detection in ICPs and to review the molecular methods used for diagnosis and the prevention measures implemented in transplant patients. During the study period, of 31,640 PCRs performed on samples from ICPs, 610 were positive (323 patients). Blood ( n …

Microbiology (medical)Microbiological Techniquesmedicine.medical_specialtyMESH: Molecular Diagnostic TechniquesAsymptomaticPolymerase Chain Reactionlaw.inventionImmunocompromised Host[SDV.MHEP.MI]Life Sciences [q-bio]/Human health and pathology/Infectious diseaseslawInternal medicinemedicineMESH: Immunocompromised HostPrevalenceHumansComputingMilieux_MISCELLANEOUSPolymerase chain reactionImmunodeficiencySurvival analysisMESH: PrevalenceRetrospective Studies[SDV.EE.SANT]Life Sciences [q-bio]/Ecology environment/HealthMESH: Humansbusiness.industryIncidence (epidemiology)MESH: ToxoplasmaMESH: Microbiological TechniquesRetrospective cohort studyMESH: Polymerase Chain ReactionMESH: Retrospective Studiesmedicine.diseaseSurvival AnalysisToxoplasmosis3. Good healthSurgeryMESH: France[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologyMolecular Diagnostic TechniquesMESH: Survival AnalysisChemoprophylaxisMESH: ToxoplasmosisParasitologyFrancemedicine.symptombusinessToxoplasmaToxoplasmosis
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Freezing and storage at -20 °C provides adequate preservation of Toxoplasma gondii DNA for retrospective molecular analysis.

2014

Equipe EA MERS; International audience; Nucleic acid-based testing has become crucial for toxoplasmosis diagnosis. For retrospective (forensic or scientific) studies, optimal methods must be employed for DNA long-term storage. We compared Toxoplasma gondii detection before and after DNA storage using real-time PCR. No significant differences were found depending on duration or storage conditions at -20 °C or -80 °C.

Microbiology (medical)Time Factors[SDV]Life Sciences [q-bio]educationBiologyReal-Time Polymerase Chain ReactionSpecimen HandlingToxoplasma gondii DNAchemistry.chemical_compoundparasitic diseasesFreezingmedicineRetrospective Studiestoxoplasma gondiiDNA storageToxoplasma gondiiamniotic fluidGeneral MedicineDNA Protozoanmedicine.diseasebiology.organism_classificationVirologyToxoplasmosisDna storageMolecular analysisInfectious DiseasesReal-time polymerase chain reaction[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologychemistryMolecular Diagnostic Techniquescongenital toxoplasmosisNucleic acidMESH: DNA Protozoan/isolation&purification; Freezing; Molecular Diagnostic Technics/methods; Specimen Handling/methods; Toxoplasmosis/diagnosisreal-Time PCRToxoplasmaDNAToxoplasmosisDiagnostic microbiology and infectious disease
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Evaluation of the Amplex eazyplex Loop-Mediated Isothermal Amplification Assay for Rapid Diagnosis of Pneumocystis jirovecii Pneumonia

2020

ABSTRACT Quantitative PCR (qPCR) assays are the gold standard for diagnosis of Pneumocystis jirovecii pneumonia (PCP). However, they are laborious and require skilled personnel. Therefore, execution outside regular working hours of the molecular biology laboratory is limited. The eazyplex P. jirovecii assay (PJA) uses loop-mediated isothermal amplification for detection of P. jirovecii. It is performed directly with respiratory specimens, without the need for special skills, and delivers a result within 3 to 25 min. The goal of our study was to compare the performance of the eazyplex PJA with that of established P. jirovecii qPCR assays. All archived bronchoalveolar lavage fluid (BALF) samp…

Microbiology (medical)Working hoursmedicine.diagnostic_testbusiness.industryPneumonia PneumocystisPneumocystis jirovecii PneumoniaLoop-mediated isothermal amplificationTime to resultMycologyGold standard (test)Pneumocystis cariniiSensitivity and SpecificityMicrobiologyReal-time polymerase chain reactionBronchoalveolar lavageMolecular Diagnostic TechniquesPneumocystis cariniiparasitic diseasesHumansMedicineProspective StudiesbusinessBronchoalveolar Lavage FluidNucleic Acid Amplification TechniquesRetrospective StudiesJournal of Clinical Microbiology
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Application of fnbA gene as new target for the species-specific and quantitative detection of Staphylococcus aureus directly from lower respiratory t…

2013

Staphylococcus aureus is a significant cause of hospital-acquired pneumonia (HAP), particularly in mechanically ventilated patients. We used the fibronectin-binding protein A gene (fnbA) for the species-specific and quantitative detection of S. aureus directly from lower respiratory tract (LRT) specimens by a Taq Man real time PCR. For this reason, a total of 269 lower respiratory tract (LRT) specimens collected from patients with hospital-acquired pneumonia were assayed. Amplification of fnbA in serial dilutions ranged from 10(9) CFU/ ml to 10(2) CFU/ml. Standard curve of triplicate every dilution had slope 3.34±0.1 and R2>0.99 with SD 0.1. Based on these data, the sensitivity and specif…

Microbiology (medical)fnbA Gene real time PCR respiratory infection Staphylococcus aureusSettore MED/07 - Microbiologia E Microbiologia ClinicaStaphylococcus aureusSerial dilutionRespiratory Systemlcsh:QR1-502medicine.disease_causeReal-Time Polymerase Chain ReactionSensitivity and SpecificityfnbA Genelcsh:MicrobiologyPathology and Forensic MedicineMicrobiologyrespiratory infectionPneumonia StaphylococcalmedicineTaqManlcsh:PathologyHumansAdhesins BacterialCross InfectionbiologyStaphylococcus. aureusRespiratory infectionGeneral Medicinemedicine.diseasePneumoniareal time PCRmedicine.anatomical_structureReal-time polymerase chain reactionMolecular Diagnostic TechniquesStaphylococcus aureusbiology.proteinProtein ARespiratory tractlcsh:RB1-214Indian journal of pathologymicrobiology
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Reverse transcriptase loop-mediated isothermal amplification (RT-LAMP) as a user-friendly system to detect SARS-CoV-2 infection: a multicentric study

2021

Although reverse transcriptase quantitative PCR remains the gold standard to perform viral detection, reverse transcriptase loop-mediated isothermal amplification (RT-LAMP) is already used to perform diagnosis of various infections. This work reports the results of a multicentric study performed in Sicily to evaluate the diagnostic power of an RT-LAMP kit for the diagnosis of SARS-CoV-2 infection on a total of 551 samples collected in January and February 2021, revealing sensitivity, specificity, accuracy, positive and negative predictive values ≥95%. Our results suggest the potential employment of this kit as a screening test to be used where fast and reliable results are demanded without …

Multicentric studyRT-LAMP.Diagnostic powerReverse Transcriptase Polymerase Chain ReactionSARS-CoV-2COVID-19RNA-Directed DNA PolymeraseSensitivity and SpecificityMolecular Diagnostic TechniquesHumansRNA ViralRNAViralNucleic Acid Amplification Techniques
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