Search results for " Levels"

showing 10 items of 483 documents

Non‐invasive haemoglobin measurement as an index test to detect pre‐operative anaemia in elective surgery patients – a prospective study

2020

Non-invasive haemoglobin measurement using absolute values lacks the precision to be the sole basis for the treatment of pre-operative anaemia. However, it can possibly serve as a screening test, indexing 'anaemia' with high sensitivity when values remain under prespecified cut-off values. Based on previous data, non-invasive haemoglobin cut-off values (146 g.l-1 for women and 152 g.l-1 for men) detect true anaemia with 99% sensitivity. An index test with these prespecified cut-off values was verified by prospective measurement of non-invasive and invasive haemoglobin pre-operatively in elective surgical patients. In 809 patients, this showed an estimated sensitivity (95%CI) of 98.9% (94.1-…

AdultMalemedicine.medical_specialtyHaemoglobin levelsSensitivity and SpecificityHemoglobins03 medical and health sciences0302 clinical medicine030202 anesthesiologyInternal medicinePreoperative CareHumansMedicineProspective Studies030212 general & internal medicineElective surgeryProspective cohort studyAgedHematologic Testsbusiness.industryNon invasiveLimits of agreementIndex testAnemiaMiddle AgedPre operativeAnesthesiology and Pain MedicineElective Surgical ProceduresFemalebusinessSurgical patientsAnaesthesia
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Evaluation of serum copper and iron levels among oral submucous fibrosis patients

2010

Objective: To estimate and compare the levels of serum copper and iron among subjects with oral submucous fibrosis (OSMF) of different clinical stages and healthy controls. Study Design: Study sample comprised of 50 patients clinically diagnosed with OSMF and 50 healthy controls who were matched for age and gender. OSMF patients were categorised by clinical staging. Serum estimation of copper and iron was done using atomic absorbtion spectrophotometry. Results: Mean copper and iron level differed significantly (p<0.000) between the patients and controls with patients exhibiting higher copper (134.1±20.16) and lower iron (114.78±23.47) levels in contrast to controls who presented lower coppe…

AdultMalemedicine.medical_specialtyPathologyAdolescentIronSerum copperchemistry.chemical_elementOral Submucous FibrosisGastroenterologyLesionYoung AdultInternal medicinemedicineHumansStage (cooking)Young adultGeneral Dentistrybusiness.industryIron levelsBuccal administrationMiddle Agedmedicine.disease:CIENCIAS MÉDICAS [UNESCO]CopperOtorhinolaryngologyOral submucous fibrosischemistryUNESCO::CIENCIAS MÉDICASSurgeryFemalemedicine.symptombusinessCopper
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Analysis of thiamine transporter genes in sporadic beriberi

2014

Abstract Objective Thiamine or vitamin B 1 deficiency diminishes thiamine-dependent enzymatic activity, alters mitochondrial function, impairs oxidative metabolism, and causes selective neuronal death. We analyzed for the first time, the role of all known mutations within three specific thiamine carrier genes, SLC19 A2, SLC19 A3 , and SLC25 A19 , in a patient with atrophic beriberi, a multiorgan nutritional disease caused by thiamine deficiency. Methods A 44-year-old male alcoholic patient from Morocco developed massive bilateral leg edema, a subacute sensorimotor neuropathy, and incontinence. Despite normal vitamin B 1 serum levels, his clinical picture was rapidly reverted by high-dose in…

AdultMalemedicine.medical_specialtySLC19 A- SLC25 A19SLC19 AEndocrinology Diabetes and MetabolismGene mutationBeriberimedicine.disease_causeMitochondrial Membrane Transport Proteinslaw.inventionBeriberilawInternal medicineGenotypemedicineThiamine transporterObjective: Thiamine or vitamin B1 deficiency diminishes thiamine-dependent enzymatic activity alters mitochondrial function impairs oxidative metabolism and causes selective neuronal death. We analyzed for the first time the role of all known mutations within three specific thiamine carrier genes SLC19 A2 SLC19 A3 and SLC25 A19 in a patient with atrophic beriberi a multiorgan nutritional disease caused by thiamine deficiency. Methods: A 44-year-old male alcoholic patient from Morocco developed massive bilateral leg edema a subacute sensorimotor neuropathy and incontinence. Despite normal vitamin B1 serum levels his clinical picture was rapidly reverted by high-dose intramuscular thiamine treatment suggesting a possible genetic resistance. We used polymerase chain reaction followed by amplicon sequencing to study all the known thiamine-related gene mutations identified within the Human Gene Mutation Database. Results: Thirty-seven mutations were tested: 29 in SLC19 A2 6 in SLC19 A3 and 2 in SLC25 A19. Mutational analyses showed a wild-type genotype for all sequences investigated. Conclusion: This is the first genetic study in beriberi disease. We did not detect any known mutation in any of the three genes in a sporadic dry beriberi patient. We cannot exclude a role for other known or unknown mutations in the same genes or in other thiamine-associated genes in the occurrence of this nutritional neuropathy.HumansThiamineGenePolymerase chain reactionGeneticsMutationNutrition and DieteticsbiologyMembrane Transport ProteinsThiamine Deficiencymedicine.diseaseAlcoholismEndocrinologyMutationbiology.proteinThiamineMutations
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Effect of changing pulse rate on profile parameters of perceptual thresholds and loudness comfort levels and relation to ECAP thresholds in recipient…

2010

Abstract: The Nucleus CI24RE Freedom device offers higher stimulation rates and lower noise levels in action potential measurements (ECAPs) than previous devices. A study including ten European implant teams showed that the effect of changes in rate from 250 to 3500 pulses per second on tilt and curvature of the T and C profiles is insignificant. When changing rate one may change the levels at all electrodes by the same amount. Using an automated procedure ECAPs could be measured quickly and reliably at a noise level of only 1 μV. However, this did not result in improved correlations between the tilt and curvature parameters of the ECAP profiles and those of the T and C profiles. Average C …

AdultPulse repetition frequencyLinguistics and Languagemedicine.medical_specialty3616 Speech and HearingLoudness Perceptionmedia_common.quotation_subjectAction PotentialsDifferential Threshold610 Medicine & health10045 Clinic for OtorhinolaryngologyStimulus (physiology)AudiologyCurvatureLanguage and LinguisticsLoudnessAutomationYoung AdultSpeech and HearingPerceptionmedicineHumansComfort levels1203 Language and LinguisticsAgedmedia_commonMathematicsPrincipal Component AnalysisAuditory ThresholdMiddle AgedElectric Stimulation3310 Linguistics and LanguageCochlear Implantsmedicine.anatomical_structurePulse rateAuditory PerceptionHuman medicineNoiseNucleus
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VITAMIN K-INDUCED MODIFICATION OF COAGULATION PHENOTYPE IN VKORC1 HOMOZYGOUS DEFICIENCY

2008

Summary.  Background: Combined vitamin K-dependent clotting factor (VKCF) deficiency type 2 (VKCFD2) is a rare bleeding disorder caused by mutated vitamin K 2,3-epoxide reductase complex subunit 1 (VKORC1) gene. Methods and results: An Italian patient with moderate to severe bleeding tendency was genotyped, and found to be homozygous for the unique VKORC1 mutation (Arg98Trp) so far detected in VKCFD2. The activity levels of VKCFs were differentially reduced, and inversely related to the previously estimated affinity of procoagulant factor propeptides for the γ-carboxylase. The normal (factor IX) or reduced antigen levels (other VKCFs) produced a gradient in specific activities. Vitamin K su…

Adultmedicine.medical_specialtycoagulation factor levelsVitamin KProtein SMixed Function OxygenasesTissue factorchemistry.chemical_compoundInternal medicineVitamin K Epoxide ReductasesmedicineVKCFD2HumansFactor IXClotting factorCoagulation factor levels; Thrombin generation; Vitamin K supplementation; VKCFD2; VKORC1 mutation;biologyFactor VIIChemistryFactor XHomozygotevitamin K supplementationHematologyBlood Coagulation DisordersEndocrinologyTreatment OutcomeCoagulationthrombin generationImmunologyMutationbiology.proteinFemaleBlood Coagulation TestsVKCFD2 VKORC1 mutation coagulation factor levels thrombin generation vitamin K supplementationProtein Cmedicine.drugHalf-LifeVKORC1 mutation
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Brain Natriuretic Peptide and Discovery of Atrial Fibrillation After Stroke

2020

Background and Purpose— Diagnosing paroxysmal atrial fibrillation (pAF) can be challenging after acute ischemic stroke. Enhanced and prolonged Holter-ECG monitoring (EPM) improves the detection rate but is not feasible for all patients. We hypothesized that brain natriuretic peptide (BNP) may help to identify patients with stroke at high risk for pAF to select patients for EPM more effectively. Methods— Patients with acute cerebral ischemia ≥60 years presenting in sinus rhythm and without history of AF were included into a prospective, randomized multicenter study to receive either EPM (3× 10-day Holter-ECG) or usual stroke care diagnostic work-up. BNP plasma levels were measured on random…

Advanced and Specialized Nursingmedicine.medical_specialtyRandomizationbusiness.industryIschemiaAtrial fibrillationPlasma levels030204 cardiovascular system & hematologymedicine.diseaseBrain natriuretic peptide3. Good healthlaw.invention03 medical and health sciences0302 clinical medicineRandomized controlled triallawInternal medicineCardiologyMedicineSinus rhythmNeurology (clinical)Cardiology and Cardiovascular MedicinebusinessStroke030217 neurology & neurosurgeryStroke
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Recent aflatoxin survey data in milk and milk products: A review

2017

Aflatoxin M1 (AFM1) occurrence in human and animal milk, infant formula, powdered milk, cheese and yoghurt represents a risk for health. The last four years (2010–2014) of data, as well as the most frequently and updated analytical methods applied for AFM1 quantification, are evaluated. Aflatoxin B1, considered the most potent toxic aflatoxin, is metabolised to form the monohydroxy derivative AFM1. This metabolized, expressed in the milk, is relatively stable, and it is not eliminated by heat treatments or pasteurisation, and thus represents a serious health concern.

AflatoxinChemistryProcess Chemistry and Technology010401 analytical chemistryfood and beveragesPasteurizationBioengineering04 agricultural and veterinary sciences040401 food science01 natural sciences0104 chemical scienceslaw.invention0404 agricultural biotechnologyMilk productsInfant formulalawFood scienceAflatoxins Food Analysis Contamination Levels Milk.Food ScienceInternational Journal of Dairy Technology
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Continuity of solutions of linear, degenerate elliptic equations

2009

We consider the simplest form of a second order, linear, degenerate, divergence structure equation in the plane. Under an integrability condition on the degenerate function, we prove that the solutions are continuous.

AlgebraMathematics (miscellaneous)Plane (geometry)Mathematical analysisStructure equationDegenerate energy levelsOrder (group theory)Function (mathematics)Divergence (statistics)Theoretical Computer ScienceMathematicsANNALI SCUOLA NORMALE SUPERIORE - CLASSE DI SCIENZE
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Ultracold Rare-Earth Magnetic Atoms with an Electric Dipole Moment

2018

We propose a new method to produce an electric and magnetic dipolar gas of ultracold dysprosium atoms. The pair of nearly degenerate energy levels of opposite parity, at 17513.33 cm$^{-1}$ with electronic angular momentum $J=10$, and at 17514.50 cm$^{-1}$ with $J=9$, can be mixed with an external electric field, thus inducing an electric dipole moment in the laboratory frame. For field amplitudes relevant to current-day experiments, we predict a magnetic dipole moment up to 13 Bohr magnetons, and an electric dipole moment up to 0.22 Debye, which is similar to the values obtained for alkali-metal diatomics. When a magnetic field is present, we show that the electric dipole moment is strongly…

Angular momentumAtomic Physics (physics.atom-ph)General Physics and AstronomyFOS: Physical sciences[PHYS.NEXP]Physics [physics]/Nuclear Experiment [nucl-ex]01 natural sciencesAtomicPhysics - Atomic Physics010305 fluids & plasmas[PHYS.QPHY]Physics [physics]/Quantum Physics [quant-ph]Electric field0103 physical sciencesPhysics::Atomic Physics010306 general physicsPhysicsQuantum PhysicsMagnetic moment[PHYS.PHYS.PHYS-ATOM-PH]Physics [physics]/Physics [physics]/Atomic Physics [physics.atom-ph]Degenerate energy levelsMolecularand Optical Physics3. Good healthMagnetic fieldElectric dipole momentDipoleAmplitudeQuantum Gases (cond-mat.quant-gas)[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Atomic physicsCondensed Matter - Quantum GasesQuantum Physics (quant-ph)
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Wulff shape characterizations in overdetermined anisotropic elliptic problems

2017

We study some overdetermined problems for possibly anisotropic degenerate elliptic PDEs, including the well-known Serrin's overdetermined problem, and we prove the corresponding Wulff shape characterizations by using some integral identities and just one pointwise inequality. Our techniques provide a somehow unified approach to this variety of problems.

Applied Mathematics010102 general mathematicsDegenerate energy levelsMathematical analysisMathematics::Analysis of PDEsElliptic pdesComputer Science::Numerical Analysis01 natural sciencesMathematics::Numerical Analysis010101 applied mathematicsOverdetermined systemMathematics - Analysis of PDEsNonlinear Sciences::Exactly Solvable and Integrable SystemsSettore MAT/05 - Analisi MatematicaOverdetermined problems. Finsler manifold. Wulff shapes. Torsion problem. CapacityFOS: MathematicsMathematics::Differential GeometryFinsler manifold0101 mathematicsAnisotropyAnalysisAnalysis of PDEs (math.AP)Mathematics
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