Search results for " DIAGNOSIS"

showing 10 items of 1378 documents

Early detection of memory impairments in older adults: standardization of a short version of the verbal and nonverbal Recognition Memory Test

2018

In several neurological conditions, in elderly and cognitively impaired subjects, memory functioning must be evaluated to early detect the cognitive deterioration processes. In particular, recognition memory assessment is an essential step in the clinical and neuropsychological evaluation of early memory impairments. The Recognition Memory Test (RMT) developed by Smirni et al. (G Ital Psicol XXXVII(1):325-343, 2010) is an effective instrument to assess verbal and nonverbal recognition memory in the Italian population. The current study provides a new, brief, and reliable RMT format to evaluate recognition memory on elderly subjects and it reports normative data in an older adult Italian pop…

Malemedicine.medical_specialtyNeurologyStandardizationDermatologyNeuropsychological TestsAudiologyMemory assessment Recognition memory Shorter form Elderly evaluation03 medical and health sciencesNonverbal communication0302 clinical medicinemedicineHumans030212 general & internal medicineAgedRecognition memoryAged 80 and overMemory DisordersSettore M-PSI/02 - Psicobiologia E Psicologia FisiologicaVerbal BehaviorNeuropsychologySettore M-PSI/03 - PsicometriaReproducibility of ResultsRecognition PsychologyRegression analysisGeneral MedicineMiddle AgedPsychiatry and Mental healthEarly DiagnosisItalyRecognition memory testNormativeFemaleNeurology (clinical)Psychology030217 neurology & neurosurgery
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Idiopathic neutropenia of infancy: Data from the Italian Neutropenia Registry.

2019

Autoimmune neutropenia of infancy (AIN) is characterized by low risk of severe infection, tendency to spontaneously resolve and typically onset at ≤4-5 years of age; it is due to auto-antibodies whose detection is often difficult. In case of negativity of 4 antineutrophils autoantibody tests, after having excluded ethnic, postinfection, drug induced, or congenital neutropenia, according to the Italian guidelines the patients will be defined as affected by "idiopathic neutropenia" (IN). We describe the characteristics of 85 IN patients enrolled in the Italian neutropenia registry: they were compared with 336 children affected by AIN. The 2 groups were clinically very similar and the main dif…

Malemedicine.medical_specialtyNeutropeniaAutoimmunityNeutropeniaDiagnosis Differential03 medical and health sciences0302 clinical medicineSex FactorsMonocytosisRisk FactorsInternal medicineDiagnosismedicineCongenital Bone Marrow Failure SyndromesHumansRegistriesCongenital NeutropeniaHematologyLeukopeniabusiness.industryAge Factors; Autoimmunity; Congenital Bone Marrow Failure Syndromes; Diagnosis Differential; Female; Humans; Infant; Italy; Leukopenia; Male; Neutropenia; Registries; Risk Factors; Sex FactorsAutoantibodyAge FactorsInfantHematologyLeukopeniamedicine.diseaseSettore MED/38Italy030220 oncology & carcinogenesisAutoimmune neutropeniaDifferentialFemalemedicine.symptomDifferential diagnosisbusiness030215 immunologyAmerican journal of hematology
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Clinical presentation of burning mouth syndrome in patients with oral lichenoid disease

2020

Background To analyze the presence of burning mouth syndrome (BMS) in a group of patients diagnosed with oral lichenoid disease (OLD). Material and Methods A retrospective study of 217 patients diagnosed with OLD; 158 (72,8%) women and 59 (27,2%) men, with an average age upon diagnosis of 56,4 years (SD 11,88). We carried out a detailed and complete characterization of symptoms, with special emphasis on BMS diagnostic data specified by the International Headache Society. Results Four patients (1.8%) presented with long-term clinical symptoms of burning mouth, indicative of BMS and they fulfilled the IHS 2018 criteria, except for criterion D, i.e.“Oral mucosa is of normal appearance”. The ob…

Malemedicine.medical_specialtyPainDiseaseBurning Mouth Syndrome03 medical and health sciences0302 clinical medicinemedicineHumansIn patientNormal appearanceMedical diagnosisOral mucosaGeneral DentistryRetrospective StudiesOral Medicine and Pathologybusiness.industryResearchMouth MucosaRetrospective cohort study030206 dentistryBurning mouth syndrome:CIENCIAS MÉDICAS [UNESCO]Dermatologystomatognathic diseasesmedicine.anatomical_structureOtorhinolaryngologyChild PreschoolUNESCO::CIENCIAS MÉDICASSurgeryFemalemedicine.symptomPresentation (obstetrics)businessMouth Diseases
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The "aRIANNA" Project: An Observational Study on a Model of Early Identification of Patients with Palliative Care Needs through the Integration betwe…

2018

Objective: The aim of this study was to illustrate the characteristics of patients with palliative care (PC) needs, early identified by general practitioners (GPS), and to analyze their care process in home PC services. Background: Early identification and service integration are key components to providing quality palliative care (PC) services ensuring the best possible service for patients and their families. However, in Italy, PC is often provided only in the last phase of life and for oncological patients, with a fragmented service. Methods: Multicenter prospective observational study, lasting in total 18 months, implemented in a sample of Italian Home Palliative Care Units (HPCUs), enr…

Malemedicine.medical_specialtyPalliative carepublic health approachDecision MakingintegrationPrimary care03 medical and health sciences0302 clinical medicineHome Health Nursingearly identificationmedicineHumansProspective Studies030212 general & internal medicineGeneral NursingNursing (all)2901 Nursing (miscellaneous)AgedAged 80 and overpalliative carePrimary Health Carebusiness.industryGeneral MedicineIdentification (information)Early DiagnosisAnesthesiology and Pain MedicineSECS-S/03 - STATISTICA ECONOMICAItaly030220 oncology & carcinogenesisFamily medicineHospice and Palliative Care NursingFemaleObservational studybusiness
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Acute painful paraplegia in a 49-year-old man with allergic asthma.

2014

We present a case of a 49-year-old man, with a 10-year history of bronchial asthma and nasal polyposis, who developed acutely painful paraplegia and paresthesias. Laboratory data showed elevated blood creatine kinase levels and myoglobinuria, which were diagnostic for rhabdomyolysis but only partially explained the neurological deficit. Electrophysiological studies revealed a sensorimotor neuropathy of multiple mononeuritis type. The patient also had leucocytosis with marked eosinophilia and antineutrophil cytoplasmic autoantibodies. Bronchial biopsies showed inflammatory infiltrates with a prevalence of eosinophils. All these findings led us to diagnose eosinophilic granulomatosis with pol…

Malemedicine.medical_specialtyPathologyChurg-Strauss SyndromeRhabdomyolysisArticleNasal PolypsEosinophilicRespiratory medicine Asthma Pneumonia Rheumatology VasculitismedicineEosinophiliaHumansParesthesiaLungAsthmaParaplegiabusiness.industryMyoglobinuriaGeneral MedicineMyalgiaMiddle Agedmedicine.diseaseDermatologyRhinitis AllergicAsthmaRadiographymedicine.symptomDifferential diagnosisGranulomatosis with polyangiitisbusinessRhabdomyolysisSystemic vasculitisBMJ case reports
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Focal cortical damage parallels cognitive impairment in minimal hepatic encephalopathy

2012

Little attention has been paid to cortical integrity in patients with minimal hepatic encephalopathy (MHE), although cognitive functions affected in early stages of liver disease are mainly allocated in different neocortical structures. Here we used cortical surface-based analysis techniques to investigate if patterns of cortical thinning accompany the mildest form of HE. To aim this goal, cortical thickness obtained from high-resolution 31 magnetic resonance imaging (MRI) was measured in patients with no MHE (NMHE), MHE, and healthy controls. Further correlation analyses were performed to examine whether scores in the critical flicker frequency (CFF) test, and blood ammonia levels accounte…

Malemedicine.medical_specialtyPathologyCognitive NeuroscienceMinimal hepatic encephalopathyPrecuneusFlicker fusion thresholdNeuropsychological TestsCortical thicknessLiver diseaseInternal medicineImage Interpretation Computer-AssistedmedicineHumansHepatic encephalopathyTemporal cortexCerebral Cortexmedicine.diagnostic_testMagnetic resonance imagingCognitionMiddle Agedmedicine.diseaseEarly diagnosisMagnetic Resonance ImagingCalcarine sulcusmedicine.anatomical_structureEarly DiagnosisCognitive impairmentNeurologyHepatic cirrhosisHepatic EncephalopathyCardiologyFemalePsychologyCognition Disordershuman activities
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Heart-type fatty acid binding protein is a sensitive biomarker for early AMI detection in troponin negative patients: a pilot study

2017

Background: Early detecting AMI in individuals presenting to the ED with chest pain continues to be a challenge. cTn is the gold standard for AMI diagnosis but early presenters (<1 hours from symptom onset) maybe cTn negative on admission. We analysed the diagnostic value of h-FABP and hs-TnI in patients presenting to ED with chest pain and no cTnI elevations. Methods: 28 AMI and 28 no-AMI individuals both presented to ED within one hour from pain onset were included. Blood donors were analysed for h-FABP cut-off identification. Among AMI patients, 55% were positive for h-FABP and 34.6% were positive for hs-TnI (p = .015), thus 21% were positive only for h-FABP. The diagnostic accuracy w…

Malemedicine.medical_specialtyPathologytroponin-negativehealth care facilities manpower and serviceshsTnIClinical BiochemistryMyocardial InfarctionPilot Projects030204 cardiovascular system & hematologyChest painClinical biochemistryGastroenterologyAMI03 medical and health sciences0302 clinical medicineRisk FactorsInternal medicineHumansMedicinecardiovascular diseases030212 general & internal medicinehealth care economics and organizationsbiologybusiness.industryTroponin IGeneral MedicineGold standard (test)Middle AgedTroponinEDEarly DiagnosisHeart-type fatty acid binding proteinbiology.proteinBiomarker (medicine)Femalemedicine.symptombusinessFatty Acid Binding Protein 3h-FABPBiomarkers
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FACTORS AFFECTING THE DIAGNOSTIC DELAY IN AMYOTROPHIC LATERAL SCLEROSIS

2012

Abstract Background Although amyotrophic lateral sclerosis (ALS) is a relentlessly progressive disorder, early diagnosis allows a prompt start with the specific drug riluzole and an accurate palliative care planning. ALS at onset may however mimic several disorders, some of them treatable ( e.g. , multifocal motor neuropathy) or epidemiologically more frequent ( e.g. , cervical myelopathy). Objective To study the delay from onset to diagnosis in a cohort of ALS patients and to the variables that may affect it. Methods We performed a retrospective analysis of the diagnostic delays in a cohort of 260 patients affected by ALS (M/F = 1.32) followed at our tertiary referral ALS Center between 20…

Malemedicine.medical_specialtyPediatricsDelayed DiagnosisPalliative careALS diagnostic delay cognitive errorsCohort StudiesHumansMedicineAge of OnsetDiagnostic ErrorsAmyotrophic lateral sclerosisAgedRetrospective Studiesbusiness.industryAmyotrophic Lateral SclerosisRetrospective cohort studyGeneral MedicineMiddle Agedmedicine.diseaseMultivariate AnalysisCohortPhysical therapyFemaleSurgerySettore MED/26 - NeurologiaNeurology (clinical)Age of onsetDifferential diagnosisbusinessCohort studyMultifocal motor neuropathy
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Fabry disease defined: baseline clinical manifestations of 366 patients in the Fabry Outcome Survey.

2004

Background  Fabry disease is a rare X-linked disorder caused by deficient activity of the lysosomal enzyme α-galactosidase A. Progressive accumulation of the substrate globotriaosylceramide in cells throughout the body leads to major organ failure and premature death. In response to the recent introduction of enzyme replacement therapy, the Fabry Outcome Survey (FOS) was established to pool data from European clinics on the natural history of this little-known disease and to monitor the long-term efficacy and safety of treatment. This paper presents the first analysis of the FOS database and provides essential baseline data against which the effects of enzyme replacement can be measured. De…

Malemedicine.medical_specialtyPediatricsGenotypeClinical BiochemistryGlobotriaosylceramideDiseaseBiochemistryCohort StudiesDiagnosis Differentialchemistry.chemical_compoundmedicineHumansCornea verticillataVascular diseasebusiness.industryAge FactorsGeneral MedicineEnzyme replacement therapymedicine.diseaseFabry diseaseSurgeryEuropeIsoenzymesTreatment Outcomechemistryalpha-GalactosidaseCohortFabry DiseaseFemaleDifferential diagnosismedicine.symptombusinessEuropean journal of clinical investigation
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Clinical Inertia in Poorly Controlled Elderly Hypertensive Patients: A Cross-Sectional Study in Spanish Physicians to Ascertain Reasons for Not Inten…

2013

Clinical inertia, the failure of physicians to initiate or intensify therapy when indicated, is a major problem in the management of hypertension and may be more prevalent in elderly patients. Overcoming clinical inertia requires understanding its causes and evaluating certain factors, particularly those related to physicians.The objective of our study was to determine the rate of clinical inertia and the physician-reported reasons for it.An observational, cross-sectional, multi-center study was carried out in a primary care setting. We included 512 physicians, with a consecutive sampling of 1,499 hypertensive patients with clinical inertia.Clinical inertia was defined when physicians did n…

Malemedicine.medical_specialtyPediatricsMedicinaCross-sectional studyTreatment outcomeAlternative medicineMEDLINEPharmacotherapyPhysiciansmedicineHumansCorPharmacology (medical)Hypertension diagnosisIntensive care medicineAntihypertensive AgentsAgedPhysician-Patient Relationsbusiness.industryGeneral MedicineMiddle AgedCross-Sectional StudiesTreatment OutcomeMulticenter studySpainHypertensionFemaleClinical CompetenceClinical competenceCardiology and Cardiovascular MedicinebusinessAmerican Journal of Cardiovascular Drugs
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