Search results for "Healthcare."

showing 10 items of 869 documents

Evaluation of two instruments of perceived symptom intensity in palliative care patients in an outpatient clinic

2015

Aims and objectives To evaluate the test–retest stability in assessments of perceived symptom intensity on the Edmonton Symptom Assessment System-revised and the European Organization for Research and Treatment of Cancer, Quality of Life Questionnaire Core 15 Palliative. The possible interchangeability between the instruments and the patients’ experiences of completing the instruments were also studied. Background The two instruments assess the same symptoms, but the symptom intensity is assessed on 11-point numerical scales on the Edmonton Symptom Assessment System-revised and on four-point verbal descriptive scales on the European Organization for Research and Treatment of Cancer, Quality…

AdultMalemedicine.medical_specialtyPalliative carePsychometricsSymptom assessmentAmbulatory Care Facilities03 medical and health sciences0302 clinical medicineQuality of life (healthcare)030502 gerontologyRating scaleNeoplasmsSurveys and QuestionnairesHumansMedicineOutpatient clinicGeneral NursingReliability (statistics)AgedSymptom intensityAged 80 and overNorwaybusiness.industryPalliative CareReproducibility of ResultsGeneral MedicineMiddle AgedClinical Practice030220 oncology & carcinogenesisQuality of LifePhysical therapyFemale0305 other medical sciencebusinessJournal of Clinical Nursing
researchProduct

Are Repeated Self-Reports of Psychological Variables Feasible for Patients Near the End of Life at a Palliative Care Unit?

2018

Patient-reported outcome (PRO) measurement is crucial to assess the benefit of psychotherapeutic interventions. Is repeated assessment of psychometric self-report data possible, as inpatient palliative care patients suffer from physical and psychological symptoms? What is the self-perceived strain caused by the assessment? Objective The main objective of this study was to investigate the feasibility of a repeated comprehensive psychometric self-assessment of inpatient palliative care patients. Secondary objectives were the PROs of the psychometric assessment.We conducted a prospective cohort study. Patients admitted to our palliative care unit (PCU) were reviewed for eligibility within 72 h…

AdultMalemedicine.medical_specialtyPalliative carePsychometricsUnit (housing)Young Adult03 medical and health sciences0302 clinical medicineQuality of life (healthcare)GermanySurveys and QuestionnairesNumeric Rating ScalemedicineHumans030212 general & internal medicineProspective cohort studyGeneral NursingDepression (differential diagnoses)AgedAged 80 and overPsychotherapeutic interventionsInpatientsbusiness.industryPalliative CareGeneral MedicineMiddle AgedhumanitiesAnesthesiology and Pain MedicinePatient Satisfaction030220 oncology & carcinogenesisQuality of LifePhysical therapyAnxietyFemalemedicine.symptombusinessJournal of Palliative Medicine
researchProduct

Quality of life in Parkinson's disease patients with motor fluctuations and dyskinesias in five European countries.

2013

Little is known about the relationship between specific subtypes of treatment-associated motor complications and different domains of health-related Quality of Life (QoL) in patients with Parkinson's disease (PD). Larger studies that investigate these aspects within a cross-cultural setting are scarce.To assess QoL and its association with on-off fluctuations, peak-dose dyskinesias, biphasic dyskinesias, and off-dystonias in PD patients from five European countries.Data from 817 PD patients were collected cross-sectionally in France, Germany, Italy, Spain, and the UK. QoL was measured with the generic EuroQoL 5-Dimension questionnaire (EQ-5D) and the disease-specific Parkinson's Disease Que…

AdultMalemedicine.medical_specialtyParkinson's diseaseNeurologyDiseaseAntiparkinson AgentsQuality of life (healthcare)Surveys and QuestionnairesActivities of Daily LivingMedicineHumansIn patientPsychiatryAgedAged 80 and overDyskinesiasbusiness.industryParkinson DiseaseMiddle Agedmedicine.diseaseEuropeNeurologyDyskinesiaQuality of LifeFemaleNeurology (clinical)Geriatrics and Gerontologymedicine.symptombusinessParkinsonismrelated disorders
researchProduct

Socio-economic cost and health-related quality of life of burn victims in Spain

2008

Abstract Objectives The aim of the study was to determine the economic burden (direct and indirect costs) of burn victims and the impact of burn on health-related quality of life in Spain. Methods In 2003, a cross-sectional study was carried out with 898 burned people. Data regarding demographic features, health resource use, informal care, indirect costs and quality of life were prospectively collected through hospital admission databases and questionnaires filled out by burn victims and caregivers. Results The mean annual cost (direct and indirect) per burn patient was US$ 99,773. The most important categories of costs were those of in-patient care and temporary and permanent disability. …

AdultMalemedicine.medical_specialtyPoison controlCritical Care and Intensive Care MedicineOccupational safety and healthIndirect costsQuality of life (healthcare)Cost of IllnessSurveys and QuestionnairesEnvironmental healthHealth caremedicineHumansProspective Studieshealth care economics and organizationsHealth policyCost–utility analysisbusiness.industryPublic healthHealth Care CostsGeneral MedicineSurgeryHospitalizationCross-Sectional StudiesCaregiversSocioeconomic FactorsSpainQuality of LifeEmergency MedicineFemaleSurgeryBurnsbusinessBurns
researchProduct

Motivation to Physical Exercise in Manual Wheelchair Users With Paraplegia

2020

Background: Motivation could be considered as a critical factor for being and staying physically active in the spinal cord–injured population. Objectives: Our goals were (1) to describe motivation to exercise in people with paraplegia, comparing those who engage in regular physical exercise with those who do not and (2) to establish whether such motivation is related to the type of physical exercise practiced. Methods: This study was quantitative, cross-sectional descriptive research. One-hundred and six participants with chronic paraplegia completed the Spanish version of the Exercise Motivations Inventory (EMI-2). Participants were divided into the non-exerciser group (NEG) and the exerc…

AdultMalemedicine.medical_specialtyPopulationPhysical Therapy Sports Therapy and RehabilitationPhysical exerciseManual wheelchairWheelchairSurveys and QuestionnairesHumansMedicineeducationExerciseSpinal Cord InjuriesParaplegiaMotivationeducation.field_of_studybusiness.industryRehabilitationFlexibility (personality)ArticlesMiddle AgedChronic paraplegiamedicine.diseaseCross-Sectional StudiesWheelchairsPhysical therapyFemaleNeurology (clinical)businessParaplegiaHealthcare providersTopics in Spinal Cord Injury Rehabilitation
researchProduct

High Prevalence of Mental Disorders and Emotional Distress in Patients with Chronic Spontaneous Urticaria

2011

Quality of life, which is impaired in patients with chronic spontaneous urticaria (CSU), is influenced by comorbid mental disorders. The aim of this study was to assess the prevalence and spectrum of mental disorders and to determine levels of emotional distress in patients with CSU. One hundred patients with CSU were investigated for mental disorders (by specialized diagnostic interviews and psychometric instruments), levels of emotional distress (by the Global Severity Index of the Symptom Check List; SCL-90R GSI) and underlying causes of their urticaria (by dermatological assessment). Forty-eight percent of patients with CSU were diagnosed with one or more psychosomatic disorders; most c…

AdultMalemedicine.medical_specialtyPsychometricsUrticariaPsychometricsEmotionsComorbidityDermatologyInterviews as TopicQuality of life (healthcare)Prevalence of mental disordersPredictive Value of TestsRisk FactorsGermanyPrevalencemedicineHumansPsychiatryDepression (differential diagnoses)Phobiasbusiness.industryMental DisordersGeneral Medicinemedicine.diseaseComorbidityChecklistClinical trialChronic DiseaseQuality of LifeAnxietyFemalemedicine.symptombusinessStress PsychologicalActa Dermato Venereologica
researchProduct

Assessing psychological and supportive care needs in glioma patients - feasibility study on the use of the Supportive Care Needs Survey Short Form (S…

2016

Neuro-oncological patients experience high symptom and psychosocial burden. The aim was to test feasibility and practicability of the Supportive Care Needs Survey Short Form (SCNS-SF34-G) and the SCNS-Screening Tool (SCNS-ST9) to assess supportive care needs of neuro-oncological patients in clinical routine. A total of 173 patients, most with a primary diagnosis of high-grade glioma (81%), were assessed first using SCNS-SF34-G in comparison to two well-established patient-reported outcome measures, the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQC30 + QLQ-BN20) and Distress Thermometer (DT). In a follow-up assessment, SCNS-ST9 was used …

AdultMalemedicine.medical_specialtyPsychometricsYoung Adult03 medical and health sciences0302 clinical medicineQuality of life (healthcare)GliomamedicineHumansScreening toolAgedHealth Services Needs and DemandBrain Neoplasmsbusiness.industrySocial SupportGliomaMiddle Agedmedicine.diseaseTest (assessment)Clinical PracticeDistressOncologyHealth Care Surveys030220 oncology & carcinogenesisNeeds assessmentPhysical therapyFeasibility StudiesFemalebusinessPsychosocialNeeds Assessment030217 neurology & neurosurgeryEuropean Journal of Cancer Care
researchProduct

Hypochondriasis and health anxiety in the German population

2007

Epidemiologic studies on hypochondriasis are very rare and have not been included in large North American community surveys until now. In order to gain information on the prevalence as well as the socio-demographic characteristics of hypochondriasis, the following community study was carried out. Analyses are based on an assessment of 1575 subjects selected by socio-demographic representation criteria for the German community. All subjects completed the Illness Attitude Scales (IAS) and responded to several additional questions on sociodemographics and diagnostic criteria pertaining to Diagnostic and Statistical Manual of Mental Disorders, fourth edition (DSM-IV) hypochondriasis. The IAS is…

AdultMalemedicine.medical_specialtySelf DisclosureAdolescentAnxietyQuality of life (healthcare)GermanySurveys and QuestionnairesEpidemiologymedicineHumansPsychiatrySocioeconomic statusApplied PsychologyAgedPublic healthSocial environmentGeneral MedicineMiddle AgedMental healthHypochondriasisQuality of LifeSelf-disclosureAnxietyFemalemedicine.symptomPsychologyClinical psychologyBritish Journal of Health Psychology
researchProduct

Resource utilization and productivity loss in persons with spina bifida—an observational study of patients in a tertiary urology clinic in Germany.

2014

Background and purpose To investigate resource use and burden associated with spina bifida (SB) in Germany. Methods A questionnaire was used to obtain information on SB-related healthcare resource use and assistive technologies used for the last 1 and 10 years. Individuals with SB were recruited at a tertiary specialist clinic. To participate, persons with SB required the cognitive ability to respond or a caregiver to answer questions on their behalf. They could use personal medical charts or other records to answer. The analyses included assessment of frequency and extent of resource use for both time frames. Results Data on 88 persons with a diagnosis of SB were collected (44% female). Du…

AdultMalemedicine.medical_specialtyTertiary Care CentersCost of IllnessGermanyHealth caremedicineHumansSpinal DysraphismHospital daysbusiness.industrySpina bifidaHealth Servicesmedicine.diseaseSelf-Help DevicesHospitalizationNeurologyPhysical therapyUrology clinicResource useObservational studyFemaleNeurology (clinical)businessHealthcare providersResource utilizationEuropean journal of neurology
researchProduct

Lifetime, 5-year and past-year prevalence of homelessness in Europe: a cross-national survey in eight European nations

2019

ObjectivesTo examine the lifetime, 5-year and past-year prevalence of homelessness among European citizens in eight European nations.DesignA nationally representative telephone survey using trained bilingual interviewers and computer-assisted telephone interview software.SettingThe study was conducted in France, Ireland, Italy, the Netherlands, Poland, Portugal, Spain and Sweden.ParticipantsEuropean adult citizens, selected from opt-in panels from March to December 2017. Total desired sample size was 5600, with 700 per country. Expected response rates of approximately 30% led to initial sample sizes of 2500 per country.Main outcome measuresHistory of homelessness was assessed for lifetime, …

AdultMalemedicine.medical_specialtyTime FactorsAdolescent[SDV]Life Sciences [q-bio]prevalenceService useSociodemographic dataHealthcare improvement science Radboud Institute for Health Sciences [Radboudumc 18]03 medical and health sciencesHealth servicesYoung Adult0302 clinical medicineRisk FactorsSurveys and QuestionnairesmedicineHumans1724030212 general & internal medicine150610. No inequalitySociodemographic datahomelessnessAgedOriginal ResearchAged 80 and overbusiness.industryeuropean adult citizensEurope; homelessness; prevalence; public healthCross national surveyPublic health1. No povertyGeneral MedicineMiddle Aged3. Good healthTelephone surveyEuropeTelephone interviewSocioeconomic FactorsSample size determinationIll-Housed PersonsLinear ModelsFemale[SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologiePublic Healthbusiness030217 neurology & neurosurgeryDemographyBMJ Open
researchProduct