Search results for "Patient rights"

showing 5 items of 5 documents

Return and Disclosure of Research Results: Parental Attitudes and Needs Over Time in Pediatric Oncology.

2017

Objectives To explore parental attitudes regarding the return and disclosure of research findings in pediatric cancer trials over time. Study design Two surveys were set up to evaluate the stability of parental attitudes. One survey was carried out among 581 parents whose child was diagnosed recently (response rate, 53.5%). A second, population-based survey was set up with a time interval of 4 years between first cancer diagnosis and survey in which 1465 parents were included (response rate, 55.1%). Results Almost all surveyed parents stated a parental right to receive aggregate research results. Fifty-five percent of the parents who recently participated in trials and 62% of those asked af…

0301 basic medicineChange over timeMaleParentsmedicine.medical_specialtyAdolescentmedia_common.quotation_subjectPopulationChild Welfare030105 genetics & heredityMedical OncologyTruth DisclosurePediatricsParental Notification03 medical and health sciences0302 clinical medicineProfessional-Family RelationsGermanyNeoplasmsmedicinePediatric oncologyHumansParent-Child RelationseducationSet (psychology)PsychiatryChildmedia_commonResponse rate (survey)education.field_of_studybusiness.industryInfant NewbornInfantPediatric cancerMaturity (psychological)First cancer diagnosisPatient Rights030220 oncology & carcinogenesisFamily medicineChild PreschoolHealth Care SurveysPediatrics Perinatology and Child HealthFemalebusinessAttitude to HealthThe Journal of pediatrics
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COVID-19 Contact Tracing and Data Protection Can Go Together

2020

We discuss the implementation of app-based contact tracing to control the coronavirus disease (COVID-19) pandemic and discuss its data protection and user acceptability aspects.

2019-20 coronavirus outbreakCoronavirus disease 2019 (COVID-19)Computer scienceSevere acute respiratory syndrome coronavirus 2 (SARS-CoV-2)Pneumonia ViralPatient rightsHealth InformaticsInformation technologyprivacycontact tracingDisease OutbreaksBetacoronavirusHuman–computer interactionHumansData Protection Act 1998Guest Editorialproximity tracingPandemicsappComputer Securitydata protectionUser acceptabilitySARS-CoV-2BluetoothCOVID-19T58.5-58.64Mobile ApplicationsPatient RightsGeographic Information SystemsSmartphonePublic aspects of medicineRA1-1270Coronavirus InfectionsContact tracingCoronavirus InfectionsJMIR mHealth and uHealth
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Market empowerment of the patient: the French experience.

2011

Through analysis of the French experience, this article explores the way economic policy has sought to encourage active, well-informed patients by giving them market power. The new status of the patient as consumer is based on two foundations: the endeavour to build a healthcare market and the activation of demand-based policies. The keystone of this new system is a conception of the market as a process constructed by economic policy. Recent measures such as the standardization of care and the introduction of incentives to respect a treatment pathway then constitute effective levers to establish a free-market rationale.

Economics and EconometricsStandardizationCompulsory insurancePatientsEconomicsmedia_common.quotation_subjectCopaymentsHealth Care SectorHistory 21st Century03 medical and health sciencesNational health insurance0302 clinical medicineHealth insurance0502 economics and businessHealth careEconomics[ SHS.ECO ] Humanities and Social Sciences/Economies and finances030212 general & internal medicineConsumer economicsMarket power050207 economicsEmpowerment[SHS.ECO] Humanities and Social Sciences/Economics and FinanceComputingMilieux_MISCELLANEOUSmedia_commonConsumer economicsPublic economics[QFIN]Quantitative Finance [q-fin]Consumer Health Informationbusiness.industry05 social sciencesPersonal empowermentNonmarket forcesStandard of CareHistory 20th Century[SHS.ECO]Humanities and Social Sciences/Economics and Finance[QFIN] Quantitative Finance [q-fin]ReimbursementIncentiveInsurance providersMarket PowerPatient RightsFranceMarketizationPower PsychologicalbusinessReview of social economy
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Sind gehörlose Patienten in Deutschland über ihren gesetzlichen Dolmetscheranspruch informiert?

2012

Gehorlose Burgerinnen und Burger stosen in einer von Horenden gestalteten gesundheitlichen Versorgung auf Barrieren. Der Gesetzgeber hat daher die Finanzierung von Gebardensprachdolmetschern zulasten der Krankenversicherungen vorgesehen. Die vorliegende Studie untersucht erstmals, inwieweit Gehorlose daruber informiert sind und Gebrauch von Dolmetschern machen. Herkommliche Erhebungen basieren auf Laut- und Schriftsprache und sind fur die Zielgruppe eher ungeeignet. Daher wurde eine Online-Querschnittsstudie durchgefuhrt, die mittels Gebardensprachvideos und visuell ausgerichteten Antwortmoglichkeiten eine barrierefreie Teilnahme ermoglichte. Mit einer multivariaten Analyse wurden Faktoren …

Political sciencePublic Health Environmental and Occupational HealthPatient rightsSign languageHumanitiesDas Gesundheitswesen
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[Recommendations for end-of-life care in patients with chronic obstructive pulmonary disease].

2009

Over the last 20 years, advances in the treatment of patients with chronic obstructive pulmonary disease (COPD) have improved survival even among patients in the most advanced stages of the disease, such as those requiring domiciliary oxygen therapy.1,2 This improvement—in principle a positive development—has given rise to considerable clinical problems associated with the establishment of a therapeutic ceiling and the difficulty of determining prognosis in some of these patients. In this situation, the clinician should consider introducing palliative care, that is, care aimed at improving symptom control, communication, physical activity, and emotional support, in order to achieve the best…

Riskmedicine.medical_specialtyPalliative careAttitude to DeathAttitude of Health PersonnelHealth PersonnelDecision MakingContext (language use)DiseaseAnxietyPulmonary Disease Chronic ObstructiveQuality of life (healthcare)Intensive careHealth caremedicineHumansTerminally IllIntensive care medicineCOPDPhysician-Patient RelationsTerminal Carebusiness.industryDepressionGeneral Medicinemedicine.diseasePrognosisDyspneaPatient RightsCaregiversSpainPractice Guidelines as TopicbusinessAdvance DirectivesEnd-of-life careArchivos de bronconeumologia
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