Browsing Artikler by Title
Now showing items 128-147 of 205
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Opioids, Pain Management, and Palliative Care in a Norwegian Nursing Home From 2013 to 2018
(Peer reviewed; Journal article, 2019)In Norway, approximately 50% of older people die in nursing homes (NH). Holistic care and pharmacological management are key factors in quality at the end of life. The purpose of this longitudinal study was to describe the ... -
Optimal Conventional Mechanical Ventilation in Full-Term Newborns
(Journal article; Peer reviewed, 2018) -
Organization of nursing care in three Nordic countries: relationships between nurses’ workload, level of involvement in direct patient care, job satisfaction, and intention to leave
(Journal article; Peer reviewed, 2014-10-06)Background: Health care systems in Finland, Norway and Sweden share many similarities, e.g. full-coverage and tax-financed, with predominately public sector hospitals. Despite similarities, there are differences in the ... -
Oxygen and ventilator treatment: perspectives on interprofessional collaboration in a neonatal intensive care unit
(Journal article; Peer reviewed, 2014-06)Abstract Background: The aim of this study was to explore perspectives on the collaboration between physicians and nurses managing oxygen and ventilator treatment of sick infants in a Norwegian neonatal intensive care ... -
Palliasjon en fremmedgjøring av fagfeltets kjerne - hvorfor ikke palliativ omsorg?
(Peer reviewed; Journal article, 2018) -
The Parent Health Literacy Questionnaire (HLQ-Parent). Adaptation and validity testing with parents of children with epilepsy
(Peer reviewed; Journal article, 2022)Aims: The aim of this study was to adapt the Health Literacy Questionnaire (HLQ) in English and Norwegian for use with parents. Methods: The research group evaluated all HLQ items and, where relevant, modified them to ... -
Parent psychological wellbeing in a single-family room versus an open bay neonatal intensive care unit
(Peer reviewed; Journal article, 2019)Background Studies of parents’ psychological well-being in single-family rooms in neonatal intensive care units have shown conflicting results. Aims To compare emotional distress in the form of depression, anxiety, ... -
Parents of children with epilepsy: Characteristics associated with high and low levels of health literacy
(Peer reviewed; Journal article, 2022)Parents of children with epilepsy play a key role in the management of their child’s condition. Their level of health literacy (HL), which refers to their ability to seek, understand, assess, remember, and utilize health ... -
Parents’ experiences of transitioning to home with a very-low-birthweight infant: A meta-ethnography
(Peer reviewed; Journal article, 2022)Medical-technological advances and neurodevelopmental care have improved the survival of extremely- and very-low-birthweight infants born before 32 weeks’ gestation. After months in neonatal care, the infants are discharged, ... -
Patient involvement in micro-decisions in intensive care
(Peer reviewed; Journal article, 2020)Objective The objective of this study was to explore how bedside micro-decisions were made between conscious patients on mechanical ventilation in intensive care and their healthcare providers. Methods Using video recordings ... -
Patient mobilisation in the intensive care unit and evaluation of a multifaceted intervention including Facebook groups: A quasi-experimental study
(Peer reviewed; Journal article, 2022)Aims: To describe prevalence and time to mobilisation in intensive care unit patients defined as a minimum sitting in an upright position in bed, and evaluate the impact of a multifaceted quality improvement campaign ... -
Patient-reported outcome measures in children, adolescents, and young adults with palliative care needs—a scoping review
(Peer reviewed; Journal article, 2023)Background: Measuring outcomes facilitates evaluation of palliative services for children, adolescents, and young adults (CAYAs) with life-limiting and/or life-threatening (LL/LT) conditions. Implementation of patient-reported, ... -
Patients experiences with a welfare technology application for remote home care: A longitudinal study
(Peer reviewed; Journal article, 2022)Aims and Objectives: To explore the longitudinal experiences using an application named remote home care for remote palliative care among patients with cancer living at home. Background: Introducing welfare technology ... -
Patients' experiences with changes in perceived control in chronic illness: A pilot study of the outcomes of a new health promotion program in community health care
(Journal article; Peer reviewed, 2016-03-12)Among the main challenges accompanying chronic illness are uncertainty and lack of perceived control, both of which put the patient at risk of developing psychological comorbidities. This qualitative study explored patients’ ... -
Patients’ Experiences of Enhanced Recovery after Surgery: A systematic review of qualitative studies
(Journal article; Peer reviewed, 2017)Aim To aggregate, interpret and synthesise findings from qualitative studies to further our knowledge regarding patients’ pre- and postoperative experiences when participating in an enhanced recovery after surgery (ERAS) ... -
Patient’s Experience of the Outcomes of Engaging in a Broadly Applicable Health Promotion Intervention for Individuals Facing Chronic Illness
(Journal article; Peer reviewed, 2015-06-29)The aim of this study was to explore the health-related outcomes of a new health promotion in- tervention designed to be broadly applicable among people diagnosed with chronic illness. Qua- litative process analysis was ... -
Pårørende til hjemmeboende med hjertesvikt: "medarbeidere" i ukjent tjenesteterreng
(Journal article; Peer reviewed, 2016-07-05)Bakgrunn: Pårørendes støtte har betydning for hvordan hjemmeboende personer som har hjertesvikt, mestrer sykdommen og hverdagen. Støtte fra pårørende kan også påvirke utfallet av sykdommen og redusere sykehusinnleggelser. ... -
Pårørendes erfaringer med kommunal hjemmetjeneste til personer med demens
(Peer reviewed; Journal article, 2016-08-22)Bakgrunn: I Norge er det cirka 75.000 personer med demens. I løpet av sykdommen vil disse ha behov for profesjonell pleie. Pårørende er ofte de første hjelperne inntil profesjonelle pleiere overtar. Studier viser at pårørende ...