13 results on '"Rosenlund, Lena"'
Search Results
2. Do presenting symptoms predict treatment decisions and survival in glioblastoma? Real-world data from 1458 patients in the Swedish brain tumor registry
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Bruhn, Helena, Tavelin, Bjorn, Rosenlund, Lena, Henriksson, Roger, Bruhn, Helena, Tavelin, Bjorn, Rosenlund, Lena, and Henriksson, Roger
- Abstract
Background Glioblastoma is the most common malignant brain tumor in adults. Non-invasive clinical parameters could play a crucial role in treatment planning and serve as predictors of patient survival. Our register-based real-life study aimed to investigate the prognostic value of presenting symptoms. Methods Data on presenting symptoms and survival, as well as known prognostic factors, were retrieved for all glioblastoma patients in Sweden registered in the Swedish Brain Tumor Registry between 2018 and 2021. The prognostic impact of different presenting symptoms was calculated using the Cox proportional hazard model. Results Data from 1458 adults with pathologically verified IDH wild-type glioblastoma were analyzed. Median survival time was 345 days. The 2-year survival rate was 21.5%. Registered presenting symptoms were focal neurological deficits, cognitive dysfunction, headache, epilepsy, signs of raised intracranial pressure, and cranial nerve symptoms, with some patients having multiple symptoms. Patients with initial cognitive dysfunction had significantly shorter survival than patients without; 265 days (245-285) vs. 409 days (365-453; P < .001). The reduced survival remained after Cox regression adjusting for known prognostic factors. Patients presenting with seizures and patients with headaches had significantly longer overall survival compared to patients without these symptoms, but the difference was not retained in multivariate analysis. Patients with cognitive deficits were less likely to have radical surgery and to receive extensive anti-neoplastic nonsurgical treatment. Conclusions This extensive real-life study reveals that initial cognitive impairment acts as an independent negative predictive factor for treatment decisions and adversely affects survival outcomes in glioblastoma patients., Funding Agencies|Swedish Brain Tumour Registry; National Cancer Foundation; Cancer Foundation Northern Sweden; Futurum Academy for Health and Care
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- 2024
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3. Inequalities in access to neuro-oncology supportive care and rehabilitation: A survey of healthcare professionals' perspectives.
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Boele, Florien, Rosenlund, Lena, Nordentoft, Sara, Melhuish, Sara, Nicklin, Emma, Rydén, Isabelle, Williamson, Aoife, Donders-Kamphuis, Marike, Preusser, Matthias, Rhun, Emilie Le, Kiesel, Barbara, Minniti, Giuseppe, Furtner, Julia, Dirven, Linda, Taphoorn, Martin, Galldiks, Norbert, Rudà, Roberta, Chalmers, Anthony, Short, Susan C, and Piil, Karin
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MEDICAL personnel , *PHYSICIANS , *NEUROREHABILITATION , *PSYCHO-oncology , *ONCOLOGY nursing , *REHABILITATION , *HEALTH equity , *BRAIN cancer - Abstract
Background Neuro-oncology patients and caregivers should have equitable access to rehabilitation, supportive-, and palliative care. To investigate existing issues and potential solutions, we surveyed neuro-oncology professionals to explore current barriers and facilitators to screening patients' needs and referral to services. Methods Members of the European Association of Neuro-Oncology and the European Organisation for Research and Treatment of Cancer Brain Tumor Group (EORTC-BTG) were invited to complete a 39-item online questionnaire covering the availability of services, screening, and referral practice. Responses were analyzed descriptively; associations between sociodemographic/clinical variables and screening/referral practice were explored. Results In total, 103 participants completed the survey (67% women and 57% medical doctors). Fifteen professions from 23 countries were represented. Various rehabilitation, supportive-, and palliative care services were available yet rated "inadequate" by 21–37% of participants. Most respondents with a clinical role (n = 94) declare to screen (78%) and to refer (83%) their patients routinely for physical/cognitive/emotional issues. Survey completers (n = 103) indicated the main reasons for not screening/referring were (1) lack of suitable referral options (50%); (2) shortage of healthcare professionals (48%); and (3) long waiting lists (42%). To improve service provision, respondents suggested there is a need for education about neuro-oncology-specific issues (75%), improving the availability of services (65%) and staff (64%), developing international guidelines (64%), and strengthening the existing evidence-base for rehabilitation (60%). Conclusions Detecting and managing neuro-oncology patients' and caregivers' rehabilitation, supportive,- and palliative care needs can be improved. Better international collaboration can help address healthcare disparities. [ABSTRACT FROM AUTHOR]
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- 2024
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4. Holistic Needs Assessment and Care Planning
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Piil, Karin, Rosenlund, Lena, and Oberg, Ingela, editor
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- 2019
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5. Regional variation in usage of TTF (Optune) Regional variation i användningen av TTF vid glioblastombehandling : [Regional variation in usage of TTF (Optune)]
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Kinhult, Sara, Tavelin, Björn, Löfgren, David, Rosenlund, Lena, Sandström, Maria, Strandeus, Michael, Henriksson, Roger, Kinhult, Sara, Tavelin, Björn, Löfgren, David, Rosenlund, Lena, Sandström, Maria, Strandeus, Michael, and Henriksson, Roger
- Abstract
The standard treatment of glioblastoma, an aggressive brain tumour, includes radiotherapy combined with temozolomide. Based on a randomised trial, showing five months increased survival, TTF has been introduced in the management of patients with good performance status. Data from the Swedish national quality registry for CNS tumours have been analysed for TTF usage. The results demonstrate that 65 percent of the patients accepted treatment with TTF. More than half of the treated patients interrupted treatment due to low compliance or their own wish. Median treatment time was 164 days, with a range from 0 to 774 days. There was a large variation between different regions in how many patients were offered TTF treatment. A non-significant trend to better survival was seen for the group of TTF-treated patients compared to individually matched controls. In summary, TTF is a new treatment for glioblastoma, with potential to prolong survival also in real world patients. Today, the treatment is not offered equally to all patients, despite national guidelines., Publicerad på Lakartidningen.se 2023-07-03
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- 2023
6. Regional variation i användningen av TTF vid glioblastombehandling : [Regional variation in usage of TTF (Optune)]
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Kinhult, Sara, Tavelin, Björn, Löfgren, David, Rosenlund, Lena, Sandström, Maria, Strandeus, Michael, Henriksson, Roger, Kinhult, Sara, Tavelin, Björn, Löfgren, David, Rosenlund, Lena, Sandström, Maria, Strandeus, Michael, and Henriksson, Roger
- Abstract
The standard treatment of glioblastoma, an aggressive brain tumour, includes radiotherapy combined with temozolomide. Based on a randomised trial, showing five months increased survival, TTF has been introduced in the management of patients with good performance status. Data from the Swedish national quality registry for CNS tumours have been analysed for TTF usage. The results demonstrate that 65 percent of the patients accepted treatment with TTF. More than half of the treated patients interrupted treatment due to low compliance or their own wish. Median treatment time was 164 days, with a range from 0 to 774 days. There was a large variation between different regions in how many patients were offered TTF treatment. A non-significant trend to better survival was seen for the group of TTF-treated patients compared to individually matched controls. In summary, TTF is a new treatment for glioblastoma, with potential to prolong survival also in real world patients. Today, the treatment is not offered equally to all patients, despite national guidelines., TTF (tumour treating fields) är en ny, nationellt godkänd utrustning, som inducerar alternerande elektriska fält och används vid behandling av hjärntumören glioblastom. Behandlingen kan vara inskränkande i vardagen, och data från det nationella registret för CNS-tumörer visar att mer än hälften av patienterna avbryter TTF på grund av dålig användningsgrad eller egen önskan. Genomsnittlig behandlingstid enligt registret är 164 dagar. Jämfört med matchade kontroller visar data från registret en trend med längre överlevnad för patienter som behandlas med TTF; dock är skillnaden inte statistiskt signifikant. Det finns en stor regional variation i andelen patienter som erbjudits behandlingen.
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- 2023
7. Person-Centered Care Item Bank
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Rosenlund, Lena, primary, Jakobsson, Sofie, additional, Lloyd, Helen, additional, Lundgren-Nilsson, Åsa, additional, Hermansson, Miriam, additional, and Dencker, Anna, additional
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- 2022
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8. Moving from clinician-defined to patient-reported outcome measures for survivors of high-grade glioma
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Rosenlund, Lena, Degsell, Eskil, and Jakola, Asgeir Store
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symptom management ,Review ,high-grade glioma ,brain tumor ,patient-reported outcome measures - Abstract
Background Persons with high-grade glioma face both neurological and cancer-related symptoms from the tumor itself and its treatment affecting their daily lives. Survival alone is not an adequate outcome, the quality of the survivorship experience needs to be regarded with equal importance. Patient-reported outcome (PRO) measures can be used to evaluate treatment effects and symptom management interventions. Purpose The aim of this review was to identify the use, challenges, and potential of PRO measures in survivors of high-grade glioma. Methods A narrative expert opinion review was performed on the subject. In addition to our own experiences we searched PubMed, Cumulative Index to Nursing and Allied Health Literature, the Cochrane Library, and PsycINFO for brain tumor-specific PRO measures used in the population of adult patients with high-grade glioma, both original articles and reviews were included. Results There are several PRO measures that have been validated for patients with primary brain tumors including high-grade glioma. PRO measures are used both in clinical trials to evaluate the effect of treatment on health-related quality of life, and in daily clinical practice for holistic needs assessment and symptom management. Common PRO measures used for patients with high-grade glioma are European Organization for Research and Treatment of Cancer general instrument for patients with cancer together with brain tumor module, Functional Assessment of Cancer Therapy-Brain, and MD Anderson Symptom Inventory for Brain Tumor. Neurologic and cognitive disorders often occur in patients with high-grade glioma, which affects patients’ ability to self-report over time, making it more challenging in this population. PRO as a primary outcome seems underutilized. Conclusion For clinical research, PRO measures need to be used together with other clinical outcome measures rather than replacing traditional outcome measures. Moving to more use of PRO measures in survivorship care has potential to improve patient-caregiver-healthcare team communication, symptom management, and quality of care. Implementing PROs in survivorship care should also involve caregivers and a response based on the results.
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- 2019
9. Measuring patient experiences of person‐centred care: Translation, cultural adaption and qualitative evaluation of item candidates for use in England and Sweden
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Rosenlund, Lena, primary, Jakobsson, Sofie, additional, Lloyd, Helen, additional, Lundgren‐Nilsson, Åsa, additional, Hermansson, Miriam, additional, and Dencker, Anna, additional
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- 2021
- Full Text
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10. Measuring patient experiences of person‐centred care: Translation, cultural adaption and qualitative evaluation of item candidates for use in England and Sweden.
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Rosenlund, Lena, Jakobsson, Sofie, Lloyd, Helen, Lundgren‐Nilsson, Åsa, Hermansson, Miriam, and Dencker, Anna
- Subjects
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EXPERIMENTAL design , *CAREGIVER attitudes , *FOCUS groups , *RESEARCH methodology , *RESEARCH methodology evaluation , *ATTITUDE (Psychology) , *PATIENT-centered care , *MEDICAL personnel , *COGNITION , *MEDICAL care , *PATIENTS , *INTERVIEWING , *PATIENTS' attitudes , *CONCEPTUAL structures , *QUESTIONNAIRES , *SCALE analysis (Psychology) , *TRANSLATIONS - Abstract
Background: To facilitate change for person‐centred care, there is a need to invest in measures to assess if and how healthcare systems are delivering care based on the principles of person‐centred care. This paper describes the first phase in developing an item bank to measure patients' experiences of person‐centred care. Aim: The aim was to translate, culturally adapt and evaluate candidate items to measure person‐centred care from the patient's perspective. Methods: The Centre for person‐centred care at Gothenburg university and the UK Person‐centred and coordinated care model informed our conceptual framework. The initial pool of item candidates originated from a previous systematic review where 855 items were identified. In this study, a mixed method design was used involving persons with experience as patients, caregivers, healthcare professionals and researchers in person‐centred care or questionnaire design (n = 84). The item analysis included two validation rounds using web questionnaires, a focus group and cognitive interviews. Results: From the initial pool, 155 items covering core domains and subdomains of person‐centred and coordinated care were selected for translation and qualitative item analysis. After translation, 44 items were excluded (duplicates). After the first validation round, 21 items were rephrased and 35 were excluded (due to low ratings, lack of comprehensibility, were duplicates or too specifically phrased). To reflect the ethical basis of person‐centred care, rewordings were also made to encompass the patient as an active partner in care and where communication and information goes two‐ways and care is co‐created. After the second round, 11 items were rephrased and 25 items were excluded (for being redundant/repetitive). Six new items were added (covering access to care, patient capabilities, mental well‐being and identifying goals). Conclusion: We have developed a first set of 57 items to proceed towards developing an item bank to measure the patient experiences of person‐centred care. [ABSTRACT FROM AUTHOR]
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- 2022
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11. Moving from clinician-defined to patient-reported outcome measures for survivors of high-grade glioma
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Rosenlund,Lena, Degsell,Eskil, Jakola,Asgeir Store, Rosenlund,Lena, Degsell,Eskil, and Jakola,Asgeir Store
- Abstract
Lena Rosenlund,1,2 Eskil Degsell,1,3,4 Asgeir Store Jakola5–71Regional Cancer Centre Stockholm, Stockholm, Sweden; 2Institute of Health and Care Sciences, Sahlgrenska Academy, Gothenburg, Sweden; 3Malignant Brain Tumor Pathway, Quality and Patient Safety Department, Karolinska University Hospital, Stockholm, Sweden; 4The Swedish Brain Tumor Association, Stockholm, Sweden; 5Department of Clinical Neurosciences, Institute of Physiology and Neuroscience, Sahlgrenska Academy, Gothenburg, Sweden; 6Department of Neurosurgery, Sahlgrenska University Hospital, Gothenburg, Sweden; 7Department of Neurosurgery, St. Olavs Hospital, Trondheim, NorwayCorrespondence: Lena RosenlundUniversity of Gothenburg, Regional Cancer Centre Stockholm, Box 6909, Stockholm 102 39, SwedenTel +46 73 668 1891Email lena.rosenlund@gu.seBackground: Persons with high-grade glioma face both neurological and cancer-related symptoms from the tumor itself and its treatment affecting their daily lives. Survival alone is not an adequate outcome, the quality of the survivorship experience needs to be regarded with equal importance. Patient-reported outcome (PRO) measures can be used to evaluate treatment effects and symptom management interventions.Purpose: The aim of this review was to identify the use, challenges, and potential of PRO measures in survivors of high-grade glioma.Methods: A narrative expert opinion review was performed on the subject. In addition to our own experiences we searched PubMed, Cumulative Index to Nursing and Allied Health Literature, the Cochrane Library, and PsycINFO for brain tumor-specific PRO measures used in the population of adult patients with high-grade glioma, both original articles and reviews were included.Results: There are several PRO measures that have been validated for patients with primary brain tumors including high-grade glioma. PRO measures are used both in clinical trials to evaluate the effect of treatment on health-related quality of life, and in d
- Published
- 2019
12. Frågeformulär med patientrapporterade utfallsmått för patienter med primär hjärntumör : en litteraturöversikt
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Rosenlund, Lena
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Funktion ,Hälsorelaterad livskvalitet ,Symptom ,Hjärntumör ,Frågeformulär ,PROM - Abstract
SAMMANFATTNING Varje år insjuknar ca 1200 personer i Sverige med primär hjärntumör (Socialstyrelsen, 2014). En hjärntumör får ofta en stor inverkan på livssituationen för patienten och dennes närstående. Att identifiera och undervisa patient och närstående att hantera symtom och biverkningar för att kunna sätta in hjälpinsatser i rätt tid är en stor del av omvårdnadsarbetet för att förbättra den hälsorelaterade livskvaliteten under och efter sjukdomsperioden (Cahill & Armstrong, 2011). PROM är en förkortning av Patient Reported Outcome Measure, som översätts till patientrapporterade utfallsmått på svenska. PROM innefattar patientens egen skattning av sjukdomssymptom, funktionsförmåga och hälsorelaterad livskvalitet. Att använda frågeformulär med PROM är ett strukturerat sätt för både symtomintervention och uppföljning av vården (Nilsson, 2014). Syftet var att sammanställa frågeformulär framtagna eller modifierade för att mäta patientrapporterade utfallsmått hos vuxna patienter med primär hjärntumör. Litteraturöversikt valdes som metod och litteratursökning gjordes i databaserna PubMed och Cinahl. I resultatet presenterades sju frågeformulär framtagna eller modifierade och validerade för patienter med hjärntumör. Frågeformulären användes i olika syften som symtomintervention, uppföljning av vården eller utfallsmått i kliniska studier. Slutsatsen var att de två vanligast förekommande frågeformulären för patienter med hjärntumör var livskvalitetsformulären EORTC QLQ-C30 med hjärntumörmodulen BN20 och FACT-Br.
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- 2015
13. [Regional variation in usage of TTF (Optune)].
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Kinhult S, Tavelin B, Löfgren D, Rosenlund L, Sandström M, Strandeus M, and Henriksson R
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- Humans, Temozolomide therapeutic use, Combined Modality Therapy, Glioblastoma drug therapy, Brain Neoplasms drug therapy
- Abstract
The standard treatment of glioblastoma, an aggressive brain tumour, includes radiotherapy combined with temozolomide. Based on a randomised trial, showing five months increased survival, TTF has been introduced in the management of patients with good performance status. Data from the Swedish national quality registry for CNS tumours have been analysed for TTF usage. The results demonstrate that 65 percent of the patients accepted treatment with TTF. More than half of the treated patients interrupted treatment due to low compliance or their own wish. Median treatment time was 164 days, with a range from 0 to 774 days. There was a large variation between different regions in how many patients were offered TTF treatment. A non-significant trend to better survival was seen for the group of TTF-treated patients compared to individually matched controls. In summary, TTF is a new treatment for glioblastoma, with potential to prolong survival also in real world patients. Today, the treatment is not offered equally to all patients, despite national guidelines.
- Published
- 2023
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