The experience of living with malignant meningioma

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Standard

The experience of living with malignant meningioma. / Maier, Andrea Daniela; Nordentoft, Sara; Mathiesen, Tiit; Guldager, Rikke.

I: Palliative and Supportive Care, Bind 22, Nr. 2, 2024, s. 338-346.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Maier, AD, Nordentoft, S, Mathiesen, T & Guldager, R 2024, 'The experience of living with malignant meningioma', Palliative and Supportive Care, bind 22, nr. 2, s. 338-346. https://doi.org/10.1017/S1478951523000585

APA

Maier, A. D., Nordentoft, S., Mathiesen, T., & Guldager, R. (2024). The experience of living with malignant meningioma. Palliative and Supportive Care, 22(2), 338-346. https://doi.org/10.1017/S1478951523000585

Vancouver

Maier AD, Nordentoft S, Mathiesen T, Guldager R. The experience of living with malignant meningioma. Palliative and Supportive Care. 2024;22(2):338-346. https://doi.org/10.1017/S1478951523000585

Author

Maier, Andrea Daniela ; Nordentoft, Sara ; Mathiesen, Tiit ; Guldager, Rikke. / The experience of living with malignant meningioma. I: Palliative and Supportive Care. 2024 ; Bind 22, Nr. 2. s. 338-346.

Bibtex

@article{9064cb783ef9493e89dbd3fd70ac73f9,
title = "The experience of living with malignant meningioma",
abstract = "Objectives Meningiomas are the most common, primary intracranial tumor and most are benign. Little is known of the rare patient group living with a malignant meningioma, comprising 1-3% of all meningiomas. Our aim was to explore how patients perceived quality of daily life after a malignant meningioma diagnosis. Methods This qualitative explorative study was composed of individual semi-structured interviews. Eligible patients (n = 12) were selected based on ability to participate in an interview, from a background population of 23 patients diagnosed with malignant meningioma at Rigshospitalet from 2000 to 2021. We performed an inductive thematic analysis following Braun and Clarke's guidelines. Results Eight patients were interviewed. The analysis revealed 4 overarching themes: (1) perceived illness and cause of symptoms, (2) identity, roles, and interaction, (3) threat and uncertainty of the future, and (4) belief in authority. The perceived quality of daily life is negatively impacted by the disease. Patients experience a shift in self-concept and close interactions, and some struggle with accepting a new everyday life. Patients have a high risk of discordant prognostic awareness in relation to health-care professionals. Significance of results We provide a much-needed patient-centered perspective of living with malignant meningioma: quality of life was affected by perception of threat and an uncertainty of the future. Perception of illness and the interpretation of the cause of symptoms varied between subjects, but a common trait was that patients' identity, roles, and interactions were affected. Shared decision-making and a strengthened continuity during follow-up could aid this rare patient group. ",
keywords = "Everyday life, Malignant meningioma, Qualitative research, WHO grade 3 meningioma",
author = "Maier, {Andrea Daniela} and Sara Nordentoft and Tiit Mathiesen and Rikke Guldager",
note = "Publisher Copyright: {\textcopyright} The Author(s), 2023. Published by Cambridge University Press.",
year = "2024",
doi = "10.1017/S1478951523000585",
language = "English",
volume = "22",
pages = "338--346",
journal = "Palliative & Supportive Care",
issn = "1478-9515",
publisher = "Cambridge University Press",
number = "2",

}

RIS

TY - JOUR

T1 - The experience of living with malignant meningioma

AU - Maier, Andrea Daniela

AU - Nordentoft, Sara

AU - Mathiesen, Tiit

AU - Guldager, Rikke

N1 - Publisher Copyright: © The Author(s), 2023. Published by Cambridge University Press.

PY - 2024

Y1 - 2024

N2 - Objectives Meningiomas are the most common, primary intracranial tumor and most are benign. Little is known of the rare patient group living with a malignant meningioma, comprising 1-3% of all meningiomas. Our aim was to explore how patients perceived quality of daily life after a malignant meningioma diagnosis. Methods This qualitative explorative study was composed of individual semi-structured interviews. Eligible patients (n = 12) were selected based on ability to participate in an interview, from a background population of 23 patients diagnosed with malignant meningioma at Rigshospitalet from 2000 to 2021. We performed an inductive thematic analysis following Braun and Clarke's guidelines. Results Eight patients were interviewed. The analysis revealed 4 overarching themes: (1) perceived illness and cause of symptoms, (2) identity, roles, and interaction, (3) threat and uncertainty of the future, and (4) belief in authority. The perceived quality of daily life is negatively impacted by the disease. Patients experience a shift in self-concept and close interactions, and some struggle with accepting a new everyday life. Patients have a high risk of discordant prognostic awareness in relation to health-care professionals. Significance of results We provide a much-needed patient-centered perspective of living with malignant meningioma: quality of life was affected by perception of threat and an uncertainty of the future. Perception of illness and the interpretation of the cause of symptoms varied between subjects, but a common trait was that patients' identity, roles, and interactions were affected. Shared decision-making and a strengthened continuity during follow-up could aid this rare patient group.

AB - Objectives Meningiomas are the most common, primary intracranial tumor and most are benign. Little is known of the rare patient group living with a malignant meningioma, comprising 1-3% of all meningiomas. Our aim was to explore how patients perceived quality of daily life after a malignant meningioma diagnosis. Methods This qualitative explorative study was composed of individual semi-structured interviews. Eligible patients (n = 12) were selected based on ability to participate in an interview, from a background population of 23 patients diagnosed with malignant meningioma at Rigshospitalet from 2000 to 2021. We performed an inductive thematic analysis following Braun and Clarke's guidelines. Results Eight patients were interviewed. The analysis revealed 4 overarching themes: (1) perceived illness and cause of symptoms, (2) identity, roles, and interaction, (3) threat and uncertainty of the future, and (4) belief in authority. The perceived quality of daily life is negatively impacted by the disease. Patients experience a shift in self-concept and close interactions, and some struggle with accepting a new everyday life. Patients have a high risk of discordant prognostic awareness in relation to health-care professionals. Significance of results We provide a much-needed patient-centered perspective of living with malignant meningioma: quality of life was affected by perception of threat and an uncertainty of the future. Perception of illness and the interpretation of the cause of symptoms varied between subjects, but a common trait was that patients' identity, roles, and interactions were affected. Shared decision-making and a strengthened continuity during follow-up could aid this rare patient group.

KW - Everyday life

KW - Malignant meningioma

KW - Qualitative research

KW - WHO grade 3 meningioma

U2 - 10.1017/S1478951523000585

DO - 10.1017/S1478951523000585

M3 - Journal article

C2 - 37221880

AN - SCOPUS:85161357909

VL - 22

SP - 338

EP - 346

JO - Palliative & Supportive Care

JF - Palliative & Supportive Care

SN - 1478-9515

IS - 2

ER -

ID: 368803373