Jaarindex Psychosociale Oncologie 2021-2022

Page 120

KWALITEIT VAN LEVEN AYA DIGESTIEVE ONCOLOGIE

PATIENTS’ PERCEPTIONS OF THE INFORMATION RECEIVED DURING DIAGNOSIS AND TREATMENT: IS THERE AN ASSOCIATION WITH LONG-TERM QUALITY OF LIFE IN COLORECTAL CANCER SURVIVORS?

PROBLEEM- EN DOELSTELLING(EN) ONDERZOEKSPROJECT

PEV PSYCHO-ONCOLOGIE

To investigate the information provided during diagnosis and treatment of colorectal cancer (CRC) as perceived by long-term survivors and its association with sociodemographic, clinical, lifestyle, psychological characteristics as well as with the long-term health-related quality of life (HRQoL).

ONDERZOEKSOPZET In 2015, CRC survivors who were followed by seven Flemish hospitals and diagnosed with CRC between 2008 and 2010, as registered by the Belgium Cancer Registry, received a written questionnaire on information provision (EORTC QLQ-INFO25) and HRQoL (EORTC QLQC30).

RESULTATEN CRC survivors indicated to receive (quite) a lot of information about their disease, medical tests and treatment, while regarding other care services they reported to have received no or little information. However, only a minority would have wanted to receive more information. The provided information was evaluated satisfying and helpful. In multiple logistic regression analyses, information provided on the disease, medical tests, self-care and the perceived helpfulness of the information varied by patient’s education. Age was significantly linked to disease and treatment information, whereas the treatment modality was associated with information on treatment, other care services, places of care and self-care. The perceived helpfulness of the provided information was related with HRQoL.

KLINISCHE- MAATSCHAPPELIJKE- EN/OF WETENSCHAPPELIJKE RELEVANTIE Although CRC survivors evaluated most of the information they obtained as helpful and satisfactory, it seems that there is room for improvement for informing patients on psychosocial, supportive and aftercare matters. The perceived quality of the information can be improved by taking individual preferences on receiving information into account, which in turn can improve HRQoL during survivorship.

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dr. Jolien Robijns, Joy Lodewijckx, dr. Katrien Wijnen, Sylvana Snoekx

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pages 152-155

Véronique Gerits

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Kaat Sioen, Inge Decock, Jana Missiaen

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Els Pazmany, Katrien Maes, Vicky De Kock, Brigitte Aerts, David Verhulst, Els Driessen

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Elke Rammant, Emile Deman, Lindsay Poppe

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dr. Steven Vanderstichelen

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dr. Naomi Dhollander, dr. Aline De Vleminck, prof. dr. Nele Michels, Else Gien Statema

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Elke Rammant, Lindsay Poppe

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Dimitri Vrancken, Marie Crabbé, Vicky Van Stappen, Ine De Clerck

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Liesbeth De Schrijver

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pages 122-127

Joke Ameryckx

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pages 120-121

Eva De Bisschop, Jill Verhoeven

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Jill Dobbelaer

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pages 118-119

Miek Goetmaeckers

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dr. Nynke Willers

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Ann Dehaese, Els Ghesquiere, Eline Decleermaecker, Sieglinde Pletinck, Sylvie De Turck, Ludo Moyersoen, Lien Agache et al

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Michael Rosskamp, Julie Verbeeck, Freija Verdoodt, Harlinde De Schutter

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Michael Rosskamp, Julie Verbeeck, Freija Verdoodt, Harlinde De Schutter

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Anne Rogiers, Christophe Leys, Justine Lauwyck , Adrian Schembri, Gil Awada, Julia Katharina Schwarze, Jennifer De Cremer, Peter Theuns, Paul Maruff, Mark De Ridder, Jan L. Bernheim, Bart Neyns

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Laurien De Roeck

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pages 84-85

A. Rogiers, C. Leys, J. De Cremer, G. Awada, A. Schembrig, P. Theuns, M. De Ridder, B. Neyns

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Gwen Schroyen

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Yasmien De Ly

1min
pages 82-83

Laura Tack

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pages 78-79

dra. Yaël Slaghmuylder

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dra. Yaël Slaghmuylder

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Eva Roose, Laurence Leysen

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Sari Illegems

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dra. Lore Dams, dra. Elien Van der Gucht

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prof. dr. Benedicte Deforche, prof. dr. Joachim Cohen

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Sigrid Dierickx, Kim Beernaert, Rigo Verhaert

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pages 56-57

dr. Liesbeth Van Humbeeck, dr. Let Dillen, drs. Charlotte Boven

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Kleo Dubois, Annemarie Coolbrandt

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Leen Ackaert, Let Dillen

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Paulien De Langhe

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pages 46-47

Kleo Dubois, Annemarie Coolbrandt, Mireille Kusters, Leen Neyens, Hadi Waelkens, Kirsten Van Nieuwerburgh-Marchand

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Deveny Vanrusselt

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pages 44-45

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Voorwoord

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