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Patient-reported Outcome Measurements on the Tolerance of Magnetic Resonance Imaging-guided Radiation Therapy.
Tetar, Shyama; Bruynzeel, Anna; Bakker, Roosje; Jeulink, Marloes; Slotman, Ben J; Oei, Swie; Haasbeek, Cornelis; De Jong, Karel; Senan, Suresh; Lagerwaard, Frank.
Afiliación
  • Tetar S; Radiation Oncology, VU University Medical Center, Amsterdam, The Netherlands.
  • Bruynzeel A; Radiation Oncology, VU University Medical Center, Amsterdam, The Netherlands.
  • Bakker R; Radiation Oncology, VU University Medical Center, Amsterdam, The Netherlands.
  • Jeulink M; Radiation Oncology, VU University Medical Center, Amsterdam, The Netherlands.
  • Slotman BJ; Radiation Oncology, VU University Medical Center, Amsterdam, The Netherlands.
  • Oei S; Radiation Oncology, VU University Medical Center, Amsterdam, The Netherlands.
  • Haasbeek C; Radiation Oncology, VU University Medical Center, Amsterdam, The Netherlands.
  • De Jong K; Radiation Oncology, VU University Medical Center, Amsterdam, The Netherlands.
  • Senan S; Radiation Oncology, VU University Medical Center, Amsterdam, The Netherlands.
  • Lagerwaard F; Radiation Oncology, VU University Medical Center, Amsterdam, The Netherlands.
Cureus ; 10(2): e2236, 2018 Feb 27.
Article en En | MEDLINE | ID: mdl-29719739
ABSTRACT
Purpose Magnetic resonance imaging-guided radiation therapy (MRgRT) requires patient positioning within the MR bore and prolonged MR imaging during delivery, both of which are new in radiation oncology. Patient tolerance of MRgRT was prospectively evaluated using patient-reported outcome questionnaires (PRO-Q). Methods Our MRgRT procedure involves daily high-resolution MR scanning, limited re-contouring, daily plan re-optimization, quality assurance (QA), and gated delivery. Patients with claustrophobia are excluded. Mean fraction duration was 45 and 60 minutes for stereotactic treatments during free-breathing and breath-hold, respectively. Patient-controlled video-feedback was used for breath-hold delivery. PRO-Qs collected in the first 150 patients treated included questions on MR-related complaints and also evaluated aspects of active participation. Results Almost one-third of patients (29%) scored at least one PRO-Q item on MR-related complaints as 'moderate' or 'very much', with noise, feeling cold, and paresthesia being the most frequently scored in this way. Considerable anxiety was reported by 5%, but no medication was required for this in any patient. Patient participation in video feedback for breath-hold delivery was appreciated by the majority of patients, all of whom completed the procedure. Only 5% of patients considered treatment duration to be unacceptably long. Conclusion Despite the lengthy MRgRT procedure, outcomes of PRO-Q indicate that it was well-tolerated by patients.
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Texto completo: 1 Colección: 01-internacional Tipo de estudio: Qualitative_research Idioma: En Revista: Cureus Año: 2018 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Colección: 01-internacional Tipo de estudio: Qualitative_research Idioma: En Revista: Cureus Año: 2018 Tipo del documento: Article País de afiliación: Países Bajos