Literature DB >> 33486637

How much time do we have? Longitudinal perception of prognosis in newly-diagnosed high grade glioma patients and caregivers compared to clinicians.

Akanksha Sharma1,2, Briant Fruth3, Celina Barrera4, Hannah N Farfour4, Maciej M Mrugala5, Mark K Edwin4, Jeff A Sloan3, Alyx B Porter5.   

Abstract

PURPOSE: Discordant prognostic awareness (PA) can cause distress, impact goals of care and future planning, especially in patients with high grade glioma (pwHGG) who have limited survival. We aimed to evaluate the feasibility of assessing PA of pwHGG, caregivers and clinicians using a single question and to evaluate these responses for discord, alignment and fluctuation over time.
METHODS: This is a sub-study of an IRB-approved pilot study evaluating early palliative care and longitudinal symptom monitoring via a smart-device tool in 16 pwHGG and their caregivers receiving treatment at the Mayo Clinic Arizona (United States). Eligible patients were ≥ 18 years, English-speaking, newly-diagnosed, and had a willing caregiver. Participants answered a multiple-choice question asking for an estimate of their own or their loved one's survival on a monthly basis.
RESULTS: All except one patient/caregiver dyad answered the question each time it was asked. The question did not appear to cause discomfort or increase conversations with clinicians around prognosis. PA of patients and caregivers fluctuated monthly, ranging from dismal to overtly optimistic, with a discordance frequency of 68%. Patients tended to be more optimistic than caregivers, and a higher QOL correlated to a more optimistic response. Clinicians' were more hopeful; their prediction tended to fluctuate less than those of patients and caregivers.
CONCLUSIONS: PA may be assessed in pwHGG and caregivers with a single, frank question. There is clear discordance between PA of patients, their caregivers and clinicians. Understanding fluctuates longitudinally through disease and treatment course. Additional studies on timing and ways of discussing prognosis in this population are needed. CLINICAL TRIAL REGISTRATION: NCT04630379.

Entities:  

Keywords:  Brain tumors; Caregivers; Glioblastoma; Glioma; Prognosis; Quality of life; Terminal disease

Year:  2021        PMID: 33486637     DOI: 10.1007/s11060-021-03700-2

Source DB:  PubMed          Journal:  J Neurooncol        ISSN: 0167-594X            Impact factor:   4.130


  23 in total

1.  Early symptoms of brain tumours.

Authors:  E Davies; C Clarke
Journal:  J Neurol Neurosurg Psychiatry       Date:  2004-08       Impact factor: 10.154

2.  Prognostic disclosure to patients with cancer near the end of life.

Authors:  E B Lamont; N A Christakis
Journal:  Ann Intern Med       Date:  2001-06-19       Impact factor: 25.391

3.  Problems of distortion in doctor-patient communications.

Authors:  J S Golden; G D Johnston
Journal:  Psychiatry Med       Date:  1970-04

4.  Collusion in doctor-patient communication about imminent death: an ethnographic study.

Authors:  A M The; T Hak; G Koëter; G van der Wal
Journal:  West J Med       Date:  2001-04

5.  Patient and caregiver perceptions of communication of prognosis in high grade glioma.

Authors:  E A Lobb; G K B Halkett; A K Nowak
Journal:  J Neurooncol       Date:  2010-12-14       Impact factor: 4.130

6.  Coping and Prognostic Awareness in Patients With Advanced Cancer.

Authors:  Ryan D Nipp; Joseph A Greer; Areej El-Jawahri; Samantha M Moran; Lara Traeger; Jamie M Jacobs; Juliet C Jacobsen; Emily R Gallagher; Elyse R Park; David P Ryan; Vicki A Jackson; William F Pirl; Jennifer S Temel
Journal:  J Clin Oncol       Date:  2017-06-02       Impact factor: 44.544

7.  Caring for someone with high-grade glioma: a time of rapid change for caregivers.

Authors:  Ruth McConigley; Georgia Halkett; Elizabeth Lobb; Anna Nowak
Journal:  Palliat Med       Date:  2010-02-01       Impact factor: 4.762

8.  Prognosis communication in serious illness: perceptions of older patients, caregivers, and clinicians.

Authors:  Terri R Fried; Elizabeth H Bradley; John O'Leary
Journal:  J Am Geriatr Soc       Date:  2003-10       Impact factor: 5.562

9.  Truth may hurt but deceit hurts more: communication in palliative care.

Authors:  L J Fallowfield; V A Jenkins; H A Beveridge
Journal:  Palliat Med       Date:  2002-07       Impact factor: 4.762

10.  Unmet supportive care needs and interest in services among patients with a brain tumour and their carers.

Authors:  Monika Janda; Suzanne Steginga; Jeff Dunn; Danette Langbecker; David Walker; Elizabeth Eakin
Journal:  Patient Educ Couns       Date:  2008-03-07
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  4 in total

Review 1.  Easing the Journey-an Updated Review of Palliative Care for the Patient with High-Grade Glioma.

Authors:  Rita C Crooms; Margaret O Johnson; Heather Leeper; Ambereen Mehta; Michelle McWhirter; Akanksha Sharma
Journal:  Curr Oncol Rep       Date:  2022-02-22       Impact factor: 5.075

2.  Development of a Patient Decision Aid to Support Shared Decision Making for Patients with Recurrent High-Grade Glioma.

Authors:  Helle Sorensen von Essen; Frantz Rom Poulsen; Rikke Hedegaard Dahlrot; Karin Piil; Karina Dahl Steffensen
Journal:  Int J Environ Res Public Health       Date:  2022-06-16       Impact factor: 4.614

3.  High grade glioma and caregiver burden.

Authors:  David O'Keeffe; Richard M Bambury; Seamus O'Reilly
Journal:  J Neurooncol       Date:  2021-04-15       Impact factor: 4.130

4.  Decisional needs of patients with recurrent high-grade glioma and their families.

Authors:  Helle Sorensen von Essen; Dawn Stacey; Karina Dahl Steffensen; Rikke Guldager; Frantz Rom Poulsen; Karin Piil
Journal:  Neurooncol Pract       Date:  2022-06-11
  4 in total

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