Literature DB >> 24292015

Assessment of a brain-tumour-specific Patient Concerns Inventory in the neuro-oncology clinic.

Alasdair G Rooney1, Anouk Netten, Shanne McNamara, Sara Erridge, Sharon Peoples, Ian Whittle, Belinda Hacking, Robin Grant.   

Abstract

PURPOSE: Brain tumour patients may struggle to express their concerns in the outpatient clinic, creating a physician-focused rather than a shared agenda. We created a simple, practical brain-tumour-specific holistic needs assessment (HNA) tool for use in the neuro-oncology outpatient clinic.
METHODS: We posted the brain tumour Patient Concerns Inventory (PCI) to a consecutive sample of adult brain tumour attendees to a neuro-oncology outpatient clinic. Participants brought the completed PCI to their clinic consultation. Patients and staff provided feedback.
RESULTS: Seventy seven patients were eligible and 53 participated (response rate = 68%). The PCI captured many problems absent from general cancer checklists. The five most frequent concerns were fatigue, fear of tumour coming back, memory, concentration, and low mood. Respondents used the PCI to formulate 105 specific questions, usually about the meaning of physical or psychological symptoms. Patients and staff found the PCI to be useful, and satisfaction with the instrument was high.
CONCLUSIONS: This study demonstrates the clinical utility of the brain tumour PCI in a neuro-oncology clinic. The combination of a brain-tumour-specific concerns checklist and an intervention to focus patient agenda creates a simple and efficient HNA tool.

Entities:  

Mesh:

Year:  2013        PMID: 24292015     DOI: 10.1007/s00520-013-2058-2

Source DB:  PubMed          Journal:  Support Care Cancer        ISSN: 0941-4355            Impact factor:   3.603


  10 in total

1.  Development and piloting of a brain tumour-specific question prompt list.

Authors:  D Langbecker; M Janda; P Yates
Journal:  Eur J Cancer Care (Engl)       Date:  2012-02-06       Impact factor: 2.520

2.  An international validation study of the EORTC brain cancer module (EORTC QLQ-BN20) for assessing health-related quality of life and symptoms in brain cancer patients.

Authors:  Martin J B Taphoorn; Lily Claassens; Neil K Aaronson; Corneel Coens; Murielle Mauer; David Osoba; Roger Stupp; René O Mirimanoff; Martin J van den Bent; Andrew Bottomley
Journal:  Eur J Cancer       Date:  2010-02-22       Impact factor: 9.162

3.  Patterns of care for adults with newly diagnosed malignant glioma.

Authors:  Susan M Chang; Ian F Parney; Wei Huang; Frederick A Anderson; Anthony L Asher; Mark Bernstein; Kevin O Lillehei; Henry Brem; Mitchel S Berger; Edward R Laws
Journal:  JAMA       Date:  2005-02-02       Impact factor: 56.272

4.  Validation of the M.D. Anderson Symptom Inventory Brain Tumor Module (MDASI-BT).

Authors:  T S Armstrong; T Mendoza; I Gning; I Gring; C Coco; M Z Cohen; L Eriksen; Ming-Ann Hsu; M R Gilbert; C Cleeland
Journal:  J Neurooncol       Date:  2006-04-06       Impact factor: 4.130

Review 5.  Patient participation in the patient-provider interaction: the effects of patient question asking on the quality of interaction, satisfaction and compliance.

Authors:  D L Roter
Journal:  Health Educ Monogr       Date:  1977

Review 6.  Primary brain tumors in adults.

Authors:  Sreenivasa R Chandana; Sujana Movva; Madan Arora; Trevor Singh
Journal:  Am Fam Physician       Date:  2008-05-15       Impact factor: 3.292

Review 7.  Ongoing transitions: the impact of a malignant brain tumour on patient and family.

Authors:  Yasmin Khalili
Journal:  Axone       Date:  2007

8.  The development of a Patients Concerns Inventory (PCI) to help reveal patients concerns in the head and neck clinic.

Authors:  S N Rogers; J El-Sheikha; D Lowe
Journal:  Oral Oncol       Date:  2008-11-22       Impact factor: 5.337

9.  Testing the feasibility, acceptability and effectiveness of a 'decision navigation' intervention for early stage prostate cancer patients in Scotland--a randomised controlled trial.

Authors:  Belinda Hacking; Louise Wallace; Sarah Scott; Joanna Kosmala-Anderson; Jeffrey Belkora; Alan McNeill
Journal:  Psychooncology       Date:  2012-05-09       Impact factor: 3.894

Review 10.  Interventions before consultations for helping patients address their information needs.

Authors:  P Kinnersley; A Edwards; K Hood; N Cadbury; R Ryan; H Prout; D Owen; F Macbeth; P Butow; C Butler
Journal:  Cochrane Database Syst Rev       Date:  2007-07-18
  10 in total
  13 in total

1.  Needs of neuro-oncological patients and their caregivers during the hospitalization and after discharge: results from a longitudinal study.

Authors:  C Scaratti; M Leonardi; A Saladino; E Anghileri; M Broggi; E Lamperti; L Fariselli; R Ayadi; G Tringali; S Schiavolin
Journal:  Support Care Cancer       Date:  2017-02-15       Impact factor: 3.603

2.  Holistic needs assessment in advanced, intensively treated multiple myeloma patients.

Authors:  E G Boland; J W Boland; Y Ezaydi; D M Greenfield; S H Ahmedzai; J A Snowden
Journal:  Support Care Cancer       Date:  2014-04-15       Impact factor: 3.603

Review 3.  Epilepsy in glioma patients: mechanisms, management, and impact of anticonvulsant therapy.

Authors:  Terri S Armstrong; Robin Grant; Mark R Gilbert; Jong Woo Lee; Andrew D Norden
Journal:  Neuro Oncol       Date:  2015-11-02       Impact factor: 12.300

4.  Psychometric validity and reliability of the Danish version of the MD Anderson Symptom Inventory Brain Tumor Module.

Authors:  Karin Piil; Meagan Whisenant; Tito Mendoza; Terri Armstrong; Charles Cleeland; Sara Nordentoft; Loretta A Williams; Mary Jarden
Journal:  Neurooncol Pract       Date:  2020-10-19

5.  Attitudes and preferences toward monitoring symptoms, distress, and quality of life in glioma patients and their informal caregivers.

Authors:  Florien W Boele; Cornelia F van Uden-Kraan; Karen Hilverda; Jaap C Reijneveld; Wilmy Cleijne; Martin Klein; Irma M Verdonck-de Leeuw
Journal:  Support Care Cancer       Date:  2016-02-15       Impact factor: 3.603

6.  Neuro-oncology family caregivers' view on keeping track of care issues using eHealth systems: it's a question of time.

Authors:  Florien W Boele; Cornelia F van Uden-Kraan; Karen Hilverda; Jason Weimer; Heidi S Donovan; Jan Drappatz; Frank S Lieberman; Irma Verdonck-de Leeuw; Paula R Sherwood
Journal:  J Neurooncol       Date:  2017-05-26       Impact factor: 4.130

7.  Internet-based guided self-help for glioma patients with depressive symptoms: a randomized controlled trial.

Authors:  Florien W Boele; Martin Klein; Irma M Verdonck-de Leeuw; Pim Cuijpers; Jan J Heimans; Tom J Snijders; Maaike Vos; Ingeborg Bosma; Cees C Tijssen; Jaap C Reijneveld
Journal:  J Neurooncol       Date:  2017-12-13       Impact factor: 4.130

8.  Formulating a Patient Concerns Inventory specific to adult burns patients: learning from the PCI concept in other specialties.

Authors:  John A G Gibson; Sally Spencer; Simon N Rogers; Kayvan Shokrollahi
Journal:  Scars Burn Heal       Date:  2018-03-03

9.  Moving from clinician-defined to patient-reported outcome measures for survivors of high-grade glioma.

Authors:  Lena Rosenlund; Eskil Degsell; Asgeir Store Jakola
Journal:  Patient Relat Outcome Meas       Date:  2019-08-23

10.  Validation of the electronic Holistic Needs Assessment.

Authors:  Austyn Snowden; Mick Fleming
Journal:  Springerplus       Date:  2015-10-19
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