Literature DB >> 23703238

Living with breathlessness: a survey of caregivers of breathless patients with lung cancer or heart failure.

Farida A Malik1, Marjolein Gysels, Irene J Higginson.   

Abstract

BACKGROUND: Breathlessness is a common, distressing symptom in patients with advanced disease. With increasing focus on home death for patients, carers are expected to support breathless people at home. Little is known about how carers experience breathlessness and the differences in caring for someone with breathlessness and malignant or non-malignant disease. AIM: To compare experiences of caring for a breathless patient with lung cancer versus those with heart failure and to examine factors associated with caregiver burden and positive caring experiences.
DESIGN: Cross-sectional survey of caregivers of breathless patients. SETTING/PARTICIPANTS: Participants were recruited from two London hospitals. INCLUSION CRITERIA: caregivers of patients with breathlessness and heart failure or lung cancer. Measures included self-completion of Short Form version of Zarit Burden Interview, a 'positive caring experiences' scale and Palliative Care Outcome Scale. We compared caregiver reports between heart failure and lung cancer. Multiple regression analyses were used to examine factors related to burden and positive caring experiences.
RESULTS: In total, 51 heart failure and 50 lung cancer caregivers were recruited. Most were spouses (72%) and women (80%). Severity of patient breathlessness was similar in both groups. Caregiver concerns were mostly similar across conditions. Higher burden was associated with poorer 'quality of patient care' and worse carer psychological health (R (2) = 0.37, F = 12.2, p = 0.01). Caregiver depression and looking after more breathless patients were associated with fewer positive caring experiences (R (2) = 0.15, F = 4.4, p = 0.04).
CONCLUSIONS: Those who care for breathless patients report high levels of unmet needs and burden, equally severe for heart failure and lung cancer caregivers. Caregivers of patients with more severe breathlessness report fewer positive caring experiences and should be targeted by services with increased support in managing this symptom.

Entities:  

Keywords:  Dyspnoea; cancer; caregiver burden; end-of-life care; family; heart disease; home; hospice; hospital; outcome; palliative

Mesh:

Year:  2013        PMID: 23703238     DOI: 10.1177/0269216313488812

Source DB:  PubMed          Journal:  Palliat Med        ISSN: 0269-2163            Impact factor:   4.762


  25 in total

1.  RDOS-family: a guided learning tool for layperson assessment of respiratory distress.

Authors:  Margaret L Campbell; Thomas N Templin
Journal:  J Palliat Med       Date:  2014-08-12       Impact factor: 2.947

Review 2.  Symptom burden in heart failure: assessment, impact on outcomes, and management.

Authors:  Craig M Alpert; Michael A Smith; Scott L Hummel; Ellen K Hummel
Journal:  Heart Fail Rev       Date:  2017-01       Impact factor: 4.214

3.  Engaging heart failure clinicians to increase palliative care referrals: overcoming barriers, improving techniques.

Authors:  Laura P Gelfman; Jill Kalman; Nathan E Goldstein
Journal:  J Palliat Med       Date:  2014-06-05       Impact factor: 2.947

Review 4.  Family caregiving for persons with heart failure at the intersection of heart failure and palliative care: a state-of-the-science review.

Authors:  J Nicholas Dionne-Odom; Stephanie A Hooker; David Bekelman; Deborah Ejem; Gwen McGhan; Lisa Kitko; Anna Strömberg; Rachel Wells; Meka Astin; Zehra Gok Metin; Gisella Mancarella; Salpy V Pamboukian; Lorraine Evangelista; Harleah G Buck; Marie A Bakitas
Journal:  Heart Fail Rev       Date:  2017-09       Impact factor: 4.214

5.  Factors influencing place of death and disenrollment among patients receiving specialist palliative care.

Authors:  Marco Di Nitto; Marco Artico; Michela Piredda; Maddalena De Maria; Caterina Magnani; Anna Marchetti; Chiara Mastroianni; Roberto Latina; Maria Grazia De Marinis; Daniela D'Angelo
Journal:  Acta Biomed       Date:  2022-05-12

6.  Comparing the symptom experience of cancer patients and non-cancer patients.

Authors:  Teresa L Deshields; Valentina Penalba; Jingxa Liu; James Avery
Journal:  Support Care Cancer       Date:  2016-12-13       Impact factor: 3.603

7.  Cancer patients' perceptions regarding the value of the physical examination: a survey study.

Authors:  Kunal C Kadakia; David Hui; Gary B Chisholm; Susan E Frisbee-Hume; Janet L Williams; Eduardo Bruera
Journal:  Cancer       Date:  2014-06-04       Impact factor: 6.860

8.  Pulmonary Rehabilitation and Palliative Care for the Lung Cancer Patient.

Authors:  Brian Tiep; Virginia Sun; Marianna Koczywas; Jae Kim; Dan Raz; Arti Hurria; Jennifer Hayter
Journal:  J Hosp Palliat Nurs       Date:  2015-10       Impact factor: 1.918

9.  Referral Practices of Cardiologists to Specialist Palliative Care in Canada.

Authors:  Michael J Bonares; Ken Mah; Jane MacIver; Lindsay Hurlburt; Ebru Kaya; Gary Rodin; Heather Ross; Camilla Zimmermann; Kirsten Wentlandt
Journal:  CJC Open       Date:  2020-12-09

10.  The experience of caregivers of people living with serious mental disorders: a study from rural Ghana.

Authors:  Kenneth Ayuurebobi Ae-Ngibise; Victor Christian Korley Doku; Kwaku Poku Asante; Seth Owusu-Agyei
Journal:  Glob Health Action       Date:  2015-05-11       Impact factor: 2.640

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.