Literature DB >> 34353345

Family reported outcomes, an unmet need in the management of a patient's disease: appraisal of the literature.

R Shah1, F M Ali2, A Y Finlay2, M S Salek3,4.   

Abstract

BACKGROUND: A person's chronic health condition or disability can have a huge impact on the quality of life (QoL) of the whole family, but this important impact is often ignored. This literature review aims to understand the impact of patients' disease on family members across all medical specialities, and appraise existing generic and disease-specific family quality of life (QoL) measures.
METHODS: The databases Medline, EMBASE, CINHAL, ASSIA, PsycINFO and Scopus were searched for original articles in English measuring the impact of health conditions on patients' family members/partner using a valid instrument.
RESULTS: Of 114 articles screened, 86 met the inclusion criteria. They explored the impact of a relative's disease on 14,661 family members, mostly 'parents' or 'mothers', using 50 different instruments across 18 specialities including neurology, oncology and dermatology, in 33 countries including the USA, China and Australia. These studies revealed a huge impact of patients' illness on family members. An appraisal of family QoL instruments identified 48 instruments, 42 disease/speciality specific and six generic measures. Five of the six generics are aimed at carers of children, people with disability or restricted to chronic disease. The only generic instrument that measures the impact of any condition on family members across all specialities is the Family Reported Outcome Measure (FROM-16). Although most instruments demonstrated good reliability and validity, only 11 reported responsiveness and only one reported the minimal clinically important difference.
CONCLUSIONS: Family members' QoL is greatly impacted by a relative's condition. To support family members, there is a need for a generic tool that offers flexibility and brevity for use in clinical settings across all areas of medicine. FROM-16 could be the tool of choice, provided its robustness is demonstrated with further validation of its psychometric properties.
© 2021. The Author(s).

Entities:  

Keywords:  FROM-16; Family member; Family quality of life; Impact of illness; Management of a patient's disease; Partner; Quality of life; Unmet need

Year:  2021        PMID: 34353345     DOI: 10.1186/s12955-021-01819-4

Source DB:  PubMed          Journal:  Health Qual Life Outcomes        ISSN: 1477-7525            Impact factor:   3.186


  116 in total

Review 1.  Quality of life: impact of chronic illness on the partner.

Authors:  J Rees; C O'Boyle; R MacDonagh
Journal:  J R Soc Med       Date:  2001-11       Impact factor: 5.344

2.  Spouses of spinal cord injury survivors: the added impact of caregiving.

Authors:  D A Weitzenkamp; K A Gerhart; S W Charlifue; G G Whiteneck; G Savic
Journal:  Arch Phys Med Rehabil       Date:  1997-08       Impact factor: 3.966

3.  A comparative study of the impairment of quality of life in Czech children with atopic dermatitis of different age groups and their families.

Authors:  Anna Jiráková; Naděžda Vojáčková; Dana Göpfertová; Jana Hercogová
Journal:  Int J Dermatol       Date:  2012-06       Impact factor: 2.736

4.  Stress, Depression, and Quality of Life Among Caregivers of Children With Osteogenesis Imperfecta.

Authors:  Margot A Lazow; Sarah S Jaser; Erin C Cobry; Melissa D Garganta; Jill H Simmons
Journal:  J Pediatr Health Care       Date:  2019-03-01       Impact factor: 1.812

5.  The family impact of skin diseases: the Greater Patient concept.

Authors:  M K A Basra; A Y Finlay
Journal:  Br J Dermatol       Date:  2007-03-23       Impact factor: 9.302

6.  Psoriasis: is it the tip of the iceberg for the quality of life of patients and their families?

Authors:  A Tadros; T Vergou; A J Stratigos; C Tzavara; M Hletsos; A Katsambas; C Antoniou
Journal:  J Eur Acad Dermatol Venereol       Date:  2011-01-17       Impact factor: 6.166

7.  Family quality of life: a qualitative inquiry.

Authors:  Denise Poston; Ann Turnbull; Jiyeon Park; Hasheem Mannan; Janet Marquis; Mian Wang
Journal:  Ment Retard       Date:  2003-10

8.  Quality of Life in Families with Children with Atopic Dermatitis.

Authors:  Nives Pustišek; Maja Vurnek Živković; Mirna Šitum
Journal:  Pediatr Dermatol       Date:  2015-10-13       Impact factor: 1.588

Review 9.  The impact of disease on family members: a critical aspect of medical care.

Authors:  Catherine Jane Golics; Mohammad Khurshid Azam Basra; Andrew Yule Finlay; Sam Salek
Journal:  J R Soc Med       Date:  2013-05-10       Impact factor: 5.344

10.  Dementia as a predictor of care-related quality of life in informal caregivers: a cross-sectional study to investigate differences in health-related outcomes between dementia and non-dementia caregivers.

Authors:  Nina Karg; Elmar Graessel; Ottilie Randzio; Anna Pendergrass
Journal:  BMC Geriatr       Date:  2018-08-23       Impact factor: 3.921

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  1 in total

1.  Using Latent Class Analyses to Examine Health Disparities among Young Children in Socially Disadvantaged Families during the COVID-19 Pandemic.

Authors:  Rosa S Wong; Keith T S Tung; Nirmala Rao; Ko Ling Chan; King-Wa Fu; Jason C Yam; Winnie W Y Tso; Wilfred H S Wong; Terry Y S Lum; Ian C K Wong; Patrick Ip
Journal:  Int J Environ Res Public Health       Date:  2022-06-27       Impact factor: 4.614

  1 in total

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