Literature DB >> 9917038

Quality of life assessment in patients undergoing head and neck surgery as evaluated by lay caregivers.

D G Deschler1, K A Walsh, S Friedman, R E Hayden.   

Abstract

OBJECTIVES/HYPOTHESIS: Rehabilitation following head and neck cancer surgery has steadily moved into the outpatient realm and become dependent on caregivers with no formal medical background (lay caregivers.) Satisfactory rehabilitation and quality of life (QOL) depend on successful relationships between patients and the lay caregivers. This study evaluates the QOL assessments of patients by themselves and their primary lay caregivers before head and neck surgery. STUDY
DESIGN: Institutional Review Board-approved study using validated QOL assessment instrument.
MATERIALS AND METHODS: The preoperative QOL status in 50 patients undergoing extensive head and neck surgery was evaluated using the self-administered Medical Outcomes Survey Short Form 36 (SF-36). The patient's primary lay caregiver (spouse, child, or friend) completed a similar questionnaire evaluating the patient's status.
RESULTS: Thirty-three (66%) questionnaires were returned. Twenty-five (50%) questionnaire sets were successfully completed by both parties and employable for comparison. Sixty percent of the caregivers were within the 90% confidence interval of the patient's assessment for six or more of the eight parameters evaluated by the SF-36. Likewise, caregiver assessments for specific parameters were consistently congruent with patient evaluation, except for the parameters of bodily pain and general health, for which caregivers demonstrated a trend for overrating pain and underestimating general health. Caregivers of the same generation as the patient demonstrated significantly higher congruence (P = .007). Similarly, a trend for higher congruence was noted in patients with recurrent disease.
CONCLUSIONS: The importance of the lay caregiver has increased in the era of greater outpatient rehabilitation. This pilot study indicates that QOL assessment by lay caregivers may be examined with existing instruments and highlights QOL parameters critical to both the head and neck surgery patient and his or her primary lay caregiver.

Entities:  

Mesh:

Year:  1999        PMID: 9917038     DOI: 10.1097/00005537-199901000-00009

Source DB:  PubMed          Journal:  Laryngoscope        ISSN: 0023-852X            Impact factor:   3.325


  9 in total

Review 1.  Systematic review of caregiver responses for patient health-related quality of life in adult cancer care.

Authors:  Jessica K Roydhouse; Ira B Wilson
Journal:  Qual Life Res       Date:  2017-03-14       Impact factor: 4.147

2.  Randomized controlled trial of a collaborative care intervention to manage cancer-related symptoms: lessons learned.

Authors:  Jennifer Steel; David A Geller; Allan Tsung; J Wallis Marsh; Mary Amanda Dew; Michael Spring; Jonathan Grady; Sonja Likumahuwa; Andrea Dunlavy; Michael Youssef; Michael Antoni; Lisa H Butterfield; Richard Schulz; Richard Day; Vicki Helgeson; Kevin H Kim; T Clark Gamblin
Journal:  Clin Trials       Date:  2011-06       Impact factor: 2.486

3.  Instruments for estimation of health-related quality of life in patients with skull base neoplasms.

Authors:  Mariana E Witgert; Tracy Veramonti; Ehab Hanna
Journal:  Skull Base       Date:  2010-01

Review 4.  Head and neck cancer pain: systematic review of prevalence and associated factors.

Authors:  Tatiana V Macfarlane; Tanja Wirth; Sriyani Ranasinghe; Kim W Ah-See; Nick Renny; David Hurman
Journal:  J Oral Maxillofac Res       Date:  2012-04-01

5.  Proxy ratings of health related quality of life in patients with hepatocellular carcinoma.

Authors:  Jennifer L Steel; David A Geller; Brian I Carr
Journal:  Qual Life Res       Date:  2005-05       Impact factor: 4.147

6.  Quality-of-Life after Anterior Skull Base Surgery: A Systematic Review.

Authors:  Matthew A Kirkman; Anouk Borg; Alaa Al-Mousa; Nikolaos Haliasos; David Choi
Journal:  J Neurol Surg B Skull Base       Date:  2013-12-11

Review 7.  Quality-of-life outcomes in head and neck cancer patients.

Authors:  Randall P Morton; Mark E Izzard
Journal:  World J Surg       Date:  2003-07       Impact factor: 3.352

8.  Late-stage HIV/AIDS patients' and their familial caregivers' agreement on the palliative care outcome scale.

Authors:  Rachel Krug; Daniel Karus; Peter A Selwyn; Victoria H Raveis
Journal:  J Pain Symptom Manage       Date:  2009-09-25       Impact factor: 3.612

9.  Confidant and breast cancer patient reports of quality of life.

Authors:  Ann K Sandgren; Amy B Mullens; Shannon C Erickson; Kathleen M Romanek; Kevin D McCaul
Journal:  Qual Life Res       Date:  2004-02       Impact factor: 4.147

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.