Literature DB >> 26503920

Palliative Care Problem Severity Score: Reliability and acceptability in a national study.

Malcolm Masso1, Samuel Frederic Allingham2, Claire Elizabeth Johnson3, Tanya Pidgeon3, Patsy Yates4, David Currow5, Kathy Eagar2.   

Abstract

BACKGROUND: The Palliative Care Problem Severity Score is a clinician-rated tool to assess problem severity in four palliative care domains (pain, other symptoms, psychological/spiritual, family/carer problems) using a 4-point categorical scale (absent, mild, moderate, severe). AIM: To test the reliability and acceptability of the Palliative Care Problem Severity Score.
DESIGN: Multi-centre, cross-sectional study involving pairs of clinicians independently rating problem severity using the tool. SETTING/PARTICIPANTS: Clinicians from 10 Australian palliative care services: 9 inpatient units and 1 mixed inpatient/community-based service.
RESULTS: A total of 102 clinicians participated, with almost 600 paired assessments completed for each domain, involving 420 patients. A total of 91% of paired assessments were undertaken within 2 h. Strength of agreement for three of the four domains was moderate: pain (Kappa = 0.42, 95% confidence interval = 0.36 to 0.49); psychological/spiritual (Kappa = 0.48, 95% confidence interval = 0.42 to 0.54); family/carer (Kappa = 0.45, 95% confidence interval = 0.40 to 0.52). Strength of agreement for the remaining domain (other symptoms) was fair (Kappa = 0.38, 95% confidence interval = 0.32 to 0.45).
CONCLUSION: The Palliative Care Problem Severity Score is an acceptable measure, with moderate reliability across three domains. Variability in inter-rater reliability across sites and participant feedback indicate that ongoing education is required to ensure that clinicians understand the purpose of the tool and each of its domains. Raters familiar with the patient they were assessing found it easier to assign problem severity, but this did not improve inter-rater reliability.
© The Author(s) 2015.

Entities:  

Keywords:  Australia; assessment of health-care needs; palliative care; patient outcome assessment; reproducibility of results

Mesh:

Year:  2015        PMID: 26503920     DOI: 10.1177/0269216315613904

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


  7 in total

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Authors:  Aaron K Wong; Lucy Demediuk; Jia Y Tay; Olivia Wawryk; Anna Collins; Rachel Everitt; Jennifer Philip; Kirsty Buising; Brian Le
Journal:  Intern Med J       Date:  2021-09       Impact factor: 2.611

2.  Phase of Illness in palliative care: Cross-sectional analysis of clinical data from community, hospital and hospice patients.

Authors:  Harriet Mather; Ping Guo; Alice Firth; Joanna M Davies; Nigel Sykes; Alison Landon; Fliss E M Murtagh
Journal:  Palliat Med       Date:  2017-08-16       Impact factor: 4.762

3.  Indigenous compared with non-Indigenous Australian patients at entry to specialist palliative care: Cross-sectional findings from a multi-jurisdictional dataset.

Authors:  John A Woods; Jade C Newton; Sandra C Thompson; Eva Malacova; Hanh T Ngo; Judith M Katzenellenbogen; Kevin Murray; Shaouli Shahid; Claire E Johnson
Journal:  PLoS One       Date:  2019-05-02       Impact factor: 3.240

4.  Describing Complexity in Palliative Home Care Through HexCom: A Cross-Sectional, Multicenter Study.

Authors:  Xavier Busquet-Duran; Eva Maria Jiménez-Zafra; Josep Maria Manresa-Domínguez; Magda Tura-Poma; Olga Bosch-delaRosa; Anna Moragas-Roca; Maria Concepción Galera Padilla; Susana Martin Moreno; Emilio Martínez-Losada; Silvia Crespo-Ramírez; Ana Isabel López-Garcia; Pere Torán-Monserrat
Journal:  J Multidiscip Healthc       Date:  2020-03-19

5.  The PCOC Symptom Assessment Scale (SAS): A valid measure for daily use at point of care and in palliative care programs.

Authors:  Barbara A Daveson; Samuel Frederic Allingham; Sabina Clapham; Claire E Johnson; David C Currow; Patsy Yates; Kathy Eagar
Journal:  PLoS One       Date:  2021-03-25       Impact factor: 3.240

6.  Assessing Face Validity of the HexCom Model for Capturing Complexity in Clinical Practice: A Delphi Study.

Authors:  Xavier Busquet-Duran; Eva Maria Jiménez-Zafra; Magda Tura-Poma; Olga Bosch-de la Rosa; Anna Moragas-Roca; Susana Martin-Moreno; Emilio Martínez-Losada; Silvia Crespo-Ramírez; Lola Lestón-Lado; Núria Salamero-Tura; Joana Llobera-Estrany; Núria Oriol-Peregrina; Eduard Moreno-Gabriel; Josep Maria Manresa-Domínguez; Pere Torán-Monserrat
Journal:  Healthcare (Basel)       Date:  2021-02-04

7.  Spiritual Care Needs of Terminal Ill Cancer Patients.

Authors:  Wasinee Wisesrith; Pilaiporn Sukcharoen; Kanittha Sripinkaew
Journal:  Asian Pac J Cancer Prev       Date:  2021-12-01
  7 in total

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