“I Don’t Need a Piece of Paper with Scores to Tell Me that Somebody’s in Pain and I Need to Do Something about it”. Nurses’ and Healthcare Assistants’ Perspectives on and Use of Pain Assessment Tools with People Dying with Advanced Dementia

Banin de witt Jansen, Kevin Brazil, Sonja McIlfatrick, Max watson, Carole Parsons

Research output: Contribution to journalArticle

Abstract

Background: The use of pain assessment tools in patientswith advanced dementia is widely recommended in healthcarepolicy but their impact on clinical outcomes for dyingDownloaded from pmj.sagepub.com at University-Ulster at Belfast on June 23, 2016NP46 Palliative Medicinepatients is unclear. Healthcare assistants have a significantrole in caring for the dying but their contribution to painrecognition is unexplored.Aims: Explore nurses’ use of pain assessment tools inpatients dying with advanced dementia in hospice, secondaryand nursing home care settings and investigate the roleof healthcare assistants in pain assessment.Methods: Semi-structured, face-to-face interviews wereconducted with 24 nurses and 14 healthcare assistants. Thematicanalysis of verbatim transcripts was used to identifyemergent themes. Three researchers confirmed final themes.Results: The Abbey Pain Scale formed part of the painassessment protocol for nurses across care settings but mostreported challenges in using it with dying patients. Scoresbased on brief observation were perceived as a poor substitutefor knowledge of the patient, observation over time andcollateral history from healthcare assistants and family.Most nurses reported pain tools resulted in no measurableclinical outcomes for patients nearing death. Healthcareassistants described methods of recognising and reportingpain and their role in observing for treatment response andside effects. Nurses and healthcare assistants describedmixed experiences discussing pain with physicians.Conclusion: Nursing staff described challenges with integratingpain assessment tools in practice and preferredpatient knowledge, observation and collateral history fromfamily and healthcare assistants to assess pain. The contributionof healthcare assistants in recognizing and reportingpain and assessing treatment response is described.These findings have important implications for healthpolicy, nurse education and healthcare provision.Funding: HSC Research and Development Division, PublicHealth Agency, Northern Ireland.
LanguageEnglish
PagesNP45-NP46
JournalPalliative Medicine
Volume30
Issue number6
Early online date11 May 2016
DOIs
Publication statusPublished - 1 Jun 2016

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Allied Health Personnel
Pain Measurement
Dementia
Nurses
Pain
Observation
Hospice and Palliative Care Nursing
History
Northern Ireland
Nursing Staff
Home Care Services
Nursing Care
Nursing Homes
Inpatients
Research Personnel
Interviews
Delivery of Health Care
Physicians
Education
Therapeutics

Keywords

  • pain assessment
  • nurses
  • dementia

Cite this

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title = "“I Don’t Need a Piece of Paper with Scores to Tell Me that Somebody’s in Pain and I Need to Do Something about it”. Nurses’ and Healthcare Assistants’ Perspectives on and Use of Pain Assessment Tools with People Dying with Advanced Dementia",
abstract = "Background: The use of pain assessment tools in patientswith advanced dementia is widely recommended in healthcarepolicy but their impact on clinical outcomes for dyingDownloaded from pmj.sagepub.com at University-Ulster at Belfast on June 23, 2016NP46 Palliative Medicinepatients is unclear. Healthcare assistants have a significantrole in caring for the dying but their contribution to painrecognition is unexplored.Aims: Explore nurses’ use of pain assessment tools inpatients dying with advanced dementia in hospice, secondaryand nursing home care settings and investigate the roleof healthcare assistants in pain assessment.Methods: Semi-structured, face-to-face interviews wereconducted with 24 nurses and 14 healthcare assistants. Thematicanalysis of verbatim transcripts was used to identifyemergent themes. Three researchers confirmed final themes.Results: The Abbey Pain Scale formed part of the painassessment protocol for nurses across care settings but mostreported challenges in using it with dying patients. Scoresbased on brief observation were perceived as a poor substitutefor knowledge of the patient, observation over time andcollateral history from healthcare assistants and family.Most nurses reported pain tools resulted in no measurableclinical outcomes for patients nearing death. Healthcareassistants described methods of recognising and reportingpain and their role in observing for treatment response andside effects. Nurses and healthcare assistants describedmixed experiences discussing pain with physicians.Conclusion: Nursing staff described challenges with integratingpain assessment tools in practice and preferredpatient knowledge, observation and collateral history fromfamily and healthcare assistants to assess pain. The contributionof healthcare assistants in recognizing and reportingpain and assessing treatment response is described.These findings have important implications for healthpolicy, nurse education and healthcare provision.Funding: HSC Research and Development Division, PublicHealth Agency, Northern Ireland.",
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