Patient self-assessment of hospital pain, mood and health-related quality of life in adults with sickle cell disease

  • KA Anie
  • , H Grocott
  • , L White
  • , M Dzingina
  • , G Rogers
  • , G Cho

Research output: Contribution to journalArticlepeer-review

Abstract

Introduction: Acute pain is a hallmark of sickle cell disease (SCD) for which frequent hospital admissions may be required, affecting the quality of life of patients.

Objectives: To characterise the relationship between adult patient self-reported sickle cell pain, mood and quality of life during and after hospital admissions.

Design: Longitudinal study across three time-points.

Setting: Secondary care, single specialist sickle cell centre.

Participants: 510 adult patients with SCD admitted to hospital daycare or inpatient units.

Outcome: measures Self-assessments of pain, mood and health-related quality of life with health utility (measured on the EQ-5D) on admission, before discharge and at 1-week postdischarge.

Results: Mood, general health and quality of life showed significant steady improvements with reduction of pain in patients with SCD on admission to hospital, before discharge and at 1-week follow-up (p
Conclusion: Examining health-related quality of life and health utility in relation to pain during hospital admissions is valuable in terms of targeting appropriate psychological interventions within the context of a multidisciplinary approach to managing sickle cell pain. This has implications for healthcare costs.
Original languageEnglish
Article numbere001274
Pages (from-to)1-6
Number of pages6
JournalBMJ Open
Volume2
Issue number4
DOIs
Publication statusPublished - 2 Jul 2012

Fingerprint

Dive into the research topics of 'Patient self-assessment of hospital pain, mood and health-related quality of life in adults with sickle cell disease'. Together they form a unique fingerprint.

Cite this