Abstract
Background and aims: Some previous studies have assessed quality of life (QoL) in home parenteral nutrition (HPN) using generic instruments or non-validated questionnaires. A systematic search of electronic databases and relevant publications identified 50 publications. This paper reviews the QoL of patients receiving HPN and discusses the factors affecting QoL.
Results: There is little available data about the QoL of HPN patients. Both HPN and the underlying disease may affect QoL, and an evaluation of QoL requires the separation of these two issues.
Conclusions: There is a need for a standardised, scientifically validated, treatment-specific instrument to measure QoL in this population. The use of a treatment-specific QoL questionnaire should become part of the routine clinical management of HPN patients. (C) 2006 Elsevier Ltd and European Society for Clinical Nutrition and Metabolism. All rights reserved.
| Original language | English |
|---|---|
| Pages (from-to) | 543-553 |
| Number of pages | 11 |
| Journal | Clinical Nutrition |
| Volume | 25 |
| Issue number | 4 |
| Early online date | 3 Jul 2006 |
| DOIs | |
| Publication status | Published - Aug 2006 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- quality of life
- parenteral nutrition
- long term
- CHRONIC INTESTINAL FAILURE
- SHORT-BOWEL SYNDROME
- ENTERAL NUTRITION
- HEALTH-STATUS
- MULTICENTER SURVEY
- CLINICAL-TRIALS
- CANCER-PATIENTS
- UNITED-KINGDOM
- HOME
- SUPPORT
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