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Home care in cystic fibrosis patients

  • W. M. van Aalderen
  • , G. P. Mannes
  • , E. S. Bosma
  • , R. J. Roorda
  • , H. S. Heymans

Research output: Contribution to journalComment/Letter to the editorAcademic

Abstract

Intravenous antibiotics and enteral tube feeding at home for the treatment of pulmonary exacerbations and underweight condition in cystic fibrosis (CF) patients have become tools that are used in many cystic fibrosis centres. The experience with home care programmes from different countries is quite conclusive. If the necessary preparations are made, such as training of staff and patients, and financial support is arranged, home care is easy to put into practice. Optimal patient compliance is also necessary. Home care is as effective as hospital treatment for selected patients, and less expensive. Experience has increased during many treatment periods in different cystic fibrosis centres, and only a few adverse events have been recorded, indicating that home care is safe. However, the most important gain for cystic fibrosis patients is the reduction of hospital admission time, which means a definite improvement in the quality of life
Original languageEnglish
Pages (from-to)172-175
JournalEuropean respiratory journal
Volume8
Issue number1
DOIs
Publication statusPublished - 1995

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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