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Peripheral long lines in cystic fibrosis
L Millar-Jones1, M C Goodchild
1Department of Child Health, University Hospital of Wales, Cardiff, UK.
Journal of Clinical Pharmacy and Therapeutics
|February 1, 1997
Summary
Peripheral long lines improve cannula survival for cystic fibrosis patients needing repeated intravenous antibiotic courses. Neonatal lines are preferred over Landmark catheters due to similar survival and less phlebitis.
Area of Science:
- Medical device evaluation
- Clinical outcomes research
- Pediatric infectious diseases
Background:
- Peripheral long lines offer improved cannula survival for patients requiring multiple intravenous (i.v.) antibiotic courses.
- These devices facilitate a more normal and mobile lifestyle for patients.
- Cystic fibrosis (CF) patients often require prolonged i.v. antibiotic therapy.
Purpose of the Study:
- To compare the performance of neonatal silastic long lines (Epicutaneo-cava-catheter) and Landmark catheters for i.v. antibiotic administration in CF patients.
- To evaluate cannula survival time and incidence of phlebitis for both catheter types.
- To determine patient preference between the two types of long lines.
Main Methods:
- Prospective data collection over 18 months on neonatal silastic long lines and Landmark catheters.
- Comparison of cannula survival times against conventional short cannulae.
- Assessment of phlebitis rates and patient preference for each catheter type.
Main Results:
- Both neonatal silastic long lines and Landmark catheters demonstrated cannula survival times that were the same and longer than conventional short cannulae.
- Patient preference favored the neonatal line.
- A trend towards increased phlebitis was observed with the Landmark catheter.
Conclusions:
- Neonatal silastic long lines are suitable for long-term i.v. antibiotic administration in cystic fibrosis patients.
- The neonatal line offers comparable cannula survival to the Landmark catheter with a lower incidence of phlebitis.
- Neonatal silastic long lines were selected for routine use in CF patients based on performance and patient preference.