Journal of Clinical Oncology, Vol 10, 1943-1948, Copyright © 1992 by American Society of Clinical Oncology
A prospective randomized trial comparing the infectious and noninfectious complications of an externalized catheter versus a subcutaneously implanted device in cancer patients
BU Mueller, J Skelton, DP Callender, D Marshall, J Gress, D Longo, J Norton, M Rubin, D Venzon and PA Pizzo
Pediatric Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.
PURPOSE: To compare the frequency of infectious episodes or other problems
occurring with an externalized catheter (Hickman) versus a subcutaneously
implanted device (Port-a-Cath, Pharmacia, Piscataway, NJ) in cancer
patients, we performed a prospective, randomized study in 100 cancer
patients (age range, 5 to 74 years). PATIENTS AND METHODS: Patients who
were chemotherapy candidates and required an indwelling catheter were
monitored prospectively and evaluated during the 180 days after the
insertion of the catheter and again at time of study closure. The frequency
of catheter use, reason for access, and any problems that might have been
related to catheter use were noted. All data were collected prospectively
and included the patient's age, sex, underlying malignancy, temperature,
and leukocyte and absolute granulocyte counts at the time of catheter
insertion and when complications occurred. The time to and reason for
removal of the catheter, as well as any intercurrent infectious or
mechanical problems, were also determined. RESULTS: Most of the infections
that occurred were caused by gram- positive organisms, especially
staphylococci or streptococci. A total of 22 complications (11 in each
group) resulted in removal of the central line. Only one infection in the
Hickman catheter group and four in the Port-a-Cath group led to removal of
the central line. All other infectious episodes were successfully treated
without removal of the catheters. The mean device life was 230 days for the
Hickman catheter and 318 days for the Port-a-Cath (not significant).
CONCLUSION: There were no differences between the two study groups
regarding incidence of documented infections or mechanical or thrombotic
complications.
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