Professional Documents
Culture Documents
Lynelle Foster has worked in the field of infusion therapy since 1992 and is the Clinical Nurse Consultant of Parenteral Therapy at
Gold Coast Hospital in Queensland, Australia.
Marianne Wallis has been the Chair of Clinical Nursing Research at Gold Coast Health Services District and Griffith University,
Queensland, Australia since January 2000.
Barbara Paterson has worked in the field of pediatrics for more than 20 years. She is the Nurse Educator in the Paediatric Unit,
Gold Coast Hospital in Queensland, Australia.
Heather James has been an Associate Lecturer in the School of Nursing, Griffith University, Queensland, Australia since 1999.
Address correspondence to: Lynelle Foster, Parental Therapy Department, Gold Coast Hospital, Office 18, 1st Floor, Southport,
Queensland, QLD 4215 (e-mail: Lynelle_Foster@health.qld.gov.au).
T
he setting used for this study was the pediatric implicated.9,10
unit at the Gold Coast Hospital (GCH), Aus- An antiseptic skin solution should always be used
tralia. This pediatric unit admits approximately before insertion of a PIV. A prospective randomized
3,700 patients each year, including neonates, trial of agents used for cutaneous antisepsis demon-
infants, and children. Neonates are defined as babies strated that 2% aqueous chlorhexidine was superior to
younger than 28 days. Infants are in the first year of life, either 10% povidone iodine or 70% alcohol in prevent-
and children are defined as 1 to 16 years of age. All ing catheter-related infection.9 However, the 2% aque-
pediatric medical and nursing services are offered at ous chlorhexidine solution is not yet available in
GCH except chemotherapy initiation, long-term venti- Australia. Direct comparisons of aqueous and alcoholic
lation, and cardiac surgery. solutions of chlorhexidine have not been undertaken.
The Infusion Nursing Standard of Practice, estab- However, an alcoholic chlorhexidine solution combines
lished by the Infusion Nurses Society (INS)1 and Guide- the benefits of rapid action and excellent residual
line for Prevention of Intravascular Device-Related antimicrobial activity.25 To maintain skin integrity and
Infection, Centers for Disease Control and Prevention prevent chlorhexidine absorption in neonates, it is sug-
([CDC]. Atlanta, Ga: US Department of Health and gested that after the solution has been allowed to dry
Human Services; 1996) are used to guide clinical infu- for 30 seconds, it should be removed completely using
sion practice at GCH. The issue of frequency of replace- sterile saline solution.10
ment of peripheral intravenous catheters (PIVs) in The most common dressing type used for PIV exit
children is, however, unresolved with both INS and the sites in adults is a sterile, transparent, semipermeable
CDC. The pediatric nursing staff at GCH identified a membrane dressing. This dressing is popular because it
number of issues related to PIV insertion, use, and dwell reliably secures the catheter, permits continuous visual
time that required further exploration. inspection of the exit site, and repels water.9,11 However,
it is not uncommon in the pediatric population to use
unsterile tape to secure PIVs.12,26,27 Infection control prac-
• LITERATURE REVIEW tices together with the type of catheter play an important
role in the prevention of complications with PIVs.
• RESULTS Complications
Demographic Patient Characteristics The most common reason for the removal of a PIV was
that it was no longer required (74.6%; n = 370), either
The sample consisted of 496 PIVs inserted into 436 pedi- because treatment had stopped or the patient was being
atric patients. No more than four different PIVs in any discharged from hospital. A total phlebitis score was
patient were included in the study. Most patients had only calculated for all the PIVs (Table 3).
TABLE 2
Frequencies and Percentages for Catheter Insertion Sites
Some degree of phlebitis was present at the removal PIV was in place longer than 72 hours, the risk was
of 33 PIVs (6.6%). Of this group, most (5.2%) were doubled. However, a PIV dwell time of 96 hours did not
associated with grade 1 phlebitis. Two PIVs (0.4%) increase the risk, and a dwell time less than 48 hours did
were associated with grade 2 phlebitis, and five PIVs not reduce the risk.
(1%) with grade 3 phlebitis. No palpable cord was doc-
umented as present for any patient. Because PIV
phlebitis has a demonstrated association with CR- Nursing Actions After Removal
BSI,35,36 blood culture reports also were reviewed.
A retrospective review of positive blood cultures Although it is clear that nurses observed signs of phlebitis
from patients in the study reported via the AUSLAB sys- when removing the 33 PIVs, no exit site skin swabs or
tem during the study period showed that a source for PIV tips were collected to confirm whether these inci-
infection was not found in most cases. Each patient dences were related to bacteria. Although a specific item
from whom a blood culture was collected had a PIV in on the form required nurses to record why a swab was
place. The most common organism isolated was coagu- not sent for culture if a catheter exit site was red or
lase-negative Staphylococcus (ie, normal skin flora). swollen, this item was completed only twice. The first of
This suggests a high rate of specimen contamination at these two completed items included the comment “did
collection, but it also could imply that a PIV may have not persist,” and the second included the comment “IV
been the source. infiltration with no obvious signs of infection.”
For this study, 29 positive blood cultures were ana-
lyzed. In two neonates, a CR-BSI may have developed
from a PIV. The first neonate, during a 32-day length of
stay in a special care nursery, had a PIV in place for 38 • DISCUSSION
hours. This neonate was recorded as having grade 3
phlebitis, and coagulase-negative Staphylococcus was The purpose of this study was to describe PIV use, man-
isolated from the blood culture 3 days after PIV removal. agement, and associated incidence of phlebitis in the
The second neonate had a 36-day length of stay in a spe- pediatric unit at GCH. The studied sample included
cial care nursery. The PIV was in place for 24 hours. neonates, infants, and children. This study was con-
Although this neonate scored zero on the phlebitis scale, cerned with the use, management, and complications of
evidence in the medical record stated that the IV exit site peripheral intravenous catheterization in a general pedi-
was pink. Coagulase-negative Staphylococcus also was atric population. It is clear from the results that most
isolated from the blood 4 days after the PIV was PIVs inserted into neonates, infants, and children are
removed. In both cases, no other source of infection was used more frequently for fluid administration than for
found. There was no record whether the clinical symp- drug administration. The most common drugs adminis-
toms of infection resolved on removal of the PIV. tered are antibiotics, but a wide range of drugs may be
The odds ratios of risk factors associated with given occasionally via the PIV.
phlebitis are shown in Table 4. These data suggest that Whereas most catheters are inserted into the left
phlebitis is related to age, administration of medications upper limb of the child, a large minority are inserted
through the catheter, and PIV dwell time. into the right upper limb. Although handedness does
Neonates and infants, as compared with children not develop until approximately the age of 3 years,41 a
older than 1 year, had more than five times the risk of large proportion of children older than 3 years still have
phlebitis. Administration of IV medication means that PIVs inserted into their dominant hand. This would
the patient had more than double the risk of phlebitis. have implications for the play and learning experiences
The data regarding dwell time is more complicated. If a in which children could engage during hospitalization.
One of the greatest difficulties in examining complica- It is acknowledged that differentiating among
tions such as phlebitis associated with PIVs is the lack of mechanical, chemical, and bacterial phlebitis can be
a common definition. The INS phlebitis scale,28 which clinically difficult, but timely collection of microbio-
ranks degree of phlebitis by how many signs or symptoms logic evidence can assist diagnosis. This study did not
are present, did not function sufficiently with this popula- prospectively assess CR-BSI. However, retrospective
tion because pain assessment in preverbal children is dif- analysis shows that CR-BSI may have developed in two
ficult. The scale developed by the authors of this study neonates from a PIV during the study period. Further-
seems to have utility for use with children. The overall more, it is necessary to educate healthcare professionals
phlebitis rate determined by this instrument was 6.6%. regarding the possible infection risks associated with
The risk of phlebitis increased according to how long the PIVs, thereby increasing their awareness of the require-
PIV had been in place, how young the child was, and ment to collect a PIV exit site skin swab and a PIV tip
whether medication had been administered. The greatest for microbiologic culture when appropriate.
risk was age. Neonates were 51/2 times more likely to have
some degree of phlebitis than non-neonates.
Although the phlebitis rate with the current sample
falls between results from other studies, it is difficult to
• RECOMMENDATIONS
make comparisons because no standardized phlebitis
FOR FUTURE RESEARCH
scale was used. One study31 in a general pediatric popu-
lation (excluding neonates) reported a 1.1% phlebitis The first recommendation from this study is for the
rate with PIVs. Another study conducted in a pediatric development of a standard definition for phlebitis asso-
intensive care unit reported a phlebitis rate of 13%.2 ciated with pediatric PIVs so that further epidemiologic