Professional Documents
Culture Documents
)
Vascular Access in Oncology Patients
Maurizio Gallieni, Mauro Pittiruti and Roberto Biffi
CA Cancer J Clin 2008;58;323-346; originally published online Oct 29, 2008;
DOI: 10.3322/CA.2008.0015
The online version of this article, along with updated information and services, is located on
the World Wide Web at:
http://caonline.amcancersoc.org/cgi/content/full/58/6/323
To subscribe to the print issue of CA: A Cancer Journal for Clinicians, go to (US
individuals only): http://caonline.amcancersoc.org/subscriptions/
CA: A Cancer Journal for Clinicians is published six times per year for the American Cancer Society by
Wiley-Blackwell. A bimonthly publication, it has been published continuously since November 1950.
CA is owned, published, and trademarked by the American Cancer Society, 250 Williams Street NW,
Atlanta GA 30303. (©American Cancer Society, Inc.) All rights reserved. Print ISSN: 0007-9235. Online
ISSN: 1542-4863.
CA Cancer J Clin 2008;58:323–346
ABSTRACT Adequate vascular access is of paramount importance in oncology patients. It is Dr. Gallieni is Coordinating Editor,
important in the initial phase of surgical treatment or chemotherapy, as well as in the chronic man- The Journal of Vascular Access; Re-
searcher, University of Milano, School
agement of advanced cancer and in the palliative care setting. We present an overview of the
agement of vascular access. Particular emphasis is given to the use of ultrasound guidance Dr. Pittiruti is Researcher, Italian Na-
tional Research Council; and Depart-
as the preferred technique of insertion, which has dramatically decreased insertion-related ment of Surgery, Catholic University,
complications. Vascular access management has considerably improved after the publication Rome, Italy.
of effective guidelines for the appropriate nursing of the vascular device, which has reduced Dr. Biffi is Director, Division of Abdomino-
Pelvic Surgery, European Institute of
the risk of late complications, such as catheter-related bloodstream infection. However, many Oncology, Milan, Italy.
areas of clinical practice are still lacking an evidence-based background, such as the choice of Published online through CA First Look
the most appropriate vascular access device in each clinical situation, as well as prevention at http://CAonline.AmCancerSoc.org.
and treatment of thrombosis. We suggest an approach to the choice of the most appropriate doi:10.3322/CA.2008.0015
vascular access device for the oncology patient, based on the literature available to date. (CA
Cancer J Clin 2008;58:323–346.) © American Cancer Society, Inc., 2008.
To earn free CME credit or nursing contact hours for successfully completing the online quiz based on this article, go to http://CME.AmCancerSoc.org.
INTRODUCTION
The use of vascular access devices (VADs) is an integral aspect of health care for neonates, children, and adults and
has moved beyond the acute care setting to chronic, long-term care. VADs have a paramount role throughout the
management of the oncology patient, as they are needed in the initial phases for surgery or chemotherapy, in the
advanced stages for chronic treatment, and in the last stages for palliative measures.
According to US data,1 approximately 150 million intravenous catheters are purchased, and at least 5 million cen-
tral venous catheters (CVCs) are inserted every year. It is difficult to estimate how many of these VADs are actually
used for oncology patients. However, it is reasonable to assume that the proportion is high, as most surgery, chemother-
apy, and radiotherapy protocols for the management of neoplastic disease require intravenous infusions, including
even those for palliative care, for which a long-term VAD usually is the best route of administration.
Data from a study commissioned by the Food and Drug Administration in the 1990s2 showed that the use of VADs
is associated with a high complication rate (10% to 25% of all patients with VADs) and a morbidity of at least 10%;
52% of the reported complications were directly related to insufficient information (for nurses, patients, and other
people dedicated to the care of the device) or inappropriate technique of VAD placement and nursing care.
In this review, we will summarize data indicating that at present, in 2008, technological developments; a new
patient-oriented, cost-effective approach to the selection of procedures and techniques; and closer attention to the impor-
tant issue of health practitioner education have decreased the complication rate, especially in the area of oncology
and palliative care. In particular, the introduction of ultrasound guidance has dramatically decreased insertion-related
complications, and the new, updated nursing guidelines related to VAD care have proved to be effective in reducing
the risk of late complications, such as catheter-related bloodstream infection.
However, at least 2 issues are still reason for concern:
(A) There is no evidence-based guide to the selection of the most appropriate VAD for each clinical situation, notwith-
standing the broad range of VADs available, both in terms of features and performance. Moreover, there is little
Disclosure: The authors report no conflicts of interest.
TABLE 1 Features, Advantages, and Disadvantages of Different Types of Vascular Access Devices
Short-term VADs
Short peripheral
cannulas Peripheral Nontunneled Teflon, silicone 72 to 96 hours Continuous Hospital Low cost Short duration
Short-term CVCs Central Nontunneled Polyurethane 1 to 3 weeks Continuous Hospital Low cost High risk for
CRBSI
Long-term VADs
Tunneled catheters Central Tunneled Polyurethane, Months to Discontinuous Outpatient Indefinite High cost
(Groshong, silicone years duration
Hickman, Broviac)
Ports Central Totally Polyurethane, Months to Discontinuous Outpatient Indefinite High cost
implanted silicone years duration
Abbreviations: CRBSI, catheter-related blood stream infection; CVC, central venous catheter; PICC, peripherally inserted central catheter;
VAD, vascular access device.
guidance addressing the problem of the therapy costs.7 However, most patients who
choice of the best VAD for the oncology require intravenous therapy for longer than
patient—a consequence of the scarcity of 1 week are not routinely assessed for inter-
randomized trials in this area. A few clear- mediate dwelling VADs. In addition, patient
cut indications come from the guidelines of satisfaction about long-term VADs has rarely
the Registered Nurses’ Association of been addressed.8,9
Ontario,3 from the guidelines of the British
Committee for Standards in Haematology,4
CLASSIFICATION AND FEATURES
and from the Standards for Infusion Therapy OF VENOUS VADS
of the Royal College of Nursing (RCN)5
and of the Infusion Nurses Society (INS).6 Venous VADs can be classified as short-term,
(B) Patients and their families still currently play intermediate (medium-term), and long-term
a minor role in the selection of VAD at the accesses. They can also be classified as central (when
onset of treatment, notwithstanding the evi- the tip of the catheter lies in the lower third of
dence showing that patient involvement is the superior vena cava [SVC], in the atrium, or in
associated with greater patient satisfaction, the upper portion of the inferior vena cava) or
fewer delays in therapy related to loss of vas- peripheral (in all the other instances). Table 1
cular access, fewer device complications, summarizes features, advantages, and disadvan-
preservation of peripheral veins, less nurs- tages of different types of VADs, which will be
ing time spent attempting to gain vascular analyzed in this review. Central venous access is
access, shorter hospital stays, fewer emer- mandatory for a number of specific solutions for
gency room visits, and decreased infusion infusion, such as those containing vesicant drugs.
oral, and nasal secretions.17 Moreover, ultrasound- The choice between a tunneled catheter and
guided placement of PICCs at midarm is asso- a port depends on many factors, mainly related
ciated with optimal nursing management of the to patient compliance, experience of the nurs-
exit site.18 ing staff, and frequency of venous access. Accord-
ing to US Centers for Disease Control and
Long-term VADs Prevention (CDC) Guidelines, 22 totally im-
plantable access devices should be reserved for
Prolonged intravenous treatment (⬎3 months) patients who require long-term, intermittent
requires a long-term venous VAD, such as a tun- vascular access. A tunneled CVC is preferable
infiltration, phlebitis, local tissue damage, and pro- and/or subsequent venous stenosis.25 This is par-
gressive loss of available peripheral veins. The INS ticularly true for PICCs,26 although it may be
standards for infusion therapy4 recommend a cen- difficult to administer blood products or high-
tral venous access (including PICC) for the admin- flow hydration with a very narrow lumen. When
istration of boluses of vesicant medications; if a a totally implanted port is used, choosing a
peripheral access is used, a new access site should catheter caliber larger than 6 to 7 French does not
be used for each administration, and its site should carry significant advantages since the main lim-
be documented to avoid repeated use. However, itation to flow is the caliber of the Huber nee-
continuous infusion of vesicants should be per- dle used to access the port.
inducing uncontrolled activation of cellular or inner diameters, are more easily blocked by pre-
plasma protein cascades. Hemocompatibility is cipitates. However, polyurethane is more prone
a complex issue: depending on how it is defined, to degradation if alcohol or other solvents are
on the patient population, disease state, catheter used to dissolve the precipitate. The patency of
entrance site, and other factors, one catheter mate- the catheters is also related to their kink-resistance
rial can be said to perform better or worse than (the ability of the catheter to maintain an open
another. For short-term applications, in general, lumen when it is bent): silicone catheters bend
there are no noticeable differences between more easily, but kink with less applied force than
polyurethane and silicone catheters. For longer- polyurethane catheters. However,silicone catheters
Teflon, silicone, and polyurethane have been Multiple Versus Single Lumen
associated with fewer catheter-related infections CVCs with multiple lumens may be associated
than polyvinyl chloride or polyethylene. However, with higher infection rates than single-lumen
all available CVCs are made either of polyure- CVCs, as shown by several randomized con-
thane or silicone, and there is no specific recom- trolled trials (RCTs) and stated by CDC guide-
mendation regarding materials for clinical practice.17 lines22; nonetheless, this contention has been
questioned by recent papers. Two recent sys-
CHOICE OF THE VAD AND RISK OF INFECTION tematic reviews and quantitative meta-analyses
have focused on the risk of CR-BSI and catheter
upper-extremity veins is needed for fistula or quite obvious. The CDC recommends not to
graft implantation. Anyway, the assumption that use routinely venous cut-down procedures as a
PICCs are safer than conventional CVCs with method to insert catheters, even for long-term
regard to the risk of infection is in question; the ones, because percutaneously placed catheters
issue should be addressed by a larger, adequately are associated with a lower infection rate than
powered RCT assessing peripheral vein throm- surgically implanted ones.22 However, in neonates
bophlebitis, PICC-related thrombosis, and pre- and in children, not routinely but in selected
mature dislodgment, as well as CR-BSI.15 cases, venous cut-down might be the safest choice.
Recognition of risk factors for difficult catheter-
in Oncology Patients method was more success- settings, such as the intensive care unit, emer-
ful than Doppler-guided cannulation for subcla- gency room,43–45 oncology,46 pediatrics,47 and
vian vein procedures (1.48; 1.03 to 2.14). An dialysis,48 leading to the conclusion that ultra-
indirect comparison of relative risks suggested sound guidance improves the success rate of vein
that 2D ultrasonography would be more success- cannulation, reducing the number of attempts,
ful than Doppler guidance for subclavian vein complications, and failures. Concerns have been
procedures in adults (0.09; 0.02 to 0.38). expressed with respect to training, as the novel
The meta-analyses have shown that ultra- techniques should be incorporated into the ultra-
sound guidance reduces complications relative sound courses that are currently being set up for
TABLE 2 Frequency of Early Complications (Expressed in % of Cases), According to the Insertion Site,
Using Anatomic Landmark Percutaneous Techniques*
experience and professional education when systematically verify position by fluoroscopy after
they choose an approach, the most important implantation; recently, an electrocardiography-
factor being their degree of familiarity with the derived method has been proposed as a radiation-
various options. While many RCTs have clearly free alternative, with initial encouraging results.52
shown that ultrasound guidance is superior to
the landmark technique—at least in terms of COMPLICATIONS OF CENTRAL VENOUS
immediate outcome—for internal jugular vein CATHETERS
cannulation in a variety of clinical settings, doubts
still persist for the subclavian insertion site, and The complications of CVCs can be classified
more studies are needed to address long-term into 2 main categories: (A) early (intraoperative
benefits and cost-effectiveness. Adequately pow- and postimplantation period to first use) and (B)
ered prospective RCTs are still lacking on sev- late complications.
eral issues, especially late complications of central
Early Complications
venous long-term accesses; for example, the
impact of different techniques and access routes Early complications are related to central
on infection and thrombosis rates in the oncol- venipuncture for catheter insertion. They include
ogy patient population is still unknown. No trial pneumothorax, hemothorax, primary malposi-
comparing the subclavian versus internal jugu- tion, arrhythmias, air embolism, and arterial per-
lar vascular access in this patient population has foration causing clinically relevant bleeding.
been published so far, although an objective need Published rates of specific complications are
for such a trial is clear.49 highly dependent on patient selection and are
based on series of several hundred patients53;
Catheter Tip Position
early complications occur in approximately 6.2%
The position of the catheter in the vascular to 11.7% of patients (Table 2). Arterial punc-
system is a major determinant of CVC-related ture and hematoma are the most common
thrombosis, and tip position has emerged as the mechanical complications during the insertion
main independent prognostic factor for mal- of CVCs, with similar rates for internal jugular
function and reduced duration of the device. and subclavian catheterization.54
Placement of the catheter tip high in the SVC Pneumothorax continues to be reported in
results in a higher incidence of thrombosis than many prospective series, while no case of signif-
low placement in the SVC or at the atriocaval icant hemorrhage related to catheter placement
junction. 50 Therefore, at least in oncology has been reported recently in the literature.
patients, the atriocaval junction appears to be
Pneumothorax
the optimal position; hemodialysis could require
full atrial positioning of the catheter tip, at least Pneumothorax is described as the most fre-
for cuffed devices.51 Thrombosis also seems to quent complication of percutaneous central ven-
be more common when catheters are inserted ous cannulation. Its prevalence is 0.5% to 12%,
entering the left subclavian vein. Many centers depending on differences in clinical features,
access site, and operator experience; this last vari- however, the routine use of this imaging tech-
able is considered by (almost) all authors as the nique does not improve the diagnostic yield.58
key deter minant of pneumothorax rate. Treatment of iatrogenic pneumothorax aims at
Consequently, the operator learning curve (maybe evacuating air from the pleural space and re-
up to 50 implants) has a major impact on com- expanding the lung. Available therapeutic options
plication rate and should be borne in mind when include simple observation; aspiration with a
the complication prevalence is assessed: inser- catheter, with or without immediate removal of
tion of a catheter by a physician who has per- the catheter after pleural air is evacuated; and
formed 50 or more catheterizations is half as insertion of a chest tube or tube-thoracostomy.59
before scheduling a procedure for CVC implan- are exchange over guidewire, removal (for non-
tation and taking alternative approaches into tunneled, short-term CVC), or an attempt at
consideration (eg, venous cut-down, ultrasound pharmacological disobstruction (for PICCs or
guidance, or peripherally inserted CVCs). long-term VADs). Disobstruction should always
be performed using a 10 mL syringe (or larger)
LATE COMPLICATIONS
so as to avoid inappropriately high pressure, which
may damage the catheter, and using the most
According to a general definition, late com- adequate solution for the presumed type of
plications are events that occur after the peri- obstruction (ethanol for lipid aggregates, uroki-
Dislocation of tunneled catheters should be (B) choice of the internal jugular vein rather than
prevented by positioning the cuff at least 2.5 cm the subclavian vein66,67; (C) appropriate position
inside the tunnel (or more, according to the man- of the tip of the catheter; (D) proper stabiliza-
ufacturer’s instructions) and securing the catheter, tion of the catheter (for external VADs); and (E)
preferably with a catheter-stabilization device, proper placement of the reservoir (for ports).
for at least 3 to 4 weeks.
Extravasation Injuries
The “pinch-off ” syndrome is due to com-
pression of a large-bore silicone catheter— Central VADs have greatly reduced the inci-
tunneled or connected to an implantable port— dence of extravasation injury, but this severe
protected from this severe complication. Patient antimicrobial catheters, and antimicrobial catheter
safety can be enhanced by incorporating guide- lock solutions. Management of catheter-related
lines17,73 into daily clinical practice. infections involves deciding on catheter removal,
Most catheter-related infections arise by 2 antimicrobial catheter lock solution, and the type
mechanisms: (A) infection of the exit site, followed and duration of systemic antimicrobial therapy
by migration of the pathogen along the exter- (Figure 1). The type of catheter involved should
nal catheter surface and (B) contamination of also be taken into account. Empirical intravenous
the catheter hub, leading to intraluminal coloniza- antimicrobial therapy should be initiated after
tion and consequent seeding of the pathogen samples for appropriate cultures have been obtained.
into the circulation. In most cases of CVC-related bacteremia and
Because diagnosis is often clinical, and clini- fungemia,nontunneled CVCs should be removed.
cal diagnostic criteria are either insensitive or On the other hand, the decision to remove a tun-
nonspecific, CVC-related infections are often neled catheter or implantable device should be
overdiagnosed; this results in unnecessary and based on several factors, such as the severity of
wasteful removal of the catheter.74 Catheter- the patient’s illness and underlying condition (neu-
sparing diagnostic methods, such as differential tropenia, thrombocytopenia); proof that the VAD
quantitative blood cultures and differential time is infected; availability of other vascular access
to positivity (DTTP), have emerged as reliable sites; assessment of the specific pathogen involved;
diagnostic techniques. Paired blood cultures (aer- and presence of complications, such as endocardi-
obic and anaerobic) from a peripheral vein and tis, septic thrombosis, and tunnel infection.
the central catheter should be obtained. If the When a catheter-related infection has been
culture from the central catheter turns positive documented and a specific pathogen has been
before the peripheral sample (diagnostic cut-off: identified, systemic antimicrobial therapy should
2 hours), this so-called DTTP can help to make be targeted, and the use of antibiotic lock ther-
the diagnosis of catheter-related infection.72 apy should be considered. Specific guidelines on
Possible preventive strategies include skin diagnosis, management, and prophylaxis of CVC-
antisepsis, maximum sterile barrier, use of related infections are available.17,73,75
McGee et al53 have suggested that selection to occur in 15% to 25% of patients with CVC-
of the subclavian site appears to minimize the related vein thrombosis. Although the throm-
risk of infectious complications. However, while bosis rate is high, only a third of the thrombosed
this statement is supported by an RCT compar- CVCs become symptomatic. Nonetheless, CVC
ing the infection rates associated with the selec- thrombosis can result in clinical symptoms, the
tion of the subclavian or femoral vein, 54 no loss of catheter function, a higher rate of infec-
RCTs comparing the infection rates associated tion, postphlebitic syndrome of the upper extrem-
with internal jugular and subclavian vein can- ity, pulmonary embolism, and greater costs.
nulation are available. Moreover, a more recent However, using totally implantable access devices,
catheter removal has been reported.82 The manda- enoxaparin 100 IU/kg) in high-risk patients,
tory indications to catheter removal in case of including those who have a family history of
thrombosis include infected thrombus, malpo- thrombotic events or previously suffered from
sition of the tip (primary or secondary to migra- idiopathic venous thrombotic events.
tion), and irreversible occlusion of the lumen. With regard to the particular type of venous
Thrombolytic drugs (urokinase or recombi- thrombosis (local or, more seldom, central), which
nant tissue plasminogen activator) should be used may occasionally be associated with PICCs, it
in acute symptomatic cases diagnosed fewer than appears to be a multifactorial phenomenon influ-
24 hours after the first symptoms. Efficacy of enced by caliber of the catheter, technique of
nursing care, renewal of the dressings, and access Transparent polyurethane film is recommended
to the catheter being the sole responsibility of for catheter-site insertion dressing by the CDC
specially trained nurses. guidelines for the prevention of infections asso-
Nowadays, much nursing time is spent car- ciated with intravascular catheters.22 It has proved
ing for patients receiving intravenous therapy. to offer the advantages of excellent adhesion,
In several countries nursing care in vascular access firm support of the catheter, good tolerability,
is very advanced, as nurses select, insert, and ease of application, and fewer replacements per
remove both peripheral and central venous catheter lifetime compared with standard gauze
devices, but in all countries their role in assess- and tape dressings.95 Regarding the risk of infec-
of smaller size are available with a traditional 10- state how to contact the hospital or health care
mL syringe diameter; they generate a signifi- professional if they have concerns.98 In selected
cantly lower pressure compared with traditional cases, it may be useful to arrange for a nurse to
3-mL syringes. visit the patient at home in order to further rein-
Flushing is recommended before and after force the retention of training information.
administration of drugs, before and after trans-
fusion of blood components, after obtaining PATIENT ISSUES: VASCULAR ACCESS AND
blood specimens, and for device maintenance QUALITY OF LIFE
when not in use.
or comparative studies with externalized tun- of use); failure of the assigned venous-access
neled systems; they have provided little infor- strategy occurred in 16 (27%) of 60 controls,
mation on quality of life and global costs, who had to cross over to receive central venous
especially when only prospective data are taken access to complete treatment. As expected, fail-
into consideration,104,105 ure was correlated with significant access-related
A paper from our group64 has provided clini- anxiety and pain according to the outcome of
cians, health care planners, and funding agencies multiple linear regression. The analysis of qual-
with data derived from a large prospective study on ity of life was based on only 92 patients com-
total cost of devices for long-term chemotherapy pleting 6 cycles of chemotherapy; although no
progression-free survival (or time to progression), access-related anxiety and pain. It is still unclear
and overall survival—as well as toxicity—were whether these benefits outweigh the overall costs
all significantly in favor of infusion over bolus of their purchase, implant, and use for the sup-
administration.108 Significantly less diarrhea, stom- portive care of an increasing number of cancer
atitis, nausea and vomiting, alopecia, lethargy, and patients. During these times of economic restraint
neutropenia (all with P ⬍.0001) were seen with and limited health care resources, further well-
5-FU infusion in a recent large multicenter trial.109 designed and sufficiently powered RCTs are
Oral medicinal products were offered as an needed to answer the question.
alternative to “unpleasant” intravenous 5-FU in
order to reduce the risk of infusion-related precautions during catheter insertion, catheter-
complications (especially extravasation). site maintenance, and hub handling. New tech-
3. Tunneled CVCs are indicated for patients in nologies and materials will be available in the
whom long-term central venous access and near future, needing appropriate trials.
intensive device use are anticipated. The Thrombosis still remains a major problem.
repeated administration of chemotherapy, When VAD-related deep vein thrombosis occurs,
antibiotics, parenteral feeding, blood prod- it seriously complicates the clinical management
ucts, and frequent blood sampling are all con- of the patient because of the need for anticoag-
ditions suggesting their preferential use. ulant treatment and sometimes the need to achieve
REFERENCES hospitals in England. J Hosp Infect 2007;65(suppl): 32. Zürcher M, Tramèr M, Walder B. Colonization
S1–S64. and bloodstream infection with single- versus multi-
1. Ryder MA. Peripheral access options. Surg 18. Pittiruti M, Migliorini I, Emoli A, et al. lumen central venous catheters: a quantitative sys-
Oncol Clin N Am 1995;4:395–427. Preventing central venous catheter related infec- tematic review. Anesth Analg 2004;99:177–182.
2. Scott WL. Central venous catheters. An overview tions: catheter site selection and insertion tech- 33. Turcotte S, Dubé S, Beauchamp G. Peripherally
of Food and Drug Administration activities. Surg nique significantly affect the chances of adequate inserted central venous catheters are not superior
Oncol Clin N Am 1995;4:377–393. catheter site care [abstract]. Intensive Care Med to central venous catheters in the acute care of sur-
3. Registered Nurses’ Association of Ontario. 2007;33(suppl):S13. gical patients on the ward. World J Surg 2006;
Nursing Best Practice Guidelines. Project: 19. Pratt RJ, Pellowe C, Loveday HP, et al. The 30:1605–1619.
Assessment and Device Selection for Vascular Access. epic project: developing national evidence-based 34. Cortelezzi A, Moia M, Falanga A, et al.
Available at: www.rnao.org/bestpractices. Accessed guidelines for preventing healthcare associated Incidence of thrombotic complications in patients
July 14, 2008. infections. Phase I: Guidelines for preventing with haematological malignancies with central
47. Verghese ST, McGill WA, Patel RI, et al. chemotherapy. A prospective study analyzing com- transplantation: results of a monocentre series of
Ultrasound-guided internal jugular venous can- plications and costs of 333 devices with a mini- 376 patients. Ann Oncol 2004;15:296–300.
nulation in infants: a prospective comparison with mum follow-up of 180 days. Ann Oncol 1998; 82. Zuha R, Price T, Powles R, Treleaven J.
the traditional palpation method. Anesthesiology 9:767–773. Paradoxical emboli after central venous catheter
1999;91:71–77. 65. Yildizeli B, Laçin T, Batirel HF, Yüksel M. removal. Ann Oncol 2000;11:885–886.
48. Gallieni M. Central vein catheterization of Complications and management of long-term cen- 83. Heaton DC, Han DY, Inder A. Minidose (1
dialysis patients with real time ultrasound guid- tral venous access catheters and ports. J Vasc Access mg) warfarin as prophylaxis for central vein catheter
ance. J Vasc Access 2000;1:10–14. 2004;5:174–178. thrombosis. Intern Med J 2002;32:84–88.
49. Hamilton HC, Foxcroft DR. Central venous 66. Araújo C, Silva JP, Antunes P, et al. A compar- 84. Monreal M, Alastrue A, Rull M, et al. Upper
access sites for the prevention of venous throm- ative study between two central veins for the intro- extremity deep venous thrombosis in cancer patients
bosis, stenosis and infection in patients requiring duction of totally implantable venous access devices with venous access devices—prophylaxis with a
long-term intravenous therapy. Cochrane Database in 1201 cancer patients. Eur J Surg Oncol 2008; low molecular weight heparin (Fragmin). Thromb
99. Bow EJ, Kilpatrick MG, Clinch JJ. Totally 103. Mueller BU, Skelton J, Callender DP. A with advanced and/or metastatic cancer. J Clin
implantable venous access ports systems for patients prospective randomized trial comparing the infec- Oncol 1998;16:2977–2985.
receiving chemotherapy for solid tissue malignan- tious and noninfectious complications of an exter- 108. Efficacy of intravenous continuous infusion
cies: A randomized controlled clinical trial exam- nalized catheter versus a subcutaneously implanted of fluorouracil compared with bolus administra-
ining the safety, efficacy, costs, and impact on quality device in cancer patients. J Clin Oncol 1992;10: tion in advanced colorectal cancer. Meta-analy-
of life. J Clin Oncol 1999;17:1267. 1943–1948. sis Group In Cancer. J Clin Oncol 1998;16:
100. Chenecky C. Satisfaction versus dissatisfac- 104. Broadwater JR, Henderson MA, Bell JL. 301–308.
tion with venous access devices in outpatient oncol- Outpatient percutaneous central venous access in
109. Chau I, Norman AR, Cunningham D, et al.
ogy: a pilot study. Oncol Nurs Forum 2001;28: cancer patients. Am J Surg 1990;160:676–680.
A randomised comparison between 6 months of
1613–1616. 105. Schuman E, Brady A, Gross G, Hayes J. Vascular bolus fluorouracil/leucovorin and 12 weeks of pro-
101. Koonings PP, Given FT Jr. Long-term expe- access options for outpatient cancer therapy. Am J tracted venous infusion fluorouracil as adjuvant
rience with a totally implanted catheter system in Surg 1987;153:487–489. treatment in colorectal cancer. Ann Oncol 2005;