Patients' attitudes to totally implantable venous access port systems for gynecological or breast malignancies
Introduction
Central venous access port devices (CVAPDs) have been used in oncology for more than 20 years. They were first described in 1982.1 In clinical practice, ports are most commonly used for the administration of long-term chemotherapy, transfusions, parenteral nutrition, blood sampling, pain therapy, and supportive cancer care involving the monthly application of intravenous bisphosphonates, for example.2, 3
The most common reason for implantation is the need to obtain secure venous access for cytotoxic oncological therapy.2, 4, 5, 6 In the treatment of breast cancer, chemotherapy regimens with a duration of up to 6 months are commonly required.7 Secure venous access is desirable for these treatments, as venous integrity may be compromised by cytostatic agents that are toxic to the veins.
The use of CVAPDs to improve the reliability of venous access, to reduce the discomfort, anxiety, and pain associated with repeated venous puncture and to avoid cancer-related morbidity has been debated.6, 8 Various types of indwelling catheter, such as externalized central venous catheters of the Hickman or Broviac type, and fully implantable central venous access ports are available for long-term venous access.9, 10, 11, 12 These systems can be placed in various vessels, such as the subclavian vein, the jugular vein, or the upper extremity veins. Totally implantable venous access port systems have several advantages over externalized indwelling catheter systems. They require only monthly flushing with heparinized solutions and are associated with fewer restrictions on activities such as bathing. In addition, the venous access is protected by the patient's skin when the port is not in use.
However, the use of CVAPD is associated with a number of complications associated with the surgery. Overall complication rates in the range of 1.8–14.4% have been reported.2, 13, 14, 15 Common complications are infections and deep venous thromboses in the upper extremity.2, 16, 17 In comparison with externalized systems, ports are associated with a lower incidence of infections and malfunctioning.16 Further complications include drug extravasation, port occlusion, catheter misplacement, pneumothorax, hematothorax, air embolism, injury to adjacent anatomic structures, disconnection, and port-membrane rupture.3, 16, 17
The overall quality of life (QoL) has been described previously in a group of patients with solid tumors.6 To date, there have been no reports describing port-specific aspects of QoL. The aim of the present study was to investigate these port-specific aspects and to correlate them to the complications associated with the CVAPD.
Section snippets
Patients and methods
The study population consisted of patients with gynecological and breast malignancies who received a CVAPD. Between April 2001 and August 2003, 362 patients underwent CVAPD placement in the department of surgery. The port catheter system used (Baxter, Munich, Germany) consists of a titanium port with a silicone membrane, which is connected to a radiopaque silicone rubber catheter. The system is implanted into the subclavian or cephalic vein. Concerning breast cancer patients the ipsilateral
Results
The results can be presented in four categories.
Concerning satisfaction and anxieties concerning the port a total of 199 of the patients were very satisfied or quite satisfied with the CVAPD (question A) and 126 patients reported that the CVAPD gave them a feeling of security (question 1). A fear of puncture of the port catheter was reported by 19 patients (question 4). Eighty percent of the patients (n = 187) confirmed that they would wish to have a port implanted again if indicated (question C).
Discussion
Implantable port catheter systems have been used for administration of chemotherapeutic agents and for blood products, infusions, and parenteral nutrition. The present study examined the safety of these systems and their impact on the port-related QoL. To date, there have been no trials describing the port-related aspects of QoL. A randomized trial examining the safety, efficacy, costs and QoL has been performed with a limited sample size (59 port implantations vs. 60 controls with peripheral
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