Background
Central venous access is essential in patients with cancer, and the need for intravenous access devices for the administration of cancer therapy has increased proportionally with the increasing number of patients diagnosed with cancer. The percutaneous approach to the subclavian or internal jugular vein is currently the most popular procedure for placing catheters in the superior vena cava both for short-term and long-term use.
Unfortunately, central venous catheter (CVC) insertion represents a risk of pneumothorax, nerve puncture and major bleeding (mechanical complications), infection and CVC-related vein thrombosis [1, 2].
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Mechanical complications of CVC insertion without ultrasound (US) guidance, such as arterial puncture and pneumothorax, are seen in up to 21% of attempts, and up to 35% of insertion attempts are not successful [3‐5].
There have been several prospective randomized trials [6‐14] and two metanalyses [15, 16] that suggest the use of US has been associated with a reduction in complication rate and an improved first-pass success when placing CVC in the internal jugular vein.
In 2001, the U.S. Agency for Healthcare Research and Quality recommended the use of ultrasound for the placement of CVC as one of their 11 practices to improve patient care [17, 18]. However a survey of 250 anesthetists in the United Kingdom found that 41% disagreed or strongly disagreed with the recommendation that ultrasound imaging should be the preferred method for insertion of a central venous catheter in the internal jugular vein [19].
In addition, a report in the United States also showed that <15% of surgery, anesthesia, internal medicine, emergency medicine and family medicine housestaff used ultrasound guidance for most CVC placements [20].
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Since in our department oncologists and hematologists have performed ultrasound imaging procedures as well as interventional ultrasound in clinical practice for patient management (diagnosis, staging, restaging and follow-up) for almost 25 years [21‐27], this procedure was early applied as a guidance for CVC insertion in the internal jugular vein in cancer patients before the recommendations from the Agency for Healthcare Research and Quality were available [17, 18]. Aims of this prospective observational study were to evaluate the safety and the efficacy of ultrasound-guided insertional CVC in patients with hematological and solid tumors, to confirm the utility of this procedure in clinical practice, and to evaluate local or systemic infection, CVC-related deep venous thrombosis (DVT) and lifespan of the CVC.
Materials and methods
Adult patients with hematologic and solid tumors admitted to the oncology-hematology department of the hospital of Piacenza, North Italy, and requiring an indwelling CVC were offered the opportunity to partecipate in the study. There were 802 women (48%) and 858 men (52%) with a mean age of 61.72 years (range 18-85).
No exclusion criteria were contemplated except patients' refusal and patients candidate to palliative care only. The study was approved by the local ethics committee as a prospective observational study, and all the patients gave informed written consent before enrolment. Three types of CVC were employed according to different indications: single-lumen 16 gauge and, double-lumen Becton Dickinson (Singapore), double-lumen 13 French Arrow International (Erding, Germany). The last one was specifically employed in leukapheresis procedures. Each CVC-positioning is considered a single procedure for the study; so a patient who need catheter insertion more than once through his clinical history was registered as a new procedure every time CVC was inserted again.
The indications of CVC were: chemotherapy delivery, transfusion, parenteral nutrition, leukapheresis, autologous and allogenic stem cell transplantation, invasive hemodynamic variables assessment and blood sampling. Patients candidate to palliative care only were excluded from this study since they were enrolled in a different study.
Operators included two physicians and a nurse with specific experience with ultrasound and ultrasonically guided procedures, so that the level of experience of the operators would not bias results.
Patients were postured in the Trendelenburg's position with the head rotated toward the opposite side. The CVC was routinely implanted on the right side; however, if conditions were unsuitable for implantation on this side, such as in the case of lymphoadenopathy, or postradiation therapy area, or at the patient's request, the CVC was placed on the left side. All procedures were performed using standard aseptic techniques and a local anesthesia with a very small, 22-gauge needle for the venipuncture was applied under ultrasound guidance.
The ultrasound examinations were performed using ESAOTE (Genova, Italy) equipped with two transducers between 3.5 to 7.5 MHZ, with a needle guide, without a sterile cover. The method that we commonly use is "the three-handed method" [28]; this method requires an assistant to hold the probe, while the operator controls the needle and performs the procedure under real-time guidance, and the nurse helps the two physicians during the maneuver.
The central vein was identified along its greater longitudinal axis and its relationship with other anatomical structures using Valsalva's maneuver which determines an increase of the diameter of the veins. Under ultrasound-guide in real time, a 16-gauge needle is introduced into the last portion of internal jugular vein. This vein was reached through the transducer placed at the point of insertion of the sternocleidomastoid muscle into the clavicular; the correct introduction of the needle was always confirmed by ultrasound guidance and by the easy aspiration of venous blood.
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The Seldinger technique was used to place the catheter, which was advanced into the superior vena cava until insertion into right atrium.
Every procedure was scheduled in order to register patient's data, pathological diagnosis, indications for CVC insertion, type of CVC, number of attempts and early complications if any failure; the procedures were observed by an independent team. Medications, CVC-related blood stream infection, symptomatic deep-vein thrombosis and CVC removal or substitution were also recorded. Within two hours after each procedure, chest radiography and ultrasound scanning were carried out to exclude pneumotorax and to evaluate correct catheter position. At the end of treatment or when required, after the removal of the catheter, the tip was sent to the laboratory for bacteriological examination.
No systemic prophylaxis against deep-vein thrombosis was adopted and no antibiotic prophylaxis was made. Each catheter at the end of its routine use was flushed with 20 ml normal sterile saline, then 5 ml heparinized saline (50 IU/ml). Follow-ups for each patient were scheduled every 10 days during the first six months, or until removal of the CVC. The follow-up consisted of: patient's clinical examination, catheters flushed with heparinized solution and catheter exit side dressing.
Assesment of endpoints
The primary endpoints were: number of pneumotorax, accidental arterial and nerve puncture; major bleeding; number of attempts; failure; local hematoma.
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Secondary endpoints were: symptomatic vein thrombosis of upper limbs (early or late), infections, malfunctioning and lifespan of the CVC.
In cases of clinical suspicion of venous thrombosis evidenced by progressive arm or facial swelling, the ultrasound criteria we considered in order to show the presence of catheter-related thrombosis included visualization of thrombus, absence of spontaneous flow, dilatation of the vein by the Valsalva maneuver and compressibility of the jugular vein as previously reported [29, 30]. Infections were defined as catheter-related bacteremia: isolation of the same organism from the catheter in the presence of more than 15 colony-forming-units (CFUs) and positive blood culture without clinical signs of infection and catheter-related septicemia: isolation of the same organism from the catheter in the presence of more than 15 CFUs and positive blood culture, with clinical signs of infection [29]. Infections with a clinically apparent focus other than exit site or catheter were excluded. Catheter malfunctioning occlusion was registered when presented.
Statistical analysis
Demographic data and clinical features were analyzed using descriptive methods. Quantitative variables were summarized using mean and standard deviation. Categorical variables were summarized as counts and percentages. Baseline analysis included all enrolled patients. Statistical tests were performed with Statview Software, latest version.
Results
From 2 December 2000 to 31 January 2009, 1,978 CVC insertional procedures were applied in 1,660 patients. The procedure was performed 580 times in hematologic malignancies and 1,398 times in solid tumors (Table 1); the majority of patients with solid tumors had gastrointestinal cancer and the majority of patients with hematologic malignancies had lymphomas (Table 2). The median platelet count at the time of CVC insertion was 236,000/mm3 while the median neutrophil count was 4,015/mm3 (Table 3). It must be emphasized that a subset of patients, especially hematological ones, had neutropenia and low platelet count; neutropenia: 254 patients (15.3%) with neutrophils below 1,500/mm3, 132 (7.95%) below 500/mm3, 88 (5.3%) below 100/mm3; low platelet count: 116 patients (6.99%) with platelet count below 50,000/mm3, 70 (4.22%) below 20,000/mm3 and 38 (2.29%) below 10,000/mm3 (Table 4).
Table 1
Patients characteristics
Noof patients | % of patients | |
|---|---|---|
Total | 1,660 | 100 |
Median age | 61.71 years (range 18-85) | |
Male | 858 | 52 |
Female | 802 | 48 |
Type of cancer | ||
Solid tumor | 1,280 | 77 |
Hematologic malignancies | 380 | 23 |
Table 2
Types of cancer
Noof procedures | % of cancer | |
|---|---|---|
Total | 1,978 | 100 |
Solid tumor
|
1,398
| 70.68 |
Gastrointestinal | 904 | 45.70 |
Lung | 64 | 3.24 |
Breast | 136 | 6.88 |
Other solid cancer | 294 | 14.86 |
Hematologic malignancies
|
580
| 29.32 |
Lymphomas | 216 | 10.82 |
Acute leukemia | 196 | 9.91 |
Multiple myeloma | 126 | 6.37 |
Other hematologic malignancies | 42 | 2.12 |
Table 3
Main Hematologic characteristics of the overall population
Median | Range | Normal range | |
|---|---|---|---|
Platelet count N/mm3 | 236,000 | 7,000-510,000/mm3 | 130,000-450,000/mm3 |
Neutrophil count N/mm3 | 4,015 | 85-10,500/mm3 | |
Prothrombin activity (%) | 60 | 30-100 | 70-120 (%) |
Fibrinogen (mg/dl) | 185 | 100-460 | 150-400 (mg/dl) |
APTT (sec) | 30 | 25-45 | 26.50-37.50 (sec) |
Table 4
Patients with impaired neutrophil/platelet count who underwent ultrasound guided internal jugular vein catheterization
Patients with neutropenia 254 of 1660 | Patients with low platelet count 116 of 1660 | ||||
|---|---|---|---|---|---|
N. Patients
|
% of patients
|
N. neutrophil/mm3
|
N. Patients
|
% of patients
|
N. Platelet/mm3
|
254 | 15.3% | <1,500 | 116 | 6.99 | <50 |
132 | 7.95 | <500 | 70 | 4.22 | <20 |
88 | 5.3 | <100 | 38 | 2.29 | <10 |
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Primary end points: a single-needle puncture of the vein was performed on 1,948 of 1,978 procedures (98.48%) and eighteen attempts of the 1,978 failed (0.9%), so the procedure revealed itself to be efficacious in 99.1% of cases. Failures were caused by arterial puncture in 6 (0.3%), mediastinum CVC dislocation in 2 (0.1%), vein collapse in 8 (0.48%) and no efficacious "eco window" in 2 (0.1%). There were no differences in mechanical complications, malposition and malfunctioning of CVC with the right (94.7% of cases) and left side (5.3% of cases) approaches.
No major bleeding and no nerve puncture were reported; four (0.2%) self-limiting hematomas at the site of CVC insertion without requiring any medical intervention were registered after arterial puncture. No pneumotorax was reported (Table 5).
Table 5
Results of ultrasound guided catheter insertion, primary endpoints and mechanical complications
No | % | |
|---|---|---|
Total procedures
| 1,978 | 100 |
Access with one attempt | 1,948 | 98.48 |
Access with two attempts | 12 | 0,6 |
Pneumothorax | 0 | 0 |
Major bleeding | 0 | 0 |
Arterial puncture | 6 | 0.3 |
Failure | 18 | 0.9 |
Local Hematoma | 4 | 0.2 |
Nerve puncture | 0 | 0 |
Secondary end points
Catheter-related infection occurred in 197/1,978 (9.96%) of the catheters inserted; CVC-related septicemia was observed in 98 cases (4.95%). No death was attributable to catheter-related infections (Table 6).
Table 6
Secondary endpoints and non-mechanical complications of ultrasound guided catheter insertion
N | % | |
|---|---|---|
Total procedures | 1,978 | 100 |
CVC-related infection | 197 | 9.96 |
Septicemia | 98 | 4.95 |
CVC-related symptomatic vein thrombosis | 45 | 2.28 |
CVC removal due infection/thrombosis or malfunctioning | 48 | 2.4 |
Mean lifespan of CVC and standard devation
|
189.7, days +/- 18.6(range 7-701 days)
| |
The organisms that caused catheter colonization were coagulase negative staphylococci 82%, Escherichia Coli 8%, Pseudomonas 6%, Enterococcus 4%.
The mean lifespan of CVC was 189.7 +/- 18.6 days (range 7-701), and CVC inserted under US guidance permitted the delivery of the planned therapy in 1,930/1,978 (97.6%) of patients.
In our 197 patients with catheter - related infection, antibiotic therapy resolved the infection: in 129 cases (65.5%) with CVC substitution and 20 cases (10.10%) without it. Only in 48 cases (24.40%) was definitive CVC removal required for associated thrombosis and for antibiotic therapy failure or for CVC malfunctioning.
Symptomatic deep-vein thrombosis of upper limbs developed in 45 cases (2.7%) mainly in the first 30 days of implantation. Clinical diagnosis suggested by progressive arm or facial swelling was confirmed by echodoppler. In 30/45 (66.7%) cases with thrombosis, CVC was removed because of associated infective complications (Table 6). No patient had any further thromboembolic complications. There was no difference in infection, bleeding or thrombosis in patients with single-lumen and double-lumen catheters; however the large - bore catheter employed in leukapheresis was generally removed after the procedure.
Discussion
The use of central venous access devices has become an essential component of the treatment of many medical disorders. Central venous access is commonly attempted in the internal jugular vein, subclavian vein, femoral vein, or arm veins using peripherally central catheters. It is estimated that several million devices are inserted each year, facilitating many emerging therapies, including long-term chemotherapy [30].
Central venous cannulation can be unsafe: the National Confidential Enquiry into perioperative deaths has reported one death resulting from a procedure-induced pneumothorax [31].
It must be emphasized that less serious discomfort (though unpleasant for the patient), clinician time, hospital stay and economic costs are variable rates for failure and complications from central venous cannulation. Ten of 328 oncological patients (3.4%) developed pneumothorax after central venous access implanted without US guidance and 6 of them (60%) required tube-thoracostomies [30].
More recently, the etiology and incidence of iatrogenic pneumothorax, which can develop after invasive procedures performed for diagnostic and for therapeutic purposes, has been reported [32]: the most frequent procedure type causing pneumotorax was central venous catheterization, with 72 patients (43.8%) of the series of 164 patients developing iatrogenic pneumothorax.
In addition, complications are more frequent when more needle passes are necessary because of anatomical variation or difficult veins (small veins; no palpable landmarkers). Anatomical variations of the internal jugular vein were found in 8% of patients studied with ultrasound-guided CVC [33]; the ease and the shorter time required to perform ultrasound-guided catheterization, together with the higher rate of success and decreased incidence of complications make using the ultrasound-guided CVC preferable to conventional CVC [34‐36].
In this large series of 1,978 CVC insertional performed procedures in 1,660 consecutive patients suffering from cancer in different phases of their disease, none of the patients experienced major complications (pneumotorax, hemothorax, nerve lesions). To our knowledge, this is the largest series of consecutive CVC insertional procedures performed in patients with hematologic malignancies and solid tumors and we have shown that this technique may be efficacious and safe both in patients with acute leukemia and with solid tumors. In addition, we emphasize that the catheter was inserted in 254 patients (15.3%) with neutrophils <1,500 ul and 116 patients (6.99%) with platelets <50 ul without complications. Individual institution data might differ from those gathered at other centers; however we think the results of this study are particularly relevant because they have been obtained through a large series of patients investigated with an accurate prospective trial performed over a long period of time. Our results can be favourably compared with a recent report where adverse events occurred in 26 cases (5.2%) of 500 US-guided CVC via subclavian vein, with two cases of pneumothorax [37].
In our study, the rate of CVC-related deep-vein thrombosis was low despite the absence of antithrombotic drugs in the practice of prophylaxis against venous thromboembolism in the patients enrolled; the incidence of symptomatic DVT was quite similar, although a bit low, with respect to the value in the control arm of previous studies which compared no systemic prophylaxis versus deltaparin or low-dose warfarin [38‐40]. The low incidence of upper-limb DVT may be explained by ultrasound guide as previously stated [41] which allowed us to achieve the following targets:
1)
to identify the exact site of CVC insertion, 2) to perform only one attempt in nearly all the patients (98.48%), causing little damage to the venous endothelium: in fact, it is well known that endothelium damage is a main risk factor in initiating thrombosis.
However the lack of venographic assessment of catheter-related thrombosis in our study is a limit to the determination of the real frequency of this complication, as previously reported [40].
The incidence of CVC infective complication was similar to previous data concerning non-tunnelled catheters, while it was higher than totally implantable central venous access ports [29, 42]. The great incidence of staphylococci reflects the classical expositional risk of this kind of catheter, although the incidence of infections, the rate of CVC withdrawal or malfunction was low when compared with previous reports [29], since prompt antibiotic therapy allowed a good control of bacterial infection. Moreover, our non-tunnelled catheters were easily replaced whenever clinical conditions suggested it. In the present study, ultrasound-guided CVC procedures were performed by our own specifically experienced oncologists and hematologists, and we agree with a recent report [28] that ultrasound is an easily learned technique that not only enhances the physical examination, but has the distinct advantage of being a portable tool that can provide real-time guidance for CVC insertion and other interventional procedures such as biopsy, abscess drainage, paracentesis, thoracentesis, etc, and for critically ill and elderly patients the procedure can be performed easily at the bedside as previously reported [21‐27]. Physicians with specific experience were defined as operators who have performed > 50 CVC insertion under ultrasound guidance [4, 28].
It must be emphasized that the use of ultrasound is not limited to radiologists. The American Medical Association policy fovours ultrasound imaging technique diffusion in medical practice [43], the American College of Emergency Physicians and the American College of Surgeons support the use of ultrasound by members of their societies and address ways to obtain and maintain competence as well as ensuring quality control [44, 45].
Conclusion
Our large study show that ultrasound-guided CVC insertion is a safe and effective technique that is sufficient to give a patient six or more months of treatment. Safety and efficacy of the procedure did not negatively impact on infective and thrombotic complications. We believe this technique can be applied easily to most practitioners in clinical oncology with relevant patient benefits.
Acknowledgements
The Authors acknowledge the following institutions for their support:
Commercianti di Agazzano, Comune di Pontenure, Roncarolo, Tramballando, Club Beppe and Dany, Marco Biolchi, Copravolley, Grande Casa Reale e Ducale di Piacenza e Parma, Pro Loco Gazzola, I Fantastici.
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Competing interests
The authors declare that they have no competing interests.
Authors' contributions
Study Concepts: LC, GC, DV. Study Design: LC, GC, DV. Data Acquisition: From LC to LT. Quality Control of Data and Algorithms: LC, GC, DV and CB. Data Analysis and Interpretation: CB and LC. Statistical analysis: DV and CB. Manuscript preparation: LC, CB, CDN. Manuscript editing: LC, CB, CDN. Manuscript review: all authors.