Keywords
Ultrasound, Central Venous Access, Internal Jugular Vein Cannulation, Mechanical complications, Puncture time
Ultrasound, Central Venous Access, Internal Jugular Vein Cannulation, Mechanical complications, Puncture time
Central venous catheters (CVC’s) are a very useful tool for the treatment of critically ill patients1. They are used for the delivery of vasoactive agents, parenteral nutrition, long-term antibiotics, blood sampling, hemodynamic monitoring, and/or venous access for haemodialysis patients2. Historically, vein cannulation has been a procedure performed with a blind approach, following only anatomical landmarks for cannulation, thus the incidence of complications has been estimated to be as high as 40%3. Consequently, the use of ultrasound-guided techniques for vein cannulation has helped to reduce the rate of complications4, and its use has been standardized in many emergency rooms around the world5.
Ultrasound-guided techniques in the emergency room have long been documented as beneficial. In fact, in 2001, the Agency for Healthcare Research and Quality Evidence Report recognized bedside-ultrasonography for central venous access as one of the eleven practices with “strength of evidence for supporting more widespread implementation”2. The American College of Emergency Physicians recommends in its Ultrasound Guidelines Policy Statement (last approved in 2016) that emergency room physicians should be trained and proficient in these techniques6. However, there is evidence that even with the recommendations to use ultrasound-guided techniques for central venous access, up to 67% of physicians do not routinely use ultrasound to guide the procedure7.
Insertion of ultrasound-guided CVCs with the conventional technique and with experienced personnel has allowed positive results with reduced costs8; nonetheless, it requires a thorough knowledge of the vascular anatomy and it is operator-dependent9. The technique is also limited in certain settings, like the emergency room, where elements such as previous vascular access, mechanical/ventilation and tracheostomy cannulas can affect access. Other factors affecting the success of the procedure are the presence of thrombosed veins, hematomas and anatomical variations10. These factors are associated with increased mechanical complications and failure rates11. This justifies the use of ultrasound to detect these possible anatomical variations before starting the procedure12.
Ultrasound-guided internal jugular venous (IJV) cannulation, one of the preferred methods for central venous access, is recognized for decreasing rates of failure and mechanical complications13. Main disadvantages of ultrasound-guided IJV cannulation access include the limited availability of the technology in low resource countries, a longer procedural time when the Doppler mode is used, and limited training from medical personnel regarding the ultrasound technique14.
The aim of this study is to determine the incidence of complications from ultrasound-guided jugular vein cannulation and compare the adverse outcomes in emergency versus planned cannulation, as well as to determine the factors that are associated with complications.
Patients’ written informed consent was obtained for the standard clinical procedure; patients were also notified through this document about the inclusion of their data in this study. All patients agreed. The Ethics Committee of Universidad San Francisco de Quito reviewed the study to the project.
This study was performed in Hospital de los Valles (HDLV), Quito, Ecuador. The emergency room department takes care of approximately 20,000 patients per year, of whom 2–4% are in critical condition. The study was designed as a prospective observational study, collecting data over a three-year period of time, between 2010 and 2013.
All patients who were admitted to the emergency room at HDLV and had an indication for CVC insertion, either emergency or planned, were eligible for the study. We excluded patients that did not consent to the CVC insertion, those with a visualized thrombus in the internal jugular vein and those who had trauma of the great vessels in the neck and thorax, according to recommendations based on previous studies11. A total of 142 consecutive patients were included in the study; informed consent for medical procedure was signed at the hospital just after the indication for CVC, either emergent or planned, was stablished. The procedure was explained to patients and/or relatives.
In order to guarantee the best possible technique for the study, physicians performing the IJV central line procedure had to fulfil the following inclusion criteria:
The technique used at the emergency room of our hospital (HDLV) starts with ultrasound-guided visualization of the internal jugular vein anatomy, using a high frequency superficial transducer (General Electric Logiq Book XP portable ultrasound). The CVC is placed with a high frequency 5–15 MHz electronic linear array. After this is done, the distance between skin to the centre of the vessel is measured using a measuring tape and it is corrected for the angulation factor that is going to be used. We mark the skin at the point of insertion. Using the Seldinger technique under sterile conditions and local anaesthesia (lidocaine 1% without epinephrine), the procedure starts with needle puncture (18–20 gauge) and visual guidance of the tip, direction and depth while advancing with continuous ultrasound monitoring. Venous blood is obtained, and the wire is introduced with visual confirmation of an intraluminal location. The dilator is positioned and the catheter is introduced. Finally, and to verify the position of the tip of the catheter, we use the saline flush test using the ultrasound subxiphoid window, to determine if the catheter is too close to the right atrium15.
Emergency CVC via IJV placement was considered in any patient that fulfilled at least one the following criteria:
1. Acute disease, with potential risk of death.
2. Hemodynamic instability.
3. Need for use of vasoactive drugs.
4. Acute decompensation from a chronic illness that puts life at risk.
5. Indication for emergent haemodialysis.
Planned CVC via IJV placement was considered in any of the following cases:
1. Stable patients with diseases that require a planned procedure for:
2. Chemotherapy.
3. Inability to place a peripheral line.
The evaluation of which patients fulfilled emergency vs planned CVC criteria was done by the emergency physicians in charge of placing the IJV central line, with help from doctors from different specialties who were also evaluating each patient for baseline medical conditions.
CVC complications are usually divided into two types: mechanical-technical and infectious. In this study, only mechanical and technical complications were evaluated since infectious require longer follow-ups and specialized studies to determine their origin. Mechanical complications were defined as either: haemothorax, pneumothorax, carotid puncture and/or hematoma at the puncture site16. Technical difficulties were defined as either: double or multiple puncture attempts, guide wire blockage and/or catheter obstruction17. All mechanical complications and/or technical difficulties were identified by the physician performing the procedures and confirmed by a second physician who was a trained observer and who was present during and after the procedure.
The data were collected prospectively, and a registry was made using a Microsoft Excel database, with access limited to the researchers. For each patient, one physician was assigned to the procedure while another one was in charge of registering the data, including demographics, type of procedure (planned vs emergent), time of the procedure, complications and technical difficulties. All the information related to the procedure was registered in the medical record of each patient.
Data is shown as number and percentage for categorical variables; for continuous variables, the mean, median and ranges were also considered. Categorical variables and proportions were compared using Fisher’s exact test, and continuous variables were compared using the Wilcoxon Rank sum test. To investigate risk factors associated with complications, a univariate and multivariate logistic regression analysis was performed in those with all the data available (N=133), and the odds ratios (ORs) with confidence intervals (CIs) and p-values were calculated. Those variables that were significant in the univariate analysis were included in the multivariate analysis. Patients who developed mechanical and technical complications were compared with those who did not present complications. STATA version 13 software was used for analysis and p-values <0.05 were considered statistically significant.
There was a total of 142 patients included in the study, among whom 55% were male and the mean age was 59 years18. Emergency procedures were performed in 36% of the cases. The main indication for CVC placement via IJV cannulation was chronic renal failure (54%), all of which were planned procedures, followed by sepsis (15%), where most procedures (91%) were done as emergencies. Approximately one third of the studied sample (35.2%) had an anatomical orientation of the internal jugular vein above the carotid artery. The median puncture time was two minutes. In most of the patients (66.2%), the time from needle puncture to the vein cannulation was less than two minutes (Table 1).
Variable | N (142) | (%) |
---|---|---|
Gender | ||
Male | 78 | 54.93 |
Female | 64 | 45.07 |
Age mean, median, SD (range) | 59, 63, 17.4 (13-94) | - |
Age (categories) | ||
13–49 years | 35 | 24.65 |
50–69 years | 64 | 45.07 |
>=70 years | 43 | 30.28 |
Type of procedure | ||
Emergency | 51 | 35.92 |
Planned | 91 | 64.08 |
Indications for procedure | ||
Chronic renal failure | 76 | 53.52 |
Acute on chronic renal failure | 2 | 1.41 |
Sepsis | 22 | 15.49 |
Cardiovascular | 11 | 7.75 |
Hematology/oncology | 11 | 7.75 |
Metabolic | 7 | 4.93 |
Acute renal failure | 7 | 4.93 |
Other | 6 | 4.23 |
Location of vessel | ||
Lateral | 55 | 38.73 |
Superior | 50 | 35.21 |
Latero-superior | 31 | 21.83 |
Other variants | 6 | 4.23 |
Puncture time mean, median, DS (range)§ | 4.9, 2, 9.52 (0-60) | - |
Puncture time (median) § | ||
0–2 min | 88 | 66.20 |
3–60 min | 45 | 33.80 |
Out of 133 patients for whom time data was available, 13 (9.8%; 95% CI: 5.3%–16.13%) had some type of complication: six patients (4.5%) had a mechanical complication, of which two (1,5%) were haematomas and four (3%) were arterial punctures, and seven patients (5.3%) had a technical complication, of which three (2.3%) were wire guide blockages and four (3%) were double punctures. Patients who developed mechanical complications were statistically younger than those who did not develop mechanical complications (40 years versus 60 years; p-value: 0.02). There were no age differences between those with and without technical complications.
Median puncture time was statistically longer in those with complications (19.9 minutes) compared to those without complications (3.3 minutes) (p-value: 0.0002). A similar pattern was found when considering mechanical or technical complications separately, where median puncture time was statistically higher in those with complications versus those without complications (Table 2).
No complications (N=120) | Complications (N=13) | P-value | |
---|---|---|---|
Age (years) | 60.4 | 50.1 | 0.17 |
Puncture time ** (min) | 3.31 | 19.9 | 0.0001 |
No mechanical complications (N=127) | Mechanical complications (N=6) | P-value | |
Age (years) | 60.3 | 40.3 | 0.02 |
Puncture time**(min) | 4.4 | 16.8 | 0.005 |
No technical difficulties (N=126) | Technical difficulties (N=7) | P-value | |
Age (years) | 59.4 | 58.6 | 0.68 |
Puncture time** (min) | 3.95 | 22.6 | 0.007 |
After univariate analysis, a puncture time longer than two minutes was statistically associated with an 8.1 times increased risk of developing complications (CI: 2.1-31; p-value: 0.002), while there was no statistical increase in complications in emergency versus planned procedures. After taking into account the effect of age, gender, type of procedure (emergency or planned) and vessel anatomical location on the association, the only independent factor associated with an increased risk of complications was a puncture time higher than two minutes (OR: 7.8; CI: 2-31; p-value: 0.004) (Table 4). When the analysis was restricted to those with mechanical or technical complications, puncture time remains the only significant predictor of mechanical complications. Other variables such as the type of procedure (emergency versus planned) and vessel localization did not reveal any statistical association (Table 3).
Complications | |||||||
---|---|---|---|---|---|---|---|
Variables | No (N=129) | Yes (N=13) | P-value | Crude OR | P-value | Adjusted OR | P-value |
Age (years) | |||||||
13–49 | 30 (85.7) | 5 (14.3) | 1 | ||||
50–69 | 59 (92.2) | 5 (7.8) | 0.51 (0.13-1.89) | 0.31 | |||
>69 | 40 (93) | 3 (7) | 0.53 | 0.45 (0.1-2.03) | 0.3 | ||
Gender (%) | |||||||
Male | 70 (89.7) | 8 (10.3) | 1 | ||||
Female | 59 (92.19) | 7 (7.8) | 0.77 | 0.74 (0.23-2.4) | 0.61 | ||
Type of procedure | |||||||
Emergency | 45 (88.2) | 6 (11.8) | 1 | 1 | |||
Planned | 84 (92.3) | 7 (7.7) | 0.54 | 0.62 (0.2-1.9) | 0.42 | 0.71 (0.21-2.36) | 0.57 |
Vessel location | |||||||
Lateral | 50 (90.9) | 5 (9.1) | 1 | 1 | |||
Superior | 47 (94) | 3 (6) | 0.64 (0.14-2.8) | 0.55 | 0.69 (0.15-3.1) | 0.62 | |
Latero-superior | 27 (87.1) | 4 (12.9) | 1.48 (0.37-5.98) | 0.58 | 1.39 (0.34-5.7) | 0.64 | |
Other variants | 5 (83.3) | 1 (16.7) | 0.5 | 2 (0.19-20.6) | 0.56 | 2.6 (0.23-29) | 0.44 |
Indication for CVC insertion | |||||||
Chronic renal failure (CRF) | 70 (92.1) | 6 (7.9) | 1 | 1 | |||
Acute over CRF | 2 (100) | 0 | na | na | |||
Sepsis | 18 (81.8) | 4 (18.2) | 2.59 (0.66-10.1) | 0.17 | 2.9 (0.68-12.2) | 0.15 | |
Cardiovascular | 11 (100) | 0 | na | na | |||
Hematology/oncology | 11 (100) | 0 | na | na | |||
Metabolic | 6 (85.7) | 1 (14.3) | 1.94 (0.2-18.9) | 0.56 | 1.25 (0.11-14) | 0.86 | |
Acute renal failure | 5 (71.4) | 2 (28.6) | 4.7 (0.74-29.4) | 0.1 | 3.7 (0.48-28.9) | 0.21 | |
Other | 6 (100) | 0 | 0.27 | na | na | ||
Puncture time * | |||||||
0–2 min | 85 (96.6) | 3 (3.4) | 1 | ||||
3–60 min | 35 (77.8) | 10 (22.2) | 0.001 | 8.1 (2.1-31) | 0.002 | 7.8 (2-31) | 0.004 |
Mechanical complications | |||||||
Puncture time * | (N=129) | (N=6) | |||||
0–2 min | 85 (98.8) | 1 (1.2) | 1 | ||||
3–60 min | 35 (87.5) | 5 (12.5) | 0.01 | 12.1 (1.4-107) | 0.03 | 12.4 (1.3-118) | 0.03 |
Type of procedure | |||||||
Emergency | 45 (93.8) | 3 (6.2) | 1 | ||||
Planned | 84 (96.6) | 3 (3.4) | 0.66 | 0.53 (0.1-2.8) | 0.45 | 0.5 (0.09-2.8) | 0.43 |
Technical complications | |||||||
Puncture time * | (N=129) | (N=7) | |||||
0–2 min | 85 (97.7) | 2 (2.3) | 1 | ||||
3–60 min | 35 (87.5) | 5 (12.5) | 0.03 | 6.1 (1-33) | 0.04 | 5.8 (1.0-33.5) | 0.05 |
Type of procedure | |||||||
Emergency | 45 (93.8) | 3 (6.2) | 1 | ||||
Planned | 84 (95.5) | 4 (4.5) | 0.7 | 0.71 (0.15-3.3) | 0.66 | 0.98 (0.20-5.13) | 0.9 |
The complication rates for central venous catheterization when using the landmark technique versus the ultrasound-guided technique have been clearly established in the literature, favoring the ultrasound-guided procedure4; nevertheless, there is no clear comparative analysis in the literature about complications during ultrasound-guided procedures in emergency versus planned situations and this is what this study tries to determine.
When the puncture time exceeded two minutes, the chance of having a mechanical complication was 12.4 times higher compared to a puncture time of less than two minutes. All other variables such as the type of procedure (emergency versus planned) and vessel location did not show any statistical differences. This finding is important for clinical practice because it advices the operator that once the two minutes puncture time interval has been surpassed, the risk of complications has increased considerably, allowing them to be primed to look for and manage the possible associated mechanical complications. Additionally, it was demonstrated that clinicians can confidently perform a CVC insertion with ultrasound, either in emergency or planned situations, since there is no significant difference in the development of complications.
The rate of mechanical complications with ultrasound-guided central venous catheterization varies widely among literature. For example, a recent study published by Björkander et al. evaluated a total of 10,949 CVC insertions and found a mechanical complication rate of 1.1%16. On the other hand, the study published by Eisen et al., showed a mechanical complication rate of 14% during ultrasound-guided central venous catheterization19. Bleedings, pneumothorax, transient nerve injuries, and self-limiting arrhythmias are described as the most common mechanical complications16. The reason for a low rate of mechanical complications in our study (4%) is thought to be related to the level of confidence and expertise of the doctors performing the procedure while using ultrasound. Other complications such as pneumothorax, hematomas and incorrect positioning reported by our study are comparable to those of others20.
Risk factors associated with mechanical complications have been described by literature: the need for help19, more than two failed punctures19, expertise of the operator21, history of previous catheterizations22, preprocedural coagulopathy and route of catheterization16. In our study, the most significant variable associated with complications was the time puncture. The need for help was not identified as a variable, and the rate of failed punctures was minimal.
The results of this study might be affected by the small number of patients chosen. However, the analysis provided was able to detect statistically significant differences between groups by complications. More patients should be recruited in future studies to confirm these findings and to guide future protocols focusing on puncture time as a predictor for mechanical complications during emergency or planned ultrasound-guided IJV cannulation.
Training in vascular access with ultrasound guidance has an enormous impact in patient safety and in the reduction of complications related to CVC. Some relevant findings were determined during the present study regarding the ultrasound-guided technique for IJV placement of a catheter. First, it was confirmed that ultrasound-guided jugular vein access is a safe strategy to perform in the emergency room. Second, it was demonstrated that the type of situation, emergency versus planned, has no influence on the outcome and complications related to the IJV access of the patient. Third, it was shown that puncture time (time from the skin puncture to the vessel cannulation) was the most predictive variable for the development of complications. The only and most important factor to predict procedural success, in this study, was a time of less than two minutes from skin puncture to IJV cannulation. A greater sample size might be necessary to confirm these findings.
Harvard Dataverse: Comparative analysis of mechanical complications of emergent versus planned ultrasound-guided internal jugular venous cannulation (IJV): data from the Emergency Room of a third-level hospital in Quito-Ecuador - RAW DATA SET ENGLISH VERSION. https://doi.org/10.7910/DVN/YAZQVA18
Data are available under the terms of the Creative Commons Zero "No rights reserved" data waiver (CC0 1.0 Public domain dedication).
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Is the work clearly and accurately presented and does it cite the current literature?
Yes
Is the study design appropriate and is the work technically sound?
Yes
Are sufficient details of methods and analysis provided to allow replication by others?
Partly
If applicable, is the statistical analysis and its interpretation appropriate?
Yes
Are all the source data underlying the results available to ensure full reproducibility?
Partly
Are the conclusions drawn adequately supported by the results?
Yes
Competing Interests: No competing interests were disclosed.
Is the work clearly and accurately presented and does it cite the current literature?
Partly
Is the study design appropriate and is the work technically sound?
Partly
Are sufficient details of methods and analysis provided to allow replication by others?
Partly
If applicable, is the statistical analysis and its interpretation appropriate?
No
Are all the source data underlying the results available to ensure full reproducibility?
No
Are the conclusions drawn adequately supported by the results?
Partly
Competing Interests: No competing interests were disclosed.
Reviewer Expertise: Medicine, Critical Care, Internal Medicine, Nutritional Support.
Alongside their report, reviewers assign a status to the article:
Invited Reviewers | ||
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1 | 2 | |
Version 1 26 Jun 20 |
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