A comparison of the clinical effects and safety between the distal radial artery and the classic radial artery approaches in percutaneous coronary intervention
Introduction
In recent years, with the development of percutaneous coronary intervention, transradial coronary intervention (TRI) has surpassed transfemoral coronary intervention to become the preferred approach for percutaneous coronary intervention (1). Existing studies demonstrate that vascular complication and bleeding incidence has a direct relationship with the postoperative short-term and long-term survival rates of patients (2,3). Compared with transfemoral coronary intervention, TRI has advantages such as low incidence of puncture vascular complications, early ambulation, less bleeding, and is easily accepted by patients. Based on selected randomized studies, TRI is considered the default technique for coronary intervention (4).
Radial artery occlusion is a common vascular complication following TRI, with an incidence of approximately 1–12% (2-5). Due to the dual arterial supply to the hand, radial artery occlusion is generally asymptomatic and overlooked, though at times it may be associated with paresthesia, pain at the site of occlusion, loss of hand function, and distal ischemia (6). Determining how to reduce vascular complications and postoperative radial artery occlusion remains an issue that requires additional research.
Compared with a classic wrist puncture for radial artery catheterization, distal radial artery puncture has the advantage of reducing the incidence of radial artery occlusion in anatomic and physiological principles (7). However, outcome comparisons between these two methods remain lacking.
In this context, the current researchers attempted to puncture the distal radial artery for coronary artery intervention compared with the classic radial artery approach to explore the clinical effects and safety of the distal radial artery approach, and to assess whether it may be a better and novel option for coronary artery intervention.
We present the following article in accordance with the STROBE reporting checklist (available at: http://dx.doi.org/10.21037/apm-19-479).
Methods
General information
A total of 620 patients who underwent percutaneous coronary intervention in our hospital for the first time from December 2017 to December 2018 were selected as study subjects. These patients were divided into two groups based on the puncture site: 312 patients who underwent percutaneous coronary intervention via the distal radial artery were enrolled in the distal radial artery puncture group; 308 patients who underwent percutaneous coronary intervention via the classic radial artery were enrolled in the radial artery puncture group. The trial was conducted in accordance with the Declaration of Helsinki (as revised in 2013). The study was approved by committee board of Tianjin Third Central Hospital and informed consent was taken from all the patients.
Distal radial artery puncture group
Prior to surgery, the Allen test was conducted on the bilateral radial artery of the patients in this group, and the bilateral blood supply recovery status was compared. The side with a faster recovery rate was selected as the operative side, and all the patients were provided with a load capacity of 300 mg of aspirin and 300 mg of clopidogrel (180 mg of ticagrelor) prior to undergoing surgery.
Following the completion of routine disinfection, the tabatiere anatomique area was selected as the puncture site (Figure 1A), and 1% lidocaine was used for local anesthesia. The Seldinger method was used to make the puncture on the distal radial artery. Following successful puncture, a 6F artery sheath was placed (Figure 1B) and 4,000 U of heparin was injected into the sheath. Next, coronary angiography was conducted. Following the completion of the intervention, the artery sheath was removed; a piece of gauze folded three times was used to cover the puncture site. Concurrently, three elastic bandages were used in a crosswise manner as a pressure bandage (Figure 1C). One elastic bandage was removed every two hours, and the compression was completely relieved after six hours (Figure 1D).
Radial artery puncture group
Prior to surgery, the Allen test was conducted on the bilateral radial artery of the patients in this group and the bilateral blood supply recovery status was compared. The side with a faster recovery rate was selected as the operative side. All patients were provided with a load capacity of 300 mg of aspirin and 300 mg of clopidogrel (180 mg of ticagrelor) prior to surgery. Following the completion of routine disinfection, the area at approximately 2 cm adjacent to the proximal end of the lateral wrinkle of the palm (the area with the highest radial artery fluctuation intensity) was used as the puncture site (Figure 2A) and 1% lidocaine was used as a local anesthetic. The Seldinger method was used to make the puncture on the radial artery. Following successful puncture, a 6F radial artery sheath was placed (Figure 2B), and 4,000 U of heparin was injected into the sheath. Then, the coronary angiography was conducted, and the contrast agent dosage used during the procedure was recorded. After completion of the intervention, the artery sheath was removed, and an air pressure tourniquet (TERUMO; Model: XX*RF06; Batch no.: 180320) was immediately used to conduct hemostasis by compression on the puncture site (Figure 2C). Air was released once every 2 hours to alleviate the pressure; compression was completely relieved after six hours (Figure 2D).
Clinical observation index and result judgment standard
The average puncture time, puncture success rate, surgery time, and implanted stent for patients in the two groups were compared. The incidence of radial artery spasm, hematoma, and artery aneurysm in patients, and the incidence of radial artery occlusion prior to discharge were also recorded. Result judgment standards are given as follows: (I) successful radial artery puncture—following the radial artery puncture, the artery sheath was inserted; (II) radial artery puncture time—the time from initial local infiltration anesthesia to sheath insertion; (III) radial artery spasm—it was impossible to conduct a radial artery puncture; alternatively, although the puncture was successful, it was impossible to complete the surgery; (IV) radial artery occlusion—color ultrasound verified that the radial artery had no forward blood flow.
Statistical analysis
The SPSS statistical software package (v.22.0) was used to conduct statistical analysis, and an χ2-test and t-test were used for the enumeration data and measurement data, respectively. Here, P<0.05 was considered to represent a statistically significant result.
Results
Comparison of the baseline data of patients in the two groups
For the distal radial artery puncture group, 160 patients were male, and 152 patients were female, and the mean age of these patients was 50.1±7.2 years old. For the radial artery puncture group, 157 patients were male, and 151 patients were female, and the mean age of these patients was 51.2±7.3 years old. There was no significant difference in the case number, gender, age, hypertension, diabetes, hyperlipemia, and blood vessel diameter of patients in the two groups (P>0.05; see Table 1). Hence, the baseline data of the two groups were comparable.
Full table
Comparison of the operative effects among patients in the two groups
There was no significant difference in the puncture success rate, average puncture time, surgery time, implanted stent, and vessel diameter of patients in these two groups (P>0.05; see Table 2).
Full table
Comparison of complications among the patients in the two groups
The radial artery occlusion rate of patients in the distal radial artery group was significantly lower than in the classic radial artery puncture group, and the difference was statistically significant (P<0.05).
The comparisons for intraoperative radial artery spasm, postoperative hematoma, arterial aneurysm, and arteriovenous fistula revealed no statistically significant difference (P>0.05; see Table 3).
Full table
Discussion
In the past two years, doctors performing coronary artery intervention have attempted to adopt the distal radial artery approach (8-11). Anatomic and physiological principles suggested the distal radial artery as an innovative approach for assessing coronary and endovascular procedures in existing studies (7). The distal radial artery, located at the tabatiere anatomique area, is relatively thick and large with fixation, with an inner diameter of approximately 2 mm. It is located at the proximal end of the thumb artery. Even when radial artery occlusion complications occur, it will not affect the blood supply to the thumb, thereby making it possible to use the distal radial artery in intervention approaches.
The reasons for radial artery occlusion primarily include extended compression time, inflammatory reaction, and thrombosis. In this study, the radial artery occlusion rate in the distal radial artery group and classic radial artery group was 1.9% and 5.19%, respectively. As expected, the radial artery occlusion rate in the distal radial artery group was much lower (P<0.05). The possible reasons for the lower occlusion rate in this group are as follows: (I) the location of the distal radial artery was relatively superficial, and the compression tension using gauze was small; (II) the distal radial artery is part of the bilateral blood supply, making it unsuitable for occlusion (7). Except for radial artery occlusion, the incidence of other complications such as radial artery spasm, hematoma, arterial aneurysm, and arteriovenous fistula was not significantly different between the two groups (P>0.05). In addition, the puncture success rate, puncture time, and operation time between the two groups were not significantly different (P>0.05). Thus, compared with classic radial artery puncture intervention, the distal radial artery intervention approach appears more convenient for hemostasis with a lower radial artery occlusion rate.
Currently, many studies pertaining to distal radial artery puncture in the coronary artery intervention process have verified the safety of this approach (5). The most recent guidance from Europe and Brazil regards the distal radial artery approach as the preferred path for coronary arterial intervention (12,13). Boncoraglio et al. (14) reported that distal radial artery puncture showed a good degree of safety in the emergency coronary artery intervention process for elderly patients. Our study also suggested that distal radial artery intervention can be used as an alternative path to the classic radial artery approach. For patients where performing a puncture on the routine radial artery site was unsuitable, an attempt to conduct a distal radial artery puncture could be made.
The present study had several limitations. Since the case number of enrolled patients in the present study was relatively low, and all patients were derived from a single health center, a bias may have been present in the patient selection. If this was the case, this study cannot be considered a randomized controlled trial (RCT). Thus, to further assess the effects and safety of distal radial artery puncture in coronary artery intervention, more theoretical evidence is required for its clinical application, alongside an RCT with a sufficient number of patients.
In conclusion, in this study, the distal radial artery approach had a lower rate of brachial artery occlusion, indicating that it can be used as an alternative to the classic radial artery approach.
Acknowledgments
We are particularly grateful to all the people who have given us help on our article.
Funding: Tianjin Science and Technology Project (No. 16ZXMJSY00200).
Footnote
Reporting Checklist: The authors have completed the STROBE reporting checklist. Available at http://dx.doi.org/10.21037/apm-19-479
Data Sharing Statement: Available at http://dx.doi.org/10.21037/apm-19-479
Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/apm-19-479). The authors have no conflicts of interest to declare.
Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved. The trial was conducted in accordance with the Declaration of Helsinki (as revised in 2013). The study was approved by committee board of Tianjin Third Central Hospital and informed consent was taken from all the patients.
Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.
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