Development of Central Venous Stenosis Upon ICD Implantation in Dialysis Patients: A Non-Negligible Issue
Rohit J Timal1*, Ioannis Karalis1, Jose M Montero Cabezas1, Joris I Rotmans2, Liselotte C R Hensen1, Maurits S. Buiten1, Mihaly K de Bie1, Lieselot van Erven1, Hein Putter3, Martin J. Schalij1, Ton J Rabelink2, J Wouter Jukema1
1Department of Cardiology, Leiden University Medical Center, Leiden, The Netherlands.
2Department of Internal Medicine, Leiden University Medical Center, Leiden, The Netherlands.
3Department of Biomedical Data Sciences, Leiden University Medical Center, Leiden, The Netherlands.
*Corresponding Author Rohit J. Timal, MD, Department of Cardiology, Leiden University Medical Center, PO Box 9600, 2300 RC Leiden, The Netherlands
Received: 22 March 2022; Accepted: 30 March 2022; Published: 14 April 2022
Rohit J Timal, Ioannis Karalis, Jose M Montero Cabezas, Joris I Rotmans, Liselotte C R Hensen, Maurits S. Buiten, Mihaly K de Bie, Lieselot van Erven, Hein Putter, Martin J. Schalij, Ton J Rabelink, J Wouter Jukema. Development of Central Venous Stenosis Upon ICD Implantation in Dialysis Patients: A Non-Negligible Issue. Cardiology and cardiovascular Medicine 6 (2022): 171-188.View / Download Pdf Share at Facebook
Background: In hemodialysis patients, implantable cardioverter-defibrillator (ICD) implantation may result in central venous stenosis (CVS) with associated symptoms, such as pain, edema of the ipsilateral arm, facial edema, and loss of dialysis access. However, literature concerning CVS in dialysis patients with a cardiac implantable electronic device is scarce.
Methods: We conducted a prospective cohort study in which we investigated the incidence of CVS in end-stage renal disease patients on chronic dialysis who received an ICD as part of participation in the randomized ICD2 trial. A venography was performed before ICD implantation and at 1 year follow-up.
Results Between 2007 and 2017, 80 patients on dialysis received an ICD according to ICD2 trial protocol. Our population mainly consisted of males (76.3%), and had a median age of 67 years. Hemodialysis was the predominant dialysis modality (71.3%). The ICD was implanted in the right pectoral region in 58 patients (72.5%). A minority of the patients (27.5%) had a history of central venous catheters use, ipsilateral to ICD implantation site. Median follow-up was 16 months (IQR 13–35). Prospective assessment of central vein patency was possible in 56 patients (70.0%). Partial obstruction of central vein at follow-up was present in 19 out of 56 patients (33.9%) and complete occlusion in 4 patients (7.1%). With a complete clinical follow-up of all patients with a median duration of 3.5 years (IQR 2.7 - 6.3), 3 patients developed clinically significant symptoms of CVS.
Conclusions Development of CVS in patients on chronic dialysis who received an ICD is a cause of concern. Prevention of such complications deserves attention and further research.
Prospective study; Subclavian vein stenosis; Central venous stenosis; Venography; Phlebography; dialysis; End-stage renal disease; Cardiac device complication; Implantable cardioverter-defibrillator; ICD; Cardiac implantable electronic device; Lead-related central vein stenosis
Prospective study articles; Subclavian vein stenosis articles; Central venous stenosis articles; Venography articles; Phlebography articles; dialysis articles; End-stage renal disease articles; Cardiac device complication articles; Implantable cardioverter-defibrillator articles; ICD articles; Cardiac implantable electronic device articles; Lead-related central vein stenosis articles.
Implantation of cardiac implantable electronic devices (CIED), such as pacemakers and implantable cardioverter-defibrillators (ICD), can be life-saving as they can restore brady – and tachyarrhythmias . End-stage renal disease patients on dialysis are at high risk for these arrhythmias and the use of CIEDs is not uncommon [2-5]. Although leadless devices are increasingly used, transvenous devices are still the most common method of implantation . However, transvenous cardiac device placement can lead to severe vascular and/or infectious complications, especially in vulnerable populations such as dialysis patients [7,8]. A well-functioning vascular access is crucial in managing patients on hemodialysis. Central venous stenosis (CVS), defined as stenosis in the brachiocephalic, subclavian or superior cava vein is associated with symptoms such as edema and pain in the ipsilateral extremity, and may result, specifically in hemodialysis patients, in a compromised usability of their arteriovenous access [9-12]. Management of central venous occlusive disease (CVOD) consists of (often repeated) percutaneous transluminal angioplasty; in refractory cases, endovascular banding/ligation of the functioning arteriovenous fistula (AVF) or removal of the ICD leads may be necessary [10,13]. Very little is known with regard to development of lead-induced CVS after CIED implantation in patients on dialysis. To the best of our knowledge, our study is the first to prospectively investigate the development of CVS upon a device implantation in dialysis patients. In this report, we aim to clarify the incidence and consequences of lead-induced CVS in this vulnerable patient group.
2.1 Study design and population
We performed a preplanned subanalysis of The Implantable Cardioverter-Defibrillator in Dialysis Patients (ICD2) trial14. In the randomized, controlled ICD2 trial we demonstrated that prophylactic ICD therapy in patients on chronic dialysis with LVEF ≥35% was not associated with a reduced rate of sudden cardiac death or all-cause death. Patients were referred from 17 dialysis centers to the Leiden University Medical Center, in Leiden, The Netherlands. Patients on dialysis for more than 90 days, with an age of ≥55 years and <81 years, and not meeting the class I indication for ICD implantation were eligible for participation. Exclusion criteria were: heart failure (New York Heart Association functional class IV); medical condition determining a life expectancy <1 year; expected kidney transplantation within 1 year; CVC in situ; patients with acute myocardial infarction in the past 40 days; known human immunodeficiency virus infection and inability to provide informed consent. Patients were randomized in a 1:1 fashion to receive an ICD (ICD group) or standard care (control group). Patients assigned to the ICD arm received a dual-chamber transvenous device (Biotronik, Berlin, Germany), which was implanted subcutaneously in the pectoral region, under local anesthesia. Baseline characteristics, such as patient demographics, comorbidity, and medication use were collected. Dialysis characteristics were extracted from the hospital’s electronic medical records. The protocol was approved by the hospital’s ethics committee in April 2007. The trial is registered at the Netherlands Trial Register (http://www.controlled-trials.com/ISRCTN20479861). All patients provided written informed consent. In October 2012 we added an amendment to the trial protocol that facilitated venography pre-randomization as standard screening procedure, as well as venography at 1-year follow-up in order to prospectively assess CVS in patients undergoing chronic dialysis. Patient enrollment ensued until January 2018. Extended clinical follow-up ensued until the ICD2 trial was stopped in February 2018 per advice of the data and safety monitoring board because of futility.
Angiographic evaluation was performed by injecting 10ml of iodine-based contrast using a peripheral venous canula, ipsilateral to the ICD-implantation site. In general, systems classifying CVS are based on anatomic location of lesion, degree of occlusion and degree of collateral flow (Supplemental eTable 1). We chose to define phlebographic images according to 2 systems. First, images were adjudicated according to the following 3 categories: completely obstructed, partially obstructed (>70%) or patent. Secondly, the degree of collateral flow was classified as ‘mild’ (residual collateral flow and/or 1 collateral vein); ‘moderate’ (moderate collateral flow with incomplete opacification of the vein proximal to the occlusion and/or 2 collateral veins can be seen) and ‘important’ (complete and rapid collateral flow and/or ≥3 collateral veins). All angiographic images were independently evaluated by two experienced interventional cardiologists (I.K. and J.M.M.C). In case of verdict discrepancy with regard to degree of stenosis or collateral flow, images were assessed by a third experienced interventional cardiologist (J.W.J).
2.3 Statistical analysis
Categorical data are presented as absolute numbers (%) and continuous data as mean ± SD, or median and interquartile range (IQR) in case of a non-normal distribution. Using relative risk (RR) statistical differences were tested for occurrence of central vein stenosis and history of ipsilateral CVC use. Statistical significance was tested using the Chi-square test. A p-value below 0.05 was considered statistically significant for this analysis. All statistical analyses were performed using SPSS version 25.0 (IBM Corp, Armonk, New York, USA).
In total, 80 patients undergoing chronic dialysis received an ICD according to the ICD2 trial protocol. Procedural characteristics such as ICD type, right atrial and ventricular leads have been described previously . All patients received dual-chamber ICDs, with the exception of 2 patients who received a device with a single right ventricular lead because of permanent atrial fibrillation. Baseline characteristics are depicted in table 1. Our population mainly consisted of males (76.3%), with a median age of 67 years, IQR 63–74 years. Hemodialysis was the predominant dialysis modality (71.3%). History of central venous catheters (CVC) ipsilateral to ICD implantation site was present in 22 out of 80 patients (27.5%). ICD was implanted in the right pectoral region in 58 patients (72.5%). Median follow-up was 16 months (IQR 13–35). Angiography at baseline was performed in 62 patients (77.5%). In the remaining 18 patients we considered the ipsilateral central venous circulation patent, as all of these patients underwent successful transvenous ICD implantation. In 7 cases (12.5%) venography images at baseline were not available. In these cases, information regarding the patency status of the central vein was extracted from the procedure report. For the patients where angiography images were available the percentage of agreement among the reviewing cardiologists was high, in more than 95% of the cases. The inter-reviewer reliability is depicted in Supplemental eTable 2.
Prospective assessment of central vein patency was not possible in 24 patients (30.0%) (Figure 1). Five out of these 24 patients (6.3%) were deceased at 1 year follow-up. The 5-year survival probability from ICD implantation is depicted in Supplemental eFigure 1. The mortality rates at 2, 3, 4 and 5 years were 11 (13.8%), 21 (26.3%), 32 (40.0%), and 33 (41.3%) out of 80, respectively. In 56 out of 80 patients (70.0%) angiography was performed at follow-up and these cases were available for prospective analysis of central vein patency (Table 2 and Table 3). Angiographic progression to CVS occurred in 22 of 56 patients (39.3%), of which 9 patients with a history of CVC use ipsilateral to ICD implantation site (40.9%) versus 13 patients without a history of ipsilateral CVC use (59.1%), relative risk 1.9; 95% confidence interval 1.0 – 3.5; p=0.055. The anatomic location of CVS ipsilateral to ICD implantation site was the subclavian vein in 20 out of 22 patients (90.9%), of which 4 cases with complete stenosis. The brachiocephalic vein was afflicted in 2 out of 22 patients (100% inter-rater reliability). In total, 11 patients with normal baseline venography developed signs of collateral flow. An example of CVS can be seen in figure 2 and figure 3. During clinical follow-up of ICD-recipients with a median duration of 3.5 years (IQR 2.7 - 6.3) from ICD implantation date, 3 patients developed clinically significant symptoms of CVS. These cases are described below.
Table 1: Baseline Characteristics
N indicates number; ICD, implantable cardioverter-defibrillator; Kt/V, K dialyser clearance of urea; t, dialysis time; V, volume of distribution of urea; LVEF, left ventricular ejection fraction.
Figure 1: Study flow chart
N indicates number.
Table 2: Central vein patency of patients with complete prospective assessment at baseline and at follow-up
* Considered patent as ICD was successfully implanted. N indicates number.
Table 3: Collateral flow of patients with complete prospective assessment at baseline and at follow-up
N indicates number.
Figure 2a: Venography: Patient (ICD 195) undergoing venography at follow-up.
* Implantable cardioverter-defibrillator; black arrows: right atrial and right ventricular leads;
+ indicates extensive collateral veins; white arrow: central vein stenosis.
Figure 2b: Venography: Patient (ICD 195) undergoing venography at follow-up.
* Implantable cardioverter-defibrillator; black arrow: right atrial and right ventricular leads;
+ indicates extensive collateral veins; white arrow: central vein stenosis.
Figure 3: Venography: Patient (ICD 47) undergoing venography at follow-up.
* Implantable cardioverter-defibrillator; black arrow: right atrial and right ventricular leads;
+ indicates extensive collateral veins; white arrow: central vein stenosis.
ICD 57: ICD was implanted via the right subclavian vein in September 2009. Patient was admitted in November 2009 for right atrial and right ventricular lead repositioning after dislocation in the context of Twiddler syndrome. Four years later, patency of the AVF in the left arm was lost following a traumatic event, after which new AVF was created, ipsilateral to ICD implantation site. Another 4 years later, the patient reported symptoms of pain and edema in the right arm, which appeared to be secondary to venous occlusion. In August and November 2017 percutaneous transluminal angioplasties were performed. Unfortunately, the complaints of pain and edema persisted, whereupon the AVF was ligated.
ICD 167: ICD was implanted right-sided in September 2014. At that time, the flow of the ipsilateral AVF was 550mL/min. Patients developed edema of the right arm in August 2015. Visualisation of the subclavian vein in August 2015 revealed a significant stenosis near the transition of the brachiocephalic vein to the superior vena cava which was left untreated as cannulation of the AVF was still possible and symptoms were mild. AVF flow and dialysis efficacy remained stable during follow-up.
ICD 195: The ICD was implanted in April 2016 in a patient treated with peritoneal dialysis. Implantation location was the right pectoral region. For clinical reasons, the dialysis modality was changed from peritoneal dialysis to hemodialysis 3 months after ICD implantation. In July 2016, an AVF was created in the right arm. Within the next month, the patient developed edema of the right arm. This was bothersome and it impeded cannulation of the fistula for dialysis. Therefore, hemodialysis was temporarily performed using a CVC. A venogram showed a mild stenosis in the transition from the subclavian vein to the vena cava superior with extensive collateral formation. The AVF had a high flow of >3 L/min, which was responsible for the edema of the arm as this venous stenosis precluded sufficient drainage of the AVF flow to the heart. During a 3-day admission the ICD and leads were removed, and an attempt was made to dilate the venous trajectory on the right-pectoral side, using rotablation and cutting balloon. The procedure was complicated by bleeding in the ICD pocket. Afterwards, a banding procedure of the fistula was performed with the aim to reduce AVF flow, whereupon the edema diminished.
We conducted a cohort study in which we prospectively evaluated the incidence of transvenous-lead-associated CVS by performing angiographic evaluation in 80 patients on chronic dialysis that received a transvenous ICD for primary prevention included in the ICD2 trial . Prospective angiographic assessment of central vein patency, with a median of 16 months from baseline angiography, revealed partial obstruction of the central vein in a third of patients, and a total occlusion of the central vein in 7.1% of patients. During clinical follow-up, with a median duration of 3.5 years from ICD implantation date, 3 patients developed CVS-related symptoms such as pain and edema of the ipsilateral arm. It is noteworthy that in 2 out of these 3 patients with complaints, the symptoms arose after the surgical creation of an AVF while an ipsilateral ICD was already in situ. This underlines the importance of the guideline recommendation that vascular access should be created in the opposite arm . Literature concerning CVOD in dialysis patients with implanted cardiac devices is scarce. This topic has previously been addressed in case reports and in (small) retrospective studies [3,11,16-22]. To the best of our knowledge, our study is the first to prospectively describe the development of CIED lead-induced CVS in patients on chronic dialysis. Importantly, in the current report central vein patency was assessed at 2 timepoints: previous to ICD insertion and at median follow-up of 16 months. Patients were referred from multiple dialysis centers in the Netherlands (n = 15), thus making the results more generalizable. Noteworthy is that, in our trial, ICD placement was performed in patients on dialysis with pre-existing and functioning vascular access of the upper extremity. Furthermore, ICD was implanted contralateral to the dialysis shunt, as was recommended in the literature [3,6,23]. Jeong and colleagues retrospectively investigated 42 patients on hemodialysis, of which 22 patients with vascular access of the upper extremity ipsilateral to transvenous CIED and 20 patients with a dialysis shunt contralateral to CIED19. After an 11 months follow-up period researchers found a CVS incidence of 27% (6 out of 22) in the ipsilateral vascular access group and 5% (1 out of 20) in the contralateral vascular access group. They concluded that transvenous device implantation, ipsilateral to vascular access should be avoided if feasible. In another retrospective study by Saad and coworkers patients, the prevalence of CIEDs was 10.5% among 1235 chronic hemodialysis patients3. Number of central venous interventions in patients with ipsilateral vascular access to CIED placement was 0.59 per access year versus 0.28 per access year in patients with contralateral vascular access, P <0.001. Adwaney et al. retrospectively assessed 2811 patient on hemodialysis, of which 120 patients (4.3%) were radiologically identified to have CVS9. Only 7 patients in this population were reported to have a pacemaker. Because of the design of this study, the CVS incidence is likely to be a considerable underestimation. CVOD in patients on dialysis without cardiac devices has been described extensively and the reported incidence varies from 4 to 41% [9,24-27]. Prevention of CVOD by minimizing exposure to well-established risk factors, such as the (duration of) use CVCs for vascular access, is of the utmost importance [11,28]. CVS after CIED implantation is a well-recognized late complication in patients without end-stage renal disease. The reported incidence varies from 14 to 64% [29-31]. Haghjoo et al. performed contrast venography in 100 non-dialysis patients who were candidates for generator change, lead revision, or device upgrade. Authors found an incidence of venous obstruction of 26% (9% total obstruction, 17% partial obstruction) after 8 ± 4.5 years since lead implantation . Da Costa et al. conducted digital subtraction venography after 6 months following pacemaker implantation among 229 non-dialysis patients . In their study, abnormal venographies were observed in 64% of the patients. In the 2 beforementioned reports baseline venography was not performed. Korkeila et al. prospectively quantified changes by contrast venography at baseline and at 6 months after CIED-implantation in 150 non-dialysis patients . The authors found an incidence of 14% for new obstructive venous lesions. The wide ranges of reported CVOD incidence may be explained by the use of various classification systems for defining CVS in studies evaluating CVOD (Supplemental eTable 1), making results difficult to compare. Some aspects of our study require further discussion. One limitation is the lack of angiographic follow-up in 30.0% of patients. It is noteworthy that only 1 of these patients developed clinical signs of CVS during extended clinical follow-up (see case 57). In the remaining 56 patients with complete angiographic follow-up, which is the largest population published to date, 41.1% showed angiographic signs of CVS. Secondly, in our study, the venographies were assessed by two independent physicians by eyeballing; no quantitative measurements were performed. Nonetheless, the percent agreement of the interrater reliability regarding CVS was >96% (Supplemental eTable 2). The development of leadless cardiac devices, such as subcutaneous ICDs and leadless pacemakers, offers opportunities to avoid lead-associated CVS in the dialysis population [32-36]. Unfortunately, with regard to complications, still little is known from these techniques in this vulnerable patients. In conclusion, prospective angiographic evaluation of central vein patency in 80 patients on chronic dialysis that received a transvenous ICD for primary prevention revealed significant progression of central vein obstruction in >40% of the patients, after a median follow-up of 16 months. Development of lead-associated CVS in ICD-recipients on chronic dialysis is a clear concern. Prevention of complications such as loss of dialysis access is of the utmost importance. Health care providers should strive for future access protection by minimizing CVC use through early referral to surgical access creation. Also, if feasible, efforts should be made to minimize transvenous lead placement. CVS in dialysis patients with CIEDs is an underexposed topic. Further research is warranted for the use of leadless cardiac devices, such as subcutaneous ICDs or leadless pacemakers, in dialysis patients.
J.W.J., M.J.S., T.J.R. and H.P. contributed to the study design. R.J.T., L.C.R.H., M.S.B., M.K.dB., J.I.R., I.K., J.M.M.C, L.vE. and J.W.J. contributed to the collection of data. R.J.T. and H.P. performed the data analyses. All authors contributed to interpretation of the data. R.J.T. wrote the first draft of the manuscript. All authors provided critical revisions to the manuscript before seeing and approving the final version.
Sources of Funding
The ICD2 trial was supported by an unrestricted educational research grant from Biotronik GmbH & Co. The study sponsors had no role in the study design, or in the collection, analysis, and interpretation of data, the writing of the report, or in the decision to submit the paper for publication.
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