Introduction
Transvenous temporary cardiac pacing (TV-TP) is a potentially life-saving therapy in patients with haemodynamically compromising arrhythmias [
1]. TV-TP therapy is primarily indicated for the treatment of symptomatic bradycardia and various types of (reversible) symptomatic heart block [
2]. In addition, TV-TP therapy may be used as a bridge to permanent cardiac pacing when permanent pacing is not immediately indicated or available, or when a permanent pacemaker cannot be implanted. Other possible indications include myocardial infarction, and injury to the conduction system following (non-)cardiac surgery (e.g. transcatheter aortic valve implantation, coronary artery bypass grafting, valve surgery) [
2‐
4].
Since the first report on its successful use by Tancredi et al. in 1967, the main concept of TV-TP therapy has not changed considerably, even though patients are at risk for procedure-related complications resulting in patient morbidity and mortality [
5]. Observed complications are related to the transvenous lead (e.g. lead dislodgement, lead malfunction, cardiac perforation) or related to the venous access and the necessity for immobilisation (e.g. bleeding, infection, thrombosis and delirium, especially in the elderly population) [
6‐
9]. These complications result in re-intervention and prolonged hospitalisation. Moreover, it is not uncommon for the pacing indication to persist after implantation of a temporary transvenous pacemaker, requiring a second procedure to implant a permanent pacemaker (PPM), often performed more than a week after implantation of the temporary pacemaker [
10]. Previous studies have investigated complication rates, yet the reported results are inconsistent and conflicting. Reported complication rates of TV-TP therapy are high, ranging from 10 to 60%, with an average of 26.5% [
8‐
11]. Consequently, current ESC guidelines recommend that TV-TP therapy should be avoided or applied as briefly as possible [
12].
Available evidence on indications, approach and complications of TV-TP therapy is limited. In addition, the need for PPM therapy following TV-TP has not yet been elucidated, but is of high clinical relevance. A substantial number of studies date back to before 1980, and it is unclear how these results translate to current clinical practice. To understand the current risks and benefits of TV-TP and the potential need for alternatives, a comprehensive review of the available evidence on TV-TP is essential. Therefore, a scoping review was performed in order to give an up-to-date overview on indications, access route and complications of TV-TP as well as the need for subsequent permanent pacemaker implantation.
Methods
A scoping review of studies reporting TV-TP indications, approaches, complications and need for PPM was conducted. Due to the scoping nature, our protocol was not eligible for assessment by PRISMA guidelines, nor for inclusion in PROSPERO. A prospectively designed protocol which defined in- and exclusion criteria, search strategy and definitions of complications and indications was developed.
Search
A systematic literature search for relevant articles published until February 2019 was carried out in the Ovid MEDLINE database. The search strategy, including terms and limits, was determined in collaboration with a medical information specialist (see Electronic Supplementary Material, Supplement 1).
Studies were eligible if they included adults requiring TV-TP therapy for bradycardia, inadequate escape rhythm or asystole. Case series with fewer than ten patients were excluded from the analysis, as were studies concerning transoesophageal, transthoracic, transcutaneous or atrial pacing. Studies without mention of complication rates were excluded. Studies were restricted to those published in English or Dutch and those conducted in humans. Studies with specific inclusion criteria regarding either patient category or complications were reviewed separately from consecutive patient series in order not to confound mean complication rates.
Two investigators (F.V.Y. Tjong, U.W. de Ruijter) independently appraised all studies and consequently extracted all relevant data from the selected studies. Differing appraisals were resolved by means of consensus. The following data were extracted: patient characteristics, indication for and duration of TV-TP therapy, definition of complications, complication rates, mortality, re-interventions, site of access and subsequent PPM implantation. A pre-specified data extraction sheet was included in the protocol.
Indications
Ten groups of indications for TV-TP therapy were defined: cardiac arrest, atrioventricular block, sinus node disease, acute myocardial infarction, permanent pacemaker failure, bradycardia, prophylactic or periprocedural use, overdrive suppression, drug toxicity and other or unknown (Tab.
1). Groups were mutually exclusive.
Table 1
Indications for transvenous temporary pacing therapy (4546 patients)
1. Asystole or cardiac arrest | 1.1% |
2. Atrioventricular block (AVB all degrees, AF with slow rate) | 62.7% |
3. Sinus node disease | 6.7% |
4. Acute myocardial infarction (underlying rhythm not specified) | 11.4% |
5. Permanent pacemaker failure | 4.4% |
6. Bradycardia (sinus bradycardia, sinus pause, sinus arrest, AV nodal escape rhythm) | 4.9% |
7. Prophylactic or periprocedural (prophylactic, diagnostic, required for procedure) | 2.7% |
8. Overdrive suppression (VPC overdrive, VT overdrive) | 2.3% |
9. Drug toxicity (medication washout, drug overdose, digitalis intoxication) | 2.4% |
10. Other or unknown | 1.5% |
A major indication for TV-TP therapy is in the setting of acute myocardial infarction, especially in previous decades [
13‐
15]. We strived to categorise this indication according to underlying arrhythmia if data were provided. In case this was not reported, the indication was categorised by default as acute myocardial infarction.
Complications
Complications were categorised in eight main groups: complicated access, cardiac perforation, device complications, infection, arrhythmia, thrombotic event, procedure-related death and other or unknown (Tab.
2). Pericardial effusion without signs of systemic infection was considered a cardiac perforation. Pericardial effusion with signs of infection was considered to be pericarditis. Malpacing and malsensing were considered to be TV-TP failure.
Table 2
Complications reported
1. Complicated access
| 0.4% | 1.0% | 2.1% | 2.8% | 4.2% | 2.0% |
Minor bleed access site | 0.2% | 0.0% | 0.0% | 1.7% | 1.0% | 0.5% |
Arterial puncture | 0.0% | 0.7% | 1.0% | 0.5% | 0.3% | 0.5% |
Brachial plexus injury | 0.0% | 0.0% | 0.3% | 0.0% | 0.0% | 0.0% |
Pneumothorax | 0.0% | 0.1% | 0.7% | 0.2% | 0.1% | 0.1% |
Excessive bleed access site | 0.2% | 0.2% | 0.0% | 0.4% | 2.7% | 0.7% |
2. Cardiac perforation
| 2.0% | 1.8% | 0.5% | 2.1% | 0.7% | 1.6% |
3. Device complications
| 21.0% | 27.1% | 25.1% | 14.7% | 12.9% | 21.1% |
TP lead dislodgement | 11.5% | 2.6% | 14.1% | 3.1% | 3.4% | 4.6% |
TP failure | 8.6% | 13.3% | 0.7% | 6.2% | 7.7% | 9.5% |
Multiple attempts | 0.3% | 0.0% | 10.3% | 5.4% | 0.9% | 1.9% |
Re-intervention | 0.6% | 11.2% | 0.0% | 0.0% | 0.9% | 5.1% |
4. Infections
| 2.8% | 5.7% | 5.2% | 5.0% | 3.6% | 4.8% |
Fever (>38 °C) | 0.4% | 0.3% | 0.0% | 1.2% | 0.0% | 0.4% |
Phlebitis | 1.4% | 1.4% | 0.0% | 0.0% | 0.2% | 0.8% |
Local wound infection | 0.8% | 1.0% | 1.0% | 1.5% | 2.4% | 1.3% |
Sepsis or systemic infection | 0.2% | 0.2% | 4.2% | 2.1% | 0.9% | 1.0% |
Pericarditis | 0.0% | 2.8% | 0.0% | 0.2% | 0.1% | 1.3% |
5. Arrhythmia
| 4.0% | 10.2% | 5.5% | 1.9% | 0.5% | 5.7% |
VT during insertion | 3.0% | 3.1% | 0.0% | 0.0% | 0.0% | 1.7% |
Arrhythmias | 1.0% | 7.2% | 5.5% | 1.9% | 0.5% | 4.0% |
6. Thrombotic event
| 0.4% | 0.2% | 0.0% | 0.7% | 0.5% | 0.3% |
Deep venous thrombosis | 0.0% | 0.0% | 0.0% | 0.7% | 0.3% | 0.2% |
Pulmonary embolism | 0.4% | 0.2% | 0.0% | 0.0% | 0.1% | 0.1% |
7. Death due to TP
| 0.4% | 0.0% | 0.2% | 0.7% | 0.2% | 0.2% |
8. Other complications
| 0.2% | 1.6% | 0.9% | 1.0% | 0.3% | 1.0% |
Total | 31.2% | 47.6% | 39.5% | 28.1% | 22.9% | 36.7% |
According to current guidelines, complications are considered serious when (re-)intervention is required [
12]. (Re-)interventions following TV-TP were not systematically documented in all published studies. We considered the following complications to warrant (re-)intervention: sepsis, cardiac perforation, excessive bleeding at access site and pulmonary embolism. We therefore defined these complications—in addition to procedure-related death—as serious complications. Procedure-related ventricular fibrillation and asystole were not included as serious complications as these usually arise during device insertion and can be corrected at this stage.
In order to assess a trend in complication rates since the introduction of TV-TP therapy we reviewed mean complication rates over the years in 10-year intervals, based on year of publication.
Statistical analysis
Continuous data were described as weighted means ± standard deviations (SD) and categorical data as weighted percentages. Statistical analysis was performed using SPSS (Version 23, 2015) and Microsoft Excel 2010. One-way analysis of variance (ANOVA) was used to assess significant changes in complication rates between the 10-year intervals.
Discussion
This systematic scoping review demonstrates that TV-TP has a wide variety of indications, but is most commonly used for patients with symptomatic atrioventricular block. The femoral vein was the most frequently used access site for TV-TP. Complication rates following TV-TP therapy remain high despite the experience gained over time, yet display a wide range amongst studies potentially related to specialist experience and quality of imaging systems used during implantation. Almost two-thirds of the patients who initially require TV-TP therapy develop a permanent need for cardiac pacing.
The published studies show a heterogeneous patient population with varying indications for TV-TP therapy. The vast majority required TV-TP because of symptomatic atrioventricular block. Severe atrioventricular block may result in haemodynamic instability and syncope and may represent a life-threatening emergency [
47]. TV-TP may re-establish normal haemodynamics that are acutely compromised in this setting [
12]. There was a relatively large number of patients requiring TV-TP in the setting of acute myocardial infarction. However, the need for cardiac pacing after myocardial infarction has declined over the past decades due to improved therapies, such as revascularisation strategies with thrombolysis and angioplasty [
48]. Of note is that in 11.6% of cases the indication for TV-TP was acute myocardial infarction without further specification of underlying rhythm. It is possible that some of these cases can also be attributed to atrioventricular block, reiterating that to be the most important indication.
The most frequently used access route for TV-TP was the femoral venous approach. This might be explained by the ease of advancing the lead to the heart and the reduced chance of complications such as pneumothorax. The best approach to the major venous access site is subject to debate. The different venous routes are associated with specific problems including lead stability, infection, haemorrhage, pneumothorax and patient discomfort [
12]. The femoral insertion site has been associated with higher infection rates than the subclavian site, yet with equal rates compared to the jugular access site with intravascular catheters [
49]. The use of chlorhexidine for skin disinfection has been shown to be superior to either povidine-iodine or 70% alcohol in reducing bacteraemia [
50]. Although less prone for infection, the subclavian insertion site has been shown to be more likely to cause thrombosis compared to the jugular site, especially considering the potential need for a future PPM, also utilising the subclavian vein as an access route. Also, the risk of pneumothorax is higher with this access site compared to the other sites [
50]. TV-TP is commonly performed in an emergency setting; hence the choice of approach is often based on individual experience [
6,
51]. Femoral placement of the pacemaker could confer benefit in the presence of thrombocytopenia and/or coagulopathy, as pressure can be easily applied and haemostasis achieved in the case of bleeding. Conversely, femoral placement may be accompanied by the least stable wire position and may restrict the patient’s mobility by requiring a horizontal position [
12]. Guidelines from the British Cardiac Society recommended the right internal jugular route as most suitable for the inexperienced operator, since this is the most direct route to the right ventricle; this route has had high success rates and few complications [
7,
52]. In patients receiving or likely to receive thrombolytic treatment, the brachial and external jugular veins could be considered in addition to the femoral vein as the routes of choice because of the potential for compression in the case of bleeding. If the probability for subsequent PPM implantation is high, it is recommended that the left subclavian approach be avoided, as this is the most frequently used route for PPM implantation [
12].
The standard approach for emergency placement of a temporary transvenous pacemaker is utilising fluoroscopic guidance. The necessary transfer to a catherisation laboratory for this procedure and the delay until therapy could be life-threatening in a haemodynamically instable patient. Echography-guided implantation of TV-TP leads could result in shorter times to therapy and avoid the risks of an emergency transfer. Two observational studies reported the feasibility of using echographic guidance in temporary transvenous pacemaker placement in a total of 130 patients [
45,
46] and showed a significant reduction in total complications in the larger study (6.8% vs 20.7%,
p = 0.03) [
45]. Also, the median time from decision to active pacing was significantly shorter for the echography-guided group (22 vs 43 min,
p < 0.01). Although these studies show positive initial results, the results need to be interpreted with caution due to their non-randomised nature, selection bias and relatively small number of patients. Larger randomised studies are needed to assess the full extent of the potential advantages of echography-guided temporary transvenous pacemaker implantation.
To our knowledge, this is the first evaluation of the trend of complication rates following TV-TP since its introduction. The mean reported complication rates have remained high (23%) over the past decades, but have shown a significant decline since its introduction. An analysis performed in the NIS database in the United States between 2003 and 2014 included 43,472 patients and showed an increasing trend in TV-TP-related periprocedural complications up to 17.7% in 2014 (Rozen et al., unpublished data). An even larger study reporting on outcomes of TV-TP in the United States included over 350,000 patients and used the same NIS database for the analysis [
16]. Although only potential complications could have been identified, a lower rate of cardiac perforations was observed (0.6%) in this large cohort. Interestingly, the incidence of this life-threatening complication has shown a rise over the last decade. Moreover, the rate of pneumothorax was higher than found in our analysis (0.9%). Non-cardiac bleeding accounted for a complication in 2.4% of patients, which is similar to the rate we found in the most recent decade. The use of echographic guidance might result in safer procedures for the implantation of a temporary transvenous pacemaker, but the risk of bleeding after insertion still remains. The total number of complications found by Metkus et al. was strikingly low at 3.9% [
16]. However, there are some important limitations to consider: no data were available on the implant procedure, and complications with no available ICD codes could have been missed (e.g. malfunction of TV-TP therapy, fever, blood-based infection, delirium). This might have resulted in an underestimation of the total complication rate. In our study the complication rates differed substantially between published studies. For instance, Shah and Awan [
44] observed a complication rate of 0.8% compared to 80.5% reported by Austin et al. [
8]. There are some important aspects in the interpretation of the differences in complication frequency that merit emphasis. First, different inclusion criteria were used, since TV-TP therapy is implemented in a heterogeneous patient population. Second, the definition of complications is different between published articles. Hospital admission following TV-TP was long, with a mean of 11.2 days. These patients are at risk for thromboembolic events, pneumonia and delirium [
12,
53]. This may result in a prolonged hospital stay, possibly resulting in an economical and logistic burden.
The high mortality rate of 14.5% indicated a sick patient population in whom TV-TP therapy is required, often to treat life-threatening situations. The mortality rate in the large US cohort (14%) was similar to that in our analysis [
16]. Another recent large study (
n = 4838) by Ng et al. showed a similar mortality rate of 11.8% during the index admission, and a strikingly high mortality rate of 53.6% during over 4 years of follow-up [
54]. In this cohort weekend admission was associated with increased mortality compared to weekdays (hazard ratio 1.15, 95% CI 1.06–1.26,
p = 0.002) and independently predicted all-cause mortality.
The need for a permanent pacing system after TV-TP therapy was high with a mean of 64.2%. A similar number of PPM implantations after TV-TP was found by Rozen et al. (unpublished data): 61.9%. These patients have to undergo two procedures and are therefore at risk for associated complications related to temporary and subsequent permanent cardiac pacemaker implantation. Patients with a TV-TP before PPM implantation are up to 2.5 times more prone to develop an infection [
12]. Therefore, the current guidelines state that TV-TP should be avoided, and if necessary should be applied as briefly as possible [
12].
These findings underline the necessity for alternative treatments for patients requiring TV-TP. New technologies, for example retrievable leadless pacemaker (LP) systems [
55,
56], could provide an alternative for selected patients who require TV-TP therapy. LP therapy has been introduced to reduce complications related to conventional PPM therapy and does not require the use of transvenous leads, likely avoiding lead-related complications associated with TV-TP and conventional PPM. In addition, LP may be an alternative approach in patients who require TV-TP and subsequent conventional PPM implantation without venous access, or who have a history of recurrent device infections [
57,
58]. However, as the LP is currently only available as a single-chamber right ventricular device, this approach could potentially be limited to a single-chamber pacemaker population. Future concepts, such as leadless VDD resulting in atrioventricular synchronous pacing [
59,
60], might broaden this patient population.
A prospective study on TV-TP complications and outcome is recommended. As the majority of TV-TP therapy patients require a PPM at a later stage and complication rates are high, upcoming techniques such as leadless pacing should be monitored closely as they might prove an alternative to TV-TP therapy and all the possible complications it entails.
Limitations
The lack of high-quality evidence resulted in the choice to perform a scoping review, but it comes with several limitations: most importantly the inability to perform a meta-analysis of the data. With the aim of providing insight into the current performance of TV-TP therapy we compiled a comprehensive descriptive overview. Due to the heterogeneity of the patients and study designs the conclusions derived from this review are restricted. Definitions of complications as well as patient characteristics differed between published studies. It is important to recognise possible under-reporting of complications (i.e. delirium, pneumonia in the elderly) as these complications might contribute to a poorer outcome and prolong hospitalisation even further. As it was not possible to differentiate asystole during insertion from postoperative asystole this was excluded as a serious complication. For these reasons, reported (serious) complication rates in this overview may be underestimations.