†These authors contributed equally.
Academic Editors: Davide Bolignano and Vincenzo Lionetti
Background: This study aimed to investigate the predictors and
prognosis of acute kidney injury (AKI) occurrence among Chinese patients
following left atrial appendage closure (LAAC). Methods: We
retrospectively enrolled 512 consecutive patients who underwent LAAC between
January 2014 and December 2019. AKI was clinically defined according to the
Kidney Disease Improving Global Outcomes serum creatinine criteria. Major adverse
cardiovascular events were defined as the composite of all-cause mortality,
readmission due to heart failure, cardiac surgery, systemic embolism, or bleeding
events. Results: The incidence of AKI was 5.3% and was highest in
patients with chronic kidney disease (CKD) stages 4–5 (25.0%), followed by
those with CKD stages 3a–3b (9.1%), and those with CKD stages 1–2 or without
CKD (3.9% only). Multivariate logistic regression showed that lower body mass
index (odds ratio [OR] = 0.889; 95% confidence interval [CI], 0.803–0.986;
p = 0.017), hypertension (OR = 5.577; 95% CI, 1.267–24.558; p = 0.023), and CKD stages 4–5 (OR = 6.729; 95% CI, 1.566–28.923; p =
0.010) were independent risk factors for AKI development after LAAC. AKI after
LAAC was associated with 3-year major adverse cardiovascular events (33.3% vs.
7.5%, p
Acute kidney injury (AKI) is commonly regarded as a complication of many cardiac interventions such as percutaneous coronary intervention (PCI) [1] and transcatheter aortic valve replacement (TAVR) [2]. Left atrial appendage closure (LAAC) is the recommended alternative for patients with nonvalvular atrial fibrillation (NVAF) who cannot tolerate long-term oral anticoagulation (OAC) treatment [3, 4]. Although LAAC is considered a safe and effective procedure, similar to other cardiac interventions that require contrast media, patients who undergo LAAC are also at risk of AKI. Recent studies have shown that in clinical practice, AKI after LAAC has implicit adverse effects [5, 6]. However, knowledge on AKI after LAAC is insufficient, and data regarding this setting remain inadequate. Furthermore, patients who undergo LAAC operation are mostly the elderly, with accompanying kidney dysfunction, diabetes, and chronic cardiopulmonary disease, all of which are risk factors for AKI [7]. Therefore, this study aimed to investigate the predictors and prognosis of AKI among Chinese patients following the LAAC procedure.
This observational study collected the clinical data of consecutive patients who
underwent LAAC between January 2014 and December 2019. The inclusion criteria
were as follows: diagnosis of paroxysmal or persistent NVAF, thrombosis risk
score (CHA
The flowchart of the study. AKI, acute kidney injury.
Baseline characteristics, including demographics and complications, LAAC
indications, CHA
The LAAC device was implanted using a catheter-based delivery system after
atrial septal puncture. Generally, closure was performed under general anesthesia
and guided by fluoroscopy combined with transesophageal echocardiography (TEE).
Left atrial appendage (LAA) angiography was performed 30° right anterior
oblique (RAO) and 20° caudal (CAU) to measure the LAA orifice. The
device was delivered through a catheter and expanded to close the LAA opening.
The device was released after confirming its stability without a large residual
shunt (
AKI was defined based on the change in serum creatinine (SCr) concentration from
the baseline to the peak value measured within 7 days after LAAC. According to
the Kidney Disease Improving Global Outcomes (KDIGO) guidelines for AKI [8], an
increase in SCr concentration by
CKD was diagnosed and staged according to the KDIGO criteria [9]: (1) regardless
of a decreased glomerular filtration rate (GFR) [10] or kidney damage lasting
Patients with CKD at baseline received prophylactic intravenous hydration with isotonic saline 12 h before LAAC and continued for at least 24 h afterwards. Renal function (SCr level and estimate glomerular filtration rate, eGFR) was monitored daily until the patient was discharged. The physician team will decide whether to use glutathione or bicarbonate, if necessary. Attention was paid on perioperative complications, especially the need for hemodialysis, during hospitalization.
Patient received warfarin with an international normalized ratio (INR) between 2.0–2.5 after LAAC and novel oral anticoagulants (NOACs) were prescribed for those with contraindications to warfarin anticoagulation.
TEE was completed 45 days after surgery to determine (
Prior to discharge, TTE was performed to rule out cardiac effusion, and SCr was tested to ensure no remarkable deterioration of renal function. The patients underwent TEE evaluation of residual leak and DRT at 6 weeks and 6 months after the procedure. Follow-up was performed during outpatient clinical visits or via telephone call. The follow up time ranged from 2 to 48 months. The comparison of the primary efficacy endpoint was defined as major adverse cardiovascular events (MACE) in terms of all-cause mortality, readmission due to heart failure, cardiac surgery, and systemic embolism, and the primary safety endpoint was defined as major periprocedural complications such as major bleedings during follow-up visits [11].
Continuous variables were presented as mean
A total of 512 eligible patients (mean age 69 years) were enrolled in this
study. Twenty-seven (5.3%) patients developed AKI according to the KDIGO SCr
criteria. The baseline clinical characteristics of the study population are shown
in Table 1. Significant differences in sex, age, or body mass index (BMI) were
not observed between the AKI and non-AKI groups. Patients with AKI were more
likely to have comorbid hypertension than that of non-AKI patients (92.6% vs.
67.2%, p = 0.006). Patients in the AKI group tend to have a higher CKD
stage (CKD stages 3a–3b, 29.6%, and CKD stages 4–5, 11.1%, and only 16.5%
and 1.9%, respectively, in the non-AKI group). The HAS-BLED score was
significantly higher in the AKI group (3.3
All | non-AKI group | AKI group | p value | ||
n = 512 | n = 485 | n = 27 | |||
Male [n (%)] | 308 (60.2%) | 296 (61.0%) | 12 (44.4%) | 0.087 | |
Age (y) | 69 |
69 |
71 |
0.151 | |
Elderly [n (%)] | 341 (66.6%) | 342 (70.5%) | 20 (74.1%) | 0.693 | |
BMI (kg/m |
24.6 |
24.7 |
22.8 |
0.094 | |
Hypertension [n (%)] | 351 (68.6%) | 326 (67.2%) | 25 (92.6%) | 0.006 | |
Diabetes [n (%)] | 112 (21.9%) | 103 (21.2%) | 9 (33.3%) | 0.139 | |
Stroke [n (%)] | 210 (41.1%) | 200 (41.3%) | 10 (37.0%) | 0.660 | |
Vascular disease [n (%)] | 48 (9.4%) | 44 (9.1%) | 4 (14.8%) | 0.319 | |
Echocardiography | |||||
LVEF (%) | 64 |
64 |
63 |
0.785 | |
LAA Diameter (mm) | 21 |
21 |
21 |
0.838 | |
LAA Length (mm) | 25 |
26 |
24 |
0.160 | |
SCr ( |
81 [69, 94] | 81 [69, 94] | 85 [73, 97] | 0.698 | |
eGFR (mL/min/1.73 m |
75.6 |
75.8 |
70.9 |
0.347 | |
CKD stage | 0.001 | ||||
no CKD/stage 1–2 [n (%)] | 412 (80.5%) | 396 (81.6%) | 16 (59.3%) | ||
stage 3a–3b [n (%)] | 88 (17.2%) | 80 (16.5%) | 8 (29.6%) | ||
stage 4–5 [n (%)] | 12 (2.3%) | 9 (1.9%) | 3 (11.1%) | ||
hs-CRP (mg/L) | 0.7 [0.3, 1.9] | 0.7 [0.3, 1.9] | 0.7 [0.3, 2.6] | 0.823 | |
D-dimer (mg/L) | 0.27 [0.19,0.74] | 0.26 [0.19, 0.72] | 0.60 [0.19, 0.97] | 0.120 | |
CHA |
3.5 |
3.5 |
4.0 |
0.079 | |
HAS-BLED | 2.9 |
2.9 |
3.3 |
0.028 | |
AKI, acute kidney injury; BMI, body mass index; LVEF, left ventricular ejection fraction; LAA, left atrial appendage; SCr, serum creatinine; eGFR, estimated glomerular filtration rate; CKD, chronic kidney disease; hs-CRP, highly sensitive C-reactive protein. |
Significant differences in LAA morphology, device type, device size, or
antithrombotic therapy between the AKI and non-AKI groups were not found. The
contrast volume administered during the procedure (154
All | non-AKI group | AKI group | p value | ||
n = 512 | n = 485 | n = 27 | |||
Procedure data | |||||
LAA morphology | 0.830 | ||||
cactus [n (%)] | 33 (6.4%) | 32 (6.6%) | 1 (3.7%) | ||
cauliflower [n (%)] | 359 (70.1%) | 340 (70.1%) | 19 (70.4%) | ||
chickenwing [n (%)] | 82 (16.0%) | 78 (16.1%) | 4 (14.8%) | ||
windsock [n (%)] | 38 (7.4%) | 35 (7.2%) | 3 (11.1%) | ||
Landing zone diameter (mm) | 26 |
26 |
23 |
0.069 | |
Device | 0.455 | ||||
Watchman [n (%)] | 366 (71.5% ) | 345 (71.1%) | 21 (77.8%) | ||
Lambre [n (%)] | 146 (28.5%) | 140 (28.9%) | 6 (22.2%) | ||
Device size (mm) | |||||
Watchman | 0.513 | ||||
21 [n (%)] | 21 (5.7%) | 19 (5.5%) | 2 (9.5%) | ||
24 [n (%)] | 41 (11.2%) | 39 (11.3%) | 2 (9.5%) | ||
27 [n (%)] | 104 (28.4%) | 96 (28.7%) | 8 (38.1%) | ||
30 [n (%)] | 88 (24.0%) | 83 (24.8%) | 5 (23.8%) | ||
33 [n (%)] | 112 (30.6%) | 108 (32.2%) | 4 (19.0%) | ||
Lambre | |||||
Umbrella size (mm) | 27.1 |
27.1 |
27.7 |
0.960 | |
Cover size (mm) | 34.8 |
34.8 |
34.7 |
0.824 | |
Contrast volume (mL) | 146 |
145 |
154 |
0.051 | |
CV/GFR ratio | 1.9 [1.6, 2.3] | 1.9 [1.6, 2.3] | 2.3 [1.8, 2.7] | 0.055 | |
Antithrombotic regimen | |||||
VKA [n (%)] | 48 (9.4%) | 46 (9.5%) | 2 (7.4%) | 0.741 | |
NOAC [n (%)] | 392 (76.6%) | 370 (76.3%) | 22 (81.5%) | 0.532 | |
DAPT [n (%)] | 72 (14.1%) | 69 (14.2%) | 3 (11.1%) | 0.288 | |
Outcomes | |||||
DRT [n (%)] | 16 (3.1%) | 13 (2.7%) | 3 (11.1%) | 0.012 | |
Residual shunt | 0.237 | ||||
None [n (%)] | 368 (71.9%) | 346 (71.3%) | 22 (81.5%) | ||
1–5 [n (%)] | 138 (26.9%) | 134 (27.6%) | 4 (14.8%) | ||
6 (1.2%) | 5 (1.0%) | 1 (3.7%) | |||
3-year MACE | |||||
HF rehospitalization [n (%)] | 12 (2.3%) | 8 (1.6%) | 4 (14.8%) | ||
Stroke/Ischemic events [n (%)] | 16 (3.1%) | 14 (2.9%) | 2 (7.4%) | ||
Cardiac surgery [n (%)] | 5 (1.0%) | 4 (0.8%) | 1 (3.7%) | ||
Major bleeding [n (%)] | 6 (1.2%) | 5 (1.0%) | 1 (3.7%) | ||
Cardiac death [n (%)] | 3 (0.6%) | 1 (0.2%) | 2 (7.4%) | ||
3-year Mortality [n (%)] | 6 (1.2%) | 3 (0.6%) | 3 (11.1%) | ||
AKI, acute kidney injury; LAA, left atrial appendage; CV/GFR, the contrast volume-to-glomerular filtration; VKA, vitamin K antagonists; NOAC, novel oral anticoagulant; DAPT, dual antiplatelet therapy; DRT, device related thrombi; MACE, major adverse cardiac event; HF, heart failure. |
The DRT ratio was significantly higher in the AKI group than that in the non-AKI
group (11.1% vs. 2.7%, p = 0.012). No significant difference in
residual shunt was observed between the two groups. The incidence of different
types of long-term MACE after the procedure was significantly higher in the AKI
group than that in the non-AKI group. Long-term all-cause mortality after the
procedure was significantly higher in the AKI group than that in the non-AKI
group (11.1% vs. 0.6%, p
The AKI incidence was highest in patients with CKD stages 4–5 (25.0%), followed by those with CKD stages 3a–3b (9.1%), and those with CKD stages 1–2 or without CKD (only 3.9%) (Fig. 2).
AKI incidence between different CKD stages. AKI, acute kidney injury; CKD, chronic kidney disease.
Variables with p
Univariate | Multivariate | ||||
OR (95% CI) | p value | OR (95% CI) | p value | ||
Male (male/female) | 0.511 (0.234–1.115) | 0.092 | |||
BMI (kg/m |
0.884 (0.798–0.978) | 0.017 | 0.889 (0.802–0.986) | 0.026 | |
Hypertension | 6.097 (1.426–26.061) | 0.015 | 5.577 (1.267–24.558) | 0.023 | |
CKD stage | |||||
no CKD/stage 1–2 | Reference | - | Reference | - | |
stage 3a–3b | 2.475 (1.024–5.979) | 0.044 | 1.997 (0.798–4.996) | 0.139 | |
stage 4–5 | 8.250 (2.037–33.421) | 0.003 | 6.729 (1.566–28.923) | 0.010 | |
CHA |
1.261 (0.972–1.636) | 0.081 | |||
HAS-BLED | 1.465 (1.039–2.067) | 0.030 | 1.184 (0.807–1.735) | 0.387 | |
Contrast volume | 1.016 (1.000–1.032) | 0.052 | |||
AKI, acute kidney injury; LAAC, left atrial appendage closure; BMI, body mass index; CKD, chronic kidney disease. |
The median (IQR) follow-up time was 15 (4–26) months. The incidence of 1-, 2-,
and 3-year MACE after the procedure was significantly higher in the AKI group
than that in the non-AKI group (11.1% vs. 2.8%, p = 0.019; 18.5% vs.
3.7%, p
All | non-AKI group | AKI group | HR (95% CI) | p value | ||
n = 512 | n = 485 | n = 27 | ||||
MACE | ||||||
1-year [n (%)] | 15 (2.9%) | 12 (2.5%) | 3 (11.1%) | 4.333 (1.146–16.391) | 0.019 | |
2-year [n (%)] | 21 (4.1%) | 16 (3.3%) | 5 (18.5%) | 5.852 (1.964–17.440) | ||
3-year [n (%)] | 42 (8.2%) | 32 (6.6%) | 10 (37.0%) | 6.203 (2.579–14.917) | ||
Mortality | ||||||
1-year [n (%)] | 2 (0.4%) | 2 (0.4%) | 0 | 0.940 (0.919–0.962) | 0.722 | |
2-year [n (%)] | 5 (1.0%) | 3 (0.6%) | 2 (7.4%) | 11.333 (1.811–37.941) | 0.001 | |
3-year [n (%)] | 6 (1.2%) | 3 (0.6%) | 3 (11.1%) | 13.250 (2.806–42.578) | ||
AKI, acute kidney injury; MACE, major adverse cardiac events. |
Kaplan-Meier curves up to 3-year follow-up for (a) MACE between AKI vs. non-AKI, log rank = 0.017; (b) all-cause of mortality between AKI vs. non-AKI, log rank = 0.001.
The principal findings of this study are as follows: (1) the incidence of AKI after LAAC in our center is relatively lower (5.3%), whereas the incidence of AKI in patients with renal insufficiency before LAAC is significantly higher (9.1% in CKD stage 3, 25% in CKD stages 4–5); (2) multivariate regression showed that low BMI, hypertension, and preoperative state of patients with CKD stages 4–5 are independent risk factors for AKI; (3) AKI after LAAC significantly increases the risk of midterm MACE and all-cause mortality, and the risk increases over the years.
The incidence of AKI ranges from 7% to 9.6% in patients undergoing PCI operation [1, 12, 13]. However, the incidence of AKI after interventional treatment for structural heart disease is much higher than that after PCI. For example, approximately 11.7% of patients develop AKI after TAVR [2], and 29% of patients after MitraClip [14] will develop AKI. Patients undergoing TAVR are usually older and frail with more comorbidities and more prone to hemodynamic disorders due to rapid cardiac pacing during the operation; therefore, the incidence of AKI is relatively higher than that in our study. Patients undergoing LAAC commonly have a venerable age, accompanied by various risk factors, such as hypertension, diabetes, and CKD. However, complications and hemodynamic instability were not observed during the LAAC procedure. Moreover, there is rare need for blood transfusion after LAAC. These may be the reasons for the lower incidence of AKI in LAAC patients than those who underwent TAVR and MitraClip.
In a previous study [5], the incidence of AKI after LAAC was 9%, whereas the overall incidence in our study was only 5.3%. Our study included much younger patients (69 years vs. 76 years), those with lower rates of hypertension (68.6% vs. 85.1%) and diabetes (21.9% vs. 33.2%) and lower rates of poor baseline renal function (CKD stages 4–5, 2.3% vs. 8.2%) than that of Nombela-Franco’s report, which may have contributed to the inconsistency of data. However, it is worth mentioning that 9% of LAAC operations in the study by Nombela-Franco et al. [5] were performed in conjunction with other operations, such as TAVR and PCI, which would increase the amount of contrast agent and theoretically increase the risk of contrast-induced kidney injury. We excluded patients who underwent combined surgery in our study. In another European multicenter study [6], the incidence of AKI after LAAC was as high as 13.7%. In this study, the subjects were older (75.1 years) and had a higher proportion of diabetes mellitus (34.7%) and CKD stages 4–5 (11.5%) at baseline. Furthermore, consistent outcomes were observed in that patients CKD stages 4–5 had the highest proportion of AKI (36.4% and 25%, respectively).
In the above two studies, the former found that the only independent predictor of AKI after LAAC was a poor baseline eGFR (HR, 1.32; 95% CI, 1.09–1.61; p = 0.004), and the latter revealed the worse renal function at baseline and a higher incidence of AKI and the CV/GFR ratio having a moderate predictive value for AKI (area under curve or AUC, 0.67; 95% CI, 0.50–0.84; p = 0.05). The CV/GFR ratio has been identified as an independent predictor of AKI, mainly in patients undergoing PCI [15]; however, in our study and Nombela-Franco’s study, no correlation was noted between the CV/GFR ratio and AKI. Contrary to our expectations, there was no significant correlation between the amount of contrast agent and the occurrence of AKI. This result is consistent with those of the two pioneering studies [5, 6]. Although the contrast volume in the AKI group had an increasing tendency compared with the non-AKI group, and the p value was very close to 0.05, it did not reach statistical significance. We would expand the sample size in further studies to confirm it. Our study suggests that low BMI, hypertension, and preoperative CKD stages 4–5 were independent risk factors for the occurrence of AKI.
Recently, a study evaluating the effect and safety of LAAC in patients with CKD and AF found that the incidence of AKI in the CKD group was 11.1%, which was significantly higher than that in the non-CKD group (0%) [16]. From the CRIC study, which is by far the largest prospective CKD cohort with nearly a decade of follow-up and systematic data collection, it is notable that incident atrial fibrillation was associated with a higher risk of developing end-stage renal disease (ESRD) in patients with CKD [17], and AKI has been recognized as a risk factor for CKD progression [18]. We previously reported [19] that the 2-year mortality and incidence of progressive CKD in patients with AKI after cardiac surgery significantly increased even after full recovery of renal function. A systematic review and meta-analysis [20] also identified AKI as an independent risk factor for CKD and ESRD. However, CKD is often considered a risk factor for AKI because of its epidemiological relationship [21]. Therefore, it is plausible to infer that patients with CKD and AF have poor prognosis after AKI.
At present, many preventive strategies for reducing the incidence of AKI have been reported, according to the recommendations for the prevention of contrast-induced nephropathy (CIN) [22], such as adequate hydration, use of low-osmolar or iso-osmolar contrast media, and minimal volume of contrast media. Adequate hydration remains the central component of CIN prevention, and this strategy should be implemented in patients with a low eGFR undergoing LAAC. A useful index to prevent CIN is the contrast volume to GFR ratio, which we strictly controlled below 3.7 in our daily practice to minimize the occurrence of AKI according to a previous study [15].
The innovation of LAA occlusion with decreased use of a contrast dye was recently described in a case report using the TrueFusion™ fusion-imaging system [23]. In turn, performing LAAC without contrast has been appealing, particularly in patients with severely reduced renal function. Sedaghat et al. [24] reported echocardiographically guided LAAC without the use of a contrast dye, and the technique appeared to be feasible without compromising the clinical effect and procedure safety. Thus, it is conceivable that completing LAAC with a reduced or no contrast agent is beneficial in special cases by decreasing AKI occurrence. The RenalGuard System has demonstrated benefits in reducing the occurrence of AKI in patients undergoing TAVR [25] and PCI [26], compared to hydration with normal saline solution, with a relative risk reduction of 79% and 74%, respectively. To the best of our knowledge, no standardized protocol for AKI prevention has been proposed for LAAC. The impact of strategies applied in PCI and TAVR on meaningful clinical outcomes in patients undergoing LAAC requires confirmation through larger and multicenter trials.
Surprisingly, these studies have consistently shown that the occurrence of AKI is related to in-hospital mortality, long-term mortality, and hospitalization due to renal and cardiac events [5, 6]. The proportion of noncardiac deaths was 68.3% in a report by Nombela-Franco. In our study, the 1-, 2-, and 3-year mortality rates were 0%, 7.6%, and 11.1%, respectively, in the AKI group, and the prognosis worsened over time. It is speculated that this poor condition is partially attributed to the deterioration of renal function after AKI.
The main limitation of this study is its retrospective nature. Conversely, the incidence of AKI could be underestimated because we may have missed an AKI diagnosis after discharge. Finally, this was a single-center, observational study. Larger, multicenter studies are warranted to confirm these results.
Like other transcatheter interventions, it is very important to assess renal function before and after LAAC to facilitate early warning, identification, and intervention in patients who are prone to develop AKI. Reducing the risk of AKI may help improve the clinical outcomes of patients receiving LAAC. In patients with a high risk of deterioration of renal function, such as low BMI, hypertension, and preoperative CKD stages 4–5, further preventive measures and close monitoring should be undertaken after surgery.
LZ and JX designed the research study. LG performed the research. WP provided help and advice on the discussion. JX and XZ analyzed the data. LZ, JX and XL wrote the manuscript. DZ provided the patients. DZ, JG and XD conceived the idea, participated in the revision. All authors contributed to editorial changes in the manuscript. All authors read and approved the final manuscript.
The study was conducted in accordance with the Declaration of Helsinki. It was approved by the Ethical Committee of Zhongshan Hospital affiliated to Fudan University (No. B2018-175).
We would like to express our sincere gratitude to our colleagues whose names do not appear on the paper but contributed diligently to the research. We also thanks to all the peer reviewers for their opinions and suggestions.
This research was funded by Shanghai Clinical Research Center for Interventional Medicine (19MC1910300); National Natural Science Foundation of China (81901939); Shanghai Municipal Hospital Frontier Technology Project supported by Shanghai Shenkang Hospital Development Center (SHDC12018127).
The authors declare no conflict of interest.
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