Literature DB >> 32802433

Efficacy and safety of airway stenting to treat anastomotic complications after lung transplant: a cohort study.

Kevin C Ma1, Mingyang Li2, Andrew R Haas1, Anthony R Lanfranco1, Edmund K Moon1, David M DiBardino1.   

Abstract

BACKGROUND: Airway complications affect roughly 15-20% of lung transplant patients. Airway stents are an attractive therapeutic option; however, no experimental or controlled observational data exists to draw firm conclusions regarding airway stent efficacy and safety in this population.
METHODS: We performed a retrospective cohort study of patients who underwent airway stent placement for post-transplant anastomotic airway complications. The primary outcomes were improvements in FEV1 and reduction in bronchoscopies post-stent.
RESULTS: We identified 36 patients who underwent airway stenting between October 2012 and October 2017. A total of 47 airways underwent stent placement. Improvement in FEV1 after stent placement was only observed in patients who ultimately were able to undergo stent removal. Patients who expired prior to stent removal had no immediate FEV1 improvement after stent placement. Among subjects who underwent stent removal, there was a statistically significant reduction in number of bronchoscopies per month after stent removal compared to pre-stent placement. Male gender was the only predictor of FEV1 improvement after stent placement while male gender and dehiscence prior to stent placement predicted increased number of bronchoscopies after stent placement. Mucous plugging and granulation tissue formation were the most common stent related complications.
CONCLUSIONS: Only select patients benefit from stent placement for airways stenosis after lung transplant. Complications related to stent placement are common. Patients with airway complications treated with airway stents undergo a high volume of repeat procedures. 2020 Journal of Thoracic Disease. All rights reserved.

Entities:  

Keywords:  Lung transplantation; bronchoscopy; self expandable metallic stents

Year:  2020        PMID: 32802433      PMCID: PMC7399444          DOI: 10.21037/jtd-20-677

Source DB:  PubMed          Journal:  J Thorac Dis        ISSN: 2072-1439            Impact factor:   2.895


Introduction

Airway complications after lung transplant continue to be a significant cause of morbidity post-transplant (1). Contemporary descriptive epidemiologic studies continue to report airway complications affecting roughly 15–20% of lung transplant patients (2,3). Much of the work in this field has centered around identifying risk factors for airway complications. Many of the non-surgical associations identified are difficult to modify, such as primary graft dysfunction, acute cellular rejection, aspergillus colonization post-transplant, prolonged post-operative mechanical ventilation, single lung transplant, post-operative hypotension, and pre-operative Pseudomonas cepacia colonization (4-10). Understanding the optimal treatment for these airway complications is critical. Research dedicated to therapeutic options has been limited by small subject numbers, a paucity of comparison arms, the historical lack of consensus definitions for the subtypes of airway complications, and institution-specific bias. These factors have led to a general lack of reproducibility and continued equipoise. Airway stents are an attractive option because airway complications often include airway stenoses that tend to recur after simple dilation techniques (7). Descriptive studies have demonstrated the feasibility of airway stents to treat certain airway complications (11-13). Improvement in FEV1 and improved respiratory symptoms after stent placement have been described (12,13). However, no experimental or controlled observational data exists to draw firm conclusions regarding airway stents in this patient population (1). In this retrospective cohort study, we report airway stent strategies and their associations with clinical outcomes in patients with post-transplant airway complications leading to airway stenosis. To our knowledge, this is the first observational study aimed at comparing airway stent techniques with clinical success. We present the following article in accordance with the STROBE reporting checklist (available at http://dx.doi.org/10.21037/jtd-20-677).

Methods

Patient population

This is a retrospective cohort study using patient data collected between October 2012 and October 2017. All consecutive post-lung transplant patients who had undergone airway stent placement for anastomotic airway complications during the study period were included in the database. Patients were excluded if airway stents were used to manage distal airways disease as previously defined in a 2018 International Society for Heart and Lung Transplantation (ISHLT) consensus statement (1). Data was gathered by reviewing the electronic medical record and imported for analyses using SAS/Stat software, Version 9.4 (SAS Institute, Cary, North Carolina, USA). For all statistical tests, significance level alpha of 0.05 was used. Descriptive statistics for patient demographics were provided on both the patient and airway level as some patients had multiple airway complications requiring stenting, and reported using median and interquartile ranges for demographic, peri-operative, and donor-recipient variables.

Statistical analysis

Primary endpoints

One sample t-test was used to evaluate the hypotheses that airway stent placement was associated with a durable change in FEV1, and a change in the number of bronchoscopies required to maintain airway patency. Co-primary endpoints were measured as improvement in FEV1 in milliliters and decrease in monthly bronchoscopy rate measured before stent placement, immediately after stent placement, and, when available, after stent removal. Bronchoscopy was performed at the discretion of the treatment team including the patient’s transplant pulmonologist as well as the interventional pulmonologist. Analyses were also repeated when stratified between airways with eventual stent removal, versus airways with permanent stent placement.

Secondary endpoints

Fisher’s exact test was used to evaluate differences in stent related complications between different stent types. Simple and multiple linear regression were used to evaluate demographic and procedure factors associated with a change in FEV1 and monthly bronchoscopy rate. Missing data points were omitted from the analysis. No patients were lost to follow up. This research was conducted with University of Pennsylvania institutional review board approval (IRB #828752). With the approval of the local IRB, informed consent was not obtained for the study due to its retrospective nature of the study. Subject data was kept secure in accordance with local IRB guidelines. The study conformed to the provisions of the Declaration of Helsinki (as revised in Edinburgh 2000).

Results

Baseline characteristics by subject and by airway are shown in . We identified 36 subjects with airway stenting after lung transplant between October 2012 and October 2017. The mean age at transplant was 61 years old. The most common indication for transplant was idiopathic pulmonary fibrosis (IPF)/interstitial lung disease (ILD) (n=23, 63.9%). Among the 36 subjects, a total of 47 airways underwent stent placement for a transplant-related anastomotic complication with a median time from transplant to stent placement of 127 (IQR 82–201) days. The preferred initial stent choice was a silicone stent (n=29, 61.7%). Specific types of anastomotic complications were categorized as cicatrix (fibrotic scar tissue), pseudomembrane (sloughing formerly necrotic airway wall), dehiscence, or malacia.
Table 1

Baseline demographics

VariableNumber
Patient level demographics (n=36)
   Number of airways stented
      1 airway28
      2 airways5
      3 airways3
   Age at transplant (mean ± SD)60.53±9.68
   Gender (male %)22 (61.1)
   BMI at time of transplant (mean ± SD)26.78±4.26
   Prior pack-years cigarette smoke exposure (mean ± SD)20.35±24.57
   Medical comorbidities (n, %)
      Essential hypertension18 (50.0)
      Atherosclerotic disease (CAD, PVD, Hx CVA/TIA)11 (30.6)
      Type 2 diabetes mellitus8 (22.2)
   Indication for lung transplant (n, %)
      COPD10 (27.8)
      IPF/ILD23 (63.9)
      PAH0 (0.0)
      CF1 (2.8)
      COPD & IPF/ILD1 (2.8)
      Other1 (2.8)
   VV/VA ECMO pre-transplant (n, %)2 (5.6)
   VV/VA ECMO post-transplant (n, %)3 (8.3)
Airway level demographics (n=47)
   Location (n, %)
      Right mainstem stenosis10 (21.3)
      Left mainstem stenosis22 (46.8)
      Bronchus intermedius11 (23.4)
      Peripheral4 (8.5)
   Days between transplant and stent placement (mean ± SD)184.51±183.12
   Days between transplant and stent placement (median, IQR)127 [82–201]
   Initial stent type (n, %)
      Silicone29 (61.7)
      Covered metallic stent6 (12.8)
      Uncovered metallic stent12 (25.5)
   Dehiscence (n, %)6 (12.8)
   Cicatrix (n, %)19 (40.4)
   Pseudomembrane (n, %)14 (29.8)
   Malacia (n, %)19 (40.4)
   FEV1 (L)1.44±0.57
   Procedures prior to stent placement (mean ± SD)
      # of dilations0.83±1.19
      # of debridements1.28±2.67
      # of aspirations for mucous plugging0.38±0.99
      # of steroid injections0.11±0.31
      # of cryotherapy treatments0.26±0.79
      # of Bronchoscopies4.62±3.38

BMI, body mass index; CAD, coronary artery disease; PVD, peripheral vascular disease; CVA/TIA, cerebral vascular attacks/transient ischemic attacks; COPD, chronic obstructive pulmonary disease; IPF/ILD, idiopathic pulmonary fibrosis/interstitial lung disease; PAH, pulmonary arterial hypertension; CF, cystic fibrosis; VV/VA, veno-venous/veno-arterial; ECMO, extra-corporeal membrane oxygenation; FEV1, forced expiratory volume in one second.

BMI, body mass index; CAD, coronary artery disease; PVD, peripheral vascular disease; CVA/TIA, cerebral vascular attacks/transient ischemic attacks; COPD, chronic obstructive pulmonary disease; IPF/ILD, idiopathic pulmonary fibrosis/interstitial lung disease; PAH, pulmonary arterial hypertension; CF, cystic fibrosis; VV/VA, veno-venous/veno-arterial; ECMO, extra-corporeal membrane oxygenation; FEV1, forced expiratory volume in one second.

Changes in pulmonary function test parameters

Among subjects who eventually had their stent removed, statistically significant improvements in FEV1 were observed immediately after placement (0.41±0.39 L, P<0.001) compared to pre-stent placement FEV1 (). Moreover, there was sustained FEV1 improvement immediately after stent removal as well as 1 year after removal. Among subjects who did not have their stent removed, no immediate improvement in FEV1 was observed after stent placement (). There was a difference in location of stented airways between those subjects who eventually underwent stent removal compared to subjects who did not (). No other differences were noted in baseline characteristics between the two groups.
Table 2

Improvement in FEV1 after stent placement and removal

VariableStent removedStent never removedAll
n∆FEV1 (L)SDP value1n∆FEV1 (L)SDP value2n∆FEV1 (L)SDP value1
Stent placement (post-stent FEV1 – pre-FEV1)210.410.39<0.001130.250.590.3278340.350.47<0.001
Stent removal, short term (stent removal FEV1 – pre-FEV1)220.350.37<0.001N/AN/AN/AN/AN/AN/AN/AN/A
Stent removal, long term (12-month stent removal FEV1 – pre-FEV1)160.370.560.019N/AN/AN/AN/AN/AN/AN/AN/A

1, t-test: H0: delta =0; 2, P value comparing (post-stent FEV1 – pre-FEV1) between patients who had stent removed vs. not removed. FEV1, forced expiratory volume in one second.

Figure 1

Change in FEV1 over time. FEV1, forced expiratory volume in one second. Short-term follow up, short-term follow up after stent removal. Long-term follow up, 1 year follow up after stent removal.

Table 3

Comparative differences between patients who underwent stent removal vs. patients who did not undergo stent removal

VariableStent removedStent never removedP value
Patient level demographics (n=36)
   Number of airways stentedNS2
      1 airway1810
      2 airways14
      3 airways30
   Age at transplant (mean ± SD)61.28±9.6959.35±9.91NS3
   Gender (male %)12 (54.5)10 (71.4)NS1
   BMI at time of transplant (mean ± SD)25.82±4.8628.29±2.58NS3
   Prior pack years cigarette smoke exposure (mean ± SD)25.45±28.7012.32±13.47NS3
   Medical comorbidities (n, %)
      Essential hypertension11 (50.0)7 (50.0)NS1
      Atherosclerotic disease CAD/PVD/stroke7 (31.8)4 (28.6)NS2
      Type 2 diabetes mellitus4 (18.2)4 (28.6)NS2
   Indication for lung transplant (n, %)NS2
      COPD8 (36.4)2 (14.3)
      IPF/ILD12 (54.5)11 (78.6)
      PAH0 (0.0)0 (0.0)
      CF1 (4.5)0 (0.0)
      COPD & ILDIPF1 (4.5)0 (0.0)
      Other0 (0.0)1 (7.1)
   VV/VA ECMO pre-transplant (n, %)0 (0.0)2 (14.3)NS2
   VV/VA ECMO post-transplant (n, %)1 (4.5)2 (14.3)NS2
Airway level demographics (n=47)
   Location (n, %)0.032
      Right mainstem stenosis9 (31.0)1 (5.6)
      Left mainstem stenosis11 (37.9)11 (61.1)
      Bronchus intermedius5 (17.2)6 (33.3)
      Peripheral4 (13.8)0 (0.0)
   Days between transplant and stent placement (mean ± SD)154.07±152.06233.56±220.29NS3
   Days between transplant and stent placement (median IQR)105 (128)144 (146)
   Initial stent type (n, %)NS2
      Silicone17 (58.6)12 (66.7)
      Covered metallic stent4 (13.8)2 (11.1)
      Uncovered metallic stent8 (27.6)4 (22.2)
   Dehiscence (n, %)5 (17.2)1 (5.6)NS2
   Cicatrix (n, %)10 (34.5)9 (50.0)NS1
   Pseudomembrane (n, %)9 (31.0)5 (27.8)NS1
   Malacia (n, %)10 (34.5)9 (50.0)NS1
   FEV1 (L) (mean ± SD)1.40±0.601.50±0.54NS3
   Procedures prior to stent placement (mean ± SD)
      # of dilations0.66±1.291.11±0.96NS3
      # of debridements1.21±2.821.39±2.48NS3
      # of aspirations for mucous plugging0.45±1.090.28±0.83NS3
      # of steroid injections0.14±0.350.06±0.24NS3
      # of cryotherapy treatments0.34±0.970.11±0.32NS3
      # of Bronchoscopies4.55±3.624.72±3.04NS3

1, Chi-square test; 2, Fisher’s exact test; 3, two-sample t-test. NS, not significant. % = n/N, where N is total counts on subject/airway level. Total counts on subject level: stent removed 22; stent never removed 14; all 36. Total counts on airway level: stent removed 29; stent never removed 18; all 47. BMI, body mass index; CAD, coronary artery disease; PVD, peripheral vascular disease; COPD, chronic obstructive pulmonary disease; IPF/ILD, idiopathic pulmonary fibrosis/interstitial lung disease; PAH, pulmonary arterial hypertension; CF, cystic fibrosis; VV/VA, veno-venous/veno-arterial; ECMO, extra-corporeal membrane oxygenation; FEV1, forced expiratory volume in one second.

1, t-test: H0: delta =0; 2, P value comparing (post-stent FEV1 – pre-FEV1) between patients who had stent removed vs. not removed. FEV1, forced expiratory volume in one second. Change in FEV1 over time. FEV1, forced expiratory volume in one second. Short-term follow up, short-term follow up after stent removal. Long-term follow up, 1 year follow up after stent removal. 1, Chi-square test; 2, Fisher’s exact test; 3, two-sample t-test. NS, not significant. % = n/N, where N is total counts on subject/airway level. Total counts on subject level: stent removed 22; stent never removed 14; all 36. Total counts on airway level: stent removed 29; stent never removed 18; all 47. BMI, body mass index; CAD, coronary artery disease; PVD, peripheral vascular disease; COPD, chronic obstructive pulmonary disease; IPF/ILD, idiopathic pulmonary fibrosis/interstitial lung disease; PAH, pulmonary arterial hypertension; CF, cystic fibrosis; VV/VA, veno-venous/veno-arterial; ECMO, extra-corporeal membrane oxygenation; FEV1, forced expiratory volume in one second.

Changes in the need for therapeutic bronchoscopy

In addition, there was no statistically significant change in the number of bronchoscopies per month before and after stent placement (). Among subjects who underwent stent removal (n=28), there was a statistically significant reduction in number of bronchoscopies per month after stent removal compared to pre-stent placement.
Table 4

Change in monthly rate of bronchoscopies after stent placement and after stent removal

VariablePatients who had stent removedPatients who did not have stent removed
n∆bronch/monthSDP value1n∆bronch/monthSDP value2
Stent placement (during-stent bronch/month − pre-stent bronch/month)29−0.071.250.754418−0.190.40.635
Stent removal (after stent removal bronch/month − pre-stent bronch/month)28−0.610.73<0.001N/AN/AN/AN/A

1, t-test: H0: delta =0; 2, P value comparing (during-stent bronch/month − pre-stent bronch/month) between patients who had stent removed vs. not removed. bronch, bronchoscopy.

1, t-test: H0: delta =0; 2, P value comparing (during-stent bronch/month − pre-stent bronch/month) between patients who had stent removed vs. not removed. bronch, bronchoscopy.

Stent related complications

Stent-related complications were common (). The total median duration of stent placement was 258±308 days. Mucous plugging (n=27, 57.5%) and granulation tissue (n=17, 36.2%) were the most common complications. When compared by type of stent placed, no differences were observed in complications.
Table 5

Stent related complications

VariableAll stents (n=47)Silicone stent (n=29)Covered metal stent (n=6)UCMS (n=12)P value
Any unplanned stent exchange
   Total stent exchanges, N (SD)1.06±1.980.55±1.121.33±3.272.17±2.52
   Stent migration (n, %)14 (29.8)9 (31.0)1 (16.7)4 (33.3)0.810
   Granulation tissue (n, %)17 (36.2)11(37.9)2 (33.3)4 (33.3)1.000
   Mucous plugging (n, %)27 (57.5)18 (62.1)4(66.7)5 (41.7)0.566
   Bleeding (n, %)4 (8.5)3 (10.3)0 (0)1 (8.3)1.000
   Fracture (n, %)0 (0)0 (0)0 (0)0 (0)
   Restenosis (n, %)9 (19.2)5 (17.24)3 (50.0)1 (8.3)0.150
   Dehiscence (n, %)2 (4.3)0 (0)0 (0)2 (16.67)0.075
Stent days (mean SD)321.26±359.18371.79±413.79130.00±85.20294.75±270.35
Stent days (median, IQR)258 [308]296 [317]108 [107]297.5 [311.5]

Predictors of improvements

After multiple linear regression, male gender was the only predictor of FEV1 improvement after stent placement (). Male gender and increase number of bronchoscopies prior to stent placement predicted continued FEV1 improvement after stent removal (). Among patients with follow up 12 months after stent removal (n=15), an increased number of bronchoscopies before stent placement continued to predict a sustained FEV1 improvement. The time from identification of an anastomotic complication to stent placement was associated with a statistically significant, but clinically insignificant, improvement in FEV1 after stent placement (). Furthermore, after multiple linear regression, male gender and the presence of a dehiscence prior to stent placement predicted increased number of bronchoscopies per month after stent placement compared to pre-stent placement (). Among subjects who ultimately underwent stent removal with available data (n=21), increased number of stent exchanges was a predictor of decreased number of bronchoscopies after stent removal compared to pre-stent placement (). Stent exchanges were typically done at the discretion of the proceduralist due to complications related to the native stent such as mucous plugging, granulation tissue or stent migrations.
Table S1

Predictors of FEV1 improvement after stent placement. Y = ΔFEV1 (post-stent − pre), n=31

PredictorsUnivariateMultivariateReduced
EstimateStandard errort-valueP valueEstimateStandard errort-valueP valueEstimateStandard errort-valueP value
Age at transplant0.010.011.850.0750.010.011.350.189
Gender0.540.143.860.0010.430.162.70.0120.540.143.860.001
Baseline FEV10.010.150.050.961
Location of stent0.352
   LMSB−0.140.25−0.560.577
   RMSB−0.480.29−1.640.112
   RBI−0.260.3−0.860.398
   PeripheralREF
Type of stent0.1180.864
   CSEMS−0.070.27−0.270.7860.090.260.350.729
   USEMS−0.460.22−2.150.04−0.080.27−0.280.78
   SiliconeREFREF
Type of airway complication
   Dehiscence−0.330.28−1.190.245
   Cicatrix Scar0.190.161.130.268
   Pseudomembrane−0.490.19−2.540.017−0.150.26−0.570.575
   Malacia−0.010.17−0.050.959
# of bronchoscopies/month pre stent−0.080.15−0.520.61
Days prior to stent placement000.620.54

FEV1, forced expiratory volume over 1 second; LMSB, left mainstem bronchus; RMSB, right mainstem bronchus; RBI, right bronchus intermedius; CSEMS, covered self expanding metallic stent; USEMS, uncovered self expanding metallic stent.

Table S2

Predictors of FEV1 improvement immediately after stent removal. Y = ΔFEV1(stent removal − pre), n=19

PredictorsUnivariateMultivariateReduced
EstimateStandard errort-valueP valueEstimateStandard errort-valueP valueEstimateStandard errort-valueP value
Age at transplant00.01−0.370.718
Gender0.350.132.590.0190.230.121.910.0750.240.122.080.054
Baseline FEV1−0.060.13−0.480.638
Location of stent0.446
   LMSB0.030.20.150.881
   RMSB−0.270.22−1.20.249
   RBI0.040.370.090.927
   PeripheralREF
Type of stent0.753
   CSEMS00.22−0.010.988
   USEMS0.150.20.740.472
   SiliconeREF
Type of airway complication
   Dehiscence0.260.211.250.23
   Cicatrix scar0.150.150.970.344
   Pseudomembrane−0.060.19−0.330.743
   Malacia−0.250.15−1.690.11−0.090.12−0.760.459
# of bronchoscopies/month pre stent−0.080.2−0.380.707
Days prior to stent placement00−1.110.282
# of days with stent00−0.60.553
# of bronchoscopies/month during stent0.190.053.530.0030.140.052.680.0170.150.053.040.008
Stent related complications
   Mucous plugging−0.010.16−0.090.931
   Migration−0.140.18−0.780.447
   Bleeding0.220.350.640.533
   Granulation tissue0.060.170.370.715
   Fracture
   Restenosis0.010.180.070.943
   Dehiscence0.020.350.060.954
Symptomatic improvement after stent0.290.340.830.419
# of stent exchanges0.080.071.220.238

FEV1, forced expiratory volume over 1 second; LMSB, left mainstem bronchus; RMSB, right mainstem bronchus; RBI, right bronchus intermedius; CSEMS, covered self expanding metallic stent; USEMS, uncovered self expanding metallic stent.

Table S3

Predictors of sustained FEV1 improvement 12 months after stent removal. Y = ΔFEV1(12-month stent removal − pre), n=15

PredictorsUnivariateMultivariateReduced
EstimateStandard errort-valueP valueEstimateStandard errort-valueP valueEstimateStandard errort-valueP value
Age at transplant−0.010.01−0.660.521
Gender0.260.251.020.328
Baseline FEV1−0.150.2−0.760.463
Location of stent0.742
   LMSB−0.110.35−0.310.759
   RMSB−0.390.39−10.341
   RBI−0.340.59−0.570.58
   PeripheralREF
Type of stent0.0960.844
   CSEMS0.250.330.770.4580.120.240.50.634
   USEMS0.660.282.370.0350.120.250.460.655
   SiliconeREFREF
Type of airway complication
   Dehiscence0.620.272.30.038
   Cicatrix scar0.070.260.290.775
   Pseudomembrane0.210.320.650.526
   Malacia−0.470.24−1.950.074−0.050.19−0.250.805
# of bronchoscopies/month pre stent−0.320.28−1.150.271
Days prior to stent placement00−2.610.02200−1.810.10800−3.070.01
# of days with stent00−2.080.057000.170.868
# of bronchoscopies/month during stent0.310.064.8300.250.073.830.0050.270.055.230
Stent related complications
   Mucous plugging−0.280.25−1.120.282
   Migration−0.130.29−0.470.648
   Bleeding0.240.510.460.65
   Granulation tissue−0.080.26−0.320.753
   Fracture
   Restenosis0.050.290.160.876
   Dehiscence−0.060.51−0.120.905
Symptomatic improvement after stent
# of stent exchanges0.080.10.810.431

FEV1, forced expiratory volume over 1 second; LMSB, left mainstem bronchus; RMSB, right mainstem bronchus; RBI, right bronchus intermedius; CSEMS, covered self expanding metallic stent; USEMS, uncovered self expanding metallic stent.

Table S4

Predictors of changes in frequency of bronchoscopy after stent placement. Y = Δbronch/month (during – pre), n=36

PredictorsUnivariateMultivariateReduced
EstimateStandard errorChi-sqP valueEstimateStandard errort-valueP valueEstimateStandard errort-valueP value
Age at transplant−0.020.02−1.030.312
Gender0.510.331.530.1350.820.332.510.0170.780.332.330.026
Baseline FEV1−0.320.31−1.050.304
Location of stent0.686
   LMSB−0.270.56−0.470.639
   RMSB−0.690.64−1.080.289
   RBI−0.170.66−0.250.803
   PeripheralREF
Type of stent0.384
   CSEMS0.440.540.810.425
   USEMS0.520.411.280.21
   SiliconeREF
Type of airway complication
   Dehiscence0.740.471.570.1261.040.462.270.031.110.472.360.024
   Cicatrix scar−0.050.34−0.140.89
   Pseudomembrane−0.250.39−0.660.515
   Malacia−0.40.34−1.190.241
Days prior to stent placement00−0.330.74
# of days with stent00−1.590.12100−1.710.096
Stent Related complications
   Mucous plugging−0.240.34−0.710.485
   Migration0.20.360.540.593
   Bleeding−0.170.54−0.310.755
   Granulation tissue−0.150.35−0.440.664
   Fracture
   Restenosis0.020.430.040.965
   Dehiscence−0.280.73−0.380.709
Symptomatic improvement after stent0.170.510.330.741
# of stent exchanges00.12−0.010.992

FEV1, forced expiratory volume over 1 second; LMSB, left mainstem bronchus; RMSB, right mainstem bronchus; RBI, right bronchus intermedius; CSEMS, covered self expanding metallic stent; USEMS, uncovered self expanding metallic stent.

Table S5

Predictors of changes in frequency of bronchoscopy after stent removal. Y = Δbronch/month (after − pre), n=21

PredictorsUnivariateMultivariateReduced
EstimateStandard errort-valueP valueEstimateStandard errort-valueP valueEstimateStandard errort-valueP value
Age at transplant−0.010.01−0.660.514
Gender0.270.241.160.259
Baseline FEV1−0.30.16−1.910.073−0.380.2−1.880.083
Location of stent0.891
   LMSB0.230.340.690.498
   RMSB0.090.390.220.827
   RBI0.010.640.010.989
   PeripheralREF
Type of stent0.981
   CSEMS−0.070.37−0.180.861
   USEMS0.010.280.040.97
   SiliconeREF
Type of airway complication
   Dehiscence0.010.310.050.963
   Cicatrix scar−0.110.24−0.470.645
   Pseudomembrane−0.330.26−1.30.208
   Malacia0.080.260.310.756
Days prior to stent placement000.970.344
# of days with stent00−1.530.14300−1.060.31
Stent related complications
   Mucous plugging−0.210.24−0.870.393
   Migration0.210.280.750.462
   Bleeding−0.050.41−0.130.9
   Granulation tissue−0.340.23−1.450.1640.020.250.090.931
   Fracture
   Restenosis−0.430.25−1.740.09800.2800.997
   Dehiscence−0.260.41−0.640.532
Symptomatic improvement after stent−0.150.57−0.270.794
# of stent exchanges−0.190.08−2.340.03−0.080.09−0.850.409−0.190.08−2.340.03

FEV1, forced expiratory volume over 1 second; LMSB, left mainstem bronchus; RMSB, right mainstem bronchus; RBI, right bronchus intermedius; CSEMS, covered self expanding metallic stent; USEMS, uncovered self expanding metallic stent.

Discussion

In this retrospective cohort study, we describe associations between patient characteristics and improvement in FEV1 and need for additional bronchoscopic interventions. Complications related to stent placement are common but treatable with repeat bronchoscopy. Patients with airway complications treated with airway stents undergo a high volume of repeat procedures. Subjects who underwent a successful period of stent placement and subsequent removal had statistically significant improvements in FEV1 both during the period of stent placement as well as sustained FEV1 improvements and decreased monthly bronchoscopies after stent removal. This data supports the notion that in a subset of stented patients airway remodeling can occur around the scaffolding of an airway stent. While the stented period often requires repeat bronchoscopy to manage complications, there is the potential decrease in airway interventions after stent removal. These benefits were not seen in patients with indefinite airway stenting. We noted that patients who could not have their stent removed were more likely to have LMSB or RBI disease. It seems plausible that patients that could not have their stent removed were likely to have more complex airway stenosis that was more difficult to treat endoscopically without full relief of their obstruction after airway stent placement. Furthermore, they may have been sicker individuals with confounding reasons leading to low FEV1, more bronchoscopy, and a perception that stent removal had prohibitive risk. In our multivariate analysis of possible predictors of stent success, only a few factors came to light. Male gender was shown to be a predictor of immediate improvement in FEV1 after stent placement and sustained improvement after stent removal. We conjecture that perhaps a larger thoracic cavity allows for more apparent improvements in FEV1 after relief of stenosis. Furthermore, larger native airway size allows for easier and more effective stenting across a stenosis. Paradoxically, male gender was also a predictor of increased need for bronchoscopy after stent placement though from the data available no inferences could be made as to the reason. Furthermore, airway dehiscence prior to stenting was a predictor of need for post-stent placement bronchoscopy. It is very possible that the major factor related to successful airway stenting is the endoscopic phenotype and anatomy of the airway complication itself. The exact anatomy and airway biology is probably an important determinant of stent related granulation tissue and mucous plugging, both of which lead to more bronchoscopies and a lower FEV1. Regardless of the success of airway stenting, frequent bronchoscopy appears to be a major feature of this patient population. While this has been observed and indirectly described in the literature previously, this is an important conclusion of the study. This observation can be used to appropriately set expectations for patients and transplant programs at the time an airway complication is diagnosed. Airway stenting may eventually decrease the need for bronchoscopy after stent removal in FEV1-responsive patients but seems unlikely to reduce that need before airway remodeling has occurred. Airway stenting was generally safe and well tolerated. All stent deployment procedures occurred without complications; however, the obvious downside is the need for frequent bronchoscopy for stent maintenance. Based on the 2007 FDA black box warning against self-expanding metal stent placement in benign disease, our practice has been to preferentially place silicone stents in this patient population. At the time of the FDA black box warning, no fully covered SEMS were commercially available. With several fully covered SEMS now available, choosing a stent that conforms to the unique anatomic constraints of the airway stenosis may be more important than the stent material. Interestingly, the risk of stent-related complications did not vary based on stent type deployed. Mucous plugging could be most closely tied to patient related factors such as intrinsic microbiome (14). Our study has several limitations. Firstly, this is a retrospective cohort analysis and therefore did not allow a priori gathering of defined exposures or outcomes of relevance. It would have been ideal to identify a clinically-meaningful outcome measure (e.g., airway luminal diameter, validated dyspnea scales, and/or patient quality of life) that could be recorded prospectively rather than spirometry values alone. FEV1 is an easy variable to use retrospectively since it is measured frequently in post-lung transplant patients and is considered an accurate measurement of airway obstruction. However, it does change due to several confounding disease processes such as acute or chronic rejection, infection, and fibrotic allograft changes. We utilized frequency of bronchoscopies as a more patient-centered outcome as frequent procedural intervention can become physically and mentally burdensome for patients. Secondly, no formalized protocol was utilized and thus decisions regarding timing and type of stent placement was left at the discretion of the bronchoscopist. Furthermore, this cohort included only those patients who had airway stenting performed. Many important questions regarding the utility of stenting compared to balloon dilation, submucosal steroid injection, debridement, and other less commonly used techniques remain unaddressed in this study. Future directions include cohort studies that include all patients with airway complications after lung transplant and can measure patient-centered outcomes as they vary between bronchoscopic treatment strategies. Such studies could also work to phenotype airway complications (dehiscence, stenosis, distal airway versus anastomosis, etc.) and describe differences in the natural evolution of these various phenotypes. Taking our airway stent data as a proof of concept, one could envision an experimental study comparing an airway stenting versus non-stenting strategy. In conclusion, our study shows that airway stenting can be an effective and durable solution in select post-transplant airway stenoses. However, patient selection remains critical and specific patient factors that predict success remain elusive. FEV1, forced expiratory volume over 1 second; LMSB, left mainstem bronchus; RMSB, right mainstem bronchus; RBI, right bronchus intermedius; CSEMS, covered self expanding metallic stent; USEMS, uncovered self expanding metallic stent. FEV1, forced expiratory volume over 1 second; LMSB, left mainstem bronchus; RMSB, right mainstem bronchus; RBI, right bronchus intermedius; CSEMS, covered self expanding metallic stent; USEMS, uncovered self expanding metallic stent. FEV1, forced expiratory volume over 1 second; LMSB, left mainstem bronchus; RMSB, right mainstem bronchus; RBI, right bronchus intermedius; CSEMS, covered self expanding metallic stent; USEMS, uncovered self expanding metallic stent. FEV1, forced expiratory volume over 1 second; LMSB, left mainstem bronchus; RMSB, right mainstem bronchus; RBI, right bronchus intermedius; CSEMS, covered self expanding metallic stent; USEMS, uncovered self expanding metallic stent. FEV1, forced expiratory volume over 1 second; LMSB, left mainstem bronchus; RMSB, right mainstem bronchus; RBI, right bronchus intermedius; CSEMS, covered self expanding metallic stent; USEMS, uncovered self expanding metallic stent. The article’s supplementary files as
  14 in total

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Authors:  Jonas Yserbyt; Christophe Dooms; Robin Vos; Lieven J Dupont; Dirk E Van Raemdonck; Geert M Verleden
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Authors:  Elfriede Ruttmann; Hanno Ulmer; Martina Marchese; Karin Dunst; Christian Geltner; Raimund Margreiter; Guenther Laufer; Ludwig C Mueller
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6.  Interventional bronchoscopy for the management of airway complications following lung transplantation.

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8.  ISHLT Consensus Statement on adult and pediatric airway complications after lung transplantation: Definitions, grading system, and therapeutics.

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9.  Airway complications after double lung transplantation. Toronto Lung Transplant Group.

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2.  Safety of hybrid bronchial stents in transplant airway complications: a single center experience.

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