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Eur J Cardiothorac Surg 1999;15:842-850
© 1999 Elsevier Science NL
a Department of Thoracic and Cardiovascular Surgery, Loyola University Medical Center, 2160 South First Avenue, Maywood, IL, 60153, USA
b Division of Pulmonary and Critical Care Medicine, Loyola University Medical Center, 2160 South First Avenue, Maywood, IL, 60153, USA
c Division of Infectious Diseases, Loyola University Medical Center, 2160 South First Avenue, Maywood, IL, 60153, USA
Received 28 February 1997; received in revised form 21 December 1998; accepted 2 March 1999.
Corresponding author. Present address: Tulane University Medical Center, Department of Surgery, SL22, 1430 Tulane Avenue, New Orleans, LA 70112,USA. Tel.: +1-504-5827998; fax: +1-504-5872141
| Abstract |
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Key Words: Lung transplantation Bronchial stricture Wire stents Silicone stents Balloon dilation Airway complication
| 1. Introduction |
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The emphasis on omentopexy and avoidance of steroids in the initial few weeks post surgery was key to the initial successes with lung transplantation [5]. Complications of airway dehiscence and strictures, however, still occur in 027% of cases [611]. Although the incidence is declining in recent series [6,7,12], it continues to be a significant surgical complication of lung transplantation.
The management of most airway problems such as stricture and/or partial dehiscence is often undertaken in a conservative fashion with the use of a flexible fiberoptic endoscope. Debridement of necrotic tissue with forceps, dilation of a stricture with a balloon [13] and surveillance biopsies can all be performed as an outpatient.
Clues to the recognition of a significant airway problem are shortness of breath, cough, fever and malaise. A drop in the spirometric measurement of the forced expiratory volume in one second (FEV1) and biconcave changes of the flow-volume loop [14,15] provides an objective measurement that indicates the development of significant post-transplant problems such as rejection, infection or airway obstruction. A chest radiograph may show an infiltrate or distal atelectasis. A CT scan may identify and estimate the severity of a bronchial dehiscence and the length and degree of a bronchial stenosis [16].
In an earlier report of our experience with 90 lung transplant patients from 1990 to 1993, we had bronchial complications in six of 66 (9%) bilateral lung transplant anastomoses and in eight of 57 (14%) single lung transplant anastomoses [17]. One post-operative death was attributed to bronchial dehiscence. During the current period (19941997), airway complications occurred in 18 of 116 (15.5%) bilateral lung transplant anastomoses and in six of 49 (13.8%) single lung transplant anastomoses. These strictures were recalcitrant to the usual treatment approach of dilation, debridement and stenting with silicone stents.
Our initial management with insertion of Hood silicone bronchial stents (Hood Laboratories, Pembroke, MA) had not been satisfactory. These stents were unforgiving and difficult to insert and maneuver into proper position. In our experience, it required frequent intervention to replace or adjust these stents. Besides migrating, they also often become inspissated with mucus and caused airway obstruction. Dumont silicone studded stents (Bryan, Woburn, MA) were utilized next because they were thought to migrate less due to the studs. But these problems recurred. Granulation tissue also built up around the orifice of the silicone stents, requiring debridement with forceps or with the Nd:YAG laser. As a result, we turned to treating these strictures and dehiscences with expandable metal stents and this is the subject of our report.
| 2. Materials and methods |
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During this period, 18 of 107 patients (16.8%) suffered airway complications of anastomotic stricture and/or dehiscence. Of 165 airway anastamoses at risk, 24 were affected (14.5%). If we separate our patients into two time periods (Phase I: 5/94 to 12/95 and Phase II: 1/967/97) we see that the incidence of airway complications declines with greater experience in lung transplantation. The overall incidence during Phase I was 18.5% (15/81 anastamoses) and during Phase II was 10.7% (9/84 anastamoses) (Table 1). The demographics of these patients are shown in Table 2.
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2.2. Technique
Patients were taken to the operating room and under general anesthesia underwent rigid bronchoscopy. The largest scope possible (usually 10.5 mm) was used. In this way, good control of the airway was ensured. Ventilation was intermittent or by use of jet inhalation. A flexible bronchoscope was then passed through the rigid bronchoscope and the airway was assessed (Fig. 1A)
, secretions suctioned and a flexible guidewire passed through the strictured area. A tapered semi-rigid rubber dilator (American Endoscopic Dilator; Bard Interventional, Billerica, MA) was passed along the guidewire to dilate the stricture. These dilators were used during our early patient experience. Sizes up to 24-26 Fr. were the maximum dilation achieved.
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The types of stents used in the early experience were silicone (Hood or Dumont). The silicone stent was placed over the end of the rigid bronchoscope, positioned and then deployed by withdrawing the scope all the while holding the stent in its place with a larger endotracheal tube loaded over the bronchoscope [1,18]. Then balloon expandable wire stents (Palmaz; Johnson & Johnson Interventional Systems, Warren, NJ) or self-expandable wire stents (Wallstent; Schneider (USA), Pfizer Hospital Products Group, Minneapolis, MN) were deployed.
The Palmaz stent was placed using fluoroscopic guidance for positioning and balloon dilation for expansion. The self-expanding radial wire stent Wallstent was first used when problems of collapse and buckling of the Palmaz stent occurred. Flexible fiberoptic bronchoscopy allowed for direct visualization of the deployment of this stent (Fig. 1C) and fluoroscopy was unnecessary for placement of this stent. Multiple stents could be placed sequentially and one stent could be deployed within another stent. The balloon used to dilate the stricture was used to further dilate the wire stent and mould it into the airway. The flared ends of the Wallstent prevented it from migrating (Fig. 1D) (as was noted with previous stents).
The purpose of dilation and stenting was to open the airway, prevent its further collapse and increase airflow across the stenotic portion of the airway. The subjective evidence of success was manifested in the immediate relief of dyspnea in the extubated patients and relief of agitation and desaturation in those that were ventilator-dependent pre-op and remained so post-stenting. The objective evidence of success was the increase in the spirometry (FEV1) after stenting [19].
2.3. Statistical analysis
Standard spirometric measurements were obtained according to a routine post-transplant testing schedule. Interventions recorded were those performed by the authors. Data were expressed as the mean±SD. Comparisons were performed using paired or non-paired t-tests using statistical software (Stat View 4.01; Abacus Concepts, Berkeley, CA); P values less than or equal to 0.05 were considered significant.
| 3. Results |
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The Palmaz was the initial wire stent placed 10 times in seven patients. It remained the ultimate stent in four of these patients. The Wallstent as the initial stent was used eight times in seven patients. Two (Patients 5 and 9) had multiple stents (right main, intermedius and lower bronchi) and another (Patient 11) required overlapping stents in the left mainstem bronchus (placed a year apart). The last four Wallstents placed were silicone covered (Permalume®). Four patients had both silicone and wire stent(s).
The YAG laser was utilized to debride granulation tissue in nine patients (50%) in this series.
It was used as the initial therapy along with balloon dilation (twice) to debulk the obstructing granulation tissue and subsequently to debride granulation tissue obstructing the silicone stents (four times) and granulation tissue growing through the wire stents (10 times).
3.2. Frequency of intervention
We compared the frequency of intervention before and after both Palmaz and Wallstent wire stent placement. Palmaz stent placement did not decrease the number of interventions required. The number of interventions before and after Palmaz stent insertion were similar. Wallstent insertion, however, tended to decrease the number of subsequent interventions required, although this did not reach statistical significance.
Comparing the total number of interventions according to the type of stent first used, we found that strictures managed primarily with Wallstent insertion required significantly fewer interventions (P<0.0008) than ones in which a Palmaz stent was initially used (Fig. 3) . An average of nearly four fewer procedures was required when a Wallstent was used. To date, there have not been any dislodgement or migration of the Wallstent in this series of patients.
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The Palmaz stent has not been without problems. In two patients, this stent buckled, deformed and obstructed the airway. In Patient 3, this was removed and replaced with another Palmaz stent. Four months later, this second stent collapsed and could not be removed. The bronchus was dilated with a balloon and a 10x20 mm Wallstent was successfully deployed over it and redilated. The patient's FEV1 improved from 0.85 to 1.33 l.
Patient 9 developed stenosis of both bronchial anastomosis 68 days after bilateral lung transplantation for cystic fibrosis. After dilation, a Dumont stent was successfully placed in the right mainstem bronchus. Placement of a stent into the left bronchus resulted in dehiscence and tension pneumothorax leading to emergent thoracotomy and re-anastomosis of the left bronchus. Three weeks later, the right Dumont stent became obstructed, was removed and a 12x8 mm Palmaz stent was placed in the bronchus intermedius and an 18x8 mm Palmaz stent was placed in the right mainstem bronchus and dilated. He subsequently required debridement of granulation tissue with the YAG laser, balloon dilation and placement of an 8x20 mm Wallstent.
There have been no operative deaths as a result of bronchoscopy or the manipulation of the airways with the dilators and stents. Four patients in this group died of various post-transplant problems. Two patients died early due to sepsis and multi-organ failure. Two patients died late due to lymphoma and progressive bronchiolitis obliterans.
3.5. Causative factors
The donor ischemia time for the patients with airway complications did not differ from those without this complication (P=n.s.) (Table 5).
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| 4. Discussion |
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Surgical technique plays a very important role in preserving healthy bronchial tissue and that consists of minimal dissection of the peribronchial tissues [26] and keeping the bronchial segment as short as possible [27]. The technique of bronchial artery re-anastomosis has been championed by a number of investigators as leading to decreased airway problems [3,28,29]. Schafers et al. [12] have shown that pharmacologic manipulation using continuous administration of heparin, prostacycline and corticosteroids improved pulmonary collateral flow and thereby promoted bronchial healing. Their subsequent experience showed an airway complication of only 4% [7]. The report of the St. Louis International Lung Transplant Registry for April 1997 (M. Pohl, personal communication) shows that the number of deaths within 60 days following transplantation due to airway dehiscence is less than 1% and is only 5% of all transplant deaths (37 of 751 patient deaths).
Our overall number of airway complications was 24 out of 165 anastomoses (14.5%) in 18 out of 107 patients (16.8%). This compares to the previously reported series at our institution from 1990 to 1993 of 14 out of 123 anastamosis (11.3%). There was a period of time in 1994 of an increased incidence of airway complications probably related to a variation of our standard harvesting technique with resultant bronchial ischemia. Although not approaching the excellent results of some centers (05%) [6,7,11], our latter experience shows a trend towards improvement and well within the range of other experienced centers [10,30].
Our approach to managing airway complications of stricture and dehiscence that are recalcitrant to conservative therapy consist of management in the operating room with rigid bronchoscopy and general anesthesia. The rigid bronchoscope provides a secure airway and gives better control in the event of untoward complications such as hemorrhage. It provides a large area through which other instruments may be passed. The flexible fiberoptic bronchoscope provides excellent visualization of the operative field and is easily passed through the rigid bronchoscope. Management decision depends on thorough evaluation of the lesion and consists of these choices: no treatment; YAG laser resection of granulation tissue; balloon dilation of stenotic segments; placement of an appropriate stent. A stent is placed if there is >50% obstruction of the lumen, or if obstruction is <50% and there is a large amount of secretion accumulating distally. If malacia is present in the bronchial wall, a stent is placed to maintain airway patency.
Use of the semi-rigid dilator is not advised as increased complications occur with its use. There are various sizes of balloons that may be inserted and under direct visualization can safely be inflated to the appropriate pressure and very successfully dilate most strictures. We used semi-rigid dilators early in our experience, but abandoned them in short order.
Silicone stents were used in the early part of our experience. The Hood stent was used initially, but we found that there were problems associated with this, especially migration of the stent and dislodgement when patients coughed vigorously. We then tried the studded Dumont stent hoping to help prevent migration, however, these were more difficult to insert, especially with distorted bronchial anatomy. We found that silicone stents often became inspissated with mucus. Others have used the silicone stents with good success [26,31]. Colt [26] and colleagues report on 270 Dumont stents placed with excellent results. They had good long term persistence of improved function. Stents were well tolerated and if secretions occluded the stent, it was replaced. Because our experience with the Dumont stents had not been good, we proceeded with the use of wire stents in the management of these difficult strictures.
The Palmaz stent was used first and was successful in achieving an open airway. Trinkle was one of the earliest to discuss the advisability of using a wire stent instead of silicone stents [10]. The problem associated with the Palmaz stent was that of deformity and buckling of the stent because of the forces of the bronchus compressing the stent. Since it has no resiliency nor an outward radial force, once the Palmaz wire stent is compressed, it cannot resume its original shape [30,32,33]. For this reason, we tried the Wallstent (Fig. 5) and found a number of advantages with its use [3436]. This self-expanding radial wire stent moulds to the shape of the bronchus and provides constant outward tension. It is easily deployable under direct vision with the use of a flexible fiberoptic bronchoscope. Another advantage is that it does not migrate. Granulation tissue that may come through the interstices of the stent have been resected using a YAG laser. The newest type of Wallstent has a silicone covering (Permalume®) that may prevent the heaping up of such granulation tissue.
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Success in any technique of stenting can be measured by bronchoscopic demonstration of a patent airway, an increase in objective measurements of airflow (FEV1), and by subjective improvement in the patient's breathing. The success of a particular procedure is related to the expediency with which it can be performed and the permanence of the therapy. Following placement of stents, the patients must continue to have surveillance bronchoscopy and routine spirometric measurements that will then guide the necessity for any further therapy. We found that with the use of the Wallstent as the primary stent, the number of re-interventions are significantly decreased. Finally, other factors have to be considered in the evaluation of the success of stent placement, as failure can be due to the disease process itself and complications such as rejection, sepsis or other organ compromise.
In summary, although the incidence of airway complications in lung transplantation is decreasing, it continues to be a significant problem. However, once a problem of airway stenosis or dehiscence occurs, management is quite effective. The Transplant Registry shows that these complications are rarely a cause of death in lung transplant recipients. The Wallstent is an excellent wire stent that may be used to successfully deal with these complications and has the potential for limiting the number of re-interventions.
| Acknowledgments |
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| Footnotes |
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| Appendix A. Conference discussion |
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Dr Lonchyna: Yes. We had a particularly bad experience in 1994 with multiple complications, but thereafter the incidence went down.
Dr Haverich: What do you think the reason for that lower incidence is? And maybe you could comment on what kind of suturing you did and you do now for the bronchial anastomosis.
Dr Lonchyna: The suturing has been fairly standard: an end-to-end anastomosis with polyglyconate, the posterior layer being continuous and the cartilaginous portion being simple interrupted. I think early on we did use Prolene and that might have contributed to the problem, but I think also that it may have been the technique of harvesting that may have caused ischemia to the donor lung that caused most of the problems.
Dr F. Venuta (Rome, Italy) : Fortunately we had only a small number of complications, only four of 36 patients undergoing lung transplantation; up to now we are happy with the Dumon stent to solve these problems, but I agree that Wallstents have a better indication, especially when the stenosis is very close to the bifurcation of the bronchus.
I didn't understand if you used covered or uncovered Wallstent, and if you used uncovered Wallstent, did you have any problem with growing of tissue through the mesh?
Dr Lonchyna: One of the slides showed the growth of granulation tissue through the interstices of the Wallstent, and this is a problem. In the last three patients that I have placed a Wallstent in I used a silicone-covered stent, which has just become available to us, and I hope that in the future we'll find that this will solve this problem.
Dr Venuta: I have one more question. You talked about stenosis but you showed also a picture of dehiscence. How did you treat these cases?
Dr Lonchyna: Most dehiscences we treat conservatively. Unless there is a massive air leak causing a pneumomediastinum or pneumothorax that needs to be treated with a chest tube, we can treat dehiscenes conservatively and hope that as time goes on the healing process will occur. This particular patient required reanastomosis of the less involved side because of a bleeding problem.
The other side continued to heal, but several months later I placed a stent in the bronchus because of stricuring. But as far as dehiscence itself is concerned, as long as there is no massive air leak, we treat it conservatively.
Dr M.A. Norgaard (Copenhagen, Denmark): I would like to ask you: There has always been a problem with silicone stents and the mucociliary clearance across the stent, but I would imagine that the problem would probably not be so big with a wire stent since the epithelium will probably overgrow the wires after a while. Have you encountered any problems with the mucociliary clearance? My other question is: How long should it stay there? Do you have the impression that the bronchus wall will stabilize after a while, so that you will be able to remove the wire stents?
Dr Lonchyna: Mucus clearing is certainly a major problem with silicone stents, which is one of the reasons that prompted us to go into something different, because even though there is great production of mucus, at least the patients are able to clear it much better with the wire stents. It's almost impossible to remove a stent once it's in. I was able to remove a Palmaz Stent when it deformed and buckled once, but when I tried it on a different patient I couldn't do it. I then ballooned it up against the wall and placed a Wallstent over it. Once it has a fair amount of tissue growing into it, it's almost impossible to take the wire stents out. So my approach is that I always look first and see if balloon dilation and lasing may open the airway sufficiently enough, and only if I feel there is malacia or buckling or it's just not opening up well enough, then I'll put a stent in.
Dr Haverich: What is your algorithm now if you are dealing with a stenosis like 4 weeks after the transplant? You would go for a laser first, then balloon, or balloon, then laser, and then stent, or put a stent in every patient? I think you have to make this very clear to the audience.
Dr Lonchyna: I always look at the area first, and I will balloon almost everything because that will open up most strictures. If there is sufficient opening with the ballooning, I'll leave it at that. The YAG laser is used as an auxiliary. If there is loose debris and I can remove it even better, I'll use the YAG laser. The Wallstent or other wire stent I will use if I feel that it's collapsing and I'm not accomplishing a patent airway. If I need to come back in a month or so, I'll do that and put a stent in.
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