| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
|
|
|
|||||||
|
|||||||||
J Thorac Cardiovasc Surg 2004;127:335-343
© 2004 The American Association for Thoracic Surgery
General thoracic surgery |
a Department of Cardiothoracic Surgery, Martin Luther University, Halle, Germany
b Department of Thoracic and Cardiovascular Surgery, University Essen, Essen, Germany
c Department of Internal Medicine, Justus Liebig University, Giessen, Germany
Received for publication August 12, 2002; revisions received September 27, 2002; accepted for publication October 18, 2002.
* Address for reprints: Dr Ivar Friedrich, Department of Cardiothoracic Surgery, Martin Luther University, Ernst Grube Str 40, D-06097 Halle, Germany
ivar.friedrich{at}medizin.uni-halle.de
 |
Abstract |
|---|
 Top Abstract MethodsResultsDiscussionConclusionReferences |
|---|
METHODS: We investigated the efficacy of bronchoscopic administration of a bovine natural lung surfactant extract (Alveofact) to improve gas exchange and lung mechanics after heterologous left lung transplantation in foxhounds (+4°C ischemia for 24 hours, conservation with Euro-Collins solution). Animals received either no surfactant therapy (untreated controls, n = 6) or 50 mg/kg body weight (prior to explantation, only graft) and 200 mg/kg body weight Alveofact (immediately after reperfusion, both lungs, n = 6). After lung transplantation, separate but synchronized ventilation of each lung was performed in a volume-controlled, pressure-limited mode for 12 hours, with the animals prone. Small catheters were inserted into the pulmonary veins of both the graft and the recipient's native lung for separate blood gas analysis. In the control group, marked protein leakage, influx of neutrophils into the alveolar space, and pulmonary edema formation (extravascular lung water; wet/dry ratio) were encountered in the transplanted lung but only to a very minor extent in the recipient's native lung.
RESULTS: Lung compliance values and arterial oxygenation progressively deteriorated in the transplanted but not in the native lungs. Pulmonary hemodynamics did not change significantly. Surfactant administration did not significantly influence the development of reperfusion edema, protein leakage, and neutrophil influx into the grafts. However, surfactant restored the surface activity and the gas exchange (PaO2/FIO2 of 201.2 ± 20.2 mm Hg vs 119.8 ± 21.7 mm Hg in controls; P < .05) in the transplanted lungs, and compliance was markedly improved in the surfactant-treated animals (18.8 ± 1.8 mL/mbar vs 11.5 ± 1.6 mL/mbar in the controls; P < .05).
CONCLUSION: Bronchoscopic surfactant administration does not prevent leukocyte influx or vascular leakage but does protect against respiratory failure and improves lung mechanics in single lung transplantation in dogs.
Transbronchial surfactant administration has been shown to improve gas exchange in a large body of experimental ARDS models and in patients suffering from severe ARDS.2
In view of the similarities between reperfusion injury and ARDS, it has been speculated that changes in the function of the pulmonary surfactant system might also be operative under conditions of pulmonary ischemia-reperfusion. Surfactant administration after lung transplantation was firstly suggested by Novick and colleagues3 in 1991. During the following years a considerable number of experimental studies have been published to verify the benefit of surfactant treatment in reperfusion injury. Natural surfactant preparations were used in different animal models such as canine, minipigs, and rats.4-9
A detailed analysis of the biochemical and biophysical surfactant properties in canine lungs undergoing 24 hours of cold ischemia and 12 hours of reperfusion was undertaken and the occurrence of severe surfactant abnormalities in the reperfusion period was demonstrated, as reported in the companion article.9a The studies were performed under conditions of separate but synchronized ventilation of the transplanted (single) lung and the native lung to avoid tidal volume shift between the graft and the native lung, which may otherwise give way to the appearance of ventilator-induced lung injury (VILI).10 We report on the impact of bronchoscopic surfactant administration on the development of posttransplantation lung injury. This maneuver was found to not affect pulmonary edema formation and neutrophil influx into the alveolar space but it strongly antagonized the loss of compliance and the deterioration of gas exchange in the transplanted lungs. Administration of surfactant to lungs subjected to severe ischemia-reperfusion may thus be suggested as a useful therapeutic regimen to improve posttransplantation lung function.
|
Methods |
|---|
|
TopAbstractMethodsResultsDiscussionConclusionReferences |
|---|
Transplantation model
Heterologous left lung transplantation was performed in foxhounds (12 donors, 12 recipients, both sexes, 27-33 kg, weight-matched) with the approval of the local authorities. The animals were randomly assigned to the control group (n = 6) and the surfactant group (n = 6). The animals received full care according to the Principles of Laboratory Animal Care (National Institutes of Health publication no. 85-23, revised 1985) and were allowed water and food ad libitum until 12 hours prior to surgery. None of the animals showed any signs of infection, as based on body temperature, peripheral blood counts, and lung auscultation. All experimental and surgical approaches were performed under sterile conditions by 1 cardiothoracic surgeon. The animals did not develop fever, and blood cultures obtained at 6 and 12 hours postreperfusion were all sterile. All animals remained hemodynamically stable; there was no need for catecholamine administration during surgery or the postoperative course. Volume (Ringer's lactate) was substituted depending on central venous (<8 mm Hg) and mean arterial (<60 mm Hg) pressures. There was no difference in warm ischemic time between the groups (Table 1).
|
Donor procedure
After intravenous anesthesia with thiopentone (30 mg/kg BW) and oropharyngeal intubation, the animals were ventilated at a frequency of 10x/min, with an FIO2 of 0.5, in a volume-controlled (tidal volume 14 mL/kg BW), pressure-limited (pmax = 30 mm Hg) fashion (Evita II, Dräger). Tidal volume was adjusted to maintain paCO2 values between 35 and 40 mm Hg. Anesthesia was maintained with fentanyl (0.7 mg/h), midazolam (5 mg/h), and rocuronium (15 mg/h) via continuous infusion, and an extra 1.5-mg dose of fentanyl was administered for thoracotomy. Left lateral thoracotomy was performed through the fifth intercostal space. After the pericardium was opened and the great vessels were dissected, a large-bore line was inserted into the pulmonary artery. In the surfactant group, 50 mg/kg BW Alveofact was instilled by bronchoscopic technique in 10 divided doses into each segment of the left lung. No transbronchial fluid administration was performed in the control group. Immediately after opening of the left atrial appendage, 60 mL/kg of cold, modified Euro-Collins solution (including 100 µg/L prostaglandin E2) were infused through the pulmonary arterial line at a temperature of 4°C and under a pressure of 30 cm H2O. The lungs were ventilated throughout the preservation period. At the end of the washout procedure, the lungs were inflated to a pressure of 20 cm H2O and the trachea was stapled. The heart-lung block was then excised, packed into sterile bags, and stored swimming in 4°C water in a refrigerator for 24 hours.
Recipient procedure
Anesthesia and ventilation were identical as described for the donors, as was left lateral thoracotomy. The left-sided lung vessels were dissected and right lung ventilation was established; the pulmonary artery was clamped with a bulldog clamp and the bronchus with an atraumatic clamp. After heparinization (50 U/kg BW) a Cooley clamp was positioned to truncate the pulmonary veins at the level of the left atrium, cutting the tissue bridge to create an opening for the left atrial cuff anastomosis of the donor lung. The donor heart-lung block was taken from the storage bag, and the left lung was prepared with a remainder of left atrial cuff containing the left pulmonary veins. Implantation sequence was left atrial cuff with 7-0 Prolene suture (Ethicon, Norderstedt, Germany), left bronchus anastomosis with 4-0 Cardiofil (Braun-Dexon, Tuttlingen, Germany) running suture, and the left pulmonary artery with 7-0 running Prolene suture. Total time from the end of cold ischemia period until reperfusion was identical for both groups (Table 1). The preserved and stored but not transplanted right donor lung was lavaged ex situ to assess storage-induced changes. After completion of left lung transplantation, a second tracheal tube (9 mm internal diameter) was positioned in the left main bronchus of the graft and secured tightly, thus allowing separate ventilation of the graft and the native lung as previously described. Upon ventilation of the graft, reperfusion was started and time was set to zero. Next, 2 small catheters were placed into the pulmonary veins of the left and the right lower lobes for withdrawal of blood samples. After insertion of a chest tube and wound closure, the animals were positioned on a vacuum-mattress and remained in the prone position until the end of the observation period (12 hours).
In the surfactant group, a second dose (200 mg/kg BW) of Alveofact was administered bronchoscopically in divided doses into each segment of both lungs, as soon as the animals were in the prone position. No transbronchial administration of fluids was performed in the control group. The animals were sacrificed by exsanguination. Both lungs were excised and samples for wet-to-dry ratio were taken from the left and right lower lobe.
Lung function
Central venous, arterial, and left and right pulmonary venous blood samples were withdrawn hourly to determine hemoglobin, potassium, and blood gases (blood gas analyzer ABL 4, Radiometer, Copenhagen, Denmark). Similarly, dynamic compliance, mean and peak ventilation pressures, as well as tidal and minute volume were read from the respirator once an hour.
Hemodynamic monitoring
A femoral artery and a pulmonary artery catheter (Swan Ganz, Baxter Healthcare, Irvine, Calif) for characterization of pulmonary and systemic hemodynamics and blood sampling were placed percutaneously; pressure transducers (Millar Micro Tip, Millar Instruments Inc, Houston, Tex) were positioned at mid-heart level and referenced to the atmospheric pressure level to record mean arterial pressure, mean pulmonary arterial pressure, central venous pressure (CVP), and pulmonary capillary wedge pressure (PCWP). Using a Sirecust 9000 Monitor (Siemens Medical Products, Erlangen, Germany), cardiac output was assessed by thermodilution. Cardiac index (CI), pulmonary vascular resistance index, and systemic vascular resistance index were calculated by standard formula. The body surface area (BSA) was estimated as follows: BSA (m2) = (0.1 · (kg body weight)2/3).
Measurement of pulmonary fluid accumulation
Two different techniques were employed. (1) The wet-to-dry ratio was determined on all excised lungs. Three lung slices, all obtained from the upper lobe, were weighed immediately after harvesting and after reaching complete dryness (65°C for 14 days). (2) Extravascular lung water (EVLW) was determined by means of a thermo-dye dilution technique (COLD Z-0-21 Monitor, Pulsion Medical Systems, Munich, Germany).11 For this purpose, an additional arterial thermistor-tipped fiberoptic catheter (Pulsiocath 4F FT PV 2024, Pulsion Medical Systems) was inserted into the femoral artery. CI, extravascular lung water index (EVLWI), and intrathoracic blood volume index (ITBVI) were determined in triplicate by injecting 8 mL of ice-cooled indocyanine green (ICG; 1 mg/mL; Pulsion Medical Systems) via the central venous line. With the thermo-dye dilution technique, ITBV and EVLW were calculated as: ITBVI = CI · MTtICG, where MTtICG is the mean transit time of indocyanine green, and EVLWI = (CI · MTtherm) - ITBV, where MTtherm is the mean thermal transit time. EVLWI was assessed at baseline (induction of anesthesia) and 1, 3, 6, 9, and 12 hours after reperfusion.
Bronchoalveolar lavage
Bronchoalveolar lavage fluid (BALF) was collected either in vivo by flexible bronchoscopy (Olympus BF P-10 bronchoscope, Olympus, Hamburg, Germany) after 6 hours of reperfusion or in vitro by whole lung lavage excluding the upper lobes. In case of bronchoscopic lavage, the instrument was placed in wedge position in the upper lobe and the lavage was performed by repetitive injection and gentle aspiration of ten 20-mL aliquots of sterile saline solution (recovery 
60%). For whole lung lavage, the main bronchus of the lower lobe was cannulated and fixed by a transbronchial suture, and lavage was done with 500 mL of sterile saline solution (recovery 70%) by passive pressure gradients of 40 cm H2O. The lavage fluids were then filtered through sterile gauze, collected on ice, and immediately centrifuged at 200g (4°C, 10 minutes) to separate cellular material. Protein content of this cell-free BALF was measured using a commercially available kit based on bicinchoninic acid.12 The remaining supernatant was aliquoted, frozen in liquid nitrogen, and stored at -85°C until subsequent measurements.
Statistics
All results are reported as means ± standard error of the mean (SEM) and were analyzed by a biostatistician (Moredata GmbH, Giessen, Germany). Statistical analysis of differences between surfactant-treated lungs and controls was performed by testing principle significant diversity first (Kruskal-Wallis H test), followed by comparison with a nonparameteric test (Mann-Whitney U test). A Wilcoxon matched-pair test was used to compare baseline values with each time point.
|
Results |
|---|
|
TopAbstractMethodsResultsDiscussionConclusionReferences |
|---|
|
|
In parallel, the transplanted lungs developed a progressive decline of gas exchange and mechanical properties under conditions of separate but synchronized mechanical ventilation. PaO2/FIO2 values (determined at an FIO2 of 0.5 after reperfusion) were 629.3 ± 11.9 mm Hg under baseline conditions, 253.5 ± 15.1 mm Hg at the onset of the reperfusion period, and dropped to 121.7 ± 25.6 mm Hg (6 hours) and 119.8 ± 21.7 mm Hg (12 hours) in the transplanted lungs (Figure 2). The graft's compliance was 19.5 ± 1.6 mL/mbar after 1 hour of reperfusion and thus significantly reduced as compared with baseline conditions (40.2 ± 5.8 mL/mbar), with a further decline to 11.5 ± 1.6 mL/mbar at the end of the 12-hour reperfusion period (Figure 3). In contrast to the graft, gas exchange and compliance of the recipient's native lung did not significantly decrease over this time span. However, as compared with the above-mentioned baseline data, compliance values of the recipient's native lung were somewhat lower (27 mL/mbar) throughout the postoperative period. This was also true for the gas exchange conditions, in particular in the early postoperative phase, with subsequent gradual increase in the PaO2 values, which nearly approached baseline data at the end of the 12-hour observation period.
|
|
|
|
Discussion |
|---|
|
TopAbstractMethodsResultsDiscussionConclusionReferences |
|---|
Model considerations
In general, the presently used left lung transplantation model in dogs followed established techniques in the field.5,7,13,14 However, some important modifications were undertaken and comprised: first, the separate but synchronized ventilation of the graft and the native lung by using 2 ventilators working in the master/slave mode; second, the insertion of small catheters into the pulmonary veins of both lungs to obtain blood samples from each lung for blood gas analysis; and third, an immediate turn of the animals to the prone position upon termination of the surgical procedures. Such experimental setting ascertained (1) full control over volume and pressure applied to each lung, and, by this, (2) prevention of any gas volume shift between graft and native lung, (3) avoidance of clamping procedures of the large pulmonary arteries, and (4) restoration of physiological gravity forces on ventilation and perfusion distribution (prone position).
Influence of surfactant administration on pulmonary and systemic hemodynamics
As anticipated from clinical15 and experimental16 data, a modest increase in pulmonary artery pressure and pulmonary vascular resistance was encountered in this single lung transplant model. This increase was not influenced by the surfactant treatment. This is in line with the previous observation that surfactant replacement improved gas exchange but did not affect pulmonary hemodynamics in patients with severe ARDS.2 Interestingly, however, the decline in systemic arterial pressure and vascular resistance, consistently noted in all transplanted animals, was only very transient and in the further course fully absent under conditions of surfactant administration. The underlying reasons for this phenomenon deserve further clarification.
Influence of surfactant administration on neutrophil recruitment, protein leakage, and pulmonary edema formation
Lung surfactant has been implicated in the regulation of alveolar fluid homeostasis and both natural surfactant preparations, and single surfactant compounds were reported to suppress inflammatory activities of immunocompetent cells, including free radical production by alveolar macrophages and monocytes, macrophage migration, and lymphocyte proliferation.17,18 However, in the present study, edema formation, protein leakage into the alveolar space, and neutrophil migration into this compartment were not significantly affected by bronchoscopic surfactant administration, though this approach established near-physiological surfactant function in the transplanted lungs. This is in line with a previous study of Novick and colleagues,5 in which surfactant instillation prior to ischemia alone or in combination with surfactant instillation after reperfusion caused only very minor (nonsignificant) reduction of reperfusion-related protein leakage. In contrast to the surfactant instillation alone, after combined therapy with aerosolized and instilled surfactant preparations the reduction in intra-alveolar protein content was more pronounced. Probably the technique of treatment has an impact on the permeability for serum proteins.13
Interestingly, neutrophil influx and plasma protein leakage also occurred to some very minor extent in the native lungs of animals undergoing single lung transplantation. In previous transplantation studies with combined lung ventilation,5,14,19 the increase in BALF protein levels in the native lungs, observed after the reperfusion period, nearly approximated that in the transplanted lungs, irregardless of the length of the ischemia period (1.5-36 hours) or the mode of ischemia (warm vs cold). It is tempting to speculate that the prevention of hyperinflation of the native lungs due to the mode of separate lung ventilation was the predominant underlying reason for the maintenance of near-physiological function including barrier properties in the native lungs in the present study.
Improvement of mechanics and gas exchange after bronchoscopic surfactant administration
A progressive impairment in gas exchange and loss of lung compliance were noticed in the graft, but not in the recipient's native lung. In accordance with previous investigations in the field, changes in surface activity and gas exchange were tightly linked, as suggested by the highly significant correlation between minimum surface tension and PaO2 in the transplanted lungs (see Figure 4).
|
VILI of the native lung under experimental conditions
Involvement of the native lung during reperfusion injury (remote injury) is well known under clinical conditions and is thought to be related to blood-borne mediators that are released by the reperfused donor lung. In addition, most entities being associated with the need for lung transplantation (eg, idiopathic pulmonary fibrosis, cystic fibrosis) are known for far-reaching alterations of the surfactant properties. In these cases, a donor lung originating from a healthy donor and thus having good surface tension-reducing properties is transplanted into a patient who has a native lung with increased alveolar surface tension. If ventilated jointly after reperfusion, the donor might be preferentially ventilated due to its better compliance, and, if reperfusion injury develops, surface tension properties might align and distribution of minute ventilation might be similar between both lungs. In experimental models of lung transplantation, however, matters might be significantly different. In this experiment, a donor organ originating from a healthy lung but being held under (mostly prolonged) ischemic conditions is transplanted into a healthy recipient with a healthy contralateral lung. This native lung, as again shown in the companion article,9a must be expected to have good surface tension–reducing properties. Due to the very good compliance, this native organ might thus be very susceptible to the deleterious effects of high tidal volume ventilation and thus VILI, once reperfusion injury develops in the graft and if jointly ventilated with the graft. It is in this line of reasoning that in a model of experimental lung transplantation,14 marked changes of gas exchange, surface tension, and surfactant composition were noted early also in the native organ. Actually, these authors did not find a difference in PaO2 values between the transplanted organ versus the native lung. In another paper addressing also surfactant properties after single lung transplantation in dogs,7 it was found that the small-to-large surfactant aggregate ratio was even higher in the native lung as compared with the graft 6 hours after reperfusion. In our present study, we were unable to detect a relevant reduction in functional properties of the native lung under separate but synchronized ventilation. Apart from an increase in extravasal water accumulation, the loss of permeability was not extended and a significant leakage of plasma proteins or a transmigration of neutrophils into the alveolar space did not occur.
VILI may substantially contribute to the severity of ARDS, as suggested from a recent multicenter trial.21 In fact, severe lung injury including neutrophil transmigration, systemic and alveolar cytokine release, impairment of surfactant function, disturbance of gas exchange, and loss of lung compliance may experimentally be provoked by ventilating otherwise healthy lungs with inappropriately high tidal volume.22 A further study of Novick and colleagues7 addressed the capability of bovine surfactant preparations to improve the function of ventilator-injured donor lungs in order to improve the donor pool. Otherwise healthy donor lungs subjected to mechanical ventilation with high tidal volumes showed decreased oxygen tension, increased intra-alveolar protein content, and a significant deterioration of the surfactant composition. After surfactant treatment a restoration of lung function and surfactant properties could be achieved.7 In view of these new insights into the impact of respirator therapy on the progression of acute lung injury, we employed separate but synchronized ventilation of the graft and the native lung. By this, we think, we avoided volume shift and thus hypoventilation of the transplanted organ graft on the one hand and overinflation of the native lung on the other hand. Moreover, this approach ascertained adequate assessment of the gas exchange properties of each lung, with mismatch of volume distribution between the 2 different organs in the single lung–transplanted animals being prevented.
|
Conclusion |
|---|
|
TopAbstractMethodsResultsDiscussionConclusionReferences |
|---|
|
Footnotes |
|---|
|
References |
|---|
|
TopAbstractMethodsResultsDiscussionConclusionReferences |
|---|
This article has been cited by other articles:
|
|
 |
|
  A. F. Isik, I. Kati, I. Bayram, and H. Ozbek A new agent for treatment of acute respiratory distress syndrome: thymoquinone. An experimental study in a rat model Eur. J. Cardiothorac. Surg., August 1, 2005; 28(2): 301 - 305. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
N. P. van der Kaaij, J. J. Haitsma, J. Kluin, B. N. Lambrecht, B. Lachmann, R. W.F. de Bruin, and A. J.J.C. Bogers Surfactant pretreatment ameliorates ischemia-reperfusion injury of the lung Eur. J. Cardiothorac. Surg., May 1, 2005; 27(5): 774 - 782. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 A. Gunther, M. Balser, R. Schmidt, P. Markart, A. Olk, J. Borgermann, F. H. Splittgerber, W. Seeger, and I. Friedrich Surfactant abnormalities after single lung transplantation in dogs: Impact of bronchoscopic surfactant administration J. Thorac. Cardiovasc. Surg., February 1, 2004; 127(2): 344 - 354. [Abstract] [Full Text] [PDF]
|
|
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| ANN THORAC SURG | ASIAN CARDIOVASC THORAC ANN | EUR J CARDIOTHORAC SURG |
| J THORAC CARDIOVASC SURG | ICVTS | ALL CTSNet JOURNALS |
